Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54583 |
| ensemblid | ENSG00000135766.9 |
| hgncid | 1232 |
| symbol | EGLN1 |
| name | egl-9 family hypoxia inducible factor 1 |
| refseq_nuc | NM_022051.3 |
| refseq_prot | NP_071334.1 |
| ensembl_nuc | ENST00000366641.4 |
| ensembl_prot | ENSP00000355601.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 231363756 |
| end | 231422287 |
| strand | - |
| ver | v1.2 |
| region | chr1:231363756-231422287 |
| region5000 | chr1:231358756-231427287 |
| regionname0 | EGLN1_chr1_231363756_231422287 |
| regionname5000 | EGLN1_chr1_231358756_231427287 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 426 | 323 | 77 | 45 | 151 | 12 | 36 | 114 | EGLN1_chr1_231358756_231427287 | EGLN1 | MANDS others(421): Show |
chr1 | 231358756 | 231427287 |
| a0002 | 0/0 | 426 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | EGLN1_chr1_231358756_231427287 | EGLN1 | MANES others(421): Show |
chr1 | 231358756 | 231427287 |
| a0003 | 0/0 | 426 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | MANDS others(421): Show |
chr1 | 231358756 | 231427287 |
| a0004 | 0/0 | 419 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | EGLN1_chr1_231358756_231427287 | EGLN1 | MANDS others(414): Show |
chr1 | 231358756 | 231427287 |
| a0005 | 0/0 | 426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | MANDS others(421): Show |
chr1 | 231358756 | 231427287 |
| a0006 | 0/0 | 426 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | MANDS others(421): Show |
chr1 | 231358756 | 231427287 |
| a0007 | 0/0 | 426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | MANDS others(421): Show |
chr1 | 231358756 | 231427287 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1278 | 321 | 76 | 45 | 150 | 12 | 36 | EGLN1_chr1_231358756_231427287 | EGLN1 | ATGGC others(1273): Show |
chr1 | 231358756 | 231427287 | ||
| a0001c0006 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | ATGGC others(1273): Show |
chr1 | 231358756 | 231427287 | ||
| a0001c0009 | 0/0 | 1278 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | ATGGC others(1273): Show |
chr1 | 231358756 | 231427287 | ||
| a0002c0002 | 0/0 | 1278 | 5 | 0 | 0 | 5 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | ATGGC others(1273): Show |
chr1 | 231358756 | 231427287 | ||
| a0003c0003 | 0/0 | 1278 | 4 | 3 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | ATGGC others(1273): Show |
chr1 | 231358756 | 231427287 | ||
| a0004c0004 | 0/0 | 1257 | 3 | 0 | 0 | 3 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | ATGGC others(1252): Show |
chr1 | 231358756 | 231427287 | ||
| a0005c0005 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | ATGGC others(1273): Show |
chr1 | 231358756 | 231427287 | ||
| a0006c0007 | 0/0 | 1278 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | ATGGC others(1273): Show |
chr1 | 231358756 | 231427287 | ||
| a0007c0008 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | ATGGC others(1273): Show |
chr1 | 231358756 | 231427287 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4336 | 128 | 19 | 22 | 65 | 6 | 16 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4331): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0002 | 1/1 | 4335 | 114 | 20 | 18 | 52 | 3 | 19 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4330): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0003 | 0/0 | 4334 | 12 | 5 | 2 | 1 | 3 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4329): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0004 | 0/0 | 4335 | 10 | 0 | 0 | 10 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4330): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0005 | 0/0 | 4336 | 8 | 8 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4331): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0006 | 0/0 | 4336 | 8 | 0 | 1 | 7 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4331): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0007 | 0/0 | 4336 | 6 | 6 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4331): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0008 | 0/0 | 4334 | 4 | 4 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4329): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0009 | 0/0 | 4332 | 4 | 1 | 0 | 3 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4327): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0010 | 0/0 | 4331 | 3 | 3 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4326): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0011 | 0/0 | 4335 | 2 | 2 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4330): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0012 | 0/0 | 4336 | 2 | 0 | 0 | 2 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4331): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0013 | 0/0 | 4335 | 2 | 2 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4330): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0014 | 0/0 | 4335 | 2 | 1 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4330): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0015 | 0/0 | 4335 | 2 | 0 | 0 | 2 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4330): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0016 | 0/0 | 4336 | 2 | 0 | 0 | 2 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4331): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0017 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4330): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0018 | 0/0 | 4334 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4329): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0019 | 0/0 | 4334 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4329): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0020 | 0/0 | 4336 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4331): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0021 | 0/0 | 4335 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4330): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0022 | 0/0 | 4336 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4331): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0023 | 0/0 | 4335 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4330): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0024 | 0/0 | 4336 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4331): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0025 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4330): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0026 | 0/0 | 4336 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4331): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0028 | 0/0 | 4335 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4330): Show |
chr1 | 231358756 | 231427287 |
| a0001c0001t0029 | 0/0 | 4335 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4330): Show |
chr1 | 231358756 | 231427287 |
| a0001c0006t0001 | 0/0 | 4336 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4331): Show |
chr1 | 231358756 | 231427287 |
| a0001c0009t0001 | 0/0 | 4336 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4331): Show |
chr1 | 231358756 | 231427287 |
| a0002c0002t0001 | 0/0 | 4336 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4331): Show |
chr1 | 231358756 | 231427287 |
| a0002c0002t0002 | 0/0 | 4335 | 3 | 0 | 0 | 3 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4330): Show |
chr1 | 231358756 | 231427287 |
| a0002c0002t0027 | 0/0 | 4335 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4330): Show |
chr1 | 231358756 | 231427287 |
| a0003c0003t0002 | 0/0 | 4335 | 4 | 3 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4330): Show |
chr1 | 231358756 | 231427287 |
| a0004c0004t0002 | 0/0 | 4314 | 3 | 0 | 0 | 3 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4309): Show |
chr1 | 231358756 | 231427287 |
| a0005c0005t0001 | 0/0 | 4336 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4331): Show |
chr1 | 231358756 | 231427287 |
| a0006c0007t0002 | 0/0 | 4335 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4330): Show |
chr1 | 231358756 | 231427287 |
| a0007c0008t0001 | 0/0 | 4336 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | GCAGA others(4331): Show |
chr1 | 231358756 | 231427287 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0005g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0006g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0006g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0009g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0009g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0009g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0009g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0010g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0010g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0010g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0011g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0011g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0012g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0012g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0013g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0013g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0014g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0014g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0015g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0016g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0016g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0017g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0018g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0019g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0020g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0021g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0022g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0023g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0024g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0025g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0026g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0028g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0001t0029g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0006t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0001c0009t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0002c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0002c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0002c0002t0027g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0003c0003t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0003c0003t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0003c0003t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0003c0003t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0004c0004t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0004c0004t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0004c0004t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0005c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0006c0007t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| a0007c0008t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0035 | EUR | GBR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | GBR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | GBR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0215 | EUR | GBR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | FIN | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0252 | EUR | FIN | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | CHS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | CHS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | CHS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00609 | hp1 | a0001 | c0001 | t0006 | g0283 | EAS | CHS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | CHS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0150 | AMR | PUR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | CHS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PUR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01243 | hp2 | a0001 | c0001 | t0014 | g0095 | AMR | PUR | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | CLM | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | CLM | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | CLM | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01358 | hp2 | a0001 | c0001 | t0028 | g0271 | AMR | CLM | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | IBS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | IBS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | ACB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01884 | hp2 | a0003 | c0003 | t0002 | g0307 | AFR | ACB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | ACB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PEL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02040 | hp2 | a0001 | c0001 | t0026 | g0100 | EAS | KHV | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0291 | AFR | ACB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02056 | hp2 | a0001 | c0001 | t0029 | g0318 | EAS | KHV | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02074 | hp1 | a0001 | c0001 | t0015 | g0018 | EAS | KHV | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0313 | EAS | KHV | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | CDX | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0033 | AFR | ACB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0278 | AFR | ACB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02258 | hp2 | a0001 | c0006 | t0001 | g0292 | AFR | ACB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02451 | hp2 | a0003 | c0003 | t0002 | g0310 | AFR | ACB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02523 | hp1 | a0001 | c0001 | t0015 | g0018 | EAS | KHV | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | KHV | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0041 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0076 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0293 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02647 | hp2 | a0001 | c0001 | t0025 | g0074 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0296 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0081 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02723 | hp2 | a0001 | c0001 | t0017 | g0047 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02809 | hp2 | a0005 | c0005 | t0001 | g0022 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0073 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02886 | hp2 | a0001 | c0001 | t0019 | g0042 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0290 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0295 | AFR | ESN | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | ESN | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0031 | AFR | MSL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0192 | AFR | ESN | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0080 | AFR | ESN | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0297 | AFR | ESN | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | MSL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | MSL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03225 | hp2 | a0001 | c0001 | t0014 | g0094 | AFR | MSL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | MSL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | MSL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03486 | hp1 | a0003 | c0003 | t0002 | g0308 | AFR | MSL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0077 | AFR | MSL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0276 | SAS | PJL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0275 | SAS | PJL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0274 | SAS | PJL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0269 | SAS | PJL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0079 | AFR | MSL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | STU | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | BEB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | BEB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | BEB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | STU | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | STU | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | BEB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | STU | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | STU | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | STU | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | STU | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | STU | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | YRI | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | CHB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | CHB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18747 | hp1 | a0001 | c0001 | t0016 | g0319 | EAS | CHB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18747 | hp2 | a0001 | c0001 | t0006 | g0127 | EAS | CHB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | YRI | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | YRI | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18942 | hp1 | a0001 | c0001 | t0006 | g0128 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18945 | hp1 | a0001 | c0001 | t0022 | g0143 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0282 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18951 | hp2 | a0004 | c0004 | t0002 | g0019 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18953 | hp1 | a0001 | c0001 | t0023 | g0258 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18953 | hp2 | a0001 | c0001 | t0009 | g0187 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18954 | hp1 | a0001 | c0001 | t0012 | g0153 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18956 | hp2 | a0001 | c0001 | t0021 | g0063 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18959 | hp1 | a0001 | c0009 | t0001 | g0312 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18961 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18961 | hp2 | a0002 | c0002 | t0027 | g0315 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18965 | hp1 | a0004 | c0004 | t0002 | g0020 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0314 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18999 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19002 | hp1 | a0001 | c0001 | t0009 | g0186 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19004 | hp2 | a0001 | c0001 | t0012 | g0104 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19005 | hp1 | a0001 | c0001 | t0006 | g0142 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19043 | hp1 | a0001 | c0001 | t0013 | g0305 | AFR | LWK | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | LWK | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19068 | hp1 | a0001 | c0001 | t0009 | g0191 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19077 | hp1 | a0006 | c0007 | t0002 | g0306 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0316 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19081 | hp2 | a0004 | c0004 | t0002 | g0021 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0317 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19085 | hp2 | a0001 | c0001 | t0020 | g0058 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | YRI | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA19240 | hp2 | a0007 | c0008 | t0001 | g0311 | AFR | YRI | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | TSI | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0224 | EUR | TSI | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | GIH | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | GIH | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01123 | hp1 | a0003 | c0003 | t0002 | g0309 | AMR | CLM | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | ACB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0294 | AFR | ACB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG02559 | hp2 | a0001 | c0001 | t0024 | g0197 | AFR | ACB | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0289 | AFR | MSL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0088 | AFR | MSL | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG06807 | hp1 | a0001 | c0001 | t0018 | g0032 | AFR | USA | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | USA | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0154 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA18955 | hp2 | a0001 | c0001 | t0016 | g0320 | EAS | JPT | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA20300 | hp1 | a0001 | c0001 | t0010 | g0279 | AFR | USA | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | USA | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | LWK | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| NA21309 | hp2 | a0001 | c0001 | t0013 | g0217 | AFR | LWK | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0214 | REF | REF | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0181 | REF | REF | EGLN1_chr1_231358756_231427287 | EGLN1 | chr1 | 231358756 | 231427287 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:231421396 | G | T | 1 | a0005 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.493C>A | p.Pro165Thr | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/5 | 892/4335 | 493/1281 | 165/426 | chr1 | 231421396 | |||
| chr1:231421496 | GGCGGCCG others(14): Show |
G | 1 | a0004 | 3 | NA18951.hp2 NA18965.hp1 NA19081.hp2 |
disruptive_inframe_deletion | MODERATE | c.372_392delGTCGCCGT others(13): Show |
p.Ser125_Ala131del | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/5 | 791/4335 | 372/1281 | 124/426 | chr1 | 231421496 | |||
| chr1:231421509 | C | G | 5 | a0001 a0002 a0003 others(2): Show |
130 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(127): Show |
missense_variant | MODERATE | c.380G>C | p.Cys127Ser | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/5 | 779/4335 | 380/1281 | 127/426 | chr1 | 231421509 | |||
| chr1:231421570 | C | A | 1 | a0006 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.319G>T | p.Ala107Ser | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/5 | 718/4335 | 319/1281 | 107/426 | chr1 | 231421570 | |||
| chr1:231421602 | G | A | 1 | a0003 | 4 | HG01123.hp1 HG01884.hp2 HG02451.hp2 others(1): Show |
missense_variant | MODERATE | c.287C>T | p.Ala96Val | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/5 | 686/4335 | 287/1281 | 96/426 | chr1 | 231421602 | |||
| chr1:231421749 | T | C | 1 | a0007 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.140A>G | p.Gln47Arg | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/5 | 539/4335 | 140/1281 | 47/426 | chr1 | 231421749 | |||
| chr1:231421877 | G | C | 1 | a0002 | 5 | HG02135.hp1 NA18961.hp2 NA18983.hp2 others(2): Show |
missense_variant | MODERATE | c.12C>G | p.Asp4Glu | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/5 | 411/4335 | 12/1281 | 4/426 | chr1 | 231421877 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:231366420 | G | A | 2 | a0001c0006 a0005c0005 |
2 | HG02258.hp2 HG02809.hp2 |
synonymous_variant | LOW | c.1272C>T | p.Asp424Asp | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 1671/4335 | 1272/1281 | 424/426 | chr1 | 231366420 | |||
| chr1:231421769 | G | A | 1 | a0001c0009 | 1 | NA18959.hp1 | synonymous_variant | LOW | c.120C>T | p.Phe40Phe | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/5 | 519/4335 | 120/1281 | 40/426 | chr1 | 231421769 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:231363793 | C | T | 1 | a0001c0001t0018 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2618G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 2618 | chr1 | 231363793 | ||||||
| chr1:231363813 | C | T | 2 | a0001c0001t0004 a0001c0001t0029 |
11 | HG02056.hp2 NA18612.hp2 NA18947.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2598G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 2598 | chr1 | 231363813 | ||||||
| chr1:231363991 | CACAA | C | 1 | a0001c0001t0009 | 4 | HG03130.hp1 NA18953.hp2 NA19002.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2416_*2419delTTGT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 2416 | chr1 | 231363991 | ||||||
| chr1:231364176 | G | C | 3 | a0001c0001t0008 a0001c0001t0018 a0001c0001t0019 |
6 | HG02257.hp1 HG02572.hp1 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2235C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 2235 | chr1 | 231364176 | ||||||
| chr1:231364286 | TCAAA | T | 1 | a0001c0001t0010 | 3 | HG02257.hp2 HG02818.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2121_*2124delTTTG | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 2121 | chr1 | 231364286 | ||||||
| chr1:231364306 | C | G | 1 | a0001c0001t0021 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2105G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 2105 | chr1 | 231364306 | ||||||
| chr1:231364350 | G | C | 1 | a0001c0001t0005 | 8 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2061C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 2061 | chr1 | 231364350 | ||||||
| chr1:231364366 | G | A | 1 | a0001c0001t0020 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2045C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 2045 | chr1 | 231364366 | ||||||
| chr1:231364492 | A | G | 2 | a0001c0001t0006 a0001c0001t0022 |
9 | HG00609.hp1 HG00642.hp2 NA18747.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1919T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 1919 | chr1 | 231364492 | ||||||
| chr1:231364531 | T | A | 3 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0011 |
16 | HG01884.hp1 HG02055.hp1 HG02486.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1880A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 1880 | chr1 | 231364531 | ||||||
| chr1:231364607 | A | AT | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(13): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*1803dupA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 1803 | chr1 | 231364607 | ||||||
| chr1:231364624 | A | C | 1 | a0001c0001t0017 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1787T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 1787 | chr1 | 231364624 | ||||||
| chr1:231364827 | C | T | 1 | a0001c0001t0014 | 2 | HG01243.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1584G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 1584 | chr1 | 231364827 | ||||||
| chr1:231365178 | T | C | 1 | a0001c0001t0013 | 2 | NA19043.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1233A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 1233 | chr1 | 231365178 | ||||||
| chr1:231365212 | T | G | 1 | a0001c0001t0019 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1199A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 1199 | chr1 | 231365212 | ||||||
| chr1:231365307 | A | G | 1 | a0001c0001t0012 | 2 | NA18954.hp1 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1104T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 1104 | chr1 | 231365307 | ||||||
| chr1:231365422 | A | G | 3 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0011 |
16 | HG01884.hp1 HG02055.hp1 HG02486.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*989T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 989 | chr1 | 231365422 | ||||||
| chr1:231365543 | T | G | 1 | a0001c0001t0022 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*868A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 868 | chr1 | 231365543 | ||||||
| chr1:231365624 | C | A | 1 | a0001c0001t0023 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*787G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 787 | chr1 | 231365624 | ||||||
| chr1:231365711 | T | C | 1 | a0001c0001t0024 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*700A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 700 | chr1 | 231365711 | ||||||
| chr1:231365762 | CA | C | 4 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0018 others(1): Show |
18 | HG00099.hp1 HG01175.hp2 HG01257.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*648delT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 648 | chr1 | 231365762 | ||||||
| chr1:231365789 | T | C | 1 | a0001c0001t0025 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*622A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 622 | chr1 | 231365789 | ||||||
| chr1:231365917 | C | T | 1 | a0001c0001t0017 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*494G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 494 | chr1 | 231365917 | ||||||
| chr1:231365959 | T | C | 1 | a0001c0001t0026 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*452A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 452 | chr1 | 231365959 | ||||||
| chr1:231365995 | T | C | 1 | a0001c0001t0014 | 2 | HG01243.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*416A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 416 | chr1 | 231365995 | ||||||
| chr1:231366033 | G | A | 1 | a0002c0002t0027 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*378C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 378 | chr1 | 231366033 | ||||||
| chr1:231366040 | T | G | 1 | a0001c0001t0028 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*371A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 5/5 | 371 | chr1 | 231366040 | ||||||
| chr1:231422265 | C | A | 1 | a0001c0001t0029 | 1 | HG02056.hp2 | 5_prime_UTR_variant | MODIFIER | c.-377G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/5 | 377 | chr1 | 231422265 | ||||||
| chr1:231422267 | T | A | 1 | a0001c0001t0016 | 2 | NA18747.hp1 NA18955.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-379A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/5 | chr1 | 231422267 | |||||||
| chr1:231422267 | T | G | 1 | a0001c0001t0015 | 2 | HG02074.hp1 HG02523.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-379A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/5 | chr1 | 231422267 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:231366484 | T | TA | 14 | a0001c0001t0002g0012 a0001c0001t0002g0065 a0001c0001t0002g0264 others(11): Show |
15 | HG01884.hp1 HG01981.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1217-10dupT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 4/4 | chr1 | 231366484 | |||||||
| chr1:231366498 | A | AG | 4 | a0001c0001t0001g0137 a0001c0001t0001g0139 a0001c0001t0001g0166 others(1): Show |
4 | HG00099.hp2 HG01258.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1217-24_1217-23ins others(1): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 4/4 | chr1 | 231366498 | |||||||
| chr1:231366498 | A | T | 9 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(6): Show |
9 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1217-23T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 4/4 | chr1 | 231366498 | |||||||
| chr1:231366499 | T | A | 156 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1217-24A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 4/4 | chr1 | 231366499 | |||||||
| chr1:231366513 | C | T | 1 | a0001c0001t0007g0078 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1217-38G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 4/4 | chr1 | 231366513 | |||||||
| chr1:231366564 | T | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(131): Show |
143 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.1217-89A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 4/4 | chr1 | 231366564 | |||||||
| chr1:231366819 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(1): Show |
5 | HG02258.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1217-344C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 4/4 | chr1 | 231366819 | |||||||
| chr1:231366980 | G | A | 1 | a0001c0001t0002g0204 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1217-505C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 4/4 | chr1 | 231366980 | |||||||
| chr1:231366999 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1217-524T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 4/4 | chr1 | 231366999 | |||||||
| chr1:231367535 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
5 | NA18948.hp2 NA18960.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1216+34C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 4/4 | chr1 | 231367535 | |||||||
| chr1:231367562 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03688.hp2 | splice_region_variant&intron_variant | LOW | c.1216+7G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 4/4 | chr1 | 231367562 | |||||||
| chr1:231367705 | G | A | 8 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0007g0078 others(5): Show |
8 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1149-69C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231367705 | |||||||
| chr1:231367794 | G | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(3): Show |
7 | HG02258.hp1 HG02735.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1149-158C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231367794 | |||||||
| chr1:231367823 | T | A | 9 | a0001c0001t0002g0065 a0001c0001t0002g0200 a0001c0001t0002g0205 others(6): Show |
9 | HG01358.hp1 HG01928.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.1149-187A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231367823 | |||||||
| chr1:231367838 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1149-202A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231367838 | |||||||
| chr1:231368086 | G | A | 1 | a0001c0001t0002g0198 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1149-450C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231368086 | |||||||
| chr1:231368194 | A | C | 2 | a0001c0001t0002g0259 a0001c0001t0002g0267 |
2 | NA18939.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.1149-558T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231368194 | |||||||
| chr1:231368311 | G | C | 3 | a0001c0001t0011g0289 a0001c0001t0011g0290 a0001c0001t0013g0305 |
3 | HG02896.hp1 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1149-675C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231368311 | |||||||
| chr1:231368351 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1149-715A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231368351 | |||||||
| chr1:231368386 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1149-750G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231368386 | |||||||
| chr1:231368491 | G | GACTT | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
150 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1149-859_1149-856d others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231368491 | |||||||
| chr1:231368565 | G | C | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
150 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1149-929C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231368565 | |||||||
| chr1:231368613 | C | T | 17 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(14): Show |
18 | HG01884.hp1 HG02258.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1149-977G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231368613 | |||||||
| chr1:231368634 | G | A | 1 | a0001c0001t0004g0284 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1149-998C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231368634 | |||||||
| chr1:231368690 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1149-1054C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231368690 | |||||||
| chr1:231368697 | G | A | 17 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1149-1061C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231368697 | |||||||
| chr1:231368704 | T | A | 16 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(13): Show |
17 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1149-1068A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231368704 | |||||||
| chr1:231368847 | A | G | 2 | a0001c0001t0011g0289 a0001c0001t0011g0290 |
2 | HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1149-1211T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231368847 | |||||||
| chr1:231369160 | C | A | 1 | a0005c0005t0001g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1148+1402G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231369160 | |||||||
| chr1:231369399 | A | T | 1 | a0001c0001t0017g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1148+1163T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231369399 | |||||||
| chr1:231369595 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(1): Show |
5 | HG02258.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1148+967G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231369595 | |||||||
| chr1:231369671 | G | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1148+891C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231369671 | |||||||
| chr1:231369679 | C | T | 4 | a0001c0001t0002g0276 a0004c0004t0002g0019 a0004c0004t0002g0020 others(1): Show |
4 | HG03490.hp2 NA18951.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1148+883G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231369679 | |||||||
| chr1:231369680 | AAC | A | 4 | a0001c0001t0002g0276 a0004c0004t0002g0019 a0004c0004t0002g0020 others(1): Show |
4 | HG03490.hp2 NA18951.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1148+880_1148+881d others(4): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231369680 | |||||||
| chr1:231369706 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1148+856G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231369706 | |||||||
| chr1:231369727 | T | C | 17 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1148+835A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231369727 | |||||||
| chr1:231369781 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1148+781C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231369781 | |||||||
| chr1:231369794 | C | A | 1 | a0001c0001t0005g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1148+768G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231369794 | |||||||
| chr1:231369801 | T | C | 1 | a0001c0001t0002g0228 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1148+761A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231369801 | |||||||
| chr1:231369841 | T | A | 156 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1148+721A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231369841 | |||||||
| chr1:231369955 | G | A | 163 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.1148+607C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231369955 | |||||||
| chr1:231369971 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1148+591A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231369971 | |||||||
| chr1:231370022 | A | G | 1 | a0001c0001t0017g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1148+540T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231370022 | |||||||
| chr1:231370109 | C | T | 1 | a0005c0005t0001g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1148+453G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231370109 | |||||||
| chr1:231370283 | C | T | 5 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0066 others(2): Show |
6 | NA18956.hp2 NA18977.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1148+279G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231370283 | |||||||
| chr1:231370288 | A | G | 1 | a0001c0001t0002g0257 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1148+274T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231370288 | |||||||
| chr1:231370398 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1148+164A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 3/4 | chr1 | 231370398 | |||||||
| chr1:231370811 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1012-113C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231370811 | |||||||
| chr1:231370854 | T | C | 17 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1012-156A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231370854 | |||||||
| chr1:231370939 | G | T | 1 | a0001c0001t0002g0199 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1012-241C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231370939 | |||||||
| chr1:231371062 | G | T | 17 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1012-364C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231371062 | |||||||
| chr1:231371160 | T | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1012-462A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231371160 | |||||||
| chr1:231371182 | C | G | 156 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1012-484G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231371182 | |||||||
| chr1:231371189 | C | T | 6 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(3): Show |
6 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1012-491G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231371189 | |||||||
| chr1:231371298 | G | C | 3 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0113 |
3 | HG02602.hp2 HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1012-600C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231371298 | |||||||
| chr1:231371508 | G | A | 156 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1012-810C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231371508 | |||||||
| chr1:231371556 | T | A | 1 | a0001c0001t0002g0004 | 2 | NA18978.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1012-858A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231371556 | |||||||
| chr1:231371671 | T | C | 1 | a0001c0001t0002g0261 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1012-973A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231371671 | |||||||
| chr1:231372059 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1012-1361A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231372059 | |||||||
| chr1:231372165 | C | A | 1 | a0001c0001t0001g0141 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1012-1467G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231372165 | |||||||
| chr1:231372214 | C | G | 1 | a0001c0001t0017g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1012-1516G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231372214 | |||||||
| chr1:231372270 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1012-1572C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231372270 | |||||||
| chr1:231372337 | C | T | 2 | a0001c0001t0002g0252 a0001c0001t0028g0271 |
2 | HG00323.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1012-1639G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231372337 | |||||||
| chr1:231372399 | T | C | 17 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1011+1581A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231372399 | |||||||
| chr1:231372537 | G | GA | 7 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(4): Show |
8 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1011+1442dupT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231372537 | |||||||
| chr1:231372932 | T | C | 1 | a0001c0001t0025g0074 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1011+1048A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231372932 | |||||||
| chr1:231372993 | T | C | 12 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0025 others(9): Show |
12 | HG00741.hp2 HG02523.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.1011+987A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231372993 | |||||||
| chr1:231373230 | T | G | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
150 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1011+750A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373230 | |||||||
| chr1:231373282 | T | C | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG01257.hp1 HG01258.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1011+698A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373282 | |||||||
| chr1:231373513 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1011+467T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373513 | |||||||
| chr1:231373654 | C | G | 1 | a0001c0001t0002g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1011+326G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373654 | |||||||
| chr1:231373662 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1011+318G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373662 | |||||||
| chr1:231373669 | CGTGTGTG others(5): Show |
C | 1 | a0001c0009t0001g0312 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1011+299_1011+310d others(14): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373669 | |||||||
| chr1:231373669 | CGTGTGTG others(7): Show |
C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0082 |
4 | HG02486.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1011+297_1011+310d others(16): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373669 | |||||||
| chr1:231373669 | CGTGTGTG others(9): Show |
C | 135 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(132): Show |
144 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.1011+295_1011+310d others(18): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373669 | |||||||
| chr1:231373677 | CGT | C | 148 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0004 others(145): Show |
154 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.1011+301_1011+302d others(4): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373677 | |||||||
| chr1:231373683 | T | C | 3 | a0001c0001t0010g0073 a0001c0001t0010g0278 a0001c0001t0010g0279 |
3 | HG02257.hp2 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1011+297A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373683 | |||||||
| chr1:231373686 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1011+294C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373686 | |||||||
| chr1:231373691 | T | C | 1 | a0001c0009t0001g0312 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1011+289A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373691 | |||||||
| chr1:231373693 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0082 |
4 | HG02486.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1011+287A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373693 | |||||||
| chr1:231373694 | GTGTGTGT others(3): Show |
G | 3 | a0001c0001t0002g0046 a0001c0001t0002g0083 a0001c0001t0005g0296 |
3 | HG02109.hp1 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1011+276_1011+285d others(12): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373694 | |||||||
| chr1:231373695 | T | C | 135 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(132): Show |
144 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.1011+285A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373695 | |||||||
| chr1:231373698 | GTGTGTA | G | 8 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0010g0073 others(5): Show |
8 | HG02257.hp2 HG02258.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1011+276_1011+281d others(8): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373698 | |||||||
| chr1:231373700 | GTGTA | G | 4 | a0001c0001t0002g0092 a0001c0001t0005g0014 a0001c0001t0011g0289 others(1): Show |
4 | HG02055.hp2 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1011+276_1011+279d others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373700 | |||||||
| chr1:231373702 | GTA | G | 6 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(3): Show |
6 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1011+276_1011+277d others(4): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373702 | |||||||
| chr1:231373704 | A | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(143): Show |
156 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1011+276T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373704 | |||||||
| chr1:231373730 | A | G | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1011+250T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373730 | |||||||
| chr1:231373771 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0006g0010 a0001c0001t0006g0127 others(6): Show |
11 | HG00609.hp1 HG00642.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.1011+209C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373771 | |||||||
| chr1:231373784 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1011+196C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373784 | |||||||
| chr1:231373941 | C | A | 1 | a0001c0001t0002g0250 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1011+39G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 2/4 | chr1 | 231373941 | |||||||
| chr1:231374180 | T | G | 3 | a0001c0001t0010g0073 a0001c0001t0010g0278 a0001c0001t0010g0279 |
3 | HG02257.hp2 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.892-81A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231374180 | |||||||
| chr1:231374521 | A | AT | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-423dupA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231374521 | |||||||
| chr1:231375000 | A | T | 4 | a0001c0001t0002g0252 a0001c0001t0002g0269 a0001c0001t0002g0275 others(1): Show |
4 | HG00323.hp2 HG01358.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.892-901T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231375000 | |||||||
| chr1:231375024 | AAAAC | A | 133 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
142 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.892-929_892-926del others(4): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231375024 | |||||||
| chr1:231375181 | G | A | 2 | a0001c0001t0002g0017 a0001c0001t0002g0304 |
3 | HG01099.hp2 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.892-1082C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231375181 | |||||||
| chr1:231375307 | CAGCCTCC others(24): Show |
C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-1239_892-1209d others(33): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231375307 | |||||||
| chr1:231375439 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-1340G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231375439 | |||||||
| chr1:231375763 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.892-1664G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231375763 | |||||||
| chr1:231376381 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-2282G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231376381 | |||||||
| chr1:231376736 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.892-2637T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231376736 | |||||||
| chr1:231376841 | G | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-2742C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231376841 | |||||||
| chr1:231376847 | T | C | 155 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.892-2748A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231376847 | |||||||
| chr1:231376913 | C | T | 1 | a0001c0001t0016g0319 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.892-2814G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231376913 | |||||||
| chr1:231377022 | C | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-2923G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231377022 | |||||||
| chr1:231377025 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-2926C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231377025 | |||||||
| chr1:231377076 | A | T | 3 | a0001c0001t0001g0137 a0001c0001t0001g0166 a0001c0001t0001g0171 |
3 | HG00099.hp2 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.892-2977T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231377076 | |||||||
| chr1:231377078 | T | C | 1 | a0001c0001t0002g0209 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.892-2979A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231377078 | |||||||
| chr1:231377179 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-3080T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231377179 | |||||||
| chr1:231377314 | T | C | 2 | a0001c0001t0002g0255 a0006c0007t0002g0306 |
2 | HG02132.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.892-3215A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231377314 | |||||||
| chr1:231377378 | T | C | 1 | a0001c0001t0002g0236 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.892-3279A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231377378 | |||||||
| chr1:231377389 | G | A | 1 | a0001c0001t0002g0206 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.892-3290C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231377389 | |||||||
| chr1:231377444 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-3345C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231377444 | |||||||
| chr1:231377478 | G | C | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.892-3379C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231377478 | |||||||
| chr1:231377685 | C | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-3586G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231377685 | |||||||
| chr1:231377736 | A | G | 1 | a0001c0001t0002g0218 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.892-3637T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231377736 | |||||||
| chr1:231377855 | A | G | 7 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(4): Show |
8 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.892-3756T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231377855 | |||||||
| chr1:231377883 | TC | T | 20 | a0001c0001t0002g0039 a0001c0001t0002g0067 a0001c0001t0003g0001 others(17): Show |
22 | HG00099.hp1 HG01175.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.892-3785delG | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231377883 | |||||||
| chr1:231377907 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-3808A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231377907 | |||||||
| chr1:231377939 | A | C | 1 | a0001c0001t0001g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.892-3840T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231377939 | |||||||
| chr1:231377993 | G | A | 1 | a0001c0001t0002g0276 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.892-3894C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231377993 | |||||||
| chr1:231378165 | C | T | 1 | a0001c0001t0005g0296 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.892-4066G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231378165 | |||||||
| chr1:231378219 | A | G | 2 | a0001c0001t0002g0237 a0001c0001t0002g0238 |
2 | HG01243.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.892-4120T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231378219 | |||||||
| chr1:231378233 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-4134T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231378233 | |||||||
| chr1:231378237 | A | G | 3 | a0001c0001t0002g0228 a0001c0001t0002g0230 a0001c0001t0002g0235 |
3 | NA18941.hp2 NA18964.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.892-4138T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231378237 | |||||||
| chr1:231378247 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-4148A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231378247 | |||||||
| chr1:231378340 | T | G | 7 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(4): Show |
8 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.892-4241A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231378340 | |||||||
| chr1:231378446 | T | C | 1 | a0001c0001t0007g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.892-4347A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231378446 | |||||||
| chr1:231378472 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-4373G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231378472 | |||||||
| chr1:231378497 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-4398G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231378497 | |||||||
| chr1:231378575 | C | T | 5 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0007g0078 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.892-4476G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231378575 | |||||||
| chr1:231378762 | G | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.892-4663C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231378762 | |||||||
| chr1:231378789 | C | CA | 41 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0048 others(38): Show |
43 | HG00642.hp1 HG00741.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.892-4691dupT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231378789 | |||||||
| chr1:231378821 | C | T | 155 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.892-4722G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231378821 | |||||||
| chr1:231378935 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-4836C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231378935 | |||||||
| chr1:231379060 | G | A | 167 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(164): Show |
178 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.892-4961C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231379060 | |||||||
| chr1:231379078 | T | C | 2 | a0001c0001t0002g0024 a0001c0001t0002g0240 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.892-4979A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231379078 | |||||||
| chr1:231379083 | G | A | 155 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.892-4984C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231379083 | |||||||
| chr1:231379166 | C | G | 1 | a0001c0001t0002g0083 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.892-5067G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231379166 | |||||||
| chr1:231379196 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-5097T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231379196 | |||||||
| chr1:231379234 | A | G | 17 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.892-5135T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231379234 | |||||||
| chr1:231379257 | T | G | 1 | a0001c0001t0002g0030 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.892-5158A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231379257 | |||||||
| chr1:231379400 | G | A | 16 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(13): Show |
17 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.892-5301C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231379400 | |||||||
| chr1:231379455 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-5356G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231379455 | |||||||
| chr1:231379813 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-5714G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231379813 | |||||||
| chr1:231379863 | G | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0131 |
3 | HG00597.hp1 HG02074.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.892-5764C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231379863 | |||||||
| chr1:231379958 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.892-5859A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231379958 | |||||||
| chr1:231380023 | C | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0179 |
2 | HG00408.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.892-5924G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380023 | |||||||
| chr1:231380057 | T | TGA | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-5959_892-5958i others(4): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380057 | |||||||
| chr1:231380114 | G | A | 1 | a0001c0001t0017g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.892-6015C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380114 | |||||||
| chr1:231380133 | G | A | 6 | a0001c0001t0008g0031 a0001c0001t0008g0033 a0001c0001t0008g0036 others(3): Show |
6 | HG02257.hp1 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.892-6034C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380133 | |||||||
| chr1:231380142 | CCA | C | 6 | a0001c0001t0001g0099 a0001c0001t0001g0103 a0001c0001t0001g0105 others(3): Show |
6 | NA18954.hp1 NA18954.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.892-6045_892-6044d others(4): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380142 | |||||||
| chr1:231380233 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.892-6134C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380233 | |||||||
| chr1:231380263 | C | T | 1 | a0001c0001t0002g0257 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.892-6164G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380263 | |||||||
| chr1:231380264 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.892-6165C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380264 | |||||||
| chr1:231380271 | G | A | 16 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(13): Show |
17 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.892-6172C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380271 | |||||||
| chr1:231380288 | C | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
142 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.892-6189G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380288 | |||||||
| chr1:231380294 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.892-6195G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380294 | |||||||
| chr1:231380315 | C | CAAA | 131 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
141 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.892-6219_892-6217d others(5): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380315 | |||||||
| chr1:231380315 | CA | C | 16 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(13): Show |
17 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.892-6217delT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380315 | |||||||
| chr1:231380348 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.892-6249G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380348 | |||||||
| chr1:231380434 | G | T | 1 | a0001c0001t0002g0083 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.892-6335C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380434 | |||||||
| chr1:231380461 | T | C | 3 | a0001c0001t0010g0073 a0001c0001t0010g0278 a0001c0001t0010g0279 |
3 | HG02257.hp2 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.892-6362A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380461 | |||||||
| chr1:231380464 | G | GTGTA | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-6366_892-6365i others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380464 | |||||||
| chr1:231380479 | A | T | 2 | a0001c0001t0002g0085 a0001c0001t0002g0086 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.892-6380T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380479 | |||||||
| chr1:231380485 | A | C | 12 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0025 others(9): Show |
12 | HG00741.hp2 HG02523.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.892-6386T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380485 | |||||||
| chr1:231380501 | A | AGATT | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-6403_892-6402i others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380501 | |||||||
| chr1:231380687 | A | G | 1 | a0001c0001t0002g0223 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.892-6588T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380687 | |||||||
| chr1:231380704 | G | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-6605C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380704 | |||||||
| chr1:231380832 | T | C | 1 | a0001c0001t0002g0227 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.892-6733A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380832 | |||||||
| chr1:231380961 | C | A | 2 | a0001c0001t0002g0070 a0001c0001t0002g0071 |
2 | HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.892-6862G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380961 | |||||||
| chr1:231380998 | C | T | 1 | a0001c0001t0014g0094 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.892-6899G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231380998 | |||||||
| chr1:231381010 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-6911A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231381010 | |||||||
| chr1:231381109 | G | A | 16 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(13): Show |
17 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.892-7010C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231381109 | |||||||
| chr1:231381230 | T | C | 2 | a0001c0001t0014g0094 a0001c0001t0014g0095 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.892-7131A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231381230 | |||||||
| chr1:231381489 | A | G | 1 | a0001c0001t0002g0240 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.892-7390T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231381489 | |||||||
| chr1:231381515 | C | A | 1 | a0001c0001t0002g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.892-7416G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231381515 | |||||||
| chr1:231381528 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.892-7429G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231381528 | |||||||
| chr1:231381662 | T | C | 2 | a0001c0001t0002g0256 a0002c0002t0027g0315 |
2 | HG00423.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.892-7563A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231381662 | |||||||
| chr1:231381692 | G | A | 317 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(314): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.892-7593C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231381692 | |||||||
| chr1:231381806 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-7707A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231381806 | |||||||
| chr1:231381832 | G | C | 1 | a0001c0001t0002g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.892-7733C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231381832 | |||||||
| chr1:231381949 | C | T | 1 | a0005c0005t0001g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.892-7850G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231381949 | |||||||
| chr1:231382019 | C | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-7920G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231382019 | |||||||
| chr1:231382108 | A | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-8009T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231382108 | |||||||
| chr1:231382212 | T | C | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.892-8113A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231382212 | |||||||
| chr1:231382270 | C | T | 16 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(13): Show |
17 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.892-8171G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231382270 | |||||||
| chr1:231382319 | G | A | 1 | a0001c0001t0006g0283 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.892-8220C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231382319 | |||||||
| chr1:231382384 | AATC | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(1): Show |
5 | HG02258.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-8288_892-8286d others(5): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231382384 | |||||||
| chr1:231382477 | A | T | 1 | a0001c0001t0002g0242 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.892-8378T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231382477 | |||||||
| chr1:231382795 | A | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
142 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.892-8696T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231382795 | |||||||
| chr1:231382795 | A | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(3): Show |
7 | HG02258.hp1 HG02735.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-8696T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231382795 | |||||||
| chr1:231382823 | C | A | 1 | a0001c0001t0005g0296 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.892-8724G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231382823 | |||||||
| chr1:231382824 | G | A | 1 | a0001c0001t0002g0233 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.892-8725C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231382824 | |||||||
| chr1:231382835 | A | G | 16 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(13): Show |
17 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.892-8736T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231382835 | |||||||
| chr1:231382919 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-8820C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231382919 | |||||||
| chr1:231382922 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(1): Show |
5 | HG02258.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-8823C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231382922 | |||||||
| chr1:231382930 | C | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
142 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.892-8831G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231382930 | |||||||
| chr1:231382958 | T | C | 2 | a0001c0001t0011g0289 a0001c0001t0011g0290 |
2 | HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.892-8859A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231382958 | |||||||
| chr1:231382980 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.892-8881G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231382980 | |||||||
| chr1:231382989 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-8890A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231382989 | |||||||
| chr1:231383057 | C | CA | 52 | a0001c0001t0001g0028 a0001c0001t0002g0013 a0001c0001t0002g0026 others(49): Show |
54 | HG00558.hp1 HG01071.hp1 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.892-8959dupT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383057 | |||||||
| chr1:231383057 | C | CAA | 8 | a0001c0001t0001g0029 a0001c0001t0002g0202 a0001c0001t0002g0213 others(5): Show |
8 | HG00597.hp2 HG00621.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.892-8960_892-8959d others(4): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383057 | |||||||
| chr1:231383057 | C | CAAAAAAA others(4): Show |
1 | a0001c0006t0001g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.892-8969_892-8959d others(13): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383057 | |||||||
| chr1:231383057 | CA | C | 12 | a0001c0001t0002g0044 a0001c0001t0002g0046 a0001c0001t0002g0083 others(9): Show |
12 | HG00323.hp2 HG01243.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.892-8959delT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383057 | |||||||
| chr1:231383057 | CAAAAAAA | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(8): Show |
12 | HG00140.hp1 HG01884.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.892-8965_892-8959d others(9): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383057 | |||||||
| chr1:231383057 | CAAAAAAA others(1): Show |
C | 126 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(123): Show |
135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.892-8966_892-8959d others(10): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383057 | |||||||
| chr1:231383057 | CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0001g0123 a0001c0001t0001g0155 a0001c0001t0001g0159 others(3): Show |
6 | HG00323.hp1 HG01943.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.892-8967_892-8959d others(11): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383057 | |||||||
| chr1:231383057 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.892-8968_892-8959d others(12): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383057 | |||||||
| chr1:231383057 | CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0002g0025 a0001c0001t0002g0027 a0001c0001t0002g0040 |
3 | HG02622.hp2 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.892-8971_892-8959d others(15): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383057 | |||||||
| chr1:231383182 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-9083C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383182 | |||||||
| chr1:231383390 | G | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.892-9291C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383390 | |||||||
| chr1:231383412 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.892-9313C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383412 | |||||||
| chr1:231383435 | G | C | 1 | a0001c0001t0002g0231 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.892-9336C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383435 | |||||||
| chr1:231383473 | G | A | 2 | a0001c0001t0014g0094 a0001c0001t0014g0095 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.892-9374C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383473 | |||||||
| chr1:231383500 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.892-9401C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383500 | |||||||
| chr1:231383502 | C | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-9403G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383502 | |||||||
| chr1:231383563 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.892-9464C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383563 | |||||||
| chr1:231383563 | G | T | 1 | a0001c0001t0002g0225 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.892-9464C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383563 | |||||||
| chr1:231383584 | C | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.892-9485G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383584 | |||||||
| chr1:231383585 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-9486T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383585 | |||||||
| chr1:231383817 | C | T | 1 | a0001c0001t0002g0259 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.892-9718G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383817 | |||||||
| chr1:231383931 | T | C | 2 | a0001c0001t0002g0260 a0001c0001t0002g0273 |
2 | NA19012.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.892-9832A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231383931 | |||||||
| chr1:231384058 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-9959T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231384058 | |||||||
| chr1:231384070 | T | C | 155 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.892-9971A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231384070 | |||||||
| chr1:231384096 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-9997T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231384096 | |||||||
| chr1:231384257 | G | C | 1 | a0001c0001t0002g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.892-10158C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231384257 | |||||||
| chr1:231384260 | C | G | 16 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(13): Show |
17 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.892-10161G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231384260 | |||||||
| chr1:231384358 | C | A | 1 | a0001c0001t0002g0040 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.892-10259G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231384358 | |||||||
| chr1:231384405 | G | GA | 131 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
140 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.892-10307dupT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231384405 | |||||||
| chr1:231384494 | C | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-10395G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231384494 | |||||||
| chr1:231384533 | A | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-10434T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231384533 | |||||||
| chr1:231384708 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.892-10609C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231384708 | |||||||
| chr1:231384747 | G | T | 1 | a0001c0001t0010g0278 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.892-10648C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231384747 | |||||||
| chr1:231384770 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0001g0054 others(2): Show |
6 | HG02040.hp1 NA18948.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.892-10671G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231384770 | |||||||
| chr1:231384777 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-10678A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231384777 | |||||||
| chr1:231385056 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-10957T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231385056 | |||||||
| chr1:231385128 | C | T | 138 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
148 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.892-11029G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231385128 | |||||||
| chr1:231385140 | A | T | 16 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(13): Show |
17 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.892-11041T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231385140 | |||||||
| chr1:231385165 | T | G | 1 | a0004c0004t0002g0020 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.892-11066A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231385165 | |||||||
| chr1:231385173 | G | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(1): Show |
5 | HG02258.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-11074C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231385173 | |||||||
| chr1:231385216 | T | A | 1 | a0001c0006t0001g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.892-11117A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231385216 | |||||||
| chr1:231385313 | G | A | 1 | a0001c0001t0007g0078 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.892-11214C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231385313 | |||||||
| chr1:231385353 | G | A | 1 | a0001c0001t0008g0031 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.892-11254C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231385353 | |||||||
| chr1:231385403 | T | A | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.892-11304A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231385403 | |||||||
| chr1:231385404 | T | G | 1 | a0004c0004t0002g0020 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.892-11305A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231385404 | |||||||
| chr1:231385732 | C | T | 167 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(164): Show |
178 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.892-11633G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231385732 | |||||||
| chr1:231385733 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.892-11634A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231385733 | |||||||
| chr1:231385751 | T | C | 6 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0007g0078 others(3): Show |
6 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.892-11652A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231385751 | |||||||
| chr1:231385882 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.892-11783C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231385882 | |||||||
| chr1:231385894 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.892-11795A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231385894 | |||||||
| chr1:231386030 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.892-11931C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231386030 | |||||||
| chr1:231386032 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-11933G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231386032 | |||||||
| chr1:231386108 | G | A | 2 | a0001c0006t0001g0292 a0005c0005t0001g0022 |
2 | HG02258.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.892-12009C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231386108 | |||||||
| chr1:231386117 | G | GT | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-12019dupA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231386117 | |||||||
| chr1:231386225 | C | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-12126G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231386225 | |||||||
| chr1:231386351 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-12252A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231386351 | |||||||
| chr1:231386385 | A | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0133 |
3 | HG00544.hp1 HG00558.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.892-12286T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231386385 | |||||||
| chr1:231386553 | CTTAA | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-12458_892-1245 others(8): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231386553 | |||||||
| chr1:231386720 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.892-12621A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231386720 | |||||||
| chr1:231386743 | T | C | 2 | a0001c0001t0006g0128 a0001c0001t0006g0154 |
2 | NA18942.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.892-12644A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231386743 | |||||||
| chr1:231386823 | C | T | 17 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.892-12724G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231386823 | |||||||
| chr1:231386847 | A | C | 1 | a0001c0001t0002g0254 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.892-12748T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231386847 | |||||||
| chr1:231386863 | T | C | 1 | a0001c0001t0005g0296 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.892-12764A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231386863 | |||||||
| chr1:231386988 | A | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
142 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.892-12889T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231386988 | |||||||
| chr1:231386994 | C | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.892-12895G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231386994 | |||||||
| chr1:231387211 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.892-13112T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387211 | |||||||
| chr1:231387236 | T | TAC | 6 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(3): Show |
7 | HG02258.hp1 HG02735.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-13139_892-1313 others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387236 | |||||||
| chr1:231387236 | T | TACAC | 120 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
129 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.892-13141_892-1313 others(8): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387236 | |||||||
| chr1:231387236 | T | TACACAC | 11 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0113 others(8): Show |
11 | HG00323.hp1 HG01071.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.892-13143_892-1313 others(10): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387236 | |||||||
| chr1:231387236 | TAC | T | 12 | a0001c0001t0005g0293 a0001c0001t0005g0296 a0001c0001t0007g0076 others(9): Show |
12 | HG01884.hp1 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.892-13139_892-1313 others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387236 | |||||||
| chr1:231387255 | ACC | A | 6 | a0001c0001t0001g0112 a0001c0001t0005g0014 a0001c0001t0005g0291 others(3): Show |
7 | HG02055.hp1 HG02486.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.892-13158_892-1315 others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387255 | |||||||
| chr1:231387257 | C | A | 183 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
196 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.892-13158G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387257 | |||||||
| chr1:231387259 | C | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-13160G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387259 | |||||||
| chr1:231387360 | A | AT | 21 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0037 others(18): Show |
23 | HG00597.hp2 HG00621.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.892-13262dupA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387360 | |||||||
| chr1:231387360 | AT | A | 19 | a0001c0001t0002g0013 a0001c0001t0002g0266 a0001c0001t0005g0014 others(16): Show |
21 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.892-13262delA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387360 | |||||||
| chr1:231387383 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-13284C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387383 | |||||||
| chr1:231387429 | G | A | 3 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0002g0245 |
3 | HG02735.hp1 NA18944.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.892-13330C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387429 | |||||||
| chr1:231387452 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-13353G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387452 | |||||||
| chr1:231387460 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-13361A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387460 | |||||||
| chr1:231387464 | A | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-13365T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387464 | |||||||
| chr1:231387517 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.892-13418C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387517 | |||||||
| chr1:231387521 | G | A | 1 | a0001c0001t0002g0223 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.892-13422C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387521 | |||||||
| chr1:231387533 | G | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(1): Show |
5 | HG02258.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-13434C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387533 | |||||||
| chr1:231387558 | G | C | 7 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(4): Show |
8 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.892-13459C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387558 | |||||||
| chr1:231387601 | T | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(3): Show |
7 | HG02258.hp1 HG02735.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-13502A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387601 | |||||||
| chr1:231387610 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(3): Show |
7 | HG02258.hp1 HG02735.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-13511G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387610 | |||||||
| chr1:231387675 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-13576C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387675 | |||||||
| chr1:231387978 | G | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-13879C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387978 | |||||||
| chr1:231387996 | C | T | 17 | a0001c0001t0002g0130 a0001c0001t0002g0218 a0001c0001t0002g0221 others(14): Show |
17 | HG00544.hp2 HG01934.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.892-13897G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231387996 | |||||||
| chr1:231388011 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-13912C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388011 | |||||||
| chr1:231388062 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-13963T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388062 | |||||||
| chr1:231388076 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.892-13977A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388076 | |||||||
| chr1:231388136 | A | T | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.892-14037T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388136 | |||||||
| chr1:231388275 | A | AAATT | 136 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
145 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.892-14180_892-1417 others(8): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388275 | |||||||
| chr1:231388275 | A | AAATTAAT others(244): Show |
3 | a0001c0001t0001g0005 a0001c0001t0001g0115 a0001c0001t0001g0117 |
4 | HG00741.hp1 HG01070.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.892-14177_892-1417 others(255): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388275 | |||||||
| chr1:231388281 | A | C | 2 | a0001c0001t0002g0039 a0001c0001t0003g0038 |
2 | HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.892-14182T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388281 | |||||||
| chr1:231388375 | T | G | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.892-14276A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388375 | |||||||
| chr1:231388421 | C | T | 2 | a0001c0001t0004g0285 a0001c0001t0004g0287 |
2 | NA18975.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.892-14322G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388421 | |||||||
| chr1:231388482 | G | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-14383C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388482 | |||||||
| chr1:231388550 | C | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.892-14451G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388550 | |||||||
| chr1:231388567 | G | A | 2 | a0001c0001t0002g0221 a0001c0001t0002g0274 |
2 | HG03491.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.892-14468C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388567 | |||||||
| chr1:231388650 | TTTG | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-14554_892-1455 others(7): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388650 | |||||||
| chr1:231388741 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-14642C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388741 | |||||||
| chr1:231388757 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-14658G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388757 | |||||||
| chr1:231388788 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-14689C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388788 | |||||||
| chr1:231388799 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-14700G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388799 | |||||||
| chr1:231388804 | A | G | 156 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.892-14705T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388804 | |||||||
| chr1:231388808 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.892-14709G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388808 | |||||||
| chr1:231388847 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-14748T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388847 | |||||||
| chr1:231388913 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-14814G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231388913 | |||||||
| chr1:231389326 | A | G | 17 | a0001c0001t0002g0039 a0001c0001t0003g0001 a0001c0001t0003g0002 others(14): Show |
19 | HG00099.hp1 HG01175.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.892-15227T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231389326 | |||||||
| chr1:231389406 | GA | G | 4 | a0001c0001t0001g0103 a0001c0001t0001g0114 a0001c0001t0001g0155 others(1): Show |
4 | HG01517.hp2 HG01943.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.892-15308delT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231389406 | |||||||
| chr1:231389412 | A | T | 135 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(132): Show |
145 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.892-15313T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231389412 | |||||||
| chr1:231389413 | A | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-15314T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231389413 | |||||||
| chr1:231389414 | A | AT | 17 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.892-15316dupA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231389414 | |||||||
| chr1:231389414 | A | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-15315T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231389414 | |||||||
| chr1:231389714 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.892-15615G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231389714 | |||||||
| chr1:231389820 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-15721G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231389820 | |||||||
| chr1:231389853 | C | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-15754G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231389853 | |||||||
| chr1:231389966 | A | C | 7 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(4): Show |
8 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.892-15867T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231389966 | |||||||
| chr1:231390062 | C | A | 1 | a0001c0001t0017g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.892-15963G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390062 | |||||||
| chr1:231390254 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-16155G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390254 | |||||||
| chr1:231390304 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.892-16205C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390304 | |||||||
| chr1:231390321 | C | A | 2 | a0001c0001t0002g0221 a0001c0001t0002g0274 |
2 | HG03491.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.892-16222G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390321 | |||||||
| chr1:231390334 | T | C | 2 | a0001c0001t0001g0105 a0001c0001t0012g0104 |
2 | NA18954.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.892-16235A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390334 | |||||||
| chr1:231390492 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-16393C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390492 | |||||||
| chr1:231390497 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-16398T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390497 | |||||||
| chr1:231390551 | C | T | 2 | a0001c0001t0002g0039 a0001c0001t0003g0038 |
2 | HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.892-16452G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390551 | |||||||
| chr1:231390707 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.892-16608G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390707 | |||||||
| chr1:231390729 | G | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(1): Show |
5 | HG02258.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-16630C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390729 | |||||||
| chr1:231390735 | A | G | 1 | a0001c0001t0002g0083 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.892-16636T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390735 | |||||||
| chr1:231390744 | G | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.892-16645C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390744 | |||||||
| chr1:231390811 | T | C | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.892-16712A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390811 | |||||||
| chr1:231390853 | A | AT | 29 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(26): Show |
30 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.892-16755dupA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390853 | |||||||
| chr1:231390853 | AT | A | 135 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(132): Show |
145 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.892-16755delA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390853 | |||||||
| chr1:231390853 | ATT | A | 6 | a0001c0001t0001g0105 a0001c0001t0001g0111 a0001c0001t0001g0299 others(3): Show |
6 | HG02735.hp1 HG03195.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.892-16756_892-1675 others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390853 | |||||||
| chr1:231390922 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0173 |
2 | NA18965.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.892-16823T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390922 | |||||||
| chr1:231390930 | G | A | 1 | a0001c0001t0004g0286 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.892-16831C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390930 | |||||||
| chr1:231390950 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-16851G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390950 | |||||||
| chr1:231390972 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-16873A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390972 | |||||||
| chr1:231390993 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.892-16894C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390993 | |||||||
| chr1:231390994 | C | A | 1 | a0001c0001t0002g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.892-16895G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231390994 | |||||||
| chr1:231391019 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-16920G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391019 | |||||||
| chr1:231391051 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-16952G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391051 | |||||||
| chr1:231391053 | C | CGT | 7 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(4): Show |
8 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.892-16956_892-1695 others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391053 | |||||||
| chr1:231391063 | T | TGTGAGAG others(142): Show |
1 | a0001c0001t0001g0145 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.892-16965_892-1696 others(153): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391063 | |||||||
| chr1:231391063 | T | TGTGTGAG others(1): Show |
66 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(63): Show |
71 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.892-16965_892-1696 others(12): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391063 | |||||||
| chr1:231391063 | T | TGTGTGAG others(132): Show |
1 | a0001c0001t0001g0124 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.892-16965_892-1696 others(143): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391063 | |||||||
| chr1:231391063 | T | TGTGTGAG others(138): Show |
1 | a0001c0001t0001g0180 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.892-16965_892-1696 others(149): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391063 | |||||||
| chr1:231391063 | T | TGTGTGAG others(140): Show |
2 | a0001c0001t0001g0119 a0001c0001t0001g0163 |
2 | HG02630.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.892-16965_892-1696 others(151): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391063 | |||||||
| chr1:231391063 | T | TGTGTGAG others(140): Show |
1 | a0001c0001t0001g0053 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.892-16965_892-1696 others(151): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391063 | |||||||
| chr1:231391063 | T | TGTGTGAG others(142): Show |
1 | a0001c0001t0001g0122 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.892-16965_892-1696 others(153): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391063 | |||||||
| chr1:231391063 | T | TGTGTGAG others(142): Show |
42 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(39): Show |
46 | HG01071.hp2 HG01099.hp1 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.892-16965_892-1696 others(153): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391063 | |||||||
| chr1:231391063 | T | TGTGTGAG others(144): Show |
21 | a0001c0001t0001g0062 a0001c0001t0001g0109 a0001c0001t0001g0129 others(18): Show |
21 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.892-16965_892-1696 others(155): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391063 | |||||||
| chr1:231391063 | T | TGTGTGAG others(146): Show |
1 | a0001c0001t0001g0015 | 2 | HG02486.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.892-16965_892-1696 others(157): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391063 | |||||||
| chr1:231391063 | T | TGTGTGAG others(148): Show |
1 | a0001c0001t0001g0172 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.892-16965_892-1696 others(159): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391063 | |||||||
| chr1:231391063 | T | TGTGTGAG others(144): Show |
1 | a0001c0001t0001g0300 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.892-16965_892-1696 others(155): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391063 | |||||||
| chr1:231391083 | G | GGTGTGTG others(122): Show |
1 | a0001c0001t0001g0108 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.892-16985_892-1698 others(133): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391083 | |||||||
| chr1:231391083 | G | GGTGTGTG others(126): Show |
1 | a0001c0001t0001g0136 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.892-16985_892-1698 others(137): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391083 | |||||||
| chr1:231391083 | G | GGTGTGTG others(126): Show |
1 | a0001c0001t0001g0135 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.892-16985_892-1698 others(137): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391083 | |||||||
| chr1:231391083 | G | GGTGTGTG others(124): Show |
13 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0054 others(10): Show |
14 | HG01257.hp1 HG01258.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.892-16985_892-1698 others(135): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391083 | |||||||
| chr1:231391083 | G | GGTGTGTG others(126): Show |
3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG02027.hp1 NA18956.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.892-16985_892-1698 others(137): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391083 | |||||||
| chr1:231391083 | G | GGTGTGTG others(126): Show |
12 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0107 others(9): Show |
13 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(10): Show |
intron_variant | MODIFIER | c.892-16985_892-1698 others(137): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391083 | |||||||
| chr1:231391083 | G | GGTGTGTG others(128): Show |
11 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0060 others(8): Show |
13 | HG00597.hp1 HG02040.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.892-16985_892-1698 others(139): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391083 | |||||||
| chr1:231391083 | G | GGTGTGTG others(129): Show |
1 | a0001c0001t0001g0164 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.892-16985_892-1698 others(140): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391083 | |||||||
| chr1:231391083 | G | GGTGTGTG others(128): Show |
3 | a0001c0001t0001g0196 a0001c0001t0001g0298 a0001c0001t0009g0192 |
3 | HG03130.hp1 HG03540.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.892-16985_892-1698 others(139): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391083 | |||||||
| chr1:231391083 | G | GGTGTGTG others(130): Show |
4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
4 | HG02451.hp1 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.892-16985_892-1698 others(141): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391083 | |||||||
| chr1:231391083 | G | GGTGTGTG others(128): Show |
1 | a0001c0001t0001g0101 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.892-16985_892-1698 others(139): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391083 | |||||||
| chr1:231391083 | G | GGTGTGTG others(130): Show |
1 | a0001c0001t0016g0320 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.892-16985_892-1698 others(141): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391083 | |||||||
| chr1:231391083 | G | GGTGTGTG others(134): Show |
1 | a0001c0001t0001g0120 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.892-16985_892-1698 others(145): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391083 | |||||||
| chr1:231391083 | G | GT | 7 | a0001c0001t0002g0030 a0001c0001t0002g0198 a0001c0001t0002g0222 others(4): Show |
7 | HG02615.hp2 HG02738.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-16985dupA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391083 | |||||||
| chr1:231391083 | G | GTT | 10 | a0001c0001t0002g0017 a0001c0001t0002g0046 a0001c0001t0002g0069 others(7): Show |
11 | HG00140.hp2 HG01934.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.892-16986_892-1698 others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391083 | |||||||
| chr1:231391083 | GTT | G | 22 | a0001c0001t0001g0062 a0001c0001t0001g0097 a0001c0001t0001g0146 others(19): Show |
22 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(19): Show |
intron_variant | MODIFIER | c.892-16986_892-1698 others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391083 | |||||||
| chr1:231391083 | GTTTT | G | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(44): Show |
52 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.892-16988_892-1698 others(8): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391083 | |||||||
| chr1:231391084 | T | A | 21 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0049 others(18): Show |
23 | HG00140.hp1 HG00597.hp1 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.892-16985A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391084 | |||||||
| chr1:231391084 | T | G | 8 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0114 others(5): Show |
8 | HG00642.hp2 HG01106.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.892-16985A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391084 | |||||||
| chr1:231391084 | T | TTGTGTGT others(132): Show |
1 | a0001c0001t0001g0299 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.892-16986_892-1698 others(143): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391084 | |||||||
| chr1:231391085 | T | C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0048 others(28): Show |
33 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.892-16986A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391085 | |||||||
| chr1:231391085 | T | TGTGTGTG others(127): Show |
1 | a0001c0001t0006g0150 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.892-16987_892-1698 others(138): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391085 | |||||||
| chr1:231391085 | T | TGTGTGTG others(132): Show |
3 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 |
3 | HG02258.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.892-16987_892-1698 others(143): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391085 | |||||||
| chr1:231391085 | T | TGTGTGTG others(134): Show |
1 | a0001c0001t0001g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.892-16987_892-1698 others(145): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391085 | |||||||
| chr1:231391085 | T | TGTGTGTG others(140): Show |
1 | a0007c0008t0001g0311 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.892-16987_892-1698 others(151): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391085 | |||||||
| chr1:231391086 | T | A | 35 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(32): Show |
38 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.892-16987A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391086 | |||||||
| chr1:231391086 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.892-16987A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391086 | |||||||
| chr1:231391086 | T | G | 15 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0114 others(12): Show |
15 | HG01106.hp2 HG01517.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.892-16987A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391086 | |||||||
| chr1:231391086 | T | TTGTGTGT others(3): Show |
1 | a0005c0005t0001g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.892-16988_892-1698 others(14): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391086 | |||||||
| chr1:231391086 | TTTTTTTT others(3): Show |
T | 1 | a0001c0001t0005g0293 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.892-16997_892-1698 others(14): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391086 | |||||||
| chr1:231391087 | T | C | 22 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0049 others(19): Show |
24 | HG00140.hp1 HG00597.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.892-16988A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391087 | |||||||
| chr1:231391088 | T | C | 1 | a0001c0001t0006g0150 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.892-16989A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391088 | |||||||
| chr1:231391088 | T | G | 52 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0062 others(49): Show |
52 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.892-16989A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391088 | |||||||
| chr1:231391088 | T | TTG | 19 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0255 others(16): Show |
21 | HG00423.hp2 HG02132.hp1 HG03490.hp2 others(18): Show |
intron_variant | MODIFIER | c.892-16990_892-1698 others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391088 | |||||||
| chr1:231391088 | T | TTGTG | 6 | a0001c0001t0002g0071 a0001c0001t0002g0259 a0001c0001t0002g0260 others(3): Show |
6 | HG03491.hp1 HG03492.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.892-16990_892-1698 others(8): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391088 | |||||||
| chr1:231391088 | T | TTGTGTGT others(5): Show |
1 | a0002c0002t0002g0316 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.892-16990_892-1698 others(16): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391088 | |||||||
| chr1:231391088 | TTTTTTGT others(3): Show |
T | 1 | a0002c0002t0002g0313 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.892-16999_892-1699 others(14): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391088 | |||||||
| chr1:231391089 | T | C | 35 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(32): Show |
38 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.892-16990A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391089 | |||||||
| chr1:231391089 | T | G | 22 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0049 others(19): Show |
24 | HG00140.hp1 HG00597.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.892-16990A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391089 | |||||||
| chr1:231391090 | T | G | 123 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(120): Show |
130 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.892-16991A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391090 | |||||||
| chr1:231391091 | T | G | 35 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(32): Show |
38 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.892-16992A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391091 | |||||||
| chr1:231391092 | T | G | 151 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(148): Show |
160 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.892-16993A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391092 | |||||||
| chr1:231391092 | T | TTG | 13 | a0001c0001t0002g0067 a0001c0001t0002g0130 a0001c0001t0002g0220 others(10): Show |
13 | HG00099.hp1 HG00544.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.892-16995_892-1699 others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391092 | |||||||
| chr1:231391092 | T | TTGTG | 9 | a0001c0001t0002g0213 a0001c0001t0002g0225 a0001c0001t0002g0226 others(6): Show |
9 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.892-16997_892-1699 others(8): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391092 | |||||||
| chr1:231391092 | T | TTTTG | 7 | a0001c0001t0002g0241 a0001c0001t0002g0304 a0001c0001t0029g0318 others(4): Show |
7 | HG01099.hp2 HG01106.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.892-16994_892-1699 others(8): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391092 | |||||||
| chr1:231391092 | T | TTTTTGTG others(8): Show |
1 | a0001c0001t0014g0095 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.892-16994_892-1699 others(19): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391092 | |||||||
| chr1:231391092 | T | TTTTTTGT others(5): Show |
1 | a0001c0001t0002g0093 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.892-16994_892-1699 others(16): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391092 | |||||||
| chr1:231391092 | TTGTGTGT others(5): Show |
T | 2 | a0001c0001t0004g0285 a0001c0001t0004g0287 |
2 | NA18975.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.892-17005_892-1699 others(16): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391092 | |||||||
| chr1:231391092 | TTGTGTGT others(7): Show |
T | 2 | a0001c0001t0002g0024 a0001c0001t0002g0240 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.892-17007_892-1699 others(18): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391092 | |||||||
| chr1:231391094 | G | GTGTGTGT others(120): Show |
1 | a0001c0001t0001g0114 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.892-16996_892-1699 others(131): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391094 | |||||||
| chr1:231391094 | G | GTGTGTGT others(122): Show |
1 | a0001c0001t0001g0052 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.892-16996_892-1699 others(133): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391094 | |||||||
| chr1:231391094 | G | GTGTGTGT others(124): Show |
2 | a0001c0001t0001g0116 a0001c0001t0012g0153 |
2 | HG01106.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.892-16996_892-1699 others(135): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391094 | |||||||
| chr1:231391094 | G | T | 48 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0004 others(45): Show |
51 | HG00558.hp1 HG00597.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.892-16995C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391094 | |||||||
| chr1:231391096 | G | GTGTGTGT others(120): Show |
2 | a0001c0001t0001g0059 a0001c0001t0020g0058 |
2 | NA19001.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.892-16998_892-1699 others(131): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391096 | |||||||
| chr1:231391096 | G | GTGTGTGT others(124): Show |
1 | a0001c0001t0001g0167 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.892-16998_892-1699 others(135): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391096 | |||||||
| chr1:231391096 | G | T | 20 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0030 others(17): Show |
21 | HG00558.hp1 HG01993.hp2 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.892-16997C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391096 | |||||||
| chr1:231391098 | G | T | 4 | a0001c0001t0002g0030 a0001c0001t0002g0040 a0001c0001t0010g0278 others(1): Show |
4 | HG02257.hp2 NA18906.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.892-16999C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391098 | |||||||
| chr1:231391133 | T | A | 19 | a0001c0001t0001g0112 a0001c0001t0001g0155 a0001c0001t0001g0156 others(16): Show |
20 | HG00099.hp2 HG01346.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.892-17034A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391133 | |||||||
| chr1:231391133 | T | TGA | 3 | a0001c0001t0007g0081 a0001c0001t0011g0289 a0001c0001t0011g0290 |
3 | HG02717.hp2 HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.892-17036_892-1703 others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391133 | |||||||
| chr1:231391133 | T | TGTGTGTG others(3): Show |
1 | a0001c0006t0001g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.892-17035_892-1703 others(14): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391133 | |||||||
| chr1:231391329 | C | T | 17 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.892-17230G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391329 | |||||||
| chr1:231391424 | C | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-17325G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391424 | |||||||
| chr1:231391468 | CTTCCT | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-17374_892-1737 others(9): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391468 | |||||||
| chr1:231391570 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-17471G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391570 | |||||||
| chr1:231391583 | T | C | 156 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.892-17484A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391583 | |||||||
| chr1:231391638 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(1): Show |
5 | HG02258.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-17539C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391638 | |||||||
| chr1:231391786 | T | C | 2 | a0001c0001t0014g0094 a0001c0001t0014g0095 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.892-17687A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231391786 | |||||||
| chr1:231392041 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-17942C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231392041 | |||||||
| chr1:231392059 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-17960C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231392059 | |||||||
| chr1:231392106 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0109 a0001c0001t0001g0115 others(1): Show |
5 | HG00642.hp1 HG00741.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-18007A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231392106 | |||||||
| chr1:231392203 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.892-18104G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231392203 | |||||||
| chr1:231392211 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-18112A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231392211 | |||||||
| chr1:231392265 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.892-18166G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231392265 | |||||||
| chr1:231392366 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-18267T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231392366 | |||||||
| chr1:231392656 | T | C | 17 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.892-18557A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231392656 | |||||||
| chr1:231392660 | G | T | 1 | a0001c0001t0001g0157 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.892-18561C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231392660 | |||||||
| chr1:231392669 | C | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-18570G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231392669 | |||||||
| chr1:231392684 | A | G | 17 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.892-18585T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231392684 | |||||||
| chr1:231392791 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.892-18692T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231392791 | |||||||
| chr1:231392866 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0298 |
3 | HG02486.hp1 HG02809.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.892-18767A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231392866 | |||||||
| chr1:231392892 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-18793T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231392892 | |||||||
| chr1:231392895 | C | A | 1 | a0001c0001t0005g0296 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.892-18796G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231392895 | |||||||
| chr1:231392956 | G | A | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG01257.hp1 HG01258.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.892-18857C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231392956 | |||||||
| chr1:231393142 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.892-19043C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231393142 | |||||||
| chr1:231393171 | G | GA | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-19073dupT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231393171 | |||||||
| chr1:231393247 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.892-19148C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231393247 | |||||||
| chr1:231393373 | TA | T | 5 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.892-19275delT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231393373 | |||||||
| chr1:231393387 | G | T | 17 | a0001c0001t0002g0039 a0001c0001t0003g0001 a0001c0001t0003g0002 others(14): Show |
19 | HG00099.hp1 HG01175.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.892-19288C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231393387 | |||||||
| chr1:231393437 | T | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-19338A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231393437 | |||||||
| chr1:231393542 | T | C | 17 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.892-19443A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231393542 | |||||||
| chr1:231393695 | C | T | 1 | a0001c0001t0002g0261 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.892-19596G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231393695 | |||||||
| chr1:231393697 | C | G | 5 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0009g0186 others(2): Show |
5 | NA18939.hp1 NA18950.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.892-19598G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231393697 | |||||||
| chr1:231393745 | A | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-19646T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231393745 | |||||||
| chr1:231393864 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-19765C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231393864 | |||||||
| chr1:231394013 | T | C | 1 | a0001c0001t0002g0236 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.892-19914A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394013 | |||||||
| chr1:231394082 | C | A | 1 | a0001c0001t0017g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.892-19983G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394082 | |||||||
| chr1:231394112 | C | T | 17 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.892-20013G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394112 | |||||||
| chr1:231394124 | T | A | 1 | a0001c0001t0002g0233 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.892-20025A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394124 | |||||||
| chr1:231394152 | T | C | 1 | a0001c0001t0002g0083 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.892-20053A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394152 | |||||||
| chr1:231394179 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-20080G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394179 | |||||||
| chr1:231394226 | T | C | 5 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.892-20127A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394226 | |||||||
| chr1:231394342 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.892-20243A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394342 | |||||||
| chr1:231394352 | C | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-20253G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394352 | |||||||
| chr1:231394382 | C | CTT | 136 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
146 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.892-20285_892-2028 others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394382 | |||||||
| chr1:231394383 | T | C | 2 | a0001c0001t0014g0094 a0001c0001t0014g0095 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.892-20284A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394383 | |||||||
| chr1:231394423 | G | C | 1 | a0001c0001t0002g0213 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.892-20324C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394423 | |||||||
| chr1:231394441 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-20342G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394441 | |||||||
| chr1:231394442 | A | G | 156 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.892-20343T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394442 | |||||||
| chr1:231394444 | T | A | 1 | a0001c0001t0013g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.892-20345A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394444 | |||||||
| chr1:231394503 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-20404G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394503 | |||||||
| chr1:231394527 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-20428G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394527 | |||||||
| chr1:231394545 | A | AT | 13 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0025 others(10): Show |
13 | HG00741.hp2 HG02056.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.892-20447dupA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394545 | |||||||
| chr1:231394545 | ATT | A | 24 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(21): Show |
25 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.892-20448_892-2044 others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394545 | |||||||
| chr1:231394545 | ATTTT | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-20450_892-2044 others(8): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394545 | |||||||
| chr1:231394669 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-20570T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394669 | |||||||
| chr1:231394680 | C | T | 1 | a0001c0001t0024g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.892-20581G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394680 | |||||||
| chr1:231394684 | T | C | 317 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(314): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.892-20585A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394684 | |||||||
| chr1:231394730 | G | T | 155 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.892-20631C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394730 | |||||||
| chr1:231394784 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.892-20685G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394784 | |||||||
| chr1:231394977 | A | G | 156 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.892-20878T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231394977 | |||||||
| chr1:231395067 | G | A | 1 | a0001c0001t0002g0238 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.892-20968C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231395067 | |||||||
| chr1:231395069 | G | A | 1 | a0001c0001t0002g0235 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.892-20970C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231395069 | |||||||
| chr1:231395229 | T | C | 2 | a0001c0001t0001g0059 a0001c0001t0020g0058 |
2 | NA19001.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.892-21130A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231395229 | |||||||
| chr1:231395363 | C | T | 1 | a0001c0001t0007g0078 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.892-21264G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231395363 | |||||||
| chr1:231395416 | CAA | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-21319_892-2131 others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231395416 | |||||||
| chr1:231395420 | C | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-21321G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231395420 | |||||||
| chr1:231395486 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-21387G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231395486 | |||||||
| chr1:231395546 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.892-21447T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231395546 | |||||||
| chr1:231395646 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-21547T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231395646 | |||||||
| chr1:231395719 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-21620G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231395719 | |||||||
| chr1:231395730 | T | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
142 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.892-21631A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231395730 | |||||||
| chr1:231395754 | G | T | 1 | a0001c0001t0001g0196 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.892-21655C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231395754 | |||||||
| chr1:231395775 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.892-21676A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231395775 | |||||||
| chr1:231395881 | T | C | 157 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.892-21782A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231395881 | |||||||
| chr1:231396030 | CT | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(124): Show |
136 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.892-21932delA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396030 | |||||||
| chr1:231396032 | T | TA | 4 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(1): Show |
5 | HG02258.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.892-21934_892-2193 others(5): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396032 | |||||||
| chr1:231396033 | T | A | 10 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0055 others(7): Show |
11 | HG02258.hp1 HG02735.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.892-21934A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396033 | |||||||
| chr1:231396039 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-21940C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396039 | |||||||
| chr1:231396186 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-22087T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396186 | |||||||
| chr1:231396202 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.892-22103G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396202 | |||||||
| chr1:231396249 | CT | C | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
150 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.892-22151delA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396249 | |||||||
| chr1:231396274 | T | C | 1 | a0001c0001t0008g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.892-22175A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396274 | |||||||
| chr1:231396274 | TTGG | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-22178_892-2217 others(7): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396274 | |||||||
| chr1:231396285 | C | T | 2 | a0001c0001t0002g0039 a0001c0001t0003g0038 |
2 | HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.892-22186G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396285 | |||||||
| chr1:231396398 | C | A | 1 | a0001c0001t0012g0153 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.892-22299G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396398 | |||||||
| chr1:231396407 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-22308G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396407 | |||||||
| chr1:231396438 | G | C | 7 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(4): Show |
7 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.892-22339C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396438 | |||||||
| chr1:231396530 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.892-22431C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396530 | |||||||
| chr1:231396541 | C | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
142 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.892-22442G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396541 | |||||||
| chr1:231396553 | C | T | 1 | a0001c0006t0001g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.892-22454G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396553 | |||||||
| chr1:231396566 | G | A | 254 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(251): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.892-22467C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396566 | |||||||
| chr1:231396605 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-22506A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396605 | |||||||
| chr1:231396740 | G | A | 4 | a0003c0003t0002g0307 a0003c0003t0002g0308 a0003c0003t0002g0309 others(1): Show |
4 | HG01123.hp1 HG01884.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.892-22641C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396740 | |||||||
| chr1:231396765 | A | G | 165 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(162): Show |
176 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.892-22666T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396765 | |||||||
| chr1:231396809 | T | C | 1 | a0001c0001t0002g0261 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.892-22710A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396809 | |||||||
| chr1:231396926 | ACTCT | A | 17 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.892-22831_892-2282 others(8): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396926 | |||||||
| chr1:231396975 | G | A | 17 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.892-22876C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396975 | |||||||
| chr1:231396979 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-22880G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396979 | |||||||
| chr1:231396980 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-22881T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231396980 | |||||||
| chr1:231397037 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-22938G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231397037 | |||||||
| chr1:231397272 | T | G | 6 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(3): Show |
6 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.892-23173A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231397272 | |||||||
| chr1:231397281 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-23182T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231397281 | |||||||
| chr1:231397354 | TA | T | 17 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.892-23256delT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231397354 | |||||||
| chr1:231397392 | G | A | 6 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0007g0078 others(3): Show |
6 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.892-23293C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231397392 | |||||||
| chr1:231397450 | C | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
142 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.892-23351G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231397450 | |||||||
| chr1:231397460 | A | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.892-23361T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231397460 | |||||||
| chr1:231397643 | A | AC | 11 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0025 others(8): Show |
11 | HG00741.hp2 HG02523.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.891+23354dupG | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231397643 | |||||||
| chr1:231397659 | G | A | 1 | a0001c0001t0025g0074 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.891+23339C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231397659 | |||||||
| chr1:231397702 | C | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.891+23296G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231397702 | |||||||
| chr1:231397736 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.891+23262A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231397736 | |||||||
| chr1:231397794 | C | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(1): Show |
5 | HG02258.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+23204G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231397794 | |||||||
| chr1:231398099 | T | G | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.891+22899A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231398099 | |||||||
| chr1:231398335 | C | CT | 135 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(132): Show |
145 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.891+22662dupA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231398335 | |||||||
| chr1:231398435 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.891+22563T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231398435 | |||||||
| chr1:231398493 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.891+22505A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231398493 | |||||||
| chr1:231398513 | C | T | 163 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.891+22485G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231398513 | |||||||
| chr1:231398643 | A | C | 165 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(162): Show |
176 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.891+22355T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231398643 | |||||||
| chr1:231398644 | T | C | 156 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
167 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.891+22354A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231398644 | |||||||
| chr1:231398647 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.891+22351T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231398647 | |||||||
| chr1:231398748 | TG | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.891+22249delC | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231398748 | |||||||
| chr1:231398797 | G | A | 1 | a0001c0001t0004g0282 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.891+22201C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231398797 | |||||||
| chr1:231398809 | A | C | 1 | a0001c0001t0002g0262 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.891+22189T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231398809 | |||||||
| chr1:231398977 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.891+22021A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231398977 | |||||||
| chr1:231399241 | T | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.891+21757A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231399241 | |||||||
| chr1:231399366 | G | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
142 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.891+21632C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231399366 | |||||||
| chr1:231399523 | A | G | 1 | a0001c0001t0002g0251 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.891+21475T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231399523 | |||||||
| chr1:231399589 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
149 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.891+21409C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231399589 | |||||||
| chr1:231399630 | ACAGTGCT others(10654): Show |
A | 2 | a0001c0001t0006g0128 a0001c0001t0006g0154 |
2 | NA18942.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.891+10707_891+2136 others(4): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231399630 | |||||||
| chr1:231399681 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+21317T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231399681 | |||||||
| chr1:231399762 | G | A | 2 | a0001c0001t0014g0094 a0001c0001t0014g0095 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.891+21236C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231399762 | |||||||
| chr1:231399838 | C | T | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+21160G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231399838 | |||||||
| chr1:231399910 | A | C | 18 | a0001c0001t0002g0130 a0001c0001t0002g0218 a0001c0001t0002g0221 others(15): Show |
18 | HG00544.hp2 HG01934.hp1 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.891+21088T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231399910 | |||||||
| chr1:231399911 | A | C | 1 | a0001c0001t0002g0301 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.891+21087T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231399911 | |||||||
| chr1:231400039 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(1): Show |
5 | HG02258.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+20959A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400039 | |||||||
| chr1:231400115 | T | C | 1 | a0001c0001t0001g0011 | 2 | NA18941.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.891+20883A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400115 | |||||||
| chr1:231400134 | A | T | 161 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(158): Show |
172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.891+20864T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400134 | |||||||
| chr1:231400137 | T | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+20861A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400137 | |||||||
| chr1:231400206 | G | A | 1 | a0001c0001t0005g0293 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.891+20792C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400206 | |||||||
| chr1:231400287 | C | T | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+20711G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400287 | |||||||
| chr1:231400303 | GTA | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+20693_891+2069 others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400303 | |||||||
| chr1:231400398 | G | C | 3 | a0001c0001t0010g0073 a0001c0001t0010g0278 a0001c0001t0010g0279 |
3 | HG02257.hp2 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.891+20600C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400398 | |||||||
| chr1:231400427 | T | A | 3 | a0001c0001t0010g0073 a0001c0001t0010g0278 a0001c0001t0010g0279 |
3 | HG02257.hp2 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.891+20571A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400427 | |||||||
| chr1:231400466 | C | T | 1 | a0001c0001t0008g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.891+20532G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400466 | |||||||
| chr1:231400491 | A | C | 1 | a0001c0001t0001g0190 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.891+20507T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400491 | |||||||
| chr1:231400517 | T | A | 1 | a0001c0001t0021g0063 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.891+20481A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400517 | |||||||
| chr1:231400528 | A | G | 2 | a0001c0001t0002g0269 a0001c0001t0002g0275 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.891+20470T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400528 | |||||||
| chr1:231400587 | C | T | 3 | a0001c0001t0010g0073 a0001c0001t0010g0278 a0001c0001t0010g0279 |
3 | HG02257.hp2 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.891+20411G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400587 | |||||||
| chr1:231400607 | A | C | 6 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(3): Show |
6 | HG02451.hp1 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.891+20391T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400607 | |||||||
| chr1:231400769 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.891+20229C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400769 | |||||||
| chr1:231400825 | A | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(158): Show |
172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.891+20173T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400825 | |||||||
| chr1:231400879 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+20119T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400879 | |||||||
| chr1:231400997 | T | TAAGAGAT others(342): Show |
1 | a0001c0001t0001g0174 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.891+20000_891+2000 others(353): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231400997 | |||||||
| chr1:231401006 | G | A | 3 | a0001c0001t0010g0073 a0001c0001t0010g0278 a0001c0001t0010g0279 |
3 | HG02257.hp2 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.891+19992C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231401006 | |||||||
| chr1:231401310 | C | T | 1 | a0001c0001t0002g0229 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.891+19688G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231401310 | |||||||
| chr1:231401381 | C | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+19617G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231401381 | |||||||
| chr1:231401474 | T | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+19524A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231401474 | |||||||
| chr1:231401485 | A | G | 1 | a0001c0001t0005g0296 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.891+19513T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231401485 | |||||||
| chr1:231401557 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+19441T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231401557 | |||||||
| chr1:231401583 | C | CTAAT | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+19414_891+1941 others(8): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231401583 | |||||||
| chr1:231401706 | C | T | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+19292G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231401706 | |||||||
| chr1:231401729 | G | T | 16 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(13): Show |
17 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.891+19269C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231401729 | |||||||
| chr1:231401797 | G | A | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+19201C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231401797 | |||||||
| chr1:231401887 | C | T | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+19111G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231401887 | |||||||
| chr1:231401992 | T | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+19006A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231401992 | |||||||
| chr1:231401998 | T | C | 17 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.891+19000A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231401998 | |||||||
| chr1:231402005 | T | A | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+18993A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231402005 | |||||||
| chr1:231402168 | C | A | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+18830G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231402168 | |||||||
| chr1:231402171 | C | A | 154 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.891+18827G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231402171 | |||||||
| chr1:231402175 | T | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+18823A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231402175 | |||||||
| chr1:231402242 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+18756T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231402242 | |||||||
| chr1:231402324 | GTTT | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+18671_891+1867 others(7): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231402324 | |||||||
| chr1:231402387 | A | G | 17 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(14): Show |
18 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.891+18611T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231402387 | |||||||
| chr1:231402437 | C | CT | 9 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0053 others(6): Show |
10 | HG00609.hp2 HG03041.hp1 HG03486.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+18560dupA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231402437 | |||||||
| chr1:231402563 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.891+18435A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231402563 | |||||||
| chr1:231402647 | C | T | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+18351G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231402647 | |||||||
| chr1:231402659 | C | T | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+18339G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231402659 | |||||||
| chr1:231402681 | G | A | 4 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0294 others(1): Show |
5 | HG02055.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+18317C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231402681 | |||||||
| chr1:231402768 | A | C | 1 | a0001c0001t0002g0026 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.891+18230T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231402768 | |||||||
| chr1:231402888 | G | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+18110C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231402888 | |||||||
| chr1:231402909 | T | TA | 138 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+18088dupT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231402909 | |||||||
| chr1:231402909 | TA | T | 16 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(13): Show |
17 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.891+18088delT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231402909 | |||||||
| chr1:231403158 | A | G | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.891+17840T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231403158 | |||||||
| chr1:231403169 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.891+17829G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231403169 | |||||||
| chr1:231403170 | T | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+17828A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231403170 | |||||||
| chr1:231403267 | T | A | 1 | a0001c0009t0001g0312 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.891+17731A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231403267 | |||||||
| chr1:231403326 | T | C | 1 | a0001c0001t0001g0008 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.891+17672A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231403326 | |||||||
| chr1:231403348 | T | G | 1 | a0001c0001t0002g0270 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.891+17650A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231403348 | |||||||
| chr1:231403499 | A | G | 155 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
166 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.891+17499T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231403499 | |||||||
| chr1:231403590 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0179 |
2 | HG00408.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.891+17408C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231403590 | |||||||
| chr1:231403705 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+17293T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231403705 | |||||||
| chr1:231403767 | C | CA | 54 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(51): Show |
56 | HG00558.hp1 HG00609.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.891+17230dupT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231403767 | |||||||
| chr1:231403767 | C | CAA | 9 | a0001c0001t0001g0178 a0001c0001t0002g0040 a0001c0001t0005g0014 others(6): Show |
9 | HG02055.hp1 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.891+17229_891+1723 others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231403767 | |||||||
| chr1:231403767 | CA | C | 7 | a0001c0001t0001g0113 a0001c0001t0001g0155 a0001c0001t0002g0267 others(4): Show |
7 | HG01943.hp2 HG02040.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+17230delT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231403767 | |||||||
| chr1:231403767 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0083 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.891+17220_891+1723 others(15): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231403767 | |||||||
| chr1:231403767 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0299 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.891+17219_891+1723 others(16): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231403767 | |||||||
| chr1:231403767 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0300 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.891+17218_891+1723 others(17): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231403767 | |||||||
| chr1:231403863 | T | G | 3 | a0001c0001t0002g0025 a0001c0001t0002g0027 a0001c0001t0002g0040 |
3 | HG02622.hp2 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.891+17135A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231403863 | |||||||
| chr1:231403882 | A | C | 1 | a0001c0001t0001g0123 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.891+17116T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231403882 | |||||||
| chr1:231403939 | A | G | 154 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.891+17059T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231403939 | |||||||
| chr1:231404049 | C | G | 1 | a0001c0001t0001g0028 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.891+16949G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231404049 | |||||||
| chr1:231404277 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.891+16721T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231404277 | |||||||
| chr1:231404298 | A | G | 2 | a0001c0001t0002g0092 a0001c0001t0002g0093 |
2 | HG02055.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.891+16700T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231404298 | |||||||
| chr1:231404397 | G | A | 1 | a0001c0001t0002g0222 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.891+16601C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231404397 | |||||||
| chr1:231404441 | A | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+16557T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231404441 | |||||||
| chr1:231404497 | G | T | 5 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0009g0186 others(2): Show |
5 | NA18939.hp1 NA18950.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+16501C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231404497 | |||||||
| chr1:231404542 | G | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.891+16456C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231404542 | |||||||
| chr1:231404752 | T | TAA | 7 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(4): Show |
8 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.891+16244_891+1624 others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231404752 | |||||||
| chr1:231404797 | A | T | 163 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.891+16201T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231404797 | |||||||
| chr1:231405126 | A | G | 1 | a0001c0001t0019g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.891+15872T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231405126 | |||||||
| chr1:231405228 | G | A | 149 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(146): Show |
159 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.891+15770C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231405228 | |||||||
| chr1:231405229 | G | T | 1 | a0001c0001t0002g0201 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.891+15769C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231405229 | |||||||
| chr1:231405316 | G | C | 1 | a0001c0001t0001g0016 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.891+15682C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231405316 | |||||||
| chr1:231405341 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.891+15657C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231405341 | |||||||
| chr1:231405419 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0082 others(1): Show |
5 | HG02258.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+15579G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231405419 | |||||||
| chr1:231405442 | G | A | 1 | a0001c0001t0002g0064 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.891+15556C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231405442 | |||||||
| chr1:231405468 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.891+15530A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231405468 | |||||||
| chr1:231405590 | T | C | 4 | a0001c0001t0002g0199 a0001c0001t0002g0201 a0001c0001t0002g0222 others(1): Show |
4 | HG00558.hp1 HG02155.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+15408A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231405590 | |||||||
| chr1:231405592 | G | A | 1 | a0001c0001t0003g0087 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.891+15406C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231405592 | |||||||
| chr1:231405594 | G | C | 1 | a0001c0001t0002g0202 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.891+15404C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231405594 | |||||||
| chr1:231405595 | T | A | 154 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.891+15403A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231405595 | |||||||
| chr1:231405609 | G | A | 1 | a0001c0001t0017g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.891+15389C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231405609 | |||||||
| chr1:231405833 | C | T | 42 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0017 others(39): Show |
45 | HG00099.hp1 HG00741.hp2 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.891+15165G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231405833 | |||||||
| chr1:231405940 | T | C | 233 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(230): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.891+15058A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231405940 | |||||||
| chr1:231405949 | G | C | 1 | a0001c0001t0002g0233 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.891+15049C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231405949 | |||||||
| chr1:231405971 | C | A | 1 | a0001c0001t0005g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.891+15027G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231405971 | |||||||
| chr1:231406029 | C | CT | 19 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0120 others(16): Show |
19 | HG00140.hp1 HG00741.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.891+14968dupA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406029 | |||||||
| chr1:231406029 | CT | C | 22 | a0001c0001t0001g0023 a0001c0001t0001g0123 a0001c0001t0001g0172 others(19): Show |
22 | HG01243.hp2 HG01358.hp2 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.891+14968delA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406029 | |||||||
| chr1:231406048 | T | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.891+14950A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406048 | |||||||
| chr1:231406097 | A | G | 9 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0007g0078 others(6): Show |
9 | HG01123.hp1 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.891+14901T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406097 | |||||||
| chr1:231406160 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0160 |
2 | NA19007.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.891+14838G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406160 | |||||||
| chr1:231406161 | G | A | 1 | a0001c0001t0002g0017 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.891+14837C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406161 | |||||||
| chr1:231406165 | C | CAAAAAAA others(4): Show |
25 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0025 others(22): Show |
26 | HG00099.hp1 HG00741.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.891+14822_891+1483 others(15): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406165 | |||||||
| chr1:231406165 | C | CAAAAAAA others(5): Show |
4 | a0001c0001t0002g0039 a0001c0001t0002g0092 a0001c0001t0003g0001 others(1): Show |
5 | HG01175.hp2 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+14821_891+1483 others(16): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406165 | |||||||
| chr1:231406165 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0014g0094 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.891+14819_891+1483 others(18): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406165 | |||||||
| chr1:231406165 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0014g0095 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.891+14832_891+1483 others(19): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406165 | |||||||
| chr1:231406165 | CA | C | 154 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.891+14832delT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406165 | |||||||
| chr1:231406170 | A | C | 1 | a0001c0001t0002g0004 | 2 | NA18978.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.891+14828T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406170 | |||||||
| chr1:231406171 | A | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
142 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.891+14827T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406171 | |||||||
| chr1:231406238 | C | T | 31 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0025 others(28): Show |
33 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.891+14760G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406238 | |||||||
| chr1:231406314 | G | A | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0265 |
3 | NA18994.hp2 NA18998.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.891+14684C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406314 | |||||||
| chr1:231406344 | T | C | 39 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(36): Show |
41 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.891+14654A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406344 | |||||||
| chr1:231406411 | G | C | 36 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(33): Show |
38 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.891+14587C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406411 | |||||||
| chr1:231406412 | T | C | 1 | a0001c0001t0017g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.891+14586A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406412 | |||||||
| chr1:231406443 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.891+14555A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406443 | |||||||
| chr1:231406447 | A | T | 1 | a0001c0001t0005g0293 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.891+14551T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406447 | |||||||
| chr1:231406469 | G | A | 36 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(33): Show |
38 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.891+14529C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406469 | |||||||
| chr1:231406540 | T | C | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.891+14458A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406540 | |||||||
| chr1:231406590 | G | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+14408C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406590 | |||||||
| chr1:231406638 | G | A | 1 | a0001c0001t0017g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.891+14360C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406638 | |||||||
| chr1:231406720 | G | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+14278C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406720 | |||||||
| chr1:231406905 | A | G | 1 | a0001c0001t0028g0271 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.891+14093T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406905 | |||||||
| chr1:231406910 | C | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+14088G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406910 | |||||||
| chr1:231406987 | C | T | 1 | a0001c0001t0002g0229 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.891+14011G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231406987 | |||||||
| chr1:231407110 | C | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+13888G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231407110 | |||||||
| chr1:231407249 | G | A | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+13749C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231407249 | |||||||
| chr1:231407313 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.891+13685T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231407313 | |||||||
| chr1:231407429 | A | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
139 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.891+13569T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231407429 | |||||||
| chr1:231407797 | G | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+13201C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231407797 | |||||||
| chr1:231407809 | G | C | 129 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(126): Show |
138 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.891+13189C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231407809 | |||||||
| chr1:231407851 | T | C | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+13147A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231407851 | |||||||
| chr1:231407876 | T | G | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+13122A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231407876 | |||||||
| chr1:231407996 | G | A | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+13002C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231407996 | |||||||
| chr1:231408016 | A | G | 1 | a0001c0001t0002g0301 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.891+12982T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231408016 | |||||||
| chr1:231408034 | G | A | 190 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.891+12964C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231408034 | |||||||
| chr1:231408077 | A | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
139 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.891+12921T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231408077 | |||||||
| chr1:231408089 | C | T | 1 | a0001c0001t0002g0206 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.891+12909G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231408089 | |||||||
| chr1:231408186 | G | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+12812C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231408186 | |||||||
| chr1:231408439 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.891+12559A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231408439 | |||||||
| chr1:231408555 | G | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+12443C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231408555 | |||||||
| chr1:231408672 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.891+12326C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231408672 | |||||||
| chr1:231408787 | G | A | 4 | a0001c0001t0011g0289 a0001c0001t0011g0290 a0001c0006t0001g0292 others(1): Show |
4 | HG02258.hp2 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+12211C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231408787 | |||||||
| chr1:231408839 | G | A | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+12159C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231408839 | |||||||
| chr1:231408861 | C | T | 189 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(186): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.891+12137G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231408861 | |||||||
| chr1:231408986 | G | A | 2 | a0001c0001t0003g0089 a0001c0001t0003g0090 |
2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.891+12012C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231408986 | |||||||
| chr1:231409015 | G | GA | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+11982dupT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231409015 | |||||||
| chr1:231409024 | C | A | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+11974G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231409024 | |||||||
| chr1:231409088 | A | G | 1 | a0001c0001t0002g0223 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.891+11910T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231409088 | |||||||
| chr1:231409241 | TAA | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+11755_891+1175 others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231409241 | |||||||
| chr1:231409249 | A | C | 1 | a0001c0001t0001g0008 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.891+11749T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231409249 | |||||||
| chr1:231409255 | AAC | A | 7 | a0001c0001t0002g0239 a0001c0001t0002g0242 a0001c0001t0002g0251 others(4): Show |
7 | HG01261.hp2 HG03491.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.891+11741_891+1174 others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231409255 | |||||||
| chr1:231409256 | AC | A | 113 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(110): Show |
118 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.891+11741delG | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231409256 | |||||||
| chr1:231409257 | C | A | 9 | a0001c0001t0001g0137 a0001c0001t0002g0024 a0001c0001t0002g0072 others(6): Show |
10 | HG01358.hp1 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+11741G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231409257 | |||||||
| chr1:231409277 | C | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0113 |
3 | HG02602.hp2 HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.891+11721G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231409277 | |||||||
| chr1:231409541 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.891+11457T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231409541 | |||||||
| chr1:231409544 | A | G | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.891+11454T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231409544 | |||||||
| chr1:231409574 | A | G | 1 | a0001c0001t0002g0223 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.891+11424T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231409574 | |||||||
| chr1:231409660 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.891+11338A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231409660 | |||||||
| chr1:231409724 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.891+11274C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231409724 | |||||||
| chr1:231409816 | T | A | 2 | a0001c0001t0014g0094 a0001c0001t0014g0095 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.891+11182A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231409816 | |||||||
| chr1:231409902 | C | CA | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+11095dupT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231409902 | |||||||
| chr1:231409957 | T | C | 126 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(123): Show |
131 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.891+11041A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231409957 | |||||||
| chr1:231409993 | A | G | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+11005T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231409993 | |||||||
| chr1:231410276 | T | C | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+10722A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231410276 | |||||||
| chr1:231410457 | G | A | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+10541C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231410457 | |||||||
| chr1:231410592 | C | A | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+10406G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231410592 | |||||||
| chr1:231410645 | T | C | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+10353A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231410645 | |||||||
| chr1:231410706 | T | C | 126 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(123): Show |
131 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.891+10292A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231410706 | |||||||
| chr1:231410855 | G | A | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+10143C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231410855 | |||||||
| chr1:231411125 | A | C | 39 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(36): Show |
41 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.891+9873T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231411125 | |||||||
| chr1:231411144 | T | C | 39 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(36): Show |
41 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.891+9854A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231411144 | |||||||
| chr1:231411277 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.891+9721G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231411277 | |||||||
| chr1:231411324 | T | C | 2 | a0001c0001t0002g0039 a0001c0001t0003g0038 |
2 | HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.891+9674A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231411324 | |||||||
| chr1:231411581 | A | C | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.891+9417T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231411581 | |||||||
| chr1:231411589 | T | C | 166 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(163): Show |
173 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.891+9409A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231411589 | |||||||
| chr1:231411635 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.891+9363T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231411635 | |||||||
| chr1:231411720 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.891+9278G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231411720 | |||||||
| chr1:231411973 | T | C | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0168 others(2): Show |
5 | HG01346.hp2 HG01928.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+9025A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231411973 | |||||||
| chr1:231411979 | T | G | 1 | a0001c0006t0001g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.891+9019A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231411979 | |||||||
| chr1:231411980 | A | C | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+9018T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231411980 | |||||||
| chr1:231412011 | C | CA | 24 | a0001c0001t0001g0015 a0001c0001t0001g0171 a0001c0001t0001g0172 others(21): Show |
26 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.891+8986dupT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412011 | C | CAA | 11 | a0001c0001t0001g0179 a0001c0001t0002g0024 a0001c0001t0002g0068 others(8): Show |
11 | HG01099.hp2 HG01106.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.891+8985_891+8986d others(4): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412011 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0005g0296 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.891+8976_891+8986d others(13): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412011 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0195 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.891+8971_891+8986d others(18): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412011 | CA | C | 88 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(85): Show |
92 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.891+8986delT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412011 | CAA | C | 35 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(32): Show |
35 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.891+8985_891+8986d others(4): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412011 | CAAA | C | 7 | a0001c0001t0001g0098 a0001c0001t0001g0108 a0001c0001t0001g0109 others(4): Show |
7 | HG00642.hp1 HG01175.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.891+8984_891+8986d others(5): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412011 | CAAAA | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0107 a0001c0001t0002g0070 others(2): Show |
6 | HG00741.hp1 HG01192.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.891+8983_891+8986d others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412011 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0014g0094 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.891+8977_891+8986d others(12): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412011 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0003c0003t0002g0309 |
3 | HG01123.hp1 HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.891+8976_891+8986d others(13): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412011 | CAAAAAAA others(5): Show |
C | 10 | a0001c0001t0001g0052 a0001c0001t0002g0040 a0001c0001t0002g0091 others(7): Show |
10 | HG01175.hp2 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+8975_891+8986d others(14): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412011 | CAAAAAAA others(6): Show |
C | 31 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(28): Show |
33 | HG00099.hp1 HG00741.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.891+8974_891+8986d others(15): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412011 | CAAAAAAA others(7): Show |
C | 17 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(14): Show |
17 | HG01257.hp1 HG01258.hp1 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.891+8973_891+8986d others(16): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412011 | CAAAAAAA others(8): Show |
C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0053 others(2): Show |
6 | NA18948.hp2 NA18960.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.891+8972_891+8986d others(17): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412011 | CAAAAAAA others(9): Show |
C | 5 | a0001c0001t0001g0196 a0001c0001t0002g0252 a0001c0001t0010g0073 others(2): Show |
5 | HG00323.hp2 HG02257.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+8971_891+8986d others(18): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412011 | CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0013g0217 a0001c0001t0013g0305 |
2 | NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.891+8970_891+8986d others(19): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412011 | CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0001g0124 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.891+8969_891+8986d others(20): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412011 | CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0001g0123 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.891+8968_891+8986d others(21): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412011 | CAAAAAAA others(15): Show |
C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0082 a0007c0008t0001g0311 |
4 | HG02258.hp1 HG02970.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+8965_891+8986d others(24): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412011 | |||||||
| chr1:231412142 | A | G | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+8856T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412142 | |||||||
| chr1:231412313 | A | C | 186 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(183): Show |
195 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.891+8685T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412313 | |||||||
| chr1:231412414 | T | A | 2 | a0001c0001t0002g0044 a0001c0001t0002g0045 |
2 | HG03041.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.891+8584A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412414 | |||||||
| chr1:231412509 | T | C | 3 | a0001c0001t0010g0073 a0001c0001t0010g0278 a0001c0001t0010g0279 |
3 | HG02257.hp2 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.891+8489A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412509 | |||||||
| chr1:231412539 | G | T | 2 | a0001c0001t0014g0094 a0001c0001t0014g0095 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.891+8459C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412539 | |||||||
| chr1:231412574 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.891+8424C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412574 | |||||||
| chr1:231412656 | G | C | 1 | a0001c0001t0002g0069 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.891+8342C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412656 | |||||||
| chr1:231412730 | T | C | 1 | a0001c0001t0002g0272 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.891+8268A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412730 | |||||||
| chr1:231412734 | A | G | 164 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(161): Show |
171 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.891+8264T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412734 | |||||||
| chr1:231412905 | C | T | 38 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0048 others(35): Show |
40 | HG00642.hp1 HG00741.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.891+8093G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412905 | |||||||
| chr1:231412912 | A | C | 316 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(313): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.891+8086T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412912 | |||||||
| chr1:231412968 | AAATATAT others(4): Show |
A | 1 | a0001c0001t0006g0010 | 2 | NA18961.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.891+8019_891+8029d others(13): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231412968 | |||||||
| chr1:231413014 | CCTA | C | 126 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(123): Show |
131 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.891+7981_891+7983d others(5): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231413014 | |||||||
| chr1:231413131 | G | A | 2 | a0001c0001t0014g0094 a0001c0001t0014g0095 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.891+7867C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231413131 | |||||||
| chr1:231413157 | G | C | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+7841C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231413157 | |||||||
| chr1:231413163 | C | A | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+7835G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231413163 | |||||||
| chr1:231413233 | G | A | 2 | a0001c0001t0002g0092 a0001c0001t0002g0093 |
2 | HG02055.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.891+7765C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231413233 | |||||||
| chr1:231413243 | T | C | 5 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0009g0186 others(2): Show |
5 | NA18939.hp1 NA18950.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.891+7755A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231413243 | |||||||
| chr1:231413296 | G | A | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+7702C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231413296 | |||||||
| chr1:231413357 | T | A | 12 | a0001c0001t0002g0017 a0001c0001t0002g0024 a0001c0001t0002g0237 others(9): Show |
13 | HG01099.hp2 HG01106.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.891+7641A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231413357 | |||||||
| chr1:231413421 | A | G | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+7577T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231413421 | |||||||
| chr1:231413500 | C | A | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+7498G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231413500 | |||||||
| chr1:231413572 | AACGTGCC others(7): Show |
A | 3 | a0001c0001t0009g0186 a0001c0001t0009g0187 a0001c0001t0009g0191 |
3 | NA18953.hp2 NA19002.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.891+7412_891+7425d others(16): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231413572 | |||||||
| chr1:231413599 | G | A | 6 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(3): Show |
6 | HG01934.hp1 NA18944.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.891+7399C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231413599 | |||||||
| chr1:231413623 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.891+7375G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231413623 | |||||||
| chr1:231413823 | T | TAAAGAAA others(325): Show |
1 | a0001c0001t0010g0073 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.891+7174_891+7175i others(334): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231413823 | |||||||
| chr1:231413823 | T | TAAAGAAA others(326): Show |
1 | a0001c0001t0010g0278 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.891+7174_891+7175i others(335): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231413823 | |||||||
| chr1:231413823 | T | TAAAGAAA others(327): Show |
1 | a0001c0001t0010g0279 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.891+7174_891+7175i others(336): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231413823 | |||||||
| chr1:231413832 | G | A | 1 | a0001c0001t0005g0296 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.891+7166C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231413832 | |||||||
| chr1:231413986 | A | AG | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+7011dupC | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231413986 | |||||||
| chr1:231414252 | A | T | 3 | a0001c0001t0010g0073 a0001c0001t0010g0278 a0001c0001t0010g0279 |
3 | HG02257.hp2 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.891+6746T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231414252 | |||||||
| chr1:231414342 | A | T | 11 | a0001c0001t0005g0014 a0001c0001t0005g0291 a0001c0001t0005g0293 others(8): Show |
12 | HG02055.hp1 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.891+6656T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231414342 | |||||||
| chr1:231414346 | T | A | 1 | a0001c0001t0002g0273 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.891+6652A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231414346 | |||||||
| chr1:231414422 | A | G | 186 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(183): Show |
195 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.891+6576T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231414422 | |||||||
| chr1:231414425 | G | A | 186 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(183): Show |
195 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.891+6573C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231414425 | |||||||
| chr1:231414489 | A | G | 1 | a0001c0001t0015g0018 | 2 | HG02074.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.891+6509T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231414489 | |||||||
| chr1:231414572 | A | G | 1 | a0001c0001t0026g0100 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.891+6426T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231414572 | |||||||
| chr1:231414659 | AG | A | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG00609.hp2 HG00621.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.891+6338delC | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231414659 | |||||||
| chr1:231414733 | C | CT | 23 | a0001c0001t0001g0016 a0001c0001t0001g0082 a0001c0001t0001g0099 others(20): Show |
25 | HG01070.hp2 HG01884.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.891+6264dupA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231414733 | |||||||
| chr1:231414733 | C | CTT | 87 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0002g0012 others(84): Show |
90 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.891+6263_891+6264d others(4): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231414733 | |||||||
| chr1:231414733 | C | CTTT | 75 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(72): Show |
79 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.891+6262_891+6264d others(5): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231414733 | |||||||
| chr1:231415013 | C | G | 1 | a0001c0001t0002g0083 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.891+5985G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231415013 | |||||||
| chr1:231415087 | A | G | 4 | a0001c0001t0011g0289 a0001c0001t0011g0290 a0001c0006t0001g0292 others(1): Show |
4 | HG02258.hp2 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.891+5911T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231415087 | |||||||
| chr1:231415186 | T | C | 4 | a0003c0003t0002g0307 a0003c0003t0002g0308 a0003c0003t0002g0309 others(1): Show |
4 | HG01123.hp1 HG01884.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+5812A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231415186 | |||||||
| chr1:231415253 | T | A | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+5745A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231415253 | |||||||
| chr1:231415270 | TA | T | 140 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0299 others(137): Show |
146 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.891+5727delT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231415270 | |||||||
| chr1:231415270 | TAAA | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+5725_891+5727d others(5): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231415270 | |||||||
| chr1:231415322 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.891+5676A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231415322 | |||||||
| chr1:231415391 | C | A | 1 | a0001c0001t0002g0276 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.891+5607G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231415391 | |||||||
| chr1:231415452 | T | TA | 37 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(34): Show |
39 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.891+5545dupT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231415452 | |||||||
| chr1:231415586 | T | C | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+5412A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231415586 | |||||||
| chr1:231415851 | C | CT | 164 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(161): Show |
171 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.891+5146dupA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231415851 | |||||||
| chr1:231415871 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.891+5127C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231415871 | |||||||
| chr1:231415940 | C | T | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.891+5058G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231415940 | |||||||
| chr1:231415996 | G | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0082 a0007c0008t0001g0311 |
4 | HG02258.hp1 HG02970.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+5002C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231415996 | |||||||
| chr1:231415997 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0082 a0007c0008t0001g0311 |
4 | HG02258.hp1 HG02970.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+5001G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231415997 | |||||||
| chr1:231416092 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.891+4906G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231416092 | |||||||
| chr1:231416094 | A | G | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+4904T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231416094 | |||||||
| chr1:231416231 | CAA | C | 5 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG02027.hp1 HG02056.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.891+4765_891+4766d others(4): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231416231 | |||||||
| chr1:231416239 | C | T | 2 | a0001c0001t0011g0289 a0001c0001t0011g0290 |
2 | HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.891+4759G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231416239 | |||||||
| chr1:231416436 | A | AAT | 36 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(33): Show |
38 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.891+4561_891+4562i others(4): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231416436 | |||||||
| chr1:231416436 | A | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0048 others(45): Show |
51 | HG00642.hp1 HG00741.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.891+4562T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231416436 | |||||||
| chr1:231416436 | AT | A | 38 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0070 others(35): Show |
40 | HG00323.hp2 HG00423.hp2 HG01358.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+4561delA | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231416436 | |||||||
| chr1:231416496 | C | T | 33 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(30): Show |
35 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.891+4502G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231416496 | |||||||
| chr1:231416531 | C | T | 2 | a0001c0001t0011g0289 a0001c0001t0011g0290 |
2 | HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.891+4467G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231416531 | |||||||
| chr1:231416558 | A | G | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+4440T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231416558 | |||||||
| chr1:231416580 | A | G | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+4418T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231416580 | |||||||
| chr1:231416596 | G | T | 1 | a0001c0001t0005g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.891+4402C>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231416596 | |||||||
| chr1:231416604 | G | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.891+4394C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231416604 | |||||||
| chr1:231416703 | G | A | 1 | a0001c0001t0009g0191 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.891+4295C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231416703 | |||||||
| chr1:231416741 | A | G | 3 | a0001c0001t0010g0073 a0001c0001t0010g0278 a0001c0001t0010g0279 |
3 | HG02257.hp2 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.891+4257T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231416741 | |||||||
| chr1:231416749 | C | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+4249G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231416749 | |||||||
| chr1:231416864 | T | C | 2 | a0001c0001t0011g0289 a0001c0001t0011g0290 |
2 | HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.891+4134A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231416864 | |||||||
| chr1:231417070 | T | G | 1 | a0001c0001t0002g0277 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.891+3928A>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231417070 | |||||||
| chr1:231417226 | TTAAC | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+3768_891+3771d others(6): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231417226 | |||||||
| chr1:231417243 | G | GA | 3 | a0001c0001t0010g0073 a0001c0001t0010g0278 a0001c0001t0010g0279 |
3 | HG02257.hp2 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.891+3754dupT | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231417243 | |||||||
| chr1:231417459 | T | C | 1 | a0001c0001t0025g0074 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.891+3539A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231417459 | |||||||
| chr1:231417673 | G | A | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+3325C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231417673 | |||||||
| chr1:231417758 | A | G | 34 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(31): Show |
36 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.891+3240T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231417758 | |||||||
| chr1:231417765 | G | A | 1 | a0001c0001t0001g0011 | 2 | NA18941.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.891+3233C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231417765 | |||||||
| chr1:231417811 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.891+3187G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231417811 | |||||||
| chr1:231417980 | T | C | 6 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(3): Show |
6 | HG02451.hp1 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.891+3018A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231417980 | |||||||
| chr1:231418041 | A | C | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0048 others(46): Show |
52 | HG00642.hp1 HG00741.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.891+2957T>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231418041 | |||||||
| chr1:231418078 | T | C | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG02735.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.891+2920A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231418078 | |||||||
| chr1:231418096 | TATA | T | 126 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(123): Show |
131 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.891+2899_891+2901d others(5): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231418096 | |||||||
| chr1:231418275 | T | A | 10 | a0001c0001t0004g0280 a0001c0001t0004g0281 a0001c0001t0004g0282 others(7): Show |
10 | HG00609.hp1 HG02056.hp2 NA18612.hp2 others(7): Show |
intron_variant | MODIFIER | c.891+2723A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231418275 | |||||||
| chr1:231418319 | C | A | 1 | a0001c0001t0002g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.891+2679G>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231418319 | |||||||
| chr1:231418404 | T | C | 1 | a0003c0003t0002g0310 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.891+2594A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231418404 | |||||||
| chr1:231418504 | C | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+2494G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231418504 | |||||||
| chr1:231418597 | T | C | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+2401A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231418597 | |||||||
| chr1:231418661 | C | T | 2 | a0001c0001t0011g0289 a0001c0001t0011g0290 |
2 | HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.891+2337G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231418661 | |||||||
| chr1:231418692 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.891+2306A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231418692 | |||||||
| chr1:231418702 | A | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | NA18944.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.891+2296T>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231418702 | |||||||
| chr1:231418785 | C | T | 126 | a0001c0001t0002g0004 a0001c0001t0002g0012 a0001c0001t0002g0013 others(123): Show |
131 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.891+2213G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231418785 | |||||||
| chr1:231418840 | C | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+2158G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231418840 | |||||||
| chr1:231418848 | C | G | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+2150G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231418848 | |||||||
| chr1:231418866 | A | AG | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+2131_891+2132i others(3): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231418866 | |||||||
| chr1:231418903 | T | C | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+2095A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231418903 | |||||||
| chr1:231419105 | G | A | 1 | a0001c0001t0002g0301 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.891+1893C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231419105 | |||||||
| chr1:231419247 | C | G | 188 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(185): Show |
198 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.891+1751G>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231419247 | |||||||
| chr1:231419266 | T | C | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+1732A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231419266 | |||||||
| chr1:231419280 | T | C | 1 | a0001c0001t0024g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.891+1718A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231419280 | |||||||
| chr1:231419409 | T | A | 2 | a0001c0001t0014g0094 a0001c0001t0014g0095 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.891+1589A>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231419409 | |||||||
| chr1:231419549 | T | C | 188 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(185): Show |
198 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.891+1449A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231419549 | |||||||
| chr1:231419574 | T | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0082 a0007c0008t0001g0311 |
4 | HG02258.hp1 HG02970.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.891+1424A>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231419574 | |||||||
| chr1:231419584 | ATTT | A | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+1411_891+1413d others(5): Show |
EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231419584 | |||||||
| chr1:231419848 | G | C | 1 | a0001c0001t0001g0302 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.891+1150C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231419848 | |||||||
| chr1:231419893 | C | T | 1 | a0001c0001t0002g0083 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.891+1105G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231419893 | |||||||
| chr1:231419962 | A | G | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(35): Show |
40 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.891+1036T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231419962 | |||||||
| chr1:231420206 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.891+792G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231420206 | |||||||
| chr1:231420489 | G | C | 1 | a0001c0001t0001g0303 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.891+509C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231420489 | |||||||
| chr1:231420605 | G | A | 2 | a0001c0001t0002g0017 a0001c0001t0002g0304 |
3 | HG01099.hp2 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.891+393C>T | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231420605 | |||||||
| chr1:231420649 | C | T | 63 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(60): Show |
67 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(64): Show |
intron_variant | MODIFIER | c.891+349G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231420649 | |||||||
| chr1:231420900 | A | G | 1 | a0001c0001t0002g0024 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.891+98T>C | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231420900 | |||||||
| chr1:231420934 | G | C | 1 | a0001c0001t0013g0305 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.891+64C>G | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231420934 | |||||||
| chr1:231420976 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.891+22G>A | EGLN1 | ENSG00000135766.9 | transcript | ENST00000366641.4 | protein_coding | 1/4 | chr1 | 231420976 |