Item | Value |
---|---|
geneid | 1508 |
ensemblid | ENSG00000164733.23 |
hgncid | 2527 |
symbol | CTSB |
name | cathepsin B |
refseq_nuc | NM_001908.5 |
refseq_prot | NP_001899.1 |
ensembl_nuc | ENST00000353047.11 |
ensembl_prot | ENSP00000345672.5 |
mane_status | MANE Select |
chr | chr8 |
start | 11842524 |
end | 11868087 |
strand | - |
ver | v1.2 |
region | chr8:11842524-11868087 |
region5000 | chr8:11837524-11873087 |
regionname0 | CTSB_chr8_11842524_11868087 |
regionname5000 | CTSB_chr8_11837524_11873087 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 339 | 226 | 51 | 44 | 91 | 11 | 28 | 70 | CTSB_chr8_11837524_11873087 | CTSB | MWQLW others(334): Show |
chr8 | 11837524 | 11873087 |
a0002 | 0/0 | 339 | 162 | 26 | 24 | 91 | 2 | 19 | 72 | CTSB_chr8_11837524_11873087 | CTSB | MWQLW others(334): Show |
chr8 | 11837524 | 11873087 |
a0003 | 0/0 | 339 | 17 | 17 | 0 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | MWQLW others(334): Show |
chr8 | 11837524 | 11873087 |
a0004 | 0/1 | 339 | 16 | 2 | 10 | 0 | 3 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | MWQLW others(334): Show |
chr8 | 11837524 | 11873087 |
a0005 | 0/0 | 339 | 7 | 0 | 0 | 7 | 0 | 0 | 7 | CTSB_chr8_11837524_11873087 | CTSB | MWQLW others(334): Show |
chr8 | 11837524 | 11873087 |
a0006 | 0/0 | 339 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CTSB_chr8_11837524_11873087 | CTSB | MWQLW others(334): Show |
chr8 | 11837524 | 11873087 |
a0007 | 0/0 | 339 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | MWQLW others(334): Show |
chr8 | 11837524 | 11873087 |
a0008 | 0/0 | 339 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CTSB_chr8_11837524_11873087 | CTSB | MWQLW others(334): Show |
chr8 | 11837524 | 11873087 |
a0009 | 0/0 | 339 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | MWQLW others(334): Show |
chr8 | 11837524 | 11873087 |
a0010 | 0/0 | 339 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | MWQLW others(334): Show |
chr8 | 11837524 | 11873087 |
a0011 | 0/0 | 339 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | MWQLW others(334): Show |
chr8 | 11837524 | 11873087 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1017 | 160 | 15 | 30 | 90 | 6 | 18 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0001c0003 | 0/0 | 1017 | 40 | 19 | 8 | 1 | 4 | 8 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0001c0004 | 0/0 | 1017 | 21 | 12 | 6 | 0 | 1 | 2 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0001c0010 | 0/0 | 1017 | 4 | 4 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0001c0018 | 0/0 | 1017 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0002c0002 | 0/0 | 1017 | 153 | 25 | 19 | 89 | 2 | 18 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0002c0006 | 0/0 | 1017 | 7 | 1 | 4 | 1 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0002c0016 | 0/0 | 1017 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0002c0022 | 0/0 | 1017 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0003c0008 | 0/0 | 1017 | 6 | 6 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0003c0009 | 0/0 | 1017 | 5 | 5 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0003c0011 | 0/0 | 1017 | 3 | 3 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0003c0012 | 0/0 | 1017 | 3 | 3 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0004c0005 | 0/1 | 1017 | 16 | 2 | 10 | 0 | 3 | 0 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0005c0007 | 0/0 | 1017 | 7 | 0 | 0 | 7 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0006c0013 | 0/0 | 1017 | 3 | 0 | 0 | 3 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0007c0017 | 0/0 | 1017 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0007c0021 | 0/0 | 1017 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0008c0014 | 0/0 | 1017 | 2 | 0 | 0 | 2 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0009c0019 | 0/0 | 1017 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0010c0015 | 0/0 | 1017 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 | ||
a0011c0020 | 0/0 | 1017 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | ATGTG others(1012): Show |
chr8 | 11837524 | 11873087 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 3730 | 62 | 5 | 15 | 26 | 3 | 13 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0003 | 0/0 | 3730 | 46 | 1 | 2 | 43 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0005 | 0/0 | 3731 | 2 | 0 | 2 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0007 | 0/0 | 3730 | 8 | 2 | 2 | 1 | 0 | 3 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0012 | 1/0 | 3733 | 5 | 3 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3728): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0015 | 0/0 | 3730 | 5 | 0 | 0 | 5 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0019 | 0/0 | 3730 | 4 | 0 | 3 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0027 | 0/0 | 3730 | 3 | 1 | 0 | 0 | 0 | 2 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0037 | 0/0 | 3730 | 2 | 0 | 0 | 0 | 2 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0038 | 0/0 | 3732 | 2 | 0 | 0 | 2 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3727): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0041 | 0/0 | 3730 | 2 | 0 | 0 | 2 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0042 | 0/0 | 3729 | 2 | 0 | 0 | 2 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3724): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0043 | 0/0 | 3729 | 2 | 0 | 0 | 2 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3724): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0044 | 0/0 | 3731 | 2 | 0 | 2 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0053 | 0/0 | 3730 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0058 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3728): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0072 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0073 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0075 | 0/0 | 3729 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3724): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0076 | 0/0 | 3730 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0078 | 0/0 | 3730 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0079 | 0/0 | 3729 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3724): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0080 | 0/0 | 3733 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3728): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0081 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0082 | 0/0 | 3731 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0083 | 0/0 | 3730 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0001t0085 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0003t0001 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0003t0003 | 0/0 | 3730 | 2 | 0 | 0 | 0 | 0 | 2 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0003t0004 | 0/0 | 3731 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0001c0003t0005 | 0/0 | 3731 | 11 | 1 | 4 | 0 | 3 | 3 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0001c0003t0009 | 0/0 | 3732 | 5 | 5 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3727): Show |
chr8 | 11837524 | 11873087 |
a0001c0003t0011 | 0/0 | 3731 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0001c0003t0013 | 0/0 | 3731 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0001c0003t0014 | 0/0 | 3729 | 5 | 5 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3724): Show |
chr8 | 11837524 | 11873087 |
a0001c0003t0018 | 0/0 | 3733 | 2 | 2 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3728): Show |
chr8 | 11837524 | 11873087 |
a0001c0003t0025 | 0/0 | 3732 | 3 | 3 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3727): Show |
chr8 | 11837524 | 11873087 |
a0001c0003t0035 | 0/0 | 3729 | 2 | 2 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3724): Show |
chr8 | 11837524 | 11873087 |
a0001c0003t0046 | 0/0 | 3732 | 2 | 0 | 1 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3727): Show |
chr8 | 11837524 | 11873087 |
a0001c0003t0047 | 0/0 | 3731 | 2 | 0 | 1 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0001c0003t0088 | 0/0 | 3731 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0001c0003t0089 | 0/0 | 3731 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0001c0004t0017 | 0/0 | 3732 | 5 | 0 | 4 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3727): Show |
chr8 | 11837524 | 11873087 |
a0001c0004t0028 | 0/0 | 3732 | 3 | 1 | 0 | 0 | 0 | 2 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3727): Show |
chr8 | 11837524 | 11873087 |
a0001c0004t0029 | 0/0 | 3744 | 3 | 3 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3739): Show |
chr8 | 11837524 | 11873087 |
a0001c0004t0034 | 0/0 | 3733 | 2 | 2 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3728): Show |
chr8 | 11837524 | 11873087 |
a0001c0004t0039 | 0/0 | 3733 | 2 | 2 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3728): Show |
chr8 | 11837524 | 11873087 |
a0001c0004t0054 | 0/0 | 3736 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3731): Show |
chr8 | 11837524 | 11873087 |
a0001c0004t0055 | 0/0 | 3735 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3730): Show |
chr8 | 11837524 | 11873087 |
a0001c0004t0077 | 0/0 | 3730 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0001c0004t0090 | 0/0 | 3731 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0001c0004t0092 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3728): Show |
chr8 | 11837524 | 11873087 |
a0001c0004t0096 | 0/0 | 3731 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0001c0010t0010 | 0/0 | 3731 | 4 | 4 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0001c0018t0010 | 0/0 | 3731 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0001 | 0/0 | 3730 | 86 | 0 | 9 | 70 | 1 | 6 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0002 | 0/0 | 3730 | 4 | 0 | 2 | 0 | 0 | 2 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0004 | 0/0 | 3731 | 6 | 4 | 0 | 0 | 0 | 2 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0006 | 0/0 | 3730 | 8 | 8 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0009 | 0/0 | 3732 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3727): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0011 | 0/0 | 3731 | 4 | 1 | 1 | 0 | 0 | 2 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0013 | 0/0 | 3731 | 3 | 0 | 1 | 1 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0016 | 0/0 | 3730 | 5 | 0 | 3 | 0 | 1 | 1 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0018 | 0/0 | 3733 | 2 | 2 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3728): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0022 | 0/0 | 3727 | 3 | 0 | 0 | 0 | 0 | 3 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3722): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0023 | 0/0 | 3731 | 3 | 3 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0026 | 0/0 | 3732 | 3 | 0 | 0 | 3 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3727): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0033 | 0/0 | 3731 | 2 | 2 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0036 | 0/0 | 3729 | 2 | 2 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3724): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0048 | 0/0 | 3733 | 2 | 2 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3728): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0050 | 0/0 | 3730 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0056 | 0/0 | 3732 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3727): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0059 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0060 | 0/0 | 3749 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3744): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0061 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0062 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0063 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0064 | 0/0 | 3730 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0065 | 0/0 | 3729 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3724): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0066 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0067 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0068 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0069 | 0/0 | 3730 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0070 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0071 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0074 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0084 | 0/0 | 3731 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0086 | 0/0 | 3728 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3723): Show |
chr8 | 11837524 | 11873087 |
a0002c0002t0087 | 0/0 | 3730 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0006t0002 | 0/0 | 3730 | 3 | 0 | 3 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0006t0003 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0006t0040 | 0/0 | 3731 | 2 | 0 | 1 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0002c0006t0095 | 0/0 | 3730 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0016t0001 | 0/0 | 3730 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0002c0022t0013 | 0/0 | 3731 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0003c0008t0020 | 0/0 | 3731 | 4 | 4 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0003c0008t0045 | 0/0 | 3733 | 2 | 2 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3728): Show |
chr8 | 11837524 | 11873087 |
a0003c0009t0021 | 0/0 | 3732 | 3 | 3 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3727): Show |
chr8 | 11837524 | 11873087 |
a0003c0009t0024 | 0/0 | 3730 | 2 | 2 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0003c0011t0024 | 0/0 | 3730 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0003c0011t0093 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3729): Show |
chr8 | 11837524 | 11873087 |
a0003c0011t0094 | 0/0 | 3730 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0003c0012t0031 | 0/0 | 3731 | 2 | 2 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0003c0012t0057 | 0/0 | 3735 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3730): Show |
chr8 | 11837524 | 11873087 |
a0004c0005t0004 | 0/1 | 3731 | 9 | 0 | 6 | 0 | 2 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0004c0005t0030 | 0/0 | 3731 | 2 | 2 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0004c0005t0032 | 0/0 | 3733 | 2 | 0 | 2 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3728): Show |
chr8 | 11837524 | 11873087 |
a0004c0005t0049 | 0/0 | 3731 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0004c0005t0052 | 0/0 | 3732 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3727): Show |
chr8 | 11837524 | 11873087 |
a0004c0005t0091 | 0/0 | 3731 | 1 | 0 | 0 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0005c0007t0008 | 0/0 | 3729 | 7 | 0 | 0 | 7 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3724): Show |
chr8 | 11837524 | 11873087 |
a0006c0013t0002 | 0/0 | 3730 | 3 | 0 | 0 | 3 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0007c0017t0051 | 0/0 | 3731 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3726): Show |
chr8 | 11837524 | 11873087 |
a0007c0021t0001 | 0/0 | 3730 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0008c0014t0002 | 0/0 | 3730 | 2 | 0 | 0 | 2 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0009c0019t0003 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0010c0015t0002 | 0/0 | 3730 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
a0011c0020t0001 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | GGCTG others(3725): Show |
chr8 | 11837524 | 11873087 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0002 | 0/0 | 17 | 0 | 6 | 9 | 0 | 2 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0005 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0005g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0007g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0007g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0007g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0007g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0007g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0007g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0007g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0012g0031 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0012g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0012g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0012g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0015g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0015g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0015g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0019g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0019g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0019g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0019g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0027g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0027g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0027g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0037g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0037g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0038g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0041g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0041g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0042g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0042g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0043g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0043g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0044g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0053g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0058g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0072g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0073g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0075g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0076g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0078g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0079g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0080g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0081g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0082g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0083g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0001t0085g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0003g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0005g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0005g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0005g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0005g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0005g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0005g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0005g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0005g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0005g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0009g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0009g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0009g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0009g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0009g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0011g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0013g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0014g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0014g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0014g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0014g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0014g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0018g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0018g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0025g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0025g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0035g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0035g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0046g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0046g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0047g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0047g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0088g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0003t0089g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0017g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0017g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0017g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0017g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0028g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0028g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0029g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0029g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0029g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0034g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0034g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0039g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0039g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0054g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0055g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0077g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0090g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0092g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0004t0096g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0010t0010g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0010t0010g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0001c0018t0010g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0001 | 0/0 | 20 | 0 | 6 | 12 | 1 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0004 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0006g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0009g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0011g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0011g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0011g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0013g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0013g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0013g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0016g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0016g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0016g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0016g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0018g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0018g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0022g0010 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0023g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0023g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0023g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0026g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0026g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0026g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0033g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0033g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0036g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0036g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0048g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0048g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0050g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0056g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0059g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0060g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0061g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0062g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0063g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0064g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0065g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0066g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0067g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0068g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0069g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0070g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0071g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0074g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0084g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0086g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0002t0087g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0006t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0006t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0006t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0006t0040g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0006t0040g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0006t0095g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0016t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0002c0022t0013g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0003c0008t0020g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0003c0008t0020g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0003c0008t0045g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0003c0009t0021g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0003c0009t0021g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0003c0009t0021g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0003c0009t0024g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0003c0009t0024g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0003c0011t0024g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0003c0011t0093g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0003c0011t0094g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0003c0012t0031g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0003c0012t0031g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0003c0012t0057g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0004c0005t0004g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0004c0005t0004g0178 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0004c0005t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0004c0005t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0004c0005t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0004c0005t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0004c0005t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0004c0005t0004g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0004c0005t0030g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0004c0005t0030g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0004c0005t0032g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0004c0005t0049g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0004c0005t0052g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0004c0005t0091g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0005c0007t0008g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0005c0007t0008g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0005c0007t0008g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0005c0007t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0005c0007t0008g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0005c0007t0008g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0005c0007t0008g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0006c0013t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0006c0013t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0006c0013t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0007c0017t0051g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0007c0021t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0008c0014t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0008c0014t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0009c0019t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0010c0015t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
a0011c0020t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0005 | g0304 | EUR | GBR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00099 | hp2 | a0004 | c0005 | t0004 | g0181 | EUR | GBR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0290 | EUR | GBR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | GBR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0256 | EUR | FIN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0246 | EUR | FIN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00323 | hp1 | a0001 | c0003 | t0005 | g0120 | EUR | FIN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00323 | hp2 | a0001 | c0001 | t0019 | g0282 | EUR | FIN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | CHS | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | CHS | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | CHS | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | CHS | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | CHS | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00558 | hp1 | a0002 | c0002 | t0066 | g0146 | EAS | CHS | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | CHS | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | CHS | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | CHS | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00639 | hp1 | a0001 | c0003 | t0005 | g0327 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0042 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00642 | hp1 | a0004 | c0005 | t0032 | g0025 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00642 | hp2 | a0001 | c0001 | t0078 | g0074 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | CHS | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00733 | hp1 | a0002 | c0002 | t0064 | g0083 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00733 | hp2 | a0002 | c0002 | t0011 | g0024 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00735 | hp1 | a0002 | c0002 | t0016 | g0014 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00735 | hp2 | a0004 | c0005 | t0032 | g0025 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00738 | hp1 | a0001 | c0001 | t0005 | g0028 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00738 | hp2 | a0002 | c0006 | t0002 | g0015 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00741 | hp1 | a0001 | c0001 | t0012 | g0235 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG00741 | hp2 | a0002 | c0006 | t0040 | g0094 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01070 | hp1 | a0002 | c0002 | t0016 | g0117 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01070 | hp2 | a0004 | c0005 | t0004 | g0038 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01071 | hp1 | a0002 | c0006 | t0002 | g0218 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01071 | hp2 | a0004 | c0005 | t0052 | g0314 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01081 | hp1 | a0002 | c0006 | t0002 | g0015 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01081 | hp2 | a0001 | c0001 | t0019 | g0322 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01099 | hp1 | a0001 | c0001 | t0007 | g0302 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01099 | hp2 | a0002 | c0016 | t0001 | g0075 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01106 | hp1 | a0004 | c0005 | t0004 | g0216 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01106 | hp2 | a0001 | c0004 | t0096 | g0332 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01109 | hp1 | a0001 | c0003 | t0004 | g0190 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01109 | hp2 | a0001 | c0001 | t0007 | g0303 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01168 | hp1 | a0001 | c0004 | t0090 | g0331 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01168 | hp2 | a0002 | c0002 | t0016 | g0014 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01169 | hp1 | a0001 | c0004 | t0017 | g0330 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01175 | hp1 | a0004 | c0005 | t0004 | g0038 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01175 | hp2 | a0001 | c0003 | t0089 | g0313 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01243 | hp1 | a0001 | c0004 | t0017 | g0333 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0028 | AMR | PUR | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01255 | hp1 | a0004 | c0005 | t0004 | g0219 | AMR | CLM | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01256 | hp1 | a0001 | c0004 | t0017 | g0040 | AMR | CLM | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01256 | hp2 | a0001 | c0003 | t0005 | g0069 | AMR | CLM | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01258 | hp1 | a0001 | c0001 | t0044 | g0034 | AMR | CLM | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01258 | hp2 | a0001 | c0004 | t0017 | g0040 | AMR | CLM | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01261 | hp1 | a0004 | c0005 | t0004 | g0213 | AMR | CLM | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01358 | hp1 | a0001 | c0003 | t0047 | g0325 | AMR | CLM | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01358 | hp2 | a0002 | c0002 | t0050 | g0099 | AMR | CLM | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0088 | AMR | CLM | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01361 | hp2 | a0001 | c0003 | t0005 | g0264 | AMR | CLM | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01433 | hp1 | a0001 | c0001 | t0044 | g0034 | AMR | CLM | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0269 | AMR | CLM | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01496 | hp1 | a0004 | c0005 | t0049 | g0212 | AMR | CLM | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01496 | hp2 | a0004 | c0005 | t0004 | g0180 | AMR | CLM | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01515 | hp1 | a0001 | c0003 | t0047 | g0192 | EUR | IBS | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01515 | hp2 | a0001 | c0001 | t0037 | g0248 | EUR | IBS | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01517 | hp1 | a0001 | c0001 | t0037 | g0247 | EUR | IBS | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01517 | hp2 | a0001 | c0003 | t0005 | g0230 | EUR | IBS | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01891 | hp1 | a0002 | c0002 | t0004 | g0046 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01891 | hp2 | a0001 | c0010 | t0010 | g0008 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0087 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01934 | hp2 | a0001 | c0003 | t0005 | g0067 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01975 | hp2 | a0002 | c0002 | t0087 | g0320 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01978 | hp1 | a0001 | c0001 | t0082 | g0291 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01978 | hp2 | a0001 | c0003 | t0046 | g0229 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0308 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01981 | hp2 | a0002 | c0002 | t0013 | g0082 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01993 | hp2 | a0001 | c0001 | t0019 | g0284 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02004 | hp2 | a0001 | c0001 | t0019 | g0255 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02055 | hp1 | a0001 | c0003 | t0005 | g0233 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02055 | hp2 | a0001 | c0003 | t0014 | g0176 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02080 | hp1 | a0002 | c0002 | t0084 | g0108 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02080 | hp2 | a0002 | c0002 | t0062 | g0103 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02129 | hp1 | a0001 | c0001 | t0007 | g0301 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02135 | hp1 | a0002 | c0002 | t0068 | g0071 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02135 | hp2 | a0002 | c0002 | t0067 | g0063 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02145 | hp1 | a0003 | c0012 | t0057 | g0158 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02155 | hp1 | a0001 | c0001 | t0073 | g0232 | EAS | CDX | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | CDX | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02165 | hp1 | a0002 | c0002 | t0059 | g0091 | EAS | CDX | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02257 | hp1 | a0001 | c0003 | t0009 | g0286 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0277 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02258 | hp1 | a0001 | c0004 | t0039 | g0317 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02258 | hp2 | a0003 | c0008 | t0020 | g0160 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02273 | hp1 | a0001 | c0001 | t0083 | g0279 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02280 | hp1 | a0001 | c0001 | t0027 | g0250 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02280 | hp2 | a0003 | c0011 | t0093 | g0342 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02451 | hp1 | a0002 | c0002 | t0036 | g0153 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02451 | hp2 | a0003 | c0012 | t0031 | g0157 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02523 | hp2 | a0009 | c0019 | t0003 | g0258 | EAS | KHV | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02572 | hp2 | a0002 | c0002 | t0004 | g0051 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0310 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02602 | hp2 | a0002 | c0002 | t0016 | g0090 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02615 | hp2 | a0001 | c0003 | t0009 | g0174 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02622 | hp1 | a0003 | c0009 | t0021 | g0220 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02622 | hp2 | a0002 | c0002 | t0006 | g0170 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02630 | hp1 | a0001 | c0004 | t0039 | g0316 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02630 | hp2 | a0001 | c0001 | t0007 | g0027 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02647 | hp1 | a0004 | c0005 | t0030 | g0215 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02647 | hp2 | a0003 | c0012 | t0031 | g0159 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0048 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0285 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02698 | hp1 | a0001 | c0003 | t0088 | g0191 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0194 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02717 | hp1 | a0001 | c0003 | t0018 | g0237 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02717 | hp2 | a0002 | c0002 | t0036 | g0149 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02723 | hp1 | a0002 | c0002 | t0048 | g0339 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02723 | hp2 | a0001 | c0004 | t0028 | g0334 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02735 | hp2 | a0002 | c0002 | t0069 | g0122 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02738 | hp1 | a0002 | c0002 | t0011 | g0207 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02738 | hp2 | a0001 | c0001 | t0007 | g0329 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02809 | hp1 | a0001 | c0001 | t0012 | g0294 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02809 | hp2 | a0003 | c0011 | t0094 | g0337 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02818 | hp1 | a0007 | c0021 | t0001 | g0136 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02818 | hp2 | a0002 | c0002 | t0004 | g0050 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02886 | hp1 | a0001 | c0004 | t0055 | g0057 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02886 | hp2 | a0003 | c0009 | t0021 | g0172 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02895 | hp1 | a0002 | c0002 | t0006 | g0022 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02895 | hp2 | a0001 | c0003 | t0025 | g0023 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02896 | hp1 | a0001 | c0001 | t0058 | g0228 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02896 | hp2 | a0001 | c0004 | t0029 | g0343 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02897 | hp1 | a0002 | c0002 | t0006 | g0022 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02897 | hp2 | a0001 | c0004 | t0029 | g0344 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02922 | hp1 | a0003 | c0008 | t0045 | g0020 | AFR | ESN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02922 | hp2 | a0002 | c0002 | t0006 | g0168 | AFR | ESN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02965 | hp1 | a0001 | c0003 | t0009 | g0175 | AFR | ESN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02965 | hp2 | a0001 | c0001 | t0012 | g0031 | AFR | ESN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02970 | hp1 | a0002 | c0002 | t0033 | g0323 | AFR | ESN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02970 | hp2 | a0001 | c0004 | t0092 | g0338 | AFR | ESN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | ESN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02976 | hp2 | a0001 | c0018 | t0010 | g0200 | AFR | ESN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03041 | hp1 | a0003 | c0009 | t0024 | g0197 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03041 | hp2 | a0002 | c0002 | t0006 | g0166 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03098 | hp1 | a0001 | c0004 | t0054 | g0319 | AFR | MSL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03098 | hp2 | a0002 | c0002 | t0048 | g0341 | AFR | MSL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03130 | hp1 | a0001 | c0010 | t0010 | g0008 | AFR | ESN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03130 | hp2 | a0001 | c0001 | t0053 | g0289 | AFR | ESN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03139 | hp1 | a0007 | c0017 | t0051 | g0041 | AFR | ESN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03139 | hp2 | a0002 | c0002 | t0023 | g0056 | AFR | ESN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03195 | hp1 | a0003 | c0008 | t0045 | g0020 | AFR | ESN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03195 | hp2 | a0002 | c0002 | t0023 | g0054 | AFR | ESN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03209 | hp1 | a0003 | c0009 | t0024 | g0196 | AFR | MSL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03209 | hp2 | a0001 | c0003 | t0014 | g0043 | AFR | MSL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03225 | hp1 | a0002 | c0002 | t0018 | g0260 | AFR | MSL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03225 | hp2 | a0001 | c0004 | t0034 | g0209 | AFR | MSL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03239 | hp1 | a0001 | c0003 | t0005 | g0193 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03453 | hp1 | a0001 | c0003 | t0014 | g0052 | AFR | MSL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03453 | hp2 | a0001 | c0004 | t0077 | g0266 | AFR | MSL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | MSL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03486 | hp2 | a0001 | c0004 | t0034 | g0186 | AFR | MSL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03490 | hp1 | a0001 | c0001 | t0007 | g0223 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03490 | hp2 | a0002 | c0002 | t0022 | g0010 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03491 | hp1 | a0001 | c0003 | t0003 | g0012 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03491 | hp2 | a0001 | c0001 | t0027 | g0124 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03492 | hp1 | a0002 | c0002 | t0022 | g0010 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03492 | hp2 | a0001 | c0003 | t0003 | g0012 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03516 | hp1 | a0003 | c0011 | t0024 | g0049 | AFR | ESN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03516 | hp2 | a0001 | c0003 | t0014 | g0150 | AFR | ESN | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03540 | hp1 | a0001 | c0003 | t0018 | g0165 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03540 | hp2 | a0001 | c0010 | t0010 | g0199 | AFR | GWD | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03579 | hp1 | a0001 | c0003 | t0014 | g0053 | AFR | MSL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03579 | hp2 | a0002 | c0002 | t0033 | g0324 | AFR | MSL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03654 | hp2 | a0002 | c0002 | t0011 | g0024 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03669 | hp2 | a0002 | c0002 | t0022 | g0010 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03688 | hp1 | a0001 | c0001 | t0027 | g0278 | SAS | STU | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03688 | hp2 | a0001 | c0003 | t0046 | g0187 | SAS | STU | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03704 | hp1 | a0002 | c0006 | t0040 | g0214 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0079 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03710 | hp2 | a0001 | c0004 | t0028 | g0039 | SAS | PJL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | BEB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03834 | hp1 | a0001 | c0001 | t0007 | g0222 | SAS | BEB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03834 | hp2 | a0001 | c0003 | t0005 | g0189 | SAS | BEB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | BEB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03927 | hp2 | a0002 | c0002 | t0004 | g0045 | SAS | BEB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03942 | hp1 | a0001 | c0003 | t0011 | g0206 | SAS | BEB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0066 | SAS | BEB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG04115 | hp1 | a0010 | c0015 | t0002 | g0309 | SAS | STU | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG04115 | hp2 | a0001 | c0003 | t0005 | g0195 | SAS | STU | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG04184 | hp1 | a0002 | c0002 | t0013 | g0102 | SAS | BEB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | BEB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0047 | SAS | STU | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0276 | SAS | STU | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG04204 | hp1 | a0001 | c0004 | t0028 | g0039 | SAS | STU | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | STU | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG04228 | hp1 | a0002 | c0002 | t0004 | g0044 | SAS | STU | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0027 | AFR | YRI | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18522 | hp2 | a0001 | c0010 | t0010 | g0008 | AFR | YRI | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | CHB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18612 | hp2 | a0011 | c0020 | t0001 | g0076 | EAS | CHB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18747 | hp1 | a0002 | c0006 | t0003 | g0259 | EAS | CHB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | CHB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18906 | hp1 | a0001 | c0003 | t0009 | g0148 | AFR | YRI | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18906 | hp2 | a0003 | c0008 | t0020 | g0007 | AFR | YRI | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18939 | hp2 | a0005 | c0007 | t0008 | g0205 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18941 | hp2 | a0001 | c0001 | t0085 | g0227 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18942 | hp2 | a0001 | c0001 | t0043 | g0297 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18943 | hp2 | a0005 | c0007 | t0008 | g0202 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18946 | hp1 | a0001 | c0001 | t0015 | g0009 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18947 | hp2 | a0002 | c0002 | t0026 | g0307 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18950 | hp1 | a0005 | c0007 | t0008 | g0203 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18951 | hp1 | a0001 | c0001 | t0038 | g0037 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18954 | hp1 | a0001 | c0001 | t0043 | g0293 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18957 | hp1 | a0008 | c0014 | t0002 | g0183 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18959 | hp2 | a0001 | c0001 | t0080 | g0224 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18970 | hp2 | a0002 | c0002 | t0063 | g0106 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18972 | hp2 | a0001 | c0001 | t0042 | g0123 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18973 | hp1 | a0001 | c0001 | t0038 | g0037 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18973 | hp2 | a0006 | c0013 | t0002 | g0236 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18982 | hp2 | a0002 | c0002 | t0065 | g0107 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18984 | hp1 | a0002 | c0002 | t0070 | g0084 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18984 | hp2 | a0001 | c0001 | t0015 | g0273 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18986 | hp2 | a0001 | c0001 | t0015 | g0009 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18987 | hp1 | a0005 | c0007 | t0008 | g0201 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18987 | hp2 | a0002 | c0002 | t0060 | g0068 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18988 | hp1 | a0002 | c0002 | t0026 | g0306 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18988 | hp2 | a0008 | c0014 | t0002 | g0182 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18993 | hp1 | a0002 | c0002 | t0013 | g0077 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18993 | hp2 | a0002 | c0002 | t0061 | g0305 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18994 | hp1 | a0005 | c0007 | t0008 | g0208 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18997 | hp1 | a0001 | c0001 | t0041 | g0154 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18997 | hp2 | a0002 | c0002 | t0071 | g0104 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18999 | hp2 | a0002 | c0002 | t0056 | g0144 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19003 | hp2 | a0002 | c0022 | t0013 | g0081 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19005 | hp2 | a0002 | c0002 | t0086 | g0072 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19009 | hp1 | a0001 | c0001 | t0015 | g0009 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19010 | hp1 | a0002 | c0002 | t0026 | g0312 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19012 | hp2 | a0001 | c0001 | t0015 | g0263 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19030 | hp1 | a0003 | c0008 | t0020 | g0007 | AFR | LWK | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19030 | hp2 | a0001 | c0004 | t0029 | g0345 | AFR | LWK | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19043 | hp1 | a0002 | c0002 | t0006 | g0167 | AFR | LWK | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19043 | hp2 | a0002 | c0002 | t0004 | g0164 | AFR | LWK | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19056 | hp1 | a0001 | c0001 | t0079 | g0268 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19057 | hp1 | a0002 | c0002 | t0074 | g0111 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19060 | hp2 | a0006 | c0013 | t0002 | g0318 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19063 | hp2 | a0001 | c0001 | t0081 | g0252 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0321 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19066 | hp2 | a0005 | c0007 | t0008 | g0315 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19068 | hp1 | a0006 | c0013 | t0002 | g0198 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19070 | hp1 | a0001 | c0003 | t0001 | g0110 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19079 | hp1 | a0001 | c0001 | t0042 | g0244 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19080 | hp1 | a0001 | c0001 | t0072 | g0272 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19081 | hp2 | a0005 | c0007 | t0008 | g0204 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19086 | hp1 | a0001 | c0001 | t0075 | g0133 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19086 | hp2 | a0001 | c0001 | t0041 | g0243 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19240 | hp1 | a0002 | c0002 | t0018 | g0163 | AFR | YRI | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA19240 | hp2 | a0001 | c0003 | t0035 | g0151 | AFR | YRI | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA20129 | hp1 | a0002 | c0002 | t0006 | g0169 | AFR | ASW | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA20129 | hp2 | a0004 | c0005 | t0030 | g0217 | AFR | ASW | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA20752 | hp1 | a0004 | c0005 | t0004 | g0211 | EUR | TSI | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA20752 | hp2 | a0001 | c0004 | t0017 | g0335 | EUR | TSI | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA20805 | hp1 | a0004 | c0005 | t0091 | g0336 | EUR | TSI | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA20805 | hp2 | a0002 | c0002 | t0016 | g0089 | EUR | TSI | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0078 | SAS | GIH | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0300 | SAS | GIH | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0288 | AMR | CLM | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02109 | hp1 | a0001 | c0001 | t0012 | g0280 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02109 | hp2 | a0001 | c0001 | t0076 | g0295 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02486 | hp1 | a0003 | c0008 | t0020 | g0007 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02486 | hp2 | a0002 | c0006 | t0095 | g0340 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02559 | hp1 | a0002 | c0002 | t0023 | g0055 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG02559 | hp2 | a0001 | c0003 | t0025 | g0171 | AFR | ACB | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03471 | hp1 | a0002 | c0002 | t0011 | g0231 | AFR | MSL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG03471 | hp2 | a0001 | c0003 | t0025 | g0023 | AFR | MSL | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG06807 | hp1 | a0001 | c0003 | t0009 | g0173 | AFR | USA | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
HG06807 | hp2 | a0002 | c0002 | t0006 | g0179 | AFR | USA | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA20300 | hp1 | a0001 | c0003 | t0035 | g0152 | AFR | USA | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA20300 | hp2 | a0002 | c0002 | t0009 | g0065 | AFR | USA | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA21309 | hp1 | a0003 | c0009 | t0021 | g0156 | AFR | LWK | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
NA21309 | hp2 | a0001 | c0003 | t0013 | g0326 | AFR | LWK | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
homoSapiens | chm13v2 | a0004 | c0005 | t0004 | g0178 | REF | REF | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
homoSapiens | grch38p0 | a0001 | c0001 | t0012 | g0031 | REF | REF | CTSB_chr8_11837524_11873087 | CTSB | chr8 | 11837524 | 11873087 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:11845144 | T | G | 1 | a0005 | 7 | NA18939.hp2 NA18943.hp2 NA18950.hp1 others(4): Show |
missense_variant | MODERATE | c.1001A>C | p.Gln334Pro | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1113/3733 | 1001/1020 | 334/339 | chr8 | 11845144 | |||
chr8:11845196 | C | T | 1 | a0006 | 3 | NA18973.hp2 NA19060.hp2 NA19068.hp1 |
missense_variant | MODERATE | c.949G>A | p.Asp317Asn | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1061/3733 | 949/1020 | 317/339 | chr8 | 11845196 | |||
chr8:11847141 | C | T | 2 | a0003 a0007 |
19 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(16): Show |
missense_variant | MODERATE | c.704G>A | p.Ser235Asn | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/10 | 816/3733 | 704/1020 | 235/339 | chr8 | 11847141 | |||
chr8:11850970 | T | C | 2 | a0006 a0009 |
4 | HG02523.hp2 NA18973.hp2 NA19060.hp2 others(1): Show |
missense_variant | MODERATE | c.223A>G | p.Thr75Ala | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/10 | 335/3733 | 223/1020 | 75/339 | chr8 | 11850970 | |||
chr8:11852631 | C | G | 1 | a0011 | 1 | NA18612.hp2 | missense_variant | MODERATE | c.191G>C | p.Gly64Ala | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/10 | 303/3733 | 191/1020 | 64/339 | chr8 | 11852631 | |||
chr8:11852665 | T | C | 1 | a0004 | 15 | HG00099.hp2 HG00642.hp1 HG00735.hp2 others(12): Show |
missense_variant | MODERATE | c.157A>G | p.Ser53Gly | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/10 | 269/3733 | 157/1020 | 53/339 | chr8 | 11852665 | |||
chr8:11852676 | T | C | 1 | a0008 | 2 | NA18957.hp1 NA18988.hp2 |
missense_variant | MODERATE | c.146A>G | p.Asn49Ser | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/10 | 258/3733 | 146/1020 | 49/339 | chr8 | 11852676 | |||
chr8:11853378 | A | G | 1 | a0007 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.77T>C | p.Leu26Pro | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/10 | 189/3733 | 77/1020 | 26/339 | chr8 | 11853378 | |||
chr8:11853379 | G | C | 5 | a0002 a0004 a0005 others(2): Show |
185 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(182): Show |
missense_variant | MODERATE | c.76C>G | p.Leu26Val | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/10 | 188/3733 | 76/1020 | 26/339 | chr8 | 11853379 | |||
chr8:11853379 | G | T | 1 | a0002 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.76C>A | p.Leu26Met | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/10 | 188/3733 | 76/1020 | 26/339 | chr8 | 11853379 | |||
chr8:11853386 | G | T | 1 | a0010 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.69C>A | p.Phe23Leu | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/10 | 181/3733 | 69/1020 | 23/339 | chr8 | 11853386 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:11847074 | C | T | 1 | a0002c0022 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.771G>A | p.Ser257Ser | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/10 | 883/3733 | 771/1020 | 257/339 | chr8 | 11847074 | |||
chr8:11847146 | G | A | 2 | a0001c0010 a0001c0018 |
5 | HG01891.hp2 HG02976.hp2 HG03130.hp1 others(2): Show |
synonymous_variant | LOW | c.699C>T | p.Ser233Ser | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/10 | 811/3733 | 699/1020 | 233/339 | chr8 | 11847146 | |||
chr8:11847158 | G | C | 1 | a0003c0011 | 3 | HG02280.hp2 HG02809.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.687C>G | p.Ser229Ser | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/10 | 799/3733 | 687/1020 | 229/339 | chr8 | 11847158 | |||
chr8:11847773 | G | A | 1 | a0003c0012 | 3 | HG02145.hp1 HG02451.hp2 HG02647.hp2 |
synonymous_variant | LOW | c.582C>T | p.Ser194Ser | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 7/10 | 694/3733 | 582/1020 | 194/339 | chr8 | 11847773 | |||
chr8:11849051 | C | T | 2 | a0003c0008 a0007c0017 |
7 | HG02258.hp2 HG02486.hp1 HG02922.hp1 others(4): Show |
synonymous_variant | LOW | c.441G>A | p.Gly147Gly | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/10 | 553/3733 | 441/1020 | 147/339 | chr8 | 11849051 | |||
chr8:11849072 | T | C | 4 | a0001c0004 a0001c0010 a0003c0008 others(1): Show |
32 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(29): Show |
synonymous_variant | LOW | c.420A>G | p.Thr140Thr | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/10 | 532/3733 | 420/1020 | 140/339 | chr8 | 11849072 | |||
chr8:11849072 | T | G | 12 | a0001c0003 a0001c0018 a0002c0002 others(9): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
synonymous_variant | LOW | c.420A>C | p.Thr140Thr | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/10 | 532/3733 | 420/1020 | 140/339 | chr8 | 11849072 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:11842592 | T | C | 45 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(42): Show |
195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*2533A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2533 | chr8 | 11842592 | ||||||
chr8:11842705 | C | G | 1 | a0002c0002t0061 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2420G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2420 | chr8 | 11842705 | ||||||
chr8:11842705 | C | T | 1 | a0004c0005t0049 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2420G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2420 | chr8 | 11842705 | ||||||
chr8:11842706 | G | C | 1 | a0002c0002t0033 | 2 | HG02970.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2419C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2419 | chr8 | 11842706 | ||||||
chr8:11842727 | C | G | 1 | a0001c0003t0035 | 2 | NA19240.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2398G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2398 | chr8 | 11842727 | ||||||
chr8:11842747 | G | A | 1 | a0002c0002t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2378C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2378 | chr8 | 11842747 | ||||||
chr8:11842793 | T | A | 1 | a0002c0002t0064 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2332A>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2332 | chr8 | 11842793 | ||||||
chr8:11842884 | G | A | 1 | a0003c0012t0031 | 2 | HG02451.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2241C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2241 | chr8 | 11842884 | ||||||
chr8:11842889 | A | G | 1 | a0003c0011t0094 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2236T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2236 | chr8 | 11842889 | ||||||
chr8:11842912 | C | T | 2 | a0001c0010t0010 a0001c0018t0010 |
5 | HG01891.hp2 HG02976.hp2 HG03130.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2213G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2213 | chr8 | 11842912 | ||||||
chr8:11842928 | C | T | 30 | a0001c0001t0038 a0001c0003t0001 a0001c0003t0013 others(27): Show |
125 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*2197G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2197 | chr8 | 11842928 | ||||||
chr8:11842935 | CCT | C | 2 | a0001c0001t0075 a0005c0007t0008 |
6 | NA18939.hp2 NA18950.hp1 NA18987.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2188_*2189delAG | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2188 | chr8 | 11842935 | ||||||
chr8:11842936 | C | CTT | 5 | a0001c0003t0011 a0001c0004t0055 a0002c0002t0011 others(2): Show |
9 | HG00733.hp2 HG02145.hp1 HG02738.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2187_*2188dupAA | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2188 | chr8 | 11842936 | ||||||
chr8:11842936 | C | CTTT | 5 | a0001c0003t0009 a0001c0003t0025 a0001c0004t0054 others(2): Show |
11 | HG02257.hp1 HG02280.hp2 HG02559.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2186_*2188dupAAA | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2188 | chr8 | 11842936 | ||||||
chr8:11842936 | CT | C | 32 | a0001c0001t0038 a0001c0001t0053 a0001c0003t0001 others(29): Show |
136 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*2188delA | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2188 | chr8 | 11842936 | ||||||
chr8:11842936 | CTT | C | 25 | a0001c0001t0005 a0001c0001t0044 a0001c0001t0082 others(22): Show |
63 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2187_*2188delAA | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2187 | chr8 | 11842936 | ||||||
chr8:11842936 | CTTT | C | 28 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(25): Show |
168 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*2186_*2188delAAA | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2186 | chr8 | 11842936 | ||||||
chr8:11842936 | CTTTT | C | 5 | a0001c0001t0042 a0001c0001t0043 a0001c0001t0079 others(2): Show |
9 | HG02451.hp1 HG02717.hp2 NA18942.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2185_*2188delAAAA | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2185 | chr8 | 11842936 | ||||||
chr8:11842940 | T | C | 1 | a0001c0001t0081 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2185A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2185 | chr8 | 11842940 | ||||||
chr8:11842943 | T | C | 1 | a0001c0001t0076 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2182A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2182 | chr8 | 11842943 | ||||||
chr8:11842959 | T | A | 1 | a0001c0001t0044 | 2 | HG01258.hp1 HG01433.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2166A>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2166 | chr8 | 11842959 | ||||||
chr8:11842961 | A | G | 2 | a0001c0001t0082 a0001c0001t0083 |
2 | HG01978.hp1 HG02273.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2164T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2164 | chr8 | 11842961 | ||||||
chr8:11842984 | T | C | 1 | a0002c0002t0067 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2141A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2141 | chr8 | 11842984 | ||||||
chr8:11842998 | G | C | 1 | a0001c0001t0027 | 3 | HG02280.hp1 HG03491.hp2 HG03688.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2127C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2127 | chr8 | 11842998 | ||||||
chr8:11843018 | G | A | 2 | a0003c0008t0020 a0003c0008t0045 |
6 | HG02258.hp2 HG02486.hp1 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2107C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2107 | chr8 | 11843018 | ||||||
chr8:11843033 | C | T | 2 | a0001c0004t0017 a0001c0004t0090 |
6 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2092G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2092 | chr8 | 11843033 | ||||||
chr8:11843034 | C | T | 1 | a0001c0001t0053 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2091G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 2091 | chr8 | 11843034 | ||||||
chr8:11843196 | C | T | 13 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0041 others(10): Show |
65 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1929G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1929 | chr8 | 11843196 | ||||||
chr8:11843218 | A | C | 37 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(34): Show |
182 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*1907T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1907 | chr8 | 11843218 | ||||||
chr8:11843227 | G | A | 1 | a0002c0002t0066 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1898C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1898 | chr8 | 11843227 | ||||||
chr8:11843236 | G | C | 115 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(112): Show |
430 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(427): Show |
3_prime_UTR_variant | MODIFIER | c.*1889C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1889 | chr8 | 11843236 | ||||||
chr8:11843238 | C | T | 1 | a0001c0003t0089 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1887G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1887 | chr8 | 11843238 | ||||||
chr8:11843296 | A | G | 1 | a0007c0017t0051 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1829T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1829 | chr8 | 11843296 | ||||||
chr8:11843319 | T | C | 1 | a0002c0002t0006 | 8 | HG02622.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1806A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1806 | chr8 | 11843319 | ||||||
chr8:11843387 | A | G | 3 | a0001c0004t0017 a0001c0004t0028 a0001c0004t0090 |
9 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1738T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1738 | chr8 | 11843387 | ||||||
chr8:11843414 | G | A | 1 | a0001c0003t0025 | 3 | HG02559.hp2 HG02895.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1711C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1711 | chr8 | 11843414 | ||||||
chr8:11843458 | T | A | 1 | a0001c0003t0047 | 2 | HG01358.hp1 HG01515.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1667A>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1667 | chr8 | 11843458 | ||||||
chr8:11843470 | C | T | 1 | a0001c0001t0037 | 2 | HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1655G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1655 | chr8 | 11843470 | ||||||
chr8:11843480 | C | G | 1 | a0001c0001t0079 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1645G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1645 | chr8 | 11843480 | ||||||
chr8:11843587 | A | C | 86 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(83): Show |
356 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(353): Show |
3_prime_UTR_variant | MODIFIER | c.*1538T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1538 | chr8 | 11843587 | ||||||
chr8:11843600 | C | G | 1 | a0001c0001t0078 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1525G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1525 | chr8 | 11843600 | ||||||
chr8:11843651 | G | C | 3 | a0001c0003t0035 a0002c0002t0006 a0002c0002t0036 |
12 | HG02451.hp1 HG02622.hp2 HG02717.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1474C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1474 | chr8 | 11843651 | ||||||
chr8:11843689 | G | A | 60 | a0001c0001t0005 a0001c0003t0001 a0001c0003t0004 others(57): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*1436C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1436 | chr8 | 11843689 | ||||||
chr8:11843715 | C | G | 1 | a0001c0004t0077 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1410G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1410 | chr8 | 11843715 | ||||||
chr8:11843744 | A | G | 9 | a0001c0001t0005 a0001c0003t0005 a0001c0003t0046 others(6): Show |
26 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1381T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1381 | chr8 | 11843744 | ||||||
chr8:11843769 | G | A | 10 | a0001c0001t0005 a0001c0003t0005 a0001c0003t0046 others(7): Show |
27 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1356C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1356 | chr8 | 11843769 | ||||||
chr8:11843779 | C | T | 1 | a0001c0001t0041 | 2 | NA18997.hp1 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1346G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1346 | chr8 | 11843779 | ||||||
chr8:11843785 | C | A | 2 | a0003c0008t0020 a0003c0008t0045 |
6 | HG02258.hp2 HG02486.hp1 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1340G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1340 | chr8 | 11843785 | ||||||
chr8:11843821 | G | A | 30 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0015 others(27): Show |
159 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*1304C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1304 | chr8 | 11843821 | ||||||
chr8:11843843 | C | CAACATGG others(11): Show |
1 | a0002c0002t0060 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1264_*1281dupACAG others(14): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1281 | chr8 | 11843843 | ||||||
chr8:11843967 | A | G | 2 | a0001c0004t0054 a0001c0004t0055 |
2 | HG02886.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1158T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1158 | chr8 | 11843967 | ||||||
chr8:11844015 | G | A | 1 | a0003c0009t0021 | 3 | HG02622.hp1 HG02886.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1110C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1110 | chr8 | 11844015 | ||||||
chr8:11844019 | TCTCA | T | 10 | a0001c0001t0075 a0001c0003t0009 a0001c0003t0011 others(7): Show |
32 | HG00733.hp2 HG02055.hp2 HG02257.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1102_*1105delTGAG | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1102 | chr8 | 11844019 | ||||||
chr8:11844055 | G | T | 1 | a0002c0002t0074 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1070C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1070 | chr8 | 11844055 | ||||||
chr8:11844093 | C | T | 2 | a0003c0008t0020 a0003c0008t0045 |
6 | HG02258.hp2 HG02486.hp1 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1032G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1032 | chr8 | 11844093 | ||||||
chr8:11844119 | G | A | 1 | a0001c0004t0092 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1006C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1006 | chr8 | 11844119 | ||||||
chr8:11844122 | G | C | 1 | a0001c0001t0085 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1003C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 1003 | chr8 | 11844122 | ||||||
chr8:11844185 | G | A | 1 | a0007c0017t0051 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*940C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 940 | chr8 | 11844185 | ||||||
chr8:11844210 | C | T | 1 | a0002c0002t0059 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*915G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 915 | chr8 | 11844210 | ||||||
chr8:11844234 | G | A | 1 | a0002c0002t0068 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*891C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 891 | chr8 | 11844234 | ||||||
chr8:11844321 | A | T | 1 | a0001c0001t0073 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*804T>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 804 | chr8 | 11844321 | ||||||
chr8:11844327 | G | A | 1 | a0001c0001t0058 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*798C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 798 | chr8 | 11844327 | ||||||
chr8:11844333 | A | C | 113 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(110): Show |
427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
3_prime_UTR_variant | MODIFIER | c.*792T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 792 | chr8 | 11844333 | ||||||
chr8:11844355 | C | G | 1 | a0001c0003t0088 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*770G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 770 | chr8 | 11844355 | ||||||
chr8:11844361 | A | T | 1 | a0001c0001t0072 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*764T>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 764 | chr8 | 11844361 | ||||||
chr8:11844378 | CTG | C | 30 | a0001c0001t0053 a0001c0003t0001 a0001c0003t0013 others(27): Show |
122 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*745_*746delCA | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 745 | chr8 | 11844378 | ||||||
chr8:11844424 | T | C | 9 | a0001c0001t0005 a0001c0003t0005 a0001c0003t0046 others(6): Show |
26 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*701A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 701 | chr8 | 11844424 | ||||||
chr8:11844497 | A | T | 84 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(81): Show |
347 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(344): Show |
3_prime_UTR_variant | MODIFIER | c.*628T>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 628 | chr8 | 11844497 | ||||||
chr8:11844541 | C | G | 1 | a0001c0003t0088 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*584G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 584 | chr8 | 11844541 | ||||||
chr8:11844613 | G | C | 1 | a0001c0001t0019 | 4 | HG00323.hp2 HG01081.hp2 HG01993.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*512C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 512 | chr8 | 11844613 | ||||||
chr8:11844632 | T | A | 1 | a0002c0002t0069 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*493A>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 493 | chr8 | 11844632 | ||||||
chr8:11844656 | G | A | 1 | a0002c0002t0070 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*469C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 469 | chr8 | 11844656 | ||||||
chr8:11844671 | G | A | 1 | a0002c0002t0006 | 8 | HG02622.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*454C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 454 | chr8 | 11844671 | ||||||
chr8:11844695 | G | A | 97 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(94): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
3_prime_UTR_variant | MODIFIER | c.*430C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 430 | chr8 | 11844695 | ||||||
chr8:11844730 | C | G | 1 | a0003c0012t0031 | 2 | HG02451.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*395G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 395 | chr8 | 11844730 | ||||||
chr8:11844768 | C | G | 13 | a0001c0001t0053 a0001c0003t0004 a0001c0003t0035 others(10): Show |
33 | HG00099.hp2 HG00642.hp1 HG00735.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*357G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 357 | chr8 | 11844768 | ||||||
chr8:11844776 | C | A | 1 | a0002c0002t0071 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*349G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 349 | chr8 | 11844776 | ||||||
chr8:11844777 | T | C | 3 | a0001c0003t0035 a0002c0002t0006 a0002c0002t0036 |
12 | HG02451.hp1 HG02622.hp2 HG02717.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*348A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 348 | chr8 | 11844777 | ||||||
chr8:11844789 | C | T | 1 | a0001c0001t0037 | 2 | HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*336G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 336 | chr8 | 11844789 | ||||||
chr8:11844804 | C | G | 19 | a0001c0001t0005 a0001c0003t0005 a0001c0003t0046 others(16): Show |
57 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*321G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 321 | chr8 | 11844804 | ||||||
chr8:11844866 | G | A | 9 | a0001c0001t0005 a0001c0003t0005 a0001c0003t0046 others(6): Show |
26 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*259C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 259 | chr8 | 11844866 | ||||||
chr8:11844922 | G | A | 1 | a0001c0001t0015 | 5 | NA18946.hp1 NA18984.hp2 NA18986.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*203C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 203 | chr8 | 11844922 | ||||||
chr8:11844932 | A | G | 9 | a0001c0004t0017 a0001c0004t0028 a0001c0004t0029 others(6): Show |
23 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*193T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 193 | chr8 | 11844932 | ||||||
chr8:11844962 | G | C | 4 | a0003c0009t0024 a0003c0011t0024 a0003c0011t0093 others(1): Show |
5 | HG02280.hp2 HG02809.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*163C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 163 | chr8 | 11844962 | ||||||
chr8:11845033 | T | C | 44 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(41): Show |
195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*92A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 92 | chr8 | 11845033 | ||||||
chr8:11845085 | G | C | 9 | a0001c0001t0005 a0001c0003t0005 a0001c0003t0046 others(6): Show |
26 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*40C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 10/10 | 40 | chr8 | 11845085 | ||||||
chr8:11853464 | C | T | 1 | a0002c0002t0050 | 1 | HG01358.hp2 | 5_prime_UTR_variant | MODIFIER | c.-10G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/10 | 10 | chr8 | 11853464 | ||||||
chr8:11853465 | G | A | 1 | a0002c0002t0016 | 5 | HG00735.hp1 HG01070.hp1 HG01168.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-11C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/10 | chr8 | 11853465 | |||||||
chr8:11853476 | C | T | 2 | a0004c0005t0030 a0004c0005t0049 |
3 | HG01496.hp1 HG02647.hp1 NA20129.hp2 |
5_prime_UTR_variant | MODIFIER | c.-22G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/10 | 22 | chr8 | 11853476 | ||||||
chr8:11868004 | G | A | 11 | a0001c0004t0017 a0001c0004t0028 a0001c0004t0029 others(8): Show |
20 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(17): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-29C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/10 | chr8 | 11868004 | |||||||
chr8:11868017 | G | GAGCCTGC others(5): Show |
1 | a0001c0004t0029 | 3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-54_-43dupGGGCTGCA others(4): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/10 | 14564 | chr8 | 11868017 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:11845258 | C | A | 7 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(4): Show |
9 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.923-36G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 9/9 | chr8 | 11845258 | |||||||
chr8:11845326 | G | A | 6 | a0003c0009t0021g0156 a0003c0009t0021g0172 a0003c0009t0021g0220 others(3): Show |
6 | HG02451.hp2 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.923-104C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 9/9 | chr8 | 11845326 | |||||||
chr8:11845331 | T | G | 22 | a0001c0001t0005g0028 a0001c0003t0005g0067 a0001c0003t0005g0069 others(19): Show |
26 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.923-109A>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 9/9 | chr8 | 11845331 | |||||||
chr8:11845369 | G | A | 1 | a0001c0003t0009g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.923-147C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 9/9 | chr8 | 11845369 | |||||||
chr8:11845493 | T | C | 20 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(17): Show |
24 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.922+168A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 9/9 | chr8 | 11845493 | |||||||
chr8:11845506 | G | A | 1 | a0002c0002t0004g0045 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.922+155C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 9/9 | chr8 | 11845506 | |||||||
chr8:11845524 | C | T | 1 | a0001c0001t0007g0027 | 2 | HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.922+137G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 9/9 | chr8 | 11845524 | |||||||
chr8:11845532 | A | G | 1 | a0001c0001t0002g0276 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.922+129T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 9/9 | chr8 | 11845532 | |||||||
chr8:11845539 | C | G | 22 | a0001c0001t0005g0028 a0001c0003t0005g0067 a0001c0003t0005g0069 others(19): Show |
26 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.922+122G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 9/9 | chr8 | 11845539 | |||||||
chr8:11845558 | C | T | 3 | a0001c0001t0003g0242 a0001c0001t0003g0271 a0001c0001t0003g0328 |
3 | HG02015.hp2 NA18957.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.922+103G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 9/9 | chr8 | 11845558 | |||||||
chr8:11845578 | T | C | 1 | a0001c0001t0002g0283 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.922+83A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 9/9 | chr8 | 11845578 | |||||||
chr8:11845596 | C | T | 1 | a0002c0002t0006g0167 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.922+65G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 9/9 | chr8 | 11845596 | |||||||
chr8:11845603 | G | A | 1 | a0001c0001t0003g0030 | 2 | NA18951.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.922+58C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 9/9 | chr8 | 11845603 | |||||||
chr8:11845608 | C | T | 2 | a0001c0003t0005g0189 a0001c0003t0005g0193 |
2 | HG03239.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.922+53G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 9/9 | chr8 | 11845608 | |||||||
chr8:11845620 | C | T | 1 | a0001c0001t0002g0276 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.922+41G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 9/9 | chr8 | 11845620 | |||||||
chr8:11845633 | T | C | 2 | a0003c0009t0024g0196 a0003c0009t0024g0197 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.922+28A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 9/9 | chr8 | 11845633 | |||||||
chr8:11845816 | C | T | 1 | a0003c0011t0094g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.794-27G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11845816 | |||||||
chr8:11845827 | C | G | 5 | a0002c0002t0001g0017 a0002c0002t0001g0113 a0002c0002t0001g0114 others(2): Show |
6 | NA18950.hp2 NA18960.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-38G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11845827 | |||||||
chr8:11845853 | C | G | 1 | a0002c0002t0001g0064 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.794-64G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11845853 | |||||||
chr8:11845855 | A | C | 2 | a0002c0002t0018g0260 a0002c0002t0048g0341 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.794-66T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11845855 | |||||||
chr8:11845860 | C | T | 1 | a0001c0001t0003g0275 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.794-71G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11845860 | |||||||
chr8:11845911 | C | T | 19 | a0001c0001t0005g0028 a0001c0003t0005g0067 a0001c0003t0005g0069 others(16): Show |
20 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.794-122G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11845911 | |||||||
chr8:11845913 | C | A | 1 | a0001c0001t0002g0296 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.794-124G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11845913 | |||||||
chr8:11845922 | G | C | 2 | a0002c0002t0004g0046 a0002c0002t0004g0050 |
2 | HG01891.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.794-133C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11845922 | |||||||
chr8:11845955 | T | G | 1 | a0007c0021t0001g0136 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.794-166A>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11845955 | |||||||
chr8:11845988 | G | T | 22 | a0001c0001t0005g0028 a0001c0003t0005g0067 a0001c0003t0005g0069 others(19): Show |
26 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.794-199C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11845988 | |||||||
chr8:11846014 | T | G | 22 | a0001c0001t0005g0028 a0001c0003t0005g0067 a0001c0003t0005g0069 others(19): Show |
26 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.794-225A>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846014 | |||||||
chr8:11846019 | C | T | 1 | a0001c0001t0002g0274 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.794-230G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846019 | |||||||
chr8:11846045 | T | C | 1 | a0001c0001t0078g0074 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.794-256A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846045 | |||||||
chr8:11846084 | G | C | 3 | a0003c0008t0020g0007 a0003c0008t0020g0160 a0003c0008t0045g0020 |
6 | HG02258.hp2 HG02486.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.794-295C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846084 | |||||||
chr8:11846143 | A | G | 114 | a0001c0001t0038g0037 a0001c0003t0001g0110 a0001c0003t0011g0206 others(111): Show |
149 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.794-354T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846143 | |||||||
chr8:11846148 | C | T | 19 | a0001c0001t0005g0028 a0001c0003t0005g0067 a0001c0003t0005g0069 others(16): Show |
20 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.794-359G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846148 | |||||||
chr8:11846150 | T | C | 22 | a0001c0001t0005g0028 a0001c0003t0005g0067 a0001c0003t0005g0069 others(19): Show |
23 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.794-361A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846150 | |||||||
chr8:11846156 | G | A | 1 | a0003c0009t0021g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.794-367C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846156 | |||||||
chr8:11846164 | G | A | 1 | a0001c0003t0005g0327 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.794-375C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846164 | |||||||
chr8:11846181 | C | T | 1 | a0002c0002t0036g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.794-392G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846181 | |||||||
chr8:11846252 | G | A | 1 | a0003c0009t0021g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.794-463C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846252 | |||||||
chr8:11846311 | C | T | 14 | a0002c0002t0006g0022 a0002c0002t0006g0166 a0002c0002t0006g0167 others(11): Show |
18 | HG02145.hp1 HG02258.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.794-522G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846311 | |||||||
chr8:11846343 | C | T | 3 | a0002c0002t0011g0231 a0002c0002t0033g0323 a0002c0002t0033g0324 |
3 | HG02970.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.794-554G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846343 | |||||||
chr8:11846344 | G | A | 5 | a0001c0001t0007g0223 a0001c0001t0007g0329 a0001c0003t0009g0148 others(2): Show |
6 | HG00735.hp1 HG01168.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-555C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846344 | |||||||
chr8:11846430 | T | G | 1 | a0001c0003t0014g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.793+622A>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846430 | |||||||
chr8:11846451 | T | C | 18 | a0002c0002t0006g0022 a0002c0002t0006g0166 a0002c0002t0006g0167 others(15): Show |
22 | HG02145.hp1 HG02258.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.793+601A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846451 | |||||||
chr8:11846460 | T | G | 18 | a0002c0002t0006g0022 a0002c0002t0006g0166 a0002c0002t0006g0167 others(15): Show |
22 | HG02145.hp1 HG02258.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.793+592A>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846460 | |||||||
chr8:11846485 | G | A | 2 | a0008c0014t0002g0182 a0008c0014t0002g0183 |
2 | NA18957.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.793+567C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846485 | |||||||
chr8:11846510 | C | T | 1 | a0002c0002t0001g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.793+542G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846510 | |||||||
chr8:11846543 | G | A | 1 | a0001c0004t0017g0335 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.793+509C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846543 | |||||||
chr8:11846555 | G | A | 17 | a0001c0003t0001g0110 a0002c0002t0001g0016 a0002c0002t0001g0017 others(14): Show |
19 | NA18948.hp1 NA18950.hp2 NA18952.hp2 others(16): Show |
intron_variant | MODIFIER | c.793+497C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846555 | |||||||
chr8:11846603 | G | C | 4 | a0001c0004t0029g0343 a0001c0004t0029g0344 a0001c0004t0029g0345 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.793+449C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846603 | |||||||
chr8:11846628 | G | A | 1 | a0002c0006t0095g0340 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.793+424C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846628 | |||||||
chr8:11846696 | G | C | 1 | a0007c0021t0001g0136 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.793+356C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846696 | |||||||
chr8:11846721 | C | T | 2 | a0001c0003t0035g0151 a0001c0003t0035g0152 |
2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.793+331G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846721 | |||||||
chr8:11846747 | G | C | 3 | a0001c0003t0018g0165 a0001c0003t0018g0237 a0002c0002t0011g0231 |
3 | HG02717.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.793+305C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846747 | |||||||
chr8:11846772 | A | C | 1 | a0001c0001t0003g0241 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.793+280T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846772 | |||||||
chr8:11846787 | G | T | 35 | a0001c0001t0005g0028 a0001c0003t0005g0067 a0001c0003t0005g0069 others(32): Show |
39 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.793+265C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846787 | |||||||
chr8:11846789 | T | C | 35 | a0001c0001t0005g0028 a0001c0003t0005g0067 a0001c0003t0005g0069 others(32): Show |
39 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.793+263A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846789 | |||||||
chr8:11846802 | G | A | 1 | a0001c0001t0053g0289 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.793+250C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846802 | |||||||
chr8:11846841 | G | C | 193 | a0001c0001t0005g0028 a0001c0001t0053g0289 a0001c0003t0001g0110 others(190): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.793+211C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846841 | |||||||
chr8:11846948 | A | C | 192 | a0001c0001t0003g0298 a0001c0001t0005g0028 a0001c0003t0001g0110 others(189): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.793+104T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846948 | |||||||
chr8:11846964 | CAGCCCTA others(2): Show |
C | 3 | a0003c0012t0031g0157 a0003c0012t0031g0159 a0003c0012t0057g0158 |
3 | HG02145.hp1 HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.793+79_793+87delAA others(7): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846964 | |||||||
chr8:11846981 | A | G | 6 | a0001c0003t0009g0173 a0001c0003t0009g0174 a0001c0003t0009g0175 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.793+71T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846981 | |||||||
chr8:11846991 | C | T | 2 | a0002c0002t0001g0080 a0002c0002t0002g0308 |
2 | HG01952.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.793+61G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846991 | |||||||
chr8:11846998 | C | G | 1 | a0001c0001t0003g0225 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.793+54G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 8/9 | chr8 | 11846998 | |||||||
chr8:11847198 | G | A | 2 | a0002c0002t0016g0014 a0002c0002t0016g0089 |
3 | HG00735.hp1 HG01168.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.677-30C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 7/9 | chr8 | 11847198 | |||||||
chr8:11847210 | C | A | 40 | a0001c0001t0005g0028 a0001c0003t0005g0067 a0001c0003t0005g0069 others(37): Show |
44 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.677-42G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 7/9 | chr8 | 11847210 | |||||||
chr8:11847211 | G | A | 2 | a0001c0001t0002g0161 a0001c0001t0002g0177 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.677-43C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 7/9 | chr8 | 11847211 | |||||||
chr8:11847221 | G | A | 1 | a0002c0002t0002g0087 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.677-53C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 7/9 | chr8 | 11847221 | |||||||
chr8:11847292 | C | T | 2 | a0002c0002t0002g0047 a0002c0002t0002g0048 |
2 | HG02683.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.677-124G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 7/9 | chr8 | 11847292 | |||||||
chr8:11847362 | G | A | 2 | a0001c0001t0003g0245 a0009c0019t0003g0258 |
2 | HG02155.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.677-194C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 7/9 | chr8 | 11847362 | |||||||
chr8:11847369 | C | G | 200 | a0001c0001t0005g0028 a0001c0001t0053g0289 a0001c0003t0001g0110 others(197): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.677-201G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 7/9 | chr8 | 11847369 | |||||||
chr8:11847388 | C | T | 35 | a0001c0001t0005g0028 a0001c0003t0005g0067 a0001c0003t0005g0069 others(32): Show |
39 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.677-220G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 7/9 | chr8 | 11847388 | |||||||
chr8:11847435 | C | T | 1 | a0002c0002t0001g0080 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.676+244G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 7/9 | chr8 | 11847435 | |||||||
chr8:11847444 | G | A | 1 | a0001c0004t0034g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.676+235C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 7/9 | chr8 | 11847444 | |||||||
chr8:11847512 | G | C | 2 | a0001c0004t0054g0319 a0001c0004t0055g0057 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.676+167C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 7/9 | chr8 | 11847512 | |||||||
chr8:11847599 | C | T | 1 | a0001c0001t0075g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.676+80G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 7/9 | chr8 | 11847599 | |||||||
chr8:11847605 | C | T | 1 | a0006c0013t0002g0198 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.676+74G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 7/9 | chr8 | 11847605 | |||||||
chr8:11847630 | C | T | 132 | a0001c0003t0001g0110 a0001c0003t0004g0190 a0001c0003t0011g0206 others(129): Show |
168 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.676+49G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 7/9 | chr8 | 11847630 | |||||||
chr8:11847652 | G | A | 1 | a0001c0003t0009g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.676+27C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 7/9 | chr8 | 11847652 | |||||||
chr8:11847658 | GCCAGGCC | G | 15 | a0003c0008t0020g0007 a0003c0008t0020g0160 a0003c0008t0045g0020 others(12): Show |
18 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.676+14_676+20delGG others(5): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 7/9 | chr8 | 11847658 | |||||||
chr8:11847833 | G | C | 179 | a0001c0001t0005g0028 a0001c0003t0001g0110 a0001c0003t0004g0190 others(176): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.533-11C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 6/9 | chr8 | 11847833 | |||||||
chr8:11847857 | C | T | 1 | a0007c0021t0001g0136 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.533-35G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 6/9 | chr8 | 11847857 | |||||||
chr8:11847871 | A | AAGCCCCA others(12): Show |
3 | a0003c0012t0031g0157 a0003c0012t0031g0159 a0003c0012t0057g0158 |
3 | HG02145.hp1 HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.533-50_533-49insGC others(17): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 6/9 | chr8 | 11847871 | |||||||
chr8:11847871 | A | AAGCCCCA others(12): Show |
169 | a0001c0001t0005g0028 a0001c0003t0001g0110 a0001c0003t0004g0190 others(166): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.533-50_533-49insGC others(17): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 6/9 | chr8 | 11847871 | |||||||
chr8:11847911 | C | T | 2 | a0002c0002t0001g0016 a0002c0002t0048g0339 |
3 | HG02723.hp1 NA18952.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.533-89G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 6/9 | chr8 | 11847911 | |||||||
chr8:11847912 | G | A | 1 | a0007c0021t0001g0136 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.533-90C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 6/9 | chr8 | 11847912 | |||||||
chr8:11847924 | C | T | 1 | a0009c0019t0003g0258 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.533-102G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 6/9 | chr8 | 11847924 | |||||||
chr8:11847933 | G | T | 122 | a0001c0003t0001g0110 a0001c0003t0004g0190 a0001c0003t0013g0326 others(119): Show |
158 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.533-111C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 6/9 | chr8 | 11847933 | |||||||
chr8:11847939 | G | A | 19 | a0001c0001t0005g0028 a0001c0003t0005g0067 a0001c0003t0005g0069 others(16): Show |
20 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.533-117C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 6/9 | chr8 | 11847939 | |||||||
chr8:11847946 | G | A | 1 | a0001c0001t0002g0256 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.532+121C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 6/9 | chr8 | 11847946 | |||||||
chr8:11847973 | C | T | 1 | a0001c0003t0009g0174 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.532+94G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 6/9 | chr8 | 11847973 | |||||||
chr8:11848026 | C | T | 6 | a0001c0001t0003g0128 a0001c0001t0003g0234 a0001c0001t0003g0240 others(3): Show |
6 | HG01433.hp2 HG02293.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.532+41G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 6/9 | chr8 | 11848026 | |||||||
chr8:11848041 | G | T | 1 | a0001c0001t0015g0263 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.532+26C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 6/9 | chr8 | 11848041 | |||||||
chr8:11848168 | C | G | 165 | a0001c0001t0002g0281 a0001c0001t0003g0269 a0001c0003t0001g0110 others(162): Show |
207 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.447-16G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848168 | |||||||
chr8:11848240 | C | T | 2 | a0002c0006t0040g0094 a0002c0006t0040g0214 |
2 | HG00741.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.447-88G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848240 | |||||||
chr8:11848245 | G | A | 6 | a0003c0009t0024g0196 a0003c0009t0024g0197 a0003c0011t0024g0049 others(3): Show |
6 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.447-93C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848245 | |||||||
chr8:11848270 | G | C | 2 | a0001c0004t0034g0186 a0001c0004t0034g0209 |
2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.447-118C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848270 | |||||||
chr8:11848288 | A | G | 1 | a0001c0001t0003g0239 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.447-136T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848288 | |||||||
chr8:11848311 | G | A | 1 | a0001c0001t0083g0279 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.447-159C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848311 | |||||||
chr8:11848361 | G | A | 17 | a0001c0003t0005g0067 a0001c0003t0005g0069 a0001c0003t0005g0120 others(14): Show |
17 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.447-209C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848361 | |||||||
chr8:11848364 | C | T | 1 | a0005c0007t0008g0201 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.447-212G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848364 | |||||||
chr8:11848375 | G | A | 14 | a0001c0001t0053g0289 a0001c0004t0017g0040 a0001c0004t0017g0330 others(11): Show |
18 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.447-223C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848375 | |||||||
chr8:11848508 | C | A | 1 | a0002c0002t0006g0022 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.447-356G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848508 | |||||||
chr8:11848539 | A | T | 1 | a0001c0001t0079g0268 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.447-387T>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848539 | |||||||
chr8:11848544 | G | C | 1 | a0002c0002t0001g0098 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.447-392C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848544 | |||||||
chr8:11848608 | A | AACACCGC others(6): Show |
2 | a0001c0001t0007g0302 a0001c0001t0007g0303 |
2 | HG01099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.446+425_446+437dup others(13): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848608 | |||||||
chr8:11848614 | G | A | 6 | a0003c0009t0024g0196 a0003c0009t0024g0197 a0003c0011t0024g0049 others(3): Show |
6 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.446+432C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848614 | |||||||
chr8:11848633 | G | A | 1 | a0002c0002t0001g0013 | 2 | HG00438.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.446+413C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848633 | |||||||
chr8:11848642 | G | A | 3 | a0001c0010t0010g0008 a0001c0010t0010g0199 a0001c0018t0010g0200 |
5 | HG01891.hp2 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.446+404C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848642 | |||||||
chr8:11848646 | G | C | 3 | a0001c0010t0010g0008 a0001c0010t0010g0199 a0001c0018t0010g0200 |
5 | HG01891.hp2 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.446+400C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848646 | |||||||
chr8:11848647 | C | T | 1 | a0003c0012t0031g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.446+399G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848647 | |||||||
chr8:11848650 | G | C | 1 | a0001c0003t0013g0326 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.446+396C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848650 | |||||||
chr8:11848655 | G | C | 1 | a0003c0012t0031g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.446+391C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848655 | |||||||
chr8:11848700 | G | A | 2 | a0002c0002t0001g0140 a0002c0002t0001g0141 |
2 | NA18959.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.446+346C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848700 | |||||||
chr8:11848720 | T | C | 184 | a0001c0001t0002g0185 a0001c0003t0001g0110 a0001c0003t0003g0012 others(181): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.446+326A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848720 | |||||||
chr8:11848726 | A | T | 2 | a0001c0004t0029g0343 a0001c0004t0029g0344 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.446+320T>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848726 | |||||||
chr8:11848821 | G | A | 1 | a0001c0004t0092g0338 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.446+225C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848821 | |||||||
chr8:11848888 | C | T | 4 | a0001c0001t0053g0289 a0001c0010t0010g0008 a0001c0010t0010g0199 others(1): Show |
6 | HG01891.hp2 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.446+158G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848888 | |||||||
chr8:11848909 | G | C | 8 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(5): Show |
10 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.446+137C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848909 | |||||||
chr8:11848919 | C | T | 1 | a0001c0004t0034g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.446+127G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11848919 | |||||||
chr8:11849004 | C | G | 18 | a0001c0003t0004g0190 a0001c0003t0005g0195 a0001c0003t0005g0327 others(15): Show |
21 | HG00639.hp1 HG01109.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.446+42G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 5/9 | chr8 | 11849004 | |||||||
chr8:11849174 | C | A | 5 | a0003c0009t0024g0196 a0003c0009t0024g0197 a0003c0011t0093g0342 others(2): Show |
5 | HG02280.hp2 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-10G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849174 | |||||||
chr8:11849191 | G | C | 1 | a0002c0002t0001g0096 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.328-27C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849191 | |||||||
chr8:11849242 | A | AG | 3 | a0002c0002t0001g0006 a0002c0002t0001g0095 a0002c0002t0086g0072 |
5 | HG00423.hp1 NA18747.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-79dupC | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849242 | |||||||
chr8:11849303 | C | T | 3 | a0003c0008t0020g0007 a0003c0008t0020g0160 a0003c0008t0045g0020 |
6 | HG02258.hp2 HG02486.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-139G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849303 | |||||||
chr8:11849325 | T | C | 171 | a0001c0003t0001g0110 a0001c0003t0003g0012 a0001c0003t0011g0206 others(168): Show |
211 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.328-161A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849325 | |||||||
chr8:11849347 | C | T | 197 | a0001c0001t0037g0247 a0001c0001t0037g0248 a0001c0003t0001g0110 others(194): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.328-183G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849347 | |||||||
chr8:11849348 | G | A | 1 | a0001c0001t0012g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.328-184C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849348 | |||||||
chr8:11849356 | G | A | 1 | a0002c0002t0011g0207 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.328-192C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849356 | |||||||
chr8:11849397 | T | C | 201 | a0001c0003t0001g0110 a0001c0003t0003g0012 a0001c0003t0004g0190 others(198): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.328-233A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849397 | |||||||
chr8:11849398 | G | A | 8 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(5): Show |
10 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.328-234C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849398 | |||||||
chr8:11849407 | A | G | 1 | a0001c0001t0027g0124 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.328-243T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849407 | |||||||
chr8:11849428 | G | C | 178 | a0001c0003t0001g0110 a0001c0003t0003g0012 a0001c0003t0004g0190 others(175): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.328-264C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849428 | |||||||
chr8:11849431 | G | A | 1 | a0001c0001t0078g0074 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.328-267C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849431 | |||||||
chr8:11849459 | ACGATTTG others(19): Show |
A | 1 | a0001c0001t0075g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.328-321_328-296del others(26): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849459 | |||||||
chr8:11849460 | CG | C | 181 | a0001c0003t0001g0110 a0001c0003t0003g0012 a0001c0003t0004g0190 others(178): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.328-297delC | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849460 | |||||||
chr8:11849464 | T | C | 343 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0021 others(340): Show |
435 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(432): Show |
intron_variant | MODIFIER | c.328-300A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849464 | |||||||
chr8:11849485 | G | A | 1 | a0002c0006t0040g0094 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.328-321C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849485 | |||||||
chr8:11849502 | G | T | 1 | a0001c0001t0080g0224 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.328-338C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849502 | |||||||
chr8:11849518 | A | G | 180 | a0001c0003t0001g0110 a0001c0003t0003g0012 a0001c0003t0004g0190 others(177): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.328-354T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849518 | |||||||
chr8:11849523 | G | C | 198 | a0001c0003t0001g0110 a0001c0003t0003g0012 a0001c0003t0004g0190 others(195): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.328-359C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849523 | |||||||
chr8:11849542 | G | A | 1 | a0004c0005t0004g0181 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.328-378C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849542 | |||||||
chr8:11849579 | G | GT | 25 | a0001c0001t0002g0126 a0001c0001t0002g0253 a0001c0001t0003g0234 others(22): Show |
27 | HG00642.hp2 HG01106.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.328-416dupA | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849579 | |||||||
chr8:11849579 | G | GTT | 140 | a0001c0001t0007g0329 a0001c0003t0001g0110 a0001c0003t0003g0012 others(137): Show |
178 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.328-417_328-416dup others(2): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849579 | |||||||
chr8:11849579 | G | GTTT | 30 | a0001c0003t0005g0067 a0001c0003t0005g0069 a0001c0003t0005g0120 others(27): Show |
30 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.328-418_328-416dup others(3): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849579 | |||||||
chr8:11849580 | T | G | 2 | a0001c0010t0010g0008 a0001c0010t0010g0199 |
4 | HG01891.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-416A>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849580 | |||||||
chr8:11849641 | C | T | 1 | a0002c0002t0004g0045 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.328-477G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849641 | |||||||
chr8:11849665 | A | G | 18 | a0001c0003t0004g0190 a0001c0003t0005g0067 a0001c0003t0005g0069 others(15): Show |
18 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.328-501T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849665 | |||||||
chr8:11849763 | T | G | 8 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(5): Show |
10 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.328-599A>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849763 | |||||||
chr8:11849784 | T | C | 2 | a0001c0004t0034g0209 a0001c0004t0092g0338 |
2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.328-620A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849784 | |||||||
chr8:11849823 | C | T | 1 | a0001c0004t0034g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.328-659G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849823 | |||||||
chr8:11849841 | A | C | 1 | a0001c0001t0003g0128 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.328-677T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849841 | |||||||
chr8:11849871 | G | A | 3 | a0001c0004t0029g0343 a0001c0004t0029g0344 a0001c0004t0029g0345 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.328-707C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849871 | |||||||
chr8:11849879 | CTG | C | 2 | a0001c0010t0010g0008 a0001c0010t0010g0199 |
4 | HG01891.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-717_328-716del others(2): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11849879 | |||||||
chr8:11850021 | A | G | 158 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0246 others(155): Show |
196 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.327+845T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850021 | |||||||
chr8:11850022 | T | C | 2 | a0001c0004t0034g0209 a0001c0004t0092g0338 |
2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.327+844A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850022 | |||||||
chr8:11850047 | G | C | 9 | a0001c0003t0088g0191 a0001c0004t0017g0040 a0001c0004t0017g0330 others(6): Show |
11 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.327+819C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850047 | |||||||
chr8:11850061 | C | T | 1 | a0001c0003t0014g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.327+805G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850061 | |||||||
chr8:11850080 | G | A | 200 | a0001c0003t0001g0110 a0001c0003t0003g0012 a0001c0003t0004g0190 others(197): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.327+786C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850080 | |||||||
chr8:11850149 | G | A | 1 | a0001c0001t0019g0284 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.327+717C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850149 | |||||||
chr8:11850159 | G | C | 1 | a0003c0011t0094g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.327+707C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850159 | |||||||
chr8:11850179 | G | C | 2 | a0001c0010t0010g0008 a0001c0010t0010g0199 |
4 | HG01891.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+687C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850179 | |||||||
chr8:11850200 | C | A | 1 | a0001c0001t0078g0074 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.327+666G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850200 | |||||||
chr8:11850283 | G | T | 4 | a0003c0008t0020g0007 a0003c0008t0020g0160 a0003c0008t0045g0020 others(1): Show |
7 | HG02258.hp2 HG02486.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.327+583C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850283 | |||||||
chr8:11850291 | T | C | 184 | a0001c0001t0019g0284 a0001c0001t0075g0133 a0001c0003t0001g0110 others(181): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.327+575A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850291 | |||||||
chr8:11850307 | T | C | 1 | a0001c0004t0034g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.327+559A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850307 | |||||||
chr8:11850337 | T | C | 3 | a0001c0001t0003g0251 a0001c0001t0003g0257 a0001c0001t0081g0252 |
3 | NA18998.hp2 NA19063.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.327+529A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850337 | |||||||
chr8:11850374 | C | T | 2 | a0001c0010t0010g0008 a0001c0010t0010g0199 |
4 | HG01891.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+492G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850374 | |||||||
chr8:11850419 | C | CA | 19 | a0001c0001t0002g0035 a0001c0001t0002g0253 a0001c0001t0002g0254 others(16): Show |
21 | HG00280.hp1 HG00323.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.327+446dupT | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850419 | |||||||
chr8:11850419 | CA | C | 7 | a0001c0001t0002g0033 a0001c0001t0002g0155 a0001c0001t0002g0300 others(4): Show |
9 | HG01993.hp1 HG02129.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.327+446delT | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850419 | |||||||
chr8:11850419 | CAAAAAAA others(4): Show |
C | 1 | a0002c0006t0003g0259 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.327+436_327+446del others(11): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850419 | |||||||
chr8:11850436 | AAAAAAG | A | 138 | a0001c0003t0001g0110 a0001c0003t0003g0012 a0001c0003t0011g0206 others(135): Show |
171 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.327+424_327+429del others(6): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850436 | |||||||
chr8:11850437 | AAAAAG | A | 20 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0064 others(17): Show |
20 | HG01175.hp1 HG02280.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.327+424_327+428del others(5): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850437 | |||||||
chr8:11850438 | AAAAG | A | 11 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(8): Show |
15 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.327+424_327+427del others(4): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850438 | |||||||
chr8:11850441 | AG | A | 17 | a0001c0003t0004g0190 a0001c0003t0005g0067 a0001c0003t0005g0069 others(14): Show |
17 | HG00099.hp1 HG00639.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.327+424delC | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850441 | |||||||
chr8:11850693 | C | T | 1 | a0003c0012t0057g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.327+173G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850693 | |||||||
chr8:11850707 | G | A | 3 | a0002c0002t0018g0163 a0002c0002t0048g0339 a0002c0006t0095g0340 |
3 | HG02486.hp2 HG02723.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.327+159C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850707 | |||||||
chr8:11850747 | CTCAGAAA others(19): Show |
C | 1 | a0002c0002t0001g0096 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.327+93_327+118delC others(25): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850747 | |||||||
chr8:11850776 | A | T | 1 | a0002c0002t0001g0096 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.327+90T>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850776 | |||||||
chr8:11850846 | G | A | 146 | a0001c0003t0001g0110 a0001c0003t0003g0012 a0001c0003t0013g0326 others(143): Show |
185 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.327+20C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850846 | |||||||
chr8:11850856 | A | T | 2 | a0001c0010t0010g0008 a0001c0010t0010g0199 |
4 | HG01891.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+10T>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 4/9 | chr8 | 11850856 | |||||||
chr8:11851100 | G | A | 14 | a0001c0003t0018g0165 a0001c0003t0018g0237 a0002c0002t0011g0024 others(11): Show |
15 | HG00733.hp2 HG02717.hp1 HG02738.hp1 others(12): Show |
intron_variant | MODIFIER | c.213-120C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851100 | |||||||
chr8:11851175 | AT | A | 17 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(14): Show |
22 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.213-196delA | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851175 | |||||||
chr8:11851206 | A | T | 150 | a0001c0003t0001g0110 a0001c0003t0003g0012 a0001c0003t0013g0326 others(147): Show |
189 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.213-226T>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851206 | |||||||
chr8:11851272 | C | T | 1 | a0001c0001t0002g0130 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.213-292G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851272 | |||||||
chr8:11851291 | T | G | 33 | a0001c0003t0004g0190 a0001c0003t0005g0067 a0001c0003t0005g0069 others(30): Show |
36 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.213-311A>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851291 | |||||||
chr8:11851321 | C | G | 19 | a0001c0003t0004g0190 a0001c0003t0005g0067 a0001c0003t0005g0069 others(16): Show |
19 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.213-341G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851321 | |||||||
chr8:11851364 | A | G | 5 | a0003c0009t0024g0196 a0003c0009t0024g0197 a0003c0011t0024g0049 others(2): Show |
5 | HG02280.hp2 HG02809.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.213-384T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851364 | |||||||
chr8:11851437 | G | C | 7 | a0001c0004t0029g0343 a0001c0004t0029g0344 a0001c0004t0029g0345 others(4): Show |
10 | HG02258.hp2 HG02486.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.213-457C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851437 | |||||||
chr8:11851450 | A | G | 1 | a0002c0002t0004g0044 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.213-470T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851450 | |||||||
chr8:11851498 | G | A | 126 | a0001c0003t0001g0110 a0001c0003t0003g0012 a0001c0003t0013g0326 others(123): Show |
163 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.213-518C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851498 | |||||||
chr8:11851600 | G | C | 2 | a0001c0004t0029g0343 a0001c0004t0029g0344 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.213-620C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851600 | |||||||
chr8:11851681 | G | A | 1 | a0001c0003t0011g0206 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.213-701C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851681 | |||||||
chr8:11851690 | G | C | 1 | a0001c0001t0002g0285 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.213-710C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851690 | |||||||
chr8:11851736 | A | C | 1 | a0002c0002t0001g0096 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.213-756T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851736 | |||||||
chr8:11851795 | T | G | 5 | a0003c0009t0021g0156 a0003c0009t0021g0220 a0003c0012t0031g0157 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.212+815A>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851795 | |||||||
chr8:11851807 | C | G | 152 | a0001c0001t0075g0133 a0001c0003t0001g0110 a0001c0003t0003g0012 others(149): Show |
191 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.212+803G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851807 | |||||||
chr8:11851811 | C | T | 2 | a0003c0009t0021g0156 a0003c0009t0021g0220 |
2 | HG02622.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.212+799G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851811 | |||||||
chr8:11851855 | C | T | 1 | a0002c0002t0013g0077 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.212+755G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851855 | |||||||
chr8:11851879 | C | G | 1 | a0001c0003t0025g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.212+731G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11851879 | |||||||
chr8:11852031 | C | T | 2 | a0001c0001t0003g0238 a0001c0001t0003g0267 |
2 | HG02074.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.212+579G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11852031 | |||||||
chr8:11852076 | G | A | 1 | a0001c0001t0053g0289 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.212+534C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11852076 | |||||||
chr8:11852162 | A | G | 9 | a0001c0004t0029g0343 a0001c0004t0029g0344 a0001c0004t0029g0345 others(6): Show |
12 | HG02258.hp2 HG02486.hp1 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.212+448T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11852162 | |||||||
chr8:11852173 | C | T | 1 | a0004c0005t0091g0336 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.212+437G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11852173 | |||||||
chr8:11852191 | C | T | 1 | a0001c0001t0078g0074 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.212+419G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11852191 | |||||||
chr8:11852295 | C | T | 31 | a0001c0001t0003g0003 a0001c0001t0003g0018 a0001c0001t0003g0026 others(28): Show |
46 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.212+315G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11852295 | |||||||
chr8:11852325 | C | T | 2 | a0001c0010t0010g0008 a0001c0010t0010g0199 |
4 | HG01891.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.212+285G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11852325 | |||||||
chr8:11852327 | T | A | 1 | a0001c0001t0075g0133 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.212+283A>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11852327 | |||||||
chr8:11852377 | A | G | 3 | a0001c0004t0029g0343 a0001c0004t0029g0344 a0001c0004t0029g0345 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.212+233T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11852377 | |||||||
chr8:11852390 | G | C | 8 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(5): Show |
10 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.212+220C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11852390 | |||||||
chr8:11852436 | G | A | 29 | a0001c0003t0004g0190 a0001c0003t0005g0067 a0001c0003t0005g0069 others(26): Show |
31 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.212+174C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11852436 | |||||||
chr8:11852448 | T | C | 56 | a0001c0003t0004g0190 a0001c0003t0005g0067 a0001c0003t0005g0069 others(53): Show |
64 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.212+162A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11852448 | |||||||
chr8:11852528 | G | C | 2 | a0003c0011t0093g0342 a0003c0011t0094g0337 |
2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.212+82C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 3/9 | chr8 | 11852528 | |||||||
chr8:11852704 | G | C | 1 | a0001c0001t0007g0301 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.127-9C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/9 | chr8 | 11852704 | |||||||
chr8:11852792 | A | G | 207 | a0001c0001t0075g0133 a0001c0003t0001g0110 a0001c0003t0004g0190 others(204): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.127-97T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/9 | chr8 | 11852792 | |||||||
chr8:11852860 | G | A | 29 | a0001c0003t0004g0190 a0001c0003t0005g0067 a0001c0003t0005g0069 others(26): Show |
31 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.127-165C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/9 | chr8 | 11852860 | |||||||
chr8:11852887 | C | T | 8 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(5): Show |
10 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-192G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/9 | chr8 | 11852887 | |||||||
chr8:11853039 | G | C | 7 | a0001c0004t0029g0343 a0001c0004t0029g0344 a0001c0004t0029g0345 others(4): Show |
10 | HG02258.hp2 HG02486.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+290C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/9 | chr8 | 11853039 | |||||||
chr8:11853047 | G | C | 1 | a0001c0003t0047g0192 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.126+282C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/9 | chr8 | 11853047 | |||||||
chr8:11853120 | T | A | 29 | a0001c0003t0004g0190 a0001c0003t0005g0067 a0001c0003t0005g0069 others(26): Show |
31 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.126+209A>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/9 | chr8 | 11853120 | |||||||
chr8:11853131 | T | A | 1 | a0001c0003t0005g0193 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.126+198A>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/9 | chr8 | 11853131 | |||||||
chr8:11853162 | A | C | 1 | a0003c0011t0094g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.126+167T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/9 | chr8 | 11853162 | |||||||
chr8:11853182 | C | T | 2 | a0006c0013t0002g0198 a0006c0013t0002g0236 |
2 | NA18973.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.126+147G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/9 | chr8 | 11853182 | |||||||
chr8:11853194 | G | A | 1 | a0001c0003t0005g0120 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.126+135C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/9 | chr8 | 11853194 | |||||||
chr8:11853219 | C | T | 2 | a0001c0001t0002g0126 a0001c0001t0002g0127 |
2 | HG01074.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.126+110G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 2/9 | chr8 | 11853219 | |||||||
chr8:11853525 | C | T | 1 | a0002c0002t0006g0167 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-25-46G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11853525 | |||||||
chr8:11853550 | C | T | 117 | a0001c0003t0013g0326 a0002c0002t0001g0001 a0002c0002t0001g0004 others(114): Show |
151 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.-25-71G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11853550 | |||||||
chr8:11853571 | C | A | 1 | a0001c0001t0002g0288 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-25-92G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11853571 | |||||||
chr8:11853604 | CT | C | 43 | a0001c0003t0004g0190 a0001c0003t0005g0067 a0001c0003t0005g0069 others(40): Show |
50 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.-25-126delA | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11853604 | |||||||
chr8:11853640 | C | A | 38 | a0001c0003t0004g0190 a0001c0003t0005g0067 a0001c0003t0005g0069 others(35): Show |
43 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.-25-161G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11853640 | |||||||
chr8:11853644 | C | T | 2 | a0001c0010t0010g0008 a0001c0010t0010g0199 |
4 | HG01891.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-165G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11853644 | |||||||
chr8:11853646 | C | T | 1 | a0001c0001t0005g0028 | 2 | HG00738.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.-25-167G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11853646 | |||||||
chr8:11853648 | A | C | 43 | a0001c0003t0004g0190 a0001c0003t0005g0067 a0001c0003t0005g0069 others(40): Show |
50 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.-25-169T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11853648 | |||||||
chr8:11853728 | G | A | 32 | a0002c0002t0004g0045 a0002c0002t0004g0046 a0002c0002t0004g0050 others(29): Show |
35 | HG00099.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-25-249C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11853728 | |||||||
chr8:11853809 | G | C | 1 | a0002c0002t0001g0092 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-25-330C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11853809 | |||||||
chr8:11853918 | G | T | 1 | a0001c0001t0007g0027 | 2 | HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-25-439C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11853918 | |||||||
chr8:11853929 | GACAA | G | 2 | a0001c0010t0010g0008 a0001c0010t0010g0199 |
4 | HG01891.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-454_-25-451del others(4): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11853929 | |||||||
chr8:11853964 | G | C | 9 | a0001c0003t0005g0067 a0001c0003t0005g0069 a0001c0003t0005g0120 others(6): Show |
9 | HG00099.hp1 HG00323.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25-485C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11853964 | |||||||
chr8:11854004 | G | A | 1 | a0002c0002t0009g0065 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-25-525C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854004 | |||||||
chr8:11854007 | G | A | 2 | a0001c0010t0010g0008 a0001c0010t0010g0199 |
4 | HG01891.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-528C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854007 | |||||||
chr8:11854039 | C | T | 2 | a0001c0004t0054g0319 a0001c0004t0055g0057 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-25-560G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854039 | |||||||
chr8:11854110 | T | C | 1 | a0001c0001t0003g0287 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-25-631A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854110 | |||||||
chr8:11854155 | C | G | 1 | a0002c0002t0016g0117 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-25-676G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854155 | |||||||
chr8:11854208 | G | T | 2 | a0001c0010t0010g0008 a0001c0010t0010g0199 |
4 | HG01891.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-729C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854208 | |||||||
chr8:11854212 | C | A | 1 | a0002c0002t0006g0167 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-25-733G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854212 | |||||||
chr8:11854243 | G | A | 1 | a0003c0009t0024g0196 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-25-764C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854243 | |||||||
chr8:11854355 | G | A | 2 | a0005c0007t0008g0203 a0005c0007t0008g0204 |
2 | NA18950.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-25-876C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854355 | |||||||
chr8:11854490 | C | CT | 27 | a0001c0001t0003g0234 a0001c0001t0003g0328 a0001c0001t0007g0027 others(24): Show |
31 | HG00741.hp1 HG02055.hp1 HG02258.hp2 others(28): Show |
intron_variant | MODIFIER | c.-25-1012dupA | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854490 | |||||||
chr8:11854493 | T | C | 1 | a0006c0013t0002g0198 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-25-1014A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854493 | |||||||
chr8:11854593 | T | TTCAAACA others(9): Show |
49 | a0001c0003t0004g0190 a0001c0003t0005g0067 a0001c0003t0005g0069 others(46): Show |
56 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.-25-1115_-25-1114i others(18): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854593 | |||||||
chr8:11854608 | G | A | 1 | a0001c0010t0010g0199 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-25-1129C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854608 | |||||||
chr8:11854629 | C | T | 3 | a0001c0003t0009g0148 a0001c0003t0035g0151 a0001c0003t0035g0152 |
3 | NA18906.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-25-1150G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854629 | |||||||
chr8:11854643 | C | A | 2 | a0002c0002t0001g0062 a0002c0002t0001g0143 |
2 | HG02523.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-25-1164G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854643 | |||||||
chr8:11854770 | C | T | 1 | a0001c0004t0034g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-25-1291G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854770 | |||||||
chr8:11854793 | C | G | 5 | a0003c0009t0021g0156 a0003c0009t0021g0220 a0003c0012t0031g0157 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25-1314G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854793 | |||||||
chr8:11854822 | G | T | 3 | a0003c0012t0031g0157 a0003c0012t0031g0159 a0003c0012t0057g0158 |
3 | HG02145.hp1 HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-25-1343C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854822 | |||||||
chr8:11854871 | C | G | 1 | a0001c0001t0078g0074 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-25-1392G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854871 | |||||||
chr8:11854885 | G | A | 8 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(5): Show |
10 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-25-1406C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854885 | |||||||
chr8:11854916 | T | C | 1 | a0001c0004t0034g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-25-1437A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854916 | |||||||
chr8:11854934 | A | C | 43 | a0001c0003t0004g0190 a0001c0003t0005g0067 a0001c0003t0005g0069 others(40): Show |
48 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-25-1455T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854934 | |||||||
chr8:11854984 | C | A | 1 | a0002c0002t0001g0093 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-25-1505G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854984 | |||||||
chr8:11854986 | G | A | 1 | a0001c0004t0034g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-25-1507C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11854986 | |||||||
chr8:11855043 | G | T | 1 | a0001c0001t0003g0026 | 2 | HG00621.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.-25-1564C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855043 | |||||||
chr8:11855045 | C | T | 1 | a0002c0002t0001g0073 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-25-1566G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855045 | |||||||
chr8:11855046 | G | A | 24 | a0002c0002t0004g0045 a0002c0002t0004g0046 a0002c0002t0004g0050 others(21): Show |
28 | HG00099.hp2 HG00642.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-25-1567C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855046 | |||||||
chr8:11855117 | G | A | 1 | a0001c0004t0092g0338 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-25-1638C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855117 | |||||||
chr8:11855117 | G | T | 1 | a0001c0001t0003g0265 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-25-1638C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855117 | |||||||
chr8:11855130 | C | T | 20 | a0001c0003t0004g0190 a0001c0003t0005g0067 a0001c0003t0005g0069 others(17): Show |
20 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.-25-1651G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855130 | |||||||
chr8:11855183 | A | G | 1 | a0002c0002t0001g0140 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-25-1704T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855183 | |||||||
chr8:11855255 | C | T | 1 | a0002c0002t0001g0096 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-25-1776G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855255 | |||||||
chr8:11855290 | G | C | 2 | a0002c0002t0002g0047 a0002c0002t0002g0048 |
2 | HG02683.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-25-1811C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855290 | |||||||
chr8:11855347 | G | T | 16 | a0001c0004t0029g0343 a0001c0004t0029g0344 a0001c0004t0029g0345 others(13): Show |
21 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.-25-1868C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855347 | |||||||
chr8:11855459 | C | T | 1 | a0002c0002t0087g0320 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-25-1980G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855459 | |||||||
chr8:11855560 | T | C | 1 | a0001c0003t0005g0195 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-25-2081A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855560 | |||||||
chr8:11855563 | A | G | 1 | a0001c0003t0009g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-25-2084T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855563 | |||||||
chr8:11855649 | G | A | 15 | a0002c0006t0040g0094 a0002c0006t0040g0214 a0004c0005t0004g0038 others(12): Show |
17 | HG00099.hp2 HG00642.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.-25-2170C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855649 | |||||||
chr8:11855654 | C | T | 3 | a0001c0001t0002g0155 a0001c0001t0007g0301 a0001c0001t0076g0295 |
3 | HG02109.hp2 HG02129.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-25-2175G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855654 | |||||||
chr8:11855696 | T | C | 3 | a0001c0001t0007g0222 a0001c0001t0007g0223 a0001c0001t0007g0329 |
3 | HG02738.hp2 HG03490.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-25-2217A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855696 | |||||||
chr8:11855800 | C | T | 9 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(6): Show |
11 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-25-2321G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855800 | |||||||
chr8:11855836 | G | A | 1 | a0007c0017t0051g0041 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-25-2357C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855836 | |||||||
chr8:11855965 | T | C | 27 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(24): Show |
34 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.-25-2486A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855965 | |||||||
chr8:11855992 | C | A | 1 | a0001c0001t0003g0125 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-25-2513G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11855992 | |||||||
chr8:11856011 | G | C | 2 | a0003c0009t0024g0196 a0003c0009t0024g0197 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-25-2532C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11856011 | |||||||
chr8:11856025 | C | CAA | 10 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(7): Show |
12 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-25-2548_-25-2547d others(4): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11856025 | |||||||
chr8:11856081 | A | C | 1 | a0001c0001t0015g0263 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-25-2602T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11856081 | |||||||
chr8:11856189 | G | C | 1 | a0004c0005t0004g0219 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-25-2710C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11856189 | |||||||
chr8:11856343 | A | G | 136 | a0001c0001t0075g0133 a0001c0001t0078g0074 a0001c0003t0001g0110 others(133): Show |
174 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.-25-2864T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11856343 | |||||||
chr8:11856504 | T | G | 3 | a0001c0004t0029g0343 a0001c0004t0029g0344 a0001c0004t0029g0345 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-25-3025A>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11856504 | |||||||
chr8:11856532 | G | C | 8 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(5): Show |
10 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-25-3053C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11856532 | |||||||
chr8:11856757 | A | C | 1 | a0001c0001t0073g0232 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-25-3278T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11856757 | |||||||
chr8:11856796 | C | T | 174 | a0001c0001t0078g0074 a0001c0003t0001g0110 a0001c0003t0004g0190 others(171): Show |
219 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.-25-3317G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11856796 | |||||||
chr8:11856855 | GA | G | 139 | a0001c0001t0075g0133 a0001c0001t0078g0074 a0001c0003t0001g0110 others(136): Show |
177 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.-25-3377delT | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11856855 | |||||||
chr8:11856896 | G | C | 1 | a0005c0007t0008g0204 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-25-3417C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11856896 | |||||||
chr8:11856914 | A | G | 14 | a0001c0003t0004g0190 a0001c0003t0005g0189 a0001c0003t0005g0193 others(11): Show |
14 | HG00639.hp1 HG01109.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.-25-3435T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11856914 | |||||||
chr8:11856941 | G | C | 1 | a0001c0001t0085g0227 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-25-3462C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11856941 | |||||||
chr8:11856952 | G | A | 2 | a0001c0010t0010g0008 a0001c0010t0010g0199 |
4 | HG01891.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-3473C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11856952 | |||||||
chr8:11857048 | G | C | 7 | a0001c0004t0017g0330 a0001c0004t0017g0333 a0001c0004t0017g0335 others(4): Show |
8 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25-3569C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857048 | |||||||
chr8:11857099 | C | G | 18 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(15): Show |
25 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-25-3620G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857099 | |||||||
chr8:11857180 | C | T | 2 | a0001c0004t0039g0316 a0002c0002t0001g0142 |
2 | HG02083.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-25-3701G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857180 | |||||||
chr8:11857189 | A | T | 4 | a0004c0005t0004g0180 a0004c0005t0004g0211 a0004c0005t0004g0216 others(1): Show |
5 | HG00642.hp1 HG00735.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25-3710T>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857189 | |||||||
chr8:11857278 | A | G | 6 | a0001c0004t0034g0209 a0002c0002t0018g0163 a0003c0009t0021g0156 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25-3799T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857278 | |||||||
chr8:11857398 | A | G | 1 | a0001c0004t0092g0338 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-25-3919T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857398 | |||||||
chr8:11857432 | T | G | 15 | a0001c0003t0004g0190 a0001c0003t0005g0189 a0001c0003t0005g0193 others(12): Show |
15 | HG00639.hp1 HG01109.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.-25-3953A>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857432 | |||||||
chr8:11857440 | G | C | 3 | a0002c0002t0048g0339 a0002c0002t0048g0341 a0002c0006t0095g0340 |
3 | HG02486.hp2 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-25-3961C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857440 | |||||||
chr8:11857469 | G | T | 8 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(5): Show |
10 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-25-3990C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857469 | |||||||
chr8:11857507 | G | C | 11 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(8): Show |
13 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-25-4028C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857507 | |||||||
chr8:11857517 | G | C | 1 | a0006c0013t0002g0318 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-25-4038C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857517 | |||||||
chr8:11857574 | G | A | 8 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(5): Show |
10 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-25-4095C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857574 | |||||||
chr8:11857591 | A | T | 112 | a0001c0001t0078g0074 a0001c0003t0001g0110 a0002c0002t0001g0001 others(109): Show |
146 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.-25-4112T>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857591 | |||||||
chr8:11857739 | C | T | 2 | a0001c0003t0005g0230 a0001c0003t0046g0229 |
2 | HG01517.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.-25-4260G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857739 | |||||||
chr8:11857784 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-25-4305G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857784 | |||||||
chr8:11857903 | A | G | 5 | a0002c0002t0018g0163 a0003c0009t0021g0156 a0003c0012t0031g0157 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25-4424T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857903 | |||||||
chr8:11857918 | G | C | 1 | a0002c0002t0074g0111 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-25-4439C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857918 | |||||||
chr8:11857920 | GC | G | 139 | a0001c0001t0078g0074 a0001c0003t0001g0110 a0001c0004t0029g0343 others(136): Show |
177 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.-25-4442delG | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857920 | |||||||
chr8:11857955 | T | C | 1 | a0001c0001t0002g0261 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-25-4476A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857955 | |||||||
chr8:11857974 | G | T | 2 | a0001c0001t0002g0184 a0001c0001t0002g0262 |
2 | NA18961.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-25-4495C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11857974 | |||||||
chr8:11858054 | A | C | 3 | a0001c0001t0053g0289 a0001c0004t0034g0186 a0001c0004t0034g0209 |
3 | HG03130.hp2 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-25-4575T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858054 | |||||||
chr8:11858124 | G | A | 1 | a0003c0011t0024g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-25-4645C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858124 | |||||||
chr8:11858141 | C | T | 1 | a0001c0001t0012g0294 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-25-4662G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858141 | |||||||
chr8:11858201 | C | T | 1 | a0001c0003t0047g0325 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-25-4722G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858201 | |||||||
chr8:11858219 | T | G | 1 | a0001c0001t0002g0288 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-25-4740A>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858219 | |||||||
chr8:11858249 | C | T | 3 | a0001c0010t0010g0008 a0001c0010t0010g0199 a0001c0018t0010g0200 |
5 | HG01891.hp2 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25-4770G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858249 | |||||||
chr8:11858451 | C | T | 1 | a0002c0002t0004g0051 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-25-4972G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858451 | |||||||
chr8:11858504 | G | A | 1 | a0003c0011t0094g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-25-5025C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858504 | |||||||
chr8:11858513 | C | G | 1 | a0003c0011t0094g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-25-5034G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858513 | |||||||
chr8:11858550 | A | G | 4 | a0002c0002t0048g0339 a0002c0002t0048g0341 a0002c0006t0095g0340 others(1): Show |
4 | HG02280.hp2 HG02486.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-5071T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858550 | |||||||
chr8:11858615 | C | T | 1 | a0003c0011t0094g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-25-5136G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858615 | |||||||
chr8:11858643 | C | T | 6 | a0002c0002t0001g0006 a0002c0002t0001g0070 a0002c0002t0001g0095 others(3): Show |
8 | HG00423.hp1 HG02132.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25-5164G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858643 | |||||||
chr8:11858679 | A | G | 8 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(5): Show |
10 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-25-5200T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858679 | |||||||
chr8:11858681 | G | C | 3 | a0001c0001t0053g0289 a0001c0004t0034g0186 a0001c0004t0034g0209 |
3 | HG03130.hp2 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-25-5202C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858681 | |||||||
chr8:11858763 | G | A | 1 | a0001c0001t0002g0292 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-25-5284C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858763 | |||||||
chr8:11858916 | C | T | 1 | a0002c0002t0001g0062 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-25-5437G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858916 | |||||||
chr8:11858952 | T | A | 1 | a0001c0003t0003g0012 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-25-5473A>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858952 | |||||||
chr8:11858954 | C | T | 1 | a0001c0003t0013g0326 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-25-5475G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858954 | |||||||
chr8:11858964 | G | C | 132 | a0001c0001t0078g0074 a0001c0003t0001g0110 a0001c0003t0035g0151 others(129): Show |
167 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.-25-5485C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11858964 | |||||||
chr8:11859035 | C | T | 1 | a0002c0002t0009g0065 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-25-5556G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859035 | |||||||
chr8:11859079 | G | A | 13 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(10): Show |
15 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-25-5600C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859079 | |||||||
chr8:11859092 | C | A | 1 | a0001c0001t0002g0290 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-25-5613G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859092 | |||||||
chr8:11859131 | G | T | 1 | a0003c0012t0057g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-25-5652C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859131 | |||||||
chr8:11859262 | G | A | 1 | a0001c0001t0043g0293 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-25-5783C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859262 | |||||||
chr8:11859294 | G | A | 3 | a0002c0002t0023g0054 a0002c0002t0023g0055 a0002c0002t0023g0056 |
3 | HG02559.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-25-5815C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859294 | |||||||
chr8:11859316 | T | C | 1 | a0002c0002t0001g0114 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-25-5837A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859316 | |||||||
chr8:11859373 | A | C | 1 | a0001c0001t0003g0188 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-25-5894T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859373 | |||||||
chr8:11859387 | G | A | 1 | a0003c0011t0094g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-25-5908C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859387 | |||||||
chr8:11859394 | G | T | 1 | a0002c0002t0006g0168 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-25-5915C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859394 | |||||||
chr8:11859434 | G | C | 14 | a0001c0003t0004g0190 a0001c0003t0005g0189 a0001c0003t0005g0193 others(11): Show |
14 | HG00639.hp1 HG01109.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.-25-5955C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859434 | |||||||
chr8:11859446 | G | C | 1 | a0003c0011t0094g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-25-5967C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859446 | |||||||
chr8:11859505 | A | G | 5 | a0002c0002t0018g0163 a0003c0009t0021g0156 a0003c0012t0031g0157 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25-6026T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859505 | |||||||
chr8:11859676 | G | A | 2 | a0003c0012t0031g0157 a0003c0012t0057g0158 |
2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-25-6197C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859676 | |||||||
chr8:11859699 | C | T | 1 | a0003c0011t0094g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-25-6220G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859699 | |||||||
chr8:11859704 | G | C | 1 | a0008c0014t0002g0183 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-25-6225C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859704 | |||||||
chr8:11859719 | G | A | 5 | a0002c0002t0018g0163 a0003c0009t0021g0156 a0003c0012t0031g0157 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25-6240C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859719 | |||||||
chr8:11859767 | C | CA | 81 | a0001c0001t0002g0002 a0001c0001t0002g0033 a0001c0001t0002g0035 others(78): Show |
109 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.-25-6289dupT | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859767 | |||||||
chr8:11859767 | C | CAA | 97 | a0001c0001t0002g0005 a0001c0001t0002g0292 a0001c0001t0002g0311 others(94): Show |
131 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.-25-6290_-25-6289d others(4): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859767 | |||||||
chr8:11859767 | C | CAAA | 49 | a0001c0003t0001g0110 a0001c0003t0014g0053 a0001c0003t0035g0152 others(46): Show |
57 | HG00639.hp2 HG00738.hp2 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.-25-6291_-25-6289d others(5): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859767 | |||||||
chr8:11859767 | C | CAAAA | 7 | a0002c0002t0001g0112 a0002c0002t0001g0113 a0002c0002t0001g0114 others(4): Show |
7 | HG02622.hp2 HG03139.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.-25-6292_-25-6289d others(6): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859767 | |||||||
chr8:11859767 | CA | C | 12 | a0001c0001t0058g0228 a0001c0003t0046g0229 a0001c0004t0017g0040 others(9): Show |
14 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-25-6289delT | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859767 | |||||||
chr8:11859767 | CAAAAAA | C | 12 | a0001c0003t0004g0190 a0001c0003t0005g0189 a0001c0003t0005g0193 others(9): Show |
12 | HG00639.hp1 HG01109.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.-25-6294_-25-6289d others(8): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859767 | |||||||
chr8:11859813 | G | C | 1 | a0007c0017t0051g0041 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-25-6334C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859813 | |||||||
chr8:11859851 | G | T | 1 | a0001c0003t0025g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-25-6372C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859851 | |||||||
chr8:11859988 | CT | C | 8 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(5): Show |
10 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-25-6510delA | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11859988 | |||||||
chr8:11860032 | A | G | 1 | a0002c0002t0001g0066 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-25-6553T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11860032 | |||||||
chr8:11860076 | A | G | 1 | a0001c0001t0002g0296 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-25-6597T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11860076 | |||||||
chr8:11860131 | G | A | 1 | a0002c0002t0001g0321 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-25-6652C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11860131 | |||||||
chr8:11860144 | G | T | 1 | a0007c0017t0051g0041 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-25-6665C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11860144 | |||||||
chr8:11860173 | C | A | 1 | a0001c0001t0002g0036 | 2 | HG00609.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.-25-6694G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11860173 | |||||||
chr8:11860211 | G | A | 1 | a0004c0005t0004g0219 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-25-6732C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11860211 | |||||||
chr8:11860314 | AT | A | 3 | a0001c0001t0012g0294 a0001c0001t0076g0295 a0003c0009t0021g0220 |
3 | HG02109.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-25-6836delA | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11860314 | |||||||
chr8:11860319 | C | G | 2 | a0001c0003t0009g0148 a0001c0003t0014g0150 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-25-6840G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11860319 | |||||||
chr8:11860334 | G | C | 6 | a0002c0002t0004g0164 a0002c0002t0018g0163 a0003c0009t0021g0156 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25-6855C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11860334 | |||||||
chr8:11860484 | G | A | 3 | a0001c0010t0010g0008 a0001c0010t0010g0199 a0001c0018t0010g0200 |
5 | HG01891.hp2 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25-7005C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11860484 | |||||||
chr8:11860619 | C | T | 1 | a0002c0002t0009g0065 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-25-7140G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11860619 | |||||||
chr8:11860620 | G | A | 3 | a0001c0001t0002g0296 a0001c0001t0038g0037 a0001c0001t0043g0297 |
4 | NA18942.hp2 NA18951.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-7141C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11860620 | |||||||
chr8:11860663 | G | A | 7 | a0005c0007t0008g0201 a0005c0007t0008g0202 a0005c0007t0008g0203 others(4): Show |
7 | NA18939.hp2 NA18943.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.-25-7184C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11860663 | |||||||
chr8:11860721 | G | A | 2 | a0002c0002t0001g0115 a0002c0002t0001g0116 |
2 | NA18960.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-25-7242C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11860721 | |||||||
chr8:11860852 | C | A | 4 | a0001c0001t0002g0021 a0001c0001t0002g0161 a0001c0001t0002g0162 others(1): Show |
5 | HG02145.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26+7149G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11860852 | |||||||
chr8:11860895 | C | T | 1 | a0007c0017t0051g0041 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-26+7106G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11860895 | |||||||
chr8:11860989 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-26+7012C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11860989 | |||||||
chr8:11861019 | T | C | 179 | a0001c0001t0002g0132 a0001c0001t0003g0298 a0001c0001t0075g0133 others(176): Show |
220 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.-26+6982A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11861019 | |||||||
chr8:11861023 | G | C | 1 | a0001c0001t0002g0299 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-26+6978C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11861023 | |||||||
chr8:11861153 | G | A | 1 | a0001c0001t0002g0300 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-26+6848C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11861153 | |||||||
chr8:11861231 | G | A | 1 | a0003c0011t0094g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-26+6770C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11861231 | |||||||
chr8:11861449 | C | A | 1 | a0001c0001t0007g0301 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-26+6552G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11861449 | |||||||
chr8:11861558 | C | T | 9 | a0002c0002t0001g0011 a0002c0002t0001g0042 a0002c0002t0001g0058 others(6): Show |
10 | HG00639.hp2 HG00673.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.-26+6443G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11861558 | |||||||
chr8:11861570 | C | T | 1 | a0001c0001t0058g0228 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-26+6431G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11861570 | |||||||
chr8:11861599 | T | C | 1 | a0002c0002t0016g0117 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-26+6402A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11861599 | |||||||
chr8:11861729 | T | C | 1 | a0002c0002t0001g0145 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-26+6272A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11861729 | |||||||
chr8:11861835 | A | G | 7 | a0001c0004t0092g0338 a0002c0002t0004g0164 a0002c0002t0018g0163 others(4): Show |
7 | HG02145.hp1 HG02451.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-26+6166T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11861835 | |||||||
chr8:11861839 | G | C | 1 | a0002c0002t0006g0179 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-26+6162C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11861839 | |||||||
chr8:11861916 | C | A | 1 | a0007c0017t0051g0041 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-26+6085G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11861916 | |||||||
chr8:11861923 | C | A | 1 | a0002c0002t0001g0118 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-26+6078G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11861923 | |||||||
chr8:11861960 | T | C | 1 | a0001c0003t0011g0206 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-26+6041A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11861960 | |||||||
chr8:11861978 | T | C | 196 | a0001c0001t0002g0132 a0001c0001t0003g0188 a0001c0001t0007g0302 others(193): Show |
239 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.-26+6023A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11861978 | |||||||
chr8:11862008 | C | G | 2 | a0001c0004t0029g0343 a0001c0004t0029g0344 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-26+5993G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11862008 | |||||||
chr8:11862021 | C | G | 4 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0080g0224 others(1): Show |
4 | NA18941.hp2 NA18954.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+5980G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11862021 | |||||||
chr8:11862070 | G | A | 1 | a0003c0012t0031g0159 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-26+5931C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11862070 | |||||||
chr8:11862156 | G | A | 8 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(5): Show |
10 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26+5845C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11862156 | |||||||
chr8:11862163 | C | T | 6 | a0001c0001t0007g0222 a0001c0001t0007g0223 a0001c0001t0007g0329 others(3): Show |
6 | HG02738.hp2 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-26+5838G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11862163 | |||||||
chr8:11862206 | C | CA | 13 | a0001c0001t0002g0310 a0001c0001t0002g0311 a0001c0003t0005g0120 others(10): Show |
13 | HG00323.hp1 HG00558.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.-26+5794dupT | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11862206 | |||||||
chr8:11862206 | C | CAAA | 9 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(6): Show |
11 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-26+5792_-26+5794d others(5): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11862206 | |||||||
chr8:11862224 | G | A | 11 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(8): Show |
13 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-26+5777C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11862224 | |||||||
chr8:11862296 | C | T | 3 | a0001c0004t0029g0345 a0001c0004t0054g0319 a0001c0004t0055g0057 |
3 | HG02886.hp1 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-26+5705G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11862296 | |||||||
chr8:11862327 | T | C | 1 | a0001c0004t0034g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-26+5674A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11862327 | |||||||
chr8:11862415 | T | C | 1 | a0004c0005t0004g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-26+5586A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11862415 | |||||||
chr8:11862416 | C | G | 1 | a0001c0004t0092g0338 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-26+5585G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11862416 | |||||||
chr8:11862574 | T | A | 1 | a0002c0002t0026g0312 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-26+5427A>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11862574 | |||||||
chr8:11862718 | G | C | 133 | a0001c0001t0078g0074 a0001c0003t0001g0110 a0001c0003t0003g0012 others(130): Show |
171 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.-26+5283C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11862718 | |||||||
chr8:11862764 | C | T | 1 | a0001c0001t0002g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-26+5237G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11862764 | |||||||
chr8:11862774 | G | A | 1 | a0001c0003t0089g0313 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-26+5227C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11862774 | |||||||
chr8:11862957 | A | C | 9 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(6): Show |
11 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-26+5044T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11862957 | |||||||
chr8:11863036 | A | G | 178 | a0001c0001t0003g0188 a0001c0001t0078g0074 a0001c0003t0001g0110 others(175): Show |
219 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.-26+4965T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863036 | |||||||
chr8:11863063 | G | C | 1 | a0002c0002t0018g0163 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-26+4938C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863063 | |||||||
chr8:11863072 | G | T | 1 | a0003c0011t0094g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-26+4929C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863072 | |||||||
chr8:11863086 | G | A | 1 | a0002c0002t0001g0134 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-26+4915C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863086 | |||||||
chr8:11863130 | T | C | 1 | a0001c0003t0089g0313 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-26+4871A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863130 | |||||||
chr8:11863276 | T | C | 12 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(9): Show |
14 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-26+4725A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863276 | |||||||
chr8:11863318 | G | T | 1 | a0002c0002t0001g0061 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-26+4683C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863318 | |||||||
chr8:11863320 | G | A | 3 | a0002c0002t0023g0054 a0002c0002t0023g0055 a0002c0002t0023g0056 |
3 | HG02559.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-26+4681C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863320 | |||||||
chr8:11863326 | G | A | 1 | a0002c0002t0001g0135 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-26+4675C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863326 | |||||||
chr8:11863331 | C | T | 1 | a0001c0003t0014g0043 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-26+4670G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863331 | |||||||
chr8:11863367 | G | A | 2 | a0004c0005t0004g0038 a0004c0005t0052g0314 |
3 | HG01070.hp2 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-26+4634C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863367 | |||||||
chr8:11863414 | ACACCACT others(2553): Show |
A | 1 | a0001c0004t0092g0338 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-26+2027_-26+4586d others(2): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863414 | |||||||
chr8:11863452 | C | T | 2 | a0002c0002t0048g0339 a0002c0006t0095g0340 |
2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-26+4549G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863452 | |||||||
chr8:11863457 | C | CA | 21 | a0001c0001t0003g0226 a0001c0001t0007g0329 a0001c0003t0089g0313 others(18): Show |
23 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.-26+4543dupT | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863457 | |||||||
chr8:11863476 | C | A | 335 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0021 others(332): Show |
427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.-26+4525G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863476 | |||||||
chr8:11863477 | C | A | 1 | a0002c0002t0001g0135 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-26+4524G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863477 | |||||||
chr8:11863532 | C | G | 1 | a0003c0011t0094g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-26+4469G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863532 | |||||||
chr8:11863571 | C | T | 135 | a0001c0001t0042g0123 a0001c0001t0078g0074 a0001c0003t0001g0110 others(132): Show |
172 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.-26+4430G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863571 | |||||||
chr8:11863639 | G | A | 1 | a0001c0001t0002g0300 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-26+4362C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863639 | |||||||
chr8:11863689 | A | C | 1 | a0002c0002t0001g0011 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-26+4312T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863689 | |||||||
chr8:11863773 | G | C | 3 | a0001c0004t0029g0343 a0001c0004t0029g0344 a0001c0004t0029g0345 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-26+4228C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863773 | |||||||
chr8:11863806 | G | A | 19 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(16): Show |
21 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.-26+4195C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863806 | |||||||
chr8:11863898 | A | T | 1 | a0001c0001t0002g0033 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-26+4103T>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863898 | |||||||
chr8:11863929 | C | G | 9 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(6): Show |
11 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-26+4072G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863929 | |||||||
chr8:11863931 | T | C | 1 | a0002c0002t0018g0163 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-26+4070A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863931 | |||||||
chr8:11863989 | T | C | 4 | a0001c0003t0035g0151 a0001c0003t0035g0152 a0002c0002t0036g0149 others(1): Show |
4 | HG02451.hp1 HG02717.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+4012A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11863989 | |||||||
chr8:11864007 | A | G | 1 | a0002c0002t0056g0144 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-26+3994T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864007 | |||||||
chr8:11864103 | A | G | 1 | a0003c0011t0094g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-26+3898T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864103 | |||||||
chr8:11864124 | C | A | 1 | a0001c0001t0002g0285 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-26+3877G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864124 | |||||||
chr8:11864314 | C | A | 343 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0021 others(340): Show |
435 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(432): Show |
intron_variant | MODIFIER | c.-26+3687G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864314 | |||||||
chr8:11864318 | G | GA | 161 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0021 others(158): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-26+3682dupT | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864318 | |||||||
chr8:11864318 | G | GAA | 52 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0021 others(49): Show |
57 | HG00621.hp1 HG00621.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.-26+3681_-26+3682d others(4): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864318 | |||||||
chr8:11864318 | GA | G | 27 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(24): Show |
31 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-26+3682delT | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864318 | |||||||
chr8:11864356 | C | G | 1 | a0001c0001t0003g0026 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-26+3645G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864356 | |||||||
chr8:11864433 | G | A | 5 | a0002c0002t0006g0022 a0002c0002t0006g0166 a0002c0002t0006g0168 others(2): Show |
6 | HG02622.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26+3568C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864433 | |||||||
chr8:11864446 | G | C | 1 | a0002c0002t0064g0083 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-26+3555C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864446 | |||||||
chr8:11864537 | A | G | 144 | a0001c0001t0003g0128 a0001c0001t0042g0123 a0001c0001t0078g0074 others(141): Show |
184 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.-26+3464T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864537 | |||||||
chr8:11864553 | G | A | 1 | a0001c0003t0018g0165 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-26+3448C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864553 | |||||||
chr8:11864566 | G | C | 1 | a0003c0011t0094g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-26+3435C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864566 | |||||||
chr8:11864581 | T | C | 3 | a0001c0004t0029g0343 a0001c0004t0029g0344 a0001c0004t0029g0345 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-26+3420A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864581 | |||||||
chr8:11864587 | G | A | 1 | a0001c0001t0019g0322 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-26+3414C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864587 | |||||||
chr8:11864600 | G | A | 1 | a0002c0016t0001g0075 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-26+3401C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864600 | |||||||
chr8:11864606 | G | C | 1 | a0007c0017t0051g0041 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-26+3395C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864606 | |||||||
chr8:11864616 | C | T | 164 | a0001c0001t0003g0125 a0001c0001t0003g0128 a0001c0001t0042g0123 others(161): Show |
204 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.-26+3385G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864616 | |||||||
chr8:11864618 | G | A | 7 | a0005c0007t0008g0201 a0005c0007t0008g0202 a0005c0007t0008g0203 others(4): Show |
7 | NA18939.hp2 NA18943.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26+3383C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864618 | |||||||
chr8:11864713 | T | C | 1 | a0001c0001t0002g0274 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-26+3288A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864713 | |||||||
chr8:11864751 | T | C | 2 | a0001c0001t0002g0184 a0001c0001t0002g0262 |
2 | NA18961.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-26+3250A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864751 | |||||||
chr8:11864791 | C | G | 5 | a0002c0002t0018g0163 a0003c0009t0021g0156 a0003c0012t0031g0157 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-26+3210G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864791 | |||||||
chr8:11864811 | G | C | 1 | a0001c0001t0003g0128 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-26+3190C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864811 | |||||||
chr8:11864846 | G | A | 120 | a0001c0001t0003g0125 a0001c0001t0003g0128 a0001c0001t0042g0123 others(117): Show |
156 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.-26+3155C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864846 | |||||||
chr8:11864903 | A | ACT | 275 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0033 others(272): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.-26+3096_-26+3097d others(4): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864903 | |||||||
chr8:11864908 | C | G | 3 | a0001c0001t0007g0027 a0002c0002t0011g0231 a0002c0002t0018g0260 |
4 | HG02630.hp2 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+3093G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11864908 | |||||||
chr8:11865070 | C | T | 1 | a0001c0001t0003g0003 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-26+2931G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865070 | |||||||
chr8:11865248 | T | C | 2 | a0001c0004t0054g0319 a0001c0004t0055g0057 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-26+2753A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865248 | |||||||
chr8:11865297 | C | T | 2 | a0002c0002t0004g0051 a0003c0009t0021g0220 |
2 | HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-26+2704G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865297 | |||||||
chr8:11865326 | C | G | 3 | a0001c0010t0010g0008 a0001c0010t0010g0199 a0001c0018t0010g0200 |
5 | HG01891.hp2 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26+2675G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865326 | |||||||
chr8:11865368 | C | G | 13 | a0001c0003t0005g0189 a0001c0003t0005g0193 a0001c0003t0005g0195 others(10): Show |
13 | HG00099.hp1 HG00639.hp1 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.-26+2633G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865368 | |||||||
chr8:11865379 | G | A | 1 | a0001c0003t0013g0326 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-26+2622C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865379 | |||||||
chr8:11865386 | T | C | 9 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(6): Show |
11 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-26+2615A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865386 | |||||||
chr8:11865396 | A | AT | 27 | a0001c0001t0002g0021 a0001c0001t0002g0161 a0001c0001t0002g0162 others(24): Show |
33 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.-26+2604dupA | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865396 | |||||||
chr8:11865410 | G | C | 1 | a0001c0004t0034g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-26+2591C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865410 | |||||||
chr8:11865418 | A | G | 3 | a0002c0002t0023g0054 a0002c0002t0023g0055 a0002c0002t0023g0056 |
3 | HG02559.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-26+2583T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865418 | |||||||
chr8:11865523 | A | AG | 343 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0021 others(340): Show |
435 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(432): Show |
intron_variant | MODIFIER | c.-26+2477dupC | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865523 | |||||||
chr8:11865567 | G | A | 1 | a0003c0011t0094g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-26+2434C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865567 | |||||||
chr8:11865587 | C | CA | 12 | a0001c0001t0002g0274 a0001c0001t0003g0241 a0001c0003t0013g0326 others(9): Show |
14 | HG00423.hp2 HG01106.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.-26+2413dupT | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865587 | |||||||
chr8:11865587 | C | CAA | 10 | a0001c0001t0002g0021 a0001c0001t0002g0161 a0001c0001t0002g0162 others(7): Show |
14 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-26+2412_-26+2413d others(4): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865587 | |||||||
chr8:11865587 | CA | C | 9 | a0002c0002t0002g0047 a0002c0002t0002g0048 a0002c0002t0004g0044 others(6): Show |
9 | HG01891.hp1 HG02559.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-26+2413delT | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865587 | |||||||
chr8:11865622 | A | G | 340 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0021 others(337): Show |
432 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(429): Show |
intron_variant | MODIFIER | c.-26+2379T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865622 | |||||||
chr8:11865649 | G | A | 3 | a0001c0004t0029g0343 a0001c0004t0029g0344 a0001c0004t0029g0345 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-26+2352C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865649 | |||||||
chr8:11865707 | C | T | 1 | a0007c0017t0051g0041 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-26+2294G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865707 | |||||||
chr8:11865733 | C | G | 1 | a0001c0003t0088g0191 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-26+2268G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865733 | |||||||
chr8:11865826 | G | C | 1 | a0001c0001t0003g0128 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-26+2175C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865826 | |||||||
chr8:11865829 | A | C | 1 | a0002c0002t0001g0147 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-26+2172T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865829 | |||||||
chr8:11865851 | AC | A | 12 | a0001c0001t0002g0021 a0001c0001t0002g0161 a0001c0001t0002g0162 others(9): Show |
16 | HG02145.hp1 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-26+2149delG | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865851 | |||||||
chr8:11865852 | C | CA | 34 | a0001c0001t0002g0261 a0001c0001t0002g0310 a0001c0001t0003g0003 others(31): Show |
36 | HG00639.hp1 HG01109.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.-26+2148dupT | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865852 | |||||||
chr8:11865852 | C | T | 8 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(5): Show |
10 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26+2149G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865852 | |||||||
chr8:11865853 | A | T | 12 | a0001c0001t0002g0021 a0001c0001t0002g0161 a0001c0001t0002g0162 others(9): Show |
16 | HG02145.hp1 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-26+2148T>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865853 | |||||||
chr8:11865854 | A | T | 1 | a0001c0001t0002g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-26+2147T>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865854 | |||||||
chr8:11865902 | C | G | 2 | a0001c0001t0007g0223 a0001c0001t0007g0329 |
2 | HG02738.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-26+2099G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865902 | |||||||
chr8:11865914 | G | C | 3 | a0001c0003t0005g0067 a0001c0003t0005g0069 a0001c0003t0005g0120 |
3 | HG00323.hp1 HG01256.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-26+2087C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11865914 | |||||||
chr8:11866006 | G | C | 1 | a0003c0011t0094g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-26+1995C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11866006 | |||||||
chr8:11866011 | T | A | 1 | a0002c0002t0001g0147 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-26+1990A>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11866011 | |||||||
chr8:11866016 | C | CA | 8 | a0001c0003t0013g0326 a0001c0004t0039g0316 a0001c0004t0039g0317 others(5): Show |
8 | HG02258.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-26+1984dupT | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11866016 | |||||||
chr8:11866016 | CA | C | 26 | a0001c0001t0002g0184 a0001c0001t0002g0185 a0001c0004t0017g0040 others(23): Show |
28 | HG00099.hp2 HG01106.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.-26+1984delT | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11866016 | |||||||
chr8:11866016 | CAA | C | 14 | a0001c0001t0002g0021 a0001c0001t0002g0161 a0001c0001t0002g0162 others(11): Show |
18 | HG02145.hp1 HG02145.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-26+1983_-26+1984d others(4): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11866016 | |||||||
chr8:11866112 | A | G | 1 | a0002c0002t0006g0022 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26+1889T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11866112 | |||||||
chr8:11866124 | A | G | 5 | a0001c0004t0092g0338 a0002c0002t0048g0339 a0002c0002t0048g0341 others(2): Show |
5 | HG02280.hp2 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26+1877T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11866124 | |||||||
chr8:11866256 | A | C | 9 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(6): Show |
11 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-26+1745T>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11866256 | |||||||
chr8:11866266 | G | A | 105 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(102): Show |
139 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.-26+1735C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11866266 | |||||||
chr8:11866423 | G | A | 6 | a0001c0004t0092g0338 a0002c0002t0048g0339 a0002c0002t0048g0341 others(3): Show |
6 | HG02280.hp2 HG02486.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26+1578C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11866423 | |||||||
chr8:11866427 | T | C | 1 | a0001c0003t0005g0327 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-26+1574A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11866427 | |||||||
chr8:11866511 | T | C | 1 | a0001c0001t0019g0322 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-26+1490A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11866511 | |||||||
chr8:11866629 | A | G | 31 | a0001c0001t0002g0021 a0001c0001t0002g0161 a0001c0001t0002g0162 others(28): Show |
37 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.-26+1372T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11866629 | |||||||
chr8:11866655 | G | A | 3 | a0001c0004t0029g0343 a0001c0004t0029g0344 a0001c0004t0029g0345 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-26+1346C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11866655 | |||||||
chr8:11866680 | T | C | 2 | a0002c0002t0033g0323 a0002c0002t0033g0324 |
2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-26+1321A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11866680 | |||||||
chr8:11866713 | A | T | 9 | a0001c0004t0029g0343 a0001c0004t0029g0344 a0001c0004t0029g0345 others(6): Show |
9 | HG02280.hp2 HG02486.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-26+1288T>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11866713 | |||||||
chr8:11866778 | T | C | 3 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 |
3 | NA18967.hp2 NA18983.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.-26+1223A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11866778 | |||||||
chr8:11866802 | G | T | 1 | a0001c0003t0009g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-26+1199C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11866802 | |||||||
chr8:11867020 | T | TG | 18 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(15): Show |
20 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.-26+980dupC | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867020 | |||||||
chr8:11867080 | T | G | 8 | a0002c0002t0001g0019 a0002c0002t0001g0140 a0002c0002t0001g0141 others(5): Show |
9 | HG00558.hp1 HG02074.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-26+921A>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867080 | |||||||
chr8:11867117 | G | A | 12 | a0001c0001t0002g0021 a0001c0001t0002g0161 a0001c0001t0002g0162 others(9): Show |
16 | HG02145.hp1 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-26+884C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867117 | |||||||
chr8:11867119 | GAC | G | 7 | a0001c0003t0009g0173 a0001c0003t0009g0174 a0001c0003t0009g0175 others(4): Show |
8 | HG02055.hp2 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26+880_-26+881del others(2): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867119 | |||||||
chr8:11867229 | C | T | 6 | a0002c0002t0006g0022 a0002c0002t0006g0166 a0002c0002t0006g0167 others(3): Show |
7 | HG02622.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26+772G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867229 | |||||||
chr8:11867233 | C | G | 1 | a0002c0002t0001g0042 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-26+768G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867233 | |||||||
chr8:11867369 | G | C | 3 | a0001c0004t0029g0343 a0001c0004t0029g0344 a0001c0004t0029g0345 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-26+632C>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867369 | |||||||
chr8:11867399 | T | C | 1 | a0001c0003t0047g0325 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-26+602A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867399 | |||||||
chr8:11867418 | C | G | 28 | a0001c0001t0002g0021 a0001c0001t0002g0161 a0001c0001t0002g0162 others(25): Show |
34 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.-26+583G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867418 | |||||||
chr8:11867426 | C | G | 1 | a0001c0001t0041g0154 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-26+575G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867426 | |||||||
chr8:11867449 | C | T | 1 | a0001c0003t0018g0165 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-26+552G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867449 | |||||||
chr8:11867467 | T | TGGGGGGG others(889): Show |
1 | a0002c0002t0001g0147 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-26+533_-26+534ins others(896): Show |
CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867467 | |||||||
chr8:11867469 | T | G | 1 | a0002c0002t0001g0147 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-26+532A>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867469 | |||||||
chr8:11867470 | C | G | 1 | a0002c0002t0001g0147 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-26+531G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867470 | |||||||
chr8:11867471 | T | G | 1 | a0002c0002t0001g0147 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-26+530A>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867471 | |||||||
chr8:11867472 | T | G | 1 | a0002c0002t0001g0147 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-26+529A>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867472 | |||||||
chr8:11867473 | C | G | 1 | a0002c0002t0001g0147 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-26+528G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867473 | |||||||
chr8:11867474 | T | G | 1 | a0002c0002t0001g0147 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-26+527A>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867474 | |||||||
chr8:11867503 | C | A | 1 | a0001c0003t0013g0326 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-26+498G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867503 | |||||||
chr8:11867542 | G | T | 9 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(6): Show |
11 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-26+459C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867542 | |||||||
chr8:11867557 | T | C | 4 | a0001c0004t0017g0040 a0001c0004t0029g0343 a0001c0004t0029g0344 others(1): Show |
5 | HG01256.hp1 HG01258.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-26+444A>G | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867557 | |||||||
chr8:11867580 | G | A | 1 | a0001c0003t0005g0327 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-26+421C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867580 | |||||||
chr8:11867596 | G | A | 1 | a0003c0011t0093g0342 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-26+405C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867596 | |||||||
chr8:11867646 | C | T | 12 | a0001c0001t0002g0021 a0001c0001t0002g0161 a0001c0001t0002g0162 others(9): Show |
16 | HG02145.hp1 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-26+355G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867646 | |||||||
chr8:11867657 | G | A | 5 | a0001c0004t0092g0338 a0002c0002t0048g0339 a0002c0002t0048g0341 others(2): Show |
5 | HG02280.hp2 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26+344C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867657 | |||||||
chr8:11867665 | C | G | 1 | a0001c0001t0002g0155 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-26+336G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867665 | |||||||
chr8:11867704 | C | G | 2 | a0001c0004t0017g0330 a0001c0004t0090g0331 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-26+297G>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867704 | |||||||
chr8:11867774 | C | T | 119 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(116): Show |
153 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.-26+227G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867774 | |||||||
chr8:11867798 | G | T | 6 | a0001c0004t0092g0338 a0002c0002t0048g0339 a0002c0002t0048g0341 others(3): Show |
6 | HG02280.hp2 HG02486.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26+203C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867798 | |||||||
chr8:11867806 | G | A | 1 | a0001c0001t0003g0328 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-26+195C>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867806 | |||||||
chr8:11867820 | A | T | 6 | a0001c0003t0009g0148 a0001c0003t0014g0150 a0001c0003t0035g0151 others(3): Show |
6 | HG02451.hp1 HG02717.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-26+181T>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867820 | |||||||
chr8:11867879 | G | T | 118 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0130 others(115): Show |
152 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-26+122C>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867879 | |||||||
chr8:11867910 | A | G | 18 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(15): Show |
20 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.-26+91T>C | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867910 | |||||||
chr8:11867916 | C | T | 9 | a0001c0004t0017g0040 a0001c0004t0017g0330 a0001c0004t0017g0333 others(6): Show |
11 | HG01106.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-26+85G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867916 | |||||||
chr8:11867934 | C | A | 1 | a0001c0001t0007g0329 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-26+67G>T | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867934 | |||||||
chr8:11867948 | C | T | 1 | a0007c0017t0051g0041 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-26+53G>A | CTSB | ENSG00000164733.23 | transcript | ENST00000353047.11 | protein_coding | 1/9 | chr8 | 11867948 |