Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80063 |
| ensemblid | ENSG00000166669.14 |
| hgncid | 20397 |
| symbol | ATF7IP2 |
| name | activating transcription factor 7 interacting protein 2 |
| refseq_nuc | NM_001393719.1 |
| refseq_prot | NP_001380648.1 |
| ensembl_nuc | ENST00000562102.6 |
| ensembl_prot | ENSP00000457731.2 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 10386061 |
| end | 10483638 |
| strand | + |
| ver | v1.2 |
| region | chr16:10386061-10483638 |
| region5000 | chr16:10381061-10488638 |
| regionname0 | ATF7IP2_chr16_10386061_10483638 |
| regionname5000 | ATF7IP2_chr16_10381061_10488638 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 682 | 169 | 42 | 40 | 60 | 6 | 20 | 54 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | MASPD others(677): Show |
chr16 | 10381061 | 10488638 |
| a0002 | 0/1 | 681 | 152 | 29 | 27 | 74 | 6 | 15 | 60 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | MASPD others(676): Show |
chr16 | 10381061 | 10488638 |
| a0003 | 0/0 | 681 | 39 | 14 | 1 | 22 | 0 | 2 | 16 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | MASPD others(676): Show |
chr16 | 10381061 | 10488638 |
| a0004 | 0/0 | 682 | 11 | 0 | 0 | 11 | 0 | 0 | 9 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | MASPD others(677): Show |
chr16 | 10381061 | 10488638 |
| a0005 | 0/0 | 682 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | MASPD others(677): Show |
chr16 | 10381061 | 10488638 |
| a0006 | 0/0 | 682 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | MASPD others(677): Show |
chr16 | 10381061 | 10488638 |
| a0007 | 0/0 | 682 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | MASPD others(677): Show |
chr16 | 10381061 | 10488638 |
| a0008 | 0/0 | 677 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | MASPD others(672): Show |
chr16 | 10381061 | 10488638 |
| a0009 | 0/0 | 682 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | MASPD others(677): Show |
chr16 | 10381061 | 10488638 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 2046 | 95 | 23 | 25 | 36 | 1 | 10 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2041): Show |
chr16 | 10381061 | 10488638 | ||
| a0001c0003 | 1/0 | 2046 | 56 | 3 | 15 | 24 | 3 | 10 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2041): Show |
chr16 | 10381061 | 10488638 | ||
| a0001c0005 | 0/0 | 2046 | 12 | 12 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2041): Show |
chr16 | 10381061 | 10488638 | ||
| a0001c0007 | 0/0 | 2046 | 4 | 4 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2041): Show |
chr16 | 10381061 | 10488638 | ||
| a0001c0013 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2041): Show |
chr16 | 10381061 | 10488638 | ||
| a0001c0016 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2041): Show |
chr16 | 10381061 | 10488638 | ||
| a0002c0001 | 0/1 | 2043 | 142 | 24 | 24 | 72 | 6 | 15 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2038): Show |
chr16 | 10381061 | 10488638 | ||
| a0002c0008 | 0/0 | 2043 | 4 | 3 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2038): Show |
chr16 | 10381061 | 10488638 | ||
| a0002c0010 | 0/0 | 2043 | 3 | 0 | 1 | 2 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2038): Show |
chr16 | 10381061 | 10488638 | ||
| a0002c0018 | 0/0 | 2043 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2038): Show |
chr16 | 10381061 | 10488638 | ||
| a0002c0019 | 0/0 | 2043 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2038): Show |
chr16 | 10381061 | 10488638 | ||
| a0002c0021 | 0/0 | 2043 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2038): Show |
chr16 | 10381061 | 10488638 | ||
| a0003c0004 | 0/0 | 2043 | 33 | 12 | 1 | 19 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2038): Show |
chr16 | 10381061 | 10488638 | ||
| a0003c0009 | 0/0 | 2043 | 3 | 0 | 0 | 3 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2038): Show |
chr16 | 10381061 | 10488638 | ||
| a0003c0011 | 0/0 | 2043 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2038): Show |
chr16 | 10381061 | 10488638 | ||
| a0003c0022 | 0/0 | 2043 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2038): Show |
chr16 | 10381061 | 10488638 | ||
| a0004c0006 | 0/0 | 2046 | 11 | 0 | 0 | 11 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2041): Show |
chr16 | 10381061 | 10488638 | ||
| a0005c0017 | 0/0 | 2046 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2041): Show |
chr16 | 10381061 | 10488638 | ||
| a0006c0014 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2041): Show |
chr16 | 10381061 | 10488638 | ||
| a0007c0015 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2041): Show |
chr16 | 10381061 | 10488638 | ||
| a0008c0020 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2026): Show |
chr16 | 10381061 | 10488638 | ||
| a0009c0012 | 0/0 | 2046 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | ATGGC others(2041): Show |
chr16 | 10381061 | 10488638 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0003 | 0/0 | 3740 | 58 | 21 | 19 | 13 | 0 | 5 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3735): Show |
chr16 | 10381061 | 10488638 |
| a0001c0002t0005 | 0/0 | 3739 | 25 | 0 | 6 | 14 | 1 | 4 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3734): Show |
chr16 | 10381061 | 10488638 |
| a0001c0002t0007 | 0/0 | 3739 | 9 | 0 | 0 | 9 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3734): Show |
chr16 | 10381061 | 10488638 |
| a0001c0002t0013 | 0/0 | 3741 | 2 | 1 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3736): Show |
chr16 | 10381061 | 10488638 |
| a0001c0002t0017 | 0/0 | 3740 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3735): Show |
chr16 | 10381061 | 10488638 |
| a0001c0003t0002 | 0/0 | 3741 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3736): Show |
chr16 | 10381061 | 10488638 |
| a0001c0003t0004 | 1/0 | 3741 | 43 | 1 | 15 | 14 | 3 | 9 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3736): Show |
chr16 | 10381061 | 10488638 |
| a0001c0003t0008 | 0/0 | 3741 | 8 | 2 | 0 | 6 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3736): Show |
chr16 | 10381061 | 10488638 |
| a0001c0003t0019 | 0/0 | 3740 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3735): Show |
chr16 | 10381061 | 10488638 |
| a0001c0003t0020 | 0/0 | 3741 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3736): Show |
chr16 | 10381061 | 10488638 |
| a0001c0003t0022 | 0/0 | 3741 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3736): Show |
chr16 | 10381061 | 10488638 |
| a0001c0005t0003 | 0/0 | 3740 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3735): Show |
chr16 | 10381061 | 10488638 |
| a0001c0005t0006 | 0/0 | 3744 | 9 | 9 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3739): Show |
chr16 | 10381061 | 10488638 |
| a0001c0005t0016 | 0/0 | 3740 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3735): Show |
chr16 | 10381061 | 10488638 |
| a0001c0005t0018 | 0/0 | 3740 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3735): Show |
chr16 | 10381061 | 10488638 |
| a0001c0007t0011 | 0/0 | 3741 | 4 | 4 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3736): Show |
chr16 | 10381061 | 10488638 |
| a0001c0013t0004 | 0/0 | 3741 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3736): Show |
chr16 | 10381061 | 10488638 |
| a0001c0016t0015 | 0/0 | 3740 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3735): Show |
chr16 | 10381061 | 10488638 |
| a0002c0001t0001 | 0/1 | 3738 | 99 | 19 | 23 | 43 | 2 | 11 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3733): Show |
chr16 | 10381061 | 10488638 |
| a0002c0001t0002 | 0/0 | 3738 | 32 | 0 | 1 | 29 | 0 | 2 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3733): Show |
chr16 | 10381061 | 10488638 |
| a0002c0001t0009 | 0/0 | 3738 | 5 | 5 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3733): Show |
chr16 | 10381061 | 10488638 |
| a0002c0001t0012 | 0/0 | 3737 | 3 | 0 | 0 | 0 | 3 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3732): Show |
chr16 | 10381061 | 10488638 |
| a0002c0001t0014 | 0/0 | 3738 | 2 | 0 | 0 | 0 | 0 | 2 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3733): Show |
chr16 | 10381061 | 10488638 |
| a0002c0001t0024 | 0/0 | 3738 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3733): Show |
chr16 | 10381061 | 10488638 |
| a0002c0008t0010 | 0/0 | 3738 | 4 | 3 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3733): Show |
chr16 | 10381061 | 10488638 |
| a0002c0010t0002 | 0/0 | 3738 | 3 | 0 | 1 | 2 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3733): Show |
chr16 | 10381061 | 10488638 |
| a0002c0018t0010 | 0/0 | 3738 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3733): Show |
chr16 | 10381061 | 10488638 |
| a0002c0019t0001 | 0/0 | 3738 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3733): Show |
chr16 | 10381061 | 10488638 |
| a0002c0021t0002 | 0/0 | 3738 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3733): Show |
chr16 | 10381061 | 10488638 |
| a0003c0004t0002 | 0/0 | 3738 | 32 | 12 | 1 | 18 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3733): Show |
chr16 | 10381061 | 10488638 |
| a0003c0004t0023 | 0/0 | 3739 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3734): Show |
chr16 | 10381061 | 10488638 |
| a0003c0009t0002 | 0/0 | 3738 | 3 | 0 | 0 | 3 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3733): Show |
chr16 | 10381061 | 10488638 |
| a0003c0011t0002 | 0/0 | 3738 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3733): Show |
chr16 | 10381061 | 10488638 |
| a0003c0022t0002 | 0/0 | 3738 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3733): Show |
chr16 | 10381061 | 10488638 |
| a0004c0006t0004 | 0/0 | 3741 | 10 | 0 | 0 | 10 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3736): Show |
chr16 | 10381061 | 10488638 |
| a0004c0006t0021 | 0/0 | 3741 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3736): Show |
chr16 | 10381061 | 10488638 |
| a0005c0017t0005 | 0/0 | 3739 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3734): Show |
chr16 | 10381061 | 10488638 |
| a0006c0014t0003 | 0/0 | 3740 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3735): Show |
chr16 | 10381061 | 10488638 |
| a0007c0015t0003 | 0/0 | 3740 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3735): Show |
chr16 | 10381061 | 10488638 |
| a0008c0020t0002 | 0/0 | 3726 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3721): Show |
chr16 | 10381061 | 10488638 |
| a0009c0012t0004 | 0/0 | 3741 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | GTTAA others(3736): Show |
chr16 | 10381061 | 10488638 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0003g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0003g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0005g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0007g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0007g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0007g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0007g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0007g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0007g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0007g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0007g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0007g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0013g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0013g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0002t0017g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0008g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0008g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0008g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0008g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0008g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0008g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0019g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0020g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0003t0022g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0005t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0005t0006g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0005t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0005t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0005t0006g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0005t0006g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0005t0006g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0005t0006g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0005t0006g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0005t0016g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0005t0018g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0007t0011g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0007t0011g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0007t0011g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0007t0011g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0013t0004g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0001c0016t0015g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0009g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0009g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0009g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0012g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0012g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0012g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0014g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0014g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0001t0024g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0008t0010g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0008t0010g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0008t0010g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0008t0010g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0010t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0010t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0010t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0018t0010g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0019t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0002c0021t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0002g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0004t0023g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0009t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0009t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0009t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0011t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0011t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0003c0022t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0004c0006t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0004c0006t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0004c0006t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0004c0006t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0004c0006t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0004c0006t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0004c0006t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0004c0006t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0004c0006t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0004c0006t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0004c0006t0021g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0005c0017t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0006c0014t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0007c0015t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0008c0020t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| a0009c0012t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0004 | g0224 | EUR | GBR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00099 | hp2 | a0002 | c0001 | t0012 | g0119 | EUR | GBR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00140 | hp1 | a0001 | c0003 | t0004 | g0262 | EUR | GBR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00140 | hp2 | a0002 | c0001 | t0012 | g0085 | EUR | GBR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00280 | hp1 | a0002 | c0001 | t0024 | g0172 | EUR | FIN | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00280 | hp2 | a0001 | c0016 | t0015 | g0323 | EUR | FIN | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00323 | hp1 | a0001 | c0003 | t0004 | g0232 | EUR | FIN | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00323 | hp2 | a0002 | c0001 | t0012 | g0092 | EUR | FIN | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00408 | hp1 | a0001 | c0003 | t0002 | g0033 | EAS | CHS | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00408 | hp2 | a0003 | c0004 | t0002 | g0076 | EAS | CHS | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00438 | hp1 | a0002 | c0001 | t0002 | g0136 | EAS | CHS | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00438 | hp2 | a0002 | c0001 | t0001 | g0093 | EAS | CHS | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00544 | hp1 | a0002 | c0001 | t0001 | g0121 | EAS | CHS | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00544 | hp2 | a0003 | c0004 | t0002 | g0074 | EAS | CHS | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00558 | hp1 | a0002 | c0001 | t0002 | g0111 | EAS | CHS | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00558 | hp2 | a0002 | c0001 | t0001 | g0059 | EAS | CHS | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00621 | hp1 | a0001 | c0003 | t0004 | g0201 | EAS | CHS | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00621 | hp2 | a0002 | c0001 | t0001 | g0095 | EAS | CHS | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00639 | hp1 | a0001 | c0002 | t0005 | g0287 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00639 | hp2 | a0002 | c0001 | t0001 | g0002 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00673 | hp1 | a0003 | c0004 | t0002 | g0079 | EAS | CHS | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00673 | hp2 | a0002 | c0001 | t0002 | g0088 | EAS | CHS | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00735 | hp1 | a0001 | c0003 | t0004 | g0261 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00735 | hp2 | a0002 | c0010 | t0002 | g0264 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00738 | hp1 | a0001 | c0003 | t0004 | g0209 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG00738 | hp2 | a0002 | c0001 | t0001 | g0122 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01069 | hp1 | a0001 | c0003 | t0004 | g0221 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01069 | hp2 | a0002 | c0019 | t0001 | g0182 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01070 | hp1 | a0001 | c0002 | t0003 | g0311 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01070 | hp2 | a0001 | c0003 | t0004 | g0238 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01071 | hp1 | a0001 | c0003 | t0004 | g0225 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0271 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01074 | hp1 | a0002 | c0001 | t0001 | g0180 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01074 | hp2 | a0003 | c0004 | t0002 | g0192 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0290 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0308 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01109 | hp1 | a0002 | c0008 | t0010 | g0196 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01109 | hp2 | a0001 | c0002 | t0005 | g0282 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01167 | hp1 | a0001 | c0002 | t0003 | g0301 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01167 | hp2 | a0002 | c0001 | t0001 | g0011 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01168 | hp1 | a0001 | c0002 | t0005 | g0317 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01168 | hp2 | a0002 | c0001 | t0001 | g0133 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01169 | hp1 | a0001 | c0002 | t0003 | g0356 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01169 | hp2 | a0001 | c0002 | t0005 | g0275 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01175 | hp1 | a0001 | c0003 | t0004 | g0206 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01175 | hp2 | a0002 | c0001 | t0001 | g0054 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01243 | hp2 | a0002 | c0001 | t0001 | g0178 | AMR | PUR | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01255 | hp1 | a0002 | c0001 | t0001 | g0039 | AMR | CLM | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01255 | hp2 | a0001 | c0003 | t0004 | g0217 | AMR | CLM | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01256 | hp1 | a0001 | c0003 | t0004 | g0223 | AMR | CLM | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0335 | AMR | CLM | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01257 | hp1 | a0002 | c0001 | t0001 | g0002 | AMR | CLM | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01257 | hp2 | a0001 | c0002 | t0003 | g0334 | AMR | CLM | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01261 | hp1 | a0002 | c0001 | t0001 | g0060 | AMR | CLM | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01261 | hp2 | a0001 | c0002 | t0005 | g0278 | AMR | CLM | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0361 | AMR | CLM | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01358 | hp2 | a0002 | c0001 | t0002 | g0089 | AMR | CLM | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01361 | hp1 | a0002 | c0001 | t0001 | g0176 | AMR | CLM | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01361 | hp2 | a0001 | c0003 | t0004 | g0218 | AMR | CLM | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0174 | AMR | CLM | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0313 | AMR | CLM | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01496 | hp1 | a0002 | c0001 | t0001 | g0165 | AMR | CLM | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01496 | hp2 | a0001 | c0003 | t0004 | g0255 | AMR | CLM | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01516 | hp1 | a0002 | c0001 | t0001 | g0057 | EUR | IBS | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01516 | hp2 | a0001 | c0013 | t0004 | g0259 | EUR | IBS | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01891 | hp1 | a0001 | c0002 | t0003 | g0272 | AFR | ACB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01891 | hp2 | a0003 | c0004 | t0002 | g0003 | AFR | ACB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01928 | hp1 | a0001 | c0002 | t0003 | g0291 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01928 | hp2 | a0002 | c0001 | t0001 | g0175 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01934 | hp1 | a0001 | c0002 | t0003 | g0341 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01934 | hp2 | a0002 | c0001 | t0001 | g0043 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01943 | hp1 | a0001 | c0003 | t0004 | g0220 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01943 | hp2 | a0002 | c0001 | t0001 | g0183 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01952 | hp1 | a0002 | c0001 | t0001 | g0023 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0296 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01975 | hp1 | a0002 | c0001 | t0001 | g0015 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01975 | hp2 | a0001 | c0002 | t0003 | g0336 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0173 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01981 | hp2 | a0001 | c0003 | t0004 | g0248 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01993 | hp1 | a0001 | c0003 | t0004 | g0258 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01993 | hp2 | a0001 | c0002 | t0003 | g0344 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02004 | hp1 | a0002 | c0001 | t0001 | g0017 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02004 | hp2 | a0001 | c0003 | t0004 | g0260 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02015 | hp1 | a0005 | c0017 | t0005 | g0302 | EAS | KHV | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02015 | hp2 | a0002 | c0001 | t0002 | g0102 | EAS | KHV | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02040 | hp1 | a0001 | c0003 | t0004 | g0250 | EAS | KHV | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0020 | EAS | KHV | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02055 | hp1 | a0002 | c0008 | t0010 | g0193 | AFR | ACB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02055 | hp2 | a0002 | c0001 | t0009 | g0167 | AFR | ACB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02071 | hp1 | a0003 | c0004 | t0002 | g0082 | EAS | KHV | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02071 | hp2 | a0001 | c0002 | t0005 | g0276 | EAS | KHV | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02080 | hp1 | a0002 | c0001 | t0002 | g0086 | EAS | KHV | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02080 | hp2 | a0001 | c0002 | t0005 | g0190 | EAS | KHV | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02129 | hp1 | a0004 | c0006 | t0004 | g0233 | EAS | KHV | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02129 | hp2 | a0002 | c0001 | t0002 | g0053 | EAS | KHV | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02145 | hp1 | a0003 | c0004 | t0002 | g0365 | AFR | ACB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02145 | hp2 | a0001 | c0005 | t0006 | g0371 | AFR | ACB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02148 | hp1 | a0002 | c0001 | t0001 | g0009 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0292 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02155 | hp1 | a0003 | c0004 | t0002 | g0073 | EAS | CDX | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02155 | hp2 | a0001 | c0002 | t0007 | g0319 | EAS | CDX | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02165 | hp1 | a0002 | c0001 | t0002 | g0083 | EAS | CDX | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02165 | hp2 | a0004 | c0006 | t0021 | g0251 | EAS | CDX | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02257 | hp1 | a0001 | c0002 | t0003 | g0312 | AFR | ACB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0362 | AFR | ACB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02258 | hp1 | a0002 | c0001 | t0001 | g0366 | AFR | ACB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02258 | hp2 | a0001 | c0003 | t0008 | g0026 | AFR | ACB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02273 | hp1 | a0001 | c0002 | t0003 | g0338 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02273 | hp2 | a0002 | c0001 | t0001 | g0177 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02280 | hp1 | a0001 | c0002 | t0003 | g0326 | AFR | ACB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02280 | hp2 | a0003 | c0004 | t0002 | g0152 | AFR | ACB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02293 | hp1 | a0001 | c0002 | t0003 | g0289 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02293 | hp2 | a0001 | c0002 | t0005 | g0351 | AMR | PEL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02451 | hp1 | a0001 | c0002 | t0003 | g0331 | AFR | ACB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0346 | AFR | ACB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02523 | hp1 | a0003 | c0004 | t0002 | g0144 | EAS | KHV | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02523 | hp2 | a0002 | c0001 | t0002 | g0137 | EAS | KHV | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02572 | hp1 | a0003 | c0004 | t0002 | g0003 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02572 | hp2 | a0002 | c0001 | t0001 | g0103 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02602 | hp1 | a0002 | c0001 | t0002 | g0143 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02602 | hp2 | a0003 | c0022 | t0002 | g0077 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02615 | hp1 | a0003 | c0004 | t0002 | g0158 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02615 | hp2 | a0002 | c0001 | t0001 | g0130 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02622 | hp1 | a0003 | c0004 | t0002 | g0153 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02622 | hp2 | a0001 | c0002 | t0003 | g0330 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02630 | hp1 | a0001 | c0002 | t0003 | g0314 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02630 | hp2 | a0002 | c0001 | t0001 | g0138 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02698 | hp1 | a0002 | c0001 | t0001 | g0037 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02698 | hp2 | a0001 | c0003 | t0004 | g0229 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02717 | hp1 | a0003 | c0004 | t0002 | g0191 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02717 | hp2 | a0003 | c0004 | t0002 | g0155 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02723 | hp1 | a0001 | c0007 | t0011 | g0355 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02723 | hp2 | a0002 | c0001 | t0001 | g0125 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02735 | hp1 | a0002 | c0001 | t0001 | g0100 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02735 | hp2 | a0001 | c0003 | t0004 | g0257 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02809 | hp1 | a0002 | c0001 | t0001 | g0056 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02809 | hp2 | a0002 | c0008 | t0010 | g0194 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02818 | hp1 | a0002 | c0001 | t0001 | g0124 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02818 | hp2 | a0001 | c0003 | t0008 | g0027 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02886 | hp1 | a0001 | c0002 | t0003 | g0359 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02886 | hp2 | a0002 | c0001 | t0001 | g0187 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02895 | hp1 | a0002 | c0008 | t0010 | g0195 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02895 | hp2 | a0001 | c0002 | t0003 | g0327 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02922 | hp1 | a0001 | c0002 | t0003 | g0328 | AFR | ESN | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02922 | hp2 | a0002 | c0001 | t0009 | g0171 | AFR | ESN | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02965 | hp1 | a0001 | c0005 | t0006 | g0368 | AFR | ESN | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02965 | hp2 | a0001 | c0007 | t0011 | g0353 | AFR | ESN | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02970 | hp1 | a0001 | c0002 | t0003 | g0347 | AFR | ESN | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02970 | hp2 | a0001 | c0002 | t0003 | g0306 | AFR | ESN | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02976 | hp1 | a0001 | c0005 | t0006 | g0005 | AFR | ESN | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02976 | hp2 | a0002 | c0001 | t0001 | g0128 | AFR | ESN | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03017 | hp1 | a0001 | c0003 | t0004 | g0228 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0273 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03041 | hp1 | a0002 | c0001 | t0001 | g0170 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03041 | hp2 | a0003 | c0011 | t0002 | g0156 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03098 | hp1 | a0001 | c0002 | t0013 | g0357 | AFR | MSL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03098 | hp2 | a0001 | c0002 | t0003 | g0283 | AFR | MSL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03130 | hp1 | a0001 | c0005 | t0006 | g0005 | AFR | ESN | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03130 | hp2 | a0003 | c0004 | t0002 | g0151 | AFR | ESN | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03139 | hp1 | a0002 | c0001 | t0001 | g0188 | AFR | ESN | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03139 | hp2 | a0003 | c0004 | t0002 | g0025 | AFR | ESN | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03209 | hp1 | a0001 | c0005 | t0006 | g0367 | AFR | MSL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03209 | hp2 | a0003 | c0011 | t0002 | g0154 | AFR | MSL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03225 | hp1 | a0001 | c0007 | t0011 | g0352 | AFR | MSL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03225 | hp2 | a0002 | c0001 | t0001 | g0163 | AFR | MSL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03239 | hp1 | a0002 | c0001 | t0001 | g0042 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03239 | hp2 | a0001 | c0003 | t0004 | g0222 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03453 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | MSL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03453 | hp2 | a0001 | c0005 | t0003 | g0032 | AFR | MSL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03486 | hp1 | a0001 | c0002 | t0003 | g0284 | AFR | MSL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03486 | hp2 | a0006 | c0014 | t0003 | g0268 | AFR | MSL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03490 | hp1 | a0002 | c0001 | t0001 | g0118 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03490 | hp2 | a0001 | c0002 | t0003 | g0270 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03491 | hp1 | a0002 | c0001 | t0014 | g0069 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03491 | hp2 | a0001 | c0002 | t0005 | g0315 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03492 | hp1 | a0002 | c0001 | t0014 | g0068 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03492 | hp2 | a0001 | c0002 | t0003 | g0269 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03516 | hp1 | a0002 | c0001 | t0001 | g0139 | AFR | ESN | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03516 | hp2 | a0001 | c0002 | t0003 | g0360 | AFR | ESN | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0363 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03540 | hp2 | a0001 | c0005 | t0006 | g0370 | AFR | GWD | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03579 | hp1 | a0001 | c0005 | t0006 | g0369 | AFR | MSL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03579 | hp2 | a0002 | c0001 | t0009 | g0169 | AFR | MSL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03669 | hp1 | a0001 | c0003 | t0004 | g0213 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03669 | hp2 | a0007 | c0015 | t0003 | g0310 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03688 | hp1 | a0001 | c0002 | t0003 | g0274 | SAS | STU | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03688 | hp2 | a0002 | c0001 | t0001 | g0179 | SAS | STU | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03704 | hp1 | a0002 | c0001 | t0002 | g0101 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03704 | hp2 | a0001 | c0003 | t0004 | g0240 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03710 | hp1 | a0001 | c0002 | t0013 | g0299 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03710 | hp2 | a0001 | c0003 | t0004 | g0239 | SAS | PJL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03831 | hp1 | a0001 | c0002 | t0005 | g0281 | SAS | BEB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03831 | hp2 | a0002 | c0001 | t0001 | g0049 | SAS | BEB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03834 | hp1 | a0002 | c0001 | t0001 | g0084 | SAS | BEB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03834 | hp2 | a0001 | c0003 | t0004 | g0245 | SAS | BEB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0298 | SAS | BEB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03942 | hp2 | a0001 | c0002 | t0005 | g0307 | SAS | BEB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG04115 | hp1 | a0002 | c0001 | t0001 | g0123 | SAS | STU | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG04115 | hp2 | a0001 | c0003 | t0022 | g0237 | SAS | STU | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG04204 | hp1 | a0001 | c0002 | t0005 | g0267 | SAS | STU | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG04204 | hp2 | a0002 | c0001 | t0001 | g0146 | SAS | STU | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG04228 | hp1 | a0003 | c0004 | t0002 | g0067 | SAS | STU | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG04228 | hp2 | a0002 | c0001 | t0001 | g0131 | SAS | STU | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18522 | hp1 | a0002 | c0001 | t0009 | g0164 | AFR | YRI | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18522 | hp2 | a0001 | c0005 | t0016 | g0031 | AFR | YRI | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18612 | hp1 | a0008 | c0020 | t0002 | g0006 | EAS | CHB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18612 | hp2 | a0002 | c0001 | t0002 | g0091 | EAS | CHB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18906 | hp1 | a0002 | c0001 | t0001 | g0120 | AFR | YRI | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18906 | hp2 | a0003 | c0004 | t0002 | g0157 | AFR | YRI | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18939 | hp1 | a0003 | c0004 | t0002 | g0129 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18939 | hp2 | a0001 | c0003 | t0002 | g0199 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18941 | hp1 | a0002 | c0001 | t0001 | g0046 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18941 | hp2 | a0001 | c0002 | t0007 | g0265 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18942 | hp1 | a0002 | c0001 | t0001 | g0094 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18942 | hp2 | a0002 | c0001 | t0002 | g0160 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18943 | hp1 | a0002 | c0001 | t0002 | g0127 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18943 | hp2 | a0004 | c0006 | t0004 | g0234 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18944 | hp1 | a0002 | c0001 | t0002 | g0159 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18944 | hp2 | a0001 | c0003 | t0008 | g0230 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18946 | hp1 | a0002 | c0001 | t0001 | g0098 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18946 | hp2 | a0001 | c0002 | t0005 | g0325 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18947 | hp1 | a0002 | c0001 | t0001 | g0016 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18947 | hp2 | a0001 | c0003 | t0004 | g0241 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18951 | hp1 | a0001 | c0002 | t0007 | g0318 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18951 | hp2 | a0002 | c0001 | t0002 | g0126 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18952 | hp1 | a0002 | c0001 | t0001 | g0051 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18952 | hp2 | a0002 | c0010 | t0002 | g0140 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18953 | hp1 | a0002 | c0001 | t0001 | g0044 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18953 | hp2 | a0001 | c0002 | t0003 | g0364 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18954 | hp1 | a0003 | c0009 | t0002 | g0063 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18954 | hp2 | a0002 | c0001 | t0001 | g0113 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18956 | hp1 | a0001 | c0002 | t0003 | g0309 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18956 | hp2 | a0002 | c0001 | t0002 | g0040 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18961 | hp1 | a0001 | c0002 | t0003 | g0345 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18961 | hp2 | a0002 | c0001 | t0001 | g0038 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18963 | hp1 | a0001 | c0003 | t0004 | g0254 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18963 | hp2 | a0002 | c0001 | t0001 | g0013 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18964 | hp1 | a0001 | c0003 | t0008 | g0256 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18964 | hp2 | a0001 | c0002 | t0003 | g0337 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18965 | hp1 | a0002 | c0001 | t0001 | g0022 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18965 | hp2 | a0001 | c0002 | t0007 | g0322 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18966 | hp1 | a0002 | c0001 | t0001 | g0114 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18966 | hp2 | a0001 | c0002 | t0005 | g0285 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18967 | hp1 | a0002 | c0010 | t0002 | g0149 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18967 | hp2 | a0002 | c0001 | t0002 | g0150 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18968 | hp1 | a0002 | c0001 | t0001 | g0058 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18968 | hp2 | a0002 | c0001 | t0001 | g0081 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18969 | hp1 | a0001 | c0002 | t0003 | g0343 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18969 | hp2 | a0002 | c0001 | t0002 | g0110 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18970 | hp1 | a0003 | c0004 | t0002 | g0065 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18970 | hp2 | a0002 | c0001 | t0001 | g0052 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18978 | hp1 | a0002 | c0001 | t0001 | g0116 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18978 | hp2 | a0001 | c0003 | t0004 | g0211 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18979 | hp1 | a0001 | c0002 | t0007 | g0320 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18979 | hp2 | a0002 | c0001 | t0002 | g0041 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18980 | hp1 | a0004 | c0006 | t0004 | g0203 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18980 | hp2 | a0001 | c0002 | t0005 | g0277 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18982 | hp1 | a0001 | c0002 | t0003 | g0342 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18982 | hp2 | a0002 | c0001 | t0002 | g0112 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18983 | hp1 | a0002 | c0001 | t0002 | g0018 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18983 | hp2 | a0003 | c0004 | t0002 | g0075 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18985 | hp1 | a0001 | c0003 | t0020 | g0214 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18985 | hp2 | a0003 | c0004 | t0002 | g0109 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18986 | hp1 | a0004 | c0006 | t0004 | g0244 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18986 | hp2 | a0002 | c0001 | t0001 | g0024 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18989 | hp1 | a0002 | c0001 | t0002 | g0148 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18989 | hp2 | a0001 | c0003 | t0004 | g0236 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18990 | hp1 | a0002 | c0001 | t0001 | g0035 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18990 | hp2 | a0001 | c0002 | t0005 | g0316 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18991 | hp1 | a0003 | c0004 | t0002 | g0072 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18991 | hp2 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18993 | hp1 | a0001 | c0002 | t0003 | g0295 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18993 | hp2 | a0002 | c0001 | t0002 | g0141 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18994 | hp1 | a0001 | c0002 | t0005 | g0304 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18994 | hp2 | a0002 | c0001 | t0001 | g0019 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0300 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18995 | hp2 | a0003 | c0009 | t0002 | g0062 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18997 | hp1 | a0001 | c0002 | t0005 | g0333 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18997 | hp2 | a0003 | c0004 | t0023 | g0106 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18998 | hp1 | a0002 | c0001 | t0002 | g0161 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18998 | hp2 | a0003 | c0004 | t0002 | g0066 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18999 | hp1 | a0001 | c0003 | t0008 | g0207 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18999 | hp2 | a0001 | c0002 | t0005 | g0266 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19000 | hp1 | a0004 | c0006 | t0004 | g0055 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19000 | hp2 | a0002 | c0001 | t0002 | g0145 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19001 | hp1 | a0002 | c0001 | t0002 | g0028 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19001 | hp2 | a0001 | c0003 | t0004 | g0204 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19002 | hp1 | a0002 | c0001 | t0001 | g0096 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19002 | hp2 | a0001 | c0002 | t0007 | g0280 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19003 | hp1 | a0004 | c0006 | t0004 | g0243 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19003 | hp2 | a0001 | c0002 | t0005 | g0303 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19004 | hp1 | a0001 | c0002 | t0005 | g0305 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19004 | hp2 | a0001 | c0003 | t0008 | g0210 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19005 | hp1 | a0009 | c0012 | t0004 | g0249 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19005 | hp2 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19006 | hp1 | a0001 | c0002 | t0003 | g0293 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19006 | hp2 | a0002 | c0001 | t0001 | g0045 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19007 | hp1 | a0001 | c0002 | t0007 | g0279 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19007 | hp2 | a0002 | c0001 | t0001 | g0021 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19011 | hp1 | a0001 | c0002 | t0005 | g0350 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19011 | hp2 | a0003 | c0004 | t0002 | g0078 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19012 | hp1 | a0002 | c0001 | t0001 | g0010 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19012 | hp2 | a0001 | c0003 | t0004 | g0252 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19030 | hp1 | a0002 | c0001 | t0001 | g0186 | AFR | LWK | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19030 | hp2 | a0002 | c0001 | t0001 | g0142 | AFR | LWK | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19043 | hp1 | a0001 | c0005 | t0006 | g0029 | AFR | LWK | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19043 | hp2 | a0003 | c0004 | t0002 | g0189 | AFR | LWK | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19055 | hp1 | a0004 | c0006 | t0004 | g0242 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19055 | hp2 | a0002 | c0001 | t0002 | g0185 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19057 | hp1 | a0002 | c0001 | t0001 | g0115 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19057 | hp2 | a0001 | c0003 | t0004 | g0247 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19058 | hp1 | a0002 | c0001 | t0001 | g0134 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19058 | hp2 | a0003 | c0004 | t0002 | g0132 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19060 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19060 | hp2 | a0001 | c0003 | t0004 | g0215 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19062 | hp1 | a0001 | c0002 | t0005 | g0348 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19062 | hp2 | a0002 | c0001 | t0001 | g0047 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19063 | hp1 | a0001 | c0002 | t0003 | g0340 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19063 | hp2 | a0002 | c0001 | t0001 | g0036 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19064 | hp1 | a0002 | c0001 | t0001 | g0099 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19064 | hp2 | a0003 | c0004 | t0002 | g0080 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19066 | hp1 | a0002 | c0001 | t0002 | g0090 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19066 | hp2 | a0001 | c0003 | t0008 | g0208 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19067 | hp1 | a0002 | c0001 | t0001 | g0070 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19067 | hp2 | a0001 | c0003 | t0004 | g0200 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19070 | hp1 | a0002 | c0001 | t0001 | g0087 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19070 | hp2 | a0004 | c0006 | t0004 | g0219 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19072 | hp1 | a0002 | c0001 | t0001 | g0061 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19072 | hp2 | a0004 | c0006 | t0004 | g0231 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19076 | hp1 | a0001 | c0003 | t0004 | g0205 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19076 | hp2 | a0003 | c0004 | t0002 | g0117 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19077 | hp1 | a0001 | c0002 | t0007 | g0286 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19077 | hp2 | a0003 | c0004 | t0002 | g0105 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19079 | hp1 | a0001 | c0002 | t0007 | g0321 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19079 | hp2 | a0001 | c0003 | t0004 | g0246 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19080 | hp1 | a0001 | c0002 | t0003 | g0297 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19080 | hp2 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19082 | hp1 | a0001 | c0003 | t0008 | g0253 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19082 | hp2 | a0002 | c0001 | t0001 | g0097 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19084 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19084 | hp2 | a0001 | c0002 | t0005 | g0349 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19086 | hp1 | a0002 | c0001 | t0002 | g0108 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19086 | hp2 | a0004 | c0006 | t0004 | g0202 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19087 | hp1 | a0002 | c0001 | t0001 | g0034 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19087 | hp2 | a0001 | c0003 | t0019 | g0235 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19088 | hp1 | a0002 | c0001 | t0002 | g0135 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19088 | hp2 | a0001 | c0002 | t0003 | g0294 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19090 | hp1 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19090 | hp2 | a0003 | c0009 | t0002 | g0064 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19091 | hp1 | a0003 | c0004 | t0002 | g0071 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19091 | hp2 | a0001 | c0002 | t0003 | g0339 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19240 | hp1 | a0002 | c0018 | t0010 | g0197 | AFR | YRI | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA19240 | hp2 | a0001 | c0005 | t0006 | g0030 | AFR | YRI | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA20752 | hp1 | a0001 | c0002 | t0005 | g0324 | EUR | TSI | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA20752 | hp2 | a0002 | c0001 | t0001 | g0048 | EUR | TSI | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA20905 | hp1 | a0001 | c0003 | t0004 | g0212 | SAS | GIH | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA20905 | hp2 | a0002 | c0001 | t0001 | g0147 | SAS | GIH | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01123 | hp1 | a0001 | c0003 | t0004 | g0198 | AMR | CLM | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG01123 | hp2 | a0002 | c0001 | t0001 | g0181 | AMR | CLM | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02486 | hp1 | a0002 | c0001 | t0001 | g0104 | AFR | ACB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0329 | AFR | ACB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02559 | hp1 | a0002 | c0001 | t0001 | g0168 | AFR | ACB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG02559 | hp2 | a0001 | c0007 | t0011 | g0354 | AFR | ACB | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03471 | hp1 | a0001 | c0002 | t0003 | g0332 | AFR | MSL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0358 | AFR | MSL | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG06807 | hp1 | a0002 | c0021 | t0002 | g0184 | AFR | USA | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| HG06807 | hp2 | a0002 | c0001 | t0009 | g0166 | AFR | USA | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18955 | hp1 | a0002 | c0001 | t0002 | g0107 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA18955 | hp2 | a0001 | c0003 | t0004 | g0216 | EAS | JPT | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA20300 | hp1 | a0001 | c0002 | t0017 | g0288 | AFR | USA | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA20300 | hp2 | a0001 | c0003 | t0004 | g0226 | AFR | USA | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA21309 | hp1 | a0002 | c0001 | t0001 | g0162 | AFR | LWK | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| NA21309 | hp2 | a0001 | c0005 | t0018 | g0263 | AFR | LWK | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| homoSapiens | chm13v2 | a0002 | c0001 | t0001 | g0050 | REF | REF | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0004 | g0227 | REF | REF | ATF7IP2_chr16_10381061_10488638 | ATF7IP2 | chr16 | 10381061 | 10488638 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:10430799 | GGAC | G | 3 | a0002 a0003 a0008 |
191 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(188): Show |
disruptive_inframe_deletion | MODERATE | c.183_185delGAC | p.Thr62del | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/14 | 486/3741 | 183/2049 | 61/682 | INFO_REALIGN_3_PRIME | chr16 | 10430799 | ||
| chr16:10431150 | T | G | 1 | a0009 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.530T>G | p.Val177Gly | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/14 | 833/3741 | 530/2049 | 177/682 | chr16 | 10431150 | |||
| chr16:10431401 | A | G | 1 | a0003 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.781A>G | p.Asn261Asp | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/14 | 1084/3741 | 781/2049 | 261/682 | chr16 | 10431401 | |||
| chr16:10433526 | C | A | 1 | a0002 | 1 | NA19240.hp1 | missense_variant&splice_region_variant | MODERATE | c.837C>A | p.Ser279Arg | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/14 | 1140/3741 | 837/2049 | 279/682 | chr16 | 10433526 | |||
| chr16:10433547 | G | A | 1 | a0006 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.858G>A | p.Met286Ile | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/14 | 1161/3741 | 858/2049 | 286/682 | chr16 | 10433547 | |||
| chr16:10433633 | C | G | 1 | a0005 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.944C>G | p.Thr315Arg | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/14 | 1247/3741 | 944/2049 | 315/682 | chr16 | 10433633 | |||
| chr16:10438107 | C | A | 1 | a0003 | 3 | NA18954.hp1 NA18995.hp2 NA19090.hp2 |
missense_variant | MODERATE | c.967C>A | p.His323Asn | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/14 | 1270/3741 | 967/2049 | 323/682 | chr16 | 10438107 | |||
| chr16:10440455 | C | A | 1 | a0007 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.1187C>A | p.Ala396Asp | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/14 | 1490/3741 | 1187/2049 | 396/682 | chr16 | 10440455 | |||
| chr16:10473936 | AACTTGAT others(5): Show |
A | 1 | a0008 | 1 | NA18612.hp1 | conservative_inframe_deletion | MODERATE | c.1498_1509delCTTGAT others(6): Show |
p.Leu500_Ile503del | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/14 | 1801/3741 | 1498/2049 | 500/682 | INFO_REALIGN_3_PRIME | chr16 | 10473936 | ||
| chr16:10480909 | C | T | 1 | a0002 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1580C>T | p.Ser527Leu | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 13/14 | 1883/3741 | 1580/2049 | 527/682 | chr16 | 10480909 | |||
| chr16:10480939 | C | T | 1 | a0003 | 39 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(36): Show |
missense_variant | MODERATE | c.1610C>T | p.Thr537Ile | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 13/14 | 1913/3741 | 1610/2049 | 537/682 | chr16 | 10480939 | |||
| chr16:10480956 | G | A | 1 | a0003 | 39 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(36): Show |
missense_variant | MODERATE | c.1627G>A | p.Ala543Thr | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 13/14 | 1930/3741 | 1627/2049 | 543/682 | chr16 | 10480956 | |||
| chr16:10482245 | C | T | 1 | a0004 | 11 | HG02129.hp1 HG02165.hp2 NA18943.hp2 others(8): Show |
missense_variant | MODERATE | c.2045C>T | p.Thr682Met | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 14/14 | 2348/3741 | 2045/2049 | 682/682 | chr16 | 10482245 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:10431097 | G | A | 2 | a0002c0008 a0002c0018 |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
synonymous_variant | LOW | c.477G>A | p.Glu159Glu | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/14 | 780/3741 | 477/2049 | 159/682 | chr16 | 10431097 | |||
| chr16:10431100 | G | T | 5 | a0001c0002 a0001c0016 a0005c0017 others(2): Show |
99 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(96): Show |
synonymous_variant | LOW | c.480G>T | p.Gly160Gly | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/14 | 783/3741 | 480/2049 | 160/682 | chr16 | 10431100 | |||
| chr16:10431205 | C | T | 1 | a0001c0013 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.585C>T | p.Asp195Asp | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/14 | 888/3741 | 585/2049 | 195/682 | chr16 | 10431205 | |||
| chr16:10431373 | T | C | 9 | a0001c0002 a0001c0005 a0001c0007 others(6): Show |
120 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(117): Show |
synonymous_variant | LOW | c.753T>C | p.Thr251Thr | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/14 | 1056/3741 | 753/2049 | 251/682 | chr16 | 10431373 | |||
| chr16:10440390 | T | C | 1 | a0002c0019 | 1 | HG01069.hp2 | synonymous_variant | LOW | c.1122T>C | p.Arg374Arg | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/14 | 1425/3741 | 1122/2049 | 374/682 | chr16 | 10440390 | |||
| chr16:10481967 | C | A | 5 | a0001c0007 a0001c0016 a0002c0001 others(2): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
synonymous_variant | LOW | c.1767C>A | p.Pro589Pro | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 14/14 | 2070/3741 | 1767/2049 | 589/682 | chr16 | 10481967 | |||
| chr16:10482168 | C | A | 1 | a0003c0011 | 2 | HG03041.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.1968C>A | p.Val656Val | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 14/14 | 2271/3741 | 1968/2049 | 656/682 | chr16 | 10482168 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:10386089 | G | C | 1 | a0002c0001t0009 | 5 | HG02055.hp2 HG02922.hp2 HG03579.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-275G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/14 | 44532 | chr16 | 10386089 | ||||||
| chr16:10428876 | CT | C | 14 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0007 others(11): Show |
115 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(112): Show |
5_prime_UTR_variant | MODIFIER | c.-140delT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/14 | 1734 | INFO_REALIGN_3_PRIME | chr16 | 10428876 | |||||
| chr16:10428905 | A | G | 33 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0007 others(30): Show |
316 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(313): Show |
5_prime_UTR_variant | MODIFIER | c.-122A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/14 | 1716 | chr16 | 10428905 | ||||||
| chr16:10428910 | G | C | 1 | a0002c0001t0014 | 2 | HG03491.hp1 HG03492.hp1 |
5_prime_UTR_variant | MODIFIER | c.-117G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/14 | 1711 | chr16 | 10428910 | ||||||
| chr16:10428955 | T | G | 16 | a0001c0003t0002 a0002c0001t0001 a0002c0001t0002 others(13): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
5_prime_UTR_variant | MODIFIER | c.-72T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/14 | 1666 | chr16 | 10428955 | ||||||
| chr16:10429005 | C | T | 1 | a0001c0003t0022 | 1 | HG04115.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-22C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/14 | chr16 | 10429005 | |||||||
| chr16:10482285 | A | C | 3 | a0001c0005t0018 a0002c0008t0010 a0002c0018t0010 |
6 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*36A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 14/14 | 36 | chr16 | 10482285 | ||||||
| chr16:10482441 | A | G | 1 | a0002c0001t0024 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*192A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 14/14 | 192 | chr16 | 10482441 | ||||||
| chr16:10482495 | G | C | 3 | a0001c0005t0018 a0002c0008t0010 a0002c0018t0010 |
6 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*246G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 14/14 | 246 | chr16 | 10482495 | ||||||
| chr16:10482533 | T | TATCA | 1 | a0001c0005t0006 | 9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*285_*288dupATCA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 14/14 | 289 | INFO_REALIGN_3_PRIME | chr16 | 10482533 | |||||
| chr16:10482682 | T | C | 1 | a0001c0005t0018 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*433T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 14/14 | 433 | chr16 | 10482682 | ||||||
| chr16:10482736 | A | AT | 3 | a0001c0002t0013 a0001c0007t0011 a0003c0004t0023 |
7 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*498dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 14/14 | 499 | INFO_REALIGN_3_PRIME | chr16 | 10482736 | |||||
| chr16:10482736 | AT | A | 5 | a0001c0002t0005 a0001c0002t0007 a0001c0003t0019 others(2): Show |
39 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*498delT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 14/14 | 498 | INFO_REALIGN_3_PRIME | chr16 | 10482736 | |||||
| chr16:10482880 | G | T | 1 | a0001c0002t0017 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*631G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 14/14 | 631 | chr16 | 10482880 | ||||||
| chr16:10482978 | T | C | 2 | a0002c0008t0010 a0002c0018t0010 |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*729T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 14/14 | 729 | chr16 | 10482978 | ||||||
| chr16:10482984 | G | T | 1 | a0004c0006t0021 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*735G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 14/14 | 735 | chr16 | 10482984 | ||||||
| chr16:10483122 | G | A | 2 | a0001c0002t0007 a0001c0003t0019 |
10 | HG02155.hp2 NA18941.hp2 NA18951.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*873G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 14/14 | 873 | chr16 | 10483122 | ||||||
| chr16:10483437 | G | T | 1 | a0001c0005t0016 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1188G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 14/14 | 1188 | chr16 | 10483437 | ||||||
| chr16:10483438 | G | A | 8 | a0001c0003t0020 a0001c0007t0011 a0001c0016t0015 others(5): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1189G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 14/14 | 1189 | chr16 | 10483438 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:10386279 | C | G | 6 | a0001c0005t0006g0005 a0001c0005t0006g0367 a0001c0005t0006g0368 others(3): Show |
7 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-242+157C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10386279 | |||||||
| chr16:10386287 | C | G | 1 | a0002c0001t0001g0366 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-242+165C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10386287 | |||||||
| chr16:10386337 | C | A | 1 | a0008c0020t0002g0006 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-242+215C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10386337 | |||||||
| chr16:10386357 | A | G | 104 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(101): Show |
105 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(102): Show |
intron_variant | MODIFIER | c.-242+235A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10386357 | |||||||
| chr16:10386406 | G | A | 18 | a0002c0001t0001g0007 a0002c0001t0001g0008 a0002c0001t0001g0009 others(15): Show |
18 | HG01167.hp2 HG01952.hp1 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.-242+284G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10386406 | |||||||
| chr16:10386413 | A | T | 1 | a0002c0001t0001g0024 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-242+291A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10386413 | |||||||
| chr16:10386443 | T | C | 1 | a0003c0004t0002g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-242+321T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10386443 | |||||||
| chr16:10386531 | C | T | 5 | a0001c0003t0004g0258 a0001c0003t0004g0260 a0001c0003t0004g0261 others(2): Show |
5 | HG00140.hp1 HG00735.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-242+409C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10386531 | |||||||
| chr16:10386603 | T | A | 305 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(302): Show |
310 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.-242+481T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10386603 | |||||||
| chr16:10386606 | C | A | 1 | a0001c0003t0004g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-242+484C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10386606 | |||||||
| chr16:10386837 | G | GA | 10 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0001c0005t0006g0029 others(7): Show |
10 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-242+718dupA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10386837 | ||||||
| chr16:10386852 | A | G | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-242+730A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10386852 | |||||||
| chr16:10386855 | A | AT | 183 | a0001c0002t0005g0190 a0002c0001t0001g0001 a0002c0001t0001g0002 others(180): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-242+741dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10386855 | ||||||
| chr16:10386897 | G | A | 1 | a0001c0003t0002g0199 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-242+775G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10386897 | |||||||
| chr16:10386918 | C | A | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-242+796C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10386918 | |||||||
| chr16:10386929 | TGTTGAAA others(5): Show |
T | 1 | a0001c0002t0003g0364 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-242+811_-242+822d others(14): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10386929 | ||||||
| chr16:10386970 | G | C | 1 | a0002c0010t0002g0264 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-242+848G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10386970 | |||||||
| chr16:10386989 | T | C | 304 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(301): Show |
309 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-242+867T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10386989 | |||||||
| chr16:10387265 | A | G | 1 | a0002c0018t0010g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-242+1143A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10387265 | |||||||
| chr16:10387324 | A | G | 2 | a0003c0004t0002g0191 a0003c0004t0002g0192 |
2 | HG01074.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-242+1202A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10387324 | |||||||
| chr16:10387451 | C | T | 1 | a0001c0002t0005g0190 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-242+1329C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10387451 | |||||||
| chr16:10387522 | G | A | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-242+1400G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10387522 | |||||||
| chr16:10387574 | A | G | 1 | a0003c0004t0002g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-242+1452A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10387574 | |||||||
| chr16:10387643 | A | G | 1 | a0002c0001t0001g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-242+1521A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10387643 | |||||||
| chr16:10387672 | A | G | 7 | a0001c0002t0003g0358 a0001c0002t0003g0359 a0001c0002t0003g0360 others(4): Show |
7 | HG01358.hp1 HG02257.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-242+1550A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10387672 | |||||||
| chr16:10387736 | G | A | 184 | a0001c0002t0005g0190 a0002c0001t0001g0001 a0002c0001t0001g0002 others(181): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-242+1614G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10387736 | |||||||
| chr16:10387824 | T | TC | 59 | a0001c0002t0003g0004 a0001c0002t0003g0306 a0001c0002t0003g0308 others(56): Show |
60 | HG00280.hp2 HG00621.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.-242+1711dupC | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10387824 | ||||||
| chr16:10387824 | T | TCC | 41 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0271 others(38): Show |
41 | HG00639.hp1 HG01071.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.-242+1710_-242+171 others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10387824 | ||||||
| chr16:10387824 | TC | T | 152 | a0001c0002t0005g0190 a0002c0001t0001g0001 a0002c0001t0001g0002 others(149): Show |
155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-242+1711delC | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10387824 | ||||||
| chr16:10387832 | C | G | 1 | a0001c0003t0004g0262 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-242+1710C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10387832 | |||||||
| chr16:10387834 | T | C | 3 | a0001c0002t0003g0364 a0001c0002t0007g0265 a0001c0003t0004g0200 |
3 | NA18941.hp2 NA18953.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-242+1712T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10387834 | |||||||
| chr16:10387837 | C | T | 4 | a0001c0002t0005g0348 a0001c0002t0005g0349 a0001c0002t0005g0350 others(1): Show |
4 | HG02293.hp2 NA19011.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.-242+1715C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10387837 | |||||||
| chr16:10387882 | G | GTTTAT | 3 | a0002c0001t0001g0186 a0002c0001t0001g0187 a0005c0017t0005g0302 |
3 | HG02015.hp1 HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-242+1775_-242+177 others(9): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10387882 | ||||||
| chr16:10387919 | G | T | 10 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(7): Show |
11 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.-242+1797G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10387919 | |||||||
| chr16:10387963 | C | T | 1 | a0001c0003t0004g0257 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-242+1841C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10387963 | |||||||
| chr16:10387995 | C | G | 1 | a0002c0001t0002g0185 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-242+1873C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10387995 | |||||||
| chr16:10388013 | C | G | 1 | a0002c0021t0002g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-242+1891C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10388013 | |||||||
| chr16:10388039 | A | G | 12 | a0002c0001t0001g0173 a0002c0001t0001g0174 a0002c0001t0001g0175 others(9): Show |
12 | HG00280.hp1 HG01069.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-242+1917A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10388039 | |||||||
| chr16:10388306 | G | C | 6 | a0001c0005t0006g0029 a0001c0005t0006g0030 a0001c0005t0006g0367 others(3): Show |
6 | HG02965.hp1 HG03209.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-242+2184G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10388306 | |||||||
| chr16:10388315 | C | T | 184 | a0001c0002t0005g0190 a0002c0001t0001g0001 a0002c0001t0001g0002 others(181): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-242+2193C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10388315 | |||||||
| chr16:10388455 | A | G | 113 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(110): Show |
115 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(112): Show |
intron_variant | MODIFIER | c.-242+2333A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10388455 | |||||||
| chr16:10388461 | T | A | 1 | a0002c0001t0001g0052 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-242+2339T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10388461 | |||||||
| chr16:10388494 | C | A | 7 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0002c0008t0010g0193 others(4): Show |
7 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-242+2372C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10388494 | |||||||
| chr16:10388517 | TATCAG | T | 4 | a0001c0002t0005g0266 a0001c0002t0005g0303 a0001c0002t0005g0304 others(1): Show |
4 | NA18994.hp1 NA18999.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.-242+2398_-242+240 others(9): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10388517 | ||||||
| chr16:10388683 | C | A | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-242+2561C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10388683 | |||||||
| chr16:10388714 | T | C | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-242+2592T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10388714 | |||||||
| chr16:10388826 | T | G | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-242+2704T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10388826 | |||||||
| chr16:10388867 | C | T | 1 | a0002c0001t0001g0051 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-242+2745C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10388867 | |||||||
| chr16:10388916 | G | C | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-242+2794G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10388916 | |||||||
| chr16:10389009 | C | CA | 7 | a0001c0003t0002g0199 a0001c0003t0004g0204 a0001c0003t0004g0205 others(4): Show |
7 | HG01175.hp2 HG02129.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.-242+2902dupA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10389009 | ||||||
| chr16:10389117 | G | T | 11 | a0002c0001t0001g0163 a0002c0001t0001g0165 a0002c0001t0001g0168 others(8): Show |
11 | HG01496.hp1 HG02055.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-242+2995G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10389117 | |||||||
| chr16:10389198 | T | C | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-242+3076T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10389198 | |||||||
| chr16:10389246 | T | C | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-242+3124T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10389246 | |||||||
| chr16:10389353 | C | T | 304 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(301): Show |
309 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-242+3231C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10389353 | |||||||
| chr16:10389509 | C | T | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-242+3387C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10389509 | |||||||
| chr16:10389716 | C | T | 1 | a0003c0004t0002g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-242+3594C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10389716 | |||||||
| chr16:10389723 | C | T | 1 | a0002c0001t0001g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-242+3601C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10389723 | |||||||
| chr16:10389758 | C | G | 3 | a0002c0001t0002g0159 a0002c0001t0002g0160 a0002c0001t0002g0161 |
3 | NA18942.hp2 NA18944.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-242+3636C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10389758 | |||||||
| chr16:10389773 | A | T | 7 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0005t0018g0263 others(4): Show |
7 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-242+3651A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10389773 | |||||||
| chr16:10389815 | G | A | 1 | a0001c0002t0003g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-242+3693G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10389815 | |||||||
| chr16:10389819 | C | T | 1 | a0002c0018t0010g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-242+3697C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10389819 | |||||||
| chr16:10389950 | T | C | 2 | a0002c0001t0001g0056 a0002c0001t0001g0057 |
2 | HG01516.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-242+3828T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10389950 | |||||||
| chr16:10389961 | T | C | 1 | a0001c0003t0004g0206 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-242+3839T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10389961 | |||||||
| chr16:10389992 | G | T | 10 | a0003c0004t0002g0003 a0003c0004t0002g0151 a0003c0004t0002g0152 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-242+3870G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10389992 | |||||||
| chr16:10390144 | T | G | 5 | a0002c0001t0001g0034 a0002c0001t0001g0035 a0002c0001t0001g0058 others(2): Show |
5 | HG00558.hp2 HG01261.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.-242+4022T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10390144 | |||||||
| chr16:10390228 | C | A | 7 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0005t0018g0263 others(4): Show |
7 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-242+4106C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10390228 | |||||||
| chr16:10390356 | G | T | 5 | a0001c0005t0006g0029 a0001c0005t0006g0030 a0001c0005t0006g0368 others(2): Show |
5 | HG02965.hp1 HG03540.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-242+4234G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10390356 | |||||||
| chr16:10390368 | C | T | 2 | a0001c0002t0003g0301 a0001c0002t0003g0356 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-242+4246C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10390368 | |||||||
| chr16:10390372 | G | A | 7 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0005t0018g0263 others(4): Show |
7 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-242+4250G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10390372 | |||||||
| chr16:10390686 | G | A | 1 | a0001c0003t0004g0201 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-242+4564G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10390686 | |||||||
| chr16:10390725 | G | A | 2 | a0001c0002t0005g0267 a0001c0002t0005g0307 |
2 | HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-242+4603G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10390725 | |||||||
| chr16:10390976 | A | G | 28 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0291 others(25): Show |
28 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.-242+4854A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10390976 | |||||||
| chr16:10391020 | C | T | 96 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(93): Show |
97 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(94): Show |
intron_variant | MODIFIER | c.-242+4898C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10391020 | |||||||
| chr16:10391091 | A | G | 96 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(93): Show |
97 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(94): Show |
intron_variant | MODIFIER | c.-242+4969A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10391091 | |||||||
| chr16:10391107 | T | C | 1 | a0003c0004t0002g0365 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-242+4985T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10391107 | |||||||
| chr16:10391156 | CA | C | 208 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0002t0005g0190 others(205): Show |
212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.-242+5049delA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10391156 | ||||||
| chr16:10391205 | C | T | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-242+5083C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10391205 | |||||||
| chr16:10391234 | T | C | 1 | a0003c0004t0002g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-242+5112T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10391234 | |||||||
| chr16:10391294 | G | A | 1 | a0001c0007t0011g0352 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-242+5172G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10391294 | |||||||
| chr16:10391302 | T | C | 2 | a0001c0003t0008g0207 a0001c0003t0008g0208 |
2 | NA18999.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-242+5180T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10391302 | |||||||
| chr16:10391473 | T | C | 2 | a0001c0002t0003g0301 a0001c0002t0003g0356 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-242+5351T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10391473 | |||||||
| chr16:10391613 | T | A | 8 | a0001c0002t0003g0358 a0001c0002t0003g0359 a0001c0002t0003g0360 others(5): Show |
8 | HG01358.hp1 HG02257.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-242+5491T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10391613 | |||||||
| chr16:10391619 | C | T | 8 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(5): Show |
9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-242+5497C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10391619 | |||||||
| chr16:10391620 | G | A | 3 | a0003c0009t0002g0062 a0003c0009t0002g0063 a0003c0009t0002g0064 |
3 | NA18954.hp1 NA18995.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-242+5498G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10391620 | |||||||
| chr16:10392054 | A | G | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-242+5932A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10392054 | |||||||
| chr16:10392056 | C | CT | 178 | a0001c0002t0003g0301 a0001c0002t0005g0190 a0001c0003t0002g0033 others(175): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.-242+5951dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10392056 | ||||||
| chr16:10392056 | C | CTT | 111 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(108): Show |
113 | HG00280.hp2 HG00639.hp1 HG00735.hp1 others(110): Show |
intron_variant | MODIFIER | c.-242+5950_-242+595 others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10392056 | ||||||
| chr16:10392056 | C | CTTT | 11 | a0001c0002t0003g0300 a0001c0002t0003g0345 a0001c0002t0003g0358 others(8): Show |
11 | HG01358.hp1 HG02257.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.-242+5949_-242+595 others(7): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10392056 | ||||||
| chr16:10392093 | C | T | 1 | a0002c0001t0001g0054 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-242+5971C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10392093 | |||||||
| chr16:10392215 | A | G | 48 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(45): Show |
49 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.-242+6093A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10392215 | |||||||
| chr16:10392225 | A | G | 304 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(301): Show |
309 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-242+6103A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10392225 | |||||||
| chr16:10392306 | C | T | 1 | a0001c0002t0003g0344 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-242+6184C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10392306 | |||||||
| chr16:10392338 | C | CT | 18 | a0001c0002t0003g0298 a0001c0002t0003g0364 a0001c0003t0004g0200 others(15): Show |
19 | HG01175.hp2 HG02145.hp2 HG02602.hp1 others(16): Show |
intron_variant | MODIFIER | c.-242+6232dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10392338 | ||||||
| chr16:10392338 | CT | C | 7 | a0001c0003t0004g0198 a0001c0003t0008g0026 a0001c0003t0008g0027 others(4): Show |
7 | HG01123.hp1 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-242+6232delT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10392338 | ||||||
| chr16:10392476 | A | G | 2 | a0002c0001t0001g0048 a0002c0001t0001g0049 |
2 | HG03831.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-242+6354A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10392476 | |||||||
| chr16:10392495 | A | C | 149 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0007 others(146): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.-242+6373A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10392495 | |||||||
| chr16:10392823 | TA | T | 11 | a0001c0002t0003g0301 a0001c0002t0005g0285 a0001c0002t0007g0286 others(8): Show |
11 | HG01069.hp2 HG01167.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.-242+6716delA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10392823 | ||||||
| chr16:10393017 | T | G | 2 | a0001c0002t0003g0346 a0001c0002t0003g0347 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-242+6895T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10393017 | |||||||
| chr16:10393076 | A | G | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-242+6954A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10393076 | |||||||
| chr16:10393127 | T | G | 16 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0271 others(13): Show |
16 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-242+7005T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10393127 | |||||||
| chr16:10393271 | A | G | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-242+7149A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10393271 | |||||||
| chr16:10393273 | G | C | 3 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0308 |
3 | HG01099.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-242+7151G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10393273 | |||||||
| chr16:10393285 | C | T | 1 | a0001c0002t0005g0333 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-242+7163C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10393285 | |||||||
| chr16:10393286 | A | G | 2 | a0002c0010t0002g0140 a0002c0010t0002g0149 |
2 | NA18952.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.-242+7164A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10393286 | |||||||
| chr16:10393314 | T | C | 2 | a0002c0001t0001g0034 a0002c0001t0001g0035 |
2 | NA18990.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-242+7192T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10393314 | |||||||
| chr16:10393315 | C | CA | 38 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0271 others(35): Show |
38 | HG00735.hp1 HG00738.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.-242+7220dupA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10393315 | ||||||
| chr16:10393315 | CA | C | 55 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(52): Show |
57 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.-242+7220delA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10393315 | ||||||
| chr16:10393315 | CAA | C | 10 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0003t0008g0026 others(7): Show |
10 | HG01109.hp1 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-242+7219_-242+722 others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10393315 | ||||||
| chr16:10393315 | CAAAAAAA | C | 28 | a0001c0002t0005g0190 a0001c0003t0002g0033 a0002c0001t0001g0081 others(25): Show |
28 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-242+7214_-242+722 others(11): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10393315 | ||||||
| chr16:10393315 | CAAAAAAA others(1): Show |
C | 152 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0007 others(149): Show |
155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-242+7213_-242+722 others(12): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10393315 | ||||||
| chr16:10393693 | A | G | 1 | a0001c0003t0008g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-242+7571A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10393693 | |||||||
| chr16:10393853 | C | T | 1 | a0001c0005t0003g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-242+7731C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10393853 | |||||||
| chr16:10393878 | A | G | 184 | a0001c0002t0005g0190 a0001c0003t0002g0033 a0002c0001t0001g0001 others(181): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-242+7756A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10393878 | |||||||
| chr16:10393917 | G | T | 1 | a0002c0001t0001g0054 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-242+7795G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10393917 | |||||||
| chr16:10394213 | C | T | 1 | a0001c0003t0004g0254 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-242+8091C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10394213 | |||||||
| chr16:10394239 | G | A | 1 | a0002c0001t0012g0085 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-242+8117G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10394239 | |||||||
| chr16:10394243 | C | G | 1 | a0003c0004t0002g0158 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-242+8121C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10394243 | |||||||
| chr16:10394327 | C | T | 1 | a0002c0001t0001g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-242+8205C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10394327 | |||||||
| chr16:10394393 | A | T | 1 | a0001c0002t0003g0347 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-242+8271A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10394393 | |||||||
| chr16:10394471 | A | C | 24 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0291 others(21): Show |
24 | HG01099.hp1 HG01256.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.-242+8349A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10394471 | |||||||
| chr16:10394560 | A | G | 14 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0003t0008g0026 others(11): Show |
14 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-242+8438A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10394560 | |||||||
| chr16:10394785 | A | G | 7 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(4): Show |
8 | HG01243.hp1 HG02451.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-242+8663A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10394785 | |||||||
| chr16:10394862 | G | T | 1 | a0001c0003t0008g0253 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-242+8740G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10394862 | |||||||
| chr16:10394979 | A | C | 1 | a0001c0005t0003g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-242+8857A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10394979 | |||||||
| chr16:10395076 | C | T | 1 | a0002c0001t0002g0083 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-242+8954C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10395076 | |||||||
| chr16:10395208 | G | C | 10 | a0003c0004t0002g0003 a0003c0004t0002g0151 a0003c0004t0002g0152 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-242+9086G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10395208 | |||||||
| chr16:10395321 | C | G | 8 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(5): Show |
9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-242+9199C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10395321 | |||||||
| chr16:10395460 | A | G | 1 | a0001c0005t0003g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-242+9338A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10395460 | |||||||
| chr16:10395482 | C | T | 3 | a0002c0001t0001g0138 a0002c0001t0001g0139 a0002c0001t0001g0188 |
3 | HG02630.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-242+9360C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10395482 | |||||||
| chr16:10395506 | C | A | 61 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0271 others(58): Show |
61 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.-242+9384C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10395506 | |||||||
| chr16:10395510 | G | A | 35 | a0001c0002t0005g0266 a0001c0002t0005g0267 a0001c0002t0005g0275 others(32): Show |
35 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.-242+9388G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10395510 | |||||||
| chr16:10395565 | A | T | 63 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(60): Show |
64 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.-242+9443A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10395565 | |||||||
| chr16:10395859 | A | C | 5 | a0001c0005t0018g0263 a0001c0007t0011g0352 a0001c0007t0011g0353 others(2): Show |
5 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-242+9737A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10395859 | |||||||
| chr16:10395956 | G | A | 1 | a0003c0004t0002g0071 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-242+9834G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10395956 | |||||||
| chr16:10395971 | G | A | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-242+9849G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10395971 | |||||||
| chr16:10396079 | A | G | 2 | a0001c0002t0003g0301 a0001c0002t0003g0356 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-242+9957A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10396079 | |||||||
| chr16:10396161 | T | C | 1 | a0001c0002t0005g0267 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-242+10039T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10396161 | |||||||
| chr16:10396208 | G | C | 3 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0002c0010t0002g0264 |
3 | HG00735.hp2 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-242+10086G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10396208 | |||||||
| chr16:10396263 | A | G | 190 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0273 others(187): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.-242+10141A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10396263 | |||||||
| chr16:10396465 | G | A | 10 | a0003c0004t0002g0003 a0003c0004t0002g0151 a0003c0004t0002g0152 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-242+10343G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10396465 | |||||||
| chr16:10396560 | T | C | 1 | a0008c0020t0002g0006 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-242+10438T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10396560 | |||||||
| chr16:10396605 | G | A | 9 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(6): Show |
10 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.-242+10483G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10396605 | |||||||
| chr16:10396818 | T | TA | 186 | a0001c0002t0005g0190 a0001c0003t0002g0033 a0001c0005t0016g0031 others(183): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.-242+10706dupA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10396818 | ||||||
| chr16:10396828 | A | AT | 111 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(108): Show |
113 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(110): Show |
intron_variant | MODIFIER | c.-242+10716dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10396828 | ||||||
| chr16:10396828 | A | T | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-242+10706A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10396828 | |||||||
| chr16:10396840 | A | C | 1 | a0001c0003t0004g0252 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-242+10718A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10396840 | |||||||
| chr16:10396987 | T | G | 37 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(34): Show |
38 | HG01099.hp1 HG01243.hp1 HG01256.hp2 others(35): Show |
intron_variant | MODIFIER | c.-242+10865T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10396987 | |||||||
| chr16:10397062 | C | T | 1 | a0001c0003t0004g0260 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-242+10940C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10397062 | |||||||
| chr16:10397068 | C | T | 1 | a0002c0001t0002g0141 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-242+10946C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10397068 | |||||||
| chr16:10397099 | G | A | 3 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0196 |
3 | HG01109.hp1 HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-242+10977G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10397099 | |||||||
| chr16:10397174 | C | G | 10 | a0003c0004t0002g0003 a0003c0004t0002g0151 a0003c0004t0002g0152 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-242+11052C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10397174 | |||||||
| chr16:10397409 | T | C | 10 | a0003c0004t0002g0003 a0003c0004t0002g0151 a0003c0004t0002g0152 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-242+11287T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10397409 | |||||||
| chr16:10397493 | C | G | 5 | a0001c0005t0018g0263 a0001c0007t0011g0352 a0001c0007t0011g0353 others(2): Show |
5 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-242+11371C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10397493 | |||||||
| chr16:10397543 | G | A | 1 | a0002c0001t0001g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-242+11421G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10397543 | |||||||
| chr16:10397576 | C | T | 3 | a0002c0001t0001g0138 a0002c0001t0001g0139 a0002c0001t0001g0188 |
3 | HG02630.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-242+11454C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10397576 | |||||||
| chr16:10397603 | G | A | 1 | a0001c0002t0005g0276 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-242+11481G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10397603 | |||||||
| chr16:10397612 | C | T | 1 | a0001c0002t0005g0325 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-242+11490C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10397612 | |||||||
| chr16:10397648 | G | A | 2 | a0001c0003t0004g0217 a0001c0003t0004g0218 |
2 | HG01255.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-242+11526G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10397648 | |||||||
| chr16:10397657 | G | A | 2 | a0001c0002t0005g0315 a0002c0001t0002g0086 |
2 | HG02080.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-242+11535G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10397657 | |||||||
| chr16:10397823 | C | A | 1 | a0001c0003t0004g0252 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-242+11701C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10397823 | |||||||
| chr16:10397857 | C | CA | 9 | a0001c0005t0018g0263 a0001c0007t0011g0352 a0001c0007t0011g0353 others(6): Show |
9 | HG00280.hp1 HG02559.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-242+11751dupA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10397857 | ||||||
| chr16:10397859 | A | C | 1 | a0004c0006t0021g0251 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-242+11737A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10397859 | |||||||
| chr16:10397875 | G | A | 3 | a0001c0002t0005g0277 a0001c0002t0005g0316 a0001c0002t0005g0325 |
3 | NA18946.hp2 NA18980.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-242+11753G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10397875 | |||||||
| chr16:10397972 | A | G | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-242+11850A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10397972 | |||||||
| chr16:10398075 | C | T | 2 | a0002c0001t0002g0137 a0002c0001t0002g0150 |
2 | HG02523.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.-242+11953C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10398075 | |||||||
| chr16:10398124 | C | T | 107 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(104): Show |
109 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(106): Show |
intron_variant | MODIFIER | c.-242+12002C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10398124 | |||||||
| chr16:10398203 | C | T | 10 | a0001c0003t0004g0200 a0001c0003t0004g0201 a0001c0003t0004g0215 others(7): Show |
10 | HG00621.hp1 HG01981.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.-242+12081C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10398203 | |||||||
| chr16:10398229 | G | A | 1 | a0004c0006t0004g0219 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-242+12107G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10398229 | |||||||
| chr16:10398260 | C | T | 1 | a0002c0021t0002g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-242+12138C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10398260 | |||||||
| chr16:10398303 | C | CA | 43 | a0001c0002t0003g0309 a0001c0002t0003g0346 a0001c0002t0003g0347 others(40): Show |
43 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.-242+12194dupA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10398303 | ||||||
| chr16:10398311 | A | T | 2 | a0003c0004t0002g0082 a0003c0004t0002g0144 |
2 | HG02071.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-242+12189A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10398311 | |||||||
| chr16:10398314 | A | AT | 60 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(57): Show |
61 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.-242+12192_-242+12 others(7): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10398314 | |||||||
| chr16:10398314 | A | T | 189 | a0001c0002t0005g0190 a0001c0003t0002g0033 a0001c0003t0004g0245 others(186): Show |
192 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-242+12192A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10398314 | |||||||
| chr16:10398316 | A | AAT | 7 | a0001c0005t0003g0032 a0001c0005t0006g0029 a0001c0005t0006g0030 others(4): Show |
7 | HG02965.hp1 HG03209.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.-242+12194_-242+12 others(8): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10398316 | |||||||
| chr16:10398317 | T | A | 7 | a0001c0005t0003g0032 a0001c0005t0006g0029 a0001c0005t0006g0030 others(4): Show |
7 | HG02965.hp1 HG03209.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.-242+12195T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10398317 | |||||||
| chr16:10398317 | T | TA | 2 | a0001c0005t0006g0005 a0001c0005t0006g0371 |
3 | HG02145.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-242+12197dupA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10398317 | ||||||
| chr16:10398363 | T | A | 2 | a0001c0002t0005g0275 a0001c0002t0005g0317 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-242+12241T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10398363 | |||||||
| chr16:10398550 | A | C | 1 | a0002c0001t0001g0181 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-242+12428A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10398550 | |||||||
| chr16:10398611 | C | T | 186 | a0001c0002t0005g0190 a0001c0003t0002g0033 a0001c0005t0016g0031 others(183): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.-242+12489C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10398611 | |||||||
| chr16:10398912 | A | G | 1 | a0004c0006t0004g0244 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-242+12790A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10398912 | |||||||
| chr16:10399062 | G | A | 1 | a0003c0004t0002g0151 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-242+12940G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10399062 | |||||||
| chr16:10399067 | T | C | 1 | a0002c0001t0002g0088 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-242+12945T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10399067 | |||||||
| chr16:10399117 | G | GA | 157 | a0001c0005t0016g0031 a0002c0001t0001g0001 a0002c0001t0001g0002 others(154): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-242+13004dupA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10399117 | ||||||
| chr16:10399150 | A | C | 6 | a0001c0005t0006g0029 a0001c0005t0006g0030 a0001c0005t0006g0367 others(3): Show |
6 | HG02965.hp1 HG03209.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-242+13028A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10399150 | |||||||
| chr16:10399178 | A | G | 4 | a0002c0001t0001g0045 a0002c0001t0001g0046 a0002c0001t0001g0047 others(1): Show |
4 | NA18941.hp1 NA18952.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-242+13056A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10399178 | |||||||
| chr16:10399260 | C | T | 292 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(289): Show |
297 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-242+13138C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10399260 | |||||||
| chr16:10399582 | A | T | 2 | a0001c0002t0003g0272 a0001c0002t0003g0312 |
2 | HG01891.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-242+13460A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10399582 | |||||||
| chr16:10399596 | A | G | 2 | a0002c0001t0002g0135 a0002c0001t0002g0136 |
2 | HG00438.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-242+13474A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10399596 | |||||||
| chr16:10399648 | C | T | 1 | a0002c0001t0002g0028 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-242+13526C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10399648 | |||||||
| chr16:10399852 | A | G | 6 | a0001c0002t0005g0275 a0001c0002t0005g0282 a0001c0002t0005g0287 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-242+13730A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10399852 | |||||||
| chr16:10399860 | T | G | 1 | a0001c0005t0003g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-242+13738T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10399860 | |||||||
| chr16:10400013 | G | A | 6 | a0001c0005t0006g0029 a0001c0005t0006g0030 a0001c0005t0006g0367 others(3): Show |
6 | HG02965.hp1 HG03209.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-242+13891G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400013 | |||||||
| chr16:10400015 | T | C | 1 | a0001c0005t0003g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-242+13893T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400015 | |||||||
| chr16:10400100 | G | A | 184 | a0001c0002t0005g0190 a0001c0005t0016g0031 a0002c0001t0001g0001 others(181): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-242+13978G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400100 | |||||||
| chr16:10400110 | G | A | 98 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(95): Show |
99 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.-242+13988G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400110 | |||||||
| chr16:10400121 | A | G | 106 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(103): Show |
108 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(105): Show |
intron_variant | MODIFIER | c.-242+13999A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400121 | |||||||
| chr16:10400171 | G | T | 2 | a0002c0001t0001g0070 a0002c0001t0001g0081 |
2 | NA18968.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-242+14049G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400171 | |||||||
| chr16:10400321 | A | G | 106 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(103): Show |
108 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(105): Show |
intron_variant | MODIFIER | c.-242+14199A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400321 | |||||||
| chr16:10400330 | C | T | 6 | a0002c0001t0001g0036 a0002c0001t0001g0044 a0002c0001t0001g0045 others(3): Show |
6 | NA18941.hp1 NA18952.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.-242+14208C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400330 | |||||||
| chr16:10400331 | G | A | 1 | a0001c0016t0015g0323 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-242+14209G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400331 | |||||||
| chr16:10400389 | A | G | 1 | a0002c0001t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-241-14185A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400389 | |||||||
| chr16:10400410 | G | C | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-241-14164G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400410 | |||||||
| chr16:10400426 | A | C | 2 | a0001c0002t0003g0339 a0001c0002t0003g0343 |
2 | NA18969.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-241-14148A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400426 | |||||||
| chr16:10400468 | T | G | 93 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(90): Show |
95 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.-241-14106T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400468 | |||||||
| chr16:10400536 | A | G | 1 | a0002c0018t0010g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-241-14038A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400536 | |||||||
| chr16:10400631 | G | T | 6 | a0001c0003t0020g0214 a0004c0006t0004g0055 a0004c0006t0004g0203 others(3): Show |
6 | NA18980.hp1 NA18985.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.-241-13943G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400631 | |||||||
| chr16:10400689 | G | A | 1 | a0001c0005t0003g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-241-13885G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400689 | |||||||
| chr16:10400705 | C | T | 2 | a0001c0002t0003g0301 a0001c0002t0003g0356 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-241-13869C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400705 | |||||||
| chr16:10400800 | G | C | 3 | a0001c0002t0005g0348 a0001c0002t0005g0349 a0001c0002t0005g0350 |
3 | NA19011.hp1 NA19062.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-241-13774G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400800 | |||||||
| chr16:10400974 | A | G | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-241-13600A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10400974 | |||||||
| chr16:10401093 | C | T | 1 | a0002c0001t0001g0134 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-241-13481C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10401093 | |||||||
| chr16:10401146 | G | A | 299 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(296): Show |
304 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.-241-13428G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10401146 | |||||||
| chr16:10401158 | T | C | 10 | a0003c0004t0002g0003 a0003c0004t0002g0151 a0003c0004t0002g0152 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-241-13416T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10401158 | |||||||
| chr16:10401292 | C | T | 1 | a0001c0002t0013g0299 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-241-13282C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10401292 | |||||||
| chr16:10401420 | G | A | 48 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(45): Show |
49 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.-241-13154G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10401420 | |||||||
| chr16:10401506 | G | A | 1 | a0002c0001t0002g0088 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-241-13068G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10401506 | |||||||
| chr16:10401609 | T | C | 1 | a0002c0001t0001g0009 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-241-12965T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10401609 | |||||||
| chr16:10401646 | T | G | 2 | a0002c0001t0002g0089 a0002c0001t0002g0143 |
2 | HG01358.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-241-12928T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10401646 | |||||||
| chr16:10401654 | C | G | 2 | a0002c0001t0001g0020 a0002c0001t0001g0021 |
2 | HG02040.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-241-12920C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10401654 | |||||||
| chr16:10401757 | CT | C | 146 | a0001c0002t0003g0326 a0001c0003t0008g0026 a0001c0003t0008g0027 others(143): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-241-12803delT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10401757 | ||||||
| chr16:10401858 | A | T | 1 | a0002c0001t0001g0131 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-241-12716A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10401858 | |||||||
| chr16:10402037 | T | G | 2 | a0002c0001t0001g0010 a0002c0001t0001g0022 |
2 | NA18965.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-241-12537T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10402037 | |||||||
| chr16:10402056 | C | T | 1 | a0001c0005t0006g0371 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-241-12518C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10402056 | |||||||
| chr16:10402087 | T | C | 5 | a0002c0001t0002g0053 a0002c0001t0002g0090 a0002c0001t0002g0091 others(2): Show |
5 | HG02129.hp2 HG02523.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.-241-12487T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10402087 | |||||||
| chr16:10402145 | A | G | 2 | a0001c0005t0006g0005 a0001c0005t0006g0371 |
3 | HG02145.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-241-12429A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10402145 | |||||||
| chr16:10402298 | A | G | 185 | a0001c0002t0005g0190 a0001c0003t0002g0033 a0001c0005t0016g0031 others(182): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-241-12276A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10402298 | |||||||
| chr16:10402316 | T | C | 1 | a0002c0001t0024g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-241-12258T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10402316 | |||||||
| chr16:10402327 | A | T | 290 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(287): Show |
295 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.-241-12247A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10402327 | |||||||
| chr16:10402475 | C | T | 2 | a0001c0002t0003g0269 a0001c0002t0003g0270 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-241-12099C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10402475 | |||||||
| chr16:10402539 | C | T | 10 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0003t0008g0026 others(7): Show |
10 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-241-12035C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10402539 | |||||||
| chr16:10402566 | C | T | 1 | a0002c0001t0001g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-241-12008C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10402566 | |||||||
| chr16:10402580 | C | T | 105 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(102): Show |
107 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(104): Show |
intron_variant | MODIFIER | c.-241-11994C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10402580 | |||||||
| chr16:10402695 | C | T | 1 | a0001c0002t0003g0297 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-241-11879C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10402695 | |||||||
| chr16:10402886 | C | G | 3 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0308 |
3 | HG01099.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-241-11688C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10402886 | |||||||
| chr16:10402886 | C | T | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-241-11688C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10402886 | |||||||
| chr16:10402907 | CA | C | 190 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0002t0005g0190 others(187): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.-241-11652delA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10402907 | ||||||
| chr16:10402907 | CAA | C | 107 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(104): Show |
109 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(106): Show |
intron_variant | MODIFIER | c.-241-11653_-241-11 others(8): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10402907 | ||||||
| chr16:10402971 | A | G | 145 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0007 others(142): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-241-11603A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10402971 | |||||||
| chr16:10402973 | G | A | 2 | a0001c0002t0003g0346 a0001c0002t0003g0347 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-241-11601G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10402973 | |||||||
| chr16:10403024 | T | C | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-241-11550T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10403024 | |||||||
| chr16:10403045 | A | G | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-241-11529A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10403045 | |||||||
| chr16:10403129 | A | G | 303 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(300): Show |
308 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-241-11445A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10403129 | |||||||
| chr16:10403228 | T | C | 1 | a0001c0005t0003g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-241-11346T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10403228 | |||||||
| chr16:10403348 | C | T | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-241-11226C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10403348 | |||||||
| chr16:10403703 | A | G | 1 | a0001c0005t0006g0030 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-241-10871A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10403703 | |||||||
| chr16:10403799 | A | T | 1 | a0002c0001t0001g0128 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-241-10775A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10403799 | |||||||
| chr16:10403802 | C | T | 2 | a0001c0002t0003g0346 a0001c0002t0003g0347 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-241-10772C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10403802 | |||||||
| chr16:10403822 | G | A | 2 | a0002c0001t0001g0056 a0002c0001t0001g0057 |
2 | HG01516.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-241-10752G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10403822 | |||||||
| chr16:10403887 | G | C | 300 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(297): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.-241-10687G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10403887 | |||||||
| chr16:10404070 | A | G | 1 | a0002c0001t0002g0127 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-241-10504A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10404070 | |||||||
| chr16:10404136 | C | T | 2 | a0002c0001t0001g0054 a0002c0001t0001g0366 |
2 | HG01175.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-241-10438C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10404136 | |||||||
| chr16:10404188 | G | C | 1 | a0003c0004t0002g0129 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-241-10386G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10404188 | |||||||
| chr16:10404378 | G | A | 8 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0001c0005t0016g0031 others(5): Show |
8 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-241-10196G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10404378 | |||||||
| chr16:10404763 | G | A | 4 | a0001c0002t0003g0293 a0001c0002t0003g0339 a0001c0002t0003g0340 others(1): Show |
4 | NA18969.hp1 NA19006.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.-241-9811G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10404763 | |||||||
| chr16:10404786 | G | A | 9 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(6): Show |
10 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.-241-9788G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10404786 | |||||||
| chr16:10404818 | C | T | 97 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(94): Show |
98 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.-241-9756C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10404818 | |||||||
| chr16:10404948 | A | G | 196 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0002t0005g0190 others(193): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-241-9626A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10404948 | |||||||
| chr16:10404998 | G | C | 1 | a0001c0002t0003g0361 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-241-9576G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10404998 | |||||||
| chr16:10405027 | C | A | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-241-9547C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10405027 | |||||||
| chr16:10405035 | T | C | 301 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(298): Show |
306 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.-241-9539T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10405035 | |||||||
| chr16:10405091 | C | T | 8 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(5): Show |
9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-241-9483C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10405091 | |||||||
| chr16:10405190 | C | T | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-241-9384C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10405190 | |||||||
| chr16:10405228 | G | A | 4 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(1): Show |
4 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-241-9346G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10405228 | |||||||
| chr16:10405347 | G | A | 1 | a0003c0004t0002g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-241-9227G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10405347 | |||||||
| chr16:10405409 | C | T | 106 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(103): Show |
108 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(105): Show |
intron_variant | MODIFIER | c.-241-9165C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10405409 | |||||||
| chr16:10405474 | C | T | 189 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0002t0005g0190 others(186): Show |
192 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-241-9100C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10405474 | |||||||
| chr16:10405531 | G | A | 48 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0271 others(45): Show |
48 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.-241-9043G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10405531 | |||||||
| chr16:10405634 | A | C | 10 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0003t0008g0026 others(7): Show |
10 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-241-8940A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10405634 | |||||||
| chr16:10405672 | G | A | 2 | a0001c0002t0005g0275 a0001c0002t0005g0317 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-241-8902G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10405672 | |||||||
| chr16:10405962 | G | T | 5 | a0002c0001t0001g0044 a0002c0001t0001g0045 a0002c0001t0001g0046 others(2): Show |
5 | NA18941.hp1 NA18952.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.-241-8612G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10405962 | |||||||
| chr16:10405963 | C | G | 10 | a0003c0004t0002g0003 a0003c0004t0002g0151 a0003c0004t0002g0152 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-241-8611C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10405963 | |||||||
| chr16:10406043 | C | G | 1 | a0001c0002t0013g0299 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-241-8531C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10406043 | |||||||
| chr16:10406088 | C | CA | 103 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(100): Show |
104 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.-241-8474dupA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10406088 | ||||||
| chr16:10406162 | G | T | 1 | a0001c0002t0005g0303 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-241-8412G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10406162 | |||||||
| chr16:10406180 | A | G | 10 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0003t0008g0026 others(7): Show |
10 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-241-8394A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10406180 | |||||||
| chr16:10406307 | C | T | 2 | a0001c0002t0003g0346 a0001c0002t0003g0347 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-241-8267C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10406307 | |||||||
| chr16:10406354 | C | T | 1 | a0003c0004t0002g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-241-8220C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10406354 | |||||||
| chr16:10406371 | G | A | 1 | a0002c0001t0001g0045 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-241-8203G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10406371 | |||||||
| chr16:10406409 | C | T | 300 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(297): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.-241-8165C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10406409 | |||||||
| chr16:10406505 | T | C | 184 | a0001c0002t0005g0190 a0001c0003t0002g0033 a0001c0005t0016g0031 others(181): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-241-8069T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10406505 | |||||||
| chr16:10406763 | C | T | 1 | a0002c0001t0001g0019 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-241-7811C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10406763 | |||||||
| chr16:10406797 | T | C | 184 | a0001c0002t0005g0190 a0001c0003t0002g0033 a0001c0005t0016g0031 others(181): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-241-7777T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10406797 | |||||||
| chr16:10406804 | A | G | 300 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(297): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.-241-7770A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10406804 | |||||||
| chr16:10406903 | C | G | 1 | a0002c0021t0002g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-241-7671C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10406903 | |||||||
| chr16:10406940 | C | T | 25 | a0001c0002t0005g0190 a0001c0003t0002g0033 a0002c0001t0001g0070 others(22): Show |
25 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.-241-7634C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10406940 | |||||||
| chr16:10406953 | A | C | 1 | a0002c0001t0001g0163 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-241-7621A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10406953 | |||||||
| chr16:10407021 | G | A | 300 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(297): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.-241-7553G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10407021 | |||||||
| chr16:10407198 | A | G | 10 | a0003c0004t0002g0003 a0003c0004t0002g0151 a0003c0004t0002g0152 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-241-7376A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10407198 | |||||||
| chr16:10407242 | G | A | 7 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0002c0008t0010g0193 others(4): Show |
7 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-241-7332G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10407242 | |||||||
| chr16:10407322 | G | C | 174 | a0001c0002t0005g0190 a0001c0003t0002g0033 a0001c0005t0016g0031 others(171): Show |
176 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-241-7252G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10407322 | |||||||
| chr16:10407520 | G | C | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-241-7054G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10407520 | |||||||
| chr16:10407546 | G | A | 9 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(6): Show |
10 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.-241-7028G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10407546 | |||||||
| chr16:10407717 | G | A | 1 | a0003c0004t0002g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-241-6857G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10407717 | |||||||
| chr16:10407735 | C | T | 2 | a0002c0001t0001g0186 a0002c0001t0001g0187 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-241-6839C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10407735 | |||||||
| chr16:10407742 | C | T | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-241-6832C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10407742 | |||||||
| chr16:10407747 | A | G | 2 | a0001c0002t0003g0346 a0001c0002t0003g0347 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-241-6827A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10407747 | |||||||
| chr16:10407815 | A | G | 1 | a0002c0001t0009g0169 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-241-6759A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10407815 | |||||||
| chr16:10407818 | G | C | 1 | a0005c0017t0005g0302 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-241-6756G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10407818 | |||||||
| chr16:10407917 | CT | C | 106 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(103): Show |
108 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(105): Show |
intron_variant | MODIFIER | c.-241-6643delT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10407917 | ||||||
| chr16:10408015 | G | A | 97 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(94): Show |
98 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.-241-6559G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10408015 | |||||||
| chr16:10408069 | A | T | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-241-6505A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10408069 | |||||||
| chr16:10408075 | C | T | 1 | a0002c0001t0001g0134 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-241-6499C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10408075 | |||||||
| chr16:10408111 | A | C | 304 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(301): Show |
309 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-241-6463A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10408111 | |||||||
| chr16:10408113 | T | C | 1 | a0002c0008t0010g0193 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-241-6461T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10408113 | |||||||
| chr16:10408118 | G | C | 1 | a0002c0001t0012g0092 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-241-6456G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10408118 | |||||||
| chr16:10408259 | G | A | 1 | a0001c0002t0013g0299 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-241-6315G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10408259 | |||||||
| chr16:10408327 | A | G | 1 | a0001c0003t0004g0241 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-241-6247A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10408327 | |||||||
| chr16:10408426 | A | T | 1 | a0002c0001t0001g0130 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-241-6148A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10408426 | |||||||
| chr16:10408462 | A | G | 6 | a0001c0005t0006g0029 a0001c0005t0006g0030 a0001c0005t0006g0367 others(3): Show |
6 | HG02965.hp1 HG03209.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-241-6112A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10408462 | |||||||
| chr16:10408463 | T | C | 29 | a0001c0002t0005g0190 a0001c0003t0002g0033 a0002c0001t0001g0070 others(26): Show |
29 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.-241-6111T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10408463 | |||||||
| chr16:10408690 | T | G | 303 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(300): Show |
308 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-241-5884T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10408690 | |||||||
| chr16:10408736 | T | C | 9 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(6): Show |
10 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.-241-5838T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10408736 | |||||||
| chr16:10408745 | T | G | 1 | a0001c0002t0003g0297 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-241-5829T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10408745 | |||||||
| chr16:10408890 | G | A | 2 | a0003c0004t0002g0003 a0003c0004t0002g0153 |
3 | HG01891.hp2 HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-241-5684G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10408890 | |||||||
| chr16:10408927 | A | G | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-241-5647A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10408927 | |||||||
| chr16:10408945 | C | T | 2 | a0001c0003t0004g0205 a0002c0001t0001g0133 |
2 | HG01168.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-241-5629C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10408945 | |||||||
| chr16:10409023 | A | G | 360 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(357): Show |
365 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.-241-5551A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409023 | |||||||
| chr16:10409033 | C | T | 3 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0196 |
3 | HG01109.hp1 HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-241-5541C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409033 | |||||||
| chr16:10409049 | C | T | 1 | a0001c0003t0004g0240 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-241-5525C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409049 | |||||||
| chr16:10409106 | C | T | 1 | a0002c0001t0001g0133 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-241-5468C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409106 | |||||||
| chr16:10409115 | G | A | 5 | a0002c0001t0001g0058 a0002c0008t0010g0193 a0002c0008t0010g0194 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-241-5459G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409115 | |||||||
| chr16:10409125 | C | T | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-241-5449C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409125 | |||||||
| chr16:10409195 | A | G | 4 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(1): Show |
4 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-241-5379A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409195 | |||||||
| chr16:10409222 | C | T | 1 | a0001c0002t0005g0266 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-241-5352C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409222 | |||||||
| chr16:10409232 | C | T | 207 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0291 others(204): Show |
210 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.-241-5342C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409232 | |||||||
| chr16:10409471 | G | A | 2 | a0002c0001t0001g0070 a0002c0001t0001g0081 |
2 | NA18968.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-241-5103G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409471 | |||||||
| chr16:10409495 | A | AT | 300 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(297): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.-241-5069dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10409495 | ||||||
| chr16:10409549 | C | T | 1 | a0002c0021t0002g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-241-5025C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409549 | |||||||
| chr16:10409562 | G | A | 1 | a0002c0001t0009g0171 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-241-5012G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409562 | |||||||
| chr16:10409640 | C | T | 9 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(6): Show |
10 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.-241-4934C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409640 | |||||||
| chr16:10409641 | G | A | 185 | a0001c0002t0005g0190 a0001c0003t0008g0026 a0001c0003t0008g0027 others(182): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-241-4933G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409641 | |||||||
| chr16:10409671 | C | T | 208 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0291 others(205): Show |
211 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.-241-4903C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409671 | |||||||
| chr16:10409873 | A | T | 208 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0291 others(205): Show |
211 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.-241-4701A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409873 | |||||||
| chr16:10409919 | T | C | 22 | a0002c0001t0001g0001 a0002c0001t0001g0034 a0002c0001t0001g0035 others(19): Show |
23 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.-241-4655T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409919 | |||||||
| chr16:10409963 | T | G | 1 | a0001c0003t0004g0209 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-241-4611T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409963 | |||||||
| chr16:10409973 | A | G | 2 | a0001c0002t0003g0301 a0001c0002t0003g0356 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-241-4601A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10409973 | |||||||
| chr16:10410017 | A | G | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-241-4557A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10410017 | |||||||
| chr16:10410116 | G | T | 6 | a0001c0005t0018g0263 a0002c0008t0010g0193 a0002c0008t0010g0194 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-241-4458G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10410116 | |||||||
| chr16:10410192 | A | C | 97 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(94): Show |
98 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.-241-4382A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10410192 | |||||||
| chr16:10410199 | C | T | 1 | a0002c0001t0002g0136 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-241-4375C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10410199 | |||||||
| chr16:10410266 | T | C | 1 | a0001c0003t0004g0258 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-241-4308T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10410266 | |||||||
| chr16:10410311 | A | AGTTTT | 9 | a0001c0003t0004g0209 a0001c0003t0004g0228 a0001c0003t0004g0229 others(6): Show |
9 | HG00738.hp1 HG02698.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.-241-4217_-241-421 others(9): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10410311 | ||||||
| chr16:10410311 | AGTTTT | A | 14 | a0001c0003t0002g0199 a0001c0003t0004g0201 a0001c0003t0004g0213 others(11): Show |
14 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.-241-4217_-241-421 others(9): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10410311 | ||||||
| chr16:10410311 | AGTTTTGT others(3): Show |
A | 44 | a0001c0002t0003g0301 a0001c0002t0003g0346 a0001c0002t0003g0347 others(41): Show |
45 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.-241-4222_-241-421 others(14): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10410311 | ||||||
| chr16:10410311 | AGTTTTGT others(8): Show |
A | 46 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(43): Show |
47 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.-241-4227_-241-421 others(19): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10410311 | ||||||
| chr16:10410311 | AGTTTTGT others(13): Show |
A | 186 | a0001c0002t0003g0293 a0001c0002t0003g0294 a0001c0002t0003g0298 others(183): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-241-4232_-241-421 others(24): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10410311 | ||||||
| chr16:10410311 | AGTTTTGT others(18): Show |
A | 28 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0291 others(25): Show |
29 | HG01099.hp1 HG01256.hp2 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-241-4237_-241-421 others(29): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10410311 | ||||||
| chr16:10410361 | T | C | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-241-4213T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10410361 | |||||||
| chr16:10410396 | G | C | 10 | a0003c0004t0002g0003 a0003c0004t0002g0151 a0003c0004t0002g0152 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-241-4178G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10410396 | |||||||
| chr16:10410470 | T | C | 300 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(297): Show |
305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.-241-4104T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10410470 | |||||||
| chr16:10410538 | T | C | 2 | a0001c0002t0003g0358 a0001c0002t0003g0362 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-241-4036T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10410538 | |||||||
| chr16:10410587 | G | C | 1 | a0001c0002t0003g0293 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-241-3987G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10410587 | |||||||
| chr16:10410725 | A | G | 1 | a0001c0002t0005g0351 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-241-3849A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10410725 | |||||||
| chr16:10410771 | G | A | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-241-3803G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10410771 | |||||||
| chr16:10410781 | A | G | 210 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0291 others(207): Show |
213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.-241-3793A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10410781 | |||||||
| chr16:10411000 | A | ATGTGG | 10 | a0003c0004t0002g0003 a0003c0004t0002g0151 a0003c0004t0002g0152 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-241-3570_-241-356 others(9): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10411000 | ||||||
| chr16:10411144 | A | T | 186 | a0001c0002t0005g0190 a0001c0003t0002g0033 a0001c0003t0008g0026 others(183): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.-241-3430A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10411144 | |||||||
| chr16:10411280 | G | T | 2 | a0002c0001t0001g0124 a0002c0001t0001g0125 |
2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-241-3294G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10411280 | |||||||
| chr16:10411314 | G | A | 1 | a0001c0005t0003g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-241-3260G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10411314 | |||||||
| chr16:10411351 | G | GT | 214 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0291 others(211): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.-241-3210dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10411351 | ||||||
| chr16:10411351 | G | GTT | 10 | a0001c0002t0003g0292 a0001c0003t0008g0026 a0001c0003t0008g0027 others(7): Show |
11 | HG01074.hp2 HG01109.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.-241-3211_-241-321 others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10411351 | ||||||
| chr16:10411370 | T | TTTG | 299 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(296): Show |
304 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.-241-3183_-241-318 others(7): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10411370 | ||||||
| chr16:10411765 | A | G | 1 | a0001c0003t0008g0256 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-241-2809A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10411765 | |||||||
| chr16:10411905 | G | GT | 17 | a0001c0002t0003g0340 a0001c0002t0003g0346 a0001c0002t0003g0347 others(14): Show |
17 | HG00735.hp2 HG01175.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-241-2656dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10411905 | ||||||
| chr16:10411908 | T | G | 1 | a0001c0002t0003g0295 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-241-2666T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10411908 | |||||||
| chr16:10411918 | TC | T | 7 | a0001c0005t0003g0032 a0002c0001t0001g0002 a0002c0001t0001g0010 others(4): Show |
8 | HG00639.hp2 HG00673.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.-241-2654delC | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10411918 | ||||||
| chr16:10411919 | C | T | 292 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(289): Show |
296 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.-241-2655C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10411919 | |||||||
| chr16:10412009 | T | TG | 30 | a0002c0001t0001g0007 a0002c0001t0001g0012 a0002c0001t0001g0013 others(27): Show |
30 | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.-241-2564dupG | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10412009 | ||||||
| chr16:10412010 | G | GGT | 6 | a0001c0003t0008g0026 a0001c0005t0003g0032 a0003c0004t0002g0151 others(3): Show |
6 | HG02258.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-241-2564_-241-256 others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10412010 | |||||||
| chr16:10412010 | G | GGTT | 6 | a0001c0003t0008g0027 a0003c0004t0002g0003 a0003c0004t0002g0152 others(3): Show |
7 | HG01891.hp2 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-241-2564_-241-256 others(7): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10412010 | |||||||
| chr16:10412010 | GT | G | 179 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(176): Show |
180 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.-241-2535delT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10412010 | ||||||
| chr16:10412010 | GTT | G | 6 | a0001c0002t0003g0289 a0001c0003t0004g0245 a0001c0003t0004g0257 others(3): Show |
6 | HG01516.hp2 HG02293.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-241-2536_-241-253 others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr16 | 10412010 | ||||||
| chr16:10412011 | T | G | 124 | a0001c0002t0003g0272 a0001c0002t0003g0295 a0001c0002t0003g0300 others(121): Show |
127 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.-241-2563T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10412011 | |||||||
| chr16:10412012 | T | G | 133 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(130): Show |
134 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.-241-2562T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10412012 | |||||||
| chr16:10412013 | T | G | 3 | a0001c0002t0003g0289 a0002c0001t0001g0103 a0002c0018t0010g0197 |
3 | HG02293.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-241-2561T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10412013 | |||||||
| chr16:10412021 | T | G | 5 | a0001c0002t0003g0272 a0001c0002t0003g0312 a0001c0002t0003g0358 others(2): Show |
5 | HG01891.hp1 HG02257.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-241-2553T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10412021 | |||||||
| chr16:10412022 | T | G | 79 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(76): Show |
80 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.-241-2552T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10412022 | |||||||
| chr16:10412028 | T | G | 16 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0271 others(13): Show |
16 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-241-2546T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10412028 | |||||||
| chr16:10412032 | T | G | 15 | a0001c0002t0003g0004 a0001c0002t0003g0272 a0001c0002t0003g0283 others(12): Show |
16 | HG01243.hp1 HG01433.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-241-2542T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10412032 | |||||||
| chr16:10412049 | A | C | 1 | a0002c0001t0001g0121 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-241-2525A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10412049 | |||||||
| chr16:10412150 | A | G | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-241-2424A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10412150 | |||||||
| chr16:10412158 | T | C | 1 | a0003c0004t0002g0129 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-241-2416T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10412158 | |||||||
| chr16:10412186 | C | G | 9 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(6): Show |
10 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.-241-2388C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10412186 | |||||||
| chr16:10412315 | G | A | 1 | a0002c0001t0001g0146 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-241-2259G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10412315 | |||||||
| chr16:10412541 | G | T | 2 | a0001c0005t0006g0005 a0001c0005t0006g0371 |
3 | HG02145.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-241-2033G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10412541 | |||||||
| chr16:10412652 | G | T | 1 | a0001c0002t0003g0363 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-241-1922G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10412652 | |||||||
| chr16:10412672 | G | A | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-241-1902G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10412672 | |||||||
| chr16:10412889 | T | C | 1 | a0003c0004t0002g0082 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-241-1685T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10412889 | |||||||
| chr16:10413124 | A | G | 304 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(301): Show |
309 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-241-1450A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10413124 | |||||||
| chr16:10413149 | C | T | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-241-1425C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10413149 | |||||||
| chr16:10413386 | C | G | 24 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0291 others(21): Show |
24 | HG01099.hp1 HG01256.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.-241-1188C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10413386 | |||||||
| chr16:10413498 | C | T | 1 | a0002c0001t0001g0054 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-241-1076C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10413498 | |||||||
| chr16:10413546 | C | G | 1 | a0001c0003t0004g0206 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-241-1028C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10413546 | |||||||
| chr16:10413684 | C | T | 1 | a0001c0003t0004g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-241-890C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10413684 | |||||||
| chr16:10413848 | T | A | 1 | a0002c0001t0001g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-241-726T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10413848 | |||||||
| chr16:10413880 | A | G | 1 | a0002c0001t0002g0101 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-241-694A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10413880 | |||||||
| chr16:10413905 | T | C | 1 | a0002c0001t0002g0150 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-241-669T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10413905 | |||||||
| chr16:10414320 | G | A | 304 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(301): Show |
309 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-241-254G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10414320 | |||||||
| chr16:10414402 | G | A | 1 | a0002c0010t0002g0264 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-241-172G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10414402 | |||||||
| chr16:10414565 | C | T | 184 | a0001c0002t0005g0190 a0001c0003t0002g0033 a0001c0005t0016g0031 others(181): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-241-9C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 1/13 | chr16 | 10414565 | |||||||
| chr16:10414627 | T | TTG | 29 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0002t0013g0357 others(26): Show |
29 | HG00558.hp2 HG00735.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.-203+49_-203+50dup others(2): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 10414627 | ||||||
| chr16:10414627 | T | TTGTG | 3 | a0001c0002t0013g0299 a0001c0003t0008g0027 a0004c0006t0004g0233 |
3 | HG02129.hp1 HG02818.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-203+47_-203+50dup others(4): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 10414627 | ||||||
| chr16:10414627 | T | TTGTGTG | 5 | a0001c0002t0003g0295 a0001c0002t0003g0297 a0001c0003t0008g0026 others(2): Show |
5 | HG02155.hp1 HG02258.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-203+45_-203+50dup others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 10414627 | ||||||
| chr16:10414627 | TTG | T | 107 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(104): Show |
109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.-203+49_-203+50del others(2): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 10414627 | ||||||
| chr16:10414627 | TTGTG | T | 8 | a0001c0002t0003g0330 a0001c0003t0008g0207 a0001c0003t0008g0208 others(5): Show |
8 | HG02559.hp2 HG02622.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-203+47_-203+50del others(4): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 10414627 | ||||||
| chr16:10414651 | G | T | 8 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(5): Show |
9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-203+39G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10414651 | |||||||
| chr16:10414653 | G | T | 1 | a0001c0005t0003g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-203+41G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10414653 | |||||||
| chr16:10414654 | T | G | 8 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(5): Show |
9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-203+42T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10414654 | |||||||
| chr16:10414655 | GTGTGTGT others(1): Show |
G | 3 | a0001c0005t0006g0030 a0001c0005t0006g0367 a0001c0005t0006g0368 |
3 | HG02965.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-203+46_-203+53del others(8): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 10414655 | ||||||
| chr16:10414656 | T | C | 5 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0369 others(2): Show |
6 | HG02145.hp2 HG02976.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-203+44T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10414656 | |||||||
| chr16:10414656 | T | G | 1 | a0001c0005t0003g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-203+44T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10414656 | |||||||
| chr16:10414657 | GTGTGTT | G | 4 | a0001c0005t0006g0005 a0001c0005t0006g0369 a0001c0005t0006g0370 others(1): Show |
5 | HG02145.hp2 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-203+48_-203+53del others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 10414657 | ||||||
| chr16:10414658 | T | C | 1 | a0001c0005t0003g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-203+46T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10414658 | |||||||
| chr16:10414664 | T | C | 3 | a0001c0005t0006g0030 a0001c0005t0006g0367 a0001c0005t0006g0368 |
3 | HG02965.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-203+52T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10414664 | |||||||
| chr16:10414664 | T | G | 5 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0369 others(2): Show |
6 | HG02145.hp2 HG02976.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-203+52T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10414664 | |||||||
| chr16:10414668 | C | CG | 248 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(245): Show |
252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.-203+63dupG | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 10414668 | ||||||
| chr16:10414668 | C | CGG | 40 | a0001c0002t0003g0274 a0001c0002t0003g0293 a0001c0002t0003g0295 others(37): Show |
40 | HG00544.hp1 HG00738.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.-203+62_-203+63dup others(2): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr16 | 10414668 | ||||||
| chr16:10414668 | C | G | 9 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(6): Show |
10 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.-203+56C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10414668 | |||||||
| chr16:10414725 | C | T | 1 | a0002c0018t0010g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-203+113C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10414725 | |||||||
| chr16:10414909 | G | C | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-203+297G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10414909 | |||||||
| chr16:10414919 | G | A | 1 | a0002c0001t0012g0085 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-203+307G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10414919 | |||||||
| chr16:10415005 | A | G | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-203+393A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10415005 | |||||||
| chr16:10415333 | G | A | 1 | a0003c0004t0002g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-203+721G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10415333 | |||||||
| chr16:10415357 | G | A | 190 | a0001c0002t0005g0190 a0001c0003t0002g0033 a0001c0003t0008g0207 others(187): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.-203+745G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10415357 | |||||||
| chr16:10415394 | A | G | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-203+782A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10415394 | |||||||
| chr16:10415990 | C | T | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-203+1378C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10415990 | |||||||
| chr16:10416084 | C | T | 1 | a0001c0003t0004g0229 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-203+1472C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10416084 | |||||||
| chr16:10416092 | G | C | 306 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(303): Show |
311 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.-203+1480G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10416092 | |||||||
| chr16:10416107 | C | G | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-203+1495C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10416107 | |||||||
| chr16:10416214 | A | T | 31 | a0001c0003t0002g0033 a0001c0003t0008g0207 a0001c0003t0008g0208 others(28): Show |
31 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.-203+1602A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10416214 | |||||||
| chr16:10416259 | C | T | 8 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(5): Show |
9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-203+1647C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10416259 | |||||||
| chr16:10416272 | C | A | 310 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(307): Show |
315 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.-203+1660C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10416272 | |||||||
| chr16:10416404 | T | A | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-203+1792T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10416404 | |||||||
| chr16:10416559 | G | A | 1 | a0002c0021t0002g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-203+1947G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10416559 | |||||||
| chr16:10416613 | C | A | 1 | a0002c0018t0010g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-203+2001C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10416613 | |||||||
| chr16:10416697 | A | T | 306 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(303): Show |
311 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.-203+2085A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10416697 | |||||||
| chr16:10416750 | T | A | 1 | a0001c0005t0003g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-203+2138T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10416750 | |||||||
| chr16:10416913 | T | C | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-203+2301T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10416913 | |||||||
| chr16:10416922 | T | C | 1 | a0001c0002t0003g0364 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-203+2310T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10416922 | |||||||
| chr16:10417155 | G | A | 1 | a0001c0003t0022g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-202-2426G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10417155 | |||||||
| chr16:10417263 | C | T | 1 | a0001c0002t0003g0312 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-202-2318C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10417263 | |||||||
| chr16:10417417 | A | G | 1 | a0003c0004t0002g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-202-2164A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10417417 | |||||||
| chr16:10417418 | G | A | 1 | a0002c0001t0001g0001 | 2 | NA19060.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-202-2163G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10417418 | |||||||
| chr16:10417438 | C | G | 32 | a0002c0001t0001g0001 a0002c0001t0001g0052 a0002c0001t0001g0054 others(29): Show |
33 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.-202-2143C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10417438 | |||||||
| chr16:10417662 | T | C | 10 | a0003c0004t0002g0003 a0003c0004t0002g0151 a0003c0004t0002g0152 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-202-1919T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10417662 | |||||||
| chr16:10417895 | A | G | 1 | a0002c0001t0001g0118 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-202-1686A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10417895 | |||||||
| chr16:10418021 | G | A | 1 | a0002c0001t0002g0083 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-202-1560G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10418021 | |||||||
| chr16:10418127 | A | C | 4 | a0003c0004t0002g0105 a0003c0004t0002g0117 a0003c0004t0002g0132 others(1): Show |
4 | NA18997.hp2 NA19058.hp2 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.-202-1454A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10418127 | |||||||
| chr16:10418176 | A | C | 1 | a0004c0006t0004g0242 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-202-1405A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10418176 | |||||||
| chr16:10418210 | A | G | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-202-1371A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10418210 | |||||||
| chr16:10418281 | G | C | 3 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0005t0018g0263 |
3 | HG02451.hp2 HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-202-1300G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10418281 | |||||||
| chr16:10418448 | A | G | 1 | a0002c0001t0001g0037 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-202-1133A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10418448 | |||||||
| chr16:10418460 | G | A | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-202-1121G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10418460 | |||||||
| chr16:10418461 | G | T | 36 | a0001c0002t0005g0266 a0001c0002t0005g0267 a0001c0002t0005g0275 others(33): Show |
36 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.-202-1120G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10418461 | |||||||
| chr16:10418470 | C | T | 1 | a0002c0008t0010g0195 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-202-1111C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10418470 | |||||||
| chr16:10418708 | C | T | 87 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(84): Show |
88 | HG00280.hp2 HG00639.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.-202-873C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10418708 | |||||||
| chr16:10418717 | T | G | 44 | a0001c0002t0003g0358 a0001c0002t0003g0359 a0001c0002t0003g0360 others(41): Show |
44 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-202-864T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10418717 | |||||||
| chr16:10418733 | A | G | 179 | a0001c0003t0002g0033 a0001c0003t0008g0207 a0001c0003t0008g0208 others(176): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.-202-848A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10418733 | |||||||
| chr16:10418778 | G | A | 2 | a0001c0002t0003g0346 a0001c0002t0003g0347 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-202-803G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10418778 | |||||||
| chr16:10418797 | C | T | 189 | a0001c0003t0002g0033 a0001c0003t0008g0207 a0001c0003t0008g0208 others(186): Show |
192 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-202-784C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10418797 | |||||||
| chr16:10418819 | G | A | 6 | a0001c0005t0006g0029 a0001c0005t0006g0030 a0001c0005t0006g0367 others(3): Show |
6 | HG02965.hp1 HG03209.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-202-762G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10418819 | |||||||
| chr16:10418975 | T | C | 207 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0003t0002g0033 others(204): Show |
211 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.-202-606T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10418975 | |||||||
| chr16:10419002 | A | G | 1 | a0005c0017t0005g0302 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-202-579A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10419002 | |||||||
| chr16:10419025 | C | A | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-202-556C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10419025 | |||||||
| chr16:10419025 | C | T | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-202-556C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10419025 | |||||||
| chr16:10419077 | G | A | 319 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0271 others(316): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-202-504G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10419077 | |||||||
| chr16:10419112 | A | C | 3 | a0001c0003t0004g0212 a0001c0003t0004g0232 a0001c0003t0004g0239 |
3 | HG00323.hp1 HG03710.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-202-469A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10419112 | |||||||
| chr16:10419152 | A | C | 3 | a0002c0001t0001g0039 a0002c0001t0001g0048 a0002c0001t0001g0049 |
3 | HG01255.hp1 HG03831.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-202-429A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10419152 | |||||||
| chr16:10419178 | C | T | 193 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0003t0002g0033 others(190): Show |
196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-202-403C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10419178 | |||||||
| chr16:10419253 | G | A | 2 | a0001c0002t0003g0346 a0001c0002t0003g0347 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-202-328G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10419253 | |||||||
| chr16:10419367 | C | T | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-202-214C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10419367 | |||||||
| chr16:10419569 | C | T | 9 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(6): Show |
10 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.-202-12C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 2/13 | chr16 | 10419569 | |||||||
| chr16:10419639 | C | T | 9 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(6): Show |
10 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.-160+16C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10419639 | |||||||
| chr16:10419696 | G | A | 1 | a0003c0004t0002g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-160+73G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10419696 | |||||||
| chr16:10419767 | A | G | 1 | a0002c0001t0002g0136 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-160+144A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10419767 | |||||||
| chr16:10419795 | A | G | 7 | a0001c0002t0003g0358 a0001c0002t0003g0359 a0001c0002t0003g0360 others(4): Show |
7 | HG01358.hp1 HG02257.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-160+172A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10419795 | |||||||
| chr16:10419803 | C | T | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+180C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10419803 | |||||||
| chr16:10419823 | C | T | 1 | a0002c0001t0001g0123 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-160+200C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10419823 | |||||||
| chr16:10420113 | G | C | 1 | a0001c0002t0005g0316 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-160+490G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10420113 | |||||||
| chr16:10420164 | C | G | 1 | a0001c0002t0003g0312 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-160+541C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10420164 | |||||||
| chr16:10420233 | T | C | 310 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(307): Show |
315 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.-160+610T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10420233 | |||||||
| chr16:10420553 | G | A | 18 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0291 others(15): Show |
18 | HG01099.hp1 HG01256.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-160+930G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10420553 | |||||||
| chr16:10420821 | C | T | 1 | a0002c0021t0002g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-160+1198C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10420821 | |||||||
| chr16:10421131 | A | G | 304 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(301): Show |
309 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-160+1508A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10421131 | |||||||
| chr16:10421145 | T | C | 2 | a0001c0002t0003g0301 a0001c0002t0003g0356 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-160+1522T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10421145 | |||||||
| chr16:10421157 | G | C | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-160+1534G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10421157 | |||||||
| chr16:10421205 | G | A | 1 | a0001c0002t0003g0334 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-160+1582G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10421205 | |||||||
| chr16:10421299 | C | G | 6 | a0002c0001t0001g0036 a0002c0001t0001g0044 a0002c0001t0001g0045 others(3): Show |
6 | NA18941.hp1 NA18952.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.-160+1676C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10421299 | |||||||
| chr16:10421335 | C | T | 1 | a0001c0007t0011g0355 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-160+1712C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10421335 | |||||||
| chr16:10421370 | G | A | 304 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(301): Show |
309 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-160+1747G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10421370 | |||||||
| chr16:10421383 | T | C | 9 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(6): Show |
10 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.-160+1760T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10421383 | |||||||
| chr16:10421406 | C | T | 1 | a0002c0001t0001g0168 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-160+1783C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10421406 | |||||||
| chr16:10421458 | G | A | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-160+1835G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10421458 | |||||||
| chr16:10421672 | A | G | 37 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(34): Show |
38 | HG01099.hp1 HG01243.hp1 HG01256.hp2 others(35): Show |
intron_variant | MODIFIER | c.-160+2049A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10421672 | |||||||
| chr16:10421701 | G | A | 9 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0271 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.-160+2078G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10421701 | |||||||
| chr16:10421788 | C | T | 1 | a0001c0002t0003g0291 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-160+2165C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10421788 | |||||||
| chr16:10421800 | T | G | 13 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(10): Show |
14 | HG01243.hp1 HG01433.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-160+2177T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10421800 | |||||||
| chr16:10421983 | A | G | 1 | a0009c0012t0004g0249 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-160+2360A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10421983 | |||||||
| chr16:10422004 | C | T | 298 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(295): Show |
303 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.-160+2381C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10422004 | |||||||
| chr16:10422087 | C | T | 1 | a0003c0004t0002g0080 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-160+2464C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10422087 | |||||||
| chr16:10422626 | A | G | 1 | a0001c0002t0005g0278 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-160+3003A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10422626 | |||||||
| chr16:10422672 | A | G | 8 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(5): Show |
9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-160+3049A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10422672 | |||||||
| chr16:10422697 | G | GT | 308 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(305): Show |
313 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.-160+3076dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 10422697 | ||||||
| chr16:10422711 | A | G | 3 | a0001c0005t0006g0368 a0001c0005t0006g0369 a0001c0005t0006g0370 |
3 | HG02965.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-160+3088A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10422711 | |||||||
| chr16:10422788 | G | A | 7 | a0002c0001t0002g0040 a0002c0001t0002g0041 a0002c0001t0002g0107 others(4): Show |
7 | NA18612.hp1 NA18955.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.-160+3165G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10422788 | |||||||
| chr16:10422837 | C | T | 303 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(300): Show |
308 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-160+3214C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10422837 | |||||||
| chr16:10422982 | C | T | 1 | a0001c0005t0003g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-160+3359C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10422982 | |||||||
| chr16:10423037 | G | A | 1 | a0001c0002t0005g0351 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-160+3414G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10423037 | |||||||
| chr16:10423049 | C | A | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-160+3426C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10423049 | |||||||
| chr16:10423165 | G | A | 96 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(93): Show |
97 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.-160+3542G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10423165 | |||||||
| chr16:10423282 | T | C | 1 | a0001c0003t0004g0232 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-160+3659T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10423282 | |||||||
| chr16:10423283 | A | T | 1 | a0001c0003t0004g0232 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-160+3660A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10423283 | |||||||
| chr16:10423284 | C | A | 1 | a0001c0003t0004g0232 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-160+3661C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10423284 | |||||||
| chr16:10423340 | T | C | 308 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(305): Show |
313 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.-160+3717T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10423340 | |||||||
| chr16:10423365 | T | C | 49 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(46): Show |
50 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.-160+3742T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10423365 | |||||||
| chr16:10423498 | G | A | 8 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(5): Show |
9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-160+3875G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10423498 | |||||||
| chr16:10423649 | G | A | 5 | a0001c0003t0004g0200 a0001c0003t0004g0215 a0001c0003t0004g0246 others(2): Show |
5 | NA19012.hp2 NA19057.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.-160+4026G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10423649 | |||||||
| chr16:10423753 | C | T | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-160+4130C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10423753 | |||||||
| chr16:10423886 | T | G | 13 | a0001c0003t0019g0235 a0001c0003t0020g0214 a0004c0006t0004g0055 others(10): Show |
13 | HG02129.hp1 HG02165.hp2 NA18943.hp2 others(10): Show |
intron_variant | MODIFIER | c.-160+4263T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10423886 | |||||||
| chr16:10423894 | A | C | 9 | a0002c0001t0002g0040 a0002c0001t0002g0041 a0002c0001t0002g0107 others(6): Show |
9 | NA18612.hp1 NA18952.hp2 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.-160+4271A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10423894 | |||||||
| chr16:10423901 | T | C | 309 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(306): Show |
314 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.-160+4278T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10423901 | |||||||
| chr16:10423902 | G | A | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-160+4279G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10423902 | |||||||
| chr16:10423976 | T | C | 7 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0005t0018g0263 others(4): Show |
7 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-160+4353T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10423976 | |||||||
| chr16:10424002 | C | T | 96 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(93): Show |
97 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.-160+4379C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10424002 | |||||||
| chr16:10424157 | T | C | 307 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(304): Show |
312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-160+4534T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10424157 | |||||||
| chr16:10424232 | C | T | 1 | a0002c0001t0009g0171 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-160+4609C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10424232 | |||||||
| chr16:10424345 | A | G | 307 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(304): Show |
312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.-159-4523A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10424345 | |||||||
| chr16:10424518 | G | A | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-159-4350G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10424518 | |||||||
| chr16:10424600 | A | G | 1 | a0001c0003t0004g0206 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-159-4268A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10424600 | |||||||
| chr16:10424630 | C | T | 1 | a0003c0004t0002g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-159-4238C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10424630 | |||||||
| chr16:10424686 | T | C | 10 | a0003c0004t0002g0003 a0003c0004t0002g0151 a0003c0004t0002g0152 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-159-4182T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10424686 | |||||||
| chr16:10424756 | G | A | 47 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0271 others(44): Show |
47 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.-159-4112G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10424756 | |||||||
| chr16:10424764 | A | C | 2 | a0001c0002t0003g0346 a0001c0002t0003g0347 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-159-4104A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10424764 | |||||||
| chr16:10425054 | A | AT | 26 | a0001c0002t0003g0295 a0001c0003t0004g0232 a0001c0003t0004g0261 others(23): Show |
26 | HG00323.hp1 HG00438.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.-159-3793dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 10425054 | ||||||
| chr16:10425054 | AT | A | 39 | a0001c0002t0003g0339 a0001c0002t0003g0358 a0001c0002t0003g0359 others(36): Show |
40 | HG00544.hp1 HG01109.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.-159-3793delT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 10425054 | ||||||
| chr16:10425054 | ATT | A | 9 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(6): Show |
10 | HG02965.hp1 HG02976.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.-159-3794_-159-379 others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 10425054 | ||||||
| chr16:10425123 | A | G | 9 | a0002c0001t0002g0040 a0002c0001t0002g0041 a0002c0001t0002g0107 others(6): Show |
9 | NA18612.hp1 NA18952.hp2 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.-159-3745A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10425123 | |||||||
| chr16:10425135 | G | A | 1 | a0002c0021t0002g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-159-3733G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10425135 | |||||||
| chr16:10425225 | G | GT | 17 | a0001c0003t0004g0211 a0001c0003t0004g0217 a0001c0005t0006g0371 others(14): Show |
17 | HG01255.hp2 HG01261.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.-159-3627dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 10425225 | ||||||
| chr16:10425225 | GT | G | 68 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(65): Show |
69 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.-159-3627delT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 10425225 | ||||||
| chr16:10425225 | GTT | G | 25 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0291 others(22): Show |
25 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-159-3628_-159-362 others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 10425225 | ||||||
| chr16:10425278 | C | A | 1 | a0003c0004t0002g0071 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-159-3590C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10425278 | |||||||
| chr16:10425351 | C | T | 2 | a0001c0003t0008g0210 a0001c0003t0008g0256 |
2 | NA18964.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-159-3517C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10425351 | |||||||
| chr16:10425576 | C | T | 9 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(6): Show |
10 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.-159-3292C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10425576 | |||||||
| chr16:10425584 | A | T | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-159-3284A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10425584 | |||||||
| chr16:10425588 | A | G | 7 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0005t0018g0263 others(4): Show |
7 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-159-3280A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10425588 | |||||||
| chr16:10425629 | C | T | 20 | a0002c0001t0001g0001 a0002c0001t0001g0052 a0002c0001t0001g0054 others(17): Show |
21 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.-159-3239C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10425629 | |||||||
| chr16:10425649 | T | A | 2 | a0002c0001t0001g0130 a0002c0001t0001g0142 |
2 | HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-159-3219T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10425649 | |||||||
| chr16:10425670 | C | A | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-159-3198C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10425670 | |||||||
| chr16:10425739 | C | A | 1 | a0001c0003t0022g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-159-3129C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10425739 | |||||||
| chr16:10425739 | C | T | 2 | a0003c0004t0002g0157 a0003c0004t0002g0365 |
2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-159-3129C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10425739 | |||||||
| chr16:10425768 | C | G | 1 | a0003c0004t0002g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-159-3100C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10425768 | |||||||
| chr16:10425783 | T | C | 302 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(299): Show |
307 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-159-3085T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10425783 | |||||||
| chr16:10425786 | G | C | 103 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(100): Show |
104 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(101): Show |
intron_variant | MODIFIER | c.-159-3082G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10425786 | |||||||
| chr16:10425895 | A | G | 1 | a0001c0002t0017g0288 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-159-2973A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10425895 | |||||||
| chr16:10426062 | G | T | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-159-2806G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10426062 | |||||||
| chr16:10426273 | G | C | 1 | a0007c0015t0003g0310 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-159-2595G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10426273 | |||||||
| chr16:10426292 | A | G | 3 | a0002c0001t0001g0138 a0002c0001t0001g0139 a0002c0001t0001g0188 |
3 | HG02630.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-159-2576A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10426292 | |||||||
| chr16:10426723 | A | G | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-159-2145A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10426723 | |||||||
| chr16:10426846 | T | G | 5 | a0001c0005t0018g0263 a0001c0007t0011g0352 a0001c0007t0011g0353 others(2): Show |
5 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-159-2022T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10426846 | |||||||
| chr16:10426852 | T | G | 1 | a0003c0004t0002g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-159-2016T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10426852 | |||||||
| chr16:10426855 | G | T | 8 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(5): Show |
9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-159-2013G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10426855 | |||||||
| chr16:10426864 | T | G | 4 | a0003c0004t0002g0082 a0003c0004t0002g0144 a0003c0004t0002g0157 others(1): Show |
4 | HG02071.hp1 HG02145.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-159-2004T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10426864 | |||||||
| chr16:10427095 | C | G | 1 | a0002c0001t0001g0045 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-159-1773C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10427095 | |||||||
| chr16:10427239 | G | C | 185 | a0001c0002t0003g0364 a0001c0005t0016g0031 a0002c0001t0001g0001 others(182): Show |
188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-159-1629G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10427239 | |||||||
| chr16:10427265 | C | G | 2 | a0002c0001t0001g0012 a0002c0001t0001g0013 |
2 | NA18963.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-159-1603C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10427265 | |||||||
| chr16:10427304 | C | G | 14 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(11): Show |
15 | HG01109.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-159-1564C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10427304 | |||||||
| chr16:10427586 | A | G | 49 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(46): Show |
50 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.-159-1282A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10427586 | |||||||
| chr16:10427625 | G | C | 1 | a0002c0001t0001g0058 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-159-1243G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10427625 | |||||||
| chr16:10427663 | G | A | 1 | a0003c0004t0002g0151 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-159-1205G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10427663 | |||||||
| chr16:10427739 | A | T | 1 | a0002c0001t0001g0180 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-159-1129A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10427739 | |||||||
| chr16:10427852 | C | CA | 10 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(7): Show |
11 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.-159-1001dupA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr16 | 10427852 | ||||||
| chr16:10427963 | C | T | 301 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(298): Show |
306 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.-159-905C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10427963 | |||||||
| chr16:10428158 | G | C | 1 | a0001c0002t0003g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-159-710G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10428158 | |||||||
| chr16:10428221 | T | C | 6 | a0001c0005t0006g0029 a0001c0005t0006g0030 a0001c0005t0006g0367 others(3): Show |
6 | HG02965.hp1 HG03209.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-159-647T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10428221 | |||||||
| chr16:10428280 | C | T | 1 | a0003c0004t0002g0192 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-159-588C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10428280 | |||||||
| chr16:10428315 | T | G | 27 | a0002c0001t0001g0070 a0002c0001t0001g0081 a0002c0010t0002g0140 others(24): Show |
27 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.-159-553T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10428315 | |||||||
| chr16:10428342 | C | T | 1 | a0003c0004t0002g0151 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-159-526C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10428342 | |||||||
| chr16:10428408 | G | T | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-159-460G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10428408 | |||||||
| chr16:10428453 | T | G | 1 | a0001c0002t0005g0285 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-159-415T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10428453 | |||||||
| chr16:10428454 | A | G | 5 | a0001c0002t0003g0271 a0001c0002t0003g0273 a0001c0002t0003g0274 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.-159-414A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10428454 | |||||||
| chr16:10428608 | G | T | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-159-260G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10428608 | |||||||
| chr16:10428663 | A | G | 1 | a0002c0001t0001g0001 | 2 | NA19060.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-159-205A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10428663 | |||||||
| chr16:10428775 | A | G | 1 | a0001c0002t0005g0281 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-159-93A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10428775 | |||||||
| chr16:10428842 | A | G | 1 | a0002c0001t0002g0089 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-159-26A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 3/13 | chr16 | 10428842 | |||||||
| chr16:10429400 | G | C | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-11+384G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429400 | |||||||
| chr16:10429695 | G | GTTTTA | 138 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0271 others(135): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-11+713_-11+717dup others(5): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 10429695 | ||||||
| chr16:10429695 | G | GTTTTATT others(3): Show |
95 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(92): Show |
98 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.-11+708_-11+717dup others(10): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 10429695 | ||||||
| chr16:10429695 | G | GTTTTATT others(8): Show |
9 | a0001c0002t0003g0313 a0001c0002t0003g0314 a0001c0002t0003g0326 others(6): Show |
9 | HG01433.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+703_-11+717dup others(15): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 10429695 | ||||||
| chr16:10429695 | GTTTTATT others(3): Show |
G | 11 | a0002c0001t0001g0163 a0002c0001t0001g0165 a0002c0001t0001g0168 others(8): Show |
11 | HG01496.hp1 HG02055.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+708_-11+717del others(10): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 10429695 | ||||||
| chr16:10429734 | A | T | 25 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0291 others(22): Show |
25 | HG01099.hp1 HG01256.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.-11+718A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429734 | |||||||
| chr16:10429735 | T | A | 25 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0291 others(22): Show |
25 | HG01099.hp1 HG01256.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.-11+719T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429735 | |||||||
| chr16:10429743 | T | A | 1 | a0001c0002t0005g0305 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-11+727T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429743 | |||||||
| chr16:10429744 | A | T | 1 | a0001c0002t0005g0305 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-11+728A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429744 | |||||||
| chr16:10429748 | A | T | 1 | a0002c0001t0001g0044 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-11+732A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429748 | |||||||
| chr16:10429749 | T | A | 1 | a0002c0001t0001g0044 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-11+733T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429749 | |||||||
| chr16:10429756 | T | A | 1 | a0001c0002t0005g0305 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-11+740T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429756 | |||||||
| chr16:10429758 | A | ATTATT | 85 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(82): Show |
87 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(84): Show |
intron_variant | MODIFIER | c.-11+756_-11+760dup others(5): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 10429758 | ||||||
| chr16:10429758 | A | ATTATTTT others(3): Show |
24 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0291 others(21): Show |
24 | HG01099.hp1 HG01256.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.-11+751_-11+760dup others(10): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 10429758 | ||||||
| chr16:10429758 | A | ATTATTTT others(11): Show |
1 | a0001c0002t0005g0315 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-11+757_-11+758ins others(18): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 10429758 | ||||||
| chr16:10429758 | A | ATTATTTT others(21): Show |
1 | a0001c0002t0003g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-11+760_-11+761ins others(28): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 10429758 | ||||||
| chr16:10429758 | A | T | 1 | a0001c0002t0005g0305 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-11+742A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429758 | |||||||
| chr16:10429761 | A | T | 1 | a0002c0001t0001g0044 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-11+745A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429761 | |||||||
| chr16:10429763 | T | A | 1 | a0002c0001t0001g0044 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-11+747T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429763 | |||||||
| chr16:10429772 | T | A | 1 | a0001c0003t0004g0245 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-11+756T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429772 | |||||||
| chr16:10429772 | TTTTAA | T | 24 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0291 others(21): Show |
24 | HG01099.hp1 HG01256.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.-11+770_-11+774del others(5): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr16 | 10429772 | ||||||
| chr16:10429777 | A | T | 26 | a0002c0001t0001g0070 a0002c0001t0001g0081 a0002c0001t0002g0083 others(23): Show |
26 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.-11+761A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429777 | |||||||
| chr16:10429782 | A | T | 26 | a0002c0001t0001g0070 a0002c0001t0001g0081 a0002c0001t0002g0083 others(23): Show |
26 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.-11+766A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429782 | |||||||
| chr16:10429808 | C | T | 303 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(300): Show |
308 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.-11+792C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429808 | |||||||
| chr16:10429914 | G | A | 1 | a0002c0001t0001g0037 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-10-697G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429914 | |||||||
| chr16:10429916 | G | A | 45 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(42): Show |
46 | HG00280.hp2 HG00639.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.-10-695G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429916 | |||||||
| chr16:10429961 | T | C | 98 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(95): Show |
99 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(96): Show |
intron_variant | MODIFIER | c.-10-650T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429961 | |||||||
| chr16:10429978 | G | A | 3 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0196 |
3 | HG01109.hp1 HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-10-633G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10429978 | |||||||
| chr16:10430066 | C | T | 9 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(6): Show |
10 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10-545C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10430066 | |||||||
| chr16:10430308 | A | G | 147 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0007 others(144): Show |
149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-10-303A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 4/13 | chr16 | 10430308 | |||||||
| chr16:10431471 | T | C | 5 | a0002c0001t0002g0111 a0002c0001t0002g0126 a0002c0001t0002g0127 others(2): Show |
5 | HG00558.hp1 NA18943.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.835+16T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10431471 | |||||||
| chr16:10431509 | A | G | 1 | a0001c0005t0003g0032 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.835+54A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10431509 | |||||||
| chr16:10431571 | A | G | 1 | a0005c0017t0005g0302 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.835+116A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10431571 | |||||||
| chr16:10431613 | T | G | 1 | a0002c0001t0001g0044 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.835+158T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10431613 | |||||||
| chr16:10431731 | A | G | 2 | a0002c0001t0001g0146 a0002c0001t0001g0147 |
2 | HG04204.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.835+276A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10431731 | |||||||
| chr16:10431736 | T | A | 1 | a0001c0002t0003g0335 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.835+281T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10431736 | |||||||
| chr16:10431786 | G | C | 21 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0271 others(18): Show |
21 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.835+331G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10431786 | |||||||
| chr16:10431820 | C | CT | 33 | a0001c0002t0003g0308 a0001c0002t0003g0336 a0001c0002t0005g0317 others(30): Show |
34 | HG01099.hp2 HG01123.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.835+386dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 10431820 | ||||||
| chr16:10431820 | C | CTT | 77 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0271 others(74): Show |
77 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(74): Show |
intron_variant | MODIFIER | c.835+385_835+386dup others(2): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 10431820 | ||||||
| chr16:10431820 | C | CTTT | 19 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(16): Show |
20 | HG01243.hp1 HG01433.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.835+384_835+386dup others(3): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 10431820 | ||||||
| chr16:10431820 | CTTTTTTT others(6): Show |
C | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.835+374_835+386del others(13): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 10431820 | ||||||
| chr16:10431847 | G | A | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.835+392G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10431847 | |||||||
| chr16:10431860 | G | A | 21 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0271 others(18): Show |
21 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.835+405G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10431860 | |||||||
| chr16:10431883 | G | T | 1 | a0001c0002t0003g0284 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.835+428G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10431883 | |||||||
| chr16:10431916 | T | C | 298 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(295): Show |
303 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.835+461T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10431916 | |||||||
| chr16:10431980 | C | T | 1 | a0001c0002t0003g0313 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.835+525C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10431980 | |||||||
| chr16:10431990 | A | AT | 285 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(282): Show |
290 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.835+555dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 10431990 | ||||||
| chr16:10431990 | A | ATT | 17 | a0001c0002t0003g0290 a0001c0002t0003g0296 a0001c0002t0003g0361 others(14): Show |
17 | HG00639.hp1 HG00738.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.835+554_835+555dup others(2): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 10431990 | ||||||
| chr16:10432195 | T | G | 5 | a0001c0005t0018g0263 a0001c0007t0011g0352 a0001c0007t0011g0353 others(2): Show |
5 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.835+740T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10432195 | |||||||
| chr16:10432424 | A | G | 1 | a0002c0021t0002g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.835+969A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10432424 | |||||||
| chr16:10432506 | C | T | 1 | a0001c0003t0008g0230 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.836-1019C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10432506 | |||||||
| chr16:10432645 | G | C | 8 | a0001c0002t0003g0358 a0001c0002t0003g0359 a0001c0002t0003g0360 others(5): Show |
8 | HG01358.hp1 HG02257.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.836-880G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10432645 | |||||||
| chr16:10432810 | G | A | 98 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(95): Show |
99 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(96): Show |
intron_variant | MODIFIER | c.836-715G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10432810 | |||||||
| chr16:10432828 | A | G | 100 | a0002c0001t0001g0002 a0002c0001t0001g0007 a0002c0001t0001g0008 others(97): Show |
101 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.836-697A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10432828 | |||||||
| chr16:10432872 | CCTT | C | 98 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(95): Show |
99 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(96): Show |
intron_variant | MODIFIER | c.836-650_836-648del others(3): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr16 | 10432872 | ||||||
| chr16:10432991 | G | A | 108 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(105): Show |
110 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(107): Show |
intron_variant | MODIFIER | c.836-534G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10432991 | |||||||
| chr16:10433010 | G | C | 1 | a0001c0003t0004g0222 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.836-515G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10433010 | |||||||
| chr16:10433093 | T | C | 2 | a0002c0001t0001g0176 a0002c0001t0024g0172 |
2 | HG00280.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.836-432T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10433093 | |||||||
| chr16:10433244 | G | T | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.836-281G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10433244 | |||||||
| chr16:10433249 | C | T | 2 | a0002c0001t0002g0135 a0002c0001t0002g0136 |
2 | HG00438.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.836-276C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10433249 | |||||||
| chr16:10433317 | G | A | 291 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(288): Show |
295 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.836-208G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10433317 | |||||||
| chr16:10433408 | T | C | 10 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(7): Show |
11 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.836-117T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 5/13 | chr16 | 10433408 | |||||||
| chr16:10433739 | C | T | 2 | a0001c0002t0003g0272 a0001c0002t0003g0312 |
2 | HG01891.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.960+90C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10433739 | |||||||
| chr16:10433756 | C | A | 153 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(150): Show |
156 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.960+107C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10433756 | |||||||
| chr16:10433794 | A | C | 1 | a0003c0004t0002g0078 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.960+145A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10433794 | |||||||
| chr16:10433955 | C | G | 1 | a0001c0013t0004g0259 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.960+306C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10433955 | |||||||
| chr16:10433975 | T | A | 10 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(7): Show |
11 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.960+326T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10433975 | |||||||
| chr16:10434065 | C | CA | 9 | a0001c0005t0003g0032 a0001c0005t0006g0005 a0001c0005t0006g0029 others(6): Show |
10 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.960+419dupA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 10434065 | ||||||
| chr16:10434179 | A | G | 99 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(96): Show |
100 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(97): Show |
intron_variant | MODIFIER | c.960+530A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10434179 | |||||||
| chr16:10434242 | G | A | 2 | a0002c0001t0001g0061 a0002c0001t0001g0097 |
2 | NA19072.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.960+593G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10434242 | |||||||
| chr16:10434251 | A | G | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.960+602A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10434251 | |||||||
| chr16:10434286 | C | G | 1 | a0001c0003t0004g0257 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.960+637C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10434286 | |||||||
| chr16:10434420 | G | A | 102 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(99): Show |
103 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(100): Show |
intron_variant | MODIFIER | c.960+771G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10434420 | |||||||
| chr16:10434434 | G | T | 2 | a0001c0003t0004g0201 a0001c0003t0004g0250 |
2 | HG00621.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.960+785G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10434434 | |||||||
| chr16:10434491 | C | A | 1 | a0002c0001t0002g0145 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.960+842C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10434491 | |||||||
| chr16:10434499 | C | G | 105 | a0002c0001t0001g0002 a0002c0001t0001g0007 a0002c0001t0001g0008 others(102): Show |
106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.960+850C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10434499 | |||||||
| chr16:10434542 | A | G | 1 | a0002c0001t0001g0179 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.960+893A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10434542 | |||||||
| chr16:10434769 | A | G | 1 | a0001c0003t0008g0026 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.960+1120A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10434769 | |||||||
| chr16:10434796 | T | TTTTG | 5 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0273 others(2): Show |
5 | HG01099.hp2 HG02895.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.960+1164_960+1167d others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 10434796 | ||||||
| chr16:10434848 | A | C | 1 | a0001c0002t0003g0332 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.960+1199A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10434848 | |||||||
| chr16:10435014 | C | T | 10 | a0003c0004t0002g0003 a0003c0004t0002g0151 a0003c0004t0002g0152 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.960+1365C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10435014 | |||||||
| chr16:10435167 | A | G | 1 | a0009c0012t0004g0249 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.960+1518A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10435167 | |||||||
| chr16:10435237 | G | A | 303 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(300): Show |
308 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.960+1588G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10435237 | |||||||
| chr16:10435254 | A | G | 6 | a0001c0003t0020g0214 a0004c0006t0004g0055 a0004c0006t0004g0203 others(3): Show |
6 | NA18980.hp1 NA18985.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+1605A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10435254 | |||||||
| chr16:10435358 | T | C | 1 | a0003c0004t0002g0132 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.960+1709T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10435358 | |||||||
| chr16:10435543 | T | C | 303 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(300): Show |
308 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.960+1894T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10435543 | |||||||
| chr16:10435635 | A | C | 2 | a0002c0001t0001g0124 a0002c0001t0001g0125 |
2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.960+1986A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10435635 | |||||||
| chr16:10435646 | C | G | 2 | a0001c0003t0004g0217 a0001c0003t0004g0218 |
2 | HG01255.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.960+1997C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10435646 | |||||||
| chr16:10435741 | C | T | 5 | a0002c0001t0001g0009 a0002c0001t0001g0011 a0002c0001t0001g0015 others(2): Show |
5 | HG01167.hp2 HG01952.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+2092C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10435741 | |||||||
| chr16:10435838 | G | T | 1 | a0001c0002t0013g0299 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.960+2189G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10435838 | |||||||
| chr16:10435844 | C | T | 286 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(283): Show |
290 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.960+2195C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10435844 | |||||||
| chr16:10435932 | G | A | 1 | a0004c0006t0004g0233 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.961-2169G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10435932 | |||||||
| chr16:10435992 | A | G | 97 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(94): Show |
98 | HG00280.hp2 HG00639.hp1 HG01099.hp1 others(95): Show |
intron_variant | MODIFIER | c.961-2109A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10435992 | |||||||
| chr16:10436086 | C | T | 8 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(5): Show |
9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.961-2015C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10436086 | |||||||
| chr16:10436096 | C | T | 1 | a0001c0003t0004g0206 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.961-2005C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10436096 | |||||||
| chr16:10436125 | C | A | 1 | a0001c0002t0005g0278 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.961-1976C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10436125 | |||||||
| chr16:10436199 | T | G | 9 | a0002c0001t0002g0040 a0002c0001t0002g0041 a0002c0001t0002g0107 others(6): Show |
9 | NA18612.hp1 NA18952.hp2 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.961-1902T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10436199 | |||||||
| chr16:10436210 | A | T | 141 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(138): Show |
143 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.961-1891A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10436210 | |||||||
| chr16:10436319 | G | A | 1 | a0002c0001t0002g0028 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.961-1782G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10436319 | |||||||
| chr16:10436348 | C | T | 1 | a0001c0002t0003g0329 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.961-1753C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10436348 | |||||||
| chr16:10436391 | C | CT | 181 | a0001c0002t0003g0271 a0001c0002t0003g0284 a0001c0002t0003g0311 others(178): Show |
184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.961-1700dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 10436391 | ||||||
| chr16:10436391 | CT | C | 18 | a0001c0002t0005g0277 a0001c0002t0005g0285 a0001c0002t0005g0316 others(15): Show |
18 | HG02015.hp1 HG02155.hp2 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.961-1700delT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 10436391 | ||||||
| chr16:10436446 | G | C | 2 | a0002c0001t0001g0054 a0002c0001t0001g0366 |
2 | HG01175.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.961-1655G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10436446 | |||||||
| chr16:10436577 | CT | C | 2 | a0002c0001t0001g0002 a0002c0001t0001g0122 |
3 | HG00639.hp2 HG00738.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.961-1522delT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 10436577 | ||||||
| chr16:10436586 | G | C | 1 | a0001c0005t0006g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.961-1515G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10436586 | |||||||
| chr16:10436860 | A | G | 1 | a0002c0001t0001g0093 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.961-1241A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10436860 | |||||||
| chr16:10436903 | C | CA | 15 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(12): Show |
16 | HG01109.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.961-1188dupA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 10436903 | ||||||
| chr16:10436940 | C | T | 296 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(293): Show |
301 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.961-1161C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10436940 | |||||||
| chr16:10436941 | A | G | 2 | a0002c0001t0002g0089 a0002c0001t0002g0143 |
2 | HG01358.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.961-1160A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10436941 | |||||||
| chr16:10437022 | A | AT | 58 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(55): Show |
59 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.961-1063dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr16 | 10437022 | ||||||
| chr16:10437138 | C | G | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.961-963C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10437138 | |||||||
| chr16:10437257 | G | T | 1 | a0002c0001t0001g0115 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.961-844G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10437257 | |||||||
| chr16:10437416 | C | A | 20 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(17): Show |
21 | HG01109.hp1 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.961-685C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10437416 | |||||||
| chr16:10437453 | C | T | 296 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(293): Show |
301 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.961-648C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10437453 | |||||||
| chr16:10437717 | T | G | 1 | a0001c0003t0004g0229 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.961-384T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10437717 | |||||||
| chr16:10437736 | C | T | 2 | a0001c0002t0003g0271 a0001c0002t0003g0311 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.961-365C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 6/13 | chr16 | 10437736 | |||||||
| chr16:10438310 | C | T | 2 | a0002c0001t0014g0068 a0002c0001t0014g0069 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1095+75C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10438310 | |||||||
| chr16:10438354 | A | C | 291 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(288): Show |
295 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1095+119A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10438354 | |||||||
| chr16:10438419 | G | GT | 29 | a0001c0002t0003g0283 a0001c0002t0003g0291 a0001c0002t0005g0266 others(26): Show |
30 | HG00140.hp1 HG01074.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1095+200dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 10438419 | ||||||
| chr16:10438626 | A | G | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1095+391A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10438626 | |||||||
| chr16:10438629 | C | T | 1 | a0001c0002t0005g0190 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1095+394C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10438629 | |||||||
| chr16:10438643 | A | G | 98 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(95): Show |
99 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.1095+408A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10438643 | |||||||
| chr16:10438690 | C | G | 4 | a0001c0002t0005g0266 a0001c0002t0005g0303 a0001c0002t0005g0304 others(1): Show |
4 | NA18994.hp1 NA18999.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+455C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10438690 | |||||||
| chr16:10438732 | C | T | 15 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0272 others(12): Show |
15 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1095+497C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10438732 | |||||||
| chr16:10438807 | C | T | 1 | a0002c0021t0002g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1095+572C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10438807 | |||||||
| chr16:10438830 | G | A | 1 | a0001c0003t0004g0262 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1095+595G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10438830 | |||||||
| chr16:10438976 | C | T | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095+741C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10438976 | |||||||
| chr16:10439037 | G | A | 1 | a0001c0002t0005g0307 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1095+802G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10439037 | |||||||
| chr16:10439049 | C | CA | 13 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0272 others(10): Show |
13 | HG01099.hp2 HG01891.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.1095+832dupA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 10439049 | ||||||
| chr16:10439049 | C | CAA | 97 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(94): Show |
98 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.1095+831_1095+832d others(4): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 10439049 | ||||||
| chr16:10439049 | C | CAAA | 171 | a0001c0002t0003g0271 a0001c0002t0003g0311 a0001c0002t0003g0313 others(168): Show |
174 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.1095+830_1095+832d others(5): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 10439049 | ||||||
| chr16:10439049 | C | CAAAA | 12 | a0002c0001t0001g0049 a0002c0001t0001g0056 a0002c0001t0001g0113 others(9): Show |
12 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(9): Show |
intron_variant | MODIFIER | c.1095+829_1095+832d others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 10439049 | ||||||
| chr16:10439156 | C | T | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1095+921C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10439156 | |||||||
| chr16:10439385 | G | A | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1096-979G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10439385 | |||||||
| chr16:10439390 | C | T | 1 | a0002c0021t0002g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1096-974C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10439390 | |||||||
| chr16:10439444 | G | C | 296 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(293): Show |
301 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1096-920G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10439444 | |||||||
| chr16:10439521 | A | G | 286 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(283): Show |
290 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1096-843A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10439521 | |||||||
| chr16:10439533 | C | CT | 108 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(105): Show |
109 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1096-811dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 10439533 | ||||||
| chr16:10439533 | CT | C | 6 | a0002c0001t0001g0056 a0002c0008t0010g0193 a0002c0008t0010g0194 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1096-811delT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr16 | 10439533 | ||||||
| chr16:10439602 | A | G | 291 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(288): Show |
295 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1096-762A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10439602 | |||||||
| chr16:10439615 | C | G | 16 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0272 others(13): Show |
16 | HG00735.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1096-749C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10439615 | |||||||
| chr16:10439785 | C | G | 1 | a0001c0002t0003g0336 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1096-579C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10439785 | |||||||
| chr16:10439834 | G | A | 1 | a0001c0002t0005g0276 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1096-530G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10439834 | |||||||
| chr16:10439901 | C | T | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1096-463C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10439901 | |||||||
| chr16:10439999 | A | G | 1 | a0002c0001t0001g0180 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1096-365A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10439999 | |||||||
| chr16:10440028 | C | T | 1 | a0002c0021t0002g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1096-336C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10440028 | |||||||
| chr16:10440029 | G | A | 1 | a0001c0002t0005g0190 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1096-335G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10440029 | |||||||
| chr16:10440133 | A | G | 2 | a0001c0002t0003g0272 a0001c0002t0003g0312 |
2 | HG01891.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1096-231A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 7/13 | chr16 | 10440133 | |||||||
| chr16:10440522 | A | G | 4 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(1): Show |
4 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1194+60A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10440522 | |||||||
| chr16:10440644 | A | G | 2 | a0002c0010t0002g0140 a0002c0010t0002g0149 |
2 | NA18952.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1194+182A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10440644 | |||||||
| chr16:10440651 | T | C | 1 | a0001c0002t0003g0294 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1194+189T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10440651 | |||||||
| chr16:10440775 | A | T | 5 | a0001c0005t0018g0263 a0001c0007t0011g0352 a0001c0007t0011g0353 others(2): Show |
5 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1194+313A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10440775 | |||||||
| chr16:10440825 | C | T | 1 | a0001c0002t0003g0291 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1194+363C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10440825 | |||||||
| chr16:10440913 | C | G | 1 | a0002c0001t0002g0088 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1194+451C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10440913 | |||||||
| chr16:10440915 | T | C | 303 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(300): Show |
308 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1194+453T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10440915 | |||||||
| chr16:10440946 | G | A | 10 | a0003c0004t0002g0003 a0003c0004t0002g0151 a0003c0004t0002g0152 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1194+484G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10440946 | |||||||
| chr16:10441013 | G | T | 1 | a0001c0003t0004g0204 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1194+551G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10441013 | |||||||
| chr16:10441086 | C | G | 4 | a0001c0002t0003g0293 a0001c0002t0003g0339 a0001c0002t0003g0340 others(1): Show |
4 | NA18969.hp1 NA19006.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1194+624C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10441086 | |||||||
| chr16:10441150 | T | C | 10 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(7): Show |
11 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.1194+688T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10441150 | |||||||
| chr16:10441192 | A | G | 16 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0272 others(13): Show |
16 | HG00735.hp2 HG01099.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1194+730A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10441192 | |||||||
| chr16:10441212 | C | T | 11 | a0001c0003t0004g0257 a0001c0005t0006g0005 a0001c0005t0006g0029 others(8): Show |
12 | HG02145.hp2 HG02735.hp2 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.1194+750C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10441212 | |||||||
| chr16:10441214 | T | C | 1 | a0001c0002t0013g0299 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1194+752T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10441214 | |||||||
| chr16:10441278 | G | C | 50 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(47): Show |
51 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.1194+816G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10441278 | |||||||
| chr16:10441299 | G | A | 3 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0002c0010t0002g0264 |
3 | HG00735.hp2 HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1194+837G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10441299 | |||||||
| chr16:10441305 | A | G | 1 | a0001c0002t0003g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1194+843A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10441305 | |||||||
| chr16:10441342 | T | C | 1 | a0002c0001t0001g0013 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1194+880T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10441342 | |||||||
| chr16:10441518 | T | C | 3 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0196 |
3 | HG01109.hp1 HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1194+1056T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10441518 | |||||||
| chr16:10441639 | C | T | 301 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(298): Show |
306 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1194+1177C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10441639 | |||||||
| chr16:10441715 | G | T | 1 | a0002c0001t0001g0120 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1194+1253G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10441715 | |||||||
| chr16:10441742 | A | C | 11 | a0002c0001t0001g0163 a0002c0001t0001g0165 a0002c0001t0001g0168 others(8): Show |
11 | HG01496.hp1 HG02055.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1194+1280A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10441742 | |||||||
| chr16:10441880 | A | T | 1 | a0002c0001t0001g0039 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1194+1418A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10441880 | |||||||
| chr16:10442063 | C | T | 183 | a0001c0002t0003g0271 a0001c0002t0003g0311 a0002c0001t0001g0001 others(180): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1194+1601C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442063 | |||||||
| chr16:10442129 | A | G | 2 | a0001c0002t0003g0004 a0001c0002t0003g0363 |
3 | HG01243.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1194+1667A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442129 | |||||||
| chr16:10442167 | A | T | 286 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(283): Show |
290 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1194+1705A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442167 | |||||||
| chr16:10442273 | T | G | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1194+1811T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442273 | |||||||
| chr16:10442275 | C | G | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1194+1813C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442275 | |||||||
| chr16:10442319 | A | G | 286 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(283): Show |
290 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1194+1857A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442319 | |||||||
| chr16:10442347 | G | C | 1 | a0001c0002t0005g0303 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1194+1885G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442347 | |||||||
| chr16:10442351 | T | G | 2 | a0001c0002t0003g0346 a0001c0002t0003g0347 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1194+1889T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442351 | |||||||
| chr16:10442430 | A | G | 1 | a0003c0004t0002g0074 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1194+1968A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442430 | |||||||
| chr16:10442471 | G | T | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1194+2009G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442471 | |||||||
| chr16:10442479 | C | T | 1 | a0001c0003t0022g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1194+2017C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442479 | |||||||
| chr16:10442592 | A | G | 1 | a0002c0001t0012g0092 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1194+2130A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442592 | |||||||
| chr16:10442626 | A | G | 1 | a0002c0001t0001g0118 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1194+2164A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442626 | |||||||
| chr16:10442645 | G | C | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1194+2183G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442645 | |||||||
| chr16:10442721 | G | A | 1 | a0003c0004t0002g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1194+2259G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442721 | |||||||
| chr16:10442727 | A | C | 8 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(5): Show |
9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1194+2265A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442727 | |||||||
| chr16:10442768 | CA | C | 286 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(283): Show |
290 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1194+2307delA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442768 | |||||||
| chr16:10442816 | T | C | 2 | a0002c0001t0001g0010 a0002c0001t0001g0022 |
2 | NA18965.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1194+2354T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442816 | |||||||
| chr16:10442931 | A | G | 303 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(300): Show |
308 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1194+2469A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442931 | |||||||
| chr16:10442969 | A | G | 1 | a0001c0003t0008g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1194+2507A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10442969 | |||||||
| chr16:10443081 | A | G | 2 | a0001c0002t0003g0301 a0001c0002t0003g0356 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1194+2619A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10443081 | |||||||
| chr16:10443154 | C | T | 288 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(285): Show |
292 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1194+2692C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10443154 | |||||||
| chr16:10443249 | A | G | 2 | a0001c0002t0003g0301 a0001c0002t0003g0356 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1194+2787A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10443249 | |||||||
| chr16:10443348 | G | T | 181 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0007 others(178): Show |
184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1194+2886G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10443348 | |||||||
| chr16:10443363 | G | A | 1 | a0001c0003t0008g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1194+2901G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10443363 | |||||||
| chr16:10443364 | A | T | 1 | a0001c0003t0008g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1194+2902A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10443364 | |||||||
| chr16:10443424 | C | T | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1194+2962C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10443424 | |||||||
| chr16:10443462 | G | A | 1 | a0002c0001t0001g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1194+3000G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10443462 | |||||||
| chr16:10443486 | C | T | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1194+3024C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10443486 | |||||||
| chr16:10443505 | A | G | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1194+3043A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10443505 | |||||||
| chr16:10443604 | T | C | 2 | a0001c0003t0019g0235 a0004c0006t0004g0233 |
2 | HG02129.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1194+3142T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10443604 | |||||||
| chr16:10443627 | T | C | 1 | a0002c0001t0001g0043 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1194+3165T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10443627 | |||||||
| chr16:10443745 | A | G | 1 | a0002c0001t0001g0084 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1194+3283A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10443745 | |||||||
| chr16:10443747 | A | C | 5 | a0001c0005t0018g0263 a0001c0007t0011g0352 a0001c0007t0011g0353 others(2): Show |
5 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1194+3285A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10443747 | |||||||
| chr16:10444009 | C | T | 40 | a0002c0001t0001g0052 a0002c0001t0001g0070 a0002c0001t0001g0081 others(37): Show |
41 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.1194+3547C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10444009 | |||||||
| chr16:10444208 | A | C | 1 | a0001c0002t0003g0327 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1194+3746A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10444208 | |||||||
| chr16:10444212 | A | C | 1 | a0001c0005t0006g0367 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1194+3750A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10444212 | |||||||
| chr16:10444218 | G | A | 288 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(285): Show |
292 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1194+3756G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10444218 | |||||||
| chr16:10444298 | G | A | 1 | a0001c0002t0003g0284 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1194+3836G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10444298 | |||||||
| chr16:10444329 | G | C | 1 | a0002c0001t0001g0019 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1194+3867G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10444329 | |||||||
| chr16:10444391 | C | T | 1 | a0001c0002t0003g0327 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1194+3929C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10444391 | |||||||
| chr16:10444392 | T | C | 1 | a0001c0003t0022g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1194+3930T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10444392 | |||||||
| chr16:10444405 | C | T | 1 | a0002c0001t0001g0035 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1194+3943C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10444405 | |||||||
| chr16:10444447 | C | T | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1194+3985C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10444447 | |||||||
| chr16:10444510 | T | A | 1 | a0002c0001t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1194+4048T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10444510 | |||||||
| chr16:10444574 | G | C | 1 | a0002c0001t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1194+4112G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10444574 | |||||||
| chr16:10444590 | C | T | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1194+4128C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10444590 | |||||||
| chr16:10444725 | T | G | 9 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(6): Show |
10 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1194+4263T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10444725 | |||||||
| chr16:10444818 | A | G | 1 | a0002c0001t0001g0052 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1194+4356A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10444818 | |||||||
| chr16:10444999 | G | C | 1 | a0002c0001t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1194+4537G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10444999 | |||||||
| chr16:10445009 | G | A | 1 | a0001c0007t0011g0355 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1194+4547G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10445009 | |||||||
| chr16:10445029 | G | A | 1 | a0002c0018t0010g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1194+4567G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10445029 | |||||||
| chr16:10445037 | G | A | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1194+4575G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10445037 | |||||||
| chr16:10445063 | C | T | 18 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0271 others(15): Show |
18 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1194+4601C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10445063 | |||||||
| chr16:10445175 | C | T | 9 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(6): Show |
10 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1194+4713C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10445175 | |||||||
| chr16:10445176 | A | G | 3 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0196 |
3 | HG01109.hp1 HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1194+4714A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10445176 | |||||||
| chr16:10445177 | A | G | 292 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(289): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.1194+4715A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10445177 | |||||||
| chr16:10445428 | T | C | 1 | a0002c0001t0001g0104 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1194+4966T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10445428 | |||||||
| chr16:10445499 | A | ATTATTTA others(1): Show |
49 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(46): Show |
50 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.1194+5052_1194+505 others(12): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 10445499 | ||||||
| chr16:10445656 | C | T | 37 | a0002c0001t0001g0052 a0003c0004t0002g0003 a0003c0004t0002g0025 others(34): Show |
38 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.1194+5194C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10445656 | |||||||
| chr16:10445668 | C | G | 9 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(6): Show |
10 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1194+5206C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10445668 | |||||||
| chr16:10445693 | G | C | 5 | a0001c0005t0018g0263 a0001c0007t0011g0352 a0001c0007t0011g0353 others(2): Show |
5 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1194+5231G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10445693 | |||||||
| chr16:10445703 | C | A | 2 | a0002c0001t0001g0054 a0002c0001t0001g0366 |
2 | HG01175.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1194+5241C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10445703 | |||||||
| chr16:10445776 | G | A | 4 | a0001c0002t0003g0293 a0001c0002t0003g0339 a0001c0002t0003g0340 others(1): Show |
4 | NA18969.hp1 NA19006.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1194+5314G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10445776 | |||||||
| chr16:10445787 | G | A | 10 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(7): Show |
11 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.1194+5325G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10445787 | |||||||
| chr16:10445970 | T | C | 1 | a0001c0002t0013g0299 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1194+5508T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10445970 | |||||||
| chr16:10446092 | C | G | 1 | a0002c0001t0001g0099 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1194+5630C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10446092 | |||||||
| chr16:10446229 | T | G | 1 | a0002c0001t0001g0104 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1194+5767T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10446229 | |||||||
| chr16:10446337 | T | G | 2 | a0002c0001t0001g0054 a0002c0001t0001g0366 |
2 | HG01175.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1194+5875T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10446337 | |||||||
| chr16:10446430 | A | G | 1 | a0002c0001t0001g0175 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1194+5968A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10446430 | |||||||
| chr16:10446454 | C | T | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1194+5992C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10446454 | |||||||
| chr16:10446463 | A | C | 3 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0196 |
3 | HG01109.hp1 HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1194+6001A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10446463 | |||||||
| chr16:10446479 | C | G | 1 | a0001c0002t0003g0327 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1194+6017C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10446479 | |||||||
| chr16:10446489 | C | A | 2 | a0002c0001t0002g0111 a0002c0001t0002g0185 |
2 | HG00558.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1194+6027C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10446489 | |||||||
| chr16:10446538 | C | T | 1 | a0002c0001t0001g0173 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1194+6076C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10446538 | |||||||
| chr16:10446553 | A | G | 9 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(6): Show |
10 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1194+6091A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10446553 | |||||||
| chr16:10446675 | G | A | 35 | a0001c0002t0005g0190 a0001c0002t0005g0266 a0001c0002t0005g0267 others(32): Show |
35 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1194+6213G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10446675 | |||||||
| chr16:10446811 | G | A | 1 | a0001c0002t0005g0303 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1194+6349G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10446811 | |||||||
| chr16:10446827 | C | T | 106 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(103): Show |
107 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(104): Show |
intron_variant | MODIFIER | c.1194+6365C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10446827 | |||||||
| chr16:10446984 | G | A | 1 | a0002c0008t0010g0195 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1194+6522G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10446984 | |||||||
| chr16:10447239 | T | C | 1 | a0002c0021t0002g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1194+6777T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10447239 | |||||||
| chr16:10447251 | C | T | 5 | a0001c0005t0018g0263 a0001c0007t0011g0352 a0001c0007t0011g0353 others(2): Show |
5 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1194+6789C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10447251 | |||||||
| chr16:10447283 | G | A | 1 | a0003c0004t0002g0132 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1194+6821G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10447283 | |||||||
| chr16:10447332 | C | T | 1 | a0001c0002t0003g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1194+6870C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10447332 | |||||||
| chr16:10447520 | G | T | 1 | a0001c0002t0005g0285 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1194+7058G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10447520 | |||||||
| chr16:10447522 | G | T | 1 | a0002c0008t0010g0195 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1194+7060G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10447522 | |||||||
| chr16:10447535 | G | T | 1 | a0001c0002t0005g0285 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1194+7073G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10447535 | |||||||
| chr16:10447782 | C | T | 1 | a0002c0001t0001g0093 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1194+7320C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10447782 | |||||||
| chr16:10447835 | G | C | 98 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(95): Show |
99 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.1194+7373G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10447835 | |||||||
| chr16:10447911 | T | C | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1194+7449T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10447911 | |||||||
| chr16:10447937 | C | T | 7 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0001c0005t0018g0263 others(4): Show |
7 | HG02258.hp2 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1194+7475C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10447937 | |||||||
| chr16:10447952 | C | G | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1194+7490C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10447952 | |||||||
| chr16:10447965 | G | A | 6 | a0001c0003t0008g0207 a0001c0003t0008g0208 a0001c0003t0008g0210 others(3): Show |
6 | NA18944.hp2 NA18964.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.1194+7503G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10447965 | |||||||
| chr16:10447985 | C | T | 1 | a0001c0002t0003g0309 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1194+7523C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10447985 | |||||||
| chr16:10448114 | C | T | 1 | a0001c0002t0003g0327 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1194+7652C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10448114 | |||||||
| chr16:10448121 | A | C | 1 | a0001c0003t0004g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1194+7659A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10448121 | |||||||
| chr16:10448200 | T | G | 1 | a0003c0004t0002g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1194+7738T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10448200 | |||||||
| chr16:10448242 | C | T | 1 | a0002c0001t0001g0042 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1194+7780C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10448242 | |||||||
| chr16:10448468 | C | T | 2 | a0001c0002t0005g0277 a0001c0002t0005g0316 |
2 | NA18980.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1194+8006C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10448468 | |||||||
| chr16:10448859 | G | C | 6 | a0002c0001t0002g0040 a0002c0001t0002g0041 a0002c0001t0002g0108 others(3): Show |
6 | NA18612.hp1 NA18956.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.1194+8397G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10448859 | |||||||
| chr16:10448867 | G | C | 1 | a0002c0008t0010g0195 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1194+8405G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10448867 | |||||||
| chr16:10448966 | T | C | 1 | a0002c0001t0002g0150 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1195-8406T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10448966 | |||||||
| chr16:10448979 | T | C | 1 | a0002c0001t0001g0052 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1195-8393T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10448979 | |||||||
| chr16:10448989 | G | A | 157 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(154): Show |
160 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(157): Show |
intron_variant | MODIFIER | c.1195-8383G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10448989 | |||||||
| chr16:10449041 | A | C | 27 | a0003c0004t0002g0025 a0003c0004t0002g0065 a0003c0004t0002g0066 others(24): Show |
27 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.1195-8331A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10449041 | |||||||
| chr16:10449138 | G | T | 1 | a0002c0001t0002g0127 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1195-8234G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10449138 | |||||||
| chr16:10449221 | T | A | 5 | a0001c0005t0018g0263 a0001c0007t0011g0352 a0001c0007t0011g0353 others(2): Show |
5 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1195-8151T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10449221 | |||||||
| chr16:10449259 | G | T | 2 | a0003c0004t0002g0157 a0003c0004t0002g0365 |
2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1195-8113G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10449259 | |||||||
| chr16:10449293 | G | T | 2 | a0001c0002t0003g0301 a0001c0002t0003g0356 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1195-8079G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10449293 | |||||||
| chr16:10449301 | A | G | 1 | a0002c0001t0002g0160 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1195-8071A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10449301 | |||||||
| chr16:10449434 | G | A | 3 | a0002c0001t0001g0070 a0002c0001t0001g0081 a0002c0001t0001g0093 |
3 | HG00438.hp2 NA18968.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1195-7938G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10449434 | |||||||
| chr16:10449687 | C | G | 1 | a0003c0004t0002g0151 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1195-7685C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10449687 | |||||||
| chr16:10449693 | TCTTTTCT others(12): Show |
T | 1 | a0002c0010t0002g0149 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1195-7678_1195-766 others(23): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10449693 | |||||||
| chr16:10449744 | T | A | 2 | a0002c0001t0001g0056 a0002c0001t0001g0057 |
2 | HG01516.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1195-7628T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10449744 | |||||||
| chr16:10449816 | A | G | 100 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(97): Show |
101 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(98): Show |
intron_variant | MODIFIER | c.1195-7556A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10449816 | |||||||
| chr16:10449925 | G | A | 1 | a0002c0001t0002g0091 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1195-7447G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10449925 | |||||||
| chr16:10449971 | C | G | 1 | a0001c0005t0006g0367 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1195-7401C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10449971 | |||||||
| chr16:10450107 | G | A | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1195-7265G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10450107 | |||||||
| chr16:10450119 | T | C | 1 | a0001c0003t0004g0229 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1195-7253T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10450119 | |||||||
| chr16:10450238 | T | C | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1195-7134T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10450238 | |||||||
| chr16:10450314 | G | A | 1 | a0001c0002t0013g0357 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1195-7058G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10450314 | |||||||
| chr16:10450337 | G | A | 5 | a0001c0003t0004g0209 a0001c0003t0004g0212 a0001c0003t0004g0232 others(2): Show |
5 | HG00323.hp1 HG00738.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.1195-7035G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10450337 | |||||||
| chr16:10450503 | C | T | 107 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(104): Show |
108 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(105): Show |
intron_variant | MODIFIER | c.1195-6869C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10450503 | |||||||
| chr16:10450548 | T | C | 100 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(97): Show |
101 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(98): Show |
intron_variant | MODIFIER | c.1195-6824T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10450548 | |||||||
| chr16:10450662 | G | T | 25 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0291 others(22): Show |
25 | HG01099.hp1 HG01256.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1195-6710G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10450662 | |||||||
| chr16:10450783 | G | A | 1 | a0002c0008t0010g0195 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1195-6589G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10450783 | |||||||
| chr16:10450869 | G | A | 2 | a0001c0002t0003g0272 a0001c0002t0003g0312 |
2 | HG01891.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1195-6503G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10450869 | |||||||
| chr16:10451079 | A | C | 2 | a0001c0003t0004g0221 a0001c0003t0004g0225 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1195-6293A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10451079 | |||||||
| chr16:10451155 | T | C | 2 | a0001c0002t0003g0346 a0001c0002t0003g0347 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1195-6217T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10451155 | |||||||
| chr16:10451335 | G | A | 1 | a0003c0004t0002g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1195-6037G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10451335 | |||||||
| chr16:10451576 | C | T | 1 | a0003c0004t0023g0106 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1195-5796C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10451576 | |||||||
| chr16:10451654 | T | A | 47 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(44): Show |
48 | HG00639.hp1 HG01109.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.1195-5718T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10451654 | |||||||
| chr16:10451682 | A | T | 1 | a0003c0004t0002g0071 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1195-5690A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10451682 | |||||||
| chr16:10451692 | A | T | 1 | a0002c0001t0001g0044 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1195-5680A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10451692 | |||||||
| chr16:10451877 | C | T | 1 | a0003c0004t0002g0065 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1195-5495C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10451877 | |||||||
| chr16:10451878 | C | G | 184 | a0001c0002t0005g0325 a0001c0003t0020g0214 a0002c0001t0001g0001 others(181): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1195-5494C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10451878 | |||||||
| chr16:10451944 | T | G | 1 | a0001c0002t0003g0336 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1195-5428T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10451944 | |||||||
| chr16:10451967 | G | A | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1195-5405G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10451967 | |||||||
| chr16:10452162 | C | T | 9 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(6): Show |
10 | HG02145.hp2 HG02717.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1195-5210C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10452162 | |||||||
| chr16:10452163 | T | G | 1 | a0001c0002t0017g0288 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1195-5209T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10452163 | |||||||
| chr16:10452199 | G | A | 24 | a0002c0001t0001g0001 a0002c0001t0001g0034 a0002c0001t0001g0035 others(21): Show |
25 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.1195-5173G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10452199 | |||||||
| chr16:10452335 | C | G | 3 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0196 |
3 | HG01109.hp1 HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1195-5037C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10452335 | |||||||
| chr16:10452612 | T | C | 7 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0005t0018g0263 others(4): Show |
7 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1195-4760T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10452612 | |||||||
| chr16:10452652 | C | T | 1 | a0003c0004t0002g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1195-4720C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10452652 | |||||||
| chr16:10452721 | C | A | 1 | a0002c0001t0001g0049 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1195-4651C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10452721 | |||||||
| chr16:10452828 | C | T | 9 | a0001c0002t0007g0265 a0001c0002t0007g0279 a0001c0002t0007g0280 others(6): Show |
9 | HG02155.hp2 NA18941.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.1195-4544C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10452828 | |||||||
| chr16:10452845 | G | T | 1 | a0002c0001t0012g0085 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1195-4527G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10452845 | |||||||
| chr16:10452851 | G | A | 8 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(5): Show |
9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1195-4521G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10452851 | |||||||
| chr16:10452858 | C | G | 191 | a0001c0002t0005g0325 a0001c0003t0020g0214 a0001c0005t0006g0005 others(188): Show |
195 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1195-4514C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10452858 | |||||||
| chr16:10452922 | A | G | 5 | a0002c0001t0002g0111 a0002c0001t0002g0126 a0002c0001t0002g0127 others(2): Show |
5 | HG00558.hp1 NA18943.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.1195-4450A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10452922 | |||||||
| chr16:10453023 | G | A | 1 | a0002c0001t0001g0138 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1195-4349G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10453023 | |||||||
| chr16:10453041 | G | A | 6 | a0002c0001t0001g0173 a0002c0001t0001g0174 a0002c0001t0001g0175 others(3): Show |
6 | HG01123.hp2 HG01433.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1195-4331G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10453041 | |||||||
| chr16:10453120 | A | G | 1 | a0001c0003t0008g0026 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1195-4252A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10453120 | |||||||
| chr16:10453121 | C | A | 8 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(5): Show |
9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1195-4251C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10453121 | |||||||
| chr16:10453153 | C | G | 203 | a0001c0002t0005g0325 a0001c0003t0008g0026 a0001c0003t0008g0027 others(200): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1195-4219C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10453153 | |||||||
| chr16:10453221 | G | C | 1 | a0002c0001t0001g0038 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1195-4151G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10453221 | |||||||
| chr16:10453281 | G | A | 1 | a0003c0004t0002g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1195-4091G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10453281 | |||||||
| chr16:10453437 | G | T | 2 | a0003c0011t0002g0154 a0003c0011t0002g0156 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1195-3935G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10453437 | |||||||
| chr16:10453490 | A | G | 5 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0003t0008g0026 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1195-3882A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10453490 | |||||||
| chr16:10453619 | G | T | 202 | a0001c0002t0005g0325 a0001c0003t0008g0026 a0001c0003t0008g0027 others(199): Show |
206 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1195-3753G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10453619 | |||||||
| chr16:10453628 | T | C | 1 | a0002c0001t0001g0034 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1195-3744T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10453628 | |||||||
| chr16:10453645 | T | C | 2 | a0003c0011t0002g0154 a0003c0011t0002g0156 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1195-3727T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10453645 | |||||||
| chr16:10453769 | C | T | 1 | a0003c0004t0002g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1195-3603C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10453769 | |||||||
| chr16:10453814 | T | G | 7 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(4): Show |
8 | HG01243.hp1 HG02451.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1195-3558T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10453814 | |||||||
| chr16:10453961 | G | C | 2 | a0002c0001t0001g0010 a0002c0001t0001g0022 |
2 | NA18965.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1195-3411G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10453961 | |||||||
| chr16:10453981 | A | C | 2 | a0002c0001t0001g0104 a0002c0001t0001g0128 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1195-3391A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10453981 | |||||||
| chr16:10454008 | GT | G | 48 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0308 others(45): Show |
49 | HG00408.hp1 HG00621.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.1195-3350delT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 10454008 | ||||||
| chr16:10454011 | T | A | 10 | a0002c0001t0001g0163 a0002c0001t0001g0165 a0002c0001t0001g0168 others(7): Show |
10 | HG01496.hp1 HG02055.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1195-3361T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10454011 | |||||||
| chr16:10454011 | T | G | 1 | a0001c0002t0003g0284 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1195-3361T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10454011 | |||||||
| chr16:10454116 | T | A | 7 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0005t0018g0263 others(4): Show |
7 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1195-3256T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10454116 | |||||||
| chr16:10454116 | T | C | 1 | a0002c0001t0001g0120 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1195-3256T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10454116 | |||||||
| chr16:10454271 | A | T | 2 | a0002c0001t0002g0135 a0002c0001t0002g0136 |
2 | HG00438.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1195-3101A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10454271 | |||||||
| chr16:10454325 | G | A | 1 | a0006c0014t0003g0268 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1195-3047G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10454325 | |||||||
| chr16:10454341 | C | T | 1 | a0002c0001t0009g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1195-3031C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10454341 | |||||||
| chr16:10454408 | C | CA | 57 | a0001c0002t0003g0269 a0001c0002t0003g0271 a0001c0002t0003g0293 others(54): Show |
57 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1195-2934dupA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 10454408 | ||||||
| chr16:10454408 | C | CAA | 22 | a0001c0002t0003g0272 a0001c0002t0003g0273 a0001c0002t0003g0274 others(19): Show |
22 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1195-2935_1195-293 others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 10454408 | ||||||
| chr16:10454408 | C | CAAA | 28 | a0001c0002t0003g0313 a0001c0002t0003g0327 a0001c0002t0003g0328 others(25): Show |
28 | HG01261.hp2 HG01433.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.1195-2936_1195-293 others(7): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 10454408 | ||||||
| chr16:10454408 | C | CAAAA | 12 | a0001c0002t0003g0306 a0001c0002t0003g0331 a0001c0002t0005g0190 others(9): Show |
12 | HG02080.hp2 HG02293.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1195-2937_1195-293 others(8): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 10454408 | ||||||
| chr16:10454408 | CA | C | 22 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0003t0004g0216 others(19): Show |
22 | HG01069.hp1 HG01167.hp2 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.1195-2934delA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 10454408 | ||||||
| chr16:10454408 | CAAAAAAA others(7): Show |
C | 1 | a0002c0001t0001g0131 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1195-2947_1195-293 others(18): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 10454408 | ||||||
| chr16:10454408 | CAAAAAAA others(12): Show |
C | 55 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(52): Show |
57 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1195-2952_1195-293 others(23): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 10454408 | ||||||
| chr16:10454512 | ATATT | A | 7 | a0002c0001t0001g0034 a0002c0001t0001g0035 a0002c0001t0001g0043 others(4): Show |
7 | HG00558.hp2 HG01261.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1195-2855_1195-285 others(8): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 10454512 | ||||||
| chr16:10454543 | G | C | 1 | a0002c0008t0010g0195 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1195-2829G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10454543 | |||||||
| chr16:10454576 | T | G | 7 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0005t0018g0263 others(4): Show |
7 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1195-2796T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10454576 | |||||||
| chr16:10454790 | A | G | 1 | a0002c0001t0001g0168 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1195-2582A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10454790 | |||||||
| chr16:10455136 | T | C | 1 | a0001c0002t0003g0360 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1195-2236T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10455136 | |||||||
| chr16:10455328 | A | G | 19 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0271 others(16): Show |
19 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1195-2044A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10455328 | |||||||
| chr16:10455388 | C | T | 47 | a0001c0005t0018g0263 a0001c0007t0011g0352 a0001c0007t0011g0353 others(44): Show |
48 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.1195-1984C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10455388 | |||||||
| chr16:10455637 | C | T | 1 | a0002c0001t0001g0058 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1195-1735C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10455637 | |||||||
| chr16:10455982 | C | CTTTTTTT others(7): Show |
266 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0271 others(263): Show |
270 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.1195-1377_1195-137 others(18): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 10455982 | ||||||
| chr16:10456043 | A | C | 2 | a0002c0008t0010g0195 a0002c0018t0010g0197 |
2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1195-1329A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10456043 | |||||||
| chr16:10456056 | T | C | 1 | a0003c0004t0002g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1195-1316T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10456056 | |||||||
| chr16:10456203 | AAG | A | 25 | a0003c0004t0002g0065 a0003c0004t0002g0066 a0003c0004t0002g0067 others(22): Show |
25 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1195-1165_1195-116 others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr16 | 10456203 | ||||||
| chr16:10456216 | A | G | 4 | a0001c0003t0004g0211 a0001c0003t0004g0236 a0001c0003t0004g0241 others(1): Show |
4 | NA18947.hp2 NA18963.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1195-1156A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10456216 | |||||||
| chr16:10456258 | T | A | 1 | a0002c0008t0010g0195 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1195-1114T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10456258 | |||||||
| chr16:10456314 | T | A | 7 | a0001c0002t0003g0358 a0001c0002t0003g0359 a0001c0002t0003g0360 others(4): Show |
7 | HG01358.hp1 HG02257.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1195-1058T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10456314 | |||||||
| chr16:10456353 | C | A | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1195-1019C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10456353 | |||||||
| chr16:10456662 | A | G | 1 | a0002c0018t0010g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1195-710A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10456662 | |||||||
| chr16:10456697 | T | C | 2 | a0002c0001t0001g0124 a0002c0001t0001g0125 |
2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1195-675T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10456697 | |||||||
| chr16:10456776 | T | C | 5 | a0001c0005t0018g0263 a0001c0007t0011g0352 a0001c0007t0011g0353 others(2): Show |
5 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1195-596T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10456776 | |||||||
| chr16:10456926 | T | A | 1 | a0001c0003t0002g0199 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1195-446T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10456926 | |||||||
| chr16:10457149 | A | T | 1 | a0001c0002t0003g0326 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1195-223A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10457149 | |||||||
| chr16:10457320 | G | T | 1 | a0003c0004t0002g0065 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1195-52G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10457320 | |||||||
| chr16:10457326 | A | G | 1 | a0003c0004t0002g0074 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1195-46A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 8/13 | chr16 | 10457326 | |||||||
| chr16:10457689 | G | GT | 12 | a0001c0003t0020g0214 a0001c0005t0018g0263 a0001c0007t0011g0352 others(9): Show |
12 | HG01175.hp2 HG02055.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1352+169dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 10457689 | ||||||
| chr16:10457689 | G | T | 10 | a0001c0002t0003g0326 a0001c0003t0002g0199 a0001c0005t0006g0005 others(7): Show |
11 | HG02145.hp2 HG02280.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.1352+160G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10457689 | |||||||
| chr16:10457690 | T | G | 1 | a0001c0002t0003g0309 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1352+161T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10457690 | |||||||
| chr16:10457705 | T | C | 1 | a0005c0017t0005g0302 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1352+176T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10457705 | |||||||
| chr16:10457745 | T | C | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1352+216T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10457745 | |||||||
| chr16:10457918 | C | T | 1 | a0001c0013t0004g0259 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1352+389C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10457918 | |||||||
| chr16:10458078 | T | C | 6 | a0003c0004t0002g0105 a0003c0004t0002g0109 a0003c0004t0002g0117 others(3): Show |
6 | NA18939.hp1 NA18985.hp2 NA18997.hp2 others(3): Show |
intron_variant | MODIFIER | c.1352+549T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10458078 | |||||||
| chr16:10458092 | C | T | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1352+563C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10458092 | |||||||
| chr16:10458124 | A | G | 51 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(48): Show |
52 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.1352+595A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10458124 | |||||||
| chr16:10458147 | A | G | 1 | a0003c0004t0002g0080 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1352+618A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10458147 | |||||||
| chr16:10458187 | C | A | 183 | a0001c0003t0020g0214 a0001c0005t0018g0263 a0002c0001t0001g0001 others(180): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1352+658C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10458187 | |||||||
| chr16:10458355 | A | C | 1 | a0001c0002t0005g0333 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1352+826A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10458355 | |||||||
| chr16:10458473 | G | A | 7 | a0002c0001t0001g0034 a0002c0001t0001g0035 a0002c0001t0001g0043 others(4): Show |
7 | HG00558.hp2 HG01261.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1352+944G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10458473 | |||||||
| chr16:10458552 | A | G | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1352+1023A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10458552 | |||||||
| chr16:10458729 | G | C | 188 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0001c0003t0020g0214 others(185): Show |
191 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1352+1200G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10458729 | |||||||
| chr16:10458913 | C | T | 10 | a0003c0004t0002g0003 a0003c0004t0002g0151 a0003c0004t0002g0152 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1352+1384C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10458913 | |||||||
| chr16:10458940 | G | A | 302 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(299): Show |
307 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1352+1411G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10458940 | |||||||
| chr16:10459027 | A | AAAT | 179 | a0001c0003t0020g0214 a0002c0001t0001g0001 a0002c0001t0001g0002 others(176): Show |
182 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.1352+1512_1352+151 others(7): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 10459027 | ||||||
| chr16:10459027 | AAAT | A | 3 | a0002c0001t0001g0060 a0002c0001t0012g0085 a0002c0001t0012g0119 |
3 | HG00099.hp2 HG00140.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1352+1512_1352+151 others(7): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 10459027 | ||||||
| chr16:10459124 | G | A | 2 | a0003c0004t0002g0157 a0003c0004t0002g0365 |
2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1352+1595G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10459124 | |||||||
| chr16:10459251 | G | A | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1352+1722G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10459251 | |||||||
| chr16:10459443 | G | A | 2 | a0002c0001t0001g0024 a0002c0001t0002g0101 |
2 | HG03704.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1352+1914G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10459443 | |||||||
| chr16:10459448 | A | G | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1352+1919A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10459448 | |||||||
| chr16:10459553 | A | T | 1 | a0003c0004t0002g0078 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1352+2024A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10459553 | |||||||
| chr16:10459603 | C | T | 1 | a0001c0003t0008g0026 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1352+2074C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10459603 | |||||||
| chr16:10459616 | C | T | 182 | a0001c0003t0020g0214 a0002c0001t0001g0001 a0002c0001t0001g0002 others(179): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1352+2087C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10459616 | |||||||
| chr16:10459761 | C | T | 2 | a0002c0008t0010g0195 a0002c0018t0010g0197 |
2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1352+2232C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10459761 | |||||||
| chr16:10459807 | T | C | 1 | a0002c0001t0001g0123 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1352+2278T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10459807 | |||||||
| chr16:10459815 | G | A | 182 | a0001c0003t0020g0214 a0002c0001t0001g0001 a0002c0001t0001g0002 others(179): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1352+2286G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10459815 | |||||||
| chr16:10459838 | G | A | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1352+2309G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10459838 | |||||||
| chr16:10460211 | G | C | 2 | a0003c0011t0002g0154 a0003c0011t0002g0156 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1352+2682G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10460211 | |||||||
| chr16:10460227 | G | C | 2 | a0003c0011t0002g0154 a0003c0011t0002g0156 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1352+2698G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10460227 | |||||||
| chr16:10460257 | G | C | 3 | a0002c0001t0001g0138 a0002c0001t0001g0139 a0002c0001t0001g0188 |
3 | HG02630.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1352+2728G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10460257 | |||||||
| chr16:10460291 | T | C | 1 | a0003c0004t0023g0106 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1352+2762T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10460291 | |||||||
| chr16:10460350 | G | A | 182 | a0001c0003t0020g0214 a0002c0001t0001g0001 a0002c0001t0001g0002 others(179): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1352+2821G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10460350 | |||||||
| chr16:10460412 | C | T | 2 | a0002c0001t0001g0054 a0002c0001t0001g0366 |
2 | HG01175.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1352+2883C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10460412 | |||||||
| chr16:10460449 | A | G | 1 | a0004c0006t0004g0244 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1352+2920A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10460449 | |||||||
| chr16:10460587 | G | A | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1352+3058G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10460587 | |||||||
| chr16:10460681 | T | C | 2 | a0002c0008t0010g0195 a0002c0018t0010g0197 |
2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1352+3152T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10460681 | |||||||
| chr16:10460760 | A | T | 182 | a0001c0003t0020g0214 a0002c0001t0001g0001 a0002c0001t0001g0002 others(179): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1352+3231A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10460760 | |||||||
| chr16:10460812 | G | A | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1352+3283G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10460812 | |||||||
| chr16:10460932 | C | A | 2 | a0003c0004t0002g0117 a0003c0004t0023g0106 |
2 | NA18997.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1352+3403C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10460932 | |||||||
| chr16:10460937 | A | G | 111 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(108): Show |
112 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(109): Show |
intron_variant | MODIFIER | c.1352+3408A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10460937 | |||||||
| chr16:10461154 | T | C | 2 | a0001c0002t0003g0339 a0001c0002t0003g0343 |
2 | NA18969.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1352+3625T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10461154 | |||||||
| chr16:10461229 | A | G | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1352+3700A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10461229 | |||||||
| chr16:10461361 | A | C | 1 | a0001c0003t0004g0228 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1352+3832A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10461361 | |||||||
| chr16:10461493 | C | T | 2 | a0001c0005t0006g0005 a0001c0005t0006g0371 |
3 | HG02145.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1352+3964C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10461493 | |||||||
| chr16:10461967 | T | G | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1352+4438T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10461967 | |||||||
| chr16:10462040 | C | T | 1 | a0002c0001t0002g0126 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1352+4511C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10462040 | |||||||
| chr16:10462143 | G | C | 2 | a0003c0011t0002g0154 a0003c0011t0002g0156 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1352+4614G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10462143 | |||||||
| chr16:10462295 | C | T | 1 | a0001c0002t0003g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1352+4766C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10462295 | |||||||
| chr16:10462378 | T | A | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1352+4849T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10462378 | |||||||
| chr16:10462456 | T | C | 68 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(65): Show |
69 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.1352+4927T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10462456 | |||||||
| chr16:10462466 | T | C | 6 | a0001c0005t0006g0029 a0001c0005t0006g0030 a0001c0005t0006g0367 others(3): Show |
6 | HG02965.hp1 HG03209.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.1352+4937T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10462466 | |||||||
| chr16:10462590 | A | G | 2 | a0002c0001t0001g0120 a0002c0001t0001g0162 |
2 | NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1352+5061A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10462590 | |||||||
| chr16:10462680 | A | T | 1 | a0002c0001t0002g0028 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1352+5151A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10462680 | |||||||
| chr16:10462767 | C | T | 1 | a0001c0003t0020g0214 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1352+5238C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10462767 | |||||||
| chr16:10462777 | T | A | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1352+5248T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10462777 | |||||||
| chr16:10462802 | A | G | 1 | a0002c0001t0001g0100 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1352+5273A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10462802 | |||||||
| chr16:10463086 | T | A | 141 | a0001c0003t0020g0214 a0002c0001t0001g0001 a0002c0001t0001g0002 others(138): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1352+5557T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10463086 | |||||||
| chr16:10463090 | T | C | 1 | a0002c0001t0001g0098 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1352+5561T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10463090 | |||||||
| chr16:10463105 | A | G | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1352+5576A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10463105 | |||||||
| chr16:10463249 | A | G | 1 | a0001c0002t0003g0291 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1352+5720A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10463249 | |||||||
| chr16:10463290 | A | G | 2 | a0002c0001t0012g0085 a0002c0001t0012g0119 |
2 | HG00099.hp2 HG00140.hp2 |
intron_variant | MODIFIER | c.1352+5761A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10463290 | |||||||
| chr16:10463325 | C | T | 1 | a0001c0003t0008g0256 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1352+5796C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10463325 | |||||||
| chr16:10463421 | T | C | 141 | a0001c0003t0020g0214 a0002c0001t0001g0001 a0002c0001t0001g0002 others(138): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1352+5892T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10463421 | |||||||
| chr16:10463442 | A | G | 34 | a0001c0002t0017g0288 a0002c0001t0001g0070 a0002c0001t0001g0081 others(31): Show |
34 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1352+5913A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10463442 | |||||||
| chr16:10463460 | C | T | 306 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(303): Show |
311 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1352+5931C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10463460 | |||||||
| chr16:10463497 | G | A | 1 | a0001c0002t0003g0364 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1352+5968G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10463497 | |||||||
| chr16:10463581 | T | G | 1 | a0002c0001t0001g0366 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1352+6052T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10463581 | |||||||
| chr16:10463904 | A | C | 306 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(303): Show |
311 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1352+6375A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10463904 | |||||||
| chr16:10463905 | T | C | 306 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(303): Show |
311 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1352+6376T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10463905 | |||||||
| chr16:10463954 | C | A | 1 | a0001c0002t0017g0288 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1352+6425C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10463954 | |||||||
| chr16:10463955 | A | G | 110 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(107): Show |
111 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(108): Show |
intron_variant | MODIFIER | c.1352+6426A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10463955 | |||||||
| chr16:10463973 | T | G | 144 | a0001c0003t0020g0214 a0002c0001t0001g0001 a0002c0001t0001g0002 others(141): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1352+6444T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10463973 | |||||||
| chr16:10463993 | C | T | 1 | a0002c0001t0002g0083 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1352+6464C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10463993 | |||||||
| chr16:10464119 | C | G | 109 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(106): Show |
110 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(107): Show |
intron_variant | MODIFIER | c.1352+6590C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10464119 | |||||||
| chr16:10464784 | A | G | 1 | a0002c0010t0002g0264 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1352+7255A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10464784 | |||||||
| chr16:10464824 | CTGTTGTT others(5): Show |
C | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1353-7278_1353-726 others(16): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 10464824 | ||||||
| chr16:10464878 | G | A | 2 | a0001c0002t0003g0293 a0001c0002t0003g0340 |
2 | NA19006.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1353-7232G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10464878 | |||||||
| chr16:10464942 | C | T | 103 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(100): Show |
104 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.1353-7168C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10464942 | |||||||
| chr16:10465043 | T | C | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1353-7067T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10465043 | |||||||
| chr16:10465247 | G | C | 237 | a0001c0002t0005g0190 a0001c0002t0005g0266 a0001c0002t0005g0267 others(234): Show |
241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1353-6863G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10465247 | |||||||
| chr16:10465281 | A | G | 10 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(7): Show |
11 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.1353-6829A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10465281 | |||||||
| chr16:10465305 | T | C | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1353-6805T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10465305 | |||||||
| chr16:10465364 | A | T | 1 | a0002c0001t0002g0083 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1353-6746A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10465364 | |||||||
| chr16:10465406 | A | G | 43 | a0002c0001t0001g0070 a0002c0001t0001g0081 a0002c0010t0002g0140 others(40): Show |
44 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1353-6704A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10465406 | |||||||
| chr16:10465565 | C | T | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1353-6545C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10465565 | |||||||
| chr16:10465835 | C | T | 1 | a0001c0003t0004g0257 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1353-6275C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10465835 | |||||||
| chr16:10465894 | C | G | 1 | a0002c0001t0001g0024 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1353-6216C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10465894 | |||||||
| chr16:10465919 | G | A | 3 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0196 |
3 | HG01109.hp1 HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1353-6191G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10465919 | |||||||
| chr16:10465969 | A | C | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1353-6141A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10465969 | |||||||
| chr16:10465978 | G | A | 304 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(301): Show |
309 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1353-6132G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10465978 | |||||||
| chr16:10466105 | A | T | 1 | a0002c0001t0001g0123 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1353-6005A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10466105 | |||||||
| chr16:10466111 | C | G | 1 | a0001c0003t0008g0230 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1353-5999C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10466111 | |||||||
| chr16:10466116 | T | C | 12 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0001c0005t0006g0005 others(9): Show |
13 | HG02145.hp2 HG02258.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.1353-5994T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10466116 | |||||||
| chr16:10466501 | G | T | 1 | a0001c0002t0007g0319 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1353-5609G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10466501 | |||||||
| chr16:10466515 | C | T | 1 | a0002c0001t0002g0112 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1353-5595C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10466515 | |||||||
| chr16:10466528 | A | G | 43 | a0002c0001t0001g0070 a0002c0001t0001g0081 a0002c0010t0002g0140 others(40): Show |
44 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1353-5582A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10466528 | |||||||
| chr16:10466535 | G | C | 1 | a0002c0001t0001g0049 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1353-5575G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10466535 | |||||||
| chr16:10466635 | T | C | 2 | a0002c0008t0010g0195 a0002c0018t0010g0197 |
2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1353-5475T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10466635 | |||||||
| chr16:10466644 | G | T | 48 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(45): Show |
49 | HG00639.hp1 HG01109.hp2 HG01168.hp1 others(46): Show |
intron_variant | MODIFIER | c.1353-5466G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10466644 | |||||||
| chr16:10466659 | T | C | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1353-5451T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10466659 | |||||||
| chr16:10466663 | G | A | 3 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0196 |
3 | HG01109.hp1 HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1353-5447G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10466663 | |||||||
| chr16:10466850 | CCTA | C | 8 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(5): Show |
9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1353-5257_1353-525 others(7): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 10466850 | ||||||
| chr16:10466881 | T | A | 41 | a0002c0010t0002g0140 a0002c0010t0002g0149 a0002c0021t0002g0184 others(38): Show |
42 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1353-5229T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10466881 | |||||||
| chr16:10467040 | A | G | 30 | a0001c0003t0002g0033 a0001c0003t0002g0199 a0001c0003t0004g0200 others(27): Show |
30 | HG00408.hp1 HG00621.hp1 HG01981.hp2 others(27): Show |
intron_variant | MODIFIER | c.1353-5070A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10467040 | |||||||
| chr16:10467221 | T | G | 1 | a0002c0001t0002g0083 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1353-4889T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10467221 | |||||||
| chr16:10467255 | AATACAAT others(3): Show |
A | 1 | a0003c0004t0002g0072 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1353-4853_1353-484 others(14): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 10467255 | ||||||
| chr16:10467347 | G | A | 1 | a0002c0001t0001g0002 | 2 | HG00639.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1353-4763G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10467347 | |||||||
| chr16:10467400 | G | A | 1 | a0003c0004t0002g0080 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1353-4710G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10467400 | |||||||
| chr16:10467404 | A | G | 1 | a0002c0019t0001g0182 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1353-4706A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10467404 | |||||||
| chr16:10467573 | A | AT | 51 | a0001c0002t0003g0314 a0001c0003t0004g0258 a0001c0003t0004g0260 others(48): Show |
52 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.1353-4522dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 10467573 | ||||||
| chr16:10467573 | AT | A | 6 | a0001c0003t0004g0257 a0002c0008t0010g0193 a0002c0008t0010g0194 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1353-4522delT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 10467573 | ||||||
| chr16:10467612 | A | G | 1 | a0001c0002t0003g0331 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1353-4498A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10467612 | |||||||
| chr16:10467670 | G | A | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1353-4440G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10467670 | |||||||
| chr16:10467743 | G | C | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1353-4367G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10467743 | |||||||
| chr16:10467781 | G | A | 1 | a0002c0001t0001g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1353-4329G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10467781 | |||||||
| chr16:10467800 | G | A | 8 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(5): Show |
9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1353-4310G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10467800 | |||||||
| chr16:10467809 | C | T | 1 | a0001c0003t0004g0257 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1353-4301C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10467809 | |||||||
| chr16:10467834 | T | C | 1 | a0001c0016t0015g0323 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1353-4276T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10467834 | |||||||
| chr16:10467845 | G | A | 1 | a0003c0004t0002g0129 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1353-4265G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10467845 | |||||||
| chr16:10467878 | CT | C | 44 | a0001c0002t0005g0325 a0001c0003t0004g0220 a0001c0003t0004g0241 others(41): Show |
45 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.1353-4214delT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 10467878 | ||||||
| chr16:10467994 | C | T | 2 | a0002c0001t0002g0137 a0002c0001t0002g0150 |
2 | HG02523.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1353-4116C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10467994 | |||||||
| chr16:10468002 | C | T | 1 | a0003c0004t0002g0072 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1353-4108C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468002 | |||||||
| chr16:10468026 | C | T | 3 | a0001c0002t0003g0309 a0002c0001t0014g0068 a0002c0001t0014g0069 |
3 | HG03491.hp1 HG03492.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1353-4084C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468026 | |||||||
| chr16:10468040 | C | T | 39 | a0002c0001t0002g0083 a0002c0021t0002g0184 a0003c0004t0002g0003 others(36): Show |
40 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.1353-4070C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468040 | |||||||
| chr16:10468071 | G | A | 38 | a0002c0021t0002g0184 a0003c0004t0002g0003 a0003c0004t0002g0025 others(35): Show |
39 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1353-4039G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468071 | |||||||
| chr16:10468120 | TCCTC | T | 38 | a0002c0021t0002g0184 a0003c0004t0002g0003 a0003c0004t0002g0025 others(35): Show |
39 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1353-3987_1353-398 others(8): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 10468120 | ||||||
| chr16:10468124 | C | A | 1 | a0008c0020t0002g0006 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1353-3986C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468124 | |||||||
| chr16:10468169 | C | T | 153 | a0001c0003t0004g0200 a0001c0003t0004g0215 a0001c0003t0004g0216 others(150): Show |
155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1353-3941C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468169 | |||||||
| chr16:10468194 | T | A | 1 | a0002c0001t0001g0051 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1353-3916T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468194 | |||||||
| chr16:10468194 | T | G | 3 | a0002c0001t0002g0159 a0002c0001t0002g0160 a0002c0001t0002g0161 |
3 | NA18942.hp2 NA18944.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1353-3916T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468194 | |||||||
| chr16:10468284 | A | T | 1 | a0001c0003t0004g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1353-3826A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468284 | |||||||
| chr16:10468290 | G | T | 1 | a0003c0004t0002g0072 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1353-3820G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468290 | |||||||
| chr16:10468291 | A | G | 1 | a0003c0004t0002g0072 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1353-3819A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468291 | |||||||
| chr16:10468293 | T | A | 1 | a0003c0004t0002g0072 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1353-3817T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468293 | |||||||
| chr16:10468313 | C | T | 1 | a0003c0004t0002g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1353-3797C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468313 | |||||||
| chr16:10468314 | A | T | 1 | a0003c0004t0002g0189 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1353-3796A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468314 | |||||||
| chr16:10468322 | C | G | 10 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(7): Show |
11 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.1353-3788C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468322 | |||||||
| chr16:10468382 | T | C | 1 | a0002c0001t0001g0009 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1353-3728T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468382 | |||||||
| chr16:10468445 | G | C | 29 | a0002c0021t0002g0184 a0003c0004t0002g0025 a0003c0004t0002g0065 others(26): Show |
29 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1353-3665G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468445 | |||||||
| chr16:10468516 | G | T | 23 | a0003c0004t0002g0065 a0003c0004t0002g0066 a0003c0004t0002g0067 others(20): Show |
23 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.1353-3594G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468516 | |||||||
| chr16:10468549 | T | C | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1353-3561T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468549 | |||||||
| chr16:10468664 | T | C | 2 | a0001c0002t0007g0318 a0001c0002t0007g0322 |
2 | NA18951.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1353-3446T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468664 | |||||||
| chr16:10468669 | C | A | 1 | a0001c0002t0003g0361 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1353-3441C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468669 | |||||||
| chr16:10468746 | T | A | 38 | a0002c0021t0002g0184 a0003c0004t0002g0003 a0003c0004t0002g0025 others(35): Show |
39 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1353-3364T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468746 | |||||||
| chr16:10468746 | T | G | 1 | a0002c0001t0002g0086 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1353-3364T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468746 | |||||||
| chr16:10468750 | G | C | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1353-3360G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468750 | |||||||
| chr16:10468881 | G | T | 102 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(99): Show |
103 | HG00639.hp1 HG00735.hp2 HG01070.hp1 others(100): Show |
intron_variant | MODIFIER | c.1353-3229G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468881 | |||||||
| chr16:10468895 | G | A | 2 | a0002c0008t0010g0195 a0002c0018t0010g0197 |
2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1353-3215G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468895 | |||||||
| chr16:10468897 | T | A | 1 | a0002c0001t0002g0083 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1353-3213T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468897 | |||||||
| chr16:10468921 | G | A | 1 | a0002c0001t0002g0086 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1353-3189G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10468921 | |||||||
| chr16:10469128 | A | G | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1353-2982A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10469128 | |||||||
| chr16:10469130 | A | G | 3 | a0001c0002t0005g0348 a0001c0002t0005g0349 a0001c0002t0005g0350 |
3 | NA19011.hp1 NA19062.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1353-2980A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10469130 | |||||||
| chr16:10469195 | C | T | 1 | a0003c0004t0002g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1353-2915C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10469195 | |||||||
| chr16:10469276 | G | A | 1 | a0003c0004t0002g0072 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1353-2834G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10469276 | |||||||
| chr16:10469602 | C | T | 2 | a0001c0002t0003g0346 a0001c0002t0003g0347 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1353-2508C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10469602 | |||||||
| chr16:10469645 | C | T | 2 | a0003c0004t0002g0082 a0003c0004t0002g0144 |
2 | HG02071.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1353-2465C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10469645 | |||||||
| chr16:10469700 | A | G | 1 | a0003c0004t0002g0192 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1353-2410A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10469700 | |||||||
| chr16:10469892 | T | A | 1 | a0001c0002t0003g0291 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1353-2218T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10469892 | |||||||
| chr16:10469892 | TA | T | 198 | a0001c0002t0003g0290 a0001c0002t0003g0301 a0001c0002t0003g0327 others(195): Show |
202 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1353-2204delA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 10469892 | ||||||
| chr16:10469892 | TAA | T | 8 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0001c0007t0011g0352 others(5): Show |
8 | HG01943.hp2 HG02258.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1353-2205_1353-220 others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 10469892 | ||||||
| chr16:10469957 | G | A | 1 | a0001c0002t0003g0339 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1353-2153G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10469957 | |||||||
| chr16:10470049 | G | C | 1 | a0001c0002t0003g0328 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1353-2061G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10470049 | |||||||
| chr16:10470132 | A | T | 1 | a0003c0004t0002g0072 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1353-1978A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10470132 | |||||||
| chr16:10470153 | G | C | 1 | a0001c0003t0008g0026 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1353-1957G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10470153 | |||||||
| chr16:10470444 | A | G | 39 | a0002c0010t0002g0140 a0002c0010t0002g0149 a0003c0004t0002g0003 others(36): Show |
40 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.1353-1666A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10470444 | |||||||
| chr16:10470568 | G | A | 1 | a0001c0002t0003g0339 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1353-1542G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10470568 | |||||||
| chr16:10470600 | A | G | 4 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0273 others(1): Show |
4 | HG01099.hp2 HG03017.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1353-1510A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10470600 | |||||||
| chr16:10470629 | T | A | 159 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(156): Show |
162 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(159): Show |
intron_variant | MODIFIER | c.1353-1481T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10470629 | |||||||
| chr16:10470746 | A | G | 304 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(301): Show |
309 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1353-1364A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10470746 | |||||||
| chr16:10470771 | C | T | 13 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0005t0006g0005 others(10): Show |
14 | HG02145.hp2 HG02451.hp2 HG02965.hp1 others(11): Show |
intron_variant | MODIFIER | c.1353-1339C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10470771 | |||||||
| chr16:10470813 | A | ATATG | 5 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0005t0016g0031 others(2): Show |
5 | HG02451.hp2 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1353-1296_1353-129 others(8): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 10470813 | ||||||
| chr16:10470813 | A | ATATGTG | 8 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(5): Show |
9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1353-1296_1353-129 others(10): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 10470813 | ||||||
| chr16:10470813 | A | G | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1353-1297A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10470813 | |||||||
| chr16:10470823 | G | A | 6 | a0001c0005t0006g0029 a0001c0005t0006g0030 a0001c0005t0006g0367 others(3): Show |
6 | HG02965.hp1 HG03209.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.1353-1287G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10470823 | |||||||
| chr16:10470823 | G | GTA | 5 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0002c0010t0002g0140 others(2): Show |
5 | HG02155.hp1 HG02258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1353-1273_1353-127 others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 10470823 | ||||||
| chr16:10470823 | GTATATAT others(17): Show |
G | 6 | a0002c0001t0001g0001 a0002c0001t0001g0061 a0002c0001t0001g0087 others(3): Show |
7 | NA18946.hp1 NA19060.hp1 NA19064.hp1 others(4): Show |
intron_variant | MODIFIER | c.1353-1279_1353-125 others(28): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 10470823 | ||||||
| chr16:10470837 | A | G | 138 | a0001c0003t0020g0214 a0001c0016t0015g0323 a0002c0001t0001g0002 others(135): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1353-1273A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10470837 | |||||||
| chr16:10470839 | G | A | 12 | a0001c0002t0003g0301 a0001c0002t0003g0356 a0001c0002t0005g0315 others(9): Show |
12 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1353-1271G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10470839 | |||||||
| chr16:10470847 | A | G | 12 | a0001c0002t0003g0301 a0001c0002t0003g0356 a0001c0002t0005g0315 others(9): Show |
12 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1353-1263A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10470847 | |||||||
| chr16:10470851 | ATATG | A | 95 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(92): Show |
96 | HG00639.hp1 HG00735.hp2 HG01070.hp1 others(93): Show |
intron_variant | MODIFIER | c.1353-1257_1353-125 others(8): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 10470851 | ||||||
| chr16:10470853 | ATG | A | 49 | a0001c0002t0003g0301 a0001c0002t0003g0346 a0001c0002t0003g0347 others(46): Show |
50 | HG00408.hp2 HG00544.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.1353-1238_1353-123 others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr16 | 10470853 | ||||||
| chr16:10470855 | G | A | 8 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0001c0005t0016g0031 others(5): Show |
8 | HG00673.hp1 HG02155.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1353-1255G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10470855 | |||||||
| chr16:10470857 | G | A | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1353-1253G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10470857 | |||||||
| chr16:10470871 | G | A | 9 | a0001c0002t0003g0358 a0001c0002t0003g0359 a0001c0002t0003g0360 others(6): Show |
9 | HG01358.hp1 HG02257.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1353-1239G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10470871 | |||||||
| chr16:10470943 | A | C | 1 | a0001c0002t0003g0284 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1353-1167A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10470943 | |||||||
| chr16:10471014 | G | A | 1 | a0001c0002t0003g0293 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1353-1096G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10471014 | |||||||
| chr16:10471075 | G | A | 1 | a0001c0002t0003g0361 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1353-1035G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10471075 | |||||||
| chr16:10471095 | G | T | 1 | a0002c0001t0002g0028 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1353-1015G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10471095 | |||||||
| chr16:10471101 | C | A | 37 | a0003c0004t0002g0003 a0003c0004t0002g0025 a0003c0004t0002g0065 others(34): Show |
38 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.1353-1009C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10471101 | |||||||
| chr16:10471254 | G | A | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1353-856G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10471254 | |||||||
| chr16:10471354 | C | A | 1 | a0002c0001t0001g0002 | 2 | HG00639.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1353-756C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10471354 | |||||||
| chr16:10471466 | T | C | 1 | a0002c0001t0001g0114 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1353-644T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10471466 | |||||||
| chr16:10471469 | G | A | 8 | a0001c0002t0003g0358 a0001c0002t0003g0359 a0001c0002t0003g0360 others(5): Show |
8 | HG01358.hp1 HG02257.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1353-641G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10471469 | |||||||
| chr16:10471512 | G | C | 183 | a0001c0003t0020g0214 a0001c0016t0015g0323 a0002c0001t0001g0001 others(180): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1353-598G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10471512 | |||||||
| chr16:10471544 | C | T | 1 | a0002c0001t0002g0185 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1353-566C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10471544 | |||||||
| chr16:10471555 | A | G | 1 | a0002c0018t0010g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1353-555A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10471555 | |||||||
| chr16:10471562 | G | T | 1 | a0002c0001t0001g0123 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1353-548G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10471562 | |||||||
| chr16:10471575 | G | C | 1 | a0001c0003t0004g0228 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1353-535G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10471575 | |||||||
| chr16:10471591 | G | A | 143 | a0001c0003t0020g0214 a0001c0016t0015g0323 a0002c0001t0001g0001 others(140): Show |
145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1353-519G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10471591 | |||||||
| chr16:10471748 | T | G | 2 | a0003c0004t0002g0003 a0003c0004t0002g0153 |
3 | HG01891.hp2 HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1353-362T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10471748 | |||||||
| chr16:10471794 | C | T | 1 | a0001c0002t0005g0303 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1353-316C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 9/13 | chr16 | 10471794 | |||||||
| chr16:10472239 | G | C | 1 | a0002c0001t0009g0164 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1426+56G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 10/13 | chr16 | 10472239 | |||||||
| chr16:10472278 | A | G | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1426+95A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 10/13 | chr16 | 10472278 | |||||||
| chr16:10472289 | G | T | 306 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(303): Show |
311 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1426+106G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 10/13 | chr16 | 10472289 | |||||||
| chr16:10472508 | G | T | 1 | a0002c0001t0002g0102 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1426+325G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 10/13 | chr16 | 10472508 | |||||||
| chr16:10472593 | C | T | 2 | a0002c0001t0002g0111 a0002c0001t0002g0185 |
2 | HG00558.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1426+410C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 10/13 | chr16 | 10472593 | |||||||
| chr16:10472638 | C | T | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1426+455C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 10/13 | chr16 | 10472638 | |||||||
| chr16:10472739 | C | A | 1 | a0002c0010t0002g0264 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1426+556C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 10/13 | chr16 | 10472739 | |||||||
| chr16:10472788 | A | G | 55 | a0001c0002t0003g0346 a0001c0002t0003g0347 a0001c0003t0008g0026 others(52): Show |
57 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1426+605A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 10/13 | chr16 | 10472788 | |||||||
| chr16:10472850 | C | G | 1 | a0002c0001t0024g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1427-629C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 10/13 | chr16 | 10472850 | |||||||
| chr16:10472855 | C | CA | 113 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(110): Show |
115 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(112): Show |
intron_variant | MODIFIER | c.1427-605dupA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr16 | 10472855 | ||||||
| chr16:10472855 | C | CAA | 14 | a0001c0002t0003g0301 a0001c0002t0003g0356 a0001c0002t0005g0282 others(11): Show |
15 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1427-606_1427-605d others(4): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr16 | 10472855 | ||||||
| chr16:10472855 | C | CAAA | 29 | a0002c0010t0002g0140 a0003c0004t0002g0065 a0003c0004t0002g0066 others(26): Show |
29 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1427-607_1427-605d others(5): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr16 | 10472855 | ||||||
| chr16:10472855 | CA | C | 7 | a0001c0003t0004g0223 a0001c0003t0004g0255 a0002c0001t0001g0036 others(4): Show |
7 | HG01256.hp1 HG01496.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1427-605delA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr16 | 10472855 | ||||||
| chr16:10472961 | C | G | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1427-518C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 10/13 | chr16 | 10472961 | |||||||
| chr16:10473059 | G | A | 2 | a0001c0002t0003g0346 a0001c0002t0003g0347 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1427-420G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 10/13 | chr16 | 10473059 | |||||||
| chr16:10473064 | G | C | 183 | a0001c0003t0020g0214 a0001c0016t0015g0323 a0002c0001t0001g0001 others(180): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1427-415G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 10/13 | chr16 | 10473064 | |||||||
| chr16:10473169 | A | G | 163 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(160): Show |
166 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(163): Show |
intron_variant | MODIFIER | c.1427-310A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 10/13 | chr16 | 10473169 | |||||||
| chr16:10473311 | A | T | 1 | a0001c0003t0004g0254 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1427-168A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 10/13 | chr16 | 10473311 | |||||||
| chr16:10473753 | A | G | 1 | a0002c0001t0001g0174 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1483-170A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 11/13 | chr16 | 10473753 | |||||||
| chr16:10473844 | T | C | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1483-79T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 11/13 | chr16 | 10473844 | |||||||
| chr16:10473885 | G | A | 1 | a0002c0001t0001g0060 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1483-38G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 11/13 | chr16 | 10473885 | |||||||
| chr16:10473894 | C | CTTTTTT | 52 | a0001c0002t0003g0334 a0001c0002t0005g0317 a0001c0003t0008g0026 others(49): Show |
54 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.1483-19_1483-14dup others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 10473894 | ||||||
| chr16:10473894 | C | CTTTTTTT | 104 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(101): Show |
105 | HG00639.hp1 HG00735.hp2 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.1483-20_1483-14dup others(7): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 10473894 | ||||||
| chr16:10473894 | C | CTTTTTTT others(1): Show |
6 | a0001c0002t0003g0309 a0001c0002t0005g0190 a0001c0002t0005g0276 others(3): Show |
6 | HG02071.hp2 HG02080.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1483-21_1483-14dup others(8): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr16 | 10473894 | ||||||
| chr16:10474030 | G | A | 1 | a0001c0003t0008g0230 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1549+41G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10474030 | |||||||
| chr16:10474050 | G | A | 1 | a0001c0003t0004g0245 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1549+61G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10474050 | |||||||
| chr16:10474066 | T | C | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1549+77T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10474066 | |||||||
| chr16:10474092 | G | A | 1 | a0002c0021t0002g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1549+103G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10474092 | |||||||
| chr16:10474127 | G | A | 103 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(100): Show |
104 | HG00639.hp1 HG00735.hp2 HG01070.hp1 others(101): Show |
intron_variant | MODIFIER | c.1549+138G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10474127 | |||||||
| chr16:10474293 | G | A | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1549+304G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10474293 | |||||||
| chr16:10474339 | A | AGT | 196 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0001c0003t0020g0214 others(193): Show |
200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1549+355_1549+356d others(4): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10474339 | ||||||
| chr16:10474374 | G | C | 107 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(104): Show |
108 | HG00639.hp1 HG00735.hp2 HG01070.hp1 others(105): Show |
intron_variant | MODIFIER | c.1549+385G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10474374 | |||||||
| chr16:10474734 | C | T | 10 | a0003c0004t0002g0003 a0003c0004t0002g0151 a0003c0004t0002g0152 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1549+745C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10474734 | |||||||
| chr16:10474883 | T | C | 50 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(47): Show |
51 | HG00639.hp1 HG01109.hp2 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.1549+894T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10474883 | |||||||
| chr16:10475024 | T | G | 1 | a0001c0005t0016g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1549+1035T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475024 | |||||||
| chr16:10475143 | G | A | 40 | a0002c0010t0002g0140 a0002c0010t0002g0149 a0003c0004t0002g0003 others(37): Show |
41 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.1549+1154G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475143 | |||||||
| chr16:10475144 | T | G | 1 | a0002c0001t0001g0180 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1549+1155T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475144 | |||||||
| chr16:10475182 | A | G | 4 | a0001c0003t0004g0220 a0001c0003t0004g0221 a0001c0003t0004g0224 others(1): Show |
4 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1549+1193A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475182 | |||||||
| chr16:10475185 | T | C | 2 | a0001c0002t0003g0339 a0001c0002t0003g0343 |
2 | NA18969.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1549+1196T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475185 | |||||||
| chr16:10475225 | A | G | 1 | a0001c0003t0004g0220 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1549+1236A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475225 | |||||||
| chr16:10475241 | G | C | 11 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0271 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.1549+1252G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475241 | |||||||
| chr16:10475275 | G | A | 103 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(100): Show |
104 | HG00639.hp1 HG00735.hp2 HG01070.hp1 others(101): Show |
intron_variant | MODIFIER | c.1549+1286G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475275 | |||||||
| chr16:10475402 | T | C | 1 | a0002c0001t0001g0054 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1549+1413T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475402 | |||||||
| chr16:10475415 | G | A | 2 | a0001c0002t0003g0346 a0001c0002t0003g0347 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1549+1426G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475415 | |||||||
| chr16:10475465 | G | T | 1 | a0002c0001t0002g0185 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1549+1476G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475465 | |||||||
| chr16:10475571 | T | C | 1 | a0001c0003t0004g0241 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1549+1582T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475571 | |||||||
| chr16:10475610 | G | A | 51 | a0001c0002t0003g0004 a0001c0002t0003g0283 a0001c0002t0003g0284 others(48): Show |
52 | HG00639.hp1 HG01109.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.1549+1621G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475610 | |||||||
| chr16:10475647 | C | T | 1 | a0001c0007t0011g0353 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1549+1658C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475647 | |||||||
| chr16:10475679 | C | T | 10 | a0003c0004t0002g0003 a0003c0004t0002g0151 a0003c0004t0002g0152 others(7): Show |
11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1549+1690C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475679 | |||||||
| chr16:10475692 | C | CA | 59 | a0001c0002t0005g0276 a0001c0002t0005g0307 a0001c0002t0005g0316 others(56): Show |
61 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.1549+1715dupA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10475692 | ||||||
| chr16:10475722 | G | GA | 68 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(65): Show |
70 | HG00673.hp1 HG00735.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.1549+1755dupA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10475722 | ||||||
| chr16:10475722 | G | GAA | 37 | a0001c0002t0003g0272 a0001c0002t0003g0283 a0001c0002t0003g0293 others(34): Show |
37 | HG00639.hp1 HG01109.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.1549+1754_1549+175 others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10475722 | ||||||
| chr16:10475722 | G | GAAA | 8 | a0001c0002t0005g0190 a0001c0002t0005g0275 a0001c0002t0005g0277 others(5): Show |
8 | HG01168.hp1 HG01169.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.1549+1753_1549+175 others(7): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10475722 | ||||||
| chr16:10475722 | G | GAAAAAAA others(5): Show |
1 | a0002c0018t0010g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1549+1744_1549+175 others(16): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10475722 | ||||||
| chr16:10475722 | G | GAAAAAAA others(6): Show |
1 | a0002c0008t0010g0195 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1549+1743_1549+175 others(17): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10475722 | ||||||
| chr16:10475722 | G | GAAAAAAA others(9): Show |
1 | a0002c0008t0010g0194 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1549+1740_1549+175 others(20): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10475722 | ||||||
| chr16:10475722 | G | GAAAAAAA others(10): Show |
2 | a0002c0008t0010g0193 a0002c0008t0010g0196 |
2 | HG01109.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1549+1739_1549+175 others(21): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10475722 | ||||||
| chr16:10475722 | GA | G | 143 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(140): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1549+1755delA | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10475722 | ||||||
| chr16:10475724 | A | G | 7 | a0002c0001t0001g0173 a0002c0001t0001g0174 a0002c0001t0001g0175 others(4): Show |
7 | HG01069.hp2 HG01123.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.1549+1735A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475724 | |||||||
| chr16:10475758 | A | T | 30 | a0002c0010t0002g0140 a0002c0010t0002g0149 a0003c0004t0002g0025 others(27): Show |
30 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.1549+1769A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475758 | |||||||
| chr16:10475761 | A | C | 53 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0001c0005t0006g0005 others(50): Show |
55 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1549+1772A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475761 | |||||||
| chr16:10475769 | T | C | 40 | a0002c0010t0002g0140 a0002c0010t0002g0149 a0003c0004t0002g0003 others(37): Show |
41 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.1549+1780T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475769 | |||||||
| chr16:10475810 | A | G | 1 | a0002c0001t0002g0143 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1549+1821A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475810 | |||||||
| chr16:10475895 | A | C | 1 | a0001c0002t0003g0296 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1549+1906A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10475895 | |||||||
| chr16:10476093 | T | C | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1549+2104T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10476093 | |||||||
| chr16:10476113 | G | A | 302 | a0001c0002t0003g0004 a0001c0002t0003g0269 a0001c0002t0003g0270 others(299): Show |
307 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1549+2124G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10476113 | |||||||
| chr16:10476210 | C | A | 1 | a0001c0002t0005g0315 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1549+2221C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10476210 | |||||||
| chr16:10476243 | A | G | 13 | a0002c0001t0001g0120 a0002c0001t0001g0162 a0002c0001t0001g0163 others(10): Show |
13 | HG01496.hp1 HG02055.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1549+2254A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10476243 | |||||||
| chr16:10476311 | A | G | 18 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0271 others(15): Show |
18 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1549+2322A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10476311 | |||||||
| chr16:10476431 | C | T | 1 | a0001c0003t0004g0211 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1549+2442C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10476431 | |||||||
| chr16:10476484 | T | TTG | 51 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(48): Show |
53 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.1549+2509_1549+251 others(6): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10476484 | ||||||
| chr16:10476500 | T | G | 77 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0291 others(74): Show |
79 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.1549+2511T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10476500 | |||||||
| chr16:10476502 | T | G | 1 | a0003c0004t0002g0072 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1549+2513T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10476502 | |||||||
| chr16:10476612 | T | G | 1 | a0002c0001t0024g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1549+2623T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10476612 | |||||||
| chr16:10476654 | A | AC | 6 | a0001c0005t0006g0029 a0001c0005t0006g0030 a0001c0005t0006g0367 others(3): Show |
6 | HG02965.hp1 HG03209.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.1549+2670dupC | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10476654 | ||||||
| chr16:10476659 | C | A | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1549+2670C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10476659 | |||||||
| chr16:10476875 | T | G | 1 | a0001c0002t0005g0315 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1549+2886T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10476875 | |||||||
| chr16:10477012 | T | C | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1549+3023T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477012 | |||||||
| chr16:10477083 | G | A | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1549+3094G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477083 | |||||||
| chr16:10477084 | C | A | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1549+3095C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477084 | |||||||
| chr16:10477092 | T | G | 58 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0001c0005t0006g0005 others(55): Show |
60 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.1549+3103T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477092 | |||||||
| chr16:10477131 | A | G | 1 | a0001c0002t0003g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1549+3142A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477131 | |||||||
| chr16:10477163 | G | C | 1 | a0002c0001t0001g0168 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1549+3174G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477163 | |||||||
| chr16:10477176 | T | A | 6 | a0001c0002t0003g0313 a0001c0002t0003g0326 a0001c0002t0003g0327 others(3): Show |
6 | HG01433.hp2 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1549+3187T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477176 | |||||||
| chr16:10477193 | A | T | 58 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0001c0005t0006g0005 others(55): Show |
60 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.1549+3204A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477193 | |||||||
| chr16:10477312 | C | G | 48 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(45): Show |
50 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1549+3323C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477312 | |||||||
| chr16:10477531 | G | A | 1 | a0002c0001t0001g0177 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1550-3348G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477531 | |||||||
| chr16:10477612 | C | T | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1550-3267C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477612 | |||||||
| chr16:10477613 | G | A | 17 | a0001c0005t0003g0032 a0001c0005t0016g0031 a0001c0005t0018g0263 others(14): Show |
17 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.1550-3266G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477613 | |||||||
| chr16:10477629 | G | A | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1550-3250G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477629 | |||||||
| chr16:10477724 | C | T | 2 | a0002c0001t0001g0128 a0002c0001t0001g0130 |
2 | HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1550-3155C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477724 | |||||||
| chr16:10477900 | G | A | 142 | a0001c0002t0005g0285 a0001c0016t0015g0323 a0002c0001t0001g0001 others(139): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1550-2979G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477900 | |||||||
| chr16:10477903 | A | G | 3 | a0002c0001t0001g0103 a0002c0001t0001g0130 a0002c0001t0001g0142 |
3 | HG02572.hp2 HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1550-2976A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477903 | |||||||
| chr16:10477920 | A | C | 1 | a0001c0002t0005g0285 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1550-2959A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477920 | |||||||
| chr16:10477950 | T | C | 144 | a0001c0016t0015g0323 a0002c0001t0001g0001 a0002c0001t0001g0002 others(141): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1550-2929T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477950 | |||||||
| chr16:10477992 | T | G | 6 | a0001c0005t0016g0031 a0002c0008t0010g0193 a0002c0008t0010g0194 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1550-2887T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477992 | |||||||
| chr16:10477998 | A | G | 1 | a0005c0017t0005g0302 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1550-2881A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10477998 | |||||||
| chr16:10478043 | A | G | 1 | a0002c0001t0001g0114 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1550-2836A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10478043 | |||||||
| chr16:10478099 | A | G | 1 | a0002c0001t0001g0087 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1550-2780A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10478099 | |||||||
| chr16:10478170 | A | C | 1 | a0002c0001t0001g0084 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1550-2709A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10478170 | |||||||
| chr16:10478186 | G | A | 4 | a0002c0001t0002g0090 a0002c0001t0002g0091 a0002c0001t0002g0137 others(1): Show |
4 | HG02523.hp2 NA18612.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1550-2693G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10478186 | |||||||
| chr16:10478190 | C | T | 2 | a0001c0003t0004g0220 a0002c0001t0001g0173 |
2 | HG01943.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1550-2689C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10478190 | |||||||
| chr16:10478191 | G | A | 4 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(1): Show |
4 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1550-2688G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10478191 | |||||||
| chr16:10478342 | T | G | 2 | a0001c0002t0003g0272 a0001c0002t0003g0312 |
2 | HG01891.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1550-2537T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10478342 | |||||||
| chr16:10478345 | C | T | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1550-2534C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10478345 | |||||||
| chr16:10478510 | G | A | 1 | a0002c0001t0001g0019 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1550-2369G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10478510 | |||||||
| chr16:10478529 | T | A | 1 | a0004c0006t0004g0203 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1550-2350T>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10478529 | |||||||
| chr16:10478762 | A | G | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1550-2117A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10478762 | |||||||
| chr16:10478780 | T | G | 28 | a0002c0010t0002g0140 a0002c0010t0002g0149 a0003c0004t0002g0065 others(25): Show |
28 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.1550-2099T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10478780 | |||||||
| chr16:10478837 | G | A | 2 | a0001c0003t0008g0210 a0001c0005t0016g0031 |
2 | NA18522.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1550-2042G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10478837 | |||||||
| chr16:10479024 | G | C | 51 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0001c0005t0006g0005 others(48): Show |
53 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.1550-1855G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479024 | |||||||
| chr16:10479054 | G | A | 2 | a0003c0004t0002g0003 a0003c0004t0002g0153 |
3 | HG01891.hp2 HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1550-1825G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479054 | |||||||
| chr16:10479080 | G | A | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1550-1799G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479080 | |||||||
| chr16:10479094 | A | G | 1 | a0001c0003t0020g0214 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1550-1785A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479094 | |||||||
| chr16:10479164 | G | C | 2 | a0001c0003t0008g0026 a0001c0003t0008g0027 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1550-1715G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479164 | |||||||
| chr16:10479253 | A | G | 58 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0001c0005t0006g0005 others(55): Show |
60 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.1550-1626A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479253 | |||||||
| chr16:10479345 | G | T | 1 | a0002c0001t0001g0134 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1550-1534G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479345 | |||||||
| chr16:10479422 | A | G | 2 | a0001c0005t0018g0263 a0002c0001t0001g0142 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1550-1457A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479422 | |||||||
| chr16:10479425 | C | T | 1 | a0001c0003t0004g0206 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1550-1454C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479425 | |||||||
| chr16:10479436 | G | A | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1550-1443G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479436 | |||||||
| chr16:10479487 | A | T | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1550-1392A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479487 | |||||||
| chr16:10479494 | C | A | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1550-1385C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479494 | |||||||
| chr16:10479502 | A | G | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1550-1377A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479502 | |||||||
| chr16:10479507 | A | G | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1550-1372A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479507 | |||||||
| chr16:10479515 | T | G | 1 | a0001c0005t0018g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1550-1364T>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479515 | |||||||
| chr16:10479653 | A | G | 1 | a0001c0002t0003g0362 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1550-1226A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479653 | |||||||
| chr16:10479661 | A | C | 12 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0001c0005t0006g0005 others(9): Show |
13 | HG02145.hp2 HG02258.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.1550-1218A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479661 | |||||||
| chr16:10479707 | G | C | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1550-1172G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479707 | |||||||
| chr16:10479768 | C | G | 1 | a0002c0018t0010g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1550-1111C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479768 | |||||||
| chr16:10479788 | A | C | 3 | a0001c0002t0003g0301 a0001c0002t0003g0356 a0001c0002t0013g0299 |
3 | HG01167.hp1 HG01169.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1550-1091A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479788 | |||||||
| chr16:10479872 | G | A | 1 | a0002c0021t0002g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1550-1007G>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479872 | |||||||
| chr16:10479872 | G | C | 2 | a0001c0002t0003g0293 a0001c0002t0003g0340 |
2 | NA19006.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1550-1007G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10479872 | |||||||
| chr16:10479958 | C | CT | 11 | a0001c0002t0003g0334 a0001c0003t0004g0200 a0001c0003t0004g0204 others(8): Show |
11 | HG01175.hp1 HG01257.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.1550-878dupT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10479958 | ||||||
| chr16:10479958 | C | CTT | 9 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0335 others(6): Show |
9 | HG01099.hp1 HG01256.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.1550-879_1550-878d others(4): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10479958 | ||||||
| chr16:10479958 | C | CTTT | 11 | a0001c0002t0003g0291 a0001c0002t0003g0292 a0001c0002t0003g0295 others(8): Show |
11 | HG01928.hp1 HG01934.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1550-880_1550-878d others(5): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10479958 | ||||||
| chr16:10479958 | CT | C | 25 | a0001c0002t0003g0284 a0001c0002t0003g0306 a0001c0002t0003g0329 others(22): Show |
25 | HG00323.hp1 HG00408.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.1550-878delT | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10479958 | ||||||
| chr16:10479958 | CTT | C | 12 | a0001c0002t0003g0274 a0001c0002t0003g0311 a0001c0002t0003g0326 others(9): Show |
12 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1550-879_1550-878d others(4): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10479958 | ||||||
| chr16:10479958 | CTTT | C | 11 | a0001c0002t0003g0271 a0001c0002t0003g0273 a0001c0002t0003g0309 others(8): Show |
11 | HG00735.hp2 HG01071.hp2 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.1550-880_1550-878d others(5): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10479958 | ||||||
| chr16:10479958 | CTTTTT | C | 22 | a0001c0002t0003g0269 a0001c0002t0003g0270 a0001c0002t0003g0272 others(19): Show |
22 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1550-882_1550-878d others(7): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10479958 | ||||||
| chr16:10479958 | CTTTTTT | C | 17 | a0001c0002t0003g0358 a0001c0002t0003g0359 a0001c0002t0003g0360 others(14): Show |
17 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1550-883_1550-878d others(8): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10479958 | ||||||
| chr16:10479958 | CTTTTTTT others(5): Show |
C | 3 | a0001c0002t0003g0313 a0002c0008t0010g0195 a0002c0018t0010g0197 |
3 | HG01433.hp2 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1550-889_1550-878d others(14): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10479958 | ||||||
| chr16:10479958 | CTTTTTTT others(6): Show |
C | 5 | a0001c0002t0003g0283 a0001c0002t0003g0328 a0002c0008t0010g0193 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1550-890_1550-878d others(15): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10479958 | ||||||
| chr16:10479958 | CTTTTTTT others(11): Show |
C | 3 | a0001c0002t0003g0346 a0001c0003t0004g0228 a0001c0005t0003g0032 |
3 | HG02451.hp2 HG03017.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1550-895_1550-878d others(20): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10479958 | ||||||
| chr16:10479958 | CTTTTTTT others(12): Show |
C | 1 | a0001c0003t0022g0237 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1550-896_1550-878d others(21): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10479958 | ||||||
| chr16:10479958 | CTTTTTTT others(14): Show |
C | 3 | a0002c0001t0001g0008 a0002c0001t0001g0036 a0002c0001t0002g0137 |
3 | HG02523.hp2 NA18991.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1550-898_1550-878d others(23): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10479958 | ||||||
| chr16:10479958 | CTTTTTTT others(15): Show |
C | 136 | a0001c0003t0020g0214 a0001c0007t0011g0352 a0001c0007t0011g0353 others(133): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1550-899_1550-878d others(24): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10479958 | ||||||
| chr16:10479958 | CTTTTTTT others(16): Show |
C | 54 | a0001c0005t0006g0005 a0001c0005t0006g0030 a0001c0005t0006g0367 others(51): Show |
56 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1550-900_1550-878d others(25): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10479958 | ||||||
| chr16:10479958 | CTTTTTTT others(17): Show |
C | 7 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0001c0005t0006g0029 others(4): Show |
7 | HG02258.hp2 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1550-901_1550-878d others(26): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr16 | 10479958 | ||||||
| chr16:10480136 | C | T | 38 | a0003c0004t0002g0003 a0003c0004t0002g0025 a0003c0004t0002g0065 others(35): Show |
39 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1550-743C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10480136 | |||||||
| chr16:10480175 | C | T | 147 | a0001c0003t0020g0214 a0001c0007t0011g0352 a0001c0007t0011g0353 others(144): Show |
149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1550-704C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10480175 | |||||||
| chr16:10480178 | C | G | 204 | a0001c0003t0008g0026 a0001c0003t0008g0027 a0001c0003t0020g0214 others(201): Show |
208 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1550-701C>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10480178 | |||||||
| chr16:10480216 | A | C | 8 | a0001c0005t0006g0005 a0001c0005t0006g0029 a0001c0005t0006g0030 others(5): Show |
9 | HG02145.hp2 HG02965.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1550-663A>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10480216 | |||||||
| chr16:10480232 | G | C | 145 | a0001c0003t0020g0214 a0001c0016t0015g0323 a0002c0001t0001g0001 others(142): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1550-647G>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10480232 | |||||||
| chr16:10480272 | C | T | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1550-607C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10480272 | |||||||
| chr16:10480276 | C | T | 4 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(1): Show |
4 | HG02559.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1550-603C>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10480276 | |||||||
| chr16:10480355 | C | A | 145 | a0001c0003t0020g0214 a0001c0016t0015g0323 a0002c0001t0001g0001 others(142): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1550-524C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10480355 | |||||||
| chr16:10480395 | C | A | 1 | a0002c0001t0001g0038 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1550-484C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10480395 | |||||||
| chr16:10480687 | G | T | 1 | a0003c0004t0002g0071 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1550-192G>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 12/13 | chr16 | 10480687 | |||||||
| chr16:10480972 | A | T | 148 | a0001c0007t0011g0352 a0001c0007t0011g0353 a0001c0007t0011g0354 others(145): Show |
150 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(147): Show |
splice_region_variant&intron_variant | LOW | c.1635+8A>T | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 13/13 | chr16 | 10480972 | |||||||
| chr16:10481182 | A | G | 5 | a0002c0008t0010g0193 a0002c0008t0010g0194 a0002c0008t0010g0195 others(2): Show |
5 | HG01109.hp1 HG02055.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1635+218A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 13/13 | chr16 | 10481182 | |||||||
| chr16:10481254 | C | A | 24 | a0001c0002t0003g0289 a0001c0002t0003g0290 a0001c0002t0003g0291 others(21): Show |
24 | HG01099.hp1 HG01256.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.1635+290C>A | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 13/13 | chr16 | 10481254 | |||||||
| chr16:10481351 | CTCCCGAG others(11): Show |
C | 8 | a0001c0002t0005g0304 a0001c0003t0008g0027 a0001c0005t0006g0029 others(5): Show |
8 | HG02818.hp2 HG02965.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1636-430_1636-413d others(20): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 10481351 | ||||||
| chr16:10481351 | CTCCCGAG others(29): Show |
C | 154 | a0001c0003t0020g0214 a0001c0007t0011g0352 a0001c0007t0011g0353 others(151): Show |
156 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.1635+424_1636-413d others(38): Show |
ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr16 | 10481351 | ||||||
| chr16:10481519 | A | G | 6 | a0003c0004t0002g0105 a0003c0004t0002g0109 a0003c0004t0002g0117 others(3): Show |
6 | NA18939.hp1 NA18985.hp2 NA18997.hp2 others(3): Show |
intron_variant | MODIFIER | c.1636-317A>G | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 13/13 | chr16 | 10481519 | |||||||
| chr16:10481605 | T | C | 1 | a0002c0021t0002g0184 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1636-231T>C | ATF7IP2 | ENSG00000166669.14 | transcript | ENST00000562102.6 | protein_coding | 13/13 | chr16 | 10481605 |