Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2516 |
| ensemblid | ENSG00000136931.10 |
| hgncid | 7983 |
| symbol | NR5A1 |
| name | nuclear receptor subfamily 5 group A member 1 |
| refseq_nuc | NM_004959.5 |
| refseq_prot | NP_004950.2 |
| ensembl_nuc | ENST00000373588.9 |
| ensembl_prot | ENSP00000362690.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 124481236 |
| end | 124507399 |
| strand | - |
| ver | v1.2 |
| region | chr9:124481236-124507399 |
| region5000 | chr9:124476236-124512399 |
| regionname0 | NR5A1_chr9_124481236_124507399 |
| regionname5000 | NR5A1_chr9_124476236_124512399 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 461 | 220 | 14 | 54 | 101 | 10 | 39 | 70 | NR5A1_chr9_124476236_124512399 | NR5A1 | MDYSY others(456): Show |
chr9 | 124476236 | 124512399 |
| a0002 | 0/0 | 461 | 134 | 82 | 4 | 42 | 0 | 6 | 31 | NR5A1_chr9_124476236_124512399 | NR5A1 | MDYSY others(456): Show |
chr9 | 124476236 | 124512399 |
| a0003 | 0/0 | 71 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | MDYSY others(66): Show |
chr9 | 124476236 | 124512399 |
| a0004 | 0/0 | 461 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | MDYSY others(456): Show |
chr9 | 124476236 | 124512399 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1383 | 219 | 13 | 54 | 101 | 10 | 39 | NR5A1_chr9_124476236_124512399 | NR5A1 | ATGGA others(1378): Show |
chr9 | 124476236 | 124512399 | ||
| a0001c0013 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | ATGGA others(1378): Show |
chr9 | 124476236 | 124512399 | ||
| a0002c0002 | 0/0 | 1383 | 95 | 45 | 2 | 42 | 0 | 6 | NR5A1_chr9_124476236_124512399 | NR5A1 | ATGGA others(1378): Show |
chr9 | 124476236 | 124512399 | ||
| a0002c0003 | 0/0 | 1383 | 26 | 24 | 2 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | ATGGA others(1378): Show |
chr9 | 124476236 | 124512399 | ||
| a0002c0004 | 0/0 | 1383 | 3 | 3 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | ATGGA others(1378): Show |
chr9 | 124476236 | 124512399 | ||
| a0002c0005 | 0/0 | 1383 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | ATGGA others(1378): Show |
chr9 | 124476236 | 124512399 | ||
| a0002c0006 | 0/0 | 1383 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | ATGGA others(1378): Show |
chr9 | 124476236 | 124512399 | ||
| a0002c0007 | 0/0 | 1383 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | ATGGA others(1378): Show |
chr9 | 124476236 | 124512399 | ||
| a0002c0008 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | ATGGA others(1378): Show |
chr9 | 124476236 | 124512399 | ||
| a0002c0009 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | ATGGA others(1378): Show |
chr9 | 124476236 | 124512399 | ||
| a0002c0010 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | ATGGA others(1378): Show |
chr9 | 124476236 | 124512399 | ||
| a0002c0011 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | ATGGA others(1378): Show |
chr9 | 124476236 | 124512399 | ||
| a0003c0014 | 0/0 | 1383 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | ATGGA others(1378): Show |
chr9 | 124476236 | 124512399 | ||
| a0004c0012 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | ATGGA others(1378): Show |
chr9 | 124476236 | 124512399 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3073 | 111 | 8 | 26 | 58 | 6 | 13 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3068): Show |
chr9 | 124476236 | 124512399 |
| a0001c0001t0002 | 1/1 | 3074 | 96 | 4 | 27 | 38 | 4 | 21 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0001c0001t0003 | 0/0 | 3074 | 8 | 1 | 0 | 3 | 0 | 4 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0001c0001t0007 | 0/0 | 3074 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0001c0001t0011 | 0/0 | 3073 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3068): Show |
chr9 | 124476236 | 124512399 |
| a0001c0001t0013 | 0/0 | 3074 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0001c0001t0016 | 0/0 | 3073 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3068): Show |
chr9 | 124476236 | 124512399 |
| a0001c0013t0002 | 0/0 | 3074 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0002c0002t0001 | 0/0 | 3073 | 66 | 30 | 0 | 33 | 0 | 3 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3068): Show |
chr9 | 124476236 | 124512399 |
| a0002c0002t0002 | 0/0 | 3074 | 6 | 2 | 0 | 2 | 0 | 2 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0002c0002t0003 | 0/0 | 3074 | 7 | 1 | 0 | 6 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0002c0002t0004 | 0/0 | 3074 | 4 | 4 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0002c0002t0005 | 0/0 | 3074 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0002c0002t0006 | 0/0 | 3075 | 3 | 3 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3070): Show |
chr9 | 124476236 | 124512399 |
| a0002c0002t0007 | 0/0 | 3074 | 2 | 1 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0002c0002t0008 | 0/0 | 3074 | 2 | 1 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0002c0002t0010 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3088): Show |
chr9 | 124476236 | 124512399 |
| a0002c0002t0012 | 0/0 | 3074 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0002c0002t0014 | 0/0 | 3074 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0002c0002t0018 | 0/0 | 3073 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3068): Show |
chr9 | 124476236 | 124512399 |
| a0002c0003t0001 | 0/0 | 3073 | 18 | 16 | 2 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3068): Show |
chr9 | 124476236 | 124512399 |
| a0002c0003t0004 | 0/0 | 3074 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0002c0003t0005 | 0/0 | 3074 | 4 | 4 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0002c0003t0006 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3070): Show |
chr9 | 124476236 | 124512399 |
| a0002c0003t0019 | 0/0 | 3073 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3068): Show |
chr9 | 124476236 | 124512399 |
| a0002c0004t0003 | 0/0 | 3074 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0002c0004t0004 | 0/0 | 3074 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0002c0004t0017 | 0/0 | 3074 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0002c0005t0001 | 0/0 | 3073 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3068): Show |
chr9 | 124476236 | 124512399 |
| a0002c0006t0002 | 0/0 | 3074 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0002c0007t0001 | 0/0 | 3073 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3068): Show |
chr9 | 124476236 | 124512399 |
| a0002c0008t0015 | 0/0 | 3074 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0002c0009t0002 | 0/0 | 3074 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0002c0010t0001 | 0/0 | 3073 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3068): Show |
chr9 | 124476236 | 124512399 |
| a0002c0011t0002 | 0/0 | 3074 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3069): Show |
chr9 | 124476236 | 124512399 |
| a0003c0014t0009 | 0/0 | 3073 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3068): Show |
chr9 | 124476236 | 124512399 |
| a0004c0012t0001 | 0/0 | 3073 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | AGCCT others(3068): Show |
chr9 | 124476236 | 124512399 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 17 | 0 | 2 | 15 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0002 | 0/0 | 12 | 0 | 4 | 4 | 2 | 2 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0003 | 0/0 | 9 | 1 | 5 | 1 | 0 | 2 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0004 | 0/0 | 9 | 0 | 2 | 4 | 0 | 3 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0022 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0049 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0003g0014 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0007g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0011g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0013g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0001t0016g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0001c0013t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0053 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0003g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0004g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0006g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0007g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0008g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0012g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0014g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0002t0018g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0003t0001g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0003t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0003t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0003t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0003t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0003t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0003t0004g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0003t0005g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0003t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0003t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0003t0019g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0004t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0004t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0004t0017g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0005t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0005t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0006t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0007t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0008t0015g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0009t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0010t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0002c0011t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0003c0014t0009g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| a0004c0012t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0221 | EUR | GBR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | GBR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | GBR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | FIN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | FIN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0212 | EAS | CHS | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | CHS | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | CHS | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00621 | hp2 | a0001 | c0001 | t0016 | g0133 | EAS | CHS | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00639 | hp2 | a0002 | c0002 | t0007 | g0202 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01099 | hp1 | a0002 | c0002 | t0008 | g0034 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01099 | hp2 | a0001 | c0001 | t0011 | g0056 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01167 | hp1 | a0002 | c0003 | t0001 | g0011 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01243 | hp1 | a0002 | c0003 | t0001 | g0093 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | CLM | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0080 | EUR | IBS | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01884 | hp1 | a0002 | c0003 | t0004 | g0052 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01884 | hp2 | a0002 | c0011 | t0002 | g0201 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0101 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01891 | hp2 | a0002 | c0009 | t0002 | g0181 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PEL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02015 | hp2 | a0002 | c0002 | t0003 | g0005 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02027 | hp2 | a0002 | c0002 | t0003 | g0005 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0058 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02083 | hp1 | a0002 | c0002 | t0003 | g0005 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02145 | hp2 | a0002 | c0003 | t0001 | g0025 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | CDX | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | CDX | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02257 | hp2 | a0002 | c0002 | t0008 | g0034 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02258 | hp1 | a0002 | c0002 | t0004 | g0021 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0094 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02280 | hp1 | a0002 | c0003 | t0005 | g0018 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0099 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0199 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | KHV | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02572 | hp2 | a0002 | c0002 | t0010 | g0055 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0083 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0207 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02622 | hp1 | a0002 | c0005 | t0001 | g0183 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0098 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02647 | hp1 | a0002 | c0003 | t0001 | g0029 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0086 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02717 | hp2 | a0002 | c0002 | t0006 | g0087 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02723 | hp1 | a0002 | c0002 | t0004 | g0088 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02723 | hp2 | a0001 | c0013 | t0002 | g0106 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02809 | hp1 | a0002 | c0007 | t0001 | g0035 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02818 | hp1 | a0002 | c0010 | t0001 | g0082 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0102 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02895 | hp1 | a0002 | c0007 | t0001 | g0035 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02895 | hp2 | a0002 | c0002 | t0006 | g0032 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02897 | hp1 | a0002 | c0002 | t0006 | g0032 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02922 | hp1 | a0002 | c0003 | t0001 | g0025 | AFR | ESN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02922 | hp2 | a0002 | c0002 | t0012 | g0206 | AFR | ESN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02965 | hp1 | a0002 | c0004 | t0017 | g0203 | AFR | ESN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0033 | AFR | ESN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02970 | hp2 | a0002 | c0005 | t0001 | g0184 | AFR | ESN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02976 | hp1 | a0002 | c0003 | t0001 | g0031 | AFR | ESN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02976 | hp2 | a0002 | c0004 | t0003 | g0200 | AFR | ESN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03017 | hp1 | a0002 | c0002 | t0014 | g0103 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03041 | hp1 | a0002 | c0002 | t0007 | g0204 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0097 | AFR | MSL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03098 | hp2 | a0002 | c0003 | t0001 | g0031 | AFR | MSL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03130 | hp1 | a0002 | c0004 | t0004 | g0194 | AFR | ESN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ESN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0095 | AFR | ESN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03139 | hp2 | a0002 | c0003 | t0005 | g0085 | AFR | ESN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03195 | hp2 | a0002 | c0003 | t0001 | g0011 | AFR | ESN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03209 | hp2 | a0002 | c0003 | t0019 | g0223 | AFR | MSL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03225 | hp1 | a0002 | c0002 | t0004 | g0021 | AFR | MSL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03225 | hp2 | a0002 | c0003 | t0001 | g0091 | AFR | MSL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03239 | hp1 | a0003 | c0014 | t0009 | g0054 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | MSL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03453 | hp2 | a0002 | c0003 | t0005 | g0018 | AFR | MSL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0053 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0053 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0104 | AFR | ESN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03516 | hp2 | a0002 | c0003 | t0001 | g0011 | AFR | ESN | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0074 | AFR | GWD | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0090 | AFR | MSL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03579 | hp2 | a0002 | c0003 | t0001 | g0028 | AFR | MSL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | STU | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | STU | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03704 | hp1 | a0001 | c0001 | t0013 | g0177 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0214 | SAS | BEB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0122 | SAS | BEB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | BEB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | BEB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | BEB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | BEB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0063 | SAS | STU | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | STU | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | STU | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0216 | SAS | STU | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | YRI | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18522 | hp2 | a0002 | c0008 | t0015 | g0182 | AFR | YRI | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | CHB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | CHB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | CHB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | YRI | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18906 | hp2 | a0002 | c0006 | t0002 | g0036 | AFR | YRI | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18957 | hp2 | a0004 | c0012 | t0001 | g0213 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18993 | hp2 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19011 | hp1 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0064 | AFR | LWK | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19030 | hp2 | a0002 | c0003 | t0006 | g0092 | AFR | LWK | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0089 | AFR | LWK | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19064 | hp1 | a0002 | c0002 | t0018 | g0069 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19082 | hp1 | a0001 | c0001 | t0007 | g0059 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19240 | hp1 | a0002 | c0003 | t0004 | g0052 | AFR | YRI | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | YRI | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA20129 | hp1 | a0002 | c0002 | t0004 | g0021 | AFR | ASW | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ASW | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | GIH | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0171 | SAS | GIH | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02109 | hp1 | a0002 | c0002 | t0005 | g0100 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02109 | hp2 | a0002 | c0003 | t0001 | g0029 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02486 | hp2 | a0002 | c0002 | t0003 | g0096 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02559 | hp1 | a0002 | c0003 | t0001 | g0011 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03471 | hp1 | a0002 | c0003 | t0001 | g0025 | AFR | MSL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0084 | AFR | MSL | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG06807 | hp1 | a0002 | c0006 | t0002 | g0036 | AFR | USA | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0028 | AFR | USA | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18955 | hp1 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | USA | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | USA | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| NA21309 | hp2 | a0002 | c0003 | t0005 | g0018 | AFR | LWK | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0049 | REF | REF | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0022 | REF | REF | NR5A1_chr9_124476236_124512399 | NR5A1 | chr9 | 124476236 | 124512399 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:124482765 | T | G | 1 | a0004 | 1 | NA18957.hp2 | missense_variant | MODERATE | c.1379A>C | p.Gln460Pro | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 7/7 | 1545/3074 | 1379/1386 | 460/461 | chr9 | 124482765 | |||
| chr9:124500523 | C | G | 2 | a0002 a0004 |
135 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(132): Show |
missense_variant | MODERATE | c.437G>C | p.Gly146Ala | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/7 | 603/3074 | 437/1386 | 146/461 | chr9 | 124500523 | |||
| chr9:124503109 | T | A | 1 | a0003 | 1 | HG03239.hp1 | stop_gained | HIGH | c.214A>T | p.Lys72* | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/7 | 380/3074 | 214/1386 | 72/461 | chr9 | 124503109 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:124482791 | C | T | 2 | a0002c0006 a0002c0008 |
3 | HG06807.hp1 NA18522.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.1353G>A | p.Leu451Leu | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 7/7 | 1519/3074 | 1353/1386 | 451/461 | chr9 | 124482791 | |||
| chr9:124500294 | G | A | 1 | a0002c0011 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.666C>T | p.Asn222Asn | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/7 | 832/3074 | 666/1386 | 222/461 | chr9 | 124500294 | |||
| chr9:124500327 | G | A | 1 | a0001c0013 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.633C>T | p.Tyr211Tyr | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/7 | 799/3074 | 633/1386 | 211/461 | chr9 | 124500327 | |||
| chr9:124500366 | C | T | 2 | a0002c0005 a0002c0007 |
4 | HG02622.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
synonymous_variant | LOW | c.594G>A | p.Pro198Pro | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/7 | 760/3074 | 594/1386 | 198/461 | chr9 | 124500366 | |||
| chr9:124500444 | G | A | 1 | a0002c0004 | 3 | HG02965.hp1 HG02976.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.516C>T | p.Ala172Ala | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/7 | 682/3074 | 516/1386 | 172/461 | chr9 | 124500444 | |||
| chr9:124500585 | C | T | 4 | a0002c0003 a0002c0006 a0002c0010 others(1): Show |
30 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
synonymous_variant | LOW | c.375G>A | p.Pro125Pro | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/7 | 541/3074 | 375/1386 | 125/461 | chr9 | 124500585 | |||
| chr9:124500684 | C | T | 1 | a0002c0010 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.276G>A | p.Arg92Arg | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/7 | 442/3074 | 276/1386 | 92/461 | chr9 | 124500684 | |||
| chr9:124503098 | C | G | 3 | a0002c0005 a0002c0008 a0002c0009 |
4 | HG01891.hp2 HG02622.hp1 HG02970.hp2 others(1): Show |
synonymous_variant | LOW | c.225G>C | p.Thr75Thr | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/7 | 391/3074 | 225/1386 | 75/461 | chr9 | 124503098 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:124481335 | G | A | 1 | a0001c0001t0013 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1423C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 7/7 | 1423 | chr9 | 124481335 | ||||||
| chr9:124481353 | C | CG | 6 | a0001c0001t0007 a0002c0002t0004 a0002c0002t0007 others(3): Show |
12 | HG00639.hp2 HG01099.hp1 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1404dupC | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 7/7 | 1404 | chr9 | 124481353 | ||||||
| chr9:124481355 | G | GT | 7 | a0001c0001t0003 a0002c0002t0003 a0002c0002t0006 others(4): Show |
22 | HG00597.hp2 HG02015.hp2 HG02027.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1402_*1403insA | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 7/7 | 1402 | chr9 | 124481355 | ||||||
| chr9:124481358 | A | G | 26 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(23): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
3_prime_UTR_variant | MODIFIER | c.*1400T>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 7/7 | 1400 | chr9 | 124481358 | ||||||
| chr9:124481478 | C | T | 1 | a0002c0002t0008 | 2 | HG01099.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1280G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 7/7 | 1280 | chr9 | 124481478 | ||||||
| chr9:124481542 | T | G | 1 | a0002c0004t0017 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1216A>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 7/7 | 1216 | chr9 | 124481542 | ||||||
| chr9:124481547 | C | T | 2 | a0002c0002t0005 a0002c0003t0005 |
5 | HG02109.hp1 HG02280.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1211G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 7/7 | 1211 | chr9 | 124481547 | ||||||
| chr9:124481816 | C | T | 1 | a0002c0002t0014 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*942G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 7/7 | 942 | chr9 | 124481816 | ||||||
| chr9:124481855 | G | A | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(22): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
3_prime_UTR_variant | MODIFIER | c.*903C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 7/7 | 903 | chr9 | 124481855 | ||||||
| chr9:124482094 | G | T | 1 | a0002c0002t0012 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*664C>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 7/7 | 664 | chr9 | 124482094 | ||||||
| chr9:124482112 | T | C | 4 | a0002c0002t0004 a0002c0002t0008 a0002c0003t0004 others(1): Show |
9 | HG01099.hp1 HG01884.hp1 HG02257.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*646A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 7/7 | 646 | chr9 | 124482112 | ||||||
| chr9:124482394 | G | A | 1 | a0002c0008t0015 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*364C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 7/7 | 364 | chr9 | 124482394 | ||||||
| chr9:124482584 | AC | A | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(19): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*173delG | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 7/7 | 173 | chr9 | 124482584 | ||||||
| chr9:124482656 | C | A | 1 | a0002c0002t0018 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*102G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 7/7 | 102 | chr9 | 124482656 | ||||||
| chr9:124482676 | G | A | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(19): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*82C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 7/7 | 82 | chr9 | 124482676 | ||||||
| chr9:124507253 | C | T | 1 | a0001c0001t0011 | 1 | HG01099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-20G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/7 | 3858 | chr9 | 124507253 | ||||||
| chr9:124507371 | C | CACGGCGG others(11): Show |
1 | a0002c0002t0010 | 1 | HG02572.hp2 | 5_prime_UTR_variant | MODIFIER | c.-156_-139dupCCGGCT others(12): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/7 | 3977 | chr9 | 124507371 | ||||||
| chr9:124507374 | G | A | 1 | a0002c0003t0019 | 1 | HG03209.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-141C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/7 | chr9 | 124507374 | |||||||
| chr9:124507380 | C | G | 1 | a0003c0014t0009 | 1 | HG03239.hp1 | 5_prime_UTR_variant | MODIFIER | c.-147G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/7 | 3985 | chr9 | 124507380 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:124483100 | C | T | 2 | a0002c0002t0001g0193 a0002c0002t0001g0195 |
2 | NA18969.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1139-95G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124483100 | |||||||
| chr9:124483117 | A | G | 5 | a0001c0013t0002g0106 a0002c0002t0005g0100 a0002c0003t0005g0018 others(2): Show |
7 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1139-112T>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124483117 | |||||||
| chr9:124483133 | C | T | 71 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(68): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.1139-128G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124483133 | |||||||
| chr9:124483166 | G | A | 1 | a0002c0002t0007g0204 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1139-161C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124483166 | |||||||
| chr9:124483250 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(148): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1139-245T>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124483250 | |||||||
| chr9:124483279 | C | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(147): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.1139-274G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124483279 | |||||||
| chr9:124483403 | G | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(146): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1139-398C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124483403 | |||||||
| chr9:124483426 | G | A | 1 | a0002c0002t0001g0072 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1139-421C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124483426 | |||||||
| chr9:124483585 | G | A | 1 | a0002c0002t0014g0103 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1139-580C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124483585 | |||||||
| chr9:124483647 | G | A | 1 | a0002c0002t0007g0202 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1139-642C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124483647 | |||||||
| chr9:124483885 | T | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0142 |
2 | HG02683.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1139-880A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124483885 | |||||||
| chr9:124483905 | G | A | 63 | a0001c0001t0001g0043 a0001c0001t0001g0077 a0001c0001t0001g0135 others(60): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.1139-900C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124483905 | |||||||
| chr9:124484019 | A | T | 1 | a0001c0001t0001g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1139-1014T>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484019 | |||||||
| chr9:124484081 | G | A | 4 | a0002c0003t0001g0084 a0002c0005t0001g0183 a0002c0005t0001g0184 others(1): Show |
5 | HG02622.hp1 HG02809.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1139-1076C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484081 | |||||||
| chr9:124484253 | G | C | 1 | a0002c0009t0002g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1139-1248C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484253 | |||||||
| chr9:124484305 | CGTG | C | 1 | a0001c0001t0002g0015 | 4 | NA18961.hp2 NA18990.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1139-1303_1139-130 others(7): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484305 | |||||||
| chr9:124484330 | G | A | 11 | a0001c0001t0001g0048 a0001c0001t0001g0129 a0001c0001t0001g0156 others(8): Show |
20 | HG00544.hp1 HG00621.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1139-1325C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484330 | |||||||
| chr9:124484338 | T | C | 1 | a0002c0002t0007g0204 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1139-1333A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484338 | |||||||
| chr9:124484365 | T | C | 66 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0129 others(63): Show |
111 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.1139-1360A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484365 | |||||||
| chr9:124484389 | C | T | 3 | a0002c0002t0001g0030 a0002c0002t0003g0096 a0002c0004t0017g0203 |
4 | HG02486.hp2 HG02965.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1139-1384G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484389 | |||||||
| chr9:124484472 | C | T | 66 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0129 others(63): Show |
111 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.1139-1467G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484472 | |||||||
| chr9:124484477 | G | A | 1 | a0002c0002t0014g0103 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1139-1472C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484477 | |||||||
| chr9:124484484 | T | C | 91 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0129 others(88): Show |
151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.1139-1479A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484484 | |||||||
| chr9:124484533 | T | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0044 others(5): Show |
14 | HG00140.hp1 HG00738.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1139-1528A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484533 | |||||||
| chr9:124484543 | G | A | 2 | a0002c0002t0001g0208 a0002c0002t0001g0209 |
2 | HG02056.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1139-1538C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484543 | |||||||
| chr9:124484549 | G | A | 1 | a0002c0005t0001g0184 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1139-1544C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484549 | |||||||
| chr9:124484551 | G | A | 1 | a0002c0002t0007g0204 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1139-1546C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484551 | |||||||
| chr9:124484562 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1139-1557G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484562 | |||||||
| chr9:124484625 | G | T | 1 | a0001c0001t0002g0078 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1139-1620C>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484625 | |||||||
| chr9:124484678 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1139-1673G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484678 | |||||||
| chr9:124484702 | C | T | 66 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0129 others(63): Show |
111 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.1139-1697G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484702 | |||||||
| chr9:124484753 | C | CTAAA | 6 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0126 others(3): Show |
9 | HG00438.hp2 HG00544.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1139-1752_1139-174 others(8): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484753 | |||||||
| chr9:124484753 | CTAAA | C | 108 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0048 others(105): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.1139-1752_1139-174 others(8): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484753 | |||||||
| chr9:124484842 | A | T | 1 | a0002c0002t0014g0103 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1139-1837T>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484842 | |||||||
| chr9:124484898 | G | A | 66 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0129 others(63): Show |
111 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.1139-1893C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484898 | |||||||
| chr9:124484995 | G | A | 2 | a0001c0001t0002g0049 a0001c0001t0002g0152 |
2 | HG00741.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1139-1990C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124484995 | |||||||
| chr9:124485016 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1139-2011G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124485016 | |||||||
| chr9:124485045 | G | A | 3 | a0002c0002t0004g0088 a0002c0006t0002g0036 a0002c0008t0015g0182 |
4 | HG02723.hp1 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1139-2040C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124485045 | |||||||
| chr9:124485397 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1139-2392G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124485397 | |||||||
| chr9:124485484 | G | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(219): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.1139-2479C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124485484 | |||||||
| chr9:124485652 | G | A | 67 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0129 others(64): Show |
112 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1139-2647C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124485652 | |||||||
| chr9:124485667 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(152): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1139-2662C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124485667 | |||||||
| chr9:124485706 | C | G | 1 | a0002c0002t0014g0103 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1139-2701G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124485706 | |||||||
| chr9:124485738 | G | C | 1 | a0002c0002t0008g0034 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1139-2733C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124485738 | |||||||
| chr9:124485765 | G | T | 1 | a0001c0001t0001g0130 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1139-2760C>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124485765 | |||||||
| chr9:124485798 | T | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0143 |
2 | HG00738.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1139-2793A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124485798 | |||||||
| chr9:124485962 | T | C | 1 | a0002c0002t0002g0216 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1139-2957A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124485962 | |||||||
| chr9:124486003 | G | A | 4 | a0002c0003t0001g0084 a0002c0005t0001g0183 a0002c0005t0001g0184 others(1): Show |
5 | HG02622.hp1 HG02809.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1139-2998C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124486003 | |||||||
| chr9:124486020 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(127): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1139-3015C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124486020 | |||||||
| chr9:124486111 | G | C | 3 | a0002c0002t0001g0037 a0002c0002t0004g0021 a0002c0004t0004g0194 |
6 | HG02258.hp1 HG02622.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1139-3106C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124486111 | |||||||
| chr9:124486145 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(156): Show |
245 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1139-3140A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124486145 | |||||||
| chr9:124486215 | G | C | 1 | a0002c0002t0007g0202 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1139-3210C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124486215 | |||||||
| chr9:124486551 | C | G | 7 | a0001c0013t0002g0106 a0002c0002t0002g0064 a0002c0002t0005g0100 others(4): Show |
9 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1139-3546G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124486551 | |||||||
| chr9:124486584 | G | A | 3 | a0002c0002t0003g0096 a0002c0004t0003g0200 a0002c0004t0017g0203 |
3 | HG02486.hp2 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1139-3579C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124486584 | |||||||
| chr9:124486647 | C | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(164): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1139-3642G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124486647 | |||||||
| chr9:124486667 | C | T | 1 | a0002c0002t0002g0064 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1139-3662G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124486667 | |||||||
| chr9:124486743 | C | T | 64 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0129 others(61): Show |
108 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1139-3738G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124486743 | |||||||
| chr9:124486763 | G | A | 12 | a0001c0001t0003g0014 a0001c0001t0003g0108 a0001c0001t0003g0122 others(9): Show |
22 | HG00597.hp2 HG01884.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1139-3758C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124486763 | |||||||
| chr9:124487064 | C | G | 68 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0129 others(65): Show |
113 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.1138+4017G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124487064 | |||||||
| chr9:124487130 | C | G | 1 | a0002c0002t0014g0103 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1138+3951G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124487130 | |||||||
| chr9:124487285 | C | A | 1 | a0002c0002t0006g0032 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1138+3796G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124487285 | |||||||
| chr9:124487589 | T | C | 6 | a0001c0001t0002g0166 a0002c0002t0001g0057 a0002c0002t0001g0071 others(3): Show |
6 | HG02083.hp2 NA18747.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.1138+3492A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124487589 | |||||||
| chr9:124487662 | G | A | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0187 |
3 | NA18939.hp2 NA18963.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1138+3419C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124487662 | |||||||
| chr9:124487664 | G | A | 2 | a0001c0001t0002g0115 a0001c0001t0002g0153 |
2 | HG01346.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1138+3417C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124487664 | |||||||
| chr9:124487717 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0114 a0001c0001t0001g0188 others(1): Show |
5 | NA18945.hp1 NA18968.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1138+3364C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124487717 | |||||||
| chr9:124488038 | A | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(157): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1138+3043T>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124488038 | |||||||
| chr9:124488062 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(151): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1138+3019C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124488062 | |||||||
| chr9:124488142 | G | GT | 153 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(150): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1138+2938dupA | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124488142 | |||||||
| chr9:124488185 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1138+2896G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124488185 | |||||||
| chr9:124488204 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(146): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1138+2877G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124488204 | |||||||
| chr9:124488222 | T | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(140): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1138+2859A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124488222 | |||||||
| chr9:124488318 | C | A | 1 | a0001c0001t0001g0048 | 2 | NA18980.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1138+2763G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124488318 | |||||||
| chr9:124488417 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1138+2664G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124488417 | |||||||
| chr9:124488481 | G | T | 34 | a0002c0002t0001g0016 a0002c0002t0001g0024 a0002c0002t0001g0026 others(31): Show |
48 | HG00423.hp1 HG01167.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.1138+2600C>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124488481 | |||||||
| chr9:124488560 | C | T | 20 | a0002c0002t0001g0016 a0002c0002t0001g0024 a0002c0002t0001g0026 others(17): Show |
28 | HG00423.hp1 HG02056.hp2 HG02135.hp2 others(25): Show |
intron_variant | MODIFIER | c.1138+2521G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124488560 | |||||||
| chr9:124488611 | C | A | 1 | a0001c0001t0002g0189 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1138+2470G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124488611 | |||||||
| chr9:124488873 | G | A | 4 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0005g0100 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1138+2208C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124488873 | |||||||
| chr9:124488881 | G | A | 2 | a0002c0002t0007g0204 a0002c0002t0014g0103 |
2 | HG03017.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1138+2200C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124488881 | |||||||
| chr9:124488963 | G | A | 5 | a0001c0001t0001g0038 a0001c0001t0001g0116 a0001c0001t0001g0143 others(2): Show |
7 | HG00738.hp1 HG00741.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1138+2118C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124488963 | |||||||
| chr9:124489073 | T | C | 7 | a0002c0003t0005g0018 a0002c0003t0005g0085 a0002c0004t0004g0194 others(4): Show |
10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1138+2008A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124489073 | |||||||
| chr9:124489105 | C | T | 2 | a0002c0002t0007g0204 a0002c0002t0014g0103 |
2 | HG03017.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1138+1976G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124489105 | |||||||
| chr9:124489178 | T | A | 3 | a0001c0001t0002g0136 a0001c0001t0002g0146 a0002c0002t0002g0063 |
3 | HG02004.hp1 HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1138+1903A>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124489178 | |||||||
| chr9:124489404 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1138+1677G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124489404 | |||||||
| chr9:124489501 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0128 |
2 | HG01261.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1138+1580G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124489501 | |||||||
| chr9:124489518 | G | A | 1 | a0002c0002t0014g0103 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1138+1563C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124489518 | |||||||
| chr9:124489570 | G | A | 1 | a0002c0002t0014g0103 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1138+1511C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124489570 | |||||||
| chr9:124489591 | G | A | 3 | a0002c0002t0007g0204 a0002c0002t0008g0034 a0002c0002t0014g0103 |
4 | HG01099.hp1 HG02257.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1138+1490C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124489591 | |||||||
| chr9:124489659 | C | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0065 a0001c0001t0001g0107 others(4): Show |
8 | HG00280.hp1 HG00280.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1138+1422G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124489659 | |||||||
| chr9:124489676 | C | T | 2 | a0002c0002t0007g0204 a0002c0002t0014g0103 |
2 | HG03017.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1138+1405G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124489676 | |||||||
| chr9:124489725 | A | C | 1 | a0001c0001t0002g0041 | 2 | HG02027.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1138+1356T>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124489725 | |||||||
| chr9:124489752 | C | A | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1138+1329G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124489752 | |||||||
| chr9:124489756 | A | C | 2 | a0002c0002t0007g0204 a0002c0002t0014g0103 |
2 | HG03017.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1138+1325T>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124489756 | |||||||
| chr9:124489757 | C | G | 2 | a0002c0002t0007g0204 a0002c0002t0014g0103 |
2 | HG03017.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1138+1324G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124489757 | |||||||
| chr9:124489795 | G | A | 1 | a0002c0002t0014g0103 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1138+1286C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124489795 | |||||||
| chr9:124490015 | T | C | 2 | a0002c0002t0007g0204 a0002c0002t0014g0103 |
2 | HG03017.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1138+1066A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124490015 | |||||||
| chr9:124490120 | T | C | 1 | a0001c0001t0002g0160 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1138+961A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124490120 | |||||||
| chr9:124490176 | C | T | 2 | a0002c0002t0001g0037 a0002c0002t0004g0021 |
5 | HG02258.hp1 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1138+905G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124490176 | |||||||
| chr9:124490271 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1138+810G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124490271 | |||||||
| chr9:124490330 | T | C | 1 | a0002c0002t0001g0053 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1138+751A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124490330 | |||||||
| chr9:124490383 | G | C | 9 | a0002c0002t0001g0020 a0002c0002t0001g0033 a0002c0002t0001g0058 others(6): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1138+698C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124490383 | |||||||
| chr9:124490438 | C | T | 1 | a0002c0002t0018g0069 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1138+643G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124490438 | |||||||
| chr9:124490441 | A | G | 2 | a0002c0002t0007g0204 a0002c0002t0014g0103 |
2 | HG03017.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1138+640T>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124490441 | |||||||
| chr9:124490578 | G | A | 1 | a0002c0002t0001g0072 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1138+503C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124490578 | |||||||
| chr9:124490632 | C | T | 4 | a0002c0003t0005g0018 a0002c0003t0005g0085 a0002c0004t0004g0194 others(1): Show |
6 | HG01891.hp2 HG02280.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1138+449G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124490632 | |||||||
| chr9:124490671 | A | G | 12 | a0001c0001t0003g0205 a0002c0002t0001g0198 a0002c0002t0002g0197 others(9): Show |
22 | HG00544.hp1 HG01884.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1138+410T>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124490671 | |||||||
| chr9:124490690 | G | A | 7 | a0002c0003t0005g0018 a0002c0003t0005g0085 a0002c0004t0004g0194 others(4): Show |
10 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1138+391C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124490690 | |||||||
| chr9:124490735 | C | T | 1 | a0002c0002t0002g0064 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1138+346G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124490735 | |||||||
| chr9:124490839 | G | A | 1 | a0002c0002t0014g0103 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1138+242C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124490839 | |||||||
| chr9:124490875 | C | G | 1 | a0002c0002t0014g0103 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1138+206G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 6/6 | chr9 | 124490875 | |||||||
| chr9:124491251 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.991-23C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491251 | |||||||
| chr9:124491269 | G | A | 1 | a0001c0001t0002g0015 | 4 | NA18961.hp2 NA18990.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.991-41C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491269 | |||||||
| chr9:124491276 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.991-48G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491276 | |||||||
| chr9:124491277 | G | A | 3 | a0002c0005t0001g0183 a0002c0005t0001g0184 a0002c0007t0001g0035 |
4 | HG02622.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.991-49C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491277 | |||||||
| chr9:124491373 | C | T | 1 | a0001c0001t0002g0162 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.991-145G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491373 | |||||||
| chr9:124491389 | A | G | 2 | a0002c0002t0008g0034 a0002c0002t0014g0103 |
3 | HG01099.hp1 HG02257.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.991-161T>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491389 | |||||||
| chr9:124491392 | A | G | 3 | a0002c0002t0002g0064 a0002c0002t0007g0202 a0002c0011t0002g0201 |
3 | HG00639.hp2 HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.991-164T>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491392 | |||||||
| chr9:124491401 | G | T | 1 | a0002c0002t0001g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.991-173C>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491401 | |||||||
| chr9:124491417 | C | T | 1 | a0001c0001t0001g0023 | 3 | HG03669.hp1 NA18987.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.991-189G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491417 | |||||||
| chr9:124491477 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.991-249G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491477 | |||||||
| chr9:124491481 | C | T | 1 | a0002c0003t0001g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.991-253G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491481 | |||||||
| chr9:124491484 | C | T | 1 | a0002c0002t0008g0034 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.991-256G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491484 | |||||||
| chr9:124491677 | T | TCACA | 2 | a0002c0002t0008g0034 a0002c0002t0014g0103 |
3 | HG01099.hp1 HG02257.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.991-453_991-450dup others(4): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491677 | |||||||
| chr9:124491763 | C | T | 7 | a0002c0002t0001g0198 a0002c0002t0002g0197 a0002c0002t0002g0216 others(4): Show |
13 | HG00544.hp1 HG02015.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.991-535G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491763 | |||||||
| chr9:124491848 | C | A | 1 | a0001c0001t0002g0189 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.991-620G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491848 | |||||||
| chr9:124491890 | G | GCA | 3 | a0001c0001t0001g0137 a0002c0003t0001g0093 a0002c0009t0002g0181 |
3 | HG01243.hp1 HG01891.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.991-664_991-663dup others(2): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491890 | |||||||
| chr9:124491892 | A | ACG | 3 | a0002c0005t0001g0183 a0002c0005t0001g0184 a0002c0007t0001g0035 |
4 | HG02622.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.991-665_991-664ins others(2): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491892 | |||||||
| chr9:124491942 | C | T | 2 | a0002c0002t0008g0034 a0002c0002t0014g0103 |
3 | HG01099.hp1 HG02257.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.991-714G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491942 | |||||||
| chr9:124491951 | G | C | 2 | a0002c0002t0008g0034 a0002c0002t0014g0103 |
3 | HG01099.hp1 HG02257.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.991-723C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124491951 | |||||||
| chr9:124492071 | A | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(146): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.991-843T>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124492071 | |||||||
| chr9:124492244 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(141): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.990+786G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124492244 | |||||||
| chr9:124492246 | C | A | 1 | a0002c0002t0006g0032 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.990+784G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124492246 | |||||||
| chr9:124492280 | G | A | 3 | a0002c0005t0001g0183 a0002c0005t0001g0184 a0002c0007t0001g0035 |
4 | HG02622.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.990+750C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124492280 | |||||||
| chr9:124492503 | C | CCATT | 3 | a0002c0002t0001g0019 a0002c0002t0001g0086 a0002c0004t0017g0203 |
5 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.990+523_990+526dup others(4): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124492503 | |||||||
| chr9:124492503 | CCATT | C | 5 | a0001c0001t0001g0079 a0002c0002t0001g0020 a0002c0002t0001g0090 others(2): Show |
8 | HG01099.hp1 HG01106.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.990+523_990+526del others(4): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124492503 | |||||||
| chr9:124492578 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(157): Show |
249 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.990+452G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124492578 | |||||||
| chr9:124492580 | T | C | 25 | a0001c0001t0003g0205 a0002c0002t0001g0193 a0002c0002t0001g0195 others(22): Show |
37 | HG00544.hp1 HG00639.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.990+450A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124492580 | |||||||
| chr9:124492587 | CCTCATCT others(4): Show |
C | 1 | a0002c0002t0001g0193 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.990+432_990+442del others(11): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124492587 | |||||||
| chr9:124492688 | C | T | 10 | a0001c0001t0001g0023 a0001c0001t0001g0067 a0001c0001t0001g0068 others(7): Show |
20 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.990+342G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124492688 | |||||||
| chr9:124493010 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG00544.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.990+20C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 5/6 | chr9 | 124493010 | |||||||
| chr9:124493162 | G | A | 1 | a0002c0002t0008g0034 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.871-13C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124493162 | |||||||
| chr9:124493169 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
140 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.871-20C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124493169 | |||||||
| chr9:124493247 | A | G | 2 | a0002c0002t0008g0034 a0002c0002t0014g0103 |
3 | HG01099.hp1 HG02257.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.871-98T>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124493247 | |||||||
| chr9:124493332 | G | C | 22 | a0001c0001t0002g0051 a0002c0002t0001g0016 a0002c0002t0001g0024 others(19): Show |
31 | HG00423.hp1 HG02056.hp2 HG02135.hp2 others(28): Show |
intron_variant | MODIFIER | c.871-183C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124493332 | |||||||
| chr9:124493335 | A | G | 2 | a0002c0002t0008g0034 a0002c0002t0014g0103 |
3 | HG01099.hp1 HG02257.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.871-186T>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124493335 | |||||||
| chr9:124493664 | C | T | 1 | a0002c0002t0002g0212 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.871-515G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124493664 | |||||||
| chr9:124493691 | C | G | 1 | a0001c0001t0002g0175 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.871-542G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124493691 | |||||||
| chr9:124493781 | G | A | 2 | a0002c0004t0004g0194 a0002c0004t0017g0203 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.871-632C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124493781 | |||||||
| chr9:124493784 | C | G | 1 | a0002c0002t0014g0103 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.871-635G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124493784 | |||||||
| chr9:124493820 | G | A | 1 | a0002c0002t0002g0216 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.871-671C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124493820 | |||||||
| chr9:124493944 | C | T | 47 | a0001c0001t0002g0051 a0001c0001t0003g0205 a0002c0002t0001g0016 others(44): Show |
71 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.871-795G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124493944 | |||||||
| chr9:124493945 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.871-796C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124493945 | |||||||
| chr9:124494224 | AG | A | 4 | a0002c0005t0001g0183 a0002c0005t0001g0184 a0002c0007t0001g0035 others(1): Show |
5 | HG01891.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-1076delC | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124494224 | |||||||
| chr9:124494227 | C | G | 4 | a0002c0005t0001g0183 a0002c0005t0001g0184 a0002c0007t0001g0035 others(1): Show |
5 | HG01891.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-1078G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124494227 | |||||||
| chr9:124494228 | ATTCCAC | A | 4 | a0002c0005t0001g0183 a0002c0005t0001g0184 a0002c0007t0001g0035 others(1): Show |
5 | HG01891.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-1085_871-1080d others(8): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124494228 | |||||||
| chr9:124494235 | T | C | 4 | a0002c0005t0001g0183 a0002c0005t0001g0184 a0002c0007t0001g0035 others(1): Show |
5 | HG01891.hp2 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-1086A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124494235 | |||||||
| chr9:124494260 | C | T | 1 | a0002c0002t0001g0098 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.871-1111G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124494260 | |||||||
| chr9:124494445 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.871-1296C>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124494445 | |||||||
| chr9:124494492 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.871-1343G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124494492 | |||||||
| chr9:124494707 | G | A | 2 | a0002c0002t0007g0202 a0002c0011t0002g0201 |
2 | HG00639.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.871-1558C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124494707 | |||||||
| chr9:124494716 | C | A | 1 | a0002c0002t0008g0034 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.871-1567G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124494716 | |||||||
| chr9:124494932 | G | A | 1 | a0002c0002t0014g0103 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.871-1783C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124494932 | |||||||
| chr9:124494959 | G | C | 1 | a0002c0002t0003g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.871-1810C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124494959 | |||||||
| chr9:124494979 | C | T | 1 | a0002c0002t0003g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.871-1830G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124494979 | |||||||
| chr9:124495004 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.871-1855G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124495004 | |||||||
| chr9:124495076 | G | A | 2 | a0001c0001t0001g0068 a0002c0002t0001g0097 |
2 | HG03098.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.871-1927C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124495076 | |||||||
| chr9:124495189 | T | TGCCCCCA others(13): Show |
1 | a0002c0002t0002g0207 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.871-2060_871-2041d others(22): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124495189 | |||||||
| chr9:124495211 | T | A | 1 | a0001c0001t0002g0170 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.871-2062A>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124495211 | |||||||
| chr9:124495223 | G | A | 1 | a0002c0002t0001g0191 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.871-2074C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124495223 | |||||||
| chr9:124495278 | T | C | 26 | a0001c0001t0001g0048 a0001c0001t0001g0156 a0001c0001t0002g0061 others(23): Show |
38 | HG00544.hp1 HG00639.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.871-2129A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124495278 | |||||||
| chr9:124495327 | C | G | 1 | a0001c0001t0001g0123 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.871-2178G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124495327 | |||||||
| chr9:124495448 | C | G | 1 | a0002c0002t0007g0204 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.871-2299G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124495448 | |||||||
| chr9:124495582 | C | T | 1 | a0001c0001t0003g0122 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.871-2433G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124495582 | |||||||
| chr9:124495603 | G | A | 1 | a0002c0004t0004g0194 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.871-2454C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124495603 | |||||||
| chr9:124495626 | C | A | 1 | a0001c0001t0002g0171 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.871-2477G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124495626 | |||||||
| chr9:124495659 | C | A | 1 | a0002c0002t0001g0024 | 3 | NA18939.hp1 NA19004.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.871-2510G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124495659 | |||||||
| chr9:124495696 | G | A | 1 | a0002c0009t0002g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.871-2547C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124495696 | |||||||
| chr9:124495756 | C | T | 3 | a0002c0003t0001g0029 a0002c0003t0001g0031 a0002c0003t0001g0091 |
5 | HG02109.hp2 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.871-2607G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124495756 | |||||||
| chr9:124495880 | T | G | 1 | a0002c0002t0001g0073 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.871-2731A>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124495880 | |||||||
| chr9:124495922 | G | A | 1 | a0002c0002t0001g0101 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.871-2773C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124495922 | |||||||
| chr9:124495936 | C | A | 9 | a0002c0002t0001g0020 a0002c0002t0001g0033 a0002c0002t0001g0058 others(6): Show |
12 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.871-2787G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124495936 | |||||||
| chr9:124496059 | T | C | 1 | a0001c0001t0002g0115 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.871-2910A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124496059 | |||||||
| chr9:124496063 | C | T | 2 | a0002c0002t0001g0210 a0002c0002t0001g0211 |
2 | NA18982.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.871-2914G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124496063 | |||||||
| chr9:124496184 | G | GCA | 27 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0002g0047 others(24): Show |
43 | HG00544.hp1 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.871-3037_871-3036d others(4): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124496184 | |||||||
| chr9:124496184 | GCA | G | 9 | a0002c0002t0002g0064 a0002c0002t0007g0202 a0002c0002t0014g0103 others(6): Show |
11 | HG00639.hp2 HG01884.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.871-3037_871-3036d others(4): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124496184 | |||||||
| chr9:124496184 | GCACACAC others(7): Show |
G | 1 | a0002c0009t0002g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.871-3049_871-3036d others(16): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124496184 | |||||||
| chr9:124496207 | C | A | 1 | a0002c0002t0008g0034 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.871-3058G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124496207 | |||||||
| chr9:124496263 | T | C | 1 | a0001c0001t0002g0172 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.871-3114A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124496263 | |||||||
| chr9:124496455 | C | A | 1 | a0002c0002t0001g0218 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.871-3306G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124496455 | |||||||
| chr9:124496757 | C | T | 2 | a0002c0003t0001g0028 a0002c0010t0001g0082 |
3 | HG02818.hp1 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.870+3333G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124496757 | |||||||
| chr9:124496769 | G | A | 2 | a0002c0002t0008g0034 a0002c0009t0002g0181 |
3 | HG01099.hp1 HG01891.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.870+3321C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124496769 | |||||||
| chr9:124497012 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.870+3078C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124497012 | |||||||
| chr9:124497072 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.870+3018A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124497072 | |||||||
| chr9:124497102 | C | T | 1 | a0002c0009t0002g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.870+2988G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124497102 | |||||||
| chr9:124497193 | T | G | 3 | a0002c0002t0007g0204 a0002c0002t0008g0034 a0002c0002t0014g0103 |
4 | HG01099.hp1 HG02257.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+2897A>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124497193 | |||||||
| chr9:124497263 | G | C | 2 | a0001c0001t0001g0190 a0001c0001t0002g0173 |
2 | HG00642.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.870+2827C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124497263 | |||||||
| chr9:124497276 | G | A | 1 | a0002c0009t0002g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.870+2814C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124497276 | |||||||
| chr9:124497290 | A | C | 2 | a0002c0002t0007g0202 a0002c0011t0002g0201 |
2 | HG00639.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.870+2800T>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124497290 | |||||||
| chr9:124497378 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.870+2712A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124497378 | |||||||
| chr9:124497397 | A | G | 1 | a0002c0004t0004g0194 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.870+2693T>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124497397 | |||||||
| chr9:124497449 | A | C | 4 | a0001c0001t0001g0065 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG00280.hp1 HG03710.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.870+2641T>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124497449 | |||||||
| chr9:124497651 | G | A | 2 | a0001c0001t0002g0155 a0001c0001t0002g0171 |
2 | HG01993.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.870+2439C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124497651 | |||||||
| chr9:124497829 | A | G | 1 | a0002c0002t0001g0053 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.870+2261T>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124497829 | |||||||
| chr9:124497887 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.870+2203C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124497887 | |||||||
| chr9:124497942 | G | A | 1 | a0002c0009t0002g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.870+2148C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124497942 | |||||||
| chr9:124498201 | C | T | 3 | a0001c0001t0002g0158 a0001c0001t0002g0159 a0001c0001t0002g0160 |
3 | HG02074.hp2 NA18612.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.870+1889G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124498201 | |||||||
| chr9:124498351 | C | A | 1 | a0002c0002t0001g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.870+1739G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124498351 | |||||||
| chr9:124498361 | T | G | 2 | a0002c0002t0007g0204 a0002c0002t0008g0034 |
3 | HG01099.hp1 HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.870+1729A>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124498361 | |||||||
| chr9:124498402 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.870+1688C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124498402 | |||||||
| chr9:124498816 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.870+1274C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124498816 | |||||||
| chr9:124499030 | T | G | 2 | a0002c0002t0014g0103 a0002c0009t0002g0181 |
2 | HG01891.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.870+1060A>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124499030 | |||||||
| chr9:124499171 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.870+919C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124499171 | |||||||
| chr9:124499296 | G | C | 1 | a0002c0002t0001g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.870+794C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124499296 | |||||||
| chr9:124499301 | C | T | 1 | a0002c0002t0001g0095 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.870+789G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124499301 | |||||||
| chr9:124499449 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.870+641G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124499449 | |||||||
| chr9:124499452 | A | G | 2 | a0002c0002t0001g0074 a0002c0002t0001g0094 |
2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.870+638T>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124499452 | |||||||
| chr9:124499614 | A | G | 20 | a0001c0001t0003g0205 a0002c0002t0001g0195 a0002c0002t0001g0196 others(17): Show |
31 | HG00544.hp1 HG00639.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.870+476T>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124499614 | |||||||
| chr9:124499764 | G | A | 1 | a0002c0002t0008g0034 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.870+326C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124499764 | |||||||
| chr9:124499852 | CAGCAGTG others(8): Show |
C | 1 | a0001c0001t0001g0174 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.870+223_870+237del others(15): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124499852 | |||||||
| chr9:124499906 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.870+184G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 4/6 | chr9 | 124499906 | |||||||
| chr9:124500789 | C | G | 1 | a0002c0002t0001g0217 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.245-74G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124500789 | |||||||
| chr9:124500791 | A | C | 1 | a0002c0002t0001g0217 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.245-76T>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124500791 | |||||||
| chr9:124500805 | G | A | 11 | a0002c0002t0001g0193 a0002c0002t0001g0195 a0002c0002t0001g0196 others(8): Show |
20 | HG00544.hp1 HG01884.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.245-90C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124500805 | |||||||
| chr9:124500953 | C | T | 2 | a0002c0002t0001g0090 a0002c0002t0010g0055 |
2 | HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.245-238G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124500953 | |||||||
| chr9:124500986 | C | A | 1 | a0002c0002t0001g0217 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.245-271G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124500986 | |||||||
| chr9:124501034 | G | A | 1 | a0002c0002t0010g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.245-319C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124501034 | |||||||
| chr9:124501177 | G | A | 1 | a0002c0002t0010g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.245-462C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124501177 | |||||||
| chr9:124501430 | C | T | 1 | a0002c0009t0002g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.245-715G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124501430 | |||||||
| chr9:124501440 | G | A | 1 | a0002c0002t0008g0034 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.245-725C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124501440 | |||||||
| chr9:124501536 | G | A | 2 | a0002c0003t0001g0199 a0002c0004t0003g0200 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.245-821C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124501536 | |||||||
| chr9:124501591 | G | A | 1 | a0001c0001t0002g0180 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.245-876C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124501591 | |||||||
| chr9:124501626 | G | T | 38 | a0001c0001t0001g0215 a0002c0002t0001g0016 a0002c0002t0001g0024 others(35): Show |
57 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.245-911C>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124501626 | |||||||
| chr9:124501717 | A | T | 1 | a0001c0001t0002g0153 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.245-1002T>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124501717 | |||||||
| chr9:124501887 | C | T | 1 | a0002c0004t0004g0194 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.245-1172G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124501887 | |||||||
| chr9:124502177 | G | C | 4 | a0002c0002t0001g0016 a0002c0002t0001g0208 a0002c0002t0001g0209 others(1): Show |
7 | HG02056.hp2 NA18942.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.244+902C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502177 | |||||||
| chr9:124502178 | G | T | 4 | a0002c0002t0001g0016 a0002c0002t0001g0208 a0002c0002t0001g0209 others(1): Show |
7 | HG02056.hp2 NA18942.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.244+901C>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502178 | |||||||
| chr9:124502233 | C | G | 1 | a0002c0002t0008g0034 | 2 | HG01099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.244+846G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502233 | |||||||
| chr9:124502234 | G | A | 1 | a0002c0002t0001g0017 | 3 | NA18942.hp2 NA18945.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.244+845C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502234 | |||||||
| chr9:124502266 | T | C | 12 | a0001c0001t0003g0205 a0002c0002t0001g0193 a0002c0002t0001g0195 others(9): Show |
20 | HG00544.hp1 HG01884.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.244+813A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502266 | |||||||
| chr9:124502289 | T | C | 1 | a0002c0002t0014g0103 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.244+790A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502289 | |||||||
| chr9:124502334 | T | C | 1 | a0001c0001t0002g0061 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.244+745A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502334 | |||||||
| chr9:124502415 | G | A | 48 | a0002c0002t0001g0007 a0002c0002t0001g0017 a0002c0002t0001g0019 others(45): Show |
72 | HG01099.hp1 HG01167.hp1 HG01243.hp1 others(69): Show |
intron_variant | MODIFIER | c.244+664C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502415 | |||||||
| chr9:124502483 | C | A | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG02698.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.244+596G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502483 | |||||||
| chr9:124502486 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.244+593G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502486 | |||||||
| chr9:124502501 | T | A | 2 | a0002c0002t0001g0037 a0002c0002t0004g0021 |
5 | HG02258.hp1 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.244+578A>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502501 | |||||||
| chr9:124502567 | G | A | 1 | a0002c0002t0014g0103 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.244+512C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502567 | |||||||
| chr9:124502609 | T | C | 2 | a0002c0002t0002g0064 a0002c0002t0010g0055 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.244+470A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502609 | |||||||
| chr9:124502643 | A | G | 1 | a0001c0001t0002g0157 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.244+436T>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502643 | |||||||
| chr9:124502648 | A | T | 1 | a0001c0001t0001g0116 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.244+431T>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502648 | |||||||
| chr9:124502657 | G | A | 2 | a0001c0001t0002g0080 a0001c0001t0013g0177 |
2 | HG01516.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.244+422C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502657 | |||||||
| chr9:124502663 | AGAGGTTA others(47): Show |
A | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.244+362_244+415del others(54): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502663 | |||||||
| chr9:124502719 | G | T | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.244+360C>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502719 | |||||||
| chr9:124502898 | T | C | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.244+181A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502898 | |||||||
| chr9:124502900 | C | T | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.244+179G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124502900 | |||||||
| chr9:124503007 | C | A | 14 | a0001c0001t0003g0205 a0002c0002t0001g0037 a0002c0002t0001g0193 others(11): Show |
25 | HG00544.hp1 HG01884.hp1 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.244+72G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124503007 | |||||||
| chr9:124503034 | C | A | 2 | a0002c0002t0002g0064 a0002c0002t0010g0055 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.244+45G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124503034 | |||||||
| chr9:124503041 | T | A | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.244+38A>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124503041 | |||||||
| chr9:124503065 | C | G | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.244+14G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 3/6 | chr9 | 124503065 | |||||||
| chr9:124503467 | C | G | 1 | a0002c0002t0014g0103 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-15-57G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124503467 | |||||||
| chr9:124503491 | C | T | 3 | a0002c0002t0001g0030 a0002c0002t0001g0089 a0002c0002t0004g0088 |
4 | HG02723.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-81G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124503491 | |||||||
| chr9:124503496 | G | A | 19 | a0001c0001t0001g0215 a0002c0002t0001g0016 a0002c0002t0001g0024 others(16): Show |
27 | HG00423.hp1 HG00558.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.-15-86C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124503496 | |||||||
| chr9:124503496 | G | C | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-15-86C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124503496 | |||||||
| chr9:124503511 | C | A | 1 | a0002c0002t0014g0103 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-15-101G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124503511 | |||||||
| chr9:124503570 | G | T | 1 | a0001c0001t0002g0115 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-15-160C>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124503570 | |||||||
| chr9:124503579 | C | T | 1 | a0001c0001t0001g0023 | 3 | HG03669.hp1 NA18987.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-15-169G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124503579 | |||||||
| chr9:124503580 | G | C | 24 | a0001c0001t0001g0215 a0001c0001t0002g0051 a0002c0002t0001g0016 others(21): Show |
33 | HG00423.hp1 HG00558.hp1 HG02056.hp2 others(30): Show |
intron_variant | MODIFIER | c.-15-170C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124503580 | |||||||
| chr9:124503616 | C | T | 1 | a0002c0002t0014g0103 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-15-206G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124503616 | |||||||
| chr9:124503825 | G | T | 2 | a0002c0002t0001g0037 a0002c0002t0004g0021 |
5 | HG02258.hp1 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-415C>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124503825 | |||||||
| chr9:124503853 | T | C | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-15-443A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124503853 | |||||||
| chr9:124503855 | C | G | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-15-445G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124503855 | |||||||
| chr9:124503887 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-15-477C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124503887 | |||||||
| chr9:124503982 | G | C | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-15-572C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124503982 | |||||||
| chr9:124503983 | C | G | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-15-573G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124503983 | |||||||
| chr9:124504024 | C | CAG | 34 | a0001c0001t0001g0008 a0001c0001t0001g0048 a0001c0001t0001g0109 others(31): Show |
49 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.-15-616_-15-615dup others(2): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504024 | |||||||
| chr9:124504024 | C | G | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-15-614G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504024 | |||||||
| chr9:124504028 | G | C | 3 | a0002c0005t0001g0183 a0002c0005t0001g0184 a0002c0008t0015g0182 |
3 | HG02622.hp1 HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-15-618C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504028 | |||||||
| chr9:124504039 | AGAGAGAG others(6): Show |
A | 3 | a0002c0002t0001g0102 a0002c0002t0001g0104 a0002c0006t0002g0036 |
4 | HG02818.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-642_-15-630del others(13): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504039 | |||||||
| chr9:124504045 | AGAGAGAC | A | 3 | a0002c0002t0001g0020 a0002c0002t0001g0098 a0002c0002t0005g0100 |
5 | HG02109.hp1 HG02630.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-642_-15-636del others(7): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504045 | |||||||
| chr9:124504047 | AGAGAC | A | 4 | a0002c0002t0001g0033 a0002c0002t0001g0089 a0002c0003t0001g0031 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-642_-15-638del others(5): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504047 | |||||||
| chr9:124504049 | AGAC | A | 7 | a0002c0002t0001g0058 a0002c0002t0001g0090 a0002c0002t0001g0097 others(4): Show |
7 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15-642_-15-640del others(3): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504049 | |||||||
| chr9:124504051 | A | AG | 5 | a0002c0002t0001g0071 a0002c0002t0010g0055 a0002c0003t0001g0093 others(2): Show |
5 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-642_-15-641ins others(1): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504051 | |||||||
| chr9:124504051 | A | AGAG | 5 | a0002c0002t0001g0007 a0002c0002t0001g0057 a0002c0002t0001g0095 others(2): Show |
5 | HG02976.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-642_-15-641ins others(3): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504051 | |||||||
| chr9:124504051 | A | AGAGAG | 4 | a0002c0003t0001g0029 a0002c0003t0001g0091 a0002c0008t0015g0182 others(1): Show |
4 | HG02647.hp1 HG02818.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-642_-15-641ins others(5): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504051 | |||||||
| chr9:124504051 | A | AGAGAGAG | 4 | a0002c0002t0001g0007 a0002c0002t0004g0021 a0002c0003t0001g0028 others(1): Show |
5 | HG02451.hp2 HG02615.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-642_-15-641ins others(7): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504051 | |||||||
| chr9:124504051 | A | AGAGAGAG others(2): Show |
3 | a0002c0002t0001g0037 a0002c0002t0004g0021 a0002c0003t0005g0085 |
3 | HG02258.hp1 HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-15-642_-15-641ins others(9): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504051 | |||||||
| chr9:124504051 | A | AGAGAGAG others(4): Show |
6 | a0002c0002t0001g0007 a0002c0002t0001g0017 a0002c0002t0001g0019 others(3): Show |
7 | HG02258.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15-642_-15-641ins others(11): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504051 | |||||||
| chr9:124504051 | A | AGAGAGAG others(6): Show |
3 | a0002c0002t0001g0072 a0002c0003t0001g0011 a0002c0005t0001g0183 |
3 | HG02559.hp1 HG02622.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-15-642_-15-641ins others(13): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504051 | |||||||
| chr9:124504051 | A | AGAGAGAG others(8): Show |
4 | a0002c0002t0001g0086 a0002c0002t0006g0087 a0002c0003t0006g0092 others(1): Show |
4 | HG02717.hp1 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-642_-15-641ins others(15): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504051 | |||||||
| chr9:124504051 | A | AGAGAGAG others(10): Show |
5 | a0002c0002t0001g0017 a0002c0002t0001g0019 a0002c0002t0001g0073 others(2): Show |
7 | HG02145.hp1 HG02486.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15-642_-15-641ins others(17): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504051 | |||||||
| chr9:124504051 | A | AGAGAGAG others(12): Show |
1 | a0002c0009t0002g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-15-642_-15-641ins others(19): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504051 | |||||||
| chr9:124504051 | A | AGAGAGAG others(14): Show |
2 | a0002c0002t0001g0019 a0002c0002t0002g0064 |
2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-15-642_-15-641ins others(21): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504051 | |||||||
| chr9:124504051 | A | AGAGAGAG others(16): Show |
3 | a0002c0002t0008g0034 a0002c0002t0014g0103 a0002c0002t0018g0069 |
3 | HG01099.hp1 HG03017.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-15-642_-15-641ins others(23): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504051 | |||||||
| chr9:124504051 | A | AGAGAGAG others(18): Show |
2 | a0002c0002t0001g0007 a0002c0002t0008g0034 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-15-642_-15-641ins others(25): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504051 | |||||||
| chr9:124504051 | AC | A | 6 | a0002c0002t0001g0030 a0002c0002t0001g0033 a0002c0002t0004g0088 others(3): Show |
9 | HG01167.hp1 HG02109.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15-642delG | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504051 | |||||||
| chr9:124504052 | C | A | 37 | a0002c0002t0001g0007 a0002c0002t0001g0017 a0002c0002t0001g0019 others(34): Show |
51 | HG01099.hp1 HG01243.hp1 HG01891.hp2 others(48): Show |
intron_variant | MODIFIER | c.-15-642G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504052 | |||||||
| chr9:124504052 | C | CGA | 5 | a0001c0001t0001g0001 a0001c0001t0001g0142 a0001c0001t0002g0009 others(2): Show |
7 | HG00558.hp2 HG00639.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15-644_-15-643dup others(2): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504052 | |||||||
| chr9:124504052 | C | G | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-15-642G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504052 | |||||||
| chr9:124504053 | G | A | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-15-643C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504053 | |||||||
| chr9:124504054 | A | C | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-15-644T>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504054 | |||||||
| chr9:124504074 | A | AG | 7 | a0001c0001t0002g0152 a0002c0002t0001g0086 a0002c0002t0006g0087 others(4): Show |
8 | HG00741.hp1 HG02109.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-665_-15-664ins others(1): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504074 | |||||||
| chr9:124504083 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-15-673C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504083 | |||||||
| chr9:124504225 | G | A | 43 | a0002c0002t0001g0007 a0002c0002t0001g0017 a0002c0002t0001g0019 others(40): Show |
65 | HG01167.hp1 HG01243.hp1 HG01891.hp1 others(62): Show |
intron_variant | MODIFIER | c.-15-815C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504225 | |||||||
| chr9:124504282 | C | T | 2 | a0002c0003t0001g0028 a0002c0010t0001g0082 |
3 | HG02818.hp1 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-15-872G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504282 | |||||||
| chr9:124504310 | C | G | 2 | a0001c0001t0002g0150 a0001c0001t0002g0151 |
2 | HG01081.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-15-900G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504310 | |||||||
| chr9:124504369 | G | T | 41 | a0002c0002t0001g0007 a0002c0002t0001g0017 a0002c0002t0001g0019 others(38): Show |
62 | HG01167.hp1 HG01243.hp1 HG01891.hp1 others(59): Show |
intron_variant | MODIFIER | c.-15-959C>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504369 | |||||||
| chr9:124504373 | C | G | 7 | a0002c0002t0001g0195 a0002c0002t0001g0196 a0002c0002t0001g0198 others(4): Show |
12 | HG00544.hp1 HG02015.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15-963G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504373 | |||||||
| chr9:124504383 | G | A | 2 | a0002c0002t0001g0037 a0002c0002t0004g0021 |
5 | HG02258.hp1 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-973C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504383 | |||||||
| chr9:124504559 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-15-1149C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504559 | |||||||
| chr9:124504631 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-15-1221G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504631 | |||||||
| chr9:124504644 | G | C | 1 | a0001c0001t0001g0149 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-15-1234C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504644 | |||||||
| chr9:124504687 | C | A | 1 | a0001c0001t0002g0050 | 2 | HG01175.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-15-1277G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504687 | |||||||
| chr9:124504873 | C | G | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-15-1463G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504873 | |||||||
| chr9:124504874 | G | C | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-15-1464C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504874 | |||||||
| chr9:124504888 | C | G | 1 | a0001c0001t0001g0079 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-15-1478G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504888 | |||||||
| chr9:124504905 | C | A | 21 | a0001c0001t0001g0215 a0001c0001t0002g0051 a0002c0002t0001g0016 others(18): Show |
30 | HG00423.hp1 HG00558.hp1 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.-15-1495G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504905 | |||||||
| chr9:124504906 | C | A | 1 | a0001c0013t0002g0106 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-15-1496G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504906 | |||||||
| chr9:124504974 | C | G | 1 | a0001c0013t0002g0106 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-15-1564G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124504974 | |||||||
| chr9:124505002 | G | A | 51 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0067 others(48): Show |
86 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.-15-1592C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505002 | |||||||
| chr9:124505002 | G | C | 1 | a0002c0002t0002g0207 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-15-1592C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505002 | |||||||
| chr9:124505024 | G | A | 21 | a0001c0001t0001g0215 a0001c0001t0002g0051 a0002c0002t0001g0016 others(18): Show |
30 | HG00423.hp1 HG00558.hp1 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.-15-1614C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505024 | |||||||
| chr9:124505068 | C | T | 1 | a0002c0004t0004g0194 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-15-1658G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505068 | |||||||
| chr9:124505071 | A | G | 1 | a0001c0001t0001g0038 | 2 | HG01243.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-15-1661T>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505071 | |||||||
| chr9:124505106 | G | GGCCCTCA others(8): Show |
1 | a0001c0001t0001g0179 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-15-1697_-15-1696i others(17): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505106 | |||||||
| chr9:124505110 | G | C | 1 | a0001c0001t0001g0179 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-15-1700C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505110 | |||||||
| chr9:124505113 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-15-1703A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505113 | |||||||
| chr9:124505410 | A | G | 94 | a0001c0001t0001g0215 a0001c0001t0002g0051 a0001c0001t0003g0205 others(91): Show |
138 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.-16+1839T>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505410 | |||||||
| chr9:124505455 | G | A | 1 | a0001c0001t0002g0180 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-16+1794C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505455 | |||||||
| chr9:124505455 | G | C | 1 | a0002c0002t0001g0219 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-16+1794C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505455 | |||||||
| chr9:124505468 | C | T | 1 | a0001c0001t0002g0081 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-16+1781G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505468 | |||||||
| chr9:124505557 | G | T | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-16+1692C>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505557 | |||||||
| chr9:124505640 | G | C | 1 | a0001c0001t0002g0080 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-16+1609C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505640 | |||||||
| chr9:124505641 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-16+1608G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505641 | |||||||
| chr9:124505642 | T | A | 1 | a0001c0001t0002g0080 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-16+1607A>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505642 | |||||||
| chr9:124505643 | G | T | 1 | a0001c0001t0002g0080 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-16+1606C>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505643 | |||||||
| chr9:124505644 | G | C | 1 | a0001c0001t0002g0080 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-16+1605C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505644 | |||||||
| chr9:124505645 | A | C | 1 | a0001c0001t0002g0080 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-16+1604T>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505645 | |||||||
| chr9:124505646 | A | C | 1 | a0001c0001t0002g0080 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-16+1603T>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505646 | |||||||
| chr9:124505648 | T | C | 4 | a0002c0005t0001g0183 a0002c0005t0001g0184 a0002c0008t0015g0182 others(1): Show |
4 | HG01891.hp2 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+1601A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505648 | |||||||
| chr9:124505649 | G | T | 1 | a0001c0001t0002g0080 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-16+1600C>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505649 | |||||||
| chr9:124505650 | G | T | 1 | a0001c0001t0002g0080 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-16+1599C>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505650 | |||||||
| chr9:124505651 | G | T | 1 | a0001c0001t0002g0080 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-16+1598C>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505651 | |||||||
| chr9:124505654 | T | A | 1 | a0001c0001t0002g0080 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-16+1595A>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505654 | |||||||
| chr9:124505655 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-16+1594G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505655 | |||||||
| chr9:124505745 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-16+1504C>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505745 | |||||||
| chr9:124505775 | G | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0185 a0001c0001t0001g0186 others(4): Show |
11 | HG00642.hp2 HG00673.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16+1474C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505775 | |||||||
| chr9:124505785 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-16+1464G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505785 | |||||||
| chr9:124505825 | T | C | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-16+1424A>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505825 | |||||||
| chr9:124505906 | C | G | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-16+1343G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505906 | |||||||
| chr9:124505907 | G | C | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-16+1342C>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505907 | |||||||
| chr9:124505960 | CAG | C | 38 | a0001c0001t0001g0215 a0001c0001t0002g0051 a0001c0001t0002g0192 others(35): Show |
55 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.-16+1287_-16+1288d others(4): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505960 | |||||||
| chr9:124505969 | T | G | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-16+1280A>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124505969 | |||||||
| chr9:124506022 | A | C | 1 | a0001c0001t0001g0077 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-16+1227T>G | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124506022 | |||||||
| chr9:124506161 | G | A | 35 | a0001c0001t0001g0215 a0001c0001t0003g0205 a0002c0002t0001g0016 others(32): Show |
49 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-16+1088C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124506161 | |||||||
| chr9:124506183 | C | A | 1 | a0001c0001t0001g0220 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-16+1066G>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124506183 | |||||||
| chr9:124506204 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-16+1045C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124506204 | |||||||
| chr9:124506224 | TCTC | T | 2 | a0001c0001t0001g0076 a0001c0001t0002g0027 |
3 | HG00438.hp1 NA19074.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-16+1022_-16+1024d others(5): Show |
NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124506224 | |||||||
| chr9:124506297 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-16+952G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124506297 | |||||||
| chr9:124506683 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | NA18963.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-16+566G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124506683 | |||||||
| chr9:124506734 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | NA18963.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-16+515C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124506734 | |||||||
| chr9:124506747 | C | T | 1 | a0002c0002t0001g0074 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-16+502G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124506747 | |||||||
| chr9:124506838 | C | T | 7 | a0002c0002t0001g0017 a0002c0002t0001g0057 a0002c0002t0001g0070 others(4): Show |
9 | NA18747.hp2 NA18942.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16+411G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124506838 | |||||||
| chr9:124506860 | C | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | NA18963.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-16+389G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124506860 | |||||||
| chr9:124506870 | C | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0066 |
6 | HG01081.hp2 HG01346.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+379G>C | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124506870 | |||||||
| chr9:124506881 | A | T | 1 | a0003c0014t0009g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-16+368T>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124506881 | |||||||
| chr9:124507006 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-16+243G>A | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124507006 | |||||||
| chr9:124507018 | G | A | 2 | a0002c0002t0002g0064 a0002c0002t0010g0055 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-16+231C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124507018 | |||||||
| chr9:124507062 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-16+187C>T | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124507062 | |||||||
| chr9:124507080 | A | AG | 8 | a0001c0001t0001g0060 a0001c0001t0002g0061 a0001c0001t0002g0062 others(5): Show |
8 | HG02055.hp2 HG03688.hp2 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.-16+168dupC | NR5A1 | ENSG00000136931.10 | transcript | ENST00000373588.9 | protein_coding | 1/6 | chr9 | 124507080 |