Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10988 |
| ensemblid | ENSG00000111142.14 |
| hgncid | 16672 |
| symbol | METAP2 |
| name | methionyl aminopeptidase 2 |
| refseq_nuc | NM_006838.4 |
| refseq_prot | NP_006829.1 |
| ensembl_nuc | ENST00000323666.10 |
| ensembl_prot | ENSP00000325312.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 95474152 |
| end | 95515839 |
| strand | + |
| ver | v1.2 |
| region | chr12:95474152-95515839 |
| region5000 | chr12:95469152-95520839 |
| regionname0 | METAP2_chr12_95474152_95515839 |
| regionname5000 | METAP2_chr12_95469152_95520839 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 478 | 380 | 86 | 74 | 160 | 16 | 42 | 126 | METAP2_chr12_95469152_95520839 | METAP2 | MAGVE others(473): Show |
chr12 | 95469152 | 95520839 |
| a0002 | 0/0 | 478 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | MAGVE others(473): Show |
chr12 | 95469152 | 95520839 |
| a0003 | 0/0 | 478 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | MAGGE others(473): Show |
chr12 | 95469152 | 95520839 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1434 | 321 | 82 | 65 | 127 | 9 | 37 | METAP2_chr12_95469152_95520839 | METAP2 | ATGGC others(1429): Show |
chr12 | 95469152 | 95520839 | ||
| a0001c0002 | 0/0 | 1434 | 47 | 3 | 7 | 29 | 4 | 4 | METAP2_chr12_95469152_95520839 | METAP2 | ATGGC others(1429): Show |
chr12 | 95469152 | 95520839 | ||
| a0001c0003 | 0/1 | 1434 | 11 | 0 | 2 | 4 | 3 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | ATGGC others(1429): Show |
chr12 | 95469152 | 95520839 | ||
| a0001c0006 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | ATGGC others(1429): Show |
chr12 | 95469152 | 95520839 | ||
| a0002c0005 | 0/0 | 1434 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | ATGGC others(1429): Show |
chr12 | 95469152 | 95520839 | ||
| a0003c0004 | 0/0 | 1434 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | ATGGC others(1429): Show |
chr12 | 95469152 | 95520839 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3400 | 232 | 44 | 58 | 100 | 6 | 23 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0001c0001t0002 | 0/0 | 3400 | 26 | 18 | 1 | 0 | 2 | 5 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0001c0001t0003 | 0/0 | 3401 | 24 | 1 | 5 | 13 | 0 | 5 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3396): Show |
chr12 | 95469152 | 95520839 |
| a0001c0001t0004 | 0/0 | 3400 | 12 | 11 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0001c0001t0005 | 0/0 | 3400 | 6 | 0 | 0 | 6 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0001c0001t0006 | 0/0 | 3400 | 4 | 4 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0001c0001t0007 | 0/0 | 3400 | 4 | 0 | 0 | 0 | 1 | 3 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0001c0001t0008 | 0/0 | 3401 | 3 | 0 | 0 | 3 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3396): Show |
chr12 | 95469152 | 95520839 |
| a0001c0001t0009 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0001c0001t0010 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0001c0001t0011 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0001c0001t0012 | 0/0 | 3400 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0001c0001t0013 | 0/0 | 3368 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3363): Show |
chr12 | 95469152 | 95520839 |
| a0001c0001t0014 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0001c0001t0015 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0001c0001t0016 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0001c0001t0017 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0001c0001t0018 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0001c0002t0001 | 0/0 | 3400 | 47 | 3 | 7 | 29 | 4 | 4 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0001c0003t0001 | 0/1 | 3400 | 11 | 0 | 2 | 4 | 3 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0001c0006t0001 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0002c0005t0001 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| a0003c0004t0001 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | CTCAT others(3395): Show |
chr12 | 95469152 | 95520839 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0123 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0007g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0007g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0007g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0008g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0008g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0008g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0009g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0010g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0011g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0012g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0013g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0014g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0015g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0016g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0017g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0001t0018g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0002 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0003t0001g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0001c0006t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0002c0005t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| a0003c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | GBR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0331 | EUR | GBR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00140 | hp1 | a0001 | c0001 | t0007 | g0255 | EUR | GBR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | GBR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0188 | EUR | FIN | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | CHS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00597 | hp2 | a0001 | c0001 | t0005 | g0275 | EAS | CHS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0177 | EAS | CHS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | CHS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0062 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0204 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0066 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0202 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0179 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0068 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0324 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0012 | EUR | IBS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0251 | EUR | IBS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0074 | EUR | IBS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0067 | EUR | IBS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0012 | EUR | IBS | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | KHV | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02055 | hp1 | a0001 | c0006 | t0001 | g0342 | AFR | ACB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | KHV | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0071 | EAS | KHV | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0261 | EAS | KHV | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | KHV | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02083 | hp2 | a0001 | c0003 | t0001 | g0073 | EAS | KHV | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CDX | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02165 | hp2 | a0001 | c0003 | t0001 | g0072 | EAS | CDX | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0327 | AFR | ACB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | ACB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | ACB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02280 | hp1 | a0001 | c0001 | t0018 | g0341 | AFR | ACB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | ACB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | KHV | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0322 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02647 | hp1 | a0001 | c0001 | t0015 | g0344 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0339 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0075 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02723 | hp1 | a0001 | c0001 | t0013 | g0343 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0328 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02735 | hp2 | a0001 | c0001 | t0007 | g0254 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0320 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0318 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0321 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0317 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | ESN | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | ESN | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0325 | AFR | ESN | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | MSL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | ESN | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | ESN | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | ESN | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | ESN | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0353 | AFR | MSL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | MSL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | MSL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0256 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0164 | AFR | MSL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0329 | AFR | MSL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0332 | AFR | ESN | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0059 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0337 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0200 | SAS | BEB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03831 | hp2 | a0001 | c0001 | t0007 | g0300 | SAS | BEB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0335 | SAS | BEB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0047 | SAS | BEB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03942 | hp1 | a0001 | c0001 | t0012 | g0336 | SAS | BEB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0054 | SAS | BEB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0172 | SAS | BEB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | STU | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0061 | SAS | STU | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0334 | SAS | STU | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0340 | SAS | STU | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0180 | AFR | YRI | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0165 | AFR | YRI | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | CHB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0163 | AFR | YRI | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0203 | AFR | YRI | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18960 | hp1 | a0001 | c0001 | t0009 | g0257 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18967 | hp2 | a0001 | c0001 | t0017 | g0314 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18968 | hp1 | a0001 | c0001 | t0005 | g0269 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18971 | hp1 | a0001 | c0001 | t0005 | g0270 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18979 | hp2 | a0001 | c0001 | t0016 | g0274 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18992 | hp1 | a0003 | c0004 | t0001 | g0159 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18992 | hp2 | a0001 | c0001 | t0005 | g0289 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | LWK | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | LWK | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19054 | hp1 | a0001 | c0001 | t0011 | g0006 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19054 | hp2 | a0001 | c0001 | t0008 | g0044 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19056 | hp2 | a0001 | c0001 | t0008 | g0046 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19059 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19068 | hp1 | a0001 | c0001 | t0014 | g0017 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19074 | hp1 | a0001 | c0001 | t0008 | g0045 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19078 | hp1 | a0001 | c0001 | t0005 | g0272 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19084 | hp1 | a0001 | c0003 | t0001 | g0070 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0330 | AFR | YRI | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ASW | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0178 | EUR | TSI | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0338 | EUR | TSI | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0069 | EUR | TSI | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0040 | SAS | GIH | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | GIH | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0166 | AFR | ACB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0333 | AFR | ACB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG02486 | hp2 | a0001 | c0001 | t0010 | g0161 | AFR | ACB | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | MSL | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | USA | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | USA | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA18955 | hp2 | a0002 | c0005 | t0001 | g0197 | EAS | JPT | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | USA | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | USA | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0076 | REF | REF | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0123 | REF | REF | METAP2_chr12_95469152_95520839 | METAP2 | chr12 | 95469152 | 95520839 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:95474190 | T | G | 1 | a0003 | 1 | NA18992.hp1 | missense_variant | MODERATE | c.11T>G | p.Val4Gly | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/11 | 39/3400 | 11/1437 | 4/478 | chr12 | 95474190 | |||
| chr12:95513687 | A | G | 1 | a0002 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1220A>G | p.Asn407Ser | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 1248/3400 | 1220/1437 | 407/478 | chr12 | 95513687 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:95485958 | C | T | 1 | a0001c0003 | 10 | HG01192.hp1 HG01433.hp2 HG01516.hp1 others(7): Show |
synonymous_variant | LOW | c.405C>T | p.Cys135Cys | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/11 | 433/3400 | 405/1437 | 135/478 | chr12 | 95485958 | |||
| chr12:95512827 | C | A | 2 | a0001c0002 a0002c0005 |
48 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(45): Show |
synonymous_variant | LOW | c.1095C>A | p.Thr365Thr | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/11 | 1123/3400 | 1095/1437 | 365/478 | chr12 | 95512827 | |||
| chr12:95513859 | G | A | 1 | a0001c0006 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1392G>A | p.Leu464Leu | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 1420/3400 | 1392/1437 | 464/478 | chr12 | 95513859 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:95514082 | G | A | 1 | a0001c0001t0009 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*178G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 178 | chr12 | 95514082 | ||||||
| chr12:95514093 | C | T | 1 | a0001c0001t0018 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*189C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 189 | chr12 | 95514093 | ||||||
| chr12:95514115 | T | G | 1 | a0001c0001t0008 | 3 | NA19054.hp2 NA19056.hp2 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*211T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 211 | chr12 | 95514115 | ||||||
| chr12:95514365 | G | A | 1 | a0001c0001t0010 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*461G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 461 | chr12 | 95514365 | ||||||
| chr12:95514445 | C | T | 1 | a0001c0001t0017 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*541C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 541 | chr12 | 95514445 | ||||||
| chr12:95514536 | G | A | 1 | a0001c0001t0011 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*632G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 632 | chr12 | 95514536 | ||||||
| chr12:95514565 | A | G | 1 | a0001c0001t0007 | 4 | HG00140.hp1 HG02735.hp2 HG03239.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*661A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 661 | chr12 | 95514565 | ||||||
| chr12:95514817 | T | C | 1 | a0001c0001t0012 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*913T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 913 | chr12 | 95514817 | ||||||
| chr12:95514826 | ATTCTTGG others(25): Show |
A | 1 | a0001c0001t0013 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*924_*955delTCTTGG others(26): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 924 | INFO_REALIGN_3_PRIME | chr12 | 95514826 | |||||
| chr12:95514879 | C | A | 2 | a0001c0001t0006 a0001c0001t0010 |
5 | HG02109.hp2 HG02486.hp2 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*975C>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 975 | chr12 | 95514879 | ||||||
| chr12:95514890 | T | TA | 2 | a0001c0001t0003 a0001c0001t0008 |
27 | HG00639.hp2 HG00673.hp2 HG00741.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*986_*987insA | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 987 | chr12 | 95514890 | ||||||
| chr12:95514947 | G | A | 1 | a0001c0001t0014 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1043G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 1043 | chr12 | 95514947 | ||||||
| chr12:95514973 | C | T | 3 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0018 |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1069C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 1069 | chr12 | 95514973 | ||||||
| chr12:95515123 | T | A | 1 | a0001c0001t0015 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1219T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 1219 | chr12 | 95515123 | ||||||
| chr12:95515262 | A | G | 1 | a0001c0001t0016 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1358A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 1358 | chr12 | 95515262 | ||||||
| chr12:95515283 | G | A | 2 | a0001c0001t0003 a0001c0001t0008 |
27 | HG00639.hp2 HG00673.hp2 HG00741.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1379G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 1379 | chr12 | 95515283 | ||||||
| chr12:95515465 | G | A | 3 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 |
39 | HG00639.hp1 HG00639.hp2 HG00673.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1561G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 1561 | chr12 | 95515465 | ||||||
| chr12:95515637 | G | T | 1 | a0001c0001t0005 | 6 | HG00597.hp2 HG02071.hp1 NA18968.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1733G>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 11/11 | 1733 | chr12 | 95515637 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:95474383 | T | A | 1 | a0001c0001t0001g0021 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.151+53T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/10 | chr12 | 95474383 | |||||||
| chr12:95474424 | G | A | 1 | a0001c0001t0001g0022 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.151+94G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/10 | chr12 | 95474424 | |||||||
| chr12:95474425 | C | T | 1 | a0001c0001t0001g0022 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.151+95C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/10 | chr12 | 95474425 | |||||||
| chr12:95474433 | AGACTGAT others(10): Show |
A | 1 | a0001c0002t0001g0023 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.151+107_151+123del others(17): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 95474433 | ||||||
| chr12:95474504 | T | A | 11 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0026 others(8): Show |
11 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.151+174T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/10 | chr12 | 95474504 | |||||||
| chr12:95474599 | A | G | 1 | a0001c0001t0004g0353 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.151+269A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/10 | chr12 | 95474599 | |||||||
| chr12:95474711 | C | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.151+381C>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/10 | chr12 | 95474711 | |||||||
| chr12:95474844 | T | C | 1 | a0001c0001t0003g0038 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.151+514T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/10 | chr12 | 95474844 | |||||||
| chr12:95475091 | T | C | 1 | a0001c0002t0001g0039 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.151+761T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/10 | chr12 | 95475091 | |||||||
| chr12:95475096 | T | C | 27 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.151+766T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/10 | chr12 | 95475096 | |||||||
| chr12:95475119 | A | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.151+789A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/10 | chr12 | 95475119 | |||||||
| chr12:95475271 | T | C | 10 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(7): Show |
10 | HG01192.hp1 HG01433.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-800T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/10 | chr12 | 95475271 | |||||||
| chr12:95475511 | A | G | 1 | a0001c0001t0001g0352 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.152-560A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/10 | chr12 | 95475511 | |||||||
| chr12:95475601 | C | T | 27 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.152-470C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/10 | chr12 | 95475601 | |||||||
| chr12:95475654 | C | T | 4 | a0001c0001t0001g0348 a0001c0001t0001g0349 a0001c0001t0001g0350 others(1): Show |
4 | NA18951.hp1 NA18964.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-417C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/10 | chr12 | 95475654 | |||||||
| chr12:95475788 | A | G | 6 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(3): Show |
6 | HG02055.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-283A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/10 | chr12 | 95475788 | |||||||
| chr12:95475828 | C | CTTT | 66 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(63): Show |
67 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.152-242_152-241ins others(3): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr12 | 95475828 | ||||||
| chr12:95475948 | CAATAAT | C | 6 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(3): Show |
6 | HG02055.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-122_152-117del others(6): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 1/10 | chr12 | 95475948 | |||||||
| chr12:95476299 | T | A | 1 | a0001c0001t0002g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.259+121T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95476299 | |||||||
| chr12:95476378 | A | G | 66 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(63): Show |
67 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.259+200A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95476378 | |||||||
| chr12:95476421 | A | C | 1 | a0001c0001t0018g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.259+243A>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95476421 | |||||||
| chr12:95476436 | C | T | 1 | a0001c0001t0001g0347 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.259+258C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95476436 | |||||||
| chr12:95476514 | A | AAAAG | 21 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(18): Show |
23 | HG00621.hp2 HG01346.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.259+360_259+363dup others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476514 | ||||||
| chr12:95476514 | A | AAAAGAAA others(5): Show |
3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+352_259+363dup others(12): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476514 | ||||||
| chr12:95476514 | A | AAAAGAAA others(25): Show |
1 | a0001c0001t0018g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.259+363_259+364ins others(32): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476514 | ||||||
| chr12:95476514 | A | G | 22 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(19): Show |
22 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.259+336A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95476514 | |||||||
| chr12:95476532 | A | AAGAAAGA others(107): Show |
1 | a0001c0001t0002g0319 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.259+361_259+362ins others(114): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476532 | ||||||
| chr12:95476532 | A | AAGAAAGA others(115): Show |
4 | a0001c0001t0002g0320 a0001c0001t0002g0321 a0001c0001t0002g0322 others(1): Show |
4 | HG02630.hp1 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+361_259+362ins others(122): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476532 | ||||||
| chr12:95476532 | A | AAGAAAGA others(119): Show |
1 | a0001c0001t0002g0324 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.259+361_259+362ins others(126): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476532 | ||||||
| chr12:95476532 | A | AAGAAAGA others(119): Show |
1 | a0001c0001t0002g0325 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.259+361_259+362ins others(126): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476532 | ||||||
| chr12:95476532 | A | AAGAAAGA others(124): Show |
1 | a0001c0001t0002g0326 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.259+361_259+362ins others(131): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476532 | ||||||
| chr12:95476532 | A | AAGAAAGA others(120): Show |
1 | a0001c0001t0002g0327 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.259+361_259+362ins others(127): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476532 | ||||||
| chr12:95476532 | A | AAGAAAGA others(123): Show |
2 | a0001c0001t0002g0328 a0001c0001t0002g0329 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.259+361_259+362ins others(130): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476532 | ||||||
| chr12:95476532 | A | AAGAAAGA others(125): Show |
1 | a0001c0001t0002g0330 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.259+361_259+362ins others(132): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476532 | ||||||
| chr12:95476532 | A | AAGAGAGA others(129): Show |
1 | a0001c0001t0002g0331 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.259+357_259+358ins others(136): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476532 | ||||||
| chr12:95476532 | A | AAGAGAGA others(120): Show |
1 | a0001c0001t0002g0332 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.259+357_259+358ins others(127): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476532 | ||||||
| chr12:95476532 | A | AAGAGAGA others(123): Show |
1 | a0001c0001t0002g0333 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.259+357_259+358ins others(130): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476532 | ||||||
| chr12:95476532 | A | AAGAGAGA others(121): Show |
1 | a0001c0001t0002g0334 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.259+357_259+358ins others(128): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476532 | ||||||
| chr12:95476532 | A | AAGAGAGA others(123): Show |
1 | a0001c0001t0002g0335 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.259+357_259+358ins others(130): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476532 | ||||||
| chr12:95476532 | A | AAGAGAGA others(125): Show |
1 | a0001c0001t0012g0336 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.259+357_259+358ins others(132): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476532 | ||||||
| chr12:95476532 | A | AAGAGAGA others(127): Show |
1 | a0001c0001t0002g0337 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.259+357_259+358ins others(134): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476532 | ||||||
| chr12:95476532 | A | AAGAGAGA others(129): Show |
1 | a0001c0001t0002g0338 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.259+357_259+358ins others(136): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476532 | ||||||
| chr12:95476532 | A | AAGAGAGA others(129): Show |
1 | a0001c0001t0002g0339 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.259+357_259+358ins others(136): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476532 | ||||||
| chr12:95476532 | A | AAGAGAGA others(133): Show |
1 | a0001c0001t0002g0340 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.259+357_259+358ins others(140): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95476532 | ||||||
| chr12:95476542 | A | G | 22 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(19): Show |
22 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.259+364A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95476542 | |||||||
| chr12:95476809 | T | C | 1 | a0001c0001t0002g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.259+631T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95476809 | |||||||
| chr12:95476899 | C | T | 264 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(261): Show |
282 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.259+721C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95476899 | |||||||
| chr12:95476913 | G | A | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.259+735G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95476913 | |||||||
| chr12:95476994 | G | A | 1 | a0001c0006t0001g0342 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.259+816G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95476994 | |||||||
| chr12:95477054 | C | G | 1 | a0001c0001t0007g0300 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.259+876C>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95477054 | |||||||
| chr12:95477083 | C | T | 11 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0026 others(8): Show |
11 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.259+905C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95477083 | |||||||
| chr12:95477084 | G | A | 1 | a0001c0001t0003g0040 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.259+906G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95477084 | |||||||
| chr12:95477104 | AT | A | 39 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(36): Show |
39 | HG00639.hp1 HG00639.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.259+937delT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95477104 | ||||||
| chr12:95477143 | G | A | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.259+965G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95477143 | |||||||
| chr12:95477172 | C | T | 1 | a0001c0001t0001g0347 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.259+994C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95477172 | |||||||
| chr12:95477253 | A | G | 263 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(260): Show |
281 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.259+1075A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95477253 | |||||||
| chr12:95477311 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.259+1133G>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95477311 | |||||||
| chr12:95477326 | A | G | 27 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.259+1148A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95477326 | |||||||
| chr12:95477442 | C | T | 11 | a0001c0001t0002g0324 a0001c0001t0002g0331 a0001c0001t0002g0332 others(8): Show |
11 | HG00099.hp2 HG01496.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+1264C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95477442 | |||||||
| chr12:95477481 | C | A | 1 | a0001c0001t0003g0041 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.259+1303C>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95477481 | |||||||
| chr12:95477548 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.259+1370T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95477548 | |||||||
| chr12:95477567 | G | A | 10 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(7): Show |
10 | HG01192.hp1 HG01433.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.259+1389G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95477567 | |||||||
| chr12:95477599 | C | T | 5 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(2): Show |
5 | HG02055.hp1 HG02647.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+1421C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95477599 | |||||||
| chr12:95477657 | T | C | 10 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(7): Show |
10 | HG01192.hp1 HG01433.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.259+1479T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95477657 | |||||||
| chr12:95477681 | C | T | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | HG00642.hp1 HG00733.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+1503C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95477681 | |||||||
| chr12:95477737 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.259+1559T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95477737 | |||||||
| chr12:95477877 | T | C | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.259+1699T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95477877 | |||||||
| chr12:95477997 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.259+1819T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95477997 | |||||||
| chr12:95478023 | G | A | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+1845G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95478023 | |||||||
| chr12:95478049 | G | C | 22 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(19): Show |
22 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.259+1871G>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95478049 | |||||||
| chr12:95478098 | T | C | 1 | a0003c0004t0001g0159 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.259+1920T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95478098 | |||||||
| chr12:95478102 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.259+1924T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95478102 | |||||||
| chr12:95478250 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.259+2072T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95478250 | |||||||
| chr12:95478260 | CAG | C | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+2085_259+2086d others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95478260 | ||||||
| chr12:95478524 | C | T | 23 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(20): Show |
23 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.259+2346C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95478524 | |||||||
| chr12:95478568 | GT | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.259+2392delT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95478568 | ||||||
| chr12:95478589 | G | C | 5 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+2411G>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95478589 | |||||||
| chr12:95478638 | A | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
133 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.259+2460A>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95478638 | |||||||
| chr12:95478668 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.259+2490G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95478668 | |||||||
| chr12:95478698 | G | T | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG02717.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.259+2520G>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95478698 | |||||||
| chr12:95478759 | C | T | 4 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+2581C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95478759 | |||||||
| chr12:95478853 | T | C | 1 | a0001c0001t0001g0301 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.259+2675T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95478853 | |||||||
| chr12:95479203 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.259+3025C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95479203 | |||||||
| chr12:95479208 | A | G | 1 | a0001c0001t0002g0329 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.259+3030A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95479208 | |||||||
| chr12:95479243 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.259+3065T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95479243 | |||||||
| chr12:95479356 | C | A | 64 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(61): Show |
65 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.259+3178C>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95479356 | |||||||
| chr12:95479400 | G | A | 6 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(3): Show |
6 | HG02055.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.259+3222G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95479400 | |||||||
| chr12:95479613 | C | CT | 6 | a0001c0001t0001g0294 a0001c0001t0001g0296 a0001c0001t0001g0297 others(3): Show |
6 | HG00642.hp1 HG00733.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.259+3450dupT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95479613 | ||||||
| chr12:95479613 | CT | C | 38 | a0001c0001t0001g0212 a0001c0001t0003g0038 a0001c0001t0003g0040 others(35): Show |
38 | HG00639.hp1 HG00639.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.259+3450delT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95479613 | ||||||
| chr12:95479851 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.260-3364C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95479851 | |||||||
| chr12:95479912 | A | G | 1 | a0001c0002t0001g0205 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.260-3303A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95479912 | |||||||
| chr12:95479957 | T | C | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG01109.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.260-3258T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95479957 | |||||||
| chr12:95479986 | G | T | 1 | a0001c0001t0001g0293 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.260-3229G>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95479986 | |||||||
| chr12:95480288 | A | G | 4 | a0001c0002t0001g0039 a0001c0002t0001g0202 a0001c0002t0001g0203 others(1): Show |
4 | HG01109.hp1 HG01192.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-2927A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95480288 | |||||||
| chr12:95480354 | A | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.260-2861A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95480354 | |||||||
| chr12:95480396 | G | T | 1 | a0001c0001t0018g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.260-2819G>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95480396 | |||||||
| chr12:95480511 | G | A | 2 | a0001c0001t0003g0042 a0001c0001t0003g0043 |
2 | NA19010.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.260-2704G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95480511 | |||||||
| chr12:95480571 | G | T | 1 | a0001c0001t0001g0292 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.260-2644G>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95480571 | |||||||
| chr12:95480877 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.260-2338G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95480877 | |||||||
| chr12:95481036 | A | G | 11 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0026 others(8): Show |
11 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.260-2179A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95481036 | |||||||
| chr12:95481042 | T | C | 1 | a0001c0001t0018g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.260-2173T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95481042 | |||||||
| chr12:95481064 | T | A | 27 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.260-2151T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95481064 | |||||||
| chr12:95481065 | T | A | 39 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(36): Show |
39 | HG00639.hp1 HG00639.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.260-2150T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95481065 | |||||||
| chr12:95481101 | A | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0151 a0001c0001t0001g0152 |
5 | NA18944.hp1 NA18952.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-2114A>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95481101 | |||||||
| chr12:95481246 | A | G | 2 | a0001c0001t0002g0332 a0001c0001t0002g0333 |
2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.260-1969A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95481246 | |||||||
| chr12:95481334 | C | T | 1 | a0001c0001t0002g0319 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.260-1881C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95481334 | |||||||
| chr12:95481425 | A | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
133 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.260-1790A>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95481425 | |||||||
| chr12:95481647 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.260-1568A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95481647 | |||||||
| chr12:95481662 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.260-1553C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95481662 | |||||||
| chr12:95481694 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0081 |
3 | HG03669.hp2 HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.260-1521T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95481694 | |||||||
| chr12:95481713 | G | A | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.260-1502G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95481713 | |||||||
| chr12:95481784 | A | G | 1 | a0001c0001t0013g0343 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.260-1431A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95481784 | |||||||
| chr12:95482016 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0347 |
2 | HG03130.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.260-1199G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95482016 | |||||||
| chr12:95482144 | C | G | 1 | a0001c0001t0001g0291 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.260-1071C>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95482144 | |||||||
| chr12:95482160 | C | T | 1 | a0001c0001t0002g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.260-1055C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95482160 | |||||||
| chr12:95482256 | C | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0211 a0001c0001t0001g0213 others(38): Show |
44 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.260-959C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95482256 | |||||||
| chr12:95482270 | C | A | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.260-945C>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95482270 | |||||||
| chr12:95482287 | A | G | 1 | a0001c0001t0009g0257 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.260-928A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95482287 | |||||||
| chr12:95482517 | C | T | 22 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(19): Show |
22 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.260-698C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95482517 | |||||||
| chr12:95482566 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.260-649G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95482566 | |||||||
| chr12:95482590 | T | TCAACATG | 6 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(3): Show |
6 | HG02055.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.260-624_260-618dup others(7): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95482590 | ||||||
| chr12:95482599 | C | T | 2 | a0001c0003t0001g0075 a0001c0006t0001g0342 |
2 | HG02055.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.260-616C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95482599 | |||||||
| chr12:95482616 | TA | T | 229 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(226): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.260-579delA | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95482616 | ||||||
| chr12:95482616 | TAA | T | 14 | a0001c0001t0001g0211 a0001c0001t0001g0290 a0001c0001t0002g0337 others(11): Show |
14 | HG00558.hp2 HG01167.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.260-580_260-579del others(2): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 95482616 | ||||||
| chr12:95482632 | A | G | 39 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(36): Show |
39 | HG00639.hp1 HG00639.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.260-583A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95482632 | |||||||
| chr12:95482648 | T | C | 11 | a0001c0001t0001g0011 a0001c0001t0001g0162 a0001c0001t0001g0207 others(8): Show |
12 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.260-567T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95482648 | |||||||
| chr12:95482748 | C | T | 22 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(19): Show |
22 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.260-467C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95482748 | |||||||
| chr12:95483067 | T | C | 1 | a0001c0001t0001g0347 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.260-148T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95483067 | |||||||
| chr12:95483132 | G | A | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.260-83G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95483132 | |||||||
| chr12:95483145 | T | C | 11 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0026 others(8): Show |
11 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.260-70T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 2/10 | chr12 | 95483145 | |||||||
| chr12:95483475 | C | CA | 37 | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0082 others(34): Show |
39 | HG00642.hp2 HG01516.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.325+218dupA | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 95483475 | ||||||
| chr12:95483475 | C | CAA | 9 | a0001c0001t0001g0157 a0001c0001t0001g0167 a0001c0001t0001g0168 others(6): Show |
9 | HG01192.hp1 HG01433.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.325+217_325+218dup others(2): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 95483475 | ||||||
| chr12:95483475 | CA | C | 52 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0078 others(49): Show |
55 | HG00140.hp1 HG00639.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.325+218delA | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 95483475 | ||||||
| chr12:95483680 | T | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0162 a0001c0001t0001g0207 others(3): Show |
7 | HG02280.hp2 HG02717.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.325+400T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95483680 | |||||||
| chr12:95483680 | T | G | 1 | a0001c0001t0013g0343 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.325+400T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95483680 | |||||||
| chr12:95483683 | C | A | 1 | a0001c0002t0001g0171 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.325+403C>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95483683 | |||||||
| chr12:95483766 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.325+486A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95483766 | |||||||
| chr12:95483853 | G | A | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.325+573G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95483853 | |||||||
| chr12:95483856 | A | T | 1 | a0001c0001t0001g0143 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.325+576A>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95483856 | |||||||
| chr12:95483859 | C | G | 1 | a0001c0001t0003g0062 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.325+579C>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95483859 | |||||||
| chr12:95484020 | C | T | 66 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(63): Show |
67 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.325+740C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95484020 | |||||||
| chr12:95484378 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.325+1098A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95484378 | |||||||
| chr12:95484403 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0085 |
3 | HG01074.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.325+1123T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95484403 | |||||||
| chr12:95484424 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.325+1144T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95484424 | |||||||
| chr12:95484541 | C | G | 39 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(36): Show |
39 | HG00639.hp1 HG00639.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.325+1261C>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95484541 | |||||||
| chr12:95484579 | G | A | 1 | a0001c0001t0005g0261 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.325+1299G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95484579 | |||||||
| chr12:95484697 | C | G | 2 | a0001c0001t0003g0063 a0001c0001t0003g0064 |
2 | NA19059.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.326-1182C>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95484697 | |||||||
| chr12:95484776 | T | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
133 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.326-1103T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95484776 | |||||||
| chr12:95484803 | A | AT | 33 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(30): Show |
34 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.326-1067dupT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 95484803 | ||||||
| chr12:95484975 | T | G | 264 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(261): Show |
282 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.326-904T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95484975 | |||||||
| chr12:95485077 | G | T | 1 | a0001c0001t0001g0142 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.326-802G>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95485077 | |||||||
| chr12:95485137 | C | G | 27 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.326-742C>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95485137 | |||||||
| chr12:95485177 | GA | G | 39 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(36): Show |
39 | HG00639.hp1 HG00639.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.326-701delA | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95485177 | |||||||
| chr12:95485392 | T | G | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 |
3 | HG01168.hp1 HG01169.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.326-487T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95485392 | |||||||
| chr12:95485457 | A | G | 39 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(36): Show |
39 | HG00639.hp1 HG00639.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.326-422A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95485457 | |||||||
| chr12:95485488 | A | G | 1 | a0001c0002t0001g0200 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.326-391A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95485488 | |||||||
| chr12:95485567 | AC | A | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0015g0344 |
3 | HG02647.hp1 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.326-310delC | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 95485567 | ||||||
| chr12:95485743 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.326-136T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 3/10 | chr12 | 95485743 | |||||||
| chr12:95486083 | A | T | 1 | a0001c0001t0001g0141 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.428+102A>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95486083 | |||||||
| chr12:95486291 | T | TA | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
152 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.428+311dupA | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95486291 | ||||||
| chr12:95486293 | T | C | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
152 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.428+312T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95486293 | |||||||
| chr12:95486643 | A | G | 1 | a0001c0001t0001g0347 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.428+662A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95486643 | |||||||
| chr12:95486672 | T | C | 1 | a0001c0001t0013g0343 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.428+691T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95486672 | |||||||
| chr12:95486728 | C | T | 1 | a0001c0001t0002g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.428+747C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95486728 | |||||||
| chr12:95486739 | C | T | 4 | a0001c0002t0001g0170 a0001c0002t0001g0171 a0001c0002t0001g0199 others(1): Show |
4 | HG02074.hp2 NA18974.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.428+758C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95486739 | |||||||
| chr12:95486760 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.428+779G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95486760 | |||||||
| chr12:95486775 | G | A | 12 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0026 others(9): Show |
12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.428+794G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95486775 | |||||||
| chr12:95486831 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.428+850C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95486831 | |||||||
| chr12:95486850 | T | C | 272 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(269): Show |
290 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.428+869T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95486850 | |||||||
| chr12:95486871 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.428+890C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95486871 | |||||||
| chr12:95487035 | G | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0258 a0001c0001t0001g0259 others(28): Show |
34 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.428+1054G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95487035 | |||||||
| chr12:95487059 | A | G | 1 | a0001c0001t0004g0353 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.428+1078A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95487059 | |||||||
| chr12:95487179 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
133 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.428+1198C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95487179 | |||||||
| chr12:95487316 | A | AT | 49 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(46): Show |
54 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.428+1346dupT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95487316 | ||||||
| chr12:95487328 | A | T | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.428+1347A>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95487328 | |||||||
| chr12:95487339 | A | G | 6 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(3): Show |
6 | HG02055.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.428+1358A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95487339 | |||||||
| chr12:95487591 | A | AT | 237 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(234): Show |
254 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.428+1625dupT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95487591 | ||||||
| chr12:95487756 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.428+1775C>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95487756 | |||||||
| chr12:95487985 | GCT | G | 10 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(7): Show |
10 | HG01192.hp1 HG01433.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.428+2005_428+2006d others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95487985 | |||||||
| chr12:95488010 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.428+2029C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95488010 | |||||||
| chr12:95488011 | T | A | 10 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(7): Show |
10 | HG01192.hp1 HG01433.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.428+2030T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95488011 | |||||||
| chr12:95488028 | G | A | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG00140.hp2 HG01074.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+2047G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95488028 | |||||||
| chr12:95488424 | G | A | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0015g0344 |
3 | HG02647.hp1 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.428+2443G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95488424 | |||||||
| chr12:95488434 | A | G | 6 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(3): Show |
6 | HG01243.hp2 HG02622.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.428+2453A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95488434 | |||||||
| chr12:95488511 | C | CA | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(62): Show |
71 | HG00408.hp2 HG00438.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.428+2558dupA | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95488511 | ||||||
| chr12:95488511 | C | CAA | 23 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0096 others(20): Show |
23 | HG00423.hp2 HG00673.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.428+2557_428+2558d others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95488511 | ||||||
| chr12:95488511 | C | CAAA | 6 | a0001c0001t0001g0011 a0001c0001t0001g0150 a0001c0001t0001g0157 others(3): Show |
7 | HG03041.hp1 HG03225.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.428+2556_428+2558d others(5): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95488511 | ||||||
| chr12:95488511 | C | CAAAAAAA others(1): Show |
7 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0026 others(4): Show |
7 | HG02257.hp2 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.428+2551_428+2558d others(10): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95488511 | ||||||
| chr12:95488511 | CAAAAAAA others(3): Show |
C | 135 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(132): Show |
146 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.428+2549_428+2558d others(12): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95488511 | ||||||
| chr12:95488540 | T | A | 2 | a0001c0001t0001g0082 a0001c0001t0004g0353 |
2 | HG02080.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.428+2559T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95488540 | |||||||
| chr12:95488663 | G | T | 22 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(19): Show |
22 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.428+2682G>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95488663 | |||||||
| chr12:95488729 | A | G | 43 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(40): Show |
48 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.428+2748A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95488729 | |||||||
| chr12:95488759 | A | T | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | HG00642.hp1 HG00733.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+2778A>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95488759 | |||||||
| chr12:95488881 | T | TAC | 79 | a0001c0001t0001g0100 a0001c0001t0002g0319 a0001c0001t0002g0320 others(76): Show |
84 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.428+2918_428+2919d others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95488881 | ||||||
| chr12:95488882 | A | T | 27 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.428+2901A>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95488882 | |||||||
| chr12:95488890 | A | T | 1 | a0001c0001t0001g0347 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.428+2909A>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95488890 | |||||||
| chr12:95488898 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.428+2917A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95488898 | |||||||
| chr12:95489020 | C | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
148 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.428+3039C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95489020 | |||||||
| chr12:95489249 | A | G | 1 | a0001c0001t0003g0061 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.428+3268A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95489249 | |||||||
| chr12:95489251 | GA | G | 23 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(20): Show |
23 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.428+3277delA | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95489251 | ||||||
| chr12:95489392 | A | C | 1 | a0001c0001t0001g0092 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.428+3411A>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95489392 | |||||||
| chr12:95489482 | C | G | 1 | a0001c0001t0018g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.428+3501C>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95489482 | |||||||
| chr12:95489513 | T | C | 70 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(67): Show |
78 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.428+3532T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95489513 | |||||||
| chr12:95489518 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.428+3537T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95489518 | |||||||
| chr12:95489519 | A | G | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.428+3538A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95489519 | |||||||
| chr12:95489532 | T | A | 1 | a0001c0001t0001g0267 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.428+3551T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95489532 | |||||||
| chr12:95489779 | G | A | 11 | a0001c0001t0002g0324 a0001c0001t0002g0331 a0001c0001t0002g0332 others(8): Show |
11 | HG00099.hp2 HG01496.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.428+3798G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95489779 | |||||||
| chr12:95489825 | T | A | 11 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0026 others(8): Show |
11 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.428+3844T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95489825 | |||||||
| chr12:95490130 | C | T | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.429-3926C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95490130 | |||||||
| chr12:95490193 | C | T | 1 | a0001c0001t0005g0275 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.429-3863C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95490193 | |||||||
| chr12:95490194 | T | TGAA | 10 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(7): Show |
10 | HG01192.hp1 HG01433.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.429-3861_429-3860i others(5): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95490194 | ||||||
| chr12:95490275 | T | G | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0015g0344 |
3 | HG02647.hp1 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.429-3781T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95490275 | |||||||
| chr12:95490289 | T | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.429-3767T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95490289 | |||||||
| chr12:95490320 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.429-3736G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95490320 | |||||||
| chr12:95490492 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.429-3564G>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95490492 | |||||||
| chr12:95490519 | C | T | 1 | a0001c0001t0018g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.429-3537C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95490519 | |||||||
| chr12:95490537 | ACT | A | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0015g0344 |
3 | HG02647.hp1 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.429-3516_429-3515d others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95490537 | ||||||
| chr12:95490566 | AT | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(65): Show |
75 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.429-3469delT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95490566 | ||||||
| chr12:95490566 | ATT | A | 206 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.429-3470_429-3469d others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95490566 | ||||||
| chr12:95490566 | ATTT | A | 10 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(7): Show |
10 | HG02015.hp2 HG02258.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.429-3471_429-3469d others(5): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95490566 | ||||||
| chr12:95490653 | C | T | 1 | a0001c0001t0002g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.429-3403C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95490653 | |||||||
| chr12:95490695 | T | C | 1 | a0001c0001t0018g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.429-3361T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95490695 | |||||||
| chr12:95490838 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.429-3218G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95490838 | |||||||
| chr12:95491028 | A | G | 3 | a0001c0002t0001g0175 a0001c0002t0001g0198 a0002c0005t0001g0197 |
3 | NA18955.hp2 NA18978.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.429-3028A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95491028 | |||||||
| chr12:95491082 | CT | C | 241 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.429-2958delT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95491082 | ||||||
| chr12:95491082 | CTT | C | 22 | a0001c0001t0002g0316 a0001c0001t0002g0319 a0001c0001t0002g0320 others(19): Show |
22 | HG00099.hp2 HG01496.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.429-2959_429-2958d others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95491082 | ||||||
| chr12:95491174 | A | G | 1 | a0001c0001t0002g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.429-2882A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95491174 | |||||||
| chr12:95491438 | T | A | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.429-2618T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95491438 | |||||||
| chr12:95491522 | T | C | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.429-2534T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95491522 | |||||||
| chr12:95491620 | C | T | 1 | a0001c0001t0001g0347 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.429-2436C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95491620 | |||||||
| chr12:95491719 | C | T | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.429-2337C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95491719 | |||||||
| chr12:95491814 | T | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
133 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.429-2242T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95491814 | |||||||
| chr12:95491941 | A | C | 18 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0047 others(15): Show |
18 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.429-2115A>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95491941 | |||||||
| chr12:95492111 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.429-1945C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95492111 | |||||||
| chr12:95492124 | A | ATG | 5 | a0001c0001t0001g0085 a0001c0001t0001g0121 a0001c0001t0002g0020 others(2): Show |
6 | HG01169.hp2 HG01258.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.429-1926_429-1925d others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95492124 | ||||||
| chr12:95492124 | A | ATGTGTGT others(3): Show |
20 | a0001c0001t0002g0316 a0001c0001t0002g0319 a0001c0001t0002g0320 others(17): Show |
20 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.429-1925_429-1924i others(12): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95492124 | ||||||
| chr12:95492124 | A | ATGTGTGT others(5): Show |
2 | a0001c0001t0002g0321 a0001c0001t0002g0330 |
2 | HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.429-1925_429-1924i others(14): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95492124 | ||||||
| chr12:95492124 | A | ATGTGTGT others(9): Show |
1 | a0001c0001t0002g0326 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.429-1925_429-1924i others(18): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95492124 | ||||||
| chr12:95492132 | T | G | 29 | a0001c0001t0001g0085 a0001c0001t0001g0121 a0001c0001t0002g0020 others(26): Show |
30 | HG00099.hp2 HG01169.hp2 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.429-1924T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95492132 | |||||||
| chr12:95492132 | T | TTGTG | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(83): Show |
93 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.429-1904_429-1901d others(6): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95492132 | ||||||
| chr12:95492132 | T | TTGTGTG | 136 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
147 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.429-1906_429-1901d others(8): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95492132 | ||||||
| chr12:95492132 | T | TTGTGTGT others(1): Show |
65 | a0001c0001t0001g0210 a0001c0001t0001g0218 a0001c0001t0001g0296 others(62): Show |
70 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.429-1908_429-1901d others(10): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95492132 | ||||||
| chr12:95492132 | T | TTGTGTGT others(3): Show |
3 | a0001c0001t0001g0346 a0001c0002t0001g0039 a0001c0002t0001g0205 |
3 | HG02965.hp1 HG03139.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.429-1910_429-1901d others(12): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95492132 | ||||||
| chr12:95492132 | T | TTGTGTGT others(5): Show |
1 | a0001c0001t0004g0353 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.429-1912_429-1901d others(14): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95492132 | ||||||
| chr12:95492132 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0001g0347 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.429-1914_429-1901d others(16): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95492132 | ||||||
| chr12:95492132 | T | TTGTGTGT others(9): Show |
11 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0026 others(8): Show |
11 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.429-1916_429-1901d others(18): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 95492132 | ||||||
| chr12:95492206 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.429-1850A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95492206 | |||||||
| chr12:95492327 | A | G | 22 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(19): Show |
22 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.429-1729A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95492327 | |||||||
| chr12:95492372 | A | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG02451.hp2 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.429-1684A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95492372 | |||||||
| chr12:95492630 | A | G | 12 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0026 others(9): Show |
12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.429-1426A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95492630 | |||||||
| chr12:95492863 | A | G | 18 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0047 others(15): Show |
18 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.429-1193A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95492863 | |||||||
| chr12:95493066 | A | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.429-990A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95493066 | |||||||
| chr12:95493083 | A | G | 6 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(3): Show |
6 | HG02055.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.429-973A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95493083 | |||||||
| chr12:95493129 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.429-927G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95493129 | |||||||
| chr12:95493245 | A | G | 125 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(122): Show |
131 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.429-811A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95493245 | |||||||
| chr12:95493341 | G | T | 1 | a0001c0001t0001g0019 | 2 | HG00621.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.429-715G>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95493341 | |||||||
| chr12:95493738 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.429-318A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 4/10 | chr12 | 95493738 | |||||||
| chr12:95494290 | T | A | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.590+73T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 5/10 | chr12 | 95494290 | |||||||
| chr12:95494383 | G | A | 2 | a0001c0001t0002g0325 a0001c0001t0002g0327 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.590+166G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 5/10 | chr12 | 95494383 | |||||||
| chr12:95494453 | A | C | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.590+236A>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 5/10 | chr12 | 95494453 | |||||||
| chr12:95494646 | T | C | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
152 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.591-311T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 5/10 | chr12 | 95494646 | |||||||
| chr12:95494685 | AAGTT | A | 43 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(40): Show |
48 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.591-269_591-266del others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 95494685 | ||||||
| chr12:95494753 | ATCAAATT others(8): Show |
A | 1 | a0001c0001t0001g0347 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.591-201_591-187del others(15): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 95494753 | ||||||
| chr12:95494778 | A | G | 14 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0162 others(11): Show |
15 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.591-179A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 5/10 | chr12 | 95494778 | |||||||
| chr12:95494827 | G | A | 10 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(7): Show |
10 | HG01192.hp1 HG01433.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.591-130G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 5/10 | chr12 | 95494827 | |||||||
| chr12:95494859 | T | G | 1 | a0001c0006t0001g0342 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.591-98T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 5/10 | chr12 | 95494859 | |||||||
| chr12:95494933 | G | A | 1 | a0001c0001t0003g0054 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.591-24G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 5/10 | chr12 | 95494933 | |||||||
| chr12:95495257 | T | C | 22 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(19): Show |
22 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.772+119T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 6/10 | chr12 | 95495257 | |||||||
| chr12:95495436 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.772+298T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 6/10 | chr12 | 95495436 | |||||||
| chr12:95495456 | CTT | C | 43 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(40): Show |
48 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.772+321_772+322del others(2): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr12 | 95495456 | ||||||
| chr12:95495660 | A | G | 40 | a0001c0001t0001g0158 a0001c0001t0003g0038 a0001c0001t0003g0040 others(37): Show |
40 | HG00639.hp1 HG00639.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.773-344A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 6/10 | chr12 | 95495660 | |||||||
| chr12:95495676 | G | T | 1 | a0001c0001t0001g0167 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.773-328G>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 6/10 | chr12 | 95495676 | |||||||
| chr12:95495830 | T | C | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.773-174T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 6/10 | chr12 | 95495830 | |||||||
| chr12:95496147 | A | G | 43 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(40): Show |
48 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.867+49A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95496147 | |||||||
| chr12:95496253 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.867+155C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95496253 | |||||||
| chr12:95496288 | T | TTTTG | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.867+206_867+209dup others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95496288 | ||||||
| chr12:95496364 | A | G | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.867+266A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95496364 | |||||||
| chr12:95496403 | T | A | 1 | a0001c0001t0002g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.867+305T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95496403 | |||||||
| chr12:95496442 | T | C | 10 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(7): Show |
10 | HG01192.hp1 HG01433.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.867+344T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95496442 | |||||||
| chr12:95496451 | T | TACCCACC others(7): Show |
1 | a0001c0001t0003g0063 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.867+355_867+368dup others(14): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95496451 | ||||||
| chr12:95496519 | T | G | 3 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0030 |
3 | HG02886.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.867+421T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95496519 | |||||||
| chr12:95496572 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.867+474G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95496572 | |||||||
| chr12:95496613 | A | G | 9 | a0001c0001t0003g0041 a0001c0001t0003g0042 a0001c0001t0003g0043 others(6): Show |
9 | HG00673.hp2 HG02056.hp1 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.867+515A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95496613 | |||||||
| chr12:95496622 | C | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.867+524C>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95496622 | |||||||
| chr12:95496637 | A | T | 10 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(7): Show |
10 | HG01192.hp1 HG01433.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.867+539A>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95496637 | |||||||
| chr12:95496695 | CCT | C | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.867+602_867+603del others(2): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95496695 | ||||||
| chr12:95496776 | TTAAA | T | 9 | a0001c0001t0003g0041 a0001c0001t0003g0042 a0001c0001t0003g0043 others(6): Show |
9 | HG00673.hp2 HG02056.hp1 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.867+679_867+682del others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95496776 | |||||||
| chr12:95496782 | TAGA | T | 9 | a0001c0001t0003g0041 a0001c0001t0003g0042 a0001c0001t0003g0043 others(6): Show |
9 | HG00673.hp2 HG02056.hp1 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.867+685_867+687del others(3): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95496782 | |||||||
| chr12:95496804 | A | G | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.867+706A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95496804 | |||||||
| chr12:95496821 | C | CT | 83 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(80): Show |
90 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.867+744dupT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95496821 | ||||||
| chr12:95496821 | C | CTT | 16 | a0001c0002t0001g0039 a0001c0002t0001g0175 a0001c0002t0001g0198 others(13): Show |
16 | HG01109.hp1 HG01192.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.867+743_867+744dup others(2): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95496821 | ||||||
| chr12:95496821 | CT | C | 28 | a0001c0001t0001g0087 a0001c0001t0001g0146 a0001c0001t0001g0224 others(25): Show |
28 | HG00099.hp2 HG01167.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.867+744delT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95496821 | ||||||
| chr12:95496825 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.867+727T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95496825 | |||||||
| chr12:95496887 | C | T | 23 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(20): Show |
23 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.867+789C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95496887 | |||||||
| chr12:95496950 | G | T | 10 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(7): Show |
10 | HG01192.hp1 HG01433.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.867+852G>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95496950 | |||||||
| chr12:95497214 | A | G | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | HG00642.hp1 HG00733.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.867+1116A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95497214 | |||||||
| chr12:95497235 | C | G | 22 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(19): Show |
22 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.867+1137C>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95497235 | |||||||
| chr12:95497351 | G | A | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.867+1253G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95497351 | |||||||
| chr12:95497429 | A | G | 27 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.867+1331A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95497429 | |||||||
| chr12:95497963 | T | C | 1 | a0001c0001t0018g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.867+1865T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95497963 | |||||||
| chr12:95497972 | C | CA | 26 | a0001c0001t0001g0097 a0001c0001t0002g0020 a0001c0001t0002g0317 others(23): Show |
27 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.867+1886dupA | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95497972 | ||||||
| chr12:95498037 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
133 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.867+1939G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95498037 | |||||||
| chr12:95498081 | C | G | 2 | a0001c0002t0001g0195 a0001c0002t0001g0196 |
2 | NA18987.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.867+1983C>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95498081 | |||||||
| chr12:95498088 | G | A | 1 | a0001c0001t0001g0019 | 2 | HG00621.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.867+1990G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95498088 | |||||||
| chr12:95498111 | C | T | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | HG00642.hp1 HG00733.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.867+2013C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95498111 | |||||||
| chr12:95498132 | C | CA | 45 | a0001c0001t0001g0022 a0001c0001t0001g0103 a0001c0001t0001g0154 others(42): Show |
45 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.867+2049dupA | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95498132 | ||||||
| chr12:95498132 | CA | C | 6 | a0001c0001t0001g0168 a0001c0001t0002g0020 a0001c0001t0002g0316 others(3): Show |
7 | HG01884.hp2 HG02258.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.867+2049delA | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95498132 | ||||||
| chr12:95498132 | CAA | C | 23 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(20): Show |
23 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.867+2048_867+2049d others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95498132 | ||||||
| chr12:95498144 | A | C | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.867+2046A>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95498144 | |||||||
| chr12:95498196 | C | T | 23 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(20): Show |
23 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.867+2098C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95498196 | |||||||
| chr12:95498277 | C | T | 1 | a0001c0006t0001g0342 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.867+2179C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95498277 | |||||||
| chr12:95498404 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.867+2306G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95498404 | |||||||
| chr12:95498531 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.867+2433C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95498531 | |||||||
| chr12:95498534 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.867+2436C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95498534 | |||||||
| chr12:95498535 | G | A | 23 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(20): Show |
23 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.867+2437G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95498535 | |||||||
| chr12:95498630 | A | G | 28 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(25): Show |
29 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.867+2532A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95498630 | |||||||
| chr12:95498779 | C | T | 28 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(25): Show |
29 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.867+2681C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95498779 | |||||||
| chr12:95498794 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.867+2696G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95498794 | |||||||
| chr12:95498834 | C | A | 1 | a0001c0001t0001g0221 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.867+2736C>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95498834 | |||||||
| chr12:95499015 | CA | C | 135 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(132): Show |
147 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.867+2930delA | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95499015 | ||||||
| chr12:95499017 | A | C | 2 | a0001c0001t0001g0267 a0001c0001t0001g0273 |
2 | NA18747.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.867+2919A>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95499017 | |||||||
| chr12:95499026 | A | G | 1 | a0001c0001t0002g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.867+2928A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95499026 | |||||||
| chr12:95499061 | T | G | 1 | a0001c0001t0018g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.867+2963T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95499061 | |||||||
| chr12:95499064 | T | C | 1 | a0001c0001t0002g0327 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.867+2966T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95499064 | |||||||
| chr12:95499155 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.867+3057G>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95499155 | |||||||
| chr12:95499297 | G | A | 1 | a0001c0001t0013g0343 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.867+3199G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95499297 | |||||||
| chr12:95499332 | A | G | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.867+3234A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95499332 | |||||||
| chr12:95499428 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.867+3330A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95499428 | |||||||
| chr12:95499509 | T | TG | 6 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(3): Show |
6 | HG02055.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.867+3411_867+3412i others(3): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95499509 | |||||||
| chr12:95499570 | A | AT | 62 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(59): Show |
63 | HG00099.hp2 HG00639.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.867+3482dupT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95499570 | ||||||
| chr12:95499609 | A | G | 1 | a0001c0001t0002g0327 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.867+3511A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95499609 | |||||||
| chr12:95499720 | A | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0081 a0001c0001t0001g0112 others(8): Show |
12 | HG00597.hp1 HG02074.hp1 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.867+3622A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95499720 | |||||||
| chr12:95499833 | G | A | 10 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(7): Show |
10 | HG01192.hp1 HG01433.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.867+3735G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95499833 | |||||||
| chr12:95499855 | T | C | 1 | a0001c0001t0001g0347 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.867+3757T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95499855 | |||||||
| chr12:95499868 | G | A | 5 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.867+3770G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95499868 | |||||||
| chr12:95500043 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.867+3945G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95500043 | |||||||
| chr12:95500151 | G | GT | 25 | a0001c0001t0002g0316 a0001c0001t0002g0319 a0001c0001t0002g0320 others(22): Show |
25 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.868-3902dupT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95500151 | ||||||
| chr12:95500231 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.868-3834G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95500231 | |||||||
| chr12:95500300 | T | C | 24 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(21): Show |
24 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.868-3765T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95500300 | |||||||
| chr12:95500403 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.868-3662T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95500403 | |||||||
| chr12:95500471 | T | C | 10 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(7): Show |
10 | HG01192.hp1 HG01433.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.868-3594T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95500471 | |||||||
| chr12:95500527 | C | A | 1 | a0001c0001t0002g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.868-3538C>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95500527 | |||||||
| chr12:95500528 | A | T | 1 | a0001c0001t0002g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.868-3537A>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95500528 | |||||||
| chr12:95500645 | A | T | 11 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0027 others(8): Show |
11 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.868-3420A>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95500645 | |||||||
| chr12:95500802 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.868-3263A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95500802 | |||||||
| chr12:95500805 | A | C | 10 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(7): Show |
10 | HG01192.hp1 HG01433.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.868-3260A>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95500805 | |||||||
| chr12:95500878 | G | A | 1 | a0001c0001t0003g0038 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.868-3187G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95500878 | |||||||
| chr12:95500928 | TGAG | T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0211 a0001c0001t0001g0213 others(37): Show |
43 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.868-3132_868-3130d others(5): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95500928 | ||||||
| chr12:95500957 | G | T | 6 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(3): Show |
6 | HG02055.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.868-3108G>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95500957 | |||||||
| chr12:95501007 | A | AT | 48 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0096 others(45): Show |
48 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.868-3034dupT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95501007 | ||||||
| chr12:95501007 | AT | A | 14 | a0001c0001t0001g0035 a0001c0001t0001g0125 a0001c0001t0001g0146 others(11): Show |
15 | HG01109.hp2 HG01167.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.868-3034delT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95501007 | ||||||
| chr12:95501007 | ATT | A | 116 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(113): Show |
127 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.868-3035_868-3034d others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95501007 | ||||||
| chr12:95501007 | ATTT | A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0162 others(12): Show |
16 | HG00423.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.868-3036_868-3034d others(5): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95501007 | ||||||
| chr12:95501126 | T | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
133 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.868-2939T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95501126 | |||||||
| chr12:95501414 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.868-2651C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95501414 | |||||||
| chr12:95501423 | T | G | 1 | a0001c0001t0002g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.868-2642T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95501423 | |||||||
| chr12:95501444 | G | A | 23 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(20): Show |
23 | HG00099.hp2 HG00741.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.868-2621G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95501444 | |||||||
| chr12:95501445 | C | T | 2 | a0001c0001t0001g0228 a0001c0001t0001g0244 |
2 | NA18944.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.868-2620C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95501445 | |||||||
| chr12:95501462 | A | T | 1 | a0001c0001t0001g0228 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.868-2603A>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95501462 | |||||||
| chr12:95501498 | C | T | 33 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0023 others(30): Show |
37 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.868-2567C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95501498 | |||||||
| chr12:95501530 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0152 |
4 | NA18944.hp1 NA18952.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.868-2535C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95501530 | |||||||
| chr12:95501594 | A | G | 28 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(25): Show |
29 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.868-2471A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95501594 | |||||||
| chr12:95501685 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0147 |
2 | NA19067.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.868-2380A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95501685 | |||||||
| chr12:95501719 | GA | G | 9 | a0001c0001t0001g0128 a0001c0001t0001g0243 a0001c0001t0001g0271 others(6): Show |
9 | HG00597.hp1 HG01256.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.868-2333delA | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95501719 | ||||||
| chr12:95501819 | C | CT | 34 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(31): Show |
35 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.868-2235dupT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95501819 | ||||||
| chr12:95501911 | C | G | 1 | a0001c0001t0005g0275 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.868-2154C>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95501911 | |||||||
| chr12:95501995 | A | AT | 17 | a0001c0001t0001g0084 a0001c0001t0001g0109 a0001c0001t0001g0116 others(14): Show |
17 | HG00621.hp1 HG01192.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.868-2052dupT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95501995 | ||||||
| chr12:95501995 | AT | A | 145 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.868-2052delT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95501995 | ||||||
| chr12:95502148 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.868-1917G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95502148 | |||||||
| chr12:95502172 | T | C | 1 | a0001c0001t0001g0347 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.868-1893T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95502172 | |||||||
| chr12:95502276 | G | T | 2 | a0001c0002t0001g0013 a0001c0002t0001g0193 |
3 | HG02132.hp1 HG02523.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.868-1789G>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95502276 | |||||||
| chr12:95502315 | T | C | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-1750T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95502315 | |||||||
| chr12:95502389 | A | C | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-1676A>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95502389 | |||||||
| chr12:95502416 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.868-1649T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95502416 | |||||||
| chr12:95502421 | A | C | 1 | a0001c0001t0001g0240 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.868-1644A>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95502421 | |||||||
| chr12:95502447 | G | A | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.868-1618G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95502447 | |||||||
| chr12:95502547 | T | A | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-1518T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95502547 | |||||||
| chr12:95502553 | T | G | 109 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(106): Show |
116 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.868-1512T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95502553 | |||||||
| chr12:95502596 | C | T | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-1469C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95502596 | |||||||
| chr12:95502642 | C | T | 6 | a0001c0001t0001g0115 a0001c0001t0001g0120 a0001c0001t0001g0129 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.868-1423C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95502642 | |||||||
| chr12:95502812 | C | CT | 43 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(40): Show |
48 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.868-1245dupT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95502812 | ||||||
| chr12:95502871 | C | T | 22 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(19): Show |
22 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.868-1194C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95502871 | |||||||
| chr12:95502916 | A | G | 10 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(7): Show |
10 | HG01192.hp1 HG01433.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.868-1149A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95502916 | |||||||
| chr12:95502926 | T | C | 12 | a0001c0002t0001g0013 a0001c0002t0001g0170 a0001c0002t0001g0171 others(9): Show |
13 | HG02015.hp1 HG02074.hp2 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.868-1139T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95502926 | |||||||
| chr12:95502949 | A | AT | 157 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
169 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.868-1102dupT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95502949 | ||||||
| chr12:95502949 | A | ATT | 33 | a0001c0001t0001g0211 a0001c0001t0001g0276 a0001c0001t0001g0345 others(30): Show |
33 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.868-1103_868-1102d others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95502949 | ||||||
| chr12:95502949 | AT | A | 12 | a0001c0002t0001g0177 a0001c0002t0001g0184 a0001c0003t0001g0066 others(9): Show |
12 | HG00621.hp1 HG01192.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.868-1102delT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 95502949 | ||||||
| chr12:95503003 | T | A | 1 | a0001c0001t0001g0283 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.868-1062T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95503003 | |||||||
| chr12:95503034 | G | A | 66 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(63): Show |
67 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.868-1031G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95503034 | |||||||
| chr12:95503038 | G | C | 1 | a0001c0001t0001g0136 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.868-1027G>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95503038 | |||||||
| chr12:95503053 | G | T | 264 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(261): Show |
282 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.868-1012G>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95503053 | |||||||
| chr12:95503149 | A | G | 10 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(7): Show |
10 | HG01192.hp1 HG01433.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.868-916A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95503149 | |||||||
| chr12:95503338 | C | T | 1 | a0001c0002t0001g0204 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.868-727C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95503338 | |||||||
| chr12:95503533 | G | A | 2 | a0001c0002t0001g0039 a0001c0002t0001g0203 |
2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.868-532G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95503533 | |||||||
| chr12:95503572 | G | A | 10 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(7): Show |
10 | HG01192.hp1 HG01433.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.868-493G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95503572 | |||||||
| chr12:95503671 | C | T | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.868-394C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95503671 | |||||||
| chr12:95503839 | A | G | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.868-226A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95503839 | |||||||
| chr12:95503877 | G | T | 1 | a0001c0002t0001g0023 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.868-188G>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 7/10 | chr12 | 95503877 | |||||||
| chr12:95504221 | T | C | 332 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(329): Show |
359 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.964+60T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95504221 | |||||||
| chr12:95504405 | A | G | 50 | a0001c0001t0001g0003 a0001c0001t0001g0210 a0001c0001t0001g0211 others(47): Show |
53 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.964+244A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95504405 | |||||||
| chr12:95504436 | G | A | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.964+275G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95504436 | |||||||
| chr12:95504549 | C | T | 1 | a0001c0001t0001g0313 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.964+388C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95504549 | |||||||
| chr12:95504550 | G | A | 10 | a0001c0001t0001g0096 a0001c0001t0001g0100 a0001c0001t0001g0101 others(7): Show |
10 | HG00673.hp1 NA18951.hp1 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.964+389G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95504550 | |||||||
| chr12:95504553 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.964+392G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95504553 | |||||||
| chr12:95505223 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.964+1062G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95505223 | |||||||
| chr12:95505282 | C | T | 3 | a0001c0001t0004g0026 a0001c0001t0004g0031 a0001c0001t0004g0032 |
3 | HG00639.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.964+1121C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95505282 | |||||||
| chr12:95505336 | AC | A | 23 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(20): Show |
23 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.964+1176delC | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95505336 | |||||||
| chr12:95505358 | C | T | 1 | a0001c0001t0002g0331 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.964+1197C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95505358 | |||||||
| chr12:95505379 | A | G | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.964+1218A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95505379 | |||||||
| chr12:95505397 | G | A | 10 | a0001c0003t0001g0066 a0001c0003t0001g0067 a0001c0003t0001g0068 others(7): Show |
10 | HG01192.hp1 HG01433.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.964+1236G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95505397 | |||||||
| chr12:95505439 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.964+1278C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95505439 | |||||||
| chr12:95505639 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.964+1478C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95505639 | |||||||
| chr12:95505751 | T | C | 68 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(65): Show |
76 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.964+1590T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95505751 | |||||||
| chr12:95505764 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.964+1603G>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95505764 | |||||||
| chr12:95505777 | G | T | 22 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(19): Show |
22 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.964+1616G>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95505777 | |||||||
| chr12:95505833 | G | A | 5 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.964+1672G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95505833 | |||||||
| chr12:95505937 | AC | A | 12 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0026 others(9): Show |
12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.964+1777delC | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95505937 | |||||||
| chr12:95505938 | C | CA | 7 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(4): Show |
7 | HG02055.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.964+1787dupA | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95505938 | ||||||
| chr12:95505985 | T | C | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.964+1824T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95505985 | |||||||
| chr12:95506012 | A | G | 1 | a0001c0001t0003g0059 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.964+1851A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506012 | |||||||
| chr12:95506152 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.964+1991C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506152 | |||||||
| chr12:95506192 | T | C | 43 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(40): Show |
48 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.964+2031T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506192 | |||||||
| chr12:95506194 | C | A | 23 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(20): Show |
23 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.964+2033C>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506194 | |||||||
| chr12:95506201 | C | G | 1 | a0001c0001t0001g0010 | 2 | HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.964+2040C>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506201 | |||||||
| chr12:95506260 | T | G | 8 | a0001c0001t0001g0079 a0001c0001t0001g0087 a0001c0001t0001g0088 others(5): Show |
8 | HG00642.hp2 HG00735.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.964+2099T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506260 | |||||||
| chr12:95506296 | C | CT | 20 | a0001c0001t0001g0106 a0001c0001t0001g0114 a0001c0001t0001g0139 others(17): Show |
20 | HG00438.hp1 HG01192.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.964+2153dupT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95506296 | ||||||
| chr12:95506296 | CT | C | 31 | a0001c0001t0001g0121 a0001c0001t0001g0141 a0001c0001t0001g0229 others(28): Show |
32 | HG00099.hp2 HG01169.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.964+2153delT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95506296 | ||||||
| chr12:95506310 | T | C | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+2149T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506310 | |||||||
| chr12:95506336 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.964+2175G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506336 | |||||||
| chr12:95506435 | T | C | 1 | a0001c0001t0002g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.964+2274T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506435 | |||||||
| chr12:95506451 | T | A | 1 | a0001c0001t0018g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.964+2290T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506451 | |||||||
| chr12:95506501 | A | G | 1 | a0001c0006t0001g0342 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.964+2340A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506501 | |||||||
| chr12:95506541 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
133 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.964+2380C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506541 | |||||||
| chr12:95506792 | A | ATATT | 11 | a0001c0001t0001g0011 a0001c0001t0001g0162 a0001c0001t0001g0207 others(8): Show |
12 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.964+2633_964+2634i others(6): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95506792 | ||||||
| chr12:95506792 | A | ATATTTAT others(5): Show |
1 | a0001c0001t0001g0167 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.964+2633_964+2634i others(14): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95506792 | ||||||
| chr12:95506795 | C | CTTAT | 14 | a0001c0001t0001g0014 a0001c0001t0001g0109 a0001c0001t0001g0119 others(11): Show |
15 | HG00558.hp1 HG00639.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.964+2664_964+2667d others(6): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95506795 | ||||||
| chr12:95506795 | C | CTTATTTA others(1): Show |
114 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
124 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.964+2660_964+2667d others(10): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95506795 | ||||||
| chr12:95506795 | C | CTTATTTA others(5): Show |
48 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0215 others(45): Show |
53 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.964+2656_964+2667d others(14): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95506795 | ||||||
| chr12:95506795 | C | CTTATTTA others(9): Show |
30 | a0001c0001t0002g0320 a0001c0001t0002g0321 a0001c0001t0002g0322 others(27): Show |
30 | HG00099.hp2 HG01192.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.964+2652_964+2667d others(18): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95506795 | ||||||
| chr12:95506795 | C | CTTATTTA others(13): Show |
3 | a0001c0001t0002g0333 a0001c0002t0001g0012 a0001c0002t0001g0200 |
4 | HG01515.hp1 HG01517.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2648_964+2667d others(22): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95506795 | ||||||
| chr12:95506795 | C | CTTATTTA others(17): Show |
1 | a0001c0002t0001g0181 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.964+2644_964+2667d others(26): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95506795 | ||||||
| chr12:95506795 | C | CTTCT | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0015g0344 |
3 | HG02647.hp1 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.964+2636_964+2637i others(6): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95506795 | ||||||
| chr12:95506795 | C | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0162 others(11): Show |
15 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.964+2634C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506795 | |||||||
| chr12:95506889 | A | G | 7 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0176 others(4): Show |
7 | HG00438.hp2 NA18962.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.964+2728A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506889 | |||||||
| chr12:95506903 | C | G | 1 | a0001c0001t0001g0211 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.964+2742C>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506903 | |||||||
| chr12:95506907 | C | T | 12 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0026 others(9): Show |
12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.964+2746C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506907 | |||||||
| chr12:95506922 | A | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0162 others(12): Show |
16 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.964+2761A>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506922 | |||||||
| chr12:95506936 | T | C | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.964+2775T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506936 | |||||||
| chr12:95506957 | C | CT | 12 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0026 others(9): Show |
12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.964+2806dupT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95506957 | ||||||
| chr12:95506985 | A | C | 1 | a0001c0002t0001g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.964+2824A>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506985 | |||||||
| chr12:95506999 | A | G | 1 | a0001c0001t0005g0275 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.964+2838A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95506999 | |||||||
| chr12:95507061 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.964+2900C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95507061 | |||||||
| chr12:95507107 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
133 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.964+2946G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95507107 | |||||||
| chr12:95507164 | G | C | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+3003G>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95507164 | |||||||
| chr12:95507189 | A | C | 12 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0026 others(9): Show |
12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.964+3028A>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95507189 | |||||||
| chr12:95507367 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0092 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.964+3206T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95507367 | |||||||
| chr12:95507372 | G | A | 3 | a0001c0001t0001g0109 a0001c0001t0001g0119 a0001c0001t0001g0147 |
3 | NA18956.hp1 NA19067.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.964+3211G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95507372 | |||||||
| chr12:95507422 | C | T | 1 | a0001c0002t0001g0200 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.964+3261C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95507422 | |||||||
| chr12:95507487 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.964+3326G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95507487 | |||||||
| chr12:95507579 | T | A | 1 | a0001c0001t0002g0327 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.964+3418T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95507579 | |||||||
| chr12:95507614 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG02451.hp2 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.964+3453G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95507614 | |||||||
| chr12:95507658 | C | A | 9 | a0001c0003t0001g0067 a0001c0003t0001g0068 a0001c0003t0001g0069 others(6): Show |
9 | HG01433.hp2 HG01516.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.964+3497C>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95507658 | |||||||
| chr12:95507693 | C | G | 24 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(21): Show |
24 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.964+3532C>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95507693 | |||||||
| chr12:95507758 | A | T | 264 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(261): Show |
282 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.964+3597A>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95507758 | |||||||
| chr12:95507765 | A | G | 2 | a0001c0001t0002g0321 a0001c0001t0002g0323 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.964+3604A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95507765 | |||||||
| chr12:95507777 | A | AT | 40 | a0001c0001t0001g0086 a0001c0001t0001g0109 a0001c0001t0001g0111 others(37): Show |
40 | HG00099.hp2 HG00733.hp2 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.964+3632dupT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95507777 | ||||||
| chr12:95507861 | C | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0217 a0001c0001t0001g0225 others(4): Show |
7 | NA18747.hp2 NA18944.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.964+3700C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95507861 | |||||||
| chr12:95507932 | G | A | 1 | a0001c0001t0003g0065 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.964+3771G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95507932 | |||||||
| chr12:95507940 | A | AT | 14 | a0001c0001t0001g0022 a0001c0001t0001g0100 a0001c0001t0001g0109 others(11): Show |
14 | HG00673.hp1 HG01255.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.964+3801dupT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95507940 | ||||||
| chr12:95507940 | A | ATTT | 12 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0026 others(9): Show |
12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.964+3799_964+3801d others(5): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95507940 | ||||||
| chr12:95507940 | AT | A | 47 | a0001c0001t0001g0017 a0001c0001t0001g0119 a0001c0001t0001g0130 others(44): Show |
48 | HG00099.hp2 HG00741.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.964+3801delT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95507940 | ||||||
| chr12:95507980 | T | C | 3 | a0001c0002t0001g0169 a0001c0002t0001g0195 a0001c0002t0001g0196 |
3 | NA18987.hp2 NA19006.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.964+3819T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95507980 | |||||||
| chr12:95507996 | G | A | 5 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(2): Show |
5 | HG02055.hp1 HG02647.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.964+3835G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95507996 | |||||||
| chr12:95508036 | C | T | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.965-3859C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95508036 | |||||||
| chr12:95508070 | C | T | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.965-3825C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95508070 | |||||||
| chr12:95508170 | A | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(138): Show |
153 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.965-3725A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95508170 | |||||||
| chr12:95508177 | T | G | 1 | a0001c0001t0002g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.965-3718T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95508177 | |||||||
| chr12:95508262 | A | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0085 |
3 | HG01074.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.965-3633A>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95508262 | |||||||
| chr12:95508279 | C | G | 1 | a0001c0001t0003g0054 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.965-3616C>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95508279 | |||||||
| chr12:95508464 | T | C | 1 | a0001c0006t0001g0342 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.965-3431T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95508464 | |||||||
| chr12:95508703 | C | A | 27 | a0001c0001t0002g0020 a0001c0001t0002g0316 a0001c0001t0002g0317 others(24): Show |
28 | HG00099.hp2 HG01496.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.965-3192C>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95508703 | |||||||
| chr12:95508718 | T | TG | 5 | a0001c0001t0001g0080 a0001c0001t0001g0086 a0001c0001t0001g0111 others(2): Show |
5 | HG01099.hp2 HG01123.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.965-3175dupG | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95508718 | ||||||
| chr12:95508780 | G | A | 1 | a0001c0001t0013g0343 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.965-3115G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95508780 | |||||||
| chr12:95508948 | CATG | C | 22 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(19): Show |
22 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.965-2944_965-2942d others(5): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95508948 | ||||||
| chr12:95509016 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG00140.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.965-2879A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95509016 | |||||||
| chr12:95509193 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.965-2702G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95509193 | |||||||
| chr12:95509356 | A | G | 26 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(23): Show |
26 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.965-2539A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95509356 | |||||||
| chr12:95509475 | T | C | 27 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.965-2420T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95509475 | |||||||
| chr12:95509555 | G | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
133 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.965-2340G>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95509555 | |||||||
| chr12:95509599 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.965-2296G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95509599 | |||||||
| chr12:95509658 | A | G | 1 | a0001c0001t0001g0312 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.965-2237A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95509658 | |||||||
| chr12:95509758 | A | G | 1 | a0001c0001t0018g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.965-2137A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95509758 | |||||||
| chr12:95509767 | C | T | 262 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
280 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.965-2128C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95509767 | |||||||
| chr12:95509836 | T | TCCC | 30 | a0001c0001t0003g0038 a0001c0001t0003g0041 a0001c0001t0003g0042 others(27): Show |
30 | HG00639.hp1 HG00639.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.965-2054_965-2052d others(5): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95509836 | ||||||
| chr12:95509841 | C | CT | 2 | a0001c0001t0002g0020 a0001c0001t0002g0318 |
3 | HG01884.hp2 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.965-2054_965-2053i others(3): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95509841 | |||||||
| chr12:95509842 | C | T | 1 | a0001c0001t0002g0317 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.965-2053C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95509842 | |||||||
| chr12:95509843 | CA | C | 22 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(19): Show |
22 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.965-2050delA | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95509843 | ||||||
| chr12:95509844 | A | C | 41 | a0001c0001t0002g0316 a0001c0001t0002g0317 a0001c0001t0003g0038 others(38): Show |
41 | HG00639.hp1 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.965-2051A>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95509844 | |||||||
| chr12:95509845 | A | C | 5 | a0001c0001t0002g0020 a0001c0001t0002g0318 a0001c0001t0003g0063 others(2): Show |
6 | HG01884.hp2 HG02717.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.965-2050A>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95509845 | |||||||
| chr12:95509846 | C | CCA | 3 | a0001c0001t0003g0063 a0001c0001t0004g0026 a0001c0001t0004g0028 |
3 | HG02717.hp2 HG02965.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.965-2048_965-2047i others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95509846 | ||||||
| chr12:95509847 | C | CT | 17 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0093 others(14): Show |
18 | HG01978.hp1 HG02071.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.965-2029dupT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95509847 | ||||||
| chr12:95509847 | C | T | 3 | a0001c0001t0001g0143 a0001c0001t0002g0020 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-2048C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95509847 | |||||||
| chr12:95509847 | CT | C | 8 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0130 others(5): Show |
8 | HG01975.hp2 NA18956.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.965-2029delT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95509847 | ||||||
| chr12:95509848 | T | C | 3 | a0001c0001t0003g0063 a0001c0001t0004g0026 a0001c0001t0004g0028 |
3 | HG02717.hp2 HG02965.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.965-2047T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95509848 | |||||||
| chr12:95509877 | C | T | 41 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0003g0038 others(38): Show |
41 | HG00639.hp1 HG00639.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.965-2018C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95509877 | |||||||
| chr12:95509888 | G | A | 38 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(35): Show |
38 | HG00639.hp1 HG00639.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.965-2007G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95509888 | |||||||
| chr12:95509994 | G | A | 1 | a0001c0001t0018g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.965-1901G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95509994 | |||||||
| chr12:95510129 | A | G | 15 | a0001c0001t0001g0011 a0001c0001t0001g0092 a0001c0001t0001g0157 others(12): Show |
16 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.965-1766A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95510129 | |||||||
| chr12:95510199 | G | C | 22 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 others(19): Show |
22 | HG00099.hp2 HG01496.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.965-1696G>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95510199 | |||||||
| chr12:95510221 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.965-1674G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95510221 | |||||||
| chr12:95510250 | T | G | 1 | a0001c0001t0013g0343 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.965-1645T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95510250 | |||||||
| chr12:95510274 | G | C | 1 | a0001c0001t0018g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.965-1621G>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95510274 | |||||||
| chr12:95510383 | A | C | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.965-1512A>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95510383 | |||||||
| chr12:95510413 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.965-1482C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95510413 | |||||||
| chr12:95510484 | T | G | 1 | a0001c0001t0004g0353 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.965-1411T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95510484 | |||||||
| chr12:95510572 | G | C | 1 | a0001c0001t0013g0343 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.965-1323G>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95510572 | |||||||
| chr12:95510821 | T | C | 2 | a0001c0001t0001g0279 a0001c0001t0002g0316 |
2 | HG02258.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.965-1074T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95510821 | |||||||
| chr12:95510917 | T | A | 1 | a0001c0001t0001g0312 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.965-978T>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95510917 | |||||||
| chr12:95510969 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.965-926A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95510969 | |||||||
| chr12:95510972 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.965-923C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95510972 | |||||||
| chr12:95511036 | C | T | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0001g0347 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-859C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95511036 | |||||||
| chr12:95511089 | G | A | 27 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.965-806G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95511089 | |||||||
| chr12:95511308 | G | GTACCTCC others(3): Show |
1 | a0001c0001t0002g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.965-576_965-567dup others(10): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95511308 | ||||||
| chr12:95511389 | G | GT | 100 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0035 others(97): Show |
104 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.965-482dupT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95511389 | ||||||
| chr12:95511389 | G | GTT | 65 | a0001c0001t0001g0016 a0001c0001t0001g0097 a0001c0001t0001g0160 others(62): Show |
66 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.965-483_965-482dup others(2): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95511389 | ||||||
| chr12:95511389 | G | GTTT | 49 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(46): Show |
56 | HG00408.hp1 HG00621.hp2 HG01175.hp1 others(53): Show |
intron_variant | MODIFIER | c.965-484_965-482dup others(3): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95511389 | ||||||
| chr12:95511389 | G | GTTTT | 10 | a0001c0001t0001g0022 a0001c0001t0001g0217 a0001c0001t0001g0219 others(7): Show |
10 | HG00558.hp1 HG01981.hp2 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.965-485_965-482dup others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95511389 | ||||||
| chr12:95511389 | GT | G | 19 | a0001c0001t0001g0118 a0001c0001t0002g0020 a0001c0001t0002g0316 others(16): Show |
21 | HG00280.hp2 HG01109.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.965-482delT | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 95511389 | ||||||
| chr12:95511401 | T | G | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-494T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95511401 | |||||||
| chr12:95511588 | C | T | 9 | a0001c0003t0001g0067 a0001c0003t0001g0068 a0001c0003t0001g0069 others(6): Show |
9 | HG01433.hp2 HG01516.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.965-307C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95511588 | |||||||
| chr12:95511590 | C | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0111 a0001c0001t0001g0122 |
3 | HG01123.hp1 HG01261.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.965-305C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95511590 | |||||||
| chr12:95511611 | C | T | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-284C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95511611 | |||||||
| chr12:95511612 | G | A | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.965-283G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95511612 | |||||||
| chr12:95511625 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.965-270C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95511625 | |||||||
| chr12:95511795 | G | A | 1 | a0001c0001t0002g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.965-100G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95511795 | |||||||
| chr12:95511829 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.965-66T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 8/10 | chr12 | 95511829 | |||||||
| chr12:95512046 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1068+48T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 9/10 | chr12 | 95512046 | |||||||
| chr12:95512065 | T | C | 1 | a0001c0001t0018g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1068+67T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 9/10 | chr12 | 95512065 | |||||||
| chr12:95512159 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1068+161A>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 9/10 | chr12 | 95512159 | |||||||
| chr12:95512223 | T | G | 5 | a0001c0001t0002g0331 a0001c0001t0002g0334 a0001c0001t0002g0335 others(2): Show |
5 | HG00099.hp2 HG03704.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068+225T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 9/10 | chr12 | 95512223 | |||||||
| chr12:95512255 | C | A | 1 | a0001c0001t0001g0080 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1068+257C>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 9/10 | chr12 | 95512255 | |||||||
| chr12:95512295 | T | G | 7 | a0001c0001t0002g0321 a0001c0001t0002g0323 a0001c0001t0002g0326 others(4): Show |
7 | HG02717.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1068+297T>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 9/10 | chr12 | 95512295 | |||||||
| chr12:95512316 | A | T | 1 | a0001c0001t0018g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1068+318A>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 9/10 | chr12 | 95512316 | |||||||
| chr12:95512317 | C | G | 1 | a0001c0001t0018g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1068+319C>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 9/10 | chr12 | 95512317 | |||||||
| chr12:95512320 | A | T | 1 | a0001c0001t0018g0341 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1068+322A>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 9/10 | chr12 | 95512320 | |||||||
| chr12:95512363 | C | T | 1 | a0001c0001t0001g0351 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1068+365C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 9/10 | chr12 | 95512363 | |||||||
| chr12:95512435 | G | C | 2 | a0001c0001t0001g0267 a0001c0001t0001g0273 |
2 | NA18747.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1069-366G>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 9/10 | chr12 | 95512435 | |||||||
| chr12:95512456 | C | T | 5 | a0001c0001t0001g0260 a0001c0001t0001g0262 a0001c0001t0001g0268 others(2): Show |
5 | HG00423.hp1 HG00558.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069-345C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 9/10 | chr12 | 95512456 | |||||||
| chr12:95512627 | G | A | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069-174G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 9/10 | chr12 | 95512627 | |||||||
| chr12:95512685 | C | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02258.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1069-116C>G | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 9/10 | chr12 | 95512685 | |||||||
| chr12:95513065 | T | C | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+149T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | chr12 | 95513065 | |||||||
| chr12:95513090 | T | TAC | 69 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0021 others(66): Show |
74 | HG00099.hp1 HG00597.hp2 HG01074.hp2 others(71): Show |
intron_variant | MODIFIER | c.1184+216_1184+217d others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 95513090 | ||||||
| chr12:95513090 | T | TACAC | 37 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0014 others(34): Show |
42 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1184+214_1184+217d others(6): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 95513090 | ||||||
| chr12:95513090 | T | TACACAC | 30 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0035 others(27): Show |
31 | HG00423.hp1 HG00673.hp2 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.1184+212_1184+217d others(8): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 95513090 | ||||||
| chr12:95513090 | T | TACACACA others(1): Show |
22 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0158 others(19): Show |
23 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.1184+210_1184+217d others(10): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 95513090 | ||||||
| chr12:95513090 | T | TACACACA others(3): Show |
11 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0250 others(8): Show |
11 | HG00733.hp1 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1184+208_1184+217d others(12): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 95513090 | ||||||
| chr12:95513090 | T | TACACACA others(5): Show |
7 | a0001c0001t0001g0259 a0001c0001t0001g0285 a0001c0001t0001g0296 others(4): Show |
7 | HG00639.hp2 HG01069.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+206_1184+217d others(14): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 95513090 | ||||||
| chr12:95513090 | T | TACACACA others(7): Show |
1 | a0001c0001t0001g0286 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1184+204_1184+217d others(16): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 95513090 | ||||||
| chr12:95513090 | T | TACACACA others(9): Show |
5 | a0001c0001t0001g0003 a0001c0001t0001g0263 a0001c0001t0001g0282 others(2): Show |
8 | HG01071.hp2 HG01099.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.1184+202_1184+217d others(18): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 95513090 | ||||||
| chr12:95513090 | T | TACACACA others(13): Show |
1 | a0001c0001t0001g0288 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1184+198_1184+217d others(22): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 95513090 | ||||||
| chr12:95513090 | TAC | T | 23 | a0001c0001t0001g0086 a0001c0001t0001g0091 a0001c0001t0001g0093 others(20): Show |
24 | HG00280.hp2 HG00423.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1184+216_1184+217d others(4): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 95513090 | ||||||
| chr12:95513090 | TACAC | T | 26 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0116 others(23): Show |
28 | HG00639.hp1 HG01192.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+214_1184+217d others(6): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 95513090 | ||||||
| chr12:95513090 | TACACAC | T | 10 | a0001c0001t0002g0331 a0001c0001t0002g0334 a0001c0001t0002g0335 others(7): Show |
10 | HG00099.hp2 HG01928.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1184+212_1184+217d others(8): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 95513090 | ||||||
| chr12:95513090 | TACACACA others(1): Show |
T | 30 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 others(27): Show |
35 | HG00438.hp2 HG00621.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1184+210_1184+217d others(10): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 95513090 | ||||||
| chr12:95513090 | TACACACA others(3): Show |
T | 2 | a0001c0002t0001g0186 a0001c0002t0001g0205 |
2 | NA19056.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1184+208_1184+217d others(12): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 95513090 | ||||||
| chr12:95513090 | TACACACA others(5): Show |
T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0167 |
2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1184+206_1184+217d others(14): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 95513090 | ||||||
| chr12:95513090 | TACACACA others(7): Show |
T | 1 | a0001c0001t0003g0059 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1184+204_1184+217d others(16): Show |
METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 95513090 | ||||||
| chr12:95513150 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0243 |
2 | HG01256.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1184+234C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | chr12 | 95513150 | |||||||
| chr12:95513220 | T | C | 264 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(261): Show |
282 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1184+304T>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | chr12 | 95513220 | |||||||
| chr12:95513326 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1185-326G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | chr12 | 95513326 | |||||||
| chr12:95513411 | C | T | 1 | a0001c0002t0001g0172 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1185-241C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | chr12 | 95513411 | |||||||
| chr12:95513417 | C | T | 27 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1185-235C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | chr12 | 95513417 | |||||||
| chr12:95513434 | A | C | 1 | a0001c0001t0007g0256 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1185-218A>C | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | chr12 | 95513434 | |||||||
| chr12:95513492 | G | A | 3 | a0001c0001t0002g0020 a0001c0001t0002g0317 a0001c0001t0002g0318 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-160G>A | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | chr12 | 95513492 | |||||||
| chr12:95513614 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0118 |
2 | HG01346.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1185-38C>T | METAP2 | ENSG00000111142.14 | transcript | ENST00000323666.10 | protein_coding | 10/10 | chr12 | 95513614 |