Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6713 |
| ensemblid | ENSG00000104549.12 |
| hgncid | 11279 |
| symbol | SQLE |
| name | squalene epoxidase |
| refseq_nuc | NM_003129.4 |
| refseq_prot | NP_003120.2 |
| ensembl_nuc | ENST00000265896.10 |
| ensembl_prot | ENSP00000265896.5 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 124998505 |
| end | 125022283 |
| strand | + |
| ver | v1.2 |
| region | chr8:124998505-125022283 |
| region5000 | chr8:124993505-125027283 |
| regionname0 | SQLE_chr8_124998505_125022283 |
| regionname5000 | SQLE_chr8_124993505_125027283 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 574 | 372 | 93 | 64 | 163 | 14 | 36 | 126 | SQLE_chr8_124993505_125027283 | SQLE | MWTFL others(569): Show |
chr8 | 124993505 | 125027283 |
| a0002 | 0/0 | 574 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | MWTFL others(569): Show |
chr8 | 124993505 | 125027283 |
| a0003 | 0/0 | 574 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SQLE_chr8_124993505_125027283 | SQLE | MWTFL others(569): Show |
chr8 | 124993505 | 125027283 |
| a0004 | 0/0 | 574 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SQLE_chr8_124993505_125027283 | SQLE | MWTFL others(569): Show |
chr8 | 124993505 | 125027283 |
| a0005 | 0/0 | 574 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | MWTFL others(569): Show |
chr8 | 124993505 | 125027283 |
| a0006 | 0/0 | 574 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | MWTFL others(569): Show |
chr8 | 124993505 | 125027283 |
| a0007 | 0/0 | 574 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | MWTFL others(569): Show |
chr8 | 124993505 | 125027283 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1722 | 315 | 73 | 61 | 140 | 12 | 27 | SQLE_chr8_124993505_125027283 | SQLE | ATGTG others(1717): Show |
chr8 | 124993505 | 125027283 | ||
| a0001c0002 | 0/0 | 1722 | 27 | 1 | 0 | 18 | 1 | 7 | SQLE_chr8_124993505_125027283 | SQLE | ATGTG others(1717): Show |
chr8 | 124993505 | 125027283 | ||
| a0001c0003 | 0/0 | 1722 | 19 | 18 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | ATGTG others(1717): Show |
chr8 | 124993505 | 125027283 | ||
| a0001c0004 | 0/0 | 1722 | 2 | 0 | 1 | 0 | 1 | 0 | SQLE_chr8_124993505_125027283 | SQLE | ATGTG others(1717): Show |
chr8 | 124993505 | 125027283 | ||
| a0001c0005 | 0/0 | 1722 | 2 | 0 | 2 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | ATGTG others(1717): Show |
chr8 | 124993505 | 125027283 | ||
| a0001c0006 | 0/0 | 1722 | 2 | 0 | 0 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | ATGTG others(1717): Show |
chr8 | 124993505 | 125027283 | ||
| a0001c0007 | 0/0 | 1722 | 2 | 0 | 0 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | ATGTG others(1717): Show |
chr8 | 124993505 | 125027283 | ||
| a0001c0008 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | ATGTG others(1717): Show |
chr8 | 124993505 | 125027283 | ||
| a0001c0009 | 0/0 | 1722 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | ATGTG others(1717): Show |
chr8 | 124993505 | 125027283 | ||
| a0001c0014 | 0/0 | 1722 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | ATGTG others(1717): Show |
chr8 | 124993505 | 125027283 | ||
| a0002c0015 | 0/0 | 1722 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | ATGTG others(1717): Show |
chr8 | 124993505 | 125027283 | ||
| a0003c0013 | 0/0 | 1722 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | ATGTG others(1717): Show |
chr8 | 124993505 | 125027283 | ||
| a0004c0012 | 0/0 | 1722 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | ATGTG others(1717): Show |
chr8 | 124993505 | 125027283 | ||
| a0005c0011 | 0/0 | 1722 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | ATGTG others(1717): Show |
chr8 | 124993505 | 125027283 | ||
| a0006c0010 | 0/0 | 1722 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | ATGTG others(1717): Show |
chr8 | 124993505 | 125027283 | ||
| a0007c0016 | 0/0 | 1722 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | ATGTG others(1717): Show |
chr8 | 124993505 | 125027283 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2962 | 227 | 31 | 45 | 117 | 10 | 23 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0001t0002 | 0/1 | 2962 | 33 | 3 | 6 | 19 | 0 | 4 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0001t0004 | 0/0 | 2962 | 13 | 7 | 4 | 0 | 2 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0001t0005 | 0/0 | 2962 | 13 | 11 | 2 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0001t0006 | 0/0 | 2962 | 13 | 11 | 2 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0001t0007 | 0/0 | 2962 | 5 | 4 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0001t0008 | 0/0 | 2962 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0001t0009 | 0/0 | 2962 | 2 | 2 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0001t0010 | 0/0 | 2962 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0001t0011 | 0/0 | 2962 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0001t0013 | 0/0 | 2962 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0001t0014 | 0/0 | 2962 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0001t0016 | 0/0 | 2962 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0001t0017 | 0/0 | 2962 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0001t0018 | 0/0 | 2962 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0001t0020 | 0/0 | 2962 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0002t0003 | 0/0 | 2962 | 25 | 1 | 0 | 17 | 1 | 6 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0002t0012 | 0/0 | 2962 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0002t0015 | 0/0 | 2962 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0003t0001 | 0/0 | 2962 | 14 | 13 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0003t0008 | 0/0 | 2962 | 3 | 3 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0003t0010 | 0/0 | 2962 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0003t0019 | 0/0 | 2962 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0004t0001 | 0/0 | 2962 | 2 | 0 | 1 | 0 | 1 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0005t0001 | 0/0 | 2962 | 2 | 0 | 2 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0006t0001 | 0/0 | 2962 | 2 | 0 | 0 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0007t0001 | 0/0 | 2962 | 2 | 0 | 0 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0008t0007 | 0/0 | 2962 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0009t0001 | 0/0 | 2962 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0001c0014t0001 | 0/0 | 2962 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0002c0015t0001 | 0/0 | 2962 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0003c0013t0001 | 0/0 | 2962 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0004c0012t0001 | 0/0 | 2962 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0005c0011t0004 | 0/0 | 2962 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0006c0010t0001 | 0/0 | 2962 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| a0007c0016t0001 | 0/0 | 2962 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | GAGAC others(2957): Show |
chr8 | 124993505 | 125027283 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 28 | 1 | 5 | 18 | 1 | 3 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0002 | 0/0 | 14 | 0 | 1 | 7 | 3 | 3 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0003 | 0/0 | 14 | 0 | 2 | 12 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0004 | 0/0 | 12 | 0 | 2 | 6 | 0 | 4 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 2 | 5 | 0 | 2 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 4 | 2 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0007 | 1/0 | 7 | 0 | 5 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0020 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0022 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0008 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0004g0021 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0005g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0005g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0005g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0006g0011 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0006g0055 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0007g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0007g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0009g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0011g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0013g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0014g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0016g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0017g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0018g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0001t0020g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0002t0003g0009 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0002t0003g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0002t0003g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0002t0003g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0002t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0002t0012g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0002t0015g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0003t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0003t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0003t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0003t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0003t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0003t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0003t0010g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0003t0019g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0004t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0005t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0005t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0006t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0007t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0008t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0009t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0001c0014t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0002c0015t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0003c0013t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0004c0012t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0005c0011t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0006c0010t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| a0007c0016t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | GBR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | GBR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00280 | hp1 | a0001 | c0004 | t0001 | g0035 | EUR | FIN | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00423 | hp1 | a0002 | c0015 | t0001 | g0001 | EAS | CHS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00438 | hp1 | a0001 | c0001 | t0013 | g0158 | EAS | CHS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00609 | hp2 | a0001 | c0002 | t0003 | g0076 | EAS | CHS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0011 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0040 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0040 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01099 | hp1 | a0001 | c0001 | t0007 | g0100 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0093 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01167 | hp1 | a0001 | c0005 | t0001 | g0134 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01169 | hp2 | a0001 | c0005 | t0001 | g0023 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01175 | hp1 | a0001 | c0001 | t0016 | g0116 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0055 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01261 | hp1 | a0001 | c0004 | t0001 | g0035 | AMR | CLM | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0103 | AMR | CLM | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | IBS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0021 | EUR | IBS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | IBS | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0027 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02027 | hp1 | a0001 | c0014 | t0001 | g0036 | EAS | KHV | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02027 | hp2 | a0001 | c0002 | t0003 | g0009 | EAS | KHV | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02040 | hp1 | a0001 | c0001 | t0011 | g0026 | EAS | KHV | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0059 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02055 | hp2 | a0001 | c0001 | t0017 | g0065 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02071 | hp2 | a0001 | c0002 | t0015 | g0072 | EAS | KHV | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02080 | hp2 | a0001 | c0002 | t0003 | g0029 | EAS | KHV | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02145 | hp1 | a0001 | c0003 | t0008 | g0088 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0009 | EAS | CDX | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0068 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0105 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0198 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0060 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0044 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0063 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02630 | hp2 | a0001 | c0002 | t0003 | g0078 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0061 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02683 | hp2 | a0003 | c0013 | t0001 | g0118 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0196 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0084 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0125 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0199 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0057 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0062 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0044 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0099 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ESN | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02922 | hp2 | a0001 | c0003 | t0008 | g0087 | AFR | ESN | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | ESN | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02965 | hp2 | a0001 | c0003 | t0010 | g0195 | AFR | ESN | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ESN | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02970 | hp2 | a0001 | c0003 | t0008 | g0086 | AFR | ESN | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02976 | hp2 | a0001 | c0003 | t0019 | g0120 | AFR | ESN | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | MSL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03098 | hp2 | a0001 | c0008 | t0007 | g0041 | AFR | MSL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | ESN | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0191 | AFR | ESN | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | MSL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | MSL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0041 | AFR | MSL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | MSL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | MSL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03486 | hp2 | a0001 | c0001 | t0018 | g0104 | AFR | MSL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0194 | AFR | ESN | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0197 | AFR | GWD | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | MSL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03669 | hp1 | a0001 | c0009 | t0001 | g0144 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0029 | SAS | PJL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0031 | SAS | BEB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0009 | SAS | BEB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG04199 | hp1 | a0001 | c0002 | t0003 | g0077 | SAS | STU | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0085 | SAS | STU | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG04228 | hp1 | a0001 | c0002 | t0003 | g0073 | SAS | STU | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG04228 | hp2 | a0004 | c0012 | t0001 | g0129 | SAS | STU | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0055 | AFR | YRI | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18906 | hp1 | a0005 | c0011 | t0004 | g0032 | AFR | YRI | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18943 | hp1 | a0001 | c0002 | t0003 | g0081 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18946 | hp2 | a0001 | c0002 | t0003 | g0075 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18948 | hp1 | a0001 | c0001 | t0014 | g0117 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18949 | hp2 | a0001 | c0002 | t0003 | g0080 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18961 | hp1 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18965 | hp1 | a0001 | c0002 | t0003 | g0071 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18968 | hp2 | a0006 | c0010 | t0001 | g0109 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18969 | hp2 | a0001 | c0006 | t0001 | g0001 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18971 | hp1 | a0007 | c0016 | t0001 | g0002 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18974 | hp2 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18984 | hp1 | a0001 | c0007 | t0001 | g0001 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18985 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18987 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18989 | hp1 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18991 | hp2 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA18994 | hp2 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19002 | hp1 | a0001 | c0007 | t0001 | g0001 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19002 | hp2 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0058 | AFR | LWK | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | LWK | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0083 | AFR | LWK | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19068 | hp2 | a0001 | c0001 | t0020 | g0001 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19080 | hp2 | a0001 | c0002 | t0003 | g0074 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19088 | hp1 | a0001 | c0006 | t0001 | g0001 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | YRI | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | YRI | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ASW | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ASW | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA20752 | hp1 | a0001 | c0002 | t0003 | g0107 | EUR | TSI | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0102 | EUR | TSI | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA20905 | hp1 | a0001 | c0002 | t0012 | g0171 | SAS | GIH | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0192 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | ACB | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | MSL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0193 | AFR | MSL | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | USA | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | USA | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0027 | AFR | USA | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | USA | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0169 | REF | REF | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0007 | REF | REF | SQLE_chr8_124993505_125027283 | SQLE | chr8 | 124993505 | 125027283 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:124999444 | A | C | 1 | a0007 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.41A>C | p.Tyr14Ser | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/11 | 940/2962 | 41/1725 | 14/574 | chr8 | 124999444 | |||
| chr8:125003176 | C | T | 1 | a0002 | 1 | HG00423.hp1 | missense_variant&splice_region_variant | MODERATE | c.292C>T | p.Arg98Cys | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/11 | 1191/2962 | 292/1725 | 98/574 | chr8 | 125003176 | |||
| chr8:125009172 | A | T | 1 | a0003 | 1 | HG02683.hp2 | missense_variant&splice_region_variant | MODERATE | c.937A>T | p.Asn313Tyr | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/11 | 1836/2962 | 937/1725 | 313/574 | chr8 | 125009172 | |||
| chr8:125009277 | A | G | 1 | a0004 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.1042A>G | p.Ile348Val | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/11 | 1941/2962 | 1042/1725 | 348/574 | chr8 | 125009277 | |||
| chr8:125011573 | A | G | 1 | a0005 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.1145A>G | p.Asn382Ser | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/11 | 2044/2962 | 1145/1725 | 382/574 | chr8 | 125011573 | |||
| chr8:125020837 | G | A | 1 | a0006 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.1498G>A | p.Glu500Lys | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/11 | 2397/2962 | 1498/1725 | 500/574 | chr8 | 125020837 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:124999493 | G | A | 1 | a0001c0008 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.90G>A | p.Leu30Leu | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/11 | 989/2962 | 90/1725 | 30/574 | chr8 | 124999493 | |||
| chr8:125003268 | C | T | 1 | a0001c0014 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.384C>T | p.Ile128Ile | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/11 | 1283/2962 | 384/1725 | 128/574 | chr8 | 125003268 | |||
| chr8:125005535 | A | G | 1 | a0001c0007 | 2 | NA18984.hp1 NA19002.hp1 |
synonymous_variant | LOW | c.555A>G | p.Glu185Glu | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/11 | 1454/2962 | 555/1725 | 185/574 | chr8 | 125005535 | |||
| chr8:125005628 | T | C | 1 | a0001c0009 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.648T>C | p.Asn216Asn | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/11 | 1547/2962 | 648/1725 | 216/574 | chr8 | 125005628 | |||
| chr8:125018159 | A | C | 1 | a0001c0006 | 2 | NA18969.hp2 NA19088.hp1 |
synonymous_variant | LOW | c.1305A>C | p.Leu435Leu | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 8/11 | 2204/2962 | 1305/1725 | 435/574 | chr8 | 125018159 | |||
| chr8:125020848 | G | T | 1 | a0001c0005 | 2 | HG01167.hp1 HG01169.hp2 |
synonymous_variant | LOW | c.1509G>T | p.Ala503Ala | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/11 | 2408/2962 | 1509/1725 | 503/574 | chr8 | 125020848 | |||
| chr8:125020854 | T | C | 1 | a0001c0002 | 27 | HG00609.hp2 HG02027.hp2 HG02071.hp2 others(24): Show |
synonymous_variant | LOW | c.1515T>C | p.Pro505Pro | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/11 | 2414/2962 | 1515/1725 | 505/574 | chr8 | 125020854 | |||
| chr8:125021810 | C | T | 2 | a0001c0002 a0001c0003 |
46 | HG00609.hp2 HG01884.hp2 HG01891.hp1 others(43): Show |
synonymous_variant | LOW | c.1590C>T | p.Ala530Ala | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 11/11 | 2489/2962 | 1590/1725 | 530/574 | chr8 | 125021810 | |||
| chr8:125021900 | A | C | 1 | a0001c0004 | 2 | HG00280.hp1 HG01261.hp1 |
synonymous_variant | LOW | c.1680A>C | p.Val560Val | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 11/11 | 2579/2962 | 1680/1725 | 560/574 | chr8 | 125021900 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:124998523 | C | T | 1 | a0001c0001t0020 | 1 | NA19068.hp2 | 5_prime_UTR_variant | MODIFIER | c.-881C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/11 | 881 | chr8 | 124998523 | ||||||
| chr8:124998563 | G | C | 4 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0013 others(1): Show |
35 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-841G>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/11 | 841 | chr8 | 124998563 | ||||||
| chr8:124998600 | A | G | 3 | a0001c0001t0007 a0001c0003t0019 a0001c0008t0007 |
7 | HG01099.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-804A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/11 | 804 | chr8 | 124998600 | ||||||
| chr8:124998603 | C | T | 2 | a0001c0001t0008 a0001c0003t0008 |
4 | HG02145.hp1 HG02647.hp1 HG02922.hp2 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-801C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/11 | chr8 | 124998603 | |||||||
| chr8:124998699 | C | G | 6 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0010 others(3): Show |
19 | HG00639.hp1 HG01192.hp2 HG01891.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-705C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/11 | 705 | chr8 | 124998699 | ||||||
| chr8:124998745 | G | A | 1 | a0001c0003t0019 | 1 | HG02976.hp2 | 5_prime_UTR_variant | MODIFIER | c.-659G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/11 | 659 | chr8 | 124998745 | ||||||
| chr8:124998751 | T | G | 1 | a0001c0001t0014 | 1 | NA18948.hp1 | 5_prime_UTR_variant | MODIFIER | c.-653T>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/11 | 653 | chr8 | 124998751 | ||||||
| chr8:124998810 | T | C | 5 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0010 others(2): Show |
18 | HG00639.hp1 HG01192.hp2 HG01891.hp2 others(15): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-594T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/11 | chr8 | 124998810 | |||||||
| chr8:124998826 | G | T | 4 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0017 others(1): Show |
16 | HG00639.hp1 HG01192.hp2 HG01891.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-578G>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/11 | 578 | chr8 | 124998826 | ||||||
| chr8:124998884 | C | T | 1 | a0001c0001t0016 | 1 | HG01175.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-520C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/11 | chr8 | 124998884 | |||||||
| chr8:124998985 | T | G | 6 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0010 others(3): Show |
19 | HG00639.hp1 HG01192.hp2 HG01891.hp2 others(16): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-419T>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/11 | chr8 | 124998985 | |||||||
| chr8:124999045 | A | T | 1 | a0001c0001t0013 | 1 | HG00438.hp1 | 5_prime_UTR_variant | MODIFIER | c.-359A>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/11 | 359 | chr8 | 124999045 | ||||||
| chr8:124999073 | A | G | 3 | a0001c0001t0006 a0001c0001t0010 a0001c0003t0010 |
15 | HG00639.hp1 HG01192.hp2 HG01891.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-331A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/11 | 331 | chr8 | 124999073 | ||||||
| chr8:124999225 | C | T | 3 | a0001c0001t0006 a0001c0001t0010 a0001c0003t0010 |
15 | HG00639.hp1 HG01192.hp2 HG01891.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-179C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/11 | 179 | chr8 | 124999225 | ||||||
| chr8:124999288 | T | G | 1 | a0001c0001t0005 | 13 | HG01070.hp2 HG01071.hp1 HG02258.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-116T>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/11 | 116 | chr8 | 124999288 | ||||||
| chr8:125022098 | G | C | 1 | a0001c0001t0011 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*153G>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 11/11 | 153 | chr8 | 125022098 | ||||||
| chr8:125022122 | T | C | 1 | a0001c0002t0015 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*177T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 11/11 | 177 | chr8 | 125022122 | ||||||
| chr8:125022133 | A | G | 3 | a0001c0002t0003 a0001c0002t0012 a0001c0002t0015 |
27 | HG00609.hp2 HG02027.hp2 HG02071.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*188A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 11/11 | 188 | chr8 | 125022133 | ||||||
| chr8:125022168 | A | G | 3 | a0001c0001t0004 a0001c0001t0006 a0005c0011t0004 |
27 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*223A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 11/11 | 223 | chr8 | 125022168 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:124999707 | C | G | 2 | a0001c0003t0001g0198 a0001c0003t0001g0199 |
2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.291+13C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 124999707 | |||||||
| chr8:124999714 | G | T | 9 | a0001c0001t0006g0011 a0001c0001t0006g0055 a0001c0001t0006g0192 others(6): Show |
15 | HG00639.hp1 HG01192.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.291+20G>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 124999714 | |||||||
| chr8:124999787 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.291+93G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 124999787 | |||||||
| chr8:124999799 | G | A | 8 | a0001c0003t0001g0014 a0001c0003t0001g0018 a0001c0003t0001g0027 others(5): Show |
14 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.291+105G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 124999799 | |||||||
| chr8:125000003 | A | C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(50): Show |
104 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.291+309A>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125000003 | |||||||
| chr8:125000034 | T | C | 6 | a0001c0001t0005g0015 a0001c0001t0005g0028 a0001c0001t0007g0063 others(3): Show |
10 | HG02615.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.291+340T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125000034 | |||||||
| chr8:125000364 | C | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0046 a0001c0001t0001g0150 others(1): Show |
9 | HG00597.hp2 HG02004.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.291+670C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125000364 | |||||||
| chr8:125000444 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.291+750A>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125000444 | |||||||
| chr8:125000536 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.291+842C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125000536 | |||||||
| chr8:125000684 | C | T | 3 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0189 |
5 | HG00621.hp1 HG00673.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.291+990C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125000684 | |||||||
| chr8:125000715 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.291+1021A>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125000715 | |||||||
| chr8:125000892 | A | G | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(24): Show |
68 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.291+1198A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125000892 | |||||||
| chr8:125000980 | C | G | 1 | a0001c0001t0002g0172 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.291+1286C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125000980 | |||||||
| chr8:125001034 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.291+1340G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125001034 | |||||||
| chr8:125001053 | C | T | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(24): Show |
68 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.291+1359C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125001053 | |||||||
| chr8:125001061 | G | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
186 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.291+1367G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125001061 | |||||||
| chr8:125001093 | C | T | 1 | a0001c0003t0001g0059 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.291+1399C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125001093 | |||||||
| chr8:125001158 | T | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
169 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.291+1464T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125001158 | |||||||
| chr8:125001371 | A | T | 1 | a0001c0001t0001g0147 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.291+1677A>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125001371 | |||||||
| chr8:125001449 | G | GGT | 27 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0020 others(24): Show |
61 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.292-1688_292-1687d others(4): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001449 | ||||||
| chr8:125001449 | G | GGTGT | 25 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0131 others(22): Show |
37 | HG01074.hp2 HG01167.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.292-1690_292-1687d others(6): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001449 | ||||||
| chr8:125001449 | G | GGTGTGT | 18 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0079 others(15): Show |
22 | HG00558.hp2 HG00609.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.292-1692_292-1687d others(8): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001449 | ||||||
| chr8:125001449 | G | GGTGTGTG others(1): Show |
8 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0143 others(5): Show |
9 | HG00140.hp2 HG01109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.292-1694_292-1687d others(10): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001449 | ||||||
| chr8:125001449 | G | GGTGTGTG others(3): Show |
2 | a0001c0001t0001g0188 a0001c0002t0003g0085 |
2 | HG04204.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.292-1696_292-1687d others(12): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001449 | ||||||
| chr8:125001449 | G | GGTGTGTG others(7): Show |
1 | a0001c0001t0001g0145 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.292-1700_292-1687d others(16): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001449 | ||||||
| chr8:125001449 | G | T | 1 | a0001c0001t0001g0146 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.292-1727G>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125001449 | |||||||
| chr8:125001449 | GGT | G | 13 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0001g0034 others(10): Show |
18 | HG00280.hp1 HG01099.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.292-1688_292-1687d others(4): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001449 | ||||||
| chr8:125001449 | GGTGT | G | 4 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG02630.hp1 NA18952.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-1690_292-1687d others(6): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001449 | ||||||
| chr8:125001449 | GGTGTGTG others(7): Show |
G | 3 | a0001c0003t0001g0018 a0001c0003t0001g0057 a0001c0003t0001g0059 |
5 | HG02055.hp1 HG02559.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.292-1700_292-1687d others(16): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001449 | ||||||
| chr8:125001468 | GTGTGTGT others(15): Show |
G | 1 | a0001c0001t0002g0152 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.292-1706_292-1685d others(24): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001468 | ||||||
| chr8:125001476 | GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0017g0065 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.292-1698_292-1685d others(16): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001476 | ||||||
| chr8:125001478 | GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0001g0004 | 2 | HG02015.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.292-1696_292-1685d others(14): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001478 | ||||||
| chr8:125001480 | GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0002g0153 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.292-1694_292-1685d others(12): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001480 | ||||||
| chr8:125001482 | GTGTGTGT others(1): Show |
G | 28 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(25): Show |
60 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.292-1692_292-1685d others(10): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001482 | ||||||
| chr8:125001484 | GTGTGTA | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
5 | HG02129.hp2 HG03490.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.292-1690_292-1685d others(8): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001484 | ||||||
| chr8:125001486 | GTGTA | G | 1 | a0001c0001t0002g0008 | 4 | NA18939.hp1 NA18984.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-1688_292-1685d others(6): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001486 | ||||||
| chr8:125001488 | GTA | G | 12 | a0001c0001t0001g0050 a0001c0001t0001g0159 a0001c0001t0001g0181 others(9): Show |
14 | HG00438.hp1 HG00673.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.292-1683_292-1682d others(4): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001488 | ||||||
| chr8:125001490 | A | G | 61 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0067 others(58): Show |
84 | HG00609.hp2 HG00621.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.292-1686A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125001490 | |||||||
| chr8:125001560 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.292-1616C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125001560 | |||||||
| chr8:125001675 | TA | T | 7 | a0001c0001t0001g0130 a0001c0001t0001g0142 a0001c0001t0002g0167 others(4): Show |
7 | HG01099.hp1 HG01168.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.292-1488delA | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001675 | ||||||
| chr8:125001689 | G | T | 1 | a0001c0001t0007g0100 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.292-1487G>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125001689 | |||||||
| chr8:125001794 | CTTGA | C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(50): Show |
104 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.292-1379_292-1376d others(6): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125001794 | ||||||
| chr8:125001795 | T | G | 1 | a0001c0001t0001g0094 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.292-1381T>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125001795 | |||||||
| chr8:125001813 | C | A | 1 | a0001c0001t0002g0153 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.292-1363C>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125001813 | |||||||
| chr8:125002002 | C | G | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | NA18946.hp1 NA18978.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.292-1174C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125002002 | |||||||
| chr8:125002112 | C | T | 6 | a0001c0001t0005g0015 a0001c0001t0005g0028 a0001c0001t0007g0063 others(3): Show |
10 | HG02615.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.292-1064C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125002112 | |||||||
| chr8:125002270 | A | C | 1 | a0001c0001t0002g0153 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.292-906A>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125002270 | |||||||
| chr8:125002274 | A | G | 6 | a0001c0001t0005g0015 a0001c0001t0005g0028 a0001c0001t0007g0063 others(3): Show |
10 | HG02615.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.292-902A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125002274 | |||||||
| chr8:125002334 | C | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
168 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.292-842C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125002334 | |||||||
| chr8:125002467 | C | G | 1 | a0001c0001t0001g0123 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.292-709C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125002467 | |||||||
| chr8:125002707 | A | T | 1 | a0001c0001t0002g0164 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.292-469A>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125002707 | |||||||
| chr8:125002735 | G | A | 1 | a0001c0001t0006g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.292-441G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125002735 | |||||||
| chr8:125002757 | A | G | 2 | a0001c0001t0006g0196 a0001c0001t0006g0197 |
2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.292-419A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125002757 | |||||||
| chr8:125003158 | C | CT | 42 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0070 others(39): Show |
63 | HG00609.hp2 HG00639.hp1 HG01192.hp2 others(60): Show |
splice_region_variant&intron_variant | LOW | c.292-7dupT | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125003158 | ||||||
| chr8:125003158 | C | CTT | 53 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(50): Show |
104 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(101): Show |
splice_region_variant&intron_variant | LOW | c.292-8_292-7dupTT | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 125003158 | ||||||
| chr8:125003158 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.292-18C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 1/10 | chr8 | 125003158 | |||||||
| chr8:125003460 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.544+32G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125003460 | |||||||
| chr8:125003502 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.544+74A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125003502 | |||||||
| chr8:125003777 | A | G | 3 | a0001c0003t0008g0086 a0001c0003t0008g0087 a0001c0003t0008g0088 |
3 | HG02145.hp1 HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.544+349A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125003777 | |||||||
| chr8:125003779 | T | G | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
169 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.544+351T>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125003779 | |||||||
| chr8:125003888 | T | TGGTGG | 8 | a0001c0003t0001g0014 a0001c0003t0001g0018 a0001c0003t0001g0027 others(5): Show |
14 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.544+478_544+482dup others(5): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr8 | 125003888 | ||||||
| chr8:125003934 | C | T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
105 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.544+506C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125003934 | |||||||
| chr8:125004150 | T | A | 1 | a0001c0001t0001g0124 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.544+722T>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125004150 | |||||||
| chr8:125004160 | C | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(50): Show |
104 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.544+732C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125004160 | |||||||
| chr8:125004325 | G | A | 15 | a0001c0002t0003g0009 a0001c0002t0003g0016 a0001c0002t0003g0029 others(12): Show |
25 | HG00609.hp2 HG02027.hp2 HG02071.hp2 others(22): Show |
intron_variant | MODIFIER | c.544+897G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125004325 | |||||||
| chr8:125004377 | C | T | 1 | a0001c0001t0010g0191 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.544+949C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125004377 | |||||||
| chr8:125004493 | A | G | 1 | a0001c0001t0017g0065 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.545-1032A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125004493 | |||||||
| chr8:125004544 | CTGT | C | 41 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0070 others(38): Show |
62 | HG00609.hp2 HG00639.hp1 HG01192.hp2 others(59): Show |
intron_variant | MODIFIER | c.545-976_545-974del others(3): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr8 | 125004544 | ||||||
| chr8:125004553 | C | A | 9 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0094 others(6): Show |
15 | HG00280.hp2 HG00735.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.545-972C>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125004553 | |||||||
| chr8:125004727 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
168 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.545-798T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125004727 | |||||||
| chr8:125004794 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.545-731A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125004794 | |||||||
| chr8:125004807 | C | T | 8 | a0001c0001t0006g0011 a0001c0001t0006g0055 a0001c0001t0006g0192 others(5): Show |
14 | HG00639.hp1 HG01192.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.545-718C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125004807 | |||||||
| chr8:125004999 | G | A | 1 | a0001c0003t0001g0027 | 2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.545-526G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125004999 | |||||||
| chr8:125005043 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.545-482T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125005043 | |||||||
| chr8:125005057 | C | G | 1 | a0001c0001t0002g0153 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.545-468C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125005057 | |||||||
| chr8:125005073 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.545-452T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125005073 | |||||||
| chr8:125005114 | A | G | 1 | a0001c0001t0017g0065 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.545-411A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125005114 | |||||||
| chr8:125005330 | T | C | 26 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0022 others(23): Show |
39 | HG00280.hp2 HG00735.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.545-195T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125005330 | |||||||
| chr8:125005335 | C | T | 27 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0070 others(24): Show |
38 | HG00609.hp2 HG01884.hp1 HG02027.hp2 others(35): Show |
intron_variant | MODIFIER | c.545-190C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125005335 | |||||||
| chr8:125005362 | C | T | 1 | a0001c0003t0001g0199 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.545-163C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | chr8 | 125005362 | |||||||
| chr8:125005370 | AT | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
168 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.545-153delT | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr8 | 125005370 | ||||||
| chr8:125005891 | T | C | 1 | a0001c0003t0008g0087 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.725+186T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125005891 | |||||||
| chr8:125006015 | C | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(23): Show |
67 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.725+310C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006015 | |||||||
| chr8:125006043 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
278 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(275): Show |
intron_variant | MODIFIER | c.725+338C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006043 | |||||||
| chr8:125006229 | T | G | 1 | a0001c0001t0009g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.725+524T>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006229 | |||||||
| chr8:125006359 | G | A | 1 | a0001c0001t0017g0065 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.725+654G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006359 | |||||||
| chr8:125006396 | A | C | 1 | a0001c0001t0010g0191 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.725+691A>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006396 | |||||||
| chr8:125006419 | A | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
170 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.725+714A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006419 | |||||||
| chr8:125006599 | C | T | 4 | a0001c0001t0007g0041 a0001c0001t0007g0044 a0001c0001t0017g0065 others(1): Show |
5 | HG02055.hp2 HG02615.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.726-792C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006599 | |||||||
| chr8:125006614 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
368 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(365): Show |
intron_variant | MODIFIER | c.726-777T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006614 | |||||||
| chr8:125006615 | G | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(97): Show |
173 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.726-776G>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006615 | |||||||
| chr8:125006620 | CA | C | 6 | a0001c0001t0001g0034 a0001c0001t0007g0041 a0001c0001t0007g0044 others(3): Show |
9 | HG00280.hp1 HG01261.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.726-756delA | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 125006620 | ||||||
| chr8:125006688 | T | C | 1 | a0001c0001t0006g0192 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.726-703T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006688 | |||||||
| chr8:125006710 | C | CT | 31 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0070 others(28): Show |
42 | HG00609.hp2 HG01884.hp1 HG02027.hp2 others(39): Show |
intron_variant | MODIFIER | c.726-678dupT | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 125006710 | ||||||
| chr8:125006721 | T | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0131 a0001c0001t0001g0137 |
5 | HG00280.hp2 HG01069.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.726-670T>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006721 | |||||||
| chr8:125006825 | C | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(23): Show |
67 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.726-566C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006825 | |||||||
| chr8:125006829 | C | T | 4 | a0001c0003t0001g0018 a0001c0003t0001g0057 a0001c0003t0001g0059 others(1): Show |
6 | HG02055.hp1 HG02559.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.726-562C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006829 | |||||||
| chr8:125006861 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.726-530C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006861 | |||||||
| chr8:125006910 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0005g0040 a0001c0003t0001g0014 |
8 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.726-481G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006910 | |||||||
| chr8:125006921 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0148 |
4 | NA18963.hp1 NA18967.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.726-470C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006921 | |||||||
| chr8:125006945 | C | T | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG02698.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.726-446C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006945 | |||||||
| chr8:125006946 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0148 |
4 | NA18963.hp1 NA18967.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.726-445G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006946 | |||||||
| chr8:125006968 | T | G | 3 | a0001c0001t0001g0106 a0001c0001t0002g0047 a0001c0001t0002g0155 |
4 | HG02602.hp1 NA18960.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.726-423T>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006968 | |||||||
| chr8:125006993 | G | A | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
233 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.726-398G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006993 | |||||||
| chr8:125006994 | T | C | 44 | a0001c0001t0001g0045 a0001c0001t0001g0108 a0001c0001t0001g0133 others(41): Show |
65 | HG00438.hp1 HG00609.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.726-397T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006994 | |||||||
| chr8:125006999 | T | A | 14 | a0001c0002t0003g0009 a0001c0002t0003g0016 a0001c0002t0003g0029 others(11): Show |
24 | HG00609.hp2 HG02027.hp2 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.726-392T>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125006999 | |||||||
| chr8:125007252 | TAAAA | T | 4 | a0001c0003t0001g0018 a0001c0003t0001g0057 a0001c0003t0001g0059 others(1): Show |
6 | HG02055.hp1 HG02559.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.726-136_726-133del others(4): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 125007252 | ||||||
| chr8:125007273 | G | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
170 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.726-118G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 3/10 | chr8 | 125007273 | |||||||
| chr8:125007684 | T | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
171 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.822+197T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 4/10 | chr8 | 125007684 | |||||||
| chr8:125008046 | G | C | 1 | a0006c0010t0001g0109 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.822+559G>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 4/10 | chr8 | 125008046 | |||||||
| chr8:125008101 | T | C | 1 | a0001c0001t0016g0116 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.822+614T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 4/10 | chr8 | 125008101 | |||||||
| chr8:125008153 | G | A | 1 | a0001c0001t0010g0191 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.822+666G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 4/10 | chr8 | 125008153 | |||||||
| chr8:125008166 | T | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | NA18963.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.822+679T>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 4/10 | chr8 | 125008166 | |||||||
| chr8:125008199 | C | G | 25 | a0001c0001t0001g0079 a0001c0001t0002g0161 a0001c0001t0004g0021 others(22): Show |
38 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.822+712C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 4/10 | chr8 | 125008199 | |||||||
| chr8:125008250 | C | T | 3 | a0001c0003t0008g0086 a0001c0003t0008g0087 a0001c0003t0008g0088 |
3 | HG02145.hp1 HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.823-721C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 4/10 | chr8 | 125008250 | |||||||
| chr8:125008251 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.823-720G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 4/10 | chr8 | 125008251 | |||||||
| chr8:125008390 | A | G | 19 | a0001c0001t0001g0079 a0001c0001t0004g0021 a0001c0001t0004g0030 others(16): Show |
28 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.823-581A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 4/10 | chr8 | 125008390 | |||||||
| chr8:125008413 | A | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
171 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.823-558A>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 4/10 | chr8 | 125008413 | |||||||
| chr8:125008446 | G | T | 16 | a0001c0002t0003g0009 a0001c0002t0003g0016 a0001c0002t0003g0029 others(13): Show |
26 | HG00609.hp2 HG02027.hp2 HG02071.hp2 others(23): Show |
intron_variant | MODIFIER | c.823-525G>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 4/10 | chr8 | 125008446 | |||||||
| chr8:125008922 | A | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
104 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.823-49A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 4/10 | chr8 | 125008922 | |||||||
| chr8:125009580 | G | A | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0185 |
3 | HG00544.hp1 NA18988.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1108+237G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/10 | chr8 | 125009580 | |||||||
| chr8:125009734 | A | G | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.1108+391A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/10 | chr8 | 125009734 | |||||||
| chr8:125010243 | G | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0094 others(2): Show |
9 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1108+900G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/10 | chr8 | 125010243 | |||||||
| chr8:125010456 | T | C | 7 | a0001c0001t0002g0161 a0001c0001t0005g0015 a0001c0001t0005g0028 others(4): Show |
11 | HG02615.hp1 HG02622.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1109-1081T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/10 | chr8 | 125010456 | |||||||
| chr8:125010473 | A | G | 3 | a0001c0001t0005g0015 a0001c0001t0005g0028 a0001c0001t0009g0062 |
7 | HG02622.hp2 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1109-1064A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/10 | chr8 | 125010473 | |||||||
| chr8:125010522 | A | T | 17 | a0001c0001t0004g0021 a0001c0001t0004g0030 a0001c0001t0004g0032 others(14): Show |
26 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1109-1015A>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/10 | chr8 | 125010522 | |||||||
| chr8:125010719 | C | G | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.1109-818C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/10 | chr8 | 125010719 | |||||||
| chr8:125010763 | G | A | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.1109-774G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/10 | chr8 | 125010763 | |||||||
| chr8:125010775 | C | CT | 17 | a0001c0002t0003g0009 a0001c0002t0003g0016 a0001c0002t0003g0029 others(14): Show |
27 | HG00609.hp2 HG02027.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1109-752dupT | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr8 | 125010775 | ||||||
| chr8:125010784 | T | C | 1 | a0001c0001t0007g0044 | 2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1109-753T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/10 | chr8 | 125010784 | |||||||
| chr8:125010882 | A | G | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.1109-655A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/10 | chr8 | 125010882 | |||||||
| chr8:125010923 | G | GCTT | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.1109-611_1109-609d others(5): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr8 | 125010923 | ||||||
| chr8:125010979 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1109-558A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/10 | chr8 | 125010979 | |||||||
| chr8:125010988 | GCACAGAA others(37): Show |
G | 1 | a0001c0005t0001g0134 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1109-548_1109-505d others(46): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/10 | chr8 | 125010988 | |||||||
| chr8:125011062 | G | T | 7 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0066 others(4): Show |
8 | HG02145.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1109-475G>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/10 | chr8 | 125011062 | |||||||
| chr8:125011094 | C | T | 1 | a0001c0001t0001g0037 | 2 | NA18983.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1109-443C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/10 | chr8 | 125011094 | |||||||
| chr8:125011112 | T | G | 1 | a0001c0001t0001g0091 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1109-425T>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/10 | chr8 | 125011112 | |||||||
| chr8:125011396 | C | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
174 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.1109-141C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 6/10 | chr8 | 125011396 | |||||||
| chr8:125011660 | A | G | 3 | a0001c0003t0008g0086 a0001c0003t0008g0087 a0001c0003t0008g0088 |
3 | HG02145.hp1 HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1204+28A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125011660 | |||||||
| chr8:125011792 | G | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
174 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.1204+160G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125011792 | |||||||
| chr8:125011810 | C | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
190 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.1204+178C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125011810 | |||||||
| chr8:125011861 | A | AGAGAAGG others(335): Show |
1 | a0001c0001t0001g0082 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1204+237_1204+238i others(344): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(321): Show |
1 | a0001c0001t0001g0168 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1204+237_1204+238i others(330): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(326): Show |
1 | a0001c0001t0001g0179 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1204+237_1204+238i others(335): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(329): Show |
15 | a0001c0001t0002g0026 a0001c0001t0002g0047 a0001c0001t0002g0053 others(12): Show |
18 | HG00733.hp1 HG01123.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.1204+237_1204+238i others(338): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(330): Show |
7 | a0001c0001t0002g0008 a0001c0001t0002g0054 a0001c0001t0002g0154 others(4): Show |
14 | HG00621.hp1 HG00673.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1204+237_1204+238i others(339): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(331): Show |
2 | a0001c0001t0013g0158 a0001c0001t0017g0065 |
2 | HG00438.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1204+237_1204+238i others(340): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(332): Show |
1 | a0001c0001t0001g0159 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1204+237_1204+238i others(341): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(333): Show |
2 | a0001c0001t0001g0048 a0001c0001t0001g0177 |
3 | NA18981.hp2 NA18988.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1204+237_1204+238i others(342): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(334): Show |
4 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0173 others(1): Show |
18 | HG00438.hp2 HG01168.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.1204+237_1204+238i others(343): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(335): Show |
7 | a0001c0001t0001g0004 a0001c0001t0001g0050 a0001c0001t0001g0175 others(4): Show |
19 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.1204+237_1204+238i others(344): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(336): Show |
6 | a0001c0001t0001g0005 a0001c0001t0001g0176 a0001c0001t0001g0178 others(3): Show |
14 | HG00558.hp1 HG01258.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.1204+237_1204+238i others(345): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(337): Show |
2 | a0001c0001t0001g0013 a0001c0001t0001g0183 |
6 | HG01943.hp2 HG01981.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1204+237_1204+238i others(346): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(338): Show |
1 | a0001c0001t0001g0051 | 2 | HG00673.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1204+237_1204+238i others(347): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(339): Show |
2 | a0001c0001t0001g0174 a0001c0001t0001g0184 |
2 | HG03710.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1204+237_1204+238i others(348): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(320): Show |
5 | a0001c0001t0002g0161 a0001c0001t0005g0015 a0001c0001t0005g0028 others(2): Show |
9 | HG02622.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1204+237_1204+238i others(329): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(320): Show |
1 | a0001c0001t0009g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1204+237_1204+238i others(329): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(321): Show |
6 | a0001c0001t0004g0021 a0001c0001t0004g0093 a0001c0001t0004g0102 others(3): Show |
14 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1204+237_1204+238i others(330): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(321): Show |
1 | a0001c0001t0007g0063 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1204+237_1204+238i others(330): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(322): Show |
9 | a0001c0001t0004g0032 a0001c0001t0004g0066 a0001c0001t0004g0068 others(6): Show |
9 | HG01346.hp1 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1204+237_1204+238i others(331): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011861 | A | AGAGAAGG others(323): Show |
3 | a0001c0001t0004g0030 a0001c0001t0004g0084 a0001c0001t0006g0197 |
4 | HG02145.hp2 HG02717.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1204+237_1204+238i others(332): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125011861 | ||||||
| chr8:125011901 | T | G | 23 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0079 others(20): Show |
33 | HG00609.hp2 HG02027.hp2 HG02071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1204+269T>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125011901 | |||||||
| chr8:125012072 | C | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
190 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.1204+440C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125012072 | |||||||
| chr8:125012137 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1204+505C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125012137 | |||||||
| chr8:125012156 | C | G | 25 | a0001c0001t0002g0161 a0001c0001t0004g0021 a0001c0001t0004g0030 others(22): Show |
38 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1204+524C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125012156 | |||||||
| chr8:125012157 | C | CTATGGCA others(37): Show |
1 | a0001c0005t0001g0134 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1204+527_1204+570d others(46): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125012157 | ||||||
| chr8:125012224 | A | G | 17 | a0001c0002t0003g0009 a0001c0002t0003g0016 a0001c0002t0003g0029 others(14): Show |
27 | HG00609.hp2 HG02027.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1204+592A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125012224 | |||||||
| chr8:125012268 | T | C | 1 | a0001c0001t0009g0060 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1204+636T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125012268 | |||||||
| chr8:125012599 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1204+967T>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125012599 | |||||||
| chr8:125012620 | T | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(52): Show |
105 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1204+988T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125012620 | |||||||
| chr8:125012935 | G | A | 3 | a0001c0003t0008g0086 a0001c0003t0008g0087 a0001c0003t0008g0088 |
3 | HG02145.hp1 HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1204+1303G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125012935 | |||||||
| chr8:125012940 | T | C | 25 | a0001c0001t0002g0161 a0001c0001t0004g0021 a0001c0001t0004g0030 others(22): Show |
38 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1204+1308T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125012940 | |||||||
| chr8:125012974 | C | G | 1 | a0001c0001t0001g0114 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1204+1342C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125012974 | |||||||
| chr8:125013074 | T | C | 3 | a0001c0001t0005g0015 a0001c0001t0005g0028 a0001c0001t0009g0062 |
7 | HG02622.hp2 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1204+1442T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125013074 | |||||||
| chr8:125013081 | T | A | 1 | a0001c0001t0001g0038 | 2 | HG00140.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1204+1449T>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125013081 | |||||||
| chr8:125013216 | C | A | 52 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(49): Show |
102 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1204+1584C>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125013216 | |||||||
| chr8:125013287 | T | C | 25 | a0001c0001t0002g0161 a0001c0001t0004g0021 a0001c0001t0004g0030 others(22): Show |
38 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1204+1655T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125013287 | |||||||
| chr8:125013319 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0148 |
4 | NA18963.hp1 NA18967.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1204+1687C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125013319 | |||||||
| chr8:125013345 | G | GTTTTCTT others(5): Show |
2 | a0001c0002t0003g0074 a0001c0002t0003g0075 |
2 | NA18946.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1204+1718_1204+172 others(16): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125013345 | ||||||
| chr8:125013356 | C | CTTTTTCT others(6): Show |
1 | a0001c0003t0001g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1204+1729_1204+173 others(17): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125013356 | ||||||
| chr8:125013356 | C | CTTTTTCT others(4): Show |
29 | a0001c0001t0001g0159 a0001c0001t0001g0177 a0001c0001t0001g0186 others(26): Show |
39 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.1204+1729_1204+173 others(15): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125013356 | ||||||
| chr8:125013356 | C | CTTTTTCT others(5): Show |
66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(63): Show |
129 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.1204+1729_1204+173 others(16): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125013356 | ||||||
| chr8:125013356 | C | CTTTTTCT others(6): Show |
11 | a0001c0001t0001g0190 a0001c0002t0015g0072 a0001c0003t0001g0014 others(8): Show |
17 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1204+1729_1204+173 others(17): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125013356 | ||||||
| chr8:125013356 | CT | C | 6 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0097 others(3): Show |
6 | HG02132.hp2 HG04199.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1204+1737delT | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125013356 | ||||||
| chr8:125013507 | C | T | 3 | a0001c0003t0008g0086 a0001c0003t0008g0087 a0001c0003t0008g0088 |
3 | HG02145.hp1 HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1204+1875C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125013507 | |||||||
| chr8:125013518 | A | G | 25 | a0001c0001t0002g0161 a0001c0001t0004g0021 a0001c0001t0004g0030 others(22): Show |
38 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1204+1886A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125013518 | |||||||
| chr8:125013564 | G | T | 32 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0079 others(29): Show |
45 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.1204+1932G>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125013564 | |||||||
| chr8:125013616 | G | A | 1 | a0001c0002t0003g0071 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1204+1984G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125013616 | |||||||
| chr8:125013634 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
190 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.1204+2002T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125013634 | |||||||
| chr8:125013651 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1204+2019C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125013651 | |||||||
| chr8:125013695 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1204+2063T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125013695 | |||||||
| chr8:125013716 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1204+2084C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125013716 | |||||||
| chr8:125013773 | G | A | 1 | a0001c0001t0005g0028 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1204+2141G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125013773 | |||||||
| chr8:125013818 | G | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
190 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.1204+2186G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125013818 | |||||||
| chr8:125014007 | A | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
171 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.1204+2375A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125014007 | |||||||
| chr8:125014051 | G | A | 1 | a0001c0003t0019g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1204+2419G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125014051 | |||||||
| chr8:125014074 | A | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
190 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.1204+2442A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125014074 | |||||||
| chr8:125014106 | CAAT | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(48): Show |
101 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1204+2475_1204+247 others(7): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125014106 | |||||||
| chr8:125014270 | C | G | 1 | a0001c0002t0003g0077 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1204+2638C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125014270 | |||||||
| chr8:125014460 | G | C | 17 | a0001c0002t0003g0009 a0001c0002t0003g0016 a0001c0002t0003g0029 others(14): Show |
27 | HG00609.hp2 HG02027.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1204+2828G>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125014460 | |||||||
| chr8:125014509 | GA | G | 3 | a0001c0003t0008g0086 a0001c0003t0008g0087 a0001c0003t0008g0088 |
3 | HG02145.hp1 HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1204+2878delA | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125014509 | |||||||
| chr8:125014566 | A | G | 1 | a0001c0003t0001g0027 | 2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1204+2934A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125014566 | |||||||
| chr8:125014762 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1204+3130G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125014762 | |||||||
| chr8:125014784 | G | T | 3 | a0001c0003t0008g0086 a0001c0003t0008g0087 a0001c0003t0008g0088 |
3 | HG02145.hp1 HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1204+3152G>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125014784 | |||||||
| chr8:125015086 | G | A | 1 | a0001c0009t0001g0144 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1205-2973G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125015086 | |||||||
| chr8:125015129 | G | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
174 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.1205-2930G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125015129 | |||||||
| chr8:125015278 | T | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
190 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.1205-2781T>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125015278 | |||||||
| chr8:125015356 | C | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
223 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.1205-2703C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125015356 | |||||||
| chr8:125015411 | G | A | 1 | a0001c0001t0001g0049 | 2 | NA18948.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1205-2648G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125015411 | |||||||
| chr8:125015582 | G | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
174 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.1205-2477G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125015582 | |||||||
| chr8:125015631 | A | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
190 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.1205-2428A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125015631 | |||||||
| chr8:125015652 | A | C | 1 | a0001c0001t0001g0182 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1205-2407A>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125015652 | |||||||
| chr8:125015706 | C | T | 17 | a0001c0002t0003g0009 a0001c0002t0003g0016 a0001c0002t0003g0029 others(14): Show |
27 | HG00609.hp2 HG02027.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1205-2353C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125015706 | |||||||
| chr8:125015901 | A | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
190 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.1205-2158A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125015901 | |||||||
| chr8:125015923 | CCT | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(48): Show |
101 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1205-2130_1205-212 others(6): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125015923 | ||||||
| chr8:125015976 | GCT | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
190 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.1205-2081_1205-208 others(6): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125015976 | ||||||
| chr8:125016098 | A | G | 17 | a0001c0002t0003g0009 a0001c0002t0003g0016 a0001c0002t0003g0029 others(14): Show |
27 | HG00609.hp2 HG02027.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1205-1961A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125016098 | |||||||
| chr8:125016121 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
190 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.1205-1938T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125016121 | |||||||
| chr8:125016208 | T | TTCTC | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
190 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.1205-1848_1205-184 others(8): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 125016208 | ||||||
| chr8:125016311 | C | A | 3 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0080 |
6 | HG00609.hp2 NA18949.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.1205-1748C>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125016311 | |||||||
| chr8:125016356 | C | G | 1 | a0001c0001t0001g0180 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1205-1703C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125016356 | |||||||
| chr8:125016512 | G | A | 7 | a0001c0001t0004g0030 a0001c0001t0004g0032 a0001c0001t0004g0066 others(4): Show |
8 | HG02145.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1205-1547G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125016512 | |||||||
| chr8:125016660 | C | G | 52 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(49): Show |
102 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1205-1399C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125016660 | |||||||
| chr8:125016743 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
190 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.1205-1316T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125016743 | |||||||
| chr8:125017087 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1205-972G>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125017087 | |||||||
| chr8:125017183 | T | A | 1 | a0001c0001t0007g0100 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1205-876T>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125017183 | |||||||
| chr8:125017587 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1205-472C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 7/10 | chr8 | 125017587 | |||||||
| chr8:125018223 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1347+22A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 8/10 | chr8 | 125018223 | |||||||
| chr8:125018341 | A | C | 3 | a0001c0003t0008g0086 a0001c0003t0008g0087 a0001c0003t0008g0088 |
3 | HG02145.hp1 HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1347+140A>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 8/10 | chr8 | 125018341 | |||||||
| chr8:125018478 | G | T | 17 | a0001c0002t0003g0009 a0001c0002t0003g0016 a0001c0002t0003g0029 others(14): Show |
27 | HG00609.hp2 HG02027.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1348-153G>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 8/10 | chr8 | 125018478 | |||||||
| chr8:125018482 | T | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(52): Show |
105 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1348-149T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 8/10 | chr8 | 125018482 | |||||||
| chr8:125018567 | T | C | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
212 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.1348-64T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 8/10 | chr8 | 125018567 | |||||||
| chr8:125018617 | T | C | 1 | a0001c0001t0017g0065 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1348-14T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 8/10 | chr8 | 125018617 | |||||||
| chr8:125018826 | T | C | 7 | a0001c0001t0002g0161 a0001c0001t0005g0015 a0001c0001t0005g0028 others(4): Show |
11 | HG02615.hp1 HG02622.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1444+99T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125018826 | |||||||
| chr8:125018893 | T | G | 1 | a0001c0001t0001g0039 | 2 | NA18965.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1444+166T>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125018893 | |||||||
| chr8:125019045 | T | A | 3 | a0001c0003t0008g0086 a0001c0003t0008g0087 a0001c0003t0008g0088 |
3 | HG02145.hp1 HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1444+318T>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125019045 | |||||||
| chr8:125019107 | G | C | 1 | a0001c0001t0017g0065 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1444+380G>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125019107 | |||||||
| chr8:125019212 | A | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
223 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.1444+485A>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125019212 | |||||||
| chr8:125019229 | C | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
223 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.1444+502C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125019229 | |||||||
| chr8:125019276 | AAGCAGTG others(204): Show |
A | 1 | a0001c0001t0001g0151 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1444+553_1444+763d others(2): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr8 | 125019276 | ||||||
| chr8:125019404 | G | C | 32 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0022 others(29): Show |
49 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.1444+677G>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125019404 | |||||||
| chr8:125019480 | G | GACT | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
212 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.1444+755_1444+757d others(5): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr8 | 125019480 | ||||||
| chr8:125019496 | A | G | 1 | a0001c0002t0003g0085 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1444+769A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125019496 | |||||||
| chr8:125019497 | C | T | 1 | a0001c0002t0003g0085 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1444+770C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125019497 | |||||||
| chr8:125019512 | A | G | 25 | a0001c0001t0001g0159 a0001c0001t0001g0168 a0001c0001t0002g0008 others(22): Show |
35 | HG00438.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1444+785A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125019512 | |||||||
| chr8:125019658 | T | C | 1 | a0003c0013t0001g0118 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1444+931T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125019658 | |||||||
| chr8:125019863 | AAAAAC | A | 13 | a0001c0003t0001g0014 a0001c0003t0001g0018 a0001c0003t0001g0027 others(10): Show |
19 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1445-911_1445-907d others(7): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr8 | 125019863 | ||||||
| chr8:125019867 | AC | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(40): Show |
91 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1445-916delC | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125019867 | |||||||
| chr8:125019868 | C | A | 49 | a0001c0001t0001g0013 a0001c0001t0001g0067 a0001c0001t0001g0070 others(46): Show |
68 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1445-916C>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125019868 | |||||||
| chr8:125019873 | C | A | 2 | a0001c0001t0017g0065 a0001c0002t0003g0085 |
2 | HG02055.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1445-911C>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125019873 | |||||||
| chr8:125020013 | T | G | 2 | a0001c0001t0001g0036 a0001c0014t0001g0036 |
2 | HG02027.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1445-771T>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125020013 | |||||||
| chr8:125020258 | A | T | 18 | a0001c0001t0004g0021 a0001c0001t0004g0030 a0001c0001t0004g0032 others(15): Show |
27 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1445-526A>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125020258 | |||||||
| chr8:125020320 | C | G | 1 | a0001c0001t0005g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1445-464C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125020320 | |||||||
| chr8:125020398 | T | C | 1 | a0001c0001t0017g0065 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1445-386T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125020398 | |||||||
| chr8:125020440 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
179 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.1445-344G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125020440 | |||||||
| chr8:125020511 | C | G | 1 | a0001c0001t0001g0111 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1445-273C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125020511 | |||||||
| chr8:125020567 | A | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(52): Show |
105 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1445-217A>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125020567 | |||||||
| chr8:125020695 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1445-89C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 9/10 | chr8 | 125020695 | |||||||
| chr8:125020909 | A | G | 1 | a0001c0001t0017g0065 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1532+38A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/10 | chr8 | 125020909 | |||||||
| chr8:125020940 | C | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0119 a0001c0001t0001g0127 |
3 | HG02083.hp2 NA18947.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1532+69C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/10 | chr8 | 125020940 | |||||||
| chr8:125020949 | T | C | 1 | a0001c0001t0001g0034 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1532+78T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/10 | chr8 | 125020949 | |||||||
| chr8:125020953 | T | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(52): Show |
105 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1532+82T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/10 | chr8 | 125020953 | |||||||
| chr8:125021008 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1532+137C>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/10 | chr8 | 125021008 | |||||||
| chr8:125021070 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1532+199G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/10 | chr8 | 125021070 | |||||||
| chr8:125021208 | G | A | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
223 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.1532+337G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/10 | chr8 | 125021208 | |||||||
| chr8:125021241 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1532+370G>A | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/10 | chr8 | 125021241 | |||||||
| chr8:125021364 | A | G | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(123): Show |
212 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.1533-389A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/10 | chr8 | 125021364 | |||||||
| chr8:125021401 | A | G | 2 | a0001c0001t0002g0154 a0001c0001t0002g0156 |
2 | HG01928.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1533-352A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/10 | chr8 | 125021401 | |||||||
| chr8:125021416 | C | T | 1 | a0001c0001t0004g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1533-337C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/10 | chr8 | 125021416 | |||||||
| chr8:125021419 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1533-334G>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/10 | chr8 | 125021419 | |||||||
| chr8:125021439 | C | CA | 7 | a0001c0001t0002g0161 a0001c0001t0005g0015 a0001c0001t0005g0028 others(4): Show |
11 | HG02615.hp1 HG02622.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1533-311dupA | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 125021439 | ||||||
| chr8:125021464 | T | C | 7 | a0001c0001t0002g0161 a0001c0001t0005g0015 a0001c0001t0005g0028 others(4): Show |
11 | HG02615.hp1 HG02622.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1533-289T>C | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/10 | chr8 | 125021464 | |||||||
| chr8:125021541 | A | AAG | 22 | a0001c0001t0001g0050 a0001c0001t0001g0181 a0001c0001t0017g0065 others(19): Show |
33 | HG00609.hp2 HG01243.hp1 HG02027.hp2 others(30): Show |
intron_variant | MODIFIER | c.1533-212_1533-211i others(4): Show |
SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/10 | chr8 | 125021541 | |||||||
| chr8:125021541 | A | AG | 60 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(57): Show |
115 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.1533-206dupG | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 125021541 | ||||||
| chr8:125021541 | A | G | 51 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0022 others(48): Show |
75 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.1533-212A>G | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/10 | chr8 | 125021541 | |||||||
| chr8:125021696 | C | T | 4 | a0001c0001t0001g0064 a0001c0001t0001g0090 a0001c0001t0001g0096 others(1): Show |
4 | HG01099.hp1 HG02630.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1533-57C>T | SQLE | ENSG00000104549.12 | transcript | ENST00000265896.10 | protein_coding | 10/10 | chr8 | 125021696 |