Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51588 |
| ensemblid | ENSG00000105229.7 |
| hgncid | 17002 |
| symbol | PIAS4 |
| name | protein inhibitor of activated STAT 4 |
| refseq_nuc | NM_015897.4 |
| refseq_prot | NP_056981.2 |
| ensembl_nuc | ENST00000262971.3 |
| ensembl_prot | ENSP00000262971.1 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 4007736 |
| end | 4039386 |
| strand | + |
| ver | v1.2 |
| region | chr19:4007736-4039386 |
| region5000 | chr19:4002736-4044386 |
| regionname0 | PIAS4_chr19_4007736_4039386 |
| regionname5000 | PIAS4_chr19_4002736_4044386 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 510 | 328 | 90 | 74 | 100 | 18 | 44 | 56 | PIAS4_chr19_4002736_4044386 | PIAS4 | MAAEL others(505): Show |
chr19 | 4002736 | 4044386 |
| a0002 | 0/0 | 510 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | MAAEL others(505): Show |
chr19 | 4002736 | 4044386 |
| a0003 | 0/0 | 510 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | MAAEL others(505): Show |
chr19 | 4002736 | 4044386 |
| a0004 | 0/0 | 510 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | MAAEL others(505): Show |
chr19 | 4002736 | 4044386 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1530 | 173 | 11 | 49 | 75 | 11 | 26 | PIAS4_chr19_4002736_4044386 | PIAS4 | ATGGC others(1525): Show |
chr19 | 4002736 | 4044386 | ||
| a0001c0002 | 0/0 | 1530 | 39 | 23 | 6 | 7 | 1 | 2 | PIAS4_chr19_4002736_4044386 | PIAS4 | ATGGC others(1525): Show |
chr19 | 4002736 | 4044386 | ||
| a0001c0003 | 0/0 | 1530 | 28 | 6 | 8 | 5 | 5 | 4 | PIAS4_chr19_4002736_4044386 | PIAS4 | ATGGC others(1525): Show |
chr19 | 4002736 | 4044386 | ||
| a0001c0004 | 0/0 | 1530 | 27 | 27 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | ATGGC others(1525): Show |
chr19 | 4002736 | 4044386 | ||
| a0001c0005 | 0/0 | 1530 | 23 | 8 | 4 | 2 | 0 | 9 | PIAS4_chr19_4002736_4044386 | PIAS4 | ATGGC others(1525): Show |
chr19 | 4002736 | 4044386 | ||
| a0001c0006 | 0/0 | 1530 | 12 | 12 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | ATGGC others(1525): Show |
chr19 | 4002736 | 4044386 | ||
| a0001c0007 | 0/0 | 1530 | 9 | 0 | 6 | 0 | 1 | 2 | PIAS4_chr19_4002736_4044386 | PIAS4 | ATGGC others(1525): Show |
chr19 | 4002736 | 4044386 | ||
| a0001c0008 | 1/0 | 1530 | 6 | 1 | 0 | 3 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | ATGGC others(1525): Show |
chr19 | 4002736 | 4044386 | ||
| a0001c0009 | 0/0 | 1530 | 5 | 0 | 0 | 5 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | ATGGC others(1525): Show |
chr19 | 4002736 | 4044386 | ||
| a0001c0012 | 0/0 | 1530 | 2 | 1 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | ATGGC others(1525): Show |
chr19 | 4002736 | 4044386 | ||
| a0001c0014 | 0/0 | 1530 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | ATGGC others(1525): Show |
chr19 | 4002736 | 4044386 | ||
| a0001c0015 | 0/0 | 1530 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | ATGGC others(1525): Show |
chr19 | 4002736 | 4044386 | ||
| a0001c0016 | 0/0 | 1530 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | ATGGC others(1525): Show |
chr19 | 4002736 | 4044386 | ||
| a0001c0017 | 0/0 | 1530 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | ATGGC others(1525): Show |
chr19 | 4002736 | 4044386 | ||
| a0002c0013 | 0/0 | 1530 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | ATGGC others(1525): Show |
chr19 | 4002736 | 4044386 | ||
| a0003c0011 | 0/0 | 1530 | 2 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | ATGGC others(1525): Show |
chr19 | 4002736 | 4044386 | ||
| a0004c0010 | 0/0 | 1530 | 2 | 0 | 0 | 0 | 0 | 2 | PIAS4_chr19_4002736_4044386 | PIAS4 | ATGGC others(1525): Show |
chr19 | 4002736 | 4044386 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3069 | 164 | 10 | 47 | 71 | 10 | 25 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0001t0009 | 0/0 | 3069 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0001t0010 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0001t0013 | 0/0 | 3069 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0001t0014 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0001t0016 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0001t0019 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0001t0021 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0001t0022 | 0/0 | 3069 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0002t0001 | 0/0 | 3069 | 16 | 5 | 5 | 5 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0002t0002 | 0/0 | 3067 | 3 | 0 | 0 | 1 | 0 | 2 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0002t0003 | 0/0 | 3067 | 4 | 3 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0002t0004 | 0/0 | 3067 | 11 | 11 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0002t0006 | 0/0 | 3067 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0002t0008 | 0/0 | 3067 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0002t0010 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0002t0018 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0002t0020 | 0/0 | 3067 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0003t0001 | 0/0 | 3069 | 4 | 0 | 2 | 1 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0003t0002 | 0/0 | 3067 | 17 | 2 | 5 | 2 | 4 | 4 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0003t0003 | 0/0 | 3067 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0003t0004 | 0/0 | 3067 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0003t0006 | 0/0 | 3067 | 4 | 2 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0003t0015 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0004t0003 | 0/0 | 3067 | 20 | 20 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0004t0004 | 0/0 | 3067 | 2 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0004t0008 | 0/0 | 3067 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0004t0011 | 0/0 | 3067 | 2 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0004t0012 | 0/0 | 3067 | 2 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0005t0001 | 0/0 | 3069 | 7 | 7 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0005t0005 | 0/0 | 3069 | 11 | 0 | 1 | 2 | 0 | 8 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0005t0007 | 0/0 | 3069 | 3 | 0 | 2 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0005t0017 | 0/0 | 3069 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0005t0023 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0006t0003 | 0/0 | 3067 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0006t0004 | 0/0 | 3067 | 10 | 10 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0006t0008 | 0/0 | 3067 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0007t0001 | 0/0 | 3069 | 4 | 0 | 1 | 0 | 1 | 2 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0007t0002 | 0/0 | 3067 | 5 | 0 | 5 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| a0001c0008t0001 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0008t0005 | 1/0 | 3069 | 5 | 0 | 0 | 3 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0009t0001 | 0/0 | 3069 | 5 | 0 | 0 | 5 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0012t0001 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0012t0005 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0014t0001 | 0/0 | 3069 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0015t0005 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0016t0001 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0001c0017t0001 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0002c0013t0001 | 0/0 | 3069 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0003c0011t0001 | 0/0 | 3069 | 2 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3064): Show |
chr19 | 4002736 | 4044386 |
| a0004c0010t0002 | 0/0 | 3067 | 2 | 0 | 0 | 0 | 0 | 2 | PIAS4_chr19_4002736_4044386 | PIAS4 | GGCGC others(3062): Show |
chr19 | 4002736 | 4044386 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0009g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0010g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0013g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0014g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0016g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0019g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0021g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0001t0022g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0008g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0010g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0018g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0002t0020g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0006g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0006g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0006g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0003t0015g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0003g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0008g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0011g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0012g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0004t0012g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0005g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0005g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0005g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0005g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0005g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0005g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0005g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0007g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0007g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0007g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0017g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0005t0023g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0006t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0006t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0006t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0006t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0006t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0006t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0006t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0006t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0006t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0006t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0006t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0006t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0007t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0007t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0007t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0007t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0007t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0007t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0007t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0007t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0008t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0008t0005g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0008t0005g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0008t0005g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0008t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0009t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0009t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0009t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0012t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0012t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0014t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0015t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0016t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0001c0017t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0002c0013t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0003c0011t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0003c0011t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0004c0010t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| a0004c0010t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | GBR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | GBR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0266 | EUR | FIN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | FIN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | FIN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | FIN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0283 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00423 | hp2 | a0001 | c0001 | t0016 | g0026 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00438 | hp1 | a0001 | c0001 | t0021 | g0094 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00558 | hp1 | a0001 | c0009 | t0001 | g0004 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00609 | hp1 | a0001 | c0012 | t0005 | g0229 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00609 | hp2 | a0001 | c0015 | t0005 | g0118 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00639 | hp1 | a0001 | c0005 | t0017 | g0022 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00642 | hp2 | a0002 | c0013 | t0001 | g0015 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00735 | hp2 | a0001 | c0014 | t0001 | g0191 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG00741 | hp2 | a0001 | c0003 | t0002 | g0265 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01070 | hp2 | a0002 | c0013 | t0001 | g0015 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0168 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01109 | hp2 | a0001 | c0002 | t0003 | g0198 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01168 | hp1 | a0001 | c0007 | t0002 | g0275 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01168 | hp2 | a0001 | c0005 | t0005 | g0263 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01169 | hp2 | a0001 | c0007 | t0002 | g0274 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0205 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01243 | hp1 | a0001 | c0003 | t0003 | g0218 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01243 | hp2 | a0001 | c0003 | t0002 | g0255 | AMR | PUR | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01255 | hp1 | a0001 | c0003 | t0002 | g0256 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01256 | hp1 | a0001 | c0001 | t0009 | g0073 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01256 | hp2 | a0001 | c0007 | t0001 | g0221 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01258 | hp2 | a0001 | c0001 | t0009 | g0076 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01261 | hp2 | a0001 | c0003 | t0002 | g0276 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01346 | hp2 | a0001 | c0003 | t0002 | g0264 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01361 | hp2 | a0001 | c0005 | t0007 | g0224 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0207 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01496 | hp1 | a0001 | c0005 | t0007 | g0227 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01515 | hp1 | a0001 | c0007 | t0001 | g0268 | EUR | IBS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01515 | hp2 | a0001 | c0003 | t0002 | g0023 | EUR | IBS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01516 | hp2 | a0001 | c0003 | t0002 | g0259 | EUR | IBS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01517 | hp1 | a0001 | c0003 | t0002 | g0023 | EUR | IBS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01517 | hp2 | a0001 | c0003 | t0002 | g0258 | EUR | IBS | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01884 | hp1 | a0001 | c0006 | t0004 | g0037 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01884 | hp2 | a0001 | c0005 | t0001 | g0251 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0167 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01891 | hp2 | a0001 | c0002 | t0004 | g0175 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02027 | hp1 | a0001 | c0008 | t0005 | g0017 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02055 | hp2 | a0001 | c0006 | t0004 | g0041 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02056 | hp1 | a0001 | c0008 | t0005 | g0113 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02071 | hp1 | a0001 | c0001 | t0014 | g0081 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02145 | hp1 | a0001 | c0004 | t0003 | g0240 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02145 | hp2 | a0001 | c0004 | t0003 | g0248 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02148 | hp2 | a0001 | c0007 | t0002 | g0025 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02155 | hp1 | a0001 | c0009 | t0001 | g0004 | EAS | CDX | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02155 | hp2 | a0001 | c0008 | t0005 | g0017 | EAS | CDX | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CDX | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02257 | hp1 | a0001 | c0006 | t0004 | g0033 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02257 | hp2 | a0001 | c0006 | t0004 | g0039 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02258 | hp1 | a0001 | c0003 | t0015 | g0206 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0179 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02280 | hp2 | a0001 | c0004 | t0003 | g0246 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02300 | hp2 | a0001 | c0007 | t0002 | g0025 | AMR | PEL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02451 | hp1 | a0001 | c0004 | t0003 | g0241 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02451 | hp2 | a0001 | c0006 | t0004 | g0029 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02572 | hp1 | a0001 | c0002 | t0004 | g0286 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02572 | hp2 | a0001 | c0002 | t0004 | g0161 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02602 | hp2 | a0001 | c0007 | t0001 | g0219 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02615 | hp1 | a0001 | c0017 | t0001 | g0030 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02615 | hp2 | a0001 | c0004 | t0003 | g0239 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02622 | hp1 | a0001 | c0002 | t0006 | g0196 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02622 | hp2 | a0001 | c0002 | t0008 | g0202 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02630 | hp1 | a0001 | c0002 | t0018 | g0125 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02630 | hp2 | a0001 | c0004 | t0003 | g0236 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02647 | hp1 | a0001 | c0006 | t0004 | g0036 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02647 | hp2 | a0001 | c0002 | t0004 | g0186 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02717 | hp1 | a0001 | c0003 | t0006 | g0279 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0216 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02738 | hp2 | a0001 | c0005 | t0005 | g0220 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02818 | hp1 | a0001 | c0006 | t0004 | g0031 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02818 | hp2 | a0001 | c0002 | t0004 | g0170 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02886 | hp1 | a0001 | c0005 | t0023 | g0232 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02886 | hp2 | a0001 | c0004 | t0003 | g0245 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02895 | hp1 | a0001 | c0005 | t0001 | g0042 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02895 | hp2 | a0003 | c0011 | t0001 | g0277 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02896 | hp1 | a0001 | c0004 | t0003 | g0292 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02896 | hp2 | a0001 | c0004 | t0004 | g0238 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02897 | hp1 | a0001 | c0004 | t0004 | g0237 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02897 | hp2 | a0003 | c0011 | t0001 | g0278 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02922 | hp1 | a0001 | c0004 | t0003 | g0244 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02922 | hp2 | a0001 | c0004 | t0012 | g0006 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02965 | hp1 | a0001 | c0005 | t0001 | g0253 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02965 | hp2 | a0001 | c0006 | t0004 | g0034 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02970 | hp1 | a0001 | c0003 | t0004 | g0217 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02970 | hp2 | a0001 | c0006 | t0004 | g0038 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02976 | hp2 | a0001 | c0002 | t0004 | g0192 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03041 | hp1 | a0001 | c0004 | t0003 | g0243 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03041 | hp2 | a0001 | c0004 | t0003 | g0007 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03098 | hp1 | a0001 | c0004 | t0003 | g0294 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03098 | hp2 | a0001 | c0002 | t0020 | g0288 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03139 | hp1 | a0001 | c0004 | t0003 | g0235 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03139 | hp2 | a0001 | c0004 | t0003 | g0007 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03209 | hp2 | a0001 | c0004 | t0011 | g0006 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03225 | hp1 | a0001 | c0006 | t0003 | g0032 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03225 | hp2 | a0001 | c0004 | t0003 | g0293 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0194 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03453 | hp2 | a0001 | c0002 | t0003 | g0197 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03486 | hp1 | a0001 | c0004 | t0003 | g0242 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03486 | hp2 | a0001 | c0004 | t0003 | g0291 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03490 | hp2 | a0004 | c0010 | t0002 | g0269 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03491 | hp1 | a0001 | c0003 | t0002 | g0261 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03491 | hp2 | a0001 | c0007 | t0001 | g0027 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03492 | hp1 | a0001 | c0003 | t0002 | g0260 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03492 | hp2 | a0004 | c0010 | t0002 | g0270 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03516 | hp1 | a0001 | c0002 | t0004 | g0154 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03516 | hp2 | a0001 | c0005 | t0001 | g0284 | AFR | ESN | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03540 | hp1 | a0001 | c0004 | t0003 | g0289 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03540 | hp2 | a0001 | c0002 | t0004 | g0287 | AFR | GWD | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03579 | hp1 | a0001 | c0004 | t0008 | g0290 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03579 | hp2 | a0001 | c0004 | t0003 | g0007 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0130 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03654 | hp2 | a0001 | c0003 | t0002 | g0024 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03688 | hp2 | a0001 | c0003 | t0002 | g0024 | SAS | STU | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03704 | hp1 | a0001 | c0001 | t0022 | g0060 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03704 | hp2 | a0001 | c0005 | t0005 | g0223 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03710 | hp1 | a0001 | c0008 | t0005 | g0061 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03834 | hp2 | a0001 | c0005 | t0005 | g0022 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03942 | hp1 | a0001 | c0005 | t0005 | g0228 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | STU | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG04184 | hp1 | a0001 | c0005 | t0005 | g0225 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0131 | SAS | BEB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG04199 | hp2 | a0001 | c0005 | t0005 | g0233 | SAS | STU | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG04204 | hp1 | a0001 | c0005 | t0005 | g0222 | SAS | STU | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18522 | hp1 | a0001 | c0004 | t0003 | g0247 | AFR | YRI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18522 | hp2 | a0001 | c0002 | t0003 | g0190 | AFR | YRI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18612 | hp2 | a0001 | c0005 | t0005 | g0230 | EAS | CHB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18747 | hp1 | a0001 | c0005 | t0005 | g0231 | EAS | CHB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | YRI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18906 | hp2 | a0001 | c0006 | t0008 | g0035 | AFR | YRI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18942 | hp1 | a0001 | c0009 | t0001 | g0004 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18968 | hp1 | a0001 | c0009 | t0001 | g0084 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18983 | hp1 | a0001 | c0003 | t0002 | g0272 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18983 | hp2 | a0001 | c0002 | t0010 | g0115 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18990 | hp2 | a0001 | c0016 | t0001 | g0111 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19007 | hp2 | a0001 | c0001 | t0010 | g0087 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19030 | hp1 | a0001 | c0006 | t0004 | g0040 | AFR | LWK | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19030 | hp2 | a0001 | c0001 | t0019 | g0183 | AFR | LWK | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19043 | hp2 | a0001 | c0005 | t0001 | g0249 | AFR | LWK | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19060 | hp2 | a0001 | c0009 | t0001 | g0085 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19079 | hp2 | a0001 | c0003 | t0006 | g0281 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19085 | hp1 | a0001 | c0003 | t0006 | g0280 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19089 | hp2 | a0001 | c0003 | t0002 | g0271 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19240 | hp1 | a0001 | c0005 | t0001 | g0250 | AFR | YRI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA19240 | hp2 | a0001 | c0002 | t0004 | g0171 | AFR | YRI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA20129 | hp1 | a0001 | c0003 | t0002 | g0257 | AFR | ASW | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA20129 | hp2 | a0001 | c0002 | t0004 | g0172 | AFR | ASW | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA20752 | hp1 | a0001 | c0001 | t0013 | g0048 | EUR | TSI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0200 | EUR | TSI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA20905 | hp1 | a0001 | c0005 | t0007 | g0267 | SAS | GIH | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA20905 | hp2 | a0001 | c0005 | t0005 | g0226 | SAS | GIH | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG01123 | hp2 | a0001 | c0007 | t0002 | g0273 | AMR | CLM | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02486 | hp1 | a0001 | c0003 | t0006 | g0282 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02486 | hp2 | a0001 | c0004 | t0011 | g0006 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02559 | hp1 | a0001 | c0008 | t0001 | g0169 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03471 | hp1 | a0001 | c0002 | t0004 | g0203 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG03471 | hp2 | a0001 | c0012 | t0001 | g0285 | AFR | MSL | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG06807 | hp1 | a0001 | c0004 | t0012 | g0234 | AFR | USA | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | USA | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA20300 | hp1 | a0001 | c0005 | t0001 | g0252 | AFR | USA | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | USA | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0182 | AFR | LWK | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| NA21309 | hp2 | a0001 | c0003 | t0002 | g0262 | AFR | LWK | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0149 | REF | REF | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| homoSapiens | grch38p0 | a0001 | c0008 | t0005 | g0079 | REF | REF | PIAS4_chr19_4002736_4044386 | PIAS4 | chr19 | 4002736 | 4044386 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:4033489 | G | A | 1 | a0004 | 2 | HG03490.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.1051G>A | p.Val351Ile | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/11 | 1076/3069 | 1051/1533 | 351/510 | chr19 | 4033489 | |||
| chr19:4033528 | A | G | 1 | a0002 | 2 | HG00642.hp2 HG01070.hp2 |
missense_variant | MODERATE | c.1090A>G | p.Met364Val | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/11 | 1115/3069 | 1090/1533 | 364/510 | chr19 | 4033528 | |||
| chr19:4037729 | G | A | 1 | a0003 | 2 | HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.1387G>A | p.Ala463Thr | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1412/3069 | 1387/1533 | 463/510 | chr19 | 4037729 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:4012973 | C | T | 3 | a0001c0004 a0001c0006 a0001c0017 |
40 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(37): Show |
synonymous_variant | LOW | c.78C>T | p.Phe26Phe | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/11 | 103/3069 | 78/1533 | 26/510 | chr19 | 4012973 | |||
| chr19:4013231 | C | T | 1 | a0001c0009 | 5 | HG00558.hp1 HG02155.hp1 NA18942.hp1 others(2): Show |
synonymous_variant | LOW | c.336C>T | p.Tyr112Tyr | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/11 | 361/3069 | 336/1533 | 112/510 | chr19 | 4013231 | |||
| chr19:4013324 | T | C | 7 | a0001c0003 a0001c0004 a0001c0005 others(4): Show |
93 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(90): Show |
synonymous_variant | LOW | c.429T>C | p.Asp143Asp | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/11 | 454/3069 | 429/1533 | 143/510 | chr19 | 4013324 | |||
| chr19:4028785 | C | T | 8 | a0001c0001 a0001c0007 a0001c0009 others(5): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
synonymous_variant | LOW | c.738C>T | p.Thr246Thr | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 6/11 | 763/3069 | 738/1533 | 246/510 | chr19 | 4028785 | |||
| chr19:4033440 | C | T | 1 | a0001c0016 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.1002C>T | p.Ser334Ser | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/11 | 1027/3069 | 1002/1533 | 334/510 | chr19 | 4033440 | |||
| chr19:4033464 | T | C | 11 | a0001c0001 a0001c0002 a0001c0003 others(8): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
synonymous_variant | LOW | c.1026T>C | p.Cys342Cys | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/11 | 1051/3069 | 1026/1533 | 342/510 | chr19 | 4033464 | |||
| chr19:4037383 | G | A | 1 | a0001c0014 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.1152G>A | p.Ser384Ser | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 10/11 | 1177/3069 | 1152/1533 | 384/510 | chr19 | 4037383 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:4037968 | T | C | 4 | a0001c0002t0002 a0001c0003t0002 a0001c0007t0002 others(1): Show |
27 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*93T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 93 | chr19 | 4037968 | ||||||
| chr19:4037973 | A | C | 3 | a0001c0002t0008 a0001c0004t0008 a0001c0006t0008 |
3 | HG02622.hp2 HG03579.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*98A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 98 | chr19 | 4037973 | ||||||
| chr19:4038047 | G | C | 1 | a0001c0001t0009 | 2 | HG01256.hp1 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*172G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 172 | chr19 | 4038047 | ||||||
| chr19:4038129 | C | T | 2 | a0001c0004t0011 a0001c0004t0012 |
4 | HG02486.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*254C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 254 | chr19 | 4038129 | ||||||
| chr19:4038187 | G | A | 1 | a0001c0005t0007 | 3 | HG01361.hp2 HG01496.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*312G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 312 | chr19 | 4038187 | ||||||
| chr19:4038275 | C | T | 1 | a0001c0005t0023 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*400C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 400 | chr19 | 4038275 | ||||||
| chr19:4038323 | A | G | 1 | a0001c0001t0022 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*448A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 448 | chr19 | 4038323 | ||||||
| chr19:4038330 | C | T | 1 | a0001c0001t0021 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*455C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 455 | chr19 | 4038330 | ||||||
| chr19:4038373 | C | T | 10 | a0001c0002t0004 a0001c0002t0006 a0001c0002t0008 others(7): Show |
33 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*498C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 498 | chr19 | 4038373 | ||||||
| chr19:4038388 | G | A | 1 | a0001c0001t0013 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*513G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 513 | chr19 | 4038388 | ||||||
| chr19:4038390 | G | A | 1 | a0001c0001t0014 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*515G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 515 | chr19 | 4038390 | ||||||
| chr19:4038643 | G | C | 1 | a0001c0003t0015 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*768G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 768 | chr19 | 4038643 | ||||||
| chr19:4038772 | G | T | 1 | a0001c0001t0019 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*897G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 897 | chr19 | 4038772 | ||||||
| chr19:4038877 | A | C | 3 | a0001c0002t0006 a0001c0002t0020 a0001c0003t0006 |
6 | HG02486.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1002A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1002 | chr19 | 4038877 | ||||||
| chr19:4038945 | G | T | 1 | a0001c0002t0018 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1070G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1070 | chr19 | 4038945 | ||||||
| chr19:4039058 | G | C | 45 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(42): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
3_prime_UTR_variant | MODIFIER | c.*1183G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1183 | chr19 | 4039058 | ||||||
| chr19:4039067 | C | T | 1 | a0001c0001t0016 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1192C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1192 | chr19 | 4039067 | ||||||
| chr19:4039104 | C | T | 1 | a0001c0004t0012 | 2 | HG02922.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1229C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1229 | chr19 | 4039104 | ||||||
| chr19:4039247 | TCA | T | 20 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0004 others(17): Show |
90 | HG00741.hp2 HG01109.hp2 HG01123.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1374_*1375delAC | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1374 | INFO_REALIGN_3_PRIME | chr19 | 4039247 | |||||
| chr19:4039261 | G | A | 1 | a0001c0002t0020 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1386G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1386 | chr19 | 4039261 | ||||||
| chr19:4039273 | G | A | 1 | a0001c0005t0017 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1398G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1398 | chr19 | 4039273 | ||||||
| chr19:4039330 | G | T | 2 | a0001c0001t0010 a0001c0002t0010 |
2 | NA18983.hp2 NA19007.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1455G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 11/11 | 1455 | chr19 | 4039330 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:4007862 | C | T | 6 | a0001c0004t0003g0289 a0001c0004t0003g0291 a0001c0004t0003g0292 others(3): Show |
6 | HG02896.hp1 HG03098.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+75C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4007862 | |||||||
| chr19:4007878 | C | T | 1 | a0001c0002t0020g0288 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.27+91C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4007878 | |||||||
| chr19:4007944 | T | TGAGGGCG others(15): Show |
1 | a0001c0007t0001g0027 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.27+159_27+180dupAG others(20): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4007944 | ||||||
| chr19:4007947 | G | A | 1 | a0001c0001t0016g0026 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.27+160G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4007947 | |||||||
| chr19:4007993 | A | G | 86 | a0001c0001t0001g0254 a0001c0002t0004g0286 a0001c0002t0004g0287 others(83): Show |
92 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.27+206A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4007993 | |||||||
| chr19:4008070 | C | T | 1 | a0001c0002t0003g0216 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.27+283C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008070 | |||||||
| chr19:4008192 | G | A | 1 | a0001c0001t0001g0028 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.27+405G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008192 | |||||||
| chr19:4008208 | C | T | 3 | a0001c0001t0001g0215 a0001c0002t0004g0286 a0001c0002t0004g0287 |
3 | HG02572.hp1 HG03540.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.27+421C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008208 | |||||||
| chr19:4008214 | C | T | 2 | a0001c0005t0001g0284 a0001c0012t0001g0285 |
2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.27+427C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008214 | |||||||
| chr19:4008387 | G | C | 13 | a0001c0006t0003g0032 a0001c0006t0004g0029 a0001c0006t0004g0031 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.27+600G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008387 | |||||||
| chr19:4008389 | C | T | 13 | a0001c0006t0003g0032 a0001c0006t0004g0029 a0001c0006t0004g0031 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.27+602C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008389 | |||||||
| chr19:4008519 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.27+732C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008519 | |||||||
| chr19:4008572 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.27+785C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008572 | |||||||
| chr19:4008590 | T | C | 2 | a0001c0002t0004g0286 a0001c0002t0004g0287 |
2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.27+803T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008590 | |||||||
| chr19:4008711 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.27+924C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4008711 | |||||||
| chr19:4009092 | A | G | 1 | a0001c0002t0020g0288 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.27+1305A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4009092 | |||||||
| chr19:4009097 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.27+1310C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4009097 | |||||||
| chr19:4009211 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.27+1424C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4009211 | |||||||
| chr19:4009260 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.27+1473A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4009260 | |||||||
| chr19:4009411 | G | C | 52 | a0001c0003t0003g0218 a0001c0003t0004g0217 a0001c0004t0003g0007 others(49): Show |
55 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.27+1624G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4009411 | |||||||
| chr19:4009437 | C | T | 2 | a0001c0002t0004g0286 a0001c0002t0004g0287 |
2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.27+1650C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4009437 | |||||||
| chr19:4009567 | C | A | 1 | a0001c0003t0004g0217 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.27+1780C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4009567 | |||||||
| chr19:4009580 | A | G | 1 | a0001c0002t0004g0287 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.27+1793A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4009580 | |||||||
| chr19:4009915 | G | A | 17 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(14): Show |
17 | HG00099.hp2 HG00735.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.27+2128G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4009915 | |||||||
| chr19:4010038 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.27+2251A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4010038 | |||||||
| chr19:4010334 | A | G | 64 | a0001c0002t0004g0286 a0001c0002t0004g0287 a0001c0003t0001g0205 others(61): Show |
67 | HG00423.hp1 HG00609.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.27+2547A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4010334 | |||||||
| chr19:4010691 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.28-2232G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4010691 | |||||||
| chr19:4010767 | C | T | 1 | a0001c0003t0001g0207 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.28-2156C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4010767 | |||||||
| chr19:4010869 | C | T | 8 | a0001c0005t0001g0042 a0001c0005t0001g0249 a0001c0005t0001g0250 others(5): Show |
8 | HG01884.hp2 HG02895.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-2054C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4010869 | |||||||
| chr19:4010939 | C | T | 1 | a0001c0003t0002g0276 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.28-1984C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4010939 | |||||||
| chr19:4011014 | C | T | 5 | a0001c0003t0001g0283 a0001c0003t0006g0279 a0001c0003t0006g0280 others(2): Show |
5 | HG00423.hp1 HG02486.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-1909C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011014 | |||||||
| chr19:4011267 | A | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0058 others(175): Show |
193 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(190): Show |
intron_variant | MODIFIER | c.28-1656A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011267 | |||||||
| chr19:4011435 | A | T | 24 | a0001c0004t0003g0007 a0001c0004t0003g0235 a0001c0004t0003g0236 others(21): Show |
27 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(24): Show |
intron_variant | MODIFIER | c.28-1488A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011435 | |||||||
| chr19:4011437 | T | G | 64 | a0001c0002t0004g0286 a0001c0002t0004g0287 a0001c0003t0001g0205 others(61): Show |
67 | HG00423.hp1 HG00609.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.28-1486T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011437 | |||||||
| chr19:4011459 | G | C | 12 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(9): Show |
12 | HG01106.hp2 HG01167.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.28-1464G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011459 | |||||||
| chr19:4011556 | C | T | 18 | a0001c0005t0005g0022 a0001c0005t0005g0220 a0001c0005t0005g0222 others(15): Show |
18 | HG00609.hp1 HG00639.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.28-1367C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011556 | |||||||
| chr19:4011574 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.28-1349C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011574 | |||||||
| chr19:4011641 | T | TGGTGTGG others(95): Show |
3 | a0001c0003t0001g0205 a0001c0003t0001g0207 a0001c0003t0015g0206 |
3 | HG01192.hp2 HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.28-1267_28-1266ins others(102): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011641 | ||||||
| chr19:4011641 | TGGTGTGG others(44): Show |
T | 1 | a0001c0002t0004g0154 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.28-1266_28-1216del others(51): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011641 | ||||||
| chr19:4011656 | T | G | 1 | a0001c0001t0001g0059 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.28-1267T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011656 | |||||||
| chr19:4011657 | T | G | 10 | a0001c0001t0001g0059 a0001c0001t0001g0150 a0001c0001t0001g0151 others(7): Show |
10 | HG01192.hp2 HG01433.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.28-1266T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011657 | |||||||
| chr19:4011658 | T | G | 10 | a0001c0001t0001g0059 a0001c0001t0001g0150 a0001c0001t0001g0151 others(7): Show |
10 | HG01192.hp2 HG01433.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.28-1265T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011658 | |||||||
| chr19:4011658 | T | TGGTGTGG others(229): Show |
1 | a0001c0004t0003g0245 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.28-1251_28-1250ins others(236): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | ||||||
| chr19:4011658 | T | TGGTGTGG others(331): Show |
2 | a0001c0004t0003g0235 a0001c0004t0003g0236 |
2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.28-1251_28-1250ins others(338): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | ||||||
| chr19:4011658 | T | TGGTGTGG others(348): Show |
11 | a0001c0004t0003g0007 a0001c0004t0003g0239 a0001c0004t0003g0240 others(8): Show |
14 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.28-1251_28-1250ins others(355): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | ||||||
| chr19:4011658 | T | TGGTGTGG others(365): Show |
2 | a0001c0004t0003g0291 a0001c0004t0008g0290 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.28-1251_28-1250ins others(372): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | ||||||
| chr19:4011658 | T | TGGTGTGG others(227): Show |
2 | a0001c0004t0003g0293 a0001c0004t0003g0294 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.28-1251_28-1250ins others(234): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | ||||||
| chr19:4011658 | T | TGGTGTGG others(363): Show |
1 | a0001c0004t0003g0292 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.28-1251_28-1250ins others(370): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | ||||||
| chr19:4011658 | T | TGGTGTGG others(586): Show |
1 | a0001c0004t0003g0246 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28-1251_28-1250ins others(593): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | ||||||
| chr19:4011658 | T | TGGTGTGG others(501): Show |
1 | a0001c0004t0003g0247 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.28-1251_28-1250ins others(508): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | ||||||
| chr19:4011658 | T | TGGTGTGG others(499): Show |
1 | a0001c0004t0003g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.28-1251_28-1250ins others(506): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | ||||||
| chr19:4011658 | T | TGGTGTGG others(142): Show |
1 | a0001c0005t0001g0253 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.28-1251_28-1250ins others(149): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | ||||||
| chr19:4011658 | TGGTGTGG others(10): Show |
T | 1 | a0001c0002t0008g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.28-1250_28-1234del others(17): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | ||||||
| chr19:4011658 | TGGTGTGG others(27): Show |
T | 1 | a0001c0002t0004g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.28-1250_28-1217del others(34): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | ||||||
| chr19:4011658 | TGGTGTGG others(44): Show |
T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.28-1250_28-1200del others(51): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | ||||||
| chr19:4011658 | TGGTGTGG others(180): Show |
T | 1 | a0001c0001t0001g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.28-1250_28-1064del | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011658 | ||||||
| chr19:4011667 | G | A | 1 | a0001c0007t0001g0219 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.28-1256G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011667 | |||||||
| chr19:4011668 | G | C | 17 | a0001c0005t0005g0022 a0001c0005t0005g0220 a0001c0005t0005g0222 others(14): Show |
17 | HG00609.hp1 HG00639.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.28-1255G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011668 | |||||||
| chr19:4011671 | TGG | T | 17 | a0001c0005t0005g0022 a0001c0005t0005g0220 a0001c0005t0005g0222 others(14): Show |
17 | HG00609.hp1 HG00639.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.28-1247_28-1246del others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011671 | ||||||
| chr19:4011673 | G | A | 6 | a0001c0003t0001g0205 a0001c0003t0001g0207 a0001c0003t0015g0206 others(3): Show |
6 | HG01192.hp2 HG01433.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-1250G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011673 | |||||||
| chr19:4011673 | G | GGGGGTGT others(10): Show |
1 | a0001c0001t0001g0003 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.28-1079_28-1063dup others(17): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011673 | ||||||
| chr19:4011673 | G | GGGGGTGT others(212): Show |
1 | a0001c0002t0004g0171 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.28-1080_28-1079ins others(219): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011673 | ||||||
| chr19:4011673 | G | T | 53 | a0001c0001t0001g0059 a0001c0001t0001g0090 a0001c0001t0001g0091 others(50): Show |
56 | HG00423.hp1 HG01243.hp1 HG01884.hp2 others(53): Show |
intron_variant | MODIFIER | c.28-1250G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011673 | |||||||
| chr19:4011673 | GGGGGTGT others(10): Show |
G | 32 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(29): Show |
37 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(34): Show |
intron_variant | MODIFIER | c.28-1079_28-1063del others(17): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011673 | ||||||
| chr19:4011673 | GGGGGTGT others(27): Show |
G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(57): Show |
66 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.28-1096_28-1063del others(34): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011673 | ||||||
| chr19:4011673 | GGGGGTGT others(44): Show |
G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0114 others(2): Show |
5 | HG00438.hp2 HG01081.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-1113_28-1063del others(51): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011673 | ||||||
| chr19:4011673 | GGGGGTGT others(61): Show |
G | 1 | a0001c0001t0001g0120 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.28-1130_28-1063del others(68): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011673 | ||||||
| chr19:4011674 | G | T | 5 | a0001c0001t0001g0201 a0001c0002t0004g0286 a0001c0002t0004g0287 others(2): Show |
5 | HG01243.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-1249G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011674 | |||||||
| chr19:4011675 | G | GGGTGTGG others(27): Show |
1 | a0003c0011t0001g0277 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.28-1234_28-1233ins others(34): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011675 | ||||||
| chr19:4011675 | G | T | 5 | a0001c0001t0001g0201 a0001c0002t0004g0286 a0001c0002t0004g0287 others(2): Show |
5 | HG01243.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-1248G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011675 | |||||||
| chr19:4011686 | T | TGTGTTTG others(298): Show |
1 | a0001c0003t0001g0283 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.28-1233_28-1232ins others(305): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011686 | ||||||
| chr19:4011687 | G | GTGTGGGG others(193): Show |
3 | a0001c0003t0002g0023 a0001c0003t0002g0255 a0001c0003t0002g0256 |
4 | HG01243.hp2 HG01255.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1205_28-1204ins others(200): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011687 | ||||||
| chr19:4011687 | G | GTGTGGGG others(244): Show |
21 | a0001c0003t0001g0266 a0001c0003t0002g0024 a0001c0003t0002g0257 others(18): Show |
23 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.28-1205_28-1204ins others(251): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011687 | ||||||
| chr19:4011690 | T | A | 1 | a0003c0011t0001g0278 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.28-1233T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011690 | |||||||
| chr19:4011690 | T | TTTGGTGT others(212): Show |
1 | a0001c0004t0012g0234 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.28-1233_28-1232ins others(219): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011690 | |||||||
| chr19:4011690 | T | TTTGGTGT others(841): Show |
1 | a0001c0004t0003g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.28-1233_28-1232ins others(848): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011690 | |||||||
| chr19:4011691 | G | T | 11 | a0001c0003t0006g0279 a0001c0003t0006g0280 a0001c0003t0006g0281 others(8): Show |
11 | HG01884.hp2 HG02486.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-1232G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011691 | |||||||
| chr19:4011692 | G | T | 11 | a0001c0003t0006g0279 a0001c0003t0006g0280 a0001c0003t0006g0281 others(8): Show |
11 | HG01884.hp2 HG02486.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-1231G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011692 | |||||||
| chr19:4011704 | G | GTGTTTGG others(72): Show |
4 | a0001c0003t0006g0279 a0001c0003t0006g0280 a0001c0003t0006g0281 others(1): Show |
4 | HG02486.hp1 HG02717.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1216_28-1215ins others(79): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011704 | ||||||
| chr19:4011704 | G | GTGTTTGG others(91): Show |
4 | a0001c0005t0001g0042 a0001c0005t0001g0249 a0001c0005t0001g0250 others(1): Show |
4 | HG01884.hp2 HG02895.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1216_28-1215ins others(98): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011704 | ||||||
| chr19:4011704 | G | GTGTTTGG others(274): Show |
1 | a0001c0005t0001g0252 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.28-1216_28-1215ins others(281): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011704 | ||||||
| chr19:4011707 | T | A | 3 | a0001c0003t0001g0205 a0001c0003t0001g0207 a0001c0003t0015g0206 |
3 | HG01192.hp2 HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.28-1216T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011707 | |||||||
| chr19:4011707 | T | G | 10 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(7): Show |
13 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(10): Show |
intron_variant | MODIFIER | c.28-1216T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011707 | |||||||
| chr19:4011707 | T | TGGGGTGT others(161): Show |
1 | a0001c0001t0001g0136 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.28-1080_28-1079ins others(168): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011707 | ||||||
| chr19:4011707 | T | TGGGGTGT others(214): Show |
1 | a0001c0001t0001g0199 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.28-1080_28-1079ins others(221): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011707 | ||||||
| chr19:4011708 | G | T | 4 | a0001c0005t0001g0284 a0001c0007t0001g0219 a0001c0012t0001g0285 others(1): Show |
4 | HG02602.hp2 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1215G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011708 | |||||||
| chr19:4011709 | G | GGGTGTGG others(76): Show |
1 | a0001c0003t0002g0276 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.28-1205_28-1204ins others(83): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011709 | ||||||
| chr19:4011709 | G | T | 4 | a0001c0005t0001g0284 a0001c0007t0001g0219 a0001c0012t0001g0285 others(1): Show |
4 | HG02602.hp2 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1214G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011709 | |||||||
| chr19:4011718 | G | A | 3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 |
3 | NA18955.hp1 NA19070.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.28-1205G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011718 | |||||||
| chr19:4011718 | G | GCTGTGGG others(325): Show |
1 | a0001c0007t0001g0219 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.28-1205_28-1204ins others(332): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011718 | |||||||
| chr19:4011718 | G | GGTGTGTG others(293): Show |
3 | a0001c0005t0005g0230 a0001c0005t0005g0231 a0001c0012t0005g0229 |
3 | HG00609.hp1 NA18612.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.28-1165_28-1164ins others(300): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011718 | ||||||
| chr19:4011721 | G | C | 2 | a0001c0005t0001g0284 a0001c0012t0001g0285 |
2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.28-1202G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011721 | |||||||
| chr19:4011721 | G | GTGTGGGG others(178): Show |
1 | a0003c0011t0001g0278 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.28-1149_28-1148ins others(185): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011721 | ||||||
| chr19:4011721 | G | GTGTGGGG others(91): Show |
12 | a0001c0005t0005g0022 a0001c0005t0005g0220 a0001c0005t0005g0222 others(9): Show |
12 | HG00639.hp1 HG01256.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.28-1165_28-1164ins others(98): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011721 | ||||||
| chr19:4011721 | G | GTGTTTGG others(8): Show |
1 | a0001c0005t0001g0253 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.28-1199_28-1198ins others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011721 | ||||||
| chr19:4011724 | T | A | 1 | a0001c0004t0003g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.28-1199T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011724 | |||||||
| chr19:4011724 | T | G | 3 | a0001c0001t0001g0067 a0001c0002t0001g0158 a0001c0002t0001g0159 |
3 | NA18964.hp2 NA19064.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.28-1199T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011724 | |||||||
| chr19:4011735 | G | GGTGTGTG others(276): Show |
1 | a0001c0005t0023g0232 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.28-1165_28-1164ins others(283): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011735 | ||||||
| chr19:4011735 | GGT | G | 9 | a0001c0003t0006g0279 a0001c0003t0006g0280 a0001c0003t0006g0281 others(6): Show |
10 | HG02486.hp1 HG02486.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.28-1182_28-1181del others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011735 | ||||||
| chr19:4011737 | T | TGTGTGGG others(610): Show |
1 | a0001c0003t0001g0205 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.28-1165_28-1164ins others(617): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011737 | ||||||
| chr19:4011738 | G | GTGTGGGG others(74): Show |
1 | a0001c0005t0005g0233 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.28-1165_28-1164ins others(81): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011738 | ||||||
| chr19:4011741 | T | A | 2 | a0001c0002t0004g0154 a0003c0011t0001g0277 |
2 | HG02895.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.28-1182T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011741 | |||||||
| chr19:4011742 | G | T | 1 | a0001c0003t0002g0276 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.28-1181G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011742 | |||||||
| chr19:4011743 | G | T | 1 | a0001c0003t0002g0276 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.28-1180G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011743 | |||||||
| chr19:4011752 | GGT | G | 13 | a0001c0004t0003g0007 a0001c0004t0003g0236 a0001c0004t0003g0239 others(10): Show |
15 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.28-1165_28-1164del others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011752 | ||||||
| chr19:4011754 | T | TGTGGGGT others(38): Show |
1 | a0001c0003t0001g0283 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.28-1166_28-1165ins others(45): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011754 | ||||||
| chr19:4011754 | T | TGTGTTTG others(8): Show |
24 | a0001c0003t0001g0266 a0001c0003t0002g0023 a0001c0003t0002g0024 others(21): Show |
27 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.28-1165_28-1164ins others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011754 | ||||||
| chr19:4011758 | T | A | 1 | a0001c0004t0003g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.28-1165T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011758 | |||||||
| chr19:4011758 | TGGGGTGT others(127): Show |
T | 1 | a0001c0002t0004g0161 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.28-1062_28-929del | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011758 | ||||||
| chr19:4011759 | G | T | 2 | a0001c0003t0001g0207 a0001c0003t0015g0206 |
2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.28-1164G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011759 | |||||||
| chr19:4011760 | G | T | 2 | a0001c0003t0001g0207 a0001c0003t0015g0206 |
2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.28-1163G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011760 | |||||||
| chr19:4011772 | G | GTGTTTGG others(25): Show |
2 | a0001c0002t0004g0286 a0001c0002t0004g0287 |
2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.28-1148_28-1147ins others(32): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011772 | ||||||
| chr19:4011775 | T | A | 1 | a0003c0011t0001g0277 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.28-1148T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011775 | |||||||
| chr19:4011775 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.28-1148T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011775 | |||||||
| chr19:4011776 | G | T | 2 | a0001c0001t0001g0021 a0001c0003t0002g0276 |
3 | HG01261.hp2 NA18944.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.28-1147G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011776 | |||||||
| chr19:4011777 | G | T | 2 | a0001c0001t0001g0021 a0001c0003t0002g0276 |
3 | HG01261.hp2 NA18944.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.28-1146G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011777 | |||||||
| chr19:4011787 | G | C | 1 | a0001c0001t0001g0021 | 2 | NA18944.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.28-1136G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011787 | |||||||
| chr19:4011789 | G | GTGTGGGG others(8): Show |
24 | a0001c0003t0001g0266 a0001c0003t0002g0023 a0001c0003t0002g0024 others(21): Show |
27 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.28-1120_28-1119ins others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011789 | ||||||
| chr19:4011789 | G | GTGTTTGG others(8): Show |
2 | a0001c0002t0001g0020 a0001c0002t0001g0200 |
3 | HG01069.hp2 HG01071.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.28-1131_28-1130ins others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011789 | ||||||
| chr19:4011790 | TGTGGGGT others(95): Show |
T | 1 | a0001c0001t0001g0021 | 2 | NA18944.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.28-1131_28-1030del | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011790 | ||||||
| chr19:4011792 | T | A | 1 | a0001c0003t0004g0217 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.28-1131T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011792 | |||||||
| chr19:4011792 | T | TGGGGTGT others(59): Show |
1 | a0001c0016t0001g0111 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.28-1097_28-1096ins others(66): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011792 | ||||||
| chr19:4011792 | T | TGGGGTGT others(42): Show |
2 | a0001c0002t0001g0018 a0001c0002t0001g0167 |
3 | HG01891.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.28-1114_28-1113ins others(49): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011792 | ||||||
| chr19:4011793 | G | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0153 a0001c0002t0006g0196 |
3 | HG02622.hp1 NA18973.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.28-1130G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011793 | |||||||
| chr19:4011794 | G | GGGTGTGG others(261): Show |
2 | a0001c0003t0001g0207 a0001c0003t0015g0206 |
2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.28-1114_28-1113ins others(268): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011794 | ||||||
| chr19:4011794 | G | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0153 a0001c0002t0006g0196 |
3 | HG02622.hp1 NA18973.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.28-1129G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011794 | |||||||
| chr19:4011806 | G | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0153 |
2 | NA18973.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.28-1117G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011806 | |||||||
| chr19:4011806 | G | GTGTTTGG others(8): Show |
6 | a0001c0001t0001g0126 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG00735.hp2 HG01074.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-1114_28-1113ins others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011806 | ||||||
| chr19:4011809 | T | A | 1 | a0001c0003t0003g0218 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.28-1114T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011809 | |||||||
| chr19:4011809 | T | G | 2 | a0001c0002t0001g0020 a0001c0002t0001g0200 |
3 | HG01069.hp2 HG01071.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.28-1114T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011809 | |||||||
| chr19:4011809 | T | TGGGGTGT others(42): Show |
1 | a0001c0001t0019g0183 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.28-1097_28-1096ins others(49): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011809 | ||||||
| chr19:4011809 | T | TTTGGTGT others(10): Show |
1 | a0001c0002t0006g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.28-1114_28-1113ins others(17): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011809 | |||||||
| chr19:4011810 | G | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0003c0011t0001g0277 |
3 | HG02895.hp2 NA18964.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.28-1113G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011810 | |||||||
| chr19:4011811 | G | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0003c0011t0001g0277 |
3 | HG02895.hp2 NA18964.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.28-1112G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011811 | |||||||
| chr19:4011819 | A | G | 1 | a0001c0001t0013g0048 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.28-1104A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011819 | |||||||
| chr19:4011823 | G | C | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | NA18964.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.28-1100G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011823 | |||||||
| chr19:4011823 | G | GTGTTTGG others(8): Show |
7 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0142 others(4): Show |
7 | HG01106.hp2 HG01167.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.28-1097_28-1096ins others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011823 | ||||||
| chr19:4011826 | T | G | 8 | a0001c0001t0001g0126 a0001c0001t0001g0140 a0001c0001t0001g0141 others(5): Show |
8 | HG00735.hp2 HG01074.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-1097T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011826 | |||||||
| chr19:4011826 | T | TTTGGTGT others(25): Show |
3 | a0001c0001t0001g0148 a0001c0001t0001g0165 a0001c0002t0004g0186 |
3 | HG01975.hp2 HG02647.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.28-1097_28-1096ins others(32): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011826 | |||||||
| chr19:4011827 | G | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(63): Show |
75 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.28-1096G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011827 | |||||||
| chr19:4011828 | G | GTGTGGAG others(59): Show |
1 | a0001c0003t0002g0276 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.28-1095_28-1094ins others(66): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011828 | |||||||
| chr19:4011828 | G | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(63): Show |
75 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.28-1095G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011828 | |||||||
| chr19:4011837 | GGT | G | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(59): Show |
70 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.28-1080_28-1079del others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011837 | ||||||
| chr19:4011838 | G | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0098 a0001c0001t0001g0144 others(1): Show |
4 | HG02523.hp2 HG03239.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1085G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011838 | |||||||
| chr19:4011840 | G | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(59): Show |
69 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.28-1083G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011840 | |||||||
| chr19:4011841 | TGTGGGGT others(44): Show |
T | 1 | a0001c0001t0001g0003 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.28-1080_28-1030del others(51): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011841 | ||||||
| chr19:4011842 | G | GGGGTGTG others(5): Show |
1 | a0001c0001t0001g0144 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.28-1081_28-1080ins others(12): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011842 | |||||||
| chr19:4011843 | T | A | 1 | a0001c0004t0003g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.28-1080T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011843 | |||||||
| chr19:4011843 | T | G | 10 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0142 others(7): Show |
10 | HG01106.hp2 HG01167.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.28-1080T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011843 | |||||||
| chr19:4011843 | TGGGGTGT others(42): Show |
T | 1 | a0001c0002t0006g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.28-1062_28-1014del others(49): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011843 | ||||||
| chr19:4011844 | G | T | 3 | a0001c0001t0001g0098 a0001c0002t0004g0154 a0001c0006t0004g0034 |
3 | HG02965.hp2 HG03516.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.28-1079G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011844 | |||||||
| chr19:4011845 | G | T | 3 | a0001c0001t0001g0098 a0001c0002t0004g0154 a0001c0006t0004g0034 |
3 | HG02965.hp2 HG03516.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.28-1078G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011845 | |||||||
| chr19:4011855 | G | C | 1 | a0001c0006t0004g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.28-1068G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011855 | |||||||
| chr19:4011857 | GTGTTTGG others(8): Show |
G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0069 others(16): Show |
21 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.28-1062_28-1048del others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011857 | ||||||
| chr19:4011858 | TGTTTGGT others(27): Show |
T | 1 | a0001c0006t0004g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.28-1063_28-1030del others(34): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011858 | ||||||
| chr19:4011860 | T | A | 1 | a0001c0003t0003g0218 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.28-1063T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011860 | |||||||
| chr19:4011860 | T | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(52): Show |
61 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.28-1063T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011860 | |||||||
| chr19:4011860 | TTTGGTGT others(25): Show |
T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0153 |
2 | HG02280.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.28-1062_28-1031del others(32): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011860 | |||||||
| chr19:4011861 | T | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
85 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.28-1062T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011861 | |||||||
| chr19:4011862 | T | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
86 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.28-1061T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011862 | |||||||
| chr19:4011862 | TGGTGTGG others(8): Show |
T | 1 | a0001c0002t0004g0154 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.28-1051_28-1037del others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011862 | ||||||
| chr19:4011871 | G | GGT | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(69): Show |
79 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.28-1052_28-1051ins others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011871 | |||||||
| chr19:4011871 | G | GGTGTGTG others(476): Show |
1 | a0001c0003t0004g0217 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.28-1052_28-1051ins others(483): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011871 | |||||||
| chr19:4011872 | C | CTGTGGGG others(10): Show |
1 | a0001c0001t0001g0063 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.28-1048_28-1032dup others(17): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011872 | ||||||
| chr19:4011872 | C | CTGTGGGG others(189): Show |
1 | a0001c0003t0006g0279 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.28-1032_28-1031ins others(196): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011872 | ||||||
| chr19:4011872 | C | CTGTGGGG others(142): Show |
4 | a0001c0003t0001g0283 a0001c0003t0006g0280 a0001c0003t0006g0281 others(1): Show |
4 | HG00423.hp1 HG02486.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1032_28-1031ins others(149): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011872 | ||||||
| chr19:4011872 | C | CTGTGGGG others(161): Show |
1 | a0001c0004t0003g0292 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.28-1032_28-1031ins others(168): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011872 | ||||||
| chr19:4011872 | C | CTGTGGGG others(463): Show |
1 | a0001c0005t0001g0249 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.28-1032_28-1031ins others(470): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011872 | ||||||
| chr19:4011872 | C | CTGTGGGG others(414): Show |
17 | a0001c0004t0003g0007 a0001c0004t0003g0235 a0001c0004t0003g0236 others(14): Show |
20 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.28-1032_28-1031ins others(421): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011872 | ||||||
| chr19:4011872 | C | CTGTGGGG others(312): Show |
1 | a0001c0005t0001g0253 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.28-1032_28-1031ins others(319): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011872 | ||||||
| chr19:4011872 | C | CTGTGGGG others(414): Show |
1 | a0001c0004t0003g0291 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.28-1032_28-1031ins others(421): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011872 | ||||||
| chr19:4011872 | C | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
121 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.28-1051C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011872 | |||||||
| chr19:4011875 | T | G | 7 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0069 others(4): Show |
8 | HG01975.hp1 HG02004.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-1048T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011875 | |||||||
| chr19:4011875 | T | TGGGGTGT others(493): Show |
1 | a0001c0007t0001g0219 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.28-1032_28-1031ins others(500): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011875 | ||||||
| chr19:4011875 | T | TGGGGTGT others(495): Show |
1 | a0001c0005t0005g0231 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.28-1032_28-1031ins others(502): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011875 | ||||||
| chr19:4011877 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.28-1046G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011877 | |||||||
| chr19:4011879 | G | A | 1 | a0003c0011t0001g0278 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.28-1044G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011879 | |||||||
| chr19:4011892 | G | A | 20 | a0001c0004t0003g0007 a0001c0004t0003g0235 a0001c0004t0003g0236 others(17): Show |
23 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.28-1031G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011892 | |||||||
| chr19:4011892 | G | GGGGGTGT others(27): Show |
1 | a0001c0002t0008g0202 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.28-1015_28-1014ins others(34): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011892 | ||||||
| chr19:4011892 | G | GGGGGTGT others(10): Show |
58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(55): Show |
68 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.28-860_28-844dupGG others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011892 | ||||||
| chr19:4011892 | G | GGGGGTGT others(27): Show |
10 | a0001c0001t0001g0173 a0001c0001t0001g0199 a0001c0001t0001g0208 others(7): Show |
10 | HG00140.hp1 HG01261.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.28-877_28-844dupGG others(32): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011892 | ||||||
| chr19:4011892 | G | GGGGGTGT others(44): Show |
5 | a0001c0006t0004g0033 a0001c0006t0004g0036 a0001c0006t0004g0037 others(2): Show |
5 | HG01884.hp1 HG02257.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-894_28-844dupGG others(49): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011892 | ||||||
| chr19:4011892 | G | GGGGGTGT others(61): Show |
1 | a0001c0006t0008g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.28-911_28-844dupGG others(66): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011892 | ||||||
| chr19:4011892 | G | GGGGGTGT others(78): Show |
1 | a0001c0006t0004g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.28-928_28-844dupGG others(83): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011892 | ||||||
| chr19:4011892 | G | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
169 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.28-1031G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011892 | |||||||
| chr19:4011892 | GGGGGTGT others(10): Show |
G | 5 | a0001c0001t0001g0054 a0001c0001t0001g0106 a0001c0001t0001g0137 others(2): Show |
6 | HG00558.hp1 HG00609.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-860_28-844delGG others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011892 | ||||||
| chr19:4011895 | G | TGTGTGGA others(10): Show |
4 | a0001c0001t0001g0028 a0001c0001t0001g0133 a0001c0001t0001g0134 others(1): Show |
4 | HG02083.hp1 NA18966.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1029_28-1028ins others(17): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011895 | |||||||
| chr19:4011909 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.28-1014T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011909 | |||||||
| chr19:4011909 | T | TGGGGTGT others(459): Show |
1 | a0001c0005t0023g0232 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.28-998_28-997insGG others(464): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011909 | ||||||
| chr19:4011909 | T | TGGGGTGT others(546): Show |
2 | a0001c0005t0005g0230 a0001c0012t0005g0229 |
2 | HG00609.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.28-998_28-997insGG others(551): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011909 | ||||||
| chr19:4011910 | G | T | 13 | a0001c0005t0005g0022 a0001c0005t0005g0220 a0001c0005t0005g0222 others(10): Show |
13 | HG00639.hp1 HG01256.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.28-1013G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011910 | |||||||
| chr19:4011911 | G | T | 13 | a0001c0005t0005g0022 a0001c0005t0005g0220 a0001c0005t0005g0222 others(10): Show |
13 | HG00639.hp1 HG01256.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.28-1012G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011911 | |||||||
| chr19:4011920 | G | A | 13 | a0001c0005t0005g0022 a0001c0005t0005g0220 a0001c0005t0005g0222 others(10): Show |
13 | HG00639.hp1 HG01256.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.28-1003G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011920 | |||||||
| chr19:4011922 | T | TGTGTGGG others(178): Show |
14 | a0001c0003t0001g0266 a0001c0003t0002g0024 a0001c0003t0002g0255 others(11): Show |
15 | HG00280.hp1 HG00741.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.28-844_28-843insGG others(183): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011922 | ||||||
| chr19:4011922 | T | TGTGTGGG others(127): Show |
1 | a0001c0003t0001g0205 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.28-878_28-877insTT others(132): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011922 | ||||||
| chr19:4011922 | T | TGTGTGGG others(763): Show |
1 | a0003c0011t0001g0277 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.28-946_28-945insTT others(768): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011922 | ||||||
| chr19:4011922 | T | TGTGTGGG others(25): Show |
2 | a0001c0003t0001g0207 a0001c0003t0015g0206 |
2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.28-980_28-979insTT others(30): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011922 | ||||||
| chr19:4011922 | T | TGTGTTTG others(612): Show |
1 | a0003c0011t0001g0278 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.28-997_28-996insTT others(617): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011922 | ||||||
| chr19:4011939 | T | TGTGTGGG others(344): Show |
1 | a0001c0003t0001g0207 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.28-952_28-951insCT others(349): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011939 | ||||||
| chr19:4011939 | T | TGTGTGGG others(178): Show |
1 | a0001c0003t0002g0023 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.28-844_28-843insGG others(183): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011939 | ||||||
| chr19:4011939 | T | TGTGTGGG others(161): Show |
11 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0001c0006t0004g0040 others(8): Show |
12 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.28-844_28-843insGG others(166): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011939 | ||||||
| chr19:4011943 | T | A | 2 | a0001c0005t0001g0249 a0001c0005t0001g0253 |
2 | HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.28-980T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011943 | |||||||
| chr19:4011943 | T | TGGGGTGT others(463): Show |
1 | a0001c0012t0001g0285 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.28-912_28-911insTT others(468): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011943 | ||||||
| chr19:4011943 | T | TGGGGTGT others(463): Show |
2 | a0001c0005t0001g0251 a0001c0005t0001g0252 |
2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.28-912_28-911insTT others(468): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011943 | ||||||
| chr19:4011943 | T | TGGGGTGT others(495): Show |
1 | a0001c0005t0001g0042 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.28-912_28-911insTT others(500): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011943 | ||||||
| chr19:4011943 | T | TGGGGTGT others(497): Show |
1 | a0001c0004t0012g0234 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.28-929_28-928insTT others(502): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011943 | ||||||
| chr19:4011943 | T | TGGGGTGT others(480): Show |
1 | a0001c0004t0003g0245 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.28-946_28-945insTT others(485): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011943 | ||||||
| chr19:4011944 | G | T | 1 | a0001c0003t0002g0276 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.28-979G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011944 | |||||||
| chr19:4011945 | G | T | 1 | a0001c0003t0002g0276 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.28-978G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011945 | |||||||
| chr19:4011956 | T | TGTGTGGG others(310): Show |
1 | a0001c0003t0015g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.28-952_28-951insCT others(315): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011956 | ||||||
| chr19:4011956 | T | TGTGTGGG others(614): Show |
1 | a0001c0004t0003g0293 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.28-929_28-928insTT others(619): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011956 | ||||||
| chr19:4011956 | T | TGTGTGGG others(597): Show |
1 | a0001c0004t0003g0294 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.28-929_28-928insTT others(602): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011956 | ||||||
| chr19:4011957 | G | GTGGGGTG others(393): Show |
1 | a0001c0003t0002g0276 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.28-964_28-963insGG others(398): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011957 | ||||||
| chr19:4011960 | T | A | 1 | a0001c0005t0005g0231 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.28-963T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011960 | |||||||
| chr19:4011960 | T | G | 2 | a0001c0002t0001g0158 a0001c0002t0001g0159 |
2 | NA18964.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.28-963T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011960 | |||||||
| chr19:4011965 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.28-958T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011965 | |||||||
| chr19:4011977 | T | A | 1 | a0001c0004t0003g0292 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.28-946T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011977 | |||||||
| chr19:4011983 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.28-940G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4011983 | |||||||
| chr19:4011990 | T | TGTGTGGG others(8): Show |
1 | a0001c0001t0001g0136 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.28-927_28-913dupGG others(13): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011990 | ||||||
| chr19:4011990 | T | TGTGTGGG others(25): Show |
3 | a0001c0005t0005g0230 a0001c0005t0023g0232 a0001c0012t0005g0229 |
3 | HG00609.hp1 HG02886.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.28-927_28-896dupGG others(30): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4011990 | ||||||
| chr19:4012007 | T | TGTGGGGT others(40): Show |
18 | a0001c0004t0003g0007 a0001c0004t0003g0235 a0001c0004t0003g0236 others(15): Show |
21 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.28-913_28-912insGG others(45): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012007 | ||||||
| chr19:4012007 | T | TGTGTGGG others(8): Show |
4 | a0001c0003t0001g0283 a0001c0003t0006g0280 a0001c0003t0006g0281 others(1): Show |
4 | HG00423.hp1 HG02486.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-910_28-896dupGG others(13): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012007 | ||||||
| chr19:4012007 | T | TGTGTGGG others(59): Show |
1 | a0001c0001t0019g0183 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.28-910_28-845dupGG others(64): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012007 | ||||||
| chr19:4012007 | T | TGTGTTTG others(561): Show |
1 | a0001c0005t0001g0284 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.28-912_28-911insTT others(566): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012007 | ||||||
| chr19:4012007 | T | TGTGTTTG others(971): Show |
1 | a0001c0005t0001g0250 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.28-912_28-911insTT others(976): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012007 | ||||||
| chr19:4012030 | G | GGGTGTGG others(776): Show |
1 | a0001c0003t0003g0218 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.28-878_28-877insTT others(781): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012030 | ||||||
| chr19:4012045 | T | G | 2 | a0001c0004t0003g0245 a0001c0004t0012g0234 |
2 | HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.28-878T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012045 | |||||||
| chr19:4012046 | G | T | 28 | a0001c0003t0004g0217 a0001c0004t0003g0007 a0001c0004t0003g0235 others(25): Show |
31 | HG00609.hp1 HG02145.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.28-877G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012046 | |||||||
| chr19:4012047 | G | GGGTGTGG others(59): Show |
1 | a0001c0005t0005g0231 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.28-862_28-861insGG others(64): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012047 | ||||||
| chr19:4012047 | G | GGGTGTGG others(59): Show |
1 | a0001c0012t0001g0285 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.28-845_28-844insGG others(64): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012047 | ||||||
| chr19:4012047 | G | GGGTGTGG others(27): Show |
6 | a0001c0004t0003g0292 a0001c0005t0001g0042 a0001c0005t0001g0249 others(3): Show |
6 | HG01884.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-872_28-839dupGT others(32): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012047 | ||||||
| chr19:4012047 | G | GGGTGTGG others(693): Show |
5 | a0001c0005t0005g0022 a0001c0005t0005g0220 a0001c0005t0005g0233 others(2): Show |
5 | HG00639.hp1 HG02738.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-861_28-860insTT others(698): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012047 | ||||||
| chr19:4012047 | G | GGGTGTGG others(710): Show |
1 | a0001c0007t0001g0221 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.28-861_28-860insTT others(715): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012047 | ||||||
| chr19:4012047 | G | GGGTGTGG others(793): Show |
1 | a0001c0005t0005g0222 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.28-861_28-860insTT others(798): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012047 | ||||||
| chr19:4012047 | G | GGGTGTGG others(810): Show |
1 | a0001c0005t0005g0223 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.28-861_28-860insTT others(815): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012047 | ||||||
| chr19:4012047 | G | GGGTGTGG others(695): Show |
5 | a0001c0005t0005g0225 a0001c0005t0005g0226 a0001c0005t0005g0228 others(2): Show |
5 | HG01361.hp2 HG01496.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-861_28-860insTT others(700): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 4012047 | ||||||
| chr19:4012047 | G | GTGTGGAG others(74): Show |
2 | a0001c0004t0003g0245 a0001c0004t0012g0234 |
2 | HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.28-876_28-875insTG others(79): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012047 | |||||||
| chr19:4012047 | G | T | 28 | a0001c0003t0004g0217 a0001c0004t0003g0007 a0001c0004t0003g0235 others(25): Show |
31 | HG00609.hp1 HG02145.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.28-876G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012047 | |||||||
| chr19:4012099 | G | A | 52 | a0001c0003t0003g0218 a0001c0003t0004g0217 a0001c0004t0003g0007 others(49): Show |
55 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.28-824G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012099 | |||||||
| chr19:4012149 | A | G | 91 | a0001c0002t0004g0286 a0001c0002t0004g0287 a0001c0003t0001g0205 others(88): Show |
97 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.28-774A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012149 | |||||||
| chr19:4012250 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.28-673C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012250 | |||||||
| chr19:4012339 | A | G | 4 | a0001c0002t0003g0197 a0001c0002t0003g0198 a0001c0002t0006g0196 others(1): Show |
4 | HG01109.hp2 HG02622.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-584A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012339 | |||||||
| chr19:4012493 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.28-430C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012493 | |||||||
| chr19:4012528 | C | T | 1 | a0001c0003t0006g0282 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.28-395C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012528 | |||||||
| chr19:4012567 | G | A | 3 | a0001c0003t0002g0257 a0001c0003t0002g0258 a0001c0003t0002g0259 |
3 | HG01516.hp2 HG01517.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.28-356G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012567 | |||||||
| chr19:4012740 | G | T | 1 | a0001c0002t0004g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.28-183G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012740 | |||||||
| chr19:4012857 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.28-66G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012857 | |||||||
| chr19:4012880 | G | A | 1 | a0001c0007t0001g0268 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.28-43G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012880 | |||||||
| chr19:4012917 | C | T | 1 | a0001c0002t0004g0203 | 1 | HG03471.hp1 | splice_region_variant&intron_variant | LOW | c.28-6C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 1/10 | chr19 | 4012917 | |||||||
| chr19:4013391 | C | T | 52 | a0001c0003t0003g0218 a0001c0003t0004g0217 a0001c0004t0003g0007 others(49): Show |
55 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.454+42C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4013391 | |||||||
| chr19:4013449 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.454+100G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4013449 | |||||||
| chr19:4013456 | A | G | 2 | a0001c0002t0004g0286 a0001c0002t0004g0287 |
2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.454+107A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4013456 | |||||||
| chr19:4013652 | C | CA | 35 | a0001c0003t0001g0205 a0001c0003t0001g0207 a0001c0003t0001g0266 others(32): Show |
38 | HG00280.hp1 HG00423.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.454+304dupA | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4013652 | ||||||
| chr19:4013685 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.454+336G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4013685 | |||||||
| chr19:4013689 | A | G | 1 | a0001c0001t0001g0021 | 2 | NA18944.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.454+340A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4013689 | |||||||
| chr19:4013707 | T | A | 5 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0075 others(2): Show |
5 | HG00323.hp2 HG01069.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.454+358T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4013707 | |||||||
| chr19:4013740 | C | T | 2 | a0001c0002t0002g0130 a0001c0002t0002g0131 |
2 | HG03654.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.454+391C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4013740 | |||||||
| chr19:4013859 | G | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG00323.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.454+510G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4013859 | |||||||
| chr19:4013901 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.454+552C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4013901 | |||||||
| chr19:4014053 | GGC | G | 3 | a0001c0005t0005g0022 a0001c0005t0005g0233 a0001c0005t0017g0022 |
3 | HG00639.hp1 HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.454+705_454+706del others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014053 | |||||||
| chr19:4014067 | G | A | 53 | a0001c0002t0004g0161 a0001c0003t0003g0218 a0001c0003t0004g0217 others(50): Show |
56 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.454+718G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014067 | |||||||
| chr19:4014112 | G | T | 24 | a0001c0004t0003g0007 a0001c0004t0003g0235 a0001c0004t0003g0236 others(21): Show |
27 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(24): Show |
intron_variant | MODIFIER | c.454+763G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014112 | |||||||
| chr19:4014177 | G | A | 1 | a0001c0002t0004g0154 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.454+828G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014177 | |||||||
| chr19:4014276 | A | G | 1 | a0001c0002t0004g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.454+927A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014276 | |||||||
| chr19:4014279 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.454+930G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014279 | |||||||
| chr19:4014284 | C | T | 1 | a0001c0002t0004g0287 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.454+935C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014284 | |||||||
| chr19:4014334 | G | T | 4 | a0001c0003t0001g0283 a0001c0003t0006g0280 a0001c0003t0006g0281 others(1): Show |
4 | HG00423.hp1 HG02486.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.454+985G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014334 | |||||||
| chr19:4014402 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.454+1053G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014402 | |||||||
| chr19:4014472 | C | T | 4 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
4 | HG00323.hp1 HG01255.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.454+1123C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014472 | |||||||
| chr19:4014664 | C | T | 3 | a0001c0007t0002g0273 a0001c0007t0002g0274 a0001c0007t0002g0275 |
3 | HG01123.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.454+1315C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014664 | |||||||
| chr19:4014665 | G | A | 2 | a0001c0003t0002g0260 a0001c0003t0002g0261 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.454+1316G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014665 | |||||||
| chr19:4014787 | C | T | 10 | a0001c0004t0003g0242 a0001c0004t0003g0243 a0001c0004t0003g0244 others(7): Show |
10 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.454+1438C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014787 | |||||||
| chr19:4014834 | G | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0001g0162 others(6): Show |
14 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.454+1485G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014834 | |||||||
| chr19:4014834 | G | T | 1 | a0001c0001t0001g0021 | 2 | NA18944.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.454+1485G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4014834 | |||||||
| chr19:4014904 | TC | T | 8 | a0001c0002t0004g0203 a0001c0003t0001g0283 a0001c0003t0006g0279 others(5): Show |
8 | HG00423.hp1 HG02486.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.454+1557delC | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4014904 | ||||||
| chr19:4015066 | A | T | 1 | a0001c0001t0001g0126 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.454+1717A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015066 | |||||||
| chr19:4015082 | G | A | 1 | a0001c0002t0004g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.454+1733G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015082 | |||||||
| chr19:4015123 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.454+1774A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015123 | |||||||
| chr19:4015411 | T | C | 20 | a0001c0002t0004g0287 a0001c0004t0003g0007 a0001c0004t0003g0235 others(17): Show |
23 | HG02145.hp1 HG02280.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.454+2062T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015411 | |||||||
| chr19:4015417 | CACCAGTG others(10): Show |
C | 2 | a0003c0011t0001g0277 a0003c0011t0001g0278 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.454+2069_454+2085d others(19): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015417 | |||||||
| chr19:4015557 | G | A | 5 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0167 others(2): Show |
7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.454+2208G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015557 | |||||||
| chr19:4015590 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG01106.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.454+2241T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015590 | |||||||
| chr19:4015751 | A | G | 7 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
7 | HG03239.hp1 HG03669.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.454+2402A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015751 | |||||||
| chr19:4015953 | A | T | 1 | a0001c0001t0001g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.454+2604A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015953 | |||||||
| chr19:4015969 | G | C | 1 | a0001c0001t0001g0021 | 2 | NA18944.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.454+2620G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015969 | |||||||
| chr19:4015986 | C | T | 1 | a0001c0003t0006g0282 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.454+2637C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4015986 | |||||||
| chr19:4016007 | T | G | 53 | a0001c0001t0001g0173 a0001c0002t0003g0216 a0001c0002t0004g0161 others(50): Show |
56 | HG00280.hp1 HG00423.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.454+2658T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4016007 | |||||||
| chr19:4016031 | C | T | 26 | a0001c0003t0001g0207 a0001c0003t0001g0266 a0001c0003t0002g0023 others(23): Show |
29 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.454+2682C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4016031 | |||||||
| chr19:4016107 | G | T | 2 | a0001c0003t0002g0260 a0001c0003t0002g0261 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.454+2758G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4016107 | |||||||
| chr19:4016141 | C | T | 1 | a0001c0007t0001g0268 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.454+2792C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4016141 | |||||||
| chr19:4016313 | C | A | 1 | a0001c0001t0001g0072 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.454+2964C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4016313 | |||||||
| chr19:4016424 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.454+3075T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4016424 | |||||||
| chr19:4016577 | T | C | 1 | a0001c0005t0001g0042 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.454+3228T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4016577 | |||||||
| chr19:4016793 | A | G | 1 | a0001c0002t0004g0286 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.454+3444A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4016793 | |||||||
| chr19:4016912 | TGCTTGCC others(7): Show |
T | 1 | a0001c0005t0001g0042 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.454+3564_454+3577d others(16): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4016912 | |||||||
| chr19:4017483 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.454+4134C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4017483 | |||||||
| chr19:4017561 | T | A | 1 | a0001c0001t0001g0133 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.454+4212T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4017561 | |||||||
| chr19:4017583 | C | T | 7 | a0001c0006t0004g0033 a0001c0006t0004g0034 a0001c0006t0004g0036 others(4): Show |
7 | HG01884.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.454+4234C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4017583 | |||||||
| chr19:4017680 | C | CT | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.454+4350dupT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4017680 | ||||||
| chr19:4017680 | C | CTT | 36 | a0001c0001t0001g0055 a0001c0001t0001g0065 a0001c0001t0001g0124 others(33): Show |
39 | HG00423.hp1 HG00741.hp1 HG02145.hp1 others(36): Show |
intron_variant | MODIFIER | c.454+4349_454+4350d others(4): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4017680 | ||||||
| chr19:4017680 | C | CTTT | 29 | a0001c0003t0001g0205 a0001c0003t0001g0207 a0001c0003t0001g0266 others(26): Show |
32 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.454+4348_454+4350d others(5): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4017680 | ||||||
| chr19:4017740 | C | T | 1 | a0001c0007t0001g0221 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.454+4391C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4017740 | |||||||
| chr19:4017921 | T | C | 87 | a0001c0002t0004g0287 a0001c0003t0001g0205 a0001c0003t0001g0207 others(84): Show |
93 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.454+4572T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4017921 | |||||||
| chr19:4017955 | G | A | 34 | a0001c0002t0003g0216 a0001c0002t0004g0170 a0001c0002t0004g0171 others(31): Show |
37 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.454+4606G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4017955 | |||||||
| chr19:4018083 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.454+4734A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018083 | |||||||
| chr19:4018096 | G | A | 1 | a0001c0001t0022g0060 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.454+4747G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018096 | |||||||
| chr19:4018102 | A | G | 87 | a0001c0002t0004g0287 a0001c0003t0001g0205 a0001c0003t0001g0207 others(84): Show |
93 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.454+4753A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018102 | |||||||
| chr19:4018107 | C | T | 1 | a0001c0003t0015g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.454+4758C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018107 | |||||||
| chr19:4018266 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.454+4917C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018266 | |||||||
| chr19:4018425 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.454+5076C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018425 | |||||||
| chr19:4018442 | T | C | 34 | a0001c0003t0001g0205 a0001c0003t0001g0207 a0001c0003t0001g0266 others(31): Show |
37 | HG00280.hp1 HG00423.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.454+5093T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018442 | |||||||
| chr19:4018483 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.454+5134G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018483 | |||||||
| chr19:4018486 | C | A | 29 | a0001c0003t0003g0218 a0001c0003t0004g0217 a0001c0004t0003g0242 others(26): Show |
29 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.454+5137C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018486 | |||||||
| chr19:4018520 | C | T | 1 | a0001c0014t0001g0191 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.454+5171C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018520 | |||||||
| chr19:4018528 | C | T | 18 | a0001c0005t0005g0022 a0001c0005t0005g0220 a0001c0005t0005g0222 others(15): Show |
18 | HG00609.hp1 HG00639.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.454+5179C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018528 | |||||||
| chr19:4018543 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG01496.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.454+5194G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018543 | |||||||
| chr19:4018579 | A | G | 18 | a0001c0005t0005g0022 a0001c0005t0005g0220 a0001c0005t0005g0222 others(15): Show |
18 | HG00609.hp1 HG00639.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.454+5230A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018579 | |||||||
| chr19:4018749 | G | C | 28 | a0001c0003t0001g0283 a0001c0003t0006g0279 a0001c0003t0006g0280 others(25): Show |
31 | HG00423.hp1 HG02145.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.455-5287G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018749 | |||||||
| chr19:4018758 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.455-5278C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018758 | |||||||
| chr19:4018880 | C | T | 9 | a0001c0004t0003g0242 a0001c0005t0001g0042 a0001c0005t0001g0249 others(6): Show |
9 | HG01884.hp2 HG02895.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.455-5156C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4018880 | |||||||
| chr19:4019258 | G | C | 2 | a0004c0010t0002g0269 a0004c0010t0002g0270 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.455-4778G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019258 | |||||||
| chr19:4019269 | C | G | 31 | a0001c0002t0003g0190 a0001c0003t0003g0218 a0001c0003t0004g0217 others(28): Show |
31 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.455-4767C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019269 | |||||||
| chr19:4019272 | C | T | 2 | a0001c0006t0004g0040 a0001c0006t0004g0041 |
2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.455-4764C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019272 | |||||||
| chr19:4019436 | G | A | 30 | a0001c0003t0003g0218 a0001c0003t0004g0217 a0001c0004t0003g0242 others(27): Show |
30 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.455-4600G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019436 | |||||||
| chr19:4019642 | C | T | 1 | a0001c0003t0003g0218 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.455-4394C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019642 | |||||||
| chr19:4019675 | C | A | 1 | a0001c0004t0008g0290 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.455-4361C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019675 | |||||||
| chr19:4019700 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.455-4336A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019700 | |||||||
| chr19:4019769 | G | A | 1 | a0001c0005t0001g0042 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.455-4267G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019769 | |||||||
| chr19:4019771 | A | C | 1 | a0001c0005t0001g0042 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.455-4265A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019771 | |||||||
| chr19:4019774 | G | A | 1 | a0001c0005t0005g0231 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.455-4262G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019774 | |||||||
| chr19:4019784 | G | T | 1 | a0001c0001t0001g0121 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.455-4252G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019784 | |||||||
| chr19:4019815 | C | T | 29 | a0001c0003t0003g0218 a0001c0003t0004g0217 a0001c0004t0003g0242 others(26): Show |
29 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.455-4221C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019815 | |||||||
| chr19:4019816 | G | T | 1 | a0001c0005t0001g0042 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.455-4220G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019816 | |||||||
| chr19:4019821 | C | T | 1 | a0001c0002t0004g0287 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.455-4215C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019821 | |||||||
| chr19:4019846 | T | G | 1 | a0001c0001t0001g0150 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.455-4190T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019846 | |||||||
| chr19:4019856 | G | T | 6 | a0001c0001t0001g0173 a0001c0002t0003g0216 a0001c0002t0004g0170 others(3): Show |
6 | HG02559.hp1 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.455-4180G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019856 | |||||||
| chr19:4019865 | G | C | 30 | a0001c0003t0003g0218 a0001c0003t0004g0217 a0001c0004t0003g0242 others(27): Show |
30 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.455-4171G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019865 | |||||||
| chr19:4019922 | CT | C | 26 | a0001c0001t0001g0080 a0001c0001t0001g0163 a0001c0004t0003g0007 others(23): Show |
29 | HG00639.hp2 HG02145.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.455-4100delT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4019922 | ||||||
| chr19:4019927 | T | C | 24 | a0001c0003t0001g0266 a0001c0003t0002g0023 a0001c0003t0002g0024 others(21): Show |
27 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.455-4109T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019927 | |||||||
| chr19:4019940 | A | G | 13 | a0001c0006t0003g0032 a0001c0006t0004g0029 a0001c0006t0004g0031 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.455-4096A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019940 | |||||||
| chr19:4019956 | G | A | 2 | a0003c0011t0001g0277 a0003c0011t0001g0278 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.455-4080G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019956 | |||||||
| chr19:4019960 | G | A | 88 | a0001c0002t0004g0287 a0001c0003t0001g0205 a0001c0003t0001g0207 others(85): Show |
94 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.455-4076G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019960 | |||||||
| chr19:4019963 | C | T | 88 | a0001c0002t0004g0287 a0001c0003t0001g0205 a0001c0003t0001g0207 others(85): Show |
94 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.455-4073C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019963 | |||||||
| chr19:4019969 | T | C | 88 | a0001c0002t0004g0287 a0001c0003t0001g0205 a0001c0003t0001g0207 others(85): Show |
94 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.455-4067T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4019969 | |||||||
| chr19:4020013 | T | C | 1 | a0001c0004t0003g0291 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.455-4023T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020013 | |||||||
| chr19:4020165 | C | G | 1 | a0001c0001t0001g0189 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.455-3871C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020165 | |||||||
| chr19:4020304 | G | A | 2 | a0003c0011t0001g0277 a0003c0011t0001g0278 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.455-3732G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020304 | |||||||
| chr19:4020370 | T | C | 2 | a0003c0011t0001g0277 a0003c0011t0001g0278 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.455-3666T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020370 | |||||||
| chr19:4020372 | C | T | 27 | a0001c0003t0001g0205 a0001c0003t0001g0207 a0001c0003t0001g0266 others(24): Show |
30 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.455-3664C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020372 | |||||||
| chr19:4020447 | T | C | 27 | a0001c0003t0001g0205 a0001c0003t0001g0207 a0001c0003t0001g0266 others(24): Show |
30 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.455-3589T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020447 | |||||||
| chr19:4020460 | G | C | 1 | a0001c0002t0004g0192 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.455-3576G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020460 | |||||||
| chr19:4020495 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.455-3541G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020495 | |||||||
| chr19:4020529 | A | G | 4 | a0001c0007t0002g0025 a0001c0007t0002g0273 a0001c0007t0002g0274 others(1): Show |
5 | HG01123.hp2 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.455-3507A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020529 | |||||||
| chr19:4020599 | C | T | 3 | a0001c0002t0004g0203 a0001c0003t0003g0218 a0001c0003t0004g0217 |
3 | HG01243.hp1 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.455-3437C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020599 | |||||||
| chr19:4020611 | T | A | 1 | a0001c0002t0003g0190 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.455-3425T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020611 | |||||||
| chr19:4020631 | A | T | 5 | a0001c0002t0003g0216 a0001c0002t0004g0170 a0001c0002t0004g0171 others(2): Show |
5 | HG02559.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.455-3405A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020631 | |||||||
| chr19:4020637 | T | G | 27 | a0001c0003t0001g0205 a0001c0003t0001g0207 a0001c0003t0001g0266 others(24): Show |
30 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.455-3399T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020637 | |||||||
| chr19:4020712 | A | T | 23 | a0001c0004t0003g0007 a0001c0004t0003g0235 a0001c0004t0003g0236 others(20): Show |
26 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.455-3324A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020712 | |||||||
| chr19:4020739 | T | C | 1 | a0001c0003t0015g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.455-3297T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020739 | |||||||
| chr19:4020793 | G | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0001g0120 others(9): Show |
17 | HG00639.hp2 HG00673.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.455-3243G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020793 | |||||||
| chr19:4020814 | TG | T | 23 | a0001c0001t0001g0173 a0001c0002t0003g0216 a0001c0002t0004g0161 others(20): Show |
23 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.455-3219delG | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4020814 | ||||||
| chr19:4020816 | G | C | 22 | a0001c0001t0001g0173 a0001c0002t0003g0216 a0001c0002t0004g0161 others(19): Show |
22 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.455-3220G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020816 | |||||||
| chr19:4020872 | G | T | 2 | a0003c0011t0001g0277 a0003c0011t0001g0278 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.455-3164G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020872 | |||||||
| chr19:4020939 | G | A | 1 | a0001c0005t0001g0042 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.455-3097G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4020939 | |||||||
| chr19:4021037 | T | A | 5 | a0001c0003t0001g0283 a0001c0003t0006g0279 a0001c0003t0006g0280 others(2): Show |
5 | HG00423.hp1 HG02486.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.455-2999T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021037 | |||||||
| chr19:4021165 | A | G | 1 | a0001c0006t0003g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.455-2871A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021165 | |||||||
| chr19:4021170 | T | C | 5 | a0001c0003t0001g0283 a0001c0003t0006g0279 a0001c0003t0006g0280 others(2): Show |
5 | HG00423.hp1 HG02486.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.455-2866T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021170 | |||||||
| chr19:4021241 | C | T | 30 | a0001c0003t0003g0218 a0001c0003t0004g0217 a0001c0004t0003g0242 others(27): Show |
30 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.455-2795C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021241 | |||||||
| chr19:4021257 | A | G | 1 | a0001c0001t0001g0005 | 3 | HG02080.hp1 HG02132.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.455-2779A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021257 | |||||||
| chr19:4021273 | C | T | 1 | a0001c0002t0020g0288 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.455-2763C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021273 | |||||||
| chr19:4021374 | T | C | 4 | a0001c0003t0001g0283 a0001c0003t0006g0280 a0001c0003t0006g0281 others(1): Show |
4 | HG00423.hp1 HG02486.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-2662T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021374 | |||||||
| chr19:4021469 | C | T | 23 | a0001c0004t0003g0007 a0001c0004t0003g0235 a0001c0004t0003g0236 others(20): Show |
26 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.455-2567C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021469 | |||||||
| chr19:4021471 | GT | G | 19 | a0001c0005t0005g0022 a0001c0005t0005g0220 a0001c0005t0005g0222 others(16): Show |
19 | HG00609.hp1 HG00639.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.455-2564delT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021471 | |||||||
| chr19:4021473 | C | G | 19 | a0001c0005t0005g0022 a0001c0005t0005g0220 a0001c0005t0005g0222 others(16): Show |
19 | HG00609.hp1 HG00639.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.455-2563C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021473 | |||||||
| chr19:4021580 | G | A | 19 | a0001c0005t0005g0022 a0001c0005t0005g0220 a0001c0005t0005g0222 others(16): Show |
19 | HG00609.hp1 HG00639.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.455-2456G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021580 | |||||||
| chr19:4021585 | T | C | 1 | a0001c0002t0004g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.455-2451T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021585 | |||||||
| chr19:4021639 | T | C | 1 | a0001c0001t0014g0081 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.455-2397T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021639 | |||||||
| chr19:4021727 | C | T | 2 | a0001c0002t0004g0186 a0001c0002t0004g0286 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.455-2309C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021727 | |||||||
| chr19:4021740 | T | G | 7 | a0001c0004t0003g0242 a0001c0005t0001g0042 a0001c0005t0001g0249 others(4): Show |
7 | HG01884.hp2 HG02895.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.455-2296T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021740 | |||||||
| chr19:4021742 | C | CT | 28 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(25): Show |
28 | HG00609.hp1 HG00639.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.455-2273dupT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4021742 | ||||||
| chr19:4021742 | CT | C | 57 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0067 others(54): Show |
60 | HG00423.hp1 HG00639.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.455-2273delT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4021742 | ||||||
| chr19:4021880 | G | C | 1 | a0001c0002t0004g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.455-2156G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021880 | |||||||
| chr19:4021955 | C | T | 1 | a0001c0004t0003g0241 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.455-2081C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4021955 | |||||||
| chr19:4022097 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.455-1939A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022097 | |||||||
| chr19:4022167 | G | A | 61 | a0001c0002t0004g0287 a0001c0003t0001g0283 a0001c0003t0003g0218 others(58): Show |
64 | HG00423.hp1 HG00609.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.455-1869G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022167 | |||||||
| chr19:4022337 | G | T | 1 | a0001c0002t0004g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.455-1699G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022337 | |||||||
| chr19:4022364 | T | C | 1 | a0001c0004t0003g0235 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.455-1672T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022364 | |||||||
| chr19:4022413 | G | A | 1 | a0001c0008t0001g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.455-1623G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022413 | |||||||
| chr19:4022453 | G | A | 1 | a0001c0003t0004g0217 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.455-1583G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022453 | |||||||
| chr19:4022465 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.455-1571C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022465 | |||||||
| chr19:4022546 | T | G | 5 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0167 others(2): Show |
7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.455-1490T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022546 | |||||||
| chr19:4022550 | T | G | 1 | a0001c0001t0001g0174 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.455-1486T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022550 | |||||||
| chr19:4022568 | G | A | 9 | a0001c0004t0003g0242 a0001c0005t0001g0042 a0001c0005t0001g0249 others(6): Show |
9 | HG01884.hp2 HG02895.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.455-1468G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022568 | |||||||
| chr19:4022617 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0148 |
2 | HG02735.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.455-1419C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022617 | |||||||
| chr19:4022629 | A | G | 88 | a0001c0002t0004g0287 a0001c0003t0001g0205 a0001c0003t0001g0207 others(85): Show |
94 | HG00280.hp1 HG00423.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.455-1407A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022629 | |||||||
| chr19:4022658 | G | A | 1 | a0001c0002t0004g0287 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.455-1378G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022658 | |||||||
| chr19:4022665 | C | T | 30 | a0001c0003t0003g0218 a0001c0003t0004g0217 a0001c0004t0003g0242 others(27): Show |
30 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.455-1371C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022665 | |||||||
| chr19:4022837 | AT | A | 29 | a0001c0003t0003g0218 a0001c0003t0004g0217 a0001c0004t0003g0242 others(26): Show |
29 | HG00609.hp1 HG00639.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.455-1185delT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4022837 | ||||||
| chr19:4022886 | C | T | 1 | a0001c0015t0005g0118 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.455-1150C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022886 | |||||||
| chr19:4022901 | G | A | 2 | a0001c0003t0002g0271 a0001c0003t0002g0272 |
2 | NA18983.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.455-1135G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4022901 | |||||||
| chr19:4023032 | G | A | 1 | a0001c0002t0004g0154 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.455-1004G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023032 | |||||||
| chr19:4023100 | A | G | 1 | a0001c0002t0001g0117 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.455-936A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023100 | |||||||
| chr19:4023140 | C | T | 1 | a0001c0002t0004g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.455-896C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023140 | |||||||
| chr19:4023172 | C | CA | 94 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0058 others(91): Show |
106 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.455-847dupA | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4023172 | ||||||
| chr19:4023172 | C | CAA | 34 | a0001c0001t0001g0215 a0001c0002t0001g0047 a0001c0002t0002g0130 others(31): Show |
37 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.455-848_455-847dup others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4023172 | ||||||
| chr19:4023172 | CA | C | 6 | a0001c0001t0001g0064 a0001c0001t0001g0129 a0001c0001t0001g0185 others(3): Show |
6 | HG01255.hp2 HG01256.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.455-847delA | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4023172 | ||||||
| chr19:4023190 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.455-846T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023190 | |||||||
| chr19:4023254 | G | A | 1 | a0001c0002t0004g0287 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.455-782G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023254 | |||||||
| chr19:4023265 | G | A | 1 | a0001c0002t0004g0192 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.455-771G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023265 | |||||||
| chr19:4023312 | C | G | 9 | a0001c0001t0001g0116 a0001c0002t0010g0115 a0001c0003t0001g0283 others(6): Show |
9 | HG00423.hp1 HG02165.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.455-724C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023312 | |||||||
| chr19:4023350 | T | C | 1 | a0001c0014t0001g0191 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.455-686T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023350 | |||||||
| chr19:4023459 | C | CCAAAA | 6 | a0001c0003t0001g0283 a0001c0003t0002g0262 a0001c0003t0006g0279 others(3): Show |
6 | HG00423.hp1 HG02717.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.455-552_455-548dup others(5): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4023459 | ||||||
| chr19:4023459 | C | CCAAAACA others(3): Show |
2 | a0001c0005t0001g0284 a0001c0012t0001g0285 |
2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.455-557_455-548dup others(10): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 4023459 | ||||||
| chr19:4023521 | C | T | 3 | a0001c0002t0004g0154 a0003c0011t0001g0277 a0003c0011t0001g0278 |
3 | HG02895.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.455-515C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023521 | |||||||
| chr19:4023748 | C | T | 1 | a0001c0003t0006g0279 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.455-288C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023748 | |||||||
| chr19:4023764 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0189 |
2 | NA18969.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.455-272C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023764 | |||||||
| chr19:4023830 | A | G | 65 | a0001c0001t0001g0021 a0001c0001t0001g0077 a0001c0001t0001g0124 others(62): Show |
69 | HG00609.hp1 HG00639.hp1 HG01168.hp2 others(66): Show |
intron_variant | MODIFIER | c.455-206A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023830 | |||||||
| chr19:4023840 | G | T | 17 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0150 others(14): Show |
18 | HG00438.hp2 HG02273.hp1 NA18944.hp1 others(15): Show |
intron_variant | MODIFIER | c.455-196G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4023840 | |||||||
| chr19:4024022 | G | A | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.455-14G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 2/10 | chr19 | 4024022 | |||||||
| chr19:4024339 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(236): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.539+219T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024339 | |||||||
| chr19:4024351 | G | T | 1 | a0001c0001t0001g0112 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.539+231G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024351 | |||||||
| chr19:4024353 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.539+233G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024353 | |||||||
| chr19:4024367 | C | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.539+247C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024367 | |||||||
| chr19:4024371 | T | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.539+251T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024371 | |||||||
| chr19:4024377 | G | A | 3 | a0001c0009t0001g0004 a0001c0009t0001g0084 a0001c0009t0001g0085 |
5 | HG00558.hp1 HG02155.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+257G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024377 | |||||||
| chr19:4024461 | A | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.539+341A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024461 | |||||||
| chr19:4024519 | G | A | 11 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(8): Show |
13 | HG01109.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.539+399G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024519 | |||||||
| chr19:4024527 | G | A | 27 | a0001c0002t0001g0047 a0001c0002t0002g0130 a0001c0002t0002g0131 others(24): Show |
30 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.539+407G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024527 | |||||||
| chr19:4024550 | G | A | 26 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(23): Show |
29 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.539+430G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024550 | |||||||
| chr19:4024655 | G | C | 1 | a0001c0009t0001g0084 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.539+535G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024655 | |||||||
| chr19:4024657 | A | G | 1 | a0001c0009t0001g0084 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.539+537A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024657 | |||||||
| chr19:4024691 | T | G | 1 | a0001c0009t0001g0084 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.539+571T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024691 | |||||||
| chr19:4024757 | T | A | 1 | a0001c0001t0001g0050 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.539+637T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024757 | |||||||
| chr19:4024762 | GT | G | 26 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(23): Show |
29 | HG01109.hp2 HG01243.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.539+654delT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4024762 | ||||||
| chr19:4024762 | GTT | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.539+653_539+654del others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4024762 | ||||||
| chr19:4024808 | C | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.539+688C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024808 | |||||||
| chr19:4024853 | C | T | 2 | a0001c0005t0005g0225 a0001c0005t0005g0228 |
2 | HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.539+733C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024853 | |||||||
| chr19:4024892 | A | G | 6 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0110 others(3): Show |
7 | HG02074.hp1 HG02080.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.539+772A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024892 | |||||||
| chr19:4024893 | G | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.539+773G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024893 | |||||||
| chr19:4024984 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.539+864C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4024984 | |||||||
| chr19:4025043 | C | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.539+923C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025043 | |||||||
| chr19:4025056 | G | T | 7 | a0001c0002t0006g0196 a0001c0002t0020g0288 a0001c0003t0001g0283 others(4): Show |
7 | HG00423.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.539+936G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025056 | |||||||
| chr19:4025062 | C | T | 7 | a0001c0002t0006g0196 a0001c0002t0020g0288 a0001c0003t0001g0283 others(4): Show |
7 | HG00423.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.539+942C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025062 | |||||||
| chr19:4025115 | T | G | 1 | a0001c0005t0005g0226 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.539+995T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025115 | |||||||
| chr19:4025147 | G | A | 26 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(23): Show |
29 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.539+1027G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025147 | |||||||
| chr19:4025156 | G | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.539+1036G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025156 | |||||||
| chr19:4025159 | C | T | 1 | a0001c0003t0006g0279 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.539+1039C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025159 | |||||||
| chr19:4025281 | G | A | 5 | a0001c0003t0002g0257 a0001c0003t0002g0258 a0001c0003t0002g0259 others(2): Show |
5 | HG01346.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.539+1161G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025281 | |||||||
| chr19:4025299 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.539+1179T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025299 | |||||||
| chr19:4025379 | C | G | 1 | a0001c0006t0004g0036 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.539+1259C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025379 | |||||||
| chr19:4025486 | C | T | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.539+1366C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025486 | |||||||
| chr19:4025539 | C | T | 2 | a0001c0003t0003g0218 a0001c0003t0004g0217 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.539+1419C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025539 | |||||||
| chr19:4025540 | G | A | 1 | a0001c0001t0010g0087 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.539+1420G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025540 | |||||||
| chr19:4025618 | G | A | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.539+1498G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025618 | |||||||
| chr19:4025669 | A | ACCTCATC others(8): Show |
1 | a0001c0002t0001g0020 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.539+1553_539+1554i others(17): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4025669 | ||||||
| chr19:4025673 | C | CGTCTTTC others(8): Show |
1 | a0001c0001t0001g0050 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.539+1567_539+1568i others(17): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4025673 | ||||||
| chr19:4025673 | C | T | 26 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(23): Show |
29 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.539+1553C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025673 | |||||||
| chr19:4025688 | C | CGTCTTTC others(8): Show |
236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.539+1573_539+1574i others(17): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4025688 | ||||||
| chr19:4025688 | C | T | 2 | a0001c0001t0001g0050 a0001c0002t0001g0020 |
3 | HG01069.hp2 HG01071.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.539+1568C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025688 | |||||||
| chr19:4025752 | G | GT | 26 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(23): Show |
29 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.539+1633dupT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4025752 | ||||||
| chr19:4025911 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.539+1791A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025911 | |||||||
| chr19:4025947 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG01496.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.539+1827G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025947 | |||||||
| chr19:4025966 | C | T | 12 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0056 others(9): Show |
15 | HG00642.hp2 HG01070.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.539+1846C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025966 | |||||||
| chr19:4025980 | A | C | 26 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(23): Show |
29 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.539+1860A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025980 | |||||||
| chr19:4025991 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.539+1871G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025991 | |||||||
| chr19:4025998 | C | T | 1 | a0001c0002t0002g0143 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.539+1878C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4025998 | |||||||
| chr19:4026006 | G | A | 26 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(23): Show |
29 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.539+1886G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026006 | |||||||
| chr19:4026073 | C | CA | 34 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(31): Show |
37 | HG01109.hp2 HG01884.hp2 HG02145.hp1 others(34): Show |
intron_variant | MODIFIER | c.539+1973dupA | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026073 | ||||||
| chr19:4026073 | C | CAAAA | 14 | a0001c0002t0004g0161 a0001c0002t0004g0192 a0001c0002t0004g0203 others(11): Show |
14 | HG02055.hp2 HG02451.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.539+1970_539+1973d others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026073 | ||||||
| chr19:4026073 | C | CAAAAA | 8 | a0001c0002t0004g0154 a0001c0002t0004g0175 a0001c0002t0004g0186 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.539+1969_539+1973d others(7): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026073 | ||||||
| chr19:4026073 | CA | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.539+1973delA | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026073 | ||||||
| chr19:4026073 | CAA | C | 27 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0143 others(24): Show |
30 | HG00280.hp1 HG00741.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.539+1972_539+1973d others(4): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026073 | ||||||
| chr19:4026158 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.540-1988T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026158 | |||||||
| chr19:4026201 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0126 a0001c0002t0018g0125 |
4 | HG02280.hp1 HG02630.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-1945C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026201 | |||||||
| chr19:4026259 | A | C | 1 | a0001c0001t0001g0055 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.540-1887A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026259 | |||||||
| chr19:4026279 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.540-1867C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026279 | |||||||
| chr19:4026295 | G | GCTAATTT others(300): Show |
1 | a0001c0002t0004g0171 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.540-1842_540-1841i others(309): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026295 | ||||||
| chr19:4026295 | G | GCTAATTT others(311): Show |
5 | a0001c0002t0004g0154 a0001c0002t0004g0172 a0001c0002t0004g0175 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.540-1842_540-1841i others(320): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026295 | ||||||
| chr19:4026295 | G | GCTAATTT others(312): Show |
7 | a0001c0002t0004g0170 a0001c0002t0004g0186 a0001c0002t0004g0192 others(4): Show |
7 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.540-1842_540-1841i others(321): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026295 | ||||||
| chr19:4026295 | G | GCTAATTT others(313): Show |
9 | a0001c0002t0003g0216 a0001c0002t0004g0161 a0001c0002t0004g0286 others(6): Show |
9 | HG02257.hp2 HG02572.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.540-1842_540-1841i others(322): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026295 | ||||||
| chr19:4026295 | G | GCTAATTT others(314): Show |
1 | a0001c0002t0004g0287 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.540-1842_540-1841i others(323): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026295 | ||||||
| chr19:4026295 | G | GCTAATTT others(315): Show |
2 | a0001c0002t0004g0203 a0001c0006t0004g0041 |
2 | HG02055.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.540-1842_540-1841i others(324): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026295 | ||||||
| chr19:4026295 | G | GCTAATTT others(316): Show |
2 | a0001c0002t0008g0202 a0001c0004t0008g0290 |
2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.540-1842_540-1841i others(325): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026295 | ||||||
| chr19:4026381 | A | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(288): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.540-1765A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026381 | |||||||
| chr19:4026397 | G | C | 1 | a0001c0001t0001g0210 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.540-1749G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026397 | |||||||
| chr19:4026411 | C | T | 2 | a0001c0005t0001g0284 a0001c0012t0001g0285 |
2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.540-1735C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026411 | |||||||
| chr19:4026478 | T | G | 1 | a0001c0001t0001g0070 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.540-1668T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026478 | |||||||
| chr19:4026550 | A | C | 27 | a0001c0002t0003g0216 a0001c0002t0004g0154 a0001c0002t0004g0161 others(24): Show |
27 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.540-1596A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026550 | |||||||
| chr19:4026571 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.540-1575A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026571 | |||||||
| chr19:4026573 | C | CCCCA | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.540-1572_540-1569d others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4026573 | ||||||
| chr19:4026769 | G | T | 27 | a0001c0002t0003g0216 a0001c0002t0004g0154 a0001c0002t0004g0161 others(24): Show |
27 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.540-1377G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026769 | |||||||
| chr19:4026810 | C | G | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(288): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.540-1336C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026810 | |||||||
| chr19:4026822 | A | T | 1 | a0001c0006t0003g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.540-1324A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026822 | |||||||
| chr19:4026922 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.540-1224A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026922 | |||||||
| chr19:4026934 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.540-1212G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4026934 | |||||||
| chr19:4027014 | A | AT | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.540-1121dupT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4027014 | ||||||
| chr19:4027110 | C | T | 6 | a0001c0002t0001g0020 a0001c0002t0001g0168 a0001c0002t0001g0200 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.540-1036C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027110 | |||||||
| chr19:4027240 | C | T | 1 | a0002c0013t0001g0015 | 2 | HG00642.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.540-906C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027240 | |||||||
| chr19:4027270 | G | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | NA18973.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.540-876G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027270 | |||||||
| chr19:4027291 | C | G | 27 | a0001c0002t0003g0216 a0001c0002t0004g0154 a0001c0002t0004g0161 others(24): Show |
27 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.540-855C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027291 | |||||||
| chr19:4027394 | G | A | 1 | a0001c0012t0005g0229 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.540-752G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027394 | |||||||
| chr19:4027501 | T | C | 2 | a0001c0003t0003g0218 a0001c0003t0004g0217 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.540-645T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027501 | |||||||
| chr19:4027562 | G | GT | 39 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0066 others(36): Show |
42 | HG00280.hp1 HG00280.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.540-579dupT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 4027562 | ||||||
| chr19:4027568 | G | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.540-578G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027568 | |||||||
| chr19:4027579 | T | G | 1 | a0001c0003t0002g0259 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.540-567T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027579 | |||||||
| chr19:4027592 | T | C | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0121 |
3 | HG02132.hp1 NA18612.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.540-554T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027592 | |||||||
| chr19:4027627 | A | G | 2 | a0001c0005t0001g0284 a0001c0012t0001g0285 |
2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.540-519A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027627 | |||||||
| chr19:4027677 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.540-469C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027677 | |||||||
| chr19:4027726 | A | T | 26 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(23): Show |
29 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.540-420A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027726 | |||||||
| chr19:4027764 | C | G | 2 | a0001c0006t0004g0040 a0001c0006t0004g0041 |
2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.540-382C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027764 | |||||||
| chr19:4027854 | C | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.540-292C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4027854 | |||||||
| chr19:4028016 | G | T | 3 | a0001c0006t0004g0037 a0001c0006t0004g0038 a0001c0006t0004g0039 |
3 | HG01884.hp1 HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.540-130G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4028016 | |||||||
| chr19:4028069 | C | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(236): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.540-77C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4028069 | |||||||
| chr19:4028075 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.540-71G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4028075 | |||||||
| chr19:4028077 | G | A | 7 | a0001c0002t0006g0196 a0001c0002t0020g0288 a0001c0003t0001g0283 others(4): Show |
7 | HG00423.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.540-69G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 3/10 | chr19 | 4028077 | |||||||
| chr19:4028292 | G | A | 27 | a0001c0001t0001g0080 a0001c0002t0001g0047 a0001c0002t0002g0130 others(24): Show |
30 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.581+105G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 4/10 | chr19 | 4028292 | |||||||
| chr19:4028636 | T | C | 16 | a0001c0001t0001g0174 a0001c0002t0001g0167 a0001c0002t0004g0175 others(13): Show |
17 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.672+36T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 5/10 | chr19 | 4028636 | |||||||
| chr19:4028692 | C | G | 67 | a0001c0002t0001g0167 a0001c0002t0003g0190 a0001c0002t0003g0197 others(64): Show |
70 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.673-28C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 5/10 | chr19 | 4028692 | |||||||
| chr19:4028862 | C | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0001g0103 others(6): Show |
14 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.801+14C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 6/10 | chr19 | 4028862 | |||||||
| chr19:4028915 | T | G | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.802-16T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 6/10 | chr19 | 4028915 | |||||||
| chr19:4028916 | T | C | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.802-15T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 6/10 | chr19 | 4028916 | |||||||
| chr19:4029058 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.907+22G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029058 | |||||||
| chr19:4029077 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.907+41C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029077 | |||||||
| chr19:4029109 | C | T | 3 | a0001c0005t0007g0224 a0001c0005t0007g0227 a0001c0005t0007g0267 |
3 | HG01361.hp2 HG01496.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.907+73C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029109 | |||||||
| chr19:4029121 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.907+85C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029121 | |||||||
| chr19:4029127 | G | A | 25 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(22): Show |
28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.907+91G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029127 | |||||||
| chr19:4029136 | G | A | 1 | a0001c0005t0005g0220 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.907+100G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029136 | |||||||
| chr19:4029146 | C | T | 2 | a0001c0005t0007g0224 a0001c0005t0007g0227 |
2 | HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.907+110C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029146 | |||||||
| chr19:4029266 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.907+230A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029266 | |||||||
| chr19:4029271 | G | T | 1 | a0001c0001t0010g0087 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.907+235G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029271 | |||||||
| chr19:4029291 | T | C | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.907+255T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029291 | |||||||
| chr19:4029345 | C | G | 4 | a0001c0003t0001g0283 a0001c0003t0006g0280 a0001c0003t0006g0281 others(1): Show |
4 | HG00423.hp1 HG02486.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.907+309C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029345 | |||||||
| chr19:4029354 | C | T | 1 | a0001c0005t0005g0230 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.907+318C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029354 | |||||||
| chr19:4029445 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0122 |
2 | HG01981.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.907+409G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029445 | |||||||
| chr19:4029455 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.907+419C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029455 | |||||||
| chr19:4029494 | G | A | 1 | a0001c0006t0004g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.907+458G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029494 | |||||||
| chr19:4029497 | C | T | 1 | a0001c0002t0004g0154 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.907+461C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029497 | |||||||
| chr19:4029571 | G | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0209 |
2 | HG03490.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.907+535G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029571 | |||||||
| chr19:4029659 | C | G | 2 | a0001c0001t0009g0073 a0001c0001t0009g0076 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.907+623C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029659 | |||||||
| chr19:4029696 | A | G | 2 | a0001c0003t0003g0218 a0001c0003t0004g0217 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.907+660A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029696 | |||||||
| chr19:4029786 | A | G | 26 | a0001c0002t0001g0047 a0001c0002t0002g0130 a0001c0002t0002g0131 others(23): Show |
29 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.907+750A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029786 | |||||||
| chr19:4029811 | AT | A | 20 | a0001c0002t0003g0198 a0001c0003t0002g0258 a0001c0003t0002g0264 others(17): Show |
21 | HG00609.hp1 HG01109.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.907+804delT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4029811 | ||||||
| chr19:4029811 | ATT | A | 72 | a0001c0001t0001g0054 a0001c0001t0001g0066 a0001c0001t0001g0072 others(69): Show |
80 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.907+803_907+804del others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4029811 | ||||||
| chr19:4029811 | ATTT | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.907+802_907+804del others(3): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4029811 | ||||||
| chr19:4029811 | ATTTT | A | 7 | a0001c0001t0001g0056 a0001c0001t0001g0068 a0001c0001t0001g0092 others(4): Show |
7 | HG01070.hp1 HG01081.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.907+801_907+804del others(4): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4029811 | ||||||
| chr19:4029811 | ATTTTTTT others(3): Show |
A | 4 | a0001c0002t0003g0216 a0001c0002t0004g0171 a0001c0002t0004g0172 others(1): Show |
4 | HG01891.hp2 HG02717.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.907+795_907+804del others(10): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4029811 | ||||||
| chr19:4029811 | ATTTTTTT others(4): Show |
A | 22 | a0001c0002t0004g0154 a0001c0002t0004g0161 a0001c0002t0004g0170 others(19): Show |
22 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.907+794_907+804del others(11): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4029811 | ||||||
| chr19:4029811 | ATTTTTTT others(5): Show |
A | 1 | a0001c0004t0004g0237 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.907+793_907+804del others(12): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4029811 | ||||||
| chr19:4029811 | ATTTTTTT others(7): Show |
A | 5 | a0001c0005t0001g0284 a0001c0008t0001g0169 a0001c0012t0001g0285 others(2): Show |
5 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.907+791_907+804del others(14): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4029811 | ||||||
| chr19:4029892 | G | A | 28 | a0001c0001t0001g0121 a0001c0002t0003g0216 a0001c0002t0004g0154 others(25): Show |
28 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.907+856G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029892 | |||||||
| chr19:4029980 | G | T | 1 | a0001c0003t0002g0256 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.907+944G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029980 | |||||||
| chr19:4029983 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.907+947C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4029983 | |||||||
| chr19:4030118 | G | C | 26 | a0001c0002t0001g0047 a0001c0002t0002g0130 a0001c0002t0002g0131 others(23): Show |
29 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.907+1082G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030118 | |||||||
| chr19:4030167 | TGCCCAGG others(208): Show |
T | 4 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0142 others(1): Show |
4 | HG01106.hp1 HG02735.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.907+1135_907+1349d others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4030167 | ||||||
| chr19:4030181 | G | T | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.907+1145G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030181 | |||||||
| chr19:4030192 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.907+1156A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030192 | |||||||
| chr19:4030345 | C | T | 11 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(8): Show |
13 | HG01109.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.907+1309C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030345 | |||||||
| chr19:4030348 | A | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.907+1312A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030348 | |||||||
| chr19:4030354 | TCA | T | 8 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0167 others(5): Show |
10 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.907+1322_907+1323d others(4): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4030354 | ||||||
| chr19:4030575 | T | C | 1 | a0001c0003t0006g0279 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.907+1539T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030575 | |||||||
| chr19:4030618 | C | CA | 11 | a0001c0001t0001g0044 a0001c0001t0001g0121 a0001c0002t0003g0216 others(8): Show |
11 | HG02055.hp1 HG02572.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.907+1596dupA | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr19 | 4030618 | ||||||
| chr19:4030628 | A | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0043 others(2): Show |
7 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(4): Show |
intron_variant | MODIFIER | c.907+1592A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030628 | |||||||
| chr19:4030777 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.907+1741A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030777 | |||||||
| chr19:4030875 | A | T | 1 | a0001c0007t0001g0219 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.907+1839A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030875 | |||||||
| chr19:4030959 | C | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.907+1923C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4030959 | |||||||
| chr19:4031046 | A | T | 1 | a0001c0002t0004g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.907+2010A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031046 | |||||||
| chr19:4031101 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.908-1999C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031101 | |||||||
| chr19:4031192 | C | G | 1 | a0001c0001t0001g0014 | 2 | HG01934.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.908-1908C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031192 | |||||||
| chr19:4031332 | T | C | 26 | a0001c0002t0001g0047 a0001c0002t0002g0130 a0001c0002t0002g0131 others(23): Show |
29 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.908-1768T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031332 | |||||||
| chr19:4031344 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.908-1756C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031344 | |||||||
| chr19:4031369 | G | A | 1 | a0001c0002t0004g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.908-1731G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031369 | |||||||
| chr19:4031428 | A | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(288): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.908-1672A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031428 | |||||||
| chr19:4031484 | T | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.908-1616T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031484 | |||||||
| chr19:4031539 | G | A | 1 | a0001c0001t0021g0094 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.908-1561G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031539 | |||||||
| chr19:4031545 | G | T | 1 | a0001c0012t0001g0285 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.908-1555G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031545 | |||||||
| chr19:4031583 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.908-1517A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031583 | |||||||
| chr19:4031632 | G | A | 1 | a0001c0003t0006g0279 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.908-1468G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031632 | |||||||
| chr19:4031771 | C | T | 26 | a0001c0002t0001g0047 a0001c0002t0002g0130 a0001c0002t0002g0131 others(23): Show |
29 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.908-1329C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031771 | |||||||
| chr19:4031812 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.908-1288C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031812 | |||||||
| chr19:4031921 | C | T | 48 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(45): Show |
55 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.908-1179C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031921 | |||||||
| chr19:4031924 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.908-1176C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4031924 | |||||||
| chr19:4032078 | G | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.908-1022G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032078 | |||||||
| chr19:4032109 | G | T | 1 | a0001c0004t0008g0290 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.908-991G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032109 | |||||||
| chr19:4032358 | C | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.908-742C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032358 | |||||||
| chr19:4032531 | T | C | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.908-569T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032531 | |||||||
| chr19:4032551 | A | G | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.908-549A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032551 | |||||||
| chr19:4032626 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.908-474T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032626 | |||||||
| chr19:4032678 | A | G | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.908-422A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032678 | |||||||
| chr19:4032683 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.908-417C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032683 | |||||||
| chr19:4032684 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.908-416A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032684 | |||||||
| chr19:4032746 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.908-354G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032746 | |||||||
| chr19:4032818 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.908-282T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032818 | |||||||
| chr19:4032943 | A | G | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.908-157A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032943 | |||||||
| chr19:4032951 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.908-149A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032951 | |||||||
| chr19:4032987 | C | T | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.908-113C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4032987 | |||||||
| chr19:4033029 | G | A | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.908-71G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4033029 | |||||||
| chr19:4033064 | A | T | 1 | a0001c0002t0004g0154 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.908-36A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 7/10 | chr19 | 4033064 | |||||||
| chr19:4033181 | G | A | 7 | a0001c0002t0006g0196 a0001c0002t0020g0288 a0001c0003t0001g0283 others(4): Show |
7 | HG00423.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.981+8G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 8/10 | chr19 | 4033181 | |||||||
| chr19:4033246 | G | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.981+73G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 8/10 | chr19 | 4033246 | |||||||
| chr19:4033281 | G | A | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.981+108G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 8/10 | chr19 | 4033281 | |||||||
| chr19:4033303 | G | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.982-117G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 8/10 | chr19 | 4033303 | |||||||
| chr19:4033616 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1142+36G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4033616 | |||||||
| chr19:4033720 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1142+140C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4033720 | |||||||
| chr19:4033751 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1142+171C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4033751 | |||||||
| chr19:4033791 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0163 |
2 | HG00639.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1142+211G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4033791 | |||||||
| chr19:4033856 | A | T | 1 | a0001c0001t0001g0124 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1142+276A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4033856 | |||||||
| chr19:4033992 | G | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1142+412G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4033992 | |||||||
| chr19:4033996 | T | TCTGG | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1142+419_1142+422d others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4033996 | ||||||
| chr19:4034136 | C | T | 5 | a0001c0005t0005g0022 a0001c0005t0005g0220 a0001c0005t0005g0233 others(2): Show |
5 | HG00639.hp1 HG02738.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1142+556C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034136 | |||||||
| chr19:4034156 | G | A | 24 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0143 others(21): Show |
27 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1142+576G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034156 | |||||||
| chr19:4034157 | C | T | 7 | a0001c0002t0006g0196 a0001c0002t0020g0288 a0001c0003t0001g0283 others(4): Show |
7 | HG00423.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1142+577C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034157 | |||||||
| chr19:4034175 | G | A | 2 | a0001c0004t0004g0237 a0001c0004t0004g0238 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1142+595G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034175 | |||||||
| chr19:4034208 | A | G | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1142+628A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034208 | |||||||
| chr19:4034215 | G | A | 1 | a0001c0002t0006g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1142+635G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034215 | |||||||
| chr19:4034225 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG00323.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1142+645C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034225 | |||||||
| chr19:4034238 | C | T | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1142+658C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034238 | |||||||
| chr19:4034258 | GGCCCTGC others(24): Show |
G | 5 | a0001c0003t0002g0257 a0001c0003t0002g0258 a0001c0003t0002g0259 others(2): Show |
5 | HG01346.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1142+684_1142+714d others(33): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4034258 | ||||||
| chr19:4034281 | G | A | 1 | a0001c0002t0020g0288 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1142+701G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034281 | |||||||
| chr19:4034343 | C | T | 1 | a0001c0006t0003g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1142+763C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034343 | |||||||
| chr19:4034379 | C | T | 2 | a0001c0004t0004g0237 a0001c0004t0004g0238 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1142+799C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034379 | |||||||
| chr19:4034385 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1142+805A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034385 | |||||||
| chr19:4034456 | A | G | 1 | a0001c0005t0005g0231 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1142+876A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034456 | |||||||
| chr19:4034471 | G | A | 2 | a0001c0003t0003g0218 a0001c0003t0004g0217 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1142+891G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034471 | |||||||
| chr19:4034710 | C | T | 25 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(22): Show |
28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1142+1130C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034710 | |||||||
| chr19:4034795 | C | T | 1 | a0001c0003t0015g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1142+1215C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034795 | |||||||
| chr19:4034844 | T | C | 25 | a0001c0002t0003g0216 a0001c0002t0004g0161 a0001c0002t0004g0170 others(22): Show |
25 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1142+1264T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034844 | |||||||
| chr19:4034909 | A | G | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1142+1329A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034909 | |||||||
| chr19:4034963 | G | A | 10 | a0001c0005t0001g0042 a0001c0005t0001g0249 a0001c0005t0001g0250 others(7): Show |
10 | HG01884.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1142+1383G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4034963 | |||||||
| chr19:4035103 | C | T | 3 | a0001c0002t0006g0196 a0001c0002t0020g0288 a0001c0003t0006g0279 |
3 | HG02622.hp1 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1142+1523C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035103 | |||||||
| chr19:4035210 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1142+1630T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035210 | |||||||
| chr19:4035278 | G | A | 27 | a0001c0002t0003g0216 a0001c0002t0004g0154 a0001c0002t0004g0161 others(24): Show |
27 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1142+1698G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035278 | |||||||
| chr19:4035300 | C | T | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1142+1720C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035300 | |||||||
| chr19:4035359 | T | C | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1142+1779T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035359 | |||||||
| chr19:4035373 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0065 others(1): Show |
6 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1142+1793G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035373 | |||||||
| chr19:4035410 | G | C | 1 | a0001c0002t0004g0286 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1142+1830G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035410 | |||||||
| chr19:4035496 | A | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1143-1878A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035496 | |||||||
| chr19:4035517 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1143-1857C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035517 | |||||||
| chr19:4035544 | G | T | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1143-1830G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035544 | |||||||
| chr19:4035568 | C | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1143-1806C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035568 | |||||||
| chr19:4035574 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1143-1800C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035574 | |||||||
| chr19:4035638 | C | G | 1 | a0001c0001t0001g0098 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1143-1736C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035638 | |||||||
| chr19:4035704 | C | T | 27 | a0001c0001t0001g0101 a0001c0002t0001g0182 a0001c0002t0001g0194 others(24): Show |
30 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.1143-1670C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035704 | |||||||
| chr19:4035752 | TCACA | T | 25 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(22): Show |
28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-1612_1143-160 others(8): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035752 | ||||||
| chr19:4035830 | TCACA | T | 4 | a0001c0002t0004g0203 a0001c0006t0004g0037 a0001c0006t0004g0038 others(1): Show |
4 | HG01884.hp1 HG02257.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143-1536_1143-153 others(8): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035830 | ||||||
| chr19:4035831 | C | A | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1143-1543C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035831 | |||||||
| chr19:4035839 | C | T | 6 | a0001c0002t0006g0196 a0001c0002t0020g0288 a0001c0003t0006g0279 others(3): Show |
6 | HG02486.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1143-1535C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035839 | |||||||
| chr19:4035864 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1143-1510C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035864 | |||||||
| chr19:4035870 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1143-1504C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035870 | |||||||
| chr19:4035872 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1143-1502C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035872 | |||||||
| chr19:4035885 | G | A | 27 | a0001c0002t0003g0216 a0001c0002t0004g0154 a0001c0002t0004g0161 others(24): Show |
27 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1143-1489G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035885 | |||||||
| chr19:4035892 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.1143-1482T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035892 | |||||||
| chr19:4035911 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1143-1463C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035911 | |||||||
| chr19:4035913 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1143-1461C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035913 | |||||||
| chr19:4035925 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1143-1449T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035925 | |||||||
| chr19:4035959 | A | ACACCCGC others(238): Show |
10 | a0001c0005t0001g0042 a0001c0005t0001g0249 a0001c0005t0001g0250 others(7): Show |
10 | HG01884.hp2 HG02559.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(249): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1246): Show |
20 | a0001c0002t0003g0190 a0001c0004t0003g0007 a0001c0004t0003g0235 others(17): Show |
23 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1257): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1246): Show |
2 | a0001c0002t0003g0197 a0001c0002t0003g0198 |
2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1257): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1360): Show |
1 | a0001c0004t0003g0236 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1371): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1246): Show |
1 | a0001c0004t0003g0243 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1257): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1246): Show |
1 | a0001c0004t0003g0291 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1257): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(521): Show |
1 | a0001c0001t0001g0110 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(532): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(238): Show |
21 | a0001c0005t0001g0284 a0001c0005t0005g0022 a0001c0005t0005g0220 others(18): Show |
22 | HG00609.hp2 HG00639.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(249): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(236): Show |
1 | a0001c0005t0005g0222 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(247): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1326): Show |
1 | a0001c0001t0001g0135 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1337): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1390): Show |
2 | a0001c0003t0002g0260 a0001c0003t0002g0261 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1401): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1326): Show |
16 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0003t0002g0023 others(13): Show |
18 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1337): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1326): Show |
1 | a0001c0003t0002g0024 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1337): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1287): Show |
2 | a0004c0010t0002g0269 a0004c0010t0002g0270 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1298): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(732): Show |
1 | a0001c0001t0001g0101 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(743): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1244): Show |
2 | a0001c0003t0003g0218 a0001c0003t0004g0217 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1255): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(238): Show |
1 | a0001c0012t0005g0229 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(249): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1367): Show |
4 | a0001c0003t0006g0279 a0001c0003t0006g0280 a0001c0003t0006g0281 others(1): Show |
4 | HG02486.hp1 HG02717.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1378): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1393): Show |
2 | a0001c0002t0006g0196 a0001c0002t0020g0288 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1404): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(204): Show |
7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(215): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(599): Show |
1 | a0001c0001t0001g0043 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(610): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(520): Show |
1 | a0001c0001t0001g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(531): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(521): Show |
62 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(59): Show |
77 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(532): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1365): Show |
1 | a0001c0001t0001g0064 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1376): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1365): Show |
1 | a0001c0001t0001g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1376): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1365): Show |
46 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(43): Show |
51 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1376): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1363): Show |
6 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0167 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1374): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1282): Show |
1 | a0001c0001t0001g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1293): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1361): Show |
1 | a0001c0001t0019g0183 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1372): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1365): Show |
5 | a0001c0001t0001g0011 a0001c0001t0001g0082 a0001c0001t0001g0112 others(2): Show |
6 | NA18994.hp2 NA19007.hp1 NA19064.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1376): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1363): Show |
26 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0058 others(23): Show |
32 | HG00438.hp2 HG00673.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1374): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1363): Show |
2 | a0001c0001t0001g0185 a0001c0014t0001g0191 |
2 | HG00735.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1374): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1361): Show |
1 | a0001c0001t0001g0103 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1372): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1363): Show |
1 | a0001c0001t0001g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1374): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(480): Show |
1 | a0001c0001t0001g0097 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(491): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1365): Show |
2 | a0001c0001t0001g0012 a0001c0001t0001g0102 |
3 | NA18973.hp1 NA19070.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1376): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1361): Show |
4 | a0001c0002t0001g0019 a0001c0002t0001g0158 a0001c0002t0001g0159 others(1): Show |
5 | HG02273.hp1 NA18955.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1372): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1359): Show |
1 | a0001c0003t0015g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1370): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(517): Show |
1 | a0001c0001t0001g0119 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(528): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1595): Show |
2 | a0001c0006t0004g0040 a0001c0006t0004g0041 |
2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1606): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1595): Show |
1 | a0001c0006t0004g0031 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1606): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1677): Show |
1 | a0001c0002t0004g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1688): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1636): Show |
3 | a0001c0002t0008g0202 a0001c0004t0008g0290 a0001c0006t0008g0035 |
3 | HG02622.hp2 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1647): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1636): Show |
6 | a0001c0002t0003g0216 a0001c0002t0004g0161 a0001c0002t0004g0170 others(3): Show |
6 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1647): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1636): Show |
8 | a0001c0002t0004g0186 a0001c0002t0004g0286 a0001c0002t0004g0287 others(5): Show |
8 | HG02257.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1647): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1633): Show |
3 | a0001c0006t0004g0037 a0001c0006t0004g0038 a0001c0006t0004g0039 |
3 | HG01884.hp1 HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1644): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1634): Show |
1 | a0001c0006t0004g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1645): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1790): Show |
1 | a0001c0002t0004g0203 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1801): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1635): Show |
1 | a0001c0002t0004g0154 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1143-1413_1143-141 others(1646): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACACCCGC others(1324): Show |
3 | a0001c0002t0002g0143 a0001c0003t0002g0271 a0001c0003t0002g0272 |
3 | NA18983.hp1 NA19087.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(1335): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035959 | A | ACCCGCAC others(1361): Show |
1 | a0001c0001t0001g0181 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1143-1414_1143-141 others(1372): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035959 | ||||||
| chr19:4035960 | C | CACCCGCA others(602): Show |
2 | a0001c0001t0001g0151 a0001c0001t0021g0094 |
2 | HG00438.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1143-1413_1143-141 others(613): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035960 | ||||||
| chr19:4035962 | T | G | 2 | a0001c0001t0001g0151 a0001c0001t0021g0094 |
2 | HG00438.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1143-1412T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035962 | |||||||
| chr19:4035971 | C | T | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1403C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035971 | |||||||
| chr19:4035975 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1143-1399G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035975 | |||||||
| chr19:4035975 | G | GTC | 4 | a0001c0004t0003g0242 a0001c0004t0003g0244 a0001c0004t0003g0245 others(1): Show |
4 | HG02145.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1143-1398_1143-139 others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035975 | ||||||
| chr19:4035979 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(123): Show |
147 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.1143-1395T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035979 | |||||||
| chr19:4035980 | A | T | 1 | a0001c0001t0001g0151 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1143-1394A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035980 | |||||||
| chr19:4035984 | A | ACACATCT others(45): Show |
24 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0143 others(21): Show |
27 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1143-1386_1143-138 others(56): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4035984 | ||||||
| chr19:4035986 | A | ATCCATAT others(4): Show |
68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
83 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1143-1388_1143-138 others(15): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035986 | |||||||
| chr19:4035986 | A | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1388A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035986 | |||||||
| chr19:4035995 | T | C | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1143-1379T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035995 | |||||||
| chr19:4035997 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1143-1377T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035997 | |||||||
| chr19:4035998 | G | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(98): Show |
119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1143-1376G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4035998 | |||||||
| chr19:4036012 | T | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(96): Show |
117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1143-1362T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036012 | |||||||
| chr19:4036012 | T | G | 2 | a0001c0001t0001g0151 a0001c0001t0021g0094 |
2 | HG00438.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1143-1362T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036012 | |||||||
| chr19:4036013 | T | TAACACAC others(7): Show |
7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1361_1143-136 others(18): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036013 | |||||||
| chr19:4036013 | T | TCACACAC others(1): Show |
70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(67): Show |
85 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1143-1355_1143-135 others(12): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036013 | ||||||
| chr19:4036022 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
83 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1143-1352C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036022 | |||||||
| chr19:4036024 | T | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
83 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1143-1350T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036024 | |||||||
| chr19:4036036 | C | T | 1 | a0001c0003t0015g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1143-1338C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036036 | |||||||
| chr19:4036037 | G | A | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1337G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036037 | |||||||
| chr19:4036039 | C | A | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1335C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036039 | |||||||
| chr19:4036040 | A | ACACACAC others(197): Show |
2 | a0001c0001t0001g0151 a0001c0001t0021g0094 |
2 | HG00438.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1143-1334_1143-133 others(208): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036040 | |||||||
| chr19:4036041 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(74): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1143-1333T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036041 | |||||||
| chr19:4036041 | T | TACACAC | 24 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0143 others(21): Show |
27 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1143-1327_1143-132 others(10): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036041 | ||||||
| chr19:4036046 | A | ACACCCG | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1325_1143-132 others(10): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036046 | ||||||
| chr19:4036055 | T | C | 9 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0001t0001g0151 others(6): Show |
9 | HG00438.hp1 HG01192.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143-1319T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036055 | |||||||
| chr19:4036056 | A | G | 24 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0143 others(21): Show |
27 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1143-1318A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036056 | |||||||
| chr19:4036067 | A | G | 2 | a0001c0001t0001g0151 a0001c0001t0021g0094 |
2 | HG00438.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1143-1307A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036067 | |||||||
| chr19:4036069 | T | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(98): Show |
119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1143-1305T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036069 | |||||||
| chr19:4036070 | G | A | 9 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0001t0001g0151 others(6): Show |
9 | HG00438.hp1 HG01192.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143-1304G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036070 | |||||||
| chr19:4036070 | G | T | 24 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0143 others(21): Show |
27 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1143-1304G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036070 | |||||||
| chr19:4036071 | T | TAACACAC others(7): Show |
7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1303_1143-130 others(18): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036071 | |||||||
| chr19:4036071 | T | TCACACAC others(1): Show |
68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
83 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1143-1297_1143-129 others(12): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036071 | ||||||
| chr19:4036081 | G | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(98): Show |
119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1143-1293G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036081 | |||||||
| chr19:4036094 | C | A | 2 | a0001c0001t0001g0151 a0001c0001t0021g0094 |
2 | HG00438.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1143-1280C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036094 | |||||||
| chr19:4036098 | A | T | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1276A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036098 | |||||||
| chr19:4036099 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1143-1275T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036099 | |||||||
| chr19:4036099 | TACAA | T | 24 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0143 others(21): Show |
27 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1143-1271_1143-126 others(8): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036099 | ||||||
| chr19:4036101 | CAA | C | 4 | a0001c0002t0003g0216 a0001c0002t0004g0170 a0001c0002t0004g0171 others(1): Show |
4 | HG02717.hp2 HG02818.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143-1271_1143-127 others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036101 | ||||||
| chr19:4036102 | A | ACACAATC others(193): Show |
68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
83 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1143-1272_1143-127 others(204): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036102 | |||||||
| chr19:4036103 | A | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(97): Show |
115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1143-1271A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036103 | |||||||
| chr19:4036108 | A | ACCCG | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1265_1143-126 others(8): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036108 | ||||||
| chr19:4036117 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1143-1257T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036117 | |||||||
| chr19:4036122 | A | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0214 |
3 | HG01192.hp1 HG02055.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1143-1252A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036122 | |||||||
| chr19:4036129 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
83 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1143-1245A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036129 | |||||||
| chr19:4036131 | C | T | 24 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0143 others(21): Show |
27 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1143-1243C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036131 | |||||||
| chr19:4036132 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1143-1242G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036132 | |||||||
| chr19:4036133 | T | TAACACAC others(7): Show |
7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1241_1143-124 others(18): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036133 | |||||||
| chr19:4036143 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1143-1231G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036143 | |||||||
| chr19:4036155 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0021g0094 |
2 | HG00438.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1143-1219C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036155 | |||||||
| chr19:4036156 | C | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
83 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.1143-1218C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036156 | |||||||
| chr19:4036157 | G | A | 9 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0001t0001g0151 others(6): Show |
9 | HG00438.hp1 HG01192.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143-1217G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036157 | |||||||
| chr19:4036161 | T | C | 9 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0001t0001g0151 others(6): Show |
9 | HG00438.hp1 HG01192.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143-1213T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036161 | |||||||
| chr19:4036161 | TACAAACA others(1): Show |
T | 26 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(23): Show |
29 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.1143-1209_1143-120 others(12): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036161 | ||||||
| chr19:4036163 | C | T | 133 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(130): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1143-1211C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036163 | |||||||
| chr19:4036164 | A | ACATCCAT others(12): Show |
1 | a0001c0001t0021g0094 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1143-1210_1143-120 others(23): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036164 | |||||||
| chr19:4036164 | A | ACATCCAT others(101): Show |
1 | a0001c0001t0001g0151 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1143-1210_1143-120 others(112): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036164 | |||||||
| chr19:4036165 | A | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
90 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1143-1209A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036165 | |||||||
| chr19:4036166 | A | T | 2 | a0001c0001t0001g0151 a0001c0001t0021g0094 |
2 | HG00438.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1143-1208A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036166 | |||||||
| chr19:4036168 | A | ATCCATAC others(12): Show |
7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1206_1143-120 others(23): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036168 | |||||||
| chr19:4036169 | C | CACACACA others(47): Show |
1 | a0001c0004t0003g0243 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1143-1170_1143-116 others(58): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036169 | ||||||
| chr19:4036179 | T | C | 8 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0001t0021g0094 others(5): Show |
8 | HG00438.hp1 HG01192.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143-1195T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036179 | |||||||
| chr19:4036180 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1143-1194A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036180 | |||||||
| chr19:4036185 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1143-1189G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036185 | |||||||
| chr19:4036194 | G | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1143-1180G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036194 | |||||||
| chr19:4036194 | G | T | 1 | a0001c0001t0001g0151 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1143-1180G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036194 | |||||||
| chr19:4036195 | T | TCA | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1174_1143-117 others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036195 | ||||||
| chr19:4036195 | T | TCACACAT others(167): Show |
64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(61): Show |
79 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1143-1170_1143-116 others(178): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036195 | ||||||
| chr19:4036195 | T | TCACACAT others(252): Show |
3 | a0001c0001t0001g0043 a0001c0001t0001g0095 a0001c0001t0001g0097 |
3 | HG00099.hp2 HG00597.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.1143-1170_1143-116 others(263): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036195 | ||||||
| chr19:4036195 | T | TCACACAT others(167): Show |
1 | a0001c0001t0001g0074 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1143-1170_1143-116 others(178): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036195 | ||||||
| chr19:4036205 | A | G | 24 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0143 others(21): Show |
27 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1143-1169A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036205 | |||||||
| chr19:4036218 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(101): Show |
122 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1143-1156T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036218 | |||||||
| chr19:4036219 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(70): Show |
88 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1143-1155G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036219 | |||||||
| chr19:4036221 | CAT | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0095 a0001c0001t0001g0097 others(1): Show |
4 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143-1151_1143-115 others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036221 | ||||||
| chr19:4036222 | A | ACACACAC others(76): Show |
1 | a0001c0002t0001g0117 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1143-1152_1143-115 others(87): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036222 | |||||||
| chr19:4036223 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(70): Show |
88 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1143-1151T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036223 | |||||||
| chr19:4036224 | A | ACACACAT others(45): Show |
65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(62): Show |
80 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.1143-1144_1143-114 others(56): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036224 | ||||||
| chr19:4036226 | A | ACACATCC others(8): Show |
7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1144_1143-114 others(19): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036226 | ||||||
| chr19:4036237 | T | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(69): Show |
87 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.1143-1137T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036237 | |||||||
| chr19:4036238 | A | G | 2 | a0001c0002t0004g0186 a0001c0002t0004g0286 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1143-1136A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036238 | |||||||
| chr19:4036252 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(62): Show |
80 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.1143-1122A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036252 | |||||||
| chr19:4036255 | ACATG | A | 5 | a0001c0001t0001g0043 a0001c0001t0001g0095 a0001c0001t0001g0097 others(2): Show |
5 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(2): Show |
intron_variant | MODIFIER | c.1143-1116_1143-111 others(8): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036255 | ||||||
| chr19:4036257 | ATG | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(62): Show |
80 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.1143-1116_1143-111 others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036257 | |||||||
| chr19:4036258 | T | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1116T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036258 | |||||||
| chr19:4036259 | G | A | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1115G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036259 | |||||||
| chr19:4036270 | T | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0095 a0001c0001t0001g0097 others(1): Show |
4 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143-1104T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036270 | |||||||
| chr19:4036271 | A | G | 1 | a0001c0001t0021g0094 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1143-1103A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036271 | |||||||
| chr19:4036272 | T | G | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1102T>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036272 | |||||||
| chr19:4036274 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(74): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1143-1100T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036274 | |||||||
| chr19:4036275 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(74): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1143-1099G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036275 | |||||||
| chr19:4036276 | G | A | 1 | a0001c0001t0021g0094 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1143-1098G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036276 | |||||||
| chr19:4036279 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(74): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1143-1095T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036279 | |||||||
| chr19:4036280 | A | G | 2 | a0001c0002t0004g0170 a0001c0002t0004g0172 |
2 | HG02818.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1143-1094A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036280 | |||||||
| chr19:4036284 | C | T | 2 | a0001c0005t0001g0284 a0001c0012t0001g0285 |
2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1143-1090C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036284 | |||||||
| chr19:4036285 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(66): Show |
84 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1143-1089G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036285 | |||||||
| chr19:4036285 | G | T | 1 | a0001c0001t0021g0094 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1143-1089G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036285 | |||||||
| chr19:4036286 | T | TCA | 121 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(118): Show |
140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1143-1075_1143-107 others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036286 | ||||||
| chr19:4036286 | T | TCACACAC others(483): Show |
1 | a0001c0001t0001g0091 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1143-1074_1143-107 others(494): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036286 | ||||||
| chr19:4036294 | A | ACATCCAT others(188): Show |
1 | a0001c0001t0021g0094 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1143-1078_1143-107 others(199): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036294 | ||||||
| chr19:4036294 | A | ACATCCAT others(43): Show |
65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(62): Show |
80 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.1143-1078_1143-107 others(54): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036294 | ||||||
| chr19:4036294 | A | ACATCTAT others(14): Show |
4 | a0001c0001t0001g0043 a0001c0001t0001g0095 a0001c0001t0001g0097 others(1): Show |
4 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143-1078_1143-107 others(25): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036294 | ||||||
| chr19:4036303 | T | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(67): Show |
85 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1143-1071T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036303 | |||||||
| chr19:4036317 | C | CG | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1057_1143-105 others(5): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036317 | |||||||
| chr19:4036317 | CT | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(67): Show |
85 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1143-1056delT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036317 | |||||||
| chr19:4036319 | G | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1055G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036319 | |||||||
| chr19:4036320 | T | A | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1054T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036320 | |||||||
| chr19:4036320 | T | TCATACAC others(1): Show |
70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(67): Show |
85 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1143-1054_1143-105 others(12): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036320 | |||||||
| chr19:4036321 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(74): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1143-1053T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036321 | |||||||
| chr19:4036325 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(74): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1143-1049T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036325 | |||||||
| chr19:4036326 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(74): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1143-1048G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036326 | |||||||
| chr19:4036335 | T | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1039T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036335 | |||||||
| chr19:4036336 | A | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(67): Show |
85 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1143-1038A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036336 | |||||||
| chr19:4036350 | G | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(67): Show |
85 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1143-1024G>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036350 | |||||||
| chr19:4036356 | C | CACACA | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1017_1143-101 others(9): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036356 | ||||||
| chr19:4036360 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(75): Show |
93 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1143-1014T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036360 | |||||||
| chr19:4036373 | C | A | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-1001C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036373 | |||||||
| chr19:4036374 | C | T | 2 | a0004c0010t0002g0269 a0004c0010t0002g0270 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1143-1000C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036374 | |||||||
| chr19:4036375 | G | A | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-999G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036375 | |||||||
| chr19:4036379 | T | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-995T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036379 | |||||||
| chr19:4036381 | C | G | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-993C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036381 | |||||||
| chr19:4036388 | A | ATCCATAT others(10): Show |
7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-986_1143-985i others(19): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036388 | |||||||
| chr19:4036390 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(74): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1143-984G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036390 | |||||||
| chr19:4036393 | T | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-981T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036393 | |||||||
| chr19:4036407 | T | C | 34 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0002t0003g0190 others(31): Show |
37 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1143-967T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036407 | |||||||
| chr19:4036408 | G | A | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-966G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036408 | |||||||
| chr19:4036409 | T | TCACACG | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-960_1143-959i others(8): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036409 | ||||||
| chr19:4036419 | G | A | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-955G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036419 | |||||||
| chr19:4036432 | T | C | 8 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0124 others(5): Show |
8 | HG01081.hp2 HG01192.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143-942T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036432 | |||||||
| chr19:4036433 | G | A | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-941G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036433 | |||||||
| chr19:4036434 | TCATA | T | 4 | a0001c0003t0002g0271 a0001c0003t0002g0272 a0004c0010t0002g0269 others(1): Show |
4 | HG03490.hp2 HG03492.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1143-937_1143-934d others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036434 | ||||||
| chr19:4036435 | CATACAA | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-937_1143-932d others(8): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036435 | ||||||
| chr19:4036437 | TACAA | T | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1143-933_1143-930d others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036437 | ||||||
| chr19:4036449 | C | T | 2 | a0001c0005t0001g0284 a0001c0012t0001g0285 |
2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1143-925C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036449 | |||||||
| chr19:4036450 | A | T | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-924A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036450 | |||||||
| chr19:4036460 | G | A | 34 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0002t0003g0190 others(31): Show |
37 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1143-914G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036460 | |||||||
| chr19:4036470 | G | A | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-904G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036470 | |||||||
| chr19:4036471 | T | TCACACA | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-902_1143-897d others(8): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036471 | ||||||
| chr19:4036480 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1143-894C>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036480 | |||||||
| chr19:4036481 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1143-893A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036481 | |||||||
| chr19:4036495 | G | A | 34 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0002t0003g0190 others(31): Show |
37 | HG01109.hp2 HG01192.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1143-879G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036495 | |||||||
| chr19:4036496 | TCATA | T | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-875_1143-872d others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036496 | ||||||
| chr19:4036503 | A | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-871A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036503 | |||||||
| chr19:4036508 | ACACACAT others(25): Show |
A | 3 | a0001c0001t0001g0097 a0001c0003t0003g0218 a0001c0003t0004g0217 |
3 | HG00621.hp2 HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1143-842_1143-811d others(34): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036508 | ||||||
| chr19:4036512 | A | T | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-862A>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036512 | |||||||
| chr19:4036531 | C | CGTCACAC others(19): Show |
25 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(22): Show |
28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-843_1143-842i others(28): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036531 | |||||||
| chr19:4036531 | CT | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-842delT | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036531 | |||||||
| chr19:4036533 | G | A | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-841G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036533 | |||||||
| chr19:4036533 | G | C | 25 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(22): Show |
28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-841G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036533 | |||||||
| chr19:4036534 | T | A | 25 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(22): Show |
28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-840T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036534 | |||||||
| chr19:4036535 | T | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-839T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036535 | |||||||
| chr19:4036539 | T | C | 32 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0002t0003g0190 others(29): Show |
35 | HG01109.hp2 HG01192.hp2 HG01256.hp2 others(32): Show |
intron_variant | MODIFIER | c.1143-835T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036539 | |||||||
| chr19:4036540 | G | A | 32 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0002t0003g0190 others(29): Show |
35 | HG01109.hp2 HG01192.hp2 HG01256.hp2 others(32): Show |
intron_variant | MODIFIER | c.1143-834G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036540 | |||||||
| chr19:4036549 | T | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-825T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036549 | |||||||
| chr19:4036550 | A | C | 25 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(22): Show |
28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-824A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036550 | |||||||
| chr19:4036561 | A | G | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-813A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036561 | |||||||
| chr19:4036564 | G | A | 32 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0002t0003g0190 others(29): Show |
35 | HG01109.hp2 HG01192.hp2 HG01256.hp2 others(32): Show |
intron_variant | MODIFIER | c.1143-810G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036564 | |||||||
| chr19:4036565 | T | TCACATGC others(1): Show |
25 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(22): Show |
28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-805_1143-804i others(10): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036565 | ||||||
| chr19:4036574 | C | T | 25 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(22): Show |
28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-800C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036574 | |||||||
| chr19:4036578 | C | T | 25 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(22): Show |
28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-796C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036578 | |||||||
| chr19:4036579 | A | G | 25 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(22): Show |
28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-795A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036579 | |||||||
| chr19:4036583 | C | T | 25 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(22): Show |
28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-791C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036583 | |||||||
| chr19:4036588 | C | A | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-786C>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036588 | |||||||
| chr19:4036588 | C | T | 2 | a0001c0004t0004g0237 a0001c0004t0004g0238 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1143-786C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036588 | |||||||
| chr19:4036593 | T | C | 25 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(22): Show |
28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-781T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036593 | |||||||
| chr19:4036593 | T | TACAC | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-773_1143-770d others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036593 | ||||||
| chr19:4036608 | A | C | 2 | a0001c0003t0003g0218 a0001c0003t0004g0217 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1143-766A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036608 | |||||||
| chr19:4036622 | G | A | 2 | a0001c0003t0003g0218 a0001c0003t0004g0217 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1143-752G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036622 | |||||||
| chr19:4036625 | T | A | 35 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0002t0003g0190 others(32): Show |
38 | HG00741.hp2 HG01109.hp2 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.1143-749T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036625 | |||||||
| chr19:4036632 | T | C | 32 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0002t0003g0190 others(29): Show |
35 | HG01109.hp2 HG01192.hp2 HG01256.hp2 others(32): Show |
intron_variant | MODIFIER | c.1143-742T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036632 | |||||||
| chr19:4036633 | A | G | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-741A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036633 | |||||||
| chr19:4036636 | C | T | 2 | a0001c0003t0003g0218 a0001c0003t0004g0217 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1143-738C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036636 | |||||||
| chr19:4036637 | A | G | 2 | a0001c0003t0003g0218 a0001c0003t0004g0217 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1143-737A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036637 | |||||||
| chr19:4036638 | G | A | 2 | a0003c0011t0001g0277 a0003c0011t0001g0278 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1143-736G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036638 | |||||||
| chr19:4036641 | C | T | 2 | a0001c0003t0003g0218 a0001c0003t0004g0217 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1143-733C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036641 | |||||||
| chr19:4036644 | ACTG | A | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-729_1143-727d others(5): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036644 | |||||||
| chr19:4036646 | T | C | 27 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(24): Show |
30 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1143-728T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036646 | |||||||
| chr19:4036651 | T | C | 2 | a0001c0003t0003g0218 a0001c0003t0004g0217 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1143-723T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036651 | |||||||
| chr19:4036651 | T | TCACACAC others(50): Show |
7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-723_1143-722i others(59): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036651 | |||||||
| chr19:4036663 | T | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0124 a0001c0003t0001g0205 others(4): Show |
7 | HG01192.hp2 HG01256.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143-711T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036663 | |||||||
| chr19:4036664 | A | C | 25 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(22): Show |
28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-710A>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036664 | |||||||
| chr19:4036678 | G | A | 25 | a0001c0002t0003g0190 a0001c0002t0003g0197 a0001c0002t0003g0198 others(22): Show |
28 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143-696G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036678 | |||||||
| chr19:4036679 | T | TCACATGC others(3): Show |
26 | a0001c0001t0001g0173 a0001c0002t0003g0190 a0001c0002t0003g0197 others(23): Show |
29 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.1143-691_1143-690i others(12): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036679 | ||||||
| chr19:4036688 | C | T | 26 | a0001c0001t0001g0173 a0001c0002t0003g0190 a0001c0002t0003g0197 others(23): Show |
29 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.1143-686C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036688 | |||||||
| chr19:4036692 | T | C | 2 | a0001c0003t0003g0218 a0001c0003t0004g0217 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1143-682T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036692 | |||||||
| chr19:4036693 | A | G | 26 | a0001c0001t0001g0173 a0001c0002t0003g0190 a0001c0002t0003g0197 others(23): Show |
29 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.1143-681A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036693 | |||||||
| chr19:4036697 | C | T | 26 | a0001c0001t0001g0173 a0001c0002t0003g0190 a0001c0002t0003g0197 others(23): Show |
29 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.1143-677C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036697 | |||||||
| chr19:4036703 | A | G | 28 | a0001c0001t0001g0173 a0001c0002t0003g0190 a0001c0002t0003g0197 others(25): Show |
31 | HG01109.hp2 HG01243.hp1 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.1143-671A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036703 | |||||||
| chr19:4036704 | T | TCA | 26 | a0001c0001t0001g0173 a0001c0002t0003g0190 a0001c0002t0003g0197 others(23): Show |
29 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.1143-669_1143-668d others(4): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036704 | ||||||
| chr19:4036707 | T | C | 26 | a0001c0001t0001g0173 a0001c0002t0003g0190 a0001c0002t0003g0197 others(23): Show |
29 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.1143-667T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036707 | |||||||
| chr19:4036717 | C | CA | 17 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0143 others(14): Show |
20 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1143-656dupA | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036717 | ||||||
| chr19:4036765 | TACACCGT others(53): Show |
T | 1 | a0001c0001t0001g0043 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1143-590_1143-531d others(62): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036765 | ||||||
| chr19:4036772 | TCACA | T | 22 | a0001c0001t0001g0173 a0001c0002t0003g0190 a0001c0002t0003g0197 others(19): Show |
24 | HG01109.hp2 HG02145.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.1143-589_1143-586d others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036772 | ||||||
| chr19:4036772 | TCACACAC others(1): Show |
T | 3 | a0001c0004t0011g0006 a0001c0004t0012g0006 a0001c0004t0012g0234 |
4 | HG02486.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143-593_1143-586d others(10): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036772 | ||||||
| chr19:4036820 | CAGTCCAC others(279): Show |
C | 1 | a0001c0001t0001g0095 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1143-550_1143-265d others(2): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036820 | ||||||
| chr19:4036853 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1143-521C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036853 | |||||||
| chr19:4036917 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1143-457T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036917 | |||||||
| chr19:4036924 | G | C | 2 | a0001c0001t0001g0177 a0001c0003t0006g0279 |
2 | HG02717.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1143-450G>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036924 | |||||||
| chr19:4036926 | TCA | T | 6 | a0001c0001t0001g0177 a0001c0001t0001g0195 a0001c0003t0001g0207 others(3): Show |
6 | HG01433.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1143-437_1143-436d others(4): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036926 | ||||||
| chr19:4036926 | TCACA | T | 3 | a0001c0004t0004g0237 a0001c0004t0004g0238 a0001c0006t0004g0034 |
3 | HG02896.hp2 HG02897.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1143-439_1143-436d others(6): Show |
PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 4036926 | ||||||
| chr19:4036974 | C | T | 2 | a0003c0011t0001g0277 a0003c0011t0001g0278 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1143-400C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036974 | |||||||
| chr19:4036995 | A | G | 2 | a0001c0002t0003g0197 a0001c0002t0003g0198 |
2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1143-379A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4036995 | |||||||
| chr19:4037014 | C | T | 1 | a0001c0006t0004g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1143-360C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4037014 | |||||||
| chr19:4037082 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(207): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1143-292T>C | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4037082 | |||||||
| chr19:4037088 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1143-286A>G | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4037088 | |||||||
| chr19:4037178 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1143-196G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4037178 | |||||||
| chr19:4037295 | T | A | 1 | a0001c0002t0010g0115 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1143-79T>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4037295 | |||||||
| chr19:4037324 | G | A | 34 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(31): Show |
36 | HG00609.hp1 HG00609.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1143-50G>A | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 9/10 | chr19 | 4037324 | |||||||
| chr19:4037527 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(109): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.1273+23C>T | PIAS4 | ENSG00000105229.7 | transcript | ENST00000262971.3 | protein_coding | 10/10 | chr19 | 4037527 |