Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 63905 |
| ensemblid | ENSG00000101363.13 |
| hgncid | 15799 |
| symbol | MANBAL |
| name | mannosidase beta like |
| refseq_nuc | NM_001003897.2 |
| refseq_prot | NP_001003897.1 |
| ensembl_nuc | ENST00000373606.8 |
| ensembl_prot | ENSP00000362708.3 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 37289655 |
| end | 37317260 |
| strand | + |
| ver | v1.2 |
| region | chr20:37289655-37317260 |
| region5000 | chr20:37284655-37322260 |
| regionname0 | MANBAL_chr20_37289655_37317260 |
| regionname5000 | MANBAL_chr20_37284655_37322260 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 255 | 270 | 78 | 48 | 94 | 16 | 32 | MANBAL_chr20_37284655_37322260 | MANBAL | ATGGC others(250): Show |
chr20 | 37284655 | 37322260 | ||
| a0001c0002 | 0/0 | 255 | 2 | 0 | 0 | 2 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ATGGC others(250): Show |
chr20 | 37284655 | 37322260 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1191 | 87 | 5 | 20 | 46 | 7 | 9 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0002 | 0/0 | 1191 | 83 | 24 | 5 | 44 | 0 | 10 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0003 | 0/1 | 1191 | 23 | 6 | 6 | 1 | 4 | 5 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0004 | 0/0 | 1191 | 12 | 8 | 3 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0005 | 0/0 | 1191 | 12 | 3 | 6 | 0 | 2 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0006 | 0/0 | 1191 | 12 | 12 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0007 | 0/0 | 1191 | 5 | 4 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0008 | 0/0 | 1191 | 4 | 0 | 3 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0009 | 0/0 | 1191 | 3 | 0 | 1 | 1 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0010 | 0/0 | 1191 | 3 | 3 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0011 | 0/0 | 1191 | 3 | 3 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0012 | 0/0 | 1191 | 2 | 2 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0013 | 0/0 | 1191 | 2 | 0 | 0 | 0 | 0 | 2 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0014 | 0/0 | 1191 | 2 | 1 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0015 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0016 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0017 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0018 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0019 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0020 | 0/0 | 1191 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0021 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0022 | 0/0 | 1191 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0023 | 1/0 | 1191 | 1 | 0 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0024 | 0/0 | 1191 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0025 | 0/0 | 1191 | 1 | 0 | 0 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0026 | 0/0 | 1191 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0027 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0028 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0029 | 0/0 | 1191 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0030 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0001t0031 | 0/0 | 1191 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| a0001c0002t0001 | 0/0 | 1191 | 2 | 0 | 0 | 2 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | ACTTC others(1186): Show |
chr20 | 37284655 | 37322260 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 40 | 2 | 7 | 25 | 0 | 6 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 2 | 0 | 4 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0002 | 0/0 | 27 | 0 | 0 | 27 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0003 | 0/0 | 9 | 6 | 0 | 0 | 0 | 3 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0003g0003 | 0/0 | 4 | 1 | 0 | 0 | 3 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0003g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0003g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0004g0001 | 0/0 | 6 | 5 | 0 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0004g0017 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0005g0003 | 0/0 | 6 | 2 | 2 | 0 | 2 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0005g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0005g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0006g0001 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0006g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0007g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0008g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0008g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0008g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0009g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0010g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0011g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0011g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0011g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0012g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0012g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0013g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0013g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0014g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0015g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0016g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0017g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0018g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0019g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0020g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0021g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0022g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0023g0001 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0024g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0025g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0026g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0027g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0028g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0029g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0030g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0001t0031g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0001 | EUR | FIN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00323 | hp1 | a0001 | c0001 | t0009 | g0001 | EUR | FIN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00323 | hp2 | a0001 | c0001 | t0025 | g0029 | EUR | FIN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | CHS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0028 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0079 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01109 | hp2 | a0001 | c0001 | t0014 | g0062 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0101 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0110 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01243 | hp2 | a0001 | c0001 | t0022 | g0113 | AMR | PUR | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01257 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01261 | hp1 | a0001 | c0001 | t0009 | g0001 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01261 | hp2 | a0001 | c0001 | t0007 | g0064 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0028 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0106 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01496 | hp2 | a0001 | c0001 | t0008 | g0111 | AMR | CLM | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0003 | EUR | IBS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | PEL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | PEL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02074 | hp2 | a0001 | c0001 | t0016 | g0088 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02145 | hp2 | a0001 | c0001 | t0019 | g0038 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02155 | hp2 | a0001 | c0001 | t0030 | g0023 | EAS | CDX | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | CDX | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CDX | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02273 | hp2 | a0001 | c0001 | t0031 | g0069 | AMR | PEL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02280 | hp2 | a0001 | c0001 | t0014 | g0037 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02602 | hp1 | a0001 | c0001 | t0020 | g0077 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0107 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02615 | hp2 | a0001 | c0001 | t0011 | g0048 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02622 | hp2 | a0001 | c0001 | t0028 | g0018 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0109 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02897 | hp1 | a0001 | c0001 | t0011 | g0001 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02897 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0003 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02970 | hp2 | a0001 | c0001 | t0021 | g0032 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03130 | hp1 | a0001 | c0001 | t0017 | g0097 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03195 | hp2 | a0001 | c0001 | t0027 | g0001 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0042 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03492 | hp2 | a0001 | c0001 | t0029 | g0006 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ESN | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0066 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03579 | hp1 | a0001 | c0001 | t0012 | g0100 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0080 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03669 | hp2 | a0001 | c0001 | t0026 | g0001 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | STU | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03688 | hp2 | a0001 | c0001 | t0013 | g0092 | SAS | STU | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03710 | hp2 | a0001 | c0001 | t0024 | g0001 | SAS | PJL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03831 | hp2 | a0001 | c0001 | t0008 | g0003 | SAS | BEB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | BEB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | STU | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | STU | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | STU | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | STU | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | YRI | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | YRI | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19002 | hp1 | a0001 | c0001 | t0009 | g0076 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | LWK | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0082 | AFR | LWK | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19240 | hp1 | a0001 | c0001 | t0012 | g0034 | AFR | YRI | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | ASW | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | ASW | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0105 | EUR | TSI | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0003 | EUR | TSI | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | TSI | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | GIH | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA20905 | hp2 | a0001 | c0001 | t0013 | g0073 | SAS | GIH | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02109 | hp1 | a0001 | c0001 | t0015 | g0004 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG02559 | hp2 | a0001 | c0001 | t0018 | g0115 | AFR | ACB | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0081 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | USA | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | USA | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0091 | AFR | LWK | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| NA21309 | hp2 | a0001 | c0001 | t0011 | g0098 | AFR | LWK | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0104 | REF | REF | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0023 | g0001 | REF | REF | MANBAL_chr20_37284655_37322260 | MANBAL | chr20 | 37284655 | 37322260 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:37316376 | G | C | 1 | a0001c0002 | 2 | HG02071.hp1 HG02165.hp1 |
synonymous_variant | LOW | c.219G>C | p.Val73Val | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 307/1191 | 219/258 | 73/85 | chr20 | 37316376 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:37316435 | T | C | 1 | a0001c0001t0012 | 2 | HG03579.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*20T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 20 | chr20 | 37316435 | ||||||
| chr20:37316483 | A | C | 1 | a0001c0001t0014 | 2 | HG01109.hp2 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*68A>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 68 | chr20 | 37316483 | ||||||
| chr20:37316530 | G | A | 1 | a0001c0001t0013 | 2 | HG03688.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*115G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 115 | chr20 | 37316530 | ||||||
| chr20:37316537 | G | T | 1 | a0001c0001t0031 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*122G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 122 | chr20 | 37316537 | ||||||
| chr20:37316540 | C | T | 1 | a0001c0001t0030 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*125C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 125 | chr20 | 37316540 | ||||||
| chr20:37316568 | C | T | 1 | a0001c0001t0029 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*153C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 153 | chr20 | 37316568 | ||||||
| chr20:37316701 | G | A | 17 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(14): Show |
207 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*286G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 286 | chr20 | 37316701 | ||||||
| chr20:37316714 | G | A | 4 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0021 others(1): Show |
7 | HG01243.hp2 HG02818.hp2 HG02896.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*299G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 299 | chr20 | 37316714 | ||||||
| chr20:37316745 | C | A | 1 | a0001c0001t0015 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*330C>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 330 | chr20 | 37316745 | ||||||
| chr20:37316750 | T | A | 1 | a0001c0001t0016 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*335T>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 335 | chr20 | 37316750 | ||||||
| chr20:37316771 | G | T | 20 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(17): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*356G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 356 | chr20 | 37316771 | ||||||
| chr20:37316819 | G | A | 1 | a0001c0001t0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*404G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 404 | chr20 | 37316819 | ||||||
| chr20:37316835 | C | G | 20 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(17): Show |
169 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*420C>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 420 | chr20 | 37316835 | ||||||
| chr20:37316855 | G | A | 1 | a0001c0001t0024 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*440G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 440 | chr20 | 37316855 | ||||||
| chr20:37316940 | T | C | 14 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(11): Show |
135 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*525T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 525 | chr20 | 37316940 | ||||||
| chr20:37316993 | A | G | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(14): Show |
153 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*578A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 578 | chr20 | 37316993 | ||||||
| chr20:37317007 | C | A | 1 | a0001c0001t0012 | 2 | HG03579.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*592C>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 592 | chr20 | 37317007 | ||||||
| chr20:37317009 | G | A | 1 | a0001c0001t0012 | 2 | HG03579.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*594G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 594 | chr20 | 37317009 | ||||||
| chr20:37317010 | C | T | 1 | a0001c0001t0012 | 2 | HG03579.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*595C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 595 | chr20 | 37317010 | ||||||
| chr20:37317018 | C | T | 1 | a0001c0001t0012 | 2 | HG03579.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*603C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 603 | chr20 | 37317018 | ||||||
| chr20:37317021 | T | G | 1 | a0001c0001t0012 | 2 | HG03579.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*606T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 606 | chr20 | 37317021 | ||||||
| chr20:37317037 | T | A | 1 | a0001c0001t0012 | 2 | HG03579.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*622T>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 622 | chr20 | 37317037 | ||||||
| chr20:37317038 | G | T | 1 | a0001c0001t0012 | 2 | HG03579.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*623G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 623 | chr20 | 37317038 | ||||||
| chr20:37317049 | T | G | 1 | a0001c0001t0019 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*634T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 634 | chr20 | 37317049 | ||||||
| chr20:37317091 | G | A | 1 | a0001c0001t0028 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*676G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 3/3 | 676 | chr20 | 37317091 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:37289713 | T | C | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-57+27T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37289713 | |||||||
| chr20:37289735 | C | G | 2 | a0001c0001t0004g0017 a0001c0001t0018g0115 |
4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+49C>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37289735 | |||||||
| chr20:37289885 | C | G | 1 | a0001c0001t0003g0114 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-57+199C>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37289885 | |||||||
| chr20:37290107 | A | C | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-57+421A>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37290107 | |||||||
| chr20:37290154 | C | T | 1 | a0001c0001t0022g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-57+468C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37290154 | |||||||
| chr20:37290414 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-57+728C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37290414 | |||||||
| chr20:37290441 | C | CT | 20 | a0001c0001t0001g0016 a0001c0001t0002g0031 a0001c0001t0002g0102 others(17): Show |
23 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.-57+768dupT | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr20 | 37290441 | ||||||
| chr20:37290583 | C | T | 1 | a0001c0001t0022g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-57+897C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37290583 | |||||||
| chr20:37290584 | G | A | 1 | a0001c0001t0021g0032 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-57+898G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37290584 | |||||||
| chr20:37290702 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-57+1016A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37290702 | |||||||
| chr20:37290725 | T | A | 1 | a0001c0001t0001g0033 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-57+1039T>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37290725 | |||||||
| chr20:37290809 | A | G | 1 | a0001c0001t0011g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-57+1123A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37290809 | |||||||
| chr20:37290920 | A | G | 1 | a0001c0001t0017g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-57+1234A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37290920 | |||||||
| chr20:37291007 | T | G | 2 | a0001c0001t0012g0034 a0001c0001t0012g0100 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-57+1321T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37291007 | |||||||
| chr20:37291013 | A | G | 2 | a0001c0001t0012g0034 a0001c0001t0012g0100 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-57+1327A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37291013 | |||||||
| chr20:37291032 | T | C | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-57+1346T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37291032 | |||||||
| chr20:37291084 | GAGA | G | 5 | a0001c0001t0002g0031 a0001c0001t0003g0030 a0001c0001t0003g0031 others(2): Show |
6 | HG01071.hp1 HG01192.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+1402_-57+1404d others(5): Show |
MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr20 | 37291084 | ||||||
| chr20:37291219 | A | T | 1 | a0001c0001t0002g0096 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-57+1533A>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37291219 | |||||||
| chr20:37291286 | A | ATGT | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-57+1601_-57+1603d others(5): Show |
MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr20 | 37291286 | ||||||
| chr20:37291616 | C | T | 1 | a0001c0001t0017g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-57+1930C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37291616 | |||||||
| chr20:37291698 | A | G | 3 | a0001c0001t0002g0027 a0001c0001t0002g0094 a0001c0001t0002g0095 |
4 | HG01192.hp1 HG02280.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+2012A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37291698 | |||||||
| chr20:37291832 | T | C | 6 | a0001c0001t0003g0011 a0001c0001t0003g0018 a0001c0001t0003g0035 others(3): Show |
8 | HG01361.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+2146T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37291832 | |||||||
| chr20:37291886 | C | T | 1 | a0001c0001t0014g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-57+2200C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37291886 | |||||||
| chr20:37292087 | C | G | 1 | a0001c0001t0002g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-57+2401C>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37292087 | |||||||
| chr20:37292098 | T | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0019g0038 |
3 | HG02145.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-57+2412T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37292098 | |||||||
| chr20:37292300 | T | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-57+2614T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37292300 | |||||||
| chr20:37292313 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-57+2627T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37292313 | |||||||
| chr20:37292340 | C | T | 1 | a0001c0001t0003g0109 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-57+2654C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37292340 | |||||||
| chr20:37292482 | A | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-57+2796A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37292482 | |||||||
| chr20:37292862 | T | C | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-57+3176T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37292862 | |||||||
| chr20:37292968 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-57+3282C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37292968 | |||||||
| chr20:37293058 | T | C | 1 | a0001c0001t0022g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-57+3372T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293058 | |||||||
| chr20:37293274 | G | T | 1 | a0001c0001t0001g0093 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-57+3588G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293274 | |||||||
| chr20:37293309 | G | A | 2 | a0001c0001t0003g0101 a0001c0001t0003g0109 |
2 | HG01175.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-57+3623G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293309 | |||||||
| chr20:37293466 | G | A | 1 | a0001c0001t0021g0032 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-57+3780G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293466 | |||||||
| chr20:37293488 | G | A | 1 | a0001c0001t0007g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-57+3802G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293488 | |||||||
| chr20:37293512 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-57+3826G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293512 | |||||||
| chr20:37293687 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-57+4001T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293687 | |||||||
| chr20:37293742 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-57+4056G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293742 | |||||||
| chr20:37293774 | G | A | 1 | a0001c0001t0001g0019 | 2 | NA19057.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-57+4088G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293774 | |||||||
| chr20:37293823 | C | T | 1 | a0001c0001t0011g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-57+4137C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37293823 | |||||||
| chr20:37294015 | G | A | 1 | a0001c0001t0002g0046 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-57+4329G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37294015 | |||||||
| chr20:37294182 | C | G | 1 | a0001c0001t0011g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-57+4496C>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37294182 | |||||||
| chr20:37294406 | T | C | 3 | a0001c0001t0002g0006 a0001c0001t0002g0096 a0001c0001t0029g0006 |
5 | HG02683.hp2 HG03239.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+4720T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37294406 | |||||||
| chr20:37294430 | C | T | 2 | a0001c0001t0012g0034 a0001c0001t0012g0100 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-57+4744C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37294430 | |||||||
| chr20:37294555 | C | T | 1 | a0001c0001t0013g0092 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-57+4869C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37294555 | |||||||
| chr20:37294697 | G | C | 1 | a0001c0001t0003g0030 | 2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-57+5011G>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37294697 | |||||||
| chr20:37294752 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-57+5066T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37294752 | |||||||
| chr20:37294923 | C | T | 1 | a0001c0001t0006g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-57+5237C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37294923 | |||||||
| chr20:37295004 | G | C | 1 | a0001c0001t0006g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-57+5318G>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37295004 | |||||||
| chr20:37295273 | A | G | 1 | a0001c0001t0003g0108 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-57+5587A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37295273 | |||||||
| chr20:37295299 | A | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-57+5613A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37295299 | |||||||
| chr20:37295545 | T | C | 1 | a0001c0001t0006g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-56-5663T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37295545 | |||||||
| chr20:37295895 | T | C | 1 | a0001c0001t0006g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-56-5313T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37295895 | |||||||
| chr20:37295981 | T | A | 1 | a0001c0001t0011g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-5227T>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37295981 | |||||||
| chr20:37296013 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-56-5195C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37296013 | |||||||
| chr20:37296049 | C | T | 2 | a0001c0001t0012g0034 a0001c0001t0012g0100 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-56-5159C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37296049 | |||||||
| chr20:37296315 | T | C | 1 | a0001c0001t0011g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-56-4893T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37296315 | |||||||
| chr20:37296429 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-56-4779G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37296429 | |||||||
| chr20:37296526 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-56-4682C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37296526 | |||||||
| chr20:37296640 | G | T | 1 | a0001c0001t0011g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-4568G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37296640 | |||||||
| chr20:37296817 | G | A | 1 | a0001c0001t0006g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-56-4391G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37296817 | |||||||
| chr20:37296893 | G | A | 47 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(44): Show |
104 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.-56-4315G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37296893 | |||||||
| chr20:37296927 | C | T | 1 | a0001c0001t0014g0037 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-56-4281C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37296927 | |||||||
| chr20:37297334 | G | A | 1 | a0001c0001t0002g0050 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-56-3874G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37297334 | |||||||
| chr20:37297542 | C | T | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-56-3666C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37297542 | |||||||
| chr20:37297803 | C | T | 1 | a0001c0001t0011g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-3405C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37297803 | |||||||
| chr20:37297804 | G | A | 1 | a0001c0001t0018g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-56-3404G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37297804 | |||||||
| chr20:37298449 | T | G | 35 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0006 others(32): Show |
88 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.-56-2759T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37298449 | |||||||
| chr20:37298523 | A | T | 2 | a0001c0001t0004g0017 a0001c0001t0018g0115 |
4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-2685A>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37298523 | |||||||
| chr20:37298542 | T | C | 1 | a0001c0001t0019g0038 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-56-2666T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37298542 | |||||||
| chr20:37298548 | C | G | 1 | a0001c0001t0002g0060 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-56-2660C>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37298548 | |||||||
| chr20:37298660 | C | T | 1 | a0001c0001t0004g0017 | 3 | HG00642.hp2 HG01167.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-56-2548C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37298660 | |||||||
| chr20:37298741 | AT | A | 3 | a0001c0001t0001g0007 a0001c0001t0002g0051 a0001c0001t0007g0007 |
5 | HG01069.hp1 HG01169.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-2452delT | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr20 | 37298741 | ||||||
| chr20:37298776 | G | A | 40 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(37): Show |
95 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.-56-2432G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37298776 | |||||||
| chr20:37299084 | G | T | 1 | a0001c0001t0021g0032 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-56-2124G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37299084 | |||||||
| chr20:37299294 | G | T | 1 | a0001c0001t0016g0088 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-56-1914G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37299294 | |||||||
| chr20:37299467 | G | A | 3 | a0001c0001t0007g0025 a0001c0001t0007g0042 a0001c0001t0007g0064 |
4 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-1741G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37299467 | |||||||
| chr20:37299608 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-56-1600G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37299608 | |||||||
| chr20:37299735 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-56-1473C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37299735 | |||||||
| chr20:37299762 | A | C | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-56-1446A>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37299762 | |||||||
| chr20:37299939 | A | G | 2 | a0001c0001t0012g0034 a0001c0001t0012g0100 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-56-1269A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37299939 | |||||||
| chr20:37299972 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-56-1236G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37299972 | |||||||
| chr20:37300041 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-56-1167C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37300041 | |||||||
| chr20:37300136 | A | C | 2 | a0001c0001t0002g0012 a0001c0001t0002g0051 |
4 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-1072A>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37300136 | |||||||
| chr20:37300190 | C | T | 2 | a0001c0001t0004g0017 a0001c0001t0018g0115 |
4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-1018C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37300190 | |||||||
| chr20:37300229 | C | A | 1 | a0001c0001t0002g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-56-979C>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37300229 | |||||||
| chr20:37300310 | C | T | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-56-898C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37300310 | |||||||
| chr20:37300958 | C | A | 1 | a0001c0001t0002g0053 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-56-250C>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37300958 | |||||||
| chr20:37300981 | A | G | 3 | a0001c0001t0002g0023 a0001c0001t0002g0050 a0001c0001t0030g0023 |
3 | HG02155.hp2 NA19057.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-56-227A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37300981 | |||||||
| chr20:37301004 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-56-204G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37301004 | |||||||
| chr20:37301006 | G | A | 1 | a0001c0001t0011g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-202G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37301006 | |||||||
| chr20:37301059 | C | T | 2 | a0001c0001t0012g0034 a0001c0001t0012g0100 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-56-149C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | chr20 | 37301059 | |||||||
| chr20:37301135 | C | CATAA | 3 | a0001c0001t0002g0054 a0001c0001t0002g0094 a0001c0001t0008g0110 |
3 | HG01192.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-56-46_-56-43dupAA others(2): Show |
MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr20 | 37301135 | ||||||
| chr20:37301135 | C | CATAAATA others(5): Show |
2 | a0001c0001t0004g0017 a0001c0001t0011g0098 |
4 | HG00642.hp2 HG01167.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-54_-56-43dupAA others(10): Show |
MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr20 | 37301135 | ||||||
| chr20:37301135 | CATAA | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0083 a0001c0001t0001g0084 others(2): Show |
8 | HG01106.hp1 HG01109.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-46_-56-43delAA others(2): Show |
MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr20 | 37301135 | ||||||
| chr20:37301881 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.150+468A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37301881 | |||||||
| chr20:37302046 | A | G | 1 | a0001c0001t0004g0017 | 3 | HG00642.hp2 HG01167.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.150+633A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37302046 | |||||||
| chr20:37302181 | C | T | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.150+768C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37302181 | |||||||
| chr20:37302226 | T | G | 2 | a0001c0001t0004g0017 a0001c0001t0018g0115 |
4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+813T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37302226 | |||||||
| chr20:37302419 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.150+1006T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37302419 | |||||||
| chr20:37302668 | G | A | 2 | a0001c0001t0004g0017 a0001c0001t0018g0115 |
4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+1255G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37302668 | |||||||
| chr20:37302766 | G | GT | 17 | a0001c0001t0002g0031 a0001c0001t0003g0029 a0001c0001t0003g0030 others(14): Show |
21 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.150+1365dupT | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37302766 | ||||||
| chr20:37303055 | G | A | 1 | a0001c0001t0011g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.150+1642G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37303055 | |||||||
| chr20:37303300 | CTA | C | 3 | a0001c0001t0007g0025 a0001c0001t0007g0042 a0001c0001t0007g0064 |
4 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+1888_150+1889d others(4): Show |
MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37303300 | |||||||
| chr20:37303325 | A | G | 1 | a0001c0001t0002g0094 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.150+1912A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37303325 | |||||||
| chr20:37303583 | G | A | 1 | a0001c0001t0006g0066 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.150+2170G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37303583 | |||||||
| chr20:37304145 | G | T | 1 | a0001c0001t0014g0062 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.150+2732G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37304145 | |||||||
| chr20:37304200 | A | G | 1 | a0001c0001t0005g0107 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.150+2787A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37304200 | |||||||
| chr20:37304228 | G | A | 1 | a0001c0001t0005g0020 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.150+2815G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37304228 | |||||||
| chr20:37304295 | A | G | 19 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0022 others(16): Show |
49 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.150+2882A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37304295 | |||||||
| chr20:37304506 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.150+3093G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37304506 | |||||||
| chr20:37304533 | C | T | 1 | a0001c0001t0002g0063 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.150+3120C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37304533 | |||||||
| chr20:37304597 | C | T | 1 | a0001c0001t0013g0092 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.150+3184C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37304597 | |||||||
| chr20:37304879 | A | C | 1 | a0001c0001t0014g0062 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.150+3466A>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37304879 | |||||||
| chr20:37304967 | C | A | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.150+3554C>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37304967 | |||||||
| chr20:37305122 | T | C | 1 | a0001c0001t0003g0011 | 3 | HG01361.hp1 HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.150+3709T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305122 | |||||||
| chr20:37305123 | T | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.150+3710T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305123 | |||||||
| chr20:37305127 | G | A | 1 | a0001c0001t0001g0014 | 3 | HG01074.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.150+3714G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305127 | |||||||
| chr20:37305213 | G | A | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.150+3800G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305213 | |||||||
| chr20:37305358 | T | C | 10 | a0001c0001t0002g0024 a0001c0001t0002g0061 a0001c0001t0002g0090 others(7): Show |
15 | HG01361.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.150+3945T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305358 | |||||||
| chr20:37305588 | C | T | 1 | a0001c0001t0021g0032 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.150+4175C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305588 | |||||||
| chr20:37305679 | C | CT | 5 | a0001c0001t0004g0080 a0001c0001t0007g0025 a0001c0001t0007g0042 others(2): Show |
6 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.150+4283dupT | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37305679 | ||||||
| chr20:37305679 | CT | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0039 a0001c0001t0001g0068 others(2): Show |
7 | HG00639.hp2 HG01433.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.150+4283delT | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37305679 | ||||||
| chr20:37305686 | T | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0033 |
3 | HG00408.hp2 NA19058.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.150+4273T>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305686 | |||||||
| chr20:37305696 | T | A | 1 | a0001c0001t0002g0045 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.150+4283T>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305696 | |||||||
| chr20:37305707 | T | C | 1 | a0001c0001t0011g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.150+4294T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305707 | |||||||
| chr20:37305801 | C | T | 2 | a0001c0001t0011g0098 a0001c0001t0018g0115 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.150+4388C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37305801 | |||||||
| chr20:37306004 | A | G | 2 | a0001c0001t0002g0012 a0001c0001t0002g0051 |
4 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+4591A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37306004 | |||||||
| chr20:37306079 | G | C | 1 | a0001c0001t0011g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.150+4666G>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37306079 | |||||||
| chr20:37306114 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0015 |
10 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.150+4701G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37306114 | |||||||
| chr20:37306688 | T | A | 1 | a0001c0001t0018g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.150+5275T>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37306688 | |||||||
| chr20:37306793 | T | C | 1 | a0001c0001t0031g0069 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.150+5380T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37306793 | |||||||
| chr20:37306836 | C | T | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.150+5423C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37306836 | |||||||
| chr20:37307212 | C | T | 1 | a0001c0001t0012g0034 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.150+5799C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307212 | |||||||
| chr20:37307229 | G | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0019g0038 |
3 | HG02145.hp2 HG02258.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.150+5816G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307229 | |||||||
| chr20:37307396 | G | A | 1 | a0001c0001t0006g0081 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.150+5983G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307396 | |||||||
| chr20:37307415 | T | C | 1 | a0001c0001t0011g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.150+6002T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307415 | |||||||
| chr20:37307531 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.150+6118C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307531 | |||||||
| chr20:37307590 | C | A | 1 | a0001c0001t0003g0105 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.150+6177C>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307590 | |||||||
| chr20:37307756 | C | CA | 5 | a0001c0001t0002g0022 a0001c0001t0002g0095 a0001c0001t0007g0025 others(2): Show |
7 | HG01261.hp2 HG02074.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.150+6357dupA | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37307756 | ||||||
| chr20:37307786 | A | G | 1 | a0001c0001t0007g0064 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.150+6373A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307786 | |||||||
| chr20:37307787 | C | T | 2 | a0001c0001t0004g0017 a0001c0001t0018g0115 |
4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+6374C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307787 | |||||||
| chr20:37307968 | C | T | 1 | a0001c0001t0004g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.150+6555C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307968 | |||||||
| chr20:37307969 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.150+6556G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307969 | |||||||
| chr20:37307996 | C | T | 1 | a0001c0001t0003g0105 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.150+6583C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37307996 | |||||||
| chr20:37308068 | C | T | 1 | a0001c0001t0004g0079 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.150+6655C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37308068 | |||||||
| chr20:37308666 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.150+7253G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37308666 | |||||||
| chr20:37308698 | T | C | 1 | a0001c0001t0002g0102 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.150+7285T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37308698 | |||||||
| chr20:37308794 | A | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.150+7381A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37308794 | |||||||
| chr20:37308909 | A | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-7399A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37308909 | |||||||
| chr20:37309152 | G | GTC | 6 | a0001c0001t0003g0011 a0001c0001t0003g0018 a0001c0001t0003g0035 others(3): Show |
8 | HG01361.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.151-7145_151-7144d others(4): Show |
MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37309152 | ||||||
| chr20:37309190 | C | T | 3 | a0001c0001t0007g0025 a0001c0001t0007g0042 a0001c0001t0007g0064 |
4 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-7118C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37309190 | |||||||
| chr20:37309496 | C | T | 3 | a0001c0001t0003g0029 a0001c0001t0003g0103 a0001c0001t0025g0029 |
3 | HG00323.hp2 HG00735.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.151-6812C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37309496 | |||||||
| chr20:37309578 | C | G | 2 | a0001c0001t0004g0017 a0001c0001t0018g0115 |
4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-6730C>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37309578 | |||||||
| chr20:37309616 | G | A | 2 | a0001c0001t0004g0017 a0001c0001t0018g0115 |
4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-6692G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37309616 | |||||||
| chr20:37309650 | A | G | 1 | a0001c0001t0018g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.151-6658A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37309650 | |||||||
| chr20:37309799 | G | A | 1 | a0001c0001t0012g0034 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.151-6509G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37309799 | |||||||
| chr20:37309976 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.151-6332G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37309976 | |||||||
| chr20:37310127 | G | A | 1 | a0001c0001t0002g0021 | 2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.151-6181G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37310127 | |||||||
| chr20:37310211 | G | A | 19 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0012 others(16): Show |
42 | HG00099.hp1 HG00738.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.151-6097G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37310211 | |||||||
| chr20:37310289 | G | A | 2 | a0001c0001t0003g0101 a0001c0001t0003g0109 |
2 | HG01175.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.151-6019G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37310289 | |||||||
| chr20:37310362 | A | G | 4 | a0001c0001t0004g0017 a0001c0001t0010g0010 a0001c0001t0011g0098 others(1): Show |
8 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.151-5946A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37310362 | |||||||
| chr20:37310432 | C | T | 1 | a0001c0001t0004g0017 | 3 | HG00642.hp2 HG01167.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.151-5876C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37310432 | |||||||
| chr20:37310737 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.151-5571C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37310737 | |||||||
| chr20:37310958 | T | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-5350T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37310958 | |||||||
| chr20:37311132 | C | T | 2 | a0001c0001t0012g0034 a0001c0001t0012g0100 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.151-5176C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37311132 | |||||||
| chr20:37311169 | G | C | 56 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(53): Show |
118 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.151-5139G>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37311169 | |||||||
| chr20:37311290 | T | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-5018T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37311290 | |||||||
| chr20:37311499 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0085 |
2 | NA18942.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.151-4809G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37311499 | |||||||
| chr20:37311612 | T | C | 59 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(56): Show |
122 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.151-4696T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37311612 | |||||||
| chr20:37311753 | C | T | 2 | a0001c0001t0012g0034 a0001c0001t0012g0100 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.151-4555C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37311753 | |||||||
| chr20:37311810 | C | A | 1 | a0001c0001t0017g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.151-4498C>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37311810 | |||||||
| chr20:37311834 | A | G | 5 | a0001c0001t0003g0011 a0001c0001t0003g0018 a0001c0001t0003g0035 others(2): Show |
7 | HG01361.hp1 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-4474A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37311834 | |||||||
| chr20:37311835 | ACT | A | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-4470_151-4469d others(4): Show |
MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37311835 | ||||||
| chr20:37311846 | C | T | 1 | a0001c0001t0018g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.151-4462C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37311846 | |||||||
| chr20:37311996 | A | AC | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-4310dupC | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37311996 | ||||||
| chr20:37312006 | C | T | 1 | a0001c0001t0002g0021 | 2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.151-4302C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37312006 | |||||||
| chr20:37312044 | A | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-4264A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37312044 | |||||||
| chr20:37312209 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.151-4099G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37312209 | |||||||
| chr20:37312480 | A | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-3828A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37312480 | |||||||
| chr20:37312671 | G | C | 1 | a0001c0001t0002g0057 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.151-3637G>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37312671 | |||||||
| chr20:37312705 | A | T | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-3603A>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37312705 | |||||||
| chr20:37312808 | G | A | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-3500G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37312808 | |||||||
| chr20:37312990 | CTTTCA | C | 3 | a0001c0001t0002g0023 a0001c0001t0002g0050 a0001c0001t0030g0023 |
3 | HG02155.hp2 NA19057.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.151-3310_151-3306d others(7): Show |
MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37312990 | ||||||
| chr20:37313147 | A | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-3161A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313147 | |||||||
| chr20:37313149 | C | T | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-3159C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313149 | |||||||
| chr20:37313161 | G | A | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-3147G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313161 | |||||||
| chr20:37313174 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.151-3134C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313174 | |||||||
| chr20:37313194 | T | C | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-3114T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313194 | |||||||
| chr20:37313210 | C | T | 2 | a0001c0001t0004g0017 a0001c0001t0018g0115 |
4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-3098C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313210 | |||||||
| chr20:37313252 | C | T | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-3056C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313252 | |||||||
| chr20:37313281 | G | C | 1 | a0001c0002t0001g0072 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.151-3027G>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313281 | |||||||
| chr20:37313288 | A | G | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-3020A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313288 | |||||||
| chr20:37313319 | C | T | 1 | a0001c0001t0020g0077 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.151-2989C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313319 | |||||||
| chr20:37313430 | C | T | 1 | a0001c0001t0009g0076 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.151-2878C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313430 | |||||||
| chr20:37313440 | C | CA | 2 | a0001c0001t0007g0025 a0001c0001t0007g0064 |
3 | HG01261.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.151-2867dupA | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37313440 | ||||||
| chr20:37313566 | C | T | 2 | a0001c0001t0003g0036 a0001c0001t0004g0080 |
2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.151-2742C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313566 | |||||||
| chr20:37313638 | G | A | 1 | a0001c0001t0011g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.151-2670G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313638 | |||||||
| chr20:37313680 | TG | T | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-2625delG | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37313680 | ||||||
| chr20:37313699 | T | C | 1 | a0001c0001t0010g0010 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.151-2609T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313699 | |||||||
| chr20:37313737 | G | C | 1 | a0001c0001t0018g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.151-2571G>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313737 | |||||||
| chr20:37313751 | G | A | 2 | a0001c0001t0012g0034 a0001c0001t0012g0100 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.151-2557G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313751 | |||||||
| chr20:37313769 | G | A | 1 | a0001c0001t0003g0035 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.151-2539G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37313769 | |||||||
| chr20:37314234 | C | T | 1 | a0001c0001t0018g0115 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.151-2074C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314234 | |||||||
| chr20:37314289 | C | T | 6 | a0001c0001t0006g0066 a0001c0001t0006g0091 a0001c0001t0007g0025 others(3): Show |
9 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.151-2019C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314289 | |||||||
| chr20:37314315 | T | C | 21 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0022 others(18): Show |
53 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.151-1993T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314315 | |||||||
| chr20:37314376 | T | G | 61 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(58): Show |
126 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.151-1932T>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314376 | |||||||
| chr20:37314401 | T | C | 22 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0022 others(19): Show |
54 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.151-1907T>C | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314401 | |||||||
| chr20:37314425 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.151-1883C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314425 | |||||||
| chr20:37314479 | G | T | 6 | a0001c0001t0006g0066 a0001c0001t0006g0091 a0001c0001t0007g0025 others(3): Show |
9 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.151-1829G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314479 | |||||||
| chr20:37314492 | G | A | 6 | a0001c0001t0006g0066 a0001c0001t0006g0091 a0001c0001t0007g0025 others(3): Show |
9 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.151-1816G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314492 | |||||||
| chr20:37314616 | G | T | 1 | a0001c0001t0017g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.151-1692G>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314616 | |||||||
| chr20:37314888 | C | T | 2 | a0001c0001t0004g0017 a0001c0001t0018g0115 |
4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-1420C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314888 | |||||||
| chr20:37314993 | C | T | 6 | a0001c0001t0006g0066 a0001c0001t0006g0091 a0001c0001t0007g0025 others(3): Show |
9 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.151-1315C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314993 | |||||||
| chr20:37314994 | C | T | 2 | a0001c0001t0012g0034 a0001c0001t0012g0100 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.151-1314C>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37314994 | |||||||
| chr20:37315034 | CA | C | 6 | a0001c0001t0006g0066 a0001c0001t0006g0091 a0001c0001t0007g0025 others(3): Show |
9 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.151-1272delA | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr20 | 37315034 | ||||||
| chr20:37315151 | A | G | 5 | a0001c0001t0006g0066 a0001c0001t0006g0091 a0001c0001t0007g0025 others(2): Show |
6 | HG01261.hp2 HG02451.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-1157A>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37315151 | |||||||
| chr20:37315378 | C | G | 1 | a0001c0001t0006g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.151-930C>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37315378 | |||||||
| chr20:37315648 | G | A | 1 | a0001c0001t0013g0073 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.151-660G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37315648 | |||||||
| chr20:37315681 | C | G | 2 | a0001c0001t0004g0017 a0001c0001t0018g0115 |
4 | HG00642.hp2 HG01167.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-627C>G | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37315681 | |||||||
| chr20:37315851 | G | A | 2 | a0001c0002t0001g0072 a0001c0002t0001g0074 |
2 | HG02071.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.151-457G>A | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37315851 | |||||||
| chr20:37315988 | A | T | 1 | a0001c0001t0001g0075 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.151-320A>T | MANBAL | ENSG00000101363.13 | transcript | ENST00000373606.8 | protein_coding | 2/2 | chr20 | 37315988 |