Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64761 |
| ensemblid | ENSG00000059378.13 |
| hgncid | 21919 |
| symbol | PARP12 |
| name | poly(ADP-ribose) polymerase family member 12 |
| refseq_nuc | NM_022750.4 |
| refseq_prot | NP_073587.1 |
| ensembl_nuc | ENST00000263549.8 |
| ensembl_prot | ENSP00000263549.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 140023749 |
| end | 140062951 |
| strand | - |
| ver | v1.2 |
| region | chr7:140023749-140062951 |
| region5000 | chr7:140018749-140067951 |
| regionname0 | PARP12_chr7_140023749_140062951 |
| regionname5000 | PARP12_chr7_140018749_140067951 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 701 | 312 | 63 | 62 | 137 | 12 | 36 | 103 | PARP12_chr7_140018749_140067951 | PARP12 | MAQAG others(696): Show |
chr7 | 140018749 | 140067951 |
| a0002 | 0/0 | 701 | 19 | 5 | 5 | 0 | 1 | 8 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | MAQAG others(696): Show |
chr7 | 140018749 | 140067951 |
| a0003 | 0/0 | 701 | 19 | 18 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | MAQAG others(696): Show |
chr7 | 140018749 | 140067951 |
| a0004 | 0/0 | 701 | 3 | 1 | 1 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | MAQAG others(696): Show |
chr7 | 140018749 | 140067951 |
| a0005 | 0/0 | 701 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | MAQAG others(696): Show |
chr7 | 140018749 | 140067951 |
| a0006 | 0/0 | 701 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | MAQAG others(696): Show |
chr7 | 140018749 | 140067951 |
| a0007 | 0/0 | 701 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | MAQAG others(696): Show |
chr7 | 140018749 | 140067951 |
| a0008 | 0/0 | 701 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | MAQAG others(696): Show |
chr7 | 140018749 | 140067951 |
| a0009 | 0/0 | 701 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | MAQAG others(696): Show |
chr7 | 140018749 | 140067951 |
| a0010 | 0/0 | 701 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | MAQAG others(696): Show |
chr7 | 140018749 | 140067951 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2103 | 144 | 15 | 28 | 62 | 9 | 29 | PARP12_chr7_140018749_140067951 | PARP12 | ATGGC others(2098): Show |
chr7 | 140018749 | 140067951 | ||
| a0001c0002 | 0/0 | 2103 | 127 | 29 | 24 | 67 | 3 | 4 | PARP12_chr7_140018749_140067951 | PARP12 | ATGGC others(2098): Show |
chr7 | 140018749 | 140067951 | ||
| a0001c0003 | 0/0 | 2103 | 22 | 19 | 2 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | ATGGC others(2098): Show |
chr7 | 140018749 | 140067951 | ||
| a0001c0006 | 0/0 | 2103 | 8 | 0 | 0 | 8 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | ATGGC others(2098): Show |
chr7 | 140018749 | 140067951 | ||
| a0001c0008 | 0/1 | 2103 | 5 | 0 | 3 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | ATGGC others(2098): Show |
chr7 | 140018749 | 140067951 | ||
| a0001c0009 | 0/0 | 2103 | 4 | 0 | 4 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | ATGGC others(2098): Show |
chr7 | 140018749 | 140067951 | ||
| a0001c0013 | 0/0 | 2103 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | ATGGC others(2098): Show |
chr7 | 140018749 | 140067951 | ||
| a0001c0014 | 0/0 | 2103 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | ATGGC others(2098): Show |
chr7 | 140018749 | 140067951 | ||
| a0002c0004 | 0/0 | 2103 | 19 | 5 | 5 | 0 | 1 | 8 | PARP12_chr7_140018749_140067951 | PARP12 | ATGGC others(2098): Show |
chr7 | 140018749 | 140067951 | ||
| a0003c0005 | 0/0 | 2103 | 12 | 11 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | ATGGC others(2098): Show |
chr7 | 140018749 | 140067951 | ||
| a0003c0007 | 0/0 | 2103 | 7 | 7 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | ATGGC others(2098): Show |
chr7 | 140018749 | 140067951 | ||
| a0004c0010 | 0/0 | 2103 | 3 | 1 | 1 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | ATGGC others(2098): Show |
chr7 | 140018749 | 140067951 | ||
| a0005c0011 | 0/0 | 2103 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | ATGGC others(2098): Show |
chr7 | 140018749 | 140067951 | ||
| a0006c0018 | 0/0 | 2103 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | ATGGC others(2098): Show |
chr7 | 140018749 | 140067951 | ||
| a0007c0015 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | ATGGC others(2098): Show |
chr7 | 140018749 | 140067951 | ||
| a0008c0016 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | ATGGC others(2098): Show |
chr7 | 140018749 | 140067951 | ||
| a0009c0017 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | ATGGC others(2098): Show |
chr7 | 140018749 | 140067951 | ||
| a0010c0012 | 0/0 | 2103 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | ATGGC others(2098): Show |
chr7 | 140018749 | 140067951 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 1/0 | 3021 | 131 | 13 | 24 | 59 | 6 | 28 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0001c0001t0003 | 0/0 | 3021 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0001c0001t0005 | 0/0 | 3021 | 6 | 0 | 4 | 0 | 1 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0001c0001t0006 | 0/0 | 3005 | 2 | 0 | 0 | 0 | 2 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3000): Show |
chr7 | 140018749 | 140067951 |
| a0001c0001t0007 | 0/0 | 3004 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(2999): Show |
chr7 | 140018749 | 140067951 |
| a0001c0001t0010 | 0/0 | 2994 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(2989): Show |
chr7 | 140018749 | 140067951 |
| a0001c0001t0011 | 0/0 | 3021 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0001c0002t0001 | 0/0 | 3021 | 126 | 29 | 23 | 67 | 3 | 4 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0001c0002t0012 | 0/0 | 3021 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0001c0003t0001 | 0/0 | 3021 | 4 | 4 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0001c0003t0003 | 0/0 | 3021 | 17 | 14 | 2 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0001c0003t0008 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0001c0006t0001 | 0/0 | 3021 | 8 | 0 | 0 | 8 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0001c0008t0002 | 0/1 | 3021 | 5 | 0 | 3 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0001c0009t0001 | 0/0 | 3021 | 4 | 0 | 4 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0001c0013t0002 | 0/0 | 3021 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0001c0014t0001 | 0/0 | 3021 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0002c0004t0003 | 0/0 | 3021 | 19 | 5 | 5 | 0 | 1 | 8 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0003c0005t0003 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0003c0005t0004 | 0/0 | 3021 | 11 | 10 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0003c0007t0003 | 0/0 | 3021 | 3 | 3 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0003c0007t0004 | 0/0 | 3021 | 3 | 3 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0003c0007t0013 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0004c0010t0002 | 0/0 | 3021 | 3 | 1 | 1 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0005c0011t0003 | 0/0 | 3021 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0006c0018t0002 | 0/0 | 3021 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0007c0015t0009 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0008c0016t0003 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0009c0017t0003 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| a0010c0012t0002 | 0/0 | 3021 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | GTTTC others(3016): Show |
chr7 | 140018749 | 140067951 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0003 | 0/0 | 5 | 0 | 0 | 1 | 0 | 4 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0006 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0192 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0006g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0007g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0010g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0001t0011g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0008 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0040 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0002t0012g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0003t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0003t0003g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0003t0003g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0003t0003g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0003t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0003t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0003t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0003t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0003t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0003t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0003t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0003t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0003t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0003t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0003t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0003t0008g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0006t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0006t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0006t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0008t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0008t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0008t0002g0080 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0008t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0008t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0009t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0009t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0009t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0009t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0013t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0001c0014t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0002c0004t0003g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0002c0004t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0002c0004t0003g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0002c0004t0003g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0002c0004t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0002c0004t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0002c0004t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0002c0004t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0002c0004t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0002c0004t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0002c0004t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0002c0004t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0002c0004t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0002c0004t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0002c0004t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0003c0005t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0003c0005t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0003c0005t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0003c0005t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0003c0005t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0003c0005t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0003c0005t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0003c0005t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0003c0005t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0003c0005t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0003c0005t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0003c0007t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0003c0007t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0003c0007t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0003c0007t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0003c0007t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0003c0007t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0003c0007t0013g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0004c0010t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0004c0010t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0004c0010t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0005c0011t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0005c0011t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0006c0018t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0007c0015t0009g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0008c0016t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0009c0017t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| a0010c0012t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0230 | EUR | GBR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0110 | EUR | GBR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0116 | EUR | GBR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00140 | hp2 | a0004 | c0010 | t0002 | g0170 | EUR | GBR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0122 | EUR | FIN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0054 | EUR | FIN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0267 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00639 | hp2 | a0002 | c0004 | t0003 | g0070 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | CHS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0222 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00735 | hp2 | a0002 | c0004 | t0003 | g0065 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00738 | hp2 | a0002 | c0004 | t0003 | g0019 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01069 | hp1 | a0002 | c0004 | t0003 | g0021 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0227 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01070 | hp1 | a0006 | c0018 | t0002 | g0272 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01071 | hp2 | a0002 | c0004 | t0003 | g0021 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01074 | hp1 | a0004 | c0010 | t0002 | g0121 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0237 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01106 | hp1 | a0001 | c0009 | t0001 | g0262 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01109 | hp1 | a0001 | c0014 | t0001 | g0243 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0252 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01175 | hp1 | a0001 | c0003 | t0003 | g0027 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01192 | hp2 | a0001 | c0008 | t0002 | g0049 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01243 | hp2 | a0001 | c0008 | t0002 | g0111 | AMR | PUR | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0169 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01261 | hp2 | a0003 | c0005 | t0004 | g0281 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01358 | hp1 | a0001 | c0008 | t0002 | g0084 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0166 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01433 | hp1 | a0001 | c0009 | t0001 | g0268 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01433 | hp2 | a0001 | c0009 | t0001 | g0259 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01496 | hp1 | a0001 | c0009 | t0001 | g0266 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0168 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0167 | EUR | IBS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0043 | EUR | IBS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0127 | EUR | IBS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0038 | EUR | IBS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01517 | hp1 | a0001 | c0001 | t0006 | g0043 | EUR | IBS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0038 | EUR | IBS | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01884 | hp1 | a0001 | c0003 | t0003 | g0189 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0226 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01952 | hp1 | a0001 | c0003 | t0003 | g0030 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02055 | hp1 | a0004 | c0010 | t0002 | g0061 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02055 | hp2 | a0005 | c0011 | t0003 | g0184 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02080 | hp1 | a0001 | c0006 | t0001 | g0002 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02083 | hp1 | a0001 | c0006 | t0001 | g0002 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02129 | hp1 | a0001 | c0006 | t0001 | g0002 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02145 | hp2 | a0003 | c0005 | t0004 | g0277 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0034 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | CDX | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | CDX | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | CDX | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | CDX | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02257 | hp2 | a0001 | c0003 | t0003 | g0030 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02258 | hp1 | a0001 | c0003 | t0003 | g0133 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0251 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0240 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0198 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0153 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PEL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0254 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02523 | hp2 | a0001 | c0006 | t0001 | g0002 | EAS | KHV | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0163 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02615 | hp1 | a0002 | c0004 | t0003 | g0020 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02615 | hp2 | a0003 | c0007 | t0003 | g0177 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02622 | hp2 | a0001 | c0003 | t0003 | g0191 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0154 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02647 | hp1 | a0001 | c0003 | t0003 | g0135 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0245 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02698 | hp1 | a0002 | c0004 | t0003 | g0071 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02717 | hp1 | a0001 | c0003 | t0003 | g0134 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0028 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02738 | hp2 | a0002 | c0004 | t0003 | g0068 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02809 | hp1 | a0003 | c0005 | t0004 | g0274 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02809 | hp2 | a0003 | c0007 | t0003 | g0183 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02818 | hp1 | a0002 | c0004 | t0003 | g0020 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02818 | hp2 | a0001 | c0003 | t0003 | g0073 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0186 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02886 | hp2 | a0003 | c0005 | t0004 | g0279 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0236 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02896 | hp1 | a0001 | c0003 | t0003 | g0031 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02897 | hp1 | a0001 | c0003 | t0003 | g0031 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02965 | hp1 | a0002 | c0004 | t0003 | g0066 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02965 | hp2 | a0003 | c0005 | t0004 | g0273 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02970 | hp1 | a0003 | c0005 | t0004 | g0280 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0255 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02976 | hp1 | a0003 | c0005 | t0003 | g0156 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02976 | hp2 | a0008 | c0016 | t0003 | g0160 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0250 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03041 | hp2 | a0003 | c0005 | t0004 | g0044 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03098 | hp2 | a0009 | c0017 | t0003 | g0271 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03130 | hp1 | a0003 | c0007 | t0004 | g0284 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03139 | hp1 | a0001 | c0003 | t0003 | g0190 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03139 | hp2 | a0003 | c0005 | t0004 | g0278 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0244 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0253 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03209 | hp1 | a0003 | c0007 | t0004 | g0285 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03225 | hp1 | a0001 | c0003 | t0008 | g0137 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0028 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0155 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03486 | hp1 | a0003 | c0005 | t0004 | g0276 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03490 | hp1 | a0001 | c0008 | t0002 | g0079 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03516 | hp1 | a0003 | c0007 | t0004 | g0282 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0256 | AFR | ESN | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0235 | AFR | GWD | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03579 | hp1 | a0001 | c0003 | t0003 | g0074 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03654 | hp2 | a0001 | c0013 | t0002 | g0051 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0164 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03688 | hp1 | a0002 | c0004 | t0003 | g0069 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03710 | hp2 | a0001 | c0003 | t0003 | g0027 | SAS | PJL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | BEB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0095 | SAS | BEB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03927 | hp2 | a0002 | c0004 | t0003 | g0067 | SAS | BEB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0239 | SAS | BEB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0173 | SAS | BEB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG04115 | hp1 | a0002 | c0004 | t0003 | g0022 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG04184 | hp1 | a0002 | c0004 | t0003 | g0072 | SAS | BEB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0180 | SAS | BEB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG04199 | hp2 | a0002 | c0004 | t0003 | g0132 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG04204 | hp2 | a0002 | c0004 | t0003 | g0022 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | STU | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18522 | hp1 | a0002 | c0004 | t0003 | g0063 | AFR | YRI | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18522 | hp2 | a0003 | c0005 | t0004 | g0044 | AFR | YRI | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | CHB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18906 | hp1 | a0001 | c0003 | t0003 | g0141 | AFR | YRI | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18906 | hp2 | a0003 | c0005 | t0004 | g0275 | AFR | YRI | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18952 | hp1 | a0001 | c0006 | t0001 | g0195 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18961 | hp2 | a0001 | c0006 | t0001 | g0002 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18969 | hp2 | a0001 | c0006 | t0001 | g0002 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19001 | hp2 | a0001 | c0001 | t0010 | g0100 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19006 | hp2 | a0001 | c0006 | t0001 | g0221 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19043 | hp1 | a0003 | c0007 | t0003 | g0176 | AFR | LWK | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | LWK | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19062 | hp2 | a0001 | c0001 | t0007 | g0089 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19080 | hp2 | a0001 | c0001 | t0011 | g0157 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19085 | hp2 | a0010 | c0012 | t0002 | g0078 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | YRI | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA19240 | hp2 | a0002 | c0004 | t0003 | g0064 | AFR | YRI | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0246 | AFR | ASW | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA20129 | hp2 | a0005 | c0011 | t0003 | g0187 | AFR | ASW | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA20805 | hp1 | a0002 | c0004 | t0003 | g0019 | EUR | TSI | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0056 | EUR | TSI | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | GIH | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | GIH | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01123 | hp1 | a0001 | c0002 | t0012 | g0247 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0165 | AMR | CLM | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02486 | hp1 | a0003 | c0007 | t0013 | g0283 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02486 | hp2 | a0007 | c0015 | t0009 | g0188 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG02559 | hp2 | a0001 | c0003 | t0003 | g0136 | AFR | ACB | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0249 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0248 | AFR | MSL | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA20300 | hp1 | a0001 | c0003 | t0003 | g0179 | AFR | USA | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | USA | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| homoSapiens | chm13v2 | a0001 | c0008 | t0002 | g0080 | REF | REF | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0192 | REF | REF | PARP12_chr7_140018749_140067951 | PARP12 | chr7 | 140018749 | 140067951 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:140024807 | G | A | 1 | a0005 | 2 | HG02055.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.1859C>T | p.Ala620Val | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 1963/3021 | 1859/2106 | 620/701 | chr7 | 140024807 | |||
| chr7:140034269 | C | T | 1 | a0002 | 19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
missense_variant | MODERATE | c.1387G>A | p.Val463Met | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/12 | 1491/3021 | 1387/2106 | 463/701 | chr7 | 140034269 | |||
| chr7:140046993 | C | T | 4 | a0003 a0005 a0008 others(1): Show |
23 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(20): Show |
missense_variant | MODERATE | c.877G>A | p.Val293Ile | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/12 | 981/3021 | 877/2106 | 293/701 | chr7 | 140046993 | |||
| chr7:140056988 | A | C | 1 | a0010 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.628T>G | p.Leu210Val | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/12 | 732/3021 | 628/2106 | 210/701 | chr7 | 140056988 | |||
| chr7:140057912 | C | A | 1 | a0004 | 3 | HG00140.hp2 HG01074.hp1 HG02055.hp1 |
missense_variant | MODERATE | c.449G>T | p.Trp150Leu | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 2/12 | 553/3021 | 449/2106 | 150/701 | chr7 | 140057912 | |||
| chr7:140057951 | T | C | 1 | a0007 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.410A>G | p.Tyr137Cys | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 2/12 | 514/3021 | 410/2106 | 137/701 | chr7 | 140057951 | |||
| chr7:140058002 | G | A | 1 | a0008 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.359C>T | p.Thr120Ile | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 2/12 | 463/3021 | 359/2106 | 120/701 | chr7 | 140058002 | |||
| chr7:140062642 | G | A | 1 | a0009 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.206C>T | p.Ala69Val | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/12 | 310/3021 | 206/2106 | 69/701 | chr7 | 140062642 | |||
| chr7:140062778 | G | C | 1 | a0006 | 1 | HG01070.hp1 | missense_variant | MODERATE | c.70C>G | p.Pro24Ala | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/12 | 174/3021 | 70/2106 | 24/701 | chr7 | 140062778 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:140024710 | C | T | 1 | a0001c0014 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.1956G>A | p.Val652Val | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 2060/3021 | 1956/2106 | 652/701 | chr7 | 140024710 | |||
| chr7:140024755 | C | G | 4 | a0003c0005 a0005c0011 a0008c0016 others(1): Show |
16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
synonymous_variant | LOW | c.1911G>C | p.Pro637Pro | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 2015/3021 | 1911/2106 | 637/701 | chr7 | 140024755 | |||
| chr7:140024755 | C | T | 6 | a0001c0002 a0001c0003 a0001c0009 others(3): Show |
162 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(159): Show |
synonymous_variant | LOW | c.1911G>A | p.Pro637Pro | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 2015/3021 | 1911/2106 | 637/701 | chr7 | 140024755 | |||
| chr7:140026321 | G | A | 2 | a0001c0008 a0001c0009 |
8 | HG01106.hp1 HG01192.hp2 HG01243.hp2 others(5): Show |
synonymous_variant | LOW | c.1656C>T | p.Asn552Asn | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/12 | 1760/3021 | 1656/2106 | 552/701 | chr7 | 140026321 | |||
| chr7:140027335 | G | A | 4 | a0001c0002 a0001c0006 a0001c0009 others(1): Show |
140 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(137): Show |
synonymous_variant | LOW | c.1569C>T | p.Phe523Phe | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/12 | 1673/3021 | 1569/2106 | 523/701 | chr7 | 140027335 | |||
| chr7:140037851 | C | G | 1 | a0001c0013 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.1188G>C | p.Thr396Thr | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/12 | 1292/3021 | 1188/2106 | 396/701 | chr7 | 140037851 | |||
| chr7:140041773 | G | A | 1 | a0008c0016 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.1053C>T | p.Tyr351Tyr | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/12 | 1157/3021 | 1053/2106 | 351/701 | chr7 | 140041773 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:140023775 | TACTCTTT others(20): Show |
T | 1 | a0001c0001t0010 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*758_*784delCTTGTG others(21): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 758 | chr7 | 140023775 | ||||||
| chr7:140023796 | G | A | 2 | a0001c0001t0005 a0001c0001t0006 |
8 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*764C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 764 | chr7 | 140023796 | ||||||
| chr7:140023874 | C | T | 1 | a0007c0015t0009 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*686G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 686 | chr7 | 140023874 | ||||||
| chr7:140023942 | C | T | 2 | a0001c0001t0005 a0001c0001t0006 |
8 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*618G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 618 | chr7 | 140023942 | ||||||
| chr7:140024020 | T | C | 1 | a0001c0002t0012 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*540A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 540 | chr7 | 140024020 | ||||||
| chr7:140024177 | A | G | 1 | a0001c0003t0008 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*383T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 383 | chr7 | 140024177 | ||||||
| chr7:140024270 | T | C | 1 | a0001c0001t0011 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*290A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 290 | chr7 | 140024270 | ||||||
| chr7:140024362 | C | T | 1 | a0003c0007t0013 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*198G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 198 | chr7 | 140024362 | ||||||
| chr7:140024369 | A | G | 21 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(18): Show |
215 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*191T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 191 | chr7 | 140024369 | ||||||
| chr7:140024472 | TAAAAGTT others(10): Show |
T | 1 | a0001c0001t0007 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*71_*87delTTTAAACA others(9): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 71 | chr7 | 140024472 | ||||||
| chr7:140024558 | G | A | 6 | a0001c0002t0001 a0001c0002t0012 a0001c0003t0001 others(3): Show |
144 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*2C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 12/12 | 2 | chr7 | 140024558 | ||||||
| chr7:140062885 | CGACGCGG others(9): Show |
C | 1 | a0001c0001t0006 | 2 | HG01515.hp2 HG01517.hp1 |
5_prime_UTR_variant | MODIFIER | c.-54_-39delCGCCGCCG others(8): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/12 | 39 | chr7 | 140062885 | ||||||
| chr7:140062915 | G | C | 3 | a0003c0005t0004 a0003c0007t0004 a0003c0007t0013 |
15 | HG01261.hp2 HG02145.hp2 HG02486.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-68C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/12 | 68 | chr7 | 140062915 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:140024942 | G | C | 17 | a0001c0002t0001g0008 a0001c0002t0001g0038 a0001c0002t0001g0163 others(14): Show |
21 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.1781-57C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/11 | chr7 | 140024942 | |||||||
| chr7:140025017 | C | T | 1 | a0001c0002t0001g0218 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1781-132G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/11 | chr7 | 140025017 | |||||||
| chr7:140025358 | C | T | 12 | a0001c0003t0003g0027 a0001c0003t0003g0031 a0001c0003t0003g0073 others(9): Show |
14 | HG01175.hp1 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1781-473G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/11 | chr7 | 140025358 | |||||||
| chr7:140025400 | A | G | 1 | a0001c0001t0003g0181 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1781-515T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/11 | chr7 | 140025400 | |||||||
| chr7:140025468 | T | C | 1 | a0003c0005t0004g0044 | 2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1781-583A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/11 | chr7 | 140025468 | |||||||
| chr7:140025508 | A | G | 11 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(8): Show |
12 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1781-623T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/11 | chr7 | 140025508 | |||||||
| chr7:140025780 | A | C | 1 | a0001c0002t0001g0014 | 3 | NA18968.hp2 NA18974.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1780+417T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/11 | chr7 | 140025780 | |||||||
| chr7:140025894 | G | A | 11 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(8): Show |
12 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1780+303C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/11 | chr7 | 140025894 | |||||||
| chr7:140026143 | T | C | 1 | a0009c0017t0003g0271 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1780+54A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 11/11 | chr7 | 140026143 | |||||||
| chr7:140026407 | G | A | 119 | a0001c0002t0001g0005 a0001c0002t0001g0007 a0001c0002t0001g0008 others(116): Show |
154 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1629-59C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026407 | |||||||
| chr7:140026420 | A | C | 1 | a0001c0001t0010g0100 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1629-72T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026420 | |||||||
| chr7:140026421 | C | A | 1 | a0001c0001t0010g0100 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1629-73G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026421 | |||||||
| chr7:140026579 | C | A | 1 | a0009c0017t0003g0271 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1629-231G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026579 | |||||||
| chr7:140026601 | A | C | 1 | a0001c0001t0010g0100 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1629-253T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026601 | |||||||
| chr7:140026605 | G | C | 1 | a0001c0001t0010g0100 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1629-257C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026605 | |||||||
| chr7:140026654 | A | C | 1 | a0001c0001t0010g0100 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1629-306T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026654 | |||||||
| chr7:140026667 | A | G | 169 | a0001c0001t0003g0131 a0001c0001t0003g0181 a0001c0001t0005g0164 others(166): Show |
215 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.1629-319T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026667 | |||||||
| chr7:140026681 | T | G | 1 | a0001c0001t0010g0100 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1629-333A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026681 | |||||||
| chr7:140026935 | C | A | 1 | a0001c0001t0002g0114 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1628+341G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026935 | |||||||
| chr7:140026973 | T | A | 2 | a0001c0001t0002g0025 a0001c0001t0002g0110 |
3 | HG00099.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1628+303A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140026973 | |||||||
| chr7:140027120 | G | C | 2 | a0001c0002t0001g0244 a0001c0002t0001g0249 |
2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1628+156C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140027120 | |||||||
| chr7:140027140 | C | A | 1 | a0001c0001t0003g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1628+136G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140027140 | |||||||
| chr7:140027155 | C | T | 1 | a0003c0007t0003g0183 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1628+121G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140027155 | |||||||
| chr7:140027243 | T | C | 15 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(12): Show |
16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1628+33A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140027243 | |||||||
| chr7:140027247 | C | G | 1 | a0001c0002t0001g0014 | 3 | NA18968.hp2 NA18974.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1628+29G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 10/11 | chr7 | 140027247 | |||||||
| chr7:140027471 | C | T | 1 | a0001c0001t0010g0100 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1498-65G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027471 | |||||||
| chr7:140027528 | C | A | 15 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(12): Show |
16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1498-122G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027528 | |||||||
| chr7:140027543 | T | C | 7 | a0003c0007t0003g0176 a0003c0007t0003g0177 a0003c0007t0003g0183 others(4): Show |
7 | HG02486.hp1 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1498-137A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027543 | |||||||
| chr7:140027567 | G | A | 2 | a0001c0001t0002g0102 a0001c0001t0002g0123 |
2 | NA18955.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1498-161C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027567 | |||||||
| chr7:140027584 | A | T | 1 | a0001c0001t0010g0100 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1498-178T>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027584 | |||||||
| chr7:140027585 | T | C | 2 | a0001c0001t0002g0239 a0001c0002t0012g0247 |
2 | HG01123.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1498-179A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027585 | |||||||
| chr7:140027703 | C | T | 2 | a0001c0001t0002g0026 a0001c0001t0002g0095 |
3 | HG03491.hp2 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1498-297G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027703 | |||||||
| chr7:140027721 | T | A | 1 | a0001c0002t0001g0202 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1498-315A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027721 | |||||||
| chr7:140027870 | T | C | 153 | a0001c0001t0002g0239 a0001c0001t0005g0164 a0001c0001t0005g0165 others(150): Show |
195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1498-464A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027870 | |||||||
| chr7:140027880 | A | G | 1 | a0001c0002t0001g0235 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1498-474T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027880 | |||||||
| chr7:140027981 | T | C | 2 | a0001c0001t0005g0165 a0001c0001t0005g0167 |
2 | HG01123.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1498-575A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140027981 | |||||||
| chr7:140028246 | T | C | 133 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0239 others(130): Show |
173 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1497+367A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140028246 | |||||||
| chr7:140028290 | C | T | 3 | a0002c0004t0003g0020 a0002c0004t0003g0065 a0002c0004t0003g0066 |
4 | HG00735.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497+323G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140028290 | |||||||
| chr7:140028518 | G | A | 1 | a0001c0003t0003g0190 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1497+95C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140028518 | |||||||
| chr7:140028600 | A | G | 3 | a0001c0002t0001g0213 a0001c0002t0001g0214 a0001c0002t0001g0219 |
3 | HG00423.hp2 HG02074.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1497+13T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 9/11 | chr7 | 140028600 | |||||||
| chr7:140028752 | G | C | 2 | a0001c0001t0002g0239 a0001c0002t0012g0247 |
2 | HG01123.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1422-64C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140028752 | |||||||
| chr7:140028784 | A | C | 124 | a0001c0001t0002g0239 a0001c0002t0001g0005 a0001c0002t0001g0007 others(121): Show |
164 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1422-96T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140028784 | |||||||
| chr7:140028916 | C | T | 15 | a0002c0004t0003g0019 a0002c0004t0003g0020 a0002c0004t0003g0021 others(12): Show |
19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1422-228G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140028916 | |||||||
| chr7:140029340 | T | C | 1 | a0002c0004t0003g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1422-652A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140029340 | |||||||
| chr7:140029414 | C | G | 15 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(12): Show |
16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1422-726G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140029414 | |||||||
| chr7:140029527 | A | G | 15 | a0002c0004t0003g0019 a0002c0004t0003g0020 a0002c0004t0003g0021 others(12): Show |
19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1422-839T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140029527 | |||||||
| chr7:140029631 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1422-943G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140029631 | |||||||
| chr7:140029762 | A | G | 12 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(9): Show |
13 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1422-1074T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140029762 | |||||||
| chr7:140029773 | G | A | 8 | a0001c0001t0005g0164 a0003c0007t0003g0176 a0003c0007t0003g0177 others(5): Show |
8 | HG02486.hp1 HG02615.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1422-1085C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140029773 | |||||||
| chr7:140030026 | G | C | 15 | a0002c0004t0003g0019 a0002c0004t0003g0020 a0002c0004t0003g0021 others(12): Show |
19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1422-1338C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030026 | |||||||
| chr7:140030230 | A | G | 1 | a0001c0001t0002g0229 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1422-1542T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030230 | |||||||
| chr7:140030451 | A | T | 1 | a0001c0002t0001g0245 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1422-1763T>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030451 | |||||||
| chr7:140030467 | G | A | 1 | a0005c0011t0003g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1422-1779C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030467 | |||||||
| chr7:140030471 | G | A | 15 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(12): Show |
16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1422-1783C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030471 | |||||||
| chr7:140030522 | C | T | 1 | a0001c0002t0001g0246 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1422-1834G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030522 | |||||||
| chr7:140030548 | A | C | 5 | a0001c0001t0002g0094 a0001c0001t0002g0103 a0001c0001t0002g0125 others(2): Show |
5 | NA18941.hp1 NA18943.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1422-1860T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030548 | |||||||
| chr7:140030605 | A | ACATACAT others(5): Show |
15 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(12): Show |
16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1422-1929_1422-191 others(16): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030605 | |||||||
| chr7:140030605 | ACATACAT others(5): Show |
A | 1 | a0001c0001t0002g0146 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1422-1929_1422-191 others(16): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030605 | |||||||
| chr7:140030700 | C | G | 138 | a0001c0001t0002g0239 a0001c0001t0005g0164 a0001c0001t0005g0165 others(135): Show |
179 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1422-2012G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030700 | |||||||
| chr7:140030702 | T | C | 3 | a0001c0002t0001g0034 a0001c0002t0001g0198 a0001c0002t0001g0207 |
4 | HG01993.hp1 HG02148.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1422-2014A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030702 | |||||||
| chr7:140030773 | A | G | 1 | a0001c0001t0002g0099 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1422-2085T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030773 | |||||||
| chr7:140030827 | G | C | 1 | a0001c0002t0001g0230 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1422-2139C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030827 | |||||||
| chr7:140030970 | T | C | 1 | a0001c0002t0001g0214 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1422-2282A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140030970 | |||||||
| chr7:140031487 | T | C | 1 | a0001c0002t0001g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1421+2748A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140031487 | |||||||
| chr7:140031730 | A | C | 2 | a0001c0002t0001g0213 a0001c0002t0001g0219 |
2 | HG00423.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1421+2505T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140031730 | |||||||
| chr7:140031838 | G | C | 1 | a0001c0001t0002g0182 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1421+2397C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140031838 | |||||||
| chr7:140031909 | G | A | 194 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0057 others(191): Show |
250 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.1421+2326C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140031909 | |||||||
| chr7:140032105 | C | G | 1 | a0003c0005t0004g0281 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1421+2130G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140032105 | |||||||
| chr7:140032153 | G | C | 2 | a0001c0001t0002g0096 a0001c0001t0002g0105 |
2 | HG01361.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1421+2082C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140032153 | |||||||
| chr7:140032160 | C | A | 1 | a0001c0001t0002g0126 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1421+2075G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140032160 | |||||||
| chr7:140032277 | A | G | 2 | a0001c0001t0003g0131 a0001c0001t0003g0181 |
2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1421+1958T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140032277 | |||||||
| chr7:140032335 | T | C | 1 | a0001c0003t0003g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1421+1900A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140032335 | |||||||
| chr7:140032349 | TA | T | 9 | a0001c0002t0001g0200 a0001c0002t0001g0203 a0003c0007t0003g0176 others(6): Show |
9 | HG02486.hp1 HG02615.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1421+1885delT | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140032349 | |||||||
| chr7:140032430 | G | C | 1 | a0001c0001t0002g0082 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1421+1805C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140032430 | |||||||
| chr7:140032467 | G | A | 1 | a0001c0002t0001g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1421+1768C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140032467 | |||||||
| chr7:140032702 | A | G | 4 | a0001c0001t0002g0024 a0001c0001t0002g0076 a0001c0001t0002g0085 others(1): Show |
5 | HG00738.hp1 HG01106.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.1421+1533T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140032702 | |||||||
| chr7:140033030 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1421+1205G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140033030 | |||||||
| chr7:140033098 | G | A | 1 | a0001c0002t0001g0260 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1421+1137C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140033098 | |||||||
| chr7:140033182 | T | G | 1 | a0003c0007t0003g0183 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1421+1053A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140033182 | |||||||
| chr7:140033371 | C | G | 1 | a0001c0001t0002g0228 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1421+864G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140033371 | |||||||
| chr7:140033454 | A | G | 2 | a0001c0001t0003g0131 a0001c0001t0003g0181 |
2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1421+781T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140033454 | |||||||
| chr7:140033612 | A | G | 3 | a0001c0003t0003g0189 a0001c0003t0003g0190 a0001c0003t0003g0191 |
3 | HG01884.hp1 HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1421+623T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140033612 | |||||||
| chr7:140033654 | C | T | 16 | a0001c0001t0002g0001 a0001c0001t0002g0077 a0001c0001t0002g0142 others(13): Show |
22 | HG00597.hp1 HG00609.hp2 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.1421+581G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140033654 | |||||||
| chr7:140033782 | G | A | 4 | a0001c0003t0003g0031 a0001c0003t0003g0189 a0001c0003t0003g0190 others(1): Show |
5 | HG01884.hp1 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1421+453C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 8/11 | chr7 | 140033782 | |||||||
| chr7:140034509 | T | C | 11 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(8): Show |
12 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1325-178A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140034509 | |||||||
| chr7:140034573 | C | T | 168 | a0001c0001t0002g0239 a0001c0001t0003g0131 a0001c0001t0003g0181 others(165): Show |
212 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.1325-242G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140034573 | |||||||
| chr7:140034633 | A | AT | 5 | a0001c0002t0001g0041 a0001c0002t0001g0231 a0001c0002t0001g0245 others(2): Show |
7 | HG01952.hp1 HG02257.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325-303dupA | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140034633 | |||||||
| chr7:140034768 | C | A | 7 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(4): Show |
8 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1325-437G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140034768 | |||||||
| chr7:140034897 | C | A | 153 | a0001c0001t0002g0239 a0001c0001t0005g0164 a0001c0001t0005g0165 others(150): Show |
195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1325-566G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140034897 | |||||||
| chr7:140035226 | A | G | 1 | a0001c0002t0001g0206 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1325-895T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035226 | |||||||
| chr7:140035276 | T | C | 13 | a0001c0003t0003g0027 a0001c0003t0003g0031 a0001c0003t0003g0073 others(10): Show |
15 | HG01175.hp1 HG01884.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1325-945A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035276 | |||||||
| chr7:140035331 | G | C | 1 | a0001c0002t0001g0217 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1325-1000C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035331 | |||||||
| chr7:140035334 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1325-1003C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035334 | |||||||
| chr7:140035483 | A | G | 1 | a0001c0001t0002g0110 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1325-1152T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035483 | |||||||
| chr7:140035793 | A | G | 1 | a0001c0001t0003g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1325-1462T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035793 | |||||||
| chr7:140035806 | T | C | 1 | a0009c0017t0003g0271 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1325-1475A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035806 | |||||||
| chr7:140035837 | A | G | 15 | a0002c0004t0003g0019 a0002c0004t0003g0020 a0002c0004t0003g0021 others(12): Show |
19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1325-1506T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035837 | |||||||
| chr7:140035842 | G | GGAGGAAG others(17): Show |
2 | a0001c0001t0003g0131 a0001c0001t0003g0181 |
2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1325-1535_1325-151 others(28): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035842 | |||||||
| chr7:140035884 | A | G | 167 | a0001c0001t0002g0239 a0001c0001t0005g0164 a0001c0001t0005g0165 others(164): Show |
213 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.1325-1553T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035884 | |||||||
| chr7:140035886 | A | G | 167 | a0001c0001t0002g0239 a0001c0001t0005g0164 a0001c0001t0005g0165 others(164): Show |
213 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.1325-1555T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035886 | |||||||
| chr7:140035890 | AGAGGAGG others(32): Show |
A | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1325-1598_1325-156 others(43): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035890 | |||||||
| chr7:140035896 | G | A | 166 | a0001c0001t0002g0239 a0001c0001t0005g0164 a0001c0001t0005g0165 others(163): Show |
212 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.1325-1565C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035896 | |||||||
| chr7:140035902 | C | A | 1 | a0002c0004t0003g0065 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1325-1571G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035902 | |||||||
| chr7:140035902 | C | G | 166 | a0001c0001t0002g0239 a0001c0001t0005g0164 a0001c0001t0005g0165 others(163): Show |
212 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.1325-1571G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035902 | |||||||
| chr7:140035908 | G | A | 152 | a0001c0001t0002g0239 a0001c0001t0005g0164 a0001c0001t0005g0165 others(149): Show |
194 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.1325-1577C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035908 | |||||||
| chr7:140035910 | A | G | 14 | a0002c0004t0003g0019 a0002c0004t0003g0020 a0002c0004t0003g0021 others(11): Show |
18 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.1325-1579T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035910 | |||||||
| chr7:140035912 | GACA | G | 16 | a0001c0002t0012g0247 a0003c0005t0003g0156 a0003c0005t0004g0044 others(13): Show |
17 | HG01123.hp1 HG01261.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1325-1584_1325-158 others(7): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035912 | |||||||
| chr7:140035914 | C | A | 150 | a0001c0001t0002g0239 a0001c0001t0005g0164 a0001c0001t0005g0165 others(147): Show |
195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1325-1583G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035914 | |||||||
| chr7:140035915 | A | G | 150 | a0001c0001t0002g0239 a0001c0001t0005g0164 a0001c0001t0005g0165 others(147): Show |
195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1325-1584T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035915 | |||||||
| chr7:140035917 | G | A | 15 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(12): Show |
16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1325-1586C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035917 | |||||||
| chr7:140035923 | G | A | 1 | a0001c0002t0012g0247 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1325-1592C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035923 | |||||||
| chr7:140035926 | C | G | 16 | a0001c0002t0012g0247 a0003c0005t0003g0156 a0003c0005t0004g0044 others(13): Show |
17 | HG01123.hp1 HG01261.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1325-1595G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035926 | |||||||
| chr7:140035926 | CAAG | C | 127 | a0001c0001t0002g0239 a0001c0001t0005g0164 a0001c0001t0005g0165 others(124): Show |
166 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.1325-1598_1325-159 others(7): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035926 | |||||||
| chr7:140035926 | CAAGGAG | C | 5 | a0001c0002t0001g0205 a0001c0002t0001g0238 a0001c0002t0001g0270 others(2): Show |
6 | HG02080.hp2 HG02165.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1325-1601_1325-159 others(10): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035926 | |||||||
| chr7:140035927 | A | G | 5 | a0001c0002t0012g0247 a0001c0003t0003g0031 a0001c0003t0003g0189 others(2): Show |
6 | HG01123.hp1 HG01884.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1325-1596T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035927 | |||||||
| chr7:140035927 | AAGG | A | 6 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0002g0118 others(3): Show |
6 | HG00438.hp1 HG00735.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.1325-1599_1325-159 others(7): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035927 | |||||||
| chr7:140035927 | AAGGAGGA others(8): Show |
A | 1 | a0002c0004t0003g0020 | 2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1325-1611_1325-159 others(19): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035927 | |||||||
| chr7:140035929 | G | A | 1 | a0001c0002t0012g0247 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1325-1598C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035929 | |||||||
| chr7:140035929 | G | C | 15 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(12): Show |
16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1325-1598C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035929 | |||||||
| chr7:140035935 | G | A | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1325-1604C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035935 | |||||||
| chr7:140035935 | G | GGAGGAGG others(11): Show |
1 | a0001c0001t0002g0148 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1325-1622_1325-160 others(22): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035935 | |||||||
| chr7:140035938 | G | C | 17 | a0001c0003t0003g0031 a0001c0003t0003g0189 a0001c0003t0003g0190 others(14): Show |
21 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.1325-1607C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035938 | |||||||
| chr7:140035939 | G | A | 17 | a0001c0003t0003g0031 a0001c0003t0003g0189 a0001c0003t0003g0190 others(14): Show |
21 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.1325-1608C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035939 | |||||||
| chr7:140035941 | G | C | 143 | a0001c0001t0002g0239 a0001c0001t0005g0164 a0001c0001t0005g0165 others(140): Show |
183 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.1325-1610C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035941 | |||||||
| chr7:140035942 | G | A | 38 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(35): Show |
41 | HG01123.hp2 HG01175.hp1 HG01261.hp1 others(38): Show |
intron_variant | MODIFIER | c.1325-1611C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035942 | |||||||
| chr7:140035944 | G | C | 5 | a0001c0002t0001g0205 a0001c0002t0001g0238 a0001c0002t0001g0270 others(2): Show |
6 | HG02080.hp2 HG02165.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1325-1613C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035944 | |||||||
| chr7:140035944 | GGAGGAGG others(2): Show |
G | 8 | a0002c0004t0003g0019 a0002c0004t0003g0066 a0002c0004t0003g0067 others(5): Show |
9 | HG00639.hp2 HG00738.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.1325-1622_1325-161 others(13): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035944 | |||||||
| chr7:140035945 | G | A | 5 | a0001c0002t0001g0205 a0001c0002t0001g0238 a0001c0002t0001g0270 others(2): Show |
6 | HG02080.hp2 HG02165.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1325-1614C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035945 | |||||||
| chr7:140035947 | GGAGGAC | G | 3 | a0002c0004t0003g0021 a0002c0004t0003g0022 a0002c0004t0003g0132 |
5 | HG01069.hp1 HG01071.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325-1622_1325-161 others(10): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035947 | |||||||
| chr7:140035949 | A | G | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1325-1618T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035949 | |||||||
| chr7:140035953 | C | A | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1325-1622G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035953 | |||||||
| chr7:140035953 | C | G | 10 | a0001c0002t0001g0205 a0001c0002t0001g0238 a0001c0002t0001g0270 others(7): Show |
12 | HG01884.hp1 HG02080.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.1325-1622G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035953 | |||||||
| chr7:140035954 | G | A | 137 | a0001c0001t0002g0239 a0001c0001t0005g0164 a0001c0001t0005g0165 others(134): Show |
175 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.1325-1623C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035954 | |||||||
| chr7:140035959 | G | A | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1325-1628C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035959 | |||||||
| chr7:140035962 | G | C | 1 | a0002c0004t0003g0063 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1325-1631C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035962 | |||||||
| chr7:140035965 | G | C | 6 | a0001c0002t0012g0247 a0001c0003t0003g0031 a0001c0003t0003g0189 others(3): Show |
7 | HG01123.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325-1634C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035965 | |||||||
| chr7:140035966 | G | A | 1 | a0001c0002t0012g0247 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1325-1635C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035966 | |||||||
| chr7:140035966 | GAGGACGA others(56): Show |
G | 1 | a0002c0004t0003g0065 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1324+1686_1325-163 others(67): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035966 | |||||||
| chr7:140035971 | C | A | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1325-1640G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035971 | |||||||
| chr7:140035971 | C | G | 148 | a0001c0001t0002g0239 a0001c0001t0005g0164 a0001c0001t0005g0165 others(145): Show |
190 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1325-1640G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035971 | |||||||
| chr7:140035971 | CGAGGAGG others(2): Show |
C | 7 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0046 others(4): Show |
9 | NA18962.hp1 NA18975.hp1 NA19003.hp1 others(6): Show |
intron_variant | MODIFIER | c.1325-1649_1325-164 others(13): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035971 | |||||||
| chr7:140035977 | G | A | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1325-1646C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035977 | |||||||
| chr7:140035977 | G | C | 8 | a0001c0009t0001g0259 a0002c0004t0003g0020 a0003c0007t0003g0176 others(5): Show |
9 | HG01433.hp2 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1325-1646C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035977 | |||||||
| chr7:140035980 | G | C | 126 | a0001c0001t0002g0239 a0001c0002t0001g0005 a0001c0002t0001g0007 others(123): Show |
165 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.1325-1649C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035980 | |||||||
| chr7:140035983 | G | C | 1 | a0003c0007t0013g0283 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1325-1652C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035983 | |||||||
| chr7:140035984 | GAGGAGGA others(38): Show |
G | 7 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(4): Show |
8 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1324+1686_1325-165 others(49): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035984 | |||||||
| chr7:140035986 | G | C | 4 | a0001c0003t0003g0031 a0001c0003t0003g0189 a0001c0003t0003g0190 others(1): Show |
5 | HG01884.hp1 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325-1655C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035986 | |||||||
| chr7:140035987 | GAGGAGGA others(8): Show |
G | 2 | a0001c0001t0003g0181 a0001c0008t0002g0049 |
2 | HG01192.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1325-1671_1325-165 others(19): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035987 | |||||||
| chr7:140035987 | GAGGAGGA others(17): Show |
G | 1 | a0001c0001t0003g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1325-1680_1325-165 others(28): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035987 | |||||||
| chr7:140035987 | GAGGAGGA others(62): Show |
G | 6 | a0001c0002t0001g0186 a0001c0002t0001g0205 a0001c0002t0001g0238 others(3): Show |
7 | HG02080.hp2 HG02165.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324+1659_1325-165 others(73): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035987 | |||||||
| chr7:140035989 | G | C | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1325-1658C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035989 | |||||||
| chr7:140035990 | GAGGAGGA others(5): Show |
G | 2 | a0004c0010t0002g0061 a0004c0010t0002g0170 |
2 | HG00140.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1325-1671_1325-166 others(16): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035990 | |||||||
| chr7:140035990 | GAGGAGGA others(14): Show |
G | 1 | a0004c0010t0002g0121 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1325-1680_1325-166 others(25): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035990 | |||||||
| chr7:140035990 | GAGGAGGA others(23): Show |
G | 2 | a0003c0007t0003g0176 a0003c0007t0003g0177 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1325-1689_1325-166 others(34): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035990 | |||||||
| chr7:140035990 | GAGGAGGA others(32): Show |
G | 1 | a0003c0007t0003g0183 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1324+1686_1325-166 others(43): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035990 | |||||||
| chr7:140035992 | G | C | 1 | a0001c0002t0012g0247 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1325-1661C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035992 | |||||||
| chr7:140035993 | G | GAGGAGGA others(2): Show |
7 | a0001c0001t0002g0006 a0001c0001t0002g0054 a0001c0001t0002g0058 others(4): Show |
7 | HG00280.hp1 HG00280.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1325-1671_1325-166 others(13): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035993 | |||||||
| chr7:140035993 | GAGGAGGA others(2): Show |
G | 30 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0010 others(27): Show |
38 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1325-1671_1325-166 others(13): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035993 | |||||||
| chr7:140035993 | GAGGAGGA others(11): Show |
G | 2 | a0001c0001t0002g0093 a0001c0001t0002g0128 |
2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1325-1680_1325-166 others(22): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035993 | |||||||
| chr7:140035993 | GAGGAGGA others(20): Show |
G | 1 | a0001c0001t0002g0087 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1325-1689_1325-166 others(31): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035993 | |||||||
| chr7:140035993 | GAGGAGGA others(38): Show |
G | 13 | a0002c0004t0003g0019 a0002c0004t0003g0020 a0002c0004t0003g0021 others(10): Show |
17 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1324+1677_1325-166 others(49): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035993 | |||||||
| chr7:140035993 | GAGGAGGA others(47): Show |
G | 2 | a0002c0004t0003g0063 a0002c0004t0003g0064 |
2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1324+1668_1325-166 others(58): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035993 | |||||||
| chr7:140035993 | GAGGAGGA others(56): Show |
G | 2 | a0001c0002t0001g0251 a0001c0009t0001g0259 |
2 | HG01433.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1324+1659_1325-166 others(67): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035993 | |||||||
| chr7:140035995 | G | C | 1 | a0003c0007t0004g0284 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1325-1664C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035995 | |||||||
| chr7:140035996 | GAGGAGAA others(8): Show |
G | 2 | a0003c0007t0004g0282 a0003c0007t0004g0285 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1325-1680_1325-166 others(19): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035996 | |||||||
| chr7:140035996 | GAGGAGAA others(26): Show |
G | 8 | a0001c0003t0003g0027 a0001c0003t0003g0073 a0001c0003t0003g0074 others(5): Show |
9 | HG01175.hp1 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1324+1686_1325-166 others(37): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035996 | |||||||
| chr7:140035996 | GAGGAGAA others(35): Show |
G | 13 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0274 others(10): Show |
14 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1324+1677_1325-166 others(46): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035996 | |||||||
| chr7:140035996 | GAGGAGAA others(44): Show |
G | 1 | a0001c0003t0003g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1324+1668_1325-166 others(55): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035996 | |||||||
| chr7:140035996 | GAGGAGAA others(53): Show |
G | 101 | a0001c0001t0002g0239 a0001c0002t0001g0005 a0001c0002t0001g0007 others(98): Show |
138 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.1324+1659_1325-166 others(64): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035996 | |||||||
| chr7:140035999 | GAGAAGGA others(5): Show |
G | 1 | a0003c0007t0004g0284 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1325-1680_1325-166 others(16): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035999 | |||||||
| chr7:140035999 | GAGAAGGA others(32): Show |
G | 1 | a0003c0005t0004g0273 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1324+1677_1325-166 others(43): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035999 | |||||||
| chr7:140035999 | GAGAAGGA others(41): Show |
G | 5 | a0001c0002t0012g0247 a0001c0003t0003g0031 a0001c0003t0003g0189 others(2): Show |
6 | HG01123.hp1 HG01884.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324+1668_1325-166 others(52): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140035999 | |||||||
| chr7:140036001 | G | C | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1325-1670C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036001 | |||||||
| chr7:140036002 | A | G | 1 | a0003c0007t0013g0283 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1325-1671T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036002 | |||||||
| chr7:140036006 | A | G | 1 | a0003c0007t0013g0283 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1325-1675T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036006 | |||||||
| chr7:140036007 | G | C | 1 | a0003c0007t0013g0283 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1325-1676C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036007 | |||||||
| chr7:140036011 | A | G | 1 | a0003c0007t0013g0283 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1325-1680T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036011 | |||||||
| chr7:140036016 | G | C | 2 | a0003c0007t0004g0282 a0003c0007t0004g0285 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1325-1685C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036016 | |||||||
| chr7:140036020 | A | G | 5 | a0003c0007t0004g0282 a0003c0007t0004g0284 a0003c0007t0004g0285 others(2): Show |
5 | HG02486.hp1 HG02486.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325-1689T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036020 | |||||||
| chr7:140036029 | A | G | 3 | a0003c0007t0004g0282 a0003c0007t0004g0285 a0007c0015t0009g0188 |
3 | HG02486.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1324+1686T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036029 | |||||||
| chr7:140036031 | G | C | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1324+1684C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036031 | |||||||
| chr7:140036034 | G | C | 8 | a0001c0003t0003g0027 a0001c0003t0003g0073 a0001c0003t0003g0074 others(5): Show |
9 | HG01175.hp1 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1324+1681C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036034 | |||||||
| chr7:140036038 | A | G | 10 | a0001c0003t0003g0027 a0001c0003t0003g0073 a0001c0003t0003g0074 others(7): Show |
11 | HG00735.hp2 HG01175.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1324+1677T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036038 | |||||||
| chr7:140036046 | G | A | 1 | a0008c0016t0003g0160 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1324+1669C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036046 | |||||||
| chr7:140036047 | A | G | 9 | a0001c0003t0003g0027 a0001c0003t0003g0073 a0001c0003t0003g0074 others(6): Show |
10 | HG01175.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1324+1668T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036047 | |||||||
| chr7:140036056 | A | G | 1 | a0001c0002t0012g0247 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1324+1659T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036056 | |||||||
| chr7:140036065 | A | G | 2 | a0001c0002t0001g0250 a0001c0002t0001g0254 |
2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1324+1650T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036065 | |||||||
| chr7:140036089 | A | G | 1 | a0005c0011t0003g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1324+1626T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036089 | |||||||
| chr7:140036116 | C | T | 1 | a0001c0001t0003g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1324+1599G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036116 | |||||||
| chr7:140036146 | G | T | 1 | a0001c0001t0002g0050 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1324+1569C>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036146 | |||||||
| chr7:140036159 | C | T | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1324+1556G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036159 | |||||||
| chr7:140036166 | C | G | 1 | a0001c0001t0002g0143 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1324+1549G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036166 | |||||||
| chr7:140036166 | C | T | 7 | a0001c0003t0003g0027 a0001c0003t0003g0073 a0001c0003t0003g0074 others(4): Show |
8 | HG01175.hp1 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1324+1549G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036166 | |||||||
| chr7:140036232 | A | C | 1 | a0009c0017t0003g0271 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1324+1483T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036232 | |||||||
| chr7:140036275 | T | A | 1 | a0009c0017t0003g0271 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1324+1440A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036275 | |||||||
| chr7:140036353 | T | G | 1 | a0001c0001t0002g0091 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1324+1362A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036353 | |||||||
| chr7:140036484 | G | A | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1324+1231C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036484 | |||||||
| chr7:140036610 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1324+1105G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036610 | |||||||
| chr7:140036634 | G | A | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1324+1081C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036634 | |||||||
| chr7:140036764 | G | C | 1 | a0009c0017t0003g0271 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1324+951C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036764 | |||||||
| chr7:140036822 | T | TA | 15 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(12): Show |
16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1324+892dupT | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036822 | |||||||
| chr7:140036822 | TA | T | 124 | a0001c0001t0002g0104 a0001c0001t0002g0239 a0001c0002t0001g0005 others(121): Show |
164 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1324+892delT | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036822 | |||||||
| chr7:140036885 | C | A | 1 | a0001c0002t0001g0261 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1324+830G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036885 | |||||||
| chr7:140036997 | T | C | 6 | a0001c0001t0002g0056 a0001c0001t0002g0102 a0001c0001t0002g0115 others(3): Show |
6 | HG01192.hp1 HG01516.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1324+718A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140036997 | |||||||
| chr7:140037034 | G | A | 17 | a0001c0002t0001g0008 a0001c0002t0001g0038 a0001c0002t0001g0163 others(14): Show |
21 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.1324+681C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140037034 | |||||||
| chr7:140037051 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1324+664C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140037051 | |||||||
| chr7:140037255 | C | T | 2 | a0001c0002t0001g0253 a0001c0002t0001g0258 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1324+460G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140037255 | |||||||
| chr7:140037256 | G | A | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1324+459C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140037256 | |||||||
| chr7:140037424 | G | A | 2 | a0001c0001t0003g0131 a0001c0001t0003g0181 |
2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1324+291C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140037424 | |||||||
| chr7:140037432 | C | A | 1 | a0001c0009t0001g0266 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1324+283G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140037432 | |||||||
| chr7:140037544 | C | T | 130 | a0001c0002t0001g0005 a0001c0002t0001g0007 a0001c0002t0001g0008 others(127): Show |
170 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1324+171G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140037544 | |||||||
| chr7:140037559 | A | G | 1 | a0001c0001t0002g0026 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1324+156T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140037559 | |||||||
| chr7:140037621 | C | T | 12 | a0002c0004t0003g0019 a0002c0004t0003g0021 a0002c0004t0003g0022 others(9): Show |
15 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.1324+94G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 7/11 | chr7 | 140037621 | |||||||
| chr7:140037992 | A | G | 12 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(9): Show |
13 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1183-136T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140037992 | |||||||
| chr7:140037998 | T | C | 15 | a0002c0004t0003g0019 a0002c0004t0003g0020 a0002c0004t0003g0021 others(12): Show |
19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1183-142A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140037998 | |||||||
| chr7:140038063 | C | T | 3 | a0002c0004t0003g0020 a0002c0004t0003g0065 a0002c0004t0003g0066 |
4 | HG00735.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1183-207G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140038063 | |||||||
| chr7:140038096 | A | C | 2 | a0001c0002t0001g0014 a0001c0002t0001g0208 |
4 | NA18968.hp2 NA18974.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1183-240T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140038096 | |||||||
| chr7:140038188 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1183-332G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140038188 | |||||||
| chr7:140038255 | C | A | 2 | a0001c0001t0003g0131 a0001c0001t0003g0181 |
2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1183-399G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140038255 | |||||||
| chr7:140038567 | A | G | 15 | a0002c0004t0003g0019 a0002c0004t0003g0020 a0002c0004t0003g0021 others(12): Show |
19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1183-711T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140038567 | |||||||
| chr7:140038707 | A | C | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1183-851T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140038707 | |||||||
| chr7:140038761 | T | C | 7 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(4): Show |
8 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1183-905A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140038761 | |||||||
| chr7:140038819 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1183-963C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140038819 | |||||||
| chr7:140039127 | T | C | 3 | a0002c0004t0003g0020 a0002c0004t0003g0065 a0002c0004t0003g0066 |
4 | HG00735.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1183-1271A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140039127 | |||||||
| chr7:140039340 | T | C | 1 | a0001c0002t0001g0161 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1183-1484A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140039340 | |||||||
| chr7:140039392 | G | T | 1 | a0001c0002t0001g0174 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1183-1536C>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140039392 | |||||||
| chr7:140039625 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1183-1769G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140039625 | |||||||
| chr7:140039778 | C | T | 16 | a0001c0002t0001g0011 a0003c0005t0003g0156 a0003c0005t0004g0044 others(13): Show |
19 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1182+1866G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140039778 | |||||||
| chr7:140039863 | C | T | 7 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(4): Show |
8 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1182+1781G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140039863 | |||||||
| chr7:140039887 | A | ACTGCT | 16 | a0001c0002t0001g0011 a0003c0005t0003g0156 a0003c0005t0004g0044 others(13): Show |
19 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1182+1752_1182+175 others(9): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140039887 | |||||||
| chr7:140040513 | C | T | 44 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0016 others(41): Show |
53 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1182+1131G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140040513 | |||||||
| chr7:140040644 | C | T | 2 | a0001c0001t0002g0055 a0001c0001t0002g0057 |
2 | NA18944.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1182+1000G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140040644 | |||||||
| chr7:140040896 | T | C | 15 | a0002c0004t0003g0019 a0002c0004t0003g0020 a0002c0004t0003g0021 others(12): Show |
19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1182+748A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140040896 | |||||||
| chr7:140040912 | C | T | 2 | a0001c0009t0001g0262 a0001c0009t0001g0268 |
2 | HG01106.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1182+732G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140040912 | |||||||
| chr7:140041064 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1182+580C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140041064 | |||||||
| chr7:140041083 | A | G | 15 | a0002c0004t0003g0019 a0002c0004t0003g0020 a0002c0004t0003g0021 others(12): Show |
19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1182+561T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140041083 | |||||||
| chr7:140041139 | T | C | 1 | a0001c0001t0002g0159 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1182+505A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140041139 | |||||||
| chr7:140041274 | A | G | 15 | a0001c0002t0001g0256 a0003c0005t0003g0156 a0003c0005t0004g0044 others(12): Show |
16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1182+370T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140041274 | |||||||
| chr7:140041306 | T | C | 16 | a0001c0002t0001g0256 a0003c0005t0003g0156 a0003c0005t0004g0044 others(13): Show |
17 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1182+338A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140041306 | |||||||
| chr7:140041430 | C | T | 2 | a0001c0002t0001g0226 a0001c0002t0001g0227 |
2 | HG01069.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1182+214G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 6/11 | chr7 | 140041430 | |||||||
| chr7:140041966 | C | T | 37 | a0001c0001t0003g0131 a0001c0001t0003g0181 a0001c0001t0005g0164 others(34): Show |
42 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.987-127G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140041966 | |||||||
| chr7:140041986 | C | T | 8 | a0001c0002t0001g0037 a0001c0002t0001g0196 a0001c0002t0001g0203 others(5): Show |
9 | HG00423.hp2 HG02074.hp1 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.987-147G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140041986 | |||||||
| chr7:140042347 | G | A | 1 | a0003c0005t0004g0281 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.987-508C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140042347 | |||||||
| chr7:140042510 | G | A | 1 | a0001c0001t0002g0087 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.987-671C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140042510 | |||||||
| chr7:140042669 | G | A | 3 | a0001c0003t0003g0030 a0001c0003t0003g0141 a0001c0003t0003g0179 |
4 | HG01952.hp1 HG02257.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.987-830C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140042669 | |||||||
| chr7:140042853 | A | G | 4 | a0001c0001t0002g0058 a0001c0001t0002g0097 a0001c0001t0002g0098 others(1): Show |
4 | HG00741.hp1 HG01070.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.987-1014T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140042853 | |||||||
| chr7:140042898 | C | T | 1 | a0003c0005t0004g0276 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.987-1059G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140042898 | |||||||
| chr7:140042922 | A | G | 10 | a0001c0002t0001g0007 a0001c0002t0001g0015 a0001c0002t0001g0153 others(7): Show |
15 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.987-1083T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140042922 | |||||||
| chr7:140042923 | T | C | 8 | a0001c0002t0001g0007 a0001c0002t0001g0015 a0001c0002t0001g0197 others(5): Show |
13 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.987-1084A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140042923 | |||||||
| chr7:140042934 | G | A | 1 | a0001c0013t0002g0051 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.987-1095C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140042934 | |||||||
| chr7:140043039 | C | CA | 3 | a0001c0003t0001g0028 a0001c0003t0001g0154 a0001c0003t0001g0155 |
4 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.987-1201dupT | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043039 | |||||||
| chr7:140043050 | C | T | 3 | a0001c0003t0001g0028 a0001c0003t0001g0154 a0001c0003t0001g0155 |
4 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.987-1211G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043050 | |||||||
| chr7:140043054 | A | C | 3 | a0001c0003t0001g0028 a0001c0003t0001g0154 a0001c0003t0001g0155 |
4 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.987-1215T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043054 | |||||||
| chr7:140043111 | A | G | 2 | a0001c0001t0002g0120 a0001c0001t0002g0229 |
2 | HG02630.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.987-1272T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043111 | |||||||
| chr7:140043173 | G | A | 1 | a0001c0001t0002g0025 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.987-1334C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043173 | |||||||
| chr7:140043234 | C | T | 1 | a0001c0002t0001g0232 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.987-1395G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043234 | |||||||
| chr7:140043249 | G | A | 1 | a0001c0001t0002g0103 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.987-1410C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043249 | |||||||
| chr7:140043653 | G | C | 1 | a0001c0002t0001g0163 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.987-1814C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043653 | |||||||
| chr7:140043687 | C | T | 8 | a0001c0001t0002g0171 a0001c0001t0005g0164 a0001c0001t0005g0165 others(5): Show |
9 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.987-1848G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043687 | |||||||
| chr7:140043704 | T | C | 1 | a0003c0007t0003g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.987-1865A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043704 | |||||||
| chr7:140043811 | C | T | 1 | a0001c0001t0003g0181 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.987-1972G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043811 | |||||||
| chr7:140043817 | C | T | 1 | a0005c0011t0003g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.987-1978G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043817 | |||||||
| chr7:140043883 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.987-2044C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043883 | |||||||
| chr7:140043949 | G | C | 3 | a0001c0003t0001g0028 a0001c0003t0001g0154 a0001c0003t0001g0155 |
4 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.987-2110C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043949 | |||||||
| chr7:140043966 | G | C | 1 | a0001c0001t0002g0229 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.987-2127C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140043966 | |||||||
| chr7:140044125 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.987-2286G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140044125 | |||||||
| chr7:140044335 | C | T | 1 | a0001c0001t0002g0145 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.987-2496G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140044335 | |||||||
| chr7:140044360 | T | C | 11 | a0001c0001t0002g0171 a0001c0001t0005g0164 a0001c0001t0005g0165 others(8): Show |
13 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.987-2521A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140044360 | |||||||
| chr7:140044367 | T | C | 2 | a0002c0004t0003g0063 a0002c0004t0003g0064 |
2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.986+2517A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140044367 | |||||||
| chr7:140044397 | A | G | 1 | a0001c0001t0002g0048 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.986+2487T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140044397 | |||||||
| chr7:140044440 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.986+2444C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140044440 | |||||||
| chr7:140044906 | T | C | 1 | a0001c0002t0001g0012 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.986+1978A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140044906 | |||||||
| chr7:140045002 | T | G | 37 | a0002c0004t0003g0019 a0002c0004t0003g0020 a0002c0004t0003g0021 others(34): Show |
42 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.986+1882A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045002 | |||||||
| chr7:140045006 | C | T | 1 | a0001c0002t0001g0240 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.986+1878G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045006 | |||||||
| chr7:140045029 | C | CT | 14 | a0002c0004t0003g0019 a0002c0004t0003g0020 a0002c0004t0003g0021 others(11): Show |
18 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.986+1854dupA | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045029 | |||||||
| chr7:140045098 | T | C | 4 | a0001c0002t0001g0162 a0001c0002t0001g0232 a0001c0002t0001g0257 others(1): Show |
4 | NA18968.hp1 NA18973.hp2 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.986+1786A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045098 | |||||||
| chr7:140045177 | G | A | 2 | a0001c0002t0001g0208 a0001c0002t0001g0209 |
2 | NA18974.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.986+1707C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045177 | |||||||
| chr7:140045203 | T | A | 1 | a0001c0001t0002g0104 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.986+1681A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045203 | |||||||
| chr7:140045246 | T | A | 2 | a0001c0002t0001g0162 a0001c0002t0001g0269 |
2 | NA18973.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.986+1638A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045246 | |||||||
| chr7:140045372 | C | G | 15 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(12): Show |
16 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.986+1512G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045372 | |||||||
| chr7:140045548 | T | C | 3 | a0001c0003t0001g0028 a0001c0003t0001g0154 a0001c0003t0001g0155 |
4 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.986+1336A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045548 | |||||||
| chr7:140045800 | C | T | 2 | a0001c0001t0002g0096 a0001c0001t0002g0105 |
2 | HG01361.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.986+1084G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045800 | |||||||
| chr7:140045805 | T | C | 1 | a0001c0001t0002g0058 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.986+1079A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045805 | |||||||
| chr7:140045983 | TGAACGAT others(1): Show |
T | 6 | a0003c0005t0004g0273 a0003c0005t0004g0274 a0003c0005t0004g0275 others(3): Show |
6 | HG01261.hp2 HG02809.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.986+893_986+900del others(8): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045983 | |||||||
| chr7:140045991 | G | A | 103 | a0001c0002t0001g0005 a0001c0002t0001g0007 a0001c0002t0001g0008 others(100): Show |
138 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.986+893C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140045991 | |||||||
| chr7:140046035 | C | A | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.986+849G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046035 | |||||||
| chr7:140046093 | A | G | 22 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(19): Show |
23 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.986+791T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046093 | |||||||
| chr7:140046195 | T | C | 1 | a0001c0001t0002g0083 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.986+689A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046195 | |||||||
| chr7:140046221 | A | C | 1 | a0001c0001t0002g0151 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.986+663T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046221 | |||||||
| chr7:140046303 | T | G | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.986+581A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046303 | |||||||
| chr7:140046503 | C | T | 1 | a0001c0001t0003g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.986+381G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046503 | |||||||
| chr7:140046721 | A | AGT | 8 | a0001c0001t0002g0050 a0001c0001t0002g0060 a0001c0001t0002g0083 others(5): Show |
8 | HG00741.hp2 HG01884.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.986+161_986+162dup others(2): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | |||||||
| chr7:140046721 | A | AGTGT | 8 | a0001c0001t0002g0171 a0001c0001t0005g0164 a0001c0001t0005g0165 others(5): Show |
9 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.986+159_986+162dup others(4): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | |||||||
| chr7:140046721 | A | AGTGTGTG others(1): Show |
5 | a0002c0004t0003g0020 a0002c0004t0003g0065 a0002c0004t0003g0066 others(2): Show |
6 | HG00639.hp2 HG00735.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.986+155_986+162dup others(8): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | |||||||
| chr7:140046721 | A | AGTGTGTG others(3): Show |
2 | a0002c0004t0003g0071 a0002c0004t0003g0072 |
2 | HG02698.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.986+153_986+162dup others(10): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | |||||||
| chr7:140046721 | A | AGTGTGTG others(5): Show |
2 | a0002c0004t0003g0069 a0002c0004t0003g0132 |
2 | HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.986+151_986+162dup others(12): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | |||||||
| chr7:140046721 | A | AGTGTGTG others(7): Show |
3 | a0002c0004t0003g0022 a0002c0004t0003g0063 a0002c0004t0003g0064 |
4 | HG04115.hp1 HG04204.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.986+149_986+162dup others(14): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | |||||||
| chr7:140046721 | A | AGTGTGTG others(11): Show |
2 | a0002c0004t0003g0021 a0002c0004t0003g0068 |
3 | HG01069.hp1 HG01071.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.986+145_986+162dup others(18): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | |||||||
| chr7:140046721 | A | AGTGTGTG others(13): Show |
1 | a0002c0004t0003g0019 | 2 | HG00738.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.986+143_986+162dup others(20): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | |||||||
| chr7:140046721 | AGT | A | 70 | a0001c0001t0002g0010 a0001c0001t0002g0016 a0001c0001t0002g0017 others(67): Show |
79 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.986+161_986+162del others(2): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | |||||||
| chr7:140046721 | AGTGT | A | 129 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0077 others(126): Show |
175 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.986+159_986+162del others(4): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | |||||||
| chr7:140046721 | AGTGTGT | A | 5 | a0001c0001t0002g0229 a0001c0001t0003g0131 a0001c0002t0001g0039 others(2): Show |
6 | HG01168.hp1 HG01169.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.986+157_986+162del others(6): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | |||||||
| chr7:140046721 | AGTGTGTG others(1): Show |
A | 3 | a0001c0002t0001g0201 a0004c0010t0002g0121 a0004c0010t0002g0170 |
3 | HG00140.hp2 HG01074.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.986+155_986+162del others(8): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046721 | |||||||
| chr7:140046799 | A | AGT | 14 | a0001c0001t0002g0006 a0001c0001t0002g0018 a0001c0001t0002g0025 others(11): Show |
19 | HG00099.hp2 HG00438.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.986+83_986+84dupAC | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | |||||||
| chr7:140046799 | A | AGTGT | 19 | a0001c0001t0002g0090 a0001c0001t0002g0139 a0001c0001t0002g0171 others(16): Show |
20 | HG00408.hp2 HG00639.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.986+81_986+84dupAC others(2): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | |||||||
| chr7:140046799 | A | AGTGTGT | 23 | a0001c0001t0003g0181 a0001c0003t0001g0028 a0001c0003t0001g0154 others(20): Show |
27 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.986+79_986+84dupAC others(4): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | |||||||
| chr7:140046799 | A | AGTGTGTG others(1): Show |
5 | a0001c0003t0003g0073 a0001c0003t0003g0074 a0001c0003t0003g0134 others(2): Show |
6 | HG00738.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.986+77_986+84dupAC others(6): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | |||||||
| chr7:140046799 | A | AGTGTGTG others(3): Show |
5 | a0001c0003t0003g0027 a0001c0003t0003g0031 a0001c0003t0003g0133 others(2): Show |
7 | HG01175.hp1 HG02258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.986+75_986+84dupAC others(8): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | |||||||
| chr7:140046799 | A | AGTGTGTG others(5): Show |
1 | a0003c0007t0003g0183 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.986+73_986+84dupAC others(10): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | |||||||
| chr7:140046799 | A | AGTGTGTG others(7): Show |
5 | a0001c0001t0003g0131 a0003c0007t0003g0176 a0003c0007t0004g0282 others(2): Show |
5 | HG02280.hp2 HG03130.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.986+71_986+84dupAC others(12): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | |||||||
| chr7:140046799 | A | AGTGTGTG others(9): Show |
1 | a0003c0007t0003g0177 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.986+69_986+84dupAC others(14): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | |||||||
| chr7:140046799 | A | AGTGTGTG others(11): Show |
1 | a0003c0007t0013g0283 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.986+67_986+84dupAC others(16): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | |||||||
| chr7:140046799 | AGTGT | A | 4 | a0001c0001t0002g0057 a0001c0001t0002g0180 a0001c0002t0001g0042 others(1): Show |
5 | HG01891.hp2 HG04184.hp2 NA19086.hp1 others(2): Show |
intron_variant | MODIFIER | c.986+81_986+84delAC others(2): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046799 | |||||||
| chr7:140046832 | G | C | 2 | a0001c0002t0001g0042 a0001c0002t0001g0246 |
3 | HG01891.hp2 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.986+52C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046832 | |||||||
| chr7:140046833 | T | A | 2 | a0001c0002t0001g0042 a0001c0002t0001g0246 |
3 | HG01891.hp2 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.986+51A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046833 | |||||||
| chr7:140046833 | T | TGTCA | 5 | a0001c0002t0001g0037 a0001c0002t0001g0185 a0001c0002t0001g0213 others(2): Show |
6 | HG00423.hp2 HG01243.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.986+50_986+51insTG others(2): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046833 | |||||||
| chr7:140046833 | T | TGTGTCA | 9 | a0001c0002t0001g0029 a0001c0002t0001g0041 a0001c0002t0001g0045 others(6): Show |
12 | HG01952.hp1 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.986+50_986+51insTG others(4): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046833 | |||||||
| chr7:140046833 | T | TGTGTGTC others(1): Show |
13 | a0001c0001t0002g0239 a0001c0002t0001g0011 a0001c0002t0001g0161 others(10): Show |
20 | HG00099.hp1 HG00673.hp2 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.986+50_986+51insTG others(6): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046833 | |||||||
| chr7:140046833 | T | TGTGTGTG others(3): Show |
20 | a0001c0002t0001g0034 a0001c0002t0001g0040 a0001c0002t0001g0162 others(17): Show |
22 | HG01106.hp1 HG01123.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.986+50_986+51insTG others(8): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046833 | |||||||
| chr7:140046833 | T | TGTGTGTG others(5): Show |
39 | a0001c0002t0001g0005 a0001c0002t0001g0007 a0001c0002t0001g0008 others(36): Show |
58 | HG00423.hp1 HG00597.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.986+50_986+51insTG others(10): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046833 | |||||||
| chr7:140046833 | T | TGTGTGTG others(7): Show |
17 | a0001c0002t0001g0015 a0001c0002t0001g0036 a0001c0002t0001g0039 others(14): Show |
21 | HG00408.hp1 HG01069.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.986+50_986+51insTG others(12): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046833 | |||||||
| chr7:140046833 | T | TGTGTGTG others(11): Show |
2 | a0001c0002t0001g0216 a0001c0002t0001g0251 |
2 | HG02258.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.986+50_986+51insTG others(16): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 5/11 | chr7 | 140046833 | |||||||
| chr7:140047123 | G | A | 2 | a0001c0001t0005g0165 a0001c0001t0005g0167 |
2 | HG01123.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.863-116C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047123 | |||||||
| chr7:140047215 | T | C | 1 | a0003c0005t0004g0273 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.863-208A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047215 | |||||||
| chr7:140047319 | G | A | 1 | a0001c0002t0012g0247 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.863-312C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047319 | |||||||
| chr7:140047334 | C | T | 1 | a0001c0001t0007g0089 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.863-327G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047334 | |||||||
| chr7:140047349 | G | T | 1 | a0001c0001t0002g0088 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.863-342C>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047349 | |||||||
| chr7:140047500 | C | T | 12 | a0001c0003t0003g0027 a0001c0003t0003g0031 a0001c0003t0003g0073 others(9): Show |
14 | HG01175.hp1 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.863-493G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047500 | |||||||
| chr7:140047502 | T | C | 1 | a0001c0001t0002g0108 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.863-495A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047502 | |||||||
| chr7:140047622 | C | A | 2 | a0001c0002t0001g0215 a0001c0002t0001g0220 |
2 | NA18983.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.863-615G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047622 | |||||||
| chr7:140047674 | G | A | 1 | a0001c0002t0001g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.863-667C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047674 | |||||||
| chr7:140047768 | C | A | 2 | a0003c0005t0004g0279 a0003c0005t0004g0280 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.863-761G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140047768 | |||||||
| chr7:140048194 | A | G | 1 | a0001c0001t0002g0124 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.863-1187T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140048194 | |||||||
| chr7:140048201 | C | T | 1 | a0001c0001t0002g0087 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.863-1194G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140048201 | |||||||
| chr7:140048258 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.863-1251G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140048258 | |||||||
| chr7:140048411 | G | A | 2 | a0001c0001t0003g0131 a0001c0001t0003g0181 |
2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.863-1404C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140048411 | |||||||
| chr7:140048531 | T | C | 1 | a0001c0001t0002g0106 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.863-1524A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140048531 | |||||||
| chr7:140048939 | C | G | 168 | a0001c0001t0002g0171 a0001c0001t0005g0164 a0001c0001t0005g0165 others(165): Show |
214 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.863-1932G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140048939 | |||||||
| chr7:140048992 | T | C | 1 | a0002c0004t0003g0020 | 2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.863-1985A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140048992 | |||||||
| chr7:140049110 | TG | T | 11 | a0001c0001t0002g0171 a0001c0001t0005g0164 a0001c0001t0005g0165 others(8): Show |
13 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.863-2104delC | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049110 | |||||||
| chr7:140049159 | T | C | 22 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(19): Show |
23 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.863-2152A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049159 | |||||||
| chr7:140049249 | C | T | 22 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(19): Show |
23 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.863-2242G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049249 | |||||||
| chr7:140049250 | C | G | 1 | a0001c0003t0003g0073 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.863-2243G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049250 | |||||||
| chr7:140049258 | G | T | 168 | a0001c0001t0002g0171 a0001c0001t0005g0164 a0001c0001t0005g0165 others(165): Show |
214 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(211): Show |
intron_variant | MODIFIER | c.863-2251C>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049258 | |||||||
| chr7:140049471 | G | C | 3 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0002g0118 |
3 | HG00438.hp1 NA18959.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.863-2464C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049471 | |||||||
| chr7:140049546 | G | A | 104 | a0001c0002t0001g0005 a0001c0002t0001g0007 a0001c0002t0001g0008 others(101): Show |
140 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.863-2539C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049546 | |||||||
| chr7:140049814 | A | G | 4 | a0001c0002t0001g0174 a0001c0002t0001g0175 a0001c0002t0001g0238 others(1): Show |
4 | HG00673.hp2 HG02074.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.863-2807T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049814 | |||||||
| chr7:140049918 | T | G | 1 | a0001c0002t0001g0227 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.863-2911A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049918 | |||||||
| chr7:140049992 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.863-2985G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049992 | |||||||
| chr7:140049993 | C | T | 2 | a0001c0009t0001g0259 a0001c0009t0001g0266 |
2 | HG01433.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.863-2986G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140049993 | |||||||
| chr7:140050148 | G | A | 3 | a0001c0002t0001g0224 a0001c0002t0001g0264 a0001c0002t0001g0265 |
3 | HG00673.hp1 NA18971.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.863-3141C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140050148 | |||||||
| chr7:140050185 | C | G | 1 | a0001c0002t0001g0237 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.863-3178G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140050185 | |||||||
| chr7:140050644 | G | A | 1 | a0001c0009t0001g0266 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.863-3637C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140050644 | |||||||
| chr7:140051159 | T | C | 1 | a0001c0001t0002g0109 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.862+3503A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051159 | |||||||
| chr7:140051198 | G | A | 11 | a0001c0001t0002g0171 a0001c0001t0005g0164 a0001c0001t0005g0165 others(8): Show |
13 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.862+3464C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051198 | |||||||
| chr7:140051205 | A | G | 2 | a0005c0011t0003g0184 a0005c0011t0003g0187 |
2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.862+3457T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051205 | |||||||
| chr7:140051217 | T | C | 11 | a0001c0001t0002g0171 a0001c0001t0005g0164 a0001c0001t0005g0165 others(8): Show |
13 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.862+3445A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051217 | |||||||
| chr7:140051270 | A | G | 2 | a0003c0005t0004g0044 a0003c0005t0004g0276 |
3 | HG03041.hp2 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.862+3392T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051270 | |||||||
| chr7:140051423 | C | T | 1 | a0001c0002t0001g0250 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.862+3239G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051423 | |||||||
| chr7:140051430 | G | A | 2 | a0001c0001t0002g0026 a0001c0001t0002g0130 |
3 | HG03491.hp2 HG03492.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.862+3232C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051430 | |||||||
| chr7:140051448 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.862+3214A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051448 | |||||||
| chr7:140051552 | A | G | 169 | a0001c0001t0002g0171 a0001c0001t0002g0239 a0001c0001t0005g0164 others(166): Show |
215 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.862+3110T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051552 | |||||||
| chr7:140051580 | A | G | 22 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(19): Show |
23 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.862+3082T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051580 | |||||||
| chr7:140051603 | C | T | 2 | a0001c0001t0002g0052 a0001c0001t0002g0086 |
2 | NA18947.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.862+3059G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051603 | |||||||
| chr7:140051643 | G | A | 1 | a0001c0001t0003g0181 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.862+3019C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051643 | |||||||
| chr7:140051861 | T | C | 8 | a0001c0001t0002g0171 a0001c0001t0005g0164 a0001c0001t0005g0165 others(5): Show |
9 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.862+2801A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051861 | |||||||
| chr7:140051922 | T | C | 1 | a0008c0016t0003g0160 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.862+2740A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140051922 | |||||||
| chr7:140052387 | A | C | 1 | a0001c0002t0001g0202 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.862+2275T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052387 | |||||||
| chr7:140052521 | T | C | 1 | a0003c0005t0004g0281 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.862+2141A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052521 | |||||||
| chr7:140052672 | GAACTCCA others(3): Show |
G | 2 | a0001c0002t0001g0235 a0001c0002t0001g0236 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.862+1980_862+1989d others(12): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052672 | |||||||
| chr7:140052732 | T | G | 1 | a0001c0001t0002g0058 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.862+1930A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | |||||||
| chr7:140052732 | T | TGTG | 3 | a0001c0002t0001g0215 a0001c0002t0001g0248 a0001c0002t0001g0249 |
3 | HG03471.hp1 HG03471.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.862+1929_862+1930i others(5): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | |||||||
| chr7:140052732 | T | TTG | 28 | a0001c0001t0002g0025 a0001c0001t0002g0047 a0001c0001t0002g0110 others(25): Show |
35 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.862+1928_862+1929d others(4): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | |||||||
| chr7:140052732 | T | TTGTG | 93 | a0001c0001t0002g0006 a0001c0001t0002g0059 a0001c0001t0002g0117 others(90): Show |
128 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.862+1926_862+1929d others(6): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | |||||||
| chr7:140052732 | T | TTGTGTG | 21 | a0001c0001t0002g0119 a0001c0002t0001g0013 a0001c0002t0001g0175 others(18): Show |
23 | HG00639.hp1 HG01167.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.862+1924_862+1929d others(8): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | |||||||
| chr7:140052732 | T | TTGTGTGT others(1): Show |
4 | a0001c0002t0001g0014 a0001c0002t0001g0162 a0001c0002t0001g0258 others(1): Show |
6 | HG03130.hp2 NA18968.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.862+1922_862+1929d others(10): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | |||||||
| chr7:140052732 | T | TTGTGTGT others(3): Show |
1 | a0003c0007t0003g0183 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.862+1920_862+1929d others(12): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | |||||||
| chr7:140052732 | TTG | T | 11 | a0001c0001t0002g0081 a0001c0001t0002g0138 a0001c0001t0003g0181 others(8): Show |
11 | HG01123.hp2 HG02273.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.862+1928_862+1929d others(4): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | |||||||
| chr7:140052732 | TTGTG | T | 4 | a0001c0001t0002g0010 a0001c0001t0002g0180 a0003c0005t0004g0281 others(1): Show |
6 | HG01261.hp2 HG02083.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.862+1926_862+1929d others(6): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | |||||||
| chr7:140052732 | TTGTGTG | T | 12 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(9): Show |
13 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.862+1924_862+1929d others(8): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140052732 | |||||||
| chr7:140053090 | T | TAA | 171 | a0001c0001t0002g0171 a0001c0001t0002g0239 a0001c0001t0003g0131 others(168): Show |
217 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.862+1571_862+1572i others(4): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140053090 | |||||||
| chr7:140053172 | G | T | 1 | a0001c0002t0001g0075 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.862+1490C>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140053172 | |||||||
| chr7:140053280 | T | C | 171 | a0001c0001t0002g0171 a0001c0001t0002g0239 a0001c0001t0003g0131 others(168): Show |
217 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.862+1382A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140053280 | |||||||
| chr7:140053631 | G | A | 171 | a0001c0001t0002g0171 a0001c0001t0002g0239 a0001c0001t0003g0131 others(168): Show |
217 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.862+1031C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140053631 | |||||||
| chr7:140053801 | A | T | 1 | a0001c0001t0003g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.862+861T>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140053801 | |||||||
| chr7:140053805 | T | C | 15 | a0002c0004t0003g0019 a0002c0004t0003g0020 a0002c0004t0003g0021 others(12): Show |
19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.862+857A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140053805 | |||||||
| chr7:140053899 | G | A | 1 | a0001c0001t0003g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.862+763C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140053899 | |||||||
| chr7:140053953 | A | C | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.862+709T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140053953 | |||||||
| chr7:140054096 | A | G | 1 | a0008c0016t0003g0160 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.862+566T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140054096 | |||||||
| chr7:140054219 | C | A | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.862+443G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140054219 | |||||||
| chr7:140054322 | C | T | 2 | a0001c0002t0001g0226 a0001c0002t0001g0227 |
2 | HG01069.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.862+340G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140054322 | |||||||
| chr7:140054473 | T | C | 7 | a0003c0007t0003g0176 a0003c0007t0003g0177 a0003c0007t0003g0183 others(4): Show |
7 | HG02486.hp1 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.862+189A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140054473 | |||||||
| chr7:140054646 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.862+16C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140054646 | |||||||
| chr7:140054651 | T | C | 169 | a0001c0001t0002g0171 a0001c0001t0002g0239 a0001c0001t0005g0164 others(166): Show |
215 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.862+11A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 4/11 | chr7 | 140054651 | |||||||
| chr7:140054885 | G | A | 11 | a0001c0001t0002g0171 a0001c0001t0005g0164 a0001c0001t0005g0165 others(8): Show |
13 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.761-122C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140054885 | |||||||
| chr7:140055019 | T | C | 169 | a0001c0001t0002g0171 a0001c0001t0002g0239 a0001c0001t0005g0164 others(166): Show |
215 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.761-256A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055019 | |||||||
| chr7:140055149 | C | G | 1 | a0003c0007t0013g0283 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.761-386G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055149 | |||||||
| chr7:140055179 | T | A | 11 | a0001c0001t0002g0171 a0001c0001t0005g0164 a0001c0001t0005g0165 others(8): Show |
13 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.761-416A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055179 | |||||||
| chr7:140055194 | A | C | 1 | a0001c0001t0002g0085 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.761-431T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055194 | |||||||
| chr7:140055372 | T | A | 1 | a0001c0001t0003g0181 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.761-609A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055372 | |||||||
| chr7:140055504 | A | C | 22 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(19): Show |
23 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.761-741T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055504 | |||||||
| chr7:140055507 | C | T | 1 | a0001c0008t0002g0084 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.761-744G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055507 | |||||||
| chr7:140055597 | C | T | 1 | a0001c0003t0003g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.761-834G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055597 | |||||||
| chr7:140055624 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.761-861G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055624 | |||||||
| chr7:140055629 | G | A | 1 | a0009c0017t0003g0271 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.761-866C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055629 | |||||||
| chr7:140055698 | A | G | 1 | a0001c0001t0002g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.761-935T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055698 | |||||||
| chr7:140055726 | A | G | 3 | a0002c0004t0003g0067 a0002c0004t0003g0071 a0002c0004t0003g0072 |
3 | HG02698.hp1 HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.761-963T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055726 | |||||||
| chr7:140055859 | C | A | 1 | a0001c0006t0001g0221 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.760+997G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140055859 | |||||||
| chr7:140056045 | A | G | 4 | a0001c0001t0002g0009 a0001c0001t0002g0081 a0001c0001t0002g0082 others(1): Show |
6 | HG01346.hp1 HG01928.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.760+811T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056045 | |||||||
| chr7:140056378 | T | C | 15 | a0002c0004t0003g0019 a0002c0004t0003g0020 a0002c0004t0003g0021 others(12): Show |
19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.760+478A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056378 | |||||||
| chr7:140056434 | T | C | 1 | a0001c0001t0002g0120 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.760+422A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056434 | |||||||
| chr7:140056545 | T | G | 8 | a0001c0003t0003g0027 a0001c0003t0003g0073 a0001c0003t0003g0074 others(5): Show |
9 | HG01175.hp1 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.760+311A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056545 | |||||||
| chr7:140056658 | A | T | 171 | a0001c0001t0002g0171 a0001c0001t0002g0239 a0001c0001t0003g0131 others(168): Show |
217 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.760+198T>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056658 | |||||||
| chr7:140056675 | T | G | 1 | a0001c0002t0001g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+181A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056675 | |||||||
| chr7:140056677 | T | A | 1 | a0001c0002t0001g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+179A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056677 | |||||||
| chr7:140056679 | C | T | 1 | a0001c0002t0001g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+177G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056679 | |||||||
| chr7:140056681 | C | G | 1 | a0001c0002t0001g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+175G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056681 | |||||||
| chr7:140056682 | A | G | 1 | a0001c0002t0001g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+174T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056682 | |||||||
| chr7:140056684 | C | T | 1 | a0001c0002t0001g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+172G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056684 | |||||||
| chr7:140056686 | C | G | 2 | a0001c0008t0002g0049 a0001c0008t0002g0079 |
2 | HG01192.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.760+170G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056686 | |||||||
| chr7:140056687 | C | T | 1 | a0001c0002t0001g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+169G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056687 | |||||||
| chr7:140056688 | G | C | 1 | a0001c0002t0001g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+168C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056688 | |||||||
| chr7:140056698 | C | T | 1 | a0001c0002t0001g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+158G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056698 | |||||||
| chr7:140056700 | TTGTTAGG others(3): Show |
T | 1 | a0001c0002t0001g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+146_760+155del others(10): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056700 | |||||||
| chr7:140056716 | A | G | 1 | a0001c0002t0001g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.760+140T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 3/11 | chr7 | 140056716 | |||||||
| chr7:140057201 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.463-48C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 2/11 | chr7 | 140057201 | |||||||
| chr7:140057271 | A | G | 1 | a0001c0001t0002g0143 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.463-118T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 2/11 | chr7 | 140057271 | |||||||
| chr7:140057336 | G | T | 154 | a0001c0001t0002g0171 a0001c0001t0002g0239 a0001c0001t0005g0164 others(151): Show |
196 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.463-183C>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 2/11 | chr7 | 140057336 | |||||||
| chr7:140057375 | C | T | 1 | a0001c0001t0003g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.463-222G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 2/11 | chr7 | 140057375 | |||||||
| chr7:140057498 | CTCA | C | 20 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(17): Show |
21 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.463-348_463-346del others(3): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 2/11 | chr7 | 140057498 | |||||||
| chr7:140057816 | A | T | 1 | a0001c0001t0002g0142 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.462+83T>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 2/11 | chr7 | 140057816 | |||||||
| chr7:140058111 | C | G | 36 | a0002c0004t0003g0019 a0002c0004t0003g0020 a0002c0004t0003g0021 others(33): Show |
41 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.327-77G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058111 | |||||||
| chr7:140058111 | C | T | 1 | a0001c0001t0002g0077 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.327-77G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058111 | |||||||
| chr7:140058180 | T | C | 29 | a0001c0002t0001g0008 a0001c0002t0001g0038 a0001c0002t0001g0163 others(26): Show |
34 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.327-146A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058180 | |||||||
| chr7:140058196 | C | T | 1 | a0001c0002t0001g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.327-162G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058196 | |||||||
| chr7:140058253 | C | T | 169 | a0001c0001t0002g0171 a0001c0001t0002g0239 a0001c0001t0005g0164 others(166): Show |
215 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.327-219G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058253 | |||||||
| chr7:140058294 | G | A | 9 | a0001c0001t0002g0171 a0001c0001t0005g0164 a0001c0001t0005g0165 others(6): Show |
10 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.327-260C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058294 | |||||||
| chr7:140058336 | C | T | 15 | a0002c0004t0003g0019 a0002c0004t0003g0020 a0002c0004t0003g0021 others(12): Show |
19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.327-302G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058336 | |||||||
| chr7:140058355 | T | C | 9 | a0002c0004t0003g0021 a0002c0004t0003g0022 a0002c0004t0003g0067 others(6): Show |
11 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.327-321A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058355 | |||||||
| chr7:140058389 | T | C | 1 | a0001c0002t0001g0225 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.327-355A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058389 | |||||||
| chr7:140058395 | C | A | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.327-361G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058395 | |||||||
| chr7:140058416 | C | A | 1 | a0001c0001t0002g0182 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.327-382G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058416 | |||||||
| chr7:140058435 | C | T | 1 | a0003c0007t0003g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.327-401G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058435 | |||||||
| chr7:140058492 | T | A | 1 | a0001c0001t0002g0150 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.327-458A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058492 | |||||||
| chr7:140058575 | G | A | 20 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(17): Show |
21 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.327-541C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058575 | |||||||
| chr7:140058619 | C | T | 1 | a0005c0011t0003g0184 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.327-585G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058619 | |||||||
| chr7:140058629 | G | C | 1 | a0001c0001t0005g0164 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.327-595C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058629 | |||||||
| chr7:140058676 | C | T | 154 | a0001c0001t0002g0171 a0001c0001t0002g0239 a0001c0001t0005g0164 others(151): Show |
196 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.327-642G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058676 | |||||||
| chr7:140058792 | A | G | 1 | a0001c0002t0001g0038 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.327-758T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058792 | |||||||
| chr7:140058815 | G | C | 120 | a0001c0001t0002g0239 a0001c0002t0001g0005 a0001c0002t0001g0007 others(117): Show |
159 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.327-781C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058815 | |||||||
| chr7:140058885 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.327-851G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058885 | |||||||
| chr7:140058894 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.327-860C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058894 | |||||||
| chr7:140058921 | A | C | 154 | a0001c0001t0002g0171 a0001c0001t0002g0239 a0001c0001t0005g0164 others(151): Show |
196 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.327-887T>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058921 | |||||||
| chr7:140058929 | C | A | 1 | a0001c0001t0002g0123 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.327-895G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058929 | |||||||
| chr7:140058959 | G | C | 1 | a0001c0001t0002g0151 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.327-925C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140058959 | |||||||
| chr7:140059026 | C | T | 122 | a0001c0001t0002g0239 a0001c0002t0001g0005 a0001c0002t0001g0007 others(119): Show |
161 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.327-992G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059026 | |||||||
| chr7:140059083 | G | A | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.327-1049C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059083 | |||||||
| chr7:140059088 | T | A | 2 | a0001c0002t0001g0226 a0001c0002t0001g0227 |
2 | HG01069.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.327-1054A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059088 | |||||||
| chr7:140059261 | T | C | 1 | a0003c0005t0004g0281 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.327-1227A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059261 | |||||||
| chr7:140059355 | C | T | 1 | a0001c0001t0005g0164 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.327-1321G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059355 | |||||||
| chr7:140059361 | T | TAC | 16 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(13): Show |
17 | HG01243.hp1 HG01346.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.327-1329_327-1328d others(4): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059361 | |||||||
| chr7:140059361 | T | TACAC | 12 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(9): Show |
13 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.327-1331_327-1328d others(6): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059361 | |||||||
| chr7:140059361 | TAC | T | 104 | a0001c0001t0002g0239 a0001c0001t0003g0131 a0001c0002t0001g0005 others(101): Show |
140 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.327-1329_327-1328d others(4): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059361 | |||||||
| chr7:140059361 | TACACACA others(1): Show |
T | 13 | a0001c0001t0002g0171 a0001c0001t0005g0164 a0001c0001t0005g0165 others(10): Show |
15 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.327-1335_327-1328d others(10): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059361 | |||||||
| chr7:140059363 | C | T | 1 | a0003c0007t0003g0183 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.327-1329G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059363 | |||||||
| chr7:140059402 | C | CTCT | 111 | a0001c0001t0002g0239 a0001c0002t0001g0005 a0001c0002t0001g0007 others(108): Show |
148 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.327-1369_327-1368i others(5): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059402 | |||||||
| chr7:140059402 | C | CTCTT | 36 | a0001c0001t0002g0171 a0001c0001t0003g0131 a0001c0001t0003g0181 others(33): Show |
43 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.327-1369_327-1368i others(6): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059402 | |||||||
| chr7:140059402 | C | CTCTTT | 24 | a0001c0003t0001g0028 a0001c0003t0001g0154 a0001c0003t0001g0155 others(21): Show |
26 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.327-1369_327-1368i others(7): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059402 | |||||||
| chr7:140059534 | G | A | 4 | a0001c0001t0002g0026 a0001c0001t0002g0128 a0001c0001t0002g0129 others(1): Show |
5 | HG02451.hp2 HG02559.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.327-1500C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059534 | |||||||
| chr7:140059778 | G | A | 1 | a0001c0002t0001g0173 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.327-1744C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059778 | |||||||
| chr7:140059795 | G | A | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.327-1761C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059795 | |||||||
| chr7:140059820 | C | T | 5 | a0001c0001t0005g0164 a0001c0001t0005g0165 a0001c0001t0005g0166 others(2): Show |
5 | HG01123.hp2 HG01361.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.327-1786G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059820 | |||||||
| chr7:140059827 | C | T | 21 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(18): Show |
22 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.327-1793G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059827 | |||||||
| chr7:140059930 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.327-1896C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140059930 | |||||||
| chr7:140060202 | C | T | 120 | a0001c0001t0002g0239 a0001c0002t0001g0005 a0001c0002t0001g0007 others(117): Show |
159 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.327-2168G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140060202 | |||||||
| chr7:140060210 | T | C | 171 | a0001c0001t0002g0171 a0001c0001t0002g0239 a0001c0001t0003g0131 others(168): Show |
217 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.327-2176A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140060210 | |||||||
| chr7:140060491 | T | C | 1 | a0001c0002t0001g0014 | 3 | NA18968.hp2 NA18974.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.326+2031A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140060491 | |||||||
| chr7:140060538 | G | C | 1 | a0001c0001t0002g0062 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.326+1984C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140060538 | |||||||
| chr7:140060740 | TCCCTGCT others(3): Show |
T | 121 | a0001c0001t0002g0239 a0001c0002t0001g0005 a0001c0002t0001g0007 others(118): Show |
160 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.326+1772_326+1781d others(12): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140060740 | |||||||
| chr7:140060849 | G | C | 1 | a0001c0001t0002g0152 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.326+1673C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140060849 | |||||||
| chr7:140060855 | C | T | 1 | a0003c0007t0003g0183 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.326+1667G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140060855 | |||||||
| chr7:140060898 | C | G | 3 | a0001c0003t0001g0028 a0001c0003t0001g0154 a0001c0003t0001g0155 |
4 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+1624G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140060898 | |||||||
| chr7:140060987 | C | T | 1 | a0001c0002t0001g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.326+1535G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140060987 | |||||||
| chr7:140061202 | T | G | 15 | a0002c0004t0003g0019 a0002c0004t0003g0020 a0002c0004t0003g0021 others(12): Show |
19 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.326+1320A>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061202 | |||||||
| chr7:140061326 | T | C | 1 | a0001c0001t0002g0182 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.326+1196A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061326 | |||||||
| chr7:140061341 | G | A | 8 | a0001c0001t0002g0171 a0001c0001t0005g0164 a0001c0001t0005g0165 others(5): Show |
9 | HG01123.hp2 HG01261.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.326+1181C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061341 | |||||||
| chr7:140061360 | T | A | 11 | a0003c0007t0003g0176 a0003c0007t0003g0177 a0003c0007t0003g0183 others(8): Show |
11 | HG02055.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.326+1162A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061360 | |||||||
| chr7:140061376 | T | A | 120 | a0001c0001t0002g0239 a0001c0002t0001g0005 a0001c0002t0001g0007 others(117): Show |
159 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.326+1146A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061376 | |||||||
| chr7:140061448 | A | G | 104 | a0001c0001t0002g0239 a0001c0002t0001g0005 a0001c0002t0001g0007 others(101): Show |
140 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.326+1074T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061448 | |||||||
| chr7:140061452 | T | TACAC | 11 | a0003c0005t0003g0156 a0003c0005t0004g0044 a0003c0005t0004g0273 others(8): Show |
12 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.326+1066_326+1069d others(6): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061452 | |||||||
| chr7:140061568 | G | T | 1 | a0001c0002t0001g0230 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.326+954C>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061568 | |||||||
| chr7:140061663 | C | T | 149 | a0001c0001t0002g0171 a0001c0001t0002g0239 a0001c0001t0005g0164 others(146): Show |
191 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.326+859G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061663 | |||||||
| chr7:140061699 | C | A | 2 | a0002c0004t0003g0071 a0002c0004t0003g0072 |
2 | HG02698.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.326+823G>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061699 | |||||||
| chr7:140061842 | T | C | 1 | a0001c0001t0002g0171 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.326+680A>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061842 | |||||||
| chr7:140061871 | GT | G | 12 | a0001c0003t0003g0027 a0001c0003t0003g0031 a0001c0003t0003g0073 others(9): Show |
14 | HG01175.hp1 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.326+650delA | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061871 | |||||||
| chr7:140061983 | CG | C | 139 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0009 others(136): Show |
178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.326+538delC | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061983 | |||||||
| chr7:140061983 | CGG | C | 70 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 others(67): Show |
87 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.326+537_326+538del others(2): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061983 | |||||||
| chr7:140061986 | G | C | 1 | a0001c0002t0001g0269 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.326+536C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061986 | |||||||
| chr7:140061989 | G | A | 1 | a0001c0002t0001g0270 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.326+533C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061989 | |||||||
| chr7:140061993 | G | C | 1 | a0007c0015t0009g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.326+529C>G | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061993 | |||||||
| chr7:140061994 | G | GA | 4 | a0001c0003t0003g0031 a0001c0003t0003g0189 a0001c0003t0003g0190 others(1): Show |
5 | HG01884.hp1 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.326+527_326+528ins others(1): Show |
PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140061994 | |||||||
| chr7:140062046 | A | G | 1 | a0001c0001t0002g0017 | 2 | NA18975.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.326+476T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062046 | |||||||
| chr7:140062096 | T | A | 167 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0142 others(164): Show |
218 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.326+426A>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062096 | |||||||
| chr7:140062318 | C | T | 4 | a0001c0001t0002g0016 a0001c0001t0002g0046 a0001c0001t0002g0047 others(1): Show |
5 | NA18962.hp1 NA19003.hp1 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.326+204G>A | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062318 | |||||||
| chr7:140062402 | G | A | 7 | a0003c0007t0003g0176 a0003c0007t0003g0177 a0003c0007t0004g0282 others(4): Show |
7 | HG02486.hp1 HG02615.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.326+120C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062402 | |||||||
| chr7:140062432 | C | G | 1 | a0001c0002t0001g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.326+90G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062432 | |||||||
| chr7:140062462 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.326+60C>T | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062462 | |||||||
| chr7:140062471 | T | TG | 7 | a0003c0007t0003g0176 a0003c0007t0003g0177 a0003c0007t0004g0282 others(4): Show |
7 | HG02486.hp1 HG02615.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.326+50dupC | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062471 | |||||||
| chr7:140062473 | A | G | 183 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(180): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.326+49T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062473 | |||||||
| chr7:140062477 | C | G | 7 | a0003c0007t0003g0176 a0003c0007t0003g0177 a0003c0007t0004g0282 others(4): Show |
7 | HG02486.hp1 HG02615.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.326+45G>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062477 | |||||||
| chr7:140062482 | A | G | 163 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(160): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.326+40T>C | PARP12 | ENSG00000059378.13 | transcript | ENST00000263549.8 | protein_coding | 1/11 | chr7 | 140062482 |