Item | Value |
---|---|
geneid | 10086 |
ensemblid | ENSG00000132297.13 |
hgncid | 4904 |
symbol | HHLA1 |
name | HHLA1 neighbor of OC90 |
refseq_nuc | NM_001145095.3 |
refseq_prot | NP_001138567.1 |
ensembl_nuc | ENST00000414222.2 |
ensembl_prot | ENSP00000388322.1 |
mane_status | MANE Select |
chr | chr8 |
start | 132061480 |
end | 132111157 |
strand | - |
ver | v1.2 |
region | chr8:132061480-132111157 |
region5000 | chr8:132056480-132116157 |
regionname0 | HHLA1_chr8_132061480_132111157 |
regionname5000 | HHLA1_chr8_132056480_132116157 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 531 | 191 | 51 | 36 | 75 | 5 | 23 | 55 | HHLA1_chr8_132056480_132116157 | HHLA1 | MLGFL others(526): Show |
chr8 | 132056480 | 132116157 |
a0002 | 1/0 | 531 | 85 | 12 | 10 | 49 | 4 | 9 | 37 | HHLA1_chr8_132056480_132116157 | HHLA1 | MLGFL others(526): Show |
chr8 | 132056480 | 132116157 |
a0003 | 0/0 | 531 | 61 | 13 | 23 | 17 | 2 | 6 | 15 | HHLA1_chr8_132056480_132116157 | HHLA1 | MLGFL others(526): Show |
chr8 | 132056480 | 132116157 |
a0004 | 0/0 | 531 | 21 | 7 | 8 | 2 | 1 | 3 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | MLGFL others(526): Show |
chr8 | 132056480 | 132116157 |
a0005 | 0/0 | 531 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | MLGFL others(526): Show |
chr8 | 132056480 | 132116157 |
a0006 | 0/0 | 531 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | HHLA1_chr8_132056480_132116157 | HHLA1 | MLGFL others(526): Show |
chr8 | 132056480 | 132116157 |
a0007 | 0/0 | 531 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | MLGFL others(526): Show |
chr8 | 132056480 | 132116157 |
a0008 | 0/0 | 531 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | MLGFL others(526): Show |
chr8 | 132056480 | 132116157 |
a0009 | 0/0 | 531 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | MLGFL others(526): Show |
chr8 | 132056480 | 132116157 |
a0010 | 0/0 | 531 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | MLGFL others(526): Show |
chr8 | 132056480 | 132116157 |
a0011 | 0/0 | 531 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | MLGFL others(526): Show |
chr8 | 132056480 | 132116157 |
a0012 | 0/0 | 531 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | MLGFL others(526): Show |
chr8 | 132056480 | 132116157 |
a0013 | 0/0 | 531 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | MLGFL others(526): Show |
chr8 | 132056480 | 132116157 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1593 | 132 | 23 | 22 | 62 | 4 | 20 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0001c0005 | 0/0 | 1593 | 32 | 13 | 8 | 10 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0001c0007 | 0/0 | 1593 | 12 | 6 | 2 | 2 | 0 | 2 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0001c0009 | 0/0 | 1593 | 6 | 6 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0001c0012 | 0/0 | 1593 | 3 | 0 | 2 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0001c0016 | 0/0 | 1593 | 2 | 2 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0001c0020 | 0/0 | 1593 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0001c0023 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0001c0024 | 0/0 | 1593 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0001c0027 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0002c0003 | 0/0 | 1593 | 42 | 11 | 4 | 21 | 1 | 5 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0002c0004 | 1/0 | 1593 | 36 | 0 | 5 | 26 | 1 | 3 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0002c0013 | 0/0 | 1593 | 3 | 0 | 0 | 0 | 2 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0002c0014 | 0/0 | 1593 | 3 | 1 | 0 | 2 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0002c0017 | 0/0 | 1593 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0003c0002 | 0/0 | 1593 | 61 | 13 | 23 | 17 | 2 | 6 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0004c0006 | 0/0 | 1593 | 21 | 7 | 8 | 2 | 1 | 3 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0005c0008 | 0/0 | 1593 | 7 | 7 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0006c0010 | 0/0 | 1593 | 3 | 0 | 0 | 3 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0006c0015 | 0/0 | 1593 | 2 | 0 | 0 | 2 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0007c0011 | 0/0 | 1593 | 3 | 3 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0008c0021 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0008c0022 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0009c0025 | 0/0 | 1593 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0010c0026 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0011c0019 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0012c0018 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 | ||
a0013c0028 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | ATGCT others(1588): Show |
chr8 | 132056480 | 132116157 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4188 | 69 | 2 | 13 | 37 | 4 | 12 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0001t0002 | 0/0 | 4188 | 30 | 2 | 3 | 18 | 0 | 7 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0001t0003 | 0/0 | 4188 | 10 | 9 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0001t0004 | 0/0 | 4188 | 9 | 0 | 2 | 6 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0001t0005 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0001t0006 | 0/0 | 4188 | 2 | 2 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0001t0009 | 0/0 | 4188 | 3 | 2 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0001t0011 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0001t0013 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0001t0014 | 0/0 | 4188 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0001t0018 | 0/0 | 4188 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0001t0019 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0001t0020 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0001t0022 | 0/0 | 4188 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0001t0024 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0005t0001 | 0/0 | 4188 | 14 | 2 | 6 | 5 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0005t0002 | 0/0 | 4188 | 6 | 1 | 0 | 5 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0005t0005 | 0/0 | 4188 | 9 | 7 | 2 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0005t0006 | 0/0 | 4188 | 2 | 2 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0005t0009 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0007t0001 | 0/0 | 4188 | 7 | 3 | 2 | 2 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0007t0002 | 0/0 | 4188 | 3 | 1 | 0 | 0 | 0 | 2 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0007t0006 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0007t0021 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0009t0002 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0009t0007 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0009t0008 | 0/0 | 4188 | 4 | 4 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0012t0001 | 0/0 | 4188 | 3 | 0 | 2 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0016t0002 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0016t0006 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0020t0001 | 0/0 | 4188 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0023t0001 | 0/0 | 4188 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0024t0001 | 0/0 | 4188 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0001c0027t0001 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0002c0003t0001 | 0/0 | 4188 | 28 | 9 | 3 | 14 | 1 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0002c0003t0002 | 0/0 | 4188 | 13 | 2 | 1 | 7 | 0 | 3 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0002c0003t0023 | 0/0 | 4188 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0002c0004t0001 | 1/0 | 4188 | 10 | 0 | 2 | 7 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0002c0004t0002 | 0/0 | 4188 | 25 | 0 | 3 | 19 | 1 | 2 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0002c0004t0015 | 0/0 | 4188 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0002c0013t0001 | 0/0 | 4188 | 3 | 0 | 0 | 0 | 2 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0002c0014t0001 | 0/0 | 4188 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0002c0014t0002 | 0/0 | 4188 | 2 | 1 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0002c0017t0002 | 0/0 | 4188 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0003c0002t0001 | 0/0 | 4188 | 39 | 2 | 17 | 14 | 2 | 4 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0003c0002t0002 | 0/0 | 4188 | 13 | 4 | 5 | 2 | 0 | 2 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0003c0002t0004 | 0/0 | 4188 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0003c0002t0006 | 0/0 | 4188 | 2 | 2 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0003c0002t0008 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0003c0002t0010 | 0/0 | 4188 | 3 | 3 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0003c0002t0012 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0003c0002t0017 | 0/0 | 4188 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0004c0006t0001 | 0/0 | 4188 | 16 | 6 | 7 | 1 | 1 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0004c0006t0002 | 0/0 | 4188 | 4 | 1 | 0 | 1 | 0 | 2 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0004c0006t0016 | 0/0 | 4188 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0005c0008t0001 | 0/0 | 4188 | 4 | 4 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0005c0008t0002 | 0/0 | 4188 | 2 | 2 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0005c0008t0009 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0006c0010t0001 | 0/0 | 4188 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0006c0010t0002 | 0/0 | 4188 | 2 | 0 | 0 | 2 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0006c0015t0001 | 0/0 | 4188 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0006c0015t0002 | 0/0 | 4188 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0007c0011t0007 | 0/0 | 4188 | 3 | 3 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0008c0021t0003 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0008c0022t0001 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0009c0025t0007 | 0/0 | 4188 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0010c0026t0001 | 0/0 | 4188 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0011c0019t0001 | 0/0 | 4188 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0012c0018t0001 | 0/0 | 4188 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
a0013c0028t0002 | 0/0 | 4188 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | TAATC others(4183): Show |
chr8 | 132056480 | 132116157 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0176 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0003g0002 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0009g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0009g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0009g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0011g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0013g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0014g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0018g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0019g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0020g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0022g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0001t0024g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0005g0003 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0005g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0005t0009g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0007t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0007t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0007t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0007t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0007t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0007t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0007t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0007t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0007t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0007t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0007t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0007t0021g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0009t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0009t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0009t0008g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0009t0008g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0009t0008g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0009t0008g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0012t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0012t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0012t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0016t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0016t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0020t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0023t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0024t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0001c0027t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0003t0023g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0001g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0002g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0002g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0004t0015g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0013t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0013t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0013t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0014t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0014t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0014t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0002c0017t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0010g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0010g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0010g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0012g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0003c0002t0017g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0004c0006t0016g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0005c0008t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0005c0008t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0005c0008t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0005c0008t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0005c0008t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0005c0008t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0005c0008t0009g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0006c0010t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0006c0010t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0006c0010t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0006c0015t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0006c0015t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0007c0011t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0007c0011t0007g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0007c0011t0007g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0008c0021t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0008c0022t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0009c0025t0007g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0010c0026t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0011c0019t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0012c0018t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
a0013c0028t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0173 | EUR | GBR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | GBR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | FIN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00280 | hp2 | a0001 | c0005 | t0001 | g0061 | EUR | FIN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00323 | hp1 | a0002 | c0003 | t0001 | g0075 | EUR | FIN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0326 | EUR | FIN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00408 | hp1 | a0001 | c0005 | t0001 | g0087 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00408 | hp2 | a0004 | c0006 | t0001 | g0036 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00423 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00438 | hp1 | a0002 | c0004 | t0002 | g0084 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00438 | hp2 | a0001 | c0005 | t0002 | g0067 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00558 | hp1 | a0002 | c0004 | t0002 | g0073 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00597 | hp1 | a0002 | c0003 | t0002 | g0348 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0333 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00639 | hp1 | a0003 | c0002 | t0001 | g0242 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00642 | hp1 | a0003 | c0002 | t0001 | g0220 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00642 | hp2 | a0004 | c0006 | t0001 | g0202 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00673 | hp1 | a0003 | c0002 | t0017 | g0228 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00673 | hp2 | a0002 | c0003 | t0002 | g0135 | EAS | CHS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00733 | hp1 | a0001 | c0005 | t0005 | g0003 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00733 | hp2 | a0004 | c0006 | t0001 | g0095 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00735 | hp1 | a0001 | c0024 | t0001 | g0194 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00735 | hp2 | a0003 | c0002 | t0001 | g0033 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00738 | hp1 | a0003 | c0002 | t0001 | g0221 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00738 | hp2 | a0002 | c0004 | t0002 | g0049 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00741 | hp1 | a0003 | c0002 | t0001 | g0199 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01069 | hp2 | a0004 | c0006 | t0001 | g0197 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01071 | hp1 | a0004 | c0006 | t0001 | g0196 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01074 | hp2 | a0003 | c0002 | t0002 | g0025 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01081 | hp1 | a0001 | c0001 | t0022 | g0327 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01081 | hp2 | a0004 | c0006 | t0016 | g0163 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01099 | hp1 | a0002 | c0004 | t0001 | g0054 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01099 | hp2 | a0001 | c0005 | t0005 | g0008 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01106 | hp1 | a0001 | c0001 | t0009 | g0302 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01106 | hp2 | a0003 | c0002 | t0004 | g0245 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01109 | hp1 | a0002 | c0017 | t0002 | g0351 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01167 | hp1 | a0009 | c0025 | t0007 | g0282 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01168 | hp1 | a0001 | c0005 | t0001 | g0069 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01169 | hp2 | a0001 | c0005 | t0001 | g0068 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01175 | hp2 | a0002 | c0004 | t0002 | g0005 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01192 | hp1 | a0002 | c0004 | t0002 | g0005 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01192 | hp2 | a0003 | c0002 | t0001 | g0246 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01243 | hp1 | a0001 | c0005 | t0001 | g0064 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01243 | hp2 | a0003 | c0002 | t0001 | g0222 | AMR | PUR | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01255 | hp1 | a0001 | c0007 | t0001 | g0263 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01255 | hp2 | a0003 | c0002 | t0001 | g0030 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01257 | hp1 | a0002 | c0004 | t0001 | g0009 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01257 | hp2 | a0003 | c0002 | t0001 | g0011 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01258 | hp2 | a0003 | c0002 | t0001 | g0011 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01261 | hp1 | a0002 | c0003 | t0001 | g0189 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0169 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01346 | hp1 | a0003 | c0002 | t0001 | g0179 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01346 | hp2 | a0004 | c0006 | t0001 | g0094 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01358 | hp1 | a0002 | c0003 | t0002 | g0190 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01361 | hp1 | a0004 | c0006 | t0001 | g0110 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01361 | hp2 | a0003 | c0002 | t0001 | g0201 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01433 | hp1 | a0004 | c0006 | t0001 | g0093 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01433 | hp2 | a0001 | c0005 | t0001 | g0062 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01496 | hp2 | a0002 | c0003 | t0001 | g0206 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01516 | hp1 | a0003 | c0002 | t0001 | g0238 | EUR | IBS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01516 | hp2 | a0002 | c0013 | t0001 | g0112 | EUR | IBS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01517 | hp1 | a0002 | c0013 | t0001 | g0113 | EUR | IBS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01517 | hp2 | a0002 | c0004 | t0002 | g0005 | EUR | IBS | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01884 | hp1 | a0005 | c0008 | t0001 | g0055 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01884 | hp2 | a0001 | c0005 | t0006 | g0046 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01891 | hp1 | a0007 | c0011 | t0007 | g0270 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01891 | hp2 | a0001 | c0005 | t0005 | g0008 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01934 | hp1 | a0003 | c0002 | t0001 | g0244 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01934 | hp2 | a0001 | c0012 | t0001 | g0154 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01943 | hp1 | a0001 | c0020 | t0001 | g0136 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01943 | hp2 | a0001 | c0001 | t0018 | g0249 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0164 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01952 | hp2 | a0003 | c0002 | t0002 | g0007 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01975 | hp1 | a0001 | c0005 | t0001 | g0101 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01975 | hp2 | a0003 | c0002 | t0001 | g0254 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01981 | hp2 | a0003 | c0002 | t0002 | g0034 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01993 | hp1 | a0003 | c0002 | t0001 | g0247 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01993 | hp2 | a0003 | c0002 | t0001 | g0241 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02004 | hp1 | a0003 | c0002 | t0002 | g0032 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02004 | hp2 | a0001 | c0007 | t0001 | g0266 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02015 | hp2 | a0006 | c0010 | t0002 | g0275 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02040 | hp1 | a0002 | c0003 | t0002 | g0298 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02040 | hp2 | a0003 | c0002 | t0001 | g0233 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02055 | hp2 | a0001 | c0009 | t0007 | g0188 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02071 | hp1 | a0002 | c0004 | t0002 | g0077 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02074 | hp1 | a0002 | c0004 | t0001 | g0053 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02080 | hp1 | a0001 | c0005 | t0001 | g0051 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02129 | hp1 | a0002 | c0004 | t0001 | g0071 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02129 | hp2 | a0002 | c0004 | t0002 | g0085 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02132 | hp2 | a0001 | c0005 | t0002 | g0086 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02145 | hp1 | a0001 | c0005 | t0005 | g0065 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | CDX | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02155 | hp2 | a0001 | c0005 | t0001 | g0059 | EAS | CDX | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02257 | hp1 | a0003 | c0002 | t0002 | g0141 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02257 | hp2 | a0001 | c0005 | t0005 | g0003 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02258 | hp1 | a0007 | c0011 | t0007 | g0042 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0330 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02273 | hp1 | a0003 | c0002 | t0001 | g0243 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02273 | hp2 | a0003 | c0002 | t0002 | g0007 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02280 | hp1 | a0001 | c0001 | t0011 | g0159 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02280 | hp2 | a0001 | c0001 | t0020 | g0027 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02293 | hp2 | a0001 | c0005 | t0001 | g0063 | AMR | PEL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02451 | hp1 | a0005 | c0008 | t0001 | g0056 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02451 | hp2 | a0005 | c0008 | t0002 | g0345 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02523 | hp1 | a0002 | c0004 | t0002 | g0076 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02572 | hp1 | a0004 | c0006 | t0001 | g0200 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02572 | hp2 | a0004 | c0006 | t0001 | g0290 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02602 | hp1 | a0002 | c0003 | t0002 | g0308 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02602 | hp2 | a0003 | c0002 | t0001 | g0038 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02622 | hp1 | a0002 | c0003 | t0001 | g0324 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0100 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02630 | hp2 | a0003 | c0002 | t0001 | g0237 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02647 | hp1 | a0004 | c0006 | t0001 | g0288 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02647 | hp2 | a0002 | c0003 | t0001 | g0335 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02683 | hp2 | a0010 | c0026 | t0001 | g0219 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02698 | hp2 | a0002 | c0003 | t0002 | g0172 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02717 | hp2 | a0001 | c0007 | t0001 | g0024 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02723 | hp1 | a0002 | c0003 | t0001 | g0336 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02723 | hp2 | a0001 | c0009 | t0008 | g0339 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02738 | hp2 | a0003 | c0002 | t0001 | g0227 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02809 | hp1 | a0001 | c0001 | t0024 | g0355 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02809 | hp2 | a0002 | c0003 | t0002 | g0325 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02818 | hp2 | a0003 | c0002 | t0002 | g0230 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02886 | hp1 | a0001 | c0005 | t0006 | g0074 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02886 | hp2 | a0002 | c0003 | t0002 | g0332 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02895 | hp1 | a0003 | c0002 | t0002 | g0142 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02895 | hp2 | a0005 | c0008 | t0001 | g0023 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02896 | hp1 | a0004 | c0006 | t0001 | g0157 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02896 | hp2 | a0001 | c0009 | t0008 | g0341 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02897 | hp1 | a0005 | c0008 | t0001 | g0022 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02897 | hp2 | a0001 | c0009 | t0008 | g0340 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02922 | hp2 | a0001 | c0001 | t0013 | g0239 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02965 | hp1 | a0011 | c0019 | t0001 | g0097 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02965 | hp2 | a0002 | c0014 | t0002 | g0267 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02970 | hp2 | a0001 | c0005 | t0002 | g0350 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02976 | hp2 | a0005 | c0008 | t0002 | g0346 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0277 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03017 | hp2 | a0012 | c0018 | t0001 | g0212 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03041 | hp1 | a0002 | c0003 | t0001 | g0315 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03041 | hp2 | a0001 | c0007 | t0006 | g0258 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03098 | hp1 | a0001 | c0005 | t0005 | g0078 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03098 | hp2 | a0001 | c0005 | t0009 | g0026 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03130 | hp1 | a0001 | c0005 | t0001 | g0066 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03130 | hp2 | a0001 | c0005 | t0005 | g0003 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03139 | hp1 | a0001 | c0007 | t0001 | g0260 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03139 | hp2 | a0003 | c0002 | t0010 | g0158 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0283 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03195 | hp2 | a0002 | c0003 | t0001 | g0029 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03209 | hp1 | a0001 | c0016 | t0006 | g0151 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03209 | hp2 | a0001 | c0007 | t0021 | g0261 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03225 | hp1 | a0004 | c0006 | t0001 | g0334 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03225 | hp2 | a0001 | c0001 | t0019 | g0304 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03239 | hp1 | a0004 | c0006 | t0002 | g0204 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03239 | hp2 | a0002 | c0013 | t0001 | g0105 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03453 | hp1 | a0003 | c0002 | t0001 | g0289 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03453 | hp2 | a0003 | c0002 | t0006 | g0147 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03486 | hp1 | a0004 | c0006 | t0001 | g0291 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03490 | hp1 | a0002 | c0004 | t0002 | g0048 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03491 | hp1 | a0001 | c0007 | t0002 | g0256 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03492 | hp1 | a0001 | c0007 | t0002 | g0262 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03492 | hp2 | a0002 | c0004 | t0002 | g0047 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03516 | hp1 | a0003 | c0002 | t0002 | g0146 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03516 | hp2 | a0001 | c0009 | t0008 | g0342 | AFR | ESN | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03540 | hp1 | a0003 | c0002 | t0010 | g0156 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03540 | hp2 | a0001 | c0007 | t0002 | g0269 | AFR | GWD | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03579 | hp1 | a0008 | c0021 | t0003 | g0191 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03654 | hp2 | a0004 | c0006 | t0001 | g0236 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03669 | hp1 | a0002 | c0003 | t0001 | g0168 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03704 | hp1 | a0002 | c0004 | t0015 | g0080 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03710 | hp1 | a0003 | c0002 | t0001 | g0187 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03831 | hp1 | a0013 | c0028 | t0002 | g0192 | SAS | BEB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03831 | hp2 | a0001 | c0012 | t0001 | g0349 | SAS | BEB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0235 | SAS | BEB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0279 | SAS | BEB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | BEB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG04115 | hp2 | a0002 | c0003 | t0002 | g0301 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG04184 | hp1 | a0003 | c0002 | t0002 | g0198 | SAS | BEB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG04184 | hp2 | a0003 | c0002 | t0001 | g0193 | SAS | BEB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG04199 | hp1 | a0003 | c0002 | t0002 | g0021 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0347 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG04204 | hp1 | a0004 | c0006 | t0002 | g0203 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG04228 | hp1 | a0002 | c0003 | t0023 | g0031 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18522 | hp1 | a0001 | c0007 | t0001 | g0259 | AFR | YRI | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | YRI | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18747 | hp1 | a0002 | c0004 | t0002 | g0079 | EAS | CHB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18906 | hp1 | a0002 | c0003 | t0001 | g0321 | AFR | YRI | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18906 | hp2 | a0001 | c0009 | t0002 | g0278 | AFR | YRI | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18940 | hp1 | a0003 | c0002 | t0001 | g0208 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18940 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18942 | hp2 | a0003 | c0002 | t0001 | g0226 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18943 | hp1 | a0004 | c0006 | t0002 | g0037 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18944 | hp1 | a0003 | c0002 | t0001 | g0224 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18944 | hp2 | a0002 | c0004 | t0002 | g0050 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18945 | hp1 | a0001 | c0005 | t0002 | g0090 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18945 | hp2 | a0003 | c0002 | t0001 | g0209 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18947 | hp2 | a0002 | c0004 | t0001 | g0091 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18951 | hp1 | a0002 | c0004 | t0002 | g0092 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0329 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18954 | hp2 | a0003 | c0002 | t0001 | g0231 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18959 | hp1 | a0001 | c0007 | t0001 | g0264 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18959 | hp2 | a0002 | c0003 | t0001 | g0310 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18960 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18962 | hp1 | a0001 | c0005 | t0001 | g0060 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18962 | hp2 | a0003 | c0002 | t0001 | g0210 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18966 | hp1 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18967 | hp2 | a0003 | c0002 | t0001 | g0223 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18968 | hp1 | a0002 | c0003 | t0001 | g0117 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18969 | hp1 | a0003 | c0002 | t0001 | g0225 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18969 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18971 | hp2 | a0003 | c0002 | t0002 | g0218 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18975 | hp2 | a0002 | c0004 | t0002 | g0052 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18977 | hp2 | a0002 | c0003 | t0001 | g0139 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18978 | hp1 | a0001 | c0005 | t0002 | g0088 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18979 | hp1 | a0002 | c0003 | t0001 | g0285 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18979 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18980 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18983 | hp1 | a0002 | c0003 | t0002 | g0125 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18983 | hp2 | a0003 | c0002 | t0001 | g0229 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18986 | hp2 | a0006 | c0010 | t0002 | g0272 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18991 | hp2 | a0002 | c0003 | t0001 | g0014 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18993 | hp1 | a0002 | c0003 | t0002 | g0126 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18994 | hp1 | a0002 | c0003 | t0002 | g0328 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18994 | hp2 | a0006 | c0015 | t0001 | g0274 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18995 | hp1 | a0002 | c0003 | t0001 | g0115 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19000 | hp1 | a0002 | c0014 | t0001 | g0257 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19002 | hp1 | a0001 | c0001 | t0014 | g0253 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19002 | hp2 | a0001 | c0001 | t0004 | g0320 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19004 | hp2 | a0003 | c0002 | t0002 | g0043 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19005 | hp2 | a0001 | c0005 | t0002 | g0082 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19010 | hp2 | a0002 | c0004 | t0001 | g0009 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19011 | hp2 | a0003 | c0002 | t0001 | g0344 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19012 | hp2 | a0002 | c0003 | t0001 | g0314 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19030 | hp1 | a0002 | c0003 | t0001 | g0152 | AFR | LWK | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19030 | hp2 | a0008 | c0022 | t0001 | g0338 | AFR | LWK | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19043 | hp1 | a0002 | c0003 | t0001 | g0153 | AFR | LWK | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19043 | hp2 | a0005 | c0008 | t0009 | g0337 | AFR | LWK | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19058 | hp1 | a0002 | c0003 | t0001 | g0114 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19060 | hp1 | a0002 | c0003 | t0001 | g0133 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19060 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19065 | hp1 | a0001 | c0001 | t0004 | g0318 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19066 | hp2 | a0003 | c0002 | t0001 | g0234 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19068 | hp2 | a0001 | c0005 | t0001 | g0072 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19070 | hp1 | a0003 | c0002 | t0001 | g0343 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19070 | hp2 | a0002 | c0004 | t0001 | g0102 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19072 | hp1 | a0002 | c0003 | t0002 | g0281 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19072 | hp2 | a0002 | c0004 | t0002 | g0083 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19076 | hp1 | a0001 | c0001 | t0004 | g0319 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19076 | hp2 | a0002 | c0004 | t0002 | g0070 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19077 | hp1 | a0002 | c0014 | t0002 | g0268 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19079 | hp1 | a0006 | c0010 | t0001 | g0276 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19079 | hp2 | a0002 | c0003 | t0001 | g0309 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19080 | hp1 | a0001 | c0023 | t0001 | g0057 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19082 | hp1 | a0002 | c0004 | t0001 | g0044 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19084 | hp1 | a0006 | c0015 | t0002 | g0273 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19084 | hp2 | a0002 | c0003 | t0001 | g0116 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19086 | hp1 | a0002 | c0004 | t0001 | g0103 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19086 | hp2 | a0002 | c0003 | t0001 | g0313 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19088 | hp1 | a0001 | c0007 | t0001 | g0265 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19088 | hp2 | a0002 | c0003 | t0001 | g0312 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19090 | hp1 | a0002 | c0003 | t0001 | g0311 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19090 | hp2 | a0003 | c0002 | t0001 | g0205 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19091 | hp1 | a0002 | c0004 | t0002 | g0089 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0240 | AFR | YRI | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA19240 | hp2 | a0001 | c0005 | t0005 | g0058 | AFR | YRI | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA20129 | hp1 | a0001 | c0016 | t0002 | g0150 | AFR | ASW | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA20129 | hp2 | a0001 | c0005 | t0001 | g0354 | AFR | ASW | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA20752 | hp1 | a0003 | c0002 | t0001 | g0195 | EUR | TSI | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA20752 | hp2 | a0004 | c0006 | t0001 | g0207 | EUR | TSI | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01123 | hp1 | a0001 | c0012 | t0001 | g0155 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG01123 | hp2 | a0002 | c0003 | t0001 | g0162 | AMR | CLM | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02486 | hp1 | a0003 | c0002 | t0006 | g0144 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02486 | hp2 | a0001 | c0001 | t0009 | g0353 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02559 | hp1 | a0007 | c0011 | t0007 | g0186 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG02559 | hp2 | a0003 | c0002 | t0010 | g0352 | AFR | ACB | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03471 | hp1 | a0003 | c0002 | t0012 | g0145 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG03471 | hp2 | a0002 | c0003 | t0001 | g0331 | AFR | MSL | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG06807 | hp1 | a0001 | c0027 | t0001 | g0045 | AFR | USA | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
HG06807 | hp2 | a0001 | c0001 | t0009 | g0305 | AFR | USA | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA20300 | hp1 | a0001 | c0005 | t0005 | g0003 | AFR | USA | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | USA | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA21309 | hp1 | a0003 | c0002 | t0008 | g0035 | AFR | LWK | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
NA21309 | hp2 | a0004 | c0006 | t0002 | g0232 | AFR | LWK | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0176 | REF | REF | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
homoSapiens | grch38p0 | a0002 | c0004 | t0001 | g0104 | REF | REF | HHLA1_chr8_132056480_132116157 | HHLA1 | chr8 | 132056480 | 132116157 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:132065886 | T | A | 2 | a0007 a0009 |
4 | HG01167.hp1 HG01891.hp1 HG02258.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1552A>T | p.Thr518Ser | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/17 | 1629/4188 | 1552/1596 | 518/531 | chr8 | 132065886 | |||
chr8:132077728 | A | G | 6 | a0001 a0003 a0006 others(3): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
missense_variant&splice_region_variant | MODERATE | c.1169T>C | p.Leu390Ser | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/17 | 1246/4188 | 1169/1596 | 390/531 | chr8 | 132077728 | |||
chr8:132079844 | A | G | 1 | a0010 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.799T>C | p.Ser267Pro | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/17 | 876/4188 | 799/1596 | 267/531 | chr8 | 132079844 | |||
chr8:132079875 | C | G | 2 | a0005 a0008 |
9 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
missense_variant | MODERATE | c.768G>C | p.Gln256His | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/17 | 845/4188 | 768/1596 | 256/531 | chr8 | 132079875 | |||
chr8:132079891 | G | A | 5 | a0003 a0004 a0010 others(2): Show |
85 | HG00408.hp2 HG00639.hp1 HG00642.hp1 others(82): Show |
missense_variant | MODERATE | c.752C>T | p.Pro251Leu | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/17 | 829/4188 | 752/1596 | 251/531 | chr8 | 132079891 | |||
chr8:132087856 | G | A | 1 | a0013 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.578C>T | p.Thr193Ile | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 9/17 | 655/4188 | 578/1596 | 193/531 | chr8 | 132087856 | |||
chr8:132095718 | C | T | 1 | a0011 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.349G>A | p.Val117Ile | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 6/17 | 426/4188 | 349/1596 | 117/531 | chr8 | 132095718 | |||
chr8:132098893 | C | G | 1 | a0006 | 5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
missense_variant | MODERATE | c.269G>C | p.Arg90Thr | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/17 | 346/4188 | 269/1596 | 90/531 | chr8 | 132098893 | |||
chr8:132098954 | C | T | 1 | a0012 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.208G>A | p.Ala70Thr | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/17 | 285/4188 | 208/1596 | 70/531 | chr8 | 132098954 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:132076512 | A | G | 1 | a0001c0024 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.1203T>C | p.Ser401Ser | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/17 | 1280/4188 | 1203/1596 | 401/531 | chr8 | 132076512 | |||
chr8:132077727 | C | T | 1 | a0001c0023 | 1 | NA19080.hp1 | splice_region_variant&synonymous_variant | LOW | c.1170G>A | p.Leu390Leu | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/17 | 1247/4188 | 1170/1596 | 390/531 | chr8 | 132077727 | |||
chr8:132077922 | C | T | 1 | a0008c0021 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.975G>A | p.Thr325Thr | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/17 | 1052/4188 | 975/1596 | 325/531 | chr8 | 132077922 | |||
chr8:132087672 | G | A | 1 | a0001c0027 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.657C>T | p.Ser219Ser | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/17 | 734/4188 | 657/1596 | 219/531 | chr8 | 132087672 | |||
chr8:132089571 | G | A | 24 | a0001c0001 a0001c0007 a0001c0009 others(21): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
synonymous_variant | LOW | c.477C>T | p.Ile159Ile | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/17 | 554/4188 | 477/1596 | 159/531 | chr8 | 132089571 | |||
chr8:132095583 | T | C | 25 | a0001c0001 a0001c0007 a0001c0009 others(22): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
synonymous_variant | LOW | c.384A>G | p.Val128Val | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/17 | 461/4188 | 384/1596 | 128/531 | chr8 | 132095583 | |||
chr8:132095758 | A | G | 2 | a0001c0012 a0002c0013 |
6 | HG01123.hp1 HG01516.hp2 HG01517.hp1 others(3): Show |
synonymous_variant | LOW | c.309T>C | p.Ser103Ser | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 6/17 | 386/4188 | 309/1596 | 103/531 | chr8 | 132095758 | |||
chr8:132098919 | T | C | 2 | a0001c0007 a0002c0014 |
15 | HG01255.hp1 HG02004.hp2 HG02717.hp2 others(12): Show |
synonymous_variant | LOW | c.243A>G | p.Thr81Thr | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/17 | 320/4188 | 243/1596 | 81/531 | chr8 | 132098919 | |||
chr8:132098934 | G | A | 7 | a0001c0007 a0001c0009 a0001c0012 others(4): Show |
30 | HG01109.hp1 HG01123.hp1 HG01255.hp1 others(27): Show |
synonymous_variant | LOW | c.228C>T | p.Ser76Ser | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/17 | 305/4188 | 228/1596 | 76/531 | chr8 | 132098934 | |||
chr8:132100076 | C | T | 2 | a0001c0009 a0002c0017 |
7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
splice_region_variant&synonymous_variant | LOW | c.198G>A | p.Thr66Thr | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/17 | 275/4188 | 198/1596 | 66/531 | chr8 | 132100076 | |||
chr8:132100100 | C | T | 1 | a0006c0015 | 2 | NA18994.hp2 NA19084.hp1 |
synonymous_variant | LOW | c.174G>A | p.Lys58Lys | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/17 | 251/4188 | 174/1596 | 58/531 | chr8 | 132100100 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:132061707 | G | A | 1 | a0001c0001t0011 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2288C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 2288 | chr8 | 132061707 | ||||||
chr8:132061841 | G | A | 1 | a0003c0002t0012 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2154C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 2154 | chr8 | 132061841 | ||||||
chr8:132061851 | C | A | 1 | a0004c0006t0016 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2144G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 2144 | chr8 | 132061851 | ||||||
chr8:132061852 | C | T | 1 | a0003c0002t0017 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2143G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 2143 | chr8 | 132061852 | ||||||
chr8:132061880 | T | C | 9 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0011 others(6): Show |
20 | HG00609.hp2 HG01106.hp2 HG01261.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2115A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 2115 | chr8 | 132061880 | ||||||
chr8:132061898 | A | C | 1 | a0002c0004t0015 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2097T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 2097 | chr8 | 132061898 | ||||||
chr8:132062009 | G | A | 1 | a0001c0001t0018 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1986C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1986 | chr8 | 132062009 | ||||||
chr8:132062071 | G | C | 1 | a0004c0006t0016 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1924C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1924 | chr8 | 132062071 | ||||||
chr8:132062230 | T | C | 15 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0011 others(12): Show |
30 | HG00733.hp1 HG01099.hp2 HG01106.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1765A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1765 | chr8 | 132062230 | ||||||
chr8:132062304 | C | A | 5 | a0001c0001t0009 a0001c0001t0019 a0001c0001t0024 others(2): Show |
7 | HG01106.hp1 HG02486.hp2 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1691G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1691 | chr8 | 132062304 | ||||||
chr8:132062331 | T | C | 15 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0011 others(12): Show |
30 | HG00733.hp1 HG01099.hp2 HG01106.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1664A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1664 | chr8 | 132062331 | ||||||
chr8:132062464 | A | G | 8 | a0001c0001t0004 a0001c0001t0006 a0001c0005t0006 others(5): Show |
19 | HG00609.hp2 HG01106.hp2 HG01261.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1531T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1531 | chr8 | 132062464 | ||||||
chr8:132062509 | A | T | 2 | a0001c0001t0003 a0008c0021t0003 |
11 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1486T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1486 | chr8 | 132062509 | ||||||
chr8:132062580 | A | G | 44 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(41): Show |
171 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*1415T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1415 | chr8 | 132062580 | ||||||
chr8:132062639 | G | A | 1 | a0003c0002t0010 | 3 | HG02559.hp2 HG03139.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1356C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1356 | chr8 | 132062639 | ||||||
chr8:132062983 | G | A | 1 | a0001c0001t0019 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1012C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 1012 | chr8 | 132062983 | ||||||
chr8:132063100 | A | G | 4 | a0001c0001t0011 a0001c0009t0007 a0007c0011t0007 others(1): Show |
6 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*895T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 895 | chr8 | 132063100 | ||||||
chr8:132063151 | G | C | 11 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0013 others(8): Show |
25 | HG00609.hp2 HG01106.hp2 HG01261.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*844C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 844 | chr8 | 132063151 | ||||||
chr8:132063168 | G | C | 1 | a0001c0001t0020 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*827C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 827 | chr8 | 132063168 | ||||||
chr8:132063415 | A | G | 2 | a0001c0001t0004 a0003c0002t0004 |
10 | HG00609.hp2 HG01106.hp2 HG01261.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*580T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 580 | chr8 | 132063415 | ||||||
chr8:132063490 | T | C | 1 | a0001c0007t0021 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*505A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 505 | chr8 | 132063490 | ||||||
chr8:132063509 | T | C | 1 | a0001c0001t0022 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*486A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 486 | chr8 | 132063509 | ||||||
chr8:132063661 | C | A | 1 | a0002c0003t0023 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*334G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 334 | chr8 | 132063661 | ||||||
chr8:132063755 | C | T | 1 | a0001c0001t0014 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*240G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 240 | chr8 | 132063755 | ||||||
chr8:132063848 | A | G | 17 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(14): Show |
41 | HG00609.hp2 HG00733.hp1 HG01099.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*147T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 17/17 | 147 | chr8 | 132063848 | ||||||
chr8:132105277 | T | C | 1 | a0001c0001t0024 | 1 | HG02809.hp1 | 5_prime_UTR_variant | MODIFIER | c.-12A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/17 | 12 | chr8 | 132105277 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:132064133 | A | G | 1 | a0001c0007t0021g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1553-95T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132064133 | |||||||
chr8:132064249 | A | C | 1 | a0001c0001t0020g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1553-211T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132064249 | |||||||
chr8:132064501 | G | A | 6 | a0001c0001t0005g0330 a0001c0005t0005g0003 a0001c0005t0005g0008 others(3): Show |
10 | HG00733.hp1 HG01099.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1553-463C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132064501 | |||||||
chr8:132064508 | C | A | 4 | a0001c0001t0001g0251 a0001c0001t0001g0300 a0001c0007t0001g0263 others(1): Show |
4 | HG00544.hp2 HG01255.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1553-470G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132064508 | |||||||
chr8:132064508 | C | G | 14 | a0001c0001t0001g0130 a0001c0001t0002g0279 a0001c0012t0001g0349 others(11): Show |
15 | HG00642.hp1 HG00673.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1553-470G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132064508 | |||||||
chr8:132064624 | CTG | C | 53 | a0001c0001t0002g0316 a0001c0001t0003g0002 a0001c0001t0003g0028 others(50): Show |
67 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1553-588_1553-587d others(4): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132064624 | |||||||
chr8:132064906 | A | T | 1 | a0001c0016t0002g0150 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1553-868T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132064906 | |||||||
chr8:132064934 | A | G | 1 | a0001c0005t0006g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1553-896T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132064934 | |||||||
chr8:132065057 | G | T | 6 | a0001c0001t0011g0159 a0001c0009t0007g0188 a0007c0011t0007g0042 others(3): Show |
6 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1552+829C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065057 | |||||||
chr8:132065068 | T | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0300 a0003c0002t0001g0234 |
3 | HG00544.hp2 NA18954.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1552+818A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065068 | |||||||
chr8:132065112 | A | G | 2 | a0003c0002t0001g0210 a0003c0002t0001g0225 |
2 | NA18962.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1552+774T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065112 | |||||||
chr8:132065124 | T | G | 95 | a0001c0001t0002g0004 a0001c0001t0002g0015 a0001c0001t0002g0016 others(92): Show |
111 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1552+762A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065124 | |||||||
chr8:132065153 | A | G | 6 | a0001c0001t0011g0159 a0001c0009t0007g0188 a0007c0011t0007g0042 others(3): Show |
6 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1552+733T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065153 | |||||||
chr8:132065192 | G | A | 1 | a0001c0001t0005g0330 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1552+694C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065192 | |||||||
chr8:132065236 | T | C | 1 | a0001c0001t0020g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1552+650A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065236 | |||||||
chr8:132065293 | G | A | 3 | a0007c0011t0007g0042 a0007c0011t0007g0270 a0009c0025t0007g0282 |
3 | HG01167.hp1 HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1552+593C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065293 | |||||||
chr8:132065442 | T | C | 5 | a0001c0001t0002g0316 a0002c0004t0002g0077 a0006c0010t0002g0272 others(2): Show |
5 | HG02015.hp2 HG02071.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1552+444A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065442 | |||||||
chr8:132065484 | A | G | 1 | a0003c0002t0001g0011 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1552+402T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065484 | |||||||
chr8:132065489 | A | G | 108 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0020 others(105): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1552+397T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065489 | |||||||
chr8:132065555 | T | C | 1 | a0003c0002t0001g0199 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1552+331A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065555 | |||||||
chr8:132065564 | G | A | 2 | a0002c0003t0002g0308 a0002c0003t0023g0031 |
2 | HG02602.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1552+322C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065564 | |||||||
chr8:132065574 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1552+312C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065574 | |||||||
chr8:132065604 | C | T | 1 | a0001c0005t0006g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1552+282G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065604 | |||||||
chr8:132065662 | G | T | 9 | a0001c0001t0002g0010 a0001c0001t0002g0149 a0001c0001t0002g0170 others(6): Show |
10 | HG01070.hp1 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.1552+224C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065662 | |||||||
chr8:132065836 | G | A | 3 | a0007c0011t0007g0042 a0007c0011t0007g0270 a0009c0025t0007g0282 |
3 | HG01167.hp1 HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1552+50C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 16/16 | chr8 | 132065836 | |||||||
chr8:132066014 | G | T | 34 | a0001c0001t0001g0299 a0001c0001t0002g0004 a0001c0001t0002g0015 others(31): Show |
36 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.1470-46C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066014 | |||||||
chr8:132066127 | T | C | 1 | a0002c0003t0001g0336 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1470-159A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066127 | |||||||
chr8:132066146 | GGAA | G | 4 | a0007c0011t0007g0042 a0007c0011t0007g0186 a0007c0011t0007g0270 others(1): Show |
4 | HG01167.hp1 HG01891.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1470-181_1470-179d others(5): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066146 | |||||||
chr8:132066178 | T | C | 1 | a0001c0007t0001g0263 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1470-210A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066178 | |||||||
chr8:132066202 | C | T | 2 | a0001c0009t0008g0342 a0002c0003t0001g0331 |
2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1470-234G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066202 | |||||||
chr8:132066245 | G | A | 6 | a0001c0001t0011g0159 a0001c0009t0007g0188 a0007c0011t0007g0042 others(3): Show |
6 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1470-277C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066245 | |||||||
chr8:132066291 | T | A | 1 | a0002c0003t0001g0114 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1470-323A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066291 | |||||||
chr8:132066362 | C | T | 5 | a0001c0001t0002g0316 a0002c0004t0002g0077 a0006c0010t0002g0272 others(2): Show |
5 | HG02015.hp2 HG02071.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1470-394G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066362 | |||||||
chr8:132066371 | T | TG | 6 | a0001c0001t0009g0302 a0001c0001t0009g0305 a0001c0001t0009g0353 others(3): Show |
6 | HG01106.hp1 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1470-404dupC | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066371 | |||||||
chr8:132066384 | CTGTT | C | 5 | a0001c0001t0002g0316 a0002c0004t0002g0077 a0006c0010t0002g0272 others(2): Show |
5 | HG02015.hp2 HG02071.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1470-420_1470-417d others(6): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066384 | |||||||
chr8:132066440 | G | C | 1 | a0007c0011t0007g0186 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1470-472C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066440 | |||||||
chr8:132066463 | T | G | 6 | a0001c0001t0011g0159 a0001c0009t0007g0188 a0007c0011t0007g0042 others(3): Show |
6 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1470-495A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066463 | |||||||
chr8:132066568 | G | A | 5 | a0001c0009t0008g0339 a0001c0009t0008g0340 a0001c0009t0008g0341 others(2): Show |
5 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1470-600C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066568 | |||||||
chr8:132066831 | C | T | 6 | a0001c0001t0011g0159 a0001c0009t0007g0188 a0007c0011t0007g0042 others(3): Show |
6 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1470-863G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066831 | |||||||
chr8:132066907 | G | A | 6 | a0001c0001t0013g0239 a0001c0009t0008g0339 a0001c0009t0008g0340 others(3): Show |
6 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1470-939C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132066907 | |||||||
chr8:132067041 | C | T | 1 | a0001c0005t0002g0086 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1470-1073G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067041 | |||||||
chr8:132067141 | C | T | 1 | a0003c0002t0001g0030 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1470-1173G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067141 | |||||||
chr8:132067218 | T | A | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1470-1250A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067218 | |||||||
chr8:132067219 | G | C | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1470-1251C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067219 | |||||||
chr8:132067220 | C | A | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1470-1252G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067220 | |||||||
chr8:132067222 | C | T | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1470-1254G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067222 | |||||||
chr8:132067224 | A | G | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1470-1256T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067224 | |||||||
chr8:132067227 | C | T | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1470-1259G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067227 | |||||||
chr8:132067228 | A | T | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1470-1260T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067228 | |||||||
chr8:132067329 | G | A | 142 | a0001c0001t0001g0299 a0001c0001t0002g0004 a0001c0001t0002g0015 others(139): Show |
162 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.1470-1361C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067329 | |||||||
chr8:132067594 | G | T | 1 | a0003c0002t0002g0230 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1470-1626C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067594 | |||||||
chr8:132067853 | G | A | 1 | a0002c0004t0002g0005 | 3 | HG01175.hp2 HG01192.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1470-1885C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132067853 | |||||||
chr8:132068053 | A | G | 6 | a0001c0001t0011g0159 a0001c0009t0007g0188 a0007c0011t0007g0042 others(3): Show |
6 | HG01167.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1470-2085T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068053 | |||||||
chr8:132068143 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1470-2175T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068143 | |||||||
chr8:132068177 | C | T | 6 | a0001c0001t0013g0239 a0001c0009t0008g0339 a0001c0009t0008g0340 others(3): Show |
6 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1470-2209G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068177 | |||||||
chr8:132068213 | C | A | 1 | a0001c0001t0020g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1470-2245G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068213 | |||||||
chr8:132068277 | A | T | 6 | a0001c0009t0002g0278 a0001c0016t0002g0150 a0001c0027t0001g0045 others(3): Show |
6 | HG02257.hp1 HG02818.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1470-2309T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068277 | |||||||
chr8:132068291 | C | T | 1 | a0002c0003t0001g0075 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1470-2323G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068291 | |||||||
chr8:132068476 | T | A | 3 | a0003c0002t0010g0156 a0003c0002t0010g0158 a0003c0002t0010g0352 |
3 | HG02559.hp2 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1470-2508A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068476 | |||||||
chr8:132068486 | G | T | 5 | a0001c0001t0002g0316 a0002c0004t0002g0077 a0006c0010t0002g0272 others(2): Show |
5 | HG02015.hp2 HG02071.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1470-2518C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068486 | |||||||
chr8:132068583 | G | T | 17 | a0001c0001t0001g0130 a0001c0001t0001g0251 a0001c0001t0001g0300 others(14): Show |
18 | HG00544.hp2 HG00642.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.1470-2615C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068583 | |||||||
chr8:132068686 | C | T | 5 | a0001c0001t0002g0316 a0002c0004t0002g0077 a0006c0010t0002g0272 others(2): Show |
5 | HG02015.hp2 HG02071.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1469+2654G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068686 | |||||||
chr8:132068690 | C | T | 5 | a0001c0001t0002g0316 a0002c0004t0002g0077 a0006c0010t0002g0272 others(2): Show |
5 | HG02015.hp2 HG02071.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1469+2650G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068690 | |||||||
chr8:132068710 | G | A | 4 | a0001c0001t0006g0240 a0001c0001t0006g0283 a0001c0005t0006g0074 others(1): Show |
4 | HG02886.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469+2630C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068710 | |||||||
chr8:132068755 | C | G | 45 | a0001c0001t0001g0020 a0001c0001t0001g0299 a0001c0001t0002g0004 others(42): Show |
47 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1469+2585G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068755 | |||||||
chr8:132068765 | T | G | 2 | a0002c0003t0002g0172 a0004c0006t0002g0204 |
2 | HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1469+2575A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068765 | |||||||
chr8:132068831 | A | G | 7 | a0001c0007t0001g0259 a0001c0007t0001g0260 a0001c0009t0008g0339 others(4): Show |
7 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1469+2509T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068831 | |||||||
chr8:132068996 | G | GGTAGAAA others(4): Show |
1 | a0002c0003t0001g0114 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1469+2343_1469+234 others(15): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132068996 | |||||||
chr8:132069007 | C | T | 1 | a0001c0001t0005g0330 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1469+2333G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069007 | |||||||
chr8:132069013 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1469+2327C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069013 | |||||||
chr8:132069199 | C | A | 17 | a0001c0001t0002g0096 a0001c0001t0004g0164 a0001c0001t0004g0169 others(14): Show |
17 | HG00609.hp2 HG01106.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.1469+2141G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069199 | |||||||
chr8:132069245 | C | A | 5 | a0001c0001t0002g0316 a0002c0004t0002g0077 a0006c0010t0002g0272 others(2): Show |
5 | HG02015.hp2 HG02071.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1469+2095G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069245 | |||||||
chr8:132069249 | A | G | 3 | a0003c0002t0010g0156 a0003c0002t0010g0158 a0003c0002t0010g0352 |
3 | HG02559.hp2 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1469+2091T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069249 | |||||||
chr8:132069355 | G | GT | 7 | a0001c0001t0009g0302 a0001c0001t0009g0305 a0001c0001t0009g0353 others(4): Show |
7 | HG01106.hp1 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1469+1984dupA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069355 | |||||||
chr8:132069360 | T | TTTG | 5 | a0001c0001t0002g0316 a0002c0004t0002g0077 a0006c0010t0002g0272 others(2): Show |
5 | HG02015.hp2 HG02071.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1469+1979_1469+198 others(7): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069360 | |||||||
chr8:132069364 | G | T | 7 | a0001c0001t0003g0100 a0001c0009t0002g0278 a0001c0027t0001g0045 others(4): Show |
7 | HG02257.hp1 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1469+1976C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069364 | |||||||
chr8:132069400 | C | T | 1 | a0001c0009t0002g0278 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1469+1940G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069400 | |||||||
chr8:132069401 | G | A | 1 | a0003c0002t0001g0254 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1469+1939C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069401 | |||||||
chr8:132069468 | G | A | 1 | a0010c0026t0001g0219 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1469+1872C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069468 | |||||||
chr8:132069594 | A | G | 1 | a0001c0001t0005g0330 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1469+1746T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069594 | |||||||
chr8:132069603 | T | G | 3 | a0001c0001t0002g0081 a0001c0001t0002g0098 a0001c0007t0002g0269 |
3 | HG02922.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1469+1737A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069603 | |||||||
chr8:132069685 | G | A | 12 | a0001c0001t0002g0096 a0001c0001t0004g0164 a0001c0001t0004g0169 others(9): Show |
12 | HG00609.hp2 HG01106.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1469+1655C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069685 | |||||||
chr8:132069736 | C | T | 1 | a0008c0022t0001g0338 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1469+1604G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069736 | |||||||
chr8:132069739 | T | G | 104 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(101): Show |
122 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1469+1601A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069739 | |||||||
chr8:132069748 | C | A | 6 | a0001c0001t0009g0302 a0001c0001t0009g0305 a0001c0001t0009g0353 others(3): Show |
6 | HG01106.hp1 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1469+1592G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069748 | |||||||
chr8:132069814 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0322 |
2 | NA18966.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1469+1526G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069814 | |||||||
chr8:132069816 | G | C | 5 | a0001c0001t0002g0316 a0002c0004t0002g0077 a0006c0010t0002g0272 others(2): Show |
5 | HG02015.hp2 HG02071.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1469+1524C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069816 | |||||||
chr8:132069898 | C | T | 1 | a0002c0003t0001g0168 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1469+1442G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069898 | |||||||
chr8:132069923 | G | A | 1 | a0007c0011t0007g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1469+1417C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069923 | |||||||
chr8:132069925 | A | G | 189 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(186): Show |
213 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.1469+1415T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132069925 | |||||||
chr8:132070010 | A | C | 3 | a0003c0002t0002g0146 a0003c0002t0006g0144 a0003c0002t0012g0145 |
3 | HG02486.hp1 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1469+1330T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070010 | |||||||
chr8:132070011 | C | A | 1 | a0001c0001t0004g0320 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1469+1329G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | |||||||
chr8:132070011 | C | CGGGGGGG others(3): Show |
14 | a0001c0001t0001g0122 a0001c0001t0001g0167 a0001c0001t0001g0252 others(11): Show |
14 | HG01358.hp2 HG01496.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1469+1319_1469+132 others(14): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | |||||||
chr8:132070011 | C | CGGGGGGG others(4): Show |
14 | a0001c0001t0001g0177 a0001c0001t0004g0333 a0001c0005t0001g0060 others(11): Show |
15 | HG00609.hp2 HG00735.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1469+1318_1469+132 others(15): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | |||||||
chr8:132070011 | C | CGGGGGGG others(5): Show |
28 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0108 others(25): Show |
28 | HG00280.hp1 HG00544.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1469+1317_1469+132 others(16): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | |||||||
chr8:132070011 | C | CGGGGGGG others(6): Show |
32 | a0001c0001t0001g0120 a0001c0001t0001g0129 a0001c0001t0001g0137 others(29): Show |
32 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.1469+1316_1469+132 others(17): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | |||||||
chr8:132070011 | C | CGGGGGGG others(7): Show |
30 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0128 others(27): Show |
30 | HG00639.hp1 HG01069.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1469+1328_1469+132 others(18): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | |||||||
chr8:132070011 | C | CGGGGGGG others(8): Show |
22 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0211 others(19): Show |
22 | HG00408.hp2 HG00642.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1469+1328_1469+132 others(19): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | |||||||
chr8:132070011 | C | CGGGGGGG others(9): Show |
11 | a0001c0001t0001g0140 a0001c0001t0004g0169 a0001c0007t0001g0264 others(8): Show |
11 | HG01070.hp2 HG01261.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.1469+1328_1469+132 others(20): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | |||||||
chr8:132070011 | C | CGGGGGGG others(10): Show |
5 | a0001c0001t0001g0250 a0001c0005t0001g0062 a0001c0005t0001g0068 others(2): Show |
5 | HG01169.hp2 HG01433.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1469+1328_1469+132 others(21): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | |||||||
chr8:132070011 | C | CGGGGGGG others(11): Show |
6 | a0001c0001t0001g0118 a0001c0001t0013g0239 a0002c0003t0001g0315 others(3): Show |
6 | HG01934.hp1 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1469+1328_1469+132 others(22): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | |||||||
chr8:132070011 | C | CGGGGGGG others(12): Show |
2 | a0001c0005t0001g0061 a0003c0002t0001g0243 |
2 | HG00280.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1469+1328_1469+132 others(23): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | |||||||
chr8:132070011 | C | CGGGGGGG others(13): Show |
4 | a0001c0001t0003g0099 a0003c0002t0001g0241 a0004c0006t0001g0095 others(1): Show |
4 | HG00733.hp2 HG01993.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1469+1328_1469+132 others(24): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | |||||||
chr8:132070011 | C | CGGGGGGG others(14): Show |
1 | a0001c0001t0004g0164 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1469+1328_1469+132 others(25): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070011 | |||||||
chr8:132070012 | GGGGGGGG others(6): Show |
G | 65 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(62): Show |
69 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1469+1315_1469+132 others(17): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070012 | |||||||
chr8:132070015 | G | GGGGGGGG others(6): Show |
1 | a0001c0009t0008g0342 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1469+1324_1469+132 others(17): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070015 | |||||||
chr8:132070016 | G | GGGGGGGG others(3): Show |
1 | a0001c0009t0008g0341 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1469+1323_1469+132 others(14): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070016 | |||||||
chr8:132070017 | G | GGGGGGGG others(3): Show |
1 | a0003c0002t0008g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1469+1322_1469+132 others(14): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070017 | |||||||
chr8:132070019 | G | T | 61 | a0001c0001t0001g0130 a0001c0001t0001g0251 a0001c0001t0001g0300 others(58): Show |
76 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1469+1321C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070019 | |||||||
chr8:132070020 | G | T | 2 | a0002c0004t0002g0070 a0004c0006t0002g0037 |
2 | NA18943.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1469+1320C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070020 | |||||||
chr8:132070020 | GGGGGA | G | 62 | a0001c0001t0001g0130 a0001c0001t0001g0251 a0001c0001t0001g0300 others(59): Show |
77 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1469+1315_1469+131 others(9): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070020 | |||||||
chr8:132070021 | G | GGGGGGGG others(7): Show |
1 | a0003c0002t0001g0227 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1469+1318_1469+131 others(18): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070021 | |||||||
chr8:132070021 | G | T | 1 | a0002c0003t0002g0135 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1469+1319C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070021 | |||||||
chr8:132070024 | GA | G | 3 | a0001c0001t0002g0010 a0001c0001t0002g0277 a0001c0001t0004g0319 |
3 | HG03017.hp1 HG03688.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1469+1315delT | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070024 | |||||||
chr8:132070025 | A | G | 42 | a0001c0001t0002g0010 a0001c0001t0002g0096 a0001c0001t0002g0149 others(39): Show |
46 | HG00609.hp2 HG00733.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.1469+1315T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070025 | |||||||
chr8:132070025 | A | T | 1 | a0001c0009t0008g0340 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1469+1315T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070025 | |||||||
chr8:132070028 | G | GGGGTGGG others(10): Show |
1 | a0001c0007t0001g0260 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1469+1311_1469+131 others(21): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070028 | |||||||
chr8:132070028 | G | GGGGTGGG others(8): Show |
1 | a0001c0009t0008g0339 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1469+1311_1469+131 others(19): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070028 | |||||||
chr8:132070028 | G | GGGTGGGG others(8): Show |
1 | a0001c0007t0001g0259 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1469+1311_1469+131 others(19): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070028 | |||||||
chr8:132070028 | G | T | 3 | a0001c0009t0008g0341 a0001c0009t0008g0342 a0003c0002t0008g0035 |
3 | HG02896.hp2 HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1469+1312C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070028 | |||||||
chr8:132070247 | T | G | 157 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(154): Show |
177 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.1469+1093A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070247 | |||||||
chr8:132070252 | G | A | 1 | a0001c0001t0002g0323 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1469+1088C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070252 | |||||||
chr8:132070381 | C | T | 3 | a0003c0002t0010g0156 a0003c0002t0010g0158 a0003c0002t0010g0352 |
3 | HG02559.hp2 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1469+959G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070381 | |||||||
chr8:132070408 | A | T | 1 | a0003c0002t0001g0011 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1469+932T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070408 | |||||||
chr8:132070568 | C | T | 1 | a0003c0002t0002g0141 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1469+772G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070568 | |||||||
chr8:132070587 | T | C | 2 | a0002c0003t0001g0315 a0004c0006t0001g0334 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1469+753A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070587 | |||||||
chr8:132070669 | G | A | 1 | a0001c0001t0011g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1469+671C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070669 | |||||||
chr8:132070676 | C | T | 1 | a0007c0011t0007g0186 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1469+664G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070676 | |||||||
chr8:132070722 | TCATCTCA others(8): Show |
T | 1 | a0001c0001t0002g0107 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1469+603_1469+617d others(17): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132070722 | |||||||
chr8:132071049 | C | T | 1 | a0002c0003t0002g0301 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1469+291G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132071049 | |||||||
chr8:132071164 | C | T | 1 | a0001c0001t0005g0330 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1469+176G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132071164 | |||||||
chr8:132071284 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0252 |
2 | NA18968.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1469+56G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 15/16 | chr8 | 132071284 | |||||||
chr8:132071554 | G | A | 20 | a0001c0001t0003g0002 a0001c0001t0003g0028 a0001c0001t0003g0099 others(17): Show |
25 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.1316-61C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071554 | |||||||
chr8:132071580 | G | A | 1 | a0001c0001t0013g0239 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1316-87C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071580 | |||||||
chr8:132071628 | A | T | 2 | a0004c0006t0001g0290 a0004c0006t0001g0291 |
2 | HG02572.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1316-135T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071628 | |||||||
chr8:132071677 | GT | G | 4 | a0001c0001t0002g0316 a0006c0010t0002g0272 a0006c0010t0002g0275 others(1): Show |
4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1316-185delA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071677 | |||||||
chr8:132071788 | G | C | 1 | a0001c0001t0001g0250 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1316-295C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071788 | |||||||
chr8:132071789 | C | A | 1 | a0001c0001t0001g0250 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1316-296G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071789 | |||||||
chr8:132071790 | A | T | 1 | a0001c0001t0001g0250 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1316-297T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071790 | |||||||
chr8:132071851 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1316-358C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071851 | |||||||
chr8:132071852 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1316-359T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071852 | |||||||
chr8:132071921 | C | T | 1 | a0001c0023t0001g0057 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1316-428G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071921 | |||||||
chr8:132071940 | G | A | 5 | a0001c0005t0005g0003 a0001c0005t0005g0008 a0001c0005t0005g0058 others(2): Show |
9 | HG00733.hp1 HG01099.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1316-447C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071940 | |||||||
chr8:132071951 | T | C | 3 | a0001c0001t0002g0081 a0001c0001t0002g0098 a0001c0007t0002g0269 |
3 | HG02922.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1316-458A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071951 | |||||||
chr8:132071960 | G | A | 1 | a0003c0002t0001g0033 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1316-467C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071960 | |||||||
chr8:132071967 | C | A | 1 | a0001c0001t0001g0250 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1316-474G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071967 | |||||||
chr8:132071968 | A | G | 4 | a0001c0001t0002g0316 a0006c0010t0002g0272 a0006c0010t0002g0275 others(1): Show |
4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1316-475T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132071968 | |||||||
chr8:132072048 | G | T | 1 | a0001c0001t0001g0250 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1316-555C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072048 | |||||||
chr8:132072078 | A | G | 1 | a0001c0001t0002g0171 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1316-585T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072078 | |||||||
chr8:132072097 | C | T | 1 | a0001c0007t0001g0263 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1316-604G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072097 | |||||||
chr8:132072249 | G | A | 48 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(45): Show |
52 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.1316-756C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072249 | |||||||
chr8:132072333 | T | C | 1 | a0001c0001t0005g0330 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1316-840A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072333 | |||||||
chr8:132072343 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1316-850C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072343 | |||||||
chr8:132072416 | A | C | 4 | a0001c0001t0002g0316 a0006c0010t0002g0272 a0006c0010t0002g0275 others(1): Show |
4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1316-923T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072416 | |||||||
chr8:132072427 | T | A | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1316-934A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072427 | |||||||
chr8:132072496 | T | C | 55 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(52): Show |
59 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.1316-1003A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072496 | |||||||
chr8:132072787 | G | T | 1 | a0001c0001t0001g0250 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1316-1294C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072787 | |||||||
chr8:132072905 | T | TA | 6 | a0001c0001t0009g0302 a0001c0001t0009g0305 a0001c0001t0009g0353 others(3): Show |
6 | HG01106.hp1 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1316-1413dupT | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132072905 | |||||||
chr8:132073064 | G | T | 1 | a0002c0003t0001g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1316-1571C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073064 | |||||||
chr8:132073074 | A | T | 1 | a0002c0003t0001g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1316-1581T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073074 | |||||||
chr8:132073214 | T | G | 1 | a0002c0004t0002g0077 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1316-1721A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073214 | |||||||
chr8:132073416 | G | T | 4 | a0001c0001t0002g0316 a0006c0010t0002g0272 a0006c0010t0002g0275 others(1): Show |
4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1316-1923C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073416 | |||||||
chr8:132073458 | T | C | 1 | a0002c0003t0001g0189 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1316-1965A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073458 | |||||||
chr8:132073556 | G | A | 1 | a0003c0002t0002g0034 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1316-2063C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073556 | |||||||
chr8:132073619 | C | G | 4 | a0001c0001t0002g0316 a0006c0010t0002g0272 a0006c0010t0002g0275 others(1): Show |
4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1316-2126G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073619 | |||||||
chr8:132073686 | A | C | 1 | a0008c0021t0003g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1316-2193T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073686 | |||||||
chr8:132073702 | C | A | 4 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0005t0001g0101 others(1): Show |
4 | HG00639.hp1 HG01496.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1316-2209G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073702 | |||||||
chr8:132073820 | G | A | 1 | a0001c0001t0005g0330 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1315+2235C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073820 | |||||||
chr8:132073836 | A | G | 2 | a0001c0005t0001g0059 a0001c0005t0001g0060 |
2 | HG02155.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1315+2219T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073836 | |||||||
chr8:132073963 | CT | C | 5 | a0001c0005t0005g0003 a0001c0005t0005g0008 a0001c0005t0005g0058 others(2): Show |
9 | HG00733.hp1 HG01099.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1315+2091delA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073963 | |||||||
chr8:132073987 | C | A | 1 | a0002c0003t0001g0315 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1315+2068G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132073987 | |||||||
chr8:132074013 | A | G | 1 | a0001c0001t0013g0239 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1315+2042T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074013 | |||||||
chr8:132074042 | C | T | 1 | a0003c0002t0001g0222 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1315+2013G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074042 | |||||||
chr8:132074115 | C | A | 63 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
67 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1315+1940G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074115 | |||||||
chr8:132074225 | T | C | 1 | a0008c0021t0003g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1315+1830A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074225 | |||||||
chr8:132074233 | C | T | 4 | a0001c0027t0001g0045 a0003c0002t0002g0141 a0003c0002t0002g0142 others(1): Show |
4 | HG02257.hp1 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1315+1822G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074233 | |||||||
chr8:132074306 | T | C | 4 | a0001c0001t0002g0316 a0006c0010t0002g0272 a0006c0010t0002g0275 others(1): Show |
4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315+1749A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074306 | |||||||
chr8:132074320 | C | A | 1 | a0002c0003t0001g0114 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1315+1735G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074320 | |||||||
chr8:132074322 | A | T | 1 | a0002c0003t0001g0114 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1315+1733T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074322 | |||||||
chr8:132074329 | CT | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0183 a0001c0001t0001g0286 others(3): Show |
8 | HG00423.hp1 HG02074.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1315+1725delA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074329 | |||||||
chr8:132074337 | T | C | 51 | a0001c0001t0001g0130 a0001c0001t0001g0251 a0001c0001t0001g0300 others(48): Show |
57 | HG00544.hp2 HG00642.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1315+1718A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074337 | |||||||
chr8:132074366 | G | A | 1 | a0002c0003t0001g0075 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1315+1689C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074366 | |||||||
chr8:132074407 | A | T | 6 | a0002c0003t0002g0281 a0002c0003t0002g0348 a0002c0004t0001g0071 others(3): Show |
6 | HG00438.hp1 HG00597.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.1315+1648T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074407 | |||||||
chr8:132074463 | T | A | 3 | a0001c0001t0002g0213 a0001c0001t0002g0215 a0001c0001t0002g0217 |
3 | NA18972.hp1 NA19003.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1315+1592A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074463 | |||||||
chr8:132074533 | G | A | 4 | a0003c0002t0001g0241 a0003c0002t0001g0243 a0003c0002t0001g0244 others(1): Show |
4 | HG01934.hp1 HG01975.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315+1522C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074533 | |||||||
chr8:132074561 | T | G | 3 | a0001c0001t0006g0240 a0001c0001t0006g0283 a0001c0007t0006g0258 |
3 | HG03041.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1315+1494A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074561 | |||||||
chr8:132074602 | A | AT | 22 | a0001c0001t0002g0096 a0001c0001t0002g0316 a0001c0001t0004g0164 others(19): Show |
22 | HG00609.hp2 HG01106.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.1315+1452dupA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074602 | |||||||
chr8:132074607 | T | A | 1 | a0002c0003t0002g0348 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1315+1448A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074607 | |||||||
chr8:132074634 | G | A | 1 | a0001c0005t0006g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1315+1421C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074634 | |||||||
chr8:132074814 | G | A | 1 | a0002c0003t0023g0031 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1315+1241C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074814 | |||||||
chr8:132074853 | G | A | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1202C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074853 | |||||||
chr8:132074854 | G | C | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1201C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074854 | |||||||
chr8:132074855 | G | A | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1200C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074855 | |||||||
chr8:132074856 | T | C | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1199A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074856 | |||||||
chr8:132074857 | A | T | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1198T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074857 | |||||||
chr8:132074858 | G | A | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1197C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074858 | |||||||
chr8:132074860 | T | A | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1195A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074860 | |||||||
chr8:132074862 | A | C | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1193T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074862 | |||||||
chr8:132074863 | A | G | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1192T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074863 | |||||||
chr8:132074864 | T | C | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1191A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074864 | |||||||
chr8:132074865 | A | G | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1190T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074865 | |||||||
chr8:132074866 | A | T | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1189T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074866 | |||||||
chr8:132074867 | A | G | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1188T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074867 | |||||||
chr8:132074869 | A | T | 1 | a0003c0002t0001g0223 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1315+1186T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132074869 | |||||||
chr8:132075124 | T | C | 4 | a0001c0001t0002g0316 a0006c0010t0002g0272 a0006c0010t0002g0275 others(1): Show |
4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315+931A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075124 | |||||||
chr8:132075241 | T | A | 4 | a0001c0001t0002g0316 a0006c0010t0002g0272 a0006c0010t0002g0275 others(1): Show |
4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315+814A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075241 | |||||||
chr8:132075275 | C | G | 1 | a0001c0001t0001g0252 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1315+780G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075275 | |||||||
chr8:132075344 | C | T | 1 | a0011c0019t0001g0097 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1315+711G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075344 | |||||||
chr8:132075404 | G | T | 1 | a0001c0005t0002g0350 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1315+651C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075404 | |||||||
chr8:132075413 | C | A | 2 | a0002c0003t0002g0332 a0002c0014t0002g0267 |
2 | HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1315+642G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075413 | |||||||
chr8:132075437 | C | T | 3 | a0007c0011t0007g0042 a0007c0011t0007g0186 a0007c0011t0007g0270 |
3 | HG01891.hp1 HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1315+618G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075437 | |||||||
chr8:132075510 | G | T | 4 | a0001c0001t0002g0316 a0006c0010t0002g0272 a0006c0010t0002g0275 others(1): Show |
4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315+545C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075510 | |||||||
chr8:132075521 | T | C | 4 | a0001c0001t0002g0316 a0006c0010t0002g0272 a0006c0010t0002g0275 others(1): Show |
4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315+534A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075521 | |||||||
chr8:132075537 | A | G | 1 | a0003c0002t0001g0233 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1315+518T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075537 | |||||||
chr8:132075589 | C | G | 1 | a0002c0004t0002g0005 | 3 | HG01175.hp2 HG01192.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1315+466G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075589 | |||||||
chr8:132075614 | T | C | 2 | a0002c0003t0001g0315 a0004c0006t0001g0334 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1315+441A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075614 | |||||||
chr8:132075780 | A | T | 8 | a0001c0001t0003g0143 a0001c0001t0013g0239 a0001c0007t0021g0261 others(5): Show |
8 | HG02055.hp1 HG02486.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1315+275T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 14/16 | chr8 | 132075780 | |||||||
chr8:132076179 | G | A | 1 | a0001c0016t0006g0151 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1241-50C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/16 | chr8 | 132076179 | |||||||
chr8:132076183 | A | G | 1 | a0003c0002t0001g0011 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1241-54T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/16 | chr8 | 132076183 | |||||||
chr8:132076204 | T | C | 4 | a0001c0001t0002g0316 a0006c0010t0002g0272 a0006c0010t0002g0275 others(1): Show |
4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-75A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/16 | chr8 | 132076204 | |||||||
chr8:132076246 | T | C | 4 | a0001c0001t0002g0316 a0006c0010t0002g0272 a0006c0010t0002g0275 others(1): Show |
4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-117A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/16 | chr8 | 132076246 | |||||||
chr8:132076289 | A | C | 4 | a0001c0001t0002g0316 a0006c0010t0002g0272 a0006c0010t0002g0275 others(1): Show |
4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-160T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/16 | chr8 | 132076289 | |||||||
chr8:132076363 | A | G | 4 | a0001c0001t0002g0316 a0006c0010t0002g0272 a0006c0010t0002g0275 others(1): Show |
4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+112T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/16 | chr8 | 132076363 | |||||||
chr8:132076388 | C | T | 1 | a0001c0001t0009g0353 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1240+87G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/16 | chr8 | 132076388 | |||||||
chr8:132076398 | C | A | 1 | a0001c0005t0006g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1240+77G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/16 | chr8 | 132076398 | |||||||
chr8:132076429 | C | T | 1 | a0001c0005t0006g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1240+46G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 13/16 | chr8 | 132076429 | |||||||
chr8:132076603 | G | A | 1 | a0011c0019t0001g0097 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1172-60C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132076603 | |||||||
chr8:132076713 | G | A | 1 | a0003c0002t0001g0199 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1172-170C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132076713 | |||||||
chr8:132076729 | G | A | 1 | a0003c0002t0001g0222 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1172-186C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132076729 | |||||||
chr8:132076757 | G | A | 1 | a0001c0005t0006g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1172-214C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132076757 | |||||||
chr8:132076907 | T | C | 1 | a0001c0001t0002g0111 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1172-364A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132076907 | |||||||
chr8:132076941 | C | T | 6 | a0002c0003t0001g0311 a0002c0003t0001g0312 a0002c0003t0001g0313 others(3): Show |
6 | HG01358.hp1 HG03704.hp1 NA19012.hp2 others(3): Show |
intron_variant | MODIFIER | c.1172-398G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132076941 | |||||||
chr8:132077042 | G | A | 1 | a0005c0008t0002g0346 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1172-499C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132077042 | |||||||
chr8:132077133 | G | C | 4 | a0001c0001t0002g0316 a0006c0010t0002g0272 a0006c0010t0002g0275 others(1): Show |
4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1172-590C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132077133 | |||||||
chr8:132077243 | A | C | 1 | a0004c0006t0001g0207 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1171+483T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132077243 | |||||||
chr8:132077468 | A | C | 1 | a0002c0003t0001g0285 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1171+258T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132077468 | |||||||
chr8:132077511 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1171+215T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132077511 | |||||||
chr8:132077581 | G | A | 1 | a0001c0009t0007g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1171+145C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132077581 | |||||||
chr8:132077667 | A | T | 1 | a0002c0004t0001g0053 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1171+59T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132077667 | |||||||
chr8:132077694 | C | T | 2 | a0001c0001t0002g0081 a0001c0001t0002g0098 |
2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1171+32G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 12/16 | chr8 | 132077694 | |||||||
chr8:132078029 | A | G | 6 | a0001c0005t0005g0003 a0001c0005t0005g0008 a0001c0005t0005g0058 others(3): Show |
10 | HG00733.hp1 HG01099.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.926-58T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078029 | |||||||
chr8:132078083 | G | A | 1 | a0001c0009t0007g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.926-112C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078083 | |||||||
chr8:132078105 | G | A | 8 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(5): Show |
8 | HG01106.hp2 HG02015.hp2 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-134C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078105 | |||||||
chr8:132078171 | A | AAC | 24 | a0001c0001t0001g0132 a0001c0001t0001g0138 a0001c0001t0001g0160 others(21): Show |
24 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.926-202_926-201dup others(2): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078171 | |||||||
chr8:132078171 | A | AACAC | 10 | a0001c0001t0001g0166 a0001c0001t0001g0173 a0001c0001t0018g0249 others(7): Show |
11 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.926-204_926-201dup others(4): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078171 | |||||||
chr8:132078171 | A | C | 1 | a0006c0015t0001g0274 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.926-200T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078171 | |||||||
chr8:132078171 | AAC | A | 34 | a0001c0001t0001g0130 a0001c0001t0001g0251 a0001c0001t0001g0271 others(31): Show |
35 | HG00323.hp2 HG00544.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.926-202_926-201del others(2): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078171 | |||||||
chr8:132078171 | AACAC | A | 58 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0018 others(55): Show |
60 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.926-204_926-201del others(4): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078171 | |||||||
chr8:132078171 | AACACAC | A | 80 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0002g0216 others(77): Show |
93 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.926-206_926-201del others(6): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078171 | |||||||
chr8:132078171 | AACACACA others(1): Show |
A | 19 | a0001c0001t0002g0170 a0001c0001t0006g0240 a0001c0001t0013g0239 others(16): Show |
19 | HG00438.hp1 HG01175.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.926-208_926-201del others(8): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078171 | |||||||
chr8:132078171 | AACACACA others(3): Show |
A | 13 | a0001c0001t0002g0010 a0001c0001t0002g0149 a0001c0001t0002g0171 others(10): Show |
14 | HG01070.hp1 HG02258.hp2 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-210_926-201del others(10): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078171 | |||||||
chr8:132078171 | AACACACA others(9): Show |
A | 4 | a0001c0001t0002g0316 a0006c0010t0002g0272 a0006c0010t0002g0275 others(1): Show |
4 | HG02015.hp2 NA18967.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-216_926-201del others(16): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078171 | |||||||
chr8:132078238 | C | T | 2 | a0002c0003t0023g0031 a0003c0002t0001g0193 |
2 | HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.926-267G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078238 | |||||||
chr8:132078249 | G | C | 3 | a0002c0013t0001g0112 a0002c0013t0001g0113 a0004c0006t0001g0110 |
3 | HG01361.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.926-278C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078249 | |||||||
chr8:132078581 | A | G | 3 | a0001c0001t0006g0240 a0001c0001t0006g0283 a0001c0001t0013g0239 |
3 | HG02922.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.926-610T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078581 | |||||||
chr8:132078620 | G | A | 3 | a0004c0006t0001g0288 a0004c0006t0001g0290 a0004c0006t0001g0291 |
3 | HG02572.hp2 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.926-649C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078620 | |||||||
chr8:132078665 | T | C | 3 | a0004c0006t0001g0288 a0004c0006t0001g0290 a0004c0006t0001g0291 |
3 | HG02572.hp2 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.926-694A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078665 | |||||||
chr8:132078800 | A | C | 1 | a0007c0011t0007g0270 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.926-829T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078800 | |||||||
chr8:132078837 | G | T | 3 | a0004c0006t0001g0288 a0004c0006t0001g0290 a0004c0006t0001g0291 |
3 | HG02572.hp2 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.926-866C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078837 | |||||||
chr8:132078861 | A | T | 2 | a0005c0008t0001g0055 a0005c0008t0001g0056 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.925+857T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078861 | |||||||
chr8:132078865 | G | T | 1 | a0001c0005t0006g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.925+853C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078865 | |||||||
chr8:132078870 | A | G | 3 | a0001c0007t0001g0259 a0001c0007t0001g0260 a0001c0007t0021g0261 |
3 | HG03139.hp1 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.925+848T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078870 | |||||||
chr8:132078904 | T | TTTTG | 7 | a0002c0013t0001g0112 a0002c0013t0001g0113 a0006c0010t0001g0276 others(4): Show |
7 | HG01516.hp2 HG01517.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+810_925+813dup others(4): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078904 | |||||||
chr8:132078904 | TTTTG | T | 4 | a0001c0009t0008g0339 a0001c0009t0008g0340 a0001c0009t0008g0341 others(1): Show |
4 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+810_925+813del others(4): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132078904 | |||||||
chr8:132079119 | C | A | 1 | a0002c0014t0002g0267 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.925+599G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079119 | |||||||
chr8:132079127 | G | T | 2 | a0005c0008t0001g0055 a0005c0008t0001g0056 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.925+591C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079127 | |||||||
chr8:132079212 | A | G | 1 | a0001c0027t0001g0045 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.925+506T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079212 | |||||||
chr8:132079327 | C | T | 4 | a0001c0009t0008g0339 a0001c0009t0008g0340 a0001c0009t0008g0341 others(1): Show |
4 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+391G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079327 | |||||||
chr8:132079342 | C | T | 2 | a0002c0013t0001g0112 a0002c0013t0001g0113 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.925+376G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079342 | |||||||
chr8:132079423 | T | C | 6 | a0001c0009t0007g0188 a0001c0009t0008g0339 a0001c0009t0008g0340 others(3): Show |
6 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+295A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079423 | |||||||
chr8:132079433 | C | T | 10 | a0001c0001t0002g0041 a0001c0007t0001g0024 a0001c0007t0001g0263 others(7): Show |
10 | HG01255.hp1 HG01891.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.925+285G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079433 | |||||||
chr8:132079460 | G | A | 10 | a0002c0004t0001g0044 a0005c0008t0001g0022 a0005c0008t0001g0023 others(7): Show |
10 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.925+258C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079460 | |||||||
chr8:132079514 | C | A | 2 | a0001c0001t0009g0353 a0007c0011t0007g0042 |
2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.925+204G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079514 | |||||||
chr8:132079565 | C | T | 1 | a0001c0005t0006g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.925+153G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079565 | |||||||
chr8:132079615 | G | C | 1 | a0010c0026t0001g0219 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.925+103C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079615 | |||||||
chr8:132079658 | C | T | 85 | a0001c0001t0005g0330 a0003c0002t0001g0011 a0003c0002t0001g0030 others(82): Show |
87 | HG00408.hp2 HG00639.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.925+60G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079658 | |||||||
chr8:132079700 | G | T | 6 | a0001c0009t0007g0188 a0001c0009t0008g0339 a0001c0009t0008g0340 others(3): Show |
6 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+18C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 11/16 | chr8 | 132079700 | |||||||
chr8:132079973 | G | A | 3 | a0001c0001t0011g0159 a0002c0003t0001g0152 a0002c0003t0001g0153 |
3 | HG02280.hp1 NA19030.hp1 NA19043.hp1 |
splice_region_variant&intron_variant | LOW | c.677-7C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132079973 | |||||||
chr8:132080080 | A | G | 1 | a0001c0001t0001g0019 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.677-114T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080080 | |||||||
chr8:132080084 | A | T | 1 | a0001c0001t0001g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.677-118T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080084 | |||||||
chr8:132080310 | T | G | 3 | a0001c0001t0001g0185 a0001c0001t0001g0252 a0001c0001t0014g0253 |
3 | NA19002.hp1 NA19012.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.677-344A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080310 | |||||||
chr8:132080327 | C | T | 1 | a0001c0009t0007g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.677-361G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080327 | |||||||
chr8:132080328 | G | A | 2 | a0001c0005t0009g0026 a0002c0003t0002g0332 |
2 | HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.677-362C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080328 | |||||||
chr8:132080411 | G | T | 1 | a0013c0028t0002g0192 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.677-445C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080411 | |||||||
chr8:132080417 | T | A | 1 | a0001c0005t0002g0350 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.677-451A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080417 | |||||||
chr8:132080531 | A | G | 301 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(298): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.677-565T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080531 | |||||||
chr8:132080581 | G | A | 25 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(22): Show |
26 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.677-615C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080581 | |||||||
chr8:132080632 | G | C | 18 | a0001c0001t0002g0041 a0001c0001t0002g0081 a0001c0001t0002g0098 others(15): Show |
23 | HG00741.hp2 HG01255.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.677-666C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080632 | |||||||
chr8:132080782 | C | T | 1 | a0002c0003t0001g0285 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.677-816G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080782 | |||||||
chr8:132080794 | G | C | 264 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(261): Show |
275 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.677-828C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080794 | |||||||
chr8:132080808 | G | A | 1 | a0001c0007t0001g0024 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.677-842C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080808 | |||||||
chr8:132080823 | G | A | 3 | a0001c0001t0006g0240 a0001c0001t0006g0283 a0001c0001t0013g0239 |
3 | HG02922.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.677-857C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080823 | |||||||
chr8:132080876 | G | A | 261 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(258): Show |
272 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.677-910C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080876 | |||||||
chr8:132080878 | G | A | 261 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(258): Show |
272 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.677-912C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080878 | |||||||
chr8:132080890 | A | T | 2 | a0005c0008t0001g0055 a0005c0008t0001g0056 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.677-924T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080890 | |||||||
chr8:132080911 | G | A | 1 | a0002c0003t0001g0139 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.677-945C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080911 | |||||||
chr8:132080923 | A | T | 264 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(261): Show |
275 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.677-957T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080923 | |||||||
chr8:132080930 | G | A | 6 | a0001c0009t0007g0188 a0001c0009t0008g0339 a0001c0009t0008g0340 others(3): Show |
6 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.677-964C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080930 | |||||||
chr8:132080935 | G | A | 2 | a0002c0013t0001g0112 a0002c0013t0001g0113 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.677-969C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080935 | |||||||
chr8:132080940 | C | T | 6 | a0001c0009t0007g0188 a0001c0009t0008g0339 a0001c0009t0008g0340 others(3): Show |
6 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.677-974G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080940 | |||||||
chr8:132080941 | A | G | 2 | a0002c0013t0001g0112 a0002c0013t0001g0113 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.677-975T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132080941 | |||||||
chr8:132081115 | G | A | 2 | a0006c0010t0002g0272 a0006c0010t0002g0275 |
2 | HG02015.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.677-1149C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081115 | |||||||
chr8:132081151 | CA | C | 301 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(298): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.677-1186delT | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081151 | |||||||
chr8:132081212 | C | T | 16 | a0001c0001t0002g0081 a0001c0001t0002g0098 a0001c0001t0003g0002 others(13): Show |
21 | HG00741.hp2 HG02145.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.677-1246G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081212 | |||||||
chr8:132081306 | T | C | 1 | a0001c0001t0001g0271 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.677-1340A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081306 | |||||||
chr8:132081309 | A | G | 2 | a0002c0003t0001g0029 a0007c0011t0007g0270 |
2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.677-1343T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081309 | |||||||
chr8:132081317 | G | A | 1 | a0001c0005t0006g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.677-1351C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081317 | |||||||
chr8:132081415 | C | T | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.677-1449G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081415 | |||||||
chr8:132081684 | G | A | 267 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(264): Show |
278 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.677-1718C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081684 | |||||||
chr8:132081762 | C | T | 85 | a0001c0001t0005g0330 a0003c0002t0001g0011 a0003c0002t0001g0030 others(82): Show |
87 | HG00408.hp2 HG00639.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.677-1796G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081762 | |||||||
chr8:132081763 | G | A | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.677-1797C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081763 | |||||||
chr8:132081780 | A | G | 1 | a0003c0002t0002g0032 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.677-1814T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081780 | |||||||
chr8:132081839 | G | A | 1 | a0001c0001t0001g0299 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.677-1873C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081839 | |||||||
chr8:132081869 | A | G | 1 | a0001c0001t0001g0299 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.677-1903T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081869 | |||||||
chr8:132081917 | G | A | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.677-1951C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081917 | |||||||
chr8:132081930 | T | C | 9 | a0005c0008t0001g0022 a0005c0008t0001g0023 a0005c0008t0001g0055 others(6): Show |
9 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.677-1964A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081930 | |||||||
chr8:132081947 | G | A | 2 | a0001c0005t0006g0046 a0001c0005t0009g0026 |
2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.677-1981C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081947 | |||||||
chr8:132081975 | T | C | 1 | a0001c0001t0024g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.677-2009A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081975 | |||||||
chr8:132081990 | A | T | 1 | a0001c0027t0001g0045 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.677-2024T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132081990 | |||||||
chr8:132082071 | A | C | 3 | a0001c0001t0009g0302 a0001c0001t0019g0304 a0001c0009t0002g0278 |
3 | HG01106.hp1 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.677-2105T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082071 | |||||||
chr8:132082112 | G | A | 1 | a0001c0001t0002g0040 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.677-2146C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082112 | |||||||
chr8:132082166 | G | A | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.677-2200C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082166 | |||||||
chr8:132082171 | T | C | 9 | a0005c0008t0001g0022 a0005c0008t0001g0023 a0005c0008t0001g0055 others(6): Show |
9 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.677-2205A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082171 | |||||||
chr8:132082185 | A | G | 9 | a0005c0008t0001g0022 a0005c0008t0001g0023 a0005c0008t0001g0055 others(6): Show |
9 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.677-2219T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082185 | |||||||
chr8:132082247 | C | A | 1 | a0001c0005t0005g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.677-2281G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082247 | |||||||
chr8:132082253 | A | G | 1 | a0001c0005t0005g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.677-2287T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082253 | |||||||
chr8:132082323 | G | A | 8 | a0001c0001t0002g0081 a0001c0001t0002g0098 a0001c0001t0003g0002 others(5): Show |
13 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.677-2357C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082323 | |||||||
chr8:132082382 | G | C | 84 | a0001c0001t0005g0330 a0003c0002t0001g0011 a0003c0002t0001g0030 others(81): Show |
86 | HG00408.hp2 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.677-2416C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082382 | |||||||
chr8:132082438 | A | G | 73 | a0003c0002t0001g0011 a0003c0002t0001g0030 a0003c0002t0001g0033 others(70): Show |
75 | HG00408.hp2 HG00639.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.677-2472T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082438 | |||||||
chr8:132082465 | T | C | 1 | a0001c0001t0024g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.677-2499A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082465 | |||||||
chr8:132082493 | T | C | 285 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(282): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.677-2527A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082493 | |||||||
chr8:132082536 | G | A | 1 | a0003c0002t0001g0038 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.677-2570C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082536 | |||||||
chr8:132082590 | G | A | 2 | a0001c0001t0001g0248 a0001c0001t0001g0317 |
2 | NA19005.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.677-2624C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082590 | |||||||
chr8:132082619 | T | A | 129 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(126): Show |
136 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.677-2653A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082619 | |||||||
chr8:132082639 | T | C | 2 | a0003c0002t0001g0233 a0003c0002t0001g0234 |
2 | HG02040.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.677-2673A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082639 | |||||||
chr8:132082651 | T | A | 228 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(225): Show |
237 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.677-2685A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082651 | |||||||
chr8:132082677 | C | T | 7 | a0001c0009t0002g0278 a0001c0009t0007g0188 a0001c0009t0008g0339 others(4): Show |
7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.677-2711G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082677 | |||||||
chr8:132082683 | C | A | 67 | a0001c0001t0001g0006 a0001c0001t0001g0109 a0001c0001t0001g0211 others(64): Show |
69 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.677-2717G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082683 | |||||||
chr8:132082683 | C | G | 74 | a0003c0002t0001g0011 a0003c0002t0001g0030 a0003c0002t0001g0033 others(71): Show |
76 | HG00408.hp2 HG00639.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.677-2717G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082683 | |||||||
chr8:132082776 | C | T | 3 | a0001c0001t0006g0240 a0001c0001t0006g0283 a0001c0001t0013g0239 |
3 | HG02922.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.677-2810G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082776 | |||||||
chr8:132082879 | A | G | 301 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(298): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.677-2913T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082879 | |||||||
chr8:132082886 | T | G | 9 | a0005c0008t0001g0022 a0005c0008t0001g0023 a0005c0008t0001g0055 others(6): Show |
9 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.677-2920A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082886 | |||||||
chr8:132082931 | G | A | 1 | a0001c0001t0024g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.677-2965C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082931 | |||||||
chr8:132082968 | T | C | 284 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(281): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.677-3002A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082968 | |||||||
chr8:132082969 | G | A | 276 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(273): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.677-3003C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082969 | |||||||
chr8:132082985 | A | G | 10 | a0001c0001t0002g0081 a0001c0001t0002g0098 a0001c0001t0003g0002 others(7): Show |
15 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.677-3019T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132082985 | |||||||
chr8:132083018 | A | G | 1 | a0001c0001t0009g0305 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.677-3052T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083018 | |||||||
chr8:132083028 | GGGTGCAT others(4): Show |
G | 8 | a0001c0001t0002g0081 a0001c0001t0002g0098 a0001c0001t0003g0002 others(5): Show |
13 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.677-3073_677-3063d others(13): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083028 | |||||||
chr8:132083039 | T | C | 3 | a0001c0007t0001g0264 a0006c0015t0001g0274 a0006c0015t0002g0273 |
3 | NA18959.hp1 NA18994.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.677-3073A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083039 | |||||||
chr8:132083044 | G | A | 8 | a0001c0001t0002g0081 a0001c0001t0002g0098 a0001c0001t0003g0002 others(5): Show |
13 | HG00741.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.677-3078C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083044 | |||||||
chr8:132083048 | A | T | 1 | a0001c0012t0001g0349 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.677-3082T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083048 | |||||||
chr8:132083056 | G | A | 3 | a0001c0001t0006g0240 a0001c0001t0006g0283 a0001c0001t0013g0239 |
3 | HG02922.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.677-3090C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083056 | |||||||
chr8:132083142 | CA | C | 25 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(22): Show |
26 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.677-3177delT | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083142 | |||||||
chr8:132083146 | G | C | 25 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(22): Show |
26 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.677-3180C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083146 | |||||||
chr8:132083200 | A | G | 259 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(256): Show |
270 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.677-3234T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083200 | |||||||
chr8:132083315 | C | A | 2 | a0001c0001t0009g0353 a0007c0011t0007g0042 |
2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.677-3349G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083315 | |||||||
chr8:132083370 | G | T | 205 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(202): Show |
209 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.677-3404C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083370 | |||||||
chr8:132083388 | C | T | 18 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(15): Show |
20 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.677-3422G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083388 | |||||||
chr8:132083393 | G | A | 100 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(97): Show |
103 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.677-3427C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083393 | |||||||
chr8:132083452 | G | A | 25 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(22): Show |
26 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.677-3486C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083452 | |||||||
chr8:132083507 | G | A | 1 | a0008c0022t0001g0338 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.677-3541C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083507 | |||||||
chr8:132083525 | G | A | 1 | a0001c0001t0024g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.677-3559C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083525 | |||||||
chr8:132083557 | C | T | 1 | a0003c0002t0002g0218 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.677-3591G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083557 | |||||||
chr8:132083570 | C | G | 1 | a0004c0006t0001g0334 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.677-3604G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083570 | |||||||
chr8:132083593 | T | A | 11 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0215 others(8): Show |
11 | HG00609.hp2 NA18951.hp2 NA18972.hp1 others(8): Show |
intron_variant | MODIFIER | c.677-3627A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083593 | |||||||
chr8:132083633 | C | T | 44 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0106 others(41): Show |
44 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.677-3667G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083633 | |||||||
chr8:132083634 | G | A | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.677-3668C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083634 | |||||||
chr8:132083635 | C | T | 248 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(245): Show |
257 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.677-3669G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083635 | |||||||
chr8:132083691 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0002g0149 |
2 | HG03669.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.677-3725T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083691 | |||||||
chr8:132083778 | G | C | 3 | a0001c0007t0001g0259 a0001c0007t0001g0260 a0001c0007t0021g0261 |
3 | HG03139.hp1 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.677-3812C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083778 | |||||||
chr8:132083931 | T | C | 7 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0002g0184 others(4): Show |
7 | HG02280.hp1 HG02683.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.676+3722A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083931 | |||||||
chr8:132083942 | A | T | 243 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(240): Show |
249 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.676+3711T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083942 | |||||||
chr8:132083944 | T | A | 243 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(240): Show |
249 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.676+3709A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083944 | |||||||
chr8:132083946 | T | C | 243 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(240): Show |
249 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.676+3707A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083946 | |||||||
chr8:132083948 | T | A | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+3705A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083948 | |||||||
chr8:132083948 | T | G | 243 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(240): Show |
249 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.676+3705A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083948 | |||||||
chr8:132083949 | T | A | 243 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(240): Show |
249 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.676+3704A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083949 | |||||||
chr8:132083992 | A | G | 260 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(257): Show |
271 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.676+3661T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083992 | |||||||
chr8:132083998 | T | C | 285 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(282): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.676+3655A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132083998 | |||||||
chr8:132084019 | C | G | 4 | a0001c0001t0006g0240 a0001c0001t0006g0283 a0001c0001t0013g0239 others(1): Show |
4 | HG02886.hp2 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+3634G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084019 | |||||||
chr8:132084058 | A | G | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0002g0184 |
3 | HG02683.hp1 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.676+3595T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084058 | |||||||
chr8:132084162 | G | C | 1 | a0001c0001t0001g0108 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.676+3491C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084162 | |||||||
chr8:132084196 | C | T | 1 | a0001c0001t0024g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+3457G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084196 | |||||||
chr8:132084197 | G | A | 14 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0165 others(11): Show |
14 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.676+3456C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084197 | |||||||
chr8:132084248 | G | A | 268 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(265): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.676+3405C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084248 | |||||||
chr8:132084259 | G | A | 1 | a0007c0011t0007g0186 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.676+3394C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084259 | |||||||
chr8:132084311 | G | A | 1 | a0001c0001t0024g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+3342C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084311 | |||||||
chr8:132084422 | C | T | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+3231G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084422 | |||||||
chr8:132084441 | A | AG | 300 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(297): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.676+3211dupC | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084441 | |||||||
chr8:132084483 | A | G | 1 | a0001c0027t0001g0045 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.676+3170T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084483 | |||||||
chr8:132084508 | G | A | 2 | a0001c0005t0006g0046 a0001c0005t0009g0026 |
2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.676+3145C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084508 | |||||||
chr8:132084632 | G | T | 1 | a0002c0003t0001g0336 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.676+3021C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084632 | |||||||
chr8:132084664 | T | C | 1 | a0005c0008t0002g0346 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.676+2989A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084664 | |||||||
chr8:132084748 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.676+2905G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084748 | |||||||
chr8:132084771 | G | A | 4 | a0001c0001t0006g0240 a0001c0001t0006g0283 a0001c0001t0013g0239 others(1): Show |
4 | HG02886.hp2 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+2882C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084771 | |||||||
chr8:132084870 | C | T | 2 | a0001c0005t0006g0046 a0001c0005t0009g0026 |
2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.676+2783G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084870 | |||||||
chr8:132084888 | C | T | 94 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(91): Show |
98 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.676+2765G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084888 | |||||||
chr8:132084930 | G | A | 1 | a0002c0003t0001g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.676+2723C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084930 | |||||||
chr8:132084960 | A | C | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+2693T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084960 | |||||||
chr8:132084969 | T | C | 297 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(294): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.676+2684A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132084969 | |||||||
chr8:132085094 | C | G | 1 | a0001c0005t0009g0026 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.676+2559G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085094 | |||||||
chr8:132085133 | C | T | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+2520G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085133 | |||||||
chr8:132085134 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.676+2519C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085134 | |||||||
chr8:132085159 | G | T | 1 | a0001c0001t0024g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+2494C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085159 | |||||||
chr8:132085232 | G | A | 2 | a0001c0016t0006g0151 a0004c0006t0001g0334 |
2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.676+2421C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085232 | |||||||
chr8:132085295 | T | C | 1 | a0001c0007t0002g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.676+2358A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085295 | |||||||
chr8:132085313 | A | G | 295 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(292): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.676+2340T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085313 | |||||||
chr8:132085461 | G | A | 1 | a0001c0001t0024g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+2192C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085461 | |||||||
chr8:132085534 | G | A | 1 | a0001c0001t0024g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+2119C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085534 | |||||||
chr8:132085560 | G | A | 9 | a0005c0008t0001g0022 a0005c0008t0001g0023 a0005c0008t0001g0055 others(6): Show |
9 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.676+2093C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085560 | |||||||
chr8:132085601 | T | C | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+2052A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085601 | |||||||
chr8:132085603 | A | T | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+2050T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085603 | |||||||
chr8:132085604 | A | G | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+2049T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085604 | |||||||
chr8:132085630 | C | T | 12 | a0001c0009t0002g0278 a0001c0009t0007g0188 a0001c0009t0008g0339 others(9): Show |
12 | HG01109.hp1 HG02015.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.676+2023G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085630 | |||||||
chr8:132085642 | G | A | 2 | a0001c0005t0006g0046 a0001c0005t0009g0026 |
2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.676+2011C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085642 | |||||||
chr8:132085679 | G | A | 4 | a0003c0002t0010g0156 a0003c0002t0010g0158 a0003c0002t0010g0352 others(1): Show |
4 | HG02559.hp2 HG02896.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.676+1974C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085679 | |||||||
chr8:132085756 | T | A | 294 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0017 others(291): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.676+1897A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085756 | |||||||
chr8:132085790 | G | C | 2 | a0001c0001t0009g0353 a0007c0011t0007g0042 |
2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.676+1863C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085790 | |||||||
chr8:132085791 | A | G | 296 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(293): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.676+1862T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085791 | |||||||
chr8:132085803 | G | A | 296 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(293): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.676+1850C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085803 | |||||||
chr8:132085830 | G | C | 199 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(196): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.676+1823C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085830 | |||||||
chr8:132085844 | C | T | 296 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(293): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.676+1809G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085844 | |||||||
chr8:132085845 | G | A | 3 | a0001c0005t0001g0051 a0001c0005t0001g0072 a0002c0004t0002g0005 |
5 | HG01175.hp2 HG01192.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+1808C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085845 | |||||||
chr8:132085951 | G | C | 1 | a0001c0001t0024g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+1702C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085951 | |||||||
chr8:132085989 | T | C | 1 | a0001c0005t0002g0086 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.676+1664A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132085989 | |||||||
chr8:132086135 | T | C | 279 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(276): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.676+1518A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086135 | |||||||
chr8:132086202 | A | T | 296 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(293): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.676+1451T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086202 | |||||||
chr8:132086283 | T | C | 66 | a0001c0001t0001g0006 a0001c0001t0001g0109 a0001c0001t0001g0211 others(63): Show |
68 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.676+1370A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086283 | |||||||
chr8:132086421 | G | A | 1 | a0002c0003t0001g0336 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.676+1232C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086421 | |||||||
chr8:132086498 | C | A | 1 | a0003c0002t0002g0025 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.676+1155G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086498 | |||||||
chr8:132086518 | A | T | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+1135T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086518 | |||||||
chr8:132086575 | G | C | 1 | a0001c0001t0024g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+1078C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086575 | |||||||
chr8:132086662 | C | A | 1 | a0003c0002t0001g0208 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.676+991G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086662 | |||||||
chr8:132086664 | C | A | 1 | a0003c0002t0001g0208 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.676+989G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086664 | |||||||
chr8:132086667 | A | T | 1 | a0003c0002t0001g0208 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.676+986T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086667 | |||||||
chr8:132086670 | A | T | 1 | a0003c0002t0001g0208 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.676+983T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086670 | |||||||
chr8:132086851 | G | GT | 29 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0118 others(26): Show |
29 | HG00323.hp1 HG00544.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.676+801dupA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086851 | |||||||
chr8:132086918 | G | C | 1 | a0003c0002t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.676+735C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086918 | |||||||
chr8:132086942 | A | G | 4 | a0001c0001t0011g0159 a0001c0027t0001g0045 a0002c0003t0001g0152 others(1): Show |
4 | HG02280.hp1 HG06807.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+711T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132086942 | |||||||
chr8:132087032 | C | T | 1 | a0001c0001t0024g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+621G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087032 | |||||||
chr8:132087052 | C | A | 1 | a0001c0001t0002g0180 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.676+601G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087052 | |||||||
chr8:132087072 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.676+581G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087072 | |||||||
chr8:132087073 | G | A | 1 | a0001c0001t0024g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.676+580C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087073 | |||||||
chr8:132087229 | G | A | 4 | a0001c0001t0011g0159 a0001c0027t0001g0045 a0002c0003t0001g0152 others(1): Show |
4 | HG02280.hp1 HG06807.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+424C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087229 | |||||||
chr8:132087240 | G | T | 11 | a0001c0001t0002g0081 a0001c0001t0002g0098 a0001c0001t0003g0002 others(8): Show |
16 | HG00741.hp2 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.676+413C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087240 | |||||||
chr8:132087274 | T | C | 4 | a0001c0001t0011g0159 a0001c0027t0001g0045 a0002c0003t0001g0152 others(1): Show |
4 | HG02280.hp1 HG06807.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+379A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087274 | |||||||
chr8:132087395 | C | G | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0002g0184 |
3 | HG02683.hp1 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.676+258G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087395 | |||||||
chr8:132087427 | A | C | 286 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(283): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.676+226T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087427 | |||||||
chr8:132087607 | C | T | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+46G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 10/16 | chr8 | 132087607 | |||||||
chr8:132087816 | A | T | 7 | a0001c0009t0002g0278 a0001c0009t0007g0188 a0001c0009t0008g0339 others(4): Show |
7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.589+29T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 9/16 | chr8 | 132087816 | |||||||
chr8:132088135 | C | T | 7 | a0001c0001t0002g0081 a0001c0001t0002g0098 a0001c0001t0003g0002 others(4): Show |
12 | HG00741.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.533-234G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088135 | |||||||
chr8:132088176 | T | C | 296 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(293): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.533-275A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088176 | |||||||
chr8:132088203 | G | T | 6 | a0001c0012t0001g0154 a0001c0012t0001g0155 a0001c0012t0001g0349 others(3): Show |
6 | HG01123.hp1 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.533-302C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088203 | |||||||
chr8:132088287 | G | A | 3 | a0001c0007t0001g0259 a0001c0007t0001g0260 a0001c0007t0021g0261 |
3 | HG03139.hp1 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.533-386C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088287 | |||||||
chr8:132088296 | G | A | 4 | a0001c0001t0011g0159 a0001c0027t0001g0045 a0002c0003t0001g0152 others(1): Show |
4 | HG02280.hp1 HG06807.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.533-395C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088296 | |||||||
chr8:132088377 | A | G | 300 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(297): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.533-476T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088377 | |||||||
chr8:132088457 | C | T | 6 | a0001c0012t0001g0154 a0001c0012t0001g0155 a0001c0012t0001g0349 others(3): Show |
6 | HG01123.hp1 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.533-556G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088457 | |||||||
chr8:132088539 | G | A | 239 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(236): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.533-638C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088539 | |||||||
chr8:132088581 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.533-680T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088581 | |||||||
chr8:132088679 | T | A | 3 | a0001c0001t0006g0240 a0001c0001t0006g0283 a0001c0001t0013g0239 |
3 | HG02922.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.533-778A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088679 | |||||||
chr8:132088744 | T | C | 1 | a0003c0002t0001g0246 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.532+772A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088744 | |||||||
chr8:132088917 | A | G | 1 | a0002c0004t0001g0102 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.532+599T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088917 | |||||||
chr8:132088981 | G | T | 4 | a0001c0001t0011g0159 a0001c0027t0001g0045 a0002c0003t0001g0152 others(1): Show |
4 | HG02280.hp1 HG06807.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.532+535C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132088981 | |||||||
chr8:132089067 | G | A | 1 | a0001c0001t0024g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.532+449C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132089067 | |||||||
chr8:132089097 | G | C | 1 | a0001c0005t0002g0350 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.532+419C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132089097 | |||||||
chr8:132089187 | A | G | 1 | a0001c0001t0024g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.532+329T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132089187 | |||||||
chr8:132089253 | G | C | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+263C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132089253 | |||||||
chr8:132089329 | T | G | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0002g0184 |
3 | HG02683.hp1 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.532+187A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132089329 | |||||||
chr8:132089359 | A | G | 7 | a0001c0001t0002g0081 a0001c0001t0002g0098 a0001c0001t0003g0002 others(4): Show |
12 | HG00741.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.532+157T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132089359 | |||||||
chr8:132089389 | T | C | 4 | a0001c0001t0011g0159 a0001c0027t0001g0045 a0002c0003t0001g0152 others(1): Show |
4 | HG02280.hp1 HG06807.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.532+127A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132089389 | |||||||
chr8:132089486 | G | A | 1 | a0003c0002t0001g0187 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.532+30C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132089486 | |||||||
chr8:132089515 | C | A | 1 | a0001c0001t0002g0015 | 1 | NA18960.hp1 | splice_donor_variant&intron_variant | HIGH | c.532+1G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 8/16 | chr8 | 132089515 | |||||||
chr8:132089741 | A | T | 3 | a0001c0001t0006g0240 a0001c0001t0006g0283 a0001c0001t0013g0239 |
3 | HG02922.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.449-142T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132089741 | |||||||
chr8:132089762 | T | C | 299 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(296): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.449-163A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132089762 | |||||||
chr8:132089929 | G | A | 1 | a0002c0003t0023g0031 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.449-330C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132089929 | |||||||
chr8:132089929 | G | C | 5 | a0005c0008t0001g0022 a0005c0008t0001g0023 a0005c0008t0002g0345 others(2): Show |
5 | HG02451.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.449-330C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132089929 | |||||||
chr8:132089931 | C | A | 1 | a0001c0001t0024g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.449-332G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132089931 | |||||||
chr8:132090059 | T | G | 1 | a0001c0001t0024g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.449-460A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090059 | |||||||
chr8:132090107 | C | G | 5 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(2): Show |
5 | HG01074.hp1 HG01167.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-508G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090107 | |||||||
chr8:132090122 | C | T | 1 | a0001c0005t0002g0350 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.449-523G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090122 | |||||||
chr8:132090328 | A | G | 4 | a0001c0012t0001g0154 a0001c0012t0001g0155 a0001c0012t0001g0349 others(1): Show |
4 | HG01123.hp1 HG01934.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-729T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090328 | |||||||
chr8:132090389 | C | T | 1 | a0001c0005t0006g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.449-790G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090389 | |||||||
chr8:132090404 | A | G | 296 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(293): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.449-805T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090404 | |||||||
chr8:132090527 | G | A | 1 | a0003c0002t0002g0198 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.449-928C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090527 | |||||||
chr8:132090684 | A | G | 1 | a0002c0003t0002g0332 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.449-1085T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090684 | |||||||
chr8:132090755 | CT | C | 254 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(251): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.449-1157delA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090755 | |||||||
chr8:132090755 | CTT | C | 15 | a0001c0001t0001g0132 a0001c0001t0002g0015 a0001c0001t0002g0217 others(12): Show |
15 | HG01069.hp2 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.449-1158_449-1157d others(4): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090755 | |||||||
chr8:132090755 | CTTTT | C | 11 | a0001c0001t0002g0081 a0001c0001t0002g0098 a0001c0001t0003g0002 others(8): Show |
16 | HG00741.hp2 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.449-1160_449-1157d others(6): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090755 | |||||||
chr8:132090756 | T | TC | 5 | a0001c0007t0001g0259 a0001c0007t0001g0260 a0001c0007t0021g0261 others(2): Show |
5 | HG02257.hp1 HG02895.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.449-1158_449-1157i others(3): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090756 | |||||||
chr8:132090757 | T | C | 14 | a0001c0001t0001g0134 a0001c0001t0001g0303 a0001c0001t0002g0041 others(11): Show |
14 | HG01255.hp1 HG01891.hp1 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.449-1158A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090757 | |||||||
chr8:132090758 | T | C | 252 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(249): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.449-1159A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090758 | |||||||
chr8:132090759 | T | C | 9 | a0001c0001t0001g0132 a0001c0001t0002g0015 a0001c0001t0002g0217 others(6): Show |
9 | HG01069.hp2 HG01516.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.449-1160A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090759 | |||||||
chr8:132090760 | T | C | 1 | a0005c0008t0001g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.449-1161A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090760 | |||||||
chr8:132090776 | T | G | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.449-1177A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090776 | |||||||
chr8:132090820 | G | A | 7 | a0001c0009t0002g0278 a0001c0009t0007g0188 a0001c0009t0008g0339 others(4): Show |
7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-1221C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090820 | |||||||
chr8:132090907 | C | T | 1 | a0001c0001t0011g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.449-1308G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090907 | |||||||
chr8:132090917 | C | T | 1 | a0001c0005t0005g0058 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.449-1318G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090917 | |||||||
chr8:132090952 | G | A | 2 | a0001c0005t0006g0046 a0001c0005t0009g0026 |
2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.449-1353C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090952 | |||||||
chr8:132090980 | C | G | 2 | a0001c0001t0009g0353 a0007c0011t0007g0042 |
2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.449-1381G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132090980 | |||||||
chr8:132091011 | G | A | 2 | a0002c0003t0001g0321 a0009c0025t0007g0282 |
2 | HG01167.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.449-1412C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132091011 | |||||||
chr8:132091020 | C | A | 2 | a0002c0003t0001g0152 a0002c0003t0001g0153 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.449-1421G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132091020 | |||||||
chr8:132091043 | T | C | 68 | a0001c0001t0001g0006 a0001c0001t0001g0109 a0001c0001t0001g0211 others(65): Show |
70 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.449-1444A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132091043 | |||||||
chr8:132091082 | CTTAG | C | 7 | a0001c0001t0002g0081 a0001c0001t0002g0098 a0001c0001t0003g0002 others(4): Show |
12 | HG00741.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.449-1487_449-1484d others(6): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132091082 | |||||||
chr8:132091534 | C | T | 2 | a0001c0016t0002g0150 a0001c0016t0006g0151 |
2 | HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.449-1935G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132091534 | |||||||
chr8:132091574 | T | C | 1 | a0002c0003t0001g0133 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.449-1975A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132091574 | |||||||
chr8:132091651 | A | G | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0002g0184 |
3 | HG02683.hp1 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.449-2052T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132091651 | |||||||
chr8:132092051 | G | T | 4 | a0001c0009t0008g0339 a0001c0009t0008g0340 a0001c0009t0008g0341 others(1): Show |
4 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-2452C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092051 | |||||||
chr8:132092068 | G | A | 295 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(292): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.449-2469C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092068 | |||||||
chr8:132092186 | G | A | 86 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(83): Show |
90 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.449-2587C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092186 | |||||||
chr8:132092359 | T | A | 1 | a0001c0001t0002g0041 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.449-2760A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092359 | |||||||
chr8:132092360 | C | A | 6 | a0001c0012t0001g0154 a0001c0012t0001g0155 a0001c0012t0001g0349 others(3): Show |
6 | HG01123.hp1 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.449-2761G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092360 | |||||||
chr8:132092361 | A | G | 7 | a0001c0009t0002g0278 a0001c0009t0007g0188 a0001c0009t0008g0339 others(4): Show |
7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.449-2762T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092361 | |||||||
chr8:132092447 | G | T | 284 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(281): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.449-2848C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092447 | |||||||
chr8:132092539 | G | A | 1 | a0002c0004t0001g0091 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.449-2940C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092539 | |||||||
chr8:132092811 | C | T | 2 | a0001c0001t0003g0028 a0001c0001t0020g0027 |
2 | HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.448+2708G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092811 | |||||||
chr8:132092830 | G | A | 4 | a0001c0001t0006g0240 a0001c0001t0006g0283 a0001c0001t0013g0239 others(1): Show |
4 | HG02886.hp2 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.448+2689C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092830 | |||||||
chr8:132092851 | C | T | 7 | a0001c0009t0002g0278 a0001c0009t0007g0188 a0001c0009t0008g0339 others(4): Show |
7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.448+2668G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092851 | |||||||
chr8:132092872 | A | G | 279 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(276): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.448+2647T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092872 | |||||||
chr8:132092900 | A | G | 1 | a0001c0001t0009g0302 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.448+2619T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092900 | |||||||
chr8:132092922 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.448+2597G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132092922 | |||||||
chr8:132093000 | T | C | 10 | a0001c0001t0002g0041 a0001c0007t0001g0024 a0001c0007t0001g0263 others(7): Show |
10 | HG01255.hp1 HG01891.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.448+2519A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093000 | |||||||
chr8:132093137 | G | C | 2 | a0001c0005t0006g0046 a0001c0005t0009g0026 |
2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.448+2382C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093137 | |||||||
chr8:132093145 | G | A | 11 | a0001c0001t0002g0081 a0001c0001t0002g0098 a0001c0001t0003g0002 others(8): Show |
16 | HG00741.hp2 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.448+2374C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093145 | |||||||
chr8:132093207 | T | C | 1 | a0001c0001t0011g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.448+2312A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093207 | |||||||
chr8:132093256 | G | A | 1 | a0001c0001t0011g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.448+2263C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093256 | |||||||
chr8:132093386 | G | A | 285 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(282): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.448+2133C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093386 | |||||||
chr8:132093493 | G | A | 1 | a0001c0007t0021g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.448+2026C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093493 | |||||||
chr8:132093527 | G | A | 9 | a0003c0002t0001g0289 a0003c0002t0010g0156 a0003c0002t0010g0158 others(6): Show |
9 | HG02559.hp2 HG02572.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.448+1992C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093527 | |||||||
chr8:132093543 | G | T | 2 | a0001c0005t0006g0046 a0001c0005t0009g0026 |
2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.448+1976C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093543 | |||||||
chr8:132093551 | T | A | 2 | a0001c0005t0006g0046 a0001c0005t0009g0026 |
2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.448+1968A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093551 | |||||||
chr8:132093586 | G | T | 45 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0106 others(42): Show |
45 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.448+1933C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093586 | |||||||
chr8:132093688 | A | C | 96 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(93): Show |
100 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.448+1831T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093688 | |||||||
chr8:132093713 | C | T | 1 | a0001c0005t0002g0350 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.448+1806G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093713 | |||||||
chr8:132093720 | A | G | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0002g0184 |
3 | HG02683.hp1 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.448+1799T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093720 | |||||||
chr8:132093818 | A | T | 68 | a0001c0001t0001g0006 a0001c0001t0001g0109 a0001c0001t0001g0211 others(65): Show |
70 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.448+1701T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093818 | |||||||
chr8:132093868 | A | T | 285 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(282): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.448+1651T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132093868 | |||||||
chr8:132094034 | T | A | 2 | a0001c0001t0001g0134 a0002c0003t0002g0135 |
2 | HG00673.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.448+1485A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094034 | |||||||
chr8:132094039 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.448+1480C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094039 | |||||||
chr8:132094093 | C | G | 9 | a0005c0008t0001g0022 a0005c0008t0001g0023 a0005c0008t0001g0055 others(6): Show |
9 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.448+1426G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094093 | |||||||
chr8:132094151 | T | C | 285 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(282): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.448+1368A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094151 | |||||||
chr8:132094153 | A | G | 1 | a0001c0005t0002g0086 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.448+1366T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094153 | |||||||
chr8:132094192 | G | GT | 285 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(282): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.448+1326_448+1327i others(3): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094192 | |||||||
chr8:132094236 | T | C | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.448+1283A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094236 | |||||||
chr8:132094292 | T | C | 300 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(297): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.448+1227A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094292 | |||||||
chr8:132094320 | C | T | 2 | a0001c0005t0006g0046 a0001c0005t0009g0026 |
2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.448+1199G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094320 | |||||||
chr8:132094357 | C | T | 1 | a0003c0002t0002g0021 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.448+1162G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094357 | |||||||
chr8:132094377 | C | A | 1 | a0001c0007t0002g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.448+1142G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094377 | |||||||
chr8:132094378 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.448+1141C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094378 | |||||||
chr8:132094490 | G | A | 68 | a0001c0001t0001g0006 a0001c0001t0001g0109 a0001c0001t0001g0211 others(65): Show |
70 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.448+1029C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094490 | |||||||
chr8:132094520 | C | A | 1 | a0001c0009t0008g0342 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.448+999G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094520 | |||||||
chr8:132094545 | G | A | 2 | a0001c0001t0001g0322 a0001c0001t0002g0323 |
2 | NA18966.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.448+974C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094545 | |||||||
chr8:132094569 | A | G | 5 | a0001c0001t0020g0027 a0002c0003t0001g0114 a0002c0003t0001g0115 others(2): Show |
5 | HG02280.hp2 NA18968.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.448+950T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094569 | |||||||
chr8:132094651 | T | C | 300 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(297): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.448+868A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094651 | |||||||
chr8:132094665 | C | T | 279 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(276): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.448+854G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094665 | |||||||
chr8:132094732 | C | T | 1 | a0002c0003t0002g0332 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.448+787G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094732 | |||||||
chr8:132094745 | C | T | 285 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(282): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.448+774G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094745 | |||||||
chr8:132094758 | A | G | 102 | a0001c0001t0001g0006 a0001c0001t0001g0109 a0001c0001t0001g0148 others(99): Show |
105 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.448+761T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094758 | |||||||
chr8:132094777 | G | T | 1 | a0001c0001t0024g0355 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.448+742C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094777 | |||||||
chr8:132094799 | G | T | 3 | a0002c0003t0001g0324 a0002c0003t0001g0335 a0002c0003t0001g0336 |
3 | HG02622.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.448+720C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094799 | |||||||
chr8:132094881 | C | T | 2 | a0001c0001t0024g0355 a0001c0005t0001g0101 |
2 | HG01975.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.448+638G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094881 | |||||||
chr8:132094898 | C | T | 1 | a0003c0002t0001g0187 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.448+621G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132094898 | |||||||
chr8:132095122 | T | C | 2 | a0001c0005t0006g0046 a0001c0005t0009g0026 |
2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.448+397A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132095122 | |||||||
chr8:132095265 | T | C | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.448+254A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132095265 | |||||||
chr8:132095277 | C | T | 1 | a0002c0004t0002g0085 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.448+242G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132095277 | |||||||
chr8:132095410 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.448+109A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132095410 | |||||||
chr8:132095421 | A | C | 2 | a0002c0014t0001g0257 a0002c0014t0002g0268 |
2 | NA19000.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.448+98T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 7/16 | chr8 | 132095421 | |||||||
chr8:132095610 | G | A | 11 | a0001c0001t0002g0081 a0001c0001t0002g0098 a0001c0001t0003g0002 others(8): Show |
16 | HG00741.hp2 HG02145.hp2 HG02280.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.365-8C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 6/16 | chr8 | 132095610 | |||||||
chr8:132095646 | A | G | 297 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(294): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.365-44T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 6/16 | chr8 | 132095646 | |||||||
chr8:132095660 | T | A | 7 | a0001c0009t0002g0278 a0001c0009t0007g0188 a0001c0009t0008g0339 others(4): Show |
7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.364+43A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 6/16 | chr8 | 132095660 | |||||||
chr8:132095860 | C | T | 9 | a0005c0008t0001g0022 a0005c0008t0001g0023 a0005c0008t0001g0055 others(6): Show |
9 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.281-74G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132095860 | |||||||
chr8:132095863 | T | C | 35 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(32): Show |
36 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.281-77A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132095863 | |||||||
chr8:132095982 | A | G | 2 | a0001c0005t0006g0046 a0001c0005t0009g0026 |
2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.281-196T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132095982 | |||||||
chr8:132096021 | G | A | 9 | a0003c0002t0001g0289 a0003c0002t0010g0156 a0003c0002t0010g0158 others(6): Show |
9 | HG02559.hp2 HG02572.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.281-235C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096021 | |||||||
chr8:132096212 | T | G | 164 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(161): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.281-426A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096212 | |||||||
chr8:132096217 | C | T | 1 | a0001c0001t0003g0143 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.281-431G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096217 | |||||||
chr8:132096304 | T | C | 7 | a0001c0001t0002g0081 a0001c0001t0002g0098 a0001c0001t0003g0002 others(4): Show |
12 | HG00741.hp2 HG02145.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.281-518A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096304 | |||||||
chr8:132096335 | C | T | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0002g0184 |
3 | HG02683.hp1 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.281-549G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096335 | |||||||
chr8:132096404 | C | T | 124 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(121): Show |
131 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.281-618G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096404 | |||||||
chr8:132096512 | A | AT | 9 | a0001c0001t0002g0081 a0001c0001t0002g0098 a0001c0001t0003g0002 others(6): Show |
14 | HG00741.hp2 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.281-727dupA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096512 | |||||||
chr8:132096696 | G | T | 1 | a0001c0001t0004g0164 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.281-910C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096696 | |||||||
chr8:132096700 | C | A | 7 | a0003c0002t0001g0289 a0003c0002t0010g0156 a0003c0002t0010g0158 others(4): Show |
7 | HG02572.hp2 HG02647.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-914G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096700 | |||||||
chr8:132096835 | G | C | 7 | a0001c0009t0002g0278 a0001c0009t0007g0188 a0001c0009t0008g0339 others(4): Show |
7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.281-1049C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096835 | |||||||
chr8:132096842 | C | T | 1 | a0001c0001t0009g0302 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.281-1056G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096842 | |||||||
chr8:132096868 | C | T | 35 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(32): Show |
36 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.281-1082G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096868 | |||||||
chr8:132096881 | C | G | 1 | a0001c0001t0001g0255 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.281-1095G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096881 | |||||||
chr8:132096895 | C | A | 5 | a0006c0010t0001g0276 a0006c0010t0002g0272 a0006c0010t0002g0275 others(2): Show |
5 | HG02015.hp2 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-1109G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096895 | |||||||
chr8:132096895 | C | G | 292 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(289): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.281-1109G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096895 | |||||||
chr8:132096939 | C | T | 262 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.281-1153G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096939 | |||||||
chr8:132096960 | C | G | 1 | a0001c0001t0001g0012 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.281-1174G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096960 | |||||||
chr8:132096965 | G | A | 2 | a0001c0001t0009g0353 a0007c0011t0007g0042 |
2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.281-1179C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132096965 | |||||||
chr8:132097000 | T | G | 3 | a0003c0002t0010g0156 a0003c0002t0010g0158 a0004c0006t0001g0157 |
3 | HG02896.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.281-1214A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097000 | |||||||
chr8:132097029 | G | A | 2 | a0001c0016t0002g0150 a0001c0016t0006g0151 |
2 | HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.281-1243C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097029 | |||||||
chr8:132097123 | T | C | 292 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(289): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.281-1337A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097123 | |||||||
chr8:132097132 | C | T | 10 | a0001c0001t0001g0280 a0001c0001t0001g0294 a0001c0001t0001g0295 others(7): Show |
10 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(7): Show |
intron_variant | MODIFIER | c.281-1346G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097132 | |||||||
chr8:132097133 | G | A | 1 | a0001c0001t0009g0353 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.281-1347C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097133 | |||||||
chr8:132097234 | A | G | 1 | a0002c0003t0002g0301 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.281-1448T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097234 | |||||||
chr8:132097394 | T | C | 2 | a0001c0001t0024g0355 a0001c0005t0001g0354 |
2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.280+1488A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097394 | |||||||
chr8:132097400 | A | T | 7 | a0005c0008t0001g0022 a0005c0008t0001g0023 a0005c0008t0002g0345 others(4): Show |
7 | HG02451.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+1482T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097400 | |||||||
chr8:132097554 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.280+1328A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097554 | |||||||
chr8:132097682 | C | T | 3 | a0001c0005t0006g0046 a0001c0005t0009g0026 a0003c0002t0010g0352 |
3 | HG01884.hp2 HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.280+1200G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097682 | |||||||
chr8:132097943 | A | T | 25 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(22): Show |
26 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.280+939T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132097943 | |||||||
chr8:132098042 | C | A | 2 | a0002c0003t0001g0324 a0002c0003t0002g0325 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.280+840G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098042 | |||||||
chr8:132098173 | G | A | 1 | a0001c0020t0001g0136 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.280+709C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098173 | |||||||
chr8:132098244 | T | C | 1 | a0002c0004t0002g0073 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.280+638A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098244 | |||||||
chr8:132098327 | A | G | 5 | a0001c0001t0002g0081 a0001c0001t0002g0098 a0001c0001t0003g0002 others(2): Show |
10 | HG00741.hp2 HG02145.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.280+555T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098327 | |||||||
chr8:132098394 | G | A | 1 | a0002c0004t0002g0052 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.280+488C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098394 | |||||||
chr8:132098425 | A | G | 4 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0002c0003t0001g0162 others(1): Show |
4 | HG00280.hp1 HG01081.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+457T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098425 | |||||||
chr8:132098623 | A | C | 5 | a0001c0005t0001g0101 a0002c0004t0001g0009 a0002c0004t0001g0054 others(2): Show |
6 | HG01099.hp1 HG01257.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.280+259T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098623 | |||||||
chr8:132098813 | A | G | 1 | a0001c0001t0002g0096 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.280+69T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098813 | |||||||
chr8:132098816 | G | T | 1 | a0003c0002t0001g0030 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.280+66C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098816 | |||||||
chr8:132098839 | GA | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0280 a0001c0001t0001g0286 others(10): Show |
15 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.280+42delT | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 5/16 | chr8 | 132098839 | |||||||
chr8:132098990 | T | C | 1 | a0001c0005t0002g0350 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.200-28A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132098990 | |||||||
chr8:132099005 | G | A | 5 | a0001c0005t0006g0074 a0003c0002t0001g0241 a0003c0002t0001g0242 others(2): Show |
5 | HG00639.hp1 HG01934.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.200-43C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099005 | |||||||
chr8:132099060 | C | G | 195 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(192): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.200-98G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099060 | |||||||
chr8:132099093 | C | T | 1 | a0001c0001t0001g0017 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.200-131G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099093 | |||||||
chr8:132099116 | G | A | 3 | a0003c0002t0010g0156 a0003c0002t0010g0158 a0004c0006t0001g0157 |
3 | HG02896.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.200-154C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099116 | |||||||
chr8:132099122 | G | A | 3 | a0001c0005t0006g0046 a0001c0005t0009g0026 a0003c0002t0010g0352 |
3 | HG01884.hp2 HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.200-160C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099122 | |||||||
chr8:132099167 | A | T | 1 | a0001c0001t0001g0292 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.200-205T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099167 | |||||||
chr8:132099182 | A | G | 2 | a0005c0008t0001g0022 a0005c0008t0001g0023 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.200-220T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099182 | |||||||
chr8:132099273 | T | C | 1 | a0001c0001t0003g0099 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.200-311A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099273 | |||||||
chr8:132099391 | A | C | 7 | a0001c0009t0002g0278 a0001c0009t0007g0188 a0001c0009t0008g0339 others(4): Show |
7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.200-429T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099391 | |||||||
chr8:132099422 | C | T | 15 | a0001c0009t0002g0278 a0001c0009t0007g0188 a0001c0009t0008g0339 others(12): Show |
15 | HG01109.hp1 HG01123.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.200-460G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099422 | |||||||
chr8:132099459 | A | G | 2 | a0001c0001t0024g0355 a0001c0005t0001g0354 |
2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.200-497T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099459 | |||||||
chr8:132099470 | A | C | 7 | a0001c0009t0002g0278 a0001c0009t0007g0188 a0001c0009t0008g0339 others(4): Show |
7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.200-508T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099470 | |||||||
chr8:132099472 | TGGAG | T | 7 | a0005c0008t0001g0022 a0005c0008t0001g0023 a0005c0008t0002g0345 others(4): Show |
7 | HG02451.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.200-514_200-511del others(4): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099472 | |||||||
chr8:132099480 | G | T | 4 | a0001c0001t0003g0028 a0001c0001t0020g0027 a0002c0003t0001g0029 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.200-518C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099480 | |||||||
chr8:132099600 | T | A | 7 | a0005c0008t0001g0022 a0005c0008t0001g0023 a0005c0008t0002g0345 others(4): Show |
7 | HG02451.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.199+475A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099600 | |||||||
chr8:132099656 | C | G | 1 | a0002c0017t0002g0351 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.199+419G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099656 | |||||||
chr8:132099683 | A | G | 180 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(177): Show |
197 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.199+392T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099683 | |||||||
chr8:132099686 | G | T | 180 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(177): Show |
197 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.199+389C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099686 | |||||||
chr8:132099760 | A | G | 3 | a0001c0001t0005g0330 a0004c0006t0001g0334 a0007c0011t0007g0186 |
3 | HG02258.hp2 HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.199+315T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099760 | |||||||
chr8:132099768 | C | T | 2 | a0003c0002t0002g0141 a0003c0002t0002g0142 |
2 | HG02257.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.199+307G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099768 | |||||||
chr8:132099846 | C | T | 1 | a0003c0002t0002g0198 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.199+229G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 4/16 | chr8 | 132099846 | |||||||
chr8:132100145 | G | A | 223 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(220): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.140-11C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100145 | |||||||
chr8:132100234 | G | A | 15 | a0001c0007t0001g0024 a0001c0007t0001g0259 a0001c0007t0001g0260 others(12): Show |
15 | HG01255.hp1 HG02004.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.140-100C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100234 | |||||||
chr8:132100362 | C | T | 3 | a0003c0002t0001g0208 a0003c0002t0001g0209 a0003c0002t0001g0210 |
3 | NA18940.hp1 NA18945.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.140-228G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100362 | |||||||
chr8:132100376 | G | A | 2 | a0001c0001t0001g0326 a0001c0001t0022g0327 |
2 | HG00323.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.140-242C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100376 | |||||||
chr8:132100416 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.140-282A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100416 | |||||||
chr8:132100513 | C | G | 118 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(115): Show |
132 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.140-379G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100513 | |||||||
chr8:132100553 | G | A | 1 | a0003c0002t0010g0158 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.140-419C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100553 | |||||||
chr8:132100555 | G | T | 1 | a0001c0001t0002g0279 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.140-421C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100555 | |||||||
chr8:132100621 | TCATTCAA others(25): Show |
T | 1 | a0001c0001t0001g0181 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.140-519_140-488del others(32): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100621 | |||||||
chr8:132100667 | G | A | 72 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0002g0081 others(69): Show |
85 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.140-533C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100667 | |||||||
chr8:132100670 | A | G | 15 | a0002c0003t0001g0206 a0003c0002t0001g0193 a0003c0002t0001g0195 others(12): Show |
15 | HG00642.hp2 HG00741.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.140-536T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100670 | |||||||
chr8:132100713 | C | T | 101 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(98): Show |
115 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.140-579G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100713 | |||||||
chr8:132100738 | G | A | 1 | a0001c0027t0001g0045 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.140-604C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100738 | |||||||
chr8:132100756 | G | A | 4 | a0001c0001t0002g0098 a0001c0001t0003g0002 a0001c0001t0003g0099 others(1): Show |
9 | HG00741.hp2 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.140-622C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100756 | |||||||
chr8:132100779 | C | T | 2 | a0001c0001t0024g0355 a0001c0005t0001g0354 |
2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.140-645G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100779 | |||||||
chr8:132100845 | A | G | 7 | a0005c0008t0001g0022 a0005c0008t0001g0023 a0005c0008t0002g0345 others(4): Show |
7 | HG02451.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.140-711T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100845 | |||||||
chr8:132100991 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.140-857A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132100991 | |||||||
chr8:132101000 | A | T | 3 | a0003c0002t0001g0195 a0004c0006t0001g0196 a0004c0006t0001g0197 |
3 | HG01069.hp2 HG01071.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.140-866T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101000 | |||||||
chr8:132101228 | G | A | 1 | a0002c0003t0002g0328 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.140-1094C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101228 | |||||||
chr8:132101235 | T | A | 1 | a0002c0003t0001g0139 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.140-1101A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101235 | |||||||
chr8:132101284 | A | T | 182 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(179): Show |
191 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(188): Show |
intron_variant | MODIFIER | c.140-1150T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101284 | |||||||
chr8:132101433 | G | C | 218 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(215): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.140-1299C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101433 | |||||||
chr8:132101434 | G | A | 1 | a0007c0011t0007g0270 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.140-1300C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101434 | |||||||
chr8:132101464 | C | T | 1 | a0002c0004t0002g0084 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.140-1330G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101464 | |||||||
chr8:132101528 | A | T | 182 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(179): Show |
191 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(188): Show |
intron_variant | MODIFIER | c.140-1394T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101528 | |||||||
chr8:132101582 | A | AT | 97 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(94): Show |
106 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.140-1449dupA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101582 | |||||||
chr8:132101582 | AT | A | 99 | a0001c0001t0001g0140 a0001c0001t0001g0148 a0001c0001t0001g0160 others(96): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.140-1449delA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101582 | |||||||
chr8:132101621 | C | T | 2 | a0001c0001t0024g0355 a0001c0005t0001g0354 |
2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.140-1487G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101621 | |||||||
chr8:132101640 | G | A | 90 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(87): Show |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.140-1506C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101640 | |||||||
chr8:132101654 | A | G | 5 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0002g0184 others(2): Show |
5 | HG02486.hp2 HG02683.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.140-1520T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101654 | |||||||
chr8:132101663 | T | C | 2 | a0001c0001t0024g0355 a0001c0005t0001g0354 |
2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.140-1529A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101663 | |||||||
chr8:132101670 | G | A | 1 | a0003c0002t0004g0245 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.140-1536C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101670 | |||||||
chr8:132101704 | G | A | 183 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(180): Show |
192 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(189): Show |
intron_variant | MODIFIER | c.140-1570C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101704 | |||||||
chr8:132101749 | T | A | 183 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(180): Show |
192 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(189): Show |
intron_variant | MODIFIER | c.140-1615A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101749 | |||||||
chr8:132101797 | C | G | 5 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0002g0184 others(2): Show |
5 | HG02486.hp2 HG02683.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.140-1663G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101797 | |||||||
chr8:132101827 | T | C | 220 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(217): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.140-1693A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101827 | |||||||
chr8:132101896 | A | G | 35 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(32): Show |
36 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.140-1762T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101896 | |||||||
chr8:132101977 | A | G | 4 | a0003c0002t0010g0156 a0003c0002t0010g0158 a0004c0006t0001g0157 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.140-1843T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132101977 | |||||||
chr8:132102065 | T | C | 1 | a0001c0001t0005g0330 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.140-1931A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102065 | |||||||
chr8:132102246 | A | G | 1 | a0006c0010t0002g0272 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.139+1862T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102246 | |||||||
chr8:132102394 | G | A | 3 | a0002c0003t0001g0152 a0002c0003t0001g0153 a0003c0002t0002g0043 |
3 | NA19004.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.139+1714C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102394 | |||||||
chr8:132102439 | C | T | 14 | a0001c0007t0001g0259 a0001c0007t0001g0260 a0001c0007t0001g0263 others(11): Show |
14 | HG01255.hp1 HG02004.hp2 HG02965.hp2 others(11): Show |
intron_variant | MODIFIER | c.139+1669G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102439 | |||||||
chr8:132102545 | G | A | 1 | a0002c0003t0001g0331 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.139+1563C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102545 | |||||||
chr8:132102568 | C | T | 4 | a0001c0001t0002g0098 a0001c0001t0003g0002 a0001c0001t0003g0099 others(1): Show |
9 | HG00741.hp2 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.139+1540G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102568 | |||||||
chr8:132102593 | A | G | 35 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(32): Show |
36 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.139+1515T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102593 | |||||||
chr8:132102602 | G | T | 2 | a0001c0001t0001g0284 a0002c0003t0001g0285 |
2 | NA18979.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.139+1506C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102602 | |||||||
chr8:132102603 | C | T | 9 | a0003c0002t0010g0156 a0003c0002t0010g0158 a0004c0006t0001g0157 others(6): Show |
9 | HG02451.hp2 HG02559.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.139+1505G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102603 | |||||||
chr8:132102604 | A | G | 221 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(218): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.139+1504T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102604 | |||||||
chr8:132102640 | G | A | 35 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(32): Show |
36 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.139+1468C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102640 | |||||||
chr8:132102686 | C | T | 7 | a0001c0009t0002g0278 a0001c0009t0007g0188 a0001c0009t0008g0339 others(4): Show |
7 | HG01109.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.139+1422G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102686 | |||||||
chr8:132102687 | G | A | 2 | a0001c0001t0009g0353 a0001c0027t0001g0045 |
2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.139+1421C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102687 | |||||||
chr8:132102706 | G | GATGCCCC others(12): Show |
2 | a0001c0001t0024g0355 a0001c0005t0001g0354 |
2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.139+1401_139+1402i others(21): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102706 | |||||||
chr8:132102710 | A | C | 350 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(347): Show |
375 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.139+1398T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102710 | |||||||
chr8:132102752 | C | T | 186 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(183): Show |
195 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(192): Show |
intron_variant | MODIFIER | c.139+1356G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102752 | |||||||
chr8:132102792 | A | AT | 5 | a0001c0005t0001g0051 a0002c0004t0001g0053 a0002c0004t0002g0005 others(2): Show |
7 | HG01175.hp2 HG01192.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.139+1315dupA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102792 | |||||||
chr8:132102792 | AT | A | 10 | a0001c0001t0002g0081 a0001c0005t0002g0350 a0001c0005t0005g0008 others(7): Show |
11 | HG01099.hp2 HG01891.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.139+1315delA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102792 | |||||||
chr8:132102792 | ATTTTTTT | A | 63 | a0001c0001t0001g0006 a0001c0001t0001g0109 a0001c0001t0001g0271 others(60): Show |
65 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.139+1309_139+1315d others(9): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102792 | |||||||
chr8:132102792 | ATTTTTTT others(3): Show |
A | 7 | a0001c0001t0009g0353 a0001c0016t0002g0150 a0001c0016t0006g0151 others(4): Show |
7 | HG02015.hp2 HG02486.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.139+1306_139+1315d others(12): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102792 | |||||||
chr8:132102792 | ATTTTTTT others(4): Show |
A | 42 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(39): Show |
43 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.139+1305_139+1315d others(13): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102792 | |||||||
chr8:132102792 | ATTTTTTT others(5): Show |
A | 177 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(174): Show |
186 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(183): Show |
intron_variant | MODIFIER | c.139+1304_139+1315d others(14): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102792 | |||||||
chr8:132102826 | T | C | 2 | a0001c0001t0024g0355 a0001c0005t0001g0354 |
2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.139+1282A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102826 | |||||||
chr8:132102844 | G | A | 4 | a0001c0001t0002g0098 a0001c0001t0003g0002 a0001c0001t0003g0099 others(1): Show |
9 | HG00741.hp2 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.139+1264C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132102844 | |||||||
chr8:132103042 | C | T | 5 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0002g0184 others(2): Show |
5 | HG02486.hp2 HG02683.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+1066G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103042 | |||||||
chr8:132103056 | A | G | 2 | a0001c0001t0024g0355 a0001c0005t0001g0354 |
2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.139+1052T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103056 | |||||||
chr8:132103110 | G | A | 1 | a0002c0014t0002g0268 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.139+998C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103110 | |||||||
chr8:132103232 | A | C | 4 | a0001c0012t0001g0154 a0001c0012t0001g0155 a0001c0012t0001g0349 others(1): Show |
4 | HG01123.hp1 HG01934.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.139+876T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103232 | |||||||
chr8:132103247 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.139+861C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103247 | |||||||
chr8:132103400 | C | T | 184 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(181): Show |
193 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.139+708G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103400 | |||||||
chr8:132103412 | G | T | 184 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(181): Show |
193 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.139+696C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103412 | |||||||
chr8:132103417 | T | A | 184 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(181): Show |
193 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.139+691A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103417 | |||||||
chr8:132103543 | T | G | 221 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(218): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.139+565A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103543 | |||||||
chr8:132103618 | A | AAAAT | 6 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0002g0184 others(3): Show |
6 | HG00735.hp1 HG02647.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.139+486_139+489dup others(4): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103618 | |||||||
chr8:132103618 | AAAATAAA others(1): Show |
A | 58 | a0001c0001t0002g0081 a0001c0005t0001g0051 a0001c0005t0001g0059 others(55): Show |
71 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.139+482_139+489del others(8): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103618 | |||||||
chr8:132103704 | A | C | 184 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(181): Show |
193 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.139+404T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103704 | |||||||
chr8:132103739 | A | T | 284 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(281): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.139+369T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103739 | |||||||
chr8:132103807 | A | G | 184 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(181): Show |
193 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.139+301T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103807 | |||||||
chr8:132103862 | G | A | 284 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(281): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.139+246C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132103862 | |||||||
chr8:132104004 | C | T | 186 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(183): Show |
195 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(192): Show |
intron_variant | MODIFIER | c.139+104G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132104004 | |||||||
chr8:132104005 | G | A | 2 | a0001c0016t0002g0150 a0001c0016t0006g0151 |
2 | HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.139+103C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132104005 | |||||||
chr8:132104055 | A | G | 1 | a0003c0002t0001g0193 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.139+53T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132104055 | |||||||
chr8:132104063 | G | T | 30 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(27): Show |
31 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.139+45C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132104063 | |||||||
chr8:132104085 | A | G | 1 | a0001c0001t0002g0016 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.139+23T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 3/16 | chr8 | 132104085 | |||||||
chr8:132104328 | G | A | 32 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(29): Show |
33 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.80-161C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104328 | |||||||
chr8:132104353 | A | G | 187 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(184): Show |
196 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(193): Show |
intron_variant | MODIFIER | c.80-186T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104353 | |||||||
chr8:132104370 | C | A | 1 | a0003c0002t0001g0246 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.80-203G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104370 | |||||||
chr8:132104487 | G | A | 14 | a0001c0007t0001g0259 a0001c0007t0001g0260 a0001c0007t0001g0263 others(11): Show |
14 | HG01255.hp1 HG02004.hp2 HG02965.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-320C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104487 | |||||||
chr8:132104523 | G | GTGAGTCT others(29): Show |
1 | a0001c0001t0001g0181 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.80-357_80-356insGC others(34): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104523 | |||||||
chr8:132104661 | A | T | 67 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0106 others(64): Show |
67 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.80-494T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104661 | |||||||
chr8:132104676 | A | G | 1 | a0013c0028t0002g0192 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.80-509T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104676 | |||||||
chr8:132104782 | A | G | 4 | a0005c0008t0002g0345 a0005c0008t0002g0346 a0005c0008t0009g0337 others(1): Show |
4 | HG02451.hp2 HG02976.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+405T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104782 | |||||||
chr8:132104786 | C | T | 2 | a0001c0005t0002g0082 a0002c0004t0002g0049 |
2 | HG00738.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.79+401G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104786 | |||||||
chr8:132104956 | G | A | 1 | a0002c0003t0002g0332 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.79+231C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104956 | |||||||
chr8:132104969 | G | A | 1 | a0001c0007t0001g0024 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.79+218C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104969 | |||||||
chr8:132104991 | G | T | 90 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(87): Show |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.79+196C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132104991 | |||||||
chr8:132105115 | T | A | 120 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(117): Show |
129 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.79+72A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 2/16 | chr8 | 132105115 | |||||||
chr8:132105356 | G | A | 74 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0106 others(71): Show |
74 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.-21-70C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132105356 | |||||||
chr8:132105623 | G | C | 94 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(91): Show |
108 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-21-337C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132105623 | |||||||
chr8:132105716 | C | T | 2 | a0001c0016t0002g0150 a0001c0016t0006g0151 |
2 | HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-21-430G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132105716 | |||||||
chr8:132105818 | G | A | 69 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0106 others(66): Show |
69 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.-21-532C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132105818 | |||||||
chr8:132105909 | TCCTTCTC others(18): Show |
T | 1 | a0001c0001t0001g0109 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21-648_-21-624del others(25): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132105909 | |||||||
chr8:132106054 | T | A | 161 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0106 others(158): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.-21-768A>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106054 | |||||||
chr8:132106106 | T | C | 1 | a0001c0001t0004g0333 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-21-820A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106106 | |||||||
chr8:132106142 | T | G | 2 | a0001c0001t0024g0355 a0001c0005t0001g0354 |
2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-21-856A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106142 | |||||||
chr8:132106169 | C | T | 67 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0106 others(64): Show |
67 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.-21-883G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106169 | |||||||
chr8:132106179 | G | T | 4 | a0001c0001t0002g0098 a0001c0001t0003g0002 a0001c0001t0003g0099 others(1): Show |
9 | HG00741.hp2 HG02145.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21-893C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106179 | |||||||
chr8:132106235 | G | A | 90 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(87): Show |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.-21-949C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106235 | |||||||
chr8:132106325 | G | C | 161 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0106 others(158): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.-21-1039C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106325 | |||||||
chr8:132106387 | C | A | 295 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(292): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-21-1101G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106387 | |||||||
chr8:132106394 | A | T | 1 | a0003c0002t0002g0025 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-21-1108T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106394 | |||||||
chr8:132106494 | A | G | 2 | a0001c0001t0009g0353 a0001c0027t0001g0045 |
2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-21-1208T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106494 | |||||||
chr8:132106506 | C | T | 161 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0106 others(158): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.-21-1220G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106506 | |||||||
chr8:132106752 | C | T | 1 | a0001c0007t0001g0024 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-21-1466G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106752 | |||||||
chr8:132106838 | G | C | 11 | a0001c0005t0001g0087 a0001c0005t0002g0082 a0001c0005t0002g0086 others(8): Show |
11 | HG00408.hp1 HG00438.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21-1552C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106838 | |||||||
chr8:132106859 | G | A | 34 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(31): Show |
35 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-21-1573C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106859 | |||||||
chr8:132106867 | A | G | 1 | a0001c0027t0001g0045 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-21-1581T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106867 | |||||||
chr8:132106913 | G | A | 1 | a0001c0007t0002g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-21-1627C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106913 | |||||||
chr8:132106944 | G | A | 34 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(31): Show |
35 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.-21-1658C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132106944 | |||||||
chr8:132107074 | C | G | 2 | a0001c0001t0024g0355 a0001c0005t0001g0354 |
2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-21-1788G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107074 | |||||||
chr8:132107356 | AGTGGTAC others(32): Show |
A | 1 | a0001c0001t0003g0100 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-21-2109_-21-2071d others(41): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107356 | |||||||
chr8:132107404 | G | T | 67 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0106 others(64): Show |
67 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.-21-2118C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107404 | |||||||
chr8:132107420 | A | C | 92 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(89): Show |
106 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-21-2134T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107420 | |||||||
chr8:132107528 | G | A | 92 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(89): Show |
106 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-21-2242C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107528 | |||||||
chr8:132107552 | A | T | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0002g0184 |
3 | HG02683.hp1 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-21-2266T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107552 | |||||||
chr8:132107568 | G | A | 92 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(89): Show |
106 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-21-2282C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107568 | |||||||
chr8:132107591 | C | T | 92 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(89): Show |
106 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-21-2305G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107591 | |||||||
chr8:132107592 | G | A | 67 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0106 others(64): Show |
67 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.-21-2306C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107592 | |||||||
chr8:132107714 | C | A | 55 | a0001c0001t0002g0081 a0001c0005t0001g0051 a0001c0005t0001g0059 others(52): Show |
68 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-21-2428G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107714 | |||||||
chr8:132107835 | T | TTTGGAGA others(1): Show |
187 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(184): Show |
196 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(193): Show |
intron_variant | MODIFIER | c.-21-2557_-21-2550d others(10): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107835 | |||||||
chr8:132107839 | G | T | 1 | a0001c0001t0001g0109 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21-2553C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107839 | |||||||
chr8:132107840 | A | AGAGTTG | 94 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(91): Show |
108 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-21-2555_-21-2554i others(8): Show |
HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132107840 | |||||||
chr8:132108188 | G | T | 2 | a0003c0002t0001g0011 a0003c0002t0001g0187 |
3 | HG01257.hp2 HG01258.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-21-2902C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108188 | |||||||
chr8:132108220 | C | T | 58 | a0001c0001t0002g0081 a0001c0001t0002g0096 a0001c0005t0001g0051 others(55): Show |
71 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.-22+2882G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108220 | |||||||
chr8:132108442 | T | G | 1 | a0001c0001t0011g0159 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-22+2660A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108442 | |||||||
chr8:132108457 | C | T | 6 | a0001c0001t0001g0271 a0006c0010t0001g0276 a0006c0010t0002g0272 others(3): Show |
6 | HG02015.hp2 NA18977.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+2645G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108457 | |||||||
chr8:132108492 | T | C | 2 | a0005c0008t0002g0345 a0005c0008t0002g0346 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-22+2610A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108492 | |||||||
chr8:132108536 | C | A | 28 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(25): Show |
29 | HG00408.hp2 HG00597.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-22+2566G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108536 | |||||||
chr8:132108537 | G | A | 44 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0106 others(41): Show |
44 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.-22+2565C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108537 | |||||||
chr8:132108630 | C | T | 2 | a0002c0004t0002g0047 a0002c0004t0002g0048 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-22+2472G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108630 | |||||||
chr8:132108641 | G | A | 2 | a0003c0002t0002g0141 a0003c0002t0002g0142 |
2 | HG02257.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-22+2461C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108641 | |||||||
chr8:132108764 | CT | C | 4 | a0001c0005t0001g0101 a0002c0004t0001g0009 a0002c0004t0001g0102 others(1): Show |
5 | HG01257.hp1 HG01975.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+2337delA | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108764 | |||||||
chr8:132108791 | G | A | 132 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(129): Show |
152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.-22+2311C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108791 | |||||||
chr8:132108845 | A | C | 25 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(22): Show |
26 | HG00408.hp2 HG00597.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.-22+2257T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108845 | |||||||
chr8:132108886 | G | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0002g0107 |
3 | HG00609.hp1 NA18968.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.-22+2216C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108886 | |||||||
chr8:132108887 | C | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0002g0107 |
3 | HG00609.hp1 NA18968.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.-22+2215G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108887 | |||||||
chr8:132108911 | C | T | 1 | a0001c0001t0002g0015 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-22+2191G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108911 | |||||||
chr8:132108948 | A | T | 221 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(218): Show |
226 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.-22+2154T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132108948 | |||||||
chr8:132109045 | T | C | 1 | a0001c0001t0001g0347 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-22+2057A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109045 | |||||||
chr8:132109047 | G | T | 45 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0106 others(42): Show |
45 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.-22+2055C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109047 | |||||||
chr8:132109063 | A | G | 1 | a0001c0001t0009g0353 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-22+2039T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109063 | |||||||
chr8:132109095 | C | A | 1 | a0002c0003t0002g0348 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-22+2007G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109095 | |||||||
chr8:132109163 | T | G | 134 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(131): Show |
154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.-22+1939A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109163 | |||||||
chr8:132109330 | C | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0002g0107 |
3 | HG00609.hp1 NA18968.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.-22+1772G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109330 | |||||||
chr8:132109331 | G | A | 24 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(21): Show |
25 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.-22+1771C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109331 | |||||||
chr8:132109345 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0002g0149 |
2 | HG03669.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-22+1757T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109345 | |||||||
chr8:132109433 | GA | G | 225 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(222): Show |
248 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.-22+1668delT | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109433 | |||||||
chr8:132109449 | C | A | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0002g0184 |
3 | HG02683.hp1 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-22+1653G>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109449 | |||||||
chr8:132109638 | A | T | 132 | a0001c0001t0001g0148 a0001c0001t0001g0160 a0001c0001t0001g0161 others(129): Show |
152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.-22+1464T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109638 | |||||||
chr8:132109717 | G | T | 63 | a0001c0001t0002g0081 a0001c0001t0002g0096 a0001c0001t0002g0098 others(60): Show |
81 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.-22+1385C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109717 | |||||||
chr8:132109774 | A | C | 1 | a0007c0011t0007g0186 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-22+1328T>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109774 | |||||||
chr8:132109937 | A | T | 27 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(24): Show |
28 | HG00408.hp2 HG00597.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-22+1165T>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132109937 | |||||||
chr8:132110007 | C | T | 221 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(218): Show |
226 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.-22+1095G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110007 | |||||||
chr8:132110047 | G | A | 221 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(218): Show |
226 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.-22+1055C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110047 | |||||||
chr8:132110147 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-22+955T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110147 | |||||||
chr8:132110155 | T | C | 5 | a0001c0001t0003g0143 a0003c0002t0002g0146 a0003c0002t0006g0144 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+947A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110155 | |||||||
chr8:132110219 | T | C | 221 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(218): Show |
226 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.-22+883A>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110219 | |||||||
chr8:132110254 | C | T | 45 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0106 others(42): Show |
45 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.-22+848G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110254 | |||||||
chr8:132110280 | C | T | 1 | a0002c0013t0001g0105 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-22+822G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110280 | |||||||
chr8:132110304 | C | G | 2 | a0001c0001t0024g0355 a0001c0005t0001g0354 |
2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-22+798G>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110304 | |||||||
chr8:132110326 | G | C | 1 | a0001c0012t0001g0349 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-22+776C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110326 | |||||||
chr8:132110537 | G | A | 3 | a0001c0005t0002g0350 a0002c0017t0002g0351 a0003c0002t0010g0352 |
3 | HG01109.hp1 HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-22+565C>T | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110537 | |||||||
chr8:132110540 | C | T | 263 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-22+562G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110540 | |||||||
chr8:132110591 | G | C | 1 | a0001c0001t0009g0353 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-22+511C>G | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110591 | |||||||
chr8:132110651 | G | T | 261 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(258): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.-22+451C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110651 | |||||||
chr8:132110713 | A | G | 27 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(24): Show |
28 | HG00408.hp2 HG00597.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-22+389T>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110713 | |||||||
chr8:132110752 | G | T | 264 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(261): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.-22+350C>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110752 | |||||||
chr8:132110794 | T | G | 263 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-22+308A>C | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110794 | |||||||
chr8:132110915 | C | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
9 | HG00558.hp2 HG02080.hp2 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22+187G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132110915 | |||||||
chr8:132111038 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0002c0003t0001g0014 |
3 | HG02071.hp2 NA18971.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-22+64G>A | HHLA1 | ENSG00000132297.13 | transcript | ENST00000414222.2 | protein_coding | 1/16 | chr8 | 132111038 |