Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8013 |
| ensemblid | ENSG00000119508.18 |
| hgncid | 7982 |
| symbol | NR4A3 |
| name | nuclear receptor subfamily 4 group A member 3 |
| refseq_nuc | NM_006981.4 |
| refseq_prot | NP_008912.2 |
| ensembl_nuc | ENST00000395097.7 |
| ensembl_prot | ENSP00000378531.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 99821885 |
| end | 99866891 |
| strand | + |
| ver | v1.2 |
| region | chr9:99821885-99866891 |
| region5000 | chr9:99816885-99871891 |
| regionname0 | NR4A3_chr9_99821885_99866891 |
| regionname5000 | NR4A3_chr9_99816885_99871891 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 626 | 160 | 41 | 26 | 71 | 4 | 16 | 52 | NR4A3_chr9_99816885_99871891 | NR4A3 | MPCVQ others(621): Show |
chr9 | 99816885 | 99871891 |
| a0002 | 0/0 | 626 | 116 | 32 | 25 | 43 | 4 | 12 | 32 | NR4A3_chr9_99816885_99871891 | NR4A3 | MPCVQ others(621): Show |
chr9 | 99816885 | 99871891 |
| a0003 | 0/0 | 626 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | MPCVQ others(621): Show |
chr9 | 99816885 | 99871891 |
| a0004 | 0/0 | 626 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | MPCVQ others(621): Show |
chr9 | 99816885 | 99871891 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1878 | 153 | 38 | 23 | 71 | 4 | 15 | NR4A3_chr9_99816885_99871891 | NR4A3 | ATGCC others(1873): Show |
chr9 | 99816885 | 99871891 | ||
| a0001c0004 | 0/0 | 1878 | 5 | 2 | 2 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | ATGCC others(1873): Show |
chr9 | 99816885 | 99871891 | ||
| a0001c0007 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | ATGCC others(1873): Show |
chr9 | 99816885 | 99871891 | ||
| a0001c0008 | 0/0 | 1878 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | ATGCC others(1873): Show |
chr9 | 99816885 | 99871891 | ||
| a0002c0002 | 0/0 | 1878 | 85 | 28 | 17 | 31 | 1 | 8 | NR4A3_chr9_99816885_99871891 | NR4A3 | ATGCC others(1873): Show |
chr9 | 99816885 | 99871891 | ||
| a0002c0003 | 0/0 | 1878 | 21 | 0 | 4 | 12 | 2 | 3 | NR4A3_chr9_99816885_99871891 | NR4A3 | ATGCC others(1873): Show |
chr9 | 99816885 | 99871891 | ||
| a0002c0005 | 0/0 | 1878 | 5 | 3 | 2 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | ATGCC others(1873): Show |
chr9 | 99816885 | 99871891 | ||
| a0002c0006 | 0/0 | 1878 | 5 | 1 | 2 | 0 | 1 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | ATGCC others(1873): Show |
chr9 | 99816885 | 99871891 | ||
| a0003c0010 | 0/0 | 1878 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | ATGCC others(1873): Show |
chr9 | 99816885 | 99871891 | ||
| a0004c0009 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | ATGCC others(1873): Show |
chr9 | 99816885 | 99871891 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5607 | 66 | 30 | 10 | 13 | 4 | 8 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5602): Show |
chr9 | 99816885 | 99871891 |
| a0001c0001t0002 | 0/0 | 5609 | 18 | 5 | 1 | 11 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5604): Show |
chr9 | 99816885 | 99871891 |
| a0001c0001t0003 | 1/0 | 5604 | 58 | 0 | 11 | 43 | 0 | 3 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5599): Show |
chr9 | 99816885 | 99871891 |
| a0001c0001t0004 | 0/0 | 5607 | 3 | 0 | 0 | 2 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5602): Show |
chr9 | 99816885 | 99871891 |
| a0001c0001t0006 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5599): Show |
chr9 | 99816885 | 99871891 |
| a0001c0001t0007 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5599): Show |
chr9 | 99816885 | 99871891 |
| a0001c0001t0008 | 0/0 | 5604 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5599): Show |
chr9 | 99816885 | 99871891 |
| a0001c0001t0009 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5602): Show |
chr9 | 99816885 | 99871891 |
| a0001c0001t0010 | 0/0 | 5561 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5556): Show |
chr9 | 99816885 | 99871891 |
| a0001c0001t0011 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5602): Show |
chr9 | 99816885 | 99871891 |
| a0001c0001t0012 | 0/0 | 5607 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5602): Show |
chr9 | 99816885 | 99871891 |
| a0001c0001t0014 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5602): Show |
chr9 | 99816885 | 99871891 |
| a0001c0004t0001 | 0/0 | 5607 | 4 | 2 | 2 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5602): Show |
chr9 | 99816885 | 99871891 |
| a0001c0004t0002 | 0/0 | 5609 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5604): Show |
chr9 | 99816885 | 99871891 |
| a0001c0007t0001 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5602): Show |
chr9 | 99816885 | 99871891 |
| a0001c0008t0002 | 0/0 | 5609 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5604): Show |
chr9 | 99816885 | 99871891 |
| a0002c0002t0001 | 0/0 | 5607 | 21 | 19 | 2 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5602): Show |
chr9 | 99816885 | 99871891 |
| a0002c0002t0002 | 0/0 | 5609 | 59 | 9 | 15 | 28 | 1 | 6 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5604): Show |
chr9 | 99816885 | 99871891 |
| a0002c0002t0003 | 0/0 | 5604 | 3 | 0 | 0 | 2 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5599): Show |
chr9 | 99816885 | 99871891 |
| a0002c0002t0004 | 0/0 | 5607 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5602): Show |
chr9 | 99816885 | 99871891 |
| a0002c0002t0013 | 0/0 | 5609 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5604): Show |
chr9 | 99816885 | 99871891 |
| a0002c0003t0002 | 0/0 | 5609 | 2 | 0 | 0 | 2 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5604): Show |
chr9 | 99816885 | 99871891 |
| a0002c0003t0004 | 0/0 | 5607 | 19 | 0 | 4 | 10 | 2 | 3 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5602): Show |
chr9 | 99816885 | 99871891 |
| a0002c0005t0001 | 0/0 | 5607 | 3 | 2 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5602): Show |
chr9 | 99816885 | 99871891 |
| a0002c0005t0004 | 0/0 | 5607 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5602): Show |
chr9 | 99816885 | 99871891 |
| a0002c0005t0005 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5602): Show |
chr9 | 99816885 | 99871891 |
| a0002c0006t0002 | 0/0 | 5609 | 5 | 1 | 2 | 0 | 1 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5604): Show |
chr9 | 99816885 | 99871891 |
| a0003c0010t0001 | 0/0 | 5607 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5602): Show |
chr9 | 99816885 | 99871891 |
| a0004c0009t0001 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | GCGCA others(5602): Show |
chr9 | 99816885 | 99871891 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0003 | 1/0 | 8 | 0 | 0 | 6 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0006 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0008g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0009g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0010g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0011g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0012g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0001t0014g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0004t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0004t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0004t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0004t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0004t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0007t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0001c0008t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0001g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0001g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0001 | 0/0 | 8 | 3 | 2 | 2 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0004 | 0/0 | 8 | 1 | 1 | 6 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0009 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0002t0013g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0003t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0003t0004g0002 | 0/0 | 9 | 0 | 2 | 4 | 1 | 2 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0003t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0003t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0003t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0003t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0003t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0003t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0003t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0003t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0003t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0005t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0005t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0005t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0005t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0005t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0006t0002g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0006t0002g0011 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0002c0006t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0003c0010t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| a0004c0009t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00099 | hp2 | a0002 | c0003 | t0004 | g0002 | EUR | GBR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00280 | hp2 | a0002 | c0003 | t0004 | g0121 | EUR | FIN | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00423 | hp1 | a0002 | c0003 | t0002 | g0021 | EAS | CHS | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | CHS | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00438 | hp2 | a0002 | c0002 | t0013 | g0012 | EAS | CHS | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00544 | hp1 | a0002 | c0003 | t0002 | g0021 | EAS | CHS | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00558 | hp2 | a0002 | c0003 | t0004 | g0002 | EAS | CHS | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | CHS | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | CHS | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | CHS | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00639 | hp1 | a0001 | c0004 | t0001 | g0196 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0054 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00642 | hp2 | a0001 | c0008 | t0002 | g0126 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG00735 | hp2 | a0002 | c0005 | t0001 | g0026 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01070 | hp1 | a0002 | c0003 | t0004 | g0002 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0041 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0046 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01074 | hp1 | a0002 | c0003 | t0004 | g0191 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01081 | hp2 | a0002 | c0005 | t0004 | g0074 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01109 | hp2 | a0001 | c0004 | t0001 | g0197 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0060 | AMR | PUR | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01257 | hp1 | a0001 | c0001 | t0010 | g0071 | AMR | CLM | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | CLM | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0039 | AMR | CLM | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01361 | hp1 | a0003 | c0010 | t0001 | g0115 | AMR | CLM | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01361 | hp2 | a0002 | c0006 | t0002 | g0001 | AMR | CLM | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01884 | hp2 | a0001 | c0001 | t0014 | g0102 | AFR | ACB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0053 | AMR | PEL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01975 | hp1 | a0002 | c0003 | t0004 | g0187 | AMR | PEL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01975 | hp2 | a0002 | c0006 | t0002 | g0045 | AMR | PEL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PEL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PEL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | PEL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02004 | hp1 | a0002 | c0003 | t0004 | g0002 | AMR | PEL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | KHV | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | KHV | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | KHV | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | KHV | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | KHV | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | KHV | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | KHV | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | CDX | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02155 | hp2 | a0002 | c0003 | t0004 | g0020 | EAS | CDX | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | CDX | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | CDX | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02257 | hp2 | a0002 | c0005 | t0001 | g0063 | AFR | ACB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PEL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0068 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0182 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02698 | hp1 | a0002 | c0006 | t0002 | g0001 | SAS | PJL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02698 | hp2 | a0002 | c0002 | t0003 | g0047 | SAS | PJL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0202 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02738 | hp2 | a0002 | c0003 | t0004 | g0002 | SAS | PJL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02818 | hp1 | a0001 | c0004 | t0001 | g0198 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0065 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0004 | AFR | ESN | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | ESN | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02976 | hp1 | a0002 | c0005 | t0001 | g0064 | AFR | ESN | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0066 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0001 | AFR | ESN | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0067 | AFR | ESN | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | ESN | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0132 | AFR | MSL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0061 | AFR | MSL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0009 | SAS | PJL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03239 | hp2 | a0002 | c0002 | t0004 | g0055 | SAS | PJL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0069 | AFR | MSL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0059 | SAS | PJL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0114 | SAS | PJL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0001 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03654 | hp2 | a0001 | c0001 | t0012 | g0154 | SAS | PJL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0009 | SAS | STU | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | STU | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0113 | SAS | PJL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03927 | hp2 | a0001 | c0004 | t0002 | g0078 | SAS | BEB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03942 | hp1 | a0001 | c0001 | t0008 | g0112 | SAS | BEB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0043 | SAS | BEB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG04184 | hp1 | a0002 | c0003 | t0004 | g0119 | SAS | BEB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0123 | SAS | BEB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0058 | SAS | STU | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | STU | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG04228 | hp2 | a0002 | c0003 | t0004 | g0002 | SAS | STU | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0038 | AFR | YRI | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | CHB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18747 | hp2 | a0002 | c0003 | t0004 | g0188 | EAS | CHB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | YRI | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18906 | hp2 | a0004 | c0009 | t0001 | g0070 | AFR | YRI | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18944 | hp2 | a0002 | c0003 | t0004 | g0002 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18945 | hp2 | a0002 | c0003 | t0004 | g0002 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18947 | hp1 | a0002 | c0003 | t0004 | g0020 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18950 | hp1 | a0001 | c0001 | t0007 | g0173 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18957 | hp1 | a0002 | c0003 | t0004 | g0122 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18960 | hp2 | a0002 | c0003 | t0004 | g0120 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18965 | hp2 | a0002 | c0002 | t0003 | g0040 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18969 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18983 | hp2 | a0002 | c0003 | t0004 | g0002 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19030 | hp2 | a0002 | c0005 | t0005 | g0062 | AFR | LWK | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | LWK | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19043 | hp2 | a0001 | c0004 | t0001 | g0199 | AFR | LWK | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19066 | hp1 | a0002 | c0003 | t0004 | g0118 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19067 | hp1 | a0002 | c0002 | t0003 | g0056 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | YRI | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | TSI | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0117 | EUR | TSI | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA20805 | hp1 | a0002 | c0006 | t0002 | g0011 | EUR | TSI | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | ACB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0031 | AFR | ACB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0057 | AFR | MSL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG03471 | hp2 | a0001 | c0007 | t0001 | g0138 | AFR | MSL | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | USA | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | USA | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| NA21309 | hp2 | a0002 | c0006 | t0002 | g0011 | AFR | LWK | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0183 | REF | REF | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0003 | REF | REF | NR4A3_chr9_99816885_99871891 | NR4A3 | chr9 | 99816885 | 99871891 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:99828708 | C | A | 1 | a0004 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.666C>A | p.Ser222Arg | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 3/8 | 1365/5604 | 666/1881 | 222/626 | chr9 | 99828708 | |||
| chr9:99828760 | A | G | 2 | a0002 a0004 |
117 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(114): Show |
missense_variant | MODERATE | c.718A>G | p.Ser240Gly | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 3/8 | 1417/5604 | 718/1881 | 240/626 | chr9 | 99828760 | |||
| chr9:99828802 | C | G | 1 | a0003 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.760C>G | p.Leu254Val | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 3/8 | 1459/5604 | 760/1881 | 254/626 | chr9 | 99828802 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:99828282 | G | A | 1 | a0001c0007 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.240G>A | p.Gln80Gln | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 3/8 | 939/5604 | 240/1881 | 80/626 | chr9 | 99828282 | |||
| chr9:99828283 | C | A | 1 | a0001c0007 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.241C>A | p.Arg81Arg | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 3/8 | 940/5604 | 241/1881 | 81/626 | chr9 | 99828283 | |||
| chr9:99828645 | C | T | 1 | a0002c0006 | 5 | HG01361.hp2 HG01975.hp2 HG02698.hp1 others(2): Show |
synonymous_variant | LOW | c.603C>T | p.Pro201Pro | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 3/8 | 1302/5604 | 603/1881 | 201/626 | chr9 | 99828645 | |||
| chr9:99828702 | G | A | 1 | a0001c0008 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.660G>A | p.Ala220Ala | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 3/8 | 1359/5604 | 660/1881 | 220/626 | chr9 | 99828702 | |||
| chr9:99832787 | G | A | 2 | a0001c0004 a0002c0003 |
26 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(23): Show |
synonymous_variant | LOW | c.1050G>A | p.Gln350Gln | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 4/8 | 1749/5604 | 1050/1881 | 350/626 | chr9 | 99832787 | |||
| chr9:99833403 | C | T | 3 | a0002c0002 a0002c0006 a0004c0009 |
91 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(88): Show |
synonymous_variant | LOW | c.1203C>T | p.Ala401Ala | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/8 | 1902/5604 | 1203/1881 | 401/626 | chr9 | 99833403 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:99822024 | C | T | 1 | a0001c0001t0014 | 1 | HG01884.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-560C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/8 | chr9 | 99822024 | |||||||
| chr9:99822081 | G | A | 1 | a0002c0005t0005 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-503G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/8 | 5962 | chr9 | 99822081 | ||||||
| chr9:99822286 | G | C | 1 | a0001c0001t0006 | 1 | NA18969.hp2 | 5_prime_UTR_variant | MODIFIER | c.-298G>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/8 | 5757 | chr9 | 99822286 | ||||||
| chr9:99863890 | C | T | 1 | a0002c0005t0005 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*23C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 8/8 | 23 | chr9 | 99863890 | ||||||
| chr9:99864091 | G | A | 1 | a0001c0001t0007 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*224G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 8/8 | 224 | chr9 | 99864091 | ||||||
| chr9:99864252 | A | G | 1 | a0002c0002t0013 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*385A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 8/8 | 385 | chr9 | 99864252 | ||||||
| chr9:99864565 | A | C | 1 | a0001c0001t0012 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*698A>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 8/8 | 698 | chr9 | 99864565 | ||||||
| chr9:99864605 | C | A | 1 | a0001c0001t0008 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*738C>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 8/8 | 738 | chr9 | 99864605 | ||||||
| chr9:99864974 | A | ATCT | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(21): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*1109_*1111dupCTT | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 8/8 | 1112 | INFO_REALIGN_3_PRIME | chr9 | 99864974 | |||||
| chr9:99865020 | A | G | 11 | a0001c0001t0002 a0001c0001t0004 a0001c0004t0002 others(8): Show |
111 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*1153A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 8/8 | 1153 | chr9 | 99865020 | ||||||
| chr9:99865301 | A | AAT | 7 | a0001c0001t0002 a0001c0004t0002 a0001c0008t0002 others(4): Show |
87 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1450_*1451dupTA | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 8/8 | 1452 | INFO_REALIGN_3_PRIME | chr9 | 99865301 | |||||
| chr9:99865308 | A | G | 1 | a0001c0001t0011 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1441A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 8/8 | 1441 | chr9 | 99865308 | ||||||
| chr9:99865613 | T | C | 1 | a0001c0001t0009 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1746T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 8/8 | 1746 | chr9 | 99865613 | ||||||
| chr9:99866121 | CATTAATT others(39): Show |
C | 1 | a0001c0001t0010 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2257_*2302delTAAT others(42): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 8/8 | 2257 | INFO_REALIGN_3_PRIME | chr9 | 99866121 | |||||
| chr9:99866799 | C | T | 1 | a0001c0001t0012 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2932C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 8/8 | 2932 | chr9 | 99866799 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:99822527 | C | G | 1 | a0002c0002t0001g0202 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-177+120C>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99822527 | |||||||
| chr9:99822838 | G | A | 1 | a0002c0002t0002g0030 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-177+431G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99822838 | |||||||
| chr9:99823073 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-177+666C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99823073 | |||||||
| chr9:99823263 | T | C | 46 | a0002c0002t0001g0007 a0002c0002t0001g0035 a0002c0002t0001g0036 others(43): Show |
80 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.-177+856T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99823263 | |||||||
| chr9:99823591 | T | C | 1 | a0002c0005t0005g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-177+1184T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99823591 | |||||||
| chr9:99823749 | C | T | 4 | a0001c0004t0001g0196 a0001c0004t0001g0197 a0001c0004t0001g0198 others(1): Show |
4 | HG00639.hp1 HG01109.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+1342C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99823749 | |||||||
| chr9:99823766 | G | C | 56 | a0002c0002t0001g0007 a0002c0002t0001g0010 a0002c0002t0001g0035 others(53): Show |
93 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.-177+1359G>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99823766 | |||||||
| chr9:99824083 | T | C | 1 | a0001c0001t0010g0071 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-176-1576T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99824083 | |||||||
| chr9:99824109 | A | C | 55 | a0002c0002t0001g0007 a0002c0002t0001g0010 a0002c0002t0001g0035 others(52): Show |
92 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.-176-1550A>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99824109 | |||||||
| chr9:99824164 | T | G | 2 | a0002c0005t0001g0063 a0002c0005t0001g0064 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-176-1495T>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99824164 | |||||||
| chr9:99824255 | C | T | 1 | a0002c0002t0001g0061 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-176-1404C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99824255 | |||||||
| chr9:99824347 | G | A | 2 | a0001c0001t0003g0072 a0001c0001t0003g0073 |
2 | NA18747.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.-176-1312G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99824347 | |||||||
| chr9:99824585 | T | C | 1 | a0002c0005t0004g0074 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-176-1074T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99824585 | |||||||
| chr9:99824767 | T | G | 53 | a0002c0002t0001g0007 a0002c0002t0001g0010 a0002c0002t0001g0035 others(50): Show |
90 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.-176-892T>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99824767 | |||||||
| chr9:99824951 | C | T | 2 | a0002c0002t0002g0059 a0002c0002t0002g0060 |
2 | HG01243.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-176-708C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99824951 | |||||||
| chr9:99825075 | T | C | 1 | a0002c0002t0002g0031 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-176-584T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99825075 | |||||||
| chr9:99825169 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-176-490C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99825169 | |||||||
| chr9:99825178 | C | A | 1 | a0001c0001t0003g0075 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-176-481C>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99825178 | |||||||
| chr9:99825372 | G | C | 1 | a0002c0002t0002g0032 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-176-287G>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99825372 | |||||||
| chr9:99825380 | G | GT | 5 | a0001c0001t0001g0193 a0001c0001t0002g0192 a0001c0001t0003g0073 others(2): Show |
5 | HG02300.hp2 HG04199.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176-269dupT | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 99825380 | ||||||
| chr9:99825390 | T | A | 1 | a0001c0001t0003g0076 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-176-269T>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99825390 | |||||||
| chr9:99825451 | C | G | 1 | a0002c0003t0004g0191 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-176-208C>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99825451 | |||||||
| chr9:99825616 | C | T | 2 | a0002c0005t0001g0063 a0002c0005t0001g0064 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-176-43C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99825616 | |||||||
| chr9:99825645 | C | T | 2 | a0001c0001t0002g0190 a0001c0001t0003g0189 |
2 | HG02056.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.-176-14C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 1/7 | chr9 | 99825645 | |||||||
| chr9:99825904 | G | A | 2 | a0001c0001t0001g0077 a0001c0004t0002g0078 |
2 | HG02145.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-3+72G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | chr9 | 99825904 | |||||||
| chr9:99826254 | A | T | 1 | a0002c0003t0004g0188 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-3+422A>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | chr9 | 99826254 | |||||||
| chr9:99826476 | A | G | 1 | a0002c0003t0004g0187 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-3+644A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | chr9 | 99826476 | |||||||
| chr9:99826696 | A | C | 1 | a0002c0002t0002g0057 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-3+864A>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | chr9 | 99826696 | |||||||
| chr9:99826937 | G | GT | 57 | a0002c0002t0001g0007 a0002c0002t0001g0010 a0002c0002t0001g0035 others(54): Show |
94 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.-2-1098dupT | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 99826937 | ||||||
| chr9:99827258 | A | ATG | 7 | a0001c0001t0001g0186 a0002c0002t0002g0009 a0002c0002t0002g0012 others(4): Show |
11 | HG00438.hp2 HG00642.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-751_-2-750dupGT | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 99827258 | ||||||
| chr9:99827258 | A | G | 1 | a0002c0002t0003g0056 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-2-783A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | chr9 | 99827258 | |||||||
| chr9:99827258 | ATG | A | 38 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(35): Show |
44 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.-2-751_-2-750delGT | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 99827258 | ||||||
| chr9:99827260 | G | A | 2 | a0002c0002t0001g0068 a0002c0002t0001g0069 |
2 | HG02572.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-2-781G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | chr9 | 99827260 | |||||||
| chr9:99827270 | G | A | 6 | a0001c0001t0002g0081 a0001c0001t0003g0015 a0001c0001t0003g0079 others(3): Show |
7 | HG00621.hp2 HG01978.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-771G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | chr9 | 99827270 | |||||||
| chr9:99827286 | GTGTGTA | G | 10 | a0001c0001t0001g0087 a0001c0001t0002g0016 a0001c0001t0002g0086 others(7): Show |
10 | HG00597.hp1 HG02155.hp1 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-753_-2-748delGT others(4): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 99827286 | ||||||
| chr9:99827290 | G | A | 13 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0002c0002t0001g0044 others(10): Show |
14 | HG02083.hp1 HG02129.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-751G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | chr9 | 99827290 | |||||||
| chr9:99827290 | GTA | G | 97 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0124 others(94): Show |
125 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-2-737_-2-736delAT | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 99827290 | ||||||
| chr9:99827292 | A | G | 8 | a0001c0001t0001g0186 a0001c0001t0003g0151 a0001c0004t0001g0196 others(5): Show |
8 | HG00639.hp1 HG01109.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-749A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | chr9 | 99827292 | |||||||
| chr9:99827294 | A | G | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0004t0002g0078 |
3 | HG02258.hp1 HG02818.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-2-747A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | chr9 | 99827294 | |||||||
| chr9:99827350 | G | A | 2 | a0002c0005t0001g0063 a0002c0005t0001g0064 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-2-691G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | chr9 | 99827350 | |||||||
| chr9:99827356 | A | G | 2 | a0002c0005t0001g0063 a0002c0005t0001g0064 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-2-685A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | chr9 | 99827356 | |||||||
| chr9:99827373 | T | C | 1 | a0001c0001t0003g0084 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-2-668T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | chr9 | 99827373 | |||||||
| chr9:99827463 | T | C | 125 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(122): Show |
177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-2-578T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | chr9 | 99827463 | |||||||
| chr9:99827532 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-2-509C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 2/7 | chr9 | 99827532 | |||||||
| chr9:99829103 | C | T | 2 | a0002c0005t0001g0063 a0002c0005t0001g0064 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.951+110C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 3/7 | chr9 | 99829103 | |||||||
| chr9:99829800 | C | T | 7 | a0002c0002t0001g0010 a0002c0002t0001g0065 a0002c0002t0001g0066 others(4): Show |
10 | HG00733.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.951+807C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 3/7 | chr9 | 99829800 | |||||||
| chr9:99830203 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.951+1210A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 3/7 | chr9 | 99830203 | |||||||
| chr9:99830406 | G | A | 56 | a0002c0002t0001g0007 a0002c0002t0001g0010 a0002c0002t0001g0035 others(53): Show |
93 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.951+1413G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 3/7 | chr9 | 99830406 | |||||||
| chr9:99830504 | G | C | 1 | a0002c0005t0005g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.951+1511G>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 3/7 | chr9 | 99830504 | |||||||
| chr9:99830505 | AT | A | 16 | a0001c0004t0001g0196 a0001c0004t0001g0197 a0001c0004t0001g0198 others(13): Show |
26 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.951+1514delT | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 99830505 | ||||||
| chr9:99831234 | A | G | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0186 |
3 | HG02809.hp2 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.952-1455A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 3/7 | chr9 | 99831234 | |||||||
| chr9:99831408 | A | G | 58 | a0002c0002t0001g0007 a0002c0002t0001g0010 a0002c0002t0001g0035 others(55): Show |
95 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.952-1281A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 3/7 | chr9 | 99831408 | |||||||
| chr9:99831430 | A | C | 1 | a0001c0001t0001g0139 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.952-1259A>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 3/7 | chr9 | 99831430 | |||||||
| chr9:99832592 | C | T | 1 | a0002c0003t0004g0188 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.952-97C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 3/7 | chr9 | 99832592 | |||||||
| chr9:99832875 | A | G | 1 | a0001c0007t0001g0138 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1081+57A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 4/7 | chr9 | 99832875 | |||||||
| chr9:99833244 | T | C | 1 | a0002c0002t0002g0033 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1082-38T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 4/7 | chr9 | 99833244 | |||||||
| chr9:99833467 | A | C | 1 | a0002c0005t0005g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1254+13A>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99833467 | |||||||
| chr9:99833484 | G | T | 1 | a0001c0001t0003g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1254+30G>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99833484 | |||||||
| chr9:99833768 | C | T | 6 | a0001c0001t0001g0029 a0001c0001t0001g0178 a0001c0001t0001g0179 others(3): Show |
7 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1254+314C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99833768 | |||||||
| chr9:99834039 | G | A | 102 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0077 others(99): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1254+585G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99834039 | |||||||
| chr9:99834134 | G | A | 1 | a0002c0005t0005g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1254+680G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99834134 | |||||||
| chr9:99834191 | G | T | 4 | a0001c0001t0001g0087 a0001c0001t0002g0088 a0001c0001t0002g0090 others(1): Show |
4 | NA18948.hp2 NA18966.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+737G>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99834191 | |||||||
| chr9:99834398 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1254+944C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99834398 | |||||||
| chr9:99834565 | C | T | 1 | a0004c0009t0001g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1254+1111C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99834565 | |||||||
| chr9:99835379 | CAAGTGTA others(8): Show |
C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG02056.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1254+1928_1254+194 others(19): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 99835379 | ||||||
| chr9:99835659 | A | C | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0186 others(2): Show |
6 | HG02280.hp1 HG02809.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+2205A>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99835659 | |||||||
| chr9:99835801 | T | A | 56 | a0002c0002t0001g0007 a0002c0002t0001g0010 a0002c0002t0001g0035 others(53): Show |
93 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.1254+2347T>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99835801 | |||||||
| chr9:99836243 | T | C | 1 | a0002c0003t0004g0118 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1254+2789T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99836243 | |||||||
| chr9:99836439 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1254+2985A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99836439 | |||||||
| chr9:99836662 | G | C | 1 | a0001c0001t0003g0194 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1254+3208G>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99836662 | |||||||
| chr9:99836839 | T | C | 57 | a0002c0002t0001g0007 a0002c0002t0001g0010 a0002c0002t0001g0035 others(54): Show |
94 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1254+3385T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99836839 | |||||||
| chr9:99836964 | T | C | 4 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0146 others(1): Show |
4 | HG00639.hp2 HG01071.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254+3510T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99836964 | |||||||
| chr9:99837582 | G | GT | 6 | a0001c0001t0001g0137 a0002c0002t0001g0010 a0002c0002t0001g0065 others(3): Show |
9 | HG00733.hp2 HG01109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1254+4137dupT | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 99837582 | ||||||
| chr9:99837781 | C | G | 1 | a0002c0002t0004g0055 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1254+4327C>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99837781 | |||||||
| chr9:99838193 | T | C | 6 | a0001c0001t0002g0081 a0001c0001t0003g0015 a0001c0001t0003g0079 others(3): Show |
7 | HG00621.hp2 HG01978.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1254+4739T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99838193 | |||||||
| chr9:99838212 | A | T | 1 | a0001c0001t0003g0177 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1254+4758A>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99838212 | |||||||
| chr9:99838221 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1254+4767G>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99838221 | |||||||
| chr9:99838313 | T | C | 1 | a0002c0002t0002g0034 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1254+4859T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99838313 | |||||||
| chr9:99838485 | G | C | 2 | a0001c0001t0002g0016 a0001c0001t0004g0016 |
2 | NA18949.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1254+5031G>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99838485 | |||||||
| chr9:99838495 | C | A | 1 | a0001c0001t0004g0123 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1254+5041C>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99838495 | |||||||
| chr9:99838536 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1254+5082A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99838536 | |||||||
| chr9:99839505 | C | A | 2 | a0001c0001t0003g0147 a0001c0001t0003g0148 |
2 | NA18942.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1255-5144C>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99839505 | |||||||
| chr9:99839518 | G | C | 1 | a0001c0001t0003g0149 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1255-5131G>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99839518 | |||||||
| chr9:99839584 | G | C | 1 | a0001c0001t0003g0150 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1255-5065G>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99839584 | |||||||
| chr9:99839752 | T | G | 1 | a0001c0001t0002g0142 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1255-4897T>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99839752 | |||||||
| chr9:99839777 | T | C | 57 | a0001c0001t0002g0022 a0002c0002t0001g0007 a0002c0002t0001g0010 others(54): Show |
95 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.1255-4872T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99839777 | |||||||
| chr9:99840264 | G | C | 1 | a0002c0002t0002g0013 | 2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1255-4385G>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99840264 | |||||||
| chr9:99840378 | A | G | 1 | a0001c0001t0004g0123 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1255-4271A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99840378 | |||||||
| chr9:99840927 | C | T | 1 | a0002c0002t0002g0052 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1255-3722C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99840927 | |||||||
| chr9:99841231 | G | GA | 69 | a0001c0001t0001g0077 a0001c0001t0001g0094 a0001c0001t0001g0124 others(66): Show |
113 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1255-3402dupA | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 99841231 | ||||||
| chr9:99841231 | G | GAA | 12 | a0001c0001t0002g0022 a0002c0002t0001g0007 a0002c0002t0001g0035 others(9): Show |
17 | HG01261.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1255-3403_1255-340 others(6): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 99841231 | ||||||
| chr9:99841284 | G | A | 6 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0109 others(3): Show |
6 | HG00544.hp2 HG02083.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.1255-3365G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99841284 | |||||||
| chr9:99841606 | A | C | 4 | a0002c0002t0002g0049 a0002c0002t0002g0050 a0002c0002t0002g0051 others(1): Show |
4 | HG02129.hp1 NA18959.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1255-3043A>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99841606 | |||||||
| chr9:99841733 | GGGAGTTC others(21): Show |
G | 17 | a0001c0001t0003g0151 a0001c0004t0001g0196 a0001c0004t0001g0197 others(14): Show |
27 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.1255-2902_1255-287 others(32): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 99841733 | ||||||
| chr9:99841737 | G | A | 1 | a0002c0005t0004g0074 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1255-2912G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99841737 | |||||||
| chr9:99841833 | G | C | 2 | a0001c0004t0001g0196 a0001c0004t0001g0197 |
2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.1255-2816G>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99841833 | |||||||
| chr9:99841860 | C | T | 2 | a0002c0002t0002g0053 a0002c0002t0002g0054 |
2 | HG00642.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1255-2789C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99841860 | |||||||
| chr9:99842108 | A | AT | 8 | a0001c0001t0003g0149 a0001c0001t0003g0174 a0001c0001t0003g0175 others(5): Show |
8 | HG01070.hp2 HG02135.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1255-2522dupT | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 99842108 | ||||||
| chr9:99842108 | A | ATT | 50 | a0001c0001t0002g0022 a0002c0002t0001g0007 a0002c0002t0001g0010 others(47): Show |
88 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.1255-2523_1255-252 others(6): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 99842108 | ||||||
| chr9:99842108 | AT | A | 6 | a0001c0001t0001g0143 a0001c0001t0003g0072 a0001c0001t0003g0073 others(3): Show |
6 | HG01071.hp1 HG01074.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255-2522delT | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 99842108 | ||||||
| chr9:99842497 | A | G | 2 | a0002c0002t0002g0014 a0002c0002t0002g0048 |
3 | NA18952.hp2 NA18977.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1255-2152A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99842497 | |||||||
| chr9:99842708 | C | T | 56 | a0001c0001t0002g0022 a0002c0002t0001g0007 a0002c0002t0001g0010 others(53): Show |
94 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.1255-1941C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99842708 | |||||||
| chr9:99842945 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0153 |
2 | HG03491.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1255-1704G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99842945 | |||||||
| chr9:99842946 | C | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0153 |
2 | HG03491.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1255-1703C>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99842946 | |||||||
| chr9:99843207 | A | G | 1 | a0002c0002t0003g0047 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1255-1442A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99843207 | |||||||
| chr9:99843374 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1255-1275G>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99843374 | |||||||
| chr9:99843557 | G | C | 1 | a0002c0005t0004g0074 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1255-1092G>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99843557 | |||||||
| chr9:99843681 | AT | A | 60 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0002g0022 others(57): Show |
98 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.1255-959delT | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 99843681 | ||||||
| chr9:99843682 | T | A | 1 | a0002c0003t0004g0119 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1255-967T>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99843682 | |||||||
| chr9:99843757 | AT | A | 59 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0002g0022 others(56): Show |
97 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.1255-879delT | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 99843757 | ||||||
| chr9:99843987 | C | T | 1 | a0002c0002t0002g0049 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1255-662C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99843987 | |||||||
| chr9:99844281 | A | G | 1 | a0001c0001t0003g0177 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1255-368A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99844281 | |||||||
| chr9:99844417 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1255-232G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 5/7 | chr9 | 99844417 | |||||||
| chr9:99844874 | T | A | 1 | a0002c0005t0005g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1454+26T>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 6/7 | chr9 | 99844874 | |||||||
| chr9:99844988 | C | T | 1 | a0002c0005t0005g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1454+140C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 6/7 | chr9 | 99844988 | |||||||
| chr9:99845092 | G | A | 1 | a0001c0001t0012g0154 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1454+244G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 6/7 | chr9 | 99845092 | |||||||
| chr9:99845228 | G | A | 1 | a0001c0001t0003g0075 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1454+380G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 6/7 | chr9 | 99845228 | |||||||
| chr9:99845393 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1454+545C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 6/7 | chr9 | 99845393 | |||||||
| chr9:99845463 | T | G | 1 | a0002c0002t0002g0013 | 2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1454+615T>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 6/7 | chr9 | 99845463 | |||||||
| chr9:99845900 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1454+1052C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 6/7 | chr9 | 99845900 | |||||||
| chr9:99846159 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1455-1278C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 6/7 | chr9 | 99846159 | |||||||
| chr9:99846781 | G | A | 1 | a0002c0005t0004g0074 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1455-656G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 6/7 | chr9 | 99846781 | |||||||
| chr9:99846970 | G | C | 17 | a0001c0001t0002g0022 a0002c0002t0001g0007 a0002c0002t0001g0010 others(14): Show |
25 | HG00733.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1455-467G>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 6/7 | chr9 | 99846970 | |||||||
| chr9:99847102 | T | C | 1 | a0001c0001t0010g0071 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1455-335T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 6/7 | chr9 | 99847102 | |||||||
| chr9:99847132 | T | C | 16 | a0001c0001t0002g0022 a0002c0002t0001g0007 a0002c0002t0001g0010 others(13): Show |
24 | HG00733.hp2 HG01891.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1455-305T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 6/7 | chr9 | 99847132 | |||||||
| chr9:99847336 | A | G | 1 | a0001c0001t0003g0177 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1455-101A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 6/7 | chr9 | 99847336 | |||||||
| chr9:99847357 | T | G | 17 | a0001c0001t0002g0022 a0002c0002t0001g0007 a0002c0002t0001g0010 others(14): Show |
25 | HG00733.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1455-80T>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 6/7 | chr9 | 99847357 | |||||||
| chr9:99847725 | A | G | 1 | a0001c0001t0009g0182 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1633+110A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99847725 | |||||||
| chr9:99847850 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1633+235A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99847850 | |||||||
| chr9:99847906 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1633+291C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99847906 | |||||||
| chr9:99848975 | C | T | 1 | a0001c0001t0012g0154 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1633+1360C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99848975 | |||||||
| chr9:99849072 | A | G | 1 | a0001c0001t0007g0173 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1633+1457A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99849072 | |||||||
| chr9:99849403 | A | T | 1 | a0001c0001t0001g0110 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1633+1788A>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99849403 | |||||||
| chr9:99849541 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1633+1926G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99849541 | |||||||
| chr9:99849780 | A | G | 18 | a0001c0001t0002g0022 a0002c0002t0001g0007 a0002c0002t0001g0010 others(15): Show |
26 | HG00733.hp2 HG01081.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1633+2165A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99849780 | |||||||
| chr9:99849922 | T | C | 5 | a0001c0001t0001g0029 a0001c0001t0001g0178 a0001c0001t0001g0179 others(2): Show |
6 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1633+2307T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99849922 | |||||||
| chr9:99850155 | A | C | 4 | a0001c0004t0001g0196 a0001c0004t0001g0197 a0001c0004t0001g0198 others(1): Show |
4 | HG00639.hp1 HG01109.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1633+2540A>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99850155 | |||||||
| chr9:99850243 | T | A | 1 | a0001c0001t0003g0075 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1633+2628T>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99850243 | |||||||
| chr9:99850247 | C | T | 1 | a0001c0001t0003g0075 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1633+2632C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99850247 | |||||||
| chr9:99850551 | G | C | 1 | a0001c0001t0002g0192 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1633+2936G>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99850551 | |||||||
| chr9:99850676 | C | T | 1 | a0002c0003t0004g0187 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1633+3061C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99850676 | |||||||
| chr9:99850771 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1633+3156T>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99850771 | |||||||
| chr9:99850912 | A | G | 1 | a0001c0001t0003g0084 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1633+3297A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99850912 | |||||||
| chr9:99851390 | T | C | 10 | a0002c0003t0004g0002 a0002c0003t0004g0020 a0002c0003t0004g0118 others(7): Show |
19 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.1633+3775T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99851390 | |||||||
| chr9:99851725 | A | T | 1 | a0001c0001t0003g0194 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1633+4110A>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99851725 | |||||||
| chr9:99852131 | G | A | 1 | a0001c0001t0003g0155 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1633+4516G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99852131 | |||||||
| chr9:99852162 | A | G | 1 | a0001c0004t0002g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1633+4547A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99852162 | |||||||
| chr9:99852682 | G | C | 1 | a0002c0005t0005g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1633+5067G>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99852682 | |||||||
| chr9:99852830 | C | T | 1 | a0001c0001t0003g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1633+5215C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99852830 | |||||||
| chr9:99852932 | T | C | 17 | a0001c0001t0002g0022 a0002c0002t0001g0007 a0002c0002t0001g0010 others(14): Show |
25 | HG00733.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1633+5317T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99852932 | |||||||
| chr9:99852949 | A | G | 17 | a0001c0001t0002g0022 a0002c0002t0001g0007 a0002c0002t0001g0010 others(14): Show |
25 | HG00733.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1633+5334A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99852949 | |||||||
| chr9:99853068 | A | G | 1 | a0001c0001t0003g0172 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1633+5453A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99853068 | |||||||
| chr9:99853168 | C | T | 14 | a0001c0001t0002g0022 a0002c0002t0001g0007 a0002c0002t0001g0010 others(11): Show |
22 | HG00733.hp2 HG01891.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1633+5553C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99853168 | |||||||
| chr9:99853321 | C | CT | 95 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0077 others(92): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1633+5725dupT | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99853321 | ||||||
| chr9:99853324 | T | C | 1 | a0001c0001t0003g0156 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1633+5709T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99853324 | |||||||
| chr9:99853417 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1633+5802C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99853417 | |||||||
| chr9:99853474 | C | T | 1 | a0002c0002t0002g0033 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1633+5859C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99853474 | |||||||
| chr9:99853478 | C | A | 2 | a0002c0005t0001g0063 a0002c0005t0001g0064 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1633+5863C>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99853478 | |||||||
| chr9:99853563 | G | A | 2 | a0002c0005t0001g0063 a0002c0005t0001g0064 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1633+5948G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99853563 | |||||||
| chr9:99853597 | C | T | 4 | a0002c0002t0001g0010 a0002c0002t0001g0065 a0002c0002t0001g0066 others(1): Show |
7 | HG00733.hp2 HG02109.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1633+5982C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99853597 | |||||||
| chr9:99853778 | G | A | 2 | a0002c0002t0001g0035 a0002c0002t0001g0036 |
2 | HG02723.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1633+6163G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99853778 | |||||||
| chr9:99853899 | G | A | 1 | a0001c0004t0001g0199 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1633+6284G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99853899 | |||||||
| chr9:99853972 | G | A | 2 | a0002c0002t0002g0053 a0002c0005t0004g0074 |
2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1633+6357G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99853972 | |||||||
| chr9:99854014 | T | C | 2 | a0002c0005t0001g0063 a0002c0005t0001g0064 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1633+6399T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99854014 | |||||||
| chr9:99854465 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1633+6850T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99854465 | |||||||
| chr9:99854522 | A | G | 17 | a0001c0001t0002g0022 a0002c0002t0001g0007 a0002c0002t0001g0010 others(14): Show |
25 | HG00733.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1633+6907A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99854522 | |||||||
| chr9:99854811 | G | A | 3 | a0001c0001t0001g0077 a0001c0001t0001g0129 a0001c0001t0001g0139 |
3 | HG02145.hp1 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1633+7196G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99854811 | |||||||
| chr9:99855114 | T | C | 2 | a0002c0002t0002g0043 a0002c0002t0002g0058 |
2 | HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1633+7499T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99855114 | |||||||
| chr9:99855327 | T | C | 1 | a0002c0003t0002g0021 | 2 | HG00423.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.1633+7712T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99855327 | |||||||
| chr9:99855412 | TGATAA | T | 3 | a0001c0001t0003g0026 a0001c0001t0003g0157 a0002c0005t0001g0026 |
3 | HG00735.hp2 HG01169.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1633+7798_1633+780 others(9): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99855412 | |||||||
| chr9:99855619 | C | T | 2 | a0002c0005t0001g0063 a0002c0005t0001g0064 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1634-8001C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99855619 | |||||||
| chr9:99855623 | T | C | 17 | a0001c0001t0002g0022 a0002c0002t0001g0007 a0002c0002t0001g0010 others(14): Show |
25 | HG00733.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1634-7997T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99855623 | |||||||
| chr9:99855636 | C | G | 16 | a0001c0001t0002g0022 a0002c0002t0001g0007 a0002c0002t0001g0010 others(13): Show |
24 | HG00733.hp2 HG01891.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1634-7984C>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99855636 | |||||||
| chr9:99855769 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1634-7851G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99855769 | |||||||
| chr9:99856016 | A | G | 1 | a0002c0002t0001g0039 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1634-7604A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99856016 | |||||||
| chr9:99856137 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0003g0100 |
2 | NA19005.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1634-7483C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99856137 | |||||||
| chr9:99856889 | G | A | 1 | a0001c0001t0003g0151 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1634-6731G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99856889 | |||||||
| chr9:99856943 | T | G | 1 | a0002c0005t0004g0074 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1634-6677T>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99856943 | |||||||
| chr9:99857173 | G | A | 1 | a0002c0005t0004g0074 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1634-6447G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99857173 | |||||||
| chr9:99857184 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1634-6436C>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99857184 | |||||||
| chr9:99857188 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1634-6432G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99857188 | |||||||
| chr9:99857405 | C | T | 2 | a0002c0002t0002g0041 a0002c0002t0002g0046 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1634-6215C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99857405 | |||||||
| chr9:99857561 | C | T | 1 | a0002c0002t0001g0037 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1634-6059C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99857561 | |||||||
| chr9:99857755 | C | CAAAT | 87 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(84): Show |
120 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.1634-5826_1634-582 others(8): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99857755 | ||||||
| chr9:99857755 | C | CAAATAAA others(1): Show |
20 | a0001c0001t0001g0029 a0001c0001t0001g0095 a0001c0001t0001g0096 others(17): Show |
24 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(21): Show |
intron_variant | MODIFIER | c.1634-5830_1634-582 others(12): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99857755 | ||||||
| chr9:99857755 | C | CAAATAAA others(5): Show |
1 | a0001c0001t0001g0153 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1634-5834_1634-582 others(16): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99857755 | ||||||
| chr9:99858229 | A | G | 2 | a0002c0002t0002g0059 a0002c0002t0002g0060 |
2 | HG01243.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1634-5391A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99858229 | |||||||
| chr9:99858641 | T | C | 1 | a0001c0001t0002g0192 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1634-4979T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99858641 | |||||||
| chr9:99858776 | T | G | 1 | a0002c0003t0004g0119 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1634-4844T>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99858776 | |||||||
| chr9:99858816 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1634-4804G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99858816 | |||||||
| chr9:99859224 | G | A | 1 | a0002c0005t0005g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1634-4396G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99859224 | |||||||
| chr9:99859671 | G | A | 6 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0181 others(3): Show |
6 | HG01243.hp1 HG02258.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634-3949G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99859671 | |||||||
| chr9:99859955 | C | T | 68 | a0001c0001t0002g0016 a0001c0001t0002g0022 a0001c0001t0002g0024 others(65): Show |
110 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1634-3665C>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99859955 | |||||||
| chr9:99860109 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1634-3511G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99860109 | |||||||
| chr9:99860214 | G | GT | 68 | a0001c0001t0002g0016 a0001c0001t0002g0022 a0001c0001t0002g0024 others(65): Show |
110 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1634-3395dupT | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99860214 | ||||||
| chr9:99860225 | T | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
7 | HG01109.hp1 HG01891.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1634-3395T>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99860225 | |||||||
| chr9:99860547 | G | A | 1 | a0001c0001t0003g0155 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1634-3073G>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99860547 | |||||||
| chr9:99860764 | G | T | 1 | a0002c0002t0001g0067 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1634-2856G>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99860764 | |||||||
| chr9:99861046 | C | A | 68 | a0001c0001t0002g0016 a0001c0001t0002g0022 a0001c0001t0002g0024 others(65): Show |
110 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1634-2574C>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99861046 | |||||||
| chr9:99861208 | G | T | 1 | a0001c0001t0003g0175 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1634-2412G>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99861208 | |||||||
| chr9:99861397 | G | T | 1 | a0001c0001t0003g0150 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1634-2223G>T | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99861397 | |||||||
| chr9:99861806 | T | C | 1 | a0001c0004t0002g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1634-1814T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99861806 | |||||||
| chr9:99861869 | T | G | 1 | a0001c0001t0002g0116 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1634-1751T>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99861869 | |||||||
| chr9:99861980 | G | C | 69 | a0001c0001t0002g0016 a0001c0001t0002g0022 a0001c0001t0002g0024 others(66): Show |
111 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1634-1640G>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99861980 | |||||||
| chr9:99862115 | T | C | 87 | a0001c0001t0002g0016 a0001c0001t0002g0022 a0001c0001t0002g0024 others(84): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1634-1505T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99862115 | |||||||
| chr9:99862214 | T | C | 87 | a0001c0001t0002g0016 a0001c0001t0002g0022 a0001c0001t0002g0024 others(84): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1634-1406T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99862214 | |||||||
| chr9:99862514 | C | A | 1 | a0001c0001t0003g0073 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1634-1106C>A | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99862514 | |||||||
| chr9:99862549 | C | CA | 16 | a0001c0001t0001g0104 a0001c0001t0001g0141 a0001c0001t0001g0181 others(13): Show |
22 | HG00735.hp2 HG01074.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.1634-1037dupA | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | C | CAA | 11 | a0001c0001t0001g0019 a0001c0001t0001g0103 a0001c0001t0001g0140 others(8): Show |
14 | HG00733.hp1 HG01891.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.1634-1038_1634-103 others(6): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | C | CAAAAA | 9 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0099 others(6): Show |
9 | HG00099.hp1 HG00423.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1634-1041_1634-103 others(9): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | C | CAAAAAA | 6 | a0001c0001t0001g0017 a0001c0001t0001g0091 a0001c0001t0001g0094 others(3): Show |
7 | HG01952.hp2 HG02056.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1634-1042_1634-103 others(10): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0164 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1634-1048_1634-103 others(16): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0127 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1634-1049_1634-103 others(17): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | C | CAAAAAAA others(8): Show |
1 | a0001c0007t0001g0138 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1634-1051_1634-103 others(19): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | C | CAAAAAAA others(9): Show |
3 | a0001c0001t0001g0087 a0001c0001t0001g0158 a0001c0001t0010g0071 |
3 | HG01257.hp1 NA18966.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1634-1052_1634-103 others(20): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | C | CAAAAAAA others(10): Show |
5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0178 others(2): Show |
5 | HG01884.hp1 HG01884.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1634-1053_1634-103 others(21): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0185 a0001c0001t0001g0200 |
2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1634-1054_1634-103 others(22): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0001g0029 a0001c0001t0001g0180 |
3 | HG02109.hp1 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1634-1055_1634-103 others(23): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | C | CAAAAAAA others(13): Show |
3 | a0001c0001t0001g0144 a0001c0001t0009g0182 a0001c0001t0011g0132 |
3 | HG02630.hp1 HG03209.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1634-1056_1634-103 others(24): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0179 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1634-1059_1634-103 others(27): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | C | CAAAAAAA others(21): Show |
1 | a0001c0001t0001g0105 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1634-1064_1634-103 others(32): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0133 |
2 | HG02129.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1634-1046_1634-103 others(14): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0108 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1634-1047_1634-103 others(15): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0003g0075 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1634-1048_1634-103 others(16): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0001g0131 a0002c0003t0004g0122 |
2 | HG01081.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1634-1050_1634-103 others(18): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | CAAAAAAA others(8): Show |
C | 14 | a0001c0001t0001g0097 a0001c0001t0004g0123 a0001c0001t0004g0161 others(11): Show |
23 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.1634-1051_1634-103 others(19): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | CAAAAAAA others(9): Show |
C | 55 | a0001c0001t0001g0134 a0001c0001t0002g0016 a0001c0001t0002g0022 others(52): Show |
88 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1634-1052_1634-103 others(20): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862549 | CAAAAAAA others(10): Show |
C | 1 | a0002c0002t0002g0042 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1634-1053_1634-103 others(21): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862549 | ||||||
| chr9:99862568 | AAAAAAAA others(9): Show |
A | 2 | a0002c0005t0001g0063 a0002c0005t0001g0064 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1634-1050_1634-103 others(20): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862568 | ||||||
| chr9:99862570 | AAAAAAAA others(7): Show |
A | 13 | a0001c0004t0001g0198 a0001c0004t0001g0199 a0002c0002t0001g0007 others(10): Show |
20 | HG00733.hp2 HG01891.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1634-1048_1634-103 others(18): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862570 | ||||||
| chr9:99862571 | AAAAAAAA others(6): Show |
A | 1 | a0001c0004t0001g0196 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1634-1047_1634-103 others(17): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862571 | ||||||
| chr9:99862572 | AAAAAAAA others(5): Show |
A | 1 | a0001c0004t0001g0197 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1634-1046_1634-103 others(16): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862572 | ||||||
| chr9:99862580 | A | G | 2 | a0001c0001t0003g0147 a0001c0001t0003g0148 |
2 | NA18942.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1634-1040A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99862580 | |||||||
| chr9:99862582 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0139 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1634-1037_1634-103 others(25): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862582 | ||||||
| chr9:99862582 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0001g0143 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1634-1037_1634-103 others(23): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862582 | ||||||
| chr9:99862582 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0107 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1634-1037_1634-103 others(20): Show |
NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 99862582 | ||||||
| chr9:99862582 | A | G | 7 | a0001c0001t0001g0133 a0001c0001t0001g0153 a0001c0001t0003g0147 others(4): Show |
8 | HG02145.hp2 HG02886.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1634-1038A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99862582 | |||||||
| chr9:99862615 | T | C | 1 | a0001c0001t0010g0071 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1634-1005T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99862615 | |||||||
| chr9:99863480 | A | G | 9 | a0001c0004t0001g0196 a0001c0004t0001g0197 a0001c0004t0001g0198 others(6): Show |
12 | HG00639.hp1 HG00733.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1634-140A>G | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99863480 | |||||||
| chr9:99863552 | T | C | 68 | a0001c0001t0002g0016 a0001c0001t0002g0022 a0001c0001t0002g0024 others(65): Show |
110 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1634-68T>C | NR4A3 | ENSG00000119508.18 | transcript | ENST00000395097.7 | protein_coding | 7/7 | chr9 | 99863552 |