Item | Value |
---|---|
geneid | 23513 |
ensemblid | ENSG00000180900.20 |
hgncid | 30377 |
symbol | SCRIB |
name | scribble planar cell polarity protein |
refseq_nuc | NM_182706.5 |
refseq_prot | NP_874365.3 |
ensembl_nuc | ENST00000356994.7 |
ensembl_prot | ENSP00000349486.2 |
mane_status | MANE Select |
chr | chr8 |
start | 143790925 |
end | 143815773 |
strand | - |
ver | v1.2 |
region | chr8:143790925-143815773 |
region5000 | chr8:143785925-143820773 |
regionname0 | SCRIB_chr8_143790925_143815773 |
regionname5000 | SCRIB_chr8_143785925_143820773 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1655 | 164 | 41 | 36 | 48 | 11 | 28 | 34 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0002 | 0/0 | 1655 | 135 | 30 | 20 | 73 | 6 | 6 | 53 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0003 | 0/0 | 1655 | 27 | 10 | 1 | 12 | 0 | 4 | 7 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0004 | 0/1 | 1655 | 8 | 0 | 1 | 4 | 0 | 2 | 4 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0005 | 0/0 | 1463 | 6 | 1 | 4 | 0 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1458): Show |
chr8 | 143785925 | 143820773 |
a0006 | 0/0 | 1655 | 5 | 0 | 4 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0007 | 0/0 | 1655 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0008 | 0/0 | 1463 | 3 | 0 | 1 | 1 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1458): Show |
chr8 | 143785925 | 143820773 |
a0009 | 0/0 | 1655 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0010 | 0/0 | 1655 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0011 | 0/0 | 1655 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0012 | 0/0 | 1655 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0013 | 0/0 | 1655 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0014 | 0/0 | 1655 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0015 | 0/0 | 1655 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0016 | 0/0 | 1655 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0017 | 0/0 | 1655 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0018 | 0/0 | 1463 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1458): Show |
chr8 | 143785925 | 143820773 |
a0019 | 0/0 | 1655 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0020 | 0/0 | 1655 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0021 | 0/0 | 1655 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0022 | 0/0 | 1655 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0023 | 0/0 | 1655 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0024 | 0/0 | 1655 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0025 | 0/0 | 1655 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0026 | 0/0 | 1655 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0027 | 0/0 | 1655 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0028 | 0/0 | 1655 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0029 | 0/0 | 1655 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0030 | 0/0 | 1655 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0031 | 0/0 | 1655 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0032 | 0/0 | 1655 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0033 | 0/0 | 1655 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0034 | 0/0 | 1655 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0035 | 0/0 | 1655 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
a0036 | 0/0 | 1655 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | MLKCI others(1650): Show |
chr8 | 143785925 | 143820773 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4965 | 112 | 8 | 29 | 42 | 9 | 24 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0004 | 0/0 | 4965 | 15 | 15 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0009 | 0/0 | 4965 | 5 | 1 | 4 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0011 | 0/0 | 4965 | 5 | 5 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0013 | 0/0 | 4965 | 4 | 4 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0016 | 0/0 | 4965 | 3 | 0 | 1 | 0 | 2 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0018 | 0/0 | 4965 | 3 | 0 | 0 | 3 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0026 | 0/0 | 4965 | 2 | 2 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0027 | 0/0 | 4965 | 2 | 0 | 0 | 2 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0028 | 0/0 | 4965 | 2 | 2 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0029 | 0/0 | 4965 | 2 | 2 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0031 | 0/0 | 4965 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0050 | 0/0 | 4965 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0059 | 0/0 | 4965 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0062 | 0/0 | 4965 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0064 | 0/0 | 4965 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0066 | 0/0 | 4965 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0068 | 0/0 | 4965 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0070 | 0/0 | 4965 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0001c0071 | 0/0 | 4965 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0002c0002 | 0/0 | 4965 | 105 | 10 | 15 | 69 | 5 | 6 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0002c0006 | 0/0 | 4965 | 9 | 9 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0002c0008 | 0/0 | 4965 | 5 | 4 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0002c0012 | 0/0 | 4965 | 4 | 4 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0002c0020 | 0/0 | 4965 | 2 | 0 | 1 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0002c0021 | 0/0 | 4965 | 2 | 1 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0002c0022 | 0/0 | 4965 | 2 | 0 | 0 | 2 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0002c0030 | 0/0 | 4965 | 2 | 0 | 2 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0002c0033 | 0/0 | 4965 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0002c0036 | 0/0 | 4965 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0002c0042 | 0/0 | 4965 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0002c0043 | 0/0 | 4965 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0003c0003 | 0/0 | 4965 | 16 | 10 | 1 | 4 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0003c0005 | 0/0 | 4965 | 10 | 0 | 0 | 8 | 0 | 2 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0003c0038 | 0/0 | 4965 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0004c0007 | 0/1 | 4965 | 7 | 0 | 1 | 3 | 0 | 2 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0004c0040 | 0/0 | 4965 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0005c0046 | 0/0 | 4966 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4961): Show |
chr8 | 143785925 | 143820773 | ||
a0005c0051 | 0/0 | 4966 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4961): Show |
chr8 | 143785925 | 143820773 | ||
a0005c0052 | 0/0 | 4966 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4961): Show |
chr8 | 143785925 | 143820773 | ||
a0005c0060 | 0/0 | 4966 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4961): Show |
chr8 | 143785925 | 143820773 | ||
a0005c0061 | 0/0 | 4966 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4961): Show |
chr8 | 143785925 | 143820773 | ||
a0005c0073 | 0/0 | 4966 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4961): Show |
chr8 | 143785925 | 143820773 | ||
a0006c0010 | 0/0 | 4965 | 5 | 0 | 4 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0007c0014 | 0/0 | 4965 | 4 | 0 | 0 | 4 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0008c0015 | 0/0 | 4966 | 3 | 0 | 1 | 1 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4961): Show |
chr8 | 143785925 | 143820773 | ||
a0009c0019 | 0/0 | 4965 | 3 | 0 | 0 | 3 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0010c0017 | 0/0 | 4965 | 3 | 0 | 0 | 3 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0011c0023 | 0/0 | 4965 | 2 | 0 | 2 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0012c0025 | 0/0 | 4965 | 2 | 1 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0013c0024 | 0/0 | 4965 | 2 | 0 | 0 | 2 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0014c0057 | 0/0 | 4965 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0015c0072 | 0/0 | 4965 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0016c0035 | 0/0 | 4965 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0017c0055 | 0/0 | 4965 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0018c0037 | 0/0 | 4966 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4961): Show |
chr8 | 143785925 | 143820773 | ||
a0019c0039 | 0/0 | 4965 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0020c0067 | 0/0 | 4965 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0021c0058 | 0/0 | 4965 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0022c0044 | 0/0 | 4965 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0023c0056 | 0/0 | 4965 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0024c0048 | 0/0 | 4965 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0025c0032 | 0/0 | 4965 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0026c0047 | 0/0 | 4965 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0027c0049 | 0/0 | 4965 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0028c0041 | 0/0 | 4965 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0029c0034 | 0/0 | 4965 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0030c0069 | 0/0 | 4965 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0031c0063 | 0/0 | 4965 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0032c0045 | 0/0 | 4965 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0033c0065 | 0/0 | 4965 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0034c0074 | 0/0 | 4965 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0035c0054 | 0/0 | 4965 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 | ||
a0036c0053 | 0/0 | 4965 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | ATGCT others(4960): Show |
chr8 | 143785925 | 143820773 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5607 | 109 | 6 | 29 | 41 | 9 | 24 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0001c0001t0002 | 0/0 | 5622 | 2 | 2 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5617): Show |
chr8 | 143785925 | 143820773 |
a0001c0001t0004 | 0/0 | 5617 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5612): Show |
chr8 | 143785925 | 143820773 |
a0001c0004t0001 | 0/0 | 5607 | 15 | 15 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0001c0009t0001 | 0/0 | 5607 | 5 | 1 | 4 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0001c0011t0001 | 0/0 | 5607 | 5 | 5 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0001c0013t0001 | 0/0 | 5607 | 4 | 4 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0001c0016t0001 | 0/0 | 5607 | 3 | 0 | 1 | 0 | 2 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0001c0018t0001 | 0/0 | 5607 | 3 | 0 | 0 | 3 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0001c0026t0002 | 0/0 | 5622 | 2 | 2 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5617): Show |
chr8 | 143785925 | 143820773 |
a0001c0027t0001 | 0/0 | 5607 | 2 | 0 | 0 | 2 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0001c0028t0001 | 0/0 | 5607 | 2 | 2 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0001c0029t0001 | 0/0 | 5607 | 2 | 2 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0001c0031t0001 | 0/0 | 5607 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0001c0050t0001 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0001c0059t0001 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0001c0062t0001 | 0/0 | 5607 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0001c0064t0001 | 0/0 | 5607 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0001c0066t0001 | 0/0 | 5607 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0001c0068t0001 | 0/0 | 5607 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0001c0070t0001 | 0/0 | 5607 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0001c0071t0001 | 0/0 | 5607 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0002c0002t0001 | 0/0 | 5607 | 103 | 10 | 15 | 67 | 5 | 6 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0002c0002t0003 | 0/0 | 5607 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0002c0002t0005 | 0/0 | 5607 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0002c0006t0001 | 0/0 | 5607 | 9 | 9 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0002c0008t0001 | 0/0 | 5607 | 5 | 4 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0002c0012t0001 | 0/0 | 5607 | 4 | 4 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0002c0020t0001 | 0/0 | 5607 | 2 | 0 | 1 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0002c0021t0001 | 0/0 | 5607 | 2 | 1 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0002c0022t0001 | 0/0 | 5607 | 2 | 0 | 0 | 2 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0002c0030t0001 | 0/0 | 5607 | 2 | 0 | 2 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0002c0033t0001 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0002c0036t0001 | 0/0 | 5607 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0002c0042t0001 | 0/0 | 5607 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0002c0043t0001 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0003c0003t0001 | 0/0 | 5607 | 15 | 10 | 0 | 4 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0003c0003t0006 | 0/0 | 5607 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0003c0005t0001 | 0/0 | 5607 | 10 | 0 | 0 | 8 | 0 | 2 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0003c0038t0001 | 0/0 | 5607 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0004c0007t0001 | 0/1 | 5607 | 7 | 0 | 1 | 3 | 0 | 2 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0004c0040t0001 | 0/0 | 5607 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0005c0046t0001 | 0/0 | 5608 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5603): Show |
chr8 | 143785925 | 143820773 |
a0005c0051t0001 | 0/0 | 5608 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5603): Show |
chr8 | 143785925 | 143820773 |
a0005c0052t0001 | 0/0 | 5608 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5603): Show |
chr8 | 143785925 | 143820773 |
a0005c0060t0001 | 0/0 | 5608 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5603): Show |
chr8 | 143785925 | 143820773 |
a0005c0061t0001 | 0/0 | 5608 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5603): Show |
chr8 | 143785925 | 143820773 |
a0005c0073t0001 | 0/0 | 5608 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5603): Show |
chr8 | 143785925 | 143820773 |
a0006c0010t0001 | 0/0 | 5607 | 5 | 0 | 4 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0007c0014t0001 | 0/0 | 5607 | 4 | 0 | 0 | 4 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0008c0015t0001 | 0/0 | 5608 | 3 | 0 | 1 | 1 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5603): Show |
chr8 | 143785925 | 143820773 |
a0009c0019t0001 | 0/0 | 5607 | 3 | 0 | 0 | 3 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0010c0017t0001 | 0/0 | 5607 | 3 | 0 | 0 | 3 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0011c0023t0001 | 0/0 | 5607 | 2 | 0 | 2 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0012c0025t0001 | 0/0 | 5607 | 2 | 1 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0013c0024t0001 | 0/0 | 5607 | 2 | 0 | 0 | 2 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0014c0057t0001 | 0/0 | 5607 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0015c0072t0001 | 0/0 | 5607 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0016c0035t0001 | 0/0 | 5607 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0017c0055t0001 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0018c0037t0001 | 0/0 | 5608 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5603): Show |
chr8 | 143785925 | 143820773 |
a0019c0039t0001 | 0/0 | 5607 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0020c0067t0001 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0021c0058t0001 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0022c0044t0001 | 0/0 | 5607 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0023c0056t0001 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0024c0048t0001 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0025c0032t0001 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0026c0047t0001 | 0/0 | 5607 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0027c0049t0001 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0028c0041t0001 | 0/0 | 5607 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0029c0034t0001 | 0/0 | 5607 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0030c0069t0001 | 0/0 | 5607 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0031c0063t0001 | 0/0 | 5607 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0032c0045t0001 | 0/0 | 5607 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0033c0065t0001 | 0/0 | 5607 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0034c0074t0001 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0035c0054t0001 | 0/0 | 5607 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
a0036c0053t0007 | 0/0 | 5607 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | GGACT others(5602): Show |
chr8 | 143785925 | 143820773 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 11 | 0 | 0 | 8 | 0 | 3 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0003 | 0/0 | 9 | 0 | 5 | 0 | 0 | 4 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0013 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0004t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0004t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0004t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0004t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0004t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0004t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0004t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0009t0001g0031 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0009t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0009t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0011t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0011t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0011t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0013t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0013t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0016t0001g0032 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0018t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0026t0002g0063 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0027t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0028t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0028t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0029t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0029t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0031t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0050t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0059t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0062t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0064t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0066t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0068t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0070t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0001c0071t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0001 | 0/0 | 13 | 0 | 1 | 12 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0005 | 0/0 | 6 | 4 | 1 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0006 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0049 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0056 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0060 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0002t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0006t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0006t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0006t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0006t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0006t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0006t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0008t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0008t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0008t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0008t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0012t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0012t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0020t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0020t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0021t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0021t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0022t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0022t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0030t0001g0062 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0033t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0036t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0042t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0002c0043t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0003c0003t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0003c0003t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0003c0003t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0003c0003t0001g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0003c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0003c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0003c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0003c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0003c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0003c0003t0006g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0003c0005t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0003c0005t0001g0029 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0003c0005t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0003c0005t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0003c0038t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0004c0007t0001g0034 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0004c0007t0001g0216 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0004c0007t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0004c0007t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0004c0007t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0004c0040t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0005c0046t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0005c0051t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0005c0052t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0005c0060t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0005c0061t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0005c0073t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0006c0010t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0006c0010t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0007c0014t0001g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0007c0014t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0008c0015t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0008c0015t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0008c0015t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0009c0019t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0009c0019t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0009c0019t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0010c0017t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0011c0023t0001g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0012c0025t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0012c0025t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0013c0024t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0014c0057t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0015c0072t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0016c0035t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0017c0055t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0018c0037t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0019c0039t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0020c0067t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0021c0058t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0022c0044t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0023c0056t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0024c0048t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0025c0032t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0026c0047t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0027c0049t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0028c0041t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0029c0034t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0030c0069t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0031c0063t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0032c0045t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0033c0065t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0034c0074t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0035c0054t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
a0036c0053t0007g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | GBR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | GBR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0168 | EUR | GBR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0171 | EUR | GBR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00280 | hp1 | a0002 | c0020 | t0001 | g0166 | EUR | FIN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0049 | EUR | FIN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00323 | hp1 | a0006 | c0010 | t0001 | g0017 | EUR | FIN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | FIN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00408 | hp2 | a0002 | c0022 | t0001 | g0169 | EAS | CHS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | CHS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00423 | hp2 | a0002 | c0022 | t0001 | g0170 | EAS | CHS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | CHS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00544 | hp1 | a0003 | c0005 | t0001 | g0011 | EAS | CHS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00544 | hp2 | a0008 | c0015 | t0001 | g0182 | EAS | CHS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | CHS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | CHS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00609 | hp2 | a0014 | c0057 | t0001 | g0143 | EAS | CHS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | CHS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0229 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0049 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00642 | hp2 | a0002 | c0020 | t0001 | g0165 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00673 | hp1 | a0002 | c0036 | t0001 | g0172 | EAS | CHS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | CHS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00733 | hp2 | a0015 | c0072 | t0001 | g0219 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG00741 | hp2 | a0002 | c0030 | t0001 | g0062 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01070 | hp2 | a0002 | c0030 | t0001 | g0062 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01074 | hp1 | a0006 | c0010 | t0001 | g0017 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01081 | hp1 | a0011 | c0023 | t0001 | g0053 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01099 | hp1 | a0005 | c0073 | t0001 | g0222 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01106 | hp1 | a0004 | c0007 | t0001 | g0217 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01106 | hp2 | a0006 | c0010 | t0001 | g0017 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01109 | hp1 | a0002 | c0021 | t0001 | g0071 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01109 | hp2 | a0005 | c0051 | t0001 | g0082 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01175 | hp1 | a0001 | c0068 | t0001 | g0065 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01175 | hp2 | a0002 | c0008 | t0001 | g0035 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01192 | hp1 | a0005 | c0052 | t0001 | g0134 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01243 | hp1 | a0008 | c0015 | t0001 | g0189 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0180 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01255 | hp2 | a0006 | c0010 | t0001 | g0039 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0060 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01257 | hp2 | a0001 | c0066 | t0001 | g0157 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01258 | hp1 | a0006 | c0010 | t0001 | g0039 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0060 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01261 | hp2 | a0016 | c0035 | t0001 | g0085 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01358 | hp1 | a0001 | c0009 | t0001 | g0031 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01361 | hp1 | a0001 | c0016 | t0001 | g0032 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0211 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01496 | hp2 | a0012 | c0025 | t0001 | g0098 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | IBS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0224 | EUR | IBS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01516 | hp2 | a0001 | c0016 | t0001 | g0032 | EUR | IBS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | IBS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01517 | hp2 | a0001 | c0016 | t0001 | g0032 | EUR | IBS | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01884 | hp1 | a0017 | c0055 | t0001 | g0137 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01884 | hp2 | a0003 | c0003 | t0001 | g0027 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01891 | hp2 | a0001 | c0011 | t0001 | g0147 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0056 | AMR | PEL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01975 | hp2 | a0003 | c0003 | t0006 | g0238 | AMR | PEL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01978 | hp2 | a0005 | c0046 | t0001 | g0204 | AMR | PEL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01981 | hp2 | a0001 | c0009 | t0001 | g0205 | AMR | PEL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01993 | hp1 | a0001 | c0009 | t0001 | g0203 | AMR | PEL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | KHV | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02027 | hp1 | a0002 | c0002 | t0003 | g0187 | EAS | KHV | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02027 | hp2 | a0003 | c0005 | t0001 | g0011 | EAS | KHV | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | KHV | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02055 | hp2 | a0018 | c0037 | t0001 | g0173 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02071 | hp1 | a0003 | c0003 | t0001 | g0028 | EAS | KHV | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02074 | hp2 | a0019 | c0039 | t0001 | g0178 | EAS | KHV | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02080 | hp1 | a0003 | c0003 | t0001 | g0028 | EAS | KHV | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02129 | hp2 | a0001 | c0018 | t0001 | g0024 | EAS | KHV | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02145 | hp1 | a0003 | c0003 | t0001 | g0201 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02145 | hp2 | a0002 | c0012 | t0001 | g0016 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | CDX | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CDX | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0086 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02258 | hp1 | a0002 | c0043 | t0001 | g0093 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02258 | hp2 | a0020 | c0067 | t0001 | g0081 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02280 | hp2 | a0001 | c0004 | t0001 | g0139 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02300 | hp1 | a0001 | c0009 | t0001 | g0031 | AMR | PEL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02523 | hp2 | a0001 | c0031 | t0001 | g0078 | EAS | KHV | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02572 | hp1 | a0003 | c0003 | t0001 | g0057 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02572 | hp2 | a0021 | c0058 | t0001 | g0144 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02622 | hp1 | a0001 | c0004 | t0001 | g0020 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02622 | hp2 | a0002 | c0012 | t0001 | g0094 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02630 | hp1 | a0002 | c0006 | t0001 | g0163 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0067 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02647 | hp2 | a0001 | c0011 | t0001 | g0015 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02683 | hp2 | a0022 | c0044 | t0001 | g0194 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02717 | hp2 | a0023 | c0056 | t0001 | g0077 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02723 | hp1 | a0002 | c0006 | t0001 | g0047 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0197 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0092 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02809 | hp2 | a0024 | c0048 | t0001 | g0121 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02818 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02818 | hp2 | a0003 | c0003 | t0001 | g0048 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02886 | hp1 | a0001 | c0013 | t0001 | g0025 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02886 | hp2 | a0001 | c0011 | t0001 | g0015 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02895 | hp1 | a0001 | c0026 | t0002 | g0063 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02895 | hp2 | a0003 | c0003 | t0001 | g0048 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02922 | hp1 | a0001 | c0004 | t0001 | g0020 | AFR | ESN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02965 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | ESN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02965 | hp2 | a0001 | c0013 | t0001 | g0025 | AFR | ESN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02970 | hp1 | a0001 | c0013 | t0001 | g0025 | AFR | ESN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02970 | hp2 | a0002 | c0006 | t0001 | g0068 | AFR | ESN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02976 | hp2 | a0002 | c0008 | t0001 | g0231 | AFR | ESN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0056 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03041 | hp1 | a0001 | c0026 | t0002 | g0063 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03041 | hp2 | a0003 | c0003 | t0001 | g0027 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03098 | hp1 | a0001 | c0011 | t0001 | g0148 | AFR | MSL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03098 | hp2 | a0001 | c0004 | t0001 | g0104 | AFR | MSL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03130 | hp2 | a0002 | c0006 | t0001 | g0047 | AFR | ESN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03139 | hp1 | a0003 | c0003 | t0001 | g0195 | AFR | ESN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | ESN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03195 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | ESN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03195 | hp2 | a0002 | c0006 | t0001 | g0026 | AFR | ESN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03209 | hp1 | a0001 | c0004 | t0001 | g0099 | AFR | MSL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03209 | hp2 | a0001 | c0050 | t0001 | g0123 | AFR | MSL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03225 | hp1 | a0001 | c0028 | t0001 | g0136 | AFR | MSL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03225 | hp2 | a0001 | c0004 | t0001 | g0223 | AFR | MSL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03453 | hp1 | a0001 | c0011 | t0001 | g0015 | AFR | MSL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03453 | hp2 | a0001 | c0004 | t0001 | g0044 | AFR | MSL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03486 | hp1 | a0002 | c0008 | t0001 | g0035 | AFR | MSL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03486 | hp2 | a0001 | c0004 | t0001 | g0010 | AFR | MSL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0038 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0038 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03516 | hp1 | a0002 | c0006 | t0001 | g0164 | AFR | ESN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03516 | hp2 | a0005 | c0060 | t0001 | g0146 | AFR | ESN | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03540 | hp1 | a0002 | c0006 | t0001 | g0228 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03540 | hp2 | a0002 | c0006 | t0001 | g0026 | AFR | GWD | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03579 | hp1 | a0002 | c0008 | t0001 | g0073 | AFR | MSL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03579 | hp2 | a0001 | c0004 | t0001 | g0044 | AFR | MSL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0207 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03669 | hp1 | a0003 | c0038 | t0001 | g0174 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03704 | hp1 | a0003 | c0005 | t0001 | g0029 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03831 | hp1 | a0005 | c0061 | t0001 | g0149 | SAS | BEB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03834 | hp1 | a0004 | c0007 | t0001 | g0218 | SAS | BEB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03834 | hp2 | a0001 | c0062 | t0001 | g0150 | SAS | BEB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03927 | hp1 | a0008 | c0015 | t0001 | g0185 | SAS | BEB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03927 | hp2 | a0026 | c0047 | t0001 | g0100 | SAS | BEB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0181 | SAS | BEB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG04184 | hp2 | a0004 | c0007 | t0001 | g0220 | SAS | BEB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG04199 | hp1 | a0003 | c0003 | t0001 | g0225 | SAS | STU | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG04204 | hp1 | a0003 | c0005 | t0001 | g0210 | SAS | STU | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG04204 | hp2 | a0001 | c0070 | t0001 | g0214 | SAS | STU | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG04228 | hp1 | a0001 | c0071 | t0001 | g0215 | SAS | STU | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18522 | hp1 | a0002 | c0021 | t0001 | g0069 | AFR | YRI | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18522 | hp2 | a0001 | c0059 | t0001 | g0145 | AFR | YRI | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18612 | hp1 | a0003 | c0005 | t0001 | g0029 | EAS | CHB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | CHB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18906 | hp1 | a0001 | c0029 | t0001 | g0140 | AFR | YRI | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18906 | hp2 | a0002 | c0006 | t0001 | g0026 | AFR | YRI | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18939 | hp2 | a0003 | c0005 | t0001 | g0011 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18943 | hp2 | a0003 | c0003 | t0001 | g0028 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18944 | hp1 | a0001 | c0018 | t0001 | g0024 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18947 | hp1 | a0003 | c0005 | t0001 | g0011 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18947 | hp2 | a0009 | c0019 | t0001 | g0162 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18951 | hp2 | a0013 | c0024 | t0001 | g0058 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18954 | hp1 | a0028 | c0041 | t0001 | g0190 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18959 | hp1 | a0029 | c0034 | t0001 | g0208 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18964 | hp2 | a0009 | c0019 | t0001 | g0153 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18965 | hp1 | a0030 | c0069 | t0001 | g0079 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18965 | hp2 | a0007 | c0014 | t0001 | g0064 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18967 | hp2 | a0010 | c0017 | t0001 | g0019 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18972 | hp1 | a0004 | c0007 | t0001 | g0034 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18972 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18974 | hp1 | a0004 | c0007 | t0001 | g0034 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18974 | hp2 | a0003 | c0005 | t0001 | g0029 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18979 | hp1 | a0007 | c0014 | t0001 | g0033 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18981 | hp2 | a0031 | c0063 | t0001 | g0151 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18984 | hp1 | a0001 | c0027 | t0001 | g0041 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18984 | hp2 | a0001 | c0018 | t0001 | g0024 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18985 | hp2 | a0010 | c0017 | t0001 | g0019 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18990 | hp1 | a0002 | c0042 | t0001 | g0212 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18994 | hp1 | a0004 | c0040 | t0001 | g0199 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18995 | hp1 | a0003 | c0005 | t0001 | g0011 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19000 | hp2 | a0003 | c0005 | t0001 | g0177 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19002 | hp2 | a0032 | c0045 | t0001 | g0095 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19005 | hp2 | a0002 | c0002 | t0005 | g0237 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19009 | hp2 | a0033 | c0065 | t0001 | g0155 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19011 | hp2 | a0003 | c0003 | t0001 | g0176 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | LWK | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19030 | hp2 | a0034 | c0074 | t0001 | g0074 | AFR | LWK | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19043 | hp1 | a0001 | c0013 | t0001 | g0160 | AFR | LWK | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19043 | hp2 | a0003 | c0003 | t0001 | g0027 | AFR | LWK | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19056 | hp2 | a0004 | c0007 | t0001 | g0034 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19062 | hp1 | a0007 | c0014 | t0001 | g0033 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19064 | hp1 | a0035 | c0054 | t0001 | g0159 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19066 | hp1 | a0009 | c0019 | t0001 | g0152 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19068 | hp1 | a0007 | c0014 | t0001 | g0033 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19085 | hp2 | a0001 | c0027 | t0001 | g0041 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19088 | hp2 | a0013 | c0024 | t0001 | g0058 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19090 | hp1 | a0010 | c0017 | t0001 | g0019 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19090 | hp2 | a0036 | c0053 | t0007 | g0239 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19240 | hp1 | a0002 | c0012 | t0001 | g0016 | AFR | YRI | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA19240 | hp2 | a0001 | c0004 | t0001 | g0020 | AFR | YRI | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA20129 | hp1 | a0001 | c0004 | t0001 | g0075 | AFR | ASW | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ASW | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0091 | EUR | TSI | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0005 | EUR | TSI | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA20905 | hp1 | a0001 | c0064 | t0001 | g0154 | SAS | GIH | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | GIH | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG01123 | hp2 | a0011 | c0023 | t0001 | g0053 | AMR | CLM | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02109 | hp1 | a0002 | c0008 | t0001 | g0070 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0198 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02486 | hp1 | a0003 | c0003 | t0001 | g0175 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02486 | hp2 | a0003 | c0003 | t0001 | g0057 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02559 | hp1 | a0002 | c0033 | t0001 | g0072 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG02559 | hp2 | a0001 | c0028 | t0001 | g0135 | AFR | ACB | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03471 | hp1 | a0002 | c0012 | t0001 | g0016 | AFR | MSL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG03471 | hp2 | a0025 | c0032 | t0001 | g0080 | AFR | MSL | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG06807 | hp1 | a0027 | c0049 | t0001 | g0206 | AFR | USA | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0202 | AFR | USA | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA20300 | hp1 | a0001 | c0009 | t0001 | g0031 | AFR | USA | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA20300 | hp2 | a0001 | c0004 | t0001 | g0010 | AFR | USA | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA21309 | hp1 | a0001 | c0029 | t0001 | g0076 | AFR | LWK | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
NA21309 | hp2 | a0012 | c0025 | t0001 | g0097 | AFR | LWK | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
homoSapiens | chm13v2 | a0004 | c0007 | t0001 | g0216 | REF | REF | SCRIB_chr8_143785925_143820773 | SCRIB | chr8 | 143785925 | 143820773 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:143791237 | C | G | 1 | a0028 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.4894G>C | p.Glu1632Gln | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 37/37 | 5295/5607 | 4894/4968 | 1632/1655 | chr8 | 143791237 | |||
chr8:143791305 | G | A | 1 | a0015 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.4826C>T | p.Pro1609Leu | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 37/37 | 5227/5607 | 4826/4968 | 1609/1655 | chr8 | 143791305 | |||
chr8:143791908 | C | T | 3 | a0004 a0015 a0023 |
9 | HG00733.hp2 HG01106.hp1 HG02717.hp2 others(6): Show |
missense_variant | MODERATE | c.4663G>A | p.Gly1555Ser | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 34/37 | 5064/5607 | 4663/4968 | 1555/1655 | chr8 | 143791908 | |||
chr8:143792317 | C | T | 1 | a0021 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.4417G>A | p.Val1473Met | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 32/37 | 4818/5607 | 4417/4968 | 1473/1655 | chr8 | 143792317 | |||
chr8:143792383 | G | GC | 3 | a0005 a0008 a0018 |
10 | HG00544.hp2 HG01099.hp1 HG01109.hp2 others(7): Show |
frameshift_variant | HIGH | c.4350_4351insG | p.Pro1451fs | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 32/37 | 4751/5607 | 4350/4968 | 1450/1655 | chr8 | 143792383 | |||
chr8:143792984 | G | A | 1 | a0036 | 1 | NA19090.hp2 | missense_variant | MODERATE | c.4009C>T | p.Pro1337Ser | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 29/37 | 4410/5607 | 4009/4968 | 1337/1655 | chr8 | 143792984 | |||
chr8:143795075 | G | C | 1 | a0021 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.3809C>G | p.Ala1270Gly | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/37 | 4210/5607 | 3809/4968 | 1270/1655 | chr8 | 143795075 | |||
chr8:143795484 | T | G | 1 | a0011 | 2 | HG01081.hp1 HG01123.hp2 |
missense_variant | MODERATE | c.3650A>C | p.His1217Pro | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 25/37 | 4051/5607 | 3650/4968 | 1217/1655 | chr8 | 143795484 | |||
chr8:143795487 | C | A | 1 | a0035 | 1 | NA19064.hp1 | missense_variant | MODERATE | c.3647G>T | p.Gly1216Val | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 25/37 | 4048/5607 | 3647/4968 | 1216/1655 | chr8 | 143795487 | |||
chr8:143803499 | G | C | 1 | a0010 | 3 | NA18967.hp2 NA18985.hp2 NA19090.hp1 |
missense_variant | MODERATE | c.3487C>G | p.Gln1163Glu | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/37 | 3888/5607 | 3487/4968 | 1163/1655 | chr8 | 143803499 | |||
chr8:143803679 | C | T | 1 | a0031 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.3382G>A | p.Asp1128Asn | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 23/37 | 3783/5607 | 3382/4968 | 1128/1655 | chr8 | 143803679 | |||
chr8:143803738 | C | T | 1 | a0019 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.3323G>A | p.Gly1108Glu | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 23/37 | 3724/5607 | 3323/4968 | 1108/1655 | chr8 | 143803738 | |||
chr8:143803916 | G | A | 1 | a0013 | 2 | NA18951.hp2 NA19088.hp2 |
missense_variant | MODERATE | c.3145C>T | p.Arg1049Cys | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 23/37 | 3546/5607 | 3145/4968 | 1049/1655 | chr8 | 143803916 | |||
chr8:143803931 | G | A | 1 | a0017 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.3130C>T | p.Arg1044Trp | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 23/37 | 3531/5607 | 3130/4968 | 1044/1655 | chr8 | 143803931 | |||
chr8:143804099 | C | T | 2 | a0009 a0031 |
4 | NA18947.hp2 NA18964.hp2 NA18981.hp2 others(1): Show |
missense_variant | MODERATE | c.3067G>A | p.Asp1023Asn | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 22/37 | 3468/5607 | 3067/4968 | 1023/1655 | chr8 | 143804099 | |||
chr8:143804639 | C | T | 4 | a0003 a0018 a0022 others(1): Show |
30 | HG00544.hp1 HG01884.hp2 HG01975.hp2 others(27): Show |
missense_variant | MODERATE | c.2938G>A | p.Gly980Arg | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 21/37 | 3339/5607 | 2938/4968 | 980/1655 | chr8 | 143804639 | |||
chr8:143804644 | G | A | 1 | a0022 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.2933C>T | p.Thr978Ile | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 21/37 | 3334/5607 | 2933/4968 | 978/1655 | chr8 | 143804644 | |||
chr8:143805258 | C | T | 1 | a0024 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.2524G>A | p.Gly842Arg | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 19/37 | 2925/5607 | 2524/4968 | 842/1655 | chr8 | 143805258 | |||
chr8:143808806 | C | T | 1 | a0034 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1918G>A | p.Val640Met | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/37 | 2319/5607 | 1918/4968 | 640/1655 | chr8 | 143808806 | |||
chr8:143809025 | G | A | 1 | a0032 | 1 | NA19002.hp2 | missense_variant&splice_region_variant | MODERATE | c.1699C>T | p.Pro567Ser | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/37 | 2100/5607 | 1699/4968 | 567/1655 | chr8 | 143809025 | |||
chr8:143809594 | G | A | 1 | a0026 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.1655C>T | p.Thr552Met | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 14/37 | 2056/5607 | 1655/4968 | 552/1655 | chr8 | 143809594 | |||
chr8:143809598 | C | T | 3 | a0006 a0016 a0026 |
7 | HG00323.hp1 HG01074.hp1 HG01106.hp2 others(4): Show |
missense_variant | MODERATE | c.1651G>A | p.Ala551Thr | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 14/37 | 2052/5607 | 1651/4968 | 551/1655 | chr8 | 143809598 | |||
chr8:143809643 | G | C | 1 | a0014 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.1606C>G | p.Pro536Ala | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 14/37 | 2007/5607 | 1606/4968 | 536/1655 | chr8 | 143809643 | |||
chr8:143810771 | G | A | 2 | a0009 a0031 |
4 | NA18947.hp2 NA18964.hp2 NA18981.hp2 others(1): Show |
missense_variant | MODERATE | c.1319C>T | p.Ala440Val | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 12/37 | 1720/5607 | 1319/4968 | 440/1655 | chr8 | 143810771 | |||
chr8:143810814 | C | T | 1 | a0012 | 2 | HG01496.hp2 NA21309.hp2 |
missense_variant&splice_region_variant | MODERATE | c.1276G>A | p.Asp426Asn | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 12/37 | 1677/5607 | 1276/4968 | 426/1655 | chr8 | 143810814 | |||
chr8:143810909 | G | A | 1 | a0033 | 1 | NA19009.hp2 | missense_variant | MODERATE | c.1270C>T | p.Leu424Phe | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 11/37 | 1671/5607 | 1270/4968 | 424/1655 | chr8 | 143810909 | |||
chr8:143810914 | G | A | 18 | a0001 a0005 a0006 others(15): Show |
195 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(192): Show |
missense_variant | MODERATE | c.1265C>T | p.Pro422Leu | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 11/37 | 1666/5607 | 1265/4968 | 422/1655 | chr8 | 143810914 | |||
chr8:143811147 | G | A | 1 | a0007 | 4 | NA18965.hp2 NA18979.hp1 NA19062.hp1 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1105C>T | p.Arg369Cys | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 10/37 | 1506/5607 | 1105/4968 | 369/1655 | chr8 | 143811147 | |||
chr8:143811269 | G | T | 1 | a0029 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.983C>A | p.Pro328Gln | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 10/37 | 1384/5607 | 983/4968 | 328/1655 | chr8 | 143811269 | |||
chr8:143812271 | G | C | 1 | a0020 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.901C>G | p.Leu301Val | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/37 | 1302/5607 | 901/4968 | 301/1655 | chr8 | 143812271 | |||
chr8:143813325 | C | T | 1 | a0025 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.553G>A | p.Asp185Asn | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 6/37 | 954/5607 | 553/4968 | 185/1655 | chr8 | 143813325 | |||
chr8:143813326 | G | T | 1 | a0030 | 1 | NA18965.hp1 | missense_variant | MODERATE | c.552C>A | p.Asn184Lys | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 6/37 | 953/5607 | 552/4968 | 184/1655 | chr8 | 143813326 | |||
chr8:143813327 | T | G | 1 | a0030 | 1 | NA18965.hp1 | missense_variant | MODERATE | c.551A>C | p.Asn184Thr | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 6/37 | 952/5607 | 551/4968 | 184/1655 | chr8 | 143813327 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:143791729 | T | C | 1 | a0001c0026 | 2 | HG02895.hp1 HG03041.hp1 |
synonymous_variant | LOW | c.4707A>G | p.Gly1569Gly | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 35/37 | 5108/5607 | 4707/4968 | 1569/1655 | chr8 | 143791729 | |||
chr8:143791909 | G | A | 4 | a0001c0004 a0001c0028 a0002c0043 others(1): Show |
19 | HG01192.hp1 HG02258.hp1 HG02280.hp2 others(16): Show |
synonymous_variant | LOW | c.4662C>T | p.Leu1554Leu | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 34/37 | 5063/5607 | 4662/4968 | 1554/1655 | chr8 | 143791909 | |||
chr8:143792115 | C | T | 1 | a0003c0038 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.4533G>A | p.Gln1511Gln | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 33/37 | 4934/5607 | 4533/4968 | 1511/1655 | chr8 | 143792115 | |||
chr8:143792249 | G | A | 1 | a0002c0042 | 1 | NA18990.hp1 | synonymous_variant | LOW | c.4485C>T | p.Ala1495Ala | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 32/37 | 4886/5607 | 4485/4968 | 1495/1655 | chr8 | 143792249 | |||
chr8:143792363 | C | T | 1 | a0013c0024 | 2 | NA18951.hp2 NA19088.hp2 |
synonymous_variant | LOW | c.4371G>A | p.Pro1457Pro | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 32/37 | 4772/5607 | 4371/4968 | 1457/1655 | chr8 | 143792363 | |||
chr8:143792384 | T | C | 65 | a0001c0001 a0001c0004 a0001c0009 others(62): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
synonymous_variant | LOW | c.4350A>G | p.Pro1450Pro | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 32/37 | 4751/5607 | 4350/4968 | 1450/1655 | chr8 | 143792384 | |||
chr8:143792384 | T | G | 8 | a0005c0046 a0005c0051 a0005c0052 others(5): Show |
10 | HG00544.hp2 HG01099.hp1 HG01109.hp2 others(7): Show |
synonymous_variant | LOW | c.4350A>C | p.Pro1450Pro | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 32/37 | 4751/5607 | 4350/4968 | 1450/1655 | chr8 | 143792384 | |||
chr8:143792601 | C | T | 1 | a0002c0021 | 2 | HG01109.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.4212G>A | p.Leu1404Leu | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 31/37 | 4613/5607 | 4212/4968 | 1404/1655 | chr8 | 143792601 | |||
chr8:143792787 | G | A | 2 | a0003c0005 a0003c0038 |
11 | HG00544.hp1 HG02027.hp2 HG03669.hp1 others(8): Show |
synonymous_variant | LOW | c.4098C>T | p.Arg1366Arg | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 30/37 | 4499/5607 | 4098/4968 | 1366/1655 | chr8 | 143792787 | |||
chr8:143792856 | A | C | 1 | a0002c0033 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.4029T>G | p.Pro1343Pro | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 30/37 | 4430/5607 | 4029/4968 | 1343/1655 | chr8 | 143792856 | |||
chr8:143793072 | C | T | 1 | a0001c0016 | 3 | HG01361.hp1 HG01516.hp2 HG01517.hp2 |
synonymous_variant | LOW | c.3921G>A | p.Pro1307Pro | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 29/37 | 4322/5607 | 3921/4968 | 1307/1655 | chr8 | 143793072 | |||
chr8:143795056 | G | A | 1 | a0001c0027 | 2 | NA18984.hp1 NA19085.hp2 |
synonymous_variant | LOW | c.3828C>T | p.Ser1276Ser | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/37 | 4229/5607 | 3828/4968 | 1276/1655 | chr8 | 143795056 | |||
chr8:143803410 | A | G | 69 | a0001c0001 a0001c0004 a0001c0009 others(66): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
synonymous_variant | LOW | c.3576T>C | p.Phe1192Phe | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/37 | 3977/5607 | 3576/4968 | 1192/1655 | chr8 | 143803410 | |||
chr8:143803431 | G | A | 2 | a0001c0028 a0002c0043 |
3 | HG02258.hp1 HG02559.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.3555C>T | p.Thr1185Thr | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/37 | 3956/5607 | 3555/4968 | 1185/1655 | chr8 | 143803431 | |||
chr8:143803782 | C | T | 1 | a0001c0059 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.3279G>A | p.Pro1093Pro | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 23/37 | 3680/5607 | 3279/4968 | 1093/1655 | chr8 | 143803782 | |||
chr8:143805316 | C | T | 1 | a0002c0036 | 1 | HG00673.hp1 | synonymous_variant | LOW | c.2466G>A | p.Ala822Ala | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 19/37 | 2867/5607 | 2466/4968 | 822/1655 | chr8 | 143805316 | |||
chr8:143805412 | G | A | 1 | a0034c0074 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.2370C>T | p.Gly790Gly | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 19/37 | 2771/5607 | 2370/4968 | 790/1655 | chr8 | 143805412 | |||
chr8:143807002 | A | G | 61 | a0001c0001 a0001c0004 a0001c0009 others(58): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
synonymous_variant | LOW | c.2190T>C | p.Thr730Thr | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 17/37 | 2591/5607 | 2190/4968 | 730/1655 | chr8 | 143807002 | |||
chr8:143807570 | A | G | 1 | a0002c0022 | 2 | HG00408.hp2 HG00423.hp2 |
synonymous_variant | LOW | c.2160T>C | p.Ala720Ala | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 16/37 | 2561/5607 | 2160/4968 | 720/1655 | chr8 | 143807570 | |||
chr8:143808768 | G | A | 1 | a0001c0071 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.1956C>T | p.Pro652Pro | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/37 | 2357/5607 | 1956/4968 | 652/1655 | chr8 | 143808768 | |||
chr8:143809011 | G | A | 1 | a0002c0012 | 4 | HG02145.hp2 HG02622.hp2 HG03471.hp1 others(1): Show |
synonymous_variant | LOW | c.1713C>T | p.Phe571Phe | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/37 | 2114/5607 | 1713/4968 | 571/1655 | chr8 | 143809011 | |||
chr8:143809584 | G | A | 1 | a0001c0018 | 3 | HG02129.hp2 NA18944.hp1 NA18984.hp2 |
synonymous_variant | LOW | c.1665C>T | p.Gly555Gly | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 14/37 | 2066/5607 | 1665/4968 | 555/1655 | chr8 | 143809584 | |||
chr8:143810497 | C | T | 2 | a0001c0009 a0005c0046 |
6 | HG01358.hp1 HG01978.hp2 HG01981.hp2 others(3): Show |
synonymous_variant | LOW | c.1512G>A | p.Ser504Ser | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 13/37 | 1913/5607 | 1512/4968 | 504/1655 | chr8 | 143810497 | |||
chr8:143810533 | C | A | 5 | a0001c0011 a0001c0013 a0001c0059 others(2): Show |
12 | HG01891.hp2 HG02572.hp2 HG02647.hp2 others(9): Show |
synonymous_variant | LOW | c.1476G>T | p.Arg492Arg | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 13/37 | 1877/5607 | 1476/4968 | 492/1655 | chr8 | 143810533 | |||
chr8:143810599 | T | C | 2 | a0001c0062 a0005c0061 |
2 | HG03831.hp1 HG03834.hp2 |
synonymous_variant | LOW | c.1410A>G | p.Leu470Leu | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 13/37 | 1811/5607 | 1410/4968 | 470/1655 | chr8 | 143810599 | |||
chr8:143810907 | G | A | 1 | a0001c0064 | 1 | NA20905.hp1 | splice_region_variant&synonymous_variant | LOW | c.1272C>T | p.Leu424Leu | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 11/37 | 1673/5607 | 1272/4968 | 424/1655 | chr8 | 143810907 | |||
chr8:143811265 | G | A | 1 | a0001c0066 | 1 | HG01257.hp2 | synonymous_variant | LOW | c.987C>T | p.Pro329Pro | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 10/37 | 1388/5607 | 987/4968 | 329/1655 | chr8 | 143811265 | |||
chr8:143812326 | G | A | 66 | a0001c0001 a0001c0004 a0001c0009 others(63): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
synonymous_variant | LOW | c.846C>T | p.Thr282Thr | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/37 | 1247/5607 | 846/4968 | 282/1655 | chr8 | 143812326 | |||
chr8:143812844 | G | A | 1 | a0001c0068 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.760C>T | p.Leu254Leu | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 8/37 | 1161/5607 | 760/4968 | 254/1655 | chr8 | 143812844 | |||
chr8:143812848 | C | T | 1 | a0002c0020 | 2 | HG00280.hp1 HG00642.hp2 |
synonymous_variant | LOW | c.756G>A | p.Gln252Gln | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 8/37 | 1157/5607 | 756/4968 | 252/1655 | chr8 | 143812848 | |||
chr8:143813490 | G | A | 2 | a0001c0070 a0001c0071 |
2 | HG04204.hp2 HG04228.hp1 |
synonymous_variant | LOW | c.483C>T | p.Asn161Asn | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 5/37 | 884/5607 | 483/4968 | 161/1655 | chr8 | 143813490 | |||
chr8:143813499 | G | A | 3 | a0002c0030 a0004c0007 a0015c0072 |
9 | HG00733.hp2 HG00741.hp2 HG01070.hp2 others(6): Show |
synonymous_variant | LOW | c.474C>T | p.Leu158Leu | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 5/37 | 875/5607 | 474/4968 | 158/1655 | chr8 | 143813499 | |||
chr8:143813829 | G | A | 1 | a0005c0073 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.345C>T | p.Asn115Asn | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 3/37 | 746/5607 | 345/4968 | 115/1655 | chr8 | 143813829 | |||
chr8:143813847 | G | A | 1 | a0034c0074 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.327C>T | p.Ile109Ile | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 3/37 | 728/5607 | 327/4968 | 109/1655 | chr8 | 143813847 | |||
chr8:143813880 | C | T | 1 | a0001c0031 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.294G>A | p.Pro98Pro | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 3/37 | 695/5607 | 294/4968 | 98/1655 | chr8 | 143813880 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:143791016 | C | CTGGGGTG others(3): Show |
1 | a0001c0001t0004 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137_*146dupCCCCAC others(4): Show |
SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 37/37 | 146 | chr8 | 143791016 | ||||||
chr8:143791103 | A | G | 1 | a0002c0002t0003 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*60T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 37/37 | 60 | chr8 | 143791103 | ||||||
chr8:143815429 | G | A | 1 | a0002c0002t0005 | 1 | NA19005.hp2 | 5_prime_UTR_variant | MODIFIER | c.-57C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/37 | 57 | chr8 | 143815429 | ||||||
chr8:143815530 | G | A | 1 | a0003c0003t0006 | 1 | HG01975.hp2 | 5_prime_UTR_variant | MODIFIER | c.-158C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/37 | 158 | chr8 | 143815530 | ||||||
chr8:143815576 | G | A | 1 | a0036c0053t0007 | 1 | NA19090.hp2 | 5_prime_UTR_variant | MODIFIER | c.-204C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/37 | 204 | chr8 | 143815576 | ||||||
chr8:143815721 | T | TGCCCCGC others(8): Show |
2 | a0001c0001t0002 a0001c0026t0002 |
4 | HG02280.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-364_-350dupGGGTGT others(9): Show |
SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/37 | 350 | chr8 | 143815721 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:143791319 | G | A | 4 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0026t0002g0063 others(1): Show |
5 | HG02280.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.4823-11C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 36/36 | chr8 | 143791319 | |||||||
chr8:143791496 | G | C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(226): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.4771-56C>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 35/36 | chr8 | 143791496 | |||||||
chr8:143791497 | G | A | 1 | a0001c0004t0001g0104 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4771-57C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 35/36 | chr8 | 143791497 | |||||||
chr8:143791574 | G | A | 1 | a0024c0048t0001g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4770+92C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 35/36 | chr8 | 143791574 | |||||||
chr8:143791791 | G | A | 1 | a0003c0003t0001g0057 | 2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.4696-51C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 34/36 | chr8 | 143791791 | |||||||
chr8:143791822 | A | AC | 57 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(54): Show |
90 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.4695+53dupG | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 34/36 | chr8 | 143791822 | |||||||
chr8:143791823 | C | A | 1 | a0001c0013t0001g0160 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4695+53G>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 34/36 | chr8 | 143791823 | |||||||
chr8:143791826 | CA | C | 11 | a0001c0001t0001g0130 a0001c0011t0001g0147 a0002c0006t0001g0163 others(8): Show |
13 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.4695+49delT | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 34/36 | chr8 | 143791826 | |||||||
chr8:143791827 | A | C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(226): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.4695+49T>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 34/36 | chr8 | 143791827 | |||||||
chr8:143791830 | C | T | 2 | a0002c0002t0001g0056 a0002c0002t0001g0168 |
3 | HG00140.hp1 HG01928.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.4695+46G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 34/36 | chr8 | 143791830 | |||||||
chr8:143791931 | G | A | 1 | a0001c0050t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4658-18C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 33/36 | chr8 | 143791931 | |||||||
chr8:143791936 | T | C | 1 | a0002c0002t0001g0090 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.4658-23A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 33/36 | chr8 | 143791936 | |||||||
chr8:143791962 | A | AC | 66 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(63): Show |
103 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.4657+28dupG | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 33/36 | chr8 | 143791962 | |||||||
chr8:143792196 | T | C | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(236): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.4514+24A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 32/36 | chr8 | 143792196 | |||||||
chr8:143792423 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4329-18G>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 31/36 | chr8 | 143792423 | |||||||
chr8:143792880 | G | A | 7 | a0001c0011t0001g0015 a0001c0011t0001g0147 a0001c0011t0001g0148 others(4): Show |
11 | HG01891.hp2 HG02647.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.4018-13C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 29/36 | chr8 | 143792880 | |||||||
chr8:143792944 | G | A | 6 | a0002c0002t0001g0180 a0002c0008t0001g0035 a0002c0008t0001g0070 others(3): Show |
7 | HG01109.hp1 HG01175.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.4017+32C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 29/36 | chr8 | 143792944 | |||||||
chr8:143792964 | G | T | 1 | a0003c0005t0001g0011 | 5 | HG00544.hp1 HG02027.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.4017+12C>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 29/36 | chr8 | 143792964 | |||||||
chr8:143793154 | C | T | 3 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0026t0002g0063 |
4 | HG02280.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3910-71G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 28/36 | chr8 | 143793154 | |||||||
chr8:143793167 | G | A | 3 | a0002c0002t0001g0008 a0002c0002t0001g0051 a0002c0002t0005g0237 |
9 | HG00438.hp1 NA18747.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.3910-84C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 28/36 | chr8 | 143793167 | |||||||
chr8:143793365 | G | A | 91 | a0001c0001t0001g0059 a0001c0001t0001g0101 a0001c0001t0001g0107 others(88): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.3910-282C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 28/36 | chr8 | 143793365 | |||||||
chr8:143793396 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3910-313T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 28/36 | chr8 | 143793396 | |||||||
chr8:143793397 | G | C | 1 | a0001c0001t0001g0233 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3910-314C>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 28/36 | chr8 | 143793397 | |||||||
chr8:143793398 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3910-315C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 28/36 | chr8 | 143793398 | |||||||
chr8:143793399 | C | G | 1 | a0001c0001t0001g0233 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3910-316G>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 28/36 | chr8 | 143793399 | |||||||
chr8:143793418 | G | A | 179 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(176): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.3910-335C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 28/36 | chr8 | 143793418 | |||||||
chr8:143793419 | G | C | 1 | a0002c0033t0001g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3910-336C>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 28/36 | chr8 | 143793419 | |||||||
chr8:143793468 | G | A | 2 | a0002c0002t0001g0056 a0002c0002t0001g0168 |
3 | HG00140.hp1 HG01928.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.3910-385C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 28/36 | chr8 | 143793468 | |||||||
chr8:143793567 | G | T | 1 | a0028c0041t0001g0190 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3909+333C>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 28/36 | chr8 | 143793567 | |||||||
chr8:143793573 | G | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(161): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.3909+327C>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 28/36 | chr8 | 143793573 | |||||||
chr8:143793633 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3909+267T>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 28/36 | chr8 | 143793633 | |||||||
chr8:143793661 | C | A | 1 | a0002c0002t0001g0191 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3909+239G>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 28/36 | chr8 | 143793661 | |||||||
chr8:143793724 | C | T | 1 | a0002c0012t0001g0094 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3909+176G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 28/36 | chr8 | 143793724 | |||||||
chr8:143793775 | G | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0021 others(40): Show |
65 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.3909+125C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 28/36 | chr8 | 143793775 | |||||||
chr8:143793806 | C | A | 1 | a0002c0002t0001g0038 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3909+94G>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 28/36 | chr8 | 143793806 | |||||||
chr8:143793989 | G | A | 34 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0022 others(31): Show |
52 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.3847-27C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/36 | chr8 | 143793989 | |||||||
chr8:143794014 | G | T | 1 | a0025c0032t0001g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3847-52C>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/36 | chr8 | 143794014 | |||||||
chr8:143794140 | C | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0224 |
2 | HG00323.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.3847-178G>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/36 | chr8 | 143794140 | |||||||
chr8:143794248 | C | T | 2 | a0002c0012t0001g0094 a0034c0074t0001g0074 |
2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3847-286G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/36 | chr8 | 143794248 | |||||||
chr8:143794260 | G | A | 1 | a0001c0009t0001g0205 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3847-298C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/36 | chr8 | 143794260 | |||||||
chr8:143794414 | C | T | 1 | a0002c0033t0001g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3847-452G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/36 | chr8 | 143794414 | |||||||
chr8:143794524 | A | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(234): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.3846+514T>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/36 | chr8 | 143794524 | |||||||
chr8:143794529 | C | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(61): Show |
103 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.3846+509G>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/36 | chr8 | 143794529 | |||||||
chr8:143794562 | T | C | 1 | a0001c0028t0001g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3846+476A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/36 | chr8 | 143794562 | |||||||
chr8:143794585 | T | A | 2 | a0002c0012t0001g0094 a0034c0074t0001g0074 |
2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3846+453A>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/36 | chr8 | 143794585 | |||||||
chr8:143794599 | A | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0021 others(38): Show |
62 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.3846+439T>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/36 | chr8 | 143794599 | |||||||
chr8:143794660 | C | G | 1 | a0001c0001t0001g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3846+378G>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/36 | chr8 | 143794660 | |||||||
chr8:143794670 | C | T | 7 | a0002c0030t0001g0062 a0004c0007t0001g0034 a0004c0007t0001g0217 others(4): Show |
10 | HG00733.hp2 HG00741.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.3846+368G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/36 | chr8 | 143794670 | |||||||
chr8:143794678 | G | A | 5 | a0001c0029t0001g0076 a0001c0029t0001g0140 a0002c0008t0001g0231 others(2): Show |
5 | HG02622.hp2 HG02976.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.3846+360C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/36 | chr8 | 143794678 | |||||||
chr8:143794842 | C | T | 1 | a0021c0058t0001g0144 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3846+196G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/36 | chr8 | 143794842 | |||||||
chr8:143794989 | A | T | 3 | a0001c0029t0001g0076 a0001c0029t0001g0140 a0002c0008t0001g0231 |
3 | HG02976.hp2 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3846+49T>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/36 | chr8 | 143794989 | |||||||
chr8:143795008 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3846+30C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 27/36 | chr8 | 143795008 | |||||||
chr8:143795212 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.3771+65G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 26/36 | chr8 | 143795212 | |||||||
chr8:143795264 | C | T | 1 | a0002c0002t0001g0191 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3771+13G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 26/36 | chr8 | 143795264 | |||||||
chr8:143795376 | C | T | 7 | a0002c0030t0001g0062 a0004c0007t0001g0034 a0004c0007t0001g0217 others(4): Show |
10 | HG00733.hp2 HG00741.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.3715-43G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 25/36 | chr8 | 143795376 | |||||||
chr8:143795559 | G | A | 1 | a0002c0012t0001g0094 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3604-29C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143795559 | |||||||
chr8:143795572 | C | T | 5 | a0002c0008t0001g0035 a0002c0008t0001g0070 a0002c0008t0001g0073 others(2): Show |
6 | HG01109.hp1 HG01175.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.3604-42G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143795572 | |||||||
chr8:143795640 | C | T | 1 | a0001c0050t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3604-110G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143795640 | |||||||
chr8:143795641 | G | A | 4 | a0001c0001t0001g0124 a0001c0001t0001g0129 a0001c0001t0001g0161 others(1): Show |
4 | HG00323.hp2 HG01069.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3604-111C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143795641 | |||||||
chr8:143795642 | C | T | 2 | a0002c0002t0001g0056 a0002c0002t0001g0168 |
3 | HG00140.hp1 HG01928.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.3604-112G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143795642 | |||||||
chr8:143795665 | G | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0021 others(37): Show |
62 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.3604-135C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143795665 | |||||||
chr8:143795693 | C | T | 3 | a0001c0050t0001g0123 a0002c0006t0001g0163 a0002c0008t0001g0231 |
3 | HG02630.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3604-163G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143795693 | |||||||
chr8:143795694 | G | A | 1 | a0001c0029t0001g0140 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3604-164C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143795694 | |||||||
chr8:143795756 | T | C | 6 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0026t0002g0063 others(3): Show |
7 | HG02257.hp2 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.3604-226A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143795756 | |||||||
chr8:143795765 | C | T | 1 | a0002c0012t0001g0094 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3604-235G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143795765 | |||||||
chr8:143795786 | C | T | 1 | a0001c0050t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3604-256G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143795786 | |||||||
chr8:143795787 | A | G | 233 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(230): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.3604-257T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143795787 | |||||||
chr8:143795792 | T | G | 1 | a0001c0001t0002g0241 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3604-262A>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143795792 | |||||||
chr8:143795881 | G | A | 1 | a0001c0029t0001g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3604-351C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143795881 | |||||||
chr8:143795917 | C | T | 1 | a0002c0002t0001g0183 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3604-387G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143795917 | |||||||
chr8:143795918 | G | A | 2 | a0002c0030t0001g0062 a0004c0007t0001g0220 |
3 | HG00741.hp2 HG01070.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.3604-388C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143795918 | |||||||
chr8:143795999 | G | A | 1 | a0001c0064t0001g0154 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3604-469C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143795999 | |||||||
chr8:143796073 | C | G | 2 | a0002c0008t0001g0070 a0002c0021t0001g0069 |
2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3604-543G>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796073 | |||||||
chr8:143796073 | C | T | 11 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0013t0001g0025 others(8): Show |
15 | HG01175.hp2 HG02257.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.3604-543G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796073 | |||||||
chr8:143796184 | G | C | 5 | a0001c0029t0001g0140 a0002c0033t0001g0072 a0004c0007t0001g0034 others(2): Show |
7 | HG01106.hp1 HG02559.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.3604-654C>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796184 | |||||||
chr8:143796237 | C | T | 1 | a0028c0041t0001g0190 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3604-707G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796237 | |||||||
chr8:143796244 | C | T | 9 | a0001c0011t0001g0015 a0001c0011t0001g0147 a0001c0011t0001g0148 others(6): Show |
13 | HG01891.hp2 HG02572.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.3604-714G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796244 | |||||||
chr8:143796280 | A | G | 1 | a0002c0002t0001g0092 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3604-750T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796280 | |||||||
chr8:143796296 | G | A | 5 | a0002c0002t0001g0037 a0002c0002t0001g0088 a0002c0002t0001g0089 others(2): Show |
6 | NA18948.hp2 NA18980.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.3604-766C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796296 | |||||||
chr8:143796302 | G | A | 1 | a0002c0008t0001g0231 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3604-772C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796302 | |||||||
chr8:143796318 | C | T | 37 | a0001c0001t0001g0130 a0001c0001t0001g0138 a0001c0001t0002g0240 others(34): Show |
51 | HG01109.hp1 HG01175.hp2 HG01192.hp1 others(48): Show |
intron_variant | MODIFIER | c.3604-788G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796318 | |||||||
chr8:143796335 | C | T | 3 | a0002c0006t0001g0026 a0002c0006t0001g0068 a0002c0006t0001g0164 |
5 | HG02970.hp2 HG03195.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3604-805G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796335 | |||||||
chr8:143796353 | C | T | 1 | a0036c0053t0007g0239 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3604-823G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796353 | |||||||
chr8:143796410 | G | C | 1 | a0017c0055t0001g0137 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3604-880C>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796410 | |||||||
chr8:143796435 | G | C | 1 | a0001c0001t0001g0036 | 2 | HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3604-905C>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796435 | |||||||
chr8:143796504 | G | C | 1 | a0001c0001t0001g0110 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3604-974C>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796504 | |||||||
chr8:143796580 | C | T | 9 | a0001c0001t0001g0059 a0001c0009t0001g0031 a0001c0009t0001g0203 others(6): Show |
14 | HG00544.hp2 HG01358.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.3604-1050G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796580 | |||||||
chr8:143796589 | A | C | 5 | a0002c0006t0001g0026 a0002c0006t0001g0047 a0002c0006t0001g0068 others(2): Show |
8 | HG02723.hp1 HG02970.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.3604-1059T>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796589 | |||||||
chr8:143796605 | C | T | 2 | a0003c0038t0001g0174 a0022c0044t0001g0194 |
2 | HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.3604-1075G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796605 | |||||||
chr8:143796838 | T | C | 3 | a0001c0029t0001g0076 a0001c0029t0001g0140 a0002c0008t0001g0231 |
3 | HG02976.hp2 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3604-1308A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796838 | |||||||
chr8:143796843 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3604-1313G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796843 | |||||||
chr8:143796963 | G | A | 2 | a0002c0002t0001g0056 a0002c0002t0001g0168 |
3 | HG00140.hp1 HG01928.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.3604-1433C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796963 | |||||||
chr8:143796992 | G | T | 1 | a0007c0014t0001g0064 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3604-1462C>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796992 | |||||||
chr8:143796994 | T | G | 1 | a0007c0014t0001g0064 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3604-1464A>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796994 | |||||||
chr8:143796995 | C | T | 1 | a0007c0014t0001g0064 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3604-1465G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143796995 | |||||||
chr8:143797092 | G | A | 1 | a0002c0002t0001g0007 | 6 | NA18939.hp1 NA18975.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.3604-1562C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143797092 | |||||||
chr8:143797095 | A | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(232): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.3604-1565T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143797095 | |||||||
chr8:143797276 | A | G | 4 | a0001c0001t0001g0124 a0001c0001t0001g0129 a0001c0001t0001g0161 others(1): Show |
4 | HG00323.hp2 HG01069.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3604-1746T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143797276 | |||||||
chr8:143797446 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3604-1916C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143797446 | |||||||
chr8:143797845 | G | A | 1 | a0011c0023t0001g0053 | 2 | HG01081.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.3604-2315C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143797845 | |||||||
chr8:143797847 | C | T | 11 | a0001c0001t0001g0096 a0002c0002t0001g0005 a0002c0002t0001g0006 others(8): Show |
22 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.3604-2317G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143797847 | |||||||
chr8:143798016 | G | A | 2 | a0002c0002t0001g0037 a0032c0045t0001g0095 |
3 | NA18948.hp2 NA18980.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.3604-2486C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143798016 | |||||||
chr8:143798041 | G | A | 1 | a0002c0033t0001g0072 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3604-2511C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143798041 | |||||||
chr8:143798084 | G | A | 1 | a0002c0012t0001g0094 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3604-2554C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143798084 | |||||||
chr8:143798119 | G | A | 2 | a0003c0003t0001g0027 a0003c0003t0001g0175 |
4 | HG01884.hp2 HG02486.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3604-2589C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143798119 | |||||||
chr8:143798148 | C | T | 1 | a0027c0049t0001g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3604-2618G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143798148 | |||||||
chr8:143798173 | T | C | 1 | a0025c0032t0001g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3604-2643A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143798173 | |||||||
chr8:143798180 | C | T | 1 | a0004c0007t0001g0217 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3604-2650G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143798180 | |||||||
chr8:143798198 | A | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0116 |
2 | HG02698.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.3604-2668T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143798198 | |||||||
chr8:143798264 | A | C | 1 | a0030c0069t0001g0079 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3604-2734T>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143798264 | |||||||
chr8:143798306 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3604-2776A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143798306 | |||||||
chr8:143798375 | A | AGGATGCG others(13): Show |
26 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0043 others(23): Show |
38 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.3604-2865_3604-284 others(24): Show |
SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143798375 | |||||||
chr8:143798505 | G | A | 1 | a0029c0034t0001g0208 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3604-2975C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143798505 | |||||||
chr8:143798562 | A | G | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(233): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.3604-3032T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143798562 | |||||||
chr8:143798569 | C | T | 2 | a0001c0029t0001g0140 a0002c0002t0001g0196 |
2 | HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3604-3039G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143798569 | |||||||
chr8:143798695 | T | C | 1 | a0002c0022t0001g0169 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3604-3165A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143798695 | |||||||
chr8:143798754 | A | C | 42 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0021 others(39): Show |
65 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.3604-3224T>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143798754 | |||||||
chr8:143798825 | G | A | 1 | a0002c0002t0001g0052 | 2 | HG00621.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.3604-3295C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143798825 | |||||||
chr8:143798839 | G | C | 5 | a0002c0008t0001g0035 a0002c0008t0001g0070 a0002c0008t0001g0073 others(2): Show |
6 | HG01109.hp1 HG01175.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.3604-3309C>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143798839 | |||||||
chr8:143799031 | A | G | 5 | a0002c0002t0001g0086 a0002c0012t0001g0016 a0002c0012t0001g0094 others(2): Show |
7 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3604-3501T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143799031 | |||||||
chr8:143799040 | C | T | 1 | a0001c0009t0001g0203 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3604-3510G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143799040 | |||||||
chr8:143799094 | G | A | 1 | a0003c0003t0001g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3604-3564C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143799094 | |||||||
chr8:143799107 | T | A | 1 | a0029c0034t0001g0208 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3604-3577A>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143799107 | |||||||
chr8:143799191 | G | C | 2 | a0002c0002t0001g0198 a0003c0003t0001g0195 |
2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3604-3661C>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143799191 | |||||||
chr8:143799289 | G | A | 2 | a0002c0002t0001g0188 a0003c0003t0001g0176 |
2 | NA19010.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.3604-3759C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143799289 | |||||||
chr8:143799534 | C | T | 1 | a0018c0037t0001g0173 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3603+3849G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143799534 | |||||||
chr8:143799584 | G | A | 1 | a0024c0048t0001g0121 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3603+3799C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143799584 | |||||||
chr8:143799631 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG01123.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.3603+3752G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143799631 | |||||||
chr8:143799754 | C | A | 1 | a0001c0001t0001g0115 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3603+3629G>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143799754 | |||||||
chr8:143799760 | CTAGAAAG others(36): Show |
C | 12 | a0001c0001t0001g0107 a0001c0001t0001g0116 a0001c0001t0001g0117 others(9): Show |
17 | HG01891.hp2 HG02572.hp2 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.3603+3580_3603+362 others(47): Show |
SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143799760 | |||||||
chr8:143799793 | GACGTGGG others(36): Show |
G | 1 | a0001c0013t0001g0160 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3603+3547_3603+358 others(47): Show |
SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143799793 | |||||||
chr8:143799796 | G | A | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(200): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.3603+3587C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143799796 | |||||||
chr8:143799961 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3603+3422C>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143799961 | |||||||
chr8:143799978 | G | T | 1 | a0001c0001t0001g0110 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3603+3405C>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143799978 | |||||||
chr8:143800036 | C | A | 4 | a0001c0001t0001g0133 a0002c0006t0001g0026 a0002c0006t0001g0068 others(1): Show |
6 | HG02970.hp2 HG03195.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.3603+3347G>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143800036 | |||||||
chr8:143800036 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3603+3347G>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143800036 | |||||||
chr8:143800211 | C | T | 1 | a0001c0001t0001g0040 | 2 | HG00609.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.3603+3172G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143800211 | |||||||
chr8:143800213 | T | C | 1 | a0011c0023t0001g0053 | 2 | HG01081.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.3603+3170A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143800213 | |||||||
chr8:143800253 | T | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(221): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.3603+3130A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143800253 | |||||||
chr8:143800257 | G | A | 1 | a0003c0005t0001g0177 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3603+3126C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143800257 | |||||||
chr8:143800317 | C | T | 1 | a0002c0002t0001g0091 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3603+3066G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143800317 | |||||||
chr8:143800505 | A | G | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(208): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.3603+2878T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143800505 | |||||||
chr8:143800540 | C | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(208): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.3603+2843G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143800540 | |||||||
chr8:143800574 | C | T | 12 | a0002c0002t0001g0005 a0002c0002t0001g0049 a0002c0002t0001g0067 others(9): Show |
19 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.3603+2809G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143800574 | |||||||
chr8:143800791 | G | A | 7 | a0001c0011t0001g0015 a0001c0011t0001g0147 a0001c0011t0001g0148 others(4): Show |
11 | HG01891.hp2 HG02647.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.3603+2592C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143800791 | |||||||
chr8:143800816 | C | T | 3 | a0002c0006t0001g0026 a0002c0006t0001g0068 a0002c0006t0001g0164 |
5 | HG02970.hp2 HG03195.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3603+2567G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143800816 | |||||||
chr8:143800817 | G | A | 217 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(214): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.3603+2566C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143800817 | |||||||
chr8:143800835 | C | A | 1 | a0001c0001t0001g0043 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3603+2548G>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143800835 | |||||||
chr8:143800857 | G | A | 1 | a0002c0002t0001g0054 | 2 | NA18969.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.3603+2526C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143800857 | |||||||
chr8:143800860 | C | T | 3 | a0001c0004t0001g0020 a0001c0004t0001g0099 a0001c0050t0001g0123 |
5 | HG02622.hp1 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.3603+2523G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143800860 | |||||||
chr8:143800955 | A | G | 1 | a0002c0002t0001g0179 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3603+2428T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143800955 | |||||||
chr8:143800966 | AT | A | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(221): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.3603+2416delA | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143800966 | |||||||
chr8:143801053 | G | A | 1 | a0008c0015t0001g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3603+2330C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143801053 | |||||||
chr8:143801182 | G | A | 1 | a0002c0002t0001g0197 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3603+2201C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143801182 | |||||||
chr8:143801190 | G | A | 1 | a0028c0041t0001g0190 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3603+2193C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143801190 | |||||||
chr8:143801207 | G | C | 6 | a0002c0030t0001g0062 a0004c0007t0001g0034 a0004c0007t0001g0217 others(3): Show |
9 | HG00733.hp2 HG00741.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.3603+2176C>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143801207 | |||||||
chr8:143801214 | C | T | 1 | a0001c0001t0004g0232 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3603+2169G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143801214 | |||||||
chr8:143801567 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3603+1816G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143801567 | |||||||
chr8:143801617 | C | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(232): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.3603+1766G>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143801617 | |||||||
chr8:143801678 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3603+1705G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143801678 | |||||||
chr8:143801691 | G | A | 3 | a0001c0029t0001g0076 a0001c0029t0001g0140 a0002c0008t0001g0231 |
3 | HG02976.hp2 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3603+1692C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143801691 | |||||||
chr8:143801811 | C | A | 1 | a0002c0002t0001g0038 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3603+1572G>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143801811 | |||||||
chr8:143801886 | C | A | 1 | a0001c0068t0001g0065 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3603+1497G>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143801886 | |||||||
chr8:143801917 | G | A | 217 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(214): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.3603+1466C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143801917 | |||||||
chr8:143801952 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3603+1431G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143801952 | |||||||
chr8:143802100 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3603+1283C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143802100 | |||||||
chr8:143802225 | C | T | 6 | a0002c0030t0001g0062 a0004c0007t0001g0034 a0004c0007t0001g0217 others(3): Show |
9 | HG00733.hp2 HG00741.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.3603+1158G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143802225 | |||||||
chr8:143802241 | G | A | 1 | a0034c0074t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3603+1142C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143802241 | |||||||
chr8:143802430 | C | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(232): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.3603+953G>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143802430 | |||||||
chr8:143802631 | A | G | 227 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(224): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.3603+752T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143802631 | |||||||
chr8:143802843 | G | A | 1 | a0007c0014t0001g0064 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3603+540C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143802843 | |||||||
chr8:143802906 | G | A | 7 | a0002c0002t0001g0030 a0002c0002t0001g0055 a0002c0002t0001g0066 others(4): Show |
10 | HG02155.hp1 NA18940.hp2 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.3603+477C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143802906 | |||||||
chr8:143802915 | G | A | 2 | a0001c0004t0001g0044 a0005c0052t0001g0134 |
3 | HG01192.hp1 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3603+468C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143802915 | |||||||
chr8:143802978 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3603+405G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 24/36 | chr8 | 143802978 | |||||||
chr8:143803584 | G | A | 2 | a0002c0002t0001g0056 a0002c0002t0001g0168 |
3 | HG00140.hp1 HG01928.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.3415-13C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 23/36 | chr8 | 143803584 | |||||||
chr8:143804004 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3120+42A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 22/36 | chr8 | 143804004 | |||||||
chr8:143804352 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3010-196C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 21/36 | chr8 | 143804352 | |||||||
chr8:143804353 | G | T | 1 | a0001c0001t0001g0158 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3010-197C>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 21/36 | chr8 | 143804353 | |||||||
chr8:143804354 | C | A | 1 | a0001c0001t0001g0158 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3010-198G>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 21/36 | chr8 | 143804354 | |||||||
chr8:143804361 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3010-205C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 21/36 | chr8 | 143804361 | |||||||
chr8:143804362 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3009+206G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 21/36 | chr8 | 143804362 | |||||||
chr8:143804363 | C | G | 1 | a0001c0001t0001g0158 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3009+205G>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 21/36 | chr8 | 143804363 | |||||||
chr8:143804364 | A | T | 1 | a0001c0001t0001g0158 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3009+204T>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 21/36 | chr8 | 143804364 | |||||||
chr8:143804365 | G | T | 1 | a0001c0001t0001g0158 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3009+203C>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 21/36 | chr8 | 143804365 | |||||||
chr8:143804441 | G | A | 1 | a0002c0002t0001g0207 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3009+127C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 21/36 | chr8 | 143804441 | |||||||
chr8:143804458 | C | T | 85 | a0001c0001t0001g0059 a0001c0009t0001g0031 a0001c0009t0001g0203 others(82): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.3009+110G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 21/36 | chr8 | 143804458 | |||||||
chr8:143804459 | C | T | 1 | a0023c0056t0001g0077 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3009+109G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 21/36 | chr8 | 143804459 | |||||||
chr8:143804509 | G | A | 1 | a0001c0001t0001g0014 | 3 | HG02602.hp1 HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.3009+59C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 21/36 | chr8 | 143804509 | |||||||
chr8:143804534 | T | C | 1 | a0002c0002t0001g0193 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3009+34A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 21/36 | chr8 | 143804534 | |||||||
chr8:143804905 | G | A | 9 | a0001c0011t0001g0015 a0001c0011t0001g0147 a0001c0011t0001g0148 others(6): Show |
13 | HG01891.hp2 HG02572.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.2751+29C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 20/36 | chr8 | 143804905 | |||||||
chr8:143805484 | A | C | 2 | a0001c0001t0001g0023 a0033c0065t0001g0155 |
4 | NA18954.hp2 NA18966.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.2347-49T>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 18/36 | chr8 | 143805484 | |||||||
chr8:143805486 | A | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0021 others(158): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.2347-51T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 18/36 | chr8 | 143805486 | |||||||
chr8:143805542 | G | A | 153 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0021 others(150): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2347-107C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 18/36 | chr8 | 143805542 | |||||||
chr8:143805550 | G | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0012 others(60): Show |
98 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.2347-115C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 18/36 | chr8 | 143805550 | |||||||
chr8:143805564 | G | A | 86 | a0001c0001t0001g0059 a0001c0009t0001g0031 a0001c0009t0001g0203 others(83): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.2347-129C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 18/36 | chr8 | 143805564 | |||||||
chr8:143805602 | G | A | 154 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0021 others(151): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2347-167C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 18/36 | chr8 | 143805602 | |||||||
chr8:143805642 | G | A | 1 | a0001c0029t0001g0140 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2347-207C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 18/36 | chr8 | 143805642 | |||||||
chr8:143805942 | G | A | 3 | a0001c0029t0001g0076 a0001c0029t0001g0140 a0002c0008t0001g0231 |
3 | HG02976.hp2 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2346+465C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 18/36 | chr8 | 143805942 | |||||||
chr8:143805977 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2346+430G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 18/36 | chr8 | 143805977 | |||||||
chr8:143806070 | T | C | 1 | a0002c0002t0001g0202 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2346+337A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 18/36 | chr8 | 143806070 | |||||||
chr8:143806079 | G | C | 1 | a0003c0003t0001g0225 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2346+328C>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 18/36 | chr8 | 143806079 | |||||||
chr8:143806132 | A | G | 1 | a0034c0074t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2346+275T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 18/36 | chr8 | 143806132 | |||||||
chr8:143806153 | T | C | 2 | a0002c0002t0001g0030 a0029c0034t0001g0208 |
4 | HG02155.hp1 NA18959.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.2346+254A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 18/36 | chr8 | 143806153 | |||||||
chr8:143806273 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2346+134G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 18/36 | chr8 | 143806273 | |||||||
chr8:143806497 | C | T | 1 | a0002c0002t0001g0171 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2269-13G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 17/36 | chr8 | 143806497 | |||||||
chr8:143806647 | G | A | 6 | a0002c0030t0001g0062 a0004c0007t0001g0034 a0004c0007t0001g0217 others(3): Show |
9 | HG00733.hp2 HG00741.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.2269-163C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 17/36 | chr8 | 143806647 | |||||||
chr8:143806768 | T | C | 1 | a0023c0056t0001g0077 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2268+156A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 17/36 | chr8 | 143806768 | |||||||
chr8:143806841 | G | A | 1 | a0002c0042t0001g0212 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2268+83C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 17/36 | chr8 | 143806841 | |||||||
chr8:143806880 | G | A | 2 | a0001c0001t0001g0138 a0001c0004t0001g0139 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2268+44C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 17/36 | chr8 | 143806880 | |||||||
chr8:143806897 | G | A | 7 | a0002c0008t0001g0035 a0002c0008t0001g0070 a0002c0008t0001g0073 others(4): Show |
8 | HG01109.hp1 HG01175.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2268+27C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 17/36 | chr8 | 143806897 | |||||||
chr8:143807120 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0105 a0033c0065t0001g0155 |
5 | HG02155.hp2 NA18954.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.2179-107C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 16/36 | chr8 | 143807120 | |||||||
chr8:143807122 | C | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0083 a0001c0001t0001g0105 others(1): Show |
6 | HG02129.hp1 HG02155.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.2179-109G>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 16/36 | chr8 | 143807122 | |||||||
chr8:143807223 | T | C | 1 | a0025c0032t0001g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2179-210A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 16/36 | chr8 | 143807223 | |||||||
chr8:143807262 | C | T | 1 | a0032c0045t0001g0095 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2179-249G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 16/36 | chr8 | 143807262 | |||||||
chr8:143807337 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2178+215C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 16/36 | chr8 | 143807337 | |||||||
chr8:143807449 | G | A | 1 | a0002c0008t0001g0231 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2178+103C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 16/36 | chr8 | 143807449 | |||||||
chr8:143807541 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2178+11C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 16/36 | chr8 | 143807541 | |||||||
chr8:143807689 | G | C | 1 | a0029c0034t0001g0208 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2116-75C>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143807689 | |||||||
chr8:143807731 | C | T | 7 | a0002c0022t0001g0169 a0002c0030t0001g0062 a0004c0007t0001g0034 others(4): Show |
10 | HG00408.hp2 HG00733.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.2116-117G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143807731 | |||||||
chr8:143807732 | G | A | 6 | a0002c0002t0001g0196 a0002c0002t0001g0197 a0002c0002t0001g0198 others(3): Show |
7 | HG01975.hp2 HG02109.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2116-118C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143807732 | |||||||
chr8:143807791 | A | T | 1 | a0001c0001t0001g0014 | 3 | HG02602.hp1 HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2116-177T>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143807791 | |||||||
chr8:143807850 | C | T | 4 | a0001c0004t0001g0010 a0001c0004t0001g0075 a0001c0004t0001g0104 others(1): Show |
8 | HG02818.hp1 HG02965.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.2116-236G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143807850 | |||||||
chr8:143807893 | A | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(232): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.2116-279T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143807893 | |||||||
chr8:143807918 | T | G | 1 | a0005c0073t0001g0222 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2116-304A>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143807918 | |||||||
chr8:143807925 | C | T | 3 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0026t0002g0063 |
4 | HG02280.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2116-311G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143807925 | |||||||
chr8:143808065 | G | A | 2 | a0002c0012t0001g0016 a0002c0012t0001g0094 |
4 | HG02145.hp2 HG02622.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2116-451C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143808065 | |||||||
chr8:143808171 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2115+438G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143808171 | |||||||
chr8:143808195 | G | A | 2 | a0002c0002t0001g0202 a0003c0003t0001g0201 |
2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2115+414C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143808195 | |||||||
chr8:143808288 | C | CACTGAGA others(34): Show |
1 | a0002c0008t0001g0231 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2115+280_2115+320d others(43): Show |
SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143808288 | |||||||
chr8:143808288 | C | CACTGAGA others(75): Show |
9 | a0002c0002t0001g0086 a0002c0008t0001g0035 a0002c0008t0001g0070 others(6): Show |
10 | HG01109.hp1 HG01175.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2115+239_2115+320d others(84): Show |
SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143808288 | |||||||
chr8:143808288 | C | CACTGAGA others(116): Show |
1 | a0034c0074t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2115+320_2115+321i others(125): Show |
SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143808288 | |||||||
chr8:143808288 | CACTGAGA others(34): Show |
C | 1 | a0002c0002t0001g0200 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2115+280_2115+320d others(43): Show |
SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143808288 | |||||||
chr8:143808306 | G | A | 1 | a0004c0040t0001g0199 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2115+303C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143808306 | |||||||
chr8:143808358 | G | GGTCCAAG others(116): Show |
1 | a0023c0056t0001g0077 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2115+250_2115+251i others(125): Show |
SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143808358 | |||||||
chr8:143808382 | CGCCAGGG others(34): Show |
C | 1 | a0013c0024t0001g0058 | 2 | NA18951.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2115+186_2115+226d others(43): Show |
SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143808382 | |||||||
chr8:143808399 | A | AGTCCAAG others(198): Show |
6 | a0002c0030t0001g0062 a0004c0007t0001g0034 a0004c0007t0001g0217 others(3): Show |
9 | HG00733.hp2 HG00741.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.2115+209_2115+210i others(207): Show |
SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143808399 | |||||||
chr8:143808399 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(136): Show |
209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.2115+210T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143808399 | |||||||
chr8:143808423 | T | C | 8 | a0002c0002t0001g0191 a0002c0030t0001g0062 a0004c0007t0001g0034 others(5): Show |
11 | HG00733.hp2 HG00741.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.2115+186A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 15/36 | chr8 | 143808423 | |||||||
chr8:143809100 | T | G | 2 | a0001c0001t0001g0023 a0033c0065t0001g0155 |
4 | NA18954.hp2 NA18966.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1699-75A>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 14/36 | chr8 | 143809100 | |||||||
chr8:143809258 | G | C | 2 | a0002c0002t0001g0008 a0002c0002t0005g0237 |
7 | HG00438.hp1 NA18948.hp1 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.1699-233C>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 14/36 | chr8 | 143809258 | |||||||
chr8:143809303 | G | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0101 others(1): Show |
9 | HG00597.hp2 HG00609.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1698+248C>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 14/36 | chr8 | 143809303 | |||||||
chr8:143809345 | C | A | 1 | a0002c0002t0001g0236 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1698+206G>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 14/36 | chr8 | 143809345 | |||||||
chr8:143809726 | G | A | 1 | a0014c0057t0001g0143 | 1 | HG00609.hp2 | splice_region_variant&intron_variant | LOW | c.1531-8C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 13/36 | chr8 | 143809726 | |||||||
chr8:143809923 | C | T | 1 | a0001c0004t0001g0099 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1531-205G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 13/36 | chr8 | 143809923 | |||||||
chr8:143809946 | G | A | 2 | a0002c0002t0001g0202 a0003c0003t0001g0201 |
2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1531-228C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 13/36 | chr8 | 143809946 | |||||||
chr8:143810041 | A | C | 8 | a0001c0011t0001g0015 a0001c0011t0001g0147 a0001c0011t0001g0148 others(5): Show |
12 | HG01891.hp2 HG02572.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1531-323T>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 13/36 | chr8 | 143810041 | |||||||
chr8:143810111 | G | A | 3 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0026t0002g0063 |
4 | HG02280.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1530+368C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 13/36 | chr8 | 143810111 | |||||||
chr8:143810295 | G | A | 1 | a0001c0001t0001g0045 | 2 | HG00099.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.1530+184C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 13/36 | chr8 | 143810295 | |||||||
chr8:143810361 | T | C | 1 | a0002c0008t0001g0231 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1530+118A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 13/36 | chr8 | 143810361 | |||||||
chr8:143810421 | C | T | 1 | a0002c0002t0001g0168 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1530+58G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 13/36 | chr8 | 143810421 | |||||||
chr8:143810871 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1273+35G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 11/36 | chr8 | 143810871 | |||||||
chr8:143810888 | C | T | 4 | a0002c0008t0001g0035 a0002c0008t0001g0070 a0002c0021t0001g0069 others(1): Show |
5 | HG01109.hp1 HG01175.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1273+18G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 11/36 | chr8 | 143810888 | |||||||
chr8:143811086 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1107-14C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 10/36 | chr8 | 143811086 | |||||||
chr8:143811359 | G | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0158 a0035c0054t0001g0159 |
4 | NA18940.hp1 NA18952.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.907-14C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143811359 | |||||||
chr8:143811361 | A | G | 6 | a0002c0008t0001g0035 a0002c0008t0001g0070 a0002c0008t0001g0073 others(3): Show |
7 | HG01109.hp1 HG01175.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.907-16T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143811361 | |||||||
chr8:143811442 | G | T | 1 | a0003c0003t0006g0238 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.907-97C>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143811442 | |||||||
chr8:143811476 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.907-131G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143811476 | |||||||
chr8:143811499 | A | C | 1 | a0002c0002t0001g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.907-154T>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143811499 | |||||||
chr8:143811564 | T | C | 1 | a0002c0008t0001g0231 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.907-219A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143811564 | |||||||
chr8:143811676 | CCT | C | 2 | a0001c0013t0001g0025 a0001c0013t0001g0160 |
4 | HG02886.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.907-333_907-332del others(2): Show |
SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143811676 | |||||||
chr8:143811780 | A | G | 1 | a0002c0006t0001g0163 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.907-435T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143811780 | |||||||
chr8:143811845 | T | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(217): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.906+421A>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143811845 | |||||||
chr8:143811932 | T | C | 1 | a0002c0002t0001g0207 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.906+334A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143811932 | |||||||
chr8:143812014 | G | A | 1 | a0002c0002t0001g0060 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.906+252C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143812014 | |||||||
chr8:143812056 | G | A | 1 | a0029c0034t0001g0208 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.906+210C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143812056 | |||||||
chr8:143812062 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.906+204G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143812062 | |||||||
chr8:143812088 | C | T | 1 | a0001c0068t0001g0065 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.906+178G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143812088 | |||||||
chr8:143812095 | G | A | 1 | a0002c0002t0001g0209 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.906+171C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143812095 | |||||||
chr8:143812177 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.906+89G>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143812177 | |||||||
chr8:143812180 | C | A | 1 | a0001c0001t0001g0235 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.906+86G>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143812180 | |||||||
chr8:143812227 | G | A | 1 | a0003c0005t0001g0210 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.906+39C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143812227 | |||||||
chr8:143812230 | G | A | 1 | a0003c0003t0006g0238 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.906+36C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 9/36 | chr8 | 143812230 | |||||||
chr8:143812398 | G | A | 1 | a0001c0071t0001g0215 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.788-14C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 8/36 | chr8 | 143812398 | |||||||
chr8:143812436 | C | G | 2 | a0002c0006t0001g0163 a0034c0074t0001g0074 |
2 | HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.788-52G>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 8/36 | chr8 | 143812436 | |||||||
chr8:143812463 | A | G | 8 | a0002c0006t0001g0163 a0002c0008t0001g0035 a0002c0008t0001g0070 others(5): Show |
9 | HG01109.hp1 HG01175.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.788-79T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 8/36 | chr8 | 143812463 | |||||||
chr8:143812471 | C | T | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(232): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.788-87G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 8/36 | chr8 | 143812471 | |||||||
chr8:143812497 | G | A | 1 | a0002c0002t0001g0061 | 2 | NA18952.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.788-113C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 8/36 | chr8 | 143812497 | |||||||
chr8:143812510 | G | C | 1 | a0009c0019t0001g0162 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.788-126C>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 8/36 | chr8 | 143812510 | |||||||
chr8:143812532 | C | CT | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(217): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.788-149_788-148ins others(1): Show |
SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 8/36 | chr8 | 143812532 | |||||||
chr8:143812533 | C | CT | 6 | a0002c0008t0001g0035 a0002c0008t0001g0070 a0002c0008t0001g0073 others(3): Show |
7 | HG01109.hp1 HG01175.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.788-150_788-149ins others(1): Show |
SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 8/36 | chr8 | 143812533 | |||||||
chr8:143812605 | G | C | 1 | a0002c0002t0001g0211 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.787+212C>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 8/36 | chr8 | 143812605 | |||||||
chr8:143812703 | G | A | 1 | a0001c0001t0001g0002 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.787+114C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 8/36 | chr8 | 143812703 | |||||||
chr8:143813121 | A | G | 7 | a0002c0008t0001g0035 a0002c0008t0001g0070 a0002c0008t0001g0073 others(4): Show |
8 | HG01109.hp1 HG01109.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.568-17T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 6/36 | chr8 | 143813121 | |||||||
chr8:143813127 | T | G | 1 | a0004c0007t0001g0220 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.568-23A>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 6/36 | chr8 | 143813127 | |||||||
chr8:143813190 | A | G | 1 | a0001c0011t0001g0015 | 3 | HG02647.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.568-86T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 6/36 | chr8 | 143813190 | |||||||
chr8:143813212 | C | T | 2 | a0001c0001t0001g0036 a0020c0067t0001g0081 |
3 | HG02258.hp2 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.567+99G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 6/36 | chr8 | 143813212 | |||||||
chr8:143813307 | G | A | 1 | a0002c0042t0001g0212 | 1 | NA18990.hp1 | splice_region_variant&intron_variant | LOW | c.567+4C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 6/36 | chr8 | 143813307 | |||||||
chr8:143813308 | C | A | 1 | a0002c0002t0001g0213 | 1 | HG00597.hp1 | splice_region_variant&intron_variant | LOW | c.567+3G>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 6/36 | chr8 | 143813308 | |||||||
chr8:143813383 | G | A | 86 | a0001c0001t0001g0059 a0001c0009t0001g0031 a0001c0009t0001g0203 others(83): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.504-9C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 5/36 | chr8 | 143813383 | |||||||
chr8:143813428 | T | C | 1 | a0004c0007t0001g0034 | 3 | NA18972.hp1 NA18974.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.503+42A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 5/36 | chr8 | 143813428 | |||||||
chr8:143813753 | G | A | 1 | a0002c0002t0001g0221 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.357-27C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 3/36 | chr8 | 143813753 | |||||||
chr8:143813799 | A | C | 1 | a0030c0069t0001g0079 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.356+19T>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 3/36 | chr8 | 143813799 | |||||||
chr8:143813801 | C | A | 1 | a0030c0069t0001g0079 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.356+17G>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 3/36 | chr8 | 143813801 | |||||||
chr8:143813802 | A | C | 1 | a0030c0069t0001g0079 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.356+16T>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 3/36 | chr8 | 143813802 | |||||||
chr8:143813924 | T | C | 1 | a0001c0004t0001g0223 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.278-28A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 2/36 | chr8 | 143813924 | |||||||
chr8:143814138 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.160-20C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143814138 | |||||||
chr8:143814260 | G | A | 1 | a0023c0056t0001g0077 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.160-142C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143814260 | |||||||
chr8:143814289 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.160-171T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143814289 | |||||||
chr8:143814356 | G | A | 1 | a0002c0002t0001g0004 | 7 | HG00558.hp1 NA18941.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-238C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143814356 | |||||||
chr8:143814363 | G | A | 1 | a0003c0003t0001g0225 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.160-245C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143814363 | |||||||
chr8:143814413 | G | T | 2 | a0001c0029t0001g0076 a0023c0056t0001g0077 |
2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.160-295C>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143814413 | |||||||
chr8:143814501 | T | G | 1 | a0001c0001t0001g0226 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.160-383A>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143814501 | |||||||
chr8:143814564 | G | A | 2 | a0001c0001t0001g0227 a0002c0006t0001g0228 |
2 | HG03492.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.160-446C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143814564 | |||||||
chr8:143814568 | G | A | 1 | a0002c0002t0001g0229 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.160-450C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143814568 | |||||||
chr8:143814622 | G | T | 1 | a0001c0004t0001g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.160-504C>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143814622 | |||||||
chr8:143814688 | A | G | 8 | a0002c0008t0001g0035 a0002c0008t0001g0070 a0002c0008t0001g0073 others(5): Show |
9 | HG01109.hp1 HG01175.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.159+526T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143814688 | |||||||
chr8:143814692 | C | T | 1 | a0002c0006t0001g0068 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.159+522G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143814692 | |||||||
chr8:143814722 | C | T | 1 | a0002c0002t0001g0067 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.159+492G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143814722 | |||||||
chr8:143814782 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.159+432C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143814782 | |||||||
chr8:143814831 | C | T | 1 | a0002c0008t0001g0231 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.159+383G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143814831 | |||||||
chr8:143814914 | A | G | 1 | a0002c0002t0001g0066 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.159+300T>C | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143814914 | |||||||
chr8:143814955 | C | T | 1 | a0001c0068t0001g0065 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.159+259G>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143814955 | |||||||
chr8:143814978 | G | A | 1 | a0002c0008t0001g0231 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.159+236C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143814978 | |||||||
chr8:143815060 | G | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
9 | NA18951.hp1 NA18966.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+154C>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143815060 | |||||||
chr8:143815078 | T | C | 1 | a0007c0014t0001g0064 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.159+136A>G | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143815078 | |||||||
chr8:143815079 | G | T | 1 | a0007c0014t0001g0064 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.159+135C>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143815079 | |||||||
chr8:143815107 | G | T | 1 | a0001c0001t0001g0014 | 3 | HG02602.hp1 HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.159+107C>A | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143815107 | |||||||
chr8:143815173 | G | A | 1 | a0002c0002t0001g0236 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.159+41C>T | SCRIB | ENSG00000180900.20 | transcript | ENST00000356994.7 | protein_coding | 1/36 | chr8 | 143815173 |