Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3163 |
| ensemblid | ENSG00000103415.12 |
| hgncid | 5014 |
| symbol | HMOX2 |
| name | heme oxygenase 2 |
| refseq_nuc | NM_002134.4 |
| refseq_prot | NP_002125.3 |
| ensembl_nuc | ENST00000570646.6 |
| ensembl_prot | ENSP00000459214.1 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 4476398 |
| end | 4510347 |
| strand | + |
| ver | v1.2 |
| region | chr16:4476398-4510347 |
| region5000 | chr16:4471398-4515347 |
| regionname0 | HMOX2_chr16_4476398_4510347 |
| regionname5000 | HMOX2_chr16_4471398_4515347 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 316 | 311 | 92 | 50 | 126 | 4 | 38 | 88 | HMOX2_chr16_4471398_4515347 | HMOX2 | MSAEV others(311): Show |
chr16 | 4471398 | 4515347 |
| a0002 | 0/0 | 316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | MSAEV others(311): Show |
chr16 | 4471398 | 4515347 |
| a0003 | 0/0 | 316 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | MSAEV others(311): Show |
chr16 | 4471398 | 4515347 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 948 | 282 | 72 | 44 | 125 | 3 | 38 | HMOX2_chr16_4471398_4515347 | HMOX2 | ATGTC others(943): Show |
chr16 | 4471398 | 4515347 | ||
| a0001c0002 | 0/1 | 948 | 26 | 17 | 6 | 1 | 1 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | ATGTC others(943): Show |
chr16 | 4471398 | 4515347 | ||
| a0001c0003 | 0/0 | 948 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | ATGTC others(943): Show |
chr16 | 4471398 | 4515347 | ||
| a0001c0006 | 0/0 | 948 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | ATGTC others(943): Show |
chr16 | 4471398 | 4515347 | ||
| a0002c0004 | 0/0 | 948 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | ATGTC others(943): Show |
chr16 | 4471398 | 4515347 | ||
| a0003c0005 | 0/0 | 948 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | ATGTC others(943): Show |
chr16 | 4471398 | 4515347 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1673 | 164 | 54 | 22 | 66 | 2 | 20 | HMOX2_chr16_4471398_4515347 | HMOX2 | GCTGG others(1668): Show |
chr16 | 4471398 | 4515347 |
| a0001c0001t0002 | 0/0 | 1673 | 111 | 11 | 22 | 59 | 1 | 18 | HMOX2_chr16_4471398_4515347 | HMOX2 | GCTGG others(1668): Show |
chr16 | 4471398 | 4515347 |
| a0001c0001t0003 | 0/0 | 1673 | 5 | 5 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | GCTGG others(1668): Show |
chr16 | 4471398 | 4515347 |
| a0001c0001t0004 | 0/0 | 1673 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | GCTGG others(1668): Show |
chr16 | 4471398 | 4515347 |
| a0001c0002t0001 | 0/1 | 1673 | 26 | 17 | 6 | 1 | 1 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | GCTGG others(1668): Show |
chr16 | 4471398 | 4515347 |
| a0001c0003t0001 | 0/0 | 1673 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | GCTGG others(1668): Show |
chr16 | 4471398 | 4515347 |
| a0001c0006t0001 | 0/0 | 1673 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | GCTGG others(1668): Show |
chr16 | 4471398 | 4515347 |
| a0002c0004t0001 | 0/0 | 1673 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | GCTGG others(1668): Show |
chr16 | 4471398 | 4515347 |
| a0003c0005t0001 | 0/0 | 1673 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | GCTGG others(1668): Show |
chr16 | 4471398 | 4515347 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0001 | 0/0 | 10 | 1 | 2 | 6 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0008 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0003t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0001c0006t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0002c0004t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| a0003c0005t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | CHS | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | CHS | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | CHS | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0049 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | CLM | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | CLM | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | CLM | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | IBS | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0102 | EUR | IBS | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0032 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CDX | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CDX | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0060 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0246 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0089 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0061 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0048 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02922 | hp1 | a0001 | c0006 | t0001 | g0145 | AFR | ESN | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | ESN | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | ESN | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | ESN | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0137 | AFR | ESN | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | MSL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | MSL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | MSL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | STU | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | STU | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | BEB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | BEB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | BEB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | STU | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | STU | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | STU | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | STU | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | STU | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | YRI | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18943 | hp1 | a0002 | c0004 | t0001 | g0215 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19004 | hp1 | a0003 | c0005 | t0001 | g0010 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | LWK | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | LWK | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | YRI | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | ASW | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ASW | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | TSI | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0044 | EUR | TSI | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | GIH | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | GIH | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | USA | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | USA | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0047 | REF | REF | HMOX2_chr16_4471398_4515347 | HMOX2 | chr16 | 4471398 | 4515347 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4507914 | G | A | 1 | a0002 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.406G>A | p.Glu136Lys | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 4/6 | 537/1673 | 406/951 | 136/316 | chr16 | 4507914 | |||
| chr16:4509667 | A | G | 1 | a0003 | 1 | NA19004.hp1 | missense_variant | MODERATE | c.862A>G | p.Met288Val | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 6/6 | 993/1673 | 862/951 | 288/316 | chr16 | 4509667 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4506910 | G | A | 1 | a0001c0002 | 25 | HG00642.hp1 HG00738.hp2 HG01081.hp1 others(22): Show |
synonymous_variant | LOW | c.102G>A | p.Ser34Ser | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 3/6 | 233/1673 | 102/951 | 34/316 | chr16 | 4506910 | |||
| chr16:4507817 | G | A | 1 | a0001c0003 | 2 | HG02572.hp2 HG03195.hp1 |
synonymous_variant | LOW | c.309G>A | p.Leu103Leu | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 4/6 | 440/1673 | 309/951 | 103/316 | chr16 | 4507817 | |||
| chr16:4509498 | C | T | 1 | a0001c0006 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.783C>T | p.Asp261Asp | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 5/6 | 914/1673 | 783/951 | 261/316 | chr16 | 4509498 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4476411 | G | T | 1 | a0001c0001t0003 | 5 | HG02723.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-118G>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/6 | 29114 | chr16 | 4476411 | ||||||
| chr16:4510267 | C | T | 1 | a0001c0001t0004 | 2 | HG02257.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*511C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 6/6 | 511 | chr16 | 4510267 | ||||||
| chr16:4510300 | G | A | 2 | a0001c0001t0002 a0001c0001t0004 |
113 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*544G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 6/6 | 544 | chr16 | 4510300 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:4476617 | C | A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(4): Show |
7 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-42+130C>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4476617 | |||||||
| chr16:4476740 | C | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(14): Show |
20 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.-42+253C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4476740 | |||||||
| chr16:4476749 | G | A | 22 | a0001c0002t0001g0007 a0001c0002t0001g0030 a0001c0002t0001g0031 others(19): Show |
24 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-42+262G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4476749 | |||||||
| chr16:4476757 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0128 others(89): Show |
115 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.-42+270G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4476757 | |||||||
| chr16:4476796 | C | G | 1 | a0001c0003t0001g0246 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-42+309C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4476796 | |||||||
| chr16:4476801 | G | A | 6 | a0001c0002t0001g0007 a0001c0002t0001g0030 a0001c0002t0001g0031 others(3): Show |
8 | HG02109.hp2 HG02145.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-42+314G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4476801 | |||||||
| chr16:4476922 | T | G | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+435T>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4476922 | |||||||
| chr16:4476952 | G | C | 1 | a0001c0001t0001g0134 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-42+465G>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4476952 | |||||||
| chr16:4477058 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-42+571G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4477058 | |||||||
| chr16:4477108 | T | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0023 others(159): Show |
190 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(187): Show |
intron_variant | MODIFIER | c.-42+621T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4477108 | |||||||
| chr16:4477212 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-42+725C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4477212 | |||||||
| chr16:4477251 | C | G | 17 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(14): Show |
20 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.-42+764C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4477251 | |||||||
| chr16:4477467 | C | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-42+980C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4477467 | |||||||
| chr16:4477497 | T | TA | 15 | a0001c0001t0001g0005 a0001c0001t0001g0135 a0001c0001t0001g0136 others(12): Show |
18 | HG00673.hp1 HG00741.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-42+1036dupA | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4477497 | ||||||
| chr16:4477497 | TA | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0128 others(104): Show |
132 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.-42+1036delA | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4477497 | ||||||
| chr16:4477497 | TAA | T | 7 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0002g0131 others(4): Show |
7 | HG01081.hp2 HG01943.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-42+1035_-42+1036d others(4): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4477497 | ||||||
| chr16:4477648 | G | C | 1 | a0001c0001t0002g0053 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-42+1161G>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4477648 | |||||||
| chr16:4477724 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-42+1237G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4477724 | |||||||
| chr16:4477748 | G | A | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+1261G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4477748 | |||||||
| chr16:4477920 | CAAAAA | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0128 others(91): Show |
117 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-42+1435_-42+1439d others(7): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4477920 | ||||||
| chr16:4477960 | G | A | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+1473G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4477960 | |||||||
| chr16:4478018 | G | A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(14): Show |
20 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.-42+1531G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4478018 | |||||||
| chr16:4478164 | C | T | 1 | a0001c0002t0001g0049 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-42+1677C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4478164 | |||||||
| chr16:4478473 | C | T | 1 | a0001c0003t0001g0137 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-42+1986C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4478473 | |||||||
| chr16:4478526 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-42+2039G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4478526 | |||||||
| chr16:4478538 | G | T | 3 | a0001c0001t0001g0168 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG01361.hp1 HG02735.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-42+2051G>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4478538 | |||||||
| chr16:4478564 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-42+2077A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4478564 | |||||||
| chr16:4478599 | T | A | 11 | a0001c0002t0001g0007 a0001c0002t0001g0030 a0001c0002t0001g0031 others(8): Show |
13 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-42+2112T>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4478599 | |||||||
| chr16:4478633 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0074 others(138): Show |
169 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.-42+2146T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4478633 | |||||||
| chr16:4478635 | T | C | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+2148T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4478635 | |||||||
| chr16:4478648 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-42+2161C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4478648 | |||||||
| chr16:4478666 | G | T | 13 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0002g0004 others(10): Show |
18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.-42+2179G>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4478666 | |||||||
| chr16:4478765 | CA | C | 7 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0002g0053 others(4): Show |
7 | HG02109.hp2 HG02818.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-42+2292delA | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4478765 | ||||||
| chr16:4478870 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-42+2383C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4478870 | |||||||
| chr16:4479000 | C | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0129 others(90): Show |
116 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.-42+2513C>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479000 | |||||||
| chr16:4479027 | T | C | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+2540T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479027 | |||||||
| chr16:4479035 | C | A | 1 | a0001c0001t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-42+2548C>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479035 | |||||||
| chr16:4479066 | G | C | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-42+2579G>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479066 | |||||||
| chr16:4479129 | C | T | 2 | a0001c0001t0002g0073 a0001c0001t0002g0120 |
2 | NA18979.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-42+2642C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479129 | |||||||
| chr16:4479132 | CAA | C | 5 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 others(2): Show |
5 | HG02723.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42+2646_-42+2647d others(4): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479132 | |||||||
| chr16:4479405 | G | T | 6 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0116 others(3): Show |
6 | HG00639.hp1 HG02602.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+2918G>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479405 | |||||||
| chr16:4479452 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-42+2965C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479452 | |||||||
| chr16:4479477 | C | T | 1 | a0001c0001t0001g0022 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-42+2990C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479477 | |||||||
| chr16:4479478 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-42+2991G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479478 | |||||||
| chr16:4479478 | G | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0002g0127 others(1): Show |
4 | NA18950.hp2 NA18980.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42+2991G>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479478 | |||||||
| chr16:4479556 | A | G | 3 | a0001c0001t0001g0134 a0001c0001t0001g0166 a0001c0001t0001g0237 |
3 | HG01934.hp1 HG01952.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-42+3069A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479556 | |||||||
| chr16:4479566 | G | A | 14 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0144 others(11): Show |
14 | HG01099.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-42+3079G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479566 | |||||||
| chr16:4479612 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0074 others(152): Show |
183 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(180): Show |
intron_variant | MODIFIER | c.-42+3125A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479612 | |||||||
| chr16:4479724 | C | G | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0146 |
3 | HG01891.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-42+3237C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479724 | |||||||
| chr16:4479726 | A | AT | 32 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(29): Show |
36 | HG00544.hp1 HG00741.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.-42+3271dupT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4479726 | ||||||
| chr16:4479726 | AT | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0022 others(10): Show |
16 | HG01891.hp2 HG01928.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.-42+3271delT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4479726 | ||||||
| chr16:4479726 | ATTTTT | A | 6 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0255 others(3): Show |
6 | HG01175.hp1 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42+3267_-42+3271d others(7): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4479726 | ||||||
| chr16:4479726 | ATTTTTT | A | 31 | a0001c0001t0001g0006 a0001c0001t0001g0174 a0001c0001t0001g0175 others(28): Show |
36 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.-42+3266_-42+3271d others(8): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4479726 | ||||||
| chr16:4479726 | ATTTTTTT others(3): Show |
A | 13 | a0001c0001t0001g0173 a0001c0001t0002g0064 a0001c0001t0002g0065 others(10): Show |
13 | HG00423.hp2 HG00558.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.-42+3262_-42+3271d others(12): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4479726 | ||||||
| chr16:4479726 | ATTTTTTT others(4): Show |
A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0128 others(76): Show |
102 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.-42+3261_-42+3271d others(13): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4479726 | ||||||
| chr16:4479726 | ATTTTTTT others(5): Show |
A | 4 | a0001c0001t0001g0029 a0001c0001t0002g0080 a0001c0001t0002g0127 others(1): Show |
4 | HG03041.hp1 HG03516.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42+3260_-42+3271d others(14): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4479726 | ||||||
| chr16:4479726 | ATTTTTTT others(6): Show |
A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+3259_-42+3271d others(15): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4479726 | ||||||
| chr16:4479726 | ATTTTTTT others(7): Show |
A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0172 |
3 | HG02896.hp2 HG03471.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-42+3258_-42+3271d others(16): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4479726 | ||||||
| chr16:4479726 | ATTTTTTT others(8): Show |
A | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG02280.hp2 HG02622.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+3257_-42+3271d others(17): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4479726 | ||||||
| chr16:4479728 | T | A | 1 | a0001c0001t0001g0018 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-42+3241T>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479728 | |||||||
| chr16:4479729 | T | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02129.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-42+3242T>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479729 | |||||||
| chr16:4479730 | T | A | 1 | a0001c0001t0001g0018 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-42+3243T>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479730 | |||||||
| chr16:4479820 | C | A | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+3333C>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479820 | |||||||
| chr16:4479825 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-42+3338G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479825 | |||||||
| chr16:4479939 | A | G | 2 | a0001c0001t0001g0147 a0001c0006t0001g0145 |
2 | HG01099.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-42+3452A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479939 | |||||||
| chr16:4479948 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-42+3461G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4479948 | |||||||
| chr16:4480025 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-42+3538C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480025 | |||||||
| chr16:4480034 | C | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+3547C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480034 | |||||||
| chr16:4480137 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-42+3650T>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480137 | |||||||
| chr16:4480223 | C | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+3736C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480223 | |||||||
| chr16:4480237 | G | T | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG02280.hp2 HG02622.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+3750G>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480237 | |||||||
| chr16:4480245 | G | A | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+3758G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480245 | |||||||
| chr16:4480334 | C | A | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0182 |
3 | NA18977.hp1 NA18980.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-42+3847C>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480334 | |||||||
| chr16:4480344 | G | A | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0183 others(1): Show |
4 | HG02074.hp2 HG02155.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42+3857G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480344 | |||||||
| chr16:4480347 | C | CT | 118 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0128 others(115): Show |
141 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.-42+3876dupT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4480347 | ||||||
| chr16:4480347 | C | CTT | 45 | a0001c0001t0001g0006 a0001c0001t0001g0163 a0001c0001t0001g0247 others(42): Show |
50 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.-42+3875_-42+3876d others(4): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4480347 | ||||||
| chr16:4480527 | T | C | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+4040T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480527 | |||||||
| chr16:4480534 | G | A | 3 | a0001c0001t0002g0054 a0001c0001t0002g0064 a0001c0001t0002g0080 |
3 | HG02486.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-42+4047G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480534 | |||||||
| chr16:4480545 | A | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-42+4058A>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480545 | |||||||
| chr16:4480575 | C | A | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+4088C>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480575 | |||||||
| chr16:4480596 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0074 others(152): Show |
183 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(180): Show |
intron_variant | MODIFIER | c.-42+4109T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480596 | |||||||
| chr16:4480651 | A | AT | 18 | a0001c0001t0001g0144 a0001c0001t0001g0148 a0001c0001t0001g0149 others(15): Show |
18 | HG00738.hp1 HG01243.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.-42+4182dupT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4480651 | ||||||
| chr16:4480651 | ATTT | A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(14): Show |
20 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.-42+4180_-42+4182d others(5): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4480651 | ||||||
| chr16:4480651 | ATTTT | A | 22 | a0001c0002t0001g0007 a0001c0002t0001g0030 a0001c0002t0001g0031 others(19): Show |
24 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-42+4179_-42+4182d others(6): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4480651 | ||||||
| chr16:4480684 | C | G | 14 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0144 others(11): Show |
14 | HG01099.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-42+4197C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480684 | |||||||
| chr16:4480693 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-42+4206C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480693 | |||||||
| chr16:4480805 | A | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0128 others(91): Show |
117 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-42+4318A>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480805 | |||||||
| chr16:4480861 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0074 others(138): Show |
169 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.-42+4374T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480861 | |||||||
| chr16:4480884 | T | C | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+4397T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480884 | |||||||
| chr16:4480918 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0074 others(138): Show |
169 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.-42+4431C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480918 | |||||||
| chr16:4480998 | A | G | 6 | a0001c0001t0001g0138 a0001c0001t0003g0139 a0001c0001t0003g0140 others(3): Show |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+4511A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4480998 | |||||||
| chr16:4481064 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0170 a0001c0001t0001g0171 |
4 | HG02129.hp2 NA18954.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42+4577G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4481064 | |||||||
| chr16:4481087 | C | G | 1 | a0001c0001t0004g0061 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-42+4600C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4481087 | |||||||
| chr16:4481145 | G | T | 22 | a0001c0002t0001g0007 a0001c0002t0001g0030 a0001c0002t0001g0031 others(19): Show |
24 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-42+4658G>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4481145 | |||||||
| chr16:4481306 | G | A | 1 | a0001c0003t0001g0246 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-42+4819G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4481306 | |||||||
| chr16:4481348 | C | CA | 114 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(111): Show |
135 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(132): Show |
intron_variant | MODIFIER | c.-42+4878dupA | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4481348 | ||||||
| chr16:4481348 | C | CAA | 12 | a0001c0001t0001g0138 a0001c0001t0001g0170 a0001c0001t0001g0173 others(9): Show |
12 | HG00423.hp2 HG00741.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-42+4877_-42+4878d others(4): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4481348 | ||||||
| chr16:4481348 | CA | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0128 others(90): Show |
116 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.-42+4878delA | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4481348 | ||||||
| chr16:4481361 | A | G | 5 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0257 others(2): Show |
5 | HG02647.hp1 HG02809.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42+4874A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4481361 | |||||||
| chr16:4481366 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-42+4879G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4481366 | |||||||
| chr16:4481374 | T | G | 2 | a0001c0001t0002g0064 a0001c0001t0002g0082 |
2 | HG01346.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-42+4887T>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4481374 | |||||||
| chr16:4481510 | G | T | 6 | a0001c0001t0001g0138 a0001c0001t0003g0139 a0001c0001t0003g0140 others(3): Show |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+5023G>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4481510 | |||||||
| chr16:4481609 | T | C | 1 | a0001c0006t0001g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-42+5122T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4481609 | |||||||
| chr16:4481658 | C | G | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+5171C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4481658 | |||||||
| chr16:4481760 | T | C | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+5273T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4481760 | |||||||
| chr16:4481782 | C | A | 1 | a0001c0001t0002g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-42+5295C>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4481782 | |||||||
| chr16:4481813 | G | C | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+5326G>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4481813 | |||||||
| chr16:4481848 | C | G | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG01891.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-42+5361C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4481848 | |||||||
| chr16:4481911 | A | G | 1 | a0001c0001t0002g0125 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-42+5424A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4481911 | |||||||
| chr16:4482066 | G | C | 1 | a0001c0001t0002g0078 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-42+5579G>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4482066 | |||||||
| chr16:4482119 | A | T | 1 | a0001c0001t0002g0110 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-42+5632A>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4482119 | |||||||
| chr16:4482186 | T | C | 17 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(14): Show |
20 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.-42+5699T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4482186 | |||||||
| chr16:4482278 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-42+5791A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4482278 | |||||||
| chr16:4482283 | A | G | 6 | a0001c0001t0001g0138 a0001c0001t0003g0139 a0001c0001t0003g0140 others(3): Show |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+5796A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4482283 | |||||||
| chr16:4482399 | C | T | 3 | a0001c0001t0002g0054 a0001c0001t0002g0064 a0001c0001t0002g0080 |
3 | HG02486.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-42+5912C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4482399 | |||||||
| chr16:4482515 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-42+6028C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4482515 | |||||||
| chr16:4482537 | G | A | 3 | a0001c0001t0002g0054 a0001c0001t0002g0064 a0001c0001t0002g0080 |
3 | HG02486.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-42+6050G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4482537 | |||||||
| chr16:4482887 | G | A | 38 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(35): Show |
43 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.-42+6400G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4482887 | |||||||
| chr16:4483034 | A | G | 1 | a0001c0001t0002g0155 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-42+6547A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4483034 | |||||||
| chr16:4483118 | A | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0244 |
3 | HG02735.hp2 HG03490.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-42+6631A>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4483118 | |||||||
| chr16:4483125 | G | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0239 |
2 | HG02735.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-42+6638G>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4483125 | |||||||
| chr16:4483134 | G | T | 2 | a0001c0001t0002g0055 a0001c0001t0002g0081 |
2 | HG02056.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.-42+6647G>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4483134 | |||||||
| chr16:4483158 | CTGGTGTG others(14): Show |
C | 1 | a0001c0001t0002g0127 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-42+6674_-42+6694d others(23): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483158 | ||||||
| chr16:4483160 | G | GGTGT | 4 | a0001c0001t0001g0134 a0001c0001t0001g0184 a0001c0001t0001g0219 others(1): Show |
4 | HG01099.hp1 HG01952.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42+6734_-42+6737d others(6): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483160 | ||||||
| chr16:4483160 | GGT | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0240 others(1): Show |
4 | HG01074.hp2 HG01109.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42+6736_-42+6737d others(4): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483160 | ||||||
| chr16:4483160 | GGTGT | G | 14 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(11): Show |
14 | HG00673.hp1 HG01123.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.-42+6734_-42+6737d others(6): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483160 | ||||||
| chr16:4483160 | GGTGTGT | G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(18): Show |
22 | HG01361.hp1 HG01975.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.-42+6732_-42+6737d others(8): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483160 | ||||||
| chr16:4483160 | GGTGTGTG others(1): Show |
G | 15 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0164 others(12): Show |
15 | HG00741.hp1 HG01943.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.-42+6730_-42+6737d others(10): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483160 | ||||||
| chr16:4483160 | GGTGTGTG others(3): Show |
G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(30): Show |
33 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.-42+6728_-42+6737d others(12): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483160 | ||||||
| chr16:4483160 | GGTGTGTG others(5): Show |
G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0019 others(17): Show |
20 | HG00423.hp2 HG01516.hp1 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-42+6726_-42+6737d others(14): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483160 | ||||||
| chr16:4483160 | GGTGTGTG others(7): Show |
G | 8 | a0001c0001t0001g0019 a0001c0001t0001g0186 a0001c0001t0001g0187 others(5): Show |
8 | HG02004.hp1 HG02155.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-42+6724_-42+6737d others(16): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483160 | ||||||
| chr16:4483160 | GGTGTGTG others(9): Show |
G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0151 others(5): Show |
9 | HG02622.hp2 HG02886.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-42+6722_-42+6737d others(18): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483160 | ||||||
| chr16:4483160 | GGTGTGTG others(11): Show |
G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0135 a0001c0001t0001g0146 others(6): Show |
10 | HG01891.hp2 HG01975.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.-42+6720_-42+6737d others(20): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483160 | ||||||
| chr16:4483160 | GGTGTGTG others(13): Show |
G | 18 | a0001c0001t0001g0001 a0001c0001t0001g0144 a0001c0001t0001g0156 others(15): Show |
19 | HG01081.hp1 HG01243.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.-42+6718_-42+6737d others(22): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483160 | ||||||
| chr16:4483160 | GGTGTGTG others(15): Show |
G | 21 | a0001c0001t0001g0147 a0001c0001t0001g0252 a0001c0001t0001g0257 others(18): Show |
25 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.-42+6716_-42+6737d others(24): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483160 | ||||||
| chr16:4483160 | GGTGTGTG others(17): Show |
G | 60 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0235 others(57): Show |
73 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.-42+6714_-42+6737d others(26): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483160 | ||||||
| chr16:4483160 | GGTGTGTG others(19): Show |
G | 12 | a0001c0001t0002g0008 a0001c0001t0002g0053 a0001c0001t0002g0064 others(9): Show |
14 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-42+6712_-42+6737d others(28): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483160 | ||||||
| chr16:4483160 | GGTGTGTG others(21): Show |
G | 13 | a0001c0001t0002g0086 a0001c0001t0002g0125 a0001c0002t0001g0035 others(10): Show |
13 | HG00738.hp2 HG01081.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-42+6710_-42+6737d others(30): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483160 | ||||||
| chr16:4483160 | GGTGTGTG others(23): Show |
G | 4 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0002t0001g0037 others(1): Show |
4 | HG00642.hp1 HG01175.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42+6708_-42+6737d others(32): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483160 | ||||||
| chr16:4483160 | GGTGTGTG others(27): Show |
G | 1 | a0001c0001t0001g0231 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-42+6704_-42+6737d others(36): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483160 | ||||||
| chr16:4483163 | GTGTGTGT others(4): Show |
G | 1 | a0001c0001t0001g0010 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-42+6677_-42+6687d others(13): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4483163 | |||||||
| chr16:4483199 | GTGTGTGT others(18): Show |
G | 2 | a0001c0001t0002g0130 a0001c0002t0001g0030 |
2 | NA18997.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-42+6714_-42+6738d others(27): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483199 | ||||||
| chr16:4483209 | GTGTGTGT others(8): Show |
G | 2 | a0001c0001t0001g0178 a0003c0005t0001g0010 |
2 | NA19004.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-42+6724_-42+6738d others(17): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483209 | ||||||
| chr16:4483211 | GTGTGTGT others(6): Show |
G | 1 | a0001c0001t0001g0228 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-42+6726_-42+6738d others(15): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483211 | ||||||
| chr16:4483213 | GTGTGTGT others(4): Show |
G | 2 | a0001c0001t0001g0149 a0001c0001t0001g0220 |
2 | HG01496.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-42+6728_-42+6738d others(13): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483213 | ||||||
| chr16:4483219 | GTGTGT | G | 4 | a0001c0001t0001g0163 a0001c0001t0001g0190 a0001c0001t0001g0194 others(1): Show |
4 | HG02004.hp2 HG02698.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42+6734_-42+6738d others(7): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483219 | ||||||
| chr16:4483297 | C | G | 1 | a0001c0001t0002g0016 | 2 | NA18971.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-42+6810C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4483297 | |||||||
| chr16:4483297 | C | T | 2 | a0001c0001t0002g0108 a0001c0001t0002g0133 |
2 | NA18982.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.-42+6810C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4483297 | |||||||
| chr16:4483403 | GTTAC | G | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+6925_-42+6928d others(6): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483403 | ||||||
| chr16:4483407 | C | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-42+6920C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4483407 | |||||||
| chr16:4483432 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-42+6945A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4483432 | |||||||
| chr16:4483512 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-42+7025A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4483512 | |||||||
| chr16:4483832 | G | A | 1 | a0001c0001t0002g0077 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-42+7345G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4483832 | |||||||
| chr16:4483898 | C | T | 1 | a0001c0001t0001g0022 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-42+7411C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4483898 | |||||||
| chr16:4483935 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-42+7448T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4483935 | |||||||
| chr16:4483973 | A | AT | 104 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0136 others(101): Show |
127 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.-42+7505dupT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483973 | ||||||
| chr16:4483973 | A | ATT | 57 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(54): Show |
62 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(59): Show |
intron_variant | MODIFIER | c.-42+7504_-42+7505d others(4): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483973 | ||||||
| chr16:4483973 | A | T | 1 | a0001c0001t0002g0055 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-42+7486A>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4483973 | |||||||
| chr16:4483973 | AT | A | 6 | a0001c0001t0001g0174 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | HG01099.hp1 HG01255.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+7505delT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4483973 | ||||||
| chr16:4484060 | C | T | 1 | a0001c0001t0004g0060 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-42+7573C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4484060 | |||||||
| chr16:4484120 | T | G | 1 | a0001c0001t0002g0068 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-42+7633T>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4484120 | |||||||
| chr16:4484124 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-42+7637G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4484124 | |||||||
| chr16:4484224 | T | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0186 a0001c0001t0001g0207 others(2): Show |
6 | HG02071.hp1 HG02155.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42+7737T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4484224 | |||||||
| chr16:4484269 | C | T | 1 | a0001c0002t0001g0048 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-42+7782C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4484269 | |||||||
| chr16:4484359 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-42+7872A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4484359 | |||||||
| chr16:4484365 | G | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0128 others(151): Show |
182 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(179): Show |
intron_variant | MODIFIER | c.-42+7878G>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4484365 | |||||||
| chr16:4484446 | GTTTCT | G | 3 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 |
3 | HG04184.hp1 HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-42+7973_-42+7977d others(7): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4484446 | ||||||
| chr16:4484460 | C | CT | 8 | a0001c0001t0001g0231 a0001c0001t0002g0015 a0001c0001t0002g0068 others(5): Show |
9 | HG01496.hp1 HG02015.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-42+7991dupT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4484460 | ||||||
| chr16:4484460 | CT | C | 72 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0135 others(69): Show |
78 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.-42+7991delT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4484460 | ||||||
| chr16:4484481 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0129 others(91): Show |
117 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-42+7994G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4484481 | |||||||
| chr16:4484482 | A | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0129 others(91): Show |
117 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-42+7995A>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4484482 | |||||||
| chr16:4484523 | C | T | 3 | a0001c0001t0002g0014 a0001c0001t0002g0070 a0001c0001t0002g0106 |
4 | NA18969.hp2 NA18977.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42+8036C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4484523 | |||||||
| chr16:4484571 | C | T | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG02280.hp2 HG02622.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+8084C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4484571 | |||||||
| chr16:4484618 | G | A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(14): Show |
20 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.-42+8131G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4484618 | |||||||
| chr16:4484680 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-42+8193C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4484680 | |||||||
| chr16:4484863 | T | C | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0211 |
3 | HG02004.hp1 HG02148.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.-42+8376T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4484863 | |||||||
| chr16:4484924 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-42+8437G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4484924 | |||||||
| chr16:4485085 | C | A | 3 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 |
3 | HG04184.hp1 HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-42+8598C>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4485085 | |||||||
| chr16:4485306 | T | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0128 others(139): Show |
170 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(167): Show |
intron_variant | MODIFIER | c.-42+8819T>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4485306 | |||||||
| chr16:4485556 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0129 others(91): Show |
117 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-42+9069C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4485556 | |||||||
| chr16:4485810 | T | G | 1 | a0001c0001t0001g0219 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-42+9323T>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4485810 | |||||||
| chr16:4485863 | T | C | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG01891.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-42+9376T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4485863 | |||||||
| chr16:4485880 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-42+9393C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4485880 | |||||||
| chr16:4485943 | C | T | 6 | a0001c0001t0001g0138 a0001c0001t0003g0139 a0001c0001t0003g0140 others(3): Show |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+9456C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4485943 | |||||||
| chr16:4486016 | G | T | 6 | a0001c0001t0001g0138 a0001c0001t0003g0139 a0001c0001t0003g0140 others(3): Show |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+9529G>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4486016 | |||||||
| chr16:4486164 | A | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0129 others(90): Show |
116 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.-42+9677A>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4486164 | |||||||
| chr16:4486166 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-42+9679C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4486166 | |||||||
| chr16:4486348 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-42+9861C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4486348 | |||||||
| chr16:4486353 | C | T | 20 | a0001c0002t0001g0007 a0001c0002t0001g0030 a0001c0002t0001g0031 others(17): Show |
22 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.-42+9866C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4486353 | |||||||
| chr16:4486468 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-42+9981C>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4486468 | |||||||
| chr16:4486516 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-42+10029T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4486516 | |||||||
| chr16:4486554 | C | T | 45 | a0001c0001t0001g0006 a0001c0001t0001g0138 a0001c0001t0001g0247 others(42): Show |
50 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.-42+10067C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4486554 | |||||||
| chr16:4486611 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-42+10124G>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4486611 | |||||||
| chr16:4486620 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0128 others(138): Show |
169 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.-42+10133T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4486620 | |||||||
| chr16:4486623 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-42+10136C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4486623 | |||||||
| chr16:4486633 | A | G | 45 | a0001c0001t0001g0006 a0001c0001t0001g0138 a0001c0001t0001g0247 others(42): Show |
50 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.-42+10146A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4486633 | |||||||
| chr16:4486933 | T | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0023 others(158): Show |
189 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(186): Show |
intron_variant | MODIFIER | c.-42+10446T>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4486933 | |||||||
| chr16:4486935 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-42+10448G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4486935 | |||||||
| chr16:4486985 | C | G | 1 | a0001c0001t0002g0015 | 2 | HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.-42+10498C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4486985 | |||||||
| chr16:4487054 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-42+10567C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487054 | |||||||
| chr16:4487103 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0129 others(91): Show |
117 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-42+10616T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487103 | |||||||
| chr16:4487118 | A | G | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG02280.hp2 HG02622.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+10631A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487118 | |||||||
| chr16:4487151 | C | G | 1 | a0001c0003t0001g0137 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-42+10664C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487151 | |||||||
| chr16:4487157 | G | A | 1 | a0001c0002t0001g0048 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-42+10670G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487157 | |||||||
| chr16:4487308 | C | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-42+10821C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487308 | |||||||
| chr16:4487359 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-42+10872G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487359 | |||||||
| chr16:4487401 | C | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(14): Show |
20 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.-42+10914C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487401 | |||||||
| chr16:4487608 | C | G | 1 | a0001c0001t0001g0211 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-42+11121C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487608 | |||||||
| chr16:4487669 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0128 others(138): Show |
169 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.-42+11182T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487669 | |||||||
| chr16:4487692 | T | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0023 others(159): Show |
190 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(187): Show |
intron_variant | MODIFIER | c.-42+11205T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487692 | |||||||
| chr16:4487693 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0146 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-42+11206G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487693 | |||||||
| chr16:4487774 | C | G | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0144 others(10): Show |
13 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-42+11287C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487774 | |||||||
| chr16:4487787 | C | CA | 17 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(14): Show |
20 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.-42+11314dupA | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4487787 | ||||||
| chr16:4487807 | C | T | 40 | a0001c0001t0001g0006 a0001c0001t0001g0231 a0001c0001t0001g0247 others(37): Show |
45 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.-42+11320C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487807 | |||||||
| chr16:4487875 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-42+11388C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487875 | |||||||
| chr16:4487892 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0129 others(88): Show |
114 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-42+11405G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487892 | |||||||
| chr16:4487895 | G | A | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG02280.hp2 HG02622.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+11408G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487895 | |||||||
| chr16:4487938 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-42+11451C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487938 | |||||||
| chr16:4487944 | T | C | 6 | a0001c0001t0001g0138 a0001c0001t0003g0139 a0001c0001t0003g0140 others(3): Show |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+11457T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4487944 | |||||||
| chr16:4487951 | C | CA | 23 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0149 others(20): Show |
23 | HG00597.hp2 HG01109.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-42+11485dupA | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4487951 | ||||||
| chr16:4487951 | CAAA | C | 37 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(34): Show |
42 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.-42+11483_-42+1148 others(7): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4487951 | ||||||
| chr16:4488007 | T | C | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+11520T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4488007 | |||||||
| chr16:4488094 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-42+11607T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4488094 | |||||||
| chr16:4488113 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0128 a0001c0001t0001g0129 others(93): Show |
119 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-42+11626G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4488113 | |||||||
| chr16:4488127 | C | CA | 44 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(41): Show |
46 | HG00639.hp1 HG00639.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.-42+11660dupA | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4488127 | ||||||
| chr16:4488127 | CAAAA | C | 19 | a0001c0001t0001g0248 a0001c0002t0001g0007 a0001c0002t0001g0030 others(16): Show |
21 | HG00642.hp1 HG01175.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-42+11657_-42+1166 others(8): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4488127 | ||||||
| chr16:4488127 | CAAAAA | C | 16 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0249 others(13): Show |
19 | HG02280.hp1 HG02559.hp2 HG02647.hp1 others(16): Show |
intron_variant | MODIFIER | c.-42+11656_-42+1166 others(9): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4488127 | ||||||
| chr16:4488147 | A | C | 1 | a0001c0001t0001g0206 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-42+11660A>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4488147 | |||||||
| chr16:4488184 | C | T | 22 | a0001c0002t0001g0007 a0001c0002t0001g0030 a0001c0002t0001g0031 others(19): Show |
24 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-42+11697C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4488184 | |||||||
| chr16:4488279 | A | C | 1 | a0001c0001t0002g0154 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-42+11792A>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4488279 | |||||||
| chr16:4488511 | C | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-42+12024C>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4488511 | |||||||
| chr16:4488560 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-42+12073C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4488560 | |||||||
| chr16:4488568 | T | C | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG02280.hp2 HG02622.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+12081T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4488568 | |||||||
| chr16:4488762 | G | A | 4 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0211 others(1): Show |
4 | HG02004.hp1 HG02148.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42+12275G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4488762 | |||||||
| chr16:4488825 | C | CT | 14 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(11): Show |
14 | HG01261.hp1 HG02486.hp1 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.-42+12355dupT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4488825 | ||||||
| chr16:4488825 | CT | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0138 others(131): Show |
162 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.-42+12355delT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4488825 | ||||||
| chr16:4488988 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0002g0001 a0001c0001t0002g0003 others(88): Show |
114 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-42+12501G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4488988 | |||||||
| chr16:4489029 | T | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0138 others(136): Show |
167 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.-42+12542T>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4489029 | |||||||
| chr16:4489155 | C | T | 7 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(4): Show |
7 | HG02486.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-42+12668C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4489155 | |||||||
| chr16:4489471 | A | T | 22 | a0001c0002t0001g0007 a0001c0002t0001g0030 a0001c0002t0001g0031 others(19): Show |
24 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-42+12984A>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4489471 | |||||||
| chr16:4489549 | C | G | 6 | a0001c0001t0001g0138 a0001c0001t0003g0139 a0001c0001t0003g0140 others(3): Show |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+13062C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4489549 | |||||||
| chr16:4489803 | G | T | 1 | a0001c0002t0001g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-42+13316G>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4489803 | |||||||
| chr16:4489831 | G | C | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+13344G>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4489831 | |||||||
| chr16:4489860 | C | T | 40 | a0001c0001t0001g0006 a0001c0001t0001g0138 a0001c0001t0001g0247 others(37): Show |
45 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.-42+13373C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4489860 | |||||||
| chr16:4489906 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-42+13419C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4489906 | |||||||
| chr16:4489941 | A | C | 2 | a0001c0001t0002g0090 a0001c0001t0002g0102 |
2 | HG01243.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-42+13454A>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4489941 | |||||||
| chr16:4490121 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-42+13634T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4490121 | |||||||
| chr16:4490226 | A | G | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42+13739A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4490226 | |||||||
| chr16:4490477 | C | T | 7 | a0001c0002t0001g0037 a0001c0002t0001g0042 a0001c0002t0001g0043 others(4): Show |
7 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.-42+13990C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4490477 | |||||||
| chr16:4490558 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-42+14071C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4490558 | |||||||
| chr16:4490599 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-42+14112G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4490599 | |||||||
| chr16:4490884 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0144 others(93): Show |
119 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-42+14397A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4490884 | |||||||
| chr16:4490956 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-42+14469G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4490956 | |||||||
| chr16:4491150 | C | G | 1 | a0001c0001t0002g0110 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-41-14334C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4491150 | |||||||
| chr16:4491213 | C | T | 1 | a0001c0002t0001g0038 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-41-14271C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4491213 | |||||||
| chr16:4491264 | C | A | 1 | a0001c0001t0001g0211 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-41-14220C>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4491264 | |||||||
| chr16:4491389 | C | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0144 a0001c0001t0001g0147 others(92): Show |
118 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.-41-14095C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4491389 | |||||||
| chr16:4491429 | C | A | 1 | a0001c0001t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-41-14055C>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4491429 | |||||||
| chr16:4491460 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-41-14024G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4491460 | |||||||
| chr16:4491600 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-41-13884C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4491600 | |||||||
| chr16:4491605 | T | C | 17 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(14): Show |
20 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.-41-13879T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4491605 | |||||||
| chr16:4491693 | C | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
44 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.-41-13791C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4491693 | |||||||
| chr16:4491830 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0144 a0001c0001t0001g0147 others(92): Show |
118 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.-41-13654C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4491830 | |||||||
| chr16:4491923 | T | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0023 others(158): Show |
189 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(186): Show |
intron_variant | MODIFIER | c.-41-13561T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4491923 | |||||||
| chr16:4492116 | T | G | 46 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(43): Show |
51 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.-41-13368T>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4492116 | |||||||
| chr16:4492295 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-41-13189C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4492295 | |||||||
| chr16:4492462 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-41-13022A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4492462 | |||||||
| chr16:4492660 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-41-12824G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4492660 | |||||||
| chr16:4492740 | C | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-41-12744C>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4492740 | |||||||
| chr16:4492782 | A | G | 1 | a0001c0002t0001g0036 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-41-12702A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4492782 | |||||||
| chr16:4492799 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-41-12685G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4492799 | |||||||
| chr16:4492812 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-41-12672G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4492812 | |||||||
| chr16:4492814 | A | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0170 others(8): Show |
13 | HG00558.hp1 HG01928.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.-41-12670A>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4492814 | |||||||
| chr16:4493201 | G | A | 5 | a0001c0001t0002g0057 a0001c0001t0002g0067 a0001c0001t0002g0092 others(2): Show |
5 | HG01123.hp1 HG01433.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41-12283G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4493201 | |||||||
| chr16:4493227 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-41-12257A>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4493227 | |||||||
| chr16:4493258 | G | A | 6 | a0001c0001t0001g0138 a0001c0001t0003g0139 a0001c0001t0003g0140 others(3): Show |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41-12226G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4493258 | |||||||
| chr16:4493295 | A | G | 1 | a0001c0006t0001g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-41-12189A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4493295 | |||||||
| chr16:4493379 | A | G | 8 | a0001c0001t0001g0138 a0001c0001t0001g0156 a0001c0001t0001g0157 others(5): Show |
8 | HG02723.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-41-12105A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4493379 | |||||||
| chr16:4493389 | G | C | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0221 |
3 | HG02630.hp2 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-41-12095G>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4493389 | |||||||
| chr16:4493576 | G | C | 1 | a0001c0001t0001g0201 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-41-11908G>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4493576 | |||||||
| chr16:4493598 | A | G | 3 | a0001c0001t0002g0054 a0001c0001t0002g0064 a0001c0001t0002g0080 |
3 | HG02486.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-41-11886A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4493598 | |||||||
| chr16:4493802 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-41-11682G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4493802 | |||||||
| chr16:4494172 | G | A | 2 | a0001c0001t0002g0090 a0001c0001t0002g0102 |
2 | HG01243.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-41-11312G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4494172 | |||||||
| chr16:4494315 | C | CA | 8 | a0001c0001t0001g0026 a0001c0001t0001g0186 a0001c0001t0001g0207 others(5): Show |
8 | HG02486.hp1 HG02572.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.-41-11154dupA | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4494315 | ||||||
| chr16:4494504 | C | T | 104 | a0001c0001t0001g0001 a0001c0001t0002g0001 a0001c0001t0002g0003 others(101): Show |
127 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.-41-10980C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4494504 | |||||||
| chr16:4494658 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-41-10826C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4494658 | |||||||
| chr16:4494673 | G | GT | 17 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(14): Show |
20 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.-41-10808dupT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4494673 | ||||||
| chr16:4494706 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0200 a0001c0001t0001g0223 others(1): Show |
6 | HG00621.hp2 HG02027.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41-10778C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4494706 | |||||||
| chr16:4494721 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-41-10763A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4494721 | |||||||
| chr16:4495126 | A | C | 17 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(14): Show |
20 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.-41-10358A>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4495126 | |||||||
| chr16:4495138 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-41-10346C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4495138 | |||||||
| chr16:4495401 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-41-10083G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4495401 | |||||||
| chr16:4495833 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-41-9651G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4495833 | |||||||
| chr16:4496079 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-41-9405T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4496079 | |||||||
| chr16:4496126 | CT | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(111): Show |
135 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.-41-9341delT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4496126 | ||||||
| chr16:4496126 | CTT | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0023 others(142): Show |
173 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(170): Show |
intron_variant | MODIFIER | c.-41-9342_-41-9341d others(4): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4496126 | ||||||
| chr16:4496156 | G | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-41-9328G>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4496156 | |||||||
| chr16:4496376 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-41-9108G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4496376 | |||||||
| chr16:4496485 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-41-8999A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4496485 | |||||||
| chr16:4496499 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0147 |
2 | HG01099.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.-41-8985T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4496499 | |||||||
| chr16:4496564 | C | G | 1 | a0001c0001t0002g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-41-8920C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4496564 | |||||||
| chr16:4496585 | G | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0002g0001 others(88): Show |
114 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-41-8899G>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4496585 | |||||||
| chr16:4496864 | A | AT | 47 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(44): Show |
52 | HG00642.hp1 HG00738.hp2 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.-41-8609dupT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4496864 | ||||||
| chr16:4496867 | T | A | 1 | a0001c0001t0002g0232 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-41-8617T>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4496867 | |||||||
| chr16:4496883 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-41-8601C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4496883 | |||||||
| chr16:4496985 | C | T | 2 | a0001c0003t0001g0137 a0001c0003t0001g0246 |
2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-41-8499C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4496985 | |||||||
| chr16:4497330 | T | G | 6 | a0001c0001t0001g0138 a0001c0001t0003g0139 a0001c0001t0003g0140 others(3): Show |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41-8154T>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4497330 | |||||||
| chr16:4497470 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0208 |
3 | HG02257.hp2 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-41-8014T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4497470 | |||||||
| chr16:4497480 | A | G | 1 | a0001c0001t0002g0015 | 2 | HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.-41-8004A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4497480 | |||||||
| chr16:4497547 | T | G | 1 | a0001c0001t0002g0130 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-41-7937T>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4497547 | |||||||
| chr16:4497753 | G | T | 1 | a0001c0001t0001g0178 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-41-7731G>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4497753 | |||||||
| chr16:4497785 | A | AG | 46 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(43): Show |
51 | HG00642.hp1 HG00738.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.-41-7694dupG | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4497785 | ||||||
| chr16:4497856 | C | T | 4 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0152 others(1): Show |
4 | HG02280.hp2 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41-7628C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4497856 | |||||||
| chr16:4497987 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-41-7497C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4497987 | |||||||
| chr16:4497994 | G | A | 1 | a0001c0002t0001g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-41-7490G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4497994 | |||||||
| chr16:4498061 | C | CT | 17 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(14): Show |
17 | HG00621.hp1 HG01891.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.-41-7400dupT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4498061 | ||||||
| chr16:4498061 | C | CTT | 11 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(8): Show |
11 | HG00639.hp1 HG02280.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.-41-7401_-41-7400d others(4): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4498061 | ||||||
| chr16:4498061 | CT | C | 10 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0001g0157 others(7): Show |
10 | HG01243.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-41-7400delT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4498061 | ||||||
| chr16:4498061 | CTTTTTT | C | 6 | a0001c0001t0001g0138 a0001c0001t0003g0139 a0001c0001t0003g0140 others(3): Show |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41-7405_-41-7400d others(8): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4498061 | ||||||
| chr16:4498102 | T | C | 1 | a0001c0002t0001g0036 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-41-7382T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4498102 | |||||||
| chr16:4498131 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0002g0001 others(88): Show |
114 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-41-7353G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4498131 | |||||||
| chr16:4498270 | T | C | 2 | a0001c0001t0001g0240 a0001c0001t0001g0242 |
2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-41-7214T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4498270 | |||||||
| chr16:4498386 | C | CT | 32 | a0001c0001t0001g0138 a0001c0001t0002g0055 a0001c0001t0003g0139 others(29): Show |
34 | HG00642.hp1 HG00738.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.-41-7085dupT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4498386 | ||||||
| chr16:4498432 | C | T | 3 | a0001c0001t0001g0168 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG01361.hp1 HG02735.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-41-7052C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4498432 | |||||||
| chr16:4498555 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-41-6929C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4498555 | |||||||
| chr16:4498831 | C | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0128 others(90): Show |
116 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.-41-6653C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4498831 | |||||||
| chr16:4498905 | C | G | 1 | a0001c0001t0001g0022 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-41-6579C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4498905 | |||||||
| chr16:4498930 | T | G | 1 | a0001c0001t0001g0194 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-41-6554T>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4498930 | |||||||
| chr16:4498991 | T | C | 9 | a0001c0001t0001g0144 a0001c0001t0001g0148 a0001c0001t0001g0149 others(6): Show |
9 | HG01243.hp1 HG02280.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-41-6493T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4498991 | |||||||
| chr16:4499086 | C | T | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0183 others(1): Show |
4 | HG02074.hp2 HG02155.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41-6398C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4499086 | |||||||
| chr16:4499225 | C | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0074 others(130): Show |
161 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.-41-6259C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4499225 | |||||||
| chr16:4499582 | G | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0002g0001 others(85): Show |
111 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.-41-5902G>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4499582 | |||||||
| chr16:4499617 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0138 others(94): Show |
120 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.-41-5867G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4499617 | |||||||
| chr16:4499727 | C | A | 1 | a0001c0001t0001g0182 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-41-5757C>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4499727 | |||||||
| chr16:4499772 | C | T | 2 | a0001c0001t0002g0088 a0001c0001t0002g0130 |
2 | NA18950.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.-41-5712C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4499772 | |||||||
| chr16:4500055 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-41-5429A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4500055 | |||||||
| chr16:4500152 | G | A | 23 | a0001c0002t0001g0007 a0001c0002t0001g0030 a0001c0002t0001g0031 others(20): Show |
25 | HG00642.hp1 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.-41-5332G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4500152 | |||||||
| chr16:4500226 | C | T | 2 | a0001c0001t0002g0117 a0001c0001t0002g0119 |
2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-41-5258C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4500226 | |||||||
| chr16:4500245 | C | G | 1 | a0001c0001t0001g0022 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-41-5239C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4500245 | |||||||
| chr16:4500377 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-41-5107G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4500377 | |||||||
| chr16:4500452 | T | C | 1 | a0001c0001t0002g0099 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-41-5032T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4500452 | |||||||
| chr16:4500691 | G | T | 1 | a0001c0001t0001g0138 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-41-4793G>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4500691 | |||||||
| chr16:4501014 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-41-4470G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4501014 | |||||||
| chr16:4501392 | G | T | 1 | a0001c0001t0002g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-41-4092G>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4501392 | |||||||
| chr16:4501405 | T | G | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0146 |
3 | HG01891.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-41-4079T>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4501405 | |||||||
| chr16:4501504 | C | G | 23 | a0001c0002t0001g0007 a0001c0002t0001g0030 a0001c0002t0001g0031 others(20): Show |
25 | HG00642.hp1 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.-41-3980C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4501504 | |||||||
| chr16:4501545 | C | T | 6 | a0001c0001t0001g0138 a0001c0001t0003g0139 a0001c0001t0003g0140 others(3): Show |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41-3939C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4501545 | |||||||
| chr16:4501680 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-41-3804A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4501680 | |||||||
| chr16:4501739 | ATGTAGCT others(10): Show |
A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(14): Show |
20 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.-41-3742_-41-3726d others(19): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4501739 | ||||||
| chr16:4501833 | G | T | 1 | a0001c0002t0001g0049 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-41-3651G>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4501833 | |||||||
| chr16:4502064 | A | C | 2 | a0001c0003t0001g0137 a0001c0003t0001g0246 |
2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-41-3420A>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4502064 | |||||||
| chr16:4502126 | T | A | 1 | a0001c0001t0001g0136 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-41-3358T>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4502126 | |||||||
| chr16:4502145 | G | A | 1 | a0001c0001t0002g0095 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-41-3339G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4502145 | |||||||
| chr16:4502176 | C | T | 6 | a0001c0002t0001g0042 a0001c0002t0001g0043 a0001c0002t0001g0044 others(3): Show |
6 | HG00738.hp2 HG01081.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41-3308C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4502176 | |||||||
| chr16:4502197 | T | C | 6 | a0001c0001t0001g0138 a0001c0001t0003g0139 a0001c0001t0003g0140 others(3): Show |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41-3287T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4502197 | |||||||
| chr16:4502514 | T | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-41-2970T>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4502514 | |||||||
| chr16:4502523 | A | G | 6 | a0001c0001t0001g0138 a0001c0001t0003g0139 a0001c0001t0003g0140 others(3): Show |
6 | HG02723.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41-2961A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4502523 | |||||||
| chr16:4502964 | G | T | 23 | a0001c0002t0001g0007 a0001c0002t0001g0030 a0001c0002t0001g0031 others(20): Show |
25 | HG00642.hp1 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.-41-2520G>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4502964 | |||||||
| chr16:4503052 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-41-2432T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4503052 | |||||||
| chr16:4503110 | C | T | 1 | a0001c0001t0002g0095 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-41-2374C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4503110 | |||||||
| chr16:4503191 | T | C | 23 | a0001c0002t0001g0007 a0001c0002t0001g0030 a0001c0002t0001g0031 others(20): Show |
25 | HG00642.hp1 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.-41-2293T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4503191 | |||||||
| chr16:4503359 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-41-2125G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4503359 | |||||||
| chr16:4503651 | T | G | 1 | a0001c0001t0001g0186 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-41-1833T>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4503651 | |||||||
| chr16:4503821 | T | G | 1 | a0001c0001t0002g0116 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-41-1663T>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4503821 | |||||||
| chr16:4503840 | C | G | 2 | a0001c0001t0001g0240 a0001c0001t0001g0242 |
2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-41-1644C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4503840 | |||||||
| chr16:4503936 | C | G | 1 | a0001c0001t0001g0197 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-41-1548C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4503936 | |||||||
| chr16:4504010 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-41-1474G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4504010 | |||||||
| chr16:4504354 | A | AT | 13 | a0001c0001t0001g0164 a0001c0001t0001g0172 a0001c0001t0001g0174 others(10): Show |
13 | HG01175.hp1 HG01361.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.-41-1106dupT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4504354 | ||||||
| chr16:4504354 | AT | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(92): Show |
115 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.-41-1106delT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4504354 | ||||||
| chr16:4504354 | ATT | A | 9 | a0001c0001t0001g0136 a0001c0001t0001g0146 a0001c0001t0001g0152 others(6): Show |
9 | HG02280.hp2 HG02723.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-41-1107_-41-1106d others(4): Show |
HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4504354 | ||||||
| chr16:4504452 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-41-1032G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4504452 | |||||||
| chr16:4504508 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-41-976G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4504508 | |||||||
| chr16:4504595 | G | A | 30 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(27): Show |
32 | HG00642.hp1 HG00738.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.-41-889G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4504595 | |||||||
| chr16:4504682 | C | CT | 28 | a0001c0001t0001g0020 a0001c0001t0001g0074 a0001c0001t0001g0135 others(25): Show |
29 | HG00423.hp2 HG00544.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.-41-776dupT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4504682 | ||||||
| chr16:4504682 | CT | C | 44 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(41): Show |
46 | HG00558.hp2 HG00642.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.-41-776delT | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr16 | 4504682 | ||||||
| chr16:4504709 | A | G | 17 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0248 others(14): Show |
20 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.-41-775A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4504709 | |||||||
| chr16:4504758 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0002g0001 a0001c0001t0002g0003 others(87): Show |
113 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.-41-726C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4504758 | |||||||
| chr16:4504760 | G | A | 3 | a0001c0002t0001g0007 a0001c0002t0001g0032 a0001c0002t0001g0034 |
5 | HG02109.hp2 HG02145.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-41-724G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4504760 | |||||||
| chr16:4505282 | A | G | 1 | a0001c0001t0002g0098 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-41-202A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 1/5 | chr16 | 4505282 | |||||||
| chr16:4505923 | G | A | 1 | a0001c0003t0001g0246 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.86+313G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 2/5 | chr16 | 4505923 | |||||||
| chr16:4505953 | A | G | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG01891.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.86+343A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 2/5 | chr16 | 4505953 | |||||||
| chr16:4505964 | G | C | 23 | a0001c0002t0001g0007 a0001c0002t0001g0030 a0001c0002t0001g0031 others(20): Show |
25 | HG00642.hp1 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.86+354G>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 2/5 | chr16 | 4505964 | |||||||
| chr16:4506156 | A | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0244 |
3 | HG02735.hp2 HG03490.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.86+546A>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 2/5 | chr16 | 4506156 | |||||||
| chr16:4506355 | C | T | 12 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0146 others(9): Show |
12 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.87-540C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 2/5 | chr16 | 4506355 | |||||||
| chr16:4506449 | A | T | 23 | a0001c0002t0001g0007 a0001c0002t0001g0030 a0001c0002t0001g0031 others(20): Show |
25 | HG00642.hp1 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.87-446A>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 2/5 | chr16 | 4506449 | |||||||
| chr16:4506683 | C | A | 1 | a0001c0006t0001g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.87-212C>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 2/5 | chr16 | 4506683 | |||||||
| chr16:4506764 | G | A | 1 | a0001c0002t0001g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.87-131G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 2/5 | chr16 | 4506764 | |||||||
| chr16:4506831 | A | G | 1 | a0001c0006t0001g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.87-64A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 2/5 | chr16 | 4506831 | |||||||
| chr16:4507210 | C | T | 1 | a0001c0003t0001g0137 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.204+198C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 3/5 | chr16 | 4507210 | |||||||
| chr16:4507211 | G | A | 1 | a0001c0001t0003g0139 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.204+199G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 3/5 | chr16 | 4507211 | |||||||
| chr16:4507315 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0001g0260 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.204+303C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 3/5 | chr16 | 4507315 | |||||||
| chr16:4507449 | C | CA | 9 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(6): Show |
9 | HG02280.hp2 HG02622.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.205-250dupA | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr16 | 4507449 | ||||||
| chr16:4507675 | G | A | 1 | a0001c0001t0001g0022 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.205-38G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 3/5 | chr16 | 4507675 | |||||||
| chr16:4508292 | T | C | 1 | a0001c0002t0001g0039 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.696+88T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 4/5 | chr16 | 4508292 | |||||||
| chr16:4508441 | C | G | 2 | a0001c0001t0001g0206 a0001c0001t0001g0222 |
2 | HG02027.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.696+237C>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 4/5 | chr16 | 4508441 | |||||||
| chr16:4508552 | C | A | 23 | a0001c0002t0001g0007 a0001c0002t0001g0030 a0001c0002t0001g0031 others(20): Show |
25 | HG00642.hp1 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.696+348C>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 4/5 | chr16 | 4508552 | |||||||
| chr16:4508556 | A | G | 10 | a0001c0001t0001g0144 a0001c0001t0001g0147 a0001c0001t0001g0148 others(7): Show |
10 | HG01099.hp2 HG01243.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.696+352A>G | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 4/5 | chr16 | 4508556 | |||||||
| chr16:4508565 | T | C | 2 | a0001c0001t0001g0218 a0001c0001t0001g0227 |
2 | HG02071.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.696+361T>C | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 4/5 | chr16 | 4508565 | |||||||
| chr16:4508577 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.696+373G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 4/5 | chr16 | 4508577 | |||||||
| chr16:4508614 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0002g0001 others(88): Show |
114 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.696+410G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 4/5 | chr16 | 4508614 | |||||||
| chr16:4508758 | A | T | 1 | a0001c0006t0001g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.696+554A>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 4/5 | chr16 | 4508758 | |||||||
| chr16:4508831 | G | A | 2 | a0001c0003t0001g0137 a0001c0003t0001g0246 |
2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.697-581G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 4/5 | chr16 | 4508831 | |||||||
| chr16:4508973 | C | T | 1 | a0001c0002t0001g0100 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.697-439C>T | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 4/5 | chr16 | 4508973 | |||||||
| chr16:4509266 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.697-146G>A | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 4/5 | chr16 | 4509266 | |||||||
| chr16:4509350 | T | TA | 10 | a0001c0001t0001g0022 a0001c0001t0001g0138 a0001c0001t0001g0256 others(7): Show |
11 | HG00642.hp2 HG01175.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.697-47dupA | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 4509350 | ||||||
| chr16:4509350 | TA | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0244 a0001c0001t0001g0255 others(2): Show |
6 | HG02735.hp2 HG03130.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.697-47delA | HMOX2 | ENSG00000103415.12 | transcript | ENST00000570646.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr16 | 4509350 |