Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3176 |
| ensemblid | ENSG00000150540.14 |
| hgncid | 5028 |
| symbol | HNMT |
| name | histamine N-methyltransferase |
| refseq_nuc | NM_006895.3 |
| refseq_prot | NP_008826.1 |
| ensembl_nuc | ENST00000280097.5 |
| ensembl_prot | ENSP00000280097.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 137964473 |
| end | 138016364 |
| strand | + |
| ver | v1.2 |
| region | chr2:137964473-138016364 |
| region5000 | chr2:137959473-138021364 |
| regionname0 | HNMT_chr2_137964473_138016364 |
| regionname5000 | HNMT_chr2_137959473_138021364 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 292 | 308 | 85 | 52 | 122 | 9 | 38 | 84 | HNMT_chr2_137959473_138021364 | HNMT | MASSM others(287): Show |
chr2 | 137959473 | 138021364 |
| a0002 | 0/0 | 292 | 23 | 0 | 8 | 8 | 1 | 6 | 6 | HNMT_chr2_137959473_138021364 | HNMT | MASSM others(287): Show |
chr2 | 137959473 | 138021364 |
| a0003 | 0/0 | 292 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | MASSM others(287): Show |
chr2 | 137959473 | 138021364 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 876 | 306 | 85 | 52 | 120 | 9 | 38 | HNMT_chr2_137959473_138021364 | HNMT | ATGGC others(871): Show |
chr2 | 137959473 | 138021364 | ||
| a0001c0004 | 0/0 | 876 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | ATGGC others(871): Show |
chr2 | 137959473 | 138021364 | ||
| a0001c0005 | 0/0 | 876 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | ATGGC others(871): Show |
chr2 | 137959473 | 138021364 | ||
| a0002c0002 | 0/0 | 876 | 23 | 0 | 8 | 8 | 1 | 6 | HNMT_chr2_137959473_138021364 | HNMT | ATGGC others(871): Show |
chr2 | 137959473 | 138021364 | ||
| a0003c0003 | 0/0 | 876 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | ATGGC others(871): Show |
chr2 | 137959473 | 138021364 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3132 | 180 | 36 | 36 | 72 | 8 | 26 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0002 | 0/0 | 3132 | 75 | 15 | 11 | 39 | 1 | 9 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0003 | 0/0 | 3132 | 18 | 18 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0004 | 0/0 | 3132 | 5 | 4 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0005 | 0/0 | 3132 | 3 | 3 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0006 | 0/0 | 3132 | 3 | 3 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0007 | 0/0 | 3132 | 3 | 0 | 0 | 3 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0008 | 0/0 | 3132 | 3 | 0 | 0 | 1 | 0 | 2 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0009 | 0/0 | 3132 | 2 | 0 | 2 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0010 | 0/0 | 3132 | 2 | 2 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0011 | 0/0 | 3132 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0012 | 0/0 | 3132 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0013 | 0/0 | 3132 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0014 | 0/0 | 3132 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0015 | 0/0 | 3132 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0016 | 0/0 | 3132 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0017 | 0/0 | 3132 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0018 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3111): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0019 | 0/0 | 3132 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0021 | 0/0 | 3132 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0001t0022 | 0/0 | 3132 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0004t0001 | 0/0 | 3132 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0001c0005t0001 | 0/0 | 3132 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0002c0002t0002 | 0/0 | 3132 | 22 | 0 | 8 | 8 | 1 | 5 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0002c0002t0020 | 0/0 | 3132 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| a0003c0003t0001 | 0/0 | 3132 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | CTTTC others(3127): Show |
chr2 | 137959473 | 138021364 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 0 | 3 | 6 | 1 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0002 | 0/0 | 10 | 3 | 2 | 5 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0003 | 0/0 | 6 | 1 | 0 | 3 | 1 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0058 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0003g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0005g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0008g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0008g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0008g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0009g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0010g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0011g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0012g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0013g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0014g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0015g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0016g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0017g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0018g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0019g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0021g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0001t0022g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0001c0005t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0002c0002t0020g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| a0003c0003t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | GBR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | GBR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | GBR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0095 | EUR | FIN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00423 | hp1 | a0001 | c0001 | t0017 | g0209 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0258 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0221 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0020 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0020 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0122 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01167 | hp2 | a0001 | c0001 | t0009 | g0011 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0011 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0218 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0256 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01361 | hp2 | a0001 | c0001 | t0019 | g0227 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | IBS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0070 | EUR | IBS | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0255 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0150 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0031 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0050 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02074 | hp1 | a0001 | c0001 | t0011 | g0005 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02135 | hp2 | a0001 | c0001 | t0011 | g0005 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02145 | hp1 | a0003 | c0003 | t0001 | g0246 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | CDX | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02165 | hp1 | a0001 | c0001 | t0008 | g0196 | EAS | CDX | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CDX | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02257 | hp2 | a0001 | c0001 | t0013 | g0139 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02300 | hp1 | a0001 | c0001 | t0022 | g0109 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02683 | hp2 | a0002 | c0002 | t0020 | g0015 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02698 | hp2 | a0001 | c0001 | t0008 | g0171 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02717 | hp1 | a0001 | c0001 | t0015 | g0250 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02965 | hp1 | a0001 | c0001 | t0021 | g0249 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02970 | hp1 | a0001 | c0001 | t0012 | g0056 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0132 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0049 | AFR | GWD | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0032 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0168 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0032 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ESN | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | STU | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0015 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03942 | hp1 | a0001 | c0001 | t0016 | g0090 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0124 | SAS | STU | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0120 | SAS | STU | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | STU | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | STU | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | STU | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | CHB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | YRI | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18974 | hp1 | a0001 | c0001 | t0007 | g0133 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18977 | hp1 | a0001 | c0001 | t0007 | g0083 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18985 | hp1 | a0001 | c0004 | t0001 | g0188 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18986 | hp2 | a0001 | c0001 | t0007 | g0081 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19002 | hp2 | a0001 | c0001 | t0014 | g0236 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | LWK | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | LWK | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | LWK | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | LWK | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19055 | hp2 | a0001 | c0005 | t0001 | g0198 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19066 | hp1 | a0001 | c0001 | t0018 | g0009 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | ASW | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | ASW | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | TSI | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | TSI | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0072 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0247 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0048 | AFR | ACB | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | USA | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| HG06807 | hp2 | a0001 | c0001 | t0010 | g0148 | AFR | USA | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | USA | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0220 | AFR | USA | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0147 | AFR | LWK | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0076 | REF | REF | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0058 | REF | REF | HNMT_chr2_137959473_138021364 | HNMT | chr2 | 137959473 | 138021364 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:138000972 | G | A | 1 | a0003 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.245G>A | p.Cys82Tyr | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/6 | 264/3132 | 245/879 | 82/292 | chr2 | 138000972 | |||
| chr2:138002079 | C | T | 1 | a0002 | 23 | HG00280.hp1 HG00558.hp2 HG01070.hp1 others(20): Show |
missense_variant | MODERATE | c.314C>T | p.Thr105Ile | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/6 | 333/3132 | 314/879 | 105/292 | chr2 | 138002079 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:138013809 | C | T | 1 | a0001c0005 | 1 | NA19055.hp2 | synonymous_variant | LOW | c.558C>T | p.Tyr186Tyr | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 577/3132 | 558/879 | 186/292 | chr2 | 138013809 | |||
| chr2:138013926 | T | C | 1 | a0001c0004 | 1 | NA18985.hp1 | synonymous_variant | LOW | c.675T>C | p.Asp225Asp | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 694/3132 | 675/879 | 225/292 | chr2 | 138013926 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:138014165 | T | C | 1 | a0001c0001t0009 | 2 | HG01167.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*35T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 35 | chr2 | 138014165 | ||||||
| chr2:138014190 | A | G | 9 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0011 others(6): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*60A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 60 | chr2 | 138014190 | ||||||
| chr2:138014348 | A | T | 9 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0011 others(6): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*218A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 218 | chr2 | 138014348 | ||||||
| chr2:138014640 | A | G | 1 | a0001c0001t0011 | 2 | HG02074.hp1 HG02135.hp2 |
3_prime_UTR_variant | MODIFIER | c.*510A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 510 | chr2 | 138014640 | ||||||
| chr2:138014765 | G | C | 1 | a0001c0001t0010 | 2 | HG06807.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*635G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 635 | chr2 | 138014765 | ||||||
| chr2:138014966 | C | T | 1 | a0001c0001t0007 | 3 | NA18974.hp1 NA18977.hp1 NA18986.hp2 |
3_prime_UTR_variant | MODIFIER | c.*836C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 836 | chr2 | 138014966 | ||||||
| chr2:138014971 | TTTATTGA others(9): Show |
T | 1 | a0001c0001t0018 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*842_*857delTTATTG others(10): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 842 | chr2 | 138014971 | ||||||
| chr2:138015124 | C | T | 9 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0011 others(6): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*994C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 994 | chr2 | 138015124 | ||||||
| chr2:138015139 | T | G | 1 | a0001c0001t0012 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1009T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1009 | chr2 | 138015139 | ||||||
| chr2:138015168 | G | C | 2 | a0001c0001t0004 a0001c0001t0010 |
7 | HG00735.hp1 HG02809.hp1 HG03130.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1038G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1038 | chr2 | 138015168 | ||||||
| chr2:138015169 | T | G | 1 | a0001c0001t0008 | 3 | HG02165.hp1 HG02698.hp2 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1039T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1039 | chr2 | 138015169 | ||||||
| chr2:138015331 | A | G | 1 | a0001c0001t0017 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1201A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1201 | chr2 | 138015331 | ||||||
| chr2:138015412 | G | A | 1 | a0001c0001t0013 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1282G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1282 | chr2 | 138015412 | ||||||
| chr2:138015418 | G | A | 1 | a0001c0001t0019 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1288G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1288 | chr2 | 138015418 | ||||||
| chr2:138015432 | A | G | 1 | a0001c0001t0016 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1302A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1302 | chr2 | 138015432 | ||||||
| chr2:138015492 | G | A | 1 | a0001c0001t0005 | 3 | HG02258.hp2 HG02486.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1362G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1362 | chr2 | 138015492 | ||||||
| chr2:138015524 | T | C | 1 | a0002c0002t0020 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1394T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1394 | chr2 | 138015524 | ||||||
| chr2:138015559 | T | C | 1 | a0001c0001t0021 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1429T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1429 | chr2 | 138015559 | ||||||
| chr2:138015659 | G | A | 9 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0011 others(6): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*1529G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1529 | chr2 | 138015659 | ||||||
| chr2:138015752 | C | T | 1 | a0001c0001t0022 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1622C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1622 | chr2 | 138015752 | ||||||
| chr2:138015899 | G | A | 1 | a0001c0001t0014 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1769G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1769 | chr2 | 138015899 | ||||||
| chr2:138015899 | G | T | 1 | a0001c0001t0006 | 3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1769G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1769 | chr2 | 138015899 | ||||||
| chr2:138016022 | G | A | 1 | a0001c0001t0015 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1892G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1892 | chr2 | 138016022 | ||||||
| chr2:138016068 | C | T | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(13): Show |
140 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*1938C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1938 | chr2 | 138016068 | ||||||
| chr2:138016113 | C | T | 1 | a0001c0001t0006 | 3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1983C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 1983 | chr2 | 138016113 | ||||||
| chr2:138016182 | T | C | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(13): Show |
140 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*2052T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 2052 | chr2 | 138016182 | ||||||
| chr2:138016241 | C | G | 9 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0011 others(6): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*2111C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 6/6 | 2111 | chr2 | 138016241 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:137964770 | C | T | 1 | a0001c0001t0005g0033 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.137+142C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137964770 | |||||||
| chr2:137964813 | G | A | 1 | a0001c0001t0005g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.137+185G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137964813 | |||||||
| chr2:137965033 | C | A | 1 | a0001c0001t0003g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.137+405C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137965033 | |||||||
| chr2:137965170 | G | T | 1 | a0001c0001t0001g0261 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.137+542G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137965170 | |||||||
| chr2:137965179 | A | T | 1 | a0002c0002t0002g0032 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.137+551A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137965179 | |||||||
| chr2:137965242 | C | CT | 14 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0002g0009 others(11): Show |
18 | HG00558.hp2 HG01346.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.137+622dupT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 137965242 | ||||||
| chr2:137965284 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.137+656G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137965284 | |||||||
| chr2:137965505 | A | G | 5 | a0001c0001t0002g0248 a0001c0001t0003g0247 a0001c0001t0015g0250 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+877A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137965505 | |||||||
| chr2:137965516 | G | A | 1 | a0001c0001t0009g0011 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.137+888G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137965516 | |||||||
| chr2:137965674 | A | G | 5 | a0001c0001t0002g0248 a0001c0001t0003g0247 a0001c0001t0015g0250 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+1046A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137965674 | |||||||
| chr2:137965718 | T | C | 5 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(2): Show |
5 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+1090T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137965718 | |||||||
| chr2:137965826 | C | T | 1 | a0001c0001t0003g0029 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.137+1198C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137965826 | |||||||
| chr2:137966043 | G | C | 5 | a0001c0001t0002g0248 a0001c0001t0003g0247 a0001c0001t0015g0250 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+1415G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137966043 | |||||||
| chr2:137966318 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.137+1690C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137966318 | |||||||
| chr2:137966416 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.137+1788C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137966416 | |||||||
| chr2:137966528 | A | T | 1 | a0001c0001t0001g0243 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.137+1900A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137966528 | |||||||
| chr2:137966766 | G | GT | 119 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(116): Show |
148 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.137+2140dupT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 137966766 | ||||||
| chr2:137966787 | A | G | 3 | a0001c0001t0001g0149 a0002c0002t0002g0020 a0002c0002t0002g0150 |
4 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+2159A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137966787 | |||||||
| chr2:137967011 | T | C | 5 | a0001c0001t0002g0248 a0001c0001t0003g0247 a0001c0001t0015g0250 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+2383T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967011 | |||||||
| chr2:137967168 | C | T | 3 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 |
3 | HG01928.hp1 HG01943.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.137+2540C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967168 | |||||||
| chr2:137967176 | T | A | 5 | a0001c0001t0002g0248 a0001c0001t0003g0247 a0001c0001t0015g0250 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+2548T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967176 | |||||||
| chr2:137967181 | C | T | 2 | a0001c0001t0010g0147 a0001c0001t0010g0148 |
2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.137+2553C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967181 | |||||||
| chr2:137967182 | G | A | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG01243.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+2554G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967182 | |||||||
| chr2:137967432 | C | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.138-2733C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967432 | |||||||
| chr2:137967526 | A | G | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02647.hp2 HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.138-2639A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967526 | |||||||
| chr2:137967546 | T | C | 2 | a0001c0001t0003g0062 a0001c0001t0003g0063 |
2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.138-2619T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967546 | |||||||
| chr2:137967608 | T | A | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG02895.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-2557T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967608 | |||||||
| chr2:137967632 | C | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.138-2533C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967632 | |||||||
| chr2:137967762 | G | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.138-2403G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137967762 | |||||||
| chr2:137968041 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.138-2124G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968041 | |||||||
| chr2:137968227 | T | C | 1 | a0001c0001t0003g0069 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.138-1938T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968227 | |||||||
| chr2:137968310 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.138-1855G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968310 | |||||||
| chr2:137968327 | A | C | 2 | a0001c0001t0003g0062 a0001c0001t0003g0063 |
2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.138-1838A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968327 | |||||||
| chr2:137968386 | C | T | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.138-1779C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968386 | |||||||
| chr2:137968421 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.138-1744G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968421 | |||||||
| chr2:137968627 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.138-1538C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968627 | |||||||
| chr2:137968712 | G | T | 6 | a0001c0001t0001g0144 a0001c0001t0002g0019 a0001c0001t0002g0145 others(3): Show |
8 | HG02055.hp2 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.138-1453G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968712 | |||||||
| chr2:137968785 | C | T | 1 | a0001c0001t0005g0033 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.138-1380C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968785 | |||||||
| chr2:137968944 | T | G | 5 | a0001c0001t0002g0248 a0001c0001t0003g0247 a0001c0001t0015g0250 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-1221T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968944 | |||||||
| chr2:137968972 | C | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(105): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.138-1193C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137968972 | |||||||
| chr2:137969045 | T | C | 1 | a0001c0001t0003g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.138-1120T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969045 | |||||||
| chr2:137969063 | A | G | 3 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 |
3 | HG01928.hp1 HG01943.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.138-1102A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969063 | |||||||
| chr2:137969202 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.138-963C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969202 | |||||||
| chr2:137969262 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.138-903A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969262 | |||||||
| chr2:137969326 | C | G | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG01074.hp1 HG01074.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.138-839C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969326 | |||||||
| chr2:137969417 | G | A | 1 | a0001c0001t0005g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.138-748G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969417 | |||||||
| chr2:137969627 | C | T | 1 | a0001c0001t0015g0250 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.138-538C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969627 | |||||||
| chr2:137969630 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.138-535G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969630 | |||||||
| chr2:137969766 | A | G | 1 | a0001c0001t0005g0033 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.138-399A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969766 | |||||||
| chr2:137969903 | C | T | 3 | a0001c0001t0004g0017 a0001c0001t0004g0138 a0001c0001t0013g0139 |
4 | HG02257.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-262C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969903 | |||||||
| chr2:137969971 | T | C | 1 | a0003c0003t0001g0246 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.138-194T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137969971 | |||||||
| chr2:137970037 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(105): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.138-128G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 1/5 | chr2 | 137970037 | |||||||
| chr2:137970597 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.190+380A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970597 | |||||||
| chr2:137970605 | T | C | 1 | a0001c0001t0003g0069 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.190+388T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970605 | |||||||
| chr2:137970641 | C | T | 2 | a0001c0001t0001g0235 a0001c0001t0014g0236 |
2 | HG02040.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.190+424C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970641 | |||||||
| chr2:137970644 | G | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
6 | HG01081.hp2 HG01256.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.190+427G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970644 | |||||||
| chr2:137970654 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.190+437C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970654 | |||||||
| chr2:137970691 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.190+474G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970691 | |||||||
| chr2:137970696 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.190+479G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970696 | |||||||
| chr2:137970781 | G | A | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG01243.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.190+564G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970781 | |||||||
| chr2:137970796 | T | G | 1 | a0001c0001t0002g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.190+579T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970796 | |||||||
| chr2:137970827 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.190+610G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970827 | |||||||
| chr2:137970828 | G | A | 24 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(21): Show |
28 | HG00558.hp2 HG01167.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.190+611G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970828 | |||||||
| chr2:137970906 | C | A | 1 | a0001c0001t0003g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.190+689C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970906 | |||||||
| chr2:137970931 | AAAAAAGA others(7): Show |
A | 1 | a0001c0001t0001g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.190+718_190+731del others(14): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970931 | ||||||
| chr2:137970933 | A | AAAAAAGA others(7): Show |
1 | a0001c0001t0003g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.190+719_190+720ins others(14): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970933 | ||||||
| chr2:137970933 | AAAAG | A | 6 | a0001c0001t0001g0144 a0001c0001t0002g0019 a0001c0001t0002g0146 others(3): Show |
8 | HG02155.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.190+752_190+755del others(4): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970933 | ||||||
| chr2:137970933 | AAAAGAAA others(1): Show |
A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(80): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.190+748_190+755del others(8): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970933 | ||||||
| chr2:137970933 | AAAAGAAA others(5): Show |
A | 14 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(11): Show |
14 | HG02145.hp2 HG02647.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.190+744_190+755del others(12): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970933 | ||||||
| chr2:137970934 | AAAGAAAG | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0087 others(11): Show |
18 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.190+720_190+726del others(7): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970934 | ||||||
| chr2:137970934 | AAAGAAAG others(4): Show |
A | 4 | a0001c0001t0001g0008 a0001c0001t0006g0048 a0001c0001t0006g0049 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+720_190+730del others(11): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970934 | ||||||
| chr2:137970934 | AAAGAAAG others(8): Show |
A | 1 | a0001c0001t0001g0210 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.190+720_190+734del others(15): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970934 | ||||||
| chr2:137970935 | AAGAAAGA others(3): Show |
A | 7 | a0001c0001t0001g0067 a0001c0001t0002g0162 a0001c0001t0002g0248 others(4): Show |
7 | HG02145.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.190+720_190+729del others(10): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970935 | ||||||
| chr2:137970935 | AAGAAAGA others(7): Show |
A | 116 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(113): Show |
142 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.190+720_190+733del others(14): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970935 | ||||||
| chr2:137970935 | AAGAAAGA others(11): Show |
A | 1 | a0001c0001t0001g0203 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.190+720_190+737del others(18): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137970935 | ||||||
| chr2:137970936 | AGAAAGAA others(2): Show |
A | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+720_190+728del others(9): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970936 | |||||||
| chr2:137970936 | AGAAAGAA others(6): Show |
A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0159 a0001c0001t0001g0169 others(5): Show |
9 | HG00140.hp1 HG01257.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.190+720_190+732del others(13): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970936 | |||||||
| chr2:137970945 | G | A | 3 | a0001c0001t0002g0073 a0001c0001t0003g0071 a0001c0001t0003g0072 |
3 | HG02109.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.190+728G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970945 | |||||||
| chr2:137970949 | G | A | 21 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(18): Show |
21 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.190+732G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970949 | |||||||
| chr2:137970965 | G | A | 1 | a0001c0001t0002g0075 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.190+748G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137970965 | |||||||
| chr2:137971117 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.190+900C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971117 | |||||||
| chr2:137971148 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.190+931T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971148 | |||||||
| chr2:137971217 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.190+1000G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971217 | |||||||
| chr2:137971388 | C | T | 3 | a0001c0001t0001g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 |
3 | NA18941.hp2 NA19083.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.190+1171C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971388 | |||||||
| chr2:137971439 | A | G | 1 | a0001c0001t0007g0133 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.190+1222A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971439 | |||||||
| chr2:137971543 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(126): Show |
158 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.190+1326G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971543 | |||||||
| chr2:137971611 | G | T | 5 | a0001c0001t0001g0144 a0001c0001t0002g0019 a0001c0001t0002g0145 others(2): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.190+1394G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971611 | |||||||
| chr2:137971664 | G | A | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.190+1447G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971664 | |||||||
| chr2:137971761 | A | G | 1 | a0001c0001t0002g0010 | 3 | HG02630.hp2 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.190+1544A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971761 | |||||||
| chr2:137971806 | TA | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(103): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.190+1590delA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971806 | |||||||
| chr2:137971880 | A | G | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.190+1663A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971880 | |||||||
| chr2:137971934 | A | G | 1 | a0001c0001t0005g0033 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.190+1717A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971934 | |||||||
| chr2:137971966 | T | C | 3 | a0001c0001t0006g0048 a0001c0001t0006g0049 a0001c0001t0006g0050 |
3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.190+1749T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137971966 | |||||||
| chr2:137972057 | A | C | 1 | a0001c0001t0001g0234 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.190+1840A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972057 | |||||||
| chr2:137972135 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02602.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.190+1918C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972135 | |||||||
| chr2:137972136 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.190+1919G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972136 | |||||||
| chr2:137972152 | T | A | 1 | a0001c0001t0003g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.190+1935T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972152 | |||||||
| chr2:137972267 | G | A | 1 | a0001c0001t0015g0250 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.190+2050G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972267 | |||||||
| chr2:137972304 | C | T | 1 | a0002c0002t0002g0032 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.190+2087C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972304 | |||||||
| chr2:137972354 | C | T | 5 | a0001c0001t0002g0248 a0001c0001t0003g0247 a0001c0001t0015g0250 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+2137C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972354 | |||||||
| chr2:137972417 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.190+2200T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972417 | |||||||
| chr2:137972419 | G | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.190+2202G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972419 | |||||||
| chr2:137972779 | G | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(102): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.190+2562G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972779 | |||||||
| chr2:137972848 | T | A | 1 | a0001c0001t0003g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.190+2631T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972848 | |||||||
| chr2:137972887 | C | T | 5 | a0001c0001t0001g0144 a0001c0001t0002g0019 a0001c0001t0002g0145 others(2): Show |
7 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.190+2670C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972887 | |||||||
| chr2:137972911 | A | T | 1 | a0001c0001t0003g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.190+2694A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972911 | |||||||
| chr2:137972913 | G | A | 1 | a0001c0001t0003g0029 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.190+2696G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137972913 | |||||||
| chr2:137973024 | A | T | 8 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(5): Show |
8 | HG02109.hp2 HG02895.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.190+2807A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973024 | |||||||
| chr2:137973091 | A | G | 1 | a0001c0001t0003g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.190+2874A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973091 | |||||||
| chr2:137973105 | T | A | 5 | a0001c0001t0002g0248 a0001c0001t0003g0247 a0001c0001t0015g0250 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+2888T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973105 | |||||||
| chr2:137973219 | C | T | 8 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(5): Show |
8 | HG02109.hp2 HG02895.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.190+3002C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973219 | |||||||
| chr2:137973596 | A | C | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG01243.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.190+3379A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973596 | |||||||
| chr2:137973712 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.190+3495A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973712 | |||||||
| chr2:137973771 | G | GT | 126 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(123): Show |
155 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.190+3562dupT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137973771 | ||||||
| chr2:137973780 | G | T | 4 | a0001c0001t0001g0230 a0001c0001t0002g0073 a0001c0001t0003g0071 others(1): Show |
4 | HG01255.hp1 HG02109.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+3563G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973780 | |||||||
| chr2:137973781 | G | T | 1 | a0001c0001t0002g0128 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.190+3564G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973781 | |||||||
| chr2:137973872 | G | A | 1 | a0001c0001t0001g0022 | 2 | NA18979.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.190+3655G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973872 | |||||||
| chr2:137973982 | C | G | 1 | a0001c0001t0001g0229 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.190+3765C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137973982 | |||||||
| chr2:137974065 | C | CAAGATTT others(40): Show |
1 | a0001c0001t0001g0229 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.190+3849_190+3850i others(49): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137974065 | ||||||
| chr2:137974067 | T | A | 1 | a0001c0001t0001g0229 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.190+3850T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974067 | |||||||
| chr2:137974195 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0037 others(21): Show |
34 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.190+3978G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974195 | |||||||
| chr2:137974353 | A | G | 4 | a0001c0001t0002g0248 a0001c0001t0003g0247 a0001c0001t0021g0249 others(1): Show |
4 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+4136A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974353 | |||||||
| chr2:137974573 | G | A | 1 | a0001c0001t0005g0033 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.190+4356G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974573 | |||||||
| chr2:137974606 | A | C | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG02895.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+4389A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974606 | |||||||
| chr2:137974624 | G | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.190+4407G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974624 | |||||||
| chr2:137974711 | C | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.190+4494C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974711 | |||||||
| chr2:137974778 | G | T | 5 | a0001c0001t0002g0248 a0001c0001t0003g0247 a0001c0001t0015g0250 others(2): Show |
5 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+4561G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974778 | |||||||
| chr2:137974848 | C | A | 3 | a0001c0001t0002g0073 a0001c0001t0003g0071 a0001c0001t0003g0072 |
3 | HG02109.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.190+4631C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974848 | |||||||
| chr2:137974850 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.190+4633C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137974850 | |||||||
| chr2:137975006 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.190+4789C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137975006 | |||||||
| chr2:137975113 | A | G | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG01243.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.190+4896A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137975113 | |||||||
| chr2:137975249 | A | T | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG02895.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+5032A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137975249 | |||||||
| chr2:137975499 | A | G | 2 | a0001c0001t0001g0235 a0001c0001t0014g0236 |
2 | HG02040.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.190+5282A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137975499 | |||||||
| chr2:137975514 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.190+5297T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137975514 | |||||||
| chr2:137975930 | G | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.190+5713G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137975930 | |||||||
| chr2:137976026 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02074.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.190+5809G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976026 | |||||||
| chr2:137976084 | T | C | 2 | a0001c0001t0003g0062 a0001c0001t0003g0063 |
2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.190+5867T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976084 | |||||||
| chr2:137976272 | AC | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0036 others(39): Show |
57 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.190+6056delC | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976272 | |||||||
| chr2:137976273 | C | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(203): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.190+6056C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976273 | |||||||
| chr2:137976280 | C | A | 20 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(17): Show |
20 | HG00280.hp1 HG00558.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.190+6063C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976280 | |||||||
| chr2:137976280 | CA | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.190+6076delA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137976280 | ||||||
| chr2:137976281 | A | C | 16 | a0001c0001t0001g0023 a0001c0001t0001g0064 a0001c0001t0001g0065 others(13): Show |
17 | HG00558.hp1 HG01261.hp2 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.190+6064A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976281 | |||||||
| chr2:137976284 | A | C | 2 | a0001c0001t0003g0062 a0001c0001t0003g0063 |
2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.190+6067A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976284 | |||||||
| chr2:137976355 | T | C | 1 | a0001c0001t0002g0070 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.190+6138T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976355 | |||||||
| chr2:137976404 | A | G | 3 | a0001c0001t0006g0048 a0001c0001t0006g0049 a0001c0001t0006g0050 |
3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.190+6187A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976404 | |||||||
| chr2:137976546 | C | T | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG02895.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+6329C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137976546 | |||||||
| chr2:137977092 | T | G | 1 | a0001c0001t0002g0051 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.190+6875T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977092 | |||||||
| chr2:137977151 | T | C | 7 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(4): Show |
7 | HG02109.hp2 HG02895.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.190+6934T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977151 | |||||||
| chr2:137977239 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.190+7022A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977239 | |||||||
| chr2:137977549 | C | T | 1 | a0001c0001t0003g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.190+7332C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977549 | |||||||
| chr2:137977552 | C | T | 1 | a0001c0001t0012g0056 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.190+7335C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977552 | |||||||
| chr2:137977600 | T | C | 1 | a0001c0001t0005g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.190+7383T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977600 | |||||||
| chr2:137977668 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0179 |
3 | HG02056.hp1 HG02080.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.190+7451A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977668 | |||||||
| chr2:137977800 | C | A | 1 | a0001c0001t0003g0029 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.190+7583C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977800 | |||||||
| chr2:137977885 | T | A | 1 | a0001c0001t0001g0180 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.190+7668T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977885 | |||||||
| chr2:137977907 | T | G | 3 | a0001c0001t0002g0073 a0001c0001t0003g0071 a0001c0001t0003g0072 |
3 | HG02109.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.190+7690T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977907 | |||||||
| chr2:137977926 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.190+7709A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977926 | |||||||
| chr2:137977945 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02647.hp2 HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.190+7728C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137977945 | |||||||
| chr2:137978033 | A | T | 1 | a0001c0001t0001g0229 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.190+7816A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978033 | |||||||
| chr2:137978101 | G | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.190+7884G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978101 | |||||||
| chr2:137978172 | C | T | 1 | a0001c0001t0003g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.190+7955C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978172 | |||||||
| chr2:137978270 | G | A | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG02895.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+8053G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978270 | |||||||
| chr2:137978289 | C | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.190+8072C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978289 | |||||||
| chr2:137978300 | G | A | 9 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(6): Show |
9 | HG01167.hp1 HG01257.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.190+8083G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978300 | |||||||
| chr2:137978317 | TATA | T | 4 | a0001c0001t0002g0248 a0001c0001t0003g0247 a0001c0001t0015g0250 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+8104_190+8106d others(5): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978317 | ||||||
| chr2:137978340 | T | C | 3 | a0001c0001t0002g0073 a0001c0001t0003g0071 a0001c0001t0003g0072 |
3 | HG02109.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.190+8123T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978340 | |||||||
| chr2:137978382 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.190+8165T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978382 | |||||||
| chr2:137978428 | A | ATATACAA others(25): Show |
3 | a0001c0001t0002g0030 a0001c0001t0002g0253 a0001c0001t0003g0071 |
4 | HG02523.hp1 HG03486.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+8263_190+8294d others(34): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978428 | ||||||
| chr2:137978480 | G | T | 4 | a0001c0001t0001g0149 a0001c0001t0013g0139 a0002c0002t0002g0020 others(1): Show |
5 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+8263G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978480 | |||||||
| chr2:137978491 | AT | A | 3 | a0001c0001t0001g0149 a0002c0002t0002g0020 a0002c0002t0002g0150 |
4 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+8276delT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978491 | ||||||
| chr2:137978510 | TATATAAT others(86): Show |
T | 1 | a0001c0001t0002g0252 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.190+8356_190+8448d others(95): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978510 | ||||||
| chr2:137978512 | T | G | 4 | a0001c0001t0001g0149 a0001c0001t0013g0139 a0002c0002t0002g0020 others(1): Show |
5 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+8295T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978512 | |||||||
| chr2:137978523 | AT | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(101): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.190+8308delT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978523 | ||||||
| chr2:137978541 | T | C | 4 | a0001c0001t0001g0149 a0001c0001t0013g0139 a0002c0002t0002g0020 others(1): Show |
5 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+8324T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978541 | |||||||
| chr2:137978553 | G | A | 4 | a0001c0001t0002g0248 a0001c0001t0003g0247 a0001c0001t0015g0250 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+8336G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978553 | |||||||
| chr2:137978571 | GACT | G | 4 | a0001c0001t0001g0149 a0001c0001t0013g0139 a0002c0002t0002g0020 others(1): Show |
5 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+8356_190+8358d others(5): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978571 | ||||||
| chr2:137978576 | G | GATAATAT others(22): Show |
3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02647.hp2 HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.190+8389_190+8417d others(31): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978576 | ||||||
| chr2:137978576 | G | T | 4 | a0001c0001t0001g0149 a0001c0001t0013g0139 a0002c0002t0002g0020 others(1): Show |
5 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+8359G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978576 | |||||||
| chr2:137978605 | T | G | 1 | a0001c0001t0002g0252 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.190+8388T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978605 | |||||||
| chr2:137978605 | T | TATAATAT others(25): Show |
1 | a0001c0001t0005g0033 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.190+8400_190+8401i others(34): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978605 | ||||||
| chr2:137978605 | T | TATAATAT others(25): Show |
108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(105): Show |
143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.190+8484_190+8515d others(34): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978605 | ||||||
| chr2:137978605 | T | TATAATAT others(57): Show |
119 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(116): Show |
149 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.190+8452_190+8515d others(66): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978605 | ||||||
| chr2:137978605 | T | TATAATAT others(89): Show |
4 | a0001c0001t0001g0157 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG01981.hp2 HG03654.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+8420_190+8515d others(98): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978605 | ||||||
| chr2:137978605 | T | TATAATAT others(153): Show |
1 | a0001c0001t0001g0182 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.190+8515_190+8516i others(162): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978605 | ||||||
| chr2:137978605 | T | TTAG | 4 | a0001c0001t0001g0149 a0001c0001t0013g0139 a0002c0002t0002g0020 others(1): Show |
5 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+8388_190+8389i others(5): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978605 | |||||||
| chr2:137978637 | G | T | 1 | a0002c0002t0002g0150 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.190+8420G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978637 | |||||||
| chr2:137978638 | A | ATAATATA others(25): Show |
4 | a0001c0001t0003g0029 a0001c0001t0006g0048 a0001c0001t0006g0049 others(1): Show |
5 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.190+8452_190+8453i others(34): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978638 | ||||||
| chr2:137978701 | G | GATAATAT others(57): Show |
2 | a0001c0001t0001g0164 a0001c0001t0003g0035 |
2 | HG02922.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.190+8515_190+8516i others(66): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978701 | ||||||
| chr2:137978701 | G | GATAATAT others(25): Show |
1 | a0001c0001t0002g0051 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.190+8533_190+8564d others(34): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978701 | ||||||
| chr2:137978701 | G | GATAATAT others(57): Show |
2 | a0001c0001t0001g0052 a0003c0003t0001g0246 |
2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.190+8501_190+8564d others(66): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137978701 | ||||||
| chr2:137978701 | G | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02647.hp2 HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.190+8484G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978701 | |||||||
| chr2:137978733 | T | G | 11 | a0001c0001t0001g0082 a0001c0001t0001g0185 a0001c0001t0002g0073 others(8): Show |
11 | HG01361.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.190+8516T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978733 | |||||||
| chr2:137978765 | T | G | 1 | a0001c0001t0002g0080 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.190+8548T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978765 | |||||||
| chr2:137978789 | T | A | 1 | a0001c0001t0002g0129 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.190+8572T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978789 | |||||||
| chr2:137978895 | G | C | 5 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 others(2): Show |
5 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+8678G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978895 | |||||||
| chr2:137978899 | A | G | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG00408.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.190+8682A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978899 | |||||||
| chr2:137978946 | T | C | 1 | a0001c0001t0010g0147 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.190+8729T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978946 | |||||||
| chr2:137978959 | A | G | 1 | a0001c0001t0005g0033 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.190+8742A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978959 | |||||||
| chr2:137978998 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.190+8781A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137978998 | |||||||
| chr2:137979100 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.190+8883A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137979100 | |||||||
| chr2:137979241 | A | G | 1 | a0003c0003t0001g0246 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.190+9024A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137979241 | |||||||
| chr2:137979356 | C | T | 4 | a0001c0001t0002g0248 a0001c0001t0003g0247 a0001c0001t0015g0250 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+9139C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137979356 | |||||||
| chr2:137979364 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.190+9147G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137979364 | |||||||
| chr2:137979388 | A | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.190+9171A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137979388 | |||||||
| chr2:137979398 | G | A | 4 | a0001c0001t0002g0248 a0001c0001t0003g0247 a0001c0001t0015g0250 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+9181G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137979398 | |||||||
| chr2:137979532 | G | A | 1 | a0001c0001t0003g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.190+9315G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137979532 | |||||||
| chr2:137979602 | T | C | 2 | a0001c0001t0003g0062 a0001c0001t0003g0063 |
2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.190+9385T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137979602 | |||||||
| chr2:137979691 | C | T | 2 | a0001c0001t0010g0147 a0001c0001t0010g0148 |
2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.190+9474C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137979691 | |||||||
| chr2:137980037 | G | GT | 31 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(28): Show |
32 | HG00280.hp1 HG00609.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.190+9836dupT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137980037 | ||||||
| chr2:137980041 | T | G | 1 | a0001c0001t0005g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.190+9824T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137980041 | |||||||
| chr2:137980099 | G | T | 4 | a0001c0001t0002g0248 a0001c0001t0003g0132 a0001c0001t0003g0247 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+9882G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137980099 | |||||||
| chr2:137980258 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.190+10041C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137980258 | |||||||
| chr2:137980288 | C | T | 5 | a0001c0001t0002g0248 a0001c0001t0003g0132 a0001c0001t0003g0247 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+10071C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137980288 | |||||||
| chr2:137980348 | T | C | 1 | a0001c0001t0007g0083 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.190+10131T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137980348 | |||||||
| chr2:137980369 | AAGAGCAA others(4): Show |
A | 1 | a0001c0001t0001g0092 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.190+10155_190+1016 others(15): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137980369 | ||||||
| chr2:137980441 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0016g0090 |
2 | HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.190+10224C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137980441 | |||||||
| chr2:137980442 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.190+10225C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137980442 | |||||||
| chr2:137980497 | G | A | 12 | a0001c0001t0001g0024 a0001c0001t0001g0181 a0001c0001t0001g0186 others(9): Show |
13 | HG00099.hp2 HG00140.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.190+10280G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137980497 | |||||||
| chr2:137980533 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.190+10316T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137980533 | |||||||
| chr2:137981119 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.190+10902A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137981119 | |||||||
| chr2:137981190 | T | C | 3 | a0001c0001t0001g0192 a0001c0001t0001g0224 a0001c0001t0001g0225 |
3 | HG00408.hp2 NA18949.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.190+10973T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137981190 | |||||||
| chr2:137981427 | CCTA | C | 3 | a0001c0001t0002g0248 a0001c0001t0003g0247 a0001c0001t0021g0249 |
3 | HG02486.hp2 HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.190+11214_190+1121 others(7): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137981427 | ||||||
| chr2:137981460 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.190+11243C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137981460 | |||||||
| chr2:137981505 | G | A | 1 | a0001c0001t0016g0090 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.190+11288G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137981505 | |||||||
| chr2:137981595 | G | A | 1 | a0001c0001t0010g0148 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.190+11378G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137981595 | |||||||
| chr2:137981731 | C | T | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG02895.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+11514C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137981731 | |||||||
| chr2:137981733 | A | G | 4 | a0001c0001t0004g0017 a0001c0001t0004g0138 a0001c0001t0004g0220 others(1): Show |
5 | HG00735.hp1 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+11516A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137981733 | |||||||
| chr2:137981821 | C | T | 1 | a0001c0001t0012g0056 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.190+11604C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137981821 | |||||||
| chr2:137982118 | G | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0094 a0001c0001t0001g0137 |
3 | HG00621.hp2 HG02129.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.190+11901G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982118 | |||||||
| chr2:137982140 | C | T | 1 | a0001c0001t0003g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.190+11923C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982140 | |||||||
| chr2:137982306 | T | G | 1 | a0001c0001t0001g0180 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.190+12089T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982306 | |||||||
| chr2:137982466 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.190+12249G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982466 | |||||||
| chr2:137982487 | A | T | 2 | a0001c0001t0010g0147 a0001c0001t0010g0148 |
2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.190+12270A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982487 | |||||||
| chr2:137982510 | C | T | 10 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(7): Show |
11 | HG00735.hp1 HG02055.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.190+12293C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982510 | |||||||
| chr2:137982606 | T | G | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+12389T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982606 | |||||||
| chr2:137982769 | C | A | 1 | a0001c0001t0001g0079 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.190+12552C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982769 | |||||||
| chr2:137982941 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.190+12724A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982941 | |||||||
| chr2:137982974 | A | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
6 | HG01256.hp2 HG02258.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.190+12757A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137982974 | |||||||
| chr2:137983196 | A | C | 1 | a0001c0001t0001g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.190+12979A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983196 | |||||||
| chr2:137983340 | A | G | 1 | a0001c0001t0003g0069 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.190+13123A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983340 | |||||||
| chr2:137983378 | T | C | 1 | a0002c0002t0002g0097 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.190+13161T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983378 | |||||||
| chr2:137983383 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.190+13166G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983383 | |||||||
| chr2:137983468 | CA | C | 5 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0069 others(2): Show |
6 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.190+13260delA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137983468 | ||||||
| chr2:137983506 | C | T | 25 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(22): Show |
36 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.190+13289C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983506 | |||||||
| chr2:137983525 | C | G | 8 | a0002c0002t0002g0015 a0002c0002t0002g0020 a0002c0002t0002g0032 others(5): Show |
10 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.190+13308C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983525 | |||||||
| chr2:137983568 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.190+13351G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983568 | |||||||
| chr2:137983606 | G | C | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG02895.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+13389G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983606 | |||||||
| chr2:137983613 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.190+13396G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983613 | |||||||
| chr2:137983866 | G | C | 1 | a0001c0001t0001g0240 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.190+13649G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137983866 | |||||||
| chr2:137984030 | G | T | 4 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0069 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+13813G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137984030 | |||||||
| chr2:137984351 | A | G | 7 | a0001c0001t0002g0051 a0001c0001t0002g0073 a0001c0001t0002g0162 others(4): Show |
7 | HG02572.hp1 HG02965.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.190+14134A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137984351 | |||||||
| chr2:137984365 | G | A | 4 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0069 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+14148G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137984365 | |||||||
| chr2:137984559 | T | C | 1 | a0001c0001t0005g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.190+14342T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137984559 | |||||||
| chr2:137984586 | A | T | 6 | a0001c0001t0002g0051 a0001c0001t0002g0073 a0001c0001t0002g0162 others(3): Show |
6 | HG02572.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.190+14369A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137984586 | |||||||
| chr2:137984650 | C | T | 1 | a0001c0001t0015g0250 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.190+14433C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137984650 | |||||||
| chr2:137984651 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.190+14434G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137984651 | |||||||
| chr2:137984916 | G | C | 1 | a0001c0001t0001g0232 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.190+14699G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137984916 | |||||||
| chr2:137985080 | T | C | 1 | a0001c0001t0005g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.190+14863T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137985080 | |||||||
| chr2:137985202 | TA | T | 87 | a0001c0001t0001g0089 a0001c0001t0001g0191 a0001c0001t0001g0240 others(84): Show |
109 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.190+15000delA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137985202 | ||||||
| chr2:137985237 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(133): Show |
172 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.190+15020T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137985237 | |||||||
| chr2:137985245 | C | T | 1 | a0001c0001t0003g0029 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.190+15028C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137985245 | |||||||
| chr2:137985334 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.190+15117G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137985334 | |||||||
| chr2:137985595 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0191 |
2 | NA18939.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.191-15323C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137985595 | |||||||
| chr2:137985596 | G | A | 93 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(90): Show |
115 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.191-15322G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137985596 | |||||||
| chr2:137985657 | G | A | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-15261G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137985657 | |||||||
| chr2:137985925 | C | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-14993C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137985925 | |||||||
| chr2:137985926 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.191-14992A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137985926 | |||||||
| chr2:137986017 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.191-14901A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137986017 | |||||||
| chr2:137986042 | T | G | 1 | a0001c0001t0003g0029 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.191-14876T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137986042 | |||||||
| chr2:137986065 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.191-14853G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137986065 | |||||||
| chr2:137986253 | T | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-14665T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137986253 | |||||||
| chr2:137986302 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.191-14616A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137986302 | |||||||
| chr2:137986756 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(128): Show |
165 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.191-14162G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137986756 | |||||||
| chr2:137986964 | A | C | 1 | a0001c0001t0003g0029 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.191-13954A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137986964 | |||||||
| chr2:137987574 | G | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(78): Show |
110 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.191-13344G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137987574 | |||||||
| chr2:137987601 | CT | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0027 others(109): Show |
147 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.191-13289delT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137987601 | ||||||
| chr2:137987601 | CTT | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.191-13290_191-1328 others(6): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137987601 | ||||||
| chr2:137987601 | CTTT | C | 12 | a0001c0001t0001g0079 a0001c0001t0001g0140 a0001c0001t0001g0173 others(9): Show |
13 | HG01074.hp1 HG02074.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.191-13291_191-1328 others(7): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137987601 | ||||||
| chr2:137987691 | C | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-13227C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137987691 | |||||||
| chr2:137987826 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.191-13092C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137987826 | |||||||
| chr2:137987943 | C | T | 3 | a0001c0001t0006g0048 a0001c0001t0006g0049 a0001c0001t0006g0050 |
3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.191-12975C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137987943 | |||||||
| chr2:137988015 | T | C | 1 | a0001c0001t0012g0056 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.191-12903T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988015 | |||||||
| chr2:137988095 | C | T | 1 | a0001c0001t0003g0042 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.191-12823C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988095 | |||||||
| chr2:137988124 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.191-12794G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988124 | |||||||
| chr2:137988280 | G | T | 2 | a0001c0001t0003g0018 a0001c0001t0003g0072 |
3 | HG02109.hp2 HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.191-12638G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988280 | |||||||
| chr2:137988469 | C | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(26): Show |
40 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.191-12449C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988469 | |||||||
| chr2:137988525 | T | C | 1 | a0002c0002t0002g0256 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.191-12393T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988525 | |||||||
| chr2:137988550 | CT | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(128): Show |
165 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.191-12360delT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137988550 | ||||||
| chr2:137988745 | C | T | 4 | a0001c0001t0003g0018 a0001c0001t0003g0029 a0001c0001t0003g0071 others(1): Show |
6 | HG02109.hp2 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.191-12173C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988745 | |||||||
| chr2:137988789 | C | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-12129C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988789 | |||||||
| chr2:137988829 | T | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.191-12089T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988829 | |||||||
| chr2:137988834 | C | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-12084C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988834 | |||||||
| chr2:137988879 | A | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(129): Show |
167 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.191-12039A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137988879 | |||||||
| chr2:137989205 | C | A | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-11713C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989205 | |||||||
| chr2:137989352 | G | A | 1 | a0001c0001t0003g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.191-11566G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989352 | |||||||
| chr2:137989586 | A | G | 1 | a0002c0002t0002g0258 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.191-11332A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989586 | |||||||
| chr2:137989634 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.191-11284A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989634 | |||||||
| chr2:137989653 | C | T | 3 | a0001c0001t0002g0019 a0001c0001t0002g0145 a0001c0001t0002g0146 |
4 | HG02615.hp2 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.191-11265C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989653 | |||||||
| chr2:137989698 | G | T | 11 | a0001c0001t0001g0024 a0001c0001t0001g0181 a0001c0001t0001g0189 others(8): Show |
12 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.191-11220G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989698 | |||||||
| chr2:137989756 | T | C | 2 | a0001c0001t0010g0147 a0001c0001t0010g0148 |
2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.191-11162T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989756 | |||||||
| chr2:137989771 | G | A | 2 | a0001c0001t0006g0048 a0001c0001t0006g0050 |
2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.191-11147G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989771 | |||||||
| chr2:137989837 | G | T | 4 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0069 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.191-11081G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989837 | |||||||
| chr2:137989953 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0144 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.191-10965G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137989953 | |||||||
| chr2:137990159 | G | A | 1 | a0001c0001t0005g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.191-10759G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990159 | |||||||
| chr2:137990470 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.191-10448C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990470 | |||||||
| chr2:137990493 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.191-10425T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990493 | |||||||
| chr2:137990540 | CT | C | 5 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0179 others(2): Show |
7 | HG02056.hp1 HG02080.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.191-10377delT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990540 | |||||||
| chr2:137990559 | C | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.191-10359C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990559 | |||||||
| chr2:137990598 | T | G | 5 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0069 others(2): Show |
5 | HG02055.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.191-10320T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990598 | |||||||
| chr2:137990696 | C | G | 1 | a0001c0001t0001g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.191-10222C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990696 | |||||||
| chr2:137990732 | T | C | 73 | a0001c0001t0001g0134 a0001c0001t0002g0005 a0001c0001t0002g0006 others(70): Show |
94 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.191-10186T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990732 | |||||||
| chr2:137990755 | T | C | 1 | a0001c0001t0003g0029 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.191-10163T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990755 | |||||||
| chr2:137990793 | A | T | 1 | a0001c0001t0013g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.191-10125A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990793 | |||||||
| chr2:137990876 | A | G | 5 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0069 others(2): Show |
5 | HG02055.hp2 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.191-10042A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990876 | |||||||
| chr2:137990939 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(133): Show |
172 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.191-9979A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137990939 | |||||||
| chr2:137991108 | T | A | 1 | a0001c0001t0005g0033 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.191-9810T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991108 | |||||||
| chr2:137991176 | C | T | 3 | a0001c0001t0008g0168 a0001c0001t0008g0171 a0001c0001t0008g0196 |
3 | HG02165.hp1 HG02698.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.191-9742C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991176 | |||||||
| chr2:137991273 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.191-9645G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991273 | |||||||
| chr2:137991320 | T | C | 107 | a0001c0001t0001g0134 a0001c0001t0001g0226 a0001c0001t0002g0005 others(104): Show |
132 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.191-9598T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991320 | |||||||
| chr2:137991325 | A | G | 2 | a0001c0001t0010g0147 a0001c0001t0010g0148 |
2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.191-9593A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991325 | |||||||
| chr2:137991375 | A | G | 1 | a0001c0001t0003g0029 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.191-9543A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991375 | |||||||
| chr2:137991487 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(127): Show |
166 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.191-9431C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991487 | |||||||
| chr2:137991692 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.191-9226A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991692 | |||||||
| chr2:137991818 | C | A | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-9100C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991818 | |||||||
| chr2:137991819 | G | A | 1 | a0001c0001t0002g0128 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.191-9099G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991819 | |||||||
| chr2:137991834 | G | A | 2 | a0001c0001t0003g0068 a0001c0001t0003g0247 |
2 | HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.191-9084G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137991834 | |||||||
| chr2:137992013 | G | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0144 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.191-8905G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992013 | |||||||
| chr2:137992014 | G | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0144 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.191-8904G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992014 | |||||||
| chr2:137992015 | G | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0144 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.191-8903G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992015 | |||||||
| chr2:137992016 | G | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0144 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.191-8902G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992016 | |||||||
| chr2:137992017 | A | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0144 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.191-8901A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992017 | |||||||
| chr2:137992024 | TC | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(122): Show |
159 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.191-8887delC | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137992024 | ||||||
| chr2:137992106 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.191-8812T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992106 | |||||||
| chr2:137992176 | G | C | 1 | a0001c0001t0003g0040 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.191-8742G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992176 | |||||||
| chr2:137992770 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.191-8148G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992770 | |||||||
| chr2:137992891 | A | T | 1 | a0001c0001t0001g0226 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.191-8027A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992891 | |||||||
| chr2:137992967 | G | GA | 3 | a0001c0001t0001g0008 a0001c0001t0001g0094 a0001c0001t0001g0199 |
6 | HG01346.hp1 HG01952.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.191-7943dupA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137992967 | ||||||
| chr2:137992988 | A | G | 1 | a0001c0001t0002g0257 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.191-7930A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137992988 | |||||||
| chr2:137993008 | C | G | 1 | a0001c0001t0001g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.191-7910C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137993008 | |||||||
| chr2:137993030 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.191-7888C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137993030 | |||||||
| chr2:137993367 | G | C | 3 | a0001c0001t0001g0175 a0001c0001t0001g0194 a0001c0001t0001g0200 |
3 | HG02109.hp1 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.191-7551G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137993367 | |||||||
| chr2:137993398 | C | T | 1 | a0001c0001t0003g0029 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.191-7520C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137993398 | |||||||
| chr2:137993448 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(133): Show |
172 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.191-7470A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137993448 | |||||||
| chr2:137993618 | A | G | 1 | a0001c0001t0019g0227 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.191-7300A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137993618 | |||||||
| chr2:137993663 | G | A | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-7255G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137993663 | |||||||
| chr2:137993832 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0137 |
2 | HG00621.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.191-7086C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137993832 | |||||||
| chr2:137994090 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-6828C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137994090 | |||||||
| chr2:137994317 | A | C | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG01243.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.191-6601A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137994317 | |||||||
| chr2:137994319 | G | A | 1 | a0003c0003t0001g0246 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.191-6599G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137994319 | |||||||
| chr2:137994527 | G | GT | 3 | a0001c0001t0006g0048 a0001c0001t0006g0049 a0001c0001t0006g0050 |
3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.191-6386dupT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137994527 | ||||||
| chr2:137994756 | C | T | 1 | a0001c0001t0013g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.191-6162C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137994756 | |||||||
| chr2:137994760 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.191-6158A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137994760 | |||||||
| chr2:137994964 | C | T | 1 | a0001c0001t0003g0018 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.191-5954C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137994964 | |||||||
| chr2:137995231 | G | C | 1 | a0001c0001t0001g0186 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.191-5687G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137995231 | |||||||
| chr2:137995249 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.191-5669T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137995249 | |||||||
| chr2:137995285 | G | T | 1 | a0002c0002t0002g0218 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.191-5633G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137995285 | |||||||
| chr2:137995350 | C | G | 1 | a0001c0001t0001g0223 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.191-5568C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137995350 | |||||||
| chr2:137995440 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.191-5478C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137995440 | |||||||
| chr2:137995556 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.191-5362G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137995556 | |||||||
| chr2:137995660 | A | G | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-5258A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137995660 | |||||||
| chr2:137995753 | A | G | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-5165A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137995753 | |||||||
| chr2:137996036 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.191-4882T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137996036 | |||||||
| chr2:137996388 | C | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(27): Show |
41 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.191-4530C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137996388 | |||||||
| chr2:137996574 | A | G | 2 | a0001c0001t0008g0168 a0001c0001t0008g0171 |
2 | HG02698.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.191-4344A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137996574 | |||||||
| chr2:137996734 | G | A | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.191-4184G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137996734 | |||||||
| chr2:137996804 | G | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(29): Show |
43 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.191-4114G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137996804 | |||||||
| chr2:137997374 | A | C | 1 | a0001c0001t0002g0114 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.191-3544A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997374 | |||||||
| chr2:137997380 | C | A | 1 | a0001c0001t0001g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.191-3538C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997380 | |||||||
| chr2:137997434 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.191-3484G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997434 | |||||||
| chr2:137997484 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(133): Show |
172 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.191-3434T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997484 | |||||||
| chr2:137997633 | G | T | 3 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0069 |
3 | HG02055.hp2 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.191-3285G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997633 | |||||||
| chr2:137997689 | A | C | 2 | a0001c0001t0001g0213 a0001c0001t0001g0238 |
2 | HG01106.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.191-3229A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997689 | |||||||
| chr2:137997859 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(126): Show |
164 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.191-3059T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997859 | |||||||
| chr2:137997942 | C | G | 6 | a0001c0001t0003g0035 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.191-2976C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997942 | |||||||
| chr2:137997989 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0001g0195 a0001c0001t0001g0212 |
3 | HG01261.hp2 HG01516.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.191-2929C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997989 | |||||||
| chr2:137997990 | G | A | 4 | a0001c0001t0004g0017 a0001c0001t0004g0138 a0001c0001t0004g0220 others(1): Show |
5 | HG00735.hp1 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.191-2928G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137997990 | |||||||
| chr2:137998077 | A | G | 4 | a0001c0001t0002g0006 a0001c0001t0002g0075 a0001c0001t0002g0114 others(1): Show |
8 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.191-2841A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998077 | |||||||
| chr2:137998117 | C | T | 1 | a0001c0001t0005g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.191-2801C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998117 | |||||||
| chr2:137998164 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0202 |
2 | NA18975.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.191-2754T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998164 | |||||||
| chr2:137998204 | A | G | 1 | a0001c0001t0003g0039 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.191-2714A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998204 | |||||||
| chr2:137998206 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.191-2712G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998206 | |||||||
| chr2:137998227 | G | A | 6 | a0001c0001t0003g0035 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.191-2691G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998227 | |||||||
| chr2:137998400 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.191-2518A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998400 | |||||||
| chr2:137998422 | T | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0036 others(128): Show |
167 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.191-2496T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998422 | |||||||
| chr2:137998672 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.191-2246G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998672 | |||||||
| chr2:137998875 | A | G | 1 | a0001c0001t0002g0113 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.191-2043A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998875 | |||||||
| chr2:137998988 | C | CT | 6 | a0001c0001t0003g0035 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.191-1923dupT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137998988 | ||||||
| chr2:137998996 | C | A | 6 | a0001c0001t0003g0035 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.191-1922C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137998996 | |||||||
| chr2:137999003 | G | A | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-1915G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137999003 | |||||||
| chr2:137999075 | T | C | 3 | a0001c0001t0006g0048 a0001c0001t0006g0049 a0001c0001t0006g0050 |
3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.191-1843T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137999075 | |||||||
| chr2:137999274 | T | C | 3 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0069 |
3 | HG02055.hp2 HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.191-1644T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137999274 | |||||||
| chr2:137999361 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.191-1557A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137999361 | |||||||
| chr2:137999430 | C | T | 1 | a0001c0001t0002g0219 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.191-1488C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137999430 | |||||||
| chr2:137999475 | A | G | 1 | a0001c0001t0002g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.191-1443A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137999475 | |||||||
| chr2:137999506 | G | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-1412G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 137999506 | |||||||
| chr2:137999918 | TA | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.191-988delA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 137999918 | ||||||
| chr2:138000021 | T | C | 6 | a0001c0001t0002g0051 a0001c0001t0002g0073 a0001c0001t0002g0162 others(3): Show |
6 | HG02572.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.191-897T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000021 | |||||||
| chr2:138000095 | C | G | 6 | a0001c0001t0003g0035 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.191-823C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000095 | |||||||
| chr2:138000148 | T | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-770T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000148 | |||||||
| chr2:138000169 | G | A | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-749G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000169 | |||||||
| chr2:138000184 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.191-734G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000184 | |||||||
| chr2:138000277 | C | A | 1 | a0002c0002t0002g0104 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.191-641C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000277 | |||||||
| chr2:138000280 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.191-638C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000280 | |||||||
| chr2:138000320 | C | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-598C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000320 | |||||||
| chr2:138000374 | G | GT | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-544_191-543ins others(1): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000374 | |||||||
| chr2:138000375 | A | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-543A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000375 | |||||||
| chr2:138000441 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0094 a0001c0001t0001g0199 others(3): Show |
9 | HG00741.hp1 HG01255.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.191-477T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000441 | |||||||
| chr2:138000455 | A | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-463A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000455 | |||||||
| chr2:138000467 | A | AT | 107 | a0001c0001t0001g0134 a0001c0001t0001g0169 a0001c0001t0001g0226 others(104): Show |
132 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.191-444dupT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 138000467 | ||||||
| chr2:138000528 | T | C | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG02895.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.191-390T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000528 | |||||||
| chr2:138000567 | TA | T | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.191-346delA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 138000567 | ||||||
| chr2:138000568 | A | T | 1 | a0001c0001t0002g0051 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.191-350A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000568 | |||||||
| chr2:138000583 | T | A | 107 | a0001c0001t0001g0134 a0001c0001t0001g0169 a0001c0001t0001g0226 others(104): Show |
132 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.191-335T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000583 | |||||||
| chr2:138000630 | T | A | 1 | a0001c0001t0004g0138 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.191-288T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000630 | |||||||
| chr2:138000698 | G | A | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-220G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000698 | |||||||
| chr2:138000757 | A | C | 1 | a0001c0001t0021g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.191-161A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000757 | |||||||
| chr2:138000789 | G | T | 1 | a0001c0001t0001g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.191-129G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 2/5 | chr2 | 138000789 | |||||||
| chr2:138001162 | C | A | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+137C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001162 | |||||||
| chr2:138001257 | G | A | 1 | a0001c0001t0005g0033 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.298+232G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001257 | |||||||
| chr2:138001275 | A | C | 3 | a0001c0001t0003g0029 a0001c0001t0010g0147 a0001c0001t0010g0148 |
4 | HG02280.hp2 HG03209.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+250A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001275 | |||||||
| chr2:138001385 | A | G | 2 | a0001c0001t0010g0147 a0001c0001t0010g0148 |
2 | HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.298+360A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001385 | |||||||
| chr2:138001445 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.298+420G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001445 | |||||||
| chr2:138001624 | A | G | 4 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0069 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-440A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001624 | |||||||
| chr2:138001693 | T | C | 3 | a0001c0001t0003g0029 a0001c0001t0010g0147 a0001c0001t0010g0148 |
4 | HG02280.hp2 HG03209.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-371T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001693 | |||||||
| chr2:138001751 | T | TATC | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-312_299-310dup others(3): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 138001751 | ||||||
| chr2:138001851 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.299-213T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001851 | |||||||
| chr2:138001900 | C | A | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-164C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001900 | |||||||
| chr2:138001921 | C | T | 1 | a0001c0001t0013g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.299-143C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001921 | |||||||
| chr2:138001951 | C | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-113C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 3/5 | chr2 | 138001951 | |||||||
| chr2:138002242 | AAT | A | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+58_429+59delTA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 138002242 | ||||||
| chr2:138002243 | A | G | 10 | a0001c0001t0002g0096 a0001c0001t0002g0105 a0001c0001t0002g0110 others(7): Show |
10 | HG00438.hp1 HG00735.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+49A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138002243 | |||||||
| chr2:138002499 | G | T | 2 | a0001c0001t0002g0007 a0001c0001t0002g0113 |
5 | HG01943.hp2 HG02273.hp2 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+305G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138002499 | |||||||
| chr2:138002535 | A | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+341A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138002535 | |||||||
| chr2:138002536 | A | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+342A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138002536 | |||||||
| chr2:138002674 | T | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+480T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138002674 | |||||||
| chr2:138002796 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.429+602A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138002796 | |||||||
| chr2:138002855 | G | T | 1 | a0001c0001t0002g0014 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.429+661G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138002855 | |||||||
| chr2:138002939 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.429+745C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138002939 | |||||||
| chr2:138002980 | A | G | 4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
4 | HG02723.hp1 HG02818.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+786A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138002980 | |||||||
| chr2:138003044 | T | C | 1 | a0002c0002t0002g0258 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.429+850T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003044 | |||||||
| chr2:138003077 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.429+883T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003077 | |||||||
| chr2:138003084 | TGG | T | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
99 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.429+893_429+894del others(2): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 138003084 | ||||||
| chr2:138003087 | G | T | 1 | a0001c0001t0002g0075 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.429+893G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003087 | |||||||
| chr2:138003096 | A | AG | 7 | a0001c0001t0001g0149 a0001c0001t0002g0051 a0001c0001t0002g0073 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+908dupG | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 138003096 | ||||||
| chr2:138003113 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.429+919T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003113 | |||||||
| chr2:138003114 | C | T | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.429+920C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003114 | |||||||
| chr2:138003147 | G | A | 3 | a0001c0001t0003g0029 a0001c0001t0010g0147 a0001c0001t0010g0148 |
4 | HG02280.hp2 HG03209.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+953G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003147 | |||||||
| chr2:138003158 | G | A | 3 | a0001c0001t0006g0048 a0001c0001t0006g0049 a0001c0001t0006g0050 |
3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.429+964G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003158 | |||||||
| chr2:138003199 | C | T | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
99 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.429+1005C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003199 | |||||||
| chr2:138003240 | T | TA | 19 | a0001c0001t0001g0226 a0001c0001t0002g0051 a0001c0001t0002g0073 others(16): Show |
20 | HG00609.hp2 HG02109.hp2 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.429+1048dupA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 138003240 | ||||||
| chr2:138003243 | T | A | 19 | a0001c0001t0001g0226 a0001c0001t0002g0051 a0001c0001t0002g0073 others(16): Show |
20 | HG00609.hp2 HG02109.hp2 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.429+1049T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003243 | |||||||
| chr2:138003243 | T | TA | 3 | a0001c0001t0003g0029 a0001c0001t0010g0147 a0001c0001t0010g0148 |
4 | HG02280.hp2 HG03209.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+1051dupA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 138003243 | ||||||
| chr2:138003246 | T | A | 109 | a0001c0001t0001g0226 a0001c0001t0002g0005 a0001c0001t0002g0006 others(106): Show |
133 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.429+1052T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003246 | |||||||
| chr2:138003275 | T | C | 2 | a0001c0001t0005g0033 a0001c0001t0005g0034 |
3 | HG02258.hp2 HG02486.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.429+1081T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003275 | |||||||
| chr2:138003433 | A | G | 103 | a0001c0001t0001g0169 a0001c0001t0001g0226 a0001c0001t0002g0005 others(100): Show |
127 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.429+1239A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003433 | |||||||
| chr2:138003483 | A | G | 2 | a0001c0001t0003g0132 a0001c0001t0013g0139 |
2 | HG02257.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.429+1289A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003483 | |||||||
| chr2:138003525 | C | A | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG01243.hp2 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+1331C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003525 | |||||||
| chr2:138003571 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.429+1377A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003571 | |||||||
| chr2:138003597 | T | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(140): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.429+1403T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003597 | |||||||
| chr2:138003653 | A | G | 6 | a0001c0001t0003g0035 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+1459A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003653 | |||||||
| chr2:138003679 | C | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0172 others(2): Show |
7 | HG02056.hp1 HG02080.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.430-1453C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003679 | |||||||
| chr2:138003689 | C | A | 4 | a0001c0001t0004g0017 a0001c0001t0004g0138 a0001c0001t0004g0220 others(1): Show |
5 | HG00735.hp1 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-1443C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003689 | |||||||
| chr2:138003729 | G | A | 21 | a0001c0001t0003g0029 a0001c0001t0003g0035 a0001c0001t0003g0038 others(18): Show |
23 | HG00735.hp1 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.430-1403G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003729 | |||||||
| chr2:138003770 | C | G | 3 | a0001c0001t0006g0048 a0001c0001t0006g0049 a0001c0001t0006g0050 |
3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.430-1362C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003770 | |||||||
| chr2:138003995 | C | T | 99 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(96): Show |
122 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.430-1137C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138003995 | |||||||
| chr2:138004107 | T | G | 1 | a0001c0001t0001g0085 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.430-1025T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004107 | |||||||
| chr2:138004134 | T | TA | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.430-997dupA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 138004134 | ||||||
| chr2:138004180 | G | C | 1 | a0001c0001t0003g0039 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.430-952G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004180 | |||||||
| chr2:138004365 | GGACAGGC others(13): Show |
G | 1 | a0001c0001t0001g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.430-764_430-745del others(20): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 138004365 | ||||||
| chr2:138004442 | G | A | 1 | a0001c0001t0003g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.430-690G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004442 | |||||||
| chr2:138004486 | C | A | 112 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(109): Show |
138 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.430-646C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004486 | |||||||
| chr2:138004486 | C | G | 2 | a0001c0001t0003g0062 a0001c0001t0003g0063 |
2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.430-646C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004486 | |||||||
| chr2:138004567 | A | T | 1 | a0001c0001t0001g0169 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.430-565A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004567 | |||||||
| chr2:138004598 | C | A | 84 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(81): Show |
105 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.430-534C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004598 | |||||||
| chr2:138004812 | C | T | 1 | a0001c0001t0002g0013 | 2 | NA18961.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.430-320C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004812 | |||||||
| chr2:138004875 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.430-257A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004875 | |||||||
| chr2:138004990 | C | T | 6 | a0001c0001t0003g0035 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-142C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 4/5 | chr2 | 138004990 | |||||||
| chr2:138005273 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.523+48G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005273 | |||||||
| chr2:138005281 | G | A | 22 | a0001c0001t0003g0018 a0001c0001t0003g0062 a0001c0001t0003g0063 others(19): Show |
25 | HG00735.hp1 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.523+56G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005281 | |||||||
| chr2:138005303 | C | CTT | 78 | a0001c0001t0001g0134 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
100 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.523+79_523+80dupTT | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138005303 | ||||||
| chr2:138005460 | T | C | 92 | a0001c0001t0001g0134 a0001c0001t0002g0005 a0001c0001t0002g0006 others(89): Show |
114 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.523+235T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005460 | |||||||
| chr2:138005571 | G | T | 5 | a0001c0001t0002g0051 a0001c0001t0002g0073 a0001c0001t0002g0162 others(2): Show |
5 | HG02572.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.523+346G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005571 | |||||||
| chr2:138005597 | T | G | 3 | a0001c0001t0001g0205 a0001c0001t0001g0228 a0001c0001t0001g0237 |
3 | HG03710.hp1 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.523+372T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005597 | |||||||
| chr2:138005717 | C | A | 91 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(88): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+492C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005717 | |||||||
| chr2:138005760 | A | G | 22 | a0001c0001t0003g0018 a0001c0001t0003g0062 a0001c0001t0003g0063 others(19): Show |
25 | HG00735.hp1 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.523+535A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005760 | |||||||
| chr2:138005850 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.523+625G>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005850 | |||||||
| chr2:138005927 | GAT | G | 91 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(88): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+704_523+705del others(2): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138005927 | ||||||
| chr2:138005943 | T | A | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+718T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005943 | |||||||
| chr2:138005976 | T | G | 91 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(88): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+751T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005976 | |||||||
| chr2:138005983 | G | A | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.523+758G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138005983 | |||||||
| chr2:138006040 | C | T | 1 | a0001c0001t0003g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.523+815C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006040 | |||||||
| chr2:138006116 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0170 |
2 | HG02071.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.523+891C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006116 | |||||||
| chr2:138006191 | C | G | 6 | a0001c0001t0003g0035 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.523+966C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006191 | |||||||
| chr2:138006245 | C | T | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
99 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.523+1020C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006245 | |||||||
| chr2:138006328 | T | G | 91 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(88): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+1103T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006328 | |||||||
| chr2:138006364 | G | A | 91 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(88): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+1139G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006364 | |||||||
| chr2:138006430 | G | A | 3 | a0001c0001t0006g0048 a0001c0001t0006g0049 a0001c0001t0006g0050 |
3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.523+1205G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006430 | |||||||
| chr2:138006575 | C | G | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.523+1350C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006575 | |||||||
| chr2:138006692 | A | G | 1 | a0001c0001t0005g0033 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.523+1467A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006692 | |||||||
| chr2:138006744 | A | G | 91 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(88): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+1519A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006744 | |||||||
| chr2:138006759 | T | A | 3 | a0001c0001t0008g0168 a0001c0001t0008g0171 a0001c0001t0008g0196 |
3 | HG02165.hp1 HG02698.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.523+1534T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006759 | |||||||
| chr2:138006808 | C | T | 12 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0068 others(9): Show |
13 | HG00735.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.523+1583C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006808 | |||||||
| chr2:138006830 | T | C | 4 | a0002c0002t0002g0031 a0002c0002t0002g0251 a0002c0002t0002g0255 others(1): Show |
5 | HG01346.hp2 HG01928.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+1605T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006830 | |||||||
| chr2:138006839 | C | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0194 a0001c0001t0001g0200 |
3 | HG02109.hp1 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.523+1614C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006839 | |||||||
| chr2:138006871 | TA | T | 91 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(88): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+1654delA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138006871 | ||||||
| chr2:138006891 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.523+1666G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006891 | |||||||
| chr2:138006901 | C | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0210 a0001c0001t0001g0223 |
8 | NA18941.hp1 NA18949.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.523+1676C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138006901 | |||||||
| chr2:138007205 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.523+1980G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007205 | |||||||
| chr2:138007235 | A | G | 1 | a0001c0001t0017g0209 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.523+2010A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007235 | |||||||
| chr2:138007250 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0172 a0001c0001t0001g0211 |
4 | NA18989.hp1 NA19001.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.523+2025C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007250 | |||||||
| chr2:138007340 | A | T | 2 | a0001c0001t0001g0228 a0001c0001t0001g0237 |
2 | HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.523+2115A>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007340 | |||||||
| chr2:138007349 | T | A | 114 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(111): Show |
140 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.523+2124T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007349 | |||||||
| chr2:138007481 | A | G | 114 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(111): Show |
140 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.523+2256A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007481 | |||||||
| chr2:138007491 | C | T | 2 | a0001c0001t0003g0062 a0001c0001t0003g0063 |
2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.523+2266C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007491 | |||||||
| chr2:138007513 | G | C | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.523+2288G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007513 | |||||||
| chr2:138007516 | C | T | 8 | a0001c0001t0002g0096 a0001c0001t0002g0110 a0001c0001t0002g0111 others(5): Show |
8 | HG00438.hp1 HG02071.hp2 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.523+2291C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007516 | |||||||
| chr2:138007637 | A | G | 2 | a0001c0001t0005g0033 a0001c0001t0005g0034 |
3 | HG02258.hp2 HG02486.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.523+2412A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007637 | |||||||
| chr2:138007698 | G | A | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+2473G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007698 | |||||||
| chr2:138007875 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.523+2650G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138007875 | |||||||
| chr2:138008092 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.523+2867T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008092 | |||||||
| chr2:138008173 | C | T | 91 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(88): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+2948C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008173 | |||||||
| chr2:138008190 | T | C | 6 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
6 | HG02145.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.523+2965T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008190 | |||||||
| chr2:138008225 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.523+3000T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008225 | |||||||
| chr2:138008301 | C | T | 5 | a0001c0001t0002g0051 a0001c0001t0002g0073 a0001c0001t0002g0162 others(2): Show |
5 | HG02572.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.523+3076C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008301 | |||||||
| chr2:138008360 | G | A | 1 | a0001c0001t0002g0096 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.523+3135G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008360 | |||||||
| chr2:138008364 | C | T | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.523+3139C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008364 | |||||||
| chr2:138008414 | T | C | 6 | a0001c0001t0003g0035 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.523+3189T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008414 | |||||||
| chr2:138008439 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.523+3214G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008439 | |||||||
| chr2:138008523 | C | T | 91 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(88): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+3298C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008523 | |||||||
| chr2:138008534 | G | A | 6 | a0001c0001t0003g0035 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.523+3309G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008534 | |||||||
| chr2:138008607 | C | T | 6 | a0001c0001t0004g0017 a0001c0001t0004g0138 a0001c0001t0004g0220 others(3): Show |
7 | HG00735.hp1 HG02809.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.523+3382C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008607 | |||||||
| chr2:138008625 | A | G | 1 | a0001c0001t0003g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.523+3400A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008625 | |||||||
| chr2:138008630 | C | T | 6 | a0001c0001t0003g0035 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.523+3405C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008630 | |||||||
| chr2:138008693 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.523+3468T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008693 | |||||||
| chr2:138008708 | T | C | 1 | a0001c0001t0003g0029 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.523+3483T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008708 | |||||||
| chr2:138008712 | T | G | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.523+3487T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008712 | |||||||
| chr2:138008906 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.523+3681G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138008906 | |||||||
| chr2:138009137 | A | G | 3 | a0001c0001t0006g0048 a0001c0001t0006g0049 a0001c0001t0006g0050 |
3 | HG02055.hp1 HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.523+3912A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009137 | |||||||
| chr2:138009270 | G | C | 22 | a0001c0001t0003g0018 a0001c0001t0003g0062 a0001c0001t0003g0063 others(19): Show |
25 | HG00735.hp1 HG02055.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.523+4045G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009270 | |||||||
| chr2:138009387 | C | T | 91 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(88): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.523+4162C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009387 | |||||||
| chr2:138009430 | C | A | 2 | a0001c0001t0005g0033 a0001c0001t0005g0034 |
3 | HG02258.hp2 HG02486.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.523+4205C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009430 | |||||||
| chr2:138009515 | A | G | 1 | a0001c0001t0005g0033 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.524-4260A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009515 | |||||||
| chr2:138009685 | T | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG00408.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.524-4090T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009685 | |||||||
| chr2:138009729 | C | G | 80 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(77): Show |
102 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.524-4046C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009729 | |||||||
| chr2:138009742 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.524-4033T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009742 | |||||||
| chr2:138009931 | T | C | 1 | a0001c0001t0003g0069 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.524-3844T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009931 | |||||||
| chr2:138009957 | T | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.524-3818T>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138009957 | |||||||
| chr2:138010016 | A | G | 1 | a0001c0001t0019g0227 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.524-3759A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010016 | |||||||
| chr2:138010181 | T | C | 1 | a0001c0001t0002g0051 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.524-3594T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010181 | |||||||
| chr2:138010240 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.524-3535T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010240 | |||||||
| chr2:138010318 | C | CA | 91 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(88): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.524-3450dupA | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010318 | ||||||
| chr2:138010434 | G | GAC | 4 | a0001c0001t0002g0070 a0001c0001t0019g0227 a0002c0002t0002g0117 others(1): Show |
4 | HG01361.hp2 HG01516.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-3336_524-3335d others(4): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010434 | ||||||
| chr2:138010434 | G | GACAC | 2 | a0001c0001t0002g0006 a0001c0001t0002g0114 |
6 | HG00408.hp1 HG00597.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.524-3338_524-3335d others(6): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010434 | ||||||
| chr2:138010434 | G | GACACACA others(3): Show |
2 | a0001c0001t0002g0106 a0001c0001t0002g0131 |
2 | NA18968.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.524-3335_524-3334i others(12): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010434 | ||||||
| chr2:138010434 | GACACACG others(5): Show |
G | 1 | a0001c0001t0002g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.524-3334_524-3323d others(14): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010434 | ||||||
| chr2:138010435 | A | ACACACAC others(1): Show |
8 | a0001c0001t0002g0014 a0001c0001t0002g0107 a0001c0001t0002g0110 others(5): Show |
9 | HG00438.hp1 HG02071.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.524-3335_524-3334i others(10): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010435 | ||||||
| chr2:138010437 | A | ACACACG | 17 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0013 others(14): Show |
24 | HG00423.hp2 HG00639.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.524-3335_524-3334i others(8): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010437 | ||||||
| chr2:138010437 | ACACG | A | 5 | a0001c0001t0002g0051 a0001c0001t0002g0073 a0001c0001t0002g0162 others(2): Show |
5 | HG02572.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.524-3334_524-3331d others(6): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010437 | ||||||
| chr2:138010439 | A | ACACG | 34 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0012 others(31): Show |
43 | HG00280.hp1 HG00558.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.524-3335_524-3334i others(6): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010439 | ||||||
| chr2:138010439 | ACG | A | 5 | a0001c0001t0002g0074 a0001c0001t0002g0115 a0001c0001t0008g0168 others(2): Show |
5 | HG01261.hp1 HG02165.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.524-3334_524-3333d others(4): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010439 | ||||||
| chr2:138010441 | G | A | 70 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(67): Show |
92 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.524-3334G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010441 | |||||||
| chr2:138010441 | G | GCA | 30 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0026 others(27): Show |
34 | HG00140.hp1 HG00738.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.524-3293_524-3292d others(4): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | ||||||
| chr2:138010441 | G | GCACA | 11 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0065 others(8): Show |
11 | HG02895.hp1 HG02965.hp2 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.524-3295_524-3292d others(6): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | ||||||
| chr2:138010441 | G | GCACACA | 7 | a0001c0001t0001g0028 a0001c0001t0001g0179 a0001c0001t0001g0200 others(4): Show |
8 | HG02056.hp1 HG02080.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.524-3297_524-3292d others(8): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | ||||||
| chr2:138010441 | GCA | G | 5 | a0001c0001t0001g0046 a0001c0001t0001g0055 a0001c0001t0001g0156 others(2): Show |
6 | HG01243.hp2 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.524-3293_524-3292d others(4): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | ||||||
| chr2:138010441 | GCACA | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0061 a0001c0001t0003g0042 |
3 | HG02647.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.524-3295_524-3292d others(6): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | ||||||
| chr2:138010441 | GCACACA | G | 8 | a0001c0001t0003g0018 a0001c0001t0003g0035 a0001c0001t0003g0038 others(5): Show |
9 | HG02109.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.524-3297_524-3292d others(8): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | ||||||
| chr2:138010441 | GCACACAC others(1): Show |
G | 4 | a0001c0001t0003g0029 a0001c0001t0003g0068 a0001c0001t0003g0071 others(1): Show |
5 | HG02280.hp2 HG02486.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.524-3299_524-3292d others(10): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | ||||||
| chr2:138010441 | GCACACAC others(3): Show |
G | 6 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0069 others(3): Show |
6 | HG00735.hp1 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.524-3301_524-3292d others(12): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | ||||||
| chr2:138010441 | GCACACAC others(5): Show |
G | 3 | a0001c0001t0004g0017 a0001c0001t0004g0138 a0001c0001t0004g0220 |
4 | HG02809.hp1 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-3303_524-3292d others(14): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | ||||||
| chr2:138010441 | GCACACAC others(7): Show |
G | 1 | a0001c0001t0010g0147 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.524-3305_524-3292d others(16): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 138010441 | ||||||
| chr2:138010443 | A | G | 5 | a0001c0001t0002g0019 a0001c0001t0002g0145 a0001c0001t0002g0146 others(2): Show |
6 | HG02300.hp1 HG02615.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.524-3332A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010443 | |||||||
| chr2:138010445 | A | G | 5 | a0001c0001t0002g0074 a0001c0001t0002g0115 a0001c0001t0008g0168 others(2): Show |
5 | HG01261.hp1 HG02165.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.524-3330A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010445 | |||||||
| chr2:138010447 | A | G | 6 | a0001c0001t0002g0051 a0001c0001t0002g0073 a0001c0001t0002g0162 others(3): Show |
6 | HG02572.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.524-3328A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010447 | |||||||
| chr2:138010449 | A | G | 6 | a0001c0001t0003g0035 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.524-3326A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010449 | |||||||
| chr2:138010451 | A | G | 5 | a0001c0001t0003g0035 a0001c0001t0003g0038 a0001c0001t0003g0039 others(2): Show |
5 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.524-3324A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010451 | |||||||
| chr2:138010455 | A | G | 1 | a0001c0001t0002g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.524-3320A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010455 | |||||||
| chr2:138010474 | CACACACA others(3): Show |
C | 1 | a0001c0001t0001g0022 | 2 | NA18979.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.524-3300_524-3291d others(12): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010474 | |||||||
| chr2:138010478 | CACACAG | C | 4 | a0001c0001t0001g0153 a0001c0001t0001g0228 a0001c0001t0007g0083 others(1): Show |
4 | HG02258.hp1 HG03710.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-3296_524-3291d others(8): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010478 | |||||||
| chr2:138010480 | CACAG | C | 11 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0024 others(8): Show |
12 | HG00639.hp2 HG01168.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.524-3294_524-3291d others(6): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010480 | |||||||
| chr2:138010482 | CAG | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
55 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.524-3292_524-3291d others(4): Show |
HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010482 | |||||||
| chr2:138010484 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0234 |
2 | HG03225.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.524-3291G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010484 | |||||||
| chr2:138010484 | G | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(73): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.524-3291G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010484 | |||||||
| chr2:138010529 | A | C | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-3246A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010529 | |||||||
| chr2:138010766 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.524-3009G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010766 | |||||||
| chr2:138010768 | T | C | 1 | a0001c0001t0002g0010 | 3 | HG02630.hp2 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.524-3007T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010768 | |||||||
| chr2:138010925 | A | C | 6 | a0001c0001t0003g0035 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.524-2850A>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138010925 | |||||||
| chr2:138011035 | C | T | 114 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(111): Show |
140 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.524-2740C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138011035 | |||||||
| chr2:138011348 | C | A | 1 | a0001c0001t0003g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.524-2427C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138011348 | |||||||
| chr2:138011422 | G | C | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-2353G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138011422 | |||||||
| chr2:138011530 | T | A | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-2245T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138011530 | |||||||
| chr2:138011566 | A | G | 6 | a0001c0001t0003g0035 a0001c0001t0003g0038 a0001c0001t0003g0039 others(3): Show |
6 | HG02451.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.524-2209A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138011566 | |||||||
| chr2:138011949 | G | A | 13 | a0001c0001t0003g0062 a0001c0001t0003g0063 a0001c0001t0003g0068 others(10): Show |
14 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.524-1826G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138011949 | |||||||
| chr2:138011953 | T | C | 3 | a0001c0001t0002g0070 a0001c0001t0002g0080 a0001c0001t0002g0143 |
3 | HG00639.hp1 HG00741.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.524-1822T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138011953 | |||||||
| chr2:138012055 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.524-1720A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012055 | |||||||
| chr2:138012099 | C | T | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-1676C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012099 | |||||||
| chr2:138012293 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.524-1482G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012293 | |||||||
| chr2:138012337 | G | C | 1 | a0001c0001t0015g0250 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.524-1438G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012337 | |||||||
| chr2:138012381 | T | C | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-1394T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012381 | |||||||
| chr2:138012397 | G | A | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-1378G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012397 | |||||||
| chr2:138012575 | T | C | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-1200T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012575 | |||||||
| chr2:138012579 | G | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0071 a0001c0001t0003g0072 |
4 | HG02109.hp2 HG02280.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.524-1196G>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012579 | |||||||
| chr2:138012695 | C | A | 46 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(43): Show |
61 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.524-1080C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012695 | |||||||
| chr2:138012741 | G | A | 1 | a0001c0001t0003g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.524-1034G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012741 | |||||||
| chr2:138012755 | T | C | 1 | a0001c0001t0003g0029 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.524-1020T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012755 | |||||||
| chr2:138012791 | A | G | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-984A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012791 | |||||||
| chr2:138012792 | T | A | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-983T>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012792 | |||||||
| chr2:138012793 | C | A | 1 | a0001c0001t0002g0051 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.524-982C>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012793 | |||||||
| chr2:138012812 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.524-963C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012812 | |||||||
| chr2:138012935 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.524-840G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138012935 | |||||||
| chr2:138013285 | C | T | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-490C>T | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138013285 | |||||||
| chr2:138013481 | C | G | 1 | a0001c0001t0005g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.524-294C>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138013481 | |||||||
| chr2:138013482 | A | G | 97 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(94): Show |
120 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.524-293A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138013482 | |||||||
| chr2:138013600 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.524-175A>G | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138013600 | |||||||
| chr2:138013649 | G | A | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.524-126G>A | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138013649 | |||||||
| chr2:138013753 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0202 |
2 | NA18975.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.524-22T>C | HNMT | ENSG00000150540.14 | transcript | ENST00000280097.5 | protein_coding | 5/5 | chr2 | 138013753 |