Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55729 |
| ensemblid | ENSG00000171681.13 |
| hgncid | 20092 |
| symbol | ATF7IP |
| name | activating transcription factor 7 interacting protein |
| refseq_nuc | NM_018179.5 |
| refseq_prot | NP_060649.3 |
| ensembl_nuc | ENST00000261168.9 |
| ensembl_prot | ENSP00000261168.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 14365682 |
| end | 14502930 |
| strand | + |
| ver | v1.2 |
| region | chr12:14365682-14502930 |
| region5000 | chr12:14360682-14507930 |
| regionname0 | ATF7IP_chr12_14365682_14502930 |
| regionname5000 | ATF7IP_chr12_14360682_14507930 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1270 | 135 | 25 | 23 | 63 | 4 | 20 | 53 | ATF7IP_chr12_14360682_14507930 | ATF7IP | MDSLE others(1265): Show |
chr12 | 14360682 | 14507930 |
| a0002 | 0/1 | 1270 | 102 | 10 | 22 | 52 | 6 | 11 | 38 | ATF7IP_chr12_14360682_14507930 | ATF7IP | MDSLE others(1265): Show |
chr12 | 14360682 | 14507930 |
| a0003 | 1/0 | 1270 | 72 | 45 | 9 | 12 | 2 | 3 | 12 | ATF7IP_chr12_14360682_14507930 | ATF7IP | MDSLE others(1265): Show |
chr12 | 14360682 | 14507930 |
| a0004 | 0/0 | 1270 | 9 | 2 | 6 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | MDSLE others(1265): Show |
chr12 | 14360682 | 14507930 |
| a0005 | 0/0 | 1270 | 9 | 0 | 2 | 3 | 0 | 4 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | MDSLE others(1265): Show |
chr12 | 14360682 | 14507930 |
| a0006 | 0/0 | 1270 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | MDSLE others(1265): Show |
chr12 | 14360682 | 14507930 |
| a0007 | 0/0 | 1270 | 3 | 0 | 0 | 0 | 3 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | MDSLE others(1265): Show |
chr12 | 14360682 | 14507930 |
| a0008 | 0/0 | 1270 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | MDSLE others(1265): Show |
chr12 | 14360682 | 14507930 |
| a0009 | 0/0 | 1270 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | MDSLE others(1265): Show |
chr12 | 14360682 | 14507930 |
| a0010 | 0/0 | 1270 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | MDSLE others(1265): Show |
chr12 | 14360682 | 14507930 |
| a0011 | 0/0 | 1270 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | MDSLE others(1265): Show |
chr12 | 14360682 | 14507930 |
| a0012 | 0/0 | 1270 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | MDSLE others(1265): Show |
chr12 | 14360682 | 14507930 |
| a0013 | 0/0 | 1270 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | MDSLE others(1265): Show |
chr12 | 14360682 | 14507930 |
| a0014 | 0/0 | 1265 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | MDSLE others(1260): Show |
chr12 | 14360682 | 14507930 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3810 | 134 | 24 | 23 | 63 | 4 | 20 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0001c0020 | 0/0 | 3810 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0002c0002 | 0/1 | 3810 | 74 | 10 | 8 | 42 | 5 | 8 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0002c0004 | 0/0 | 3810 | 15 | 0 | 14 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0002c0006 | 0/0 | 3810 | 13 | 0 | 0 | 10 | 0 | 3 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0003c0003 | 1/0 | 3810 | 57 | 33 | 8 | 10 | 2 | 3 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0003c0005 | 0/0 | 3810 | 13 | 12 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0003c0014 | 0/0 | 3810 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0004c0008 | 0/0 | 3810 | 8 | 2 | 5 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0004c0018 | 0/0 | 3810 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0005c0007 | 0/0 | 3810 | 9 | 0 | 2 | 3 | 0 | 4 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0006c0009 | 0/0 | 3810 | 6 | 6 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0007c0010 | 0/0 | 3810 | 3 | 0 | 0 | 0 | 3 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0008c0012 | 0/0 | 3810 | 2 | 0 | 2 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0009c0011 | 0/0 | 3810 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0010c0013 | 0/0 | 3810 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0011c0016 | 0/0 | 3810 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0012c0015 | 0/0 | 3810 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0013c0017 | 0/0 | 3810 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3805): Show |
chr12 | 14360682 | 14507930 | ||
| a0014c0019 | 0/0 | 3795 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | ATGGA others(3790): Show |
chr12 | 14360682 | 14507930 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 8818 | 57 | 4 | 6 | 32 | 1 | 14 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8813): Show |
chr12 | 14360682 | 14507930 |
| a0001c0001t0003 | 0/0 | 8818 | 47 | 3 | 14 | 24 | 3 | 3 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8813): Show |
chr12 | 14360682 | 14507930 |
| a0001c0001t0006 | 0/0 | 8819 | 11 | 11 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8814): Show |
chr12 | 14360682 | 14507930 |
| a0001c0001t0014 | 0/0 | 8823 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8818): Show |
chr12 | 14360682 | 14507930 |
| a0001c0001t0016 | 0/0 | 8819 | 3 | 3 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8814): Show |
chr12 | 14360682 | 14507930 |
| a0001c0001t0017 | 0/0 | 8818 | 3 | 0 | 0 | 3 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8813): Show |
chr12 | 14360682 | 14507930 |
| a0001c0001t0019 | 0/0 | 8823 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8818): Show |
chr12 | 14360682 | 14507930 |
| a0001c0001t0021 | 0/0 | 8818 | 2 | 0 | 2 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8813): Show |
chr12 | 14360682 | 14507930 |
| a0001c0001t0022 | 0/0 | 8818 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8813): Show |
chr12 | 14360682 | 14507930 |
| a0001c0001t0027 | 0/0 | 8818 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8813): Show |
chr12 | 14360682 | 14507930 |
| a0001c0001t0029 | 0/0 | 8818 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8813): Show |
chr12 | 14360682 | 14507930 |
| a0001c0001t0030 | 0/0 | 8818 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8813): Show |
chr12 | 14360682 | 14507930 |
| a0001c0001t0031 | 0/0 | 8818 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8813): Show |
chr12 | 14360682 | 14507930 |
| a0001c0001t0032 | 0/0 | 8818 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8813): Show |
chr12 | 14360682 | 14507930 |
| a0001c0001t0033 | 0/0 | 8818 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8813): Show |
chr12 | 14360682 | 14507930 |
| a0001c0001t0040 | 0/0 | 8825 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8820): Show |
chr12 | 14360682 | 14507930 |
| a0001c0020t0036 | 0/0 | 8824 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0002c0002t0001 | 0/1 | 8824 | 61 | 1 | 7 | 40 | 5 | 7 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0002c0002t0009 | 0/0 | 8824 | 10 | 9 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0002c0002t0026 | 0/0 | 8824 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0002c0002t0037 | 0/0 | 8824 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0002c0004t0001 | 0/0 | 8824 | 15 | 0 | 14 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0002c0006t0008 | 0/0 | 8825 | 11 | 0 | 0 | 8 | 0 | 3 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8820): Show |
chr12 | 14360682 | 14507930 |
| a0002c0006t0019 | 0/0 | 8823 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8818): Show |
chr12 | 14360682 | 14507930 |
| a0003c0003t0004 | 0/0 | 8824 | 19 | 5 | 2 | 10 | 0 | 2 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0003c0003t0005 | 0/0 | 8824 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0003c0003t0011 | 0/0 | 8824 | 6 | 6 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0003c0003t0012 | 0/0 | 8824 | 7 | 7 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0003c0003t0013 | 0/0 | 8823 | 4 | 0 | 4 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8818): Show |
chr12 | 14360682 | 14507930 |
| a0003c0003t0014 | 0/0 | 8823 | 4 | 4 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8818): Show |
chr12 | 14360682 | 14507930 |
| a0003c0003t0015 | 0/0 | 8823 | 5 | 5 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8818): Show |
chr12 | 14360682 | 14507930 |
| a0003c0003t0018 | 1/0 | 8823 | 3 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8818): Show |
chr12 | 14360682 | 14507930 |
| a0003c0003t0023 | 0/0 | 8823 | 2 | 0 | 2 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8818): Show |
chr12 | 14360682 | 14507930 |
| a0003c0003t0025 | 0/0 | 8824 | 2 | 0 | 0 | 0 | 2 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0003c0003t0028 | 0/0 | 8824 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0003c0003t0034 | 0/0 | 8823 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8818): Show |
chr12 | 14360682 | 14507930 |
| a0003c0003t0035 | 0/0 | 8823 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8818): Show |
chr12 | 14360682 | 14507930 |
| a0003c0005t0007 | 0/0 | 8825 | 11 | 11 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8820): Show |
chr12 | 14360682 | 14507930 |
| a0003c0005t0038 | 0/0 | 8825 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8820): Show |
chr12 | 14360682 | 14507930 |
| a0003c0005t0041 | 0/0 | 8825 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8820): Show |
chr12 | 14360682 | 14507930 |
| a0003c0014t0013 | 0/0 | 8823 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8818): Show |
chr12 | 14360682 | 14507930 |
| a0004c0008t0005 | 0/0 | 8824 | 8 | 2 | 5 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0004c0018t0005 | 0/0 | 8824 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0005c0007t0010 | 0/0 | 8824 | 9 | 0 | 2 | 3 | 0 | 4 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0006c0009t0005 | 0/0 | 8824 | 6 | 6 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0007c0010t0002 | 0/0 | 8818 | 3 | 0 | 0 | 0 | 3 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8813): Show |
chr12 | 14360682 | 14507930 |
| a0008c0012t0011 | 0/0 | 8824 | 2 | 0 | 2 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0009c0011t0024 | 0/0 | 8824 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0010c0013t0020 | 0/0 | 8818 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8813): Show |
chr12 | 14360682 | 14507930 |
| a0011c0016t0039 | 0/0 | 8824 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0012c0015t0003 | 0/0 | 8818 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8813): Show |
chr12 | 14360682 | 14507930 |
| a0013c0017t0001 | 0/0 | 8824 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8819): Show |
chr12 | 14360682 | 14507930 |
| a0014c0019t0001 | 0/0 | 8809 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | GAATC others(8804): Show |
chr12 | 14360682 | 14507930 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0014g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0016g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0016g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0016g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0017g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0017g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0017g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0019g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0021g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0021g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0022g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0022g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0027g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0029g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0030g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0031g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0032g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0033g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0001t0040g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0001c0020t0036g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0302 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0009g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0026g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0002t0037g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0004t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0008g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0019g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0002c0006t0019g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0011g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0011g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0011g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0011g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0011g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0011g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0012g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0012g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0012g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0012g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0012g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0013g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0013g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0013g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0013g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0014g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0014g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0014g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0014g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0015g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0015g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0015g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0015g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0018g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0018g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0018g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0023g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0023g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0025g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0025g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0028g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0034g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0003t0035g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0007g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0038g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0005t0041g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0014t0013g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0003c0014t0013g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0004c0008t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0004c0008t0005g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0004c0008t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0004c0008t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0004c0008t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0004c0008t0005g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0004c0008t0005g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0004c0008t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0004c0018t0005g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0005c0007t0010g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0005c0007t0010g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0005c0007t0010g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0005c0007t0010g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0005c0007t0010g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0005c0007t0010g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0005c0007t0010g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0005c0007t0010g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0006c0009t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0006c0009t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0006c0009t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0006c0009t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0006c0009t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0006c0009t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0007c0010t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0007c0010t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0007c0010t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0008c0012t0011g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0008c0012t0011g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0009c0011t0024g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0009c0011t0024g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0010c0013t0020g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0010c0013t0020g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0011c0016t0039g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0012c0015t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0013c0017t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| a0014c0019t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0025 | g0173 | EUR | GBR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0282 | EUR | GBR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0234 | EUR | GBR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0098 | EUR | GBR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00280 | hp1 | a0003 | c0003 | t0025 | g0172 | EUR | FIN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00280 | hp2 | a0004 | c0008 | t0005 | g0251 | EUR | FIN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00438 | hp2 | a0002 | c0006 | t0008 | g0226 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0294 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00609 | hp2 | a0005 | c0007 | t0010 | g0316 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00639 | hp1 | a0003 | c0003 | t0013 | g0162 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00639 | hp2 | a0002 | c0004 | t0001 | g0337 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00673 | hp1 | a0001 | c0001 | t0032 | g0106 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00673 | hp2 | a0002 | c0006 | t0008 | g0220 | EAS | CHS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0281 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00733 | hp2 | a0003 | c0003 | t0004 | g0195 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0217 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG00741 | hp2 | a0003 | c0003 | t0013 | g0164 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0102 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01069 | hp2 | a0002 | c0004 | t0001 | g0288 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01071 | hp1 | a0002 | c0004 | t0001 | g0215 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0104 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01074 | hp2 | a0002 | c0004 | t0001 | g0232 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01081 | hp1 | a0004 | c0008 | t0005 | g0252 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01099 | hp1 | a0003 | c0003 | t0023 | g0154 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0112 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01106 | hp2 | a0002 | c0004 | t0001 | g0241 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01109 | hp2 | a0002 | c0002 | t0009 | g0008 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01167 | hp1 | a0008 | c0012 | t0011 | g0335 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0295 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01168 | hp1 | a0004 | c0008 | t0005 | g0277 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01169 | hp1 | a0004 | c0008 | t0005 | g0280 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01169 | hp2 | a0008 | c0012 | t0011 | g0336 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01175 | hp2 | a0002 | c0004 | t0001 | g0230 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01243 | hp1 | a0001 | c0001 | t0029 | g0063 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01243 | hp2 | a0002 | c0004 | t0001 | g0228 | AMR | PUR | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0208 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01257 | hp1 | a0001 | c0001 | t0021 | g0032 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0287 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01258 | hp1 | a0001 | c0001 | t0021 | g0039 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0209 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01261 | hp1 | a0002 | c0004 | t0001 | g0237 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01261 | hp2 | a0003 | c0003 | t0013 | g0163 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01346 | hp1 | a0005 | c0007 | t0010 | g0315 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0124 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01358 | hp1 | a0002 | c0004 | t0001 | g0240 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01361 | hp2 | a0004 | c0008 | t0005 | g0290 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01496 | hp2 | a0004 | c0018 | t0005 | g0273 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0305 | EUR | IBS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01515 | hp2 | a0007 | c0010 | t0002 | g0052 | EUR | IBS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0103 | EUR | IBS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01516 | hp2 | a0007 | c0010 | t0002 | g0014 | EUR | IBS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01517 | hp1 | a0007 | c0010 | t0002 | g0025 | EUR | IBS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0306 | EUR | IBS | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01884 | hp1 | a0001 | c0001 | t0016 | g0130 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01884 | hp2 | a0003 | c0003 | t0005 | g0313 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01891 | hp1 | a0009 | c0011 | t0024 | g0150 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01891 | hp2 | a0003 | c0003 | t0018 | g0158 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01934 | hp1 | a0003 | c0005 | t0041 | g0334 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01934 | hp2 | a0002 | c0004 | t0001 | g0239 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0303 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01993 | hp1 | a0002 | c0004 | t0001 | g0229 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02004 | hp1 | a0002 | c0004 | t0001 | g0231 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02004 | hp2 | a0003 | c0003 | t0013 | g0165 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02055 | hp1 | a0003 | c0003 | t0015 | g0002 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02055 | hp2 | a0001 | c0020 | t0036 | g0134 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | KHV | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | KHV | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | KHV | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | KHV | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0275 | EAS | KHV | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02132 | hp2 | a0005 | c0007 | t0010 | g0317 | EAS | KHV | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02135 | hp1 | a0002 | c0006 | t0019 | g0227 | EAS | KHV | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02135 | hp2 | a0001 | c0001 | t0019 | g0065 | EAS | KHV | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0135 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02145 | hp2 | a0003 | c0005 | t0007 | g0325 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02148 | hp1 | a0005 | c0007 | t0010 | g0314 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02148 | hp2 | a0002 | c0004 | t0001 | g0242 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | CDX | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CDX | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02165 | hp1 | a0001 | c0001 | t0040 | g0142 | EAS | CDX | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | CDX | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02257 | hp1 | a0003 | c0003 | t0004 | g0200 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02257 | hp2 | a0003 | c0003 | t0014 | g0161 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02273 | hp2 | a0002 | c0004 | t0001 | g0238 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02280 | hp1 | a0003 | c0003 | t0011 | g0311 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02280 | hp2 | a0003 | c0003 | t0015 | g0002 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02300 | hp1 | a0003 | c0003 | t0023 | g0155 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | PEL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02451 | hp1 | a0003 | c0003 | t0011 | g0312 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02451 | hp2 | a0003 | c0005 | t0007 | g0322 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02572 | hp1 | a0002 | c0002 | t0009 | g0210 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02572 | hp2 | a0003 | c0005 | t0007 | g0327 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0304 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02615 | hp1 | a0002 | c0002 | t0009 | g0212 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0137 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02622 | hp1 | a0001 | c0001 | t0022 | g0085 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02622 | hp2 | a0002 | c0002 | t0009 | g0286 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02630 | hp1 | a0003 | c0003 | t0012 | g0001 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02630 | hp2 | a0003 | c0003 | t0014 | g0159 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0132 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02647 | hp2 | a0003 | c0005 | t0007 | g0333 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02683 | hp2 | a0011 | c0016 | t0039 | g0244 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02717 | hp1 | a0003 | c0003 | t0014 | g0171 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02717 | hp2 | a0001 | c0001 | t0014 | g0128 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02723 | hp1 | a0006 | c0009 | t0005 | g0177 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02723 | hp2 | a0010 | c0013 | t0020 | g0118 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02735 | hp2 | a0001 | c0001 | t0027 | g0026 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02738 | hp2 | a0003 | c0003 | t0034 | g0153 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02818 | hp2 | a0003 | c0005 | t0038 | g0328 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02895 | hp1 | a0003 | c0003 | t0018 | g0156 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0136 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02896 | hp1 | a0006 | c0009 | t0005 | g0179 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02897 | hp1 | a0006 | c0009 | t0005 | g0178 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0140 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02922 | hp1 | a0003 | c0003 | t0015 | g0169 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02922 | hp2 | a0003 | c0003 | t0012 | g0001 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02965 | hp1 | a0003 | c0005 | t0007 | g0323 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02965 | hp2 | a0003 | c0003 | t0012 | g0183 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02970 | hp1 | a0003 | c0003 | t0012 | g0180 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02970 | hp2 | a0003 | c0003 | t0004 | g0198 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02976 | hp1 | a0002 | c0002 | t0009 | g0284 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0079 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03041 | hp1 | a0002 | c0002 | t0009 | g0214 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03098 | hp1 | a0006 | c0009 | t0005 | g0174 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03098 | hp2 | a0003 | c0003 | t0015 | g0170 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03130 | hp1 | a0001 | c0001 | t0016 | g0078 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03130 | hp2 | a0003 | c0005 | t0007 | g0326 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03139 | hp1 | a0003 | c0005 | t0007 | g0331 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03139 | hp2 | a0006 | c0009 | t0005 | g0175 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03195 | hp1 | a0004 | c0008 | t0005 | g0006 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03195 | hp2 | a0003 | c0003 | t0012 | g0181 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03209 | hp2 | a0003 | c0005 | t0007 | g0332 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03225 | hp1 | a0003 | c0005 | t0007 | g0324 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0138 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0131 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03239 | hp2 | a0012 | c0015 | t0003 | g0097 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03453 | hp1 | a0003 | c0005 | t0007 | g0329 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03453 | hp2 | a0003 | c0003 | t0035 | g0340 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03486 | hp1 | a0003 | c0003 | t0011 | g0338 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03486 | hp2 | a0003 | c0003 | t0004 | g0197 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03490 | hp1 | a0001 | c0001 | t0033 | g0096 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03490 | hp2 | a0005 | c0007 | t0010 | g0005 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03491 | hp1 | a0003 | c0003 | t0004 | g0189 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03491 | hp2 | a0002 | c0006 | t0008 | g0219 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03492 | hp1 | a0005 | c0007 | t0010 | g0005 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03492 | hp2 | a0003 | c0003 | t0004 | g0191 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03516 | hp1 | a0006 | c0009 | t0005 | g0176 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03516 | hp2 | a0002 | c0002 | t0009 | g0285 | AFR | ESN | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03540 | hp1 | a0002 | c0002 | t0009 | g0009 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03540 | hp2 | a0001 | c0001 | t0022 | g0084 | AFR | GWD | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03579 | hp1 | a0003 | c0003 | t0004 | g0196 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03579 | hp2 | a0003 | c0003 | t0011 | g0185 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0123 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03704 | hp2 | a0002 | c0006 | t0008 | g0292 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03710 | hp1 | a0002 | c0006 | t0008 | g0207 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03831 | hp1 | a0002 | c0002 | t0037 | g0236 | SAS | BEB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | BEB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0245 | SAS | BEB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0115 | SAS | BEB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0270 | SAS | BEB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | BEB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | STU | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG04115 | hp2 | a0005 | c0007 | t0010 | g0320 | SAS | STU | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0205 | SAS | STU | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | STU | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG04204 | hp1 | a0001 | c0001 | t0030 | g0043 | SAS | STU | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0235 | SAS | STU | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | STU | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG04228 | hp2 | a0005 | c0007 | t0010 | g0318 | SAS | STU | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18522 | hp1 | a0002 | c0002 | t0009 | g0211 | AFR | YRI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18522 | hp2 | a0003 | c0003 | t0004 | g0199 | AFR | YRI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | CHB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | CHB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0250 | EAS | CHB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18747 | hp2 | a0002 | c0006 | t0019 | g0221 | EAS | CHB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18906 | hp1 | a0003 | c0003 | t0005 | g0160 | AFR | YRI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18906 | hp2 | a0003 | c0003 | t0028 | g0184 | AFR | YRI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18939 | hp1 | a0003 | c0003 | t0004 | g0188 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18945 | hp2 | a0002 | c0002 | t0026 | g0004 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18946 | hp1 | a0001 | c0001 | t0017 | g0031 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18946 | hp2 | a0002 | c0006 | t0008 | g0216 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18947 | hp2 | a0001 | c0001 | t0017 | g0049 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18950 | hp2 | a0013 | c0017 | t0001 | g0265 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18967 | hp1 | a0001 | c0001 | t0031 | g0012 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18967 | hp2 | a0003 | c0003 | t0004 | g0187 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18968 | hp1 | a0003 | c0003 | t0004 | g0193 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18977 | hp2 | a0002 | c0006 | t0008 | g0223 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18981 | hp2 | a0002 | c0006 | t0008 | g0224 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18986 | hp1 | a0003 | c0003 | t0004 | g0201 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19002 | hp1 | a0014 | c0019 | t0001 | g0310 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19003 | hp2 | a0003 | c0014 | t0013 | g0166 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19007 | hp2 | a0003 | c0003 | t0004 | g0003 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19010 | hp2 | a0005 | c0007 | t0010 | g0319 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19030 | hp1 | a0003 | c0003 | t0012 | g0182 | AFR | LWK | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0139 | AFR | LWK | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19043 | hp1 | a0003 | c0003 | t0011 | g0321 | AFR | LWK | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19043 | hp2 | a0010 | c0013 | t0020 | g0120 | AFR | LWK | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19056 | hp1 | a0003 | c0003 | t0004 | g0202 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19057 | hp2 | a0002 | c0006 | t0008 | g0218 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19067 | hp1 | a0002 | c0006 | t0008 | g0225 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19072 | hp1 | a0003 | c0003 | t0004 | g0003 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19074 | hp2 | a0003 | c0014 | t0013 | g0167 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19079 | hp2 | a0002 | c0002 | t0026 | g0004 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19084 | hp2 | a0001 | c0001 | t0017 | g0051 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19088 | hp2 | a0002 | c0006 | t0008 | g0255 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19090 | hp1 | a0003 | c0003 | t0004 | g0190 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19091 | hp1 | a0003 | c0003 | t0004 | g0186 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19240 | hp1 | a0003 | c0003 | t0014 | g0152 | AFR | YRI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0141 | AFR | YRI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA20129 | hp1 | a0003 | c0003 | t0015 | g0168 | AFR | ASW | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA20129 | hp2 | a0004 | c0008 | t0005 | g0291 | AFR | ASW | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0044 | EUR | TSI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0274 | EUR | TSI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA20805 | hp1 | a0002 | c0004 | t0001 | g0246 | EUR | TSI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0149 | EUR | TSI | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | GIH | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0243 | SAS | GIH | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01123 | hp1 | a0004 | c0008 | t0005 | g0276 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG01123 | hp2 | a0003 | c0003 | t0004 | g0194 | AMR | CLM | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02109 | hp1 | a0001 | c0001 | t0016 | g0129 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02109 | hp2 | a0002 | c0002 | t0009 | g0213 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02486 | hp1 | a0003 | c0005 | t0007 | g0330 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02486 | hp2 | a0003 | c0003 | t0011 | g0203 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02559 | hp1 | a0009 | c0011 | t0024 | g0151 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0073 | AFR | ACB | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | MSL | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG06807 | hp1 | a0003 | c0003 | t0012 | g0001 | AFR | USA | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | USA | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA18955 | hp2 | a0003 | c0003 | t0004 | g0192 | EAS | JPT | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0233 | AFR | LWK | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0133 | AFR | LWK | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0302 | REF | REF | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0018 | g0157 | REF | REF | ATF7IP_chr12_14360682_14507930 | ATF7IP | chr12 | 14360682 | 14507930 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:14424423 | GCCTCTGG others(8): Show |
G | 1 | a0014 | 1 | NA19002.hp1 | disruptive_inframe_deletion | MODERATE | c.522_536delAACCTCTG others(7): Show |
p.Thr175_Ala179del | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/15 | 675/8823 | 522/3813 | 174/1270 | INFO_REALIGN_3_PRIME | chr12 | 14424423 | ||
| chr12:14424573 | A | G | 1 | a0010 | 2 | HG02723.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.658A>G | p.Ile220Val | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/15 | 811/8823 | 658/3813 | 220/1270 | chr12 | 14424573 | |||
| chr12:14424747 | G | A | 1 | a0005 | 9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
missense_variant | MODERATE | c.832G>A | p.Glu278Lys | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/15 | 985/8823 | 832/3813 | 278/1270 | chr12 | 14424747 | |||
| chr12:14424838 | C | G | 1 | a0008 | 2 | HG01167.hp1 HG01169.hp2 |
missense_variant | MODERATE | c.923C>G | p.Pro308Arg | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/15 | 1076/8823 | 923/3813 | 308/1270 | chr12 | 14424838 | |||
| chr12:14424958 | A | T | 5 | a0002 a0004 a0011 others(2): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(110): Show |
missense_variant | MODERATE | c.1043A>T | p.Asn348Ile | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/15 | 1196/8823 | 1043/3813 | 348/1270 | chr12 | 14424958 | |||
| chr12:14425420 | C | T | 1 | a0007 | 3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
missense_variant | MODERATE | c.1505C>T | p.Ser502Leu | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/15 | 1658/8823 | 1505/3813 | 502/1270 | chr12 | 14425420 | |||
| chr12:14434367 | A | G | 5 | a0001 a0004 a0007 others(2): Show |
150 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(147): Show |
missense_variant | MODERATE | c.1589A>G | p.Lys530Arg | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/15 | 1742/8823 | 1589/3813 | 530/1270 | chr12 | 14434367 | |||
| chr12:14460537 | G | A | 1 | a0006 | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
missense_variant | MODERATE | c.2201G>A | p.Ser734Asn | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/15 | 2354/8823 | 2201/3813 | 734/1270 | chr12 | 14460537 | |||
| chr12:14460845 | T | C | 1 | a0009 | 2 | HG01891.hp1 HG02559.hp1 |
missense_variant | MODERATE | c.2509T>C | p.Ser837Pro | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/15 | 2662/8823 | 2509/3813 | 837/1270 | chr12 | 14460845 | |||
| chr12:14481110 | G | A | 1 | a0011 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.3205G>A | p.Ala1069Thr | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/15 | 3358/8823 | 3205/3813 | 1069/1270 | chr12 | 14481110 | |||
| chr12:14481185 | A | G | 1 | a0012 | 1 | HG03239.hp2 | missense_variant&splice_region_variant | MODERATE | c.3280A>G | p.Ser1094Gly | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/15 | 3433/8823 | 3280/3813 | 1094/1270 | chr12 | 14481185 | |||
| chr12:14497663 | C | T | 1 | a0013 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.3403C>T | p.Arg1135Cys | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 3556/8823 | 3403/3813 | 1135/1270 | chr12 | 14497663 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:14424338 | C | T | 1 | a0003c0014 | 2 | NA19003.hp2 NA19074.hp2 |
synonymous_variant | LOW | c.423C>T | p.Ala141Ala | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/15 | 576/8823 | 423/3813 | 141/1270 | chr12 | 14424338 | |||
| chr12:14424360 | C | T | 1 | a0001c0020 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.445C>T | p.Leu149Leu | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/15 | 598/8823 | 445/3813 | 149/1270 | chr12 | 14424360 | |||
| chr12:14424917 | A | T | 1 | a0009c0011 | 2 | HG01891.hp1 HG02559.hp1 |
synonymous_variant | LOW | c.1002A>T | p.Ser334Ser | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/15 | 1155/8823 | 1002/3813 | 334/1270 | chr12 | 14424917 | |||
| chr12:14460697 | A | G | 1 | a0004c0018 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.2361A>G | p.Val787Val | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/15 | 2514/8823 | 2361/3813 | 787/1270 | chr12 | 14460697 | |||
| chr12:14460766 | A | G | 1 | a0002c0006 | 13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
synonymous_variant | LOW | c.2430A>G | p.Pro810Pro | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/15 | 2583/8823 | 2430/3813 | 810/1270 | chr12 | 14460766 | |||
| chr12:14478405 | G | A | 1 | a0003c0005 | 13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
synonymous_variant | LOW | c.3030G>A | p.Pro1010Pro | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/15 | 3183/8823 | 3030/3813 | 1010/1270 | chr12 | 14478405 | |||
| chr12:14496262 | A | G | 1 | a0002c0004 | 15 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(12): Show |
synonymous_variant | LOW | c.3312A>G | p.Thr1104Thr | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/15 | 3465/8823 | 3312/3813 | 1104/1270 | chr12 | 14496262 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:14365687 | T | C | 1 | a0001c0001t0027 | 1 | HG02735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-148T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/15 | 58229 | chr12 | 14365687 | ||||||
| chr12:14498115 | T | G | 1 | a0003c0003t0028 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*42T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 42 | chr12 | 14498115 | ||||||
| chr12:14498214 | A | G | 1 | a0002c0002t0026 | 2 | NA18945.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*141A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 141 | chr12 | 14498214 | ||||||
| chr12:14498482 | A | G | 1 | a0003c0005t0041 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*409A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 409 | chr12 | 14498482 | ||||||
| chr12:14498533 | GAAAT | G | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(13): Show |
137 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*468_*471delTAAA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 468 | INFO_REALIGN_3_PRIME | chr12 | 14498533 | |||||
| chr12:14498654 | C | T | 1 | a0001c0001t0017 | 3 | NA18946.hp1 NA18947.hp2 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*581C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 581 | chr12 | 14498654 | ||||||
| chr12:14498658 | A | G | 2 | a0003c0003t0012 a0005c0007t0010 |
16 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*585A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 585 | chr12 | 14498658 | ||||||
| chr12:14498814 | C | T | 2 | a0003c0003t0012 a0005c0007t0010 |
16 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*741C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 741 | chr12 | 14498814 | ||||||
| chr12:14498851 | A | AT | 24 | a0001c0020t0036 a0002c0002t0001 a0002c0002t0009 others(21): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*790dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 791 | INFO_REALIGN_3_PRIME | chr12 | 14498851 | |||||
| chr12:14498851 | A | ATT | 2 | a0001c0001t0040 a0002c0006t0008 |
12 | HG00438.hp2 HG00673.hp2 HG02165.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*789_*790dupTT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 791 | INFO_REALIGN_3_PRIME | chr12 | 14498851 | |||||
| chr12:14498864 | A | T | 28 | a0001c0001t0019 a0001c0001t0040 a0001c0020t0036 others(25): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*791A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 791 | chr12 | 14498864 | ||||||
| chr12:14499037 | G | A | 5 | a0001c0020t0036 a0003c0003t0004 a0003c0003t0011 others(2): Show |
29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*964G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 964 | chr12 | 14499037 | ||||||
| chr12:14499121 | C | T | 6 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0027 others(3): Show |
53 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1048C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 1048 | chr12 | 14499121 | ||||||
| chr12:14499147 | A | G | 1 | a0003c0003t0015 | 5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1074A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 1074 | chr12 | 14499147 | ||||||
| chr12:14499238 | G | A | 2 | a0003c0003t0013 a0003c0014t0013 |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1165G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 1165 | chr12 | 14499238 | ||||||
| chr12:14499547 | G | C | 1 | a0002c0002t0037 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1474G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 1474 | chr12 | 14499547 | ||||||
| chr12:14499576 | T | C | 1 | a0010c0013t0020 | 2 | HG02723.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1503T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 1503 | chr12 | 14499576 | ||||||
| chr12:14499738 | C | T | 3 | a0001c0001t0019 a0002c0006t0008 a0002c0006t0019 |
14 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1665C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 1665 | chr12 | 14499738 | ||||||
| chr12:14499824 | C | CA | 3 | a0003c0005t0007 a0003c0005t0038 a0003c0005t0041 |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1761dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 1762 | INFO_REALIGN_3_PRIME | chr12 | 14499824 | |||||
| chr12:14499898 | T | G | 1 | a0001c0001t0022 | 2 | HG02622.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1825T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 1825 | chr12 | 14499898 | ||||||
| chr12:14500090 | C | G | 4 | a0003c0003t0025 a0003c0005t0007 a0003c0005t0038 others(1): Show |
15 | HG00099.hp1 HG00280.hp1 HG01934.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2017C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 2017 | chr12 | 14500090 | ||||||
| chr12:14500137 | C | G | 1 | a0001c0001t0006 | 11 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2064C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 2064 | chr12 | 14500137 | ||||||
| chr12:14500449 | T | C | 2 | a0003c0003t0023 a0003c0003t0034 |
3 | HG01099.hp1 HG02300.hp1 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2376T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 2376 | chr12 | 14500449 | ||||||
| chr12:14500657 | G | A | 1 | a0001c0001t0021 | 2 | HG01257.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2584G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 2584 | chr12 | 14500657 | ||||||
| chr12:14500666 | A | G | 1 | a0001c0001t0033 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2593A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 2593 | chr12 | 14500666 | ||||||
| chr12:14500733 | T | A | 36 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(33): Show |
222 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*2660T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 2660 | chr12 | 14500733 | ||||||
| chr12:14500922 | C | T | 1 | a0003c0003t0012 | 7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2849C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 2849 | chr12 | 14500922 | ||||||
| chr12:14500933 | C | T | 7 | a0002c0002t0001 a0002c0002t0026 a0002c0002t0037 others(4): Show |
81 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2860C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 2860 | chr12 | 14500933 | ||||||
| chr12:14501142 | G | C | 1 | a0003c0003t0035 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3069G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 3069 | chr12 | 14501142 | ||||||
| chr12:14501196 | G | A | 1 | a0003c0003t0004 | 19 | HG00733.hp2 HG01123.hp2 HG02257.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3123G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 3123 | chr12 | 14501196 | ||||||
| chr12:14501481 | T | C | 1 | a0001c0001t0029 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3408T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 3408 | chr12 | 14501481 | ||||||
| chr12:14501575 | G | T | 1 | a0001c0001t0040 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3502G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 3502 | chr12 | 14501575 | ||||||
| chr12:14501675 | C | T | 1 | a0009c0011t0024 | 2 | HG01891.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3602C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 3602 | chr12 | 14501675 | ||||||
| chr12:14501848 | C | T | 1 | a0001c0001t0030 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3775C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 3775 | chr12 | 14501848 | ||||||
| chr12:14502422 | CA | C | 14 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0017 others(11): Show |
123 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*4352delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 4352 | INFO_REALIGN_3_PRIME | chr12 | 14502422 | |||||
| chr12:14502700 | A | T | 1 | a0003c0003t0023 | 2 | HG01099.hp1 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4627A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 4627 | chr12 | 14502700 | ||||||
| chr12:14502809 | T | C | 1 | a0011c0016t0039 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4736T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 15/15 | 4736 | chr12 | 14502809 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:14365929 | C | T | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8+102C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14365929 | |||||||
| chr12:14365961 | C | T | 1 | a0001c0001t0002g0339 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-8+134C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14365961 | |||||||
| chr12:14366282 | A | G | 1 | a0003c0003t0011g0338 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8+455A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14366282 | |||||||
| chr12:14366615 | C | T | 1 | a0002c0004t0001g0337 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-8+788C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14366615 | |||||||
| chr12:14366622 | A | G | 2 | a0008c0012t0011g0335 a0008c0012t0011g0336 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-8+795A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14366622 | |||||||
| chr12:14366802 | T | G | 1 | a0004c0008t0005g0006 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-8+975T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14366802 | |||||||
| chr12:14366833 | TAAAAA | T | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8+1010_-8+1014del others(5): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14366833 | ||||||
| chr12:14366843 | C | A | 1 | a0002c0002t0001g0007 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-8+1016C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14366843 | |||||||
| chr12:14366865 | G | A | 2 | a0002c0002t0009g0008 a0002c0002t0009g0009 |
2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-8+1038G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14366865 | |||||||
| chr12:14366909 | A | T | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8+1082A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14366909 | |||||||
| chr12:14367192 | T | C | 1 | a0001c0001t0002g0010 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-8+1365T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14367192 | |||||||
| chr12:14367307 | T | C | 141 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(138): Show |
141 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.-8+1480T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14367307 | |||||||
| chr12:14367497 | G | T | 1 | a0001c0001t0003g0149 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-8+1670G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14367497 | |||||||
| chr12:14367571 | A | T | 2 | a0001c0001t0002g0147 a0001c0001t0002g0148 |
2 | HG03669.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-8+1744A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14367571 | |||||||
| chr12:14367646 | T | C | 1 | a0001c0001t0003g0011 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-8+1819T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14367646 | |||||||
| chr12:14367767 | A | G | 142 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(139): Show |
142 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.-8+1940A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14367767 | |||||||
| chr12:14367836 | T | C | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-8+2009T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14367836 | |||||||
| chr12:14367867 | A | G | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+2040A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14367867 | |||||||
| chr12:14368014 | A | C | 14 | a0003c0003t0035g0340 a0003c0005t0007g0322 a0003c0005t0007g0323 others(11): Show |
14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+2187A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368014 | |||||||
| chr12:14368125 | T | G | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-8+2298T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368125 | |||||||
| chr12:14368243 | A | C | 1 | a0001c0001t0002g0146 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-8+2416A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368243 | |||||||
| chr12:14368248 | T | C | 141 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(138): Show |
141 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.-8+2421T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368248 | |||||||
| chr12:14368285 | C | G | 2 | a0003c0003t0011g0311 a0003c0003t0011g0312 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-8+2458C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368285 | |||||||
| chr12:14368442 | G | T | 176 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(173): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.-8+2615G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368442 | |||||||
| chr12:14368490 | C | T | 112 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(109): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-8+2663C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368490 | |||||||
| chr12:14368653 | A | G | 28 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(25): Show |
29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.-8+2826A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368653 | |||||||
| chr12:14368870 | G | C | 1 | a0001c0001t0031g0012 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-8+3043G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368870 | |||||||
| chr12:14368875 | T | C | 1 | a0001c0001t0031g0012 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-8+3048T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368875 | |||||||
| chr12:14368876 | T | G | 1 | a0001c0001t0031g0012 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-8+3049T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368876 | |||||||
| chr12:14368877 | T | C | 1 | a0001c0001t0031g0012 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-8+3050T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368877 | |||||||
| chr12:14368878 | A | G | 1 | a0001c0001t0031g0012 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-8+3051A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368878 | |||||||
| chr12:14368879 | A | T | 1 | a0001c0001t0031g0012 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-8+3052A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368879 | |||||||
| chr12:14368880 | A | G | 1 | a0001c0001t0031g0012 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-8+3053A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368880 | |||||||
| chr12:14368881 | A | T | 1 | a0001c0001t0031g0012 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-8+3054A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368881 | |||||||
| chr12:14368891 | A | G | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+3064A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14368891 | |||||||
| chr12:14369118 | CT | C | 170 | a0001c0001t0002g0013 a0001c0001t0003g0015 a0002c0002t0001g0007 others(167): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.-8+3307delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14369118 | ||||||
| chr12:14369125 | T | C | 2 | a0002c0002t0001g0204 a0002c0002t0001g0205 |
2 | HG00621.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-8+3298T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369125 | |||||||
| chr12:14369175 | A | G | 16 | a0002c0002t0001g0293 a0002c0002t0001g0294 a0002c0002t0001g0295 others(13): Show |
16 | HG00597.hp2 HG01167.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8+3348A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369175 | |||||||
| chr12:14369199 | C | T | 1 | a0002c0006t0008g0292 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-8+3372C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369199 | |||||||
| chr12:14369383 | C | T | 4 | a0003c0003t0015g0002 a0003c0003t0015g0168 a0003c0003t0015g0169 others(1): Show |
5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+3556C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369383 | |||||||
| chr12:14369432 | G | T | 7 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(4): Show |
9 | HG01891.hp1 HG02559.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+3605G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369432 | |||||||
| chr12:14369549 | G | C | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-8+3722G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369549 | |||||||
| chr12:14369587 | C | G | 1 | a0002c0002t0001g0307 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-8+3760C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369587 | |||||||
| chr12:14369707 | T | C | 65 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(62): Show |
65 | HG01175.hp1 HG01243.hp1 HG01257.hp1 others(62): Show |
intron_variant | MODIFIER | c.-8+3880T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369707 | |||||||
| chr12:14369761 | GCTAGTTT others(18): Show |
G | 14 | a0003c0003t0035g0340 a0003c0005t0007g0322 a0003c0005t0007g0323 others(11): Show |
14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+3946_-8+3970del others(25): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14369761 | ||||||
| chr12:14369783 | A | G | 1 | a0003c0003t0005g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-8+3956A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369783 | |||||||
| chr12:14369939 | A | AT | 8 | a0001c0001t0002g0072 a0002c0002t0001g0309 a0003c0003t0012g0001 others(5): Show |
10 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+4127dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14369939 | ||||||
| chr12:14369967 | C | T | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+4140C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369967 | |||||||
| chr12:14369968 | G | A | 1 | a0001c0001t0006g0073 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-8+4141G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14369968 | |||||||
| chr12:14370001 | G | A | 1 | a0002c0002t0001g0206 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-8+4174G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370001 | |||||||
| chr12:14370135 | C | T | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+4308C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370135 | |||||||
| chr12:14370197 | A | G | 2 | a0004c0008t0005g0290 a0004c0008t0005g0291 |
2 | HG01361.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-8+4370A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370197 | |||||||
| chr12:14370213 | A | G | 183 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(180): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-8+4386A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370213 | |||||||
| chr12:14370302 | T | C | 2 | a0002c0006t0008g0207 a0002c0006t0008g0292 |
2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-8+4475T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370302 | |||||||
| chr12:14370315 | G | A | 1 | a0002c0002t0001g0309 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-8+4488G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370315 | |||||||
| chr12:14370384 | C | T | 1 | a0001c0001t0003g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-8+4557C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370384 | |||||||
| chr12:14370474 | G | A | 182 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(179): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-8+4647G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370474 | |||||||
| chr12:14370540 | A | C | 1 | a0001c0001t0002g0071 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-8+4713A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370540 | |||||||
| chr12:14370633 | A | G | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-8+4806A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370633 | |||||||
| chr12:14370740 | A | G | 41 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(38): Show |
42 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.-8+4913A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370740 | |||||||
| chr12:14370796 | A | C | 1 | a0001c0001t0003g0144 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8+4969A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370796 | |||||||
| chr12:14370811 | C | A | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-8+4984C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370811 | |||||||
| chr12:14370899 | A | G | 1 | a0003c0003t0004g0200 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8+5072A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370899 | |||||||
| chr12:14370957 | C | A | 2 | a0003c0003t0011g0185 a0003c0003t0028g0184 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-8+5130C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14370957 | |||||||
| chr12:14371004 | G | A | 2 | a0001c0001t0002g0016 a0001c0001t0002g0017 |
2 | NA18953.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-8+5177G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14371004 | |||||||
| chr12:14371038 | G | T | 177 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(174): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.-8+5211G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14371038 | |||||||
| chr12:14371136 | A | G | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-8+5309A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14371136 | |||||||
| chr12:14371507 | T | C | 2 | a0002c0002t0001g0208 a0002c0002t0001g0209 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-8+5680T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14371507 | |||||||
| chr12:14371564 | A | G | 183 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(180): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-8+5737A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14371564 | |||||||
| chr12:14371565 | A | C | 183 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(180): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-8+5738A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14371565 | |||||||
| chr12:14371613 | A | G | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-8+5786A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14371613 | |||||||
| chr12:14371987 | A | G | 183 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(180): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-8+6160A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14371987 | |||||||
| chr12:14372164 | C | T | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+6337C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14372164 | |||||||
| chr12:14372215 | C | T | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+6388C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14372215 | |||||||
| chr12:14372232 | T | A | 1 | a0003c0003t0014g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-8+6405T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14372232 | |||||||
| chr12:14372360 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-8+6533C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14372360 | |||||||
| chr12:14372460 | C | CA | 143 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0018 others(140): Show |
146 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.-8+6649dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14372460 | ||||||
| chr12:14372460 | C | CAA | 14 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(11): Show |
16 | HG01071.hp1 HG01109.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8+6648_-8+6649dup others(2): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14372460 | ||||||
| chr12:14372993 | G | A | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+7166G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14372993 | |||||||
| chr12:14373092 | C | T | 4 | a0003c0003t0015g0002 a0003c0003t0015g0168 a0003c0003t0015g0169 others(1): Show |
5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+7265C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373092 | |||||||
| chr12:14373255 | C | T | 1 | a0001c0001t0002g0339 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-8+7428C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373255 | |||||||
| chr12:14373305 | CAT | C | 141 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(138): Show |
141 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.-8+7479_-8+7480del others(2): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373305 | |||||||
| chr12:14373386 | C | A | 4 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(1): Show |
4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+7559C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373386 | |||||||
| chr12:14373446 | A | G | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-8+7619A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373446 | |||||||
| chr12:14373450 | G | C | 2 | a0008c0012t0011g0335 a0008c0012t0011g0336 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-8+7623G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373450 | |||||||
| chr12:14373516 | A | C | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+7689A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373516 | |||||||
| chr12:14373535 | T | A | 1 | a0002c0006t0008g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-8+7708T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373535 | |||||||
| chr12:14373595 | G | C | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+7768G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373595 | |||||||
| chr12:14373674 | A | G | 2 | a0003c0003t0011g0311 a0003c0003t0011g0312 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-8+7847A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373674 | |||||||
| chr12:14373789 | T | C | 2 | a0003c0003t0011g0185 a0003c0003t0028g0184 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-8+7962T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373789 | |||||||
| chr12:14373816 | C | T | 1 | a0003c0003t0025g0173 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-8+7989C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373816 | |||||||
| chr12:14373926 | G | A | 1 | a0001c0001t0003g0076 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-8+8099G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373926 | |||||||
| chr12:14373946 | A | G | 2 | a0003c0014t0013g0166 a0003c0014t0013g0167 |
2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-8+8119A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373946 | |||||||
| chr12:14373969 | A | C | 63 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(60): Show |
64 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.-8+8142A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14373969 | |||||||
| chr12:14374033 | A | AT | 142 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(139): Show |
142 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.-8+8215dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14374033 | ||||||
| chr12:14374036 | T | A | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8+8209T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374036 | |||||||
| chr12:14374076 | T | C | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+8249T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374076 | |||||||
| chr12:14374096 | A | AC | 3 | a0002c0002t0001g0247 a0002c0002t0001g0248 a0002c0002t0001g0308 |
3 | NA18947.hp1 NA18979.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-8+8270dupC | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14374096 | ||||||
| chr12:14374107 | T | C | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+8280T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374107 | |||||||
| chr12:14374154 | G | C | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+8327G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374154 | |||||||
| chr12:14374272 | A | AT | 40 | a0001c0001t0002g0022 a0001c0001t0002g0067 a0001c0001t0002g0068 others(37): Show |
40 | HG00280.hp2 HG00438.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-8+8466dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14374272 | ||||||
| chr12:14374272 | A | ATT | 84 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(81): Show |
85 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-8+8465_-8+8466dup others(2): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14374272 | ||||||
| chr12:14374272 | AT | A | 10 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0014t0013g0166 others(7): Show |
11 | HG00609.hp2 HG00639.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8+8466delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14374272 | ||||||
| chr12:14374378 | T | C | 5 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0023g0154 others(2): Show |
5 | HG01099.hp1 HG02300.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+8551T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374378 | |||||||
| chr12:14374460 | T | C | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+8633T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374460 | |||||||
| chr12:14374578 | A | C | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+8751A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374578 | |||||||
| chr12:14374711 | G | A | 2 | a0002c0006t0008g0207 a0002c0006t0008g0292 |
2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-8+8884G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374711 | |||||||
| chr12:14374727 | C | G | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+8900C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374727 | |||||||
| chr12:14374805 | A | G | 1 | a0001c0001t0040g0142 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-8+8978A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374805 | |||||||
| chr12:14374819 | T | C | 1 | a0001c0001t0003g0077 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-8+8992T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374819 | |||||||
| chr12:14374835 | A | G | 112 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(109): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-8+9008A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374835 | |||||||
| chr12:14374988 | T | TTTTTTTT others(2060): Show |
1 | a0001c0001t0002g0072 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-8+9161_-8+9162ins others(2067): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374988 | |||||||
| chr12:14374988 | T | TTTTTTTT others(2063): Show |
1 | a0001c0001t0002g0064 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-8+9161_-8+9162ins others(2070): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374988 | |||||||
| chr12:14374988 | T | TTTTTTTT others(2060): Show |
1 | a0001c0001t0019g0065 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-8+9161_-8+9162ins others(2067): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374988 | |||||||
| chr12:14374988 | T | TTTTTTTT others(2059): Show |
1 | a0001c0001t0002g0066 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-8+9161_-8+9162ins others(2066): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374988 | |||||||
| chr12:14374989 | A | C | 4 | a0001c0001t0002g0064 a0001c0001t0002g0066 a0001c0001t0002g0072 others(1): Show |
4 | HG02135.hp2 NA18977.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+9162A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374989 | |||||||
| chr12:14374990 | A | G | 4 | a0001c0001t0002g0064 a0001c0001t0002g0066 a0001c0001t0002g0072 others(1): Show |
4 | HG02135.hp2 NA18977.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+9163A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374990 | |||||||
| chr12:14374993 | C | CG | 4 | a0001c0001t0002g0064 a0001c0001t0002g0066 a0001c0001t0002g0072 others(1): Show |
4 | HG02135.hp2 NA18977.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+9166_-8+9167ins others(1): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14374993 | |||||||
| chr12:14375222 | T | A | 3 | a0003c0003t0004g0197 a0003c0003t0004g0198 a0003c0003t0004g0199 |
3 | HG02970.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-8+9395T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14375222 | |||||||
| chr12:14375271 | G | C | 2 | a0001c0001t0006g0079 a0001c0001t0016g0078 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-8+9444G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14375271 | |||||||
| chr12:14375319 | G | A | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+9492G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14375319 | |||||||
| chr12:14375526 | G | A | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-8+9699G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14375526 | |||||||
| chr12:14375587 | A | T | 2 | a0002c0002t0001g0205 a0002c0002t0001g0283 |
2 | HG00438.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-8+9760A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14375587 | |||||||
| chr12:14375768 | C | T | 1 | a0002c0002t0001g0282 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-8+9941C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14375768 | |||||||
| chr12:14375860 | G | A | 182 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(179): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-8+10033G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14375860 | |||||||
| chr12:14375905 | G | A | 1 | a0001c0001t0003g0080 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-8+10078G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14375905 | |||||||
| chr12:14376121 | T | C | 4 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(1): Show |
4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+10294T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14376121 | |||||||
| chr12:14376336 | C | T | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+10509C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14376336 | |||||||
| chr12:14376386 | C | T | 1 | a0002c0002t0001g0293 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-8+10559C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14376386 | |||||||
| chr12:14376638 | A | G | 2 | a0006c0009t0005g0178 a0006c0009t0005g0179 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-8+10811A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14376638 | |||||||
| chr12:14376692 | G | T | 1 | a0005c0007t0010g0319 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-8+10865G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14376692 | |||||||
| chr12:14376713 | T | C | 11 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(8): Show |
12 | HG03491.hp1 HG03492.hp2 NA18939.hp1 others(9): Show |
intron_variant | MODIFIER | c.-8+10886T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14376713 | |||||||
| chr12:14376791 | T | C | 2 | a0003c0003t0011g0185 a0003c0003t0028g0184 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-8+10964T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14376791 | |||||||
| chr12:14376979 | A | C | 1 | a0002c0004t0001g0246 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-8+11152A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14376979 | |||||||
| chr12:14376992 | T | G | 14 | a0003c0003t0035g0340 a0003c0005t0007g0322 a0003c0005t0007g0323 others(11): Show |
14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+11165T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14376992 | |||||||
| chr12:14377126 | C | T | 2 | a0002c0006t0008g0226 a0002c0006t0019g0227 |
2 | HG00438.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.-8+11299C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377126 | |||||||
| chr12:14377135 | C | A | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8+11308C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377135 | |||||||
| chr12:14377192 | A | G | 1 | a0003c0005t0041g0334 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-8+11365A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377192 | |||||||
| chr12:14377271 | A | G | 18 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(15): Show |
19 | HG00733.hp2 HG01123.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8+11444A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377271 | |||||||
| chr12:14377334 | C | T | 3 | a0003c0003t0005g0160 a0003c0003t0014g0159 a0003c0003t0014g0161 |
3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+11507C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377334 | |||||||
| chr12:14377357 | A | AT | 11 | a0001c0001t0002g0339 a0001c0001t0003g0075 a0001c0001t0003g0080 others(8): Show |
13 | HG01243.hp1 HG02080.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+11546dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14377357 | ||||||
| chr12:14377379 | G | T | 10 | a0001c0001t0006g0073 a0001c0001t0006g0079 a0001c0001t0006g0135 others(7): Show |
10 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+11552G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377379 | |||||||
| chr12:14377516 | C | T | 11 | a0001c0001t0006g0073 a0001c0001t0006g0079 a0001c0001t0006g0132 others(8): Show |
11 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8+11689C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377516 | |||||||
| chr12:14377644 | C | T | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+11817C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377644 | |||||||
| chr12:14377674 | C | T | 1 | a0001c0001t0002g0062 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-8+11847C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377674 | |||||||
| chr12:14377675 | G | A | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+11848G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377675 | |||||||
| chr12:14377814 | A | G | 5 | a0001c0001t0002g0061 a0001c0001t0002g0064 a0001c0001t0002g0066 others(2): Show |
5 | HG02135.hp2 NA18977.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+11987A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377814 | |||||||
| chr12:14377931 | C | T | 1 | a0003c0003t0011g0338 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8+12104C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377931 | |||||||
| chr12:14377948 | T | C | 2 | a0001c0001t0003g0081 a0001c0001t0003g0082 |
2 | NA18955.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-8+12121T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14377948 | |||||||
| chr12:14378100 | C | CT | 140 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(137): Show |
145 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-8+12288dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14378100 | ||||||
| chr12:14378100 | C | CTT | 25 | a0002c0002t0001g0222 a0002c0002t0001g0248 a0002c0002t0001g0281 others(22): Show |
25 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8+12287_-8+12288d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14378100 | ||||||
| chr12:14378105 | T | TC | 14 | a0003c0003t0035g0340 a0003c0005t0007g0322 a0003c0005t0007g0323 others(11): Show |
14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+12278_-8+12279i others(3): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378105 | |||||||
| chr12:14378137 | G | A | 1 | a0001c0001t0002g0023 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-8+12310G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378137 | |||||||
| chr12:14378178 | A | G | 18 | a0003c0003t0011g0203 a0003c0003t0011g0311 a0003c0003t0011g0312 others(15): Show |
18 | HG01934.hp1 HG02145.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8+12351A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378178 | |||||||
| chr12:14378277 | A | T | 183 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(180): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-8+12450A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378277 | |||||||
| chr12:14378377 | C | T | 2 | a0003c0014t0013g0166 a0003c0014t0013g0167 |
2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-8+12550C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378377 | |||||||
| chr12:14378403 | T | C | 1 | a0001c0001t0003g0083 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-8+12576T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378403 | |||||||
| chr12:14378562 | A | G | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+12735A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378562 | |||||||
| chr12:14378611 | G | A | 182 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(179): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-8+12784G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378611 | |||||||
| chr12:14378630 | T | C | 14 | a0003c0003t0035g0340 a0003c0005t0007g0322 a0003c0005t0007g0323 others(11): Show |
14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+12803T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378630 | |||||||
| chr12:14378857 | T | C | 1 | a0003c0003t0011g0338 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8+13030T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14378857 | |||||||
| chr12:14379102 | C | G | 4 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(1): Show |
4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+13275C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14379102 | |||||||
| chr12:14379250 | T | G | 2 | a0003c0003t0012g0001 a0003c0003t0012g0180 |
4 | HG02630.hp1 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+13423T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14379250 | |||||||
| chr12:14379331 | C | T | 1 | a0003c0014t0013g0167 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-8+13504C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14379331 | |||||||
| chr12:14379391 | A | C | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+13564A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14379391 | |||||||
| chr12:14379767 | C | T | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+13940C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14379767 | |||||||
| chr12:14380242 | A | G | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8+14415A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14380242 | |||||||
| chr12:14380287 | GTC | G | 4 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(1): Show |
4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+14464_-8+14465d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14380287 | ||||||
| chr12:14380474 | A | T | 1 | a0001c0001t0002g0060 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-8+14647A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14380474 | |||||||
| chr12:14380556 | G | A | 176 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(173): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.-8+14729G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14380556 | |||||||
| chr12:14380612 | T | G | 5 | a0001c0001t0002g0087 a0001c0001t0003g0086 a0001c0001t0022g0084 others(2): Show |
5 | HG02622.hp1 HG02896.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+14785T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14380612 | |||||||
| chr12:14380631 | T | C | 1 | a0001c0001t0003g0088 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-8+14804T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14380631 | |||||||
| chr12:14380839 | C | T | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+15012C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14380839 | |||||||
| chr12:14380867 | C | G | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-8+15040C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14380867 | |||||||
| chr12:14380916 | G | A | 1 | a0003c0003t0011g0185 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-8+15089G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14380916 | |||||||
| chr12:14381258 | G | T | 5 | a0001c0001t0003g0077 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02165.hp1 HG03239.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+15431G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14381258 | |||||||
| chr12:14381264 | T | C | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.-8+15437T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14381264 | |||||||
| chr12:14381492 | G | A | 176 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(173): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.-8+15665G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14381492 | |||||||
| chr12:14381526 | C | T | 8 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0013g0162 others(5): Show |
10 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+15699C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14381526 | |||||||
| chr12:14381590 | GT | G | 4 | a0003c0003t0015g0002 a0003c0003t0015g0168 a0003c0003t0015g0169 others(1): Show |
5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+15770delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14381590 | ||||||
| chr12:14381867 | G | GT | 331 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(328): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-8+16051dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14381867 | ||||||
| chr12:14381929 | A | G | 2 | a0002c0002t0001g0245 a0011c0016t0039g0244 |
2 | HG02683.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-8+16102A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14381929 | |||||||
| chr12:14382066 | G | A | 1 | a0002c0002t0001g0294 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-8+16239G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14382066 | |||||||
| chr12:14382201 | A | G | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+16374A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14382201 | |||||||
| chr12:14382328 | T | C | 1 | a0001c0001t0006g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-8+16501T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14382328 | |||||||
| chr12:14382373 | C | T | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+16546C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14382373 | |||||||
| chr12:14382531 | T | A | 1 | a0001c0001t0002g0070 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-8+16704T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14382531 | |||||||
| chr12:14382617 | A | G | 102 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(99): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-8+16790A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14382617 | |||||||
| chr12:14382945 | G | A | 181 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(178): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.-8+17118G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14382945 | |||||||
| chr12:14382974 | T | G | 141 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(138): Show |
141 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.-8+17147T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14382974 | |||||||
| chr12:14383071 | C | G | 177 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(174): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.-8+17244C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383071 | |||||||
| chr12:14383105 | G | A | 1 | a0001c0001t0003g0089 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-8+17278G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383105 | |||||||
| chr12:14383115 | A | T | 1 | a0009c0011t0024g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-8+17288A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383115 | |||||||
| chr12:14383116 | C | T | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+17289C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383116 | |||||||
| chr12:14383350 | G | T | 1 | a0001c0001t0002g0066 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-8+17523G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383350 | |||||||
| chr12:14383416 | G | A | 9 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(6): Show |
11 | HG00099.hp1 HG00280.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+17589G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383416 | |||||||
| chr12:14383472 | C | G | 1 | a0001c0001t0003g0011 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-8+17645C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383472 | |||||||
| chr12:14383503 | A | G | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+17676A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383503 | |||||||
| chr12:14383613 | A | G | 13 | a0002c0002t0001g0222 a0002c0006t0008g0207 a0002c0006t0008g0216 others(10): Show |
13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+17786A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383613 | |||||||
| chr12:14383724 | T | A | 102 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(99): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-8+17897T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383724 | |||||||
| chr12:14383732 | T | G | 142 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(139): Show |
142 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.-8+17905T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383732 | |||||||
| chr12:14383778 | T | G | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-8+17951T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383778 | |||||||
| chr12:14383808 | C | T | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-8+17981C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383808 | |||||||
| chr12:14383817 | C | T | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-8+17990C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383817 | |||||||
| chr12:14383939 | A | G | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+18112A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14383939 | |||||||
| chr12:14384101 | G | A | 1 | a0001c0001t0003g0076 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-8+18274G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14384101 | |||||||
| chr12:14384330 | C | G | 1 | a0001c0001t0003g0082 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-8+18503C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14384330 | |||||||
| chr12:14384331 | C | A | 1 | a0001c0001t0003g0082 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-8+18504C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14384331 | |||||||
| chr12:14384379 | A | C | 1 | a0002c0002t0001g0307 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-8+18552A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14384379 | |||||||
| chr12:14384578 | T | C | 1 | a0001c0001t0002g0061 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-8+18751T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14384578 | |||||||
| chr12:14384787 | TAATC | T | 8 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 others(5): Show |
8 | HG02486.hp2 NA18946.hp2 NA19003.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+18967_-8+18970d others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14384787 | ||||||
| chr12:14384841 | G | A | 1 | a0002c0002t0001g0204 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-8+19014G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14384841 | |||||||
| chr12:14384872 | T | TA | 250 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(247): Show |
251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.-8+19059dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14384872 | ||||||
| chr12:14384872 | T | TAA | 7 | a0001c0001t0003g0093 a0001c0001t0003g0094 a0001c0001t0006g0135 others(4): Show |
7 | HG01243.hp2 HG02083.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+19058_-8+19059d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14384872 | ||||||
| chr12:14384872 | TA | T | 18 | a0003c0003t0005g0313 a0003c0003t0013g0162 a0003c0003t0013g0163 others(15): Show |
19 | HG00609.hp2 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-8+19059delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14384872 | ||||||
| chr12:14384906 | C | CT | 7 | a0001c0001t0014g0128 a0001c0001t0016g0078 a0001c0001t0016g0129 others(4): Show |
8 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+19094dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14384906 | ||||||
| chr12:14384988 | A | C | 13 | a0002c0002t0001g0222 a0002c0006t0008g0207 a0002c0006t0008g0216 others(10): Show |
13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+19161A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14384988 | |||||||
| chr12:14385001 | C | G | 4 | a0001c0001t0002g0087 a0001c0001t0003g0086 a0001c0001t0022g0084 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+19174C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14385001 | |||||||
| chr12:14385140 | C | T | 3 | a0002c0002t0009g0284 a0002c0002t0009g0285 a0002c0002t0009g0286 |
3 | HG02622.hp2 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-8+19313C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14385140 | |||||||
| chr12:14385195 | C | T | 1 | a0002c0002t0001g0243 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-8+19368C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14385195 | |||||||
| chr12:14385431 | A | G | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-8+19604A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14385431 | |||||||
| chr12:14385453 | A | G | 1 | a0002c0004t0001g0242 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-8+19626A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14385453 | |||||||
| chr12:14385557 | A | G | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+19730A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14385557 | |||||||
| chr12:14385683 | G | T | 3 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0062 |
3 | NA18612.hp2 NA18993.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-8+19856G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14385683 | |||||||
| chr12:14385782 | G | C | 4 | a0002c0004t0001g0229 a0002c0004t0001g0230 a0002c0004t0001g0231 others(1): Show |
4 | HG01074.hp2 HG01175.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+19955G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14385782 | |||||||
| chr12:14385797 | T | C | 1 | a0002c0002t0001g0206 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-8+19970T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14385797 | |||||||
| chr12:14386385 | C | CTTA | 3 | a0003c0003t0005g0160 a0003c0003t0014g0159 a0003c0003t0014g0161 |
3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+20558_-8+20559i others(5): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386385 | |||||||
| chr12:14386387 | G | A | 3 | a0003c0003t0005g0160 a0003c0003t0014g0159 a0003c0003t0014g0161 |
3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+20560G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386387 | |||||||
| chr12:14386390 | CCTG | C | 3 | a0003c0003t0005g0160 a0003c0003t0014g0159 a0003c0003t0014g0161 |
3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+20564_-8+20566d others(5): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386390 | |||||||
| chr12:14386438 | G | A | 14 | a0003c0003t0035g0340 a0003c0005t0007g0322 a0003c0005t0007g0323 others(11): Show |
14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+20611G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386438 | |||||||
| chr12:14386443 | G | A | 1 | a0003c0003t0034g0153 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-8+20616G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386443 | |||||||
| chr12:14386469 | A | G | 11 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+20642A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386469 | |||||||
| chr12:14386616 | A | C | 1 | a0003c0003t0011g0321 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-8+20789A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386616 | |||||||
| chr12:14386774 | C | T | 3 | a0002c0002t0009g0284 a0002c0002t0009g0285 a0002c0002t0009g0286 |
3 | HG02622.hp2 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-8+20947C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386774 | |||||||
| chr12:14386797 | G | A | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+20970G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386797 | |||||||
| chr12:14386945 | A | C | 2 | a0008c0012t0011g0335 a0008c0012t0011g0336 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-8+21118A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386945 | |||||||
| chr12:14386972 | A | T | 2 | a0003c0003t0012g0001 a0003c0003t0012g0180 |
4 | HG02630.hp1 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+21145A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14386972 | |||||||
| chr12:14386972 | AT | A | 6 | a0001c0001t0003g0088 a0001c0001t0003g0095 a0001c0001t0003g0131 others(3): Show |
6 | HG00741.hp1 HG01993.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+21153delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14386972 | ||||||
| chr12:14387023 | A | G | 4 | a0002c0002t0001g0222 a0002c0006t0008g0223 a0002c0006t0008g0224 others(1): Show |
4 | NA18977.hp2 NA18981.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+21196A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387023 | |||||||
| chr12:14387070 | C | T | 1 | a0003c0005t0041g0334 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-8+21243C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387070 | |||||||
| chr12:14387153 | C | T | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+21326C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387153 | |||||||
| chr12:14387203 | A | C | 183 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(180): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-8+21376A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387203 | |||||||
| chr12:14387207 | AAAAAAG | A | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+21392_-8+21397d others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14387207 | ||||||
| chr12:14387245 | A | C | 2 | a0003c0003t0011g0185 a0003c0003t0028g0184 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-8+21418A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387245 | |||||||
| chr12:14387478 | T | G | 2 | a0003c0005t0038g0328 a0003c0005t0041g0334 |
2 | HG01934.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-8+21651T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387478 | |||||||
| chr12:14387561 | G | C | 183 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(180): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-8+21734G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387561 | |||||||
| chr12:14387646 | T | A | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+21819T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387646 | |||||||
| chr12:14387694 | G | A | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8+21867G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387694 | |||||||
| chr12:14387760 | G | A | 1 | a0001c0001t0002g0024 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-8+21933G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14387760 | |||||||
| chr12:14388014 | CT | C | 171 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(168): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.-8+22203delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14388014 | ||||||
| chr12:14388077 | T | G | 177 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(174): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.-8+22250T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388077 | |||||||
| chr12:14388078 | T | A | 177 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(174): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.-8+22251T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388078 | |||||||
| chr12:14388104 | C | T | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+22277C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388104 | |||||||
| chr12:14388123 | C | G | 2 | a0004c0008t0005g0277 a0004c0008t0005g0280 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-8+22296C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388123 | |||||||
| chr12:14388174 | C | T | 4 | a0004c0008t0005g0006 a0004c0008t0005g0276 a0004c0008t0005g0290 others(1): Show |
4 | HG01123.hp1 HG01361.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+22347C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388174 | |||||||
| chr12:14388229 | T | C | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | NA18980.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-8+22402T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388229 | |||||||
| chr12:14388294 | C | T | 1 | a0002c0002t0001g0243 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-8+22467C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388294 | |||||||
| chr12:14388297 | G | A | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+22470G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388297 | |||||||
| chr12:14388471 | C | T | 1 | a0002c0002t0001g0243 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-8+22644C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388471 | |||||||
| chr12:14388589 | C | T | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+22762C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388589 | |||||||
| chr12:14388590 | G | A | 1 | a0003c0005t0038g0328 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-8+22763G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388590 | |||||||
| chr12:14388669 | C | T | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+22842C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388669 | |||||||
| chr12:14388739 | G | C | 1 | a0003c0003t0011g0338 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8+22912G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388739 | |||||||
| chr12:14388828 | C | T | 1 | a0002c0002t0001g0304 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-8+23001C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14388828 | |||||||
| chr12:14389033 | A | G | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+23206A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14389033 | |||||||
| chr12:14389045 | T | C | 1 | a0007c0010t0002g0025 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-8+23218T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14389045 | |||||||
| chr12:14389142 | T | G | 1 | a0003c0003t0018g0156 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-8+23315T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14389142 | |||||||
| chr12:14389194 | A | G | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+23367A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14389194 | |||||||
| chr12:14389315 | G | A | 1 | a0002c0002t0001g0282 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-8+23488G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14389315 | |||||||
| chr12:14389607 | A | G | 177 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(174): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.-8+23780A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14389607 | |||||||
| chr12:14389697 | G | A | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+23870G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14389697 | |||||||
| chr12:14389764 | T | A | 177 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(174): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.-8+23937T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14389764 | |||||||
| chr12:14389866 | C | T | 1 | a0001c0001t0003g0127 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-8+24039C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14389866 | |||||||
| chr12:14390053 | C | T | 4 | a0001c0001t0003g0015 a0001c0001t0003g0124 a0001c0001t0003g0125 others(1): Show |
4 | HG01074.hp1 HG01168.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+24226C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390053 | |||||||
| chr12:14390081 | C | T | 4 | a0003c0003t0015g0002 a0003c0003t0015g0168 a0003c0003t0015g0169 others(1): Show |
5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+24254C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390081 | |||||||
| chr12:14390112 | G | A | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-8+24285G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390112 | |||||||
| chr12:14390113 | C | T | 112 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(109): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-8+24286C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390113 | |||||||
| chr12:14390114 | G | A | 1 | a0006c0009t0005g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-8+24287G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390114 | |||||||
| chr12:14390137 | T | TTA | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+24311_-8+24312d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14390137 | ||||||
| chr12:14390282 | A | G | 1 | a0005c0007t0010g0319 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-8+24455A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390282 | |||||||
| chr12:14390316 | T | A | 1 | a0002c0006t0008g0255 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-8+24489T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390316 | |||||||
| chr12:14390371 | A | G | 1 | a0003c0003t0005g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-8+24544A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390371 | |||||||
| chr12:14390386 | G | A | 1 | a0001c0001t0002g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-8+24559G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390386 | |||||||
| chr12:14390624 | C | G | 5 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0023g0154 others(2): Show |
5 | HG01099.hp1 HG02300.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+24797C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14390624 | |||||||
| chr12:14391142 | A | G | 13 | a0002c0002t0001g0222 a0002c0006t0008g0207 a0002c0006t0008g0216 others(10): Show |
13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+25315A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14391142 | |||||||
| chr12:14391391 | T | C | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+25564T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14391391 | |||||||
| chr12:14391484 | C | G | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.-8+25657C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14391484 | |||||||
| chr12:14391778 | A | G | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-8+25951A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14391778 | |||||||
| chr12:14391806 | C | T | 27 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(24): Show |
28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8+25979C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14391806 | |||||||
| chr12:14391871 | G | A | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8+26044G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14391871 | |||||||
| chr12:14391911 | G | A | 1 | a0003c0003t0028g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-8+26084G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14391911 | |||||||
| chr12:14392044 | T | C | 2 | a0003c0003t0011g0185 a0003c0003t0028g0184 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-8+26217T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392044 | |||||||
| chr12:14392082 | T | G | 1 | a0001c0020t0036g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-8+26255T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392082 | |||||||
| chr12:14392224 | C | CT | 30 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(27): Show |
31 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8+26407dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14392224 | ||||||
| chr12:14392227 | TTTTTTTT others(1): Show |
T | 11 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+26408_-8+26415d others(10): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14392227 | ||||||
| chr12:14392472 | C | G | 1 | a0002c0002t0001g0303 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-8+26645C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392472 | |||||||
| chr12:14392534 | A | G | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+26707A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392534 | |||||||
| chr12:14392541 | G | T | 1 | a0001c0001t0002g0058 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-8+26714G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392541 | |||||||
| chr12:14392646 | T | C | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+26819T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392646 | |||||||
| chr12:14392776 | A | C | 1 | a0002c0002t0001g0309 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-8+26949A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392776 | |||||||
| chr12:14392809 | A | G | 1 | a0003c0003t0011g0338 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8+26982A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392809 | |||||||
| chr12:14392870 | A | G | 1 | a0002c0004t0001g0232 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-8+27043A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392870 | |||||||
| chr12:14392906 | C | G | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-8+27079C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14392906 | |||||||
| chr12:14393013 | G | A | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+27186G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14393013 | |||||||
| chr12:14393239 | A | T | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+27412A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14393239 | |||||||
| chr12:14393262 | T | C | 1 | a0001c0001t0003g0083 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-8+27435T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14393262 | |||||||
| chr12:14393419 | T | C | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-8+27592T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14393419 | |||||||
| chr12:14393423 | A | G | 3 | a0003c0003t0005g0160 a0003c0003t0014g0159 a0003c0003t0014g0161 |
3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+27596A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14393423 | |||||||
| chr12:14393435 | C | G | 4 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(1): Show |
6 | HG02630.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+27608C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14393435 | |||||||
| chr12:14393537 | TAA | T | 15 | a0002c0004t0001g0215 a0002c0004t0001g0228 a0002c0004t0001g0229 others(12): Show |
15 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8+27711_-8+27712d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14393537 | |||||||
| chr12:14393774 | G | A | 1 | a0001c0001t0003g0098 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-8+27947G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14393774 | |||||||
| chr12:14394447 | A | G | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+28620A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14394447 | |||||||
| chr12:14394704 | G | C | 1 | a0001c0001t0002g0339 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-8+28877G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14394704 | |||||||
| chr12:14394768 | A | G | 1 | a0001c0020t0036g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-8+28941A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14394768 | |||||||
| chr12:14394958 | G | A | 26 | a0002c0002t0001g0208 a0002c0002t0001g0209 a0002c0002t0001g0217 others(23): Show |
26 | HG00140.hp1 HG00639.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.-7-28951G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14394958 | |||||||
| chr12:14395074 | A | G | 1 | a0002c0002t0001g0275 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-7-28835A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14395074 | |||||||
| chr12:14395380 | A | C | 178 | a0001c0001t0002g0070 a0002c0002t0001g0007 a0002c0002t0001g0204 others(175): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.-7-28529A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14395380 | |||||||
| chr12:14395471 | G | T | 1 | a0002c0002t0001g0205 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-7-28438G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14395471 | |||||||
| chr12:14395891 | C | A | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.-7-28018C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14395891 | |||||||
| chr12:14395934 | TA | T | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-27974delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14395934 | |||||||
| chr12:14396050 | A | G | 1 | a0002c0002t0037g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-7-27859A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396050 | |||||||
| chr12:14396066 | G | A | 3 | a0003c0003t0004g0197 a0003c0003t0004g0198 a0003c0003t0004g0199 |
3 | HG02970.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-7-27843G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396066 | |||||||
| chr12:14396172 | G | A | 1 | a0003c0003t0011g0338 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-7-27737G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396172 | |||||||
| chr12:14396250 | CTT | C | 18 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(15): Show |
19 | HG00733.hp2 HG01123.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-7-27657_-7-27656d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14396250 | ||||||
| chr12:14396287 | C | G | 14 | a0003c0003t0035g0340 a0003c0005t0007g0322 a0003c0005t0007g0323 others(11): Show |
14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7-27622C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396287 | |||||||
| chr12:14396380 | G | C | 1 | a0001c0001t0003g0090 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-7-27529G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396380 | |||||||
| chr12:14396434 | A | G | 1 | a0003c0003t0004g0201 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-7-27475A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396434 | |||||||
| chr12:14396437 | T | TA | 13 | a0003c0003t0005g0313 a0003c0003t0013g0162 a0003c0003t0013g0163 others(10): Show |
14 | HG00609.hp2 HG00639.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7-27461dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14396437 | ||||||
| chr12:14396438 | A | T | 3 | a0003c0003t0005g0160 a0003c0003t0014g0159 a0003c0003t0014g0161 |
3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-7-27471A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396438 | |||||||
| chr12:14396901 | C | T | 4 | a0003c0003t0015g0002 a0003c0003t0015g0168 a0003c0003t0015g0169 others(1): Show |
5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-27008C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396901 | |||||||
| chr12:14396926 | C | T | 3 | a0002c0002t0001g0274 a0002c0002t0001g0281 a0002c0002t0001g0282 |
3 | HG00099.hp2 HG00733.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-7-26983C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396926 | |||||||
| chr12:14396971 | A | C | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-26938A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396971 | |||||||
| chr12:14396998 | T | A | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-26911T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14396998 | |||||||
| chr12:14397118 | C | T | 1 | a0002c0002t0001g0204 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-7-26791C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14397118 | |||||||
| chr12:14397617 | TTCTG | T | 5 | a0002c0002t0001g0206 a0002c0002t0001g0253 a0002c0002t0001g0256 others(2): Show |
5 | HG02083.hp1 NA18942.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-26282_-7-26279d others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14397617 | ||||||
| chr12:14397659 | A | G | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-26250A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14397659 | |||||||
| chr12:14397660 | T | A | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-26249T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14397660 | |||||||
| chr12:14397718 | AAATATC | A | 89 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.-7-26184_-7-26179d others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14397718 | ||||||
| chr12:14398037 | A | G | 4 | a0002c0002t0001g0206 a0002c0002t0001g0256 a0002c0002t0001g0257 others(1): Show |
4 | NA18942.hp1 NA18973.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-25872A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398037 | |||||||
| chr12:14398066 | C | T | 13 | a0002c0002t0001g0222 a0002c0006t0008g0207 a0002c0006t0008g0216 others(10): Show |
13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-25843C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398066 | |||||||
| chr12:14398091 | T | C | 192 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(189): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-7-25818T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398091 | |||||||
| chr12:14398276 | C | A | 2 | a0003c0014t0013g0166 a0003c0014t0013g0167 |
2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-7-25633C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398276 | |||||||
| chr12:14398387 | G | GT | 122 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(119): Show |
124 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.-7-25511dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14398387 | ||||||
| chr12:14398431 | T | A | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-25478T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398431 | |||||||
| chr12:14398474 | GT | G | 147 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(144): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.-7-25423delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14398474 | ||||||
| chr12:14398476 | T | G | 1 | a0003c0003t0015g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-7-25433T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398476 | |||||||
| chr12:14398551 | G | A | 184 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(181): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-7-25358G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398551 | |||||||
| chr12:14398592 | C | T | 1 | a0001c0001t0031g0012 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-7-25317C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398592 | |||||||
| chr12:14398676 | T | C | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.-7-25233T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398676 | |||||||
| chr12:14398757 | A | G | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-25152A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398757 | |||||||
| chr12:14398948 | C | T | 14 | a0003c0003t0035g0340 a0003c0005t0007g0322 a0003c0005t0007g0323 others(11): Show |
14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7-24961C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14398948 | |||||||
| chr12:14399185 | CTTATAT | C | 16 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(13): Show |
17 | HG01123.hp2 HG02257.hp1 HG02970.hp2 others(14): Show |
intron_variant | MODIFIER | c.-7-24717_-7-24712d others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14399185 | ||||||
| chr12:14399258 | C | T | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-24651C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14399258 | |||||||
| chr12:14399340 | GT | G | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-24559delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14399340 | ||||||
| chr12:14399556 | G | T | 2 | a0008c0012t0011g0335 a0008c0012t0011g0336 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-7-24353G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14399556 | |||||||
| chr12:14399586 | T | A | 1 | a0003c0003t0011g0203 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-7-24323T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14399586 | |||||||
| chr12:14399593 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-7-24316C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14399593 | |||||||
| chr12:14399786 | T | A | 1 | a0003c0003t0011g0321 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-7-24123T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14399786 | |||||||
| chr12:14399786 | T | C | 26 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(23): Show |
27 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.-7-24123T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14399786 | |||||||
| chr12:14399809 | T | A | 1 | a0002c0002t0001g0289 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-7-24100T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14399809 | |||||||
| chr12:14399836 | A | G | 1 | a0003c0005t0038g0328 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-7-24073A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14399836 | |||||||
| chr12:14399911 | G | C | 141 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(138): Show |
141 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.-7-23998G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14399911 | |||||||
| chr12:14400441 | T | C | 7 | a0001c0001t0003g0083 a0001c0001t0003g0090 a0001c0001t0003g0091 others(4): Show |
7 | HG00597.hp1 NA18959.hp1 NA19010.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-23468T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14400441 | |||||||
| chr12:14400569 | A | AT | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-23330dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14400569 | ||||||
| chr12:14400777 | C | T | 186 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(183): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-7-23132C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14400777 | |||||||
| chr12:14400784 | C | T | 12 | a0001c0001t0006g0073 a0001c0001t0006g0079 a0001c0001t0006g0132 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7-23125C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14400784 | |||||||
| chr12:14400920 | T | G | 2 | a0005c0007t0010g0314 a0005c0007t0010g0315 |
2 | HG01346.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-7-22989T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14400920 | |||||||
| chr12:14401100 | T | G | 1 | a0001c0001t0002g0339 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-7-22809T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401100 | |||||||
| chr12:14401157 | A | G | 1 | a0002c0006t0019g0221 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-7-22752A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401157 | |||||||
| chr12:14401193 | G | A | 4 | a0003c0003t0015g0002 a0003c0003t0015g0168 a0003c0003t0015g0169 others(1): Show |
5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-22716G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401193 | |||||||
| chr12:14401282 | G | A | 89 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.-7-22627G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401282 | |||||||
| chr12:14401288 | TG | T | 186 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(183): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-7-22617delG | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14401288 | ||||||
| chr12:14401291 | G | A | 2 | a0003c0003t0011g0311 a0003c0003t0011g0312 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-7-22618G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401291 | |||||||
| chr12:14401358 | G | A | 1 | a0002c0004t0001g0238 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-7-22551G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401358 | |||||||
| chr12:14401471 | A | G | 2 | a0001c0001t0002g0055 a0001c0001t0002g0056 |
2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-7-22438A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401471 | |||||||
| chr12:14401570 | ATT | A | 4 | a0002c0002t0001g0247 a0002c0002t0001g0248 a0002c0002t0001g0259 others(1): Show |
4 | NA18947.hp1 NA18979.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-22338_-7-22337d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401570 | |||||||
| chr12:14401573 | C | A | 4 | a0002c0002t0001g0247 a0002c0002t0001g0248 a0002c0002t0001g0259 others(1): Show |
4 | NA18947.hp1 NA18979.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-22336C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401573 | |||||||
| chr12:14401583 | CT | C | 52 | a0001c0001t0002g0143 a0001c0001t0003g0015 a0001c0001t0003g0074 others(49): Show |
52 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.-7-22315delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14401583 | ||||||
| chr12:14401604 | A | G | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-22305A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401604 | |||||||
| chr12:14401714 | C | CT | 33 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0042 others(30): Show |
33 | HG01175.hp1 HG01358.hp2 HG01515.hp2 others(30): Show |
intron_variant | MODIFIER | c.-7-22174dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14401714 | ||||||
| chr12:14401714 | CT | C | 176 | a0001c0001t0002g0023 a0001c0001t0003g0089 a0001c0001t0003g0100 others(173): Show |
182 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.-7-22174delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14401714 | ||||||
| chr12:14401714 | CTT | C | 8 | a0002c0002t0001g0274 a0002c0002t0001g0281 a0002c0002t0001g0282 others(5): Show |
8 | HG00099.hp2 HG00733.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7-22175_-7-22174d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14401714 | ||||||
| chr12:14401739 | A | G | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7-22170A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401739 | |||||||
| chr12:14401756 | C | T | 4 | a0003c0003t0015g0002 a0003c0003t0015g0168 a0003c0003t0015g0169 others(1): Show |
5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-22153C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401756 | |||||||
| chr12:14401841 | G | A | 1 | a0002c0002t0001g0295 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-7-22068G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401841 | |||||||
| chr12:14401931 | C | T | 3 | a0005c0007t0010g0316 a0005c0007t0010g0317 a0005c0007t0010g0319 |
3 | HG00609.hp2 HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-7-21978C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401931 | |||||||
| chr12:14401963 | C | T | 1 | a0004c0008t0005g0291 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-7-21946C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401963 | |||||||
| chr12:14401971 | A | C | 14 | a0003c0003t0035g0340 a0003c0005t0007g0322 a0003c0005t0007g0323 others(11): Show |
14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7-21938A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14401971 | |||||||
| chr12:14402044 | A | G | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-21865A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14402044 | |||||||
| chr12:14402118 | T | C | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-21791T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14402118 | |||||||
| chr12:14402127 | C | CT | 65 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0017 others(62): Show |
65 | HG01175.hp1 HG01243.hp1 HG01257.hp1 others(62): Show |
intron_variant | MODIFIER | c.-7-21764dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14402127 | ||||||
| chr12:14402127 | CT | C | 152 | a0001c0001t0003g0090 a0001c0001t0003g0102 a0001c0001t0014g0128 others(149): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.-7-21764delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14402127 | ||||||
| chr12:14402127 | CTT | C | 21 | a0002c0002t0001g0256 a0002c0002t0001g0283 a0002c0006t0008g0218 others(18): Show |
22 | HG00438.hp1 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7-21765_-7-21764d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14402127 | ||||||
| chr12:14402218 | C | G | 1 | a0003c0003t0011g0338 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-7-21691C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14402218 | |||||||
| chr12:14402367 | A | G | 3 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0131 |
3 | HG03239.hp1 NA18955.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-7-21542A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14402367 | |||||||
| chr12:14402608 | AT | A | 297 | a0001c0001t0002g0010 a0001c0001t0002g0016 a0001c0001t0002g0017 others(294): Show |
302 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.-7-21283delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14402608 | ||||||
| chr12:14402608 | ATT | A | 30 | a0002c0002t0001g0306 a0003c0003t0004g0003 a0003c0003t0004g0186 others(27): Show |
31 | HG00733.hp2 HG01099.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.-7-21284_-7-21283d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14402608 | ||||||
| chr12:14402637 | C | G | 3 | a0003c0003t0011g0311 a0003c0003t0011g0312 a0003c0003t0011g0321 |
3 | HG02280.hp1 HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-7-21272C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14402637 | |||||||
| chr12:14402711 | C | T | 2 | a0001c0001t0006g0073 a0001c0001t0006g0141 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-7-21198C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14402711 | |||||||
| chr12:14402766 | T | C | 1 | a0003c0003t0011g0321 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-7-21143T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14402766 | |||||||
| chr12:14403104 | G | T | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-7-20805G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14403104 | |||||||
| chr12:14403214 | T | C | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-20695T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14403214 | |||||||
| chr12:14403324 | G | A | 2 | a0003c0003t0004g0194 a0003c0003t0004g0200 |
2 | HG01123.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-7-20585G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14403324 | |||||||
| chr12:14403386 | G | A | 1 | a0001c0001t0003g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-7-20523G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14403386 | |||||||
| chr12:14403460 | A | G | 2 | a0003c0005t0007g0324 a0003c0005t0007g0333 |
2 | HG02647.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-7-20449A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14403460 | |||||||
| chr12:14403500 | G | A | 2 | a0001c0001t0003g0077 a0001c0001t0040g0142 |
2 | HG02165.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-7-20409G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14403500 | |||||||
| chr12:14403550 | G | A | 1 | a0002c0002t0001g0260 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-7-20359G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14403550 | |||||||
| chr12:14403967 | A | T | 1 | a0004c0018t0005g0273 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-7-19942A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14403967 | |||||||
| chr12:14404019 | A | AT | 10 | a0001c0001t0002g0059 a0003c0003t0005g0313 a0005c0007t0010g0005 others(7): Show |
11 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7-19879dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14404019 | ||||||
| chr12:14404132 | C | CT | 174 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0206 others(171): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.-7-19763dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14404132 | ||||||
| chr12:14404132 | CT | C | 141 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(138): Show |
141 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.-7-19763delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14404132 | ||||||
| chr12:14404158 | C | T | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-7-19751C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404158 | |||||||
| chr12:14404162 | C | T | 1 | a0001c0001t0016g0078 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-7-19747C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404162 | |||||||
| chr12:14404175 | A | G | 3 | a0003c0003t0004g0003 a0003c0003t0004g0192 a0003c0003t0004g0193 |
4 | NA18955.hp2 NA18968.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-19734A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404175 | |||||||
| chr12:14404435 | A | G | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-19474A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404435 | |||||||
| chr12:14404597 | G | T | 2 | a0002c0002t0001g0309 a0014c0019t0001g0310 |
2 | NA19002.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.-7-19312G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404597 | |||||||
| chr12:14404630 | G | A | 1 | a0014c0019t0001g0310 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-7-19279G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404630 | |||||||
| chr12:14404746 | C | T | 112 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(109): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-7-19163C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404746 | |||||||
| chr12:14404834 | A | AT | 102 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(99): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-7-19072dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14404834 | ||||||
| chr12:14404838 | G | T | 102 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(99): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-7-19071G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404838 | |||||||
| chr12:14404839 | A | T | 102 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(99): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-7-19070A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404839 | |||||||
| chr12:14404994 | T | G | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.-7-18915T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404994 | |||||||
| chr12:14404996 | T | G | 1 | a0003c0005t0007g0329 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-7-18913T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14404996 | |||||||
| chr12:14405032 | C | T | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7-18877C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405032 | |||||||
| chr12:14405165 | G | GTAGTAGA others(2): Show |
4 | a0002c0002t0001g0295 a0002c0002t0001g0304 a0002c0002t0001g0305 others(1): Show |
4 | HG01167.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-18742_-7-18734d others(11): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405165 | ||||||
| chr12:14405232 | T | G | 1 | a0002c0002t0001g0204 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-7-18677T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405232 | |||||||
| chr12:14405272 | A | G | 1 | a0005c0007t0010g0319 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-7-18637A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405272 | |||||||
| chr12:14405403 | C | CT | 41 | a0001c0001t0002g0021 a0001c0001t0002g0038 a0001c0001t0002g0040 others(38): Show |
41 | HG00597.hp1 HG01099.hp2 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.-7-18477dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405403 | ||||||
| chr12:14405403 | CT | C | 6 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(3): Show |
6 | HG01496.hp1 HG01981.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-18477delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405403 | ||||||
| chr12:14405403 | CTTT | C | 20 | a0002c0002t0001g0235 a0002c0002t0001g0245 a0002c0002t0001g0272 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.-7-18479_-7-18477d others(5): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405403 | ||||||
| chr12:14405403 | CTTTT | C | 113 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(110): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.-7-18480_-7-18477d others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405403 | ||||||
| chr12:14405403 | CTTTTT | C | 24 | a0002c0002t0001g0222 a0002c0002t0009g0008 a0002c0002t0009g0009 others(21): Show |
24 | HG00673.hp2 HG01109.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.-7-18481_-7-18477d others(7): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405403 | ||||||
| chr12:14405403 | CTTTTTT | C | 18 | a0001c0001t0003g0081 a0003c0003t0005g0313 a0003c0003t0025g0172 others(15): Show |
18 | HG00099.hp1 HG00280.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.-7-18482_-7-18477d others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405403 | ||||||
| chr12:14405403 | CTTTTTTT | C | 11 | a0001c0001t0003g0077 a0001c0001t0003g0082 a0001c0001t0003g0131 others(8): Show |
12 | HG00609.hp2 HG01934.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7-18483_-7-18477d others(9): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405403 | ||||||
| chr12:14405403 | CTTTTTTT others(3): Show |
C | 8 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-18486_-7-18477d others(12): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405403 | ||||||
| chr12:14405403 | CTTTTTTT others(4): Show |
C | 10 | a0001c0001t0006g0073 a0001c0001t0006g0079 a0001c0001t0006g0135 others(7): Show |
10 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-18487_-7-18477d others(13): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14405403 | ||||||
| chr12:14405505 | C | T | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-18404C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405505 | |||||||
| chr12:14405546 | C | T | 12 | a0001c0001t0003g0015 a0001c0001t0003g0088 a0001c0001t0003g0095 others(9): Show |
12 | HG00140.hp2 HG00735.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-18363C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405546 | |||||||
| chr12:14405622 | G | A | 150 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(147): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.-7-18287G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405622 | |||||||
| chr12:14405673 | C | G | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-18236C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405673 | |||||||
| chr12:14405739 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-7-18170C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405739 | |||||||
| chr12:14405767 | G | A | 27 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(24): Show |
28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-7-18142G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405767 | |||||||
| chr12:14405784 | G | C | 1 | a0001c0001t0003g0090 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-7-18125G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14405784 | |||||||
| chr12:14406130 | C | T | 1 | a0003c0003t0014g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-7-17779C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406130 | |||||||
| chr12:14406173 | A | G | 1 | a0002c0004t0001g0241 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-7-17736A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406173 | |||||||
| chr12:14406256 | G | A | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-17653G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406256 | |||||||
| chr12:14406318 | C | T | 2 | a0008c0012t0011g0335 a0008c0012t0011g0336 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-7-17591C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406318 | |||||||
| chr12:14406373 | A | T | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-17536A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406373 | |||||||
| chr12:14406447 | C | T | 1 | a0001c0001t0003g0088 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-7-17462C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406447 | |||||||
| chr12:14406493 | GA | G | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-17415delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406493 | |||||||
| chr12:14406514 | G | C | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7-17395G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406514 | |||||||
| chr12:14406543 | T | C | 1 | a0003c0005t0007g0324 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-7-17366T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406543 | |||||||
| chr12:14406552 | G | A | 141 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(138): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.-7-17357G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406552 | |||||||
| chr12:14406565 | A | G | 2 | a0005c0007t0010g0316 a0005c0007t0010g0317 |
2 | HG00609.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.-7-17344A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406565 | |||||||
| chr12:14406592 | TA | T | 10 | a0001c0001t0002g0121 a0001c0001t0003g0108 a0002c0002t0001g0289 others(7): Show |
12 | HG00735.hp1 HG02630.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7-17304delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14406592 | ||||||
| chr12:14406665 | G | GT | 17 | a0001c0001t0002g0037 a0001c0001t0002g0040 a0001c0001t0002g0041 others(14): Show |
17 | HG02135.hp1 HG02486.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.-7-17227dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14406665 | ||||||
| chr12:14406721 | A | G | 1 | a0002c0002t0001g0303 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-7-17188A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406721 | |||||||
| chr12:14406749 | C | T | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-17160C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14406749 | |||||||
| chr12:14407035 | T | C | 1 | a0004c0008t0005g0251 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-7-16874T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14407035 | |||||||
| chr12:14407257 | A | G | 27 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(24): Show |
28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-7-16652A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14407257 | |||||||
| chr12:14407333 | T | C | 1 | a0002c0002t0001g0217 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-7-16576T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14407333 | |||||||
| chr12:14407585 | A | G | 1 | a0003c0003t0015g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-7-16324A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14407585 | |||||||
| chr12:14407672 | T | C | 2 | a0003c0003t0004g0195 a0003c0003t0004g0196 |
2 | HG00733.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-7-16237T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14407672 | |||||||
| chr12:14407752 | CT | C | 11 | a0001c0001t0006g0073 a0001c0001t0006g0079 a0001c0001t0006g0132 others(8): Show |
11 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7-16156delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14407752 | |||||||
| chr12:14407769 | T | A | 11 | a0001c0001t0006g0073 a0001c0001t0006g0079 a0001c0001t0006g0132 others(8): Show |
11 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7-16140T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14407769 | |||||||
| chr12:14407847 | T | TAAAAAAA others(321): Show |
1 | a0002c0002t0001g0243 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-7-16045_-7-16044i others(330): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14407847 | ||||||
| chr12:14407942 | T | C | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-15967T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14407942 | |||||||
| chr12:14408116 | G | GCA | 167 | a0001c0001t0002g0010 a0001c0001t0002g0016 a0001c0001t0002g0017 others(164): Show |
168 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(165): Show |
intron_variant | MODIFIER | c.-7-15768_-7-15767d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14408116 | ||||||
| chr12:14408116 | G | GCACA | 125 | a0001c0001t0002g0050 a0001c0001t0002g0056 a0001c0001t0003g0114 others(122): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.-7-15770_-7-15767d others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14408116 | ||||||
| chr12:14408116 | G | GCACACA | 17 | a0002c0002t0001g0247 a0002c0002t0001g0248 a0002c0002t0001g0259 others(14): Show |
18 | HG00609.hp2 HG00639.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.-7-15772_-7-15767d others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14408116 | ||||||
| chr12:14408116 | G | GCACACAC others(5): Show |
3 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0183 |
5 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-15778_-7-15767d others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14408116 | ||||||
| chr12:14408116 | G | GCACACAC others(7): Show |
2 | a0003c0003t0012g0181 a0003c0003t0012g0182 |
2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-7-15780_-7-15767d others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14408116 | ||||||
| chr12:14408141 | C | CACAA | 8 | a0003c0003t0014g0171 a0003c0003t0015g0002 a0003c0003t0015g0168 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-15767_-7-15766i others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14408141 | ||||||
| chr12:14408168 | C | T | 1 | a0001c0001t0003g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-7-15741C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14408168 | |||||||
| chr12:14408211 | A | G | 4 | a0003c0003t0015g0002 a0003c0003t0015g0168 a0003c0003t0015g0169 others(1): Show |
5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-15698A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14408211 | |||||||
| chr12:14408296 | GT | G | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-15608delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14408296 | ||||||
| chr12:14408369 | A | G | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-15540A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14408369 | |||||||
| chr12:14408477 | T | C | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.-7-15432T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14408477 | |||||||
| chr12:14408485 | A | G | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-7-15424A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14408485 | |||||||
| chr12:14408518 | A | G | 1 | a0009c0011t0024g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-7-15391A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14408518 | |||||||
| chr12:14408581 | T | C | 1 | a0003c0003t0014g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-7-15328T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14408581 | |||||||
| chr12:14408592 | G | A | 14 | a0003c0003t0035g0340 a0003c0005t0007g0322 a0003c0005t0007g0323 others(11): Show |
14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7-15317G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14408592 | |||||||
| chr12:14408714 | G | GT | 4 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(1): Show |
4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-15191dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14408714 | ||||||
| chr12:14409040 | T | C | 1 | a0001c0001t0002g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-7-14869T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14409040 | |||||||
| chr12:14409064 | A | G | 2 | a0010c0013t0020g0118 a0010c0013t0020g0120 |
2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-7-14845A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14409064 | |||||||
| chr12:14409165 | A | G | 1 | a0002c0004t0001g0231 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-7-14744A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14409165 | |||||||
| chr12:14409317 | A | G | 1 | a0001c0020t0036g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-7-14592A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14409317 | |||||||
| chr12:14409487 | G | A | 7 | a0003c0003t0011g0338 a0006c0009t0005g0174 a0006c0009t0005g0175 others(4): Show |
7 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-14422G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14409487 | |||||||
| chr12:14409733 | A | G | 1 | a0001c0001t0002g0027 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-7-14176A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14409733 | |||||||
| chr12:14409790 | A | C | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-14119A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14409790 | |||||||
| chr12:14409908 | T | A | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-14001T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14409908 | |||||||
| chr12:14409915 | T | C | 1 | a0001c0001t0002g0071 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-7-13994T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14409915 | |||||||
| chr12:14410038 | C | T | 3 | a0002c0002t0009g0284 a0002c0002t0009g0285 a0002c0002t0009g0286 |
3 | HG02622.hp2 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-7-13871C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410038 | |||||||
| chr12:14410175 | C | T | 1 | a0003c0003t0011g0338 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-7-13734C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410175 | |||||||
| chr12:14410177 | C | T | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-13732C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410177 | |||||||
| chr12:14410195 | C | G | 1 | a0003c0003t0004g0201 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-7-13714C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410195 | |||||||
| chr12:14410228 | C | T | 7 | a0003c0003t0011g0338 a0006c0009t0005g0174 a0006c0009t0005g0175 others(4): Show |
7 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-13681C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410228 | |||||||
| chr12:14410240 | T | G | 13 | a0002c0002t0001g0222 a0002c0006t0008g0207 a0002c0006t0008g0216 others(10): Show |
13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-13669T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410240 | |||||||
| chr12:14410271 | A | G | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-7-13638A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410271 | |||||||
| chr12:14410373 | C | T | 2 | a0001c0001t0003g0113 a0001c0001t0003g0114 |
2 | HG01106.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-7-13536C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410373 | |||||||
| chr12:14410375 | G | T | 1 | a0001c0001t0002g0055 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-7-13534G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410375 | |||||||
| chr12:14410387 | T | G | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-13522T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410387 | |||||||
| chr12:14410393 | C | T | 1 | a0001c0001t0002g0058 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-7-13516C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410393 | |||||||
| chr12:14410461 | G | A | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-13448G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410461 | |||||||
| chr12:14410660 | G | C | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-13249G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410660 | |||||||
| chr12:14410714 | A | G | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-7-13195A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410714 | |||||||
| chr12:14410715 | A | G | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-13194A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410715 | |||||||
| chr12:14410721 | T | C | 1 | a0002c0002t0001g0283 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-7-13188T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410721 | |||||||
| chr12:14410725 | G | C | 1 | a0001c0001t0003g0109 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-7-13184G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410725 | |||||||
| chr12:14410744 | A | AATGT | 27 | a0001c0020t0036g0134 a0003c0003t0004g0003 a0003c0003t0004g0186 others(24): Show |
28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-7-13146_-7-13143d others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14410744 | ||||||
| chr12:14410777 | A | G | 112 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(109): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-7-13132A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410777 | |||||||
| chr12:14410908 | T | C | 184 | a0001c0020t0036g0134 a0002c0002t0001g0007 a0002c0002t0001g0204 others(181): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.-7-13001T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14410908 | |||||||
| chr12:14411069 | C | T | 1 | a0003c0005t0007g0332 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-7-12840C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411069 | |||||||
| chr12:14411274 | A | C | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.-7-12635A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411274 | |||||||
| chr12:14411277 | G | A | 26 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(23): Show |
27 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.-7-12632G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411277 | |||||||
| chr12:14411545 | T | A | 2 | a0002c0002t0001g0260 a0002c0002t0001g0295 |
2 | HG01167.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-7-12364T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411545 | |||||||
| chr12:14411570 | A | G | 1 | a0001c0001t0002g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-7-12339A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411570 | |||||||
| chr12:14411607 | T | G | 1 | a0003c0003t0011g0338 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-7-12302T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411607 | |||||||
| chr12:14411634 | T | C | 1 | a0003c0005t0007g0327 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7-12275T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411634 | |||||||
| chr12:14411711 | C | T | 1 | a0001c0001t0002g0020 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-7-12198C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411711 | |||||||
| chr12:14411730 | C | G | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-12179C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411730 | |||||||
| chr12:14411778 | T | A | 3 | a0007c0010t0002g0014 a0007c0010t0002g0025 a0007c0010t0002g0052 |
3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-7-12131T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411778 | |||||||
| chr12:14411812 | T | C | 7 | a0003c0003t0011g0338 a0006c0009t0005g0174 a0006c0009t0005g0175 others(4): Show |
7 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-12097T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411812 | |||||||
| chr12:14411857 | T | C | 27 | a0001c0020t0036g0134 a0003c0003t0004g0003 a0003c0003t0004g0186 others(24): Show |
28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-7-12052T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411857 | |||||||
| chr12:14411976 | G | A | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-11933G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14411976 | |||||||
| chr12:14412000 | T | A | 2 | a0003c0014t0013g0166 a0003c0014t0013g0167 |
2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-7-11909T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412000 | |||||||
| chr12:14412090 | C | A | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-11819C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412090 | |||||||
| chr12:14412170 | C | T | 2 | a0003c0003t0004g0189 a0003c0003t0004g0191 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-7-11739C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412170 | |||||||
| chr12:14412307 | T | C | 1 | a0001c0020t0036g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-7-11602T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412307 | |||||||
| chr12:14412369 | AAG | A | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-11537_-7-11536d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14412369 | ||||||
| chr12:14412420 | C | A | 12 | a0002c0002t0001g0206 a0002c0002t0001g0249 a0002c0002t0001g0253 others(9): Show |
12 | HG02083.hp1 NA18942.hp1 NA18952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-11489C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412420 | |||||||
| chr12:14412760 | T | A | 1 | a0003c0003t0005g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-7-11149T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412760 | |||||||
| chr12:14412798 | G | A | 112 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(109): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-7-11111G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412798 | |||||||
| chr12:14412843 | G | A | 2 | a0002c0006t0019g0221 a0003c0003t0014g0171 |
2 | HG02717.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.-7-11066G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412843 | |||||||
| chr12:14412912 | G | T | 1 | a0001c0001t0022g0085 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-7-10997G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412912 | |||||||
| chr12:14412918 | G | A | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-10991G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14412918 | |||||||
| chr12:14413065 | C | T | 1 | a0002c0002t0001g0260 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-7-10844C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413065 | |||||||
| chr12:14413079 | T | A | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-10830T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413079 | |||||||
| chr12:14413107 | G | A | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-7-10802G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413107 | |||||||
| chr12:14413277 | A | G | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-10632A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413277 | |||||||
| chr12:14413437 | A | G | 1 | a0001c0001t0002g0070 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-7-10472A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413437 | |||||||
| chr12:14413495 | G | A | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-10414G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413495 | |||||||
| chr12:14413686 | G | T | 27 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(24): Show |
28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-7-10223G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413686 | |||||||
| chr12:14413714 | A | G | 27 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(24): Show |
28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-7-10195A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413714 | |||||||
| chr12:14413726 | G | C | 1 | a0001c0001t0002g0013 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-7-10183G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413726 | |||||||
| chr12:14413852 | C | T | 1 | a0003c0003t0034g0153 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-7-10057C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14413852 | |||||||
| chr12:14414082 | G | A | 1 | a0002c0002t0001g0253 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-7-9827G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14414082 | |||||||
| chr12:14414316 | T | C | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-9593T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14414316 | |||||||
| chr12:14414458 | A | G | 1 | a0001c0001t0003g0112 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-7-9451A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14414458 | |||||||
| chr12:14414580 | T | C | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-9329T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14414580 | |||||||
| chr12:14415408 | C | G | 1 | a0003c0003t0005g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-7-8501C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14415408 | |||||||
| chr12:14415518 | G | A | 174 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(171): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.-7-8391G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14415518 | |||||||
| chr12:14415573 | C | T | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-8336C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14415573 | |||||||
| chr12:14415691 | G | GT | 219 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(216): Show |
224 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(221): Show |
intron_variant | MODIFIER | c.-7-8203dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14415691 | ||||||
| chr12:14415691 | G | GTT | 109 | a0001c0001t0003g0123 a0001c0001t0031g0012 a0002c0002t0001g0007 others(106): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.-7-8204_-7-8203dup others(2): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14415691 | ||||||
| chr12:14415792 | A | G | 2 | a0002c0002t0001g0305 a0002c0002t0001g0306 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-7-8117A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14415792 | |||||||
| chr12:14415857 | G | A | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-8052G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14415857 | |||||||
| chr12:14415893 | A | G | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-8016A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14415893 | |||||||
| chr12:14415917 | T | G | 1 | a0001c0001t0003g0113 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-7-7992T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14415917 | |||||||
| chr12:14415950 | T | C | 1 | a0002c0002t0001g0254 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-7-7959T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14415950 | |||||||
| chr12:14416008 | A | C | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7-7901A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14416008 | |||||||
| chr12:14416242 | G | A | 3 | a0003c0003t0004g0003 a0003c0003t0004g0192 a0003c0003t0004g0193 |
4 | NA18955.hp2 NA18968.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-7667G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14416242 | |||||||
| chr12:14416259 | G | C | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-7650G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14416259 | |||||||
| chr12:14416270 | TTATTTAA | T | 103 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(100): Show |
104 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.-7-7630_-7-7624del others(7): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14416270 | ||||||
| chr12:14416343 | G | T | 18 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(15): Show |
19 | HG00733.hp2 HG01123.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-7-7566G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14416343 | |||||||
| chr12:14416399 | AATGCCTT others(4): Show |
A | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-7508_-7-7498del others(11): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14416399 | ||||||
| chr12:14416553 | T | C | 13 | a0002c0002t0001g0222 a0002c0006t0008g0207 a0002c0006t0008g0216 others(10): Show |
13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-7356T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14416553 | |||||||
| chr12:14416741 | G | A | 1 | a0003c0003t0011g0203 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-7-7168G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14416741 | |||||||
| chr12:14416819 | G | T | 3 | a0003c0003t0005g0160 a0003c0003t0014g0159 a0003c0003t0014g0161 |
3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-7-7090G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14416819 | |||||||
| chr12:14416937 | G | A | 1 | a0002c0004t0001g0238 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-7-6972G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14416937 | |||||||
| chr12:14417142 | T | G | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-6767T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14417142 | |||||||
| chr12:14417296 | C | G | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-6613C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14417296 | |||||||
| chr12:14417370 | C | A | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-6539C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14417370 | |||||||
| chr12:14417500 | A | G | 2 | a0002c0002t0001g0305 a0002c0002t0001g0306 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-7-6409A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14417500 | |||||||
| chr12:14417517 | G | A | 168 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(165): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-7-6392G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14417517 | |||||||
| chr12:14417645 | A | G | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-6264A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14417645 | |||||||
| chr12:14417705 | T | C | 103 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(100): Show |
104 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.-7-6204T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14417705 | |||||||
| chr12:14417832 | T | C | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-6077T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14417832 | |||||||
| chr12:14418022 | T | G | 3 | a0001c0001t0002g0087 a0001c0001t0002g0121 a0001c0001t0002g0122 |
3 | HG02818.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-7-5887T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418022 | |||||||
| chr12:14418126 | A | C | 7 | a0002c0002t0001g0247 a0002c0002t0001g0248 a0002c0002t0001g0259 others(4): Show |
8 | NA18612.hp1 NA18945.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7-5783A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418126 | |||||||
| chr12:14418185 | C | T | 2 | a0003c0003t0004g0003 a0003c0003t0004g0193 |
3 | NA18968.hp1 NA19007.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.-7-5724C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418185 | |||||||
| chr12:14418211 | T | C | 175 | a0001c0020t0036g0134 a0002c0002t0001g0007 a0002c0002t0001g0204 others(172): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.-7-5698T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418211 | |||||||
| chr12:14418295 | C | G | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-7-5614C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418295 | |||||||
| chr12:14418497 | C | G | 152 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(149): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-7-5412C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418497 | |||||||
| chr12:14418539 | T | C | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-5370T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418539 | |||||||
| chr12:14418563 | A | C | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-5346A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418563 | |||||||
| chr12:14418737 | A | G | 2 | a0003c0003t0011g0185 a0003c0003t0028g0184 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-7-5172A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418737 | |||||||
| chr12:14418795 | A | G | 1 | a0002c0002t0001g0217 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-7-5114A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418795 | |||||||
| chr12:14418880 | G | A | 177 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(174): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.-7-5029G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14418880 | |||||||
| chr12:14419025 | C | A | 1 | a0013c0017t0001g0265 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-7-4884C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14419025 | |||||||
| chr12:14419056 | A | G | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-4853A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14419056 | |||||||
| chr12:14419294 | CAGAGTTC others(63): Show |
C | 1 | a0002c0002t0001g0249 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-7-4581_-7-4512del others(70): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14419294 | ||||||
| chr12:14419333 | A | G | 17 | a0001c0001t0002g0017 a0001c0001t0002g0028 a0001c0001t0002g0029 others(14): Show |
17 | HG01257.hp1 HG01258.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.-7-4576A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14419333 | |||||||
| chr12:14419496 | C | T | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-4413C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14419496 | |||||||
| chr12:14419685 | C | T | 1 | a0003c0003t0004g0201 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-7-4224C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14419685 | |||||||
| chr12:14419956 | C | A | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-7-3953C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14419956 | |||||||
| chr12:14419959 | T | C | 1 | a0009c0011t0024g0150 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-7-3950T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14419959 | |||||||
| chr12:14420427 | A | G | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-3482A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14420427 | |||||||
| chr12:14420565 | C | G | 105 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(102): Show |
106 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-7-3344C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14420565 | |||||||
| chr12:14420569 | C | T | 2 | a0003c0003t0011g0185 a0003c0003t0028g0184 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-7-3340C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14420569 | |||||||
| chr12:14420585 | C | T | 1 | a0002c0002t0001g0234 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-7-3324C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14420585 | |||||||
| chr12:14420586 | G | A | 2 | a0010c0013t0020g0118 a0010c0013t0020g0120 |
2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-7-3323G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14420586 | |||||||
| chr12:14420634 | GA | G | 168 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(165): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-7-3265delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14420634 | ||||||
| chr12:14420851 | TTTTC | T | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-3048_-7-3045del others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14420851 | ||||||
| chr12:14420874 | G | T | 2 | a0001c0001t0002g0116 a0001c0001t0027g0026 |
2 | HG02735.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-7-3035G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14420874 | |||||||
| chr12:14420908 | A | G | 2 | a0001c0001t0003g0077 a0001c0001t0040g0142 |
2 | HG02165.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-7-3001A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14420908 | |||||||
| chr12:14421342 | G | T | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-2567G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14421342 | |||||||
| chr12:14421459 | C | T | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-2450C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14421459 | |||||||
| chr12:14421584 | C | T | 2 | a0003c0003t0011g0185 a0003c0003t0028g0184 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-7-2325C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14421584 | |||||||
| chr12:14422225 | C | G | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-1684C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14422225 | |||||||
| chr12:14422248 | G | A | 1 | a0001c0001t0030g0043 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-7-1661G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14422248 | |||||||
| chr12:14422312 | T | TAC | 28 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0054 others(25): Show |
28 | HG00099.hp1 HG00741.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.-7-1553_-7-1552dup others(2): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | ||||||
| chr12:14422312 | T | TACAC | 14 | a0001c0001t0003g0083 a0001c0001t0003g0093 a0001c0001t0003g0094 others(11): Show |
15 | HG01099.hp1 HG01109.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.-7-1555_-7-1552dup others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | ||||||
| chr12:14422312 | T | TACACAC | 3 | a0001c0001t0002g0058 a0002c0002t0009g0212 a0003c0003t0014g0171 |
3 | HG02615.hp1 HG02717.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-7-1557_-7-1552dup others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | ||||||
| chr12:14422312 | T | TACACACA others(1): Show |
3 | a0001c0001t0003g0119 a0002c0002t0009g0008 a0002c0002t0009g0009 |
3 | HG01109.hp2 HG03540.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.-7-1559_-7-1552dup others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | ||||||
| chr12:14422312 | TAC | T | 55 | a0001c0001t0002g0016 a0001c0001t0002g0027 a0001c0001t0002g0033 others(52): Show |
55 | HG00140.hp2 HG01074.hp1 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.-7-1553_-7-1552del others(2): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | ||||||
| chr12:14422312 | TACAC | T | 56 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0028 others(53): Show |
57 | HG00735.hp1 HG00741.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.-7-1555_-7-1552del others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | ||||||
| chr12:14422312 | TACACAC | T | 93 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(90): Show |
93 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.-7-1557_-7-1552del others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | ||||||
| chr12:14422312 | TACACACA others(1): Show |
T | 21 | a0001c0001t0003g0099 a0002c0002t0009g0210 a0002c0002t0009g0211 others(18): Show |
22 | HG00597.hp1 HG00733.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-7-1559_-7-1552del others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | ||||||
| chr12:14422312 | TACACACA others(3): Show |
T | 7 | a0002c0002t0001g0253 a0002c0002t0009g0213 a0003c0003t0011g0311 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-1561_-7-1552del others(10): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | ||||||
| chr12:14422312 | TACACACA others(5): Show |
T | 12 | a0003c0003t0011g0185 a0003c0003t0012g0001 a0003c0003t0012g0180 others(9): Show |
14 | HG02630.hp1 HG02723.hp1 HG02896.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7-1563_-7-1552del others(12): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | ||||||
| chr12:14422312 | TACACACA others(7): Show |
T | 9 | a0003c0003t0011g0203 a0003c0003t0012g0183 a0005c0007t0010g0005 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-1565_-7-1552del others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | ||||||
| chr12:14422312 | TACACACA others(9): Show |
T | 2 | a0003c0003t0012g0181 a0003c0005t0007g0326 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-7-1567_-7-1552del others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | ||||||
| chr12:14422312 | TACACACA others(11): Show |
T | 2 | a0003c0003t0014g0152 a0003c0003t0018g0156 |
2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-7-1569_-7-1552del others(18): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14422312 | ||||||
| chr12:14422378 | A | T | 16 | a0001c0001t0006g0073 a0001c0001t0006g0079 a0001c0001t0006g0132 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-7-1531A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14422378 | |||||||
| chr12:14422525 | A | G | 178 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(175): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.-7-1384A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14422525 | |||||||
| chr12:14422579 | A | G | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-7-1330A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14422579 | |||||||
| chr12:14422814 | G | C | 3 | a0003c0003t0005g0160 a0003c0003t0014g0159 a0003c0003t0014g0161 |
3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-7-1095G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14422814 | |||||||
| chr12:14423029 | A | G | 1 | a0009c0011t0024g0150 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-7-880A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14423029 | |||||||
| chr12:14423102 | T | A | 1 | a0002c0002t0026g0004 | 2 | NA18945.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-7-807T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14423102 | |||||||
| chr12:14423293 | T | C | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.-7-616T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14423293 | |||||||
| chr12:14423548 | T | C | 150 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(147): Show |
150 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(147): Show |
intron_variant | MODIFIER | c.-7-361T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14423548 | |||||||
| chr12:14423574 | C | CT | 122 | a0001c0001t0002g0040 a0001c0001t0002g0057 a0001c0001t0002g0143 others(119): Show |
124 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.-7-311dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14423574 | ||||||
| chr12:14423574 | C | CTT | 22 | a0001c0001t0016g0130 a0002c0002t0001g0204 a0002c0002t0001g0217 others(19): Show |
23 | HG00621.hp1 HG00621.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.-7-312_-7-311dupTT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14423574 | ||||||
| chr12:14423574 | CT | C | 10 | a0001c0001t0002g0023 a0001c0001t0003g0103 a0003c0003t0004g0192 others(7): Show |
12 | HG01167.hp1 HG01168.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-311delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14423574 | ||||||
| chr12:14423574 | CTTTTT | C | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-315_-7-311delTT others(3): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14423574 | ||||||
| chr12:14423651 | A | T | 1 | a0001c0001t0029g0063 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-7-258A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14423651 | |||||||
| chr12:14423655 | G | GA | 22 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(19): Show |
24 | HG00099.hp1 HG00280.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.-7-245dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 14423655 | ||||||
| chr12:14423719 | A | T | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-190A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14423719 | |||||||
| chr12:14423788 | A | G | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-7-121A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14423788 | |||||||
| chr12:14423809 | A | G | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.-7-100A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 1/14 | chr12 | 14423809 | |||||||
| chr12:14425545 | A | G | 1 | a0001c0001t0002g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1558+72A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14425545 | |||||||
| chr12:14425585 | G | A | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1558+112G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14425585 | |||||||
| chr12:14425640 | G | A | 2 | a0005c0007t0010g0314 a0005c0007t0010g0315 |
2 | HG01346.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1558+167G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14425640 | |||||||
| chr12:14425918 | A | G | 1 | a0002c0002t0001g0299 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1558+445A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14425918 | |||||||
| chr12:14425947 | T | C | 9 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(6): Show |
11 | HG00099.hp1 HG00280.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1558+474T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14425947 | |||||||
| chr12:14426035 | A | G | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1558+562A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426035 | |||||||
| chr12:14426079 | A | G | 1 | a0011c0016t0039g0244 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1558+606A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426079 | |||||||
| chr12:14426084 | C | A | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1558+611C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426084 | |||||||
| chr12:14426164 | T | A | 2 | a0002c0006t0008g0207 a0002c0006t0008g0292 |
2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1558+691T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426164 | |||||||
| chr12:14426301 | A | C | 184 | a0001c0020t0036g0134 a0002c0002t0001g0007 a0002c0002t0001g0204 others(181): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1558+828A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426301 | |||||||
| chr12:14426319 | G | C | 1 | a0003c0005t0007g0329 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1558+846G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426319 | |||||||
| chr12:14426464 | A | G | 1 | a0001c0001t0002g0035 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1558+991A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426464 | |||||||
| chr12:14426529 | C | CT | 26 | a0001c0001t0002g0021 a0001c0001t0002g0030 a0001c0001t0002g0033 others(23): Show |
26 | HG01261.hp1 HG01358.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.1558+1071dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 14426529 | ||||||
| chr12:14426637 | G | C | 1 | a0001c0001t0002g0028 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1558+1164G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426637 | |||||||
| chr12:14426653 | C | G | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1558+1180C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426653 | |||||||
| chr12:14426686 | C | T | 2 | a0004c0008t0005g0277 a0004c0008t0005g0280 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1558+1213C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426686 | |||||||
| chr12:14426712 | G | C | 28 | a0001c0020t0036g0134 a0003c0003t0004g0003 a0003c0003t0004g0186 others(25): Show |
29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1558+1239G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426712 | |||||||
| chr12:14426788 | T | C | 2 | a0002c0002t0001g0305 a0002c0002t0001g0306 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1558+1315T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426788 | |||||||
| chr12:14426823 | C | CAAAAAAA others(3): Show |
1 | a0003c0014t0013g0166 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1558+1368_1558+137 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 14426823 | ||||||
| chr12:14426823 | C | CAAAAAAA others(4): Show |
1 | a0003c0014t0013g0167 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1558+1367_1558+137 others(15): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 14426823 | ||||||
| chr12:14426823 | C | CAAAAAAA others(5): Show |
1 | a0003c0003t0013g0164 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1558+1366_1558+137 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 14426823 | ||||||
| chr12:14426847 | AAAAG | A | 15 | a0002c0002t0009g0009 a0002c0002t0009g0211 a0002c0002t0009g0212 others(12): Show |
15 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.1558+1375_1558+137 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426847 | |||||||
| chr12:14426848 | AAAG | A | 103 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0206 others(100): Show |
106 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1558+1376_1558+137 others(7): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426848 | |||||||
| chr12:14426849 | AAG | A | 34 | a0002c0002t0001g0205 a0002c0002t0001g0217 a0002c0002t0001g0254 others(31): Show |
34 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.1558+1377_1558+137 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426849 | |||||||
| chr12:14426850 | AG | A | 130 | a0001c0001t0002g0013 a0001c0001t0002g0016 a0001c0001t0002g0017 others(127): Show |
130 | HG00280.hp2 HG00673.hp1 HG00733.hp2 others(127): Show |
intron_variant | MODIFIER | c.1558+1379delG | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 14426850 | ||||||
| chr12:14426851 | G | A | 59 | a0001c0001t0002g0010 a0001c0001t0002g0027 a0001c0001t0002g0035 others(56): Show |
59 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.1558+1378G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426851 | |||||||
| chr12:14426881 | A | G | 14 | a0003c0003t0035g0340 a0003c0005t0007g0322 a0003c0005t0007g0323 others(11): Show |
14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1558+1408A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426881 | |||||||
| chr12:14426887 | C | A | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1558+1414C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426887 | |||||||
| chr12:14426973 | C | T | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1558+1500C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14426973 | |||||||
| chr12:14427106 | C | CAT | 28 | a0001c0020t0036g0134 a0003c0003t0004g0003 a0003c0003t0004g0186 others(25): Show |
29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1558+1634_1558+163 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 14427106 | ||||||
| chr12:14427204 | C | T | 103 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(100): Show |
104 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1558+1731C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427204 | |||||||
| chr12:14427213 | T | C | 14 | a0003c0003t0035g0340 a0003c0005t0007g0322 a0003c0005t0007g0323 others(11): Show |
14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1558+1740T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427213 | |||||||
| chr12:14427232 | C | G | 7 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(4): Show |
9 | HG00099.hp1 HG00280.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558+1759C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427232 | |||||||
| chr12:14427332 | C | T | 1 | a0003c0005t0007g0322 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1558+1859C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427332 | |||||||
| chr12:14427358 | T | C | 28 | a0001c0020t0036g0134 a0003c0003t0004g0003 a0003c0003t0004g0186 others(25): Show |
29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1558+1885T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427358 | |||||||
| chr12:14427394 | G | A | 4 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(1): Show |
4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558+1921G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427394 | |||||||
| chr12:14427479 | A | T | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1558+2006A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427479 | |||||||
| chr12:14427514 | C | T | 1 | a0002c0002t0001g0007 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1558+2041C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427514 | |||||||
| chr12:14427515 | G | A | 3 | a0001c0001t0002g0087 a0001c0001t0002g0121 a0001c0001t0002g0122 |
3 | HG02818.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1558+2042G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427515 | |||||||
| chr12:14427656 | G | A | 2 | a0001c0001t0003g0089 a0001c0001t0003g0100 |
2 | HG01081.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1558+2183G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427656 | |||||||
| chr12:14427749 | C | G | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1558+2276C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427749 | |||||||
| chr12:14427755 | T | C | 28 | a0001c0020t0036g0134 a0003c0003t0004g0003 a0003c0003t0004g0186 others(25): Show |
29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1558+2282T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427755 | |||||||
| chr12:14427804 | T | A | 1 | a0012c0015t0003g0097 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1558+2331T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427804 | |||||||
| chr12:14427915 | A | G | 13 | a0001c0001t0002g0027 a0001c0001t0003g0074 a0001c0001t0003g0075 others(10): Show |
13 | HG00609.hp1 HG00673.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.1558+2442A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427915 | |||||||
| chr12:14427954 | A | T | 1 | a0003c0003t0014g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1558+2481A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427954 | |||||||
| chr12:14427975 | C | T | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1558+2502C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14427975 | |||||||
| chr12:14428183 | A | G | 2 | a0004c0008t0005g0277 a0004c0008t0005g0280 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1558+2710A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14428183 | |||||||
| chr12:14428245 | G | A | 1 | a0001c0001t0003g0080 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1558+2772G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14428245 | |||||||
| chr12:14428515 | C | T | 141 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(138): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1558+3042C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14428515 | |||||||
| chr12:14428681 | A | G | 3 | a0002c0002t0001g0298 a0002c0002t0001g0299 a0002c0002t0001g0300 |
3 | NA18943.hp1 NA18949.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1558+3208A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14428681 | |||||||
| chr12:14428753 | T | G | 4 | a0001c0001t0014g0128 a0001c0001t0016g0078 a0001c0001t0016g0129 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558+3280T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14428753 | |||||||
| chr12:14428805 | C | T | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1558+3332C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14428805 | |||||||
| chr12:14428817 | CTATTTTA others(4): Show |
C | 1 | a0002c0006t0019g0221 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1558+3347_1558+335 others(15): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 14428817 | ||||||
| chr12:14428831 | C | G | 1 | a0002c0006t0019g0221 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1558+3358C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14428831 | |||||||
| chr12:14428831 | C | T | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558+3358C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14428831 | |||||||
| chr12:14428855 | A | C | 7 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(4): Show |
9 | HG00099.hp1 HG00280.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558+3382A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14428855 | |||||||
| chr12:14429173 | C | T | 1 | a0004c0008t0005g0276 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1558+3700C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14429173 | |||||||
| chr12:14429183 | A | T | 1 | a0013c0017t0001g0265 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1558+3710A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14429183 | |||||||
| chr12:14429207 | A | G | 25 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(22): Show |
26 | HG00733.hp2 HG01123.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.1558+3734A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14429207 | |||||||
| chr12:14429213 | A | G | 3 | a0002c0002t0001g0247 a0002c0002t0001g0248 a0002c0002t0001g0308 |
3 | NA18947.hp1 NA18979.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1558+3740A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14429213 | |||||||
| chr12:14429403 | G | A | 1 | a0002c0002t0001g0233 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1558+3930G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14429403 | |||||||
| chr12:14429906 | A | G | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1559-4431A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14429906 | |||||||
| chr12:14429941 | T | G | 1 | a0001c0001t0003g0112 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1559-4396T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14429941 | |||||||
| chr12:14429966 | A | G | 1 | a0002c0004t0001g0239 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1559-4371A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14429966 | |||||||
| chr12:14430176 | G | A | 36 | a0001c0001t0002g0017 a0001c0001t0002g0028 a0001c0001t0002g0029 others(33): Show |
36 | HG01175.hp1 HG01257.hp1 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.1559-4161G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14430176 | |||||||
| chr12:14430556 | T | C | 7 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(4): Show |
9 | HG00099.hp1 HG00280.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1559-3781T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14430556 | |||||||
| chr12:14430654 | A | G | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1559-3683A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14430654 | |||||||
| chr12:14430776 | A | G | 1 | a0002c0002t0001g0294 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1559-3561A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14430776 | |||||||
| chr12:14430947 | T | C | 1 | a0002c0002t0001g0283 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1559-3390T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14430947 | |||||||
| chr12:14431062 | A | G | 1 | a0006c0009t0005g0175 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1559-3275A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431062 | |||||||
| chr12:14431165 | A | G | 3 | a0003c0003t0004g0197 a0003c0003t0004g0198 a0003c0003t0004g0199 |
3 | HG02970.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1559-3172A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431165 | |||||||
| chr12:14431196 | C | G | 1 | a0003c0003t0011g0203 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1559-3141C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431196 | |||||||
| chr12:14431258 | T | G | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1559-3079T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431258 | |||||||
| chr12:14431318 | A | G | 3 | a0007c0010t0002g0014 a0007c0010t0002g0025 a0007c0010t0002g0052 |
3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1559-3019A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431318 | |||||||
| chr12:14431359 | A | G | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1559-2978A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431359 | |||||||
| chr12:14431398 | C | CT | 30 | a0002c0002t0037g0236 a0003c0003t0004g0003 a0003c0003t0004g0186 others(27): Show |
31 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.1559-2925dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 14431398 | ||||||
| chr12:14431420 | C | A | 176 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(173): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1559-2917C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431420 | |||||||
| chr12:14431420 | C | T | 4 | a0001c0001t0014g0128 a0001c0001t0016g0078 a0001c0001t0016g0129 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1559-2917C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431420 | |||||||
| chr12:14431445 | A | G | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1559-2892A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431445 | |||||||
| chr12:14431457 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1559-2880C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431457 | |||||||
| chr12:14431504 | C | T | 1 | a0001c0001t0003g0080 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1559-2833C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431504 | |||||||
| chr12:14431604 | C | G | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1559-2733C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431604 | |||||||
| chr12:14431640 | C | T | 3 | a0003c0003t0005g0160 a0003c0003t0014g0159 a0003c0003t0014g0161 |
3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1559-2697C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431640 | |||||||
| chr12:14431669 | T | C | 149 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(146): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1559-2668T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431669 | |||||||
| chr12:14431673 | T | C | 149 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(146): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1559-2664T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431673 | |||||||
| chr12:14431678 | G | A | 149 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(146): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1559-2659G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431678 | |||||||
| chr12:14431683 | C | T | 149 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(146): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1559-2654C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431683 | |||||||
| chr12:14431684 | A | G | 149 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(146): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1559-2653A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431684 | |||||||
| chr12:14431686 | A | G | 149 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(146): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1559-2651A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431686 | |||||||
| chr12:14431689 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1559-2648C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431689 | |||||||
| chr12:14431722 | T | G | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1559-2615T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431722 | |||||||
| chr12:14431899 | G | A | 4 | a0002c0002t0001g0266 a0002c0002t0001g0268 a0002c0002t0001g0275 others(1): Show |
4 | HG02132.hp1 NA18941.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1559-2438G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431899 | |||||||
| chr12:14431914 | T | A | 1 | a0001c0001t0002g0037 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1559-2423T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431914 | |||||||
| chr12:14431953 | C | T | 1 | a0002c0002t0001g0295 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1559-2384C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14431953 | |||||||
| chr12:14432145 | G | A | 183 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(180): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.1559-2192G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432145 | |||||||
| chr12:14432150 | T | C | 337 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(334): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1559-2187T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432150 | |||||||
| chr12:14432257 | C | G | 1 | a0001c0001t0002g0059 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1559-2080C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432257 | |||||||
| chr12:14432269 | G | A | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1559-2068G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432269 | |||||||
| chr12:14432395 | G | C | 4 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(1): Show |
4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1559-1942G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432395 | |||||||
| chr12:14432400 | C | G | 2 | a0008c0012t0011g0335 a0008c0012t0011g0336 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1559-1937C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432400 | |||||||
| chr12:14432549 | T | C | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1559-1788T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432549 | |||||||
| chr12:14432559 | G | A | 1 | a0001c0001t0002g0143 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1559-1778G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432559 | |||||||
| chr12:14432584 | G | A | 1 | a0003c0003t0005g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1559-1753G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432584 | |||||||
| chr12:14432899 | T | C | 16 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(13): Show |
17 | HG01123.hp2 HG02257.hp1 HG02970.hp2 others(14): Show |
intron_variant | MODIFIER | c.1559-1438T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432899 | |||||||
| chr12:14432970 | G | A | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1559-1367G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14432970 | |||||||
| chr12:14433007 | A | G | 3 | a0002c0002t0001g0208 a0002c0002t0001g0209 a0002c0002t0037g0236 |
3 | HG01256.hp1 HG01258.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1559-1330A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433007 | |||||||
| chr12:14433086 | G | A | 2 | a0003c0003t0011g0185 a0003c0003t0028g0184 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1559-1251G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433086 | |||||||
| chr12:14433106 | C | T | 13 | a0002c0006t0008g0207 a0002c0006t0008g0216 a0002c0006t0008g0218 others(10): Show |
13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1559-1231C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433106 | |||||||
| chr12:14433211 | A | G | 1 | a0011c0016t0039g0244 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1559-1126A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433211 | |||||||
| chr12:14433319 | A | G | 4 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(1): Show |
4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1559-1018A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433319 | |||||||
| chr12:14433420 | G | A | 2 | a0001c0001t0002g0037 a0001c0001t0002g0038 |
2 | HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1559-917G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433420 | |||||||
| chr12:14433424 | G | C | 1 | a0003c0003t0011g0185 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1559-913G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433424 | |||||||
| chr12:14433466 | C | T | 2 | a0003c0003t0004g0195 a0003c0003t0004g0196 |
2 | HG00733.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1559-871C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433466 | |||||||
| chr12:14433538 | C | T | 1 | a0001c0001t0003g0131 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1559-799C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433538 | |||||||
| chr12:14433641 | G | T | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1559-696G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433641 | |||||||
| chr12:14433748 | G | T | 1 | a0001c0001t0002g0037 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1559-589G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433748 | |||||||
| chr12:14433937 | C | T | 7 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1559-400C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14433937 | |||||||
| chr12:14434083 | T | A | 176 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(173): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1559-254T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 2/14 | chr12 | 14434083 | |||||||
| chr12:14434474 | G | A | 1 | a0002c0002t0009g0213 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1645+51G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14434474 | |||||||
| chr12:14434513 | A | G | 2 | a0001c0001t0003g0113 a0001c0001t0003g0114 |
2 | HG01106.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1645+90A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14434513 | |||||||
| chr12:14434678 | G | T | 12 | a0001c0001t0003g0074 a0001c0001t0003g0075 a0001c0001t0003g0080 others(9): Show |
12 | HG00609.hp1 HG00673.hp1 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.1645+255G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14434678 | |||||||
| chr12:14434793 | C | T | 167 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(164): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1645+370C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14434793 | |||||||
| chr12:14434939 | T | A | 1 | a0003c0005t0041g0334 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1645+516T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14434939 | |||||||
| chr12:14435116 | A | G | 1 | a0002c0004t0001g0241 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1645+693A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14435116 | |||||||
| chr12:14435117 | C | G | 1 | a0002c0004t0001g0241 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1645+694C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14435117 | |||||||
| chr12:14435122 | AGGAAGGA others(4): Show |
A | 3 | a0002c0002t0001g0297 a0003c0014t0013g0166 a0003c0014t0013g0167 |
3 | NA18984.hp2 NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1645+709_1645+719d others(13): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 14435122 | ||||||
| chr12:14435133 | G | GGGAA | 4 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(1): Show |
4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1645+727_1645+730d others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 14435133 | ||||||
| chr12:14435151 | G | A | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1645+728G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14435151 | |||||||
| chr12:14435276 | T | C | 1 | a0014c0019t0001g0310 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1646-830T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14435276 | |||||||
| chr12:14435436 | T | C | 1 | a0003c0003t0004g0192 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1646-670T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14435436 | |||||||
| chr12:14435457 | A | C | 4 | a0003c0003t0014g0171 a0003c0003t0023g0154 a0003c0003t0023g0155 others(1): Show |
4 | HG01099.hp1 HG02300.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1646-649A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14435457 | |||||||
| chr12:14435470 | C | G | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1646-636C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14435470 | |||||||
| chr12:14435507 | A | G | 1 | a0012c0015t0003g0097 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1646-599A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14435507 | |||||||
| chr12:14435877 | C | T | 41 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(38): Show |
42 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.1646-229C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14435877 | |||||||
| chr12:14436063 | A | G | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1646-43A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 3/14 | chr12 | 14436063 | |||||||
| chr12:14436582 | C | T | 1 | a0002c0002t0001g0270 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1791+331C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14436582 | |||||||
| chr12:14436599 | G | A | 14 | a0003c0003t0035g0340 a0003c0005t0007g0322 a0003c0005t0007g0323 others(11): Show |
14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1791+348G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14436599 | |||||||
| chr12:14436640 | C | T | 1 | a0001c0001t0003g0090 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1791+389C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14436640 | |||||||
| chr12:14436782 | CT | C | 164 | a0001c0001t0002g0036 a0001c0001t0003g0011 a0001c0001t0003g0075 others(161): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.1791+544delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr12 | 14436782 | ||||||
| chr12:14436793 | T | A | 2 | a0006c0009t0005g0174 a0006c0009t0005g0175 |
2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1791+542T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14436793 | |||||||
| chr12:14436794 | T | A | 7 | a0002c0002t0001g0256 a0006c0009t0005g0174 a0006c0009t0005g0175 others(4): Show |
7 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1791+543T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14436794 | |||||||
| chr12:14436795 | T | A | 109 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(106): Show |
110 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1791+544T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14436795 | |||||||
| chr12:14437055 | G | A | 167 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(164): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1791+804G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437055 | |||||||
| chr12:14437585 | G | A | 2 | a0008c0012t0011g0335 a0008c0012t0011g0336 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1792-545G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437585 | |||||||
| chr12:14437674 | G | A | 1 | a0002c0004t0001g0241 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1792-456G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437674 | |||||||
| chr12:14437797 | T | C | 1 | a0001c0001t0002g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1792-333T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437797 | |||||||
| chr12:14437829 | G | A | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1792-301G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437829 | |||||||
| chr12:14437878 | C | A | 1 | a0002c0002t0001g0283 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1792-252C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437878 | |||||||
| chr12:14437910 | G | A | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1792-220G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437910 | |||||||
| chr12:14437916 | A | G | 2 | a0001c0001t0021g0032 a0001c0001t0021g0039 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1792-214A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437916 | |||||||
| chr12:14437926 | G | A | 4 | a0003c0003t0014g0171 a0003c0003t0023g0154 a0003c0003t0023g0155 others(1): Show |
4 | HG01099.hp1 HG02300.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1792-204G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437926 | |||||||
| chr12:14437929 | T | G | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1792-201T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437929 | |||||||
| chr12:14437977 | C | T | 1 | a0001c0001t0006g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1792-153C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437977 | |||||||
| chr12:14437978 | G | A | 11 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1792-152G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14437978 | |||||||
| chr12:14438047 | T | C | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1792-83T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14438047 | |||||||
| chr12:14438052 | C | T | 1 | a0001c0001t0003g0081 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1792-78C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 4/14 | chr12 | 14438052 | |||||||
| chr12:14438286 | G | A | 174 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(171): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1929+19G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14438286 | |||||||
| chr12:14438779 | G | T | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1929+512G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14438779 | |||||||
| chr12:14439272 | T | C | 4 | a0001c0001t0003g0088 a0001c0001t0003g0095 a0001c0001t0033g0096 others(1): Show |
4 | HG00741.hp1 HG01993.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1929+1005T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14439272 | |||||||
| chr12:14439325 | C | T | 1 | a0001c0001t0003g0112 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1929+1058C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14439325 | |||||||
| chr12:14439539 | C | T | 5 | a0001c0001t0003g0077 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02165.hp1 HG03239.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.1929+1272C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14439539 | |||||||
| chr12:14439583 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1929+1316C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14439583 | |||||||
| chr12:14439593 | G | T | 2 | a0001c0001t0003g0077 a0001c0001t0040g0142 |
2 | HG02165.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1929+1326G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14439593 | |||||||
| chr12:14439840 | A | AATCC | 44 | a0001c0001t0002g0017 a0001c0001t0002g0037 a0001c0001t0002g0038 others(41): Show |
45 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1929+1618_1929+162 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14439840 | ||||||
| chr12:14439840 | A | AATCCATC others(1): Show |
13 | a0001c0001t0002g0041 a0001c0001t0002g0044 a0001c0001t0002g0045 others(10): Show |
13 | HG01175.hp1 HG01358.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.1929+1614_1929+162 others(12): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14439840 | ||||||
| chr12:14439840 | AATCC | A | 125 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0018 others(122): Show |
127 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.1929+1618_1929+162 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14439840 | ||||||
| chr12:14439840 | AATCCATC others(5): Show |
A | 14 | a0001c0001t0002g0087 a0001c0001t0002g0121 a0001c0001t0002g0122 others(11): Show |
14 | HG01167.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1929+1610_1929+162 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14439840 | ||||||
| chr12:14439840 | AATCCATC others(13): Show |
A | 1 | a0002c0006t0008g0218 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1929+1602_1929+162 others(24): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14439840 | ||||||
| chr12:14439840 | AATCCATC others(17): Show |
A | 7 | a0002c0002t0001g0297 a0003c0003t0013g0162 a0003c0003t0013g0163 others(4): Show |
7 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.1929+1598_1929+162 others(28): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14439840 | ||||||
| chr12:14439889 | T | A | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1929+1622T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14439889 | |||||||
| chr12:14439909 | A | G | 92 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(89): Show |
93 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1929+1642A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14439909 | |||||||
| chr12:14439945 | A | G | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1929+1678A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14439945 | |||||||
| chr12:14440086 | G | A | 174 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(171): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1929+1819G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14440086 | |||||||
| chr12:14440140 | A | G | 1 | a0003c0005t0041g0334 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1929+1873A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14440140 | |||||||
| chr12:14440239 | A | G | 13 | a0001c0001t0002g0027 a0001c0001t0003g0074 a0001c0001t0003g0075 others(10): Show |
13 | HG00609.hp1 HG00673.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.1929+1972A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14440239 | |||||||
| chr12:14440353 | C | G | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1929+2086C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14440353 | |||||||
| chr12:14440636 | AC | A | 102 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(99): Show |
103 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1929+2371delC | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14440636 | ||||||
| chr12:14440751 | G | A | 2 | a0003c0003t0011g0185 a0003c0003t0028g0184 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1929+2484G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14440751 | |||||||
| chr12:14440968 | T | C | 79 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(76): Show |
80 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1929+2701T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14440968 | |||||||
| chr12:14441007 | C | G | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1929+2740C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441007 | |||||||
| chr12:14441035 | T | C | 1 | a0002c0006t0019g0221 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1929+2768T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441035 | |||||||
| chr12:14441054 | T | G | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1929+2787T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441054 | |||||||
| chr12:14441108 | T | C | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1929+2841T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441108 | |||||||
| chr12:14441143 | A | G | 1 | a0003c0003t0013g0164 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1929+2876A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441143 | |||||||
| chr12:14441283 | A | G | 1 | a0003c0003t0005g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1929+3016A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441283 | |||||||
| chr12:14441421 | AT | A | 4 | a0003c0003t0014g0171 a0003c0003t0023g0154 a0003c0003t0023g0155 others(1): Show |
4 | HG01099.hp1 HG02300.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1929+3157delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14441421 | ||||||
| chr12:14441487 | C | CT | 93 | a0001c0001t0002g0010 a0001c0001t0002g0016 a0001c0001t0002g0019 others(90): Show |
97 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1929+3240dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14441487 | ||||||
| chr12:14441487 | CTTTTTTT others(3): Show |
C | 7 | a0002c0002t0001g0247 a0002c0002t0001g0248 a0002c0002t0001g0259 others(4): Show |
8 | NA18612.hp1 NA18945.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.1929+3231_1929+324 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14441487 | ||||||
| chr12:14441591 | G | A | 2 | a0003c0003t0004g0195 a0003c0003t0004g0196 |
2 | HG00733.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1929+3324G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441591 | |||||||
| chr12:14441678 | A | T | 1 | a0003c0003t0005g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1929+3411A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441678 | |||||||
| chr12:14441800 | A | C | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1929+3533A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441800 | |||||||
| chr12:14441806 | C | T | 167 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(164): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1929+3539C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441806 | |||||||
| chr12:14441870 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1929+3603G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14441870 | |||||||
| chr12:14442127 | T | C | 4 | a0003c0003t0011g0203 a0003c0003t0011g0311 a0003c0003t0011g0312 others(1): Show |
4 | HG02280.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1929+3860T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14442127 | |||||||
| chr12:14442136 | A | G | 13 | a0002c0006t0008g0207 a0002c0006t0008g0216 a0002c0006t0008g0218 others(10): Show |
13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1929+3869A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14442136 | |||||||
| chr12:14442235 | A | G | 1 | a0002c0002t0001g0217 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1929+3968A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14442235 | |||||||
| chr12:14442406 | A | G | 27 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(24): Show |
28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1929+4139A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14442406 | |||||||
| chr12:14442459 | C | T | 4 | a0001c0001t0014g0128 a0001c0001t0016g0078 a0001c0001t0016g0129 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1929+4192C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14442459 | |||||||
| chr12:14442522 | G | A | 176 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(173): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1929+4255G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14442522 | |||||||
| chr12:14442677 | A | G | 1 | a0003c0005t0007g0326 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1930-4311A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14442677 | |||||||
| chr12:14442822 | G | A | 141 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(138): Show |
141 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.1930-4166G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14442822 | |||||||
| chr12:14443032 | G | C | 1 | a0003c0003t0011g0338 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1930-3956G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14443032 | |||||||
| chr12:14443255 | A | T | 1 | a0010c0013t0020g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1930-3733A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14443255 | |||||||
| chr12:14443382 | G | GA | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1930-3599dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14443382 | ||||||
| chr12:14443414 | A | C | 1 | a0002c0002t0001g0304 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1930-3574A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14443414 | |||||||
| chr12:14443568 | G | A | 1 | a0002c0002t0037g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1930-3420G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14443568 | |||||||
| chr12:14443592 | G | C | 1 | a0002c0002t0001g0297 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1930-3396G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14443592 | |||||||
| chr12:14443691 | G | A | 11 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1930-3297G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14443691 | |||||||
| chr12:14443697 | T | G | 1 | a0003c0003t0034g0153 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1930-3291T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14443697 | |||||||
| chr12:14443846 | T | G | 1 | a0002c0002t0001g0272 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1930-3142T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14443846 | |||||||
| chr12:14444022 | A | G | 2 | a0001c0001t0003g0089 a0001c0001t0003g0100 |
2 | HG01081.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1930-2966A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14444022 | |||||||
| chr12:14444221 | T | A | 1 | a0002c0002t0001g0296 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1930-2767T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14444221 | |||||||
| chr12:14444508 | A | AAAT | 7 | a0002c0002t0001g0204 a0002c0002t0001g0222 a0002c0002t0001g0254 others(4): Show |
7 | HG00099.hp2 HG00621.hp2 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.1930-2479_1930-247 others(7): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14444508 | ||||||
| chr12:14444533 | A | T | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1930-2455A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14444533 | |||||||
| chr12:14444542 | C | T | 4 | a0003c0003t0015g0002 a0003c0003t0015g0168 a0003c0003t0015g0169 others(1): Show |
5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1930-2446C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14444542 | |||||||
| chr12:14444755 | C | A | 2 | a0003c0003t0004g0195 a0003c0003t0004g0196 |
2 | HG00733.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1930-2233C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14444755 | |||||||
| chr12:14444841 | C | T | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1930-2147C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14444841 | |||||||
| chr12:14444901 | T | C | 1 | a0001c0001t0002g0071 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1930-2087T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14444901 | |||||||
| chr12:14444987 | C | G | 2 | a0003c0003t0011g0185 a0003c0003t0028g0184 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1930-2001C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14444987 | |||||||
| chr12:14444990 | G | GT | 31 | a0001c0001t0003g0123 a0001c0001t0006g0132 a0003c0003t0004g0003 others(28): Show |
32 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.1930-1979dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14444990 | ||||||
| chr12:14444995 | T | G | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1930-1993T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14444995 | |||||||
| chr12:14445041 | G | C | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1930-1947G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445041 | |||||||
| chr12:14445054 | C | A | 1 | a0001c0001t0003g0112 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1930-1934C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445054 | |||||||
| chr12:14445055 | G | A | 4 | a0003c0003t0015g0002 a0003c0003t0015g0168 a0003c0003t0015g0169 others(1): Show |
5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1930-1933G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445055 | |||||||
| chr12:14445060 | C | T | 2 | a0003c0003t0011g0185 a0003c0003t0028g0184 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1930-1928C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445060 | |||||||
| chr12:14445107 | C | T | 3 | a0003c0003t0005g0160 a0003c0003t0014g0159 a0003c0003t0014g0161 |
3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1930-1881C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445107 | |||||||
| chr12:14445116 | G | A | 140 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(137): Show |
140 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.1930-1872G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445116 | |||||||
| chr12:14445153 | G | A | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1930-1835G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445153 | |||||||
| chr12:14445165 | A | G | 4 | a0003c0003t0015g0002 a0003c0003t0015g0168 a0003c0003t0015g0169 others(1): Show |
5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1930-1823A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445165 | |||||||
| chr12:14445222 | CT | C | 4 | a0003c0003t0015g0002 a0003c0003t0015g0168 a0003c0003t0015g0169 others(1): Show |
5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1930-1764delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14445222 | ||||||
| chr12:14445298 | G | T | 3 | a0003c0003t0005g0160 a0003c0003t0014g0159 a0003c0003t0014g0161 |
3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1930-1690G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445298 | |||||||
| chr12:14445393 | C | CT | 14 | a0003c0003t0005g0313 a0003c0003t0012g0001 a0003c0003t0012g0180 others(11): Show |
17 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1930-1585dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14445393 | ||||||
| chr12:14445793 | A | T | 2 | a0003c0003t0004g0003 a0003c0003t0004g0193 |
3 | NA18968.hp1 NA19007.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1930-1195A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445793 | |||||||
| chr12:14445927 | C | T | 1 | a0005c0007t0010g0319 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1930-1061C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14445927 | |||||||
| chr12:14446155 | G | GT | 8 | a0002c0006t0019g0227 a0003c0003t0012g0181 a0006c0009t0005g0174 others(5): Show |
8 | HG02135.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1930-823dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14446155 | ||||||
| chr12:14446158 | T | C | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1930-830T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14446158 | |||||||
| chr12:14446195 | T | G | 13 | a0002c0006t0008g0207 a0002c0006t0008g0216 a0002c0006t0008g0218 others(10): Show |
13 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1930-793T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14446195 | |||||||
| chr12:14446208 | C | T | 1 | a0003c0003t0011g0338 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1930-780C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14446208 | |||||||
| chr12:14446210 | C | T | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1930-778C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14446210 | |||||||
| chr12:14446374 | T | A | 1 | a0002c0002t0009g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1930-614T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14446374 | |||||||
| chr12:14446835 | A | C | 1 | a0003c0003t0011g0185 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1930-153A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14446835 | |||||||
| chr12:14446906 | T | C | 1 | a0003c0003t0005g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1930-82T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14446906 | |||||||
| chr12:14446912 | A | G | 1 | a0002c0002t0001g0283 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1930-76A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | chr12 | 14446912 | |||||||
| chr12:14446921 | G | GT | 11 | a0001c0001t0002g0143 a0002c0002t0009g0008 a0002c0002t0009g0009 others(8): Show |
11 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1930-56dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14446921 | ||||||
| chr12:14446921 | GT | G | 8 | a0002c0002t0001g0293 a0002c0002t0001g0297 a0003c0005t0007g0322 others(5): Show |
8 | HG02145.hp2 HG02451.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1930-56delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14446921 | ||||||
| chr12:14446970 | C | CT | 305 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0028 others(302): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
splice_region_variant&intron_variant | LOW | c.1930-4dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14446970 | ||||||
| chr12:14446970 | C | CTT | 29 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0018 others(26): Show |
29 | HG00639.hp1 HG01243.hp1 HG01261.hp2 others(26): Show |
splice_region_variant&intron_variant | LOW | c.1930-5_1930-4dupTT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 14446970 | ||||||
| chr12:14447067 | A | G | 1 | a0003c0003t0011g0321 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1995+14A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14447067 | |||||||
| chr12:14447281 | CT | C | 180 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(177): Show |
182 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(179): Show |
intron_variant | MODIFIER | c.1995+248delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 14447281 | ||||||
| chr12:14447281 | CTT | C | 53 | a0001c0001t0002g0035 a0001c0001t0002g0059 a0001c0001t0002g0072 others(50): Show |
56 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1995+247_1995+248d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 14447281 | ||||||
| chr12:14447281 | CTTT | C | 90 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(87): Show |
91 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1995+246_1995+248d others(5): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 14447281 | ||||||
| chr12:14447502 | G | A | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995+449G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14447502 | |||||||
| chr12:14447508 | C | T | 1 | a0003c0005t0041g0334 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1995+455C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14447508 | |||||||
| chr12:14447591 | T | C | 4 | a0003c0003t0011g0203 a0003c0003t0011g0311 a0003c0003t0011g0312 others(1): Show |
4 | HG02280.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1995+538T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14447591 | |||||||
| chr12:14447629 | A | T | 28 | a0001c0020t0036g0134 a0003c0003t0004g0003 a0003c0003t0004g0186 others(25): Show |
29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1995+576A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14447629 | |||||||
| chr12:14447698 | C | T | 1 | a0002c0002t0001g0243 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1995+645C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14447698 | |||||||
| chr12:14447745 | A | G | 26 | a0001c0020t0036g0134 a0003c0003t0004g0003 a0003c0003t0004g0186 others(23): Show |
27 | HG00733.hp2 HG01123.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1995+692A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14447745 | |||||||
| chr12:14447815 | A | G | 2 | a0003c0003t0004g0186 a0003c0003t0004g0187 |
2 | NA18967.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1995+762A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14447815 | |||||||
| chr12:14448044 | T | C | 1 | a0001c0001t0002g0339 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1995+991T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14448044 | |||||||
| chr12:14448060 | AT | A | 140 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(137): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.1995+1015delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 14448060 | ||||||
| chr12:14448316 | T | C | 3 | a0002c0004t0001g0238 a0002c0004t0001g0239 a0002c0004t0001g0242 |
3 | HG01934.hp2 HG02148.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1995+1263T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14448316 | |||||||
| chr12:14448466 | C | T | 1 | a0003c0003t0014g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1995+1413C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14448466 | |||||||
| chr12:14448725 | C | G | 3 | a0003c0003t0005g0160 a0003c0003t0014g0159 a0003c0003t0014g0161 |
3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1995+1672C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14448725 | |||||||
| chr12:14448804 | C | T | 4 | a0003c0003t0015g0002 a0003c0003t0015g0168 a0003c0003t0015g0169 others(1): Show |
5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1995+1751C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14448804 | |||||||
| chr12:14448998 | C | T | 1 | a0002c0002t0001g0270 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1995+1945C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14448998 | |||||||
| chr12:14449058 | CTT | C | 9 | a0003c0003t0035g0340 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1995+2006_1995+200 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14449058 | |||||||
| chr12:14449427 | T | C | 1 | a0002c0002t0001g0204 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1995+2374T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14449427 | |||||||
| chr12:14449495 | T | C | 1 | a0002c0002t0001g0243 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1995+2442T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14449495 | |||||||
| chr12:14449529 | A | G | 1 | a0001c0001t0003g0117 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1995+2476A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14449529 | |||||||
| chr12:14449791 | G | C | 4 | a0003c0003t0011g0203 a0003c0003t0011g0311 a0003c0003t0011g0312 others(1): Show |
4 | HG02280.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1995+2738G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14449791 | |||||||
| chr12:14449965 | TG | T | 4 | a0003c0003t0015g0002 a0003c0003t0015g0168 a0003c0003t0015g0169 others(1): Show |
5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1995+2913delG | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14449965 | |||||||
| chr12:14450011 | G | A | 1 | a0001c0001t0002g0016 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1995+2958G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14450011 | |||||||
| chr12:14450045 | T | C | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1995+2992T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14450045 | |||||||
| chr12:14450159 | CT | C | 92 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(89): Show |
93 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1995+3111delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 14450159 | ||||||
| chr12:14450212 | A | C | 11 | a0001c0001t0006g0073 a0001c0001t0006g0079 a0001c0001t0006g0132 others(8): Show |
11 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1995+3159A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14450212 | |||||||
| chr12:14450585 | AT | A | 7 | a0002c0002t0001g0297 a0003c0003t0013g0162 a0003c0003t0013g0163 others(4): Show |
7 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.1995+3533delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14450585 | |||||||
| chr12:14450758 | T | C | 7 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1995+3705T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14450758 | |||||||
| chr12:14451086 | T | C | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1995+4033T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14451086 | |||||||
| chr12:14451222 | T | C | 1 | a0002c0002t0001g0271 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1995+4169T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14451222 | |||||||
| chr12:14451285 | T | C | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1995+4232T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14451285 | |||||||
| chr12:14451518 | C | T | 2 | a0002c0002t0009g0008 a0002c0002t0009g0009 |
2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1995+4465C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14451518 | |||||||
| chr12:14451619 | G | GT | 8 | a0001c0001t0031g0012 a0002c0002t0001g0297 a0003c0003t0013g0162 others(5): Show |
8 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.1995+4577dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 14451619 | ||||||
| chr12:14451706 | A | G | 1 | a0001c0020t0036g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1995+4653A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14451706 | |||||||
| chr12:14451891 | A | G | 2 | a0008c0012t0011g0335 a0008c0012t0011g0336 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1996-4670A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14451891 | |||||||
| chr12:14451967 | A | G | 27 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(24): Show |
28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1996-4594A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14451967 | |||||||
| chr12:14451978 | G | T | 92 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(89): Show |
93 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1996-4583G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14451978 | |||||||
| chr12:14452190 | T | C | 1 | a0001c0001t0003g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1996-4371T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14452190 | |||||||
| chr12:14452288 | A | C | 7 | a0002c0002t0001g0297 a0003c0003t0013g0162 a0003c0003t0013g0163 others(4): Show |
7 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.1996-4273A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14452288 | |||||||
| chr12:14452308 | G | A | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1996-4253G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14452308 | |||||||
| chr12:14453209 | G | A | 1 | a0002c0004t0001g0238 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1996-3352G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14453209 | |||||||
| chr12:14453384 | G | T | 3 | a0005c0007t0010g0005 a0005c0007t0010g0318 a0005c0007t0010g0320 |
4 | HG03490.hp2 HG03492.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1996-3177G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14453384 | |||||||
| chr12:14453452 | G | A | 1 | a0003c0003t0014g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1996-3109G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14453452 | |||||||
| chr12:14453599 | C | T | 1 | a0003c0003t0011g0338 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1996-2962C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14453599 | |||||||
| chr12:14453676 | G | A | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1996-2885G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14453676 | |||||||
| chr12:14453788 | C | G | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1996-2773C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14453788 | |||||||
| chr12:14453850 | C | T | 2 | a0008c0012t0011g0335 a0008c0012t0011g0336 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1996-2711C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14453850 | |||||||
| chr12:14453871 | C | T | 1 | a0003c0003t0011g0321 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1996-2690C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14453871 | |||||||
| chr12:14453872 | G | T | 1 | a0003c0003t0004g0200 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1996-2689G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14453872 | |||||||
| chr12:14454208 | T | C | 28 | a0001c0020t0036g0134 a0003c0003t0004g0003 a0003c0003t0004g0186 others(25): Show |
29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1996-2353T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14454208 | |||||||
| chr12:14454423 | A | G | 3 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0062 |
3 | NA18612.hp2 NA18993.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1996-2138A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14454423 | |||||||
| chr12:14454498 | G | A | 1 | a0003c0003t0018g0156 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1996-2063G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14454498 | |||||||
| chr12:14454552 | G | A | 1 | a0001c0001t0003g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1996-2009G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14454552 | |||||||
| chr12:14454637 | G | C | 175 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(172): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1996-1924G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14454637 | |||||||
| chr12:14454697 | A | G | 27 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(24): Show |
28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1996-1864A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14454697 | |||||||
| chr12:14454787 | C | A | 139 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(136): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.1996-1774C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14454787 | |||||||
| chr12:14454892 | A | G | 3 | a0002c0004t0001g0239 a0002c0004t0001g0242 a0003c0003t0014g0152 |
3 | HG01934.hp2 HG02148.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1996-1669A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14454892 | |||||||
| chr12:14455000 | A | G | 183 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(180): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.1996-1561A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14455000 | |||||||
| chr12:14455036 | G | A | 3 | a0001c0001t0003g0102 a0001c0001t0003g0103 a0001c0001t0003g0104 |
3 | HG01069.hp1 HG01071.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1996-1525G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14455036 | |||||||
| chr12:14455125 | C | G | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1996-1436C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14455125 | |||||||
| chr12:14455138 | G | A | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1996-1423G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14455138 | |||||||
| chr12:14455182 | C | CA | 16 | a0001c0001t0002g0053 a0001c0001t0002g0059 a0001c0001t0002g0061 others(13): Show |
16 | HG00741.hp1 HG01099.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1996-1360dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 14455182 | ||||||
| chr12:14455182 | CA | C | 25 | a0001c0001t0003g0098 a0001c0001t0003g0108 a0001c0001t0003g0149 others(22): Show |
27 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.1996-1360delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 14455182 | ||||||
| chr12:14455439 | A | G | 4 | a0001c0001t0003g0086 a0001c0001t0003g0117 a0001c0001t0022g0084 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1996-1122A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14455439 | |||||||
| chr12:14455468 | A | C | 1 | a0003c0003t0011g0185 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1996-1093A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14455468 | |||||||
| chr12:14455741 | C | T | 3 | a0003c0003t0005g0160 a0003c0003t0014g0159 a0003c0003t0014g0161 |
3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1996-820C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14455741 | |||||||
| chr12:14455789 | G | A | 2 | a0001c0001t0002g0057 a0001c0001t0002g0058 |
2 | NA18612.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1996-772G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14455789 | |||||||
| chr12:14455865 | G | A | 149 | a0001c0001t0002g0021 a0002c0002t0001g0007 a0002c0002t0001g0204 others(146): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1996-696G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14455865 | |||||||
| chr12:14456148 | G | C | 187 | a0001c0001t0003g0119 a0001c0020t0036g0134 a0002c0002t0001g0007 others(184): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1996-413G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14456148 | |||||||
| chr12:14456319 | AT | A | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1996-240delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 14456319 | ||||||
| chr12:14456410 | A | T | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1996-151A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 6/14 | chr12 | 14456410 | |||||||
| chr12:14456645 | A | G | 1 | a0001c0001t0002g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2069+11A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 7/14 | chr12 | 14456645 | |||||||
| chr12:14457160 | C | G | 2 | a0003c0014t0013g0166 a0003c0014t0013g0167 |
2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2070-47C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 7/14 | chr12 | 14457160 | |||||||
| chr12:14457505 | A | G | 183 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(180): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.2158+210A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14457505 | |||||||
| chr12:14457536 | A | T | 1 | a0003c0003t0011g0321 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2158+241A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14457536 | |||||||
| chr12:14457628 | T | C | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.2158+333T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14457628 | |||||||
| chr12:14457657 | A | G | 1 | a0001c0001t0003g0117 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2158+362A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14457657 | |||||||
| chr12:14457726 | G | T | 112 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(109): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.2158+431G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14457726 | |||||||
| chr12:14457740 | G | A | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.2158+445G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14457740 | |||||||
| chr12:14457772 | A | T | 1 | a0002c0002t0001g0247 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2158+477A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14457772 | |||||||
| chr12:14457870 | G | A | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.2158+575G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14457870 | |||||||
| chr12:14458045 | G | A | 4 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(1): Show |
4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2158+750G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458045 | |||||||
| chr12:14458055 | C | T | 2 | a0001c0001t0003g0080 a0001c0001t0003g0105 |
2 | NA18949.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.2158+760C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458055 | |||||||
| chr12:14458095 | CA | C | 8 | a0002c0004t0001g0228 a0003c0003t0013g0162 a0003c0003t0013g0163 others(5): Show |
8 | HG00639.hp1 HG00741.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.2158+811delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 14458095 | ||||||
| chr12:14458106 | AT | A | 7 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2158+812delT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458106 | |||||||
| chr12:14458107 | T | A | 13 | a0002c0002t0009g0284 a0002c0002t0009g0285 a0002c0002t0009g0286 others(10): Show |
14 | HG00609.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2158+812T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458107 | |||||||
| chr12:14458150 | C | G | 4 | a0001c0001t0003g0086 a0001c0001t0003g0117 a0001c0001t0022g0084 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2158+855C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458150 | |||||||
| chr12:14458372 | T | A | 7 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(4): Show |
9 | HG00099.hp1 HG00280.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2158+1077T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458372 | |||||||
| chr12:14458547 | C | T | 3 | a0003c0003t0023g0154 a0003c0003t0023g0155 a0003c0003t0034g0153 |
3 | HG01099.hp1 HG02300.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2158+1252C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458547 | |||||||
| chr12:14458588 | C | T | 140 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(137): Show |
140 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.2158+1293C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458588 | |||||||
| chr12:14458920 | A | G | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2159-1575A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458920 | |||||||
| chr12:14458970 | A | G | 1 | a0002c0002t0001g0300 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2159-1525A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14458970 | |||||||
| chr12:14459020 | A | G | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2159-1475A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459020 | |||||||
| chr12:14459032 | T | C | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2159-1463T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459032 | |||||||
| chr12:14459096 | A | G | 1 | a0001c0001t0002g0116 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2159-1399A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459096 | |||||||
| chr12:14459282 | G | C | 1 | a0001c0001t0002g0339 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2159-1213G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459282 | |||||||
| chr12:14459332 | T | TA | 27 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(24): Show |
28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.2159-1162dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 14459332 | ||||||
| chr12:14459389 | A | G | 142 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(139): Show |
142 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.2159-1106A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459389 | |||||||
| chr12:14459452 | T | G | 1 | a0001c0001t0016g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2159-1043T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459452 | |||||||
| chr12:14459505 | C | G | 1 | a0001c0001t0003g0112 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2159-990C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459505 | |||||||
| chr12:14459570 | T | A | 183 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(180): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.2159-925T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459570 | |||||||
| chr12:14459672 | C | T | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.2159-823C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459672 | |||||||
| chr12:14459695 | T | G | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2159-800T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459695 | |||||||
| chr12:14459780 | T | C | 12 | a0002c0002t0001g0272 a0003c0005t0007g0322 a0003c0005t0007g0323 others(9): Show |
12 | HG00621.hp1 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2159-715T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459780 | |||||||
| chr12:14459938 | G | A | 1 | a0002c0006t0019g0227 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2159-557G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459938 | |||||||
| chr12:14459958 | A | G | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2159-537A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459958 | |||||||
| chr12:14459961 | G | C | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2159-534G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459961 | |||||||
| chr12:14459997 | A | C | 2 | a0008c0012t0011g0335 a0008c0012t0011g0336 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2159-498A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14459997 | |||||||
| chr12:14460244 | C | T | 1 | a0003c0003t0011g0185 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2159-251C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14460244 | |||||||
| chr12:14460271 | C | A | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2159-224C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14460271 | |||||||
| chr12:14460311 | T | C | 3 | a0003c0003t0023g0154 a0003c0003t0023g0155 a0003c0003t0034g0153 |
3 | HG01099.hp1 HG02300.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2159-184T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14460311 | |||||||
| chr12:14460457 | TAACCATT others(2): Show |
T | 14 | a0003c0003t0035g0340 a0003c0005t0007g0322 a0003c0005t0007g0323 others(11): Show |
14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2159-34_2159-26del others(9): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 14460457 | ||||||
| chr12:14460463 | T | A | 1 | a0001c0001t0003g0098 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2159-32T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14460463 | |||||||
| chr12:14460469 | C | A | 1 | a0001c0001t0003g0098 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2159-26C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 8/14 | chr12 | 14460469 | |||||||
| chr12:14461210 | A | G | 1 | a0003c0005t0007g0331 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2797+77A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14461210 | |||||||
| chr12:14461270 | T | A | 11 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2797+137T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14461270 | |||||||
| chr12:14461290 | A | G | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2797+157A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14461290 | |||||||
| chr12:14461397 | T | C | 2 | a0003c0003t0011g0185 a0003c0003t0028g0184 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2797+264T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14461397 | |||||||
| chr12:14461413 | G | A | 1 | a0003c0003t0018g0156 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2797+280G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14461413 | |||||||
| chr12:14461453 | C | T | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2797+320C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14461453 | |||||||
| chr12:14461543 | C | G | 11 | a0002c0002t0001g0247 a0002c0002t0001g0248 a0002c0002t0001g0259 others(8): Show |
12 | HG02132.hp1 NA18612.hp1 NA18941.hp1 others(9): Show |
intron_variant | MODIFIER | c.2797+410C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14461543 | |||||||
| chr12:14461546 | T | C | 3 | a0001c0001t0002g0047 a0001c0001t0002g0055 a0001c0001t0002g0056 |
3 | HG02602.hp1 HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2797+413T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14461546 | |||||||
| chr12:14461982 | C | T | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2797+849C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14461982 | |||||||
| chr12:14462159 | CTA | C | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2797+1027_2797+102 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14462159 | |||||||
| chr12:14462192 | A | G | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2797+1059A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14462192 | |||||||
| chr12:14462743 | T | C | 1 | a0001c0001t0002g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2797+1610T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14462743 | |||||||
| chr12:14462931 | G | A | 1 | a0001c0001t0003g0117 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2797+1798G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14462931 | |||||||
| chr12:14463103 | T | C | 4 | a0003c0003t0011g0203 a0003c0003t0011g0311 a0003c0003t0011g0312 others(1): Show |
4 | HG02280.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2797+1970T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14463103 | |||||||
| chr12:14463346 | T | C | 1 | a0002c0002t0001g0254 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2797+2213T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14463346 | |||||||
| chr12:14463497 | T | C | 2 | a0003c0014t0013g0166 a0003c0014t0013g0167 |
2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2797+2364T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14463497 | |||||||
| chr12:14463625 | T | G | 1 | a0001c0001t0002g0116 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2797+2492T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14463625 | |||||||
| chr12:14463845 | T | C | 1 | a0003c0003t0012g0180 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2798-2681T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14463845 | |||||||
| chr12:14463960 | C | T | 2 | a0003c0014t0013g0166 a0003c0014t0013g0167 |
2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2798-2566C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14463960 | |||||||
| chr12:14463979 | T | A | 326 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(323): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.2798-2547T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14463979 | |||||||
| chr12:14463979 | T | G | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2798-2547T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14463979 | |||||||
| chr12:14464226 | G | A | 11 | a0002c0006t0008g0216 a0002c0006t0008g0218 a0002c0006t0008g0219 others(8): Show |
11 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.2798-2300G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14464226 | |||||||
| chr12:14464433 | C | T | 1 | a0002c0002t0001g0297 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2798-2093C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14464433 | |||||||
| chr12:14464435 | A | G | 2 | a0001c0001t0002g0041 a0001c0001t0002g0045 |
2 | HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2798-2091A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14464435 | |||||||
| chr12:14464511 | G | A | 1 | a0005c0007t0010g0319 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2798-2015G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14464511 | |||||||
| chr12:14464527 | G | A | 2 | a0001c0001t0003g0077 a0001c0001t0040g0142 |
2 | HG02165.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.2798-1999G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14464527 | |||||||
| chr12:14464534 | A | G | 14 | a0003c0003t0035g0340 a0003c0005t0007g0322 a0003c0005t0007g0323 others(11): Show |
14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2798-1992A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14464534 | |||||||
| chr12:14464610 | T | C | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2798-1916T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14464610 | |||||||
| chr12:14464703 | G | C | 1 | a0003c0003t0028g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2798-1823G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14464703 | |||||||
| chr12:14465041 | G | A | 1 | a0003c0003t0014g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2798-1485G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465041 | |||||||
| chr12:14465253 | T | C | 2 | a0010c0013t0020g0118 a0010c0013t0020g0120 |
2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2798-1273T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465253 | |||||||
| chr12:14465300 | A | G | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2798-1226A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465300 | |||||||
| chr12:14465304 | T | G | 4 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(1): Show |
4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2798-1222T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465304 | |||||||
| chr12:14465345 | A | G | 3 | a0001c0001t0003g0015 a0001c0001t0003g0125 a0001c0001t0003g0126 |
3 | HG01074.hp1 HG01168.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.2798-1181A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465345 | |||||||
| chr12:14465489 | A | C | 1 | a0003c0003t0011g0338 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2798-1037A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465489 | |||||||
| chr12:14465499 | C | T | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2798-1027C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465499 | |||||||
| chr12:14465548 | T | A | 4 | a0003c0003t0015g0002 a0003c0003t0015g0168 a0003c0003t0015g0169 others(1): Show |
5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2798-978T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465548 | |||||||
| chr12:14465579 | G | A | 297 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(294): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.2798-947G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465579 | |||||||
| chr12:14465667 | C | T | 1 | a0009c0011t0024g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2798-859C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465667 | |||||||
| chr12:14465726 | GTTTAAC | G | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.2798-797_2798-792d others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 14465726 | ||||||
| chr12:14465738 | G | T | 1 | a0004c0008t0005g0291 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2798-788G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14465738 | |||||||
| chr12:14466034 | T | C | 1 | a0003c0003t0015g0169 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2798-492T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14466034 | |||||||
| chr12:14466138 | C | G | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2798-388C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14466138 | |||||||
| chr12:14466161 | G | T | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2798-365G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14466161 | |||||||
| chr12:14466163 | C | A | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2798-363C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14466163 | |||||||
| chr12:14466165 | T | A | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2798-361T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14466165 | |||||||
| chr12:14466387 | G | A | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2798-139G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14466387 | |||||||
| chr12:14466507 | G | A | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2798-19G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 9/14 | chr12 | 14466507 | |||||||
| chr12:14466697 | T | A | 1 | a0003c0003t0025g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2862+107T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14466697 | |||||||
| chr12:14467165 | G | A | 4 | a0002c0004t0001g0229 a0002c0004t0001g0230 a0002c0004t0001g0231 others(1): Show |
4 | HG01074.hp2 HG01175.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2862+575G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14467165 | |||||||
| chr12:14467364 | C | T | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2862+774C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14467364 | |||||||
| chr12:14467414 | A | C | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2862+824A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14467414 | |||||||
| chr12:14467443 | G | C | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.2862+853G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14467443 | |||||||
| chr12:14467486 | G | T | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.2862+896G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14467486 | |||||||
| chr12:14467672 | G | GT | 95 | a0001c0001t0003g0113 a0001c0001t0003g0114 a0002c0002t0001g0007 others(92): Show |
96 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.2862+1095dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14467672 | ||||||
| chr12:14467844 | A | AAAT | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.2862+1256_2862+125 others(7): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14467844 | ||||||
| chr12:14467990 | G | A | 16 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(13): Show |
17 | HG01123.hp2 HG02257.hp1 HG02970.hp2 others(14): Show |
intron_variant | MODIFIER | c.2862+1400G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14467990 | |||||||
| chr12:14467995 | G | A | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2862+1405G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14467995 | |||||||
| chr12:14468101 | T | C | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2862+1511T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468101 | |||||||
| chr12:14468272 | C | CA | 19 | a0001c0001t0003g0077 a0002c0002t0001g0208 a0002c0002t0001g0209 others(16): Show |
22 | HG00609.hp2 HG01256.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2862+1699dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14468272 | ||||||
| chr12:14468272 | CA | C | 10 | a0002c0004t0001g0229 a0002c0004t0001g0288 a0002c0006t0008g0216 others(7): Show |
10 | HG01069.hp2 HG01993.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2862+1699delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14468272 | ||||||
| chr12:14468276 | A | G | 1 | a0001c0001t0002g0021 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2862+1686A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468276 | |||||||
| chr12:14468289 | A | G | 1 | a0003c0003t0011g0321 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2862+1699A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468289 | |||||||
| chr12:14468384 | T | G | 3 | a0001c0001t0003g0102 a0001c0001t0003g0103 a0001c0001t0003g0104 |
3 | HG01069.hp1 HG01071.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2862+1794T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468384 | |||||||
| chr12:14468398 | T | G | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2862+1808T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468398 | |||||||
| chr12:14468401 | G | A | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.2862+1811G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468401 | |||||||
| chr12:14468439 | G | A | 3 | a0005c0007t0010g0316 a0005c0007t0010g0317 a0005c0007t0010g0319 |
3 | HG00609.hp2 HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2862+1849G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468439 | |||||||
| chr12:14468444 | C | G | 16 | a0003c0003t0025g0172 a0003c0003t0025g0173 a0003c0003t0035g0340 others(13): Show |
16 | HG00099.hp1 HG00280.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.2862+1854C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468444 | |||||||
| chr12:14468493 | TA | T | 231 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(228): Show |
236 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.2862+1918delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14468493 | ||||||
| chr12:14468493 | TAA | T | 103 | a0001c0001t0006g0079 a0002c0002t0001g0007 a0002c0002t0001g0204 others(100): Show |
104 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.2862+1917_2862+191 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14468493 | ||||||
| chr12:14468607 | G | T | 2 | a0005c0007t0010g0314 a0005c0007t0010g0315 |
2 | HG01346.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.2862+2017G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468607 | |||||||
| chr12:14468783 | A | C | 103 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(100): Show |
104 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.2862+2193A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468783 | |||||||
| chr12:14468785 | A | G | 93 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(90): Show |
94 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.2862+2195A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468785 | |||||||
| chr12:14468801 | A | G | 1 | a0003c0003t0014g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2862+2211A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468801 | |||||||
| chr12:14468810 | T | C | 4 | a0002c0006t0008g0223 a0002c0006t0008g0224 a0002c0006t0008g0225 others(1): Show |
4 | NA18977.hp2 NA18981.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.2862+2220T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468810 | |||||||
| chr12:14468995 | A | T | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.2862+2405A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14468995 | |||||||
| chr12:14469052 | T | C | 1 | a0002c0002t0001g0235 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2862+2462T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14469052 | |||||||
| chr12:14469068 | A | G | 62 | a0001c0001t0002g0016 a0001c0001t0002g0027 a0001c0001t0002g0143 others(59): Show |
62 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.2862+2478A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14469068 | |||||||
| chr12:14469330 | A | G | 3 | a0007c0010t0002g0014 a0007c0010t0002g0025 a0007c0010t0002g0052 |
3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2862+2740A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14469330 | |||||||
| chr12:14469346 | C | G | 1 | a0001c0001t0003g0108 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2862+2756C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14469346 | |||||||
| chr12:14469362 | CA | C | 190 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(187): Show |
193 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(190): Show |
intron_variant | MODIFIER | c.2862+2793delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14469362 | ||||||
| chr12:14469362 | CAA | C | 122 | a0001c0001t0002g0023 a0001c0001t0003g0077 a0001c0001t0003g0081 others(119): Show |
125 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.2862+2792_2862+279 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14469362 | ||||||
| chr12:14469368 | A | C | 3 | a0003c0003t0005g0160 a0003c0003t0014g0159 a0003c0003t0014g0161 |
3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2862+2778A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14469368 | |||||||
| chr12:14469378 | A | C | 1 | a0003c0003t0034g0153 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2862+2788A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14469378 | |||||||
| chr12:14469383 | A | C | 80 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(77): Show |
81 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.2862+2793A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14469383 | |||||||
| chr12:14469420 | G | A | 1 | a0003c0005t0007g0325 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2862+2830G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14469420 | |||||||
| chr12:14469540 | TTTA | T | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2862+2954_2862+295 others(7): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14469540 | ||||||
| chr12:14469587 | AAAAC | A | 4 | a0003c0003t0014g0171 a0003c0003t0023g0154 a0003c0003t0023g0155 others(1): Show |
4 | HG01099.hp1 HG02300.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2862+3001_2862+300 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14469587 | ||||||
| chr12:14470054 | C | G | 1 | a0001c0001t0002g0027 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2862+3464C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470054 | |||||||
| chr12:14470128 | A | C | 1 | a0002c0002t0001g0204 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2862+3538A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470128 | |||||||
| chr12:14470198 | C | A | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2862+3608C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470198 | |||||||
| chr12:14470241 | C | T | 1 | a0003c0003t0014g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2862+3651C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470241 | |||||||
| chr12:14470327 | C | T | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2862+3737C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470327 | |||||||
| chr12:14470370 | A | T | 107 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(104): Show |
108 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.2862+3780A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470370 | |||||||
| chr12:14470381 | A | G | 1 | a0001c0001t0003g0117 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2862+3791A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470381 | |||||||
| chr12:14470435 | G | A | 1 | a0001c0001t0002g0061 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2862+3845G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470435 | |||||||
| chr12:14470490 | C | T | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2862+3900C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470490 | |||||||
| chr12:14470646 | G | A | 11 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2862+4056G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470646 | |||||||
| chr12:14470653 | T | C | 1 | a0003c0003t0011g0203 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2862+4063T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470653 | |||||||
| chr12:14470771 | A | G | 311 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.2862+4181A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14470771 | |||||||
| chr12:14471072 | G | A | 2 | a0003c0003t0004g0202 a0003c0003t0014g0152 |
2 | NA19056.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2862+4482G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14471072 | |||||||
| chr12:14471385 | C | T | 1 | a0001c0001t0003g0083 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2863-4505C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14471385 | |||||||
| chr12:14471640 | A | C | 141 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(138): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.2863-4250A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14471640 | |||||||
| chr12:14471837 | T | C | 1 | a0001c0001t0003g0077 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2863-4053T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14471837 | |||||||
| chr12:14471842 | G | A | 1 | a0002c0006t0008g0292 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2863-4048G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14471842 | |||||||
| chr12:14471877 | C | G | 1 | a0001c0001t0002g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2863-4013C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14471877 | |||||||
| chr12:14471919 | G | A | 3 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0032g0106 |
3 | HG00673.hp1 NA19060.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.2863-3971G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14471919 | |||||||
| chr12:14471955 | A | G | 9 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(6): Show |
10 | NA18939.hp1 NA18955.hp2 NA18967.hp2 others(7): Show |
intron_variant | MODIFIER | c.2863-3935A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14471955 | |||||||
| chr12:14472044 | G | T | 2 | a0003c0003t0004g0195 a0003c0003t0004g0196 |
2 | HG00733.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2863-3846G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472044 | |||||||
| chr12:14472119 | TA | T | 149 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(146): Show |
149 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.2863-3770delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472119 | |||||||
| chr12:14472214 | A | T | 1 | a0009c0011t0024g0150 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2863-3676A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472214 | |||||||
| chr12:14472308 | GAAAAGCA others(3): Show |
G | 4 | a0003c0003t0011g0203 a0003c0003t0011g0311 a0003c0003t0011g0312 others(1): Show |
4 | HG02280.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2863-3571_2863-356 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14472308 | ||||||
| chr12:14472337 | T | G | 3 | a0003c0003t0004g0003 a0003c0003t0004g0192 a0003c0003t0004g0193 |
4 | NA18955.hp2 NA18968.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.2863-3553T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472337 | |||||||
| chr12:14472350 | C | T | 4 | a0001c0001t0003g0086 a0001c0001t0003g0117 a0001c0001t0022g0084 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2863-3540C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472350 | |||||||
| chr12:14472480 | A | G | 1 | a0001c0001t0002g0062 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2863-3410A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472480 | |||||||
| chr12:14472609 | C | G | 1 | a0003c0003t0004g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2863-3281C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472609 | |||||||
| chr12:14472618 | G | A | 1 | a0002c0002t0001g0204 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2863-3272G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472618 | |||||||
| chr12:14472624 | T | C | 1 | a0012c0015t0003g0097 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2863-3266T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472624 | |||||||
| chr12:14472637 | C | A | 1 | a0001c0001t0002g0023 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2863-3253C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472637 | |||||||
| chr12:14472694 | C | T | 2 | a0003c0014t0013g0166 a0003c0014t0013g0167 |
2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2863-3196C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472694 | |||||||
| chr12:14472718 | C | G | 1 | a0001c0001t0002g0046 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2863-3172C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472718 | |||||||
| chr12:14472722 | G | A | 2 | a0001c0001t0003g0089 a0001c0001t0003g0100 |
2 | HG01081.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.2863-3168G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472722 | |||||||
| chr12:14472729 | T | G | 1 | a0001c0001t0002g0023 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2863-3161T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472729 | |||||||
| chr12:14472777 | T | A | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.2863-3113T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472777 | |||||||
| chr12:14472820 | G | GCA | 160 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(157): Show |
161 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(158): Show |
intron_variant | MODIFIER | c.2863-3058_2863-305 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14472820 | ||||||
| chr12:14472820 | G | GCACA | 3 | a0001c0001t0029g0063 a0003c0003t0018g0156 a0003c0003t0018g0158 |
3 | HG01243.hp1 HG01891.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2863-3060_2863-305 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14472820 | ||||||
| chr12:14472871 | C | T | 1 | a0001c0001t0002g0021 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2863-3019C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14472871 | |||||||
| chr12:14473081 | A | T | 1 | a0001c0001t0002g0023 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2863-2809A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473081 | |||||||
| chr12:14473200 | C | G | 2 | a0003c0003t0018g0156 a0003c0003t0018g0158 |
2 | HG01891.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2863-2690C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473200 | |||||||
| chr12:14473274 | C | T | 1 | a0003c0003t0012g0183 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2863-2616C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473274 | |||||||
| chr12:14473275 | GCT | G | 56 | a0001c0001t0003g0015 a0001c0001t0003g0074 a0001c0001t0003g0075 others(53): Show |
56 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2863-2600_2863-259 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473275 | ||||||
| chr12:14473277 | T | G | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2863-2613T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473277 | |||||||
| chr12:14473280 | C | CTG | 10 | a0001c0001t0002g0016 a0003c0003t0005g0160 a0003c0003t0013g0162 others(7): Show |
10 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.2863-2609_2863-260 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473280 | ||||||
| chr12:14473282 | C | G | 107 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0017 others(104): Show |
108 | HG01099.hp1 HG01099.hp2 HG01123.hp1 others(105): Show |
intron_variant | MODIFIER | c.2863-2608C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473282 | |||||||
| chr12:14473284 | C | G | 52 | a0001c0001t0003g0015 a0001c0001t0003g0074 a0001c0001t0003g0075 others(49): Show |
52 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.2863-2606C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473284 | |||||||
| chr12:14473288 | C | CTGTA | 29 | a0001c0001t0002g0027 a0001c0001t0002g0035 a0001c0001t0006g0073 others(26): Show |
29 | HG00735.hp2 HG01099.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.2863-2601_2863-260 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | ||||||
| chr12:14473288 | C | CTGTATG | 57 | a0001c0001t0002g0013 a0001c0001t0002g0020 a0001c0001t0002g0071 others(54): Show |
58 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.2863-2601_2863-260 others(10): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | ||||||
| chr12:14473288 | C | CTGTATGT others(1): Show |
68 | a0001c0001t0002g0010 a0001c0001t0002g0018 a0001c0001t0002g0019 others(65): Show |
68 | HG00438.hp1 HG01071.hp1 HG01074.hp2 others(65): Show |
intron_variant | MODIFIER | c.2863-2601_2863-260 others(12): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | ||||||
| chr12:14473288 | C | CTGTATGT others(3): Show |
29 | a0001c0001t0002g0017 a0001c0001t0002g0034 a0001c0001t0002g0040 others(26): Show |
29 | HG01361.hp1 HG01884.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.2863-2601_2863-260 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | ||||||
| chr12:14473288 | C | CTGTATGT others(5): Show |
22 | a0001c0001t0002g0060 a0001c0001t0002g0064 a0001c0001t0002g0066 others(19): Show |
23 | HG00438.hp2 HG00673.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.2863-2601_2863-260 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | ||||||
| chr12:14473288 | C | CTGTATGT others(7): Show |
6 | a0002c0006t0008g0216 a0002c0006t0008g0219 a0003c0003t0018g0156 others(3): Show |
6 | HG01515.hp2 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.2863-2601_2863-260 others(18): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | ||||||
| chr12:14473288 | C | CTGTATGT others(9): Show |
6 | a0001c0001t0002g0033 a0003c0003t0011g0312 a0003c0003t0015g0002 others(3): Show |
7 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2863-2601_2863-260 others(20): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | ||||||
| chr12:14473288 | C | CTGTATGT others(11): Show |
1 | a0003c0003t0011g0311 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2863-2601_2863-260 others(22): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | ||||||
| chr12:14473288 | C | CTGTG | 4 | a0003c0003t0004g0195 a0003c0003t0004g0196 a0008c0012t0011g0335 others(1): Show |
4 | HG00733.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.2863-2601_2863-260 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | ||||||
| chr12:14473288 | C | G | 12 | a0001c0001t0002g0016 a0003c0003t0005g0160 a0003c0003t0013g0162 others(9): Show |
12 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.2863-2602C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473288 | |||||||
| chr12:14473288 | CTCTG | C | 5 | a0001c0001t0002g0143 a0001c0001t0003g0077 a0001c0001t0027g0026 others(2): Show |
5 | HG00597.hp2 HG02735.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.2863-2600_2863-259 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | ||||||
| chr12:14473288 | CTCTGTG | C | 6 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0003g0112 others(3): Show |
6 | HG01099.hp2 HG03239.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2863-2600_2863-259 others(10): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | ||||||
| chr12:14473288 | CTCTGTGT others(1): Show |
C | 11 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2863-2600_2863-259 others(12): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | ||||||
| chr12:14473288 | CTCTGTGT others(3): Show |
C | 11 | a0003c0003t0011g0185 a0003c0003t0012g0001 a0003c0003t0012g0180 others(8): Show |
13 | HG00099.hp1 HG00280.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.2863-2600_2863-259 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473288 | ||||||
| chr12:14473290 | C | A | 11 | a0001c0001t0002g0016 a0003c0003t0005g0160 a0003c0003t0013g0162 others(8): Show |
11 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.2863-2600C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473290 | |||||||
| chr12:14473290 | C | G | 237 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0017 others(234): Show |
241 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(238): Show |
intron_variant | MODIFIER | c.2863-2600C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473290 | |||||||
| chr12:14473292 | G | A | 13 | a0001c0001t0003g0101 a0001c0001t0003g0114 a0001c0001t0003g0115 others(10): Show |
14 | HG00140.hp1 HG00609.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.2863-2598G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473292 | |||||||
| chr12:14473294 | G | A | 56 | a0001c0001t0003g0015 a0001c0001t0003g0074 a0001c0001t0003g0075 others(53): Show |
56 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2863-2596G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473294 | |||||||
| chr12:14473296 | G | A | 5 | a0001c0001t0002g0143 a0001c0001t0003g0077 a0001c0001t0027g0026 others(2): Show |
5 | HG00597.hp2 HG02735.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.2863-2594G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473296 | |||||||
| chr12:14473298 | G | A | 6 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0003g0112 others(3): Show |
6 | HG01099.hp2 HG03239.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2863-2592G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473298 | |||||||
| chr12:14473300 | G | A | 11 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2863-2590G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473300 | |||||||
| chr12:14473302 | G | A | 6 | a0003c0003t0011g0185 a0003c0003t0025g0172 a0003c0003t0025g0173 others(3): Show |
6 | HG00099.hp1 HG00280.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2863-2588G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473302 | |||||||
| chr12:14473330 | T | G | 2 | a0001c0001t0002g0016 a0001c0001t0003g0011 |
2 | NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.2863-2560T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473330 | |||||||
| chr12:14473332 | T | G | 2 | a0001c0001t0002g0016 a0001c0001t0003g0011 |
2 | NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.2863-2558T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473332 | |||||||
| chr12:14473487 | A | C | 163 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(160): Show |
164 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(161): Show |
intron_variant | MODIFIER | c.2863-2403A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473487 | |||||||
| chr12:14473512 | A | T | 1 | a0003c0005t0041g0334 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2863-2378A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473512 | |||||||
| chr12:14473586 | C | A | 4 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(1): Show |
4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2863-2304C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473586 | |||||||
| chr12:14473632 | T | C | 1 | a0001c0001t0003g0081 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2863-2258T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473632 | |||||||
| chr12:14473648 | A | G | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2863-2242A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473648 | |||||||
| chr12:14473681 | C | T | 1 | a0001c0001t0003g0092 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2863-2209C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473681 | |||||||
| chr12:14473734 | T | C | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2863-2156T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473734 | |||||||
| chr12:14473804 | A | AG | 4 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(1): Show |
4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2863-2084dupG | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14473804 | ||||||
| chr12:14473806 | G | A | 4 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0182 others(1): Show |
6 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2863-2084G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473806 | |||||||
| chr12:14473807 | T | G | 305 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(302): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.2863-2083T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473807 | |||||||
| chr12:14473808 | T | G | 1 | a0002c0002t0001g0301 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2863-2082T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473808 | |||||||
| chr12:14473913 | C | T | 3 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0062 |
3 | NA18612.hp2 NA18993.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2863-1977C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473913 | |||||||
| chr12:14473983 | T | C | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2863-1907T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14473983 | |||||||
| chr12:14474078 | T | G | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2863-1812T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474078 | |||||||
| chr12:14474211 | T | G | 2 | a0003c0003t0018g0156 a0003c0003t0018g0158 |
2 | HG01891.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2863-1679T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474211 | |||||||
| chr12:14474214 | C | T | 3 | a0003c0003t0004g0186 a0003c0003t0004g0187 a0003c0003t0004g0190 |
3 | NA18967.hp2 NA19090.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2863-1676C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474214 | |||||||
| chr12:14474259 | C | T | 1 | a0003c0003t0011g0321 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2863-1631C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474259 | |||||||
| chr12:14474387 | A | G | 1 | a0001c0001t0029g0063 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2863-1503A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474387 | |||||||
| chr12:14474403 | A | AT | 12 | a0001c0001t0003g0080 a0002c0002t0001g0234 a0003c0003t0004g0186 others(9): Show |
12 | HG00140.hp1 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.2863-1472dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 14474403 | ||||||
| chr12:14474456 | A | G | 18 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(15): Show |
19 | HG00733.hp2 HG01123.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2863-1434A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474456 | |||||||
| chr12:14474459 | C | T | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2863-1431C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474459 | |||||||
| chr12:14474475 | A | T | 4 | a0002c0002t0009g0210 a0002c0002t0009g0211 a0002c0002t0009g0213 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2863-1415A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474475 | |||||||
| chr12:14474510 | C | A | 1 | a0002c0002t0001g0304 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2863-1380C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474510 | |||||||
| chr12:14474521 | C | T | 2 | a0001c0001t0002g0041 a0001c0001t0002g0045 |
2 | HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2863-1369C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474521 | |||||||
| chr12:14474838 | A | T | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2863-1052A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14474838 | |||||||
| chr12:14475055 | C | T | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2863-835C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475055 | |||||||
| chr12:14475092 | G | A | 1 | a0002c0006t0008g0292 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2863-798G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475092 | |||||||
| chr12:14475111 | A | G | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2863-779A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475111 | |||||||
| chr12:14475135 | A | G | 112 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(109): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.2863-755A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475135 | |||||||
| chr12:14475195 | A | G | 1 | a0003c0003t0005g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2863-695A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475195 | |||||||
| chr12:14475212 | A | G | 4 | a0003c0003t0014g0171 a0003c0003t0023g0154 a0003c0003t0023g0155 others(1): Show |
4 | HG01099.hp1 HG02300.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2863-678A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475212 | |||||||
| chr12:14475313 | C | T | 1 | a0002c0002t0001g0267 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2863-577C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475313 | |||||||
| chr12:14475478 | G | C | 4 | a0003c0003t0014g0171 a0003c0003t0023g0154 a0003c0003t0023g0155 others(1): Show |
4 | HG01099.hp1 HG02300.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2863-412G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475478 | |||||||
| chr12:14475511 | C | T | 103 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(100): Show |
104 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.2863-379C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475511 | |||||||
| chr12:14475543 | A | G | 1 | a0002c0002t0001g0294 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2863-347A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475543 | |||||||
| chr12:14475591 | C | T | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2863-299C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475591 | |||||||
| chr12:14475610 | C | G | 310 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(307): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2863-280C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475610 | |||||||
| chr12:14475761 | C | A | 3 | a0003c0003t0005g0160 a0003c0003t0014g0159 a0003c0003t0014g0161 |
3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2863-129C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475761 | |||||||
| chr12:14475771 | A | G | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.2863-119A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475771 | |||||||
| chr12:14475839 | C | T | 148 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(145): Show |
148 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.2863-51C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475839 | |||||||
| chr12:14475842 | A | G | 4 | a0003c0003t0015g0002 a0003c0003t0015g0168 a0003c0003t0015g0169 others(1): Show |
5 | HG02055.hp1 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2863-48A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 10/14 | chr12 | 14475842 | |||||||
| chr12:14475985 | T | C | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2941+17T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14475985 | |||||||
| chr12:14476229 | C | T | 3 | a0002c0002t0001g0204 a0002c0002t0001g0222 a0002c0002t0001g0267 |
3 | HG00621.hp2 HG02155.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2941+261C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14476229 | |||||||
| chr12:14476230 | G | A | 1 | a0003c0003t0011g0185 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2941+262G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14476230 | |||||||
| chr12:14476239 | C | A | 2 | a0003c0003t0004g0194 a0003c0003t0004g0200 |
2 | HG01123.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.2941+271C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14476239 | |||||||
| chr12:14476241 | G | A | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2941+273G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14476241 | |||||||
| chr12:14476411 | CA | C | 32 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0072 others(29): Show |
34 | HG00609.hp2 HG00733.hp2 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.2941+467delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 14476411 | ||||||
| chr12:14476411 | CAA | C | 252 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(249): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2941+466_2941+467d others(4): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 14476411 | ||||||
| chr12:14476411 | CAAA | C | 33 | a0001c0001t0002g0054 a0001c0001t0003g0075 a0001c0001t0003g0088 others(30): Show |
34 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.2941+465_2941+467d others(5): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 14476411 | ||||||
| chr12:14476411 | CAAAA | C | 11 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(8): Show |
11 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2941+464_2941+467d others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 14476411 | ||||||
| chr12:14476724 | G | A | 2 | a0003c0014t0013g0166 a0003c0014t0013g0167 |
2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2941+756G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14476724 | |||||||
| chr12:14476726 | A | G | 3 | a0003c0003t0005g0160 a0003c0003t0014g0159 a0003c0003t0014g0161 |
3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2941+758A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14476726 | |||||||
| chr12:14477075 | G | A | 1 | a0003c0003t0005g0160 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2941+1107G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14477075 | |||||||
| chr12:14477330 | C | T | 1 | a0002c0002t0001g0304 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2942-987C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14477330 | |||||||
| chr12:14477374 | ATTATCTC others(12): Show |
A | 1 | a0001c0001t0003g0086 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2942-922_2942-904d others(21): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 14477374 | ||||||
| chr12:14477383 | A | G | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2942-934A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14477383 | |||||||
| chr12:14477762 | C | A | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2942-555C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14477762 | |||||||
| chr12:14477779 | GTTTT | G | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2942-536_2942-533d others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr12 | 14477779 | ||||||
| chr12:14477862 | A | G | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2942-455A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14477862 | |||||||
| chr12:14477922 | G | A | 168 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(165): Show |
169 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.2942-395G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14477922 | |||||||
| chr12:14477966 | T | C | 2 | a0010c0013t0020g0118 a0010c0013t0020g0120 |
2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2942-351T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14477966 | |||||||
| chr12:14478050 | T | C | 1 | a0003c0003t0011g0321 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2942-267T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14478050 | |||||||
| chr12:14478093 | C | T | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2942-224C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14478093 | |||||||
| chr12:14478127 | A | G | 1 | a0002c0002t0009g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2942-190A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14478127 | |||||||
| chr12:14478177 | T | C | 163 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(160): Show |
164 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(161): Show |
intron_variant | MODIFIER | c.2942-140T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14478177 | |||||||
| chr12:14478249 | A | G | 1 | a0002c0002t0001g0257 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2942-68A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14478249 | |||||||
| chr12:14478264 | G | A | 1 | a0003c0003t0015g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2942-53G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 11/14 | chr12 | 14478264 | |||||||
| chr12:14478558 | A | G | 1 | a0003c0005t0007g0323 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3097+86A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14478558 | |||||||
| chr12:14478576 | G | T | 1 | a0003c0005t0007g0323 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3097+104G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14478576 | |||||||
| chr12:14478599 | T | C | 1 | a0001c0001t0002g0148 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3097+127T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14478599 | |||||||
| chr12:14478612 | G | A | 1 | a0001c0001t0002g0143 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3097+140G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14478612 | |||||||
| chr12:14478819 | G | C | 2 | a0001c0001t0002g0037 a0001c0001t0002g0038 |
2 | HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.3097+347G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14478819 | |||||||
| chr12:14478994 | C | T | 3 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0032g0106 |
3 | HG00673.hp1 NA19060.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.3097+522C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14478994 | |||||||
| chr12:14478995 | G | A | 1 | a0001c0001t0003g0098 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3097+523G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14478995 | |||||||
| chr12:14479272 | T | C | 1 | a0002c0002t0001g0217 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3097+800T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479272 | |||||||
| chr12:14479323 | C | T | 103 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(100): Show |
104 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.3097+851C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479323 | |||||||
| chr12:14479368 | A | G | 1 | a0002c0002t0001g0303 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3097+896A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479368 | |||||||
| chr12:14479405 | A | G | 14 | a0003c0003t0005g0313 a0003c0003t0012g0001 a0003c0003t0012g0180 others(11): Show |
17 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.3097+933A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479405 | |||||||
| chr12:14479516 | T | A | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3097+1044T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479516 | |||||||
| chr12:14479559 | A | T | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3097+1087A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479559 | |||||||
| chr12:14479571 | G | A | 311 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.3097+1099G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479571 | |||||||
| chr12:14479671 | T | G | 5 | a0001c0001t0003g0077 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02165.hp1 HG03239.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.3097+1199T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479671 | |||||||
| chr12:14479672 | AG | A | 5 | a0001c0001t0003g0077 a0001c0001t0003g0081 a0001c0001t0003g0082 others(2): Show |
5 | HG02165.hp1 HG03239.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.3097+1201delG | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479672 | |||||||
| chr12:14479778 | C | T | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3098-1225C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14479778 | |||||||
| chr12:14480050 | C | T | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3098-953C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14480050 | |||||||
| chr12:14480115 | C | T | 1 | a0003c0003t0005g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3098-888C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14480115 | |||||||
| chr12:14480122 | T | C | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3098-881T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14480122 | |||||||
| chr12:14480289 | A | G | 103 | a0001c0001t0019g0065 a0002c0002t0001g0007 a0002c0002t0001g0204 others(100): Show |
104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.3098-714A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14480289 | |||||||
| chr12:14480511 | A | T | 26 | a0001c0020t0036g0134 a0003c0003t0004g0003 a0003c0003t0004g0186 others(23): Show |
27 | HG00733.hp2 HG01123.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.3098-492A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14480511 | |||||||
| chr12:14480653 | A | G | 11 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3098-350A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14480653 | |||||||
| chr12:14480806 | T | C | 2 | a0008c0012t0011g0335 a0008c0012t0011g0336 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3098-197T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14480806 | |||||||
| chr12:14480973 | T | C | 1 | a0002c0002t0001g0266 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.3098-30T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 12/14 | chr12 | 14480973 | |||||||
| chr12:14481296 | T | A | 42 | a0001c0020t0036g0134 a0003c0003t0004g0003 a0003c0003t0004g0186 others(39): Show |
43 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.3280+111T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481296 | |||||||
| chr12:14481332 | C | T | 1 | a0001c0001t0003g0149 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3280+147C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481332 | |||||||
| chr12:14481454 | A | G | 1 | a0003c0003t0013g0165 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3280+269A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481454 | |||||||
| chr12:14481458 | C | CAGTT | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.3280+275_3280+276i others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14481458 | ||||||
| chr12:14481458 | C | T | 1 | a0003c0003t0013g0165 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3280+273C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481458 | |||||||
| chr12:14481489 | A | G | 1 | a0001c0001t0002g0057 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3280+304A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481489 | |||||||
| chr12:14481498 | A | T | 1 | a0001c0001t0003g0112 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3280+313A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481498 | |||||||
| chr12:14481738 | A | G | 9 | a0003c0003t0005g0313 a0005c0007t0010g0005 a0005c0007t0010g0314 others(6): Show |
10 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+553A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481738 | |||||||
| chr12:14481758 | G | A | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.3280+573G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481758 | |||||||
| chr12:14481758 | G | T | 3 | a0002c0002t0001g0254 a0002c0002t0001g0293 a0002c0002t0001g0294 |
3 | HG00597.hp2 HG02080.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.3280+573G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481758 | |||||||
| chr12:14481794 | A | C | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+609A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481794 | |||||||
| chr12:14481876 | TAAAG | T | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3280+696_3280+699d others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14481876 | ||||||
| chr12:14481888 | G | C | 1 | a0001c0001t0002g0070 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3280+703G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14481888 | |||||||
| chr12:14481923 | C | CATATGTT others(4): Show |
185 | a0001c0001t0019g0065 a0001c0020t0036g0134 a0002c0002t0001g0007 others(182): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.3280+739_3280+749d others(13): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14481923 | ||||||
| chr12:14482078 | C | T | 1 | a0001c0001t0014g0128 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3280+893C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482078 | |||||||
| chr12:14482183 | A | G | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+998A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482183 | |||||||
| chr12:14482336 | A | G | 14 | a0003c0003t0035g0340 a0003c0005t0007g0322 a0003c0005t0007g0323 others(11): Show |
14 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.3280+1151A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482336 | |||||||
| chr12:14482388 | G | C | 4 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0325 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3280+1203G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482388 | |||||||
| chr12:14482576 | C | G | 1 | a0001c0001t0006g0138 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3280+1391C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482576 | |||||||
| chr12:14482601 | T | C | 1 | a0002c0006t0008g0219 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3280+1416T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482601 | |||||||
| chr12:14482696 | A | T | 5 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(2): Show |
7 | HG02630.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.3280+1511A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482696 | |||||||
| chr12:14482721 | T | G | 4 | a0004c0008t0005g0006 a0004c0008t0005g0276 a0004c0008t0005g0290 others(1): Show |
4 | HG01123.hp1 HG01361.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3280+1536T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482721 | |||||||
| chr12:14482869 | A | G | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3280+1684A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482869 | |||||||
| chr12:14482937 | A | C | 1 | a0002c0002t0001g0272 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3280+1752A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482937 | |||||||
| chr12:14482987 | G | A | 1 | a0003c0003t0012g0181 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3280+1802G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14482987 | |||||||
| chr12:14483088 | A | G | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.3280+1903A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483088 | |||||||
| chr12:14483152 | T | C | 1 | a0001c0001t0017g0031 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3280+1967T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483152 | |||||||
| chr12:14483180 | C | A | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3280+1995C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483180 | |||||||
| chr12:14483292 | A | G | 1 | a0003c0003t0004g0200 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3280+2107A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483292 | |||||||
| chr12:14483348 | G | A | 1 | a0003c0003t0011g0203 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3280+2163G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483348 | |||||||
| chr12:14483384 | C | T | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3280+2199C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483384 | |||||||
| chr12:14483389 | C | G | 2 | a0003c0003t0004g0194 a0003c0003t0004g0200 |
2 | HG01123.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.3280+2204C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483389 | |||||||
| chr12:14483422 | G | T | 2 | a0001c0001t0002g0147 a0001c0001t0002g0148 |
2 | HG03669.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.3280+2237G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483422 | |||||||
| chr12:14483441 | A | G | 2 | a0008c0012t0011g0335 a0008c0012t0011g0336 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3280+2256A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483441 | |||||||
| chr12:14483447 | G | T | 2 | a0008c0012t0011g0335 a0008c0012t0011g0336 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3280+2262G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483447 | |||||||
| chr12:14483507 | G | A | 1 | a0002c0002t0001g0269 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3280+2322G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483507 | |||||||
| chr12:14483620 | G | A | 2 | a0003c0014t0013g0166 a0003c0014t0013g0167 |
2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3280+2435G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483620 | |||||||
| chr12:14483622 | T | C | 2 | a0003c0014t0013g0166 a0003c0014t0013g0167 |
2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3280+2437T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483622 | |||||||
| chr12:14483810 | T | G | 2 | a0003c0003t0011g0185 a0003c0003t0028g0184 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3280+2625T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483810 | |||||||
| chr12:14483899 | G | A | 2 | a0001c0001t0002g0147 a0001c0001t0002g0148 |
2 | HG03669.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.3280+2714G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483899 | |||||||
| chr12:14483976 | G | C | 1 | a0002c0002t0001g0205 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3280+2791G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14483976 | |||||||
| chr12:14484089 | C | A | 104 | a0001c0001t0019g0065 a0002c0002t0001g0007 a0002c0002t0001g0204 others(101): Show |
105 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.3280+2904C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484089 | |||||||
| chr12:14484091 | C | T | 11 | a0001c0001t0006g0073 a0001c0001t0006g0079 a0001c0001t0006g0132 others(8): Show |
11 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.3280+2906C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484091 | |||||||
| chr12:14484476 | C | G | 3 | a0003c0003t0004g0186 a0003c0003t0004g0187 a0003c0003t0004g0190 |
3 | NA18967.hp2 NA19090.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.3280+3291C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484476 | |||||||
| chr12:14484528 | T | G | 186 | a0001c0001t0019g0065 a0001c0001t0040g0142 a0001c0020t0036g0134 others(183): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.3280+3343T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484528 | |||||||
| chr12:14484626 | A | C | 5 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0211 others(2): Show |
5 | HG01109.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.3280+3441A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484626 | |||||||
| chr12:14484652 | G | C | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3280+3467G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484652 | |||||||
| chr12:14484656 | C | G | 2 | a0003c0005t0007g0324 a0003c0005t0007g0333 |
2 | HG02647.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3280+3471C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484656 | |||||||
| chr12:14484720 | C | G | 337 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(334): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.3280+3535C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484720 | |||||||
| chr12:14484852 | G | A | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.3280+3667G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484852 | |||||||
| chr12:14484929 | A | T | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+3744A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14484929 | |||||||
| chr12:14485060 | G | A | 184 | a0001c0001t0019g0065 a0002c0002t0001g0007 a0002c0002t0001g0204 others(181): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.3280+3875G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485060 | |||||||
| chr12:14485223 | A | C | 4 | a0003c0003t0011g0203 a0003c0003t0011g0311 a0003c0003t0011g0312 others(1): Show |
4 | HG02280.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3280+4038A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485223 | |||||||
| chr12:14485470 | T | C | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3280+4285T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485470 | |||||||
| chr12:14485473 | G | A | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3280+4288G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485473 | |||||||
| chr12:14485479 | T | C | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3280+4294T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485479 | |||||||
| chr12:14485511 | C | T | 3 | a0001c0001t0002g0040 a0001c0001t0002g0042 a0001c0001t0002g0046 |
3 | NA18957.hp1 NA19057.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.3280+4326C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485511 | |||||||
| chr12:14485570 | C | G | 1 | a0002c0002t0001g0245 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3280+4385C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485570 | |||||||
| chr12:14485571 | C | T | 1 | a0002c0002t0001g0245 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3280+4386C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485571 | |||||||
| chr12:14485607 | G | A | 1 | a0003c0003t0004g0192 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3280+4422G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485607 | |||||||
| chr12:14485724 | C | T | 139 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(136): Show |
139 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.3280+4539C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485724 | |||||||
| chr12:14485741 | C | T | 3 | a0001c0001t0003g0107 a0001c0001t0003g0110 a0001c0001t0032g0106 |
3 | HG00673.hp1 NA19060.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.3280+4556C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485741 | |||||||
| chr12:14485807 | A | G | 3 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0003c0003t0011g0338 |
3 | HG03486.hp1 NA18980.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.3280+4622A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485807 | |||||||
| chr12:14485920 | C | T | 80 | a0002c0002t0001g0007 a0002c0002t0001g0204 a0002c0002t0001g0205 others(77): Show |
81 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.3280+4735C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485920 | |||||||
| chr12:14485922 | C | T | 1 | a0002c0002t0001g0249 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3280+4737C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14485922 | |||||||
| chr12:14485958 | TCTC | T | 4 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(1): Show |
4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.3280+4777_3280+477 others(7): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14485958 | ||||||
| chr12:14486003 | T | C | 2 | a0002c0002t0001g0235 a0006c0009t0005g0176 |
2 | HG03516.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.3280+4818T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486003 | |||||||
| chr12:14486063 | C | T | 30 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(27): Show |
31 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.3280+4878C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486063 | |||||||
| chr12:14486081 | A | G | 1 | a0003c0003t0034g0153 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3280+4896A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486081 | |||||||
| chr12:14486109 | T | G | 1 | a0001c0001t0003g0107 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3280+4924T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486109 | |||||||
| chr12:14486165 | T | G | 14 | a0003c0003t0005g0313 a0003c0003t0012g0001 a0003c0003t0012g0180 others(11): Show |
17 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.3280+4980T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486165 | |||||||
| chr12:14486188 | T | G | 3 | a0001c0001t0003g0083 a0001c0001t0003g0093 a0001c0001t0003g0094 |
3 | NA18959.hp1 NA19010.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.3280+5003T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486188 | |||||||
| chr12:14486261 | T | G | 1 | a0001c0001t0003g0127 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3280+5076T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486261 | |||||||
| chr12:14486499 | A | C | 1 | a0001c0001t0002g0061 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3280+5314A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486499 | |||||||
| chr12:14486618 | A | G | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+5433A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486618 | |||||||
| chr12:14486815 | G | C | 1 | a0003c0003t0011g0321 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3280+5630G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486815 | |||||||
| chr12:14486818 | C | G | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+5633C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486818 | |||||||
| chr12:14486826 | A | G | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+5641A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486826 | |||||||
| chr12:14486827 | A | C | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+5642A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486827 | |||||||
| chr12:14486828 | G | A | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+5643G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486828 | |||||||
| chr12:14486829 | G | A | 1 | a0002c0002t0001g0007 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3280+5644G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486829 | |||||||
| chr12:14486835 | A | G | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+5650A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486835 | |||||||
| chr12:14486837 | C | T | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+5652C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486837 | |||||||
| chr12:14486838 | G | A | 20 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(17): Show |
21 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.3280+5653G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486838 | |||||||
| chr12:14486853 | C | T | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+5668C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486853 | |||||||
| chr12:14486858 | A | T | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3280+5673A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486858 | |||||||
| chr12:14486881 | A | T | 1 | a0002c0002t0001g0295 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3280+5696A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486881 | |||||||
| chr12:14486887 | C | G | 1 | a0002c0006t0008g0220 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3280+5702C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486887 | |||||||
| chr12:14486946 | C | T | 3 | a0006c0009t0005g0177 a0006c0009t0005g0178 a0006c0009t0005g0179 |
3 | HG02723.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3280+5761C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486946 | |||||||
| chr12:14486951 | C | G | 1 | a0002c0002t0001g0297 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3280+5766C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14486951 | |||||||
| chr12:14487125 | C | CT | 145 | a0001c0001t0019g0065 a0001c0001t0040g0142 a0002c0002t0001g0007 others(142): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.3280+5949dupT | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14487125 | ||||||
| chr12:14487125 | C | CTT | 30 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(27): Show |
31 | HG00733.hp2 HG01123.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.3280+5948_3280+594 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14487125 | ||||||
| chr12:14487125 | C | T | 1 | a0003c0005t0041g0334 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3280+5940C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487125 | |||||||
| chr12:14487215 | T | C | 103 | a0001c0001t0019g0065 a0001c0001t0040g0142 a0002c0002t0001g0007 others(100): Show |
104 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.3280+6030T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487215 | |||||||
| chr12:14487222 | C | T | 1 | a0001c0001t0040g0142 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3280+6037C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487222 | |||||||
| chr12:14487224 | T | C | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+6039T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487224 | |||||||
| chr12:14487233 | T | C | 15 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(12): Show |
15 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.3280+6048T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487233 | |||||||
| chr12:14487253 | C | T | 105 | a0001c0001t0019g0065 a0001c0001t0040g0142 a0002c0002t0001g0007 others(102): Show |
106 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.3280+6068C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487253 | |||||||
| chr12:14487266 | C | T | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+6081C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487266 | |||||||
| chr12:14487267 | T | C | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+6082T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487267 | |||||||
| chr12:14487270 | G | A | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+6085G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487270 | |||||||
| chr12:14487278 | T | A | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+6093T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487278 | |||||||
| chr12:14487282 | G | T | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+6097G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487282 | |||||||
| chr12:14487284 | A | G | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+6099A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487284 | |||||||
| chr12:14487290 | G | A | 13 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(10): Show |
13 | HG01934.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3280+6105G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487290 | |||||||
| chr12:14487307 | C | T | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3280+6122C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487307 | |||||||
| chr12:14487382 | G | T | 2 | a0001c0001t0003g0015 a0001c0001t0003g0125 |
2 | HG01074.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.3280+6197G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487382 | |||||||
| chr12:14487542 | A | G | 1 | a0001c0001t0003g0109 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3280+6357A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487542 | |||||||
| chr12:14487543 | T | C | 105 | a0001c0001t0019g0065 a0001c0001t0040g0142 a0002c0002t0001g0007 others(102): Show |
106 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.3280+6358T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487543 | |||||||
| chr12:14487570 | G | C | 1 | a0002c0002t0001g0204 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3280+6385G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487570 | |||||||
| chr12:14487576 | G | A | 1 | a0002c0002t0001g0279 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3280+6391G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487576 | |||||||
| chr12:14487742 | G | A | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.3280+6557G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487742 | |||||||
| chr12:14487773 | T | G | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3280+6588T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487773 | |||||||
| chr12:14487899 | G | A | 1 | a0003c0003t0004g0200 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3280+6714G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14487899 | |||||||
| chr12:14488114 | C | T | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3280+6929C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14488114 | |||||||
| chr12:14488241 | TA | T | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3280+7057delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14488241 | |||||||
| chr12:14488308 | A | G | 3 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 |
3 | NA19056.hp2 NA19066.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.3280+7123A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14488308 | |||||||
| chr12:14488332 | G | A | 1 | a0001c0001t0003g0099 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3280+7147G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14488332 | |||||||
| chr12:14488378 | C | G | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3280+7193C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14488378 | |||||||
| chr12:14488461 | G | A | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3280+7276G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14488461 | |||||||
| chr12:14488594 | G | T | 27 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(24): Show |
28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.3280+7409G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14488594 | |||||||
| chr12:14488659 | G | A | 1 | a0013c0017t0001g0265 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3280+7474G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14488659 | |||||||
| chr12:14488677 | A | G | 27 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(24): Show |
28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.3280+7492A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14488677 | |||||||
| chr12:14489009 | C | A | 2 | a0003c0003t0011g0311 a0003c0003t0011g0312 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3281-7222C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489009 | |||||||
| chr12:14489069 | AGTG | A | 14 | a0001c0001t0019g0065 a0002c0006t0008g0207 a0002c0006t0008g0216 others(11): Show |
14 | HG00438.hp2 HG00673.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.3281-7159_3281-715 others(7): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14489069 | ||||||
| chr12:14489138 | C | T | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3281-7093C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489138 | |||||||
| chr12:14489248 | A | G | 1 | a0001c0001t0003g0108 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3281-6983A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489248 | |||||||
| chr12:14489291 | G | T | 9 | a0003c0003t0014g0152 a0003c0003t0014g0171 a0003c0003t0015g0002 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3281-6940G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489291 | |||||||
| chr12:14489372 | T | C | 6 | a0006c0009t0005g0174 a0006c0009t0005g0175 a0006c0009t0005g0176 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3281-6859T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489372 | |||||||
| chr12:14489454 | C | A | 2 | a0003c0003t0025g0172 a0003c0003t0025g0173 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.3281-6777C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489454 | |||||||
| chr12:14489481 | A | C | 14 | a0003c0003t0005g0313 a0003c0003t0012g0001 a0003c0003t0012g0180 others(11): Show |
17 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.3281-6750A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489481 | |||||||
| chr12:14489701 | G | A | 66 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(63): Show |
66 | HG01175.hp1 HG01243.hp1 HG01257.hp1 others(63): Show |
intron_variant | MODIFIER | c.3281-6530G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489701 | |||||||
| chr12:14489729 | A | G | 1 | a0003c0003t0005g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3281-6502A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489729 | |||||||
| chr12:14489793 | G | A | 2 | a0002c0002t0001g0245 a0011c0016t0039g0244 |
2 | HG02683.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3281-6438G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489793 | |||||||
| chr12:14489993 | A | C | 1 | a0002c0002t0001g0205 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3281-6238A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14489993 | |||||||
| chr12:14490084 | T | G | 1 | a0001c0001t0003g0107 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3281-6147T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490084 | |||||||
| chr12:14490147 | T | C | 15 | a0003c0003t0025g0172 a0003c0003t0025g0173 a0003c0005t0007g0322 others(12): Show |
15 | HG00099.hp1 HG00280.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.3281-6084T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490147 | |||||||
| chr12:14490539 | T | G | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.3281-5692T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490539 | |||||||
| chr12:14490567 | G | C | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.3281-5664G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490567 | |||||||
| chr12:14490576 | T | G | 179 | a0001c0001t0019g0065 a0001c0001t0040g0142 a0001c0020t0036g0134 others(176): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.3281-5655T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490576 | |||||||
| chr12:14490594 | T | C | 185 | a0001c0001t0019g0065 a0001c0001t0040g0142 a0001c0020t0036g0134 others(182): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.3281-5637T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490594 | |||||||
| chr12:14490596 | C | T | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3281-5635C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490596 | |||||||
| chr12:14490614 | A | C | 2 | a0001c0001t0002g0013 a0001c0001t0002g0020 |
2 | HG02083.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.3281-5617A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490614 | |||||||
| chr12:14490639 | C | A | 14 | a0003c0003t0005g0313 a0003c0003t0012g0001 a0003c0003t0012g0180 others(11): Show |
17 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.3281-5592C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490639 | |||||||
| chr12:14490676 | C | G | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3281-5555C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490676 | |||||||
| chr12:14490783 | T | G | 185 | a0001c0001t0019g0065 a0001c0001t0040g0142 a0001c0020t0036g0134 others(182): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.3281-5448T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490783 | |||||||
| chr12:14490806 | A | G | 1 | a0002c0002t0001g0245 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3281-5425A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490806 | |||||||
| chr12:14490821 | C | G | 28 | a0001c0020t0036g0134 a0003c0003t0004g0003 a0003c0003t0004g0186 others(25): Show |
29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.3281-5410C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490821 | |||||||
| chr12:14490953 | C | A | 1 | a0004c0008t0005g0252 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3281-5278C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490953 | |||||||
| chr12:14490954 | T | G | 1 | a0004c0008t0005g0252 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3281-5277T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14490954 | |||||||
| chr12:14491012 | G | A | 13 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(10): Show |
16 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.3281-5219G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14491012 | |||||||
| chr12:14491236 | A | G | 1 | a0001c0001t0002g0070 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3281-4995A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14491236 | |||||||
| chr12:14491298 | C | G | 2 | a0010c0013t0020g0118 a0010c0013t0020g0120 |
2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3281-4933C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14491298 | |||||||
| chr12:14491349 | A | G | 28 | a0001c0020t0036g0134 a0003c0003t0004g0003 a0003c0003t0004g0186 others(25): Show |
29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.3281-4882A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14491349 | |||||||
| chr12:14491408 | A | T | 1 | a0003c0003t0011g0321 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3281-4823A>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14491408 | |||||||
| chr12:14491519 | A | G | 11 | a0001c0001t0006g0073 a0001c0001t0006g0079 a0001c0001t0006g0132 others(8): Show |
11 | HG02145.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.3281-4712A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14491519 | |||||||
| chr12:14491885 | A | G | 28 | a0001c0020t0036g0134 a0003c0003t0004g0003 a0003c0003t0004g0186 others(25): Show |
29 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.3281-4346A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14491885 | |||||||
| chr12:14491947 | G | A | 1 | a0002c0002t0001g0283 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3281-4284G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14491947 | |||||||
| chr12:14492069 | T | C | 1 | a0004c0008t0005g0276 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3281-4162T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492069 | |||||||
| chr12:14492092 | G | A | 2 | a0003c0003t0011g0311 a0003c0003t0011g0312 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3281-4139G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492092 | |||||||
| chr12:14492145 | G | C | 66 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(63): Show |
66 | HG01175.hp1 HG01243.hp1 HG01257.hp1 others(63): Show |
intron_variant | MODIFIER | c.3281-4086G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492145 | |||||||
| chr12:14492149 | A | G | 1 | a0001c0001t0002g0035 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3281-4082A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492149 | |||||||
| chr12:14492171 | G | T | 1 | a0003c0003t0013g0164 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3281-4060G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492171 | |||||||
| chr12:14492183 | T | C | 2 | a0002c0002t0001g0245 a0003c0003t0013g0164 |
2 | HG00741.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3281-4048T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492183 | |||||||
| chr12:14492187 | C | T | 14 | a0003c0003t0005g0313 a0003c0003t0012g0001 a0003c0003t0012g0180 others(11): Show |
17 | HG00609.hp2 HG01346.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.3281-4044C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492187 | |||||||
| chr12:14492240 | T | C | 3 | a0003c0003t0023g0154 a0003c0003t0023g0155 a0003c0003t0034g0153 |
3 | HG01099.hp1 HG02300.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.3281-3991T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492240 | |||||||
| chr12:14492241 | G | C | 3 | a0003c0003t0023g0154 a0003c0003t0023g0155 a0003c0003t0034g0153 |
3 | HG01099.hp1 HG02300.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.3281-3990G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492241 | |||||||
| chr12:14492243 | A | G | 3 | a0003c0003t0023g0154 a0003c0003t0023g0155 a0003c0003t0034g0153 |
3 | HG01099.hp1 HG02300.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.3281-3988A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492243 | |||||||
| chr12:14492332 | A | G | 2 | a0002c0002t0001g0305 a0002c0002t0001g0306 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3281-3899A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492332 | |||||||
| chr12:14492335 | G | A | 2 | a0002c0002t0001g0305 a0002c0002t0001g0306 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3281-3896G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492335 | |||||||
| chr12:14492341 | T | C | 2 | a0002c0002t0001g0305 a0002c0002t0001g0306 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3281-3890T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492341 | |||||||
| chr12:14492347 | G | C | 2 | a0002c0002t0001g0305 a0002c0002t0001g0306 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3281-3884G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492347 | |||||||
| chr12:14492350 | A | G | 2 | a0002c0002t0001g0305 a0002c0002t0001g0306 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3281-3881A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492350 | |||||||
| chr12:14492416 | A | G | 185 | a0001c0001t0019g0065 a0001c0001t0040g0142 a0001c0020t0036g0134 others(182): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.3281-3815A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492416 | |||||||
| chr12:14492455 | G | A | 1 | a0001c0001t0029g0063 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3281-3776G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492455 | |||||||
| chr12:14492457 | C | T | 11 | a0003c0005t0007g0322 a0003c0005t0007g0323 a0003c0005t0007g0324 others(8): Show |
11 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3281-3774C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492457 | |||||||
| chr12:14492473 | T | C | 10 | a0002c0002t0009g0008 a0002c0002t0009g0009 a0002c0002t0009g0210 others(7): Show |
10 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.3281-3758T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492473 | |||||||
| chr12:14492494 | A | G | 179 | a0001c0001t0019g0065 a0001c0001t0040g0142 a0001c0020t0036g0134 others(176): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.3281-3737A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492494 | |||||||
| chr12:14492513 | AATTG | A | 138 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(135): Show |
138 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.3281-3712_3281-370 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14492513 | ||||||
| chr12:14492525 | G | A | 1 | a0003c0003t0011g0338 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3281-3706G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492525 | |||||||
| chr12:14492558 | C | T | 3 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0022 |
3 | NA18943.hp2 NA19074.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.3281-3673C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492558 | |||||||
| chr12:14492578 | A | C | 2 | a0003c0003t0005g0160 a0003c0003t0014g0161 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3281-3653A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492578 | |||||||
| chr12:14492650 | A | G | 2 | a0008c0012t0011g0335 a0008c0012t0011g0336 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3281-3581A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492650 | |||||||
| chr12:14492800 | G | A | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3281-3431G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492800 | |||||||
| chr12:14492836 | G | A | 1 | a0003c0003t0025g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3281-3395G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492836 | |||||||
| chr12:14492855 | AGAGTC | A | 13 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(10): Show |
16 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.3281-3372_3281-336 others(9): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14492855 | ||||||
| chr12:14492882 | G | A | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3281-3349G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492882 | |||||||
| chr12:14492952 | G | A | 1 | a0001c0001t0029g0063 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3281-3279G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492952 | |||||||
| chr12:14492952 | G | C | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3281-3279G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14492952 | |||||||
| chr12:14493064 | T | A | 1 | a0003c0003t0005g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3281-3167T>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14493064 | |||||||
| chr12:14493078 | A | G | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3281-3153A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14493078 | |||||||
| chr12:14493344 | A | G | 13 | a0003c0003t0012g0001 a0003c0003t0012g0180 a0003c0003t0012g0181 others(10): Show |
16 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.3281-2887A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14493344 | |||||||
| chr12:14493446 | A | C | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.3281-2785A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14493446 | |||||||
| chr12:14493550 | G | A | 2 | a0008c0012t0011g0335 a0008c0012t0011g0336 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3281-2681G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14493550 | |||||||
| chr12:14493592 | C | T | 1 | a0001c0001t0031g0012 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3281-2639C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14493592 | |||||||
| chr12:14493720 | C | G | 1 | a0001c0001t0002g0038 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3281-2511C>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14493720 | |||||||
| chr12:14493821 | A | G | 3 | a0002c0006t0008g0223 a0002c0006t0008g0224 a0002c0006t0008g0225 |
3 | NA18977.hp2 NA18981.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.3281-2410A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14493821 | |||||||
| chr12:14493929 | A | G | 1 | a0003c0003t0004g0199 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3281-2302A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14493929 | |||||||
| chr12:14494124 | T | C | 1 | a0001c0001t0003g0123 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3281-2107T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494124 | |||||||
| chr12:14494234 | C | A | 1 | a0001c0020t0036g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3281-1997C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494234 | |||||||
| chr12:14494284 | A | AAT | 15 | a0001c0001t0002g0041 a0001c0001t0002g0045 a0001c0001t0002g0047 others(12): Show |
15 | HG00140.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.3281-1898_3281-189 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | A | AATAT | 11 | a0001c0001t0002g0020 a0001c0001t0002g0029 a0001c0001t0002g0030 others(8): Show |
11 | HG00673.hp1 HG00735.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.3281-1900_3281-189 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | A | AATATAT | 8 | a0001c0001t0002g0021 a0001c0001t0002g0146 a0001c0001t0002g0339 others(5): Show |
8 | HG01516.hp1 HG01993.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.3281-1902_3281-189 others(10): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | A | AATATATA others(1): Show |
11 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0038 others(8): Show |
11 | HG00597.hp1 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.3281-1904_3281-189 others(12): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | A | AATATATA others(3): Show |
3 | a0001c0001t0003g0074 a0001c0001t0003g0126 a0012c0015t0003g0097 |
3 | HG01168.hp2 HG03239.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.3281-1906_3281-189 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | A | AATATATA others(5): Show |
3 | a0001c0001t0002g0068 a0001c0001t0003g0075 a0003c0003t0011g0185 |
3 | HG03579.hp2 NA18981.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.3281-1908_3281-189 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | A | AATATATA others(7): Show |
7 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0053 others(4): Show |
7 | HG03453.hp2 HG03490.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.3281-1910_3281-189 others(18): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | AAT | A | 26 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0022 others(23): Show |
26 | HG00099.hp2 HG00280.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.3281-1898_3281-189 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | AATAT | A | 21 | a0001c0001t0002g0027 a0001c0001t0003g0092 a0001c0001t0003g0093 others(18): Show |
21 | HG00140.hp1 HG00639.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.3281-1900_3281-189 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | AATATAT | A | 35 | a0001c0001t0002g0058 a0001c0001t0002g0121 a0001c0001t0003g0094 others(32): Show |
36 | HG00621.hp2 HG00733.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.3281-1902_3281-189 others(10): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | AATATATA others(1): Show |
A | 12 | a0001c0001t0002g0062 a0002c0002t0001g0300 a0002c0002t0009g0211 others(9): Show |
14 | HG01496.hp2 HG02572.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.3281-1904_3281-189 others(12): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | AATATATA others(3): Show |
A | 18 | a0001c0001t0002g0057 a0001c0001t0002g0064 a0001c0001t0002g0066 others(15): Show |
18 | HG00639.hp1 HG00741.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.3281-1906_3281-189 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | AATATATA others(5): Show |
A | 5 | a0001c0001t0002g0028 a0002c0002t0009g0008 a0002c0002t0009g0285 others(2): Show |
5 | HG01109.hp2 HG01496.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3281-1908_3281-189 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | AATATATA others(7): Show |
A | 11 | a0001c0001t0002g0116 a0001c0001t0002g0147 a0001c0001t0003g0080 others(8): Show |
11 | HG02257.hp2 HG02630.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.3281-1910_3281-189 others(18): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | AATATATA others(9): Show |
A | 5 | a0001c0001t0002g0148 a0001c0001t0003g0123 a0001c0001t0016g0130 others(2): Show |
5 | HG01346.hp1 HG01884.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.3281-1912_3281-189 others(20): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | AATATATA others(11): Show |
A | 1 | a0001c0001t0016g0078 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3281-1914_3281-189 others(22): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | AATATATA others(13): Show |
A | 3 | a0001c0001t0006g0139 a0001c0001t0014g0128 a0001c0001t0016g0129 |
3 | HG02109.hp1 HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3281-1916_3281-189 others(24): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | AATATATA others(15): Show |
A | 13 | a0001c0001t0003g0144 a0001c0001t0006g0073 a0001c0001t0006g0079 others(10): Show |
13 | HG02055.hp2 HG02145.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.3281-1918_3281-189 others(26): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | AATATATA others(17): Show |
A | 1 | a0002c0002t0001g0206 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3281-1920_3281-189 others(28): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | AATATATA others(21): Show |
A | 5 | a0001c0001t0003g0145 a0003c0003t0015g0002 a0003c0003t0015g0168 others(2): Show |
6 | HG00609.hp1 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.3281-1924_3281-189 others(32): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | AATATATA others(23): Show |
A | 1 | a0001c0001t0003g0124 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3281-1926_3281-189 others(34): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494284 | AATATATA others(27): Show |
A | 4 | a0003c0003t0025g0172 a0003c0003t0025g0173 a0009c0011t0024g0150 others(1): Show |
4 | HG00099.hp1 HG00280.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.3281-1930_3281-189 others(38): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494284 | ||||||
| chr12:14494309 | ATATATAT others(19): Show |
A | 2 | a0003c0003t0004g0194 a0003c0003t0004g0200 |
2 | HG01123.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.3281-1920_3281-189 others(30): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494309 | ||||||
| chr12:14494319 | ATATATAT others(9): Show |
A | 1 | a0003c0003t0004g0202 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3281-1910_3281-189 others(20): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494319 | ||||||
| chr12:14494323 | A | G | 3 | a0002c0004t0001g0230 a0002c0004t0001g0237 a0002c0004t0001g0246 |
3 | HG01175.hp2 HG01261.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3281-1908A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494323 | |||||||
| chr12:14494325 | A | ATG | 4 | a0002c0004t0001g0215 a0002c0004t0001g0229 a0002c0004t0001g0242 others(1): Show |
4 | HG01071.hp1 HG01993.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.3281-1905_3281-190 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494325 | ||||||
| chr12:14494325 | A | G | 13 | a0002c0004t0001g0228 a0002c0004t0001g0230 a0002c0004t0001g0231 others(10): Show |
13 | HG00639.hp2 HG01069.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.3281-1906A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494325 | |||||||
| chr12:14494325 | ATATATAT others(3): Show |
A | 1 | a0003c0003t0004g0188 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3281-1904_3281-189 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494325 | ||||||
| chr12:14494327 | A | G | 38 | a0002c0002t0001g0208 a0002c0002t0001g0209 a0002c0002t0001g0217 others(35): Show |
38 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.3281-1904A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494327 | |||||||
| chr12:14494329 | A | ATGTGTG | 3 | a0002c0004t0001g0238 a0002c0004t0001g0239 a0002c0004t0001g0241 |
3 | HG01106.hp2 HG01934.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.3281-1901_3281-190 others(10): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494329 | ||||||
| chr12:14494329 | A | G | 105 | a0001c0001t0040g0142 a0002c0002t0001g0007 a0002c0002t0001g0204 others(102): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.3281-1902A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494329 | |||||||
| chr12:14494331 | A | G | 125 | a0001c0001t0040g0142 a0002c0002t0001g0007 a0002c0002t0001g0204 others(122): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.3281-1900A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494331 | |||||||
| chr12:14494331 | ATATG | A | 4 | a0003c0003t0004g0003 a0003c0003t0004g0189 a0003c0003t0004g0191 others(1): Show |
4 | HG03491.hp1 HG03492.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.3281-1898_3281-189 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494331 | ||||||
| chr12:14494333 | A | ATATATAT others(15): Show |
1 | a0001c0001t0017g0049 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3281-1897_3281-189 others(26): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | ||||||
| chr12:14494333 | A | ATATATAT others(7): Show |
1 | a0007c0010t0002g0052 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3281-1897_3281-189 others(18): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | ||||||
| chr12:14494333 | A | ATATATAT others(5): Show |
5 | a0001c0001t0003g0090 a0001c0001t0017g0031 a0001c0001t0017g0051 others(2): Show |
5 | HG01516.hp2 HG01517.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.3281-1897_3281-189 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | ||||||
| chr12:14494333 | A | ATATATAT others(7): Show |
1 | a0005c0007t0010g0317 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3281-1897_3281-189 others(18): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | ||||||
| chr12:14494333 | A | ATATATAT others(9): Show |
1 | a0002c0006t0008g0225 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.3281-1897_3281-189 others(20): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | ||||||
| chr12:14494333 | A | ATATATAT others(3): Show |
1 | a0001c0001t0003g0109 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3281-1897_3281-189 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | ||||||
| chr12:14494333 | A | ATATATAT others(5): Show |
1 | a0005c0007t0010g0319 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3281-1897_3281-189 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | ||||||
| chr12:14494333 | A | ATATATAT others(7): Show |
1 | a0002c0006t0008g0220 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3281-1897_3281-189 others(18): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | ||||||
| chr12:14494333 | A | ATATATAT others(5): Show |
2 | a0002c0006t0008g0223 a0005c0007t0010g0316 |
2 | HG00609.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.3281-1897_3281-189 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | ||||||
| chr12:14494333 | A | ATATATAT others(7): Show |
1 | a0003c0005t0007g0330 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3281-1897_3281-189 others(18): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | ||||||
| chr12:14494333 | A | ATATATGT others(3): Show |
4 | a0002c0006t0008g0224 a0002c0006t0008g0226 a0002c0006t0008g0255 others(1): Show |
4 | HG00438.hp2 HG02135.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.3281-1897_3281-189 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | ||||||
| chr12:14494333 | A | ATATATGT others(5): Show |
3 | a0003c0005t0007g0322 a0003c0005t0007g0329 a0003c0005t0007g0331 |
3 | HG02451.hp2 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3281-1897_3281-189 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | ||||||
| chr12:14494333 | A | ATATG | 3 | a0001c0001t0003g0125 a0001c0001t0022g0084 a0001c0001t0022g0085 |
3 | HG01256.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3281-1897_3281-189 others(8): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | ||||||
| chr12:14494333 | A | ATATGTG | 2 | a0005c0007t0010g0005 a0005c0007t0010g0318 |
3 | HG03490.hp2 HG03492.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3281-1897_3281-189 others(10): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | ||||||
| chr12:14494333 | A | ATATGTGT others(1): Show |
5 | a0002c0002t0001g0272 a0002c0006t0008g0216 a0002c0006t0019g0221 others(2): Show |
5 | HG00621.hp1 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.3281-1897_3281-189 others(12): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | ||||||
| chr12:14494333 | A | ATATGTGT others(5): Show |
1 | a0003c0005t0007g0325 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3281-1897_3281-189 others(16): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | ||||||
| chr12:14494333 | A | ATGTGTGT others(3): Show |
1 | a0003c0005t0041g0334 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3281-1896_3281-188 others(14): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | ||||||
| chr12:14494333 | A | ATGTGTGT others(11): Show |
1 | a0003c0003t0005g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3281-1887_3281-188 others(22): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494333 | ||||||
| chr12:14494333 | A | G | 146 | a0001c0001t0002g0028 a0001c0001t0002g0054 a0001c0001t0002g0121 others(143): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.3281-1898A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494333 | |||||||
| chr12:14494335 | G | A | 2 | a0003c0003t0004g0190 a0003c0003t0004g0192 |
2 | NA18955.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.3281-1896G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494335 | |||||||
| chr12:14494345 | A | G | 1 | a0003c0003t0035g0340 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3281-1886A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494345 | |||||||
| chr12:14494440 | A | G | 6 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(3): Show |
6 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3281-1791A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494440 | |||||||
| chr12:14494520 | A | G | 104 | a0001c0001t0019g0065 a0002c0002t0001g0007 a0002c0002t0001g0204 others(101): Show |
105 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.3281-1711A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494520 | |||||||
| chr12:14494716 | T | G | 27 | a0003c0003t0004g0003 a0003c0003t0004g0186 a0003c0003t0004g0187 others(24): Show |
28 | HG00733.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.3281-1515T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494716 | |||||||
| chr12:14494751 | C | T | 3 | a0001c0001t0003g0102 a0001c0001t0003g0103 a0001c0001t0003g0104 |
3 | HG01069.hp1 HG01071.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.3281-1480C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494751 | |||||||
| chr12:14494908 | G | A | 3 | a0003c0003t0005g0160 a0003c0003t0014g0159 a0003c0003t0014g0161 |
3 | HG02257.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3281-1323G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14494908 | |||||||
| chr12:14494932 | C | CA | 8 | a0003c0003t0004g0193 a0003c0003t0004g0200 a0003c0003t0015g0002 others(5): Show |
9 | HG01169.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.3281-1276dupA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494932 | ||||||
| chr12:14494932 | CA | C | 149 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(146): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.3281-1276delA | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494932 | ||||||
| chr12:14494932 | CAA | C | 124 | a0001c0001t0002g0036 a0001c0001t0002g0042 a0001c0001t0003g0102 others(121): Show |
126 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.3281-1277_3281-127 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14494932 | ||||||
| chr12:14495051 | G | C | 1 | a0002c0006t0008g0218 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3281-1180G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495051 | |||||||
| chr12:14495115 | G | A | 2 | a0001c0001t0022g0084 a0001c0001t0022g0085 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3281-1116G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495115 | |||||||
| chr12:14495213 | ATC | A | 8 | a0005c0007t0010g0005 a0005c0007t0010g0314 a0005c0007t0010g0315 others(5): Show |
9 | HG00609.hp2 HG01346.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.3281-1014_3281-101 others(6): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14495213 | ||||||
| chr12:14495375 | T | C | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3281-856T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495375 | |||||||
| chr12:14495536 | C | T | 1 | a0001c0020t0036g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3281-695C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495536 | |||||||
| chr12:14495566 | A | G | 336 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(333): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.3281-665A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495566 | |||||||
| chr12:14495652 | G | T | 1 | a0003c0003t0014g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3281-579G>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495652 | |||||||
| chr12:14495807 | C | A | 2 | a0003c0003t0004g0194 a0003c0003t0004g0200 |
2 | HG01123.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.3281-424C>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495807 | |||||||
| chr12:14495846 | C | T | 2 | a0001c0001t0002g0069 a0001c0001t0002g0071 |
2 | HG01175.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.3281-385C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495846 | |||||||
| chr12:14495876 | A | C | 2 | a0008c0012t0011g0335 a0008c0012t0011g0336 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3281-355A>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495876 | |||||||
| chr12:14495938 | G | A | 1 | a0001c0001t0003g0115 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3281-293G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14495938 | |||||||
| chr12:14495996 | AGAAAGGG others(28): Show |
A | 1 | a0001c0001t0002g0030 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3281-233_3281-199d others(37): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr12 | 14495996 | ||||||
| chr12:14496038 | A | G | 1 | a0001c0001t0003g0101 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3281-193A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14496038 | |||||||
| chr12:14496088 | C | T | 2 | a0003c0003t0011g0311 a0003c0003t0011g0312 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3281-143C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14496088 | |||||||
| chr12:14496217 | T | G | 2 | a0003c0003t0011g0311 a0003c0003t0011g0312 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3281-14T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 13/14 | chr12 | 14496217 | |||||||
| chr12:14496458 | G | C | 1 | a0003c0003t0011g0203 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3393+115G>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/14 | chr12 | 14496458 | |||||||
| chr12:14496525 | GATCATTT others(19): Show |
G | 1 | a0002c0002t0001g0309 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3393+183_3393+208d others(28): Show |
ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/14 | chr12 | 14496525 | |||||||
| chr12:14496679 | G | A | 1 | a0003c0003t0005g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3393+336G>A | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/14 | chr12 | 14496679 | |||||||
| chr12:14496773 | C | T | 1 | a0003c0003t0012g0183 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3393+430C>T | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/14 | chr12 | 14496773 | |||||||
| chr12:14496910 | A | G | 2 | a0009c0011t0024g0150 a0009c0011t0024g0151 |
2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3393+567A>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/14 | chr12 | 14496910 | |||||||
| chr12:14497044 | T | C | 4 | a0003c0003t0013g0162 a0003c0003t0013g0163 a0003c0003t0013g0164 others(1): Show |
4 | HG00639.hp1 HG00741.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.3394-610T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/14 | chr12 | 14497044 | |||||||
| chr12:14497138 | T | C | 75 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0016 others(72): Show |
75 | HG00280.hp2 HG01081.hp1 HG01123.hp1 others(72): Show |
intron_variant | MODIFIER | c.3394-516T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/14 | chr12 | 14497138 | |||||||
| chr12:14497279 | T | C | 177 | a0001c0001t0019g0065 a0001c0001t0040g0142 a0001c0020t0036g0134 others(174): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.3394-375T>C | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/14 | chr12 | 14497279 | |||||||
| chr12:14497533 | T | G | 2 | a0001c0001t0002g0040 a0001c0001t0002g0042 |
2 | NA18957.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.3394-121T>G | ATF7IP | ENSG00000171681.13 | transcript | ENST00000261168.9 | protein_coding | 14/14 | chr12 | 14497533 |