Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7182 |
| ensemblid | ENSG00000177463.16 |
| hgncid | 7972 |
| symbol | NR2C2 |
| name | nuclear receptor subfamily 2 group C member 2 |
| refseq_nuc | NM_001291694.2 |
| refseq_prot | NP_001278623.1 |
| ensembl_nuc | ENST00000425241.6 |
| ensembl_prot | ENSP00000388387.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 14947583 |
| end | 15049273 |
| strand | + |
| ver | v1.2 |
| region | chr3:14947583-15049273 |
| region5000 | chr3:14942583-15054273 |
| regionname0 | NR2C2_chr3_14947583_15049273 |
| regionname5000 | NR2C2_chr3_14942583_15054273 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 596 | 307 | 84 | 65 | 108 | 10 | 38 | 78 | NR2C2_chr3_14942583_15054273 | NR2C2 | MTSPS others(591): Show |
chr3 | 14942583 | 15054273 |
| a0002 | 0/0 | 596 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | MTSPS others(591): Show |
chr3 | 14942583 | 15054273 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1788 | 262 | 51 | 59 | 106 | 7 | 37 | NR2C2_chr3_14942583_15054273 | NR2C2 | ATGAC others(1783): Show |
chr3 | 14942583 | 15054273 | ||
| a0001c0002 | 0/0 | 1788 | 16 | 13 | 3 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | ATGAC others(1783): Show |
chr3 | 14942583 | 15054273 | ||
| a0001c0003 | 0/0 | 1788 | 14 | 7 | 3 | 0 | 3 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | ATGAC others(1783): Show |
chr3 | 14942583 | 15054273 | ||
| a0001c0004 | 0/0 | 1788 | 8 | 8 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | ATGAC others(1783): Show |
chr3 | 14942583 | 15054273 | ||
| a0001c0005 | 0/0 | 1788 | 3 | 3 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | ATGAC others(1783): Show |
chr3 | 14942583 | 15054273 | ||
| a0001c0006 | 0/0 | 1788 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | ATGAC others(1783): Show |
chr3 | 14942583 | 15054273 | ||
| a0001c0007 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | ATGAC others(1783): Show |
chr3 | 14942583 | 15054273 | ||
| a0001c0009 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | ATGAC others(1783): Show |
chr3 | 14942583 | 15054273 | ||
| a0002c0008 | 0/0 | 1788 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | ATGAC others(1783): Show |
chr3 | 14942583 | 15054273 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 8419 | 128 | 12 | 25 | 66 | 2 | 21 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0002 | 0/0 | 8423 | 35 | 0 | 13 | 18 | 1 | 3 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8418): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0003 | 0/0 | 8419 | 25 | 3 | 6 | 13 | 0 | 3 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0004 | 0/0 | 8419 | 16 | 14 | 2 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0008 | 0/0 | 8418 | 5 | 0 | 2 | 0 | 3 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8413): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0009 | 0/0 | 8419 | 5 | 0 | 3 | 1 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0010 | 0/0 | 8423 | 4 | 0 | 0 | 4 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8418): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0011 | 0/0 | 8423 | 4 | 0 | 2 | 0 | 0 | 2 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8418): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0012 | 0/0 | 8419 | 4 | 4 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0015 | 0/0 | 8423 | 3 | 0 | 0 | 0 | 0 | 3 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8418): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0016 | 0/0 | 8419 | 2 | 2 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0017 | 0/0 | 8419 | 2 | 2 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0018 | 0/0 | 8423 | 2 | 1 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8418): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0019 | 0/0 | 8419 | 2 | 2 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0020 | 0/0 | 8419 | 2 | 0 | 2 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0021 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0022 | 0/0 | 8419 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0023 | 0/0 | 8419 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0024 | 0/0 | 8423 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8418): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0025 | 0/0 | 8423 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8418): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0026 | 0/0 | 8423 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8418): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0027 | 0/0 | 8423 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8418): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0028 | 0/0 | 8423 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8418): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0029 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0030 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0031 | 0/0 | 8423 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8418): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0032 | 0/0 | 8423 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8418): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0033 | 0/0 | 8419 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0034 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0035 | 0/0 | 8419 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0036 | 0/0 | 8419 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0037 | 0/0 | 8419 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0038 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0039 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0040 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0041 | 0/0 | 8419 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0042 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0001t0043 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0002t0005 | 0/0 | 8423 | 14 | 12 | 2 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8418): Show |
chr3 | 14942583 | 15054273 |
| a0001c0002t0014 | 0/0 | 8423 | 2 | 1 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8418): Show |
chr3 | 14942583 | 15054273 |
| a0001c0003t0006 | 0/0 | 8419 | 10 | 3 | 3 | 0 | 3 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0003t0013 | 0/0 | 8419 | 4 | 4 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0004t0007 | 0/0 | 8419 | 8 | 8 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0005t0002 | 0/0 | 8423 | 3 | 3 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8418): Show |
chr3 | 14942583 | 15054273 |
| a0001c0006t0001 | 0/0 | 8419 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0001c0007t0014 | 0/0 | 8423 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8418): Show |
chr3 | 14942583 | 15054273 |
| a0001c0009t0001 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| a0002c0008t0001 | 0/0 | 8419 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | GAACA others(8414): Show |
chr3 | 14942583 | 15054273 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0014 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0008g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0008g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0008g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0008g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0008g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0009g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0009g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0009g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0009g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0009g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0010g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0010g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0010g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0010g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0011g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0011g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0011g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0011g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0012g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0012g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0012g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0012g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0015g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0015g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0016g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0016g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0017g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0017g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0018g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0018g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0019g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0019g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0020g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0020g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0021g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0022g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0023g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0024g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0025g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0026g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0027g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0028g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0029g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0030g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0031g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0032g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0033g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0034g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0035g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0036g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0037g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0038g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0039g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0040g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0041g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0042g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0001t0043g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0014g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0002t0014g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0006g0006 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0006g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0006g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0006g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0006g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0006g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0013g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0013g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0013g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0003t0013g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0004t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0004t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0004t0007g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0004t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0004t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0004t0007g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0004t0007g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0004t0007g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0005t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0005t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0005t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0006t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0006t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0007t0014g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0001c0009t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| a0002c0008t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0003 | t0006 | g0006 | EUR | GBR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | GBR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00280 | hp1 | a0001 | c0001 | t0008 | g0177 | EUR | FIN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00280 | hp2 | a0001 | c0001 | t0037 | g0160 | EUR | FIN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00609 | hp1 | a0001 | c0001 | t0010 | g0060 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00639 | hp2 | a0001 | c0001 | t0008 | g0176 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00642 | hp1 | a0001 | c0001 | t0011 | g0214 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00642 | hp2 | a0001 | c0003 | t0006 | g0007 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00733 | hp1 | a0001 | c0003 | t0006 | g0269 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00733 | hp2 | a0001 | c0001 | t0018 | g0067 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00735 | hp1 | a0001 | c0001 | t0009 | g0117 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01081 | hp1 | a0001 | c0001 | t0009 | g0115 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01081 | hp2 | a0001 | c0002 | t0014 | g0008 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01109 | hp1 | a0001 | c0002 | t0005 | g0020 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0119 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01168 | hp1 | a0001 | c0002 | t0005 | g0022 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01168 | hp2 | a0001 | c0001 | t0020 | g0222 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01169 | hp2 | a0001 | c0001 | t0020 | g0223 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01175 | hp1 | a0001 | c0001 | t0033 | g0148 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0234 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01192 | hp2 | a0001 | c0001 | t0025 | g0066 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01258 | hp2 | a0001 | c0001 | t0008 | g0210 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0217 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01496 | hp1 | a0001 | c0001 | t0024 | g0053 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01515 | hp1 | a0001 | c0003 | t0006 | g0007 | EUR | IBS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01515 | hp2 | a0001 | c0001 | t0008 | g0158 | EUR | IBS | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01884 | hp1 | a0001 | c0004 | t0007 | g0278 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01891 | hp1 | a0001 | c0004 | t0007 | g0276 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0243 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0242 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02055 | hp1 | a0001 | c0001 | t0012 | g0076 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02071 | hp1 | a0001 | c0001 | t0010 | g0047 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02129 | hp1 | a0001 | c0001 | t0023 | g0094 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02132 | hp2 | a0001 | c0001 | t0036 | g0172 | EAS | KHV | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | CDX | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CDX | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CDX | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02257 | hp1 | a0001 | c0004 | t0007 | g0274 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02258 | hp1 | a0001 | c0003 | t0013 | g0248 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02273 | hp2 | a0002 | c0008 | t0001 | g0152 | AMR | PEL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02615 | hp1 | a0001 | c0001 | t0034 | g0114 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02622 | hp1 | a0001 | c0003 | t0013 | g0247 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02622 | hp2 | a0001 | c0001 | t0039 | g0288 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02630 | hp1 | a0001 | c0002 | t0005 | g0099 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02630 | hp2 | a0001 | c0001 | t0019 | g0289 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02683 | hp2 | a0001 | c0001 | t0032 | g0056 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02717 | hp1 | a0001 | c0002 | t0005 | g0028 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0227 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02723 | hp1 | a0001 | c0003 | t0013 | g0246 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0244 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02735 | hp2 | a0001 | c0001 | t0035 | g0142 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02809 | hp1 | a0001 | c0001 | t0017 | g0292 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02809 | hp2 | a0001 | c0001 | t0012 | g0297 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02886 | hp2 | a0001 | c0001 | t0019 | g0290 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02895 | hp1 | a0001 | c0002 | t0005 | g0026 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02895 | hp2 | a0001 | c0001 | t0038 | g0287 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02896 | hp1 | a0001 | c0001 | t0012 | g0282 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0238 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02897 | hp1 | a0001 | c0002 | t0005 | g0029 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02897 | hp2 | a0001 | c0001 | t0012 | g0281 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0232 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0241 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02965 | hp2 | a0001 | c0002 | t0005 | g0021 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02970 | hp2 | a0001 | c0002 | t0014 | g0009 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0240 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03098 | hp1 | a0001 | c0004 | t0007 | g0271 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03098 | hp2 | a0001 | c0001 | t0042 | g0230 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03130 | hp1 | a0001 | c0002 | t0005 | g0019 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03130 | hp2 | a0001 | c0001 | t0040 | g0079 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03139 | hp1 | a0001 | c0002 | t0005 | g0031 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03195 | hp1 | a0001 | c0005 | t0002 | g0295 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03209 | hp1 | a0001 | c0001 | t0016 | g0273 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03209 | hp2 | a0001 | c0002 | t0005 | g0023 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03225 | hp1 | a0001 | c0001 | t0029 | g0296 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0231 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03486 | hp2 | a0001 | c0001 | t0043 | g0235 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03491 | hp1 | a0001 | c0001 | t0015 | g0003 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03491 | hp2 | a0001 | c0001 | t0009 | g0267 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03492 | hp2 | a0001 | c0001 | t0015 | g0003 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03516 | hp1 | a0001 | c0001 | t0016 | g0272 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03516 | hp2 | a0001 | c0005 | t0002 | g0293 | AFR | ESN | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03540 | hp1 | a0001 | c0003 | t0006 | g0006 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03540 | hp2 | a0001 | c0004 | t0007 | g0275 | AFR | GWD | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03579 | hp2 | a0001 | c0002 | t0005 | g0030 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0254 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03669 | hp2 | a0001 | c0001 | t0015 | g0059 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | STU | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0255 | SAS | STU | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03710 | hp1 | a0001 | c0001 | t0011 | g0215 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03710 | hp2 | a0001 | c0001 | t0041 | g0156 | SAS | PJL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | BEB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | BEB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03834 | hp2 | a0001 | c0001 | t0031 | g0218 | SAS | BEB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0095 | SAS | BEB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | STU | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG04184 | hp2 | a0001 | c0001 | t0011 | g0216 | SAS | BEB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | STU | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18522 | hp1 | a0001 | c0001 | t0027 | g0072 | AFR | YRI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18522 | hp2 | a0001 | c0003 | t0013 | g0245 | AFR | YRI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | YRI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18906 | hp2 | a0001 | c0005 | t0002 | g0294 | AFR | YRI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18957 | hp2 | a0001 | c0006 | t0001 | g0203 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18988 | hp1 | a0001 | c0001 | t0026 | g0034 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18994 | hp2 | a0001 | c0006 | t0001 | g0128 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18998 | hp2 | a0001 | c0001 | t0010 | g0048 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19005 | hp2 | a0001 | c0001 | t0022 | g0179 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19030 | hp1 | a0001 | c0001 | t0030 | g0077 | AFR | LWK | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19030 | hp2 | a0001 | c0004 | t0007 | g0280 | AFR | LWK | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19043 | hp1 | a0001 | c0001 | t0021 | g0283 | AFR | LWK | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19043 | hp2 | a0001 | c0009 | t0001 | g0016 | AFR | LWK | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19082 | hp2 | a0001 | c0001 | t0009 | g0196 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19085 | hp1 | a0001 | c0001 | t0010 | g0268 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19240 | hp1 | a0001 | c0004 | t0007 | g0279 | AFR | YRI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | YRI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0239 | AFR | ASW | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20129 | hp2 | a0001 | c0003 | t0006 | g0251 | AFR | ASW | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20752 | hp2 | a0001 | c0003 | t0006 | g0250 | EUR | TSI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0258 | EUR | TSI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20805 | hp2 | a0001 | c0001 | t0008 | g0173 | EUR | TSI | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20905 | hp1 | a0001 | c0003 | t0006 | g0252 | SAS | GIH | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | GIH | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG01123 | hp2 | a0001 | c0003 | t0006 | g0253 | AMR | CLM | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0233 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02109 | hp2 | a0001 | c0004 | t0007 | g0277 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02486 | hp1 | a0001 | c0001 | t0018 | g0068 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02486 | hp2 | a0001 | c0002 | t0005 | g0024 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02559 | hp1 | a0001 | c0003 | t0006 | g0249 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0237 | AFR | ACB | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03471 | hp1 | a0001 | c0007 | t0014 | g0270 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG03471 | hp2 | a0001 | c0001 | t0028 | g0065 | AFR | MSL | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG06807 | hp1 | a0001 | c0001 | t0017 | g0291 | AFR | USA | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| HG06807 | hp2 | a0001 | c0002 | t0005 | g0025 | AFR | USA | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20300 | hp1 | a0001 | c0002 | t0005 | g0027 | AFR | USA | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | USA | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0014 | REF | REF | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0118 | REF | REF | NR2C2_chr3_14942583_15054273 | NR2C2 | chr3 | 14942583 | 15054273 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15016206 | C | T | 1 | a0002 | 1 | HG02273.hp2 | missense_variant | MODERATE | c.328C>T | p.Arg110Trp | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/14 | 691/8419 | 328/1791 | 110/596 | chr3 | 15016206 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15003971 | A | T | 1 | a0001c0009 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.57A>T | p.Ser19Ser | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/14 | 420/8419 | 57/1791 | 19/596 | chr3 | 15003971 | |||
| chr3:15020931 | A | G | 1 | a0001c0006 | 2 | NA18957.hp2 NA18994.hp2 |
splice_region_variant&synonymous_variant | LOW | c.555A>G | p.Glu185Glu | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/14 | 918/8419 | 555/1791 | 185/596 | chr3 | 15020931 | |||
| chr3:15023282 | C | A | 1 | a0001c0007 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.639C>A | p.Ile213Ile | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 6/14 | 1002/8419 | 639/1791 | 213/596 | chr3 | 15023282 | |||
| chr3:15023315 | T | A | 1 | a0001c0004 | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
synonymous_variant | LOW | c.672T>A | p.Thr224Thr | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 6/14 | 1035/8419 | 672/1791 | 224/596 | chr3 | 15023315 | |||
| chr3:15030395 | G | A | 1 | a0001c0005 | 3 | HG03195.hp1 HG03516.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.1053G>A | p.Ser351Ser | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/14 | 1416/8419 | 1053/1791 | 351/596 | chr3 | 15030395 | |||
| chr3:15038076 | G | A | 2 | a0001c0002 a0001c0007 |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
synonymous_variant | LOW | c.1449G>A | p.Ala483Ala | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/14 | 1812/8419 | 1449/1791 | 483/596 | chr3 | 15038076 | |||
| chr3:15039189 | G | A | 1 | a0001c0003 | 14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
synonymous_variant | LOW | c.1578G>A | p.Gln526Gln | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/14 | 1941/8419 | 1578/1791 | 526/596 | chr3 | 15039189 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:14947745 | G | A | 3 | a0001c0001t0016 a0001c0001t0021 a0001c0004t0007 |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-201G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/14 | 56170 | chr3 | 14947745 | ||||||
| chr3:14947778 | C | T | 3 | a0001c0001t0004 a0001c0001t0042 a0001c0001t0043 |
18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-168C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/14 | 56137 | chr3 | 14947778 | ||||||
| chr3:14947803 | C | A | 2 | a0001c0002t0014 a0001c0007t0014 |
3 | HG01081.hp2 HG02970.hp2 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-143C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/14 | 56112 | chr3 | 14947803 | ||||||
| chr3:15043044 | C | T | 1 | a0001c0001t0041 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*36C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 36 | chr3 | 15043044 | ||||||
| chr3:15043108 | T | C | 1 | a0001c0001t0022 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*100T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 100 | chr3 | 15043108 | ||||||
| chr3:15043169 | G | T | 3 | a0001c0001t0038 a0001c0001t0039 a0001c0001t0040 |
3 | HG02622.hp2 HG02895.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*161G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 161 | chr3 | 15043169 | ||||||
| chr3:15043362 | A | G | 2 | a0001c0001t0009 a0001c0001t0037 |
6 | HG00280.hp2 HG00735.hp1 HG01081.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*354A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 354 | chr3 | 15043362 | ||||||
| chr3:15043373 | T | A | 31 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(28): Show |
141 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*365T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 365 | chr3 | 15043373 | ||||||
| chr3:15043450 | A | G | 1 | a0001c0001t0032 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*442A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 442 | chr3 | 15043450 | ||||||
| chr3:15043465 | T | C | 1 | a0001c0001t0038 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*457T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 457 | chr3 | 15043465 | ||||||
| chr3:15043640 | G | A | 2 | a0001c0001t0038 a0001c0001t0039 |
2 | HG02622.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*632G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 632 | chr3 | 15043640 | ||||||
| chr3:15043687 | G | A | 1 | a0001c0001t0023 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*679G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 679 | chr3 | 15043687 | ||||||
| chr3:15043916 | G | A | 1 | a0001c0003t0013 | 4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*908G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 908 | chr3 | 15043916 | ||||||
| chr3:15044063 | C | T | 3 | a0001c0002t0005 a0001c0002t0014 a0001c0007t0014 |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1055C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 1055 | chr3 | 15044063 | ||||||
| chr3:15044085 | A | T | 5 | a0001c0001t0003 a0001c0001t0023 a0001c0001t0038 others(2): Show |
29 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1077A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 1077 | chr3 | 15044085 | ||||||
| chr3:15044093 | G | A | 1 | a0001c0001t0017 | 2 | HG02809.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1085G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 1085 | chr3 | 15044093 | ||||||
| chr3:15044189 | G | A | 1 | a0001c0001t0033 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1181G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 1181 | chr3 | 15044189 | ||||||
| chr3:15044242 | T | A | 1 | a0001c0001t0024 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1234T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 1234 | chr3 | 15044242 | ||||||
| chr3:15044338 | C | T | 3 | a0001c0001t0004 a0001c0001t0042 a0001c0001t0043 |
18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1330C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 1330 | chr3 | 15044338 | ||||||
| chr3:15044399 | G | A | 1 | a0001c0001t0018 | 2 | HG00733.hp2 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1391G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 1391 | chr3 | 15044399 | ||||||
| chr3:15044618 | G | T | 1 | a0001c0001t0021 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1610G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 1610 | chr3 | 15044618 | ||||||
| chr3:15044745 | C | T | 2 | a0001c0003t0006 a0001c0003t0013 |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1737C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 1737 | chr3 | 15044745 | ||||||
| chr3:15045549 | CT | C | 1 | a0001c0001t0008 | 5 | HG00280.hp1 HG00639.hp2 HG01258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2544delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 2544 | INFO_REALIGN_3_PRIME | chr3 | 15045549 | |||||
| chr3:15045630 | G | A | 1 | a0001c0001t0042 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2622G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 2622 | chr3 | 15045630 | ||||||
| chr3:15045720 | C | G | 1 | a0001c0001t0031 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2712C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 2712 | chr3 | 15045720 | ||||||
| chr3:15045965 | C | CAGAT | 16 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0011 others(13): Show |
75 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2962_*2965dupAGAT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 2966 | INFO_REALIGN_3_PRIME | chr3 | 15045965 | |||||
| chr3:15046083 | G | C | 1 | a0001c0001t0017 | 2 | HG02809.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3075G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 3075 | chr3 | 15046083 | ||||||
| chr3:15046088 | T | C | 1 | a0001c0004t0007 | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3080T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 3080 | chr3 | 15046088 | ||||||
| chr3:15046724 | G | T | 1 | a0001c0001t0028 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3716G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 3716 | chr3 | 15046724 | ||||||
| chr3:15046914 | G | A | 1 | a0001c0001t0010 | 4 | HG00609.hp1 HG02071.hp1 NA18998.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3906G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 3906 | chr3 | 15046914 | ||||||
| chr3:15046984 | G | A | 1 | a0001c0001t0019 | 2 | HG02630.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3976G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 3976 | chr3 | 15046984 | ||||||
| chr3:15047197 | T | C | 1 | a0001c0001t0025 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4189T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4189 | chr3 | 15047197 | ||||||
| chr3:15047208 | A | G | 1 | a0001c0001t0015 | 3 | HG03491.hp1 HG03492.hp2 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4200A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4200 | chr3 | 15047208 | ||||||
| chr3:15047260 | T | C | 1 | a0001c0001t0017 | 2 | HG02809.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4252T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4252 | chr3 | 15047260 | ||||||
| chr3:15047274 | C | G | 1 | a0001c0002t0005 | 14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4266C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4266 | chr3 | 15047274 | ||||||
| chr3:15047445 | T | C | 1 | a0001c0001t0034 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4437T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4437 | chr3 | 15047445 | ||||||
| chr3:15047515 | A | G | 1 | a0001c0001t0017 | 2 | HG02809.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4507A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4507 | chr3 | 15047515 | ||||||
| chr3:15047631 | T | C | 1 | a0001c0001t0017 | 2 | HG02809.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4623T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4623 | chr3 | 15047631 | ||||||
| chr3:15047639 | C | T | 1 | a0001c0001t0037 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4631C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4631 | chr3 | 15047639 | ||||||
| chr3:15047696 | C | G | 2 | a0001c0001t0011 a0001c0001t0031 |
5 | HG00642.hp1 HG01361.hp1 HG03710.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4688C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4688 | chr3 | 15047696 | ||||||
| chr3:15047924 | C | T | 1 | a0001c0001t0030 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4916C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4916 | chr3 | 15047924 | ||||||
| chr3:15047953 | C | T | 1 | a0001c0001t0020 | 2 | HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4945C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 4945 | chr3 | 15047953 | ||||||
| chr3:15048121 | T | A | 1 | a0001c0001t0026 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5113T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5113 | chr3 | 15048121 | ||||||
| chr3:15048155 | G | A | 1 | a0001c0001t0035 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5147G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5147 | chr3 | 15048155 | ||||||
| chr3:15048471 | C | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5463C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5463 | chr3 | 15048471 | ||||||
| chr3:15048477 | A | G | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5469A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5469 | chr3 | 15048477 | ||||||
| chr3:15048483 | T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5475T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5475 | chr3 | 15048483 | ||||||
| chr3:15048484 | T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5476T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5476 | chr3 | 15048484 | ||||||
| chr3:15048486 | G | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5478G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5478 | chr3 | 15048486 | ||||||
| chr3:15048486 | G | T | 1 | a0001c0001t0027 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5478G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5478 | chr3 | 15048486 | ||||||
| chr3:15048491 | T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5483T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5483 | chr3 | 15048491 | ||||||
| chr3:15048492 | T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5484T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5484 | chr3 | 15048492 | ||||||
| chr3:15048493 | G | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5485G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5485 | chr3 | 15048493 | ||||||
| chr3:15048495 | T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5487T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5487 | chr3 | 15048495 | ||||||
| chr3:15048500 | A | C | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5492A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5492 | chr3 | 15048500 | ||||||
| chr3:15048501 | T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5493T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5493 | chr3 | 15048501 | ||||||
| chr3:15048506 | G | T | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5498G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5498 | chr3 | 15048506 | ||||||
| chr3:15048507 | C | T | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5499C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5499 | chr3 | 15048507 | ||||||
| chr3:15048508 | A | G | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5500A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5500 | chr3 | 15048508 | ||||||
| chr3:15048510 | A | C | 1 | a0001c0001t0029 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5502A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5502 | chr3 | 15048510 | ||||||
| chr3:15048511 | A | C | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5503A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5503 | chr3 | 15048511 | ||||||
| chr3:15048513 | A | G | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5505A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5505 | chr3 | 15048513 | ||||||
| chr3:15048514 | G | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5506G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5506 | chr3 | 15048514 | ||||||
| chr3:15048519 | A | T | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5511A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5511 | chr3 | 15048519 | ||||||
| chr3:15048522 | A | C | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5514A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5514 | chr3 | 15048522 | ||||||
| chr3:15048536 | T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5528T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5528 | chr3 | 15048536 | ||||||
| chr3:15048564 | T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5556T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5556 | chr3 | 15048564 | ||||||
| chr3:15048578 | T | C | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5570T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5570 | chr3 | 15048578 | ||||||
| chr3:15048579 | G | T | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5571G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5571 | chr3 | 15048579 | ||||||
| chr3:15048583 | G | T | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5575G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5575 | chr3 | 15048583 | ||||||
| chr3:15048594 | T | G | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5586T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5586 | chr3 | 15048594 | ||||||
| chr3:15048595 | G | C | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5587G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5587 | chr3 | 15048595 | ||||||
| chr3:15048596 | C | T | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5588C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5588 | chr3 | 15048596 | ||||||
| chr3:15048611 | T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5603T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5603 | chr3 | 15048611 | ||||||
| chr3:15048637 | T | A | 1 | a0001c0001t0036 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5629T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 5629 | chr3 | 15048637 | ||||||
| chr3:15049109 | G | A | 1 | a0001c0001t0043 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6101G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 14/14 | 6101 | chr3 | 15049109 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:14947913 | T | C | 2 | a0001c0002t0014g0008 a0001c0002t0014g0009 |
2 | HG01081.hp2 HG02970.hp2 |
splice_region_variant&intron_variant | LOW | c.-40+7T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14947913 | |||||||
| chr3:14947954 | G | A | 1 | a0001c0001t0003g0010 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-40+48G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14947954 | |||||||
| chr3:14947983 | C | T | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-40+77C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14947983 | |||||||
| chr3:14948143 | G | T | 1 | a0001c0001t0001g0298 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-40+237G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948143 | |||||||
| chr3:14948250 | C | T | 2 | a0001c0001t0012g0297 a0001c0001t0029g0296 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-40+344C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948250 | |||||||
| chr3:14948257 | C | T | 3 | a0001c0005t0002g0293 a0001c0005t0002g0294 a0001c0005t0002g0295 |
3 | HG03195.hp1 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-40+351C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948257 | |||||||
| chr3:14948329 | C | T | 2 | a0001c0001t0012g0297 a0001c0001t0029g0296 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-40+423C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948329 | |||||||
| chr3:14948427 | A | G | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+521A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948427 | |||||||
| chr3:14948476 | C | T | 2 | a0001c0001t0019g0289 a0001c0001t0019g0290 |
2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-40+570C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948476 | |||||||
| chr3:14948487 | G | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+581G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948487 | |||||||
| chr3:14948567 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0009t0001g0016 |
3 | HG03139.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-40+661G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948567 | |||||||
| chr3:14948647 | T | A | 1 | a0001c0009t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-40+741T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948647 | |||||||
| chr3:14948739 | T | C | 13 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(10): Show |
13 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-40+833T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948739 | |||||||
| chr3:14948748 | C | T | 2 | a0001c0001t0038g0287 a0001c0001t0039g0288 |
2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-40+842C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948748 | |||||||
| chr3:14948777 | C | G | 2 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
2 | HG03704.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-40+871C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948777 | |||||||
| chr3:14948865 | A | T | 1 | a0001c0001t0001g0284 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-40+959A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948865 | |||||||
| chr3:14948872 | G | T | 13 | a0001c0001t0012g0281 a0001c0001t0012g0282 a0001c0001t0016g0272 others(10): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-40+966G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948872 | |||||||
| chr3:14948878 | G | A | 50 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(47): Show |
51 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.-40+972G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948878 | |||||||
| chr3:14948927 | T | G | 2 | a0001c0001t0012g0297 a0001c0001t0029g0296 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-40+1021T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14948927 | |||||||
| chr3:14949011 | C | T | 1 | a0001c0001t0021g0283 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-40+1105C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949011 | |||||||
| chr3:14949029 | G | A | 1 | a0001c0002t0005g0019 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-40+1123G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949029 | |||||||
| chr3:14949055 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-40+1149G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949055 | |||||||
| chr3:14949076 | C | T | 2 | a0001c0001t0012g0297 a0001c0001t0029g0296 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-40+1170C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949076 | |||||||
| chr3:14949115 | T | C | 3 | a0001c0001t0038g0287 a0001c0001t0039g0288 a0001c0001t0040g0079 |
3 | HG02622.hp2 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-40+1209T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949115 | |||||||
| chr3:14949117 | A | G | 3 | a0001c0001t0038g0287 a0001c0001t0039g0288 a0001c0001t0040g0079 |
3 | HG02622.hp2 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-40+1211A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949117 | |||||||
| chr3:14949168 | CTAGAGTT others(17): Show |
C | 24 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(21): Show |
26 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-40+1267_-40+1290d others(26): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14949168 | ||||||
| chr3:14949209 | G | T | 3 | a0001c0002t0014g0008 a0001c0002t0014g0009 a0001c0007t0014g0270 |
3 | HG01081.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-40+1303G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949209 | |||||||
| chr3:14949244 | A | G | 1 | a0001c0003t0006g0269 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-40+1338A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949244 | |||||||
| chr3:14949248 | C | T | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+1342C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949248 | |||||||
| chr3:14949298 | C | T | 12 | a0001c0002t0005g0019 a0001c0002t0005g0021 a0001c0002t0005g0022 others(9): Show |
12 | HG01168.hp1 HG02486.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-40+1392C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949298 | |||||||
| chr3:14949682 | C | T | 1 | a0001c0001t0010g0268 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-40+1776C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949682 | |||||||
| chr3:14949745 | CAT | C | 3 | a0001c0001t0003g0096 a0001c0001t0003g0097 a0001c0001t0003g0098 |
3 | HG00438.hp1 HG00544.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.-40+1840_-40+1841d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949745 | |||||||
| chr3:14949756 | G | GATTT | 14 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(11): Show |
14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40+1871_-40+1874d others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14949756 | ||||||
| chr3:14949756 | GATTT | G | 7 | a0001c0001t0009g0267 a0001c0001t0012g0076 a0001c0001t0012g0281 others(4): Show |
7 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40+1871_-40+1874d others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14949756 | ||||||
| chr3:14949833 | C | T | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+1927C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949833 | |||||||
| chr3:14949862 | C | G | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+1956C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949862 | |||||||
| chr3:14949954 | T | C | 4 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40+2048T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949954 | |||||||
| chr3:14949968 | C | G | 1 | a0001c0001t0001g0266 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-40+2062C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14949968 | |||||||
| chr3:14950065 | G | A | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40+2159G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950065 | |||||||
| chr3:14950132 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-40+2226C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950132 | |||||||
| chr3:14950136 | G | A | 4 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(1): Show |
4 | NA18946.hp1 NA18978.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40+2230G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950136 | |||||||
| chr3:14950481 | C | G | 1 | a0001c0001t0001g0265 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-40+2575C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950481 | |||||||
| chr3:14950493 | C | T | 4 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(1): Show |
4 | HG01243.hp1 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40+2587C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950493 | |||||||
| chr3:14950557 | A | G | 1 | a0001c0001t0002g0074 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-40+2651A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950557 | |||||||
| chr3:14950628 | C | T | 54 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(51): Show |
55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-40+2722C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950628 | |||||||
| chr3:14950707 | C | T | 26 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(23): Show |
28 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-40+2801C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950707 | |||||||
| chr3:14950846 | GA | G | 14 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(11): Show |
14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40+2941delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950846 | |||||||
| chr3:14950850 | C | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+2944C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14950850 | |||||||
| chr3:14951122 | G | A | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+3216G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951122 | |||||||
| chr3:14951498 | T | C | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+3592T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951498 | |||||||
| chr3:14951504 | T | C | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+3598T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951504 | |||||||
| chr3:14951543 | A | G | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+3637A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951543 | |||||||
| chr3:14951559 | A | G | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+3653A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951559 | |||||||
| chr3:14951666 | T | G | 1 | a0001c0001t0002g0036 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-40+3760T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951666 | |||||||
| chr3:14951697 | T | C | 1 | a0001c0001t0029g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-40+3791T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951697 | |||||||
| chr3:14951705 | C | T | 146 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(143): Show |
151 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-40+3799C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951705 | |||||||
| chr3:14951754 | G | GT | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+3857dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14951754 | ||||||
| chr3:14951967 | C | G | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+4061C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951967 | |||||||
| chr3:14951988 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-40+4082C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951988 | |||||||
| chr3:14951992 | T | C | 1 | a0001c0004t0007g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-40+4086T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14951992 | |||||||
| chr3:14952030 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-40+4124G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952030 | |||||||
| chr3:14952037 | C | T | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+4131C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952037 | |||||||
| chr3:14952038 | G | A | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+4132G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952038 | |||||||
| chr3:14952145 | C | G | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+4239C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952145 | |||||||
| chr3:14952160 | C | T | 2 | a0001c0001t0004g0243 a0001c0001t0004g0244 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-40+4254C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952160 | |||||||
| chr3:14952270 | G | T | 14 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(11): Show |
14 | HG00140.hp2 HG00642.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40+4364G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952270 | |||||||
| chr3:14952325 | T | TCTC | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+4421_-40+4422i others(5): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14952325 | ||||||
| chr3:14952369 | C | G | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-40+4463C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952369 | |||||||
| chr3:14952501 | A | G | 1 | a0001c0001t0002g0073 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-40+4595A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952501 | |||||||
| chr3:14952847 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-40+4941G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952847 | |||||||
| chr3:14952863 | A | G | 3 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0298 |
3 | HG00673.hp2 NA18991.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-40+4957A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952863 | |||||||
| chr3:14952919 | G | C | 14 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(11): Show |
14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40+5013G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14952919 | |||||||
| chr3:14953027 | C | G | 1 | a0001c0001t0004g0242 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-40+5121C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953027 | |||||||
| chr3:14953087 | A | G | 1 | a0001c0001t0027g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-40+5181A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953087 | |||||||
| chr3:14953110 | C | A | 2 | a0001c0001t0012g0281 a0001c0001t0012g0282 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-40+5204C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953110 | |||||||
| chr3:14953155 | TGAAAG | T | 7 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0250 others(4): Show |
9 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.-40+5250_-40+5254d others(7): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953155 | |||||||
| chr3:14953193 | G | A | 4 | a0001c0003t0013g0245 a0001c0003t0013g0246 a0001c0003t0013g0247 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40+5287G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953193 | |||||||
| chr3:14953245 | G | A | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+5339G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953245 | |||||||
| chr3:14953284 | C | G | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+5378C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953284 | |||||||
| chr3:14953442 | T | G | 1 | a0001c0001t0001g0102 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-40+5536T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953442 | |||||||
| chr3:14953518 | A | G | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+5612A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953518 | |||||||
| chr3:14953609 | C | T | 18 | a0001c0001t0004g0227 a0001c0001t0004g0228 a0001c0001t0004g0229 others(15): Show |
18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-40+5703C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953609 | |||||||
| chr3:14953610 | G | A | 1 | a0001c0001t0027g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-40+5704G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953610 | |||||||
| chr3:14953621 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-40+5715C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953621 | |||||||
| chr3:14953622 | G | A | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+5716G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953622 | |||||||
| chr3:14953663 | A | G | 14 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(11): Show |
14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40+5757A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953663 | |||||||
| chr3:14953671 | G | A | 5 | a0001c0001t0011g0214 a0001c0001t0011g0215 a0001c0001t0011g0216 others(2): Show |
5 | HG00642.hp1 HG01361.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40+5765G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953671 | |||||||
| chr3:14953756 | G | A | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+5850G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953756 | |||||||
| chr3:14953894 | C | CA | 54 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(51): Show |
56 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.-40+6005dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14953894 | ||||||
| chr3:14953912 | C | A | 3 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 |
3 | HG02615.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-40+6006C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953912 | |||||||
| chr3:14953977 | C | A | 1 | a0001c0001t0029g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-40+6071C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953977 | |||||||
| chr3:14953978 | A | G | 1 | a0001c0001t0029g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-40+6072A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14953978 | |||||||
| chr3:14954203 | C | T | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+6297C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14954203 | |||||||
| chr3:14954213 | G | C | 1 | a0001c0004t0007g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-40+6307G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14954213 | |||||||
| chr3:14954308 | TAAAC | T | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+6405_-40+6408d others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14954308 | ||||||
| chr3:14954326 | G | A | 2 | a0001c0002t0014g0008 a0001c0002t0014g0009 |
2 | HG01081.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-40+6420G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14954326 | |||||||
| chr3:14954596 | A | G | 1 | a0001c0001t0003g0095 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-40+6690A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14954596 | |||||||
| chr3:14954647 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-40+6741A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14954647 | |||||||
| chr3:14954695 | T | A | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+6789T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14954695 | |||||||
| chr3:14954729 | G | C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | NA18945.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-40+6823G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14954729 | |||||||
| chr3:14955070 | G | T | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+7164G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955070 | |||||||
| chr3:14955106 | C | T | 1 | a0001c0001t0008g0210 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-40+7200C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955106 | |||||||
| chr3:14955250 | T | C | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+7344T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955250 | |||||||
| chr3:14955251 | G | A | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+7345G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955251 | |||||||
| chr3:14955289 | G | A | 5 | a0001c0001t0001g0078 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG01106.hp2 HG01361.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40+7383G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955289 | |||||||
| chr3:14955574 | G | A | 4 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40+7668G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955574 | |||||||
| chr3:14955583 | C | T | 2 | a0001c0001t0002g0071 a0001c0001t0002g0260 |
2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-40+7677C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955583 | |||||||
| chr3:14955705 | A | C | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+7799A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955705 | |||||||
| chr3:14955762 | T | C | 2 | a0001c0001t0002g0032 a0001c0001t0002g0033 |
2 | NA18978.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-40+7856T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955762 | |||||||
| chr3:14955826 | T | TATGTAGT others(356): Show |
1 | a0001c0001t0001g0209 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-40+7936_-40+7937i others(365): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14955826 | ||||||
| chr3:14955850 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-40+7944G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955850 | |||||||
| chr3:14955879 | C | G | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40+7973C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955879 | |||||||
| chr3:14955958 | A | G | 1 | a0001c0001t0002g0070 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-40+8052A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14955958 | |||||||
| chr3:14956058 | C | G | 1 | a0001c0003t0006g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-40+8152C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14956058 | |||||||
| chr3:14956178 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0034g0114 |
2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-40+8272T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14956178 | |||||||
| chr3:14956353 | A | G | 1 | a0001c0001t0002g0069 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-40+8447A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14956353 | |||||||
| chr3:14956422 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-40+8516G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14956422 | |||||||
| chr3:14956567 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-40+8661G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14956567 | |||||||
| chr3:14956760 | C | T | 9 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(6): Show |
9 | HG01099.hp2 NA18957.hp2 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.-40+8854C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14956760 | |||||||
| chr3:14956899 | G | C | 102 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(99): Show |
105 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.-40+8993G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14956899 | |||||||
| chr3:14957049 | A | G | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+9143A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957049 | |||||||
| chr3:14957068 | C | T | 3 | a0001c0001t0018g0067 a0001c0001t0018g0068 a0001c0001t0025g0066 |
3 | HG00733.hp2 HG01192.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-40+9162C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957068 | |||||||
| chr3:14957331 | T | C | 1 | a0001c0001t0009g0115 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-40+9425T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957331 | |||||||
| chr3:14957477 | G | A | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+9571G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957477 | |||||||
| chr3:14957488 | T | C | 18 | a0001c0001t0004g0227 a0001c0001t0004g0228 a0001c0001t0004g0229 others(15): Show |
18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-40+9582T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957488 | |||||||
| chr3:14957493 | C | T | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40+9587C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957493 | |||||||
| chr3:14957533 | T | C | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+9627T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957533 | |||||||
| chr3:14957709 | T | C | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+9803T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957709 | |||||||
| chr3:14957764 | A | G | 1 | a0001c0002t0005g0020 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-40+9858A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957764 | |||||||
| chr3:14957805 | AT | A | 27 | a0001c0001t0001g0116 a0001c0001t0003g0001 a0001c0001t0003g0010 others(24): Show |
29 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.-40+9910delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14957805 | ||||||
| chr3:14957927 | T | TTGCC | 293 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(290): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.-40+10022_-40+1002 others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14957927 | ||||||
| chr3:14957975 | A | G | 1 | a0001c0002t0005g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-40+10069A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14957975 | |||||||
| chr3:14958114 | G | A | 54 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(51): Show |
55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-40+10208G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958114 | |||||||
| chr3:14958275 | A | G | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+10369A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958275 | |||||||
| chr3:14958336 | A | G | 1 | a0001c0007t0014g0270 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-40+10430A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958336 | |||||||
| chr3:14958340 | C | CT | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+10445dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14958340 | ||||||
| chr3:14958431 | G | A | 49 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(46): Show |
50 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-40+10525G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958431 | |||||||
| chr3:14958506 | G | A | 18 | a0001c0001t0004g0227 a0001c0001t0004g0228 a0001c0001t0004g0229 others(15): Show |
18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-40+10600G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958506 | |||||||
| chr3:14958530 | T | G | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+10624T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958530 | |||||||
| chr3:14958563 | T | C | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+10657T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958563 | |||||||
| chr3:14958614 | G | T | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40+10708G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958614 | |||||||
| chr3:14958674 | T | G | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+10768T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958674 | |||||||
| chr3:14958687 | T | A | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+10781T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958687 | |||||||
| chr3:14958758 | T | A | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+10852T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958758 | |||||||
| chr3:14958844 | C | T | 1 | a0001c0001t0002g0064 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-40+10938C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958844 | |||||||
| chr3:14958956 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-40+11050C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958956 | |||||||
| chr3:14958970 | G | A | 7 | a0001c0001t0001g0121 a0001c0001t0012g0076 a0001c0001t0012g0281 others(4): Show |
7 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40+11064G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14958970 | |||||||
| chr3:14959137 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-40+11231T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14959137 | |||||||
| chr3:14959682 | C | G | 3 | a0001c0002t0014g0008 a0001c0002t0014g0009 a0001c0007t0014g0270 |
3 | HG01081.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-40+11776C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14959682 | |||||||
| chr3:14960334 | G | A | 18 | a0001c0001t0004g0227 a0001c0001t0004g0228 a0001c0001t0004g0229 others(15): Show |
18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-40+12428G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14960334 | |||||||
| chr3:14960372 | C | A | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+12466C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14960372 | |||||||
| chr3:14960476 | T | C | 31 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(28): Show |
33 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-40+12570T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14960476 | |||||||
| chr3:14960752 | A | G | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+12846A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14960752 | |||||||
| chr3:14960952 | TTG | T | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40+13050_-40+1305 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14960952 | ||||||
| chr3:14961062 | A | G | 1 | a0001c0002t0005g0024 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-40+13156A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961062 | |||||||
| chr3:14961157 | A | T | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+13251A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961157 | |||||||
| chr3:14961285 | G | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-40+13379G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961285 | |||||||
| chr3:14961384 | G | A | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+13478G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961384 | |||||||
| chr3:14961435 | A | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0009t0001g0016 |
3 | HG03139.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-40+13529A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961435 | |||||||
| chr3:14961501 | T | G | 18 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(15): Show |
20 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-40+13595T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961501 | |||||||
| chr3:14961544 | T | A | 2 | a0001c0001t0003g0254 a0001c0001t0003g0255 |
2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-40+13638T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961544 | |||||||
| chr3:14961550 | A | G | 3 | a0001c0002t0014g0008 a0001c0002t0014g0009 a0001c0007t0014g0270 |
3 | HG01081.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-40+13644A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961550 | |||||||
| chr3:14961617 | C | T | 1 | a0001c0001t0009g0119 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-40+13711C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961617 | |||||||
| chr3:14961873 | G | A | 2 | a0001c0001t0012g0297 a0001c0001t0029g0296 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-40+13967G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961873 | |||||||
| chr3:14961918 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-40+14012C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14961918 | |||||||
| chr3:14962541 | A | G | 18 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(15): Show |
20 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-40+14635A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14962541 | |||||||
| chr3:14962602 | C | T | 18 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(15): Show |
20 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-40+14696C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14962602 | |||||||
| chr3:14962655 | C | CT | 31 | a0001c0001t0001g0106 a0001c0001t0001g0120 a0001c0001t0001g0198 others(28): Show |
31 | HG00544.hp1 HG01081.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-40+14769dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14962655 | ||||||
| chr3:14962655 | CT | C | 25 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0107 others(22): Show |
27 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.-40+14769delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14962655 | ||||||
| chr3:14962686 | G | T | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40+14780G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14962686 | |||||||
| chr3:14962809 | C | T | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+14903C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14962809 | |||||||
| chr3:14962845 | G | T | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-40+14939G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14962845 | |||||||
| chr3:14962919 | T | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | NA18960.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-40+15013T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14962919 | |||||||
| chr3:14963023 | T | A | 54 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(51): Show |
55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-40+15117T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14963023 | |||||||
| chr3:14963024 | C | T | 54 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(51): Show |
55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-40+15118C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14963024 | |||||||
| chr3:14963224 | G | C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(37): Show |
42 | HG01070.hp2 HG01071.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.-40+15318G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14963224 | |||||||
| chr3:14963269 | A | G | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+15363A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14963269 | |||||||
| chr3:14963336 | ATAAG | A | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+15434_-40+1543 others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14963336 | ||||||
| chr3:14963389 | C | T | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+15483C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14963389 | |||||||
| chr3:14963460 | CATTTTTT | C | 9 | a0001c0001t0001g0105 a0001c0001t0001g0197 a0001c0001t0009g0196 others(6): Show |
9 | HG00438.hp2 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-40+15576_-40+1558 others(11): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14963460 | ||||||
| chr3:14963618 | G | A | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+15712G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14963618 | |||||||
| chr3:14963671 | T | C | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+15765T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14963671 | |||||||
| chr3:14963910 | G | A | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 |
3 | HG01884.hp2 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-40+16004G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14963910 | |||||||
| chr3:14963917 | A | G | 1 | a0001c0001t0035g0142 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-40+16011A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14963917 | |||||||
| chr3:14964161 | A | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0195 |
2 | NA18951.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.-40+16255A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964161 | |||||||
| chr3:14964255 | A | G | 1 | a0001c0005t0002g0293 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-40+16349A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964255 | |||||||
| chr3:14964423 | G | A | 1 | a0001c0009t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-40+16517G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964423 | |||||||
| chr3:14964496 | TTATTTTC | T | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+16597_-40+1660 others(11): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14964496 | ||||||
| chr3:14964503 | CTATTTTA | C | 288 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(285): Show |
296 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.-40+16604_-40+1661 others(11): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14964503 | ||||||
| chr3:14964503 | CTATTTTA others(7): Show |
C | 1 | a0001c0001t0018g0067 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-40+16604_-40+1661 others(18): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14964503 | ||||||
| chr3:14964510 | A | T | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+16604A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964510 | |||||||
| chr3:14964577 | C | T | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+16671C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964577 | |||||||
| chr3:14964615 | C | T | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+16709C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964615 | |||||||
| chr3:14964660 | G | A | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+16754G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964660 | |||||||
| chr3:14964676 | G | A | 1 | a0001c0001t0040g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-40+16770G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964676 | |||||||
| chr3:14964681 | A | AT | 20 | a0001c0001t0001g0106 a0001c0001t0002g0033 a0001c0002t0005g0019 others(17): Show |
20 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-40+16790dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14964681 | ||||||
| chr3:14964724 | G | A | 1 | a0001c0001t0002g0040 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-40+16818G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964724 | |||||||
| chr3:14964726 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-40+16820G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964726 | |||||||
| chr3:14964765 | G | A | 7 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0250 others(4): Show |
9 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.-40+16859G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964765 | |||||||
| chr3:14964802 | G | A | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+16896G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964802 | |||||||
| chr3:14964811 | C | T | 11 | a0001c0001t0004g0234 a0001c0001t0004g0236 a0001c0001t0004g0237 others(8): Show |
11 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.-40+16905C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14964811 | |||||||
| chr3:14965030 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-40+17124A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965030 | |||||||
| chr3:14965090 | A | G | 18 | a0001c0001t0004g0227 a0001c0001t0004g0228 a0001c0001t0004g0229 others(15): Show |
18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-40+17184A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965090 | |||||||
| chr3:14965140 | A | C | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+17234A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965140 | |||||||
| chr3:14965141 | C | CT | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+17242dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965141 | ||||||
| chr3:14965273 | C | T | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+17367C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965273 | |||||||
| chr3:14965380 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-40+17474G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965380 | |||||||
| chr3:14965451 | G | A | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+17545G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965451 | |||||||
| chr3:14965522 | C | CA | 71 | a0001c0001t0001g0078 a0001c0001t0001g0116 a0001c0001t0001g0146 others(68): Show |
72 | HG00609.hp1 HG00642.hp1 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.-40+17640dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965522 | ||||||
| chr3:14965522 | C | CAA | 34 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0001g0211 others(31): Show |
34 | HG00673.hp1 HG00735.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.-40+17639_-40+1764 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965522 | ||||||
| chr3:14965522 | CA | C | 6 | a0001c0001t0001g0113 a0001c0001t0001g0145 a0001c0001t0001g0193 others(3): Show |
6 | HG01169.hp2 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40+17640delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965522 | ||||||
| chr3:14965522 | CAAA | C | 22 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(19): Show |
24 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.-40+17638_-40+1764 others(7): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965522 | ||||||
| chr3:14965522 | CAAAAAA | C | 7 | a0001c0001t0001g0103 a0001c0001t0001g0125 a0001c0001t0001g0126 others(4): Show |
7 | HG02723.hp2 HG02809.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40+17635_-40+1764 others(10): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965522 | ||||||
| chr3:14965522 | CAAAAAAA | C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(37): Show |
42 | HG01070.hp2 HG01071.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.-40+17634_-40+1764 others(11): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965522 | ||||||
| chr3:14965522 | CAAAAAAA others(3): Show |
C | 16 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(13): Show |
16 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-40+17631_-40+1764 others(14): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965522 | ||||||
| chr3:14965522 | CAAAAAAA others(4): Show |
C | 11 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(8): Show |
13 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.-40+17630_-40+1764 others(15): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965522 | ||||||
| chr3:14965522 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0224 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-40+17629_-40+1764 others(16): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965522 | ||||||
| chr3:14965637 | GCT | G | 3 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 |
3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-40+17732_-40+1773 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965637 | |||||||
| chr3:14965640 | G | GT | 111 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(108): Show |
116 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-40+17742dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965640 | ||||||
| chr3:14965640 | G | T | 3 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 |
3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-40+17734G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965640 | |||||||
| chr3:14965648 | T | G | 3 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 |
3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-40+17742T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965648 | |||||||
| chr3:14965648 | T | TG | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40+17743dupG | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14965648 | ||||||
| chr3:14965649 | G | T | 1 | a0001c0003t0006g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-40+17743G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965649 | |||||||
| chr3:14965825 | G | A | 2 | a0001c0002t0005g0028 a0001c0002t0005g0031 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-40+17919G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965825 | |||||||
| chr3:14965862 | G | A | 6 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0049 others(3): Show |
6 | NA18945.hp2 NA18972.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+17956G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965862 | |||||||
| chr3:14965910 | C | G | 71 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(68): Show |
72 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.-40+18004C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14965910 | |||||||
| chr3:14966195 | A | G | 4 | a0001c0003t0013g0245 a0001c0003t0013g0246 a0001c0003t0013g0247 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40+18289A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14966195 | |||||||
| chr3:14966207 | A | C | 54 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(51): Show |
55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-40+18301A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14966207 | |||||||
| chr3:14966227 | A | G | 146 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(143): Show |
151 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-40+18321A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14966227 | |||||||
| chr3:14966657 | A | G | 1 | a0001c0001t0002g0062 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-40+18751A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14966657 | |||||||
| chr3:14966711 | A | G | 1 | a0001c0002t0005g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-40+18805A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14966711 | |||||||
| chr3:14966823 | A | G | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+18917A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14966823 | |||||||
| chr3:14966900 | A | C | 4 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40+18994A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14966900 | |||||||
| chr3:14966927 | A | G | 2 | a0001c0001t0004g0232 a0001c0001t0004g0233 |
2 | HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-40+19021A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14966927 | |||||||
| chr3:14967075 | A | T | 2 | a0001c0004t0007g0277 a0001c0004t0007g0278 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-40+19169A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967075 | |||||||
| chr3:14967288 | T | G | 1 | a0001c0001t0002g0041 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-40+19382T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967288 | |||||||
| chr3:14967361 | T | C | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+19455T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967361 | |||||||
| chr3:14967403 | T | A | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40+19497T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967403 | |||||||
| chr3:14967558 | T | A | 1 | a0001c0001t0029g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-40+19652T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967558 | |||||||
| chr3:14967622 | G | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-40+19716G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967622 | |||||||
| chr3:14967747 | G | C | 3 | a0001c0005t0002g0293 a0001c0005t0002g0294 a0001c0005t0002g0295 |
3 | HG03195.hp1 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-40+19841G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967747 | |||||||
| chr3:14967793 | T | C | 1 | a0001c0007t0014g0270 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-40+19887T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967793 | |||||||
| chr3:14967851 | T | G | 1 | a0001c0001t0041g0156 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-40+19945T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967851 | |||||||
| chr3:14967981 | A | ATCAGTTC | 3 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 |
3 | HG02055.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-40+20078_-40+2007 others(11): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14967981 | ||||||
| chr3:14967985 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-40+20079A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14967985 | |||||||
| chr3:14968068 | A | G | 3 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 |
3 | HG02615.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-40+20162A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968068 | |||||||
| chr3:14968172 | G | A | 1 | a0001c0001t0003g0084 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-40+20266G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968172 | |||||||
| chr3:14968209 | A | T | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+20303A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968209 | |||||||
| chr3:14968234 | G | A | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+20328G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968234 | |||||||
| chr3:14968544 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-40+20638A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968544 | |||||||
| chr3:14968568 | A | T | 18 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(15): Show |
20 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-40+20662A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968568 | |||||||
| chr3:14968570 | A | G | 18 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(15): Show |
20 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.-40+20664A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968570 | |||||||
| chr3:14968573 | G | A | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40+20667G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968573 | |||||||
| chr3:14968720 | G | T | 9 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
9 | HG00140.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-40+20814G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968720 | |||||||
| chr3:14968728 | C | A | 35 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(32): Show |
37 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.-40+20822C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968728 | |||||||
| chr3:14968787 | A | G | 1 | a0001c0001t0029g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-40+20881A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968787 | |||||||
| chr3:14968876 | A | C | 1 | a0001c0002t0005g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-40+20970A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968876 | |||||||
| chr3:14968906 | A | G | 1 | a0001c0003t0006g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-40+21000A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14968906 | |||||||
| chr3:14969059 | C | G | 3 | a0001c0002t0014g0008 a0001c0002t0014g0009 a0001c0007t0014g0270 |
3 | HG01081.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-40+21153C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969059 | |||||||
| chr3:14969059 | C | T | 3 | a0001c0001t0010g0047 a0001c0001t0010g0048 a0001c0001t0010g0060 |
3 | HG00609.hp1 HG02071.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-40+21153C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969059 | |||||||
| chr3:14969134 | A | T | 1 | a0001c0001t0001g0013 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-40+21228A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969134 | |||||||
| chr3:14969200 | T | C | 54 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(51): Show |
55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-40+21294T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969200 | |||||||
| chr3:14969244 | C | CT | 28 | a0001c0001t0001g0013 a0001c0001t0001g0106 a0001c0001t0001g0109 others(25): Show |
28 | HG01081.hp1 HG01106.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-40+21357dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14969244 | ||||||
| chr3:14969244 | CT | C | 65 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0001g0157 others(62): Show |
66 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.-40+21357delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14969244 | ||||||
| chr3:14969244 | CTT | C | 8 | a0001c0001t0002g0073 a0001c0004t0007g0271 a0001c0004t0007g0274 others(5): Show |
8 | HG01891.hp1 HG01993.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40+21356_-40+2135 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14969244 | ||||||
| chr3:14969354 | C | T | 1 | a0001c0001t0010g0048 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-40+21448C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969354 | |||||||
| chr3:14969430 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-40+21524A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969430 | |||||||
| chr3:14969442 | T | C | 1 | a0001c0001t0040g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-40+21536T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969442 | |||||||
| chr3:14969457 | G | T | 3 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 |
3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-40+21551G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969457 | |||||||
| chr3:14969503 | A | G | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-40+21597A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969503 | |||||||
| chr3:14969560 | C | T | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+21654C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969560 | |||||||
| chr3:14969719 | C | G | 6 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 others(3): Show |
6 | NA18960.hp1 NA18964.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+21813C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14969719 | |||||||
| chr3:14970152 | T | G | 1 | a0001c0001t0002g0071 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-40+22246T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14970152 | |||||||
| chr3:14970269 | G | A | 1 | a0001c0001t0009g0196 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-40+22363G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14970269 | |||||||
| chr3:14970277 | T | TG | 15 | a0001c0001t0001g0105 a0001c0001t0001g0120 a0001c0001t0001g0127 others(12): Show |
15 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.-40+22378dupG | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14970277 | ||||||
| chr3:14970327 | G | A | 1 | a0001c0001t0019g0290 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-40+22421G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14970327 | |||||||
| chr3:14970787 | C | T | 2 | a0001c0001t0016g0272 a0001c0001t0016g0273 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-40+22881C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14970787 | |||||||
| chr3:14971005 | G | T | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+23099G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971005 | |||||||
| chr3:14971111 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0129 |
2 | NA18954.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-40+23205T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971111 | |||||||
| chr3:14971124 | T | G | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-40+23218T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971124 | |||||||
| chr3:14971156 | CGCCCAGG others(684): Show |
C | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40+23268_-40+2395 others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14971156 | ||||||
| chr3:14971203 | T | C | 140 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(137): Show |
145 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-40+23297T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971203 | |||||||
| chr3:14971308 | G | A | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+23402G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971308 | |||||||
| chr3:14971457 | A | G | 1 | a0001c0001t0008g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-40+23551A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971457 | |||||||
| chr3:14971571 | C | T | 1 | a0001c0001t0002g0038 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-40+23665C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971571 | |||||||
| chr3:14971574 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-40+23668C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971574 | |||||||
| chr3:14971670 | A | G | 1 | a0001c0002t0005g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-40+23764A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971670 | |||||||
| chr3:14971730 | A | C | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40+23824A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971730 | |||||||
| chr3:14971810 | C | CT | 44 | a0001c0001t0001g0103 a0001c0001t0001g0110 a0001c0001t0001g0127 others(41): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.-40+23919dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14971810 | ||||||
| chr3:14971810 | CT | C | 9 | a0001c0001t0001g0102 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01433.hp1 NA18942.hp1 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.-40+23919delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14971810 | ||||||
| chr3:14971841 | T | G | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+23935T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14971841 | |||||||
| chr3:14972128 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-40+24222A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972128 | |||||||
| chr3:14972129 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-40+24223G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972129 | |||||||
| chr3:14972132 | A | G | 7 | a0001c0001t0004g0227 a0001c0001t0004g0228 a0001c0001t0004g0229 others(4): Show |
7 | HG02109.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40+24226A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972132 | |||||||
| chr3:14972286 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-40+24380T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972286 | |||||||
| chr3:14972310 | G | A | 1 | a0001c0001t0003g0087 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-40+24404G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972310 | |||||||
| chr3:14972486 | A | G | 4 | a0001c0003t0013g0245 a0001c0003t0013g0246 a0001c0003t0013g0247 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40+24580A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972486 | |||||||
| chr3:14972602 | T | G | 1 | a0001c0007t0014g0270 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-40+24696T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972602 | |||||||
| chr3:14972669 | G | A | 14 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(11): Show |
14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40+24763G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972669 | |||||||
| chr3:14972698 | A | G | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40+24792A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972698 | |||||||
| chr3:14972843 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-40+24937G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972843 | |||||||
| chr3:14972925 | C | T | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+25019C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972925 | |||||||
| chr3:14972929 | C | G | 1 | a0001c0001t0001g0213 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-40+25023C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14972929 | |||||||
| chr3:14973047 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0127 |
2 | HG02683.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-40+25141T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14973047 | |||||||
| chr3:14973235 | G | A | 1 | a0001c0001t0035g0142 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-40+25329G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14973235 | |||||||
| chr3:14973397 | T | TA | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+25502dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14973397 | ||||||
| chr3:14973408 | A | T | 10 | a0001c0001t0003g0086 a0001c0001t0041g0156 a0001c0004t0007g0271 others(7): Show |
10 | HG00408.hp2 HG01884.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40+25502A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14973408 | |||||||
| chr3:14973600 | GTTA | G | 26 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(23): Show |
28 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-40+25696_-40+2569 others(7): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14973600 | ||||||
| chr3:14973606 | C | T | 43 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(40): Show |
45 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-40+25700C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14973606 | |||||||
| chr3:14973607 | G | T | 26 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(23): Show |
28 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-40+25701G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14973607 | |||||||
| chr3:14973725 | A | C | 1 | a0001c0001t0003g0082 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-40+25819A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14973725 | |||||||
| chr3:14973826 | G | A | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+25920G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14973826 | |||||||
| chr3:14973834 | G | A | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40+25928G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14973834 | |||||||
| chr3:14973836 | A | G | 1 | a0001c0001t0004g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-40+25930A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14973836 | |||||||
| chr3:14974020 | C | T | 1 | a0001c0001t0012g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-40+26114C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14974020 | |||||||
| chr3:14974068 | A | T | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+26162A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14974068 | |||||||
| chr3:14974133 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-40+26227A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14974133 | |||||||
| chr3:14974189 | T | C | 1 | a0001c0001t0003g0097 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-40+26283T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14974189 | |||||||
| chr3:14974229 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0004g0237 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-40+26323G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14974229 | |||||||
| chr3:14974564 | A | G | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40+26658A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14974564 | |||||||
| chr3:14974595 | T | C | 2 | a0001c0001t0012g0297 a0001c0001t0029g0296 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-40+26689T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14974595 | |||||||
| chr3:14974609 | G | GT | 19 | a0001c0001t0001g0106 a0001c0001t0001g0127 a0001c0001t0001g0141 others(16): Show |
21 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-40+26717dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14974609 | ||||||
| chr3:14974764 | C | T | 21 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0102 others(18): Show |
22 | HG01255.hp1 HG01346.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.-40+26858C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14974764 | |||||||
| chr3:14975088 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0199 |
2 | HG00544.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.-40+27182A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14975088 | |||||||
| chr3:14975203 | A | G | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-40+27297A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14975203 | |||||||
| chr3:14975408 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-40+27502C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14975408 | |||||||
| chr3:14975665 | A | G | 103 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0001g0188 others(100): Show |
106 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.-40+27759A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14975665 | |||||||
| chr3:14975819 | C | T | 2 | a0001c0001t0015g0003 a0001c0001t0015g0059 |
3 | HG03491.hp1 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-40+27913C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14975819 | |||||||
| chr3:14975870 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-40+27964C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14975870 | |||||||
| chr3:14976085 | T | A | 49 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(46): Show |
50 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-39-27791T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14976085 | |||||||
| chr3:14976187 | T | C | 3 | a0001c0001t0003g0084 a0001c0001t0003g0085 a0001c0001t0003g0087 |
3 | NA18949.hp1 NA18978.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-39-27689T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14976187 | |||||||
| chr3:14976291 | A | G | 14 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(11): Show |
14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39-27585A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14976291 | |||||||
| chr3:14976388 | A | C | 2 | a0001c0001t0012g0297 a0001c0001t0029g0296 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-39-27488A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14976388 | |||||||
| chr3:14976592 | T | G | 3 | a0001c0001t0003g0088 a0001c0001t0017g0291 a0001c0001t0017g0292 |
3 | HG02809.hp1 HG06807.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.-39-27284T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14976592 | |||||||
| chr3:14976602 | C | CT | 9 | a0001c0001t0001g0116 a0001c0001t0001g0153 a0001c0001t0001g0154 others(6): Show |
9 | HG01081.hp1 HG01109.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.-39-27252dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14976602 | ||||||
| chr3:14976602 | C | CTTTT | 7 | a0001c0001t0002g0050 a0001c0001t0002g0074 a0001c0001t0026g0034 others(4): Show |
7 | HG01069.hp1 HG01081.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-39-27255_-39-2725 others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14976602 | ||||||
| chr3:14976602 | C | CTTTTT | 68 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(65): Show |
69 | HG00673.hp1 HG00733.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.-39-27256_-39-2725 others(9): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14976602 | ||||||
| chr3:14976602 | C | CTTTTTT | 14 | a0001c0001t0002g0058 a0001c0001t0002g0259 a0001c0001t0003g0080 others(11): Show |
16 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.-39-27257_-39-2725 others(10): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14976602 | ||||||
| chr3:14976602 | C | CTTTTTTT | 19 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0081 others(16): Show |
21 | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.-39-27258_-39-2725 others(11): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14976602 | ||||||
| chr3:14976602 | C | CTTTTTTT others(1): Show |
6 | a0001c0001t0003g0086 a0001c0001t0003g0093 a0001c0001t0012g0281 others(3): Show |
6 | HG00408.hp2 HG02129.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-27259_-39-2725 others(12): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14976602 | ||||||
| chr3:14976602 | C | CTTTTTTT others(3): Show |
6 | a0001c0001t0003g0095 a0001c0004t0007g0271 a0001c0004t0007g0275 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-27261_-39-2725 others(14): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14976602 | ||||||
| chr3:14976602 | CT | C | 6 | a0001c0001t0001g0113 a0001c0001t0001g0124 a0001c0001t0001g0145 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-27252delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14976602 | ||||||
| chr3:14976705 | T | C | 5 | a0001c0001t0001g0078 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG01106.hp2 HG01361.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39-27171T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14976705 | |||||||
| chr3:14976833 | T | C | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-27043T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14976833 | |||||||
| chr3:14976897 | A | G | 14 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(11): Show |
14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39-26979A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14976897 | |||||||
| chr3:14977115 | T | G | 1 | a0001c0001t0002g0256 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-39-26761T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14977115 | |||||||
| chr3:14977367 | A | G | 3 | a0001c0005t0002g0293 a0001c0005t0002g0294 a0001c0005t0002g0295 |
3 | HG03195.hp1 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-39-26509A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14977367 | |||||||
| chr3:14977370 | GTGGCAGA others(13): Show |
G | 1 | a0001c0001t0001g0198 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-39-26501_-39-2648 others(24): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14977370 | ||||||
| chr3:14977378 | T | C | 1 | a0001c0001t0012g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-39-26498T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14977378 | |||||||
| chr3:14977825 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-39-26051C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14977825 | |||||||
| chr3:14977948 | C | CA | 60 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(57): Show |
61 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.-39-25913dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14977948 | ||||||
| chr3:14977961 | AAAG | A | 13 | a0001c0001t0021g0283 a0001c0003t0006g0006 a0001c0003t0006g0007 others(10): Show |
15 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.-39-25897_-39-2589 others(7): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14977961 | ||||||
| chr3:14977964 | G | A | 86 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(83): Show |
87 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.-39-25912G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14977964 | |||||||
| chr3:14977967 | G | A | 15 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(12): Show |
17 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.-39-25909G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14977967 | |||||||
| chr3:14977967 | G | T | 1 | a0001c0002t0005g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-39-25909G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14977967 | |||||||
| chr3:14978005 | AAATATGA others(6): Show |
A | 1 | a0001c0001t0001g0124 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-39-25870_-39-2585 others(17): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978005 | |||||||
| chr3:14978060 | A | T | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-25816A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978060 | |||||||
| chr3:14978088 | G | C | 7 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0250 others(4): Show |
9 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.-39-25788G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978088 | |||||||
| chr3:14978182 | C | T | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-25694C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978182 | |||||||
| chr3:14978399 | G | A | 102 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(99): Show |
105 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.-39-25477G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978399 | |||||||
| chr3:14978589 | C | A | 1 | a0001c0001t0002g0038 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-39-25287C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978589 | |||||||
| chr3:14978630 | A | G | 1 | a0001c0001t0012g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-39-25246A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978630 | |||||||
| chr3:14978713 | A | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | NA18968.hp1 NA18990.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-39-25163A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978713 | |||||||
| chr3:14978800 | T | C | 1 | a0001c0001t0012g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-39-25076T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978800 | |||||||
| chr3:14978842 | A | G | 29 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(26): Show |
31 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.-39-25034A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978842 | |||||||
| chr3:14978869 | A | G | 102 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(99): Show |
105 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.-39-25007A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14978869 | |||||||
| chr3:14979088 | T | C | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-24788T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979088 | |||||||
| chr3:14979093 | G | A | 3 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 |
3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-39-24783G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979093 | |||||||
| chr3:14979199 | TAAGGTGG others(7): Show |
T | 9 | a0001c0001t0001g0102 a0001c0001t0001g0125 a0001c0001t0001g0129 others(6): Show |
9 | HG01433.hp1 NA18942.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.-39-24672_-39-2465 others(18): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14979199 | ||||||
| chr3:14979233 | G | A | 18 | a0001c0001t0004g0227 a0001c0001t0004g0228 a0001c0001t0004g0229 others(15): Show |
18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-39-24643G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979233 | |||||||
| chr3:14979292 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-39-24584T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979292 | |||||||
| chr3:14979318 | A | G | 2 | a0001c0001t0015g0003 a0001c0001t0015g0059 |
3 | HG03491.hp1 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-39-24558A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979318 | |||||||
| chr3:14979506 | A | G | 54 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(51): Show |
55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-39-24370A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979506 | |||||||
| chr3:14979603 | A | G | 14 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(11): Show |
14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39-24273A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979603 | |||||||
| chr3:14979621 | G | A | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-24255G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979621 | |||||||
| chr3:14979776 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-39-24100C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979776 | |||||||
| chr3:14979794 | C | T | 14 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(11): Show |
14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39-24082C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979794 | |||||||
| chr3:14979821 | G | A | 1 | a0001c0003t0013g0246 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-39-24055G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979821 | |||||||
| chr3:14979928 | G | A | 1 | a0001c0007t0014g0270 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-39-23948G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14979928 | |||||||
| chr3:14980049 | GA | G | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-23825delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14980049 | ||||||
| chr3:14980087 | T | C | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-23789T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14980087 | |||||||
| chr3:14980317 | T | TA | 15 | a0001c0001t0001g0120 a0001c0001t0016g0272 a0001c0001t0016g0273 others(12): Show |
17 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.-39-23543dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14980317 | ||||||
| chr3:14980318 | A | T | 1 | a0001c0001t0001g0284 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-39-23558A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14980318 | |||||||
| chr3:14980439 | A | G | 1 | a0001c0001t0003g0095 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-39-23437A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14980439 | |||||||
| chr3:14980541 | C | T | 1 | a0001c0003t0013g0245 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-39-23335C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14980541 | |||||||
| chr3:14980558 | TAAGA | T | 49 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(46): Show |
50 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-39-23314_-39-2331 others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14980558 | ||||||
| chr3:14980621 | G | A | 1 | a0001c0001t0037g0160 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-39-23255G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14980621 | |||||||
| chr3:14980667 | A | C | 1 | a0001c0001t0021g0283 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-39-23209A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14980667 | |||||||
| chr3:14980756 | C | T | 3 | a0001c0001t0038g0287 a0001c0001t0039g0288 a0001c0001t0040g0079 |
3 | HG02622.hp2 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-39-23120C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14980756 | |||||||
| chr3:14980804 | A | G | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-23072A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14980804 | |||||||
| chr3:14981126 | G | C | 1 | a0001c0001t0001g0208 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-39-22750G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981126 | |||||||
| chr3:14981190 | G | A | 1 | a0001c0001t0041g0156 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-39-22686G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981190 | |||||||
| chr3:14981236 | G | A | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-22640G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981236 | |||||||
| chr3:14981275 | C | T | 2 | a0001c0001t0038g0287 a0001c0001t0039g0288 |
2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-39-22601C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981275 | |||||||
| chr3:14981336 | C | G | 129 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(126): Show |
134 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.-39-22540C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981336 | |||||||
| chr3:14981374 | C | T | 3 | a0001c0001t0003g0096 a0001c0001t0003g0097 a0001c0001t0003g0098 |
3 | HG00438.hp1 HG00544.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.-39-22502C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981374 | |||||||
| chr3:14981593 | G | A | 102 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(99): Show |
105 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.-39-22283G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981593 | |||||||
| chr3:14981597 | T | C | 102 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(99): Show |
105 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.-39-22279T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981597 | |||||||
| chr3:14981602 | C | CA | 11 | a0001c0001t0001g0103 a0001c0001t0001g0110 a0001c0001t0001g0113 others(8): Show |
11 | HG01361.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-39-22253dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14981602 | ||||||
| chr3:14981623 | A | AAAG | 12 | a0001c0001t0016g0273 a0001c0002t0014g0008 a0001c0002t0014g0009 others(9): Show |
12 | HG01081.hp2 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-39-22253_-39-2225 others(7): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981623 | |||||||
| chr3:14981623 | A | AAG | 33 | a0001c0001t0002g0038 a0001c0001t0002g0041 a0001c0001t0002g0051 others(30): Show |
35 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.-39-22253_-39-2225 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981623 | |||||||
| chr3:14981623 | A | AG | 57 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(54): Show |
58 | HG00609.hp1 HG00673.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.-39-22252dupG | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14981623 | ||||||
| chr3:14981690 | GA | G | 3 | a0001c0001t0004g0228 a0001c0001t0004g0229 a0001c0001t0042g0230 |
3 | HG02886.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-39-22184delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14981690 | ||||||
| chr3:14981885 | G | C | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-21991G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981885 | |||||||
| chr3:14981916 | G | A | 14 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(11): Show |
14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39-21960G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981916 | |||||||
| chr3:14981954 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-39-21922G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981954 | |||||||
| chr3:14981990 | T | A | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-21886T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14981990 | |||||||
| chr3:14982047 | T | C | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-21829T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14982047 | |||||||
| chr3:14982159 | G | A | 5 | a0001c0001t0027g0072 a0001c0001t0028g0065 a0001c0005t0002g0293 others(2): Show |
5 | HG03195.hp1 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39-21717G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14982159 | |||||||
| chr3:14982404 | G | A | 1 | a0001c0001t0003g0090 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-39-21472G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14982404 | |||||||
| chr3:14982526 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-39-21350T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14982526 | |||||||
| chr3:14982592 | C | T | 9 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
9 | HG00140.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-39-21284C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14982592 | |||||||
| chr3:14982662 | C | G | 3 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 |
3 | HG02055.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-39-21214C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14982662 | |||||||
| chr3:14982764 | C | T | 10 | a0001c0001t0001g0127 a0001c0001t0001g0219 a0001c0001t0001g0220 others(7): Show |
10 | HG00140.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-39-21112C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14982764 | |||||||
| chr3:14983158 | T | C | 2 | a0001c0002t0005g0026 a0001c0002t0005g0029 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-39-20718T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983158 | |||||||
| chr3:14983304 | G | A | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-20572G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983304 | |||||||
| chr3:14983318 | CT | C | 8 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(5): Show |
8 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-39-20549delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983318 | ||||||
| chr3:14983462 | T | TAC | 54 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0100 others(51): Show |
54 | HG00140.hp2 HG01081.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.-39-20382_-39-2038 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983462 | ||||||
| chr3:14983462 | T | TACAC | 46 | a0001c0001t0001g0005 a0001c0001t0001g0061 a0001c0001t0001g0105 others(43): Show |
47 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.-39-20384_-39-2038 others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983462 | ||||||
| chr3:14983462 | T | TACACAC | 85 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0120 others(82): Show |
88 | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.-39-20386_-39-2038 others(10): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983462 | ||||||
| chr3:14983462 | T | TACACACA others(1): Show |
9 | a0001c0001t0001g0075 a0001c0001t0002g0036 a0001c0001t0002g0037 others(6): Show |
9 | HG00408.hp2 HG00673.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-39-20388_-39-2038 others(12): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983462 | ||||||
| chr3:14983462 | T | TACACACA others(3): Show |
4 | a0001c0001t0002g0051 a0001c0001t0002g0070 a0001c0001t0003g0083 others(1): Show |
4 | HG00558.hp2 HG02165.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-20390_-39-2038 others(14): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983462 | ||||||
| chr3:14983462 | TAC | T | 3 | a0001c0001t0004g0236 a0001c0001t0004g0242 a0001c0003t0006g0252 |
3 | HG01934.hp1 HG03453.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-39-20382_-39-2038 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983462 | ||||||
| chr3:14983462 | TACAC | T | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(3): Show |
6 | HG01884.hp2 HG02055.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-20384_-39-2038 others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983462 | ||||||
| chr3:14983462 | TACACACA others(13): Show |
T | 1 | a0001c0001t0041g0156 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-39-20400_-39-2038 others(24): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983462 | ||||||
| chr3:14983491 | A | ACACG | 4 | a0001c0003t0013g0245 a0001c0003t0013g0246 a0001c0003t0013g0247 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39-20382_-39-2038 others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983491 | ||||||
| chr3:14983491 | A | ACG | 7 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(4): Show |
9 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.-39-20384_-39-2038 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14983491 | ||||||
| chr3:14983491 | A | G | 1 | a0001c0003t0006g0252 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-39-20385A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983491 | |||||||
| chr3:14983548 | G | T | 4 | a0001c0003t0013g0245 a0001c0003t0013g0246 a0001c0003t0013g0247 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39-20328G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983548 | |||||||
| chr3:14983602 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-39-20274G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983602 | |||||||
| chr3:14983638 | G | A | 7 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0250 others(4): Show |
9 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.-39-20238G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983638 | |||||||
| chr3:14983756 | G | A | 5 | a0001c0001t0002g0037 a0001c0001t0012g0076 a0001c0001t0012g0281 others(2): Show |
5 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39-20120G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983756 | |||||||
| chr3:14983817 | C | G | 54 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(51): Show |
55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-39-20059C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983817 | |||||||
| chr3:14983863 | A | G | 3 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 |
3 | HG02615.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-39-20013A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983863 | |||||||
| chr3:14983911 | G | T | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-19965G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983911 | |||||||
| chr3:14983945 | A | G | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-19931A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983945 | |||||||
| chr3:14983984 | G | C | 1 | a0001c0001t0009g0196 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-39-19892G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14983984 | |||||||
| chr3:14984118 | C | T | 12 | a0001c0001t0001g0116 a0001c0001t0001g0187 a0001c0001t0001g0195 others(9): Show |
12 | HG01123.hp1 HG01243.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.-39-19758C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14984118 | |||||||
| chr3:14984169 | T | C | 27 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(24): Show |
29 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.-39-19707T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14984169 | |||||||
| chr3:14984324 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-39-19552A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14984324 | |||||||
| chr3:14984361 | A | G | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39-19515A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14984361 | |||||||
| chr3:14984376 | T | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | NA18945.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-39-19500T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14984376 | |||||||
| chr3:14984423 | T | C | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-19453T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14984423 | |||||||
| chr3:14984544 | TAAAG | T | 54 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(51): Show |
55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-39-19328_-39-1932 others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14984544 | ||||||
| chr3:14984832 | G | GT | 6 | a0001c0001t0001g0266 a0001c0001t0008g0210 a0001c0001t0012g0076 others(3): Show |
6 | HG01258.hp2 HG02055.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-19033dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14984832 | ||||||
| chr3:14984935 | C | T | 4 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-18941C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14984935 | |||||||
| chr3:14985190 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-39-18686A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14985190 | |||||||
| chr3:14985262 | T | C | 1 | a0001c0007t0014g0270 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-39-18614T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14985262 | |||||||
| chr3:14985446 | TCA | T | 3 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 |
3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-39-18427_-39-1842 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14985446 | ||||||
| chr3:14985463 | G | A | 1 | a0001c0001t0012g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-39-18413G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14985463 | |||||||
| chr3:14985613 | C | T | 2 | a0001c0001t0020g0222 a0001c0001t0020g0223 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-39-18263C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14985613 | |||||||
| chr3:14985620 | T | C | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-18256T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14985620 | |||||||
| chr3:14985709 | C | A | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-39-18167C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14985709 | |||||||
| chr3:14985975 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-39-17901A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14985975 | |||||||
| chr3:14986139 | A | G | 1 | a0001c0003t0006g0250 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-39-17737A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14986139 | |||||||
| chr3:14986865 | A | G | 1 | a0001c0001t0029g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-39-17011A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14986865 | |||||||
| chr3:14986955 | T | A | 54 | a0001c0001t0001g0061 a0001c0001t0001g0075 a0001c0001t0002g0032 others(51): Show |
55 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-39-16921T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14986955 | |||||||
| chr3:14986971 | A | G | 27 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(24): Show |
29 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.-39-16905A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14986971 | |||||||
| chr3:14987136 | C | T | 2 | a0001c0001t0003g0096 a0001c0001t0003g0097 |
2 | HG00438.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.-39-16740C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987136 | |||||||
| chr3:14987234 | C | T | 1 | a0001c0003t0006g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-39-16642C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987234 | |||||||
| chr3:14987274 | G | A | 3 | a0001c0002t0005g0025 a0001c0002t0005g0027 a0001c0002t0005g0030 |
3 | HG03579.hp2 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-39-16602G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987274 | |||||||
| chr3:14987329 | C | T | 1 | a0001c0003t0006g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-39-16547C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987329 | |||||||
| chr3:14987453 | G | C | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-16423G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987453 | |||||||
| chr3:14987625 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-39-16251T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987625 | |||||||
| chr3:14987626 | C | T | 1 | a0001c0001t0021g0283 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-39-16250C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987626 | |||||||
| chr3:14987646 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-39-16230A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987646 | |||||||
| chr3:14987826 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-39-16050C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987826 | |||||||
| chr3:14987861 | C | T | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-16015C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987861 | |||||||
| chr3:14987867 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0034g0114 |
2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-39-16009G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987867 | |||||||
| chr3:14987945 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-39-15931C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14987945 | |||||||
| chr3:14988043 | A | G | 1 | a0001c0001t0003g0089 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-39-15833A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14988043 | |||||||
| chr3:14988066 | A | G | 1 | a0001c0001t0003g0097 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-39-15810A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14988066 | |||||||
| chr3:14988248 | C | G | 2 | a0001c0001t0016g0272 a0001c0001t0016g0273 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-39-15628C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14988248 | |||||||
| chr3:14988351 | G | A | 1 | a0001c0001t0010g0268 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-39-15525G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14988351 | |||||||
| chr3:14988384 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0219 |
2 | HG02683.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-39-15492A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14988384 | |||||||
| chr3:14988502 | G | A | 1 | a0001c0001t0039g0288 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-39-15374G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14988502 | |||||||
| chr3:14988575 | C | G | 3 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 |
3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-39-15301C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14988575 | |||||||
| chr3:14988763 | C | T | 126 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(123): Show |
128 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.-39-15113C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14988763 | |||||||
| chr3:14988884 | A | C | 1 | a0001c0003t0006g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-39-14992A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14988884 | |||||||
| chr3:14989038 | T | A | 29 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(26): Show |
31 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.-39-14838T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14989038 | |||||||
| chr3:14989141 | G | T | 1 | a0001c0001t0029g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-39-14735G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14989141 | |||||||
| chr3:14989307 | G | A | 1 | a0001c0007t0014g0270 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-39-14569G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14989307 | |||||||
| chr3:14989404 | G | C | 2 | a0001c0002t0005g0026 a0001c0002t0005g0029 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-39-14472G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14989404 | |||||||
| chr3:14989825 | G | A | 1 | a0001c0001t0011g0215 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-39-14051G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14989825 | |||||||
| chr3:14989924 | C | CA | 31 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0061 others(28): Show |
31 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.-39-13923dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14989924 | ||||||
| chr3:14989924 | C | CAA | 13 | a0001c0001t0001g0104 a0001c0001t0001g0187 a0001c0001t0001g0212 others(10): Show |
13 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.-39-13924_-39-1392 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14989924 | ||||||
| chr3:14989924 | CA | C | 76 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0102 others(73): Show |
78 | HG00609.hp1 HG00673.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.-39-13923delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14989924 | ||||||
| chr3:14989924 | CAA | C | 24 | a0001c0001t0002g0055 a0001c0001t0004g0227 a0001c0001t0004g0229 others(21): Show |
24 | HG01884.hp1 HG01934.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-39-13924_-39-1392 others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14989924 | ||||||
| chr3:14989924 | CAAA | C | 7 | a0001c0001t0004g0236 a0001c0001t0004g0239 a0001c0001t0012g0297 others(4): Show |
7 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-39-13925_-39-1392 others(7): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14989924 | ||||||
| chr3:14989924 | CAAAAA | C | 11 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(8): Show |
11 | HG01109.hp1 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-39-13927_-39-1392 others(9): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14989924 | ||||||
| chr3:14989924 | CAAAAAAA others(1): Show |
C | 16 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0084 others(13): Show |
20 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.-39-13930_-39-1392 others(12): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14989924 | ||||||
| chr3:14989924 | CAAAAAAA others(5): Show |
C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.-39-13934_-39-1392 others(16): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14989924 | ||||||
| chr3:14989954 | T | A | 4 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0182 others(1): Show |
4 | NA18941.hp2 NA18960.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39-13922T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14989954 | |||||||
| chr3:14990132 | A | C | 4 | a0001c0003t0013g0245 a0001c0003t0013g0246 a0001c0003t0013g0247 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39-13744A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14990132 | |||||||
| chr3:14990216 | A | C | 1 | a0001c0003t0006g0269 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-39-13660A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14990216 | |||||||
| chr3:14990489 | G | A | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-39-13387G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14990489 | |||||||
| chr3:14990525 | C | T | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-13351C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14990525 | |||||||
| chr3:14990636 | G | A | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39-13240G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14990636 | |||||||
| chr3:14990741 | T | A | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-13135T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14990741 | |||||||
| chr3:14990811 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0129 |
2 | NA18954.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-39-13065A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14990811 | |||||||
| chr3:14991047 | G | A | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-12829G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14991047 | |||||||
| chr3:14991345 | C | T | 1 | a0001c0001t0008g0210 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-39-12531C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14991345 | |||||||
| chr3:14991445 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-39-12431G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14991445 | |||||||
| chr3:14991518 | A | G | 1 | a0001c0001t0002g0058 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-39-12358A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14991518 | |||||||
| chr3:14991533 | A | G | 5 | a0001c0001t0011g0214 a0001c0001t0011g0215 a0001c0001t0011g0216 others(2): Show |
5 | HG00642.hp1 HG01361.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.-39-12343A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14991533 | |||||||
| chr3:14991768 | C | CT | 26 | a0001c0001t0001g0151 a0001c0001t0001g0157 a0001c0001t0001g0171 others(23): Show |
26 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-39-12094dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14991768 | ||||||
| chr3:14991971 | A | G | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-11905A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14991971 | |||||||
| chr3:14992049 | G | A | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-11827G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14992049 | |||||||
| chr3:14992364 | C | T | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-11512C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14992364 | |||||||
| chr3:14992413 | G | C | 2 | a0001c0001t0001g0154 a0001c0001t0036g0172 |
2 | HG02027.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.-39-11463G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14992413 | |||||||
| chr3:14992461 | C | G | 2 | a0001c0001t0018g0067 a0001c0001t0018g0068 |
2 | HG00733.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-39-11415C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14992461 | |||||||
| chr3:14992727 | G | T | 1 | a0001c0001t0001g0185 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-39-11149G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14992727 | |||||||
| chr3:14992920 | G | T | 3 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0298 |
3 | HG00673.hp2 NA18991.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-39-10956G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14992920 | |||||||
| chr3:14993454 | CA | C | 31 | a0001c0001t0001g0116 a0001c0001t0001g0195 a0001c0001t0012g0076 others(28): Show |
33 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-39-10408delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14993454 | ||||||
| chr3:14993631 | A | G | 1 | a0001c0003t0006g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-39-10245A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14993631 | |||||||
| chr3:14993673 | AT | A | 18 | a0001c0001t0004g0227 a0001c0001t0004g0228 a0001c0001t0004g0229 others(15): Show |
18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-39-10199delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14993673 | ||||||
| chr3:14993840 | A | G | 1 | a0001c0003t0006g0252 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-39-10036A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14993840 | |||||||
| chr3:14993932 | G | A | 100 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(97): Show |
103 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.-39-9944G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14993932 | |||||||
| chr3:14994075 | A | G | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-9801A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994075 | |||||||
| chr3:14994076 | T | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-9800T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994076 | |||||||
| chr3:14994154 | ATT | A | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39-9718_-39-9717d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14994154 | ||||||
| chr3:14994183 | T | C | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39-9693T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994183 | |||||||
| chr3:14994197 | A | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0195 |
2 | NA18951.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.-39-9679A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994197 | |||||||
| chr3:14994218 | C | T | 1 | a0001c0001t0029g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-39-9658C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994218 | |||||||
| chr3:14994306 | T | C | 4 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-9570T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994306 | |||||||
| chr3:14994419 | G | T | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-9457G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994419 | |||||||
| chr3:14994427 | T | C | 1 | a0001c0001t0008g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-39-9449T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994427 | |||||||
| chr3:14994439 | C | CT | 69 | a0001c0001t0001g0015 a0001c0001t0001g0104 a0001c0001t0001g0116 others(66): Show |
71 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-39-9415dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14994439 | ||||||
| chr3:14994439 | C | CTT | 77 | a0001c0001t0001g0146 a0001c0001t0001g0298 a0001c0001t0002g0032 others(74): Show |
80 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.-39-9416_-39-9415d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14994439 | ||||||
| chr3:14994439 | C | CTTT | 9 | a0001c0001t0002g0033 a0001c0001t0002g0041 a0001c0001t0002g0046 others(6): Show |
9 | HG01175.hp2 HG01891.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-39-9417_-39-9415d others(5): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14994439 | ||||||
| chr3:14994547 | A | G | 1 | a0001c0001t0035g0142 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-39-9329A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994547 | |||||||
| chr3:14994684 | G | A | 1 | a0001c0002t0005g0027 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-39-9192G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994684 | |||||||
| chr3:14994725 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-39-9151G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994725 | |||||||
| chr3:14994733 | A | G | 153 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0298 others(150): Show |
158 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.-39-9143A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994733 | |||||||
| chr3:14994752 | T | TA | 95 | a0001c0001t0001g0078 a0001c0001t0001g0109 a0001c0001t0001g0110 others(92): Show |
97 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.-39-9108dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14994752 | ||||||
| chr3:14994830 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-39-9046G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994830 | |||||||
| chr3:14994945 | A | G | 30 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0298 others(27): Show |
32 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.-39-8931A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14994945 | |||||||
| chr3:14994977 | C | CT | 32 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0113 others(29): Show |
32 | HG01081.hp2 HG02027.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.-39-8878dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14994977 | ||||||
| chr3:14994977 | C | CTT | 22 | a0001c0001t0001g0208 a0001c0002t0005g0019 a0001c0002t0005g0020 others(19): Show |
22 | HG01109.hp1 HG01168.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.-39-8879_-39-8878d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14994977 | ||||||
| chr3:14994977 | CT | C | 75 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(72): Show |
79 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.-39-8878delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14994977 | ||||||
| chr3:14995033 | T | G | 1 | a0001c0001t0001g0224 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-39-8843T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995033 | |||||||
| chr3:14995097 | C | G | 1 | a0001c0001t0001g0166 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-39-8779C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995097 | |||||||
| chr3:14995172 | T | A | 5 | a0001c0001t0002g0039 a0001c0001t0002g0042 a0001c0001t0002g0043 others(2): Show |
5 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39-8704T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995172 | |||||||
| chr3:14995255 | C | T | 6 | a0001c0001t0001g0078 a0001c0001t0001g0109 a0001c0001t0001g0110 others(3): Show |
6 | HG01106.hp2 HG01361.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39-8621C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995255 | |||||||
| chr3:14995282 | C | G | 4 | a0001c0001t0028g0065 a0001c0005t0002g0293 a0001c0005t0002g0294 others(1): Show |
4 | HG03195.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-8594C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995282 | |||||||
| chr3:14995320 | C | CA | 34 | a0001c0001t0001g0104 a0001c0001t0001g0133 a0001c0001t0001g0151 others(31): Show |
34 | HG00642.hp1 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-39-8539dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995320 | ||||||
| chr3:14995383 | C | A | 254 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(251): Show |
261 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.-39-8493C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995383 | |||||||
| chr3:14995401 | TA | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0009t0001g0016 |
3 | HG03139.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-39-8474delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995401 | |||||||
| chr3:14995498 | A | G | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-8378A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995498 | |||||||
| chr3:14995668 | C | CGCGTGTG others(9): Show |
1 | a0001c0002t0005g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-39-8207_-39-8206i others(18): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | ||||||
| chr3:14995668 | C | CGTGTGT | 8 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0017g0291 others(5): Show |
8 | HG01175.hp2 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-39-8189_-39-8184d others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | ||||||
| chr3:14995668 | C | CGTGTGTG others(1): Show |
43 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(40): Show |
44 | HG00609.hp1 HG00642.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.-39-8191_-39-8184d others(10): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | ||||||
| chr3:14995668 | C | CGTGTGTG others(3): Show |
26 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(23): Show |
26 | HG01192.hp1 HG01243.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-39-8193_-39-8184d others(12): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | ||||||
| chr3:14995668 | C | CGTGTGTG others(5): Show |
9 | a0001c0001t0002g0036 a0001c0001t0003g0080 a0001c0001t0003g0081 others(6): Show |
9 | HG00673.hp1 HG01192.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-39-8195_-39-8184d others(14): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | ||||||
| chr3:14995668 | C | CGTGTGTG others(7): Show |
10 | a0001c0001t0043g0235 a0001c0003t0006g0006 a0001c0003t0006g0007 others(7): Show |
12 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.-39-8197_-39-8184d others(16): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | ||||||
| chr3:14995668 | C | CGTGTGTG others(9): Show |
13 | a0001c0001t0012g0076 a0001c0002t0005g0019 a0001c0002t0005g0020 others(10): Show |
13 | HG01109.hp1 HG01168.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-39-8199_-39-8184d others(18): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | ||||||
| chr3:14995668 | C | CGTGTGTG others(11): Show |
14 | a0001c0001t0003g0083 a0001c0001t0003g0085 a0001c0001t0003g0093 others(11): Show |
14 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39-8201_-39-8184d others(20): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | ||||||
| chr3:14995668 | C | CGTGTGTG others(13): Show |
20 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0084 others(17): Show |
22 | HG00408.hp2 HG00639.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.-39-8203_-39-8184d others(22): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | ||||||
| chr3:14995668 | C | CGTGTGTG others(15): Show |
3 | a0001c0001t0003g0091 a0001c0001t0003g0254 a0001c0001t0003g0255 |
3 | HG01069.hp2 HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-39-8205_-39-8184d others(24): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | ||||||
| chr3:14995668 | C | CGTGTGTG others(17): Show |
2 | a0001c0001t0003g0088 a0001c0001t0030g0077 |
2 | NA18951.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-39-8207_-39-8184d others(26): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | ||||||
| chr3:14995668 | C | CGTGTGTG others(19): Show |
1 | a0001c0001t0012g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-39-8184_-39-8183i others(28): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14995668 | ||||||
| chr3:14995669 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-39-8207G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995669 | |||||||
| chr3:14995670 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-39-8206T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995670 | |||||||
| chr3:14995824 | T | G | 1 | a0001c0001t0021g0283 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-39-8052T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995824 | |||||||
| chr3:14995894 | C | T | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-39-7982C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14995894 | |||||||
| chr3:14996084 | G | A | 105 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(102): Show |
108 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.-39-7792G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14996084 | |||||||
| chr3:14996192 | G | T | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-7684G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14996192 | |||||||
| chr3:14996278 | A | G | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-7598A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14996278 | |||||||
| chr3:14996344 | C | G | 57 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(54): Show |
58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.-39-7532C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14996344 | |||||||
| chr3:14996695 | C | T | 23 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(20): Show |
25 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.-39-7181C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14996695 | |||||||
| chr3:14996708 | C | T | 4 | a0001c0003t0013g0245 a0001c0003t0013g0246 a0001c0003t0013g0247 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39-7168C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14996708 | |||||||
| chr3:14996715 | C | T | 1 | a0001c0007t0014g0270 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-39-7161C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14996715 | |||||||
| chr3:14996884 | G | A | 18 | a0001c0001t0004g0227 a0001c0001t0004g0228 a0001c0001t0004g0229 others(15): Show |
18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-39-6992G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14996884 | |||||||
| chr3:14997024 | G | T | 18 | a0001c0001t0004g0227 a0001c0001t0004g0228 a0001c0001t0004g0229 others(15): Show |
18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-39-6852G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14997024 | |||||||
| chr3:14997075 | G | T | 1 | a0001c0001t0021g0283 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-39-6801G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14997075 | |||||||
| chr3:14997951 | A | AC | 4 | a0001c0001t0001g0211 a0001c0001t0001g0266 a0001c0001t0009g0119 others(1): Show |
4 | HG01109.hp2 HG02080.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-5921dupC | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14997951 | ||||||
| chr3:14998061 | C | T | 1 | a0001c0001t0027g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-39-5815C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14998061 | |||||||
| chr3:14998062 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-5814G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14998062 | |||||||
| chr3:14998569 | G | T | 2 | a0001c0001t0004g0232 a0001c0001t0004g0233 |
2 | HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-39-5307G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14998569 | |||||||
| chr3:14998659 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-39-5217T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14998659 | |||||||
| chr3:14998774 | G | T | 1 | a0001c0001t0001g0108 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-39-5102G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14998774 | |||||||
| chr3:14998875 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-39-5001G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14998875 | |||||||
| chr3:14998954 | C | T | 6 | a0001c0001t0002g0041 a0001c0001t0002g0063 a0001c0001t0002g0256 others(3): Show |
6 | HG01070.hp1 HG01099.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39-4922C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14998954 | |||||||
| chr3:14999025 | T | A | 75 | a0001c0001t0001g0139 a0001c0001t0002g0032 a0001c0001t0002g0033 others(72): Show |
76 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.-39-4851T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999025 | |||||||
| chr3:14999026 | T | A | 1 | a0001c0001t0027g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-39-4850T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999026 | |||||||
| chr3:14999270 | C | T | 2 | a0001c0001t0004g0243 a0001c0001t0004g0244 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-39-4606C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999270 | |||||||
| chr3:14999281 | A | AC | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-4594dupC | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14999281 | ||||||
| chr3:14999455 | C | T | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-39-4421C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999455 | |||||||
| chr3:14999460 | T | C | 2 | a0001c0001t0020g0222 a0001c0001t0020g0223 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-39-4416T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999460 | |||||||
| chr3:14999497 | A | C | 1 | a0001c0007t0014g0270 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-39-4379A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999497 | |||||||
| chr3:14999547 | A | G | 1 | a0001c0001t0012g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-39-4329A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999547 | |||||||
| chr3:14999592 | T | C | 2 | a0001c0006t0001g0128 a0001c0006t0001g0203 |
2 | NA18957.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-39-4284T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999592 | |||||||
| chr3:14999669 | A | AT | 9 | a0001c0001t0001g0103 a0001c0004t0007g0271 a0001c0004t0007g0274 others(6): Show |
9 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-39-4195dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14999669 | ||||||
| chr3:14999669 | AT | A | 70 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(67): Show |
73 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.-39-4195delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 14999669 | ||||||
| chr3:14999695 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-39-4181G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999695 | |||||||
| chr3:14999891 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-39-3985T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999891 | |||||||
| chr3:14999916 | G | T | 2 | a0001c0001t0002g0058 a0001c0001t0002g0069 |
2 | HG02015.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.-39-3960G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999916 | |||||||
| chr3:14999938 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-39-3938G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999938 | |||||||
| chr3:14999951 | G | A | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-3925G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999951 | |||||||
| chr3:14999965 | T | A | 1 | a0001c0001t0001g0263 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-39-3911T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999965 | |||||||
| chr3:14999984 | A | G | 1 | a0001c0001t0041g0156 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-39-3892A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 14999984 | |||||||
| chr3:15000108 | T | TA | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-3759dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15000108 | ||||||
| chr3:15000108 | T | TAA | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-3760_-39-3759d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15000108 | ||||||
| chr3:15000158 | C | G | 4 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-3718C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000158 | |||||||
| chr3:15000449 | G | A | 14 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(11): Show |
14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39-3427G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000449 | |||||||
| chr3:15000513 | A | C | 1 | a0001c0001t0026g0034 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-39-3363A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000513 | |||||||
| chr3:15000529 | C | T | 103 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(100): Show |
106 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.-39-3347C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000529 | |||||||
| chr3:15000571 | C | T | 4 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-3305C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000571 | |||||||
| chr3:15000758 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-39-3118G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000758 | |||||||
| chr3:15000764 | T | C | 1 | a0001c0001t0002g0071 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-39-3112T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000764 | |||||||
| chr3:15000814 | G | GT | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(68): Show |
75 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.-39-3042dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15000814 | ||||||
| chr3:15000814 | GT | G | 43 | a0001c0001t0002g0039 a0001c0001t0002g0042 a0001c0001t0002g0043 others(40): Show |
43 | HG00609.hp1 HG00642.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.-39-3042delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15000814 | ||||||
| chr3:15000814 | GTT | G | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0250 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-39-3043_-39-3042d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15000814 | ||||||
| chr3:15000818 | T | G | 1 | a0001c0001t0001g0192 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-39-3058T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000818 | |||||||
| chr3:15000884 | G | A | 1 | a0001c0001t0033g0148 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-39-2992G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000884 | |||||||
| chr3:15000895 | A | G | 1 | a0001c0001t0009g0117 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-39-2981A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000895 | |||||||
| chr3:15000959 | C | T | 1 | a0001c0006t0001g0203 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-39-2917C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000959 | |||||||
| chr3:15000983 | T | A | 57 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(54): Show |
58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.-39-2893T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15000983 | |||||||
| chr3:15001094 | G | A | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-39-2782G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15001094 | |||||||
| chr3:15001104 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-39-2772G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15001104 | |||||||
| chr3:15001151 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-39-2725T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15001151 | |||||||
| chr3:15001318 | G | GT | 48 | a0001c0001t0001g0154 a0001c0001t0001g0161 a0001c0001t0001g0171 others(45): Show |
50 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-39-2538dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15001318 | ||||||
| chr3:15001318 | GT | G | 41 | a0001c0001t0010g0048 a0001c0001t0010g0060 a0001c0001t0012g0076 others(38): Show |
43 | HG00140.hp1 HG00609.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.-39-2538delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15001318 | ||||||
| chr3:15001318 | GTT | G | 6 | a0001c0001t0012g0281 a0001c0001t0012g0282 a0001c0001t0012g0297 others(3): Show |
6 | HG02809.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39-2539_-39-2538d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15001318 | ||||||
| chr3:15001328 | TTTTTTTT others(5): Show |
T | 1 | a0001c0001t0002g0045 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-39-2535_-39-2524d others(14): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15001328 | ||||||
| chr3:15001338 | T | G | 1 | a0001c0001t0010g0047 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-39-2538T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15001338 | |||||||
| chr3:15001340 | G | GT | 8 | a0001c0001t0001g0017 a0001c0001t0001g0136 a0001c0001t0001g0159 others(5): Show |
8 | HG02165.hp2 HG02273.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-2526dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15001340 | ||||||
| chr3:15001340 | G | T | 1 | a0001c0001t0010g0047 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-39-2536G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15001340 | |||||||
| chr3:15001820 | G | T | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39-2056G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15001820 | |||||||
| chr3:15002187 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-39-1689G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002187 | |||||||
| chr3:15002195 | T | C | 3 | a0001c0001t0003g0086 a0001c0001t0003g0093 a0001c0001t0023g0094 |
3 | HG00408.hp2 HG02129.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-39-1681T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002195 | |||||||
| chr3:15002198 | T | C | 59 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(56): Show |
60 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.-39-1678T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002198 | |||||||
| chr3:15002278 | T | A | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-1598T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002278 | |||||||
| chr3:15002364 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-39-1512G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002364 | |||||||
| chr3:15002433 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-39-1443C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002433 | |||||||
| chr3:15002477 | A | T | 150 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(147): Show |
155 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.-39-1399A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002477 | |||||||
| chr3:15002542 | G | T | 1 | a0001c0001t0012g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-39-1334G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002542 | |||||||
| chr3:15002645 | C | CT | 91 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0061 others(88): Show |
92 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-39-1201dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15002645 | ||||||
| chr3:15002645 | C | CTT | 20 | a0001c0001t0001g0104 a0001c0001t0001g0120 a0001c0001t0001g0127 others(17): Show |
20 | HG00140.hp2 HG00609.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.-39-1202_-39-1201d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15002645 | ||||||
| chr3:15002645 | CT | C | 33 | a0001c0001t0001g0017 a0001c0001t0001g0123 a0001c0001t0001g0145 others(30): Show |
35 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.-39-1201delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15002645 | ||||||
| chr3:15002645 | CTT | C | 12 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0038 others(9): Show |
12 | HG00733.hp1 HG02683.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.-39-1202_-39-1201d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15002645 | ||||||
| chr3:15002645 | CTTT | C | 56 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 others(53): Show |
59 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.-39-1203_-39-1201d others(5): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15002645 | ||||||
| chr3:15002645 | CTTTTTTT others(8): Show |
C | 13 | a0001c0001t0012g0297 a0001c0001t0016g0272 a0001c0001t0016g0273 others(10): Show |
13 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-39-1215_-39-1201d others(17): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15002645 | ||||||
| chr3:15002863 | G | C | 4 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-1013G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002863 | |||||||
| chr3:15002890 | T | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0105 a0001c0001t0001g0107 others(27): Show |
31 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.-39-986T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002890 | |||||||
| chr3:15002909 | C | T | 27 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(24): Show |
29 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.-39-967C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002909 | |||||||
| chr3:15002946 | C | T | 4 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39-930C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002946 | |||||||
| chr3:15002947 | C | T | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-39-929C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002947 | |||||||
| chr3:15002953 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-39-923C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15002953 | |||||||
| chr3:15002967 | CT | C | 57 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(54): Show |
58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.-39-897delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15002967 | ||||||
| chr3:15003112 | A | AT | 63 | a0001c0001t0001g0005 a0001c0001t0001g0061 a0001c0001t0001g0101 others(60): Show |
64 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.-39-747dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | 15003112 | ||||||
| chr3:15003121 | T | C | 3 | a0001c0001t0004g0227 a0001c0001t0004g0232 a0001c0001t0004g0233 |
3 | HG02109.hp1 HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-39-755T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15003121 | |||||||
| chr3:15003143 | A | G | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39-733A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15003143 | |||||||
| chr3:15003258 | C | T | 1 | a0001c0001t0027g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-39-618C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15003258 | |||||||
| chr3:15003534 | A | G | 2 | a0001c0001t0002g0058 a0001c0001t0002g0069 |
2 | HG02015.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.-39-342A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15003534 | |||||||
| chr3:15003816 | A | T | 4 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(1): Show |
4 | NA18946.hp1 NA18978.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39-60A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 1/13 | chr3 | 15003816 | |||||||
| chr3:15004066 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.72+80A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004066 | |||||||
| chr3:15004206 | A | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+220A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004206 | |||||||
| chr3:15004239 | T | C | 1 | a0001c0001t0040g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.72+253T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004239 | |||||||
| chr3:15004581 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.72+595T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004581 | |||||||
| chr3:15004627 | G | A | 4 | a0001c0001t0010g0047 a0001c0001t0010g0048 a0001c0001t0010g0060 others(1): Show |
4 | HG00609.hp1 HG02071.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+641G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004627 | |||||||
| chr3:15004661 | A | C | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.72+675A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004661 | |||||||
| chr3:15004758 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.72+772G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004758 | |||||||
| chr3:15004869 | G | T | 4 | a0001c0001t0028g0065 a0001c0005t0002g0293 a0001c0005t0002g0294 others(1): Show |
4 | HG03195.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+883G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004869 | |||||||
| chr3:15004927 | A | G | 57 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(54): Show |
58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.72+941A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004927 | |||||||
| chr3:15004978 | C | G | 1 | a0001c0001t0028g0065 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.72+992C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15004978 | |||||||
| chr3:15005041 | C | T | 3 | a0001c0001t0003g0096 a0001c0001t0003g0097 a0001c0001t0003g0098 |
3 | HG00438.hp1 HG00544.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.72+1055C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15005041 | |||||||
| chr3:15005122 | A | C | 4 | a0001c0003t0013g0245 a0001c0003t0013g0246 a0001c0003t0013g0247 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+1136A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15005122 | |||||||
| chr3:15005368 | C | CT | 33 | a0001c0001t0001g0015 a0001c0001t0001g0100 a0001c0001t0001g0104 others(30): Show |
33 | HG00438.hp2 HG01109.hp2 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.72+1407dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15005368 | ||||||
| chr3:15005368 | CT | C | 42 | a0001c0001t0001g0185 a0001c0001t0001g0198 a0001c0001t0012g0297 others(39): Show |
44 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.72+1407delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15005368 | ||||||
| chr3:15005368 | CTTT | C | 54 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(51): Show |
55 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.72+1405_72+1407del others(3): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15005368 | ||||||
| chr3:15005519 | C | CT | 103 | a0001c0001t0001g0135 a0001c0001t0001g0149 a0001c0001t0001g0163 others(100): Show |
104 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(101): Show |
intron_variant | MODIFIER | c.72+1553dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15005519 | ||||||
| chr3:15005519 | C | CTT | 47 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0298 others(44): Show |
51 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.72+1552_72+1553dup others(2): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15005519 | ||||||
| chr3:15005519 | C | CTTT | 6 | a0001c0001t0002g0033 a0001c0001t0003g0093 a0001c0001t0016g0272 others(3): Show |
6 | HG03098.hp1 HG03209.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+1551_72+1553dup others(3): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15005519 | ||||||
| chr3:15005519 | CT | C | 12 | a0001c0001t0001g0116 a0001c0001t0001g0133 a0001c0001t0001g0195 others(9): Show |
12 | HG01243.hp1 HG01496.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.72+1553delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15005519 | ||||||
| chr3:15005611 | A | C | 1 | a0001c0001t0001g0199 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.72+1625A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15005611 | |||||||
| chr3:15005845 | C | T | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.72+1859C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15005845 | |||||||
| chr3:15006067 | C | A | 1 | a0001c0001t0001g0213 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.72+2081C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15006067 | |||||||
| chr3:15006149 | G | A | 1 | a0001c0001t0003g0080 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.72+2163G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15006149 | |||||||
| chr3:15006234 | T | G | 2 | a0001c0001t0002g0071 a0001c0001t0002g0260 |
2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.72+2248T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15006234 | |||||||
| chr3:15006455 | T | C | 27 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(24): Show |
29 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.72+2469T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15006455 | |||||||
| chr3:15006577 | T | C | 1 | a0001c0001t0029g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.72+2591T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15006577 | |||||||
| chr3:15006747 | A | G | 1 | a0001c0001t0002g0070 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.72+2761A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15006747 | |||||||
| chr3:15006776 | CT | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0001g0163 others(12): Show |
15 | HG01069.hp1 HG01169.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.72+2808delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15006776 | ||||||
| chr3:15006811 | T | C | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.72+2825T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15006811 | |||||||
| chr3:15006845 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0224 |
2 | HG00140.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.72+2859G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15006845 | |||||||
| chr3:15007151 | G | A | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.72+3165G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15007151 | |||||||
| chr3:15007379 | G | C | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.72+3393G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15007379 | |||||||
| chr3:15007717 | G | A | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.72+3731G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15007717 | |||||||
| chr3:15007863 | C | G | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.72+3877C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15007863 | |||||||
| chr3:15007967 | G | A | 3 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 |
3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.72+3981G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15007967 | |||||||
| chr3:15008029 | G | A | 23 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(20): Show |
25 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.72+4043G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008029 | |||||||
| chr3:15008035 | C | T | 1 | a0001c0001t0004g0234 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.72+4049C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008035 | |||||||
| chr3:15008101 | G | A | 12 | a0001c0001t0002g0039 a0001c0001t0002g0042 a0001c0001t0002g0043 others(9): Show |
12 | HG00642.hp1 HG00735.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+4115G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008101 | |||||||
| chr3:15008134 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.72+4148A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008134 | |||||||
| chr3:15008181 | C | T | 2 | a0001c0001t0008g0158 a0001c0001t0008g0177 |
2 | HG00280.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.72+4195C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008181 | |||||||
| chr3:15008214 | TTG | T | 3 | a0001c0001t0012g0281 a0001c0001t0012g0282 a0001c0001t0030g0077 |
3 | HG02896.hp1 HG02897.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.72+4230_72+4231del others(2): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15008214 | ||||||
| chr3:15008219 | TG | T | 99 | a0001c0001t0001g0112 a0001c0001t0002g0032 a0001c0001t0002g0033 others(96): Show |
102 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.72+4234delG | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008219 | |||||||
| chr3:15008220 | G | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
170 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.72+4234G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008220 | |||||||
| chr3:15008224 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.72+4238T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008224 | |||||||
| chr3:15008232 | A | T | 10 | a0001c0001t0001g0104 a0001c0001t0001g0178 a0001c0001t0008g0158 others(7): Show |
10 | HG00280.hp1 HG00639.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+4246A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008232 | |||||||
| chr3:15008382 | C | T | 23 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(20): Show |
25 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.72+4396C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008382 | |||||||
| chr3:15008383 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0017g0291 others(1): Show |
5 | HG02015.hp1 HG02155.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+4397G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008383 | |||||||
| chr3:15008392 | C | T | 1 | a0001c0001t0002g0036 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.72+4406C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008392 | |||||||
| chr3:15008524 | GA | G | 74 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0197 others(71): Show |
78 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.72+4550delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15008524 | ||||||
| chr3:15008537 | C | A | 1 | a0001c0001t0024g0053 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.72+4551C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008537 | |||||||
| chr3:15008568 | C | G | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.72+4582C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008568 | |||||||
| chr3:15008644 | C | T | 4 | a0001c0001t0001g0121 a0001c0001t0001g0146 a0001c0001t0001g0150 others(1): Show |
4 | HG02698.hp1 NA18946.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+4658C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008644 | |||||||
| chr3:15008690 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.72+4704A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008690 | |||||||
| chr3:15008963 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0102 others(35): Show |
39 | HG00140.hp2 HG01099.hp2 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.73-4626A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008963 | |||||||
| chr3:15008987 | G | C | 1 | a0001c0001t0019g0289 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.73-4602G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15008987 | |||||||
| chr3:15009011 | G | C | 1 | a0001c0007t0014g0270 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.73-4578G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009011 | |||||||
| chr3:15009077 | C | CG | 56 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(53): Show |
57 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.73-4508dupG | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15009077 | ||||||
| chr3:15009178 | T | C | 4 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-4411T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009178 | |||||||
| chr3:15009218 | G | A | 4 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-4371G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009218 | |||||||
| chr3:15009271 | A | T | 132 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(129): Show |
137 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.73-4318A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009271 | |||||||
| chr3:15009281 | G | C | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.73-4308G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009281 | |||||||
| chr3:15009558 | T | TTGAGGGC others(21): Show |
1 | a0001c0001t0001g0155 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.73-4030_73-4003dup others(28): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15009558 | ||||||
| chr3:15009615 | C | G | 1 | a0001c0001t0034g0114 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73-3974C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009615 | |||||||
| chr3:15009619 | C | G | 1 | a0001c0001t0002g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.73-3970C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009619 | |||||||
| chr3:15009621 | G | A | 292 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(289): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.73-3968G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009621 | |||||||
| chr3:15009716 | T | G | 7 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0250 others(4): Show |
9 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.73-3873T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009716 | |||||||
| chr3:15009908 | G | C | 3 | a0001c0001t0038g0287 a0001c0001t0039g0288 a0001c0001t0040g0079 |
3 | HG02622.hp2 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.73-3681G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15009908 | |||||||
| chr3:15010045 | G | A | 18 | a0001c0001t0004g0227 a0001c0001t0004g0228 a0001c0001t0004g0229 others(15): Show |
18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-3544G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15010045 | |||||||
| chr3:15010103 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.73-3486C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15010103 | |||||||
| chr3:15010353 | TA | T | 30 | a0001c0001t0002g0045 a0001c0001t0012g0076 a0001c0001t0012g0281 others(27): Show |
32 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.73-3224delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15010353 | ||||||
| chr3:15010563 | A | T | 1 | a0001c0007t0014g0270 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.73-3026A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15010563 | |||||||
| chr3:15010711 | C | CA | 41 | a0001c0001t0001g0015 a0001c0001t0001g0181 a0001c0001t0015g0059 others(38): Show |
43 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.73-2861dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15010711 | ||||||
| chr3:15010998 | T | C | 132 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(129): Show |
137 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.73-2591T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15010998 | |||||||
| chr3:15011114 | C | T | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.73-2475C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15011114 | |||||||
| chr3:15011211 | C | T | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-2378C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15011211 | |||||||
| chr3:15011425 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0182 |
2 | NA18941.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.73-2164C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15011425 | |||||||
| chr3:15011472 | T | C | 1 | a0001c0001t0004g0231 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.73-2117T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15011472 | |||||||
| chr3:15011576 | C | T | 31 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(28): Show |
33 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.73-2013C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15011576 | |||||||
| chr3:15011990 | C | T | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.73-1599C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15011990 | |||||||
| chr3:15012054 | A | T | 2 | a0001c0001t0012g0297 a0001c0001t0029g0296 |
2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.73-1535A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012054 | |||||||
| chr3:15012161 | G | A | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.73-1428G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012161 | |||||||
| chr3:15012194 | G | C | 1 | a0001c0003t0006g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-1395G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012194 | |||||||
| chr3:15012230 | C | CT | 57 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(54): Show |
58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.73-1347dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr3 | 15012230 | ||||||
| chr3:15012248 | C | T | 10 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(7): Show |
10 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.73-1341C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012248 | |||||||
| chr3:15012382 | C | T | 1 | a0001c0001t0003g0255 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.73-1207C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012382 | |||||||
| chr3:15012517 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.73-1072C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012517 | |||||||
| chr3:15012521 | C | T | 14 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(11): Show |
14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.73-1068C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012521 | |||||||
| chr3:15012544 | T | TCTGTCAA others(3): Show |
105 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(102): Show |
108 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.73-1045_73-1044ins others(10): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012544 | |||||||
| chr3:15012584 | T | G | 1 | a0001c0001t0012g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.73-1005T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012584 | |||||||
| chr3:15012614 | A | G | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 |
3 | HG01884.hp2 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.73-975A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012614 | |||||||
| chr3:15012643 | C | G | 2 | a0001c0001t0001g0149 a0001c0001t0001g0167 |
2 | NA18990.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.73-946C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15012643 | |||||||
| chr3:15013132 | T | C | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.73-457T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15013132 | |||||||
| chr3:15013307 | C | T | 105 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(102): Show |
108 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.73-282C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15013307 | |||||||
| chr3:15013337 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.73-252A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15013337 | |||||||
| chr3:15013463 | G | T | 27 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(24): Show |
29 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.73-126G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 2/13 | chr3 | 15013463 | |||||||
| chr3:15013916 | C | T | 1 | a0001c0001t0003g0093 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.273+127C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15013916 | |||||||
| chr3:15013918 | G | A | 2 | a0001c0002t0014g0008 a0001c0002t0014g0009 |
2 | HG01081.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.273+129G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15013918 | |||||||
| chr3:15013972 | G | A | 1 | a0001c0001t0003g0080 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.273+183G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15013972 | |||||||
| chr3:15014073 | T | C | 2 | a0001c0001t0020g0222 a0001c0001t0020g0223 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.273+284T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15014073 | |||||||
| chr3:15014147 | G | A | 3 | a0001c0005t0002g0293 a0001c0005t0002g0294 a0001c0005t0002g0295 |
3 | HG03195.hp1 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.273+358G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15014147 | |||||||
| chr3:15014392 | A | C | 3 | a0001c0001t0018g0067 a0001c0001t0018g0068 a0001c0001t0025g0066 |
3 | HG00733.hp2 HG01192.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.273+603A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15014392 | |||||||
| chr3:15014398 | A | G | 49 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(46): Show |
50 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.273+609A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15014398 | |||||||
| chr3:15014470 | A | AT | 27 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(24): Show |
29 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.273+692dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 15014470 | ||||||
| chr3:15014470 | A | T | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.273+681A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15014470 | |||||||
| chr3:15014470 | AT | A | 23 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(20): Show |
25 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.273+692delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr3 | 15014470 | ||||||
| chr3:15014604 | C | T | 3 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 |
3 | HG03209.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.273+815C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15014604 | |||||||
| chr3:15014971 | C | G | 1 | a0001c0002t0005g0025 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.274-1181C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15014971 | |||||||
| chr3:15015088 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.274-1064G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15015088 | |||||||
| chr3:15015178 | C | T | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.274-974C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15015178 | |||||||
| chr3:15015351 | G | A | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.274-801G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15015351 | |||||||
| chr3:15015352 | C | T | 2 | a0001c0001t0003g0254 a0001c0001t0003g0255 |
2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.274-800C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15015352 | |||||||
| chr3:15015464 | A | G | 1 | a0001c0001t0002g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.274-688A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15015464 | |||||||
| chr3:15015918 | C | T | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-234C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15015918 | |||||||
| chr3:15015968 | A | T | 1 | a0001c0001t0001g0175 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.274-184A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 3/13 | chr3 | 15015968 | |||||||
| chr3:15016648 | GTA | G | 8 | a0001c0001t0001g0061 a0001c0001t0001g0149 a0001c0001t0001g0163 others(5): Show |
8 | HG02071.hp2 NA18942.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.376+395_376+396del others(2): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15016648 | |||||||
| chr3:15016794 | A | G | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.376+540A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15016794 | |||||||
| chr3:15016896 | A | T | 23 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(20): Show |
25 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.376+642A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15016896 | |||||||
| chr3:15016925 | G | A | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.376+671G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15016925 | |||||||
| chr3:15017059 | T | G | 1 | a0001c0001t0009g0267 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.376+805T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15017059 | |||||||
| chr3:15017230 | T | C | 1 | a0001c0001t0029g0296 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.376+976T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15017230 | |||||||
| chr3:15017408 | T | C | 1 | a0001c0003t0006g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.376+1154T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15017408 | |||||||
| chr3:15017412 | G | T | 21 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0102 others(18): Show |
22 | HG01255.hp1 HG01346.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.376+1158G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15017412 | |||||||
| chr3:15017449 | A | G | 49 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(46): Show |
50 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.376+1195A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15017449 | |||||||
| chr3:15017809 | A | T | 1 | a0001c0001t0035g0142 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.376+1555A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15017809 | |||||||
| chr3:15017823 | T | C | 33 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(30): Show |
35 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.376+1569T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15017823 | |||||||
| chr3:15018092 | A | G | 292 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(289): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.376+1838A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15018092 | |||||||
| chr3:15018277 | A | G | 7 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0250 others(4): Show |
9 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.376+2023A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15018277 | |||||||
| chr3:15018361 | C | T | 1 | a0001c0001t0027g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.376+2107C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15018361 | |||||||
| chr3:15018372 | T | C | 2 | a0001c0002t0014g0008 a0001c0002t0014g0009 |
2 | HG01081.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.376+2118T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15018372 | |||||||
| chr3:15018381 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.376+2127C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15018381 | |||||||
| chr3:15018388 | C | T | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.376+2134C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15018388 | |||||||
| chr3:15018488 | C | T | 1 | a0001c0001t0028g0065 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.376+2234C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15018488 | |||||||
| chr3:15018679 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.377-2074C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15018679 | |||||||
| chr3:15019016 | T | TA | 77 | a0001c0001t0001g0018 a0001c0001t0001g0061 a0001c0001t0001g0078 others(74): Show |
80 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.377-1714dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 15019016 | ||||||
| chr3:15019016 | T | TAA | 8 | a0001c0001t0002g0035 a0001c0001t0002g0038 a0001c0001t0002g0041 others(5): Show |
8 | HG01175.hp2 HG02129.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.377-1715_377-1714d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 15019016 | ||||||
| chr3:15019016 | TA | T | 28 | a0001c0001t0001g0185 a0001c0001t0002g0054 a0001c0001t0016g0272 others(25): Show |
28 | HG01168.hp1 HG01255.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.377-1714delA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 15019016 | ||||||
| chr3:15019032 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.377-1721A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15019032 | |||||||
| chr3:15019033 | A | T | 6 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0133 others(3): Show |
6 | NA18942.hp1 NA18948.hp2 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.377-1720A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15019033 | |||||||
| chr3:15019035 | AAAAAGAT others(9): Show |
A | 9 | a0001c0001t0001g0102 a0001c0001t0001g0124 a0001c0001t0001g0125 others(6): Show |
9 | HG01433.hp1 NA18942.hp1 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.377-1716_377-1701d others(18): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 15019035 | ||||||
| chr3:15019036 | AAAAGATT others(8): Show |
A | 1 | a0001c0001t0001g0129 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.377-1715_377-1701d others(17): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 15019036 | ||||||
| chr3:15019157 | T | C | 2 | a0001c0001t0001g0213 a0001c0001t0001g0298 |
2 | NA18991.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.377-1596T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15019157 | |||||||
| chr3:15019283 | G | A | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.377-1470G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15019283 | |||||||
| chr3:15019472 | C | T | 1 | a0001c0001t0003g0083 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.377-1281C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15019472 | |||||||
| chr3:15019714 | T | C | 1 | a0001c0003t0006g0252 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.377-1039T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15019714 | |||||||
| chr3:15019865 | T | G | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.377-888T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15019865 | |||||||
| chr3:15019981 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.377-772C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15019981 | |||||||
| chr3:15020160 | C | T | 3 | a0001c0001t0018g0067 a0001c0001t0018g0068 a0001c0001t0025g0066 |
3 | HG00733.hp2 HG01192.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.377-593C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15020160 | |||||||
| chr3:15020174 | C | CT | 29 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(26): Show |
31 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.377-575dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr3 | 15020174 | ||||||
| chr3:15020201 | G | A | 37 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0102 others(34): Show |
38 | HG00140.hp2 HG01099.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.377-552G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15020201 | |||||||
| chr3:15020499 | G | T | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.377-254G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15020499 | |||||||
| chr3:15020540 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.377-213C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 4/13 | chr3 | 15020540 | |||||||
| chr3:15021016 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.556+84G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15021016 | |||||||
| chr3:15021380 | C | G | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(3): Show |
6 | HG01884.hp2 HG02055.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.556+448C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15021380 | |||||||
| chr3:15021396 | C | A | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.556+464C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15021396 | |||||||
| chr3:15021665 | GGCATGCA others(4): Show |
G | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.556+750_556+760del others(11): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 15021665 | ||||||
| chr3:15021745 | C | T | 2 | a0001c0001t0016g0272 a0001c0001t0016g0273 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.556+813C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15021745 | |||||||
| chr3:15022019 | A | G | 57 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(54): Show |
58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.556+1087A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022019 | |||||||
| chr3:15022335 | C | T | 1 | a0001c0003t0006g0249 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.557-865C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022335 | |||||||
| chr3:15022382 | TTTTTTC | T | 7 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.557-808_557-803del others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 15022382 | ||||||
| chr3:15022392 | T | C | 1 | a0001c0004t0007g0280 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.557-808T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022392 | |||||||
| chr3:15022398 | C | CCT | 3 | a0001c0001t0028g0065 a0001c0005t0002g0293 a0001c0005t0002g0294 |
3 | HG03471.hp2 HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.557-802_557-801ins others(2): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022398 | |||||||
| chr3:15022398 | C | CT | 65 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(62): Show |
68 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.557-780dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 15022398 | ||||||
| chr3:15022398 | CT | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
142 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.557-780delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 15022398 | ||||||
| chr3:15022398 | CTT | C | 20 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0195 others(17): Show |
20 | HG01192.hp1 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.557-781_557-780del others(2): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr3 | 15022398 | ||||||
| chr3:15022402 | T | C | 3 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 |
3 | HG02615.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.557-798T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022402 | |||||||
| chr3:15022403 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.557-797T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022403 | |||||||
| chr3:15022474 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-726G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022474 | |||||||
| chr3:15022491 | G | A | 1 | a0001c0006t0001g0128 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.557-709G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022491 | |||||||
| chr3:15022685 | G | T | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.557-515G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022685 | |||||||
| chr3:15022797 | G | A | 1 | a0001c0001t0021g0283 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.557-403G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022797 | |||||||
| chr3:15022976 | G | A | 10 | a0001c0001t0001g0102 a0001c0001t0001g0124 a0001c0001t0001g0125 others(7): Show |
10 | HG01433.hp1 NA18942.hp1 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.557-224G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15022976 | |||||||
| chr3:15023045 | T | G | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.557-155T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 5/13 | chr3 | 15023045 | |||||||
| chr3:15023485 | C | A | 3 | a0001c0001t0004g0227 a0001c0001t0004g0232 a0001c0001t0004g0233 |
3 | HG02109.hp1 HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.704+138C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 6/13 | chr3 | 15023485 | |||||||
| chr3:15023801 | A | G | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.705-314A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 6/13 | chr3 | 15023801 | |||||||
| chr3:15024278 | G | A | 16 | a0001c0001t0002g0039 a0001c0001t0002g0042 a0001c0001t0002g0043 others(13): Show |
16 | HG00609.hp1 HG00642.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.798+70G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024278 | |||||||
| chr3:15024332 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.798+124C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024332 | |||||||
| chr3:15024463 | G | T | 1 | a0001c0001t0002g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.798+255G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024463 | |||||||
| chr3:15024485 | T | C | 3 | a0001c0001t0004g0227 a0001c0001t0004g0232 a0001c0001t0004g0233 |
3 | HG02109.hp1 HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.798+277T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024485 | |||||||
| chr3:15024493 | C | G | 3 | a0001c0001t0004g0227 a0001c0001t0004g0232 a0001c0001t0004g0233 |
3 | HG02109.hp1 HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.798+285C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024493 | |||||||
| chr3:15024615 | A | G | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.798+407A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024615 | |||||||
| chr3:15024672 | A | G | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.798+464A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024672 | |||||||
| chr3:15024750 | G | C | 16 | a0001c0001t0001g0140 a0001c0001t0001g0200 a0001c0001t0001g0201 others(13): Show |
16 | HG00140.hp2 HG01099.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.798+542G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024750 | |||||||
| chr3:15024807 | G | A | 3 | a0001c0001t0003g0096 a0001c0001t0003g0097 a0001c0001t0003g0098 |
3 | HG00438.hp1 HG00544.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.798+599G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024807 | |||||||
| chr3:15024951 | A | C | 1 | a0001c0001t0021g0283 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.798+743A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15024951 | |||||||
| chr3:15025081 | T | A | 57 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(54): Show |
58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.798+873T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15025081 | |||||||
| chr3:15025121 | T | G | 3 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 |
3 | HG02055.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.798+913T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15025121 | |||||||
| chr3:15025508 | T | A | 16 | a0001c0001t0001g0140 a0001c0001t0001g0200 a0001c0001t0001g0201 others(13): Show |
16 | HG00140.hp2 HG01099.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.798+1300T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15025508 | |||||||
| chr3:15025763 | T | C | 3 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 |
3 | HG02055.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.798+1555T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15025763 | |||||||
| chr3:15025880 | A | G | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.798+1672A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15025880 | |||||||
| chr3:15026025 | C | CT | 21 | a0001c0001t0018g0067 a0001c0001t0018g0068 a0001c0001t0025g0066 others(18): Show |
21 | HG00733.hp2 HG01081.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.798+1828dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr3 | 15026025 | ||||||
| chr3:15026159 | T | C | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.798+1951T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15026159 | |||||||
| chr3:15026303 | G | A | 1 | a0001c0001t0012g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.798+2095G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15026303 | |||||||
| chr3:15026426 | A | G | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-2160A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15026426 | |||||||
| chr3:15026705 | GT | G | 74 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(71): Show |
75 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.799-1872delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr3 | 15026705 | ||||||
| chr3:15026721 | A | G | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.799-1865A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15026721 | |||||||
| chr3:15026726 | T | C | 17 | a0001c0001t0001g0127 a0001c0001t0001g0140 a0001c0001t0001g0200 others(14): Show |
17 | HG00140.hp2 HG01099.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.799-1860T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15026726 | |||||||
| chr3:15026776 | T | G | 5 | a0001c0001t0001g0151 a0001c0001t0001g0157 a0001c0001t0001g0171 others(2): Show |
5 | HG01981.hp2 HG02148.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.799-1810T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15026776 | |||||||
| chr3:15026824 | C | T | 4 | a0001c0003t0013g0245 a0001c0003t0013g0246 a0001c0003t0013g0247 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-1762C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15026824 | |||||||
| chr3:15026930 | G | A | 2 | a0001c0001t0003g0254 a0001c0001t0003g0255 |
2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.799-1656G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15026930 | |||||||
| chr3:15027116 | C | T | 6 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-1470C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15027116 | |||||||
| chr3:15027145 | G | A | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.799-1441G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15027145 | |||||||
| chr3:15027222 | C | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-1364C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15027222 | |||||||
| chr3:15027422 | C | A | 1 | a0001c0001t0002g0046 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.799-1164C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15027422 | |||||||
| chr3:15027476 | G | A | 2 | a0001c0001t0009g0115 a0001c0001t0009g0119 |
2 | HG01081.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.799-1110G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15027476 | |||||||
| chr3:15027779 | G | A | 3 | a0001c0002t0014g0008 a0001c0002t0014g0009 a0001c0007t0014g0270 |
3 | HG01081.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.799-807G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15027779 | |||||||
| chr3:15028139 | C | G | 1 | a0001c0001t0031g0218 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.799-447C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15028139 | |||||||
| chr3:15028425 | G | C | 74 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(71): Show |
75 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.799-161G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15028425 | |||||||
| chr3:15028462 | C | A | 1 | a0001c0001t0012g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.799-124C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 7/13 | chr3 | 15028462 | |||||||
| chr3:15028735 | G | A | 1 | a0001c0001t0003g0092 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.932+16G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15028735 | |||||||
| chr3:15028750 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.932+31C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15028750 | |||||||
| chr3:15029037 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.932+318T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029037 | |||||||
| chr3:15029066 | C | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.932+347C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029066 | |||||||
| chr3:15029096 | ATTTTTCT | A | 18 | a0001c0001t0004g0227 a0001c0001t0004g0228 a0001c0001t0004g0229 others(15): Show |
18 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.932+390_932+396del others(7): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029096 | ||||||
| chr3:15029164 | A | G | 1 | a0001c0001t0002g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.932+445A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029164 | |||||||
| chr3:15029171 | T | C | 132 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(129): Show |
137 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.932+452T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029171 | |||||||
| chr3:15029287 | A | C | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.932+568A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029287 | |||||||
| chr3:15029369 | A | G | 1 | a0001c0001t0025g0066 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.932+650A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029369 | |||||||
| chr3:15029515 | A | G | 14 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(11): Show |
14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.933-760A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029515 | |||||||
| chr3:15029627 | A | G | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.933-648A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029627 | |||||||
| chr3:15029792 | A | AATAC | 36 | a0001c0001t0002g0035 a0001c0001t0002g0039 a0001c0001t0002g0041 others(33): Show |
36 | HG00438.hp1 HG00609.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.933-480_933-479ins others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029792 | ||||||
| chr3:15029792 | A | AATACATA others(1): Show |
19 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0042 others(16): Show |
21 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.933-480_933-479ins others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029792 | ||||||
| chr3:15029792 | A | AATACATA others(5): Show |
1 | a0001c0001t0002g0045 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.933-480_933-479ins others(12): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029792 | ||||||
| chr3:15029792 | A | AATAG | 41 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
44 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.933-435_933-432dup others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029792 | ||||||
| chr3:15029792 | A | AATAGATA others(1): Show |
9 | a0001c0001t0001g0018 a0001c0001t0001g0129 a0001c0001t0001g0141 others(6): Show |
9 | HG00673.hp2 HG00735.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.933-439_933-432dup others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029792 | ||||||
| chr3:15029792 | A | AATAGATA others(5): Show |
1 | a0001c0001t0001g0209 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.933-443_933-432dup others(12): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029792 | ||||||
| chr3:15029792 | AATAG | A | 33 | a0001c0001t0001g0078 a0001c0001t0001g0100 a0001c0001t0001g0102 others(30): Show |
33 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.933-435_933-432del others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029792 | ||||||
| chr3:15029792 | AATAGATA others(1): Show |
A | 8 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0189 others(5): Show |
8 | HG00609.hp2 HG02698.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.933-439_933-432del others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029792 | ||||||
| chr3:15029796 | G | C | 73 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0036 others(70): Show |
76 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.933-479G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029796 | |||||||
| chr3:15029826 | TAGATAGA others(3): Show |
T | 2 | a0001c0001t0012g0281 a0001c0001t0012g0282 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.933-447_933-438del others(10): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029826 | ||||||
| chr3:15029830 | TAGATAG | T | 3 | a0001c0001t0012g0076 a0001c0001t0017g0291 a0001c0001t0017g0292 |
3 | HG02055.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.933-443_933-438del others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029830 | ||||||
| chr3:15029834 | TAG | T | 8 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0004g0229 others(5): Show |
8 | HG02559.hp2 HG02615.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.933-439_933-438del others(2): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029834 | ||||||
| chr3:15029840 | G | T | 21 | a0001c0001t0003g0080 a0001c0001t0003g0093 a0001c0001t0004g0234 others(18): Show |
21 | HG01109.hp1 HG01168.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.933-435G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029840 | |||||||
| chr3:15029840 | GAT | G | 13 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0004g0229 others(10): Show |
13 | HG02055.hp1 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.933-431_933-430del others(2): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029840 | ||||||
| chr3:15029842 | T | G | 21 | a0001c0001t0003g0080 a0001c0001t0003g0093 a0001c0001t0004g0234 others(18): Show |
21 | HG01109.hp1 HG01168.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.933-433T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029842 | |||||||
| chr3:15029842 | T | TAGATAGA others(9): Show |
1 | a0001c0001t0004g0227 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.933-432_933-431ins others(16): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029842 | ||||||
| chr3:15029842 | T | TAGATAGA others(5): Show |
1 | a0001c0001t0004g0242 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.933-432_933-431ins others(12): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029842 | ||||||
| chr3:15029842 | T | TAGATATA others(1): Show |
3 | a0001c0001t0004g0236 a0001c0001t0004g0240 a0001c0001t0004g0241 |
3 | HG02965.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.933-432_933-431ins others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029842 | ||||||
| chr3:15029848 | T | C | 39 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(36): Show |
39 | HG01109.hp1 HG01168.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.933-427T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029848 | |||||||
| chr3:15029848 | T | TAGAC | 109 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(106): Show |
114 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.933-426_933-423dup others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029848 | ||||||
| chr3:15029943 | GAGAA | G | 7 | a0001c0001t0001g0102 a0001c0001t0001g0125 a0001c0001t0001g0132 others(4): Show |
7 | HG01433.hp1 NA18954.hp2 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.933-326_933-323del others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr3 | 15029943 | ||||||
| chr3:15029947 | A | G | 3 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 |
3 | HG02615.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.933-328A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029947 | |||||||
| chr3:15029975 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.933-300G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15029975 | |||||||
| chr3:15030063 | G | A | 1 | a0001c0001t0012g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.933-212G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15030063 | |||||||
| chr3:15030115 | A | G | 2 | a0001c0001t0016g0272 a0001c0001t0016g0273 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.933-160A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 8/13 | chr3 | 15030115 | |||||||
| chr3:15030459 | G | A | 3 | a0001c0002t0014g0008 a0001c0002t0014g0009 a0001c0007t0014g0270 |
3 | HG01081.hp2 HG02970.hp2 HG03471.hp1 |
splice_region_variant&intron_variant | LOW | c.1110+7G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15030459 | |||||||
| chr3:15030505 | T | C | 1 | a0001c0001t0003g0089 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1110+53T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15030505 | |||||||
| chr3:15030609 | C | G | 3 | a0001c0002t0014g0008 a0001c0002t0014g0009 a0001c0007t0014g0270 |
3 | HG01081.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1110+157C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15030609 | |||||||
| chr3:15030640 | C | A | 33 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(30): Show |
35 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1110+188C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15030640 | |||||||
| chr3:15030729 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1110+277G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15030729 | |||||||
| chr3:15030839 | A | G | 3 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 |
3 | HG02055.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1110+387A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15030839 | |||||||
| chr3:15031034 | A | T | 3 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0298 |
3 | HG00673.hp2 NA18991.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1110+582A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031034 | |||||||
| chr3:15031263 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1110+811G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031263 | |||||||
| chr3:15031370 | AT | A | 148 | a0001c0001t0001g0061 a0001c0001t0002g0032 a0001c0001t0002g0033 others(145): Show |
153 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1110+932delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr3 | 15031370 | ||||||
| chr3:15031395 | A | G | 1 | a0001c0001t0017g0291 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1110+943A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031395 | |||||||
| chr3:15031406 | C | T | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1110+954C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031406 | |||||||
| chr3:15031416 | T | A | 57 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(54): Show |
58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.1111-963T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031416 | |||||||
| chr3:15031712 | A | G | 5 | a0001c0001t0027g0072 a0001c0001t0028g0065 a0001c0005t0002g0293 others(2): Show |
5 | HG03195.hp1 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111-667A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031712 | |||||||
| chr3:15031723 | C | G | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1111-656C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031723 | |||||||
| chr3:15031819 | C | T | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1111-560C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031819 | |||||||
| chr3:15031832 | A | G | 58 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(55): Show |
62 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1111-547A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031832 | |||||||
| chr3:15031876 | A | G | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1111-503A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15031876 | |||||||
| chr3:15032020 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1111-359G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15032020 | |||||||
| chr3:15032023 | C | T | 4 | a0001c0003t0013g0245 a0001c0003t0013g0246 a0001c0003t0013g0247 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-356C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15032023 | |||||||
| chr3:15032042 | A | G | 1 | a0001c0001t0003g0096 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1111-337A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15032042 | |||||||
| chr3:15032063 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0199 |
2 | HG00544.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.1111-316A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 9/13 | chr3 | 15032063 | |||||||
| chr3:15032541 | C | A | 1 | a0001c0001t0001g0165 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1232+41C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15032541 | |||||||
| chr3:15032548 | C | T | 1 | a0001c0001t0043g0235 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1232+48C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15032548 | |||||||
| chr3:15032816 | C | T | 29 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(26): Show |
31 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1232+316C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15032816 | |||||||
| chr3:15032964 | A | AC | 26 | a0001c0001t0001g0178 a0001c0001t0003g0001 a0001c0001t0003g0010 others(23): Show |
28 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.1232+474dupC | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 15032964 | ||||||
| chr3:15033014 | C | T | 1 | a0001c0001t0001g0298 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1232+514C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033014 | |||||||
| chr3:15033262 | C | T | 12 | a0001c0001t0001g0116 a0001c0001t0001g0187 a0001c0001t0001g0195 others(9): Show |
12 | HG01123.hp1 HG01243.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1232+762C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033262 | |||||||
| chr3:15033351 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1232+851C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033351 | |||||||
| chr3:15033517 | C | T | 132 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(129): Show |
137 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1232+1017C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033517 | |||||||
| chr3:15033619 | G | C | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1233-1051G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033619 | |||||||
| chr3:15033623 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1233-1047G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033623 | |||||||
| chr3:15033628 | G | A | 23 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(20): Show |
25 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.1233-1042G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033628 | |||||||
| chr3:15033639 | C | CT | 93 | a0001c0001t0001g0116 a0001c0001t0001g0134 a0001c0001t0001g0155 others(90): Show |
97 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.1233-1006dupT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 15033639 | ||||||
| chr3:15033639 | CT | C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0112 others(25): Show |
28 | HG01109.hp1 HG01167.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.1233-1006delT | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr3 | 15033639 | ||||||
| chr3:15033808 | G | A | 1 | a0001c0001t0002g0046 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1233-862G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033808 | |||||||
| chr3:15033853 | A | G | 283 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(280): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1233-817A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033853 | |||||||
| chr3:15033970 | T | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1233-700T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15033970 | |||||||
| chr3:15034041 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1233-629C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15034041 | |||||||
| chr3:15034046 | G | A | 1 | a0001c0004t0007g0271 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1233-624G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15034046 | |||||||
| chr3:15034291 | T | A | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1233-379T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15034291 | |||||||
| chr3:15034350 | T | C | 132 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(129): Show |
137 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1233-320T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15034350 | |||||||
| chr3:15034390 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1233-280G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15034390 | |||||||
| chr3:15034636 | C | T | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1233-34C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15034636 | |||||||
| chr3:15034669 | G | A | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1233-1G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 10/13 | chr3 | 15034669 | |||||||
| chr3:15034908 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1372+99C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15034908 | |||||||
| chr3:15035004 | G | A | 282 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(279): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1372+195G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15035004 | |||||||
| chr3:15035173 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1372+364G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15035173 | |||||||
| chr3:15035183 | C | T | 3 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 |
3 | HG02615.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1372+374C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15035183 | |||||||
| chr3:15035294 | G | C | 17 | a0001c0001t0001g0127 a0001c0001t0001g0140 a0001c0001t0001g0200 others(14): Show |
17 | HG00140.hp2 HG01099.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.1372+485G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15035294 | |||||||
| chr3:15035581 | G | C | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1372+772G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15035581 | |||||||
| chr3:15035657 | G | T | 1 | a0001c0001t0001g0265 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1372+848G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15035657 | |||||||
| chr3:15035843 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1372+1034A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15035843 | |||||||
| chr3:15035982 | C | G | 4 | a0001c0003t0013g0245 a0001c0003t0013g0246 a0001c0003t0013g0247 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372+1173C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15035982 | |||||||
| chr3:15036083 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1372+1274G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15036083 | |||||||
| chr3:15036133 | T | G | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1372+1324T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15036133 | |||||||
| chr3:15036859 | C | G | 12 | a0001c0001t0001g0116 a0001c0001t0001g0187 a0001c0001t0001g0195 others(9): Show |
12 | HG01123.hp1 HG01243.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1373-1141C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15036859 | |||||||
| chr3:15036860 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1373-1140G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15036860 | |||||||
| chr3:15036982 | CATG | C | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1373-1017_1373-101 others(7): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15036982 | |||||||
| chr3:15037113 | C | CA | 6 | a0001c0001t0001g0137 a0001c0001t0003g0083 a0001c0001t0024g0053 others(3): Show |
6 | HG00558.hp2 HG01175.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.1373-874dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037113 | ||||||
| chr3:15037127 | C | A | 11 | a0001c0001t0016g0272 a0001c0001t0016g0273 a0001c0001t0021g0283 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1373-873C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037127 | |||||||
| chr3:15037207 | G | GTT | 17 | a0001c0001t0012g0076 a0001c0001t0016g0272 a0001c0001t0016g0273 others(14): Show |
17 | HG01109.hp1 HG01168.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1373-791_1373-790d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037207 | ||||||
| chr3:15037209 | T | TTG | 36 | a0001c0001t0001g0061 a0001c0001t0001g0164 a0001c0001t0001g0170 others(33): Show |
38 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1373-761_1373-760d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | ||||||
| chr3:15037209 | T | TTGTG | 3 | a0001c0001t0003g0096 a0001c0001t0003g0097 a0001c0001t0003g0098 |
3 | HG00438.hp1 HG00544.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1373-763_1373-760d others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | ||||||
| chr3:15037209 | T | TTTTGTG | 34 | a0001c0001t0002g0032 a0001c0001t0002g0035 a0001c0001t0002g0036 others(31): Show |
34 | HG00609.hp1 HG00673.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.1373-790_1373-789i others(8): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | ||||||
| chr3:15037209 | T | TTTTGTGT others(1): Show |
16 | a0001c0001t0002g0033 a0001c0001t0002g0039 a0001c0001t0002g0042 others(13): Show |
16 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1373-790_1373-789i others(10): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | ||||||
| chr3:15037209 | T | TTTTGTGT others(3): Show |
8 | a0001c0001t0002g0055 a0001c0001t0002g0259 a0001c0001t0011g0214 others(5): Show |
9 | HG00642.hp1 HG01099.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.1373-790_1373-789i others(12): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | ||||||
| chr3:15037209 | T | TTTTGTGT others(5): Show |
1 | a0001c0001t0011g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1373-790_1373-789i others(14): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | ||||||
| chr3:15037209 | TTG | T | 13 | a0001c0001t0001g0110 a0001c0001t0001g0153 a0001c0001t0012g0281 others(10): Show |
15 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.1373-761_1373-760d others(4): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | ||||||
| chr3:15037209 | TTGTG | T | 7 | a0001c0001t0001g0018 a0001c0001t0012g0297 a0001c0001t0029g0296 others(4): Show |
7 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1373-763_1373-760d others(6): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | ||||||
| chr3:15037209 | TTGTGTGT others(3): Show |
T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0130 |
4 | HG01167.hp1 HG01169.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1373-769_1373-760d others(12): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | ||||||
| chr3:15037209 | TTGTGTGT others(5): Show |
T | 8 | a0001c0001t0001g0113 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1373-771_1373-760d others(14): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | ||||||
| chr3:15037209 | TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1373-773_1373-760d others(16): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr3 | 15037209 | ||||||
| chr3:15037211 | G | T | 11 | a0001c0002t0014g0008 a0001c0002t0014g0009 a0001c0004t0007g0271 others(8): Show |
11 | HG01081.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1373-789G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037211 | |||||||
| chr3:15037213 | G | T | 11 | a0001c0001t0012g0281 a0001c0001t0012g0282 a0001c0001t0030g0077 others(8): Show |
13 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.1373-787G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037213 | |||||||
| chr3:15037215 | G | T | 6 | a0001c0001t0012g0297 a0001c0001t0029g0296 a0001c0003t0013g0245 others(3): Show |
6 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1373-785G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037215 | |||||||
| chr3:15037239 | G | T | 1 | a0001c0001t0004g0228 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1373-761G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037239 | |||||||
| chr3:15037241 | T | G | 4 | a0001c0001t0001g0100 a0001c0001t0003g0092 a0001c0001t0004g0232 others(1): Show |
4 | HG02083.hp2 HG02109.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1373-759T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037241 | |||||||
| chr3:15037523 | C | T | 3 | a0001c0001t0038g0287 a0001c0001t0039g0288 a0001c0001t0040g0079 |
3 | HG02622.hp2 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1373-477C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037523 | |||||||
| chr3:15037535 | T | C | 1 | a0001c0001t0030g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1373-465T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037535 | |||||||
| chr3:15037581 | A | C | 2 | a0001c0001t0016g0272 a0001c0001t0016g0273 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1373-419A>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037581 | |||||||
| chr3:15037661 | T | C | 7 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0250 others(4): Show |
9 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.1373-339T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037661 | |||||||
| chr3:15037700 | A | G | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1373-300A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037700 | |||||||
| chr3:15037726 | T | C | 4 | a0001c0001t0012g0076 a0001c0001t0012g0281 a0001c0001t0012g0282 others(1): Show |
4 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1373-274T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 11/13 | chr3 | 15037726 | |||||||
| chr3:15038192 | T | C | 3 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0090 |
5 | HG00639.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+55T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | chr3 | 15038192 | |||||||
| chr3:15038543 | A | G | 2 | a0001c0002t0014g0008 a0001c0002t0014g0009 |
2 | HG01081.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1510+406A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | chr3 | 15038543 | |||||||
| chr3:15038574 | G | T | 1 | a0001c0001t0001g0265 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1510+437G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | chr3 | 15038574 | |||||||
| chr3:15038637 | C | G | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1511-485C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | chr3 | 15038637 | |||||||
| chr3:15038693 | T | C | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1511-429T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | chr3 | 15038693 | |||||||
| chr3:15038854 | A | AG | 17 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1511-266dupG | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 15038854 | ||||||
| chr3:15039095 | T | TGG | 26 | a0001c0001t0003g0001 a0001c0001t0003g0080 a0001c0001t0003g0081 others(23): Show |
28 | HG00408.hp2 HG00438.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1511-19_1511-18dup others(2): Show |
NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr3 | 15039095 | ||||||
| chr3:15039097 | G | C | 1 | a0001c0001t0001g0141 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1511-25G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | chr3 | 15039097 | |||||||
| chr3:15039098 | G | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0186 a0001c0001t0001g0266 |
3 | HG02027.hp1 HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1511-24G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | chr3 | 15039098 | |||||||
| chr3:15039109 | T | C | 1 | a0001c0001t0010g0268 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1511-13T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 12/13 | chr3 | 15039109 | |||||||
| chr3:15039233 | G | A | 2 | a0001c0002t0014g0008 a0001c0002t0014g0009 |
2 | HG01081.hp2 HG02970.hp2 |
splice_region_variant&intron_variant | LOW | c.1616+6G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15039233 | |||||||
| chr3:15039364 | C | T | 3 | a0001c0002t0014g0008 a0001c0002t0014g0009 a0001c0007t0014g0270 |
3 | HG01081.hp2 HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1616+137C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15039364 | |||||||
| chr3:15039367 | G | A | 1 | a0001c0001t0011g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1616+140G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15039367 | |||||||
| chr3:15039568 | G | T | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1616+341G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15039568 | |||||||
| chr3:15039845 | T | C | 58 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(55): Show |
62 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1616+618T>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15039845 | |||||||
| chr3:15039932 | G | C | 150 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(147): Show |
155 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1616+705G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15039932 | |||||||
| chr3:15039940 | C | A | 132 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(129): Show |
137 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1616+713C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15039940 | |||||||
| chr3:15039977 | C | T | 8 | a0001c0004t0007g0271 a0001c0004t0007g0274 a0001c0004t0007g0275 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1616+750C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15039977 | |||||||
| chr3:15039997 | A | T | 3 | a0001c0001t0001g0213 a0001c0001t0016g0272 a0001c0001t0016g0273 |
3 | HG03209.hp1 HG03516.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1616+770A>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15039997 | |||||||
| chr3:15040006 | T | A | 14 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(11): Show |
14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1616+779T>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040006 | |||||||
| chr3:15040018 | G | A | 2 | a0001c0001t0019g0289 a0001c0001t0019g0290 |
2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1616+791G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040018 | |||||||
| chr3:15040116 | C | T | 60 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(57): Show |
61 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.1616+889C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040116 | |||||||
| chr3:15040166 | C | CA | 65 | a0001c0001t0001g0061 a0001c0001t0001g0078 a0001c0001t0001g0109 others(62): Show |
66 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.1616+950dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr3 | 15040166 | ||||||
| chr3:15040178 | C | A | 1 | a0001c0001t0004g0228 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1616+951C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040178 | |||||||
| chr3:15040181 | C | CA | 6 | a0001c0001t0001g0015 a0001c0001t0001g0137 a0001c0001t0001g0213 others(3): Show |
6 | HG01981.hp1 HG04115.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1616+963dupA | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr3 | 15040181 | ||||||
| chr3:15040199 | C | A | 1 | a0001c0001t0002g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1616+972C>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040199 | |||||||
| chr3:15040200 | G | C | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1616+973G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040200 | |||||||
| chr3:15040294 | A | G | 3 | a0001c0001t0038g0287 a0001c0001t0039g0288 a0001c0001t0040g0079 |
3 | HG02622.hp2 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1616+1067A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040294 | |||||||
| chr3:15040413 | C | T | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1616+1186C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040413 | |||||||
| chr3:15040447 | G | A | 3 | a0001c0001t0038g0287 a0001c0001t0039g0288 a0001c0001t0040g0079 |
3 | HG02622.hp2 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1616+1220G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040447 | |||||||
| chr3:15040463 | C | T | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1616+1236C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040463 | |||||||
| chr3:15040496 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1616+1269G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040496 | |||||||
| chr3:15040546 | C | T | 57 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(54): Show |
58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.1616+1319C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040546 | |||||||
| chr3:15040627 | G | A | 3 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0298 |
3 | HG00673.hp2 NA18991.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1616+1400G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040627 | |||||||
| chr3:15040689 | G | A | 227 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(224): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.1616+1462G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040689 | |||||||
| chr3:15040813 | T | G | 5 | a0001c0001t0004g0234 a0001c0001t0004g0236 a0001c0001t0004g0237 others(2): Show |
5 | HG01192.hp1 HG01934.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1616+1586T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040813 | |||||||
| chr3:15040959 | G | A | 4 | a0001c0003t0013g0245 a0001c0003t0013g0246 a0001c0003t0013g0247 others(1): Show |
4 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1616+1732G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15040959 | |||||||
| chr3:15041043 | G | C | 29 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(26): Show |
31 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1617-1791G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15041043 | |||||||
| chr3:15041814 | A | G | 132 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(129): Show |
137 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1617-1020A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15041814 | |||||||
| chr3:15041870 | C | T | 2 | a0001c0001t0009g0115 a0001c0001t0009g0119 |
2 | HG01081.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.1617-964C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15041870 | |||||||
| chr3:15041909 | C | T | 27 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(24): Show |
29 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1617-925C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15041909 | |||||||
| chr3:15041946 | G | C | 12 | a0001c0003t0006g0006 a0001c0003t0006g0007 a0001c0003t0006g0249 others(9): Show |
14 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1617-888G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15041946 | |||||||
| chr3:15042105 | G | C | 14 | a0001c0002t0005g0019 a0001c0002t0005g0020 a0001c0002t0005g0021 others(11): Show |
14 | HG01109.hp1 HG01168.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1617-729G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15042105 | |||||||
| chr3:15042257 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1617-577T>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15042257 | |||||||
| chr3:15042277 | C | G | 33 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(30): Show |
35 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1617-557C>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15042277 | |||||||
| chr3:15042417 | C | T | 57 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0035 others(54): Show |
58 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.1617-417C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15042417 | |||||||
| chr3:15042507 | C | T | 33 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0080 others(30): Show |
35 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1617-327C>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15042507 | |||||||
| chr3:15042528 | A | G | 2 | a0001c0001t0017g0291 a0001c0001t0017g0292 |
2 | HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1617-306A>G | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15042528 | |||||||
| chr3:15042591 | G | C | 1 | a0001c0001t0001g0174 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1617-243G>C | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15042591 | |||||||
| chr3:15042710 | G | T | 2 | a0001c0001t0009g0115 a0001c0001t0009g0119 |
2 | HG01081.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.1617-124G>T | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15042710 | |||||||
| chr3:15042755 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1617-79G>A | NR2C2 | ENSG00000177463.16 | transcript | ENST00000425241.6 | protein_coding | 13/13 | chr3 | 15042755 |