Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3162 |
| ensemblid | ENSG00000100292.18 |
| hgncid | 5013 |
| symbol | HMOX1 |
| name | heme oxygenase 1 |
| refseq_nuc | NM_002133.3 |
| refseq_prot | NP_002124.1 |
| ensembl_nuc | ENST00000216117.9 |
| ensembl_prot | ENSP00000216117.8 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 35381096 |
| end | 35394207 |
| strand | + |
| ver | v1.2 |
| region | chr22:35381096-35394207 |
| region5000 | chr22:35376096-35399207 |
| regionname0 | HMOX1_chr22_35381096_35394207 |
| regionname5000 | HMOX1_chr22_35376096_35399207 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 288 | 362 | 76 | 62 | 167 | 16 | 39 | 128 | HMOX1_chr22_35376096_35399207 | HMOX1 | MERPQ others(283): Show |
chr22 | 35376096 | 35399207 |
| a0002 | 0/0 | 288 | 17 | 3 | 0 | 14 | 0 | 0 | 11 | HMOX1_chr22_35376096_35399207 | HMOX1 | MERPQ others(283): Show |
chr22 | 35376096 | 35399207 |
| a0003 | 0/0 | 288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | MERPQ others(283): Show |
chr22 | 35376096 | 35399207 |
| a0004 | 0/0 | 288 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | MERPQ others(283): Show |
chr22 | 35376096 | 35399207 |
| a0005 | 0/0 | 288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | MERPQ others(283): Show |
chr22 | 35376096 | 35399207 |
| a0006 | 0/0 | 288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | MERPQ others(283): Show |
chr22 | 35376096 | 35399207 |
| a0007 | 0/0 | 288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | MERPQ others(283): Show |
chr22 | 35376096 | 35399207 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 864 | 354 | 68 | 62 | 167 | 16 | 39 | HMOX1_chr22_35376096_35399207 | HMOX1 | ATGGA others(859): Show |
chr22 | 35376096 | 35399207 | ||
| a0001c0003 | 0/0 | 864 | 4 | 4 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | ATGGA others(859): Show |
chr22 | 35376096 | 35399207 | ||
| a0001c0004 | 0/0 | 864 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | ATGGA others(859): Show |
chr22 | 35376096 | 35399207 | ||
| a0001c0006 | 0/0 | 864 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | ATGGA others(859): Show |
chr22 | 35376096 | 35399207 | ||
| a0001c0011 | 0/0 | 864 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | ATGGA others(859): Show |
chr22 | 35376096 | 35399207 | ||
| a0002c0002 | 0/0 | 864 | 17 | 3 | 0 | 14 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | ATGGA others(859): Show |
chr22 | 35376096 | 35399207 | ||
| a0003c0008 | 0/0 | 864 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | ATGGA others(859): Show |
chr22 | 35376096 | 35399207 | ||
| a0004c0009 | 0/0 | 864 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | ATGGA others(859): Show |
chr22 | 35376096 | 35399207 | ||
| a0005c0005 | 0/0 | 864 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | ATGGA others(859): Show |
chr22 | 35376096 | 35399207 | ||
| a0006c0007 | 0/0 | 864 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | ATGGA others(859): Show |
chr22 | 35376096 | 35399207 | ||
| a0007c0010 | 0/0 | 864 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | ATGGA others(859): Show |
chr22 | 35376096 | 35399207 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1554 | 315 | 36 | 60 | 163 | 16 | 38 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0001c0001t0002 | 0/0 | 1554 | 24 | 23 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0001c0001t0003 | 0/0 | 1554 | 5 | 5 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0001c0001t0004 | 0/0 | 1562 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1557): Show |
chr22 | 35376096 | 35399207 |
| a0001c0001t0005 | 0/0 | 1554 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0001c0001t0006 | 0/0 | 1562 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1557): Show |
chr22 | 35376096 | 35399207 |
| a0001c0001t0007 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0001c0001t0008 | 0/0 | 1554 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0001c0001t0009 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0001c0001t0010 | 0/0 | 1554 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0001c0001t0012 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0001c0003t0001 | 0/0 | 1554 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0001c0003t0002 | 0/0 | 1554 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0001c0004t0004 | 0/0 | 1562 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1557): Show |
chr22 | 35376096 | 35399207 |
| a0001c0006t0002 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0001c0011t0001 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0002c0002t0001 | 0/0 | 1554 | 15 | 1 | 0 | 14 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0002c0002t0002 | 0/0 | 1554 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0003c0008t0001 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0004c0009t0001 | 0/0 | 1554 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0005c0005t0001 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0006c0007t0011 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| a0007c0010t0001 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | AACGC others(1549): Show |
chr22 | 35376096 | 35399207 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 38 | 5 | 10 | 12 | 3 | 7 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0002 | 0/0 | 13 | 6 | 2 | 1 | 2 | 2 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0003 | 0/0 | 12 | 0 | 3 | 9 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0004 | 0/0 | 10 | 1 | 2 | 4 | 2 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0006 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0007 | 0/0 | 8 | 1 | 0 | 7 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 2 | 1 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0010 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0186 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0003g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0007g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0010g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0001t0012g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0003t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0004t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0004t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0006t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0001c0011t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0002c0002t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0002c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0002c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0002c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0002c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0003c0008t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0004c0009t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0005c0005t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0006c0007t0011g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| a0007c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01496 | hp1 | a0001 | c0001 | t0010 | g0144 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | IBS | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0079 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0074 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CDX | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CDX | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02257 | hp1 | a0001 | c0011 | t0001 | g0054 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0080 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02630 | hp1 | a0001 | c0004 | t0004 | g0153 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0145 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02717 | hp1 | a0003 | c0008 | t0001 | g0225 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0199 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02818 | hp1 | a0001 | c0004 | t0004 | g0152 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02896 | hp1 | a0001 | c0003 | t0002 | g0016 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02897 | hp1 | a0001 | c0003 | t0002 | g0016 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0197 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0198 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | ESN | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0058 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03710 | hp2 | a0004 | c0009 | t0001 | g0040 | SAS | PJL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03834 | hp2 | a0001 | c0001 | t0008 | g0001 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | STU | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | STU | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | YRI | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18962 | hp1 | a0001 | c0001 | t0007 | g0100 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18963 | hp1 | a0001 | c0001 | t0005 | g0097 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18969 | hp1 | a0005 | c0005 | t0001 | g0206 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18986 | hp1 | a0006 | c0007 | t0011 | g0114 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0124 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19009 | hp2 | a0001 | c0001 | t0012 | g0041 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | LWK | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | LWK | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19079 | hp1 | a0007 | c0010 | t0001 | g0001 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | YRI | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA20129 | hp1 | a0001 | c0006 | t0002 | g0230 | AFR | ASW | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | TSI | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | GIH | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | GIH | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | ACB | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | USA | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | USA | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | USA | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | LWK | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0186 | REF | REF | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | HMOX1_chr22_35376096_35399207 | HMOX1 | chr22 | 35376096 | 35399207 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:35381192 | G | C | 1 | a0002 | 17 | HG00544.hp2 HG00621.hp2 HG00673.hp1 others(14): Show |
missense_variant | MODERATE | c.19G>C | p.Asp7His | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/5 | 97/1554 | 19/867 | 7/288 | chr22 | 35381192 | |||
| chr22:35383131 | C | A | 1 | a0005 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.49C>A | p.Leu17Met | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/5 | 127/1554 | 49/867 | 17/288 | chr22 | 35383131 | |||
| chr22:35386997 | A | C | 1 | a0007 | 1 | NA19079.hp1 | missense_variant | MODERATE | c.457A>C | p.Lys153Gln | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/5 | 535/1554 | 457/867 | 153/288 | chr22 | 35386997 | |||
| chr22:35386998 | A | T | 1 | a0007 | 1 | NA19079.hp1 | missense_variant | MODERATE | c.458A>T | p.Lys153Ile | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/5 | 536/1554 | 458/867 | 153/288 | chr22 | 35386998 | |||
| chr22:35386999 | A | C | 1 | a0007 | 1 | NA19079.hp1 | missense_variant | MODERATE | c.459A>C | p.Lys153Asn | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/5 | 537/1554 | 459/867 | 153/288 | chr22 | 35386999 | |||
| chr22:35387156 | G | T | 1 | a0005 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.616G>T | p.Ala206Ser | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/5 | 694/1554 | 616/867 | 206/288 | chr22 | 35387156 | |||
| chr22:35389903 | A | G | 1 | a0004 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.676A>G | p.Lys226Glu | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/5 | 754/1554 | 676/867 | 226/288 | chr22 | 35389903 | |||
| chr22:35393479 | G | C | 1 | a0006 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.748G>C | p.Val250Leu | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 826/1554 | 748/867 | 250/288 | chr22 | 35393479 | |||
| chr22:35393480 | T | G | 1 | a0006 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.749T>G | p.Val250Gly | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 827/1554 | 749/867 | 250/288 | chr22 | 35393480 | |||
| chr22:35393483 | A | T | 1 | a0006 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.752A>T | p.Glu251Val | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 830/1554 | 752/867 | 251/288 | chr22 | 35393483 | |||
| chr22:35393567 | C | T | 1 | a0003 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.836C>T | p.Ala279Val | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 914/1554 | 836/867 | 279/288 | chr22 | 35393567 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:35386918 | C | T | 1 | a0001c0011 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.378C>T | p.Pro126Pro | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/5 | 456/1554 | 378/867 | 126/288 | chr22 | 35386918 | |||
| chr22:35387143 | A | G | 1 | a0001c0003 | 4 | HG02055.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
synonymous_variant | LOW | c.603A>G | p.Glu201Glu | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/5 | 681/1554 | 603/867 | 201/288 | chr22 | 35387143 | |||
| chr22:35387158 | G | A | 1 | a0001c0006 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.618G>A | p.Ala206Ala | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/5 | 696/1554 | 618/867 | 206/288 | chr22 | 35387158 | |||
| chr22:35393481 | G | T | 1 | a0006c0007 | 1 | NA18986.hp1 | synonymous_variant | LOW | c.750G>T | p.Val250Val | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 828/1554 | 750/867 | 250/288 | chr22 | 35393481 | |||
| chr22:35393571 | A | G | 1 | a0001c0004 | 2 | HG02630.hp1 HG02818.hp1 |
synonymous_variant | LOW | c.840A>G | p.Thr280Thr | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 918/1554 | 840/867 | 280/288 | chr22 | 35393571 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:35381102 | T | G | 1 | a0001c0001t0006 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-72T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/5 | 72 | chr22 | 35381102 | ||||||
| chr22:35381137 | C | G | 1 | a0001c0001t0012 | 1 | NA19009.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/5 | 37 | chr22 | 35381137 | ||||||
| chr22:35393662 | G | C | 1 | a0001c0001t0005 | 2 | NA18963.hp1 NA18998.hp1 |
3_prime_UTR_variant | MODIFIER | c.*64G>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 64 | chr22 | 35393662 | ||||||
| chr22:35393692 | G | T | 1 | a0006c0007t0011 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*94G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 94 | chr22 | 35393692 | ||||||
| chr22:35393701 | A | C | 1 | a0006c0007t0011 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*103A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 103 | chr22 | 35393701 | ||||||
| chr22:35393732 | G | T | 1 | a0006c0007t0011 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*134G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 134 | chr22 | 35393732 | ||||||
| chr22:35393733 | T | C | 1 | a0006c0007t0011 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*135T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 135 | chr22 | 35393733 | ||||||
| chr22:35393842 | C | T | 3 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0010 |
7 | HG01496.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*244C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 244 | chr22 | 35393842 | ||||||
| chr22:35393876 | A | G | 5 | a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 others(2): Show |
34 | HG01192.hp2 HG02055.hp1 HG02258.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*278A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 278 | chr22 | 35393876 | ||||||
| chr22:35393915 | C | T | 1 | a0006c0007t0011 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*317C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 317 | chr22 | 35393915 | ||||||
| chr22:35393916 | T | G | 1 | a0006c0007t0011 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*318T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 318 | chr22 | 35393916 | ||||||
| chr22:35393917 | G | A | 1 | a0006c0007t0011 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*319G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 319 | chr22 | 35393917 | ||||||
| chr22:35393978 | T | G | 1 | a0001c0001t0007 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*380T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 380 | chr22 | 35393978 | ||||||
| chr22:35394089 | T | A | 1 | a0006c0007t0011 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*491T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 491 | chr22 | 35394089 | ||||||
| chr22:35394154 | T | TTAAAGTT others(1): Show |
3 | a0001c0001t0004 a0001c0001t0006 a0001c0004t0004 |
5 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*556_*557insTAAAGT others(2): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 557 | chr22 | 35394154 | ||||||
| chr22:35394181 | A | G | 1 | a0001c0001t0008 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*583A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 583 | chr22 | 35394181 | ||||||
| chr22:35394202 | A | T | 1 | a0001c0001t0010 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*604A>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 5/5 | 604 | chr22 | 35394202 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:35381210 | G | A | 1 | a0004c0009t0001g0040 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.23+14G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381210 | |||||||
| chr22:35381230 | C | G | 1 | a0001c0006t0002g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.23+34C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381230 | |||||||
| chr22:35381268 | C | T | 3 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 |
3 | NA18947.hp2 NA19062.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.23+72C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381268 | |||||||
| chr22:35381301 | G | C | 1 | a0001c0001t0012g0041 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.23+105G>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381301 | |||||||
| chr22:35381302 | C | G | 1 | a0001c0001t0012g0041 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.23+106C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381302 | |||||||
| chr22:35381357 | C | A | 1 | a0001c0001t0001g0042 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.23+161C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381357 | |||||||
| chr22:35381358 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0043 a0001c0001t0001g0044 |
4 | HG00408.hp1 NA18953.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.23+162G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381358 | |||||||
| chr22:35381466 | A | AT | 7 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0222 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.23+280dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 35381466 | ||||||
| chr22:35381466 | A | T | 1 | a0001c0001t0001g0226 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.23+270A>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381466 | |||||||
| chr22:35381569 | G | GGTGGCAT others(113): Show |
1 | a0001c0001t0001g0042 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.23+375_23+494dupTG others(118): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 35381569 | ||||||
| chr22:35381579 | G | A | 6 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(3): Show |
6 | HG01192.hp2 HG02258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.23+383G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381579 | |||||||
| chr22:35381625 | G | A | 138 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(135): Show |
190 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.23+429G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381625 | |||||||
| chr22:35381772 | A | AT | 24 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0038 others(21): Show |
36 | HG00408.hp2 HG01081.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.23+587dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 35381772 | ||||||
| chr22:35381863 | C | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(47): Show |
65 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.23+667C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381863 | |||||||
| chr22:35381910 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG00099.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.23+714G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381910 | |||||||
| chr22:35381957 | G | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0001t0001g0052 |
6 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.23+761G>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381957 | |||||||
| chr22:35381991 | A | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.23+795A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35381991 | |||||||
| chr22:35382007 | C | A | 5 | a0001c0001t0001g0039 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.23+811C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382007 | |||||||
| chr22:35382164 | T | C | 1 | a0004c0009t0001g0040 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.24-942T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382164 | |||||||
| chr22:35382184 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.24-922C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382184 | |||||||
| chr22:35382201 | C | G | 1 | a0001c0006t0002g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.24-905C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382201 | |||||||
| chr22:35382269 | T | C | 5 | a0001c0001t0001g0039 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.24-837T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382269 | |||||||
| chr22:35382285 | A | G | 49 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(46): Show |
64 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.24-821A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382285 | |||||||
| chr22:35382372 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG00735.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.24-734G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382372 | |||||||
| chr22:35382395 | A | G | 1 | a0001c0001t0006g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.24-711A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382395 | |||||||
| chr22:35382413 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.24-693G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382413 | |||||||
| chr22:35382497 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.24-609G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382497 | |||||||
| chr22:35382512 | C | T | 137 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(134): Show |
189 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.24-594C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382512 | |||||||
| chr22:35382517 | A | AT | 48 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(45): Show |
67 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.24-572dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 35382517 | ||||||
| chr22:35382517 | A | ATT | 6 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0071 others(3): Show |
11 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.24-573_24-572dupTT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 35382517 | ||||||
| chr22:35382517 | AT | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0039 others(11): Show |
15 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.24-572delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 35382517 | ||||||
| chr22:35382535 | G | A | 5 | a0001c0001t0001g0039 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.24-571G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382535 | |||||||
| chr22:35382609 | C | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.24-497C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382609 | |||||||
| chr22:35382663 | C | CT | 96 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
139 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.24-436dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 35382663 | ||||||
| chr22:35382663 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.24-443C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382663 | |||||||
| chr22:35382671 | C | CT | 7 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(4): Show |
7 | HG01192.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.24-426dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 35382671 | ||||||
| chr22:35382671 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0006g0145 |
2 | HG02647.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.24-435C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382671 | |||||||
| chr22:35382734 | T | A | 48 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(45): Show |
63 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.24-372T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382734 | |||||||
| chr22:35382760 | C | G | 49 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(46): Show |
64 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.24-346C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382760 | |||||||
| chr22:35382846 | C | T | 34 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(31): Show |
48 | HG00408.hp1 HG00597.hp1 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.24-260C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382846 | |||||||
| chr22:35382872 | G | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0002g0150 |
3 | HG03516.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.24-234G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382872 | |||||||
| chr22:35382968 | A | C | 9 | a0002c0002t0001g0011 a0002c0002t0001g0037 a0002c0002t0001g0199 others(6): Show |
14 | HG00544.hp2 HG00621.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.24-138A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 1/4 | chr22 | 35382968 | |||||||
| chr22:35383230 | T | C | 5 | a0001c0001t0001g0039 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.144+4T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383230 | |||||||
| chr22:35383261 | G | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0226 |
2 | HG00597.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.144+35G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383261 | |||||||
| chr22:35383323 | C | T | 1 | a0004c0009t0001g0040 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.144+97C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383323 | |||||||
| chr22:35383438 | A | AAAAAAAG others(31): Show |
1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+212_144+213ins others(38): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383438 | |||||||
| chr22:35383443 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+217C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383443 | |||||||
| chr22:35383444 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+218T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383444 | |||||||
| chr22:35383449 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+223C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383449 | |||||||
| chr22:35383451 | GCAGTGCC others(65): Show |
G | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+227_144+298del others(72): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35383451 | ||||||
| chr22:35383492 | T | G | 1 | a0001c0001t0006g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.144+266T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383492 | |||||||
| chr22:35383524 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+298C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383524 | |||||||
| chr22:35383525 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+299T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383525 | |||||||
| chr22:35383528 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+302C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383528 | |||||||
| chr22:35383529 | G | T | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+303G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383529 | |||||||
| chr22:35383535 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+309G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383535 | |||||||
| chr22:35383537 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+311T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383537 | |||||||
| chr22:35383538 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+312G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383538 | |||||||
| chr22:35383539 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+313A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383539 | |||||||
| chr22:35383540 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+314G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383540 | |||||||
| chr22:35383548 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+322A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383548 | |||||||
| chr22:35383549 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+323G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383549 | |||||||
| chr22:35383551 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.144+325C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383551 | |||||||
| chr22:35383575 | G | A | 47 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(44): Show |
62 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.144+349G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383575 | |||||||
| chr22:35383622 | C | T | 1 | a0002c0002t0001g0202 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.144+396C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383622 | |||||||
| chr22:35383637 | A | G | 1 | a0001c0001t0002g0073 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.144+411A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383637 | |||||||
| chr22:35383642 | T | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0002g0005 others(7): Show |
17 | HG02055.hp1 HG02486.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.144+416T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383642 | |||||||
| chr22:35383655 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | NA18950.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.144+429C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383655 | |||||||
| chr22:35383851 | T | A | 35 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(32): Show |
49 | HG00408.hp1 HG00597.hp1 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.144+625T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383851 | |||||||
| chr22:35383914 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.144+688C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383914 | |||||||
| chr22:35383951 | AAGAGCTT others(39): Show |
A | 1 | a0001c0001t0001g0138 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.144+728_144+773del others(46): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35383951 | ||||||
| chr22:35383981 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.144+755G>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35383981 | |||||||
| chr22:35384024 | G | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01243.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.144+798G>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35384024 | |||||||
| chr22:35384056 | C | G | 1 | a0001c0001t0001g0072 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.144+830C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35384056 | |||||||
| chr22:35384192 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0137 |
3 | HG00733.hp1 HG01175.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.144+966C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35384192 | |||||||
| chr22:35384284 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.144+1058A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35384284 | |||||||
| chr22:35384371 | AC | A | 6 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(3): Show |
6 | HG01192.hp2 HG02258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.144+1147delC | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35384371 | ||||||
| chr22:35384701 | T | A | 1 | a0001c0001t0001g0227 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.144+1475T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35384701 | |||||||
| chr22:35385122 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.145-1563C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35385122 | |||||||
| chr22:35385213 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.145-1472G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35385213 | |||||||
| chr22:35385214 | T | C | 88 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
125 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.145-1471T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35385214 | |||||||
| chr22:35385221 | C | T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(44): Show |
62 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.145-1464C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35385221 | |||||||
| chr22:35385227 | G | A | 2 | a0001c0004t0004g0152 a0001c0004t0004g0153 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.145-1458G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35385227 | |||||||
| chr22:35385271 | C | A | 1 | a0001c0001t0001g0084 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.145-1414C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35385271 | |||||||
| chr22:35385433 | A | AT | 58 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(55): Show |
74 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.145-1234dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35385433 | ||||||
| chr22:35385433 | A | ATT | 8 | a0001c0001t0001g0039 a0001c0001t0001g0070 a0001c0001t0001g0071 others(5): Show |
9 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.145-1235_145-1234d others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35385433 | ||||||
| chr22:35385433 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0138 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.145-1247_145-1234d others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35385433 | ||||||
| chr22:35385574 | GGACTATA others(60): Show |
G | 1 | a0001c0001t0001g0131 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.145-1109_145-1043d others(69): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35385574 | ||||||
| chr22:35385609 | C | CT | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(31): Show |
41 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.145-1054dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35385609 | ||||||
| chr22:35385609 | CT | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(79): Show |
116 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.145-1054delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35385609 | ||||||
| chr22:35385609 | CTT | C | 40 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(37): Show |
52 | HG00408.hp1 HG00597.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.145-1055_145-1054d others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35385609 | ||||||
| chr22:35385617 | T | TTTTTTTT others(4): Show |
1 | a0001c0001t0001g0138 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.145-1058_145-1057i others(13): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35385617 | ||||||
| chr22:35385673 | T | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0154 a0001c0001t0001g0187 others(1): Show |
8 | NA18948.hp1 NA18967.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.145-1012T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35385673 | |||||||
| chr22:35385936 | G | GTTTA | 14 | a0001c0001t0001g0039 a0001c0001t0001g0222 a0001c0001t0001g0223 others(11): Show |
15 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.145-729_145-726dup others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35385936 | ||||||
| chr22:35386017 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.145-668G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35386017 | |||||||
| chr22:35386056 | C | T | 1 | a0004c0009t0001g0040 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.145-629C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35386056 | |||||||
| chr22:35386149 | G | C | 1 | a0004c0009t0001g0040 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.145-536G>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35386149 | |||||||
| chr22:35386339 | T | TTAAGCAA others(31): Show |
1 | a0001c0001t0001g0130 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.145-345_145-308dup others(38): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr22 | 35386339 | ||||||
| chr22:35386380 | TACAGGGG others(15): Show |
T | 1 | a0001c0001t0001g0129 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.145-304_145-283del others(22): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35386380 | |||||||
| chr22:35386494 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.145-191T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35386494 | |||||||
| chr22:35386515 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG02738.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.145-170A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35386515 | |||||||
| chr22:35386520 | C | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(32): Show |
49 | HG00408.hp1 HG00597.hp1 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.145-165C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35386520 | |||||||
| chr22:35386666 | C | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.145-19C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 2/4 | chr22 | 35386666 | |||||||
| chr22:35387293 | C | T | 7 | a0001c0001t0001g0216 a0001c0001t0002g0045 a0001c0001t0002g0046 others(4): Show |
7 | HG01192.hp2 HG02056.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.636+117C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387293 | |||||||
| chr22:35387371 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.636+195A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387371 | |||||||
| chr22:35387410 | G | A | 1 | a0005c0005t0001g0206 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.636+234G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387410 | |||||||
| chr22:35387420 | A | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
263 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.636+244A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387420 | |||||||
| chr22:35387558 | C | T | 1 | a0001c0011t0001g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.636+382C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387558 | |||||||
| chr22:35387559 | A | C | 1 | a0001c0001t0001g0183 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.636+383A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387559 | |||||||
| chr22:35387592 | T | TACAGGTG others(65): Show |
1 | a0001c0001t0001g0138 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.636+418_636+489dup others(72): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35387592 | ||||||
| chr22:35387624 | G | A | 48 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(45): Show |
63 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.636+448G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387624 | |||||||
| chr22:35387626 | CTAGCCAG others(25): Show |
C | 1 | a0001c0001t0001g0182 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.636+452_636+483del others(32): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35387626 | ||||||
| chr22:35387721 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.636+545G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387721 | |||||||
| chr22:35387783 | C | T | 6 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(3): Show |
6 | HG01192.hp2 HG02258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.636+607C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387783 | |||||||
| chr22:35387853 | A | C | 1 | a0001c0001t0004g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.636+677A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35387853 | |||||||
| chr22:35388002 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0155 others(2): Show |
8 | NA18968.hp2 NA18972.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.636+826G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388002 | |||||||
| chr22:35388030 | G | T | 1 | a0001c0001t0001g0151 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.636+854G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388030 | |||||||
| chr22:35388042 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.636+866T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388042 | |||||||
| chr22:35388061 | T | G | 2 | a0002c0002t0002g0197 a0002c0002t0002g0198 |
2 | HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.636+885T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388061 | |||||||
| chr22:35388096 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.636+920T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388096 | |||||||
| chr22:35388107 | TA | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0215 a0001c0001t0001g0219 |
3 | NA18956.hp1 NA19012.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.636+937delA | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35388107 | ||||||
| chr22:35388126 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.636+950T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388126 | |||||||
| chr22:35388131 | G | GA | 51 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(48): Show |
66 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(63): Show |
intron_variant | MODIFIER | c.636+962dupA | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35388131 | ||||||
| chr22:35388287 | C | CA | 9 | a0002c0002t0001g0011 a0002c0002t0001g0037 a0002c0002t0001g0199 others(6): Show |
14 | HG00544.hp2 HG00621.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.636+1116dupA | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35388287 | ||||||
| chr22:35388324 | C | T | 88 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
125 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.636+1148C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388324 | |||||||
| chr22:35388394 | G | A | 1 | a0001c0011t0001g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.636+1218G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388394 | |||||||
| chr22:35388415 | G | A | 3 | a0002c0002t0001g0160 a0002c0002t0001g0161 a0002c0002t0001g0162 |
3 | NA18975.hp2 NA19012.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.636+1239G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388415 | |||||||
| chr22:35388466 | AAAAAAC | A | 7 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(4): Show |
7 | HG01192.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.636+1308_636+1313d others(8): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35388466 | ||||||
| chr22:35388484 | C | CA | 15 | a0001c0001t0001g0020 a0001c0001t0001g0083 a0001c0001t0001g0084 others(12): Show |
17 | HG00323.hp1 HG00741.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.636+1317dupA | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35388484 | ||||||
| chr22:35388510 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.636+1334G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388510 | |||||||
| chr22:35388525 | C | T | 1 | a0001c0011t0001g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-1339C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388525 | |||||||
| chr22:35388553 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.637-1311C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388553 | |||||||
| chr22:35388554 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | NA18983.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.637-1310G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388554 | |||||||
| chr22:35388562 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.637-1302T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388562 | |||||||
| chr22:35388614 | C | A | 1 | a0001c0001t0001g0219 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.637-1250C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388614 | |||||||
| chr22:35388624 | A | G | 5 | a0001c0001t0001g0039 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-1240A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388624 | |||||||
| chr22:35388752 | G | A | 34 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(31): Show |
48 | HG00408.hp1 HG00597.hp1 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.637-1112G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388752 | |||||||
| chr22:35388754 | G | A | 7 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | HG01109.hp2 HG02922.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-1110G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388754 | |||||||
| chr22:35388763 | C | T | 1 | a0004c0009t0001g0040 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.637-1101C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388763 | |||||||
| chr22:35388802 | C | CA | 3 | a0001c0001t0001g0039 a0001c0001t0001g0223 a0001c0001t0001g0224 |
4 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-1056dupA | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35388802 | ||||||
| chr22:35388809 | C | A | 5 | a0001c0001t0001g0039 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-1055C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388809 | |||||||
| chr22:35388809 | C | CA | 20 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(17): Show |
24 | HG00597.hp1 HG01168.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.637-1052dupA | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35388809 | ||||||
| chr22:35388809 | C | CAA | 9 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0057 others(6): Show |
16 | HG00408.hp1 HG02486.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.637-1053_637-1052d others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35388809 | ||||||
| chr22:35388812 | A | AAC | 7 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(4): Show |
7 | HG01192.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-1052_637-1051i others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388812 | |||||||
| chr22:35388813 | C | A | 48 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(45): Show |
63 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.637-1051C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388813 | |||||||
| chr22:35388813 | C | CA | 10 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0159 others(7): Show |
10 | HG00621.hp2 HG01106.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.637-1042dupA | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35388813 | ||||||
| chr22:35388990 | A | G | 2 | a0001c0001t0005g0097 a0001c0001t0005g0124 |
2 | NA18963.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.637-874A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388990 | |||||||
| chr22:35388996 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.637-868T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35388996 | |||||||
| chr22:35389005 | A | G | 43 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(40): Show |
57 | HG00408.hp1 HG00597.hp1 HG01168.hp2 others(54): Show |
intron_variant | MODIFIER | c.637-859A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389005 | |||||||
| chr22:35389113 | G | A | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-751G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389113 | |||||||
| chr22:35389140 | A | G | 1 | a0001c0011t0001g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-724A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389140 | |||||||
| chr22:35389141 | T | C | 13 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(10): Show |
16 | HG00408.hp1 HG00597.hp1 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.637-723T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389141 | |||||||
| chr22:35389189 | T | TTTTC | 24 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0028 others(21): Show |
33 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.637-653_637-650dup others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389189 | ||||||
| chr22:35389189 | T | TTTTCTTT others(1): Show |
21 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0029 others(18): Show |
35 | HG00733.hp1 HG01106.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.637-657_637-650dup others(8): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389189 | ||||||
| chr22:35389189 | T | TTTTCTTT others(5): Show |
15 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(12): Show |
24 | HG01069.hp2 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.637-661_637-650dup others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389189 | ||||||
| chr22:35389189 | T | TTTTCTTT others(9): Show |
6 | a0001c0001t0001g0019 a0001c0001t0001g0075 a0001c0001t0001g0120 others(3): Show |
8 | HG00558.hp2 HG01070.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.637-665_637-650dup others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389189 | ||||||
| chr22:35389189 | T | TTTTCTTT others(13): Show |
3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG00438.hp1 NA18957.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.637-669_637-650dup others(20): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389189 | ||||||
| chr22:35389211 | TTCTC | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0027 a0001c0001t0001g0085 others(1): Show |
5 | NA19011.hp1 NA19074.hp1 NA20752.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-649_637-646del others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389211 | ||||||
| chr22:35389215 | C | CTCTT | 15 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(12): Show |
28 | HG00544.hp1 HG00544.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.637-627_637-624dup others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389215 | ||||||
| chr22:35389215 | C | T | 133 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(130): Show |
183 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.637-649C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389215 | |||||||
| chr22:35389215 | CTCTT | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(11): Show |
17 | HG00140.hp1 HG00642.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.637-627_637-624del others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389215 | ||||||
| chr22:35389223 | TTCTTTC | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-639_637-634del others(6): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389223 | ||||||
| chr22:35389229 | C | CTTTCTT | 2 | a0001c0001t0001g0012 a0001c0001t0001g0052 |
3 | HG01168.hp2 HG01169.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.637-633_637-628dup others(6): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389229 | ||||||
| chr22:35389229 | C | CTTTCTTT others(3): Show |
6 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0001t0001g0060 others(3): Show |
7 | HG01884.hp1 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-622_637-613dup others(10): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389229 | ||||||
| chr22:35389229 | C | CTTTCTTT others(7): Show |
15 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(12): Show |
21 | HG00408.hp1 HG02486.hp2 HG02622.hp2 others(18): Show |
intron_variant | MODIFIER | c.637-624_637-623ins others(14): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389229 | ||||||
| chr22:35389229 | C | CTTTCTTT others(10): Show |
1 | a0001c0001t0002g0059 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.637-624_637-623ins others(17): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389229 | ||||||
| chr22:35389229 | C | CTTTCTTT others(11): Show |
9 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0044 others(6): Show |
12 | HG00597.hp1 HG02135.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.637-624_637-623ins others(18): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389229 | ||||||
| chr22:35389229 | C | CTTTCTTT others(23): Show |
1 | a0001c0011t0001g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-624_637-623ins others(30): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389229 | ||||||
| chr22:35389229 | C | CTTTCTTT others(16): Show |
2 | a0001c0001t0002g0047 a0001c0001t0002g0050 |
2 | HG01192.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.637-624_637-623ins others(23): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389229 | ||||||
| chr22:35389229 | C | CTTTCTTT others(12): Show |
3 | a0001c0001t0002g0046 a0001c0001t0002g0048 a0001c0001t0002g0049 |
3 | HG02258.hp2 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.637-624_637-623ins others(19): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389229 | ||||||
| chr22:35389229 | C | CTTTCTTT others(8): Show |
1 | a0001c0001t0002g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.637-623_637-622ins others(15): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389229 | ||||||
| chr22:35389237 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.637-627C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389237 | |||||||
| chr22:35389238 | T | TTTCTTTC others(8): Show |
1 | a0001c0001t0001g0091 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.637-624_637-623ins others(15): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389238 | ||||||
| chr22:35389239 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.637-625T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389239 | |||||||
| chr22:35389239 | T | TTC | 4 | a0001c0001t0001g0064 a0001c0001t0001g0131 a0001c0001t0010g0144 others(1): Show |
4 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-624_637-623ins others(2): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389239 | ||||||
| chr22:35389239 | T | TTCTTTCT others(3): Show |
1 | a0001c0004t0004g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.637-624_637-623ins others(10): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389239 | ||||||
| chr22:35389241 | T | C | 4 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0227 others(1): Show |
4 | HG02738.hp2 NA18963.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-623T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389241 | |||||||
| chr22:35389243 | C | T | 4 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0227 others(1): Show |
4 | HG02738.hp2 NA18963.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-621C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389243 | |||||||
| chr22:35389250 | T | C | 2 | a0001c0001t0001g0096 a0001c0001t0010g0144 |
2 | HG01496.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.637-614T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389250 | |||||||
| chr22:35389250 | T | TC | 4 | a0001c0001t0001g0127 a0001c0001t0001g0156 a0001c0001t0001g0165 others(1): Show |
4 | HG02738.hp2 NA18612.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-614_637-613ins others(1): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389250 | |||||||
| chr22:35389250 | T | TTC | 9 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0164 others(6): Show |
14 | HG00642.hp1 HG01109.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-591_637-590dup others(2): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389250 | ||||||
| chr22:35389250 | TTC | T | 4 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(1): Show |
4 | HG03831.hp2 NA18944.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-591_637-590del others(2): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389250 | ||||||
| chr22:35389250 | TTCTC | T | 14 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0076 others(11): Show |
16 | HG00735.hp2 HG01109.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.637-593_637-590del others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389250 | ||||||
| chr22:35389250 | TTCTCTCT others(7): Show |
T | 1 | a0001c0001t0001g0217 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.637-603_637-590del others(14): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389250 | ||||||
| chr22:35389251 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.637-613T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389251 | |||||||
| chr22:35389252 | C | T | 4 | a0001c0001t0001g0096 a0001c0001t0001g0129 a0001c0001t0001g0131 others(1): Show |
4 | HG02738.hp1 HG02818.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-612C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389252 | |||||||
| chr22:35389253 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-611T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389253 | |||||||
| chr22:35389254 | C | T | 6 | a0001c0001t0001g0064 a0001c0001t0001g0072 a0001c0001t0001g0086 others(3): Show |
6 | HG01243.hp2 HG02055.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-610C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389254 | |||||||
| chr22:35389256 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.637-608C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389256 | |||||||
| chr22:35389258 | C | T | 2 | a0001c0001t0001g0072 a0001c0003t0001g0074 |
2 | HG02055.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.637-606C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389258 | |||||||
| chr22:35389260 | C | T | 2 | a0001c0001t0001g0064 a0001c0003t0001g0074 |
2 | HG01243.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.637-604C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389260 | |||||||
| chr22:35389264 | C | T | 2 | a0001c0001t0001g0064 a0001c0003t0001g0074 |
2 | HG01243.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.637-600C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389264 | |||||||
| chr22:35389265 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-599T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389265 | |||||||
| chr22:35389266 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.637-598C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389266 | |||||||
| chr22:35389268 | CT | C | 3 | a0001c0001t0001g0104 a0001c0001t0001g0141 a0001c0001t0001g0226 |
3 | HG00597.hp2 NA18948.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.637-595delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389268 | |||||||
| chr22:35389269 | T | TC | 67 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): Show |
102 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.637-594dupC | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389269 | ||||||
| chr22:35389270 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.637-594C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389270 | |||||||
| chr22:35389271 | TCTC | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0025 others(14): Show |
23 | HG00597.hp1 HG02135.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.637-589_637-587del others(3): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389271 | ||||||
| chr22:35389273 | T | C | 3 | a0001c0001t0001g0082 a0001c0001t0001g0103 a0001c0001t0001g0127 |
3 | HG01358.hp2 HG02738.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.637-591T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389273 | |||||||
| chr22:35389273 | TC | T | 80 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(77): Show |
119 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.637-589delC | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389273 | ||||||
| chr22:35389274 | C | CT | 17 | a0001c0001t0001g0026 a0001c0001t0001g0063 a0001c0001t0001g0071 others(14): Show |
18 | HG02055.hp1 HG02055.hp2 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.637-590_637-589ins others(1): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389274 | |||||||
| chr22:35389274 | C | T | 4 | a0001c0001t0001g0064 a0001c0001t0001g0082 a0001c0001t0001g0103 others(1): Show |
4 | HG01243.hp2 HG01358.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-590C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389274 | |||||||
| chr22:35389275 | C | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0064 a0001c0001t0001g0180 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.637-589C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389275 | |||||||
| chr22:35389276 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.637-588T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389276 | |||||||
| chr22:35389276 | T | C | 6 | a0001c0001t0001g0039 a0001c0001t0001g0180 a0001c0001t0001g0222 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.637-588T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389276 | |||||||
| chr22:35389281 | CTCTCTCT others(51): Show |
C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0222 |
3 | HG01070.hp2 HG01071.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.637-578_637-521del others(58): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389281 | ||||||
| chr22:35389282 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-582T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389282 | |||||||
| chr22:35389284 | T | TC | 3 | a0001c0001t0002g0046 a0001c0001t0002g0048 a0001c0001t0002g0049 |
3 | HG02258.hp2 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.637-579dupC | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389284 | ||||||
| chr22:35389285 | CTCTCTTC others(29): Show |
C | 1 | a0001c0001t0001g0224 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.637-578_637-543del others(36): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389285 | |||||||
| chr22:35389285 | CTCTCTTC others(37): Show |
C | 1 | a0003c0008t0001g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.637-578_637-535del others(44): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389285 | |||||||
| chr22:35389286 | TCTC | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0170 a0001c0001t0001g0176 others(2): Show |
5 | HG00438.hp2 NA18949.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-577_637-575del others(3): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389286 | |||||||
| chr22:35389287 | C | T | 70 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(67): Show |
104 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.637-577C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389287 | |||||||
| chr22:35389288 | T | C | 69 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(66): Show |
103 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.637-576T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389288 | |||||||
| chr22:35389288 | TCTTCTTT others(46): Show |
T | 1 | a0001c0001t0001g0223 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.637-575_637-523del others(53): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389288 | |||||||
| chr22:35389289 | C | CT | 3 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0006g0145 |
3 | HG01891.hp1 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.637-573dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389289 | ||||||
| chr22:35389289 | C | CTTCT | 6 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0096 others(3): Show |
6 | HG02135.hp1 HG02738.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-569_637-566dup others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389289 | ||||||
| chr22:35389289 | C | T | 70 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(67): Show |
104 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.637-575C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389289 | |||||||
| chr22:35389289 | CT | C | 9 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
11 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.637-573delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389289 | ||||||
| chr22:35389289 | CTTCTTTC others(5): Show |
C | 1 | a0001c0001t0002g0068 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.637-573_637-562del others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389289 | ||||||
| chr22:35389290 | T | C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0025 others(22): Show |
35 | HG00408.hp1 HG00597.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.637-574T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389290 | |||||||
| chr22:35389290 | T | TC | 7 | a0001c0001t0001g0012 a0001c0001t0002g0046 a0001c0001t0002g0047 others(4): Show |
7 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-574_637-573ins others(1): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389290 | |||||||
| chr22:35389291 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0012g0041 |
2 | HG04228.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.637-573T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389291 | |||||||
| chr22:35389294 | T | C | 40 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(37): Show |
54 | HG00408.hp1 HG00597.hp1 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.637-570T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389294 | |||||||
| chr22:35389295 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0180 a0001c0001t0010g0144 |
3 | HG01496.hp1 NA18940.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.637-569T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389295 | |||||||
| chr22:35389296 | C | CTCTCTCT others(3): Show |
1 | a0001c0001t0002g0050 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.637-567_637-566ins others(10): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389296 | ||||||
| chr22:35389296 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0180 a0001c0001t0002g0047 |
3 | HG02809.hp1 NA18940.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.637-568C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389296 | |||||||
| chr22:35389296 | CT | C | 27 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(24): Show |
35 | HG00408.hp1 HG00597.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.637-566delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389296 | ||||||
| chr22:35389296 | CTTCT | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0159 a0001c0001t0001g0183 |
3 | HG01517.hp2 HG03041.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.637-546_637-543del others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389296 | ||||||
| chr22:35389297 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0072 a0001c0001t0010g0144 |
3 | HG01496.hp1 HG04228.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.637-567T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389297 | |||||||
| chr22:35389297 | T | TC | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0002g0005 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-567_637-566ins others(1): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389297 | |||||||
| chr22:35389298 | T | C | 7 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0001t0001g0052 others(4): Show |
9 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.637-566T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389298 | |||||||
| chr22:35389299 | C | T | 10 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0089 others(7): Show |
12 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.637-565C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389299 | |||||||
| chr22:35389300 | T | C | 7 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0089 others(4): Show |
9 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.637-564T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389300 | |||||||
| chr22:35389301 | T | C | 34 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(31): Show |
45 | HG00408.hp1 HG00597.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.637-563T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389301 | |||||||
| chr22:35389302 | T | G | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-562T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389302 | |||||||
| chr22:35389305 | T | C | 34 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0025 others(31): Show |
45 | HG00408.hp1 HG00597.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.637-559T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389305 | |||||||
| chr22:35389305 | TTC | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0020 others(2): Show |
7 | HG00323.hp1 HG01081.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-557_637-556del others(2): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389305 | ||||||
| chr22:35389306 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-558T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389306 | |||||||
| chr22:35389306 | TCTTTCTT others(82): Show |
T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0051 |
3 | HG01884.hp1 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.637-542_637-454del others(89): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389306 | ||||||
| chr22:35389309 | T | C | 33 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0025 others(30): Show |
44 | HG00408.hp1 HG00597.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.637-555T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389309 | |||||||
| chr22:35389310 | TCTTTCTT others(78): Show |
T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0052 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.637-542_637-458del others(85): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389310 | ||||||
| chr22:35389311 | CTTTCTTT others(89): Show |
C | 1 | a0001c0001t0002g0069 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.637-552_637-457del others(96): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389311 | |||||||
| chr22:35389312 | T | G | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-552T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389312 | |||||||
| chr22:35389313 | T | C | 32 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0025 others(29): Show |
43 | HG00408.hp1 HG00597.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.637-551T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389313 | |||||||
| chr22:35389314 | TCTTTCTT others(74): Show |
T | 1 | a0001c0001t0001g0012 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.637-542_637-462del others(81): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389314 | ||||||
| chr22:35389315 | CTTTCTTC others(97): Show |
C | 1 | a0001c0001t0002g0005 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.637-548_637-445del | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389315 | |||||||
| chr22:35389316 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-548T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389316 | |||||||
| chr22:35389317 | T | C | 32 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0025 others(29): Show |
42 | HG00408.hp1 HG00597.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.637-547T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389317 | |||||||
| chr22:35389318 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0002 |
2 | HG01516.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.637-546T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389318 | |||||||
| chr22:35389318 | TCTTCTTT others(70): Show |
T | 1 | a0001c0001t0002g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.637-542_637-466del others(77): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389318 | ||||||
| chr22:35389319 | C | CT | 5 | a0001c0001t0001g0031 a0001c0001t0001g0083 a0001c0001t0001g0120 others(2): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-543dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389319 | ||||||
| chr22:35389319 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0002 |
2 | HG01516.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.637-545C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389319 | |||||||
| chr22:35389319 | CT | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0070 others(1): Show |
4 | HG02135.hp2 HG03927.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-543delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389319 | ||||||
| chr22:35389319 | CTTCTTTC others(77): Show |
C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0060 others(1): Show |
4 | HG00408.hp1 HG03490.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-544_637-461del others(84): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389319 | |||||||
| chr22:35389319 | CTTCTTTC others(79): Show |
C | 1 | a0001c0001t0001g0026 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.637-523_637-438del others(86): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389319 | ||||||
| chr22:35389319 | CTTCTTTC others(85): Show |
C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0061 a0001c0001t0001g0062 |
4 | HG00597.hp1 NA18941.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-544_637-453del others(92): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389319 | |||||||
| chr22:35389319 | CTTCTTTC others(89): Show |
C | 4 | a0001c0001t0002g0005 a0001c0001t0002g0024 a0001c0001t0002g0059 others(1): Show |
5 | HG03139.hp2 HG03453.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-544_637-449del others(96): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389319 | |||||||
| chr22:35389319 | CTTCTTTC others(93): Show |
C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0002g0005 others(3): Show |
8 | HG02647.hp1 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.637-544_637-445del others(100): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389319 | |||||||
| chr22:35389319 | CTTCTTTC others(97): Show |
C | 3 | a0001c0001t0003g0005 a0001c0003t0001g0016 a0001c0003t0002g0016 |
4 | HG02622.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-544_637-441del | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389319 | |||||||
| chr22:35389320 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.637-544T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389320 | |||||||
| chr22:35389320 | TTCTTTCT others(68): Show |
T | 1 | a0001c0001t0001g0026 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.637-543_637-469del others(75): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389320 | |||||||
| chr22:35389321 | T | C | 8 | a0001c0001t0001g0044 a0001c0001t0002g0055 a0001c0001t0002g0065 others(5): Show |
8 | HG02055.hp1 HG02486.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.637-543T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389321 | |||||||
| chr22:35389321 | T | TTTCTTC | 3 | a0001c0001t0002g0046 a0001c0001t0002g0048 a0001c0001t0002g0049 |
3 | HG02258.hp2 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.637-543_637-542ins others(6): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389321 | |||||||
| chr22:35389322 | C | T | 83 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(80): Show |
118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.637-542C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389322 | |||||||
| chr22:35389323 | T | C | 84 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(81): Show |
119 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.637-541T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389323 | |||||||
| chr22:35389324 | T | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0064 others(4): Show |
7 | HG01243.hp2 HG01496.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-540T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389324 | |||||||
| chr22:35389325 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.637-539T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389325 | |||||||
| chr22:35389326 | CTTTCTTT others(70): Show |
C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0070 |
2 | HG02135.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.637-537_637-461del others(77): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389326 | |||||||
| chr22:35389326 | CTTTCTTT others(74): Show |
C | 1 | a0001c0001t0001g0072 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.637-537_637-457del others(81): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389326 | |||||||
| chr22:35389326 | CTTTCTTT others(82): Show |
C | 1 | a0001c0003t0001g0074 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.637-537_637-449del others(89): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389326 | |||||||
| chr22:35389328 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0010g0144 |
3 | HG01243.hp2 HG01496.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.637-536T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389328 | |||||||
| chr22:35389329 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.637-535T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389329 | |||||||
| chr22:35389329 | T | G | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-535T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389329 | |||||||
| chr22:35389330 | CT | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0120 a0001c0001t0001g0134 others(1): Show |
5 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-531delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389330 | ||||||
| chr22:35389330 | CTTTCTTT others(66): Show |
C | 1 | a0001c0001t0001g0063 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.637-533_637-461del others(73): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389330 | |||||||
| chr22:35389331 | T | C | 1 | a0002c0002t0001g0201 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.637-533T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389331 | |||||||
| chr22:35389331 | TTTCTTTC others(57): Show |
T | 1 | a0001c0001t0001g0064 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.637-532_637-469del others(64): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389331 | |||||||
| chr22:35389332 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-532T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389332 | |||||||
| chr22:35389332 | TTCTTTCT others(91): Show |
T | 5 | a0001c0001t0002g0055 a0001c0001t0002g0065 a0001c0001t0002g0066 others(2): Show |
5 | HG02055.hp1 HG02486.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-523_637-426del others(98): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389332 | ||||||
| chr22:35389333 | T | C | 3 | a0001c0001t0001g0224 a0001c0001t0010g0144 a0003c0008t0001g0225 |
3 | HG01168.hp1 HG01496.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.637-531T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389333 | |||||||
| chr22:35389335 | T | C | 2 | a0001c0001t0001g0143 a0002c0002t0001g0201 |
2 | HG00735.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.637-529T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389335 | |||||||
| chr22:35389336 | T | C | 1 | a0001c0011t0001g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-528T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389336 | |||||||
| chr22:35389337 | T | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0224 others(1): Show |
4 | HG01168.hp1 HG01516.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-527T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389337 | |||||||
| chr22:35389337 | TCTTCTCC others(51): Show |
T | 1 | a0001c0001t0002g0068 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.637-523_637-466del others(58): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389337 | ||||||
| chr22:35389339 | T | C | 3 | a0001c0001t0001g0143 a0001c0001t0010g0144 a0002c0002t0001g0201 |
3 | HG00735.hp2 HG01496.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.637-525T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389339 | |||||||
| chr22:35389339 | T | TTTCTTTC others(88): Show |
1 | a0001c0001t0002g0047 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.637-524_637-523ins others(95): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389339 | ||||||
| chr22:35389339 | T | TTTCTTTC others(94): Show |
1 | a0001c0001t0002g0046 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.637-524_637-523ins others(101): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389339 | ||||||
| chr22:35389339 | T | TTTCTTTC others(86): Show |
1 | a0001c0001t0002g0050 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.637-524_637-523ins others(93): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389339 | ||||||
| chr22:35389339 | TTC | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0120 a0001c0001t0001g0134 others(2): Show |
6 | HG01109.hp1 HG01168.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-522_637-521del others(2): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389339 | ||||||
| chr22:35389340 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.637-524T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389340 | |||||||
| chr22:35389340 | T | TTCTTCTT others(14): Show |
1 | a0001c0001t0001g0194 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.637-524_637-523ins others(21): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389340 | |||||||
| chr22:35389340 | T | TTCTTTCT others(96): Show |
1 | a0001c0001t0002g0048 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.637-524_637-523ins others(103): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389340 | |||||||
| chr22:35389340 | T | TTCTTTCT others(88): Show |
1 | a0001c0001t0002g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.637-524_637-523ins others(95): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389340 | |||||||
| chr22:35389340 | TCTCCTTC others(83): Show |
T | 2 | a0001c0001t0001g0044 a0001c0001t0012g0041 |
2 | NA18953.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.637-523_637-434del others(90): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389340 | |||||||
| chr22:35389341 | C | CTCCT | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(9): Show |
18 | HG00408.hp2 HG00621.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.637-469_637-466dup others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | ||||||
| chr22:35389341 | C | CTCCTTCC others(1): Show |
8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(5): Show |
9 | HG00673.hp2 HG01256.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.637-473_637-466dup others(8): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | ||||||
| chr22:35389341 | C | CTCCTTCC others(5): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0213 |
2 | HG01433.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.637-477_637-466dup others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | ||||||
| chr22:35389341 | C | CTCCTTCC others(9): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0209 |
3 | HG03209.hp2 NA18944.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.637-481_637-466dup others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | ||||||
| chr22:35389341 | C | CTCCTTCC others(13): Show |
1 | a0002c0002t0001g0200 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.637-485_637-466dup others(20): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | ||||||
| chr22:35389341 | C | CTCCTTCC others(37): Show |
1 | a0001c0001t0001g0122 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.637-509_637-466dup others(44): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | ||||||
| chr22:35389341 | C | CTCCTTCC others(73): Show |
1 | a0001c0001t0001g0142 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.637-476_637-475ins others(80): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | ||||||
| chr22:35389341 | C | T | 3 | a0001c0001t0001g0194 a0001c0001t0002g0048 a0002c0002t0001g0162 |
3 | HG00642.hp2 HG02258.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.637-523C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389341 | |||||||
| chr22:35389341 | CTCCT | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(12): Show |
20 | HG00323.hp1 HG00544.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.637-469_637-466del others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | ||||||
| chr22:35389341 | CTCCTTCC others(1): Show |
C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(9): Show |
14 | HG01978.hp1 HG02027.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-473_637-466del others(8): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | ||||||
| chr22:35389341 | CTCCTTCC others(5): Show |
C | 19 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(16): Show |
20 | HG00544.hp2 HG00609.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.637-477_637-466del others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | ||||||
| chr22:35389341 | CTCCTTCC others(9): Show |
C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(4): Show |
7 | HG00423.hp1 HG02976.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.637-481_637-466del others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | ||||||
| chr22:35389341 | CTCCTTCC others(17): Show |
C | 1 | a0002c0002t0001g0011 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.637-489_637-466del others(24): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389341 | ||||||
| chr22:35389342 | T | C | 1 | a0001c0001t0001g0007 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.637-522T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389342 | |||||||
| chr22:35389343 | C | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0120 a0001c0001t0001g0134 others(1): Show |
5 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-521C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389343 | |||||||
| chr22:35389343 | CCTTCCTT others(3): Show |
C | 1 | a0001c0001t0001g0170 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.637-520_637-511del others(10): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389343 | |||||||
| chr22:35389344 | C | T | 1 | a0001c0011t0001g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-520C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389344 | |||||||
| chr22:35389345 | T | C | 3 | a0001c0001t0001g0171 a0001c0001t0010g0144 a0001c0011t0001g0054 |
3 | HG00423.hp2 HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-519T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389345 | |||||||
| chr22:35389347 | C | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0120 others(1): Show |
6 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-517C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389347 | |||||||
| chr22:35389348 | C | G | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-516C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389348 | |||||||
| chr22:35389348 | C | T | 1 | a0001c0011t0001g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-516C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389348 | |||||||
| chr22:35389349 | T | C | 2 | a0001c0001t0010g0144 a0001c0011t0001g0054 |
2 | HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-515T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389349 | |||||||
| chr22:35389351 | C | CCTTCCTT others(8): Show |
1 | a0001c0001t0001g0159 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.637-511_637-497dup others(15): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389351 | ||||||
| chr22:35389351 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0180 |
3 | NA18940.hp2 NA19011.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.637-513C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389351 | |||||||
| chr22:35389351 | CCT | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0120 a0001c0001t0001g0134 others(1): Show |
5 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-512_637-511del others(2): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389351 | |||||||
| chr22:35389352 | C | T | 1 | a0001c0011t0001g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-512C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389352 | |||||||
| chr22:35389353 | T | C | 1 | a0001c0011t0001g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-511T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389353 | |||||||
| chr22:35389355 | C | T | 1 | a0001c0001t0001g0027 | 2 | NA19011.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.637-509C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389355 | |||||||
| chr22:35389356 | C | T | 1 | a0001c0011t0001g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-508C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389356 | |||||||
| chr22:35389357 | T | C | 2 | a0001c0001t0010g0144 a0001c0011t0001g0054 |
2 | HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-507T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389357 | |||||||
| chr22:35389360 | C | G | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-504C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389360 | |||||||
| chr22:35389361 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-503T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389361 | |||||||
| chr22:35389361 | TTCCTTCC others(27): Show |
T | 1 | a0001c0011t0001g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.637-502_637-469del others(34): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389361 | |||||||
| chr22:35389367 | CCTTCCTT others(37): Show |
C | 1 | a0001c0004t0004g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.637-493_637-450del others(44): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389367 | ||||||
| chr22:35389369 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-495T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389369 | |||||||
| chr22:35389372 | C | G | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-492C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389372 | |||||||
| chr22:35389373 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-491T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389373 | |||||||
| chr22:35389375 | C | T | 2 | a0002c0002t0001g0011 a0002c0002t0001g0204 |
3 | NA18957.hp2 NA18989.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.637-489C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389375 | |||||||
| chr22:35389379 | C | T | 1 | a0002c0002t0001g0011 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.637-485C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389379 | |||||||
| chr22:35389379 | CCTTCCTT others(13): Show |
C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(6): Show |
9 | HG00597.hp2 HG01256.hp1 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.637-481_637-462del others(20): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389379 | ||||||
| chr22:35389379 | CCTTCCTT others(29): Show |
C | 1 | a0001c0001t0001g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.637-481_637-446del others(36): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389379 | ||||||
| chr22:35389380 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.637-484C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389380 | |||||||
| chr22:35389381 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-483T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389381 | |||||||
| chr22:35389382 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.637-482T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389382 | |||||||
| chr22:35389383 | C | CCTTT | 4 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0140 others(1): Show |
4 | HG01070.hp1 NA18952.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-478_637-477ins others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389383 | ||||||
| chr22:35389383 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0096 a0001c0001t0001g0105 others(1): Show |
4 | NA18971.hp2 NA18990.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-481C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389383 | |||||||
| chr22:35389383 | CCTTCCTT others(9): Show |
C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(5): Show |
11 | HG01069.hp2 HG01255.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.637-477_637-462del others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389383 | ||||||
| chr22:35389383 | CCTTCCTT others(13): Show |
C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0001g0130 others(1): Show |
4 | HG00438.hp2 HG02602.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-477_637-458del others(20): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389383 | ||||||
| chr22:35389383 | CCTTCCTT others(21): Show |
C | 1 | a0001c0004t0004g0153 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.637-477_637-450del others(28): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389383 | ||||||
| chr22:35389384 | C | G | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-480C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389384 | |||||||
| chr22:35389384 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.637-480C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389384 | |||||||
| chr22:35389385 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-479T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389385 | |||||||
| chr22:35389387 | C | CCCTCCCT others(87): Show |
1 | a0006c0007t0011g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.637-476_637-475ins others(94): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389387 | ||||||
| chr22:35389387 | C | CCCTCCCT others(91): Show |
1 | a0001c0001t0001g0116 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.637-476_637-475ins others(98): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389387 | ||||||
| chr22:35389387 | C | CCCTCCCT others(85): Show |
1 | a0001c0001t0001g0115 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.637-476_637-475ins others(92): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389387 | ||||||
| chr22:35389387 | C | T | 17 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0017 others(14): Show |
19 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.637-477C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389387 | |||||||
| chr22:35389387 | CCTTCCTT others(5): Show |
C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(1): Show |
4 | HG00609.hp1 HG02004.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-473_637-462del others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389387 | ||||||
| chr22:35389387 | CCTTCCTT others(9): Show |
C | 1 | a0001c0001t0001g0212 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.637-473_637-458del others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389387 | ||||||
| chr22:35389389 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.637-475T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389389 | |||||||
| chr22:35389390 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-474T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389390 | |||||||
| chr22:35389391 | C | CCTTCCTT others(21): Show |
1 | a0001c0001t0001g0099 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(28): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389391 | ||||||
| chr22:35389391 | C | CCTTTCTT others(17): Show |
1 | a0001c0001t0004g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.637-470_637-469ins others(24): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389391 | ||||||
| chr22:35389391 | C | CCTTTCTT others(9): Show |
1 | a0001c0001t0001g0103 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.637-470_637-469ins others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389391 | ||||||
| chr22:35389391 | C | CCTTTCTT others(13): Show |
1 | a0001c0001t0001g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.637-470_637-469ins others(20): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389391 | ||||||
| chr22:35389391 | C | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(35): Show |
41 | HG01070.hp1 HG01167.hp2 HG01169.hp2 others(38): Show |
intron_variant | MODIFIER | c.637-473C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389391 | |||||||
| chr22:35389391 | CCTTCCTT others(1): Show |
C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(9): Show |
14 | HG00558.hp2 HG00733.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.637-469_637-462del others(8): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389391 | ||||||
| chr22:35389391 | CCTTCCTT others(5): Show |
C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0205 a0001c0001t0001g0221 |
3 | HG02132.hp1 HG03130.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.637-469_637-458del others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389391 | ||||||
| chr22:35389391 | CCTTCCTT others(9): Show |
C | 1 | a0001c0001t0001g0002 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.637-469_637-454del others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389391 | ||||||
| chr22:35389394 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-470T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389394 | |||||||
| chr22:35389394 | TCCTTTCT others(29): Show |
T | 1 | a0001c0001t0001g0226 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.637-469_637-434del others(36): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389394 | |||||||
| chr22:35389395 | C | CCTTCCTT others(40): Show |
1 | a0001c0001t0001g0007 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(47): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(69): Show |
1 | a0001c0001t0001g0111 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(76): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(85): Show |
1 | a0001c0001t0001g0108 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(92): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(73): Show |
1 | a0001c0001t0005g0124 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(80): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(97): Show |
1 | a0001c0001t0001g0129 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(104): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(53): Show |
1 | a0001c0001t0001g0147 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(60): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(61): Show |
1 | a0001c0001t0001g0123 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(68): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(57): Show |
1 | a0001c0001t0005g0097 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(64): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(53): Show |
1 | a0001c0001t0001g0019 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(60): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(89): Show |
1 | a0001c0001t0001g0007 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(96): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(38): Show |
1 | a0001c0001t0001g0121 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(45): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(33): Show |
1 | a0001c0001t0001g0220 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(40): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(49): Show |
1 | a0001c0001t0001g0146 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(56): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(17): Show |
1 | a0001c0001t0001g0207 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(24): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(25): Show |
1 | a0001c0001t0001g0101 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(32): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(33): Show |
1 | a0001c0001t0001g0135 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(40): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(45): Show |
1 | a0001c0001t0001g0008 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(52): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(60): Show |
1 | a0001c0001t0001g0110 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(67): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(9): Show |
1 | a0001c0001t0001g0010 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(13): Show |
1 | a0001c0001t0001g0003 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.637-466_637-465ins others(20): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(5): Show |
1 | a0001c0001t0001g0010 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(53): Show |
1 | a0001c0001t0001g0028 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(60): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(1): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(1): Show |
5 | HG00140.hp2 HG04184.hp2 NA19087.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-466_637-465ins others(8): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(21): Show |
1 | a0001c0001t0006g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.637-466_637-465ins others(28): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTCCTT others(5): Show |
2 | a0001c0001t0001g0001 a0007c0010t0001g0001 |
2 | HG01081.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.637-466_637-465ins others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTT | 6 | a0001c0001t0001g0020 a0001c0001t0001g0174 a0001c0001t0001g0214 others(3): Show |
6 | HG03831.hp2 HG04228.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-438_637-435dup others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTTCTT others(1): Show |
4 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0004g0080 others(1): Show |
4 | HG01358.hp2 HG02258.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-442_637-435dup others(8): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | CCTTTCTT others(5): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0081 a0001c0001t0001g0143 |
3 | HG00735.hp1 HG00735.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.637-446_637-435dup others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | C | G | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-469C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389395 | |||||||
| chr22:35389395 | C | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0014 others(27): Show |
43 | HG00544.hp2 HG00558.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.637-469C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389395 | |||||||
| chr22:35389395 | CCTTT | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(8): Show |
12 | HG00099.hp2 HG00140.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.637-438_637-435del others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389395 | CCTTTCTT others(1): Show |
C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-442_637-435del others(8): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389395 | ||||||
| chr22:35389396 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.637-468C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389396 | |||||||
| chr22:35389398 | T | C | 4 | a0001c0001t0001g0026 a0001c0001t0001g0064 a0001c0001t0010g0144 others(1): Show |
4 | HG01243.hp2 HG01496.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-466T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389398 | |||||||
| chr22:35389399 | T | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(35): Show |
52 | HG00408.hp2 HG00733.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.637-465T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389399 | |||||||
| chr22:35389401 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0010g0144 |
2 | HG01496.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.637-463T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389401 | |||||||
| chr22:35389402 | T | C | 4 | a0001c0001t0001g0064 a0001c0001t0010g0144 a0001c0006t0002g0230 others(1): Show |
4 | HG01243.hp2 HG01496.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-462T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389402 | |||||||
| chr22:35389403 | T | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(35): Show |
47 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.637-461T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389403 | |||||||
| chr22:35389405 | T | G | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-459T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389405 | |||||||
| chr22:35389406 | T | C | 3 | a0001c0001t0001g0064 a0001c0001t0010g0144 a0001c0011t0001g0054 |
3 | HG01243.hp2 HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-458T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389406 | |||||||
| chr22:35389407 | T | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(27): Show |
37 | HG00597.hp2 HG00733.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.637-457T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389407 | |||||||
| chr22:35389407 | T | G | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-457T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389407 | |||||||
| chr22:35389410 | T | C | 3 | a0001c0001t0001g0064 a0001c0001t0010g0144 a0001c0011t0001g0054 |
3 | HG01243.hp2 HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-454T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389410 | |||||||
| chr22:35389410 | TTCTTTCT others(13): Show |
T | 1 | a0001c0006t0002g0230 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.637-434_637-415del others(20): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389410 | ||||||
| chr22:35389411 | T | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0001g0099 others(10): Show |
13 | HG01192.hp2 HG02258.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.637-453T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389411 | |||||||
| chr22:35389414 | T | C | 3 | a0001c0001t0001g0064 a0001c0001t0010g0144 a0001c0011t0001g0054 |
3 | HG01243.hp2 HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-450T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389414 | |||||||
| chr22:35389414 | TTCTTTCT others(9): Show |
T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0104 |
2 | HG02922.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.637-434_637-419del others(16): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389414 | ||||||
| chr22:35389415 | T | C | 4 | a0001c0001t0002g0046 a0001c0001t0002g0048 a0001c0001t0002g0049 others(1): Show |
4 | HG01192.hp2 HG02258.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-449T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389415 | |||||||
| chr22:35389416 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.637-448C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389416 | |||||||
| chr22:35389418 | T | C | 2 | a0001c0001t0010g0144 a0001c0011t0001g0054 |
2 | HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-446T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389418 | |||||||
| chr22:35389418 | TTCTTTCT others(5): Show |
T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0090 a0001c0001t0001g0127 others(2): Show |
6 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-434_637-423del others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389418 | ||||||
| chr22:35389419 | T | C | 5 | a0001c0001t0001g0064 a0001c0001t0002g0046 a0001c0001t0002g0048 others(2): Show |
5 | HG01243.hp2 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-445T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389419 | |||||||
| chr22:35389420 | CTTTCTTT others(22): Show |
C | 1 | a0001c0001t0001g0039 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.637-434_637-406del others(29): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389420 | ||||||
| chr22:35389421 | T | TTTTTTCC others(58): Show |
1 | a0001c0001t0001g0131 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.637-441_637-440ins others(65): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389421 | ||||||
| chr22:35389422 | T | C | 2 | a0001c0001t0010g0144 a0001c0011t0001g0054 |
2 | HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-442T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389422 | |||||||
| chr22:35389422 | TTCTTTCT others(1): Show |
T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0098 others(2): Show |
6 | HG02451.hp1 HG03017.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-434_637-427del others(8): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389422 | ||||||
| chr22:35389423 | T | C | 2 | a0001c0001t0001g0075 a0001c0001t0002g0046 |
2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.637-441T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389423 | |||||||
| chr22:35389426 | T | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0193 |
3 | HG01106.hp1 HG01192.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.637-438T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389426 | |||||||
| chr22:35389426 | T | C | 2 | a0001c0001t0010g0144 a0001c0011t0001g0054 |
2 | HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-438T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389426 | |||||||
| chr22:35389426 | TTCTA | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0034 others(1): Show |
5 | HG01175.hp1 HG01257.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-434_637-431del others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389426 | ||||||
| chr22:35389428 | CTATCTTT others(14): Show |
C | 1 | a0001c0001t0001g0222 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.637-434_637-414del others(21): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389428 | ||||||
| chr22:35389430 | A | C | 2 | a0001c0001t0010g0144 a0001c0011t0001g0054 |
2 | HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-434A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389430 | |||||||
| chr22:35389430 | A | T | 125 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(122): Show |
174 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.637-434A>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389430 | |||||||
| chr22:35389434 | T | A | 1 | a0001c0001t0001g0210 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.637-430T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389434 | |||||||
| chr22:35389434 | T | C | 2 | a0001c0001t0010g0144 a0001c0011t0001g0054 |
2 | HG01496.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.637-430T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389434 | |||||||
| chr22:35389438 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-426T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389438 | |||||||
| chr22:35389440 | C | CTTTCT | 3 | a0001c0001t0001g0036 a0001c0001t0001g0178 a0001c0001t0001g0193 |
4 | HG01106.hp1 HG01192.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-421_637-417dup others(5): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389440 | ||||||
| chr22:35389441 | T | G | 1 | a0001c0001t0002g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.637-423T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389441 | |||||||
| chr22:35389442 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-422T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389442 | |||||||
| chr22:35389445 | T | G | 1 | a0001c0001t0002g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.637-419T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389445 | |||||||
| chr22:35389445 | TTTCTTTT others(5): Show |
T | 1 | a0004c0009t0001g0040 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.637-416_637-405del others(12): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389445 | ||||||
| chr22:35389446 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-418T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389446 | |||||||
| chr22:35389448 | CT | C | 45 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(42): Show |
59 | HG00408.hp1 HG00597.hp1 HG01168.hp1 others(56): Show |
intron_variant | MODIFIER | c.637-412delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 35389448 | ||||||
| chr22:35389450 | T | G | 1 | a0001c0001t0002g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.637-414T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389450 | |||||||
| chr22:35389451 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-413T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389451 | |||||||
| chr22:35389452 | T | C | 9 | a0001c0001t0001g0104 a0001c0001t0001g0108 a0001c0001t0001g0115 others(6): Show |
9 | HG00597.hp2 NA18948.hp2 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.637-412T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389452 | |||||||
| chr22:35389453 | C | T | 6 | a0001c0001t0001g0108 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | NA18968.hp1 NA18971.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-411C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389453 | |||||||
| chr22:35389455 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-409T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389455 | |||||||
| chr22:35389459 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.637-405T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389459 | |||||||
| chr22:35389464 | G | T | 3 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0049 |
3 | HG02258.hp2 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.637-400G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389464 | |||||||
| chr22:35389466 | A | T | 3 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0049 |
3 | HG02258.hp2 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.637-398A>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389466 | |||||||
| chr22:35389474 | G | A | 5 | a0002c0002t0001g0011 a0002c0002t0001g0199 a0002c0002t0001g0204 others(2): Show |
9 | HG00544.hp2 HG00673.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.637-390G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389474 | |||||||
| chr22:35389486 | G | A | 49 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(46): Show |
64 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.637-378G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389486 | |||||||
| chr22:35389517 | A | T | 1 | a0004c0009t0001g0040 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.637-347A>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389517 | |||||||
| chr22:35389675 | C | CT | 138 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(135): Show |
190 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.637-189_637-188ins others(1): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389675 | |||||||
| chr22:35389681 | T | C | 5 | a0001c0001t0001g0039 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.637-183T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389681 | |||||||
| chr22:35389706 | G | A | 1 | a0004c0009t0001g0040 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.637-158G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389706 | |||||||
| chr22:35389710 | G | A | 48 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(45): Show |
63 | HG00408.hp1 HG00597.hp1 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.637-154G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 3/4 | chr22 | 35389710 | |||||||
| chr22:35390010 | GGACTTGG others(6): Show |
G | 5 | a0002c0002t0001g0011 a0002c0002t0001g0199 a0002c0002t0001g0204 others(2): Show |
9 | HG00544.hp2 HG00673.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.736+52_736+64delTG others(11): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35390010 | ||||||
| chr22:35390022 | C | G | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.736+59C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390022 | |||||||
| chr22:35390117 | G | T | 2 | a0001c0004t0004g0152 a0001c0004t0004g0153 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.736+154G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390117 | |||||||
| chr22:35390123 | G | A | 5 | a0001c0001t0001g0108 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | NA18968.hp1 NA18971.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.736+160G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390123 | |||||||
| chr22:35390189 | A | G | 145 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(142): Show |
201 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.736+226A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390189 | |||||||
| chr22:35390233 | T | C | 89 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+270T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390233 | |||||||
| chr22:35390272 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.736+309G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390272 | |||||||
| chr22:35390618 | T | G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0029 a0001c0001t0001g0096 others(4): Show |
11 | HG00423.hp1 HG00609.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.736+655T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390618 | |||||||
| chr22:35390620 | T | C | 1 | a0002c0002t0001g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.736+657T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390620 | |||||||
| chr22:35390666 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.736+703A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390666 | |||||||
| chr22:35390713 | A | G | 89 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+750A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390713 | |||||||
| chr22:35390720 | A | C | 89 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+757A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390720 | |||||||
| chr22:35390729 | T | C | 138 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(135): Show |
190 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.736+766T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390729 | |||||||
| chr22:35390748 | T | C | 89 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+785T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390748 | |||||||
| chr22:35390880 | A | G | 89 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+917A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390880 | |||||||
| chr22:35390970 | G | A | 42 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(39): Show |
56 | HG00408.hp1 HG00597.hp1 HG01168.hp2 others(53): Show |
intron_variant | MODIFIER | c.736+1007G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390970 | |||||||
| chr22:35390994 | T | G | 1 | a0001c0001t0001g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.736+1031T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35390994 | |||||||
| chr22:35391012 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.736+1049G>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391012 | |||||||
| chr22:35391072 | T | C | 5 | a0001c0001t0001g0039 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.736+1109T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391072 | |||||||
| chr22:35391106 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.736+1143C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391106 | |||||||
| chr22:35391171 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.736+1208C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391171 | |||||||
| chr22:35391173 | C | A | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.736+1210C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391173 | |||||||
| chr22:35391174 | C | G | 89 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+1211C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391174 | |||||||
| chr22:35391218 | G | T | 1 | a0001c0001t0001g0154 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.736+1255G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391218 | |||||||
| chr22:35391242 | C | T | 89 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+1279C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391242 | |||||||
| chr22:35391257 | CA | C | 89 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+1297delA | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391257 | ||||||
| chr22:35391283 | ATTTTTTT others(11): Show |
A | 89 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+1324_736+1341d others(20): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391283 | ||||||
| chr22:35391292 | G | GT | 18 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(15): Show |
21 | HG00140.hp2 HG00597.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.736+1341dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391292 | ||||||
| chr22:35391292 | GT | G | 7 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(4): Show |
7 | HG01192.hp2 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.736+1341delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391292 | ||||||
| chr22:35391327 | A | G | 88 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
125 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.736+1364A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391327 | |||||||
| chr22:35391328 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.736+1365C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391328 | |||||||
| chr22:35391337 | G | A | 5 | a0001c0001t0001g0088 a0002c0002t0001g0011 a0002c0002t0001g0204 others(2): Show |
9 | HG00544.hp2 HG00673.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.736+1374G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391337 | |||||||
| chr22:35391356 | C | T | 89 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+1393C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391356 | |||||||
| chr22:35391373 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.736+1410C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391373 | |||||||
| chr22:35391413 | G | A | 2 | a0001c0001t0010g0144 a0004c0009t0001g0040 |
2 | HG01496.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.736+1450G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391413 | |||||||
| chr22:35391437 | G | A | 2 | a0001c0001t0010g0144 a0004c0009t0001g0040 |
2 | HG01496.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.736+1474G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391437 | |||||||
| chr22:35391444 | T | C | 2 | a0001c0001t0010g0144 a0004c0009t0001g0040 |
2 | HG01496.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.736+1481T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391444 | |||||||
| chr22:35391508 | C | T | 1 | a0004c0009t0001g0040 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.736+1545C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391508 | |||||||
| chr22:35391522 | T | C | 2 | a0001c0001t0010g0144 a0004c0009t0001g0040 |
2 | HG01496.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.736+1559T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391522 | |||||||
| chr22:35391557 | A | C | 2 | a0001c0001t0010g0144 a0004c0009t0001g0040 |
2 | HG01496.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.736+1594A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391557 | |||||||
| chr22:35391579 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.736+1616G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391579 | |||||||
| chr22:35391582 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
7 | HG01168.hp2 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.736+1619C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391582 | |||||||
| chr22:35391585 | C | CAT | 48 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(45): Show |
79 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.736+1622_736+1623i others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391585 | |||||||
| chr22:35391585 | C | CATT | 29 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0028 others(26): Show |
34 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.736+1622_736+1623i others(5): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391585 | |||||||
| chr22:35391585 | C | CATTT | 9 | a0001c0001t0001g0030 a0001c0001t0001g0084 a0001c0001t0001g0096 others(6): Show |
10 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.736+1622_736+1623i others(6): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391585 | |||||||
| chr22:35391586 | C | CT | 41 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0015 others(38): Show |
61 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.736+1648dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391586 | ||||||
| chr22:35391586 | C | CTT | 26 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0023 others(23): Show |
37 | HG00408.hp1 HG01168.hp2 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.736+1647_736+1648d others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391586 | ||||||
| chr22:35391586 | C | CTTT | 21 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0064 others(18): Show |
24 | HG01175.hp2 HG01243.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.736+1646_736+1648d others(5): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391586 | ||||||
| chr22:35391586 | C | T | 89 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+1623C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391586 | |||||||
| chr22:35391586 | CT | C | 8 | a0001c0001t0001g0159 a0001c0001t0001g0165 a0001c0001t0001g0173 others(5): Show |
12 | HG00544.hp2 HG00673.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.736+1648delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391586 | ||||||
| chr22:35391625 | G | A | 89 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.736+1662G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391625 | |||||||
| chr22:35391755 | A | C | 1 | a0001c0001t0001g0154 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.737-1713A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391755 | |||||||
| chr22:35391757 | A | AT | 37 | a0001c0001t0001g0012 a0001c0001t0001g0023 a0001c0001t0001g0025 others(34): Show |
45 | HG00408.hp1 HG00423.hp2 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.737-1697dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391757 | ||||||
| chr22:35391757 | AT | A | 81 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.737-1697delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35391757 | ||||||
| chr22:35391758 | T | A | 1 | a0001c0001t0001g0154 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.737-1710T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391758 | |||||||
| chr22:35391771 | T | G | 1 | a0001c0001t0001g0138 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.737-1697T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391771 | |||||||
| chr22:35391773 | G | C | 1 | a0001c0001t0001g0138 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.737-1695G>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391773 | |||||||
| chr22:35391774 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.737-1694C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391774 | |||||||
| chr22:35391966 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.737-1502T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391966 | |||||||
| chr22:35391990 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.737-1478T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35391990 | |||||||
| chr22:35392149 | G | A | 5 | a0001c0001t0001g0039 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.737-1319G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392149 | |||||||
| chr22:35392221 | C | CA | 88 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(85): Show |
125 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.737-1231dupA | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35392221 | ||||||
| chr22:35392221 | C | CAA | 6 | a0001c0001t0001g0083 a0001c0001t0001g0117 a0001c0001t0001g0119 others(3): Show |
6 | HG01069.hp2 HG01243.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.737-1232_737-1231d others(4): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35392221 | ||||||
| chr22:35392256 | A | AAGAATTT others(24): Show |
1 | a0006c0007t0011g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-1210_737-1180d others(33): Show |
HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35392256 | ||||||
| chr22:35392606 | G | A | 1 | a0004c0009t0001g0040 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.737-862G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392606 | |||||||
| chr22:35392607 | G | T | 1 | a0001c0001t0010g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.737-861G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392607 | |||||||
| chr22:35392717 | C | CT | 10 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0087 others(7): Show |
11 | HG01070.hp2 HG01071.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.737-733dupT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35392717 | ||||||
| chr22:35392717 | CT | C | 9 | a0001c0001t0001g0057 a0001c0001t0001g0083 a0001c0001t0001g0104 others(6): Show |
9 | HG01168.hp1 HG01517.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.737-733delT | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 35392717 | ||||||
| chr22:35392779 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.737-689G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392779 | |||||||
| chr22:35392841 | C | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0168 a0001c0001t0001g0179 others(1): Show |
6 | HG02027.hp1 HG02056.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.737-627C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392841 | |||||||
| chr22:35392891 | T | A | 1 | a0006c0007t0011g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-577T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392891 | |||||||
| chr22:35392892 | A | T | 1 | a0006c0007t0011g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-576A>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392892 | |||||||
| chr22:35392893 | T | A | 1 | a0006c0007t0011g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-575T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392893 | |||||||
| chr22:35392916 | C | T | 86 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(83): Show |
123 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.737-552C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392916 | |||||||
| chr22:35392976 | A | T | 1 | a0006c0007t0011g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-492A>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392976 | |||||||
| chr22:35392988 | T | G | 3 | a0001c0001t0001g0205 a0001c0001t0001g0210 a0001c0001t0001g0212 |
3 | HG01175.hp2 HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.737-480T>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35392988 | |||||||
| chr22:35393011 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.737-457C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393011 | |||||||
| chr22:35393053 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.737-415G>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393053 | |||||||
| chr22:35393114 | A | C | 1 | a0006c0007t0011g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-354A>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393114 | |||||||
| chr22:35393115 | C | G | 1 | a0006c0007t0011g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-353C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393115 | |||||||
| chr22:35393116 | G | T | 1 | a0006c0007t0011g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-352G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393116 | |||||||
| chr22:35393149 | C | G | 1 | a0002c0002t0001g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.737-319C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393149 | |||||||
| chr22:35393207 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.737-261C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393207 | |||||||
| chr22:35393251 | G | T | 1 | a0006c0007t0011g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-217G>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393251 | |||||||
| chr22:35393268 | T | A | 3 | a0002c0002t0001g0199 a0002c0002t0002g0197 a0002c0002t0002g0198 |
3 | HG02809.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.737-200T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393268 | |||||||
| chr22:35393270 | A | G | 143 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(140): Show |
195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.737-198A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393270 | |||||||
| chr22:35393288 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.737-180C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393288 | |||||||
| chr22:35393325 | C | A | 1 | a0006c0007t0011g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-143C>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393325 | |||||||
| chr22:35393386 | C | T | 3 | a0002c0002t0001g0199 a0002c0002t0002g0197 a0002c0002t0002g0198 |
3 | HG02809.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.737-82C>T | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393386 | |||||||
| chr22:35393399 | T | A | 1 | a0006c0007t0011g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-69T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393399 | |||||||
| chr22:35393400 | T | C | 1 | a0001c0001t0009g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.737-68T>C | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393400 | |||||||
| chr22:35393405 | A | G | 1 | a0004c0009t0001g0040 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.737-63A>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393405 | |||||||
| chr22:35393406 | T | A | 1 | a0006c0007t0011g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-62T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393406 | |||||||
| chr22:35393448 | T | A | 1 | a0006c0007t0011g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-20T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393448 | |||||||
| chr22:35393452 | C | G | 1 | a0001c0001t0001g0106 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.737-16C>G | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393452 | |||||||
| chr22:35393457 | T | A | 1 | a0006c0007t0011g0114 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.737-11T>A | HMOX1 | ENSG00000100292.18 | transcript | ENST00000216117.9 | protein_coding | 4/4 | chr22 | 35393457 |