Search by Gene
| Item | Value |
|---|---|
| geneid | 401138 |
| ensemblid | ENSG00000187689.10 |
| hgncid | 33188 |
| symbol | AMTN |
| name | amelotin |
| refseq_nuc | NM_212557.4 |
| refseq_prot | NP_997722.1 |
| ensembl_nuc | ENST00000339336.9 |
| ensembl_prot | ENSP00000341013.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 70518569 |
| end | 70532743 |
| strand | + |
| ver | v1.2 |
| region | chr4:70518569-70532743 |
| region5000 | chr4:70513569-70537743 |
| regionname0 | AMTN_chr4_70518569_70532743 |
| regionname5000 | AMTN_chr4_70513569_70537743 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 209 | 314 | 82 | 62 | 129 | 11 | 28 | AMTN_chr4_70513569_70537743 | AMTN | MRSTI others(204): Show |
chr4 | 70513569 | 70537743 |
| a0002 | 0/0 | 209 | 67 | 2 | 7 | 44 | 3 | 11 | AMTN_chr4_70513569_70537743 | AMTN | MRSTI others(204): Show |
chr4 | 70513569 | 70537743 |
| a0003 | 0/0 | 209 | 58 | 0 | 5 | 47 | 1 | 5 | AMTN_chr4_70513569_70537743 | AMTN | MRSTI others(204): Show |
chr4 | 70513569 | 70537743 |
| a0004 | 0/0 | 209 | 8 | 6 | 1 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | MRSTI others(204): Show |
chr4 | 70513569 | 70537743 |
| a0005 | 0/0 | 209 | 3 | 2 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | MRSTI others(204): Show |
chr4 | 70513569 | 70537743 |
| a0006 | 0/0 | 209 | 2 | 0 | 0 | 0 | 1 | 1 | AMTN_chr4_70513569_70537743 | AMTN | MRSTI others(204): Show |
chr4 | 70513569 | 70537743 |
| a0007 | 0/0 | 209 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | MRSTI others(204): Show |
chr4 | 70513569 | 70537743 |
| a0008 | 0/0 | 209 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | MRSTI others(204): Show |
chr4 | 70513569 | 70537743 |
| a0009 | 0/0 | 209 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | MRSTI others(204): Show |
chr4 | 70513569 | 70537743 |
| a0010 | 0/0 | 209 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | MRSTI others(204): Show |
chr4 | 70513569 | 70537743 |
| a0011 | 0/0 | 209 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | MRSTI others(204): Show |
chr4 | 70513569 | 70537743 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 627 | 193 | 63 | 25 | 82 | 8 | 14 | AMTN_chr4_70513569_70537743 | AMTN | ATGAG others(622): Show |
chr4 | 70513569 | 70537743 | ||
| a0001c0002 | 0/1 | 627 | 121 | 19 | 37 | 47 | 3 | 14 | AMTN_chr4_70513569_70537743 | AMTN | ATGAG others(622): Show |
chr4 | 70513569 | 70537743 | ||
| a0002c0003 | 0/0 | 627 | 67 | 2 | 7 | 44 | 3 | 11 | AMTN_chr4_70513569_70537743 | AMTN | ATGAG others(622): Show |
chr4 | 70513569 | 70537743 | ||
| a0003c0004 | 0/0 | 627 | 57 | 0 | 5 | 46 | 1 | 5 | AMTN_chr4_70513569_70537743 | AMTN | ATGAG others(622): Show |
chr4 | 70513569 | 70537743 | ||
| a0003c0009 | 0/0 | 627 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | ATGAG others(622): Show |
chr4 | 70513569 | 70537743 | ||
| a0004c0005 | 0/0 | 627 | 8 | 6 | 1 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | ATGAG others(622): Show |
chr4 | 70513569 | 70537743 | ||
| a0005c0006 | 0/0 | 627 | 3 | 2 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | ATGAG others(622): Show |
chr4 | 70513569 | 70537743 | ||
| a0006c0008 | 0/0 | 627 | 2 | 0 | 0 | 0 | 1 | 1 | AMTN_chr4_70513569_70537743 | AMTN | ATGAG others(622): Show |
chr4 | 70513569 | 70537743 | ||
| a0007c0007 | 0/0 | 627 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | ATGAG others(622): Show |
chr4 | 70513569 | 70537743 | ||
| a0008c0012 | 0/0 | 627 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | ATGAG others(622): Show |
chr4 | 70513569 | 70537743 | ||
| a0009c0010 | 0/0 | 627 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | ATGAG others(622): Show |
chr4 | 70513569 | 70537743 | ||
| a0010c0011 | 0/0 | 627 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | ATGAG others(622): Show |
chr4 | 70513569 | 70537743 | ||
| a0011c0013 | 0/0 | 627 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | ATGAG others(622): Show |
chr4 | 70513569 | 70537743 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1009 | 105 | 47 | 14 | 29 | 4 | 11 | AMTN_chr4_70513569_70537743 | AMTN | ATTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| a0001c0001t0002 | 1/0 | 1009 | 71 | 1 | 9 | 53 | 4 | 3 | AMTN_chr4_70513569_70537743 | AMTN | ATTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| a0001c0001t0003 | 0/0 | 1009 | 15 | 13 | 2 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | ACTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| a0001c0001t0004 | 0/0 | 1009 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | ATTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| a0001c0002t0001 | 0/1 | 1009 | 120 | 19 | 36 | 47 | 3 | 14 | AMTN_chr4_70513569_70537743 | AMTN | ATTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| a0001c0002t0006 | 0/0 | 1009 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | ATTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| a0002c0003t0001 | 0/0 | 1009 | 66 | 2 | 7 | 44 | 3 | 10 | AMTN_chr4_70513569_70537743 | AMTN | ATTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| a0002c0003t0005 | 0/0 | 1009 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | ATTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| a0003c0004t0001 | 0/0 | 1009 | 57 | 0 | 5 | 46 | 1 | 5 | AMTN_chr4_70513569_70537743 | AMTN | ATTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| a0003c0009t0001 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | ATTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| a0004c0005t0001 | 0/0 | 1009 | 7 | 6 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | ATTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| a0004c0005t0002 | 0/0 | 1009 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | ATTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| a0005c0006t0001 | 0/0 | 1009 | 3 | 2 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | ATTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| a0006c0008t0001 | 0/0 | 1009 | 2 | 0 | 0 | 0 | 1 | 1 | AMTN_chr4_70513569_70537743 | AMTN | ATTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| a0007c0007t0002 | 0/0 | 1009 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | ATTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| a0008c0012t0001 | 0/0 | 1009 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | ATTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| a0009c0010t0001 | 0/0 | 1009 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | ATTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| a0010c0011t0002 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | ATTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| a0011c0013t0001 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | ATTGA others(1004): Show |
chr4 | 70513569 | 70537743 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 36 | 6 | 6 | 15 | 3 | 6 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0006 | 0/0 | 13 | 10 | 3 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0014 | 0/0 | 5 | 1 | 0 | 2 | 0 | 2 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0037 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0005 | 0/0 | 18 | 0 | 1 | 16 | 1 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0007 | 0/0 | 12 | 0 | 3 | 9 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0013 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0021 | 1/0 | 4 | 0 | 1 | 0 | 2 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0032 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0036 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0001 | 0/0 | 73 | 7 | 28 | 28 | 3 | 7 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0011 | 0/0 | 6 | 3 | 2 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0015 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0018 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0024 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0073 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0001c0002t0006g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0004 | 0/0 | 18 | 1 | 1 | 14 | 0 | 2 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0008 | 0/0 | 8 | 1 | 0 | 7 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0019 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0026 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0027 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0002c0003t0005g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0003 | 0/0 | 26 | 0 | 0 | 25 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0009 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0034 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0050 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0003c0009t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0004c0005t0001g0035 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0004c0005t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0004c0005t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0004c0005t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0004c0005t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0005c0006t0001g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0005c0006t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0006c0008t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0007c0007t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0007c0007t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0008c0012t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0009c0010t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0010c0011t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| a0011c0013t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | GBR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00099 | hp2 | a0003 | c0004 | t0001 | g0034 | EUR | GBR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | GBR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | GBR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | FIN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0036 | EUR | FIN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00323 | hp2 | a0002 | c0003 | t0001 | g0026 | EUR | FIN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00423 | hp1 | a0002 | c0003 | t0001 | g0076 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00423 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00438 | hp1 | a0003 | c0004 | t0001 | g0009 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00544 | hp2 | a0003 | c0004 | t0001 | g0009 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00597 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00621 | hp1 | a0003 | c0009 | t0001 | g0003 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00642 | hp1 | a0002 | c0003 | t0001 | g0027 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00642 | hp2 | a0003 | c0004 | t0001 | g0050 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00673 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00733 | hp2 | a0002 | c0003 | t0001 | g0085 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00735 | hp1 | a0008 | c0012 | t0001 | g0001 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00735 | hp2 | a0003 | c0004 | t0001 | g0124 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00741 | hp1 | a0003 | c0004 | t0001 | g0049 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01109 | hp2 | a0002 | c0003 | t0001 | g0081 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01168 | hp1 | a0003 | c0004 | t0001 | g0034 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01169 | hp1 | a0003 | c0004 | t0001 | g0034 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01192 | hp1 | a0004 | c0005 | t0001 | g0035 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0068 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01243 | hp1 | a0005 | c0006 | t0001 | g0002 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01255 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01257 | hp1 | a0002 | c0003 | t0001 | g0027 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01261 | hp1 | a0002 | c0003 | t0001 | g0043 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01358 | hp2 | a0009 | c0010 | t0001 | g0069 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0021 | EUR | IBS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01515 | hp2 | a0002 | c0003 | t0001 | g0027 | EUR | IBS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0021 | EUR | IBS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01517 | hp2 | a0002 | c0003 | t0001 | g0019 | EUR | IBS | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01943 | hp1 | a0002 | c0003 | t0001 | g0084 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01981 | hp2 | a0001 | c0002 | t0006 | g0071 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02015 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02027 | hp1 | a0002 | c0003 | t0001 | g0019 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02055 | hp2 | a0010 | c0011 | t0002 | g0117 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02071 | hp2 | a0003 | c0004 | t0001 | g0009 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02074 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02080 | hp2 | a0002 | c0003 | t0001 | g0012 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02083 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02129 | hp2 | a0002 | c0003 | t0001 | g0079 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02132 | hp2 | a0002 | c0003 | t0001 | g0008 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02135 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02155 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | CDX | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02155 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | CDX | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | CDX | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02165 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | CDX | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0088 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0095 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02615 | hp2 | a0005 | c0006 | t0001 | g0014 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02717 | hp1 | a0004 | c0005 | t0001 | g0035 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0094 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02735 | hp1 | a0002 | c0003 | t0001 | g0019 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0018 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02738 | hp2 | a0002 | c0003 | t0001 | g0042 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02818 | hp2 | a0005 | c0006 | t0001 | g0002 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02922 | hp1 | a0004 | c0005 | t0001 | g0051 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02922 | hp2 | a0011 | c0013 | t0001 | g0008 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0089 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03239 | hp2 | a0002 | c0003 | t0001 | g0043 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03453 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03491 | hp2 | a0002 | c0003 | t0001 | g0004 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03492 | hp1 | a0002 | c0003 | t0001 | g0004 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03669 | hp2 | a0004 | c0005 | t0002 | g0118 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0058 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03688 | hp2 | a0003 | c0004 | t0001 | g0050 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03704 | hp2 | a0002 | c0003 | t0001 | g0026 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03710 | hp2 | a0003 | c0004 | t0001 | g0122 | SAS | PJL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03831 | hp1 | a0003 | c0004 | t0001 | g0009 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0080 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03927 | hp1 | a0002 | c0003 | t0001 | g0042 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0074 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03942 | hp1 | a0002 | c0003 | t0001 | g0026 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04115 | hp1 | a0003 | c0004 | t0001 | g0003 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0024 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0018 | SAS | BEB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04199 | hp1 | a0002 | c0003 | t0005 | g0004 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04228 | hp1 | a0002 | c0003 | t0001 | g0078 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG04228 | hp2 | a0006 | c0008 | t0001 | g0045 | SAS | STU | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | CHB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | CHB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | YRI | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18906 | hp2 | a0004 | c0005 | t0001 | g0035 | AFR | YRI | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18941 | hp2 | a0003 | c0004 | t0001 | g0016 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18942 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18943 | hp1 | a0002 | c0003 | t0001 | g0083 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18944 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18946 | hp1 | a0003 | c0004 | t0001 | g0016 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18947 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18949 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18951 | hp1 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18951 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18953 | hp1 | a0002 | c0003 | t0001 | g0077 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18954 | hp1 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18956 | hp1 | a0003 | c0004 | t0001 | g0009 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18957 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18959 | hp1 | a0002 | c0003 | t0001 | g0086 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18961 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18961 | hp2 | a0007 | c0007 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18962 | hp1 | a0003 | c0004 | t0001 | g0009 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18963 | hp1 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18963 | hp2 | a0003 | c0004 | t0001 | g0127 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18965 | hp1 | a0002 | c0003 | t0001 | g0082 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18965 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18969 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18969 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18973 | hp2 | a0007 | c0007 | t0002 | g0031 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18974 | hp1 | a0003 | c0004 | t0001 | g0016 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18975 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18977 | hp1 | a0003 | c0004 | t0001 | g0016 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18978 | hp2 | a0002 | c0003 | t0001 | g0019 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18979 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18982 | hp1 | a0003 | c0004 | t0001 | g0128 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18984 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18986 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18986 | hp2 | a0003 | c0004 | t0001 | g0104 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18987 | hp2 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18988 | hp2 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18989 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18990 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18992 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18994 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18994 | hp2 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18995 | hp1 | a0003 | c0004 | t0001 | g0121 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18995 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18997 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18999 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19000 | hp2 | a0003 | c0004 | t0001 | g0009 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19001 | hp2 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19002 | hp1 | a0003 | c0004 | t0001 | g0123 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19005 | hp2 | a0003 | c0004 | t0001 | g0147 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19007 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19010 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19011 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19012 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | LWK | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19059 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19060 | hp1 | a0002 | c0003 | t0001 | g0044 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19062 | hp2 | a0003 | c0004 | t0001 | g0131 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19063 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19064 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19065 | hp2 | a0003 | c0004 | t0001 | g0016 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19068 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19070 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19072 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19074 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19075 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19075 | hp2 | a0003 | c0004 | t0001 | g0009 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19076 | hp2 | a0003 | c0004 | t0001 | g0103 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19079 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19080 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19080 | hp2 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19082 | hp2 | a0003 | c0004 | t0001 | g0009 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19085 | hp1 | a0002 | c0003 | t0001 | g0008 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19086 | hp1 | a0002 | c0003 | t0001 | g0044 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19086 | hp2 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19088 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19240 | hp1 | a0004 | c0005 | t0001 | g0129 | AFR | YRI | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA19240 | hp2 | a0004 | c0005 | t0001 | g0051 | AFR | YRI | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0008 | AFR | ASW | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ASW | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | TSI | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20805 | hp1 | a0006 | c0008 | t0001 | g0045 | EUR | TSI | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20905 | hp1 | a0003 | c0004 | t0001 | g0049 | SAS | GIH | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | GIH | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | MSL | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | USA | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20300 | hp1 | a0004 | c0005 | t0001 | g0130 | AFR | USA | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | USA | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0073 | REF | REF | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0021 | REF | REF | AMTN_chr4_70513569_70537743 | AMTN | chr4 | 70513569 | 70537743 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70518820 | C | T | 1 | a0002 | 67 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(64): Show |
missense_variant | MODERATE | c.43C>T | p.Arg15Trp | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/9 | 144/1009 | 43/630 | 15/209 | chr4 | 70518820 | |||
| chr4:70518829 | C | T | 1 | a0011 | 1 | HG02922.hp2 | missense_variant&splice_region_variant | MODERATE | c.52C>T | p.Pro18Ser | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/9 | 153/1009 | 52/630 | 18/209 | chr4 | 70518829 | |||
| chr4:70522834 | A | G | 2 | a0003a0006 | 60 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(57): Show |
missense_variant | MODERATE | c.134A>G | p.Asn45Ser | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/9 | 235/1009 | 134/630 | 45/209 | chr4 | 70522834 | |||
| chr4:70523868 | G | T | 1 | a0008 | 1 | HG00735.hp1 | missense_variant&splice_region_variant | MODERATE | c.139G>T | p.Val47Phe | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/9 | 240/1009 | 139/630 | 47/209 | chr4 | 70523868 | |||
| chr4:70523877 | T | C | 1 | a0004 | 8 | HG01192.hp1 HG02717.hp1 HG02922.hp1 others(5): Show |
missense_variant | MODERATE | c.148T>C | p.Ser50Pro | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/9 | 249/1009 | 148/630 | 50/209 | chr4 | 70523877 | |||
| chr4:70524930 | G | A | 1 | a0009 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.263G>A | p.Gly88Glu | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/9 | 364/1009 | 263/630 | 88/209 | chr4 | 70524930 | |||
| chr4:70528753 | G | A | 1 | a0006 | 2 | HG04228.hp2 NA20805.hp1 |
missense_variant | MODERATE | c.325G>A | p.Ala109Thr | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 6/9 | 426/1009 | 325/630 | 109/209 | chr4 | 70528753 | |||
| chr4:70531066 | C | T | 1 | a0010 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.385C>T | p.His129Tyr | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/9 | 486/1009 | 385/630 | 129/209 | chr4 | 70531066 | |||
| chr4:70531193 | G | A | 1 | a0007 | 2 | NA18961.hp2 NA18973.hp2 |
missense_variant | MODERATE | c.512G>A | p.Arg171His | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/9 | 613/1009 | 512/630 | 171/209 | chr4 | 70531193 | |||
| chr4:70531211 | G | T | 1 | a0005 | 3 | HG01243.hp1 HG02615.hp2 HG02818.hp2 |
missense_variant | MODERATE | c.530G>T | p.Gly177Val | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/9 | 631/1009 | 530/630 | 177/209 | chr4 | 70531211 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70518789 | G | A | 1 | a0003c0009 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.12G>A | p.Thr4Thr | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/9 | 113/1009 | 12/630 | 4/209 | chr4 | 70518789 | |||
| chr4:70531272 | C | T | 3 | a0001c0002a0008c0012a0009c0010 | 122 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(119): Show |
synonymous_variant | LOW | c.591C>T | p.Ile197Ile | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/9 | 692/1009 | 591/630 | 197/209 | chr4 | 70531272 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70518570 | T | C | 1 | a0001c0001t0003 | 15 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(12): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-100T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 1/9 | chr4 | 70518570 | |||||||
| chr4:70518615 | G | A | 1 | a0002c0003t0005 | 1 | HG04199.hp1 | 5_prime_UTR_variant | MODIFIER | c.-55G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 1/9 | 163 | chr4 | 70518615 | ||||||
| chr4:70518771 | C | T | 15 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(12): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-7C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/9 | chr4 | 70518771 | |||||||
| chr4:70532504 | G | T | 1 | a0001c0001t0004 | 2 | HG02258.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*39G>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 9/9 | 39 | chr4 | 70532504 | ||||||
| chr4:70532622 | A | C | 1 | a0001c0002t0006 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*157A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 9/9 | 157 | chr4 | 70532622 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:70518739 | A | AGTAACAC others(6): Show |
5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0038others(2): Show | 10 | HG02145.hp2 HG02886.hp1 HG02896.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.-15-21_-15-9dupAAC others(10): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 70518739 | ||||||
| chr4:70518862 | G | A | 28 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(25): Show | 122 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.54+31G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70518862 | |||||||
| chr4:70518896 | C | T | 1 | a0001c0002t0001g0075 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.54+65C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70518896 | |||||||
| chr4:70518922 | GCT | G | 2 | a0001c0001t0003g0055a0001c0001t0003g0148 | 3 | HG01891.hp2 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.54+94_54+95delCT | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70518922 | ||||||
| chr4:70518975 | A | G | 1 | a0001c0002t0001g0074 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.54+144A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70518975 | |||||||
| chr4:70519014 | A | G | 1 | a0003c0004t0001g0147 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.54+183A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519014 | |||||||
| chr4:70519063 | A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.54+232A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519063 | |||||||
| chr4:70519078 | G | A | 25 | a0001c0001t0001g0010a0002c0003t0001g0004a0002c0003t0001g0008others(22): Show | 69 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.54+247G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519078 | |||||||
| chr4:70519123 | G | T | 28 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(25): Show | 122 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.54+292G>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519123 | |||||||
| chr4:70519190 | G | A | 28 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(25): Show | 122 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.54+359G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519190 | |||||||
| chr4:70519217 | G | A | 12 | a0001c0001t0001g0090a0001c0001t0003g0020a0001c0001t0003g0028others(9): Show | 18 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.54+386G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519217 | |||||||
| chr4:70519284 | T | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.54+453T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519284 | |||||||
| chr4:70519319 | A | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.54+488A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519319 | |||||||
| chr4:70519345 | T | C | 12 | a0001c0001t0001g0090a0001c0001t0003g0020a0001c0001t0003g0028others(9): Show | 18 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.54+514T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519345 | |||||||
| chr4:70519380 | C | T | 1 | a0001c0001t0002g0036 | 3 | HG00323.hp1 HG01081.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.54+549C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519380 | |||||||
| chr4:70519409 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.54+578G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519409 | |||||||
| chr4:70519438 | T | C | 3 | a0001c0001t0001g0090a0001c0001t0004g0088a0001c0001t0004g0089 | 3 | HG02258.hp2 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.54+607T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519438 | |||||||
| chr4:70519450 | T | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.54+619T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519450 | |||||||
| chr4:70519473 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.54+642A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519473 | |||||||
| chr4:70519512 | TAAAA | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.54+682_54+685delAA others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519512 | |||||||
| chr4:70519572 | C | A | 1 | a0006c0008t0001g0045 | 2 | HG04228.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.54+741C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519572 | |||||||
| chr4:70519617 | T | C | 12 | a0001c0001t0001g0090a0001c0001t0003g0020a0001c0001t0003g0028others(9): Show | 18 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.54+786T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519617 | |||||||
| chr4:70519698 | A | AT | 11 | a0001c0001t0001g0090a0001c0001t0003g0020a0001c0001t0003g0028others(8): Show | 17 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.54+877dupT | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70519698 | ||||||
| chr4:70519699 | T | TTTTTTTA | 60 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(57): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.54+874_54+875insAT others(5): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70519699 | ||||||
| chr4:70519711 | CT | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.54+889delT | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70519711 | ||||||
| chr4:70519730 | A | C | 7 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0091others(4): Show | 12 | HG01346.hp2 HG01891.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.54+899A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519730 | |||||||
| chr4:70519872 | G | A | 1 | a0001c0002t0001g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.54+1041G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519872 | |||||||
| chr4:70519913 | C | CGT | 26 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0002t0001g0001others(23): Show | 112 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.54+1101_54+1102dup others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70519913 | ||||||
| chr4:70519913 | C | CGTGT | 3 | a0001c0002t0001g0015a0001c0002t0001g0041a0001c0002t0001g0072 | 8 | HG00558.hp1 HG01175.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.54+1099_54+1102dup others(4): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70519913 | ||||||
| chr4:70519913 | CGT | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0101a0001c0001t0001g0102 | 4 | HG02109.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+1101_54+1102del others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70519913 | ||||||
| chr4:70519932 | GTC | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(4): Show | 22 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.54+1103_54+1104del others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70519932 | ||||||
| chr4:70519934 | C | G | 28 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(25): Show | 122 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.54+1103C>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70519934 | |||||||
| chr4:70520010 | AT | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.54+1186delT | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70520010 | ||||||
| chr4:70520075 | T | TAC | 73 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(70): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.54+1245_54+1246ins others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70520075 | ||||||
| chr4:70520137 | T | C | 3 | a0003c0004t0001g0016a0003c0004t0001g0103a0003c0004t0001g0104 | 7 | NA18941.hp2 NA18946.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.54+1306T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520137 | |||||||
| chr4:70520145 | T | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(70): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.54+1314T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520145 | |||||||
| chr4:70520183 | C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.54+1352C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520183 | |||||||
| chr4:70520257 | GAGGCGAC others(7): Show |
G | 1 | a0003c0004t0001g0131 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.54+1427_54+1440del others(14): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520257 | |||||||
| chr4:70520261 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.54+1430C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520261 | |||||||
| chr4:70520311 | C | A | 1 | a0001c0001t0001g0105 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.54+1480C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520311 | |||||||
| chr4:70520311 | C | G | 66 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(63): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.54+1480C>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520311 | |||||||
| chr4:70520352 | G | T | 126 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(123): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.54+1521G>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520352 | |||||||
| chr4:70520374 | A | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.54+1543A>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520374 | |||||||
| chr4:70520458 | C | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.54+1627C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520458 | |||||||
| chr4:70520531 | A | T | 1 | a0003c0004t0001g0131 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.54+1700A>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520531 | |||||||
| chr4:70520560 | C | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.54+1729C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520560 | |||||||
| chr4:70520684 | A | C | 2 | a0001c0001t0003g0055a0001c0001t0003g0148 | 3 | HG01891.hp2 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.54+1853A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520684 | |||||||
| chr4:70520687 | A | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0145 | 3 | NA18941.hp1 NA18998.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.54+1856A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520687 | |||||||
| chr4:70520946 | C | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.55-1809C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70520946 | |||||||
| chr4:70521001 | A | G | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.55-1754A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521001 | |||||||
| chr4:70521119 | C | T | 23 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0018others(20): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.55-1636C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521119 | |||||||
| chr4:70521142 | G | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0101a0001c0001t0001g0102 | 4 | HG02109.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-1613G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521142 | |||||||
| chr4:70521151 | G | C | 12 | a0001c0001t0001g0090a0001c0001t0003g0020a0001c0001t0003g0028others(9): Show | 18 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.55-1604G>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521151 | |||||||
| chr4:70521153 | C | T | 3 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0095 | 8 | HG01891.hp1 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.55-1602C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521153 | |||||||
| chr4:70521173 | G | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.55-1582G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521173 | |||||||
| chr4:70521205 | A | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(70): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.55-1550A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521205 | |||||||
| chr4:70521211 | C | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.55-1544C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521211 | |||||||
| chr4:70521255 | C | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0101a0001c0001t0001g0102 | 4 | HG02109.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-1500C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521255 | |||||||
| chr4:70521302 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.55-1453C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521302 | |||||||
| chr4:70521320 | C | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.55-1435C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521320 | |||||||
| chr4:70521344 | C | T | 1 | a0001c0001t0001g0030 | 3 | HG02630.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.55-1411C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521344 | |||||||
| chr4:70521378 | TA | T | 70 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(67): Show | 232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.55-1361delA | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521378 | ||||||
| chr4:70521415 | G | GAA | 34 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(31): Show | 144 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.55-1333_55-1332dup others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521415 | ||||||
| chr4:70521470 | C | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.55-1285C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521470 | |||||||
| chr4:70521519 | G | A | 7 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0091others(4): Show | 12 | HG01346.hp2 HG01891.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.55-1236G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521519 | |||||||
| chr4:70521525 | G | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(4): Show | 23 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.55-1230G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521525 | |||||||
| chr4:70521604 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.55-1151G>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521604 | |||||||
| chr4:70521640 | C | CT | 10 | a0001c0001t0002g0005a0001c0001t0002g0013a0001c0001t0002g0036others(7): Show | 35 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.55-1079dupT | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | ||||||
| chr4:70521640 | C | CTT | 10 | a0001c0001t0001g0046a0001c0001t0001g0102a0001c0001t0001g0125others(7): Show | 22 | HG00408.hp2 HG00609.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.55-1080_55-1079dup others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | ||||||
| chr4:70521640 | C | CTTT | 5 | a0001c0001t0001g0126a0001c0001t0002g0032a0001c0001t0002g0100others(2): Show | 7 | HG01952.hp2 HG02055.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-1081_55-1079dup others(3): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | ||||||
| chr4:70521640 | C | CTTTTT | 8 | a0002c0003t0001g0008a0002c0003t0001g0012a0002c0003t0001g0026others(5): Show | 24 | HG00323.hp2 HG01192.hp1 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.55-1083_55-1079dup others(5): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | ||||||
| chr4:70521640 | C | CTTTTTT | 8 | a0002c0003t0001g0004a0002c0003t0001g0027a0002c0003t0001g0043others(5): Show | 29 | HG00642.hp1 HG01255.hp2 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.55-1084_55-1079dup others(6): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | ||||||
| chr4:70521640 | C | CTTTTTTT | 6 | a0001c0001t0001g0010a0002c0003t0001g0010a0002c0003t0001g0081others(3): Show | 11 | HG01109.hp2 HG01261.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.55-1085_55-1079dup others(7): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | ||||||
| chr4:70521640 | C | CTTTTTTT others(3): Show |
2 | a0002c0003t0001g0019a0002c0003t0001g0087 | 5 | HG01517.hp2 HG02027.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.55-1088_55-1079dup others(10): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | ||||||
| chr4:70521640 | C | CTTTTTTT others(4): Show |
1 | a0002c0003t0001g0085 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.55-1089_55-1079dup others(11): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | ||||||
| chr4:70521640 | C | T | 1 | a0001c0001t0002g0033 | 3 | NA18948.hp1 NA18985.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.55-1115C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521640 | |||||||
| chr4:70521640 | CTT | C | 6 | a0001c0001t0001g0105a0003c0004t0001g0009a0003c0004t0001g0049others(3): Show | 16 | HG00438.hp1 HG00544.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.55-1080_55-1079del others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | ||||||
| chr4:70521640 | CTTT | C | 11 | a0003c0004t0001g0003a0003c0004t0001g0016a0003c0004t0001g0034others(8): Show | 43 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.55-1081_55-1079del others(3): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | ||||||
| chr4:70521640 | CTTTTT | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0038others(4): Show | 15 | HG02074.hp2 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.55-1083_55-1079del others(5): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | ||||||
| chr4:70521640 | CTTTTTT | C | 27 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0022others(24): Show | 88 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.55-1084_55-1079del others(6): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | ||||||
| chr4:70521640 | CTTTTTTT | C | 7 | a0001c0001t0001g0096a0001c0001t0001g0135a0001c0001t0001g0136others(4): Show | 10 | HG01346.hp2 HG01934.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.55-1085_55-1079del others(7): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | ||||||
| chr4:70521640 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0047 | 2 | NA18987.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.55-1089_55-1079del others(11): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | ||||||
| chr4:70521640 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0090a0001c0001t0004g0088 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.55-1093_55-1079del others(15): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | ||||||
| chr4:70521640 | CTTTTTTT others(9): Show |
C | 3 | a0001c0001t0003g0055a0001c0001t0003g0148a0001c0001t0004g0089 | 4 | HG01891.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.55-1094_55-1079del others(16): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | ||||||
| chr4:70521640 | CTTTTTTT others(10): Show |
C | 4 | a0001c0002t0001g0018a0001c0002t0001g0070a0001c0002t0006g0071others(1): Show | 7 | HG00423.hp1 HG01981.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-1095_55-1079del others(17): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | ||||||
| chr4:70521640 | CTTTTTTT others(11): Show |
C | 25 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(22): Show | 116 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.55-1096_55-1079del others(18): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70521640 | ||||||
| chr4:70521643 | T | C | 1 | a0003c0004t0001g0131 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.55-1112T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521643 | |||||||
| chr4:70521644 | T | C | 5 | a0003c0004t0001g0009a0003c0004t0001g0049a0003c0004t0001g0050others(2): Show | 15 | HG00438.hp1 HG00544.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.55-1111T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521644 | |||||||
| chr4:70521645 | T | C | 12 | a0003c0004t0001g0003a0003c0004t0001g0016a0003c0004t0001g0034others(9): Show | 44 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.55-1110T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521645 | |||||||
| chr4:70521646 | T | C | 6 | a0003c0004t0001g0009a0003c0004t0001g0049a0003c0004t0001g0050others(3): Show | 16 | HG00438.hp1 HG00544.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.55-1109T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521646 | |||||||
| chr4:70521647 | T | C | 16 | a0001c0001t0001g0014a0001c0001t0001g0038a0001c0001t0001g0053others(13): Show | 54 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.55-1108T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521647 | |||||||
| chr4:70521648 | T | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(17): Show | 64 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.55-1107T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521648 | |||||||
| chr4:70521649 | T | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG01934.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.55-1106T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521649 | |||||||
| chr4:70521713 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.55-1042G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521713 | |||||||
| chr4:70521733 | C | G | 5 | a0004c0005t0001g0035a0004c0005t0001g0051a0004c0005t0001g0129others(2): Show | 8 | HG01192.hp1 HG02717.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.55-1022C>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521733 | |||||||
| chr4:70521772 | A | T | 1 | a0003c0004t0001g0131 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.55-983A>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521772 | |||||||
| chr4:70521823 | T | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 147 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.55-932T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521823 | |||||||
| chr4:70521863 | G | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(33): Show | 147 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.55-892G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521863 | |||||||
| chr4:70521867 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.55-888G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521867 | |||||||
| chr4:70521936 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.55-819C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70521936 | |||||||
| chr4:70522009 | G | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.55-746G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522009 | |||||||
| chr4:70522032 | T | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.55-723T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522032 | |||||||
| chr4:70522045 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.55-710A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522045 | |||||||
| chr4:70522121 | G | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(35): Show | 94 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.55-634G>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522121 | |||||||
| chr4:70522189 | C | T | 1 | a0009c0010t0001g0069 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.55-566C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522189 | |||||||
| chr4:70522200 | GA | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(35): Show | 94 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.55-548delA | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70522200 | ||||||
| chr4:70522326 | C | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.55-429C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522326 | |||||||
| chr4:70522327 | G | A | 3 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0095 | 8 | HG01891.hp1 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.55-428G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522327 | |||||||
| chr4:70522333 | G | GC | 38 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(35): Show | 94 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.55-421dupC | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 70522333 | ||||||
| chr4:70522347 | A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.55-408A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522347 | |||||||
| chr4:70522412 | A | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG02896.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.55-343A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522412 | |||||||
| chr4:70522512 | A | G | 28 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(25): Show | 122 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.55-243A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522512 | |||||||
| chr4:70522519 | C | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(70): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.55-236C>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522519 | |||||||
| chr4:70522545 | C | A | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.55-210C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522545 | |||||||
| chr4:70522662 | A | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.55-93A>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522662 | |||||||
| chr4:70522677 | T | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(70): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.55-78T>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 2/8 | chr4 | 70522677 | |||||||
| chr4:70522856 | TGGAACAT others(23): Show |
T | 1 | a0002c0003t0001g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.138+46_138+75delTA others(28): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 70522856 | ||||||
| chr4:70522872 | C | T | 2 | a0001c0001t0004g0088a0001c0001t0004g0089 | 2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.138+34C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70522872 | |||||||
| chr4:70522924 | C | T | 1 | a0002c0003t0001g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.138+86C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70522924 | |||||||
| chr4:70522949 | C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(4): Show | 23 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.138+111C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70522949 | |||||||
| chr4:70522969 | G | T | 1 | a0001c0001t0001g0098 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.138+131G>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70522969 | |||||||
| chr4:70522989 | G | A | 12 | a0001c0001t0001g0090a0001c0001t0003g0020a0001c0001t0003g0028others(9): Show | 18 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.138+151G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70522989 | |||||||
| chr4:70523132 | C | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(70): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.138+294C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523132 | |||||||
| chr4:70523205 | A | T | 18 | a0003c0004t0001g0003a0003c0004t0001g0009a0003c0004t0001g0016others(15): Show | 60 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.138+367A>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523205 | |||||||
| chr4:70523241 | T | G | 1 | a0001c0002t0001g0039 | 2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.138+403T>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523241 | |||||||
| chr4:70523476 | C | T | 1 | a0001c0001t0002g0107 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.139-392C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523476 | |||||||
| chr4:70523513 | C | T | 1 | a0001c0001t0002g0110 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.139-355C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523513 | |||||||
| chr4:70523514 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.139-354G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523514 | |||||||
| chr4:70523548 | C | A | 5 | a0001c0002t0001g0061a0003c0004t0001g0121a0003c0004t0001g0123others(2): Show | 5 | HG01358.hp2 HG01433.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-320C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523548 | |||||||
| chr4:70523629 | C | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(70): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.139-239C>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523629 | |||||||
| chr4:70523665 | G | A | 1 | a0001c0001t0003g0095 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.139-203G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523665 | |||||||
| chr4:70523780 | C | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(35): Show | 94 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.139-88C>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 3/8 | chr4 | 70523780 | |||||||
| chr4:70523940 | G | C | 1 | a0001c0002t0001g0059 | 1 | HG02572.hp2 | splice_region_variant&intron_variant | LOW | c.204+7G>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70523940 | |||||||
| chr4:70523952 | T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(35): Show | 94 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.204+19T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70523952 | |||||||
| chr4:70524059 | C | T | 5 | a0004c0005t0001g0035a0004c0005t0001g0051a0004c0005t0001g0129others(2): Show | 8 | HG01192.hp1 HG02717.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.204+126C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524059 | |||||||
| chr4:70524077 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.204+144G>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524077 | |||||||
| chr4:70524148 | T | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0014others(60): Show | 163 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.204+215T>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524148 | |||||||
| chr4:70524199 | C | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0101a0001c0001t0001g0102 | 4 | HG02109.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+266C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524199 | |||||||
| chr4:70524220 | T | C | 125 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(122): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.204+287T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524220 | |||||||
| chr4:70524352 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.204+419G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524352 | |||||||
| chr4:70524431 | T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.205-441T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524431 | |||||||
| chr4:70524463 | C | T | 7 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0091others(4): Show | 12 | HG01346.hp2 HG01891.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.205-409C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524463 | |||||||
| chr4:70524467 | A | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.205-405A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524467 | |||||||
| chr4:70524499 | T | A | 1 | a0001c0001t0004g0089 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.205-373T>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524499 | |||||||
| chr4:70524604 | C | G | 1 | a0002c0003t0001g0027 | 3 | HG00642.hp1 HG01257.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.205-268C>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524604 | |||||||
| chr4:70524658 | GAA | G | 28 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(25): Show | 122 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.205-211_205-210del others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 70524658 | ||||||
| chr4:70524684 | C | T | 25 | a0001c0001t0001g0010a0002c0003t0001g0004a0002c0003t0001g0008others(22): Show | 69 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.205-188C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524684 | |||||||
| chr4:70524754 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.205-118G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524754 | |||||||
| chr4:70524814 | T | G | 1 | a0001c0001t0002g0111 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.205-58T>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524814 | |||||||
| chr4:70524865 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03540.hp2 | splice_region_variant&intron_variant | LOW | c.205-7C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 4/8 | chr4 | 70524865 | |||||||
| chr4:70525064 | A | G | 7 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0091others(4): Show | 12 | HG01346.hp2 HG01891.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.294+103A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525064 | |||||||
| chr4:70525078 | C | A | 40 | a0001c0001t0001g0090a0001c0001t0003g0020a0001c0001t0003g0028others(37): Show | 140 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.294+117C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525078 | |||||||
| chr4:70525105 | A | G | 12 | a0001c0001t0001g0090a0001c0001t0003g0020a0001c0001t0003g0028others(9): Show | 18 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.294+144A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525105 | |||||||
| chr4:70525174 | T | C | 127 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(124): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.294+213T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525174 | |||||||
| chr4:70525343 | G | A | 4 | a0004c0005t0001g0035a0004c0005t0001g0051a0004c0005t0001g0129others(1): Show | 7 | HG01192.hp1 HG02717.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+382G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525343 | |||||||
| chr4:70525388 | C | T | 12 | a0001c0001t0001g0090a0001c0001t0003g0020a0001c0001t0003g0028others(9): Show | 18 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.294+427C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525388 | |||||||
| chr4:70525389 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.294+428G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525389 | |||||||
| chr4:70525471 | A | T | 1 | a0004c0005t0001g0129 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.294+510A>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525471 | |||||||
| chr4:70525760 | C | A | 1 | a0001c0001t0001g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.294+799C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525760 | |||||||
| chr4:70525760 | C | T | 1 | a0001c0002t0001g0011 | 6 | HG00738.hp1 HG01099.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+799C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525760 | |||||||
| chr4:70525769 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.294+808G>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525769 | |||||||
| chr4:70525939 | T | C | 3 | a0003c0004t0001g0034a0003c0004t0001g0049a0003c0004t0001g0050 | 7 | HG00099.hp2 HG00642.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+978T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525939 | |||||||
| chr4:70525941 | C | T | 1 | a0004c0005t0001g0129 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.294+980C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70525941 | |||||||
| chr4:70526164 | C | T | 1 | a0001c0002t0001g0068 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.294+1203C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526164 | |||||||
| chr4:70526182 | A | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(4): Show | 23 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.294+1221A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526182 | |||||||
| chr4:70526340 | A | C | 25 | a0001c0001t0001g0010a0002c0003t0001g0004a0002c0003t0001g0008others(22): Show | 69 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.294+1379A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526340 | |||||||
| chr4:70526360 | T | C | 1 | a0001c0002t0001g0059 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.294+1399T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526360 | |||||||
| chr4:70526436 | A | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(4): Show | 23 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.294+1475A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526436 | |||||||
| chr4:70526491 | T | A | 4 | a0002c0003t0001g0026a0002c0003t0001g0042a0002c0003t0001g0043others(1): Show | 8 | HG00323.hp2 HG01261.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.294+1530T>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526491 | |||||||
| chr4:70526544 | A | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(70): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.294+1583A>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526544 | |||||||
| chr4:70526588 | C | T | 25 | a0001c0001t0001g0010a0002c0003t0001g0004a0002c0003t0001g0008others(22): Show | 69 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.294+1627C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526588 | |||||||
| chr4:70526800 | C | G | 1 | a0010c0011t0002g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.294+1839C>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526800 | |||||||
| chr4:70526886 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.295-1837C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70526886 | |||||||
| chr4:70527019 | G | A | 2 | a0001c0002t0001g0062a0001c0002t0001g0074 | 2 | HG03927.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.295-1704G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527019 | |||||||
| chr4:70527229 | A | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(70): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.295-1494A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527229 | |||||||
| chr4:70527233 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.295-1490G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527233 | |||||||
| chr4:70527266 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.295-1457C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527266 | |||||||
| chr4:70527277 | GA | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0056a0001c0001t0001g0057 | 5 | HG02886.hp1 HG02896.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-1440delA | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 70527277 | ||||||
| chr4:70527284 | G | T | 4 | a0004c0005t0001g0035a0004c0005t0001g0051a0004c0005t0001g0129others(1): Show | 7 | HG01192.hp1 HG02717.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.295-1439G>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527284 | |||||||
| chr4:70527465 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.295-1258C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527465 | |||||||
| chr4:70527560 | C | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(121): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.295-1163C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527560 | |||||||
| chr4:70527713 | C | T | 7 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0091others(4): Show | 12 | HG01346.hp2 HG01891.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.295-1010C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527713 | |||||||
| chr4:70527727 | T | C | 2 | a0001c0002t0001g0040a0001c0002t0001g0072 | 3 | HG00558.hp1 NA18971.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.295-996T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527727 | |||||||
| chr4:70527757 | G | T | 1 | a0001c0001t0003g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.295-966G>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527757 | |||||||
| chr4:70527871 | T | A | 1 | a0001c0001t0001g0105 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.295-852T>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527871 | |||||||
| chr4:70527875 | A | G | 25 | a0001c0001t0001g0010a0002c0003t0001g0004a0002c0003t0001g0008others(22): Show | 69 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.295-848A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70527875 | |||||||
| chr4:70528023 | T | C | 1 | a0001c0001t0003g0091 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.295-700T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528023 | |||||||
| chr4:70528041 | C | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(58): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.295-682C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528041 | |||||||
| chr4:70528072 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.295-651T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528072 | |||||||
| chr4:70528151 | A | AT | 5 | a0001c0001t0001g0037a0001c0001t0001g0053a0001c0001t0001g0138others(2): Show | 8 | HG02074.hp2 HG02083.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.295-563dupT | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 70528151 | ||||||
| chr4:70528158 | T | G | 2 | a0001c0002t0001g0064a0001c0002t0001g0070 | 2 | NA18991.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.295-565T>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528158 | |||||||
| chr4:70528226 | C | T | 1 | a0001c0002t0001g0041 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.295-497C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528226 | |||||||
| chr4:70528227 | T | TC | 73 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(70): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.295-496_295-495ins others(1): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528227 | |||||||
| chr4:70528303 | A | T | 7 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0091others(4): Show | 12 | HG01346.hp2 HG01891.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.295-420A>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528303 | |||||||
| chr4:70528467 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.295-256G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528467 | |||||||
| chr4:70528616 | C | T | 12 | a0001c0001t0001g0090a0001c0001t0003g0020a0001c0001t0003g0028others(9): Show | 18 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.295-107C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528616 | |||||||
| chr4:70528646 | T | A | 1 | a0001c0001t0002g0112 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.295-77T>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528646 | |||||||
| chr4:70528682 | C | G | 1 | a0001c0002t0001g0041 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.295-41C>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 5/8 | chr4 | 70528682 | |||||||
| chr4:70528771 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.330+13C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 6/8 | chr4 | 70528771 | |||||||
| chr4:70528948 | A | G | 28 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(25): Show | 122 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.330+190A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 6/8 | chr4 | 70528948 | |||||||
| chr4:70529022 | G | A | 1 | a0002c0003t0001g0081 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.331-162G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 6/8 | chr4 | 70529022 | |||||||
| chr4:70529042 | T | C | 7 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0091others(4): Show | 12 | HG01346.hp2 HG01891.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.331-142T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 6/8 | chr4 | 70529042 | |||||||
| chr4:70529068 | A | G | 1 | a0001c0001t0002g0116 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.331-116A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 6/8 | chr4 | 70529068 | |||||||
| chr4:70529256 | A | G | 3 | a0001c0001t0001g0090a0001c0001t0004g0088a0001c0001t0004g0089 | 3 | HG02258.hp2 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.357+46A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529256 | |||||||
| chr4:70529313 | T | C | 1 | a0003c0004t0001g0122 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.357+103T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529313 | |||||||
| chr4:70529432 | G | A | 1 | a0002c0003t0001g0079 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.357+222G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529432 | |||||||
| chr4:70529473 | C | A | 1 | a0001c0001t0001g0139 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.357+263C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529473 | |||||||
| chr4:70529528 | A | G | 1 | a0003c0004t0001g0124 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.357+318A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529528 | |||||||
| chr4:70529571 | G | A | 1 | a0001c0001t0002g0106 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.357+361G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529571 | |||||||
| chr4:70529633 | G | A | 2 | a0001c0001t0003g0055a0001c0001t0003g0148 | 3 | HG01891.hp2 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.357+423G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529633 | |||||||
| chr4:70529722 | T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.357+512T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529722 | |||||||
| chr4:70529725 | G | A | 1 | a0001c0002t0001g0065 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.357+515G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529725 | |||||||
| chr4:70529772 | T | C | 1 | a0001c0001t0002g0047 | 2 | NA18987.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.357+562T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529772 | |||||||
| chr4:70529775 | T | C | 7 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0091others(4): Show | 12 | HG01346.hp2 HG01891.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.357+565T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529775 | |||||||
| chr4:70529778 | C | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.357+568C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529778 | |||||||
| chr4:70529805 | G | A | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.357+595G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529805 | |||||||
| chr4:70529827 | A | G | 35 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(32): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.357+617A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529827 | |||||||
| chr4:70529854 | T | C | 23 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0018others(20): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.357+644T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70529854 | |||||||
| chr4:70529991 | T | TA | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(23): Show | 76 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.357+782dupA | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 70529991 | ||||||
| chr4:70530003 | T | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(70): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.357+793T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530003 | |||||||
| chr4:70530203 | C | T | 1 | a0002c0003t0001g0084 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.358-836C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530203 | |||||||
| chr4:70530221 | GCA | G | 52 | a0001c0001t0001g0010a0001c0001t0001g0046a0001c0001t0001g0105others(49): Show | 185 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.358-793_358-792del others(2): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 70530221 | ||||||
| chr4:70530221 | GCACA | G | 44 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(41): Show | 119 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.358-795_358-792del others(4): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 70530221 | ||||||
| chr4:70530221 | GCACACA | G | 2 | a0001c0001t0003g0055a0001c0001t0003g0148 | 3 | HG01891.hp2 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.358-797_358-792del others(6): Show |
AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 70530221 | ||||||
| chr4:70530256 | A | G | 2 | a0001c0002t0001g0025a0001c0002t0001g0075 | 4 | NA18947.hp1 NA18985.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-783A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530256 | |||||||
| chr4:70530318 | G | A | 3 | a0001c0001t0001g0090a0001c0001t0004g0088a0001c0001t0004g0089 | 3 | HG02258.hp2 HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.358-721G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530318 | |||||||
| chr4:70530371 | G | A | 1 | a0004c0005t0001g0130 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.358-668G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530371 | |||||||
| chr4:70530381 | G | T | 1 | a0001c0002t0001g0041 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.358-658G>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530381 | |||||||
| chr4:70530492 | A | G | 3 | a0002c0003t0001g0012a0002c0003t0001g0044a0002c0003t0001g0083 | 9 | HG02080.hp2 NA18943.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.358-547A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530492 | |||||||
| chr4:70530596 | T | C | 1 | a0003c0004t0001g0049 | 2 | HG00741.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.358-443T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530596 | |||||||
| chr4:70530642 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.358-397T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530642 | |||||||
| chr4:70530649 | A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(151): Show | 452 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(449): Show |
intron_variant | MODIFIER | c.358-390A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 7/8 | chr4 | 70530649 | |||||||
| chr4:70531349 | G | T | 2 | a0001c0001t0003g0055a0001c0001t0003g0148 | 3 | HG01891.hp2 HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.619+49G>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531349 | |||||||
| chr4:70531478 | C | T | 2 | a0001c0001t0002g0048a0001c0001t0002g0115 | 3 | NA18964.hp1 NA19003.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.619+178C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531478 | |||||||
| chr4:70531598 | C | T | 1 | a0001c0001t0003g0091 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.619+298C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531598 | |||||||
| chr4:70531640 | T | A | 1 | a0001c0002t0001g0066 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.619+340T>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531640 | |||||||
| chr4:70531647 | G | A | 1 | a0001c0002t0001g0059 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.619+347G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531647 | |||||||
| chr4:70531656 | C | T | 7 | a0001c0001t0003g0020a0001c0001t0003g0028a0001c0001t0003g0091others(4): Show | 12 | HG01346.hp2 HG01891.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.619+356C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531656 | |||||||
| chr4:70531763 | C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0056a0001c0001t0001g0057 | 5 | HG02886.hp1 HG02896.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.619+463C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531763 | |||||||
| chr4:70531796 | G | A | 3 | a0001c0001t0002g0013a0001c0001t0002g0112a0001c0001t0002g0114 | 8 | HG00408.hp2 HG02523.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.619+496G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531796 | |||||||
| chr4:70531876 | G | A | 2 | a0001c0001t0004g0088a0001c0001t0004g0089 | 2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.619+576G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531876 | |||||||
| chr4:70531978 | A | T | 1 | a0002c0003t0001g0082 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.620-477A>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531978 | |||||||
| chr4:70531981 | A | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0101a0001c0001t0001g0102 | 4 | HG02109.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.620-474A>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70531981 | |||||||
| chr4:70532064 | A | G | 2 | a0001c0001t0004g0088a0001c0001t0004g0089 | 2 | HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.620-391A>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70532064 | |||||||
| chr4:70532146 | C | A | 12 | a0001c0001t0001g0090a0001c0001t0003g0020a0001c0001t0003g0028others(9): Show | 18 | HG01346.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.620-309C>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70532146 | |||||||
| chr4:70532181 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.620-274G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70532181 | |||||||
| chr4:70532225 | G | A | 28 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(25): Show | 122 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.620-230G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70532225 | |||||||
| chr4:70532240 | C | T | 66 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(63): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.620-215C>T | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70532240 | |||||||
| chr4:70532347 | G | A | 28 | a0001c0002t0001g0001a0001c0002t0001g0011a0001c0002t0001g0015others(25): Show | 122 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.620-108G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70532347 | |||||||
| chr4:70532355 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.620-100T>C | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70532355 | |||||||
| chr4:70532384 | T | G | 1 | a0002c0003t0001g0077 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.620-71T>G | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70532384 | |||||||
| chr4:70532438 | G | A | 1 | a0001c0002t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.620-17G>A | AMTN | ENSG00000187689.10 | transcript | ENST00000339336.9 | protein_coding | 8/8 | chr4 | 70532438 |