Item | Value |
---|---|
geneid | 55501 |
ensemblid | ENSG00000136213.10 |
hgncid | 17423 |
symbol | CHST12 |
name | carbohydrate sulfotransferase 12 |
refseq_nuc | NM_018641.5 |
refseq_prot | NP_061111.1 |
ensembl_nuc | ENST00000618655.2 |
ensembl_prot | ENSP00000481912.1 |
mane_status | MANE Select |
chr | chr7 |
start | 2403611 |
end | 2448484 |
strand | + |
ver | v1.2 |
region | chr7:2403611-2448484 |
region5000 | chr7:2398611-2453484 |
regionname0 | CHST12_chr7_2403611_2448484 |
regionname5000 | CHST12_chr7_2398611_2453484 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 414 | 238 | 77 | 57 | 59 | 12 | 31 | 39 | CHST12_chr7_2398611_2453484 | CHST12 | MTKAR others(409): Show |
chr7 | 2398611 | 2453484 |
a0002 | 0/0 | 414 | 39 | 1 | 4 | 27 | 0 | 7 | 18 | CHST12_chr7_2398611_2453484 | CHST12 | MTKAR others(409): Show |
chr7 | 2398611 | 2453484 |
a0003 | 0/0 | 414 | 33 | 0 | 6 | 27 | 0 | 0 | 18 | CHST12_chr7_2398611_2453484 | CHST12 | MTKAR others(409): Show |
chr7 | 2398611 | 2453484 |
a0004 | 0/0 | 414 | 18 | 1 | 4 | 12 | 0 | 1 | 8 | CHST12_chr7_2398611_2453484 | CHST12 | MTKAR others(409): Show |
chr7 | 2398611 | 2453484 |
a0005 | 0/0 | 414 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | MTKAR others(409): Show |
chr7 | 2398611 | 2453484 |
a0006 | 0/0 | 414 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | MTKAR others(409): Show |
chr7 | 2398611 | 2453484 |
a0007 | 0/0 | 414 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | MTKAR others(409): Show |
chr7 | 2398611 | 2453484 |
a0008 | 0/0 | 414 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | MTKAR others(409): Show |
chr7 | 2398611 | 2453484 |
a0009 | 0/0 | 414 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | MTKAR others(409): Show |
chr7 | 2398611 | 2453484 |
a0010 | 0/0 | 414 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | MTKAR others(409): Show |
chr7 | 2398611 | 2453484 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1242 | 232 | 73 | 57 | 59 | 10 | 31 | CHST12_chr7_2398611_2453484 | CHST12 | ATGAC others(1237): Show |
chr7 | 2398611 | 2453484 | ||
a0001c0006 | 0/0 | 1242 | 3 | 3 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | ATGAC others(1237): Show |
chr7 | 2398611 | 2453484 | ||
a0001c0009 | 0/0 | 1242 | 2 | 0 | 0 | 0 | 2 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | ATGAC others(1237): Show |
chr7 | 2398611 | 2453484 | ||
a0001c0012 | 0/0 | 1242 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | ATGAC others(1237): Show |
chr7 | 2398611 | 2453484 | ||
a0002c0002 | 0/0 | 1242 | 38 | 1 | 4 | 26 | 0 | 7 | CHST12_chr7_2398611_2453484 | CHST12 | ATGAC others(1237): Show |
chr7 | 2398611 | 2453484 | ||
a0002c0010 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | ATGAC others(1237): Show |
chr7 | 2398611 | 2453484 | ||
a0003c0003 | 0/0 | 1242 | 33 | 0 | 6 | 27 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | ATGAC others(1237): Show |
chr7 | 2398611 | 2453484 | ||
a0004c0004 | 0/0 | 1242 | 18 | 1 | 4 | 12 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | ATGAC others(1237): Show |
chr7 | 2398611 | 2453484 | ||
a0005c0005 | 0/0 | 1242 | 8 | 8 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | ATGAC others(1237): Show |
chr7 | 2398611 | 2453484 | ||
a0006c0007 | 0/0 | 1242 | 3 | 2 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | ATGAC others(1237): Show |
chr7 | 2398611 | 2453484 | ||
a0007c0008 | 0/0 | 1242 | 2 | 0 | 0 | 1 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | ATGAC others(1237): Show |
chr7 | 2398611 | 2453484 | ||
a0008c0014 | 0/0 | 1242 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | ATGAC others(1237): Show |
chr7 | 2398611 | 2453484 | ||
a0009c0013 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | ATGAC others(1237): Show |
chr7 | 2398611 | 2453484 | ||
a0010c0011 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | ATGAC others(1237): Show |
chr7 | 2398611 | 2453484 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0003 | 0/0 | 15989 | 3 | 0 | 0 | 3 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0005 | 0/0 | 15979 | 4 | 3 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0006 | 0/0 | 15989 | 3 | 0 | 2 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0007 | 0/0 | 15989 | 3 | 0 | 3 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0009 | 0/0 | 15993 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15988): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0011 | 0/0 | 15990 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0014 | 0/0 | 15990 | 2 | 1 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0015 | 0/0 | 15990 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0016 | 0/0 | 15988 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15983): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0018 | 0/0 | 15991 | 2 | 0 | 1 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15986): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0019 | 0/0 | 15985 | 2 | 0 | 0 | 0 | 0 | 2 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15980): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0020 | 0/0 | 15985 | 2 | 2 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15980): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0021 | 0/0 | 15978 | 2 | 0 | 2 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0025 | 0/0 | 15973 | 2 | 0 | 2 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15968): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0026 | 0/0 | 15978 | 2 | 0 | 2 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0027 | 0/0 | 15978 | 2 | 0 | 0 | 0 | 0 | 2 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0028 | 0/0 | 15979 | 2 | 0 | 2 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0029 | 0/0 | 15978 | 2 | 2 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0030 | 0/0 | 15979 | 2 | 2 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0031 | 0/0 | 15980 | 2 | 2 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0034 | 0/1 | 15989 | 1 | 0 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0036 | 0/0 | 15995 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15990): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0037 | 0/0 | 15990 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0038 | 0/0 | 15991 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15986): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0040 | 0/0 | 16000 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15995): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0041 | 0/0 | 15999 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15994): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0042 | 0/0 | 15997 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15992): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0043 | 0/0 | 15995 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15990): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0045 | 0/0 | 15996 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15991): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0046 | 0/0 | 15992 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15987): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0047 | 0/0 | 15995 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15990): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0049 | 0/0 | 15993 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15988): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0050 | 0/0 | 15994 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15989): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0051 | 0/0 | 15993 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15988): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0052 | 0/0 | 15992 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15987): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0053 | 0/0 | 15991 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15986): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0054 | 0/0 | 15993 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15988): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0058 | 0/0 | 15991 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15986): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0059 | 0/0 | 15992 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15987): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0061 | 0/0 | 15991 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15986): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0062 | 0/0 | 15993 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15988): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0063 | 0/0 | 15993 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15988): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0064 | 0/0 | 15993 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15988): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0066 | 0/0 | 15992 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15987): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0067 | 0/0 | 15995 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15990): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0068 | 0/0 | 15993 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15988): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0069 | 0/0 | 15993 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15988): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0070 | 0/0 | 15991 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15986): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0071 | 0/0 | 15990 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0072 | 0/0 | 15989 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0073 | 0/0 | 15991 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15986): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0074 | 0/0 | 15990 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0076 | 0/0 | 15992 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15987): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0077 | 0/0 | 15990 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0078 | 0/0 | 15990 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0079 | 0/0 | 15990 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0081 | 0/0 | 15992 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15987): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0084 | 0/0 | 15989 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0085 | 0/0 | 15991 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15986): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0086 | 0/0 | 15985 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15980): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0087 | 0/0 | 15989 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0088 | 0/0 | 15991 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15986): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0089 | 0/0 | 15990 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0090 | 0/0 | 15991 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15986): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0091 | 0/0 | 15992 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15987): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0092 | 0/0 | 15992 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15987): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0093 | 0/0 | 15992 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15987): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0094 | 0/0 | 15990 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0095 | 0/0 | 15987 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15982): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0096 | 0/0 | 15989 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0097 | 0/0 | 15989 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0098 | 0/0 | 15989 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0099 | 0/0 | 15989 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0100 | 0/0 | 15989 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0101 | 0/0 | 15989 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0106 | 0/0 | 15989 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0107 | 0/0 | 15990 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0109 | 0/0 | 15990 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0111 | 0/0 | 15991 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15986): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0112 | 0/0 | 15992 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15987): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0113 | 0/0 | 15989 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0114 | 0/0 | 15990 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0115 | 0/0 | 15991 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15986): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0116 | 0/0 | 15990 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0117 | 0/0 | 15991 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15986): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0118 | 0/0 | 15993 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15988): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0120 | 0/0 | 15991 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15986): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0126 | 0/0 | 15981 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15976): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0127 | 0/0 | 15986 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15981): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0132 | 0/0 | 15984 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15979): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0133 | 1/0 | 15985 | 1 | 0 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15980): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0134 | 0/0 | 15986 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15981): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0135 | 0/0 | 15980 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0136 | 0/0 | 15984 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15979): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0137 | 0/0 | 15980 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0138 | 0/0 | 15979 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0139 | 0/0 | 15986 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15981): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0140 | 0/0 | 15985 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15980): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0142 | 0/0 | 15984 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15979): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0143 | 0/0 | 15982 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15977): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0144 | 0/0 | 15984 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15979): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0145 | 0/0 | 15980 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0146 | 0/0 | 15983 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15978): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0147 | 0/0 | 15980 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0149 | 0/0 | 15984 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15979): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0150 | 0/0 | 15979 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0151 | 0/0 | 15978 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0152 | 0/0 | 15983 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15978): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0153 | 0/0 | 15983 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15978): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0154 | 0/0 | 15984 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15979): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0155 | 0/0 | 15980 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0156 | 0/0 | 15979 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0157 | 0/0 | 15979 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0158 | 0/0 | 15982 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15977): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0159 | 0/0 | 15981 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15976): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0160 | 0/0 | 15980 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0168 | 0/0 | 15976 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15971): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0169 | 0/0 | 15977 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15972): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0181 | 0/0 | 15978 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0182 | 0/0 | 15977 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15972): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0183 | 0/0 | 15977 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15972): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0184 | 0/0 | 15975 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15970): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0185 | 0/0 | 15968 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15963): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0186 | 0/0 | 15974 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15969): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0187 | 0/0 | 15969 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15964): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0188 | 0/0 | 15969 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15964): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0189 | 0/0 | 15972 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15967): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0190 | 0/0 | 15974 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15969): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0191 | 0/0 | 15971 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15966): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0193 | 0/0 | 15972 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15967): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0194 | 0/0 | 15971 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15966): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0196 | 0/0 | 15979 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0197 | 0/0 | 15968 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15963): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0198 | 0/0 | 15982 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15977): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0199 | 0/0 | 15977 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15972): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0200 | 0/0 | 15980 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0201 | 0/0 | 15980 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0202 | 0/0 | 15981 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15976): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0203 | 0/0 | 15980 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0204 | 0/0 | 15979 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0205 | 0/0 | 15980 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0206 | 0/0 | 15980 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0207 | 0/0 | 15980 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0208 | 0/0 | 15976 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15971): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0209 | 0/0 | 15978 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0210 | 0/0 | 15979 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0211 | 0/0 | 15979 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0212 | 0/0 | 15979 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0213 | 0/0 | 15980 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0214 | 0/0 | 15981 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15976): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0215 | 0/0 | 15980 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0216 | 0/0 | 15978 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0217 | 0/0 | 15978 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0218 | 0/0 | 15977 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15972): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0219 | 0/0 | 15978 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0220 | 0/0 | 15978 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0221 | 0/0 | 15982 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15977): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0222 | 0/0 | 15979 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0223 | 0/0 | 15981 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15976): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0224 | 0/0 | 15980 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0225 | 0/0 | 15979 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0226 | 0/0 | 15979 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0227 | 0/0 | 15980 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0228 | 0/0 | 15979 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0229 | 0/0 | 15978 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0230 | 0/0 | 15979 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0231 | 0/0 | 15981 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15976): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0232 | 0/0 | 15979 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0233 | 0/0 | 15980 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0234 | 0/0 | 15975 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15970): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0236 | 0/0 | 15976 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15971): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0237 | 0/0 | 15978 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0238 | 0/0 | 15979 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0239 | 0/0 | 15974 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15969): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0240 | 0/0 | 15980 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0241 | 0/0 | 15980 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0242 | 0/0 | 15980 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0243 | 0/0 | 15977 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15972): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0244 | 0/0 | 15981 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15976): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0245 | 0/0 | 15980 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0246 | 0/0 | 15978 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0247 | 0/0 | 15978 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0248 | 0/0 | 15978 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0249 | 0/0 | 15978 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0250 | 0/0 | 15979 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0251 | 0/0 | 15970 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15965): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0252 | 0/0 | 15992 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15987): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0263 | 0/0 | 15984 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15979): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0264 | 0/0 | 15978 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0269 | 0/0 | 15991 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15986): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0270 | 0/0 | 15979 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0271 | 0/0 | 15979 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0273 | 0/0 | 15961 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15956): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0275 | 0/0 | 15959 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15954): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0276 | 0/0 | 15973 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15968): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0277 | 0/0 | 15976 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15971): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0278 | 0/0 | 15973 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15968): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0280 | 0/0 | 15983 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15978): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0281 | 0/0 | 15977 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15972): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0282 | 0/0 | 15977 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15972): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0283 | 0/0 | 15977 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15972): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0284 | 0/0 | 15975 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15970): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0285 | 0/0 | 15973 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15968): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0286 | 0/0 | 15971 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15966): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0287 | 0/0 | 15964 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15959): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0288 | 0/0 | 15956 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15951): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0289 | 0/0 | 15955 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15950): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0290 | 0/0 | 15955 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15950): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0291 | 0/0 | 15952 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15947): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0292 | 0/0 | 15951 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15946): Show |
chr7 | 2398611 | 2453484 |
a0001c0001t0293 | 0/0 | 15979 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0006t0035 | 0/0 | 15979 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15974): Show |
chr7 | 2398611 | 2453484 |
a0001c0006t0267 | 0/0 | 15981 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15976): Show |
chr7 | 2398611 | 2453484 |
a0001c0006t0268 | 0/0 | 15978 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0001c0009t0102 | 0/0 | 15989 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0001c0009t0105 | 0/0 | 15985 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15980): Show |
chr7 | 2398611 | 2453484 |
a0001c0012t0192 | 0/0 | 15972 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15967): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0001 | 0/0 | 15976 | 8 | 0 | 0 | 6 | 0 | 2 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15971): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0004 | 0/0 | 15977 | 4 | 0 | 1 | 3 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15972): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0022 | 0/0 | 15976 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15971): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0023 | 0/0 | 15977 | 2 | 0 | 0 | 2 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15972): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0024 | 0/0 | 15975 | 2 | 0 | 0 | 1 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15970): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0065 | 0/0 | 15992 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15987): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0122 | 0/0 | 15986 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15981): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0161 | 0/0 | 15976 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15971): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0162 | 0/0 | 15977 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15972): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0163 | 0/0 | 15978 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0164 | 0/0 | 15976 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15971): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0165 | 0/0 | 15975 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15970): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0166 | 0/0 | 15978 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15973): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0167 | 0/0 | 15977 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15972): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0170 | 0/0 | 15977 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15972): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0171 | 0/0 | 15975 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15970): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0172 | 0/0 | 15975 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15970): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0173 | 0/0 | 15977 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15972): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0174 | 0/0 | 15977 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15972): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0175 | 0/0 | 15976 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15971): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0176 | 0/0 | 15976 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15971): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0177 | 0/0 | 15960 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15955): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0178 | 0/0 | 15976 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15971): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0179 | 0/0 | 15972 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15967): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0180 | 0/0 | 15975 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15970): Show |
chr7 | 2398611 | 2453484 |
a0002c0002t0195 | 0/0 | 15966 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15961): Show |
chr7 | 2398611 | 2453484 |
a0002c0010t0022 | 0/0 | 15976 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15971): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0003 | 0/0 | 15989 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0009 | 0/0 | 15993 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15988): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0010 | 0/0 | 15994 | 2 | 0 | 0 | 2 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15989): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0011 | 0/0 | 15990 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0012 | 0/0 | 15990 | 2 | 0 | 0 | 2 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0013 | 0/0 | 15990 | 2 | 0 | 1 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0016 | 0/0 | 15988 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15983): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0017 | 0/0 | 15989 | 2 | 0 | 2 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0039 | 0/0 | 15999 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15994): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0044 | 0/0 | 15996 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15991): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0048 | 0/0 | 15993 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15988): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0055 | 0/0 | 15993 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15988): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0056 | 0/0 | 15992 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15987): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0057 | 0/0 | 15993 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15988): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0060 | 0/0 | 15994 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15989): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0075 | 0/0 | 15991 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15986): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0080 | 0/0 | 15992 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15987): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0082 | 0/0 | 15991 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15986): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0103 | 0/0 | 15990 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0104 | 0/0 | 15989 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0108 | 0/0 | 15991 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15986): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0110 | 0/0 | 15989 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0119 | 0/0 | 15989 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15984): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0124 | 0/0 | 15986 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15981): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0125 | 0/0 | 15985 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15980): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0128 | 0/0 | 15986 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15981): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0129 | 0/0 | 15983 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15978): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0253 | 0/0 | 16000 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15995): Show |
chr7 | 2398611 | 2453484 |
a0003c0003t0279 | 0/0 | 15990 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0004c0004t0008 | 0/0 | 15986 | 3 | 0 | 1 | 2 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15981): Show |
chr7 | 2398611 | 2453484 |
a0004c0004t0032 | 0/0 | 15987 | 2 | 1 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15982): Show |
chr7 | 2398611 | 2453484 |
a0004c0004t0033 | 0/0 | 15987 | 2 | 0 | 0 | 2 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15982): Show |
chr7 | 2398611 | 2453484 |
a0004c0004t0235 | 0/0 | 15975 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15970): Show |
chr7 | 2398611 | 2453484 |
a0004c0004t0255 | 0/0 | 15984 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15979): Show |
chr7 | 2398611 | 2453484 |
a0004c0004t0256 | 0/0 | 15988 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15983): Show |
chr7 | 2398611 | 2453484 |
a0004c0004t0257 | 0/0 | 15988 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15983): Show |
chr7 | 2398611 | 2453484 |
a0004c0004t0258 | 0/0 | 15983 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15978): Show |
chr7 | 2398611 | 2453484 |
a0004c0004t0259 | 0/0 | 15986 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15981): Show |
chr7 | 2398611 | 2453484 |
a0004c0004t0260 | 0/0 | 15987 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15982): Show |
chr7 | 2398611 | 2453484 |
a0004c0004t0261 | 0/0 | 15986 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15981): Show |
chr7 | 2398611 | 2453484 |
a0004c0004t0262 | 0/0 | 15985 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15980): Show |
chr7 | 2398611 | 2453484 |
a0004c0004t0265 | 0/0 | 15970 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15965): Show |
chr7 | 2398611 | 2453484 |
a0004c0004t0266 | 0/0 | 15971 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15966): Show |
chr7 | 2398611 | 2453484 |
a0005c0005t0002 | 0/0 | 15985 | 5 | 5 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15980): Show |
chr7 | 2398611 | 2453484 |
a0005c0005t0123 | 0/0 | 15985 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15980): Show |
chr7 | 2398611 | 2453484 |
a0005c0005t0130 | 0/0 | 15986 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15981): Show |
chr7 | 2398611 | 2453484 |
a0005c0005t0131 | 0/0 | 15985 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15980): Show |
chr7 | 2398611 | 2453484 |
a0006c0007t0121 | 0/0 | 15982 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15977): Show |
chr7 | 2398611 | 2453484 |
a0006c0007t0141 | 0/0 | 15981 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15976): Show |
chr7 | 2398611 | 2453484 |
a0006c0007t0148 | 0/0 | 15980 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15975): Show |
chr7 | 2398611 | 2453484 |
a0007c0008t0272 | 0/0 | 15973 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15968): Show |
chr7 | 2398611 | 2453484 |
a0007c0008t0274 | 0/0 | 15973 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15968): Show |
chr7 | 2398611 | 2453484 |
a0008c0014t0254 | 0/0 | 15960 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15955): Show |
chr7 | 2398611 | 2453484 |
a0009c0013t0015 | 0/0 | 15990 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15985): Show |
chr7 | 2398611 | 2453484 |
a0010c0011t0083 | 0/0 | 15988 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | AGTCG others(15983): Show |
chr7 | 2398611 | 2453484 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0005g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0006g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0006g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0007g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0007g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0007g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0009g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0011g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0014g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0014g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0015g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0016g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0018g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0018g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0019g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0019g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0020g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0021g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0021g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0025g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0025g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0026g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0027g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0027g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0028g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0028g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0029g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0029g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0030g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0030g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0031g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0031g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0034g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0036g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0037g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0038g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0040g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0041g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0042g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0043g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0045g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0046g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0047g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0049g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0050g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0051g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0052g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0053g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0054g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0058g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0059g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0061g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0062g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0063g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0064g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0066g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0067g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0068g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0069g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0070g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0071g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0072g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0073g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0074g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0076g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0077g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0078g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0079g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0081g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0084g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0085g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0086g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0087g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0088g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0089g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0090g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0091g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0092g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0093g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0094g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0095g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0096g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0097g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0098g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0099g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0100g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0101g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0106g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0107g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0109g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0111g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0112g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0113g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0114g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0115g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0116g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0117g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0118g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0120g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0126g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0127g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0132g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0133g0014 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0134g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0135g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0136g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0137g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0138g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0139g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0140g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0142g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0143g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0144g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0145g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0146g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0147g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0149g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0150g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0151g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0152g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0153g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0154g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0155g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0156g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0157g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0158g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0159g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0160g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0168g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0169g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0181g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0182g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0183g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0184g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0185g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0186g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0187g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0188g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0189g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0190g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0191g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0193g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0194g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0196g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0197g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0198g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0199g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0200g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0201g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0202g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0203g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0204g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0205g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0206g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0207g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0208g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0209g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0210g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0211g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0212g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0213g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0214g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0215g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0216g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0217g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0218g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0219g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0220g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0221g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0222g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0223g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0224g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0225g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0226g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0227g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0228g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0229g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0230g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0231g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0232g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0233g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0234g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0236g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0237g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0238g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0239g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0240g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0241g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0242g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0243g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0244g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0245g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0246g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0247g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0248g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0249g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0250g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0251g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0252g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0263g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0264g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0269g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0270g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0271g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0273g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0275g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0276g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0277g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0278g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0280g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0281g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0282g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0283g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0284g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0285g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0286g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0287g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0288g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0289g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0290g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0291g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0292g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0001t0293g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0006t0035g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0006t0267g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0006t0268g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0009t0102g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0009t0105g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0001c0012t0192g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0022g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0023g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0023g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0024g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0024g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0065g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0122g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0161g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0162g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0163g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0164g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0165g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0166g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0167g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0170g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0171g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0172g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0173g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0174g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0175g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0176g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0177g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0178g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0179g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0180g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0002t0195g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0002c0010t0022g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0009g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0010g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0010g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0011g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0012g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0013g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0013g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0016g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0017g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0017g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0039g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0044g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0048g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0055g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0056g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0057g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0060g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0075g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0080g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0082g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0103g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0104g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0108g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0110g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0119g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0124g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0125g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0128g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0129g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0253g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0003c0003t0279g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0004c0004t0008g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0004c0004t0008g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0004c0004t0032g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0004c0004t0032g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0004c0004t0033g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0004c0004t0033g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0004c0004t0235g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0004c0004t0255g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0004c0004t0256g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0004c0004t0257g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0004c0004t0258g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0004c0004t0259g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0004c0004t0260g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0004c0004t0261g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0004c0004t0262g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0004c0004t0265g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0004c0004t0266g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0005c0005t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0005c0005t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0005c0005t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0005c0005t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0005c0005t0123g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0005c0005t0130g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0005c0005t0131g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0006c0007t0121g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0006c0007t0141g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0006c0007t0148g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0007c0008t0272g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0007c0008t0274g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0008c0014t0254g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0009c0013t0015g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
a0010c0011t0083g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0293 | g0247 | EUR | GBR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00099 | hp2 | a0001 | c0009 | t0105 | g0027 | EUR | GBR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00280 | hp1 | a0001 | c0009 | t0102 | g0262 | EUR | FIN | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00280 | hp2 | a0001 | c0001 | t0144 | g0233 | EUR | FIN | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00408 | hp1 | a0003 | c0003 | t0009 | g0025 | EAS | CHS | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | CHS | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00423 | hp1 | a0004 | c0004 | t0255 | g0001 | EAS | CHS | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00438 | hp1 | a0003 | c0003 | t0108 | g0199 | EAS | CHS | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00438 | hp2 | a0001 | c0001 | t0154 | g0232 | EAS | CHS | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00544 | hp1 | a0001 | c0001 | t0223 | g0042 | EAS | CHS | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00544 | hp2 | a0002 | c0002 | t0164 | g0030 | EAS | CHS | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00597 | hp1 | a0001 | c0001 | t0269 | g0006 | EAS | CHS | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00597 | hp2 | a0004 | c0004 | t0033 | g0064 | EAS | CHS | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00609 | hp1 | a0001 | c0001 | t0084 | g0038 | EAS | CHS | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00609 | hp2 | a0002 | c0002 | t0004 | g0287 | EAS | CHS | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00639 | hp1 | a0001 | c0001 | t0212 | g0091 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00639 | hp2 | a0004 | c0004 | t0032 | g0001 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00642 | hp1 | a0001 | c0001 | t0076 | g0266 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00642 | hp2 | a0001 | c0001 | t0140 | g0014 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00673 | hp1 | a0001 | c0001 | t0155 | g0259 | EAS | CHS | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00673 | hp2 | a0003 | c0003 | t0044 | g0263 | EAS | CHS | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00733 | hp1 | a0001 | c0001 | t0077 | g0142 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00733 | hp2 | a0001 | c0001 | t0143 | g0231 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00735 | hp1 | a0001 | c0001 | t0061 | g0006 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00735 | hp2 | a0001 | c0001 | t0070 | g0017 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00738 | hp1 | a0001 | c0001 | t0249 | g0061 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG00738 | hp2 | a0001 | c0001 | t0219 | g0005 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01069 | hp1 | a0001 | c0001 | t0071 | g0017 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01069 | hp2 | a0001 | c0001 | t0026 | g0005 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01070 | hp1 | a0002 | c0002 | t0178 | g0292 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01070 | hp2 | a0001 | c0001 | t0098 | g0167 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01071 | hp1 | a0001 | c0001 | t0026 | g0005 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01071 | hp2 | a0001 | c0001 | t0074 | g0021 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01074 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01074 | hp2 | a0001 | c0001 | t0072 | g0115 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01081 | hp1 | a0001 | c0001 | t0078 | g0129 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01081 | hp2 | a0006 | c0007 | t0121 | g0026 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01099 | hp1 | a0001 | c0001 | t0246 | g0054 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01099 | hp2 | a0001 | c0001 | t0160 | g0271 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01106 | hp1 | a0001 | c0001 | t0285 | g0136 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01106 | hp2 | a0001 | c0001 | t0217 | g0031 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01109 | hp1 | a0001 | c0001 | t0046 | g0177 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01109 | hp2 | a0001 | c0001 | t0190 | g0194 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01167 | hp1 | a0001 | c0001 | t0242 | g0097 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01167 | hp2 | a0001 | c0001 | t0153 | g0243 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01168 | hp1 | a0001 | c0001 | t0113 | g0123 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01168 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01169 | hp1 | a0001 | c0001 | t0191 | g0125 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01169 | hp2 | a0001 | c0001 | t0159 | g0238 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01192 | hp1 | a0001 | c0001 | t0014 | g0265 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01192 | hp2 | a0001 | c0001 | t0231 | g0305 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01243 | hp1 | a0001 | c0001 | t0169 | g0172 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01243 | hp2 | a0002 | c0002 | t0004 | g0285 | AMR | PUR | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01255 | hp1 | a0001 | c0001 | t0087 | g0171 | AMR | CLM | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01255 | hp2 | a0001 | c0001 | t0220 | g0055 | AMR | CLM | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01256 | hp1 | a0003 | c0003 | t0017 | g0155 | AMR | CLM | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01256 | hp2 | a0001 | c0001 | t0021 | g0236 | AMR | CLM | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01257 | hp1 | a0001 | c0001 | t0236 | g0060 | AMR | CLM | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01257 | hp2 | a0001 | c0001 | t0025 | g0138 | AMR | CLM | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01258 | hp1 | a0001 | c0001 | t0025 | g0002 | AMR | CLM | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01258 | hp2 | a0003 | c0003 | t0017 | g0119 | AMR | CLM | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01261 | hp1 | a0003 | c0003 | t0103 | g0154 | AMR | CLM | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01261 | hp2 | a0001 | c0001 | t0050 | g0141 | AMR | CLM | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01346 | hp1 | a0001 | c0001 | t0136 | g0235 | AMR | CLM | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01346 | hp2 | a0001 | c0001 | t0216 | g0058 | AMR | CLM | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01361 | hp1 | a0002 | c0002 | t0165 | g0291 | AMR | CLM | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01361 | hp2 | a0001 | c0001 | t0239 | g0088 | AMR | CLM | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01515 | hp1 | a0001 | c0001 | t0101 | g0159 | EUR | IBS | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01515 | hp2 | a0001 | c0001 | t0208 | g0077 | EUR | IBS | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01517 | hp1 | a0001 | c0001 | t0199 | g0009 | EUR | IBS | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01517 | hp2 | a0001 | c0001 | t0006 | g0019 | EUR | IBS | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01884 | hp1 | a0001 | c0001 | t0116 | g0022 | AFR | ACB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01884 | hp2 | a0001 | c0001 | t0097 | g0021 | AFR | ACB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01891 | hp1 | a0001 | c0001 | t0201 | g0041 | AFR | ACB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01891 | hp2 | a0001 | c0001 | t0292 | g0261 | AFR | ACB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01928 | hp1 | a0001 | c0001 | t0118 | g0210 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01928 | hp2 | a0003 | c0003 | t0013 | g0157 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01934 | hp1 | a0001 | c0001 | t0106 | g0158 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01934 | hp2 | a0001 | c0001 | t0021 | g0237 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01943 | hp1 | a0001 | c0001 | t0218 | g0050 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01943 | hp2 | a0001 | c0001 | t0132 | g0197 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01952 | hp1 | a0001 | c0001 | t0028 | g0049 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01952 | hp2 | a0001 | c0001 | t0007 | g0135 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01975 | hp1 | a0001 | c0001 | t0028 | g0053 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01975 | hp2 | a0001 | c0001 | t0018 | g0150 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01978 | hp1 | a0001 | c0001 | t0232 | g0080 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01978 | hp2 | a0001 | c0001 | t0036 | g0246 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01981 | hp1 | a0004 | c0004 | t0257 | g0066 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01981 | hp2 | a0001 | c0001 | t0149 | g0267 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01993 | hp1 | a0001 | c0001 | t0007 | g0034 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG01993 | hp2 | a0004 | c0004 | t0008 | g0004 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02004 | hp1 | a0001 | c0001 | t0007 | g0148 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02004 | hp2 | a0002 | c0002 | t0161 | g0007 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02015 | hp1 | a0001 | c0001 | t0286 | g0146 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02015 | hp2 | a0001 | c0001 | t0146 | g0126 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02027 | hp1 | a0002 | c0002 | t0122 | g0298 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02027 | hp2 | a0001 | c0001 | t0066 | g0016 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02040 | hp1 | a0003 | c0003 | t0119 | g0111 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02040 | hp2 | a0001 | c0001 | t0226 | g0032 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02055 | hp1 | a0001 | c0001 | t0030 | g0099 | AFR | ACB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02055 | hp2 | a0005 | c0005 | t0002 | g0277 | AFR | ACB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02056 | hp1 | a0001 | c0001 | t0225 | g0081 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02056 | hp2 | a0002 | c0002 | t0173 | g0029 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02071 | hp1 | a0001 | c0001 | t0150 | g0248 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02071 | hp2 | a0002 | c0002 | t0065 | g0207 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02074 | hp1 | a0003 | c0003 | t0125 | g0200 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02080 | hp2 | a0004 | c0004 | t0260 | g0073 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02083 | hp1 | a0001 | c0001 | t0068 | g0140 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02083 | hp2 | a0003 | c0003 | t0012 | g0020 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02129 | hp1 | a0001 | c0001 | t0009 | g0122 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02129 | hp2 | a0003 | c0003 | t0110 | g0190 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02132 | hp2 | a0001 | c0001 | t0227 | g0062 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02135 | hp1 | a0004 | c0004 | t0256 | g0065 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02135 | hp2 | a0001 | c0001 | t0079 | g0249 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02145 | hp1 | a0001 | c0001 | t0014 | g0181 | AFR | ACB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02145 | hp2 | a0001 | c0001 | t0271 | g0163 | AFR | ACB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02148 | hp1 | a0003 | c0003 | t0039 | g0153 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02148 | hp2 | a0001 | c0001 | t0092 | g0015 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02165 | hp1 | a0002 | c0002 | t0162 | g0007 | EAS | CDX | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02165 | hp2 | a0003 | c0003 | t0057 | g0187 | EAS | CDX | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02257 | hp1 | a0002 | c0002 | t0174 | g0003 | AFR | ACB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02257 | hp2 | a0001 | c0001 | t0276 | g0162 | AFR | ACB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02258 | hp1 | a0001 | c0001 | t0120 | g0211 | AFR | ACB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02258 | hp2 | a0001 | c0001 | t0194 | g0131 | AFR | ACB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02273 | hp1 | a0003 | c0003 | t0003 | g0156 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02273 | hp2 | a0004 | c0004 | t0261 | g0040 | AMR | PEL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02280 | hp1 | a0001 | c0001 | t0275 | g0108 | AFR | ACB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02280 | hp2 | a0001 | c0001 | t0089 | g0168 | AFR | ACB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02523 | hp1 | a0001 | c0001 | t0096 | g0152 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02523 | hp2 | a0002 | c0002 | t0023 | g0299 | EAS | KHV | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02572 | hp1 | a0005 | c0005 | t0131 | g0276 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02572 | hp2 | a0001 | c0001 | t0252 | g0205 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02602 | hp1 | a0001 | c0001 | t0139 | g0114 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02602 | hp2 | a0001 | c0001 | t0228 | g0059 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02615 | hp1 | a0001 | c0001 | t0183 | g0101 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02615 | hp2 | a0001 | c0001 | t0152 | g0227 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02622 | hp1 | a0001 | c0001 | t0115 | g0169 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02622 | hp2 | a0001 | c0001 | t0238 | g0084 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02630 | hp1 | a0001 | c0001 | t0037 | g0204 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02630 | hp2 | a0001 | c0001 | t0052 | g0254 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02647 | hp1 | a0001 | c0001 | t0280 | g0132 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02647 | hp2 | a0001 | c0001 | t0202 | g0079 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02698 | hp1 | a0001 | c0001 | t0281 | g0218 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02698 | hp2 | a0002 | c0002 | t0170 | g0007 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02723 | hp1 | a0001 | c0001 | t0099 | g0264 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02723 | hp2 | a0001 | c0001 | t0278 | g0160 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02735 | hp1 | a0001 | c0001 | t0247 | g0008 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02735 | hp2 | a0001 | c0001 | t0157 | g0241 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02738 | hp1 | a0001 | c0001 | t0069 | g0220 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02738 | hp2 | a0001 | c0001 | t0135 | g0244 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02809 | hp1 | a0001 | c0001 | t0270 | g0272 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02809 | hp2 | a0001 | c0001 | t0288 | g0102 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02818 | hp1 | a0001 | c0001 | t0020 | g0023 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02818 | hp2 | a0001 | c0006 | t0268 | g0250 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02886 | hp1 | a0001 | c0001 | t0213 | g0013 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02886 | hp2 | a0001 | c0001 | t0189 | g0120 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02896 | hp1 | a0001 | c0001 | t0273 | g0106 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02896 | hp2 | a0001 | c0001 | t0250 | g0095 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02897 | hp1 | a0001 | c0001 | t0031 | g0096 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02897 | hp2 | a0001 | c0001 | t0042 | g0047 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02922 | hp1 | a0001 | c0001 | t0054 | g0173 | AFR | ESN | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02922 | hp2 | a0001 | c0006 | t0035 | g0252 | AFR | ESN | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02965 | hp1 | a0001 | c0001 | t0114 | g0206 | AFR | ESN | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02965 | hp2 | a0001 | c0001 | t0031 | g0012 | AFR | ESN | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02970 | hp1 | a0001 | c0001 | t0264 | g0078 | AFR | ESN | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02970 | hp2 | a0001 | c0001 | t0200 | g0090 | AFR | ESN | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02976 | hp1 | a0001 | c0001 | t0263 | g0107 | AFR | ESN | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02976 | hp2 | a0001 | c0001 | t0211 | g0052 | AFR | ESN | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03017 | hp1 | a0001 | c0001 | t0047 | g0221 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03017 | hp2 | a0001 | c0001 | t0206 | g0051 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03098 | hp1 | a0001 | c0001 | t0182 | g0036 | AFR | MSL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03098 | hp2 | a0005 | c0005 | t0002 | g0275 | AFR | MSL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03130 | hp1 | a0006 | c0007 | t0148 | g0026 | AFR | ESN | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03130 | hp2 | a0001 | c0001 | t0117 | g0022 | AFR | ESN | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03139 | hp1 | a0001 | c0001 | t0214 | g0098 | AFR | ESN | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03139 | hp2 | a0001 | c0001 | t0207 | g0011 | AFR | ESN | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03195 | hp1 | a0001 | c0001 | t0241 | g0012 | AFR | ESN | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03195 | hp2 | a0001 | c0001 | t0029 | g0076 | AFR | ESN | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03209 | hp1 | a0001 | c0001 | t0209 | g0046 | AFR | MSL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03209 | hp2 | a0001 | c0001 | t0038 | g0203 | AFR | MSL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03225 | hp1 | a0001 | c0001 | t0020 | g0023 | AFR | MSL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03225 | hp2 | a0001 | c0001 | t0291 | g0105 | AFR | MSL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03239 | hp1 | a0001 | c0001 | t0015 | g0151 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03239 | hp2 | a0002 | c0002 | t0167 | g0304 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | MSL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03453 | hp2 | a0001 | c0001 | t0277 | g0161 | AFR | MSL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03486 | hp1 | a0001 | c0001 | t0245 | g0010 | AFR | MSL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03486 | hp2 | a0001 | c0001 | t0240 | g0100 | AFR | MSL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03490 | hp1 | a0002 | c0002 | t0024 | g0300 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03490 | hp2 | a0001 | c0001 | t0156 | g0240 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03491 | hp1 | a0001 | c0001 | t0019 | g0113 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03491 | hp2 | a0001 | c0001 | t0051 | g0219 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03492 | hp2 | a0001 | c0001 | t0019 | g0112 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03516 | hp1 | a0001 | c0001 | t0229 | g0164 | AFR | ESN | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03516 | hp2 | a0005 | c0005 | t0130 | g0037 | AFR | ESN | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03540 | hp1 | a0001 | c0006 | t0267 | g0251 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03540 | hp2 | a0001 | c0001 | t0053 | g0253 | AFR | GWD | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03579 | hp1 | a0005 | c0005 | t0123 | g0274 | AFR | MSL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0069 | AFR | MSL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03669 | hp1 | a0001 | c0001 | t0073 | g0166 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03669 | hp2 | a0007 | c0008 | t0272 | g0269 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03704 | hp1 | a0001 | c0001 | t0243 | g0214 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03704 | hp2 | a0004 | c0004 | t0235 | g0010 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03710 | hp1 | a0001 | c0001 | t0085 | g0215 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03710 | hp2 | a0001 | c0001 | t0287 | g0056 | SAS | PJL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03831 | hp1 | a0001 | c0001 | t0081 | g0130 | SAS | BEB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03831 | hp2 | a0001 | c0001 | t0027 | g0093 | SAS | BEB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03834 | hp1 | a0001 | c0001 | t0094 | g0016 | SAS | BEB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03834 | hp2 | a0001 | c0001 | t0086 | g0216 | SAS | BEB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03927 | hp1 | a0001 | c0001 | t0041 | g0116 | SAS | BEB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03927 | hp2 | a0002 | c0002 | t0175 | g0302 | SAS | BEB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03942 | hp1 | a0001 | c0001 | t0142 | g0226 | SAS | BEB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03942 | hp2 | a0001 | c0001 | t0284 | g0134 | SAS | BEB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG04115 | hp1 | a0001 | c0001 | t0027 | g0094 | SAS | STU | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG04115 | hp2 | a0002 | c0002 | t0179 | g0295 | SAS | STU | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG04204 | hp1 | a0001 | c0001 | t0151 | g0239 | SAS | STU | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG04204 | hp2 | a0001 | c0001 | t0205 | g0008 | SAS | STU | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG04228 | hp1 | a0001 | c0001 | t0185 | g0124 | SAS | STU | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG04228 | hp2 | a0001 | c0001 | t0193 | g0006 | SAS | STU | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18522 | hp1 | a0005 | c0005 | t0002 | g0028 | AFR | YRI | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18522 | hp2 | a0001 | c0001 | t0233 | g0048 | AFR | YRI | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18747 | hp1 | a0003 | c0003 | t0012 | g0020 | EAS | CHB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18747 | hp2 | a0001 | c0001 | t0040 | g0018 | EAS | CHB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18906 | hp1 | a0001 | c0001 | t0289 | g0103 | AFR | YRI | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18906 | hp2 | a0001 | c0001 | t0127 | g0260 | AFR | YRI | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18939 | hp1 | a0003 | c0003 | t0129 | g0183 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18939 | hp2 | a0002 | c0002 | t0177 | g0296 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18940 | hp1 | a0001 | c0001 | t0224 | g0045 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18940 | hp2 | a0002 | c0002 | t0163 | g0284 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18942 | hp1 | a0002 | c0002 | t0023 | g0303 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18942 | hp2 | a0002 | c0002 | t0004 | g0288 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18943 | hp1 | a0003 | c0003 | t0124 | g0182 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18943 | hp2 | a0001 | c0001 | t0234 | g0043 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18947 | hp1 | a0007 | c0008 | t0274 | g0268 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18947 | hp2 | a0002 | c0002 | t0172 | g0297 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18948 | hp1 | a0001 | c0001 | t0100 | g0255 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18948 | hp2 | a0001 | c0001 | t0138 | g0228 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18950 | hp1 | a0001 | c0001 | t0137 | g0229 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18950 | hp2 | a0003 | c0003 | t0060 | g0209 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18951 | hp1 | a0001 | c0001 | t0222 | g0057 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18951 | hp2 | a0001 | c0001 | t0067 | g0149 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18954 | hp1 | a0001 | c0001 | t0109 | g0174 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18959 | hp1 | a0004 | c0004 | t0266 | g0004 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18959 | hp2 | a0003 | c0003 | t0048 | g0121 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18960 | hp1 | a0001 | c0001 | t0058 | g0127 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18961 | hp1 | a0001 | c0001 | t0111 | g0175 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18961 | hp2 | a0003 | c0003 | t0082 | g0189 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18962 | hp1 | a0003 | c0003 | t0016 | g0024 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18962 | hp2 | a0002 | c0002 | t0180 | g0301 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18964 | hp1 | a0003 | c0003 | t0128 | g0198 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18964 | hp2 | a0001 | c0001 | t0145 | g0245 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18966 | hp1 | a0003 | c0003 | t0253 | g0184 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18966 | hp2 | a0004 | c0004 | t0265 | g0004 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18969 | hp1 | a0003 | c0003 | t0011 | g0188 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18969 | hp2 | a0001 | c0001 | t0168 | g0180 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18971 | hp1 | a0004 | c0004 | t0262 | g0067 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18971 | hp2 | a0001 | c0001 | t0016 | g0019 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18979 | hp1 | a0004 | c0004 | t0259 | g0085 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18979 | hp2 | a0002 | c0002 | t0022 | g0293 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18980 | hp1 | a0004 | c0004 | t0008 | g0001 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18980 | hp2 | a0002 | c0010 | t0022 | g0294 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18983 | hp1 | a0001 | c0001 | t0064 | g0018 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18983 | hp2 | a0001 | c0001 | t0011 | g0147 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18984 | hp1 | a0009 | c0013 | t0015 | g0143 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18984 | hp2 | a0003 | c0003 | t0279 | g0202 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18993 | hp1 | a0001 | c0001 | t0244 | g0072 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18993 | hp2 | a0002 | c0002 | t0024 | g0039 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18995 | hp1 | a0001 | c0001 | t0187 | g0212 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18995 | hp2 | a0001 | c0001 | t0186 | g0144 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18997 | hp1 | a0001 | c0001 | t0063 | g0117 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18997 | hp2 | a0002 | c0002 | t0176 | g0286 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18998 | hp2 | a0003 | c0003 | t0056 | g0213 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18999 | hp1 | a0001 | c0001 | t0126 | g0234 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18999 | hp2 | a0001 | c0001 | t0107 | g0133 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19000 | hp1 | a0002 | c0002 | t0195 | g0282 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19000 | hp2 | a0001 | c0001 | t0198 | g0044 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19002 | hp1 | a0001 | c0001 | t0248 | g0071 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19002 | hp2 | a0002 | c0002 | t0004 | g0289 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19003 | hp1 | a0001 | c0001 | t0197 | g0208 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19003 | hp2 | a0001 | c0001 | t0059 | g0195 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19004 | hp1 | a0002 | c0002 | t0166 | g0279 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19004 | hp2 | a0001 | c0001 | t0230 | g0063 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19007 | hp1 | a0001 | c0001 | t0049 | g0223 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19007 | hp2 | a0001 | c0001 | t0062 | g0145 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19009 | hp1 | a0001 | c0001 | t0188 | g0193 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19009 | hp2 | a0001 | c0001 | t0221 | g0087 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19011 | hp1 | a0001 | c0001 | t0147 | g0230 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19012 | hp1 | a0003 | c0003 | t0010 | g0025 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19012 | hp2 | a0004 | c0004 | t0033 | g0068 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19030 | hp1 | a0001 | c0001 | t0029 | g0089 | AFR | LWK | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19030 | hp2 | a0001 | c0001 | t0290 | g0104 | AFR | LWK | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19043 | hp1 | a0001 | c0001 | t0283 | g0110 | AFR | LWK | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19043 | hp2 | a0001 | c0001 | t0251 | g0270 | AFR | LWK | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19063 | hp2 | a0001 | c0001 | t0093 | g0224 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19065 | hp1 | a0001 | c0001 | t0018 | g0015 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19065 | hp2 | a0004 | c0004 | t0008 | g0001 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19068 | hp1 | a0001 | c0001 | t0112 | g0176 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19068 | hp2 | a0003 | c0003 | t0075 | g0024 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19079 | hp1 | a0010 | c0011 | t0083 | g0178 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19079 | hp2 | a0004 | c0004 | t0258 | g0074 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19081 | hp1 | a0001 | c0001 | t0237 | g0070 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19081 | hp2 | a0003 | c0003 | t0013 | g0186 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19086 | hp1 | a0003 | c0003 | t0010 | g0196 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19086 | hp2 | a0002 | c0002 | t0171 | g0003 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19088 | hp1 | a0003 | c0003 | t0055 | g0225 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19088 | hp2 | a0001 | c0001 | t0091 | g0222 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19090 | hp1 | a0003 | c0003 | t0080 | g0201 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19090 | hp2 | a0001 | c0001 | t0203 | g0086 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19240 | hp1 | a0001 | c0001 | t0090 | g0118 | AFR | YRI | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA19240 | hp2 | a0006 | c0007 | t0141 | g0242 | AFR | YRI | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | ASW | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA20129 | hp2 | a0005 | c0005 | t0002 | g0028 | AFR | ASW | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA20752 | hp1 | a0001 | c0001 | t0184 | g0139 | EUR | TSI | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA20752 | hp2 | a0001 | c0001 | t0095 | g0256 | EUR | TSI | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA20805 | hp1 | a0001 | c0001 | t0158 | g0258 | EUR | TSI | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA20805 | hp2 | a0001 | c0001 | t0043 | g0165 | EUR | TSI | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | GIH | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA20905 | hp2 | a0001 | c0001 | t0282 | g0217 | SAS | GIH | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02109 | hp1 | a0005 | c0005 | t0002 | g0273 | AFR | ACB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02109 | hp2 | a0001 | c0001 | t0204 | g0075 | AFR | ACB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02559 | hp1 | a0001 | c0001 | t0134 | g0179 | AFR | ACB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG02559 | hp2 | a0001 | c0001 | t0210 | g0092 | AFR | ACB | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03471 | hp1 | a0001 | c0001 | t0196 | g0109 | AFR | MSL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG03471 | hp2 | a0001 | c0001 | t0181 | g0035 | AFR | MSL | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG06807 | hp1 | a0008 | c0014 | t0254 | g0191 | AFR | USA | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
HG06807 | hp2 | a0001 | c0001 | t0045 | g0027 | AFR | USA | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18955 | hp1 | a0003 | c0003 | t0104 | g0185 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA18955 | hp2 | a0001 | c0001 | t0088 | g0170 | EAS | JPT | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA20300 | hp1 | a0001 | c0001 | t0030 | g0013 | AFR | USA | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA20300 | hp2 | a0004 | c0004 | t0032 | g0083 | AFR | USA | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA21309 | hp1 | a0001 | c0012 | t0192 | g0192 | AFR | LWK | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
NA21309 | hp2 | a0001 | c0001 | t0215 | g0082 | AFR | LWK | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
homoSapiens | chm13v2 | a0001 | c0001 | t0034 | g0257 | REF | REF | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
homoSapiens | grch38p0 | a0001 | c0001 | t0133 | g0014 | REF | REF | CHST12_chr7_2398611_2453484 | CHST12 | chr7 | 2398611 | 2453484 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:2432794 | C | A | 1 | a0002 | 39 | HG00544.hp2 HG00609.hp2 HG01070.hp1 others(36): Show |
missense_variant | MODERATE | c.155C>A | p.Pro52His | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 295/15985 | 155/1245 | 52/414 | chr7 | 2432794 | |||
chr7:2432817 | C | T | 1 | a0008 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.178C>T | p.Leu60Phe | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 318/15985 | 178/1245 | 60/414 | chr7 | 2432817 | |||
chr7:2432820 | A | T | 1 | a0002 | 39 | HG00544.hp2 HG00609.hp2 HG01070.hp1 others(36): Show |
missense_variant | MODERATE | c.181A>T | p.Thr61Ser | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 321/15985 | 181/1245 | 61/414 | chr7 | 2432820 | |||
chr7:2432920 | C | T | 1 | a0004 | 18 | HG00423.hp1 HG00597.hp2 HG00639.hp2 others(15): Show |
missense_variant | MODERATE | c.281C>T | p.Pro94Leu | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 421/15985 | 281/1245 | 94/414 | chr7 | 2432920 | |||
chr7:2432964 | C | A | 1 | a0005 | 8 | HG02055.hp2 HG02109.hp1 HG02572.hp1 others(5): Show |
missense_variant | MODERATE | c.325C>A | p.Arg109Ser | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 465/15985 | 325/1245 | 109/414 | chr7 | 2432964 | |||
chr7:2433027 | G | C | 1 | a0005 | 8 | HG02055.hp2 HG02109.hp1 HG02572.hp1 others(5): Show |
missense_variant | MODERATE | c.388G>C | p.Gly130Arg | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 528/15985 | 388/1245 | 130/414 | chr7 | 2433027 | |||
chr7:2433072 | G | C | 1 | a0003 | 33 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(30): Show |
missense_variant | MODERATE | c.433G>C | p.Ala145Pro | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 573/15985 | 433/1245 | 145/414 | chr7 | 2433072 | |||
chr7:2433268 | C | G | 1 | a0006 | 3 | HG01081.hp2 HG03130.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.629C>G | p.Ala210Gly | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 769/15985 | 629/1245 | 210/414 | chr7 | 2433268 | |||
chr7:2433304 | G | T | 1 | a0009 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.665G>T | p.Arg222Leu | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 805/15985 | 665/1245 | 222/414 | chr7 | 2433304 | |||
chr7:2433342 | C | G | 1 | a0010 | 1 | NA19079.hp1 | missense_variant | MODERATE | c.703C>G | p.Leu235Val | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 843/15985 | 703/1245 | 235/414 | chr7 | 2433342 | |||
chr7:2433495 | G | C | 1 | a0007 | 2 | HG03669.hp2 NA18947.hp1 |
missense_variant | MODERATE | c.856G>C | p.Ala286Pro | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 996/15985 | 856/1245 | 286/414 | chr7 | 2433495 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:2432882 | C | T | 1 | a0001c0009 | 2 | HG00099.hp2 HG00280.hp1 |
synonymous_variant | LOW | c.243C>T | p.Ser81Ser | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 383/15985 | 243/1245 | 81/414 | chr7 | 2432882 | |||
chr7:2432927 | C | T | 1 | a0009c0013 | 1 | NA18984.hp1 | synonymous_variant | LOW | c.288C>T | p.Ser96Ser | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 428/15985 | 288/1245 | 96/414 | chr7 | 2432927 | |||
chr7:2433095 | G | A | 1 | a0001c0006 | 3 | HG02818.hp2 HG02922.hp2 HG03540.hp1 |
synonymous_variant | LOW | c.456G>A | p.Ser152Ser | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 596/15985 | 456/1245 | 152/414 | chr7 | 2433095 | |||
chr7:2433248 | G | A | 1 | a0002c0010 | 1 | NA18980.hp2 | synonymous_variant | LOW | c.609G>A | p.Pro203Pro | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 749/15985 | 609/1245 | 203/414 | chr7 | 2433248 | |||
chr7:2433257 | C | T | 1 | a0001c0012 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.618C>T | p.His206His | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 758/15985 | 618/1245 | 206/414 | chr7 | 2433257 | |||
chr7:2433452 | C | T | 1 | a0007c0008 | 2 | HG03669.hp2 NA18947.hp1 |
synonymous_variant | LOW | c.813C>T | p.Ala271Ala | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 953/15985 | 813/1245 | 271/414 | chr7 | 2433452 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:2403624 | C | T | 1 | a0001c0001t0293 | 1 | HG00099.hp1 | 5_prime_UTR_variant | MODIFIER | c.-127C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/2 | 29016 | chr7 | 2403624 | ||||||
chr7:2403636 | CGGGCGCG others(7): Show |
C | 5 | a0001c0001t0288 a0001c0001t0289 a0001c0001t0290 others(2): Show |
5 | HG01891.hp2 HG02809.hp2 HG03225.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-98_-85delGCGCGAGG others(6): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/2 | 28974 | INFO_REALIGN_3_PRIME | chr7 | 2403636 | |||||
chr7:2403653 | GCGCGAGG others(7): Show |
G | 8 | a0001c0001t0280 a0001c0001t0281 a0001c0001t0282 others(5): Show |
8 | HG01106.hp1 HG02015.hp1 HG02647.hp1 others(5): Show |
splice_donor_variant&splice_region_variant&5_prime_UTR_variant&intron_variant | HIGH | c.-84_-78+7delTCGCGA others(8): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/2 | 28960 | INFO_REALIGN_3_PRIME | chr7 | 2403653 | |||||
chr7:2403667 | T | G | 171 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(168): Show |
202 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(199): Show |
5_prime_UTR_variant | MODIFIER | c.-84T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/2 | 28973 | chr7 | 2403667 | ||||||
chr7:2432620 | C | T | 1 | a0003c0003t0279 | 1 | NA18984.hp2 | 5_prime_UTR_variant | MODIFIER | c.-20C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 20 | chr7 | 2432620 | ||||||
chr7:2432632 | G | A | 1 | a0001c0006t0035 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-8G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8 | chr7 | 2432632 | ||||||
chr7:2433924 | A | C | 12 | a0001c0001t0270 a0001c0001t0271 a0001c0001t0273 others(9): Show |
12 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*40A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 40 | chr7 | 2433924 | ||||||
chr7:2434076 | C | T | 1 | a0001c0001t0269 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*192C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 192 | chr7 | 2434076 | ||||||
chr7:2434088 | A | C | 12 | a0001c0001t0270 a0001c0001t0271 a0001c0001t0273 others(9): Show |
12 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*204A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 204 | chr7 | 2434088 | ||||||
chr7:2434101 | T | TCCGCCCG others(1): Show |
11 | a0004c0004t0008 a0004c0004t0032 a0004c0004t0033 others(8): Show |
15 | HG00423.hp1 HG00597.hp2 HG00639.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*220_*227dupGCCCGC others(2): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 228 | INFO_REALIGN_3_PRIME | chr7 | 2434101 | |||||
chr7:2434101 | T | TCCGCCCG others(5): Show |
2 | a0001c0001t0263 a0001c0001t0264 |
2 | HG02970.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*227_*228insGCCCGC others(6): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 228 | INFO_REALIGN_3_PRIME | chr7 | 2434101 | |||||
chr7:2434103 | C | T | 2 | a0001c0006t0267 a0001c0006t0268 |
2 | HG02818.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*219C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 219 | chr7 | 2434103 | ||||||
chr7:2434104 | GCCCGCCC others(1): Show |
G | 16 | a0001c0001t0270 a0001c0001t0271 a0001c0001t0273 others(13): Show |
16 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*228_*235delACCCGC others(2): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 228 | INFO_REALIGN_3_PRIME | chr7 | 2434104 | |||||
chr7:2434112 | A | ACCCG | 3 | a0001c0001t0113 a0001c0001t0159 a0001c0001t0185 |
3 | HG01168.hp1 HG01169.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*238_*241dupCCGC | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 242 | INFO_REALIGN_3_PRIME | chr7 | 2434112 | |||||
chr7:2434112 | A | ACCCGCCC others(1): Show |
3 | a0001c0001t0145 a0001c0001t0191 a0001c0001t0193 |
3 | HG01169.hp1 HG04228.hp2 NA18964.hp2 |
3_prime_UTR_variant | MODIFIER | c.*234_*241dupCCGCCC others(2): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 242 | INFO_REALIGN_3_PRIME | chr7 | 2434112 | |||||
chr7:2434112 | A | G | 79 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0027 others(76): Show |
92 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*228A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 228 | chr7 | 2434112 | ||||||
chr7:2434114 | CCGCCCGC others(5): Show |
C | 1 | a0008c0014t0254 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*238_*249delCCGCTC others(6): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 238 | INFO_REALIGN_3_PRIME | chr7 | 2434114 | |||||
chr7:2434117 | C | A | 9 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0028 others(6): Show |
12 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*233C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 233 | chr7 | 2434117 | ||||||
chr7:2434118 | C | CCGCCCGC others(9): Show |
1 | a0003c0003t0056 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*241_*242insCCGCCC others(10): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 242 | INFO_REALIGN_3_PRIME | chr7 | 2434118 | |||||
chr7:2434118 | C | CCGCCCGC others(25): Show |
1 | a0004c0004t0235 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*241_*242insCCGCCC others(26): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 242 | INFO_REALIGN_3_PRIME | chr7 | 2434118 | |||||
chr7:2434118 | C | CCGCCCGC others(1): Show |
30 | a0001c0001t0059 a0001c0001t0087 a0001c0001t0089 others(27): Show |
32 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*252_*259dupGCCCGC others(2): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 260 | INFO_REALIGN_3_PRIME | chr7 | 2434118 | |||||
chr7:2434122 | C | T | 12 | a0001c0001t0270 a0001c0001t0271 a0001c0001t0273 others(9): Show |
12 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*238C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 238 | chr7 | 2434122 | ||||||
chr7:2434126 | T | C | 1 | a0004c0004t0265 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*242T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 242 | chr7 | 2434126 | ||||||
chr7:2434126 | T | TCGCCCGC others(1): Show |
59 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0027 others(56): Show |
67 | HG00544.hp1 HG00639.hp1 HG00738.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*249_*250insCCGCCC others(2): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 250 | INFO_REALIGN_3_PRIME | chr7 | 2434126 | |||||
chr7:2434126 | T | TCGCCCGC others(5): Show |
2 | a0001c0001t0202 a0001c0001t0214 |
2 | HG02647.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*249_*250insCCGCCC others(6): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 250 | INFO_REALIGN_3_PRIME | chr7 | 2434126 | |||||
chr7:2434128 | G | A | 12 | a0001c0001t0270 a0001c0001t0271 a0001c0001t0273 others(9): Show |
12 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*244G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 244 | chr7 | 2434128 | ||||||
chr7:2434128 | G | GCCCCGCT others(3): Show |
1 | a0001c0001t0036 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*247_*248insCGCTCG others(4): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 248 | INFO_REALIGN_3_PRIME | chr7 | 2434128 | |||||
chr7:2434128 | G | GCTCCGCT others(3): Show |
1 | a0003c0003t0253 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*245_*246insTCCGCT others(4): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 246 | INFO_REALIGN_3_PRIME | chr7 | 2434128 | |||||
chr7:2434134 | T | C | 1 | a0004c0004t0265 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*250T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 250 | chr7 | 2434134 | ||||||
chr7:2434135 | C | T | 1 | a0001c0001t0252 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*251C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 251 | chr7 | 2434135 | ||||||
chr7:2434169 | G | T | 75 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0027 others(72): Show |
88 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*285G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 285 | chr7 | 2434169 | ||||||
chr7:2434259 | G | A | 2 | a0001c0001t0037 a0001c0001t0038 |
2 | HG02630.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*375G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 375 | chr7 | 2434259 | ||||||
chr7:2434285 | C | G | 1 | a0001c0001t0197 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*401C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 401 | chr7 | 2434285 | ||||||
chr7:2434335 | A | C | 2 | a0001c0001t0277 a0001c0001t0278 |
2 | HG02723.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*451A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 451 | chr7 | 2434335 | ||||||
chr7:2434468 | C | G | 1 | a0001c0001t0196 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*584C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 584 | chr7 | 2434468 | ||||||
chr7:2434579 | T | TAAAA | 38 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(35): Show |
46 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*729_*732dupAAAA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 733 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | T | TAAAAA | 32 | a0001c0001t0014 a0001c0001t0070 a0001c0001t0071 others(29): Show |
35 | HG00609.hp1 HG00642.hp1 HG00733.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*728_*732dupAAAAA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 733 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | T | TAAAAAA | 15 | a0001c0001t0011 a0001c0001t0037 a0001c0001t0038 others(12): Show |
15 | HG00735.hp1 HG02027.hp2 HG02071.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*727_*732dupAAAAAA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 733 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | T | TAAAAAAA | 6 | a0001c0001t0058 a0001c0001t0059 a0003c0003t0055 others(3): Show |
6 | HG02165.hp2 NA18950.hp2 NA18960.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*726_*732dupAAAAAA others(1): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 733 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | T | TAAAAAAA others(1): Show |
10 | a0001c0001t0009 a0001c0001t0049 a0001c0001t0050 others(7): Show |
11 | HG00408.hp1 HG01261.hp2 HG02129.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*725_*732dupAAAAAA others(2): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 733 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | T | TAAAAAAA others(3): Show |
6 | a0001c0001t0043 a0001c0001t0045 a0001c0001t0046 others(3): Show |
6 | HG00673.hp2 HG01109.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*723_*732dupAAAAAA others(4): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 733 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | T | TAAAAAAA others(5): Show |
1 | a0001c0001t0042 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*721_*732dupAAAAAA others(6): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 733 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | T | TAAAAAAA others(6): Show |
1 | a0001c0001t0041 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*720_*732dupAAAAAA others(7): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 733 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | T | TAAAAAAA others(7): Show |
2 | a0001c0001t0040 a0003c0003t0039 |
2 | HG02148.hp1 NA18747.hp2 |
3_prime_UTR_variant | MODIFIER | c.*719_*732dupAAAAAA others(8): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 733 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | TA | T | 6 | a0001c0001t0135 a0001c0001t0136 a0001c0001t0137 others(3): Show |
6 | HG00642.hp2 HG01346.hp1 HG02602.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*732delA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 732 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | TAA | T | 12 | a0001c0001t0021 a0001c0001t0036 a0001c0001t0142 others(9): Show |
13 | HG00280.hp2 HG00733.hp2 HG01256.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*731_*732delAA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 731 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | TAAA | T | 19 | a0001c0001t0149 a0001c0001t0150 a0001c0001t0151 others(16): Show |
19 | HG00099.hp1 HG00438.hp2 HG00673.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*730_*732delAAA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 730 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | TAAAA | T | 19 | a0001c0001t0203 a0001c0001t0204 a0001c0001t0205 others(16): Show |
20 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*729_*732delAAAA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 729 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | TAAAAA | T | 47 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0027 others(44): Show |
59 | HG00544.hp1 HG00597.hp2 HG00738.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*728_*732delAAAAA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 728 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | TAAAAAA | T | 13 | a0001c0001t0160 a0001c0001t0246 a0001c0001t0247 others(10): Show |
13 | HG00738.hp1 HG01099.hp1 HG01099.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*727_*732delAAAAAA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 727 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | TAAAAAAA others(1): Show |
T | 15 | a0001c0001t0168 a0001c0001t0169 a0001c0001t0196 others(12): Show |
19 | HG00544.hp2 HG00609.hp2 HG01243.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*725_*732delAAAAAA others(2): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 725 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | TAAAAAAA others(2): Show |
T | 14 | a0001c0001t0181 a0001c0001t0182 a0001c0001t0183 others(11): Show |
21 | HG01070.hp1 HG02056.hp2 HG02074.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*724_*732delAAAAAA others(3): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 724 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | TAAAAAAA others(3): Show |
T | 1 | a0002c0002t0024 | 2 | HG03490.hp1 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*723_*732delAAAAAA others(4): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 723 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | TAAAAAAA others(4): Show |
T | 3 | a0001c0001t0184 a0001c0001t0185 a0001c0001t0290 |
3 | HG04228.hp1 NA19030.hp2 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*722_*732delAAAAAA others(5): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 722 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | TAAAAAAA others(5): Show |
T | 5 | a0001c0001t0025 a0001c0001t0186 a0001c0001t0187 others(2): Show |
6 | HG01257.hp2 HG01258.hp1 HG03225.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*721_*732delAAAAAA others(6): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 721 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | TAAAAAAA others(6): Show |
T | 8 | a0001c0001t0189 a0001c0001t0190 a0001c0001t0191 others(5): Show |
8 | HG01109.hp2 HG01169.hp1 HG01891.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*720_*732delAAAAAA others(7): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 720 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | TAAAAAAA others(7): Show |
T | 1 | a0001c0001t0194 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*719_*732delAAAAAA others(8): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 719 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | TAAAAAAA others(8): Show |
T | 1 | a0001c0001t0251 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*718_*732delAAAAAA others(9): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 718 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434579 | TAAAAAAA others(14): Show |
T | 1 | a0002c0002t0195 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*712_*732delAAAAAA others(15): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 712 | INFO_REALIGN_3_PRIME | chr7 | 2434579 | |||||
chr7:2434623 | G | A | 5 | a0001c0001t0290 a0001c0001t0291 a0001c0001t0292 others(2): Show |
5 | HG01891.hp2 HG03225.hp2 HG03669.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*739G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 739 | chr7 | 2434623 | ||||||
chr7:2434749 | A | G | 6 | a0001c0001t0020 a0001c0001t0042 a0001c0001t0052 others(3): Show |
7 | HG02559.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*865A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 865 | chr7 | 2434749 | ||||||
chr7:2434796 | T | C | 3 | a0001c0001t0290 a0001c0001t0291 a0001c0001t0292 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*912T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 912 | chr7 | 2434796 | ||||||
chr7:2434801 | A | G | 3 | a0001c0001t0290 a0001c0001t0291 a0001c0001t0292 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*917A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 917 | chr7 | 2434801 | ||||||
chr7:2434920 | C | T | 1 | a0001c0001t0120 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1036C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 1036 | chr7 | 2434920 | ||||||
chr7:2434976 | G | C | 7 | a0001c0001t0270 a0001c0001t0271 a0001c0001t0273 others(4): Show |
7 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1092G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 1092 | chr7 | 2434976 | ||||||
chr7:2435020 | A | G | 1 | a0001c0001t0276 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1136A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 1136 | chr7 | 2435020 | ||||||
chr7:2435324 | G | C | 1 | a0001c0001t0120 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1440G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 1440 | chr7 | 2435324 | ||||||
chr7:2435744 | G | T | 1 | a0001c0001t0245 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1860G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 1860 | chr7 | 2435744 | ||||||
chr7:2435810 | A | C | 1 | a0001c0001t0196 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1926A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 1926 | chr7 | 2435810 | ||||||
chr7:2435873 | G | C | 2 | a0001c0001t0070 a0001c0001t0071 |
2 | HG00735.hp2 HG01069.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1989G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 1989 | chr7 | 2435873 | ||||||
chr7:2436001 | A | T | 2 | a0001c0001t0263 a0001c0001t0264 |
2 | HG02970.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2117A>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 2117 | chr7 | 2436001 | ||||||
chr7:2436016 | G | A | 1 | a0001c0001t0096 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2132G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 2132 | chr7 | 2436016 | ||||||
chr7:2436121 | G | A | 9 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0028 others(6): Show |
12 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2237G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 2237 | chr7 | 2436121 | ||||||
chr7:2436388 | A | T | 86 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0027 others(83): Show |
99 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*2504A>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 2504 | chr7 | 2436388 | ||||||
chr7:2436401 | A | G | 2 | a0001c0001t0273 a0001c0001t0275 |
2 | HG02280.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2517A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 2517 | chr7 | 2436401 | ||||||
chr7:2436554 | T | A | 1 | a0001c0001t0285 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2670T>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 2670 | chr7 | 2436554 | ||||||
chr7:2436713 | G | A | 2 | a0007c0008t0272 a0007c0008t0274 |
2 | HG03669.hp2 NA18947.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2829G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 2829 | chr7 | 2436713 | ||||||
chr7:2436738 | G | A | 1 | a0001c0001t0189 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2854G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 2854 | chr7 | 2436738 | ||||||
chr7:2436819 | G | C | 2 | a0001c0001t0288 a0001c0001t0289 |
2 | HG02809.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2935G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 2935 | chr7 | 2436819 | ||||||
chr7:2436962 | C | T | 5 | a0001c0001t0270 a0001c0001t0271 a0001c0001t0276 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3078C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 3078 | chr7 | 2436962 | ||||||
chr7:2437011 | C | T | 5 | a0001c0001t0051 a0001c0001t0069 a0001c0001t0095 others(2): Show |
5 | HG02698.hp1 HG02738.hp1 HG03491.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3127C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 3127 | chr7 | 2437011 | ||||||
chr7:2437049 | A | G | 1 | a0001c0001t0215 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3165A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 3165 | chr7 | 2437049 | ||||||
chr7:2437161 | C | T | 1 | a0001c0001t0290 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3277C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 3277 | chr7 | 2437161 | ||||||
chr7:2437706 | G | A | 1 | a0001c0001t0221 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3822G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 3822 | chr7 | 2437706 | ||||||
chr7:2437726 | ACG | A | 77 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0027 others(74): Show |
90 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*3848_*3849delGC | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 3848 | INFO_REALIGN_3_PRIME | chr7 | 2437726 | |||||
chr7:2437728 | G | A | 1 | a0002c0002t0001 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3844G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 3844 | chr7 | 2437728 | ||||||
chr7:2437732 | G | A | 8 | a0001c0001t0221 a0001c0001t0263 a0001c0001t0264 others(5): Show |
8 | HG02145.hp2 HG02257.hp2 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3848G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 3848 | chr7 | 2437732 | ||||||
chr7:2437732 | GCA | G | 171 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(168): Show |
200 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*3870_*3871delAC | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 3870 | INFO_REALIGN_3_PRIME | chr7 | 2437732 | |||||
chr7:2437732 | GCACA | G | 6 | a0001c0001t0069 a0001c0001t0135 a0001c0001t0146 others(3): Show |
6 | HG02015.hp2 HG02738.hp1 HG02738.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3868_*3871delACAC | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 3868 | INFO_REALIGN_3_PRIME | chr7 | 2437732 | |||||
chr7:2437734 | A | G | 2 | a0002c0002t0001 a0003c0003t0128 |
2 | NA18964.hp1 NA19063.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3850A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 3850 | chr7 | 2437734 | ||||||
chr7:2437736 | A | G | 8 | a0001c0001t0014 a0001c0001t0087 a0001c0001t0099 others(5): Show |
9 | HG01192.hp1 HG01255.hp1 HG01884.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3852A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 3852 | chr7 | 2437736 | ||||||
chr7:2437756 | T | A | 73 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0027 others(70): Show |
86 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*3872T>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 3872 | chr7 | 2437756 | ||||||
chr7:2437762 | T | A | 1 | a0001c0001t0221 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3878T>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 3878 | chr7 | 2437762 | ||||||
chr7:2437766 | A | C | 1 | a0003c0003t0013 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3882A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 3882 | chr7 | 2437766 | ||||||
chr7:2437981 | G | A | 1 | a0001c0001t0135 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4097G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4097 | chr7 | 2437981 | ||||||
chr7:2438004 | G | A | 3 | a0001c0001t0283 a0001c0001t0288 a0001c0001t0289 |
3 | HG02809.hp2 NA18906.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4120G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4120 | chr7 | 2438004 | ||||||
chr7:2438086 | G | A | 1 | a0001c0001t0194 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4202G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4202 | chr7 | 2438086 | ||||||
chr7:2438160 | C | T | 1 | a0001c0001t0289 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4276C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4276 | chr7 | 2438160 | ||||||
chr7:2438162 | C | T | 9 | a0001c0001t0030 a0001c0001t0031 a0001c0001t0213 others(6): Show |
11 | HG01167.hp1 HG02055.hp1 HG02886.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4278C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4278 | chr7 | 2438162 | ||||||
chr7:2438218 | A | T | 1 | a0001c0001t0293 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4334A>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4334 | chr7 | 2438218 | ||||||
chr7:2438233 | A | C | 1 | a0001c0001t0280 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4349A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4349 | chr7 | 2438233 | ||||||
chr7:2438307 | C | T | 4 | a0001c0001t0263 a0001c0001t0264 a0001c0001t0273 others(1): Show |
4 | HG02280.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4423C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4423 | chr7 | 2438307 | ||||||
chr7:2438364 | T | G | 295 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(292): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
3_prime_UTR_variant | MODIFIER | c.*4480T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4480 | chr7 | 2438364 | ||||||
chr7:2438385 | C | T | 77 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0027 others(74): Show |
89 | HG00423.hp1 HG00597.hp2 HG00639.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*4501C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4501 | chr7 | 2438385 | ||||||
chr7:2438424 | C | T | 3 | a0001c0001t0290 a0001c0001t0291 a0001c0001t0292 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4540C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4540 | chr7 | 2438424 | ||||||
chr7:2438489 | C | T | 3 | a0001c0001t0290 a0001c0001t0291 a0001c0001t0292 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4605C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4605 | chr7 | 2438489 | ||||||
chr7:2438586 | C | G | 2 | a0001c0001t0029 a0001c0001t0204 |
3 | HG02109.hp2 HG03195.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4702C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4702 | chr7 | 2438586 | ||||||
chr7:2438632 | A | G | 1 | a0002c0002t0170 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4748A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4748 | chr7 | 2438632 | ||||||
chr7:2438638 | G | A | 26 | a0002c0002t0001 a0002c0002t0004 a0002c0002t0022 others(23): Show |
38 | HG00544.hp2 HG00609.hp2 HG01070.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*4754G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4754 | chr7 | 2438638 | ||||||
chr7:2438671 | C | T | 1 | a0001c0001t0054 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4787C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4787 | chr7 | 2438671 | ||||||
chr7:2438725 | C | T | 4 | a0001c0001t0263 a0001c0001t0264 a0001c0001t0273 others(1): Show |
4 | HG02280.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4841C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4841 | chr7 | 2438725 | ||||||
chr7:2438836 | CCATGGTT others(7): Show |
C | 4 | a0001c0001t0263 a0001c0001t0264 a0001c0001t0273 others(1): Show |
4 | HG02280.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4953_*4966delCATG others(10): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4953 | chr7 | 2438836 | ||||||
chr7:2438853 | C | T | 1 | a0001c0001t0068 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4969C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4969 | chr7 | 2438853 | ||||||
chr7:2438876 | C | T | 3 | a0001c0001t0290 a0001c0001t0291 a0001c0001t0292 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4992C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 4992 | chr7 | 2438876 | ||||||
chr7:2438971 | G | C | 1 | a0001c0001t0285 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5087G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 5087 | chr7 | 2438971 | ||||||
chr7:2438978 | C | T | 3 | a0001c0001t0290 a0001c0001t0291 a0001c0001t0292 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5094C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 5094 | chr7 | 2438978 | ||||||
chr7:2438979 | G | A | 1 | a0005c0005t0123 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5095G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 5095 | chr7 | 2438979 | ||||||
chr7:2439032 | C | G | 1 | a0003c0003t0119 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5148C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 5148 | chr7 | 2439032 | ||||||
chr7:2439078 | C | T | 1 | a0001c0001t0094 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5194C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 5194 | chr7 | 2439078 | ||||||
chr7:2439099 | G | A | 2 | a0001c0001t0288 a0001c0001t0289 |
2 | HG02809.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5215G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 5215 | chr7 | 2439099 | ||||||
chr7:2439188 | A | G | 1 | a0001c0001t0292 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5304A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 5304 | chr7 | 2439188 | ||||||
chr7:2439394 | T | C | 81 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0027 others(78): Show |
93 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*5510T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 5510 | chr7 | 2439394 | ||||||
chr7:2439422 | T | C | 1 | a0002c0002t0161 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5538T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 5538 | chr7 | 2439422 | ||||||
chr7:2439521 | C | T | 1 | a0001c0001t0221 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5637C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 5637 | chr7 | 2439521 | ||||||
chr7:2439524 | A | T | 1 | a0001c0001t0221 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5640A>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 5640 | chr7 | 2439524 | ||||||
chr7:2439572 | C | T | 16 | a0001c0001t0030 a0001c0001t0031 a0001c0001t0160 others(13): Show |
18 | HG00639.hp1 HG01099.hp2 HG01167.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5688C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 5688 | chr7 | 2439572 | ||||||
chr7:2439608 | G | A | 1 | a0001c0001t0200 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5724G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 5724 | chr7 | 2439608 | ||||||
chr7:2439630 | G | C | 1 | a0001c0001t0269 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5746G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 5746 | chr7 | 2439630 | ||||||
chr7:2439703 | C | A | 1 | a0001c0001t0018 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5819C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 5819 | chr7 | 2439703 | ||||||
chr7:2439735 | C | T | 4 | a0001c0001t0263 a0001c0001t0264 a0001c0001t0273 others(1): Show |
4 | HG02280.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5851C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 5851 | chr7 | 2439735 | ||||||
chr7:2439772 | G | A | 5 | a0001c0001t0043 a0001c0001t0073 a0001c0001t0074 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG01884.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5888G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 5888 | chr7 | 2439772 | ||||||
chr7:2439774 | G | A | 2 | a0001c0001t0142 a0001c0001t0149 |
2 | HG01981.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5890G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 5890 | chr7 | 2439774 | ||||||
chr7:2440134 | C | T | 1 | a0001c0001t0047 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6250C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 6250 | chr7 | 2440134 | ||||||
chr7:2440250 | G | A | 2 | a0001c0001t0203 a0001c0001t0222 |
2 | NA18951.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6366G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 6366 | chr7 | 2440250 | ||||||
chr7:2440330 | G | GGT | 6 | a0001c0001t0018 a0001c0001t0067 a0001c0001t0091 others(3): Show |
7 | HG01928.hp1 HG01975.hp2 HG02148.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6456_*6457dupTG | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 6458 | INFO_REALIGN_3_PRIME | chr7 | 2440330 | |||||
chr7:2440391 | T | C | 3 | a0001c0001t0290 a0001c0001t0291 a0001c0001t0292 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6507T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 6507 | chr7 | 2440391 | ||||||
chr7:2440404 | AAT | A | 5 | a0001c0001t0288 a0001c0001t0289 a0001c0006t0035 others(2): Show |
5 | HG02809.hp2 HG02818.hp2 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6521_*6522delAT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 6521 | chr7 | 2440404 | ||||||
chr7:2440436 | C | T | 6 | a0001c0001t0196 a0001c0001t0290 a0001c0001t0291 others(3): Show |
6 | HG01891.hp2 HG03225.hp2 HG03471.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6552C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 6552 | chr7 | 2440436 | ||||||
chr7:2440670 | G | A | 2 | a0001c0001t0205 a0001c0001t0247 |
2 | HG02735.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6786G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 6786 | chr7 | 2440670 | ||||||
chr7:2440823 | G | A | 2 | a0001c0001t0099 a0001c0001t0143 |
2 | HG00733.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6939G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 6939 | chr7 | 2440823 | ||||||
chr7:2440832 | C | T | 1 | a0004c0004t0265 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6948C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 6948 | chr7 | 2440832 | ||||||
chr7:2440843 | G | A | 1 | a0001c0001t0026 | 2 | HG01069.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6959G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 6959 | chr7 | 2440843 | ||||||
chr7:2440881 | G | A | 1 | a0001c0001t0143 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6997G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 6997 | chr7 | 2440881 | ||||||
chr7:2440922 | T | C | 2 | a0007c0008t0272 a0007c0008t0274 |
2 | HG03669.hp2 NA18947.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7038T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 7038 | chr7 | 2440922 | ||||||
chr7:2440931 | G | A | 2 | a0007c0008t0272 a0007c0008t0274 |
2 | HG03669.hp2 NA18947.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7047G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 7047 | chr7 | 2440931 | ||||||
chr7:2441094 | C | T | 45 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0019 others(42): Show |
54 | HG01070.hp2 HG01071.hp2 HG01106.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*7210C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 7210 | chr7 | 2441094 | ||||||
chr7:2441100 | C | T | 1 | a0001c0001t0040 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7216C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 7216 | chr7 | 2441100 | ||||||
chr7:2441115 | C | T | 2 | a0003c0003t0010 a0003c0003t0060 |
3 | NA18950.hp2 NA19012.hp1 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7231C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 7231 | chr7 | 2441115 | ||||||
chr7:2441134 | C | T | 2 | a0007c0008t0272 a0007c0008t0274 |
2 | HG03669.hp2 NA18947.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7250C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 7250 | chr7 | 2441134 | ||||||
chr7:2441191 | T | C | 3 | a0001c0001t0270 a0001c0001t0271 a0001c0001t0276 |
3 | HG02145.hp2 HG02257.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7307T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 7307 | chr7 | 2441191 | ||||||
chr7:2441210 | C | T | 5 | a0001c0001t0085 a0001c0001t0086 a0006c0007t0121 others(2): Show |
5 | HG01081.hp2 HG03130.hp1 HG03710.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7326C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 7326 | chr7 | 2441210 | ||||||
chr7:2441257 | A | G | 2 | a0001c0001t0239 a0001c0001t0249 |
2 | HG00738.hp1 HG01361.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7373A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 7373 | chr7 | 2441257 | ||||||
chr7:2441296 | T | C | 1 | a0001c0001t0100 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7412T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 7412 | chr7 | 2441296 | ||||||
chr7:2441446 | A | G | 2 | a0007c0008t0272 a0007c0008t0274 |
2 | HG03669.hp2 NA18947.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7562A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 7562 | chr7 | 2441446 | ||||||
chr7:2441450 | T | G | 2 | a0001c0001t0277 a0001c0001t0278 |
2 | HG02723.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7566T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 7566 | chr7 | 2441450 | ||||||
chr7:2441457 | T | C | 7 | a0001c0001t0263 a0001c0001t0264 a0001c0001t0273 others(4): Show |
7 | HG01891.hp2 HG02280.hp1 HG02896.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7573T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 7573 | chr7 | 2441457 | ||||||
chr7:2441692 | T | TA | 8 | a0001c0001t0036 a0001c0001t0063 a0001c0001t0076 others(5): Show |
8 | HG00544.hp1 HG00642.hp1 HG01978.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7829dupA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 7830 | INFO_REALIGN_3_PRIME | chr7 | 2441692 | |||||
chr7:2441692 | TA | T | 115 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0009 others(112): Show |
144 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*7829delA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 7829 | INFO_REALIGN_3_PRIME | chr7 | 2441692 | |||||
chr7:2441692 | TAA | T | 8 | a0001c0001t0086 a0001c0001t0090 a0001c0001t0132 others(5): Show |
8 | HG01081.hp2 HG01943.hp2 HG03669.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7828_*7829delAA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 7828 | INFO_REALIGN_3_PRIME | chr7 | 2441692 | |||||
chr7:2441835 | G | C | 1 | a0001c0001t0189 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7951G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 7951 | chr7 | 2441835 | ||||||
chr7:2441925 | A | C | 1 | a0001c0001t0242 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8041A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8041 | chr7 | 2441925 | ||||||
chr7:2442000 | T | TA | 6 | a0001c0001t0086 a0001c0001t0205 a0001c0001t0206 others(3): Show |
6 | HG02602.hp2 HG02735.hp1 HG03017.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8117dupA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8118 | INFO_REALIGN_3_PRIME | chr7 | 2442000 | |||||
chr7:2442001 | A | AG | 199 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(196): Show |
235 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*8117_*8118insG | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8118 | chr7 | 2442001 | ||||||
chr7:2442060 | C | T | 1 | a0001c0001t0290 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8176C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8176 | chr7 | 2442060 | ||||||
chr7:2442062 | C | T | 5 | a0001c0001t0046 a0001c0001t0074 a0001c0001t0098 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8178C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8178 | chr7 | 2442062 | ||||||
chr7:2442075 | C | T | 1 | a0004c0004t0260 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8191C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8191 | chr7 | 2442075 | ||||||
chr7:2442202 | G | A | 3 | a0001c0001t0221 a0001c0001t0230 a0001c0001t0237 |
3 | NA19004.hp2 NA19009.hp2 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8318G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8318 | chr7 | 2442202 | ||||||
chr7:2442236 | G | A | 1 | a0001c0001t0077 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8352G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8352 | chr7 | 2442236 | ||||||
chr7:2442306 | C | G | 3 | a0001c0001t0113 a0001c0001t0191 a0004c0004t0235 |
3 | HG01168.hp1 HG01169.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8422C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8422 | chr7 | 2442306 | ||||||
chr7:2442395 | G | A | 1 | a0001c0006t0268 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8511G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8511 | chr7 | 2442395 | ||||||
chr7:2442433 | A | G | 1 | a0001c0001t0240 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8549A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8549 | chr7 | 2442433 | ||||||
chr7:2442524 | T | C | 3 | a0006c0007t0121 a0006c0007t0141 a0006c0007t0148 |
3 | HG01081.hp2 HG03130.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8640T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8640 | chr7 | 2442524 | ||||||
chr7:2442525 | G | A | 3 | a0006c0007t0121 a0006c0007t0141 a0006c0007t0148 |
3 | HG01081.hp2 HG03130.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8641G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8641 | chr7 | 2442525 | ||||||
chr7:2442655 | G | A | 4 | a0001c0001t0027 a0001c0001t0041 a0001c0001t0072 others(1): Show |
5 | HG01074.hp2 HG01934.hp1 HG03831.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8771G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8771 | chr7 | 2442655 | ||||||
chr7:2442669 | C | G | 24 | a0001c0001t0021 a0001c0001t0046 a0001c0001t0086 others(21): Show |
25 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*8785C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8785 | chr7 | 2442669 | ||||||
chr7:2442720 | A | G | 6 | a0001c0001t0027 a0001c0001t0041 a0001c0001t0072 others(3): Show |
7 | HG01074.hp2 HG01361.hp1 HG01934.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8836A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8836 | chr7 | 2442720 | ||||||
chr7:2442793 | C | T | 6 | a0001c0001t0029 a0001c0001t0183 a0001c0001t0204 others(3): Show |
7 | HG01081.hp2 HG02109.hp2 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8909C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8909 | chr7 | 2442793 | ||||||
chr7:2442808 | C | T | 1 | a0001c0001t0225 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8924C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8924 | chr7 | 2442808 | ||||||
chr7:2442820 | G | A | 4 | a0001c0001t0045 a0001c0001t0078 a0001c0001t0097 others(1): Show |
4 | HG01081.hp1 HG01884.hp2 HG02615.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8936G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8936 | chr7 | 2442820 | ||||||
chr7:2442823 | G | C | 4 | a0001c0001t0090 a0001c0001t0114 a0001c0001t0252 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8939G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 8939 | chr7 | 2442823 | ||||||
chr7:2442933 | T | G | 9 | a0001c0001t0115 a0001c0001t0116 a0001c0001t0240 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*9049T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 9049 | chr7 | 2442933 | ||||||
chr7:2442961 | G | A | 1 | a0001c0001t0189 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9077G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 9077 | chr7 | 2442961 | ||||||
chr7:2442991 | G | A | 1 | a0001c0001t0101 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9107G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 9107 | chr7 | 2442991 | ||||||
chr7:2442993 | C | G | 1 | a0001c0001t0193 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9109C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 9109 | chr7 | 2442993 | ||||||
chr7:2443077 | A | G | 1 | a0001c0001t0293 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9193A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 9193 | chr7 | 2443077 | ||||||
chr7:2443103 | T | G | 2 | a0001c0001t0271 a0001c0001t0276 |
2 | HG02145.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9219T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 9219 | chr7 | 2443103 | ||||||
chr7:2443146 | G | C | 161 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(158): Show |
194 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*9262G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 9262 | chr7 | 2443146 | ||||||
chr7:2443151 | G | T | 12 | a0001c0001t0031 a0001c0001t0064 a0001c0001t0089 others(9): Show |
13 | HG01167.hp1 HG02258.hp1 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*9267G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 9267 | chr7 | 2443151 | ||||||
chr7:2443396 | A | G | 1 | a0001c0001t0219 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9512A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 9512 | chr7 | 2443396 | ||||||
chr7:2443476 | C | T | 2 | a0001c0001t0202 a0001c0001t0211 |
2 | HG02647.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9592C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 9592 | chr7 | 2443476 | ||||||
chr7:2443500 | C | A | 16 | a0001c0001t0027 a0001c0001t0041 a0001c0001t0072 others(13): Show |
17 | HG01074.hp2 HG01361.hp1 HG01884.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*9616C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 9616 | chr7 | 2443500 | ||||||
chr7:2443796 | G | A | 1 | a0001c0001t0198 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9912G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 9912 | chr7 | 2443796 | ||||||
chr7:2443807 | C | T | 6 | a0001c0001t0027 a0001c0001t0041 a0001c0001t0072 others(3): Show |
7 | HG01074.hp2 HG01361.hp1 HG01934.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*9923C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 9923 | chr7 | 2443807 | ||||||
chr7:2443866 | C | T | 1 | a0001c0001t0019 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9982C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 9982 | chr7 | 2443866 | ||||||
chr7:2443912 | G | T | 10 | a0001c0001t0115 a0001c0001t0116 a0001c0001t0240 others(7): Show |
10 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*10028G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10028 | chr7 | 2443912 | ||||||
chr7:2443919 | C | T | 2 | a0001c0001t0271 a0001c0001t0276 |
2 | HG02145.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10035C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10035 | chr7 | 2443919 | ||||||
chr7:2443978 | G | A | 1 | a0001c0001t0252 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10094G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10094 | chr7 | 2443978 | ||||||
chr7:2444048 | G | T | 2 | a0002c0002t0167 a0002c0002t0178 |
2 | HG01070.hp1 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10164G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10164 | chr7 | 2444048 | ||||||
chr7:2444101 | G | C | 1 | a0001c0001t0209 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10217G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10217 | chr7 | 2444101 | ||||||
chr7:2444163 | A | C | 163 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(160): Show |
196 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*10279A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10279 | chr7 | 2444163 | ||||||
chr7:2444262 | C | T | 1 | a0001c0001t0196 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10378C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10378 | chr7 | 2444262 | ||||||
chr7:2444271 | G | A | 2 | a0001c0001t0127 a0001c0001t0291 |
2 | HG03225.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10387G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10387 | chr7 | 2444271 | ||||||
chr7:2444283 | C | CA | 77 | a0001c0001t0031 a0001c0001t0050 a0001c0001t0062 others(74): Show |
78 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*10424dupA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10425 | INFO_REALIGN_3_PRIME | chr7 | 2444283 | |||||
chr7:2444283 | C | CAA | 10 | a0001c0001t0090 a0001c0001t0112 a0001c0001t0115 others(7): Show |
10 | HG01167.hp1 HG01192.hp2 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*10423_*10424dupAA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10425 | INFO_REALIGN_3_PRIME | chr7 | 2444283 | |||||
chr7:2444283 | CA | C | 12 | a0001c0001t0053 a0001c0001t0072 a0001c0001t0096 others(9): Show |
12 | HG01074.hp2 HG01257.hp1 HG01361.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*10424delA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10424 | INFO_REALIGN_3_PRIME | chr7 | 2444283 | |||||
chr7:2444283 | CAAAAAAA others(9): Show |
C | 1 | a0002c0002t0177 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10409_*10424delAA others(14): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10409 | INFO_REALIGN_3_PRIME | chr7 | 2444283 | |||||
chr7:2444322 | T | C | 10 | a0001c0001t0115 a0001c0001t0116 a0001c0001t0240 others(7): Show |
10 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*10438T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10438 | chr7 | 2444322 | ||||||
chr7:2444341 | C | A | 1 | a0001c0001t0049 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10457C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10457 | chr7 | 2444341 | ||||||
chr7:2444381 | G | A | 2 | a0001c0001t0199 a0001c0001t0208 |
2 | HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10497G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10497 | chr7 | 2444381 | ||||||
chr7:2444383 | T | C | 2 | a0001c0001t0127 a0001c0001t0291 |
2 | HG03225.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10499T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10499 | chr7 | 2444383 | ||||||
chr7:2444444 | C | A | 2 | a0001c0001t0271 a0001c0001t0276 |
2 | HG02145.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10560C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10560 | chr7 | 2444444 | ||||||
chr7:2444500 | G | A | 2 | a0001c0001t0271 a0001c0001t0276 |
2 | HG02145.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10616G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10616 | chr7 | 2444500 | ||||||
chr7:2444506 | C | T | 1 | a0001c0001t0157 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10622C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10622 | chr7 | 2444506 | ||||||
chr7:2444549 | A | T | 4 | a0001c0001t0090 a0001c0001t0114 a0001c0001t0252 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10665A>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10665 | chr7 | 2444549 | ||||||
chr7:2444663 | A | G | 6 | a0001c0001t0027 a0001c0001t0041 a0001c0001t0072 others(3): Show |
7 | HG01074.hp2 HG01361.hp1 HG01934.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*10779A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10779 | chr7 | 2444663 | ||||||
chr7:2444681 | T | G | 1 | a0003c0003t0080 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10797T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10797 | chr7 | 2444681 | ||||||
chr7:2444703 | G | A | 1 | a0005c0005t0131 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10819G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10819 | chr7 | 2444703 | ||||||
chr7:2444743 | G | A | 1 | a0001c0001t0233 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10859G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10859 | chr7 | 2444743 | ||||||
chr7:2444756 | A | G | 4 | a0001c0001t0189 a0001c0001t0196 a0001c0001t0209 others(1): Show |
4 | HG02809.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10872A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10872 | chr7 | 2444756 | ||||||
chr7:2444816 | G | A | 2 | a0001c0001t0221 a0001c0001t0237 |
2 | NA19009.hp2 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10932G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10932 | chr7 | 2444816 | ||||||
chr7:2444848 | C | T | 1 | a0001c0001t0147 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10964C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10964 | chr7 | 2444848 | ||||||
chr7:2444873 | C | A | 1 | a0001c0001t0147 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10989C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 10989 | chr7 | 2444873 | ||||||
chr7:2444913 | G | A | 2 | a0001c0001t0271 a0001c0001t0276 |
2 | HG02145.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11029G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 11029 | chr7 | 2444913 | ||||||
chr7:2444919 | T | A | 16 | a0001c0001t0027 a0001c0001t0041 a0001c0001t0072 others(13): Show |
17 | HG01074.hp2 HG01361.hp1 HG01884.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*11035T>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 11035 | chr7 | 2444919 | ||||||
chr7:2444923 | C | T | 6 | a0001c0001t0090 a0001c0001t0114 a0001c0001t0252 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*11039C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 11039 | chr7 | 2444923 | ||||||
chr7:2445069 | G | A | 1 | a0001c0001t0088 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11185G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 11185 | chr7 | 2445069 | ||||||
chr7:2445103 | G | C | 1 | a0001c0001t0086 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11219G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 11219 | chr7 | 2445103 | ||||||
chr7:2445165 | G | A | 1 | a0001c0001t0205 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11281G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 11281 | chr7 | 2445165 | ||||||
chr7:2445196 | A | G | 1 | a0008c0014t0254 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11312A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 11312 | chr7 | 2445196 | ||||||
chr7:2445281 | C | T | 10 | a0001c0001t0115 a0001c0001t0116 a0001c0001t0240 others(7): Show |
10 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*11397C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 11397 | chr7 | 2445281 | ||||||
chr7:2445451 | G | A | 3 | a0001c0001t0085 a0001c0001t0094 a0002c0002t0175 |
3 | HG03710.hp1 HG03834.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11567G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 11567 | chr7 | 2445451 | ||||||
chr7:2445588 | A | T | 31 | a0001c0001t0021 a0001c0001t0046 a0001c0001t0086 others(28): Show |
32 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*11704A>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 11704 | chr7 | 2445588 | ||||||
chr7:2445628 | T | C | 1 | a0001c0001t0289 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11744T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 11744 | chr7 | 2445628 | ||||||
chr7:2445666 | G | A | 1 | a0001c0001t0111 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11782G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 11782 | chr7 | 2445666 | ||||||
chr7:2445790 | C | T | 1 | a0003c0003t0044 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11906C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 11906 | chr7 | 2445790 | ||||||
chr7:2445870 | G | A | 2 | a0001c0001t0182 a0001c0001t0213 |
2 | HG02886.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11986G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 11986 | chr7 | 2445870 | ||||||
chr7:2445957 | G | C | 1 | a0001c0001t0284 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12073G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 12073 | chr7 | 2445957 | ||||||
chr7:2445978 | C | T | 1 | a0001c0001t0209 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12094C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 12094 | chr7 | 2445978 | ||||||
chr7:2446097 | C | A | 1 | a0003c0003t0082 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12213C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 12213 | chr7 | 2446097 | ||||||
chr7:2446138 | A | G | 5 | a0001c0001t0126 a0001c0001t0150 a0001c0001t0151 others(2): Show |
5 | HG00423.hp1 HG00673.hp1 HG02071.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*12254A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 12254 | chr7 | 2446138 | ||||||
chr7:2446221 | C | T | 2 | a0001c0001t0127 a0001c0001t0291 |
2 | HG03225.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*12337C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 12337 | chr7 | 2446221 | ||||||
chr7:2446298 | T | C | 240 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(237): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*12414T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 12414 | chr7 | 2446298 | ||||||
chr7:2446369 | C | T | 172 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(169): Show |
206 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*12485C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 12485 | chr7 | 2446369 | ||||||
chr7:2446479 | ATGTC | A | 31 | a0001c0001t0021 a0001c0001t0046 a0001c0001t0086 others(28): Show |
32 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*12599_*12602delCT others(2): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 12599 | INFO_REALIGN_3_PRIME | chr7 | 2446479 | |||||
chr7:2446552 | T | C | 165 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(162): Show |
199 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*12668T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 12668 | chr7 | 2446552 | ||||||
chr7:2446580 | T | C | 1 | a0004c0004t0235 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12696T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 12696 | chr7 | 2446580 | ||||||
chr7:2446614 | C | G | 1 | a0001c0001t0278 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12730C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 12730 | chr7 | 2446614 | ||||||
chr7:2446655 | G | A | 2 | a0002c0002t0176 a0002c0002t0195 |
2 | NA18997.hp2 NA19000.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12771G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 12771 | chr7 | 2446655 | ||||||
chr7:2446733 | G | C | 169 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(166): Show |
203 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*12849G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 12849 | chr7 | 2446733 | ||||||
chr7:2446807 | C | T | 1 | a0001c0001t0202 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12923C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 12923 | chr7 | 2446807 | ||||||
chr7:2446957 | A | G | 295 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(292): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
3_prime_UTR_variant | MODIFIER | c.*13073A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 13073 | chr7 | 2446957 | ||||||
chr7:2447084 | A | T | 169 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(166): Show |
203 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*13200A>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 13200 | chr7 | 2447084 | ||||||
chr7:2447115 | C | T | 1 | a0001c0001t0198 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13231C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 13231 | chr7 | 2447115 | ||||||
chr7:2447175 | G | A | 228 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(225): Show |
265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
3_prime_UTR_variant | MODIFIER | c.*13291G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 13291 | chr7 | 2447175 | ||||||
chr7:2447197 | C | T | 2 | a0001c0001t0271 a0001c0001t0276 |
2 | HG02145.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13313C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 13313 | chr7 | 2447197 | ||||||
chr7:2447228 | T | C | 6 | a0001c0001t0027 a0001c0001t0041 a0001c0001t0072 others(3): Show |
7 | HG01074.hp2 HG01361.hp1 HG01934.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*13344T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 13344 | chr7 | 2447228 | ||||||
chr7:2447332 | G | T | 1 | a0001c0001t0196 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13448G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 13448 | chr7 | 2447332 | ||||||
chr7:2447336 | C | A | 10 | a0001c0001t0115 a0001c0001t0116 a0001c0001t0240 others(7): Show |
10 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*13452C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 13452 | chr7 | 2447336 | ||||||
chr7:2447703 | C | T | 1 | a0001c0001t0236 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13819C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 13819 | chr7 | 2447703 | ||||||
chr7:2447709 | G | A | 40 | a0001c0001t0026 a0001c0001t0045 a0001c0001t0074 others(37): Show |
42 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*13825G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 13825 | chr7 | 2447709 | ||||||
chr7:2447828 | A | C | 6 | a0001c0001t0027 a0001c0001t0041 a0001c0001t0072 others(3): Show |
7 | HG01074.hp2 HG01361.hp1 HG01934.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*13944A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 13944 | chr7 | 2447828 | ||||||
chr7:2447831 | T | C | 1 | a0001c0001t0194 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13947T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 13947 | chr7 | 2447831 | ||||||
chr7:2447900 | C | G | 31 | a0001c0001t0021 a0001c0001t0046 a0001c0001t0086 others(28): Show |
32 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*14016C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 14016 | chr7 | 2447900 | ||||||
chr7:2448073 | G | T | 6 | a0001c0001t0027 a0001c0001t0041 a0001c0001t0072 others(3): Show |
7 | HG01074.hp2 HG01361.hp1 HG01934.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*14189G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 14189 | chr7 | 2448073 | ||||||
chr7:2448076 | C | T | 1 | a0001c0001t0269 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14192C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 14192 | chr7 | 2448076 | ||||||
chr7:2448114 | C | G | 1 | a0003c0003t0017 | 2 | HG01256.hp1 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*14230C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 14230 | chr7 | 2448114 | ||||||
chr7:2448198 | G | A | 1 | a0001c0001t0091 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14314G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 14314 | chr7 | 2448198 | ||||||
chr7:2448365 | C | T | 1 | a0001c0001t0275 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14481C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 14481 | chr7 | 2448365 | ||||||
chr7:2448389 | C | T | 1 | a0007c0008t0272 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14505C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 14505 | chr7 | 2448389 | ||||||
chr7:2448415 | C | T | 10 | a0001c0001t0115 a0001c0001t0116 a0001c0001t0240 others(7): Show |
10 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*14531C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 2/2 | 14531 | chr7 | 2448415 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:2403800 | T | C | 1 | a0002c0002t0164g0030 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-78+127T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2403800 | |||||||
chr7:2403876 | C | T | 1 | a0001c0001t0231g0305 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-78+203C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2403876 | |||||||
chr7:2404156 | G | A | 1 | a0001c0001t0217g0031 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-78+483G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2404156 | |||||||
chr7:2404194 | G | T | 36 | a0002c0002t0001g0003 a0002c0002t0001g0029 a0002c0002t0001g0278 others(33): Show |
37 | HG00544.hp2 HG00609.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.-78+521G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2404194 | |||||||
chr7:2404349 | C | G | 7 | a0001c0001t0270g0272 a0005c0005t0002g0028 a0005c0005t0002g0273 others(4): Show |
8 | HG02055.hp2 HG02109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-78+676C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2404349 | |||||||
chr7:2404457 | G | C | 1 | a0001c0001t0226g0032 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-78+784G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2404457 | |||||||
chr7:2404462 | C | T | 2 | a0001c0001t0160g0271 a0001c0001t0251g0270 |
2 | HG01099.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-78+789C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2404462 | |||||||
chr7:2404484 | G | A | 1 | a0001c0001t0005g0033 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-78+811G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2404484 | |||||||
chr7:2404704 | C | G | 2 | a0007c0008t0272g0269 a0007c0008t0274g0268 |
2 | HG03669.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-78+1031C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2404704 | |||||||
chr7:2404712 | C | T | 1 | a0001c0001t0149g0267 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-78+1039C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2404712 | |||||||
chr7:2404947 | C | T | 1 | a0001c0001t0076g0266 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-78+1274C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2404947 | |||||||
chr7:2404957 | G | T | 2 | a0001c0001t0014g0265 a0001c0001t0099g0264 |
2 | HG01192.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-78+1284G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2404957 | |||||||
chr7:2404960 | T | C | 1 | a0001c0001t0007g0034 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-78+1287T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2404960 | |||||||
chr7:2404993 | GCGACATT others(3): Show |
G | 3 | a0001c0001t0181g0035 a0001c0001t0182g0036 a0005c0005t0130g0037 |
3 | HG03098.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-78+1332_-78+1341d others(12): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2404993 | ||||||
chr7:2405150 | G | C | 1 | a0001c0001t0084g0038 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-78+1477G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2405150 | |||||||
chr7:2405191 | T | G | 5 | a0002c0002t0001g0278 a0002c0002t0001g0280 a0002c0002t0001g0281 others(2): Show |
5 | HG02080.hp1 NA18954.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.-78+1518T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2405191 | |||||||
chr7:2405313 | T | G | 87 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(84): Show |
89 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-78+1640T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2405313 | |||||||
chr7:2405675 | G | T | 1 | a0003c0003t0044g0263 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-78+2002G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2405675 | |||||||
chr7:2405685 | A | G | 3 | a0001c0001t0045g0027 a0001c0009t0102g0262 a0001c0009t0105g0027 |
3 | HG00099.hp2 HG00280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-78+2012A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2405685 | |||||||
chr7:2405835 | G | A | 2 | a0007c0008t0272g0269 a0007c0008t0274g0268 |
2 | HG03669.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-78+2162G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2405835 | |||||||
chr7:2406048 | C | T | 1 | a0001c0001t0292g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-78+2375C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2406048 | |||||||
chr7:2406180 | A | T | 1 | a0001c0001t0127g0260 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-78+2507A>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2406180 | |||||||
chr7:2406375 | CACAGTTG others(39): Show |
C | 2 | a0001c0001t0288g0102 a0001c0001t0289g0103 |
2 | HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-78+2748_-78+2793d others(48): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2406375 | ||||||
chr7:2406387 | T | C | 1 | a0001c0001t0094g0016 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-78+2714T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2406387 | |||||||
chr7:2406397 | G | A | 1 | a0001c0001t0096g0152 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-78+2724G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2406397 | |||||||
chr7:2406421 | A | C | 3 | a0001c0001t0290g0104 a0001c0001t0291g0105 a0001c0001t0292g0261 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-78+2748A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2406421 | |||||||
chr7:2406433 | T | C | 5 | a0001c0001t0288g0102 a0001c0001t0289g0103 a0001c0001t0290g0104 others(2): Show |
5 | HG01891.hp2 HG02809.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-78+2760T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2406433 | |||||||
chr7:2406433 | TGGGGTGG others(39): Show |
T | 88 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(85): Show |
90 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.-78+2795_-78+2840d others(48): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2406433 | ||||||
chr7:2406444 | C | A | 5 | a0001c0001t0288g0102 a0001c0001t0289g0103 a0001c0001t0290g0104 others(2): Show |
5 | HG01891.hp2 HG02809.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-78+2771C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2406444 | |||||||
chr7:2406456 | C | T | 2 | a0001c0001t0288g0102 a0001c0001t0289g0103 |
2 | HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-78+2783C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2406456 | |||||||
chr7:2406734 | C | T | 1 | a0001c0001t0095g0256 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-78+3061C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2406734 | |||||||
chr7:2406741 | C | T | 1 | a0001c0001t0100g0255 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-78+3068C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2406741 | |||||||
chr7:2406742 | G | A | 6 | a0001c0001t0196g0109 a0001c0001t0263g0107 a0001c0001t0273g0106 others(3): Show |
6 | HG02280.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78+3069G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2406742 | |||||||
chr7:2406772 | G | A | 1 | a0001c0001t0273g0106 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-78+3099G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2406772 | |||||||
chr7:2406794 | A | C | 7 | a0001c0001t0052g0254 a0001c0001t0053g0253 a0001c0001t0160g0271 others(4): Show |
7 | HG01099.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-78+3121A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2406794 | |||||||
chr7:2406932 | G | A | 1 | a0001c0001t0283g0110 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-78+3259G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2406932 | |||||||
chr7:2406943 | C | T | 11 | a0001c0001t0030g0013 a0001c0001t0030g0099 a0001c0001t0031g0012 others(8): Show |
11 | HG01167.hp1 HG02055.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-78+3270C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2406943 | |||||||
chr7:2406952 | C | T | 1 | a0001c0001t0079g0249 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-78+3279C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2406952 | |||||||
chr7:2407037 | T | TA | 6 | a0001c0001t0052g0254 a0001c0001t0053g0253 a0001c0006t0035g0252 others(3): Show |
6 | HG02040.hp1 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-78+3376dupA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2407037 | ||||||
chr7:2407045 | A | T | 28 | a0001c0001t0021g0236 a0001c0001t0021g0237 a0001c0001t0036g0246 others(25): Show |
28 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.-78+3372A>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2407045 | |||||||
chr7:2407199 | G | C | 130 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(127): Show |
132 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.-78+3526G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2407199 | |||||||
chr7:2407226 | G | A | 1 | a0001c0001t0290g0104 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-78+3553G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2407226 | |||||||
chr7:2407288 | A | G | 1 | a0002c0002t0167g0304 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-78+3615A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2407288 | |||||||
chr7:2407412 | C | T | 2 | a0007c0008t0272g0269 a0007c0008t0274g0268 |
2 | HG03669.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-78+3739C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2407412 | |||||||
chr7:2407484 | A | G | 3 | a0001c0001t0290g0104 a0001c0001t0291g0105 a0001c0001t0292g0261 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-78+3811A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2407484 | |||||||
chr7:2407502 | A | G | 1 | a0001c0001t0293g0247 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-78+3829A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2407502 | |||||||
chr7:2407675 | G | T | 3 | a0001c0001t0290g0104 a0001c0001t0291g0105 a0001c0001t0292g0261 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-78+4002G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2407675 | |||||||
chr7:2407867 | G | A | 2 | a0001c0001t0160g0271 a0001c0001t0251g0270 |
2 | HG01099.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-78+4194G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2407867 | |||||||
chr7:2408096 | G | A | 2 | a0001c0001t0019g0112 a0001c0001t0019g0113 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-78+4423G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2408096 | |||||||
chr7:2408211 | A | C | 3 | a0001c0001t0181g0035 a0001c0001t0182g0036 a0005c0005t0130g0037 |
3 | HG03098.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-78+4538A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2408211 | |||||||
chr7:2408293 | C | T | 4 | a0001c0001t0160g0271 a0001c0001t0251g0270 a0001c0006t0035g0252 others(1): Show |
4 | HG01099.hp2 HG02922.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-78+4620C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2408293 | |||||||
chr7:2408302 | C | T | 1 | a0003c0003t0055g0225 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-78+4629C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2408302 | |||||||
chr7:2408362 | CAA | C | 6 | a0001c0001t0127g0260 a0001c0001t0291g0105 a0002c0002t0001g0278 others(3): Show |
6 | HG02080.hp1 HG03225.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.-78+4716_-78+4717d others(4): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2408362 | ||||||
chr7:2408362 | CAAA | C | 33 | a0001c0001t0196g0109 a0001c0001t0263g0107 a0001c0001t0273g0106 others(30): Show |
34 | HG00544.hp2 HG00609.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.-78+4715_-78+4717d others(5): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2408362 | ||||||
chr7:2408362 | CAAAA | C | 19 | a0001c0001t0041g0116 a0001c0001t0042g0047 a0001c0001t0198g0044 others(16): Show |
19 | HG00544.hp1 HG01106.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.-78+4714_-78+4717d others(6): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2408362 | ||||||
chr7:2408362 | CAAAAA | C | 77 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(74): Show |
79 | HG00423.hp1 HG00597.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.-78+4713_-78+4717d others(7): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2408362 | ||||||
chr7:2408362 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0063g0117 a0001c0001t0090g0118 |
2 | NA18997.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-78+4706_-78+4717d others(14): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2408362 | ||||||
chr7:2408362 | CAAAAAAA others(6): Show |
C | 161 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(158): Show |
165 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.-78+4705_-78+4717d others(15): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2408362 | ||||||
chr7:2408362 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0093g0224 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-78+4704_-78+4717d others(16): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2408362 | ||||||
chr7:2408411 | A | G | 2 | a0002c0002t0023g0299 a0002c0002t0023g0303 |
2 | HG02523.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.-78+4738A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2408411 | |||||||
chr7:2408547 | G | T | 5 | a0001c0001t0026g0005 a0001c0001t0027g0093 a0001c0001t0027g0094 others(2): Show |
6 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78+4874G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2408547 | |||||||
chr7:2408630 | C | T | 3 | a0001c0001t0290g0104 a0001c0001t0291g0105 a0001c0001t0292g0261 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-78+4957C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2408630 | |||||||
chr7:2408682 | A | C | 213 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(210): Show |
218 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.-78+5009A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2408682 | |||||||
chr7:2408739 | T | C | 1 | a0002c0002t0195g0282 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-78+5066T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2408739 | |||||||
chr7:2408768 | G | T | 2 | a0001c0001t0288g0102 a0001c0001t0289g0103 |
2 | HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-78+5095G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2408768 | |||||||
chr7:2408858 | T | C | 210 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(207): Show |
215 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-78+5185T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2408858 | |||||||
chr7:2408964 | A | T | 1 | a0001c0001t0049g0223 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-78+5291A>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2408964 | |||||||
chr7:2408989 | T | C | 2 | a0001c0001t0142g0226 a0001c0001t0149g0267 |
2 | HG01981.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-78+5316T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2408989 | |||||||
chr7:2409075 | G | A | 1 | a0001c0001t0028g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-78+5402G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2409075 | |||||||
chr7:2409129 | C | T | 1 | a0001c0001t0091g0222 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-78+5456C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2409129 | |||||||
chr7:2409132 | C | A | 1 | a0001c0001t0263g0107 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-78+5459C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2409132 | |||||||
chr7:2409263 | C | CAAGCTGA others(22): Show |
1 | a0003c0003t0017g0119 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-78+5591_-78+5619d others(31): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2409263 | ||||||
chr7:2409332 | G | T | 3 | a0001c0001t0290g0104 a0001c0001t0291g0105 a0001c0001t0292g0261 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-78+5659G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2409332 | |||||||
chr7:2409354 | C | T | 86 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(83): Show |
88 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-78+5681C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2409354 | |||||||
chr7:2409390 | G | A | 1 | a0003c0003t0119g0111 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-78+5717G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2409390 | |||||||
chr7:2409435 | C | T | 4 | a0002c0002t0001g0280 a0002c0002t0001g0281 a0002c0002t0024g0039 others(1): Show |
4 | NA18954.hp2 NA18993.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-78+5762C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2409435 | |||||||
chr7:2409472 | A | T | 2 | a0007c0008t0272g0269 a0007c0008t0274g0268 |
2 | HG03669.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-78+5799A>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2409472 | |||||||
chr7:2409480 | T | C | 1 | a0001c0001t0189g0120 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-78+5807T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2409480 | |||||||
chr7:2409522 | G | A | 208 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(205): Show |
213 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.-78+5849G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2409522 | |||||||
chr7:2409540 | C | A | 1 | a0001c0001t0231g0305 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-78+5867C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2409540 | |||||||
chr7:2409571 | C | T | 3 | a0001c0001t0042g0047 a0001c0001t0209g0046 a0001c0001t0233g0048 |
3 | HG02897.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-78+5898C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2409571 | |||||||
chr7:2409625 | GA | G | 296 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(293): Show |
303 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.-78+5967delA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2409625 | ||||||
chr7:2409627 | A | G | 1 | a0003c0003t0048g0121 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-78+5954A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2409627 | |||||||
chr7:2409628 | A | G | 207 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(204): Show |
212 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.-78+5955A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2409628 | |||||||
chr7:2409774 | GGGAACAG others(25): Show |
G | 1 | a0003c0003t0017g0119 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-78+6106_-78+6137d others(34): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2409774 | ||||||
chr7:2409955 | T | C | 210 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(207): Show |
215 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-78+6282T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2409955 | |||||||
chr7:2410037 | A | G | 2 | a0001c0001t0085g0215 a0001c0001t0086g0216 |
2 | HG03710.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-78+6364A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2410037 | |||||||
chr7:2410037 | A | T | 6 | a0001c0001t0047g0221 a0001c0001t0051g0219 a0001c0001t0069g0220 others(3): Show |
6 | HG02698.hp1 HG02738.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78+6364A>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2410037 | |||||||
chr7:2410050 | A | G | 1 | a0001c0001t0047g0221 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-78+6377A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2410050 | |||||||
chr7:2410098 | C | T | 86 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(83): Show |
88 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-78+6425C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2410098 | |||||||
chr7:2410105 | C | T | 218 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(215): Show |
223 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.-78+6432C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2410105 | |||||||
chr7:2410174 | A | G | 1 | a0001c0001t0243g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-78+6501A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2410174 | |||||||
chr7:2410345 | T | C | 304 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(301): Show |
311 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.-78+6672T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2410345 | |||||||
chr7:2410347 | G | A | 1 | a0001c0001t0009g0122 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-78+6674G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2410347 | |||||||
chr7:2410382 | T | A | 2 | a0007c0008t0272g0269 a0007c0008t0274g0268 |
2 | HG03669.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-78+6709T>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2410382 | |||||||
chr7:2410785 | C | T | 3 | a0001c0001t0200g0090 a0001c0001t0210g0092 a0001c0001t0212g0091 |
3 | HG00639.hp1 HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-78+7112C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2410785 | |||||||
chr7:2410815 | G | A | 2 | a0001c0001t0160g0271 a0001c0001t0251g0270 |
2 | HG01099.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-78+7142G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2410815 | |||||||
chr7:2411062 | T | A | 3 | a0001c0001t0113g0123 a0001c0001t0185g0124 a0001c0001t0191g0125 |
3 | HG01168.hp1 HG01169.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-78+7389T>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2411062 | |||||||
chr7:2411124 | G | C | 1 | a0001c0001t0146g0126 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-78+7451G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2411124 | |||||||
chr7:2411159 | T | A | 202 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(199): Show |
207 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.-78+7486T>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2411159 | |||||||
chr7:2411490 | C | CTTTTTTT | 84 | a0001c0001t0003g0002 a0001c0001t0003g0137 a0001c0001t0006g0002 others(81): Show |
85 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.-78+7829_-78+7835d others(9): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2411490 | ||||||
chr7:2411490 | C | CTTTTTTT others(1): Show |
177 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(174): Show |
183 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.-78+7828_-78+7835d others(10): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2411490 | ||||||
chr7:2411490 | C | CTTTTTTT others(2): Show |
33 | a0001c0001t0014g0265 a0001c0001t0027g0094 a0001c0001t0029g0089 others(30): Show |
33 | HG01192.hp1 HG01192.hp2 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.-78+7827_-78+7835d others(11): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2411490 | ||||||
chr7:2411490 | C | CTTTTTTT others(3): Show |
3 | a0001c0006t0267g0251 a0001c0006t0268g0250 a0003c0003t0056g0213 |
3 | HG02818.hp2 HG03540.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-78+7826_-78+7835d others(12): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2411490 | ||||||
chr7:2411490 | C | CTTTTTTT others(4): Show |
1 | a0001c0006t0035g0252 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-78+7825_-78+7835d others(13): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2411490 | ||||||
chr7:2411583 | G | T | 2 | a0001c0001t0052g0254 a0001c0001t0053g0253 |
2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-78+7910G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2411583 | |||||||
chr7:2411614 | C | T | 1 | a0003c0003t0055g0225 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-78+7941C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2411614 | |||||||
chr7:2411657 | T | C | 1 | a0003c0003t0012g0020 | 2 | HG02083.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.-78+7984T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2411657 | |||||||
chr7:2411798 | C | G | 1 | a0001c0001t0196g0109 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-78+8125C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2411798 | |||||||
chr7:2411826 | C | T | 198 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(195): Show |
203 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.-78+8153C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2411826 | |||||||
chr7:2411893 | C | T | 1 | a0002c0002t0122g0298 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-78+8220C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2411893 | |||||||
chr7:2412019 | A | G | 1 | a0001c0006t0035g0252 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-78+8346A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2412019 | |||||||
chr7:2412042 | CTG | C | 7 | a0001c0001t0038g0203 a0001c0001t0200g0090 a0001c0001t0201g0041 others(4): Show |
7 | HG00639.hp1 HG01891.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-78+8372_-78+8373d others(4): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2412042 | ||||||
chr7:2412061 | C | T | 1 | a0002c0002t0177g0296 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-78+8388C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2412061 | |||||||
chr7:2412157 | G | C | 1 | a0001c0001t0283g0110 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-78+8484G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2412157 | |||||||
chr7:2412287 | G | A | 3 | a0002c0002t0004g0288 a0002c0002t0004g0289 a0002c0002t0164g0030 |
3 | HG00544.hp2 NA18942.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-78+8614G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2412287 | |||||||
chr7:2412301 | C | T | 1 | a0001c0001t0155g0259 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-78+8628C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2412301 | |||||||
chr7:2412592 | A | G | 1 | a0001c0001t0187g0212 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-78+8919A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2412592 | |||||||
chr7:2412738 | G | C | 84 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(81): Show |
86 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-78+9065G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2412738 | |||||||
chr7:2412898 | G | GT | 11 | a0001c0001t0041g0116 a0001c0001t0270g0272 a0001c0001t0271g0163 others(8): Show |
11 | HG02080.hp1 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-78+9238dupT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2412898 | ||||||
chr7:2412898 | GT | G | 87 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(84): Show |
89 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-78+9238delT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2412898 | ||||||
chr7:2412979 | A | G | 1 | a0004c0004t0258g0074 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-78+9306A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2412979 | |||||||
chr7:2412989 | C | T | 87 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(84): Show |
89 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-78+9316C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2412989 | |||||||
chr7:2413026 | T | G | 95 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(92): Show |
97 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.-78+9353T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2413026 | |||||||
chr7:2413091 | G | T | 3 | a0001c0001t0270g0272 a0001c0001t0271g0163 a0001c0001t0276g0162 |
3 | HG02145.hp2 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-78+9418G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2413091 | |||||||
chr7:2413144 | G | A | 3 | a0001c0001t0270g0272 a0001c0001t0271g0163 a0001c0001t0276g0162 |
3 | HG02145.hp2 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-78+9471G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2413144 | |||||||
chr7:2413208 | C | A | 3 | a0001c0001t0137g0229 a0001c0001t0138g0228 a0001c0001t0147g0230 |
3 | NA18948.hp2 NA18950.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-78+9535C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2413208 | |||||||
chr7:2413245 | G | A | 6 | a0001c0001t0200g0090 a0001c0001t0201g0041 a0001c0001t0202g0079 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-78+9572G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2413245 | |||||||
chr7:2413419 | G | A | 1 | a0002c0002t0001g0290 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-78+9746G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2413419 | |||||||
chr7:2413579 | A | T | 1 | a0003c0003t0279g0202 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-78+9906A>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2413579 | |||||||
chr7:2413613 | C | T | 1 | a0003c0003t0279g0202 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-78+9940C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2413613 | |||||||
chr7:2413723 | C | CT | 39 | a0001c0001t0027g0094 a0001c0001t0029g0089 a0001c0001t0036g0246 others(36): Show |
39 | HG00099.hp1 HG00438.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.-78+10073dupT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2413723 | ||||||
chr7:2413723 | CT | C | 12 | a0001c0001t0150g0248 a0001c0001t0158g0258 a0001c0001t0232g0080 others(9): Show |
12 | HG01978.hp1 HG02027.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.-78+10073delT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2413723 | ||||||
chr7:2413897 | T | A | 2 | a0001c0001t0031g0012 a0001c0001t0241g0012 |
2 | HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-78+10224T>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2413897 | |||||||
chr7:2413981 | G | A | 4 | a0001c0001t0200g0090 a0001c0001t0201g0041 a0001c0001t0210g0092 others(1): Show |
4 | HG00639.hp1 HG01891.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78+10308G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2413981 | |||||||
chr7:2414064 | T | C | 100 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(97): Show |
102 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.-78+10391T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2414064 | |||||||
chr7:2414091 | C | A | 5 | a0001c0001t0273g0106 a0001c0001t0275g0108 a0001c0001t0290g0104 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-78+10418C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2414091 | |||||||
chr7:2414111 | CTTCTT | C | 6 | a0003c0003t0003g0156 a0003c0003t0013g0157 a0003c0003t0017g0119 others(3): Show |
6 | HG01256.hp1 HG01258.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78+10441_-78+1044 others(9): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2414111 | ||||||
chr7:2414125 | C | T | 2 | a0001c0001t0263g0107 a0001c0001t0264g0078 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-78+10452C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2414125 | |||||||
chr7:2414153 | T | A | 1 | a0001c0001t0143g0231 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-78+10480T>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2414153 | |||||||
chr7:2414275 | A | C | 4 | a0001c0001t0081g0130 a0001c0001t0290g0104 a0001c0001t0291g0105 others(1): Show |
4 | HG01891.hp2 HG03225.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-78+10602A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2414275 | |||||||
chr7:2414281 | C | A | 1 | a0001c0001t0248g0071 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-78+10608C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2414281 | |||||||
chr7:2414378 | G | T | 1 | a0003c0003t0080g0201 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-78+10705G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2414378 | |||||||
chr7:2414526 | C | G | 8 | a0001c0001t0059g0195 a0003c0003t0009g0025 a0003c0003t0010g0025 others(5): Show |
8 | HG00408.hp1 HG02074.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78+10853C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2414526 | |||||||
chr7:2414582 | G | A | 1 | a0001c0001t0185g0124 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-78+10909G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2414582 | |||||||
chr7:2414804 | C | T | 1 | a0001c0001t0196g0109 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-78+11131C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2414804 | |||||||
chr7:2414820 | A | G | 1 | a0001c0001t0190g0194 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-78+11147A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2414820 | |||||||
chr7:2415000 | T | C | 106 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(103): Show |
108 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.-78+11327T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2415000 | |||||||
chr7:2415086 | C | T | 1 | a0001c0001t0209g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-78+11413C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2415086 | |||||||
chr7:2415314 | G | A | 93 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(90): Show |
95 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.-78+11641G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2415314 | |||||||
chr7:2415319 | T | A | 2 | a0001c0001t0019g0112 a0001c0001t0019g0113 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-78+11646T>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2415319 | |||||||
chr7:2415365 | C | CA | 98 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(95): Show |
100 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.-78+11706dupA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2415365 | ||||||
chr7:2415480 | C | A | 2 | a0001c0001t0290g0104 a0001c0001t0292g0261 |
2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-78+11807C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2415480 | |||||||
chr7:2415618 | C | CT | 40 | a0001c0001t0041g0116 a0001c0001t0127g0260 a0001c0001t0135g0244 others(37): Show |
40 | HG00544.hp2 HG00609.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.-78+11959dupT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2415618 | ||||||
chr7:2415652 | G | A | 93 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(90): Show |
95 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.-78+11979G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2415652 | |||||||
chr7:2415705 | C | T | 11 | a0001c0001t0113g0123 a0001c0001t0185g0124 a0001c0001t0187g0212 others(8): Show |
11 | HG01109.hp2 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-78+12032C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2415705 | |||||||
chr7:2415860 | C | T | 2 | a0001c0001t0189g0120 a0001c0001t0190g0194 |
2 | HG01109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-78+12187C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2415860 | |||||||
chr7:2416033 | T | C | 3 | a0001c0001t0290g0104 a0001c0001t0291g0105 a0001c0001t0292g0261 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-78+12360T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2416033 | |||||||
chr7:2416120 | C | T | 32 | a0003c0003t0003g0156 a0003c0003t0009g0025 a0003c0003t0010g0025 others(29): Show |
33 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.-78+12447C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2416120 | |||||||
chr7:2416266 | C | G | 2 | a0001c0001t0263g0107 a0001c0001t0264g0078 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-78+12593C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2416266 | |||||||
chr7:2416313 | G | A | 1 | a0003c0003t0039g0153 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-78+12640G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2416313 | |||||||
chr7:2416323 | ACTC | A | 3 | a0001c0001t0270g0272 a0001c0001t0271g0163 a0001c0001t0276g0162 |
3 | HG02145.hp2 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-78+12654_-78+1265 others(7): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2416323 | ||||||
chr7:2416372 | A | T | 1 | a0001c0001t0263g0107 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-78+12699A>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2416372 | |||||||
chr7:2416431 | A | T | 93 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(90): Show |
95 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.-78+12758A>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2416431 | |||||||
chr7:2416433 | G | A | 90 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(87): Show |
92 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.-78+12760G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2416433 | |||||||
chr7:2416504 | C | T | 1 | a0001c0001t0188g0193 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-78+12831C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2416504 | |||||||
chr7:2416567 | C | T | 1 | a0001c0001t0137g0229 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-78+12894C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2416567 | |||||||
chr7:2416672 | G | C | 3 | a0001c0001t0270g0272 a0001c0001t0271g0163 a0001c0001t0276g0162 |
3 | HG02145.hp2 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-78+12999G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2416672 | |||||||
chr7:2416703 | G | C | 1 | a0001c0001t0290g0104 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-78+13030G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2416703 | |||||||
chr7:2416758 | G | A | 2 | a0001c0001t0288g0102 a0001c0001t0289g0103 |
2 | HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-78+13085G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2416758 | |||||||
chr7:2416768 | A | T | 1 | a0001c0001t0086g0216 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-78+13095A>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2416768 | |||||||
chr7:2416858 | G | A | 2 | a0002c0002t0024g0039 a0002c0002t0166g0279 |
2 | NA18993.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-78+13185G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2416858 | |||||||
chr7:2416931 | A | G | 1 | a0001c0001t0028g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-78+13258A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2416931 | |||||||
chr7:2416954 | G | C | 2 | a0001c0001t0288g0102 a0001c0001t0289g0103 |
2 | HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-78+13281G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2416954 | |||||||
chr7:2416973 | C | T | 1 | a0001c0001t0160g0271 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-78+13300C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2416973 | |||||||
chr7:2417036 | A | G | 2 | a0001c0001t0273g0106 a0001c0001t0275g0108 |
2 | HG02280.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-78+13363A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2417036 | |||||||
chr7:2417093 | A | G | 1 | a0001c0001t0120g0211 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-78+13420A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2417093 | |||||||
chr7:2417164 | A | G | 303 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(300): Show |
310 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(307): Show |
intron_variant | MODIFIER | c.-78+13491A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2417164 | |||||||
chr7:2417176 | G | C | 1 | a0002c0002t0001g0283 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-78+13503G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2417176 | |||||||
chr7:2417226 | C | CT | 13 | a0001c0001t0003g0128 a0001c0001t0005g0069 a0001c0001t0014g0181 others(10): Show |
13 | HG00438.hp1 HG01081.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.-78+13569dupT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2417226 | ||||||
chr7:2417226 | CT | C | 6 | a0001c0001t0089g0168 a0001c0001t0120g0211 a0001c0001t0187g0212 others(3): Show |
6 | HG02258.hp1 HG02280.hp2 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78+13569delT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2417226 | ||||||
chr7:2417261 | G | C | 1 | a0001c0001t0115g0169 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-78+13588G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2417261 | |||||||
chr7:2417387 | C | CT | 11 | a0001c0001t0069g0220 a0001c0001t0081g0130 a0001c0001t0132g0197 others(8): Show |
11 | HG00544.hp1 HG01361.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.-78+13734dupT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2417387 | ||||||
chr7:2417387 | CT | C | 17 | a0001c0001t0028g0049 a0001c0001t0028g0053 a0001c0001t0059g0195 others(14): Show |
17 | HG01099.hp1 HG01255.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-78+13734delT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2417387 | ||||||
chr7:2417556 | A | G | 11 | a0001c0001t0030g0013 a0001c0001t0030g0099 a0001c0001t0031g0012 others(8): Show |
11 | HG01167.hp1 HG02055.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.-78+13883A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2417556 | |||||||
chr7:2417811 | C | G | 3 | a0001c0006t0035g0252 a0001c0006t0267g0251 a0001c0006t0268g0250 |
3 | HG02818.hp2 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-78+14138C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2417811 | |||||||
chr7:2417845 | C | T | 1 | a0003c0003t0013g0157 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-78+14172C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2417845 | |||||||
chr7:2417858 | G | A | 1 | a0001c0001t0291g0105 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-78+14185G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2417858 | |||||||
chr7:2418020 | G | A | 5 | a0001c0001t0107g0133 a0001c0001t0196g0109 a0001c0001t0290g0104 others(2): Show |
5 | HG01891.hp2 HG03225.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-78+14347G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2418020 | |||||||
chr7:2418047 | G | A | 38 | a0001c0001t0005g0009 a0001c0001t0026g0005 a0001c0001t0027g0093 others(35): Show |
39 | HG00544.hp1 HG00738.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.-78+14374G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2418047 | |||||||
chr7:2418074 | T | C | 303 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(300): Show |
310 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(307): Show |
intron_variant | MODIFIER | c.-78+14401T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2418074 | |||||||
chr7:2418090 | C | T | 1 | a0001c0001t0243g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-78+14417C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2418090 | |||||||
chr7:2418151 | G | A | 1 | a0001c0001t0088g0170 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-77-14412G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2418151 | |||||||
chr7:2418210 | G | A | 2 | a0007c0008t0272g0269 a0007c0008t0274g0268 |
2 | HG03669.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-77-14353G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2418210 | |||||||
chr7:2418343 | G | A | 3 | a0001c0001t0029g0076 a0001c0001t0029g0089 a0001c0001t0204g0075 |
3 | HG02109.hp2 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-77-14220G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2418343 | |||||||
chr7:2418343 | G | T | 2 | a0001c0001t0288g0102 a0001c0001t0289g0103 |
2 | HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-77-14220G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2418343 | |||||||
chr7:2418346 | G | A | 1 | a0001c0001t0181g0035 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-77-14217G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2418346 | |||||||
chr7:2418441 | C | T | 1 | a0001c0001t0160g0271 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-77-14122C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2418441 | |||||||
chr7:2418468 | C | T | 99 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(96): Show |
101 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.-77-14095C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2418468 | |||||||
chr7:2418494 | G | C | 97 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(94): Show |
99 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.-77-14069G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2418494 | |||||||
chr7:2418518 | G | C | 1 | a0001c0001t0154g0232 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-77-14045G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2418518 | |||||||
chr7:2418563 | C | T | 1 | a0001c0001t0078g0129 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-77-14000C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2418563 | |||||||
chr7:2418661 | G | A | 1 | a0003c0003t0119g0111 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-77-13902G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2418661 | |||||||
chr7:2418764 | T | C | 99 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(96): Show |
101 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.-77-13799T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2418764 | |||||||
chr7:2418789 | TTGC | T | 3 | a0001c0001t0290g0104 a0001c0001t0291g0105 a0001c0001t0292g0261 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-77-13771_-77-1376 others(7): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2418789 | ||||||
chr7:2418792 | CTGT | C | 96 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(93): Show |
98 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.-77-13760_-77-1375 others(7): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2418792 | ||||||
chr7:2418972 | ATTAT | A | 85 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(82): Show |
87 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-77-13588_-77-1358 others(8): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2418972 | ||||||
chr7:2419039 | C | T | 1 | a0003c0003t0011g0188 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-77-13524C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2419039 | |||||||
chr7:2419186 | A | T | 2 | a0001c0001t0273g0106 a0001c0001t0275g0108 |
2 | HG02280.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-77-13377A>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2419186 | |||||||
chr7:2419389 | G | A | 8 | a0001c0001t0196g0109 a0001c0001t0273g0106 a0001c0001t0275g0108 others(5): Show |
8 | HG01891.hp2 HG02280.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77-13174G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2419389 | |||||||
chr7:2419401 | CA | C | 15 | a0001c0001t0137g0229 a0001c0001t0138g0228 a0001c0001t0142g0226 others(12): Show |
15 | HG00099.hp1 HG00673.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.-77-13140delA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2419401 | ||||||
chr7:2419401 | CAA | C | 33 | a0001c0001t0018g0015 a0001c0001t0029g0076 a0001c0001t0029g0089 others(30): Show |
33 | HG00597.hp2 HG01081.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.-77-13141_-77-1314 others(6): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2419401 | ||||||
chr7:2419401 | CAAA | C | 275 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(272): Show |
282 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.-77-13142_-77-1314 others(7): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2419401 | ||||||
chr7:2419444 | C | T | 11 | a0001c0001t0196g0109 a0001c0001t0270g0272 a0001c0001t0271g0163 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-77-13119C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2419444 | |||||||
chr7:2419707 | C | CA | 88 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(85): Show |
90 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.-77-12838dupA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2419707 | ||||||
chr7:2419707 | CA | C | 33 | a0001c0001t0007g0148 a0001c0001t0015g0151 a0001c0001t0018g0150 others(30): Show |
33 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.-77-12838delA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2419707 | ||||||
chr7:2419783 | A | G | 8 | a0001c0001t0196g0109 a0001c0001t0273g0106 a0001c0001t0275g0108 others(5): Show |
8 | HG01891.hp2 HG02280.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77-12780A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2419783 | |||||||
chr7:2419877 | C | A | 1 | a0001c0001t0158g0258 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-77-12686C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2419877 | |||||||
chr7:2419968 | C | CT | 91 | a0001c0001t0007g0034 a0001c0001t0007g0135 a0001c0001t0007g0148 others(88): Show |
94 | HG01070.hp1 HG01106.hp1 HG01109.hp2 others(91): Show |
intron_variant | MODIFIER | c.-77-12572dupT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2419968 | ||||||
chr7:2419968 | C | CTT | 108 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(105): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-77-12573_-77-1257 others(6): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2419968 | ||||||
chr7:2419968 | CT | C | 9 | a0001c0001t0031g0096 a0001c0001t0158g0258 a0001c0001t0209g0046 others(6): Show |
9 | HG01081.hp2 HG02647.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-77-12572delT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2419968 | ||||||
chr7:2420035 | A | G | 1 | a0001c0001t0277g0161 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-77-12528A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2420035 | |||||||
chr7:2420066 | C | T | 5 | a0001c0001t0146g0126 a0001c0001t0270g0272 a0001c0001t0271g0163 others(2): Show |
5 | HG02015.hp2 HG02145.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.-77-12497C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2420066 | |||||||
chr7:2420134 | C | T | 7 | a0001c0001t0187g0212 a0001c0001t0188g0193 a0001c0001t0189g0120 others(4): Show |
7 | HG01109.hp2 HG02886.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.-77-12429C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2420134 | |||||||
chr7:2420194 | TGA | T | 8 | a0001c0001t0196g0109 a0001c0001t0273g0106 a0001c0001t0275g0108 others(5): Show |
8 | HG01891.hp2 HG02280.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77-12368_-77-1236 others(6): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2420194 | |||||||
chr7:2420211 | G | T | 3 | a0001c0001t0270g0272 a0001c0001t0271g0163 a0001c0001t0276g0162 |
3 | HG02145.hp2 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-77-12352G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2420211 | |||||||
chr7:2420239 | C | G | 1 | a0001c0001t0196g0109 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-77-12324C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2420239 | |||||||
chr7:2420260 | G | A | 8 | a0001c0001t0196g0109 a0001c0001t0273g0106 a0001c0001t0275g0108 others(5): Show |
8 | HG01891.hp2 HG02280.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77-12303G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2420260 | |||||||
chr7:2420268 | G | A | 3 | a0001c0001t0270g0272 a0001c0001t0271g0163 a0001c0001t0276g0162 |
3 | HG02145.hp2 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-77-12295G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2420268 | |||||||
chr7:2420311 | A | G | 2 | a0004c0004t0033g0068 a0004c0004t0259g0085 |
2 | NA18979.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-77-12252A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2420311 | |||||||
chr7:2420335 | G | C | 1 | a0001c0001t0003g0137 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-77-12228G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2420335 | |||||||
chr7:2420398 | G | A | 2 | a0007c0008t0272g0269 a0007c0008t0274g0268 |
2 | HG03669.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-77-12165G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2420398 | |||||||
chr7:2420447 | C | A | 1 | a0001c0001t0189g0120 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-77-12116C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2420447 | |||||||
chr7:2420555 | C | T | 3 | a0001c0001t0011g0147 a0001c0001t0058g0127 a0001c0001t0168g0180 |
3 | NA18960.hp1 NA18969.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-77-12008C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2420555 | |||||||
chr7:2420785 | A | G | 2 | a0007c0008t0272g0269 a0007c0008t0274g0268 |
2 | HG03669.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-77-11778A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2420785 | |||||||
chr7:2420887 | C | T | 1 | a0001c0001t0196g0109 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-77-11676C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2420887 | |||||||
chr7:2420888 | G | A | 1 | a0001c0001t0109g0174 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-77-11675G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2420888 | |||||||
chr7:2420990 | G | T | 89 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(86): Show |
91 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.-77-11573G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2420990 | |||||||
chr7:2420997 | G | A | 1 | a0001c0001t0106g0158 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-77-11566G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2420997 | |||||||
chr7:2421227 | CT | C | 266 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(263): Show |
272 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.-77-11313delT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2421227 | ||||||
chr7:2421227 | CTT | C | 11 | a0001c0001t0028g0053 a0001c0001t0189g0120 a0001c0001t0196g0109 others(8): Show |
11 | HG01975.hp1 HG02809.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.-77-11314_-77-1131 others(6): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2421227 | ||||||
chr7:2421253 | A | AT | 6 | a0001c0001t0196g0109 a0001c0001t0290g0104 a0001c0001t0291g0105 others(3): Show |
6 | HG01891.hp2 HG03225.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-77-11302dupT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2421253 | ||||||
chr7:2421314 | T | G | 1 | a0001c0001t0106g0158 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-77-11249T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2421314 | |||||||
chr7:2421350 | A | G | 2 | a0001c0001t0003g0128 a0001c0001t0286g0146 |
2 | HG02015.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.-77-11213A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2421350 | |||||||
chr7:2421355 | C | G | 3 | a0001c0006t0035g0252 a0001c0006t0267g0251 a0001c0006t0268g0250 |
3 | HG02818.hp2 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-77-11208C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2421355 | |||||||
chr7:2421395 | A | G | 8 | a0001c0001t0059g0195 a0003c0003t0009g0025 a0003c0003t0010g0025 others(5): Show |
8 | HG00408.hp1 HG02074.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.-77-11168A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2421395 | |||||||
chr7:2421425 | G | T | 1 | a0001c0001t0293g0247 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-77-11138G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2421425 | |||||||
chr7:2421576 | A | G | 86 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(83): Show |
88 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-77-10987A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2421576 | |||||||
chr7:2421600 | C | T | 3 | a0001c0001t0090g0118 a0001c0001t0114g0206 a0001c0001t0252g0205 |
3 | HG02572.hp2 HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-77-10963C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2421600 | |||||||
chr7:2421813 | G | A | 1 | a0001c0001t0049g0223 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-77-10750G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2421813 | |||||||
chr7:2421861 | T | G | 1 | a0001c0001t0196g0109 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-77-10702T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2421861 | |||||||
chr7:2422093 | G | A | 1 | a0001c0001t0196g0109 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-77-10470G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2422093 | |||||||
chr7:2422127 | C | T | 2 | a0001c0001t0101g0159 a0001c0001t0106g0158 |
2 | HG01515.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-77-10436C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2422127 | |||||||
chr7:2422144 | C | T | 1 | a0001c0001t0169g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-77-10419C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2422144 | |||||||
chr7:2422275 | C | G | 6 | a0001c0001t0196g0109 a0001c0001t0290g0104 a0001c0001t0291g0105 others(3): Show |
6 | HG01891.hp2 HG03225.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-77-10288C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2422275 | |||||||
chr7:2422311 | C | T | 2 | a0001c0001t0037g0204 a0001c0001t0038g0203 |
2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-77-10252C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2422311 | |||||||
chr7:2422345 | A | C | 1 | a0001c0001t0091g0222 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-77-10218A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2422345 | |||||||
chr7:2422433 | A | C | 201 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(198): Show |
206 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.-77-10130A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2422433 | |||||||
chr7:2422497 | G | A | 3 | a0001c0001t0090g0118 a0001c0001t0114g0206 a0001c0001t0252g0205 |
3 | HG02572.hp2 HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-77-10066G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2422497 | |||||||
chr7:2422611 | C | T | 3 | a0001c0001t0290g0104 a0001c0001t0291g0105 a0001c0001t0292g0261 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-77-9952C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2422611 | |||||||
chr7:2422629 | G | A | 3 | a0001c0001t0029g0076 a0001c0001t0029g0089 a0001c0001t0204g0075 |
3 | HG02109.hp2 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-77-9934G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2422629 | |||||||
chr7:2422682 | C | T | 3 | a0001c0001t0181g0035 a0001c0001t0182g0036 a0001c0001t0183g0101 |
3 | HG02615.hp1 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-77-9881C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2422682 | |||||||
chr7:2422723 | A | T | 1 | a0001c0001t0196g0109 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-77-9840A>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2422723 | |||||||
chr7:2422800 | C | T | 1 | a0001c0001t0052g0254 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-77-9763C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2422800 | |||||||
chr7:2422843 | TGC | T | 8 | a0001c0001t0196g0109 a0001c0001t0273g0106 a0001c0001t0275g0108 others(5): Show |
8 | HG01891.hp2 HG02280.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77-9719_-77-9718d others(4): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2422843 | |||||||
chr7:2422848 | T | G | 8 | a0001c0001t0196g0109 a0001c0001t0273g0106 a0001c0001t0275g0108 others(5): Show |
8 | HG01891.hp2 HG02280.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77-9715T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2422848 | |||||||
chr7:2422850 | T | TAAGAA | 8 | a0001c0001t0196g0109 a0001c0001t0273g0106 a0001c0001t0275g0108 others(5): Show |
8 | HG01891.hp2 HG02280.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77-9713_-77-9712i others(7): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2422850 | |||||||
chr7:2422851 | T | A | 8 | a0001c0001t0196g0109 a0001c0001t0273g0106 a0001c0001t0275g0108 others(5): Show |
8 | HG01891.hp2 HG02280.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77-9712T>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2422851 | |||||||
chr7:2422866 | C | CT | 6 | a0001c0001t0014g0181 a0001c0001t0231g0305 a0001c0001t0270g0272 others(3): Show |
6 | HG01192.hp2 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-77-9680dupT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2422866 | ||||||
chr7:2422866 | CT | C | 8 | a0001c0001t0025g0138 a0001c0001t0029g0076 a0001c0001t0029g0089 others(5): Show |
8 | HG01257.hp2 HG02015.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-77-9680delT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2422866 | ||||||
chr7:2423073 | A | C | 304 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(301): Show |
311 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.-77-9490A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2423073 | |||||||
chr7:2423281 | T | A | 2 | a0001c0001t0273g0106 a0001c0001t0275g0108 |
2 | HG02280.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-77-9282T>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2423281 | |||||||
chr7:2423327 | G | A | 3 | a0001c0001t0270g0272 a0001c0001t0271g0163 a0001c0001t0276g0162 |
3 | HG02145.hp2 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-77-9236G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2423327 | |||||||
chr7:2423345 | G | A | 3 | a0001c0001t0270g0272 a0001c0001t0271g0163 a0001c0001t0276g0162 |
3 | HG02145.hp2 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-77-9218G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2423345 | |||||||
chr7:2423811 | G | A | 1 | a0002c0002t0024g0039 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-77-8752G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2423811 | |||||||
chr7:2423939 | C | T | 1 | a0001c0001t0127g0260 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-77-8624C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2423939 | |||||||
chr7:2423996 | G | A | 1 | a0001c0001t0292g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-77-8567G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2423996 | |||||||
chr7:2424343 | TAAAG | T | 3 | a0001c0001t0290g0104 a0001c0001t0291g0105 a0001c0001t0292g0261 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-77-8213_-77-8210d others(6): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2424343 | ||||||
chr7:2424361 | T | TAAGAATC others(296): Show |
1 | a0001c0001t0244g0072 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-77-8192_-77-8191i others(305): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2424361 | ||||||
chr7:2424361 | T | TAAGAATC others(312): Show |
6 | a0001c0001t0203g0086 a0001c0001t0222g0057 a0001c0001t0223g0042 others(3): Show |
6 | HG00544.hp1 HG02040.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.-77-8192_-77-8191i others(321): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2424361 | ||||||
chr7:2424361 | T | TAAGAATC others(313): Show |
1 | a0001c0001t0224g0045 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-77-8192_-77-8191i others(322): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2424361 | ||||||
chr7:2424361 | T | TAAGAATC others(316): Show |
1 | a0001c0001t0239g0088 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-77-8192_-77-8191i others(325): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2424361 | ||||||
chr7:2424361 | T | TAAGAATC others(320): Show |
1 | a0001c0001t0249g0061 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-77-8192_-77-8191i others(329): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2424361 | ||||||
chr7:2424361 | T | TAAGAATC others(333): Show |
2 | a0001c0001t0234g0043 a0001c0001t0248g0071 |
2 | NA18943.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-77-8192_-77-8191i others(342): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2424361 | ||||||
chr7:2424459 | G | C | 1 | a0001c0001t0144g0233 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-77-8104G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2424459 | |||||||
chr7:2424581 | A | G | 1 | a0001c0001t0160g0271 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-77-7982A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2424581 | |||||||
chr7:2424585 | G | T | 1 | a0001c0001t0264g0078 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-77-7978G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2424585 | |||||||
chr7:2424759 | T | G | 202 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(199): Show |
207 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.-77-7804T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2424759 | |||||||
chr7:2424784 | G | A | 2 | a0001c0001t0183g0101 a0004c0004t0033g0064 |
2 | HG00597.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-77-7779G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2424784 | |||||||
chr7:2424848 | T | G | 3 | a0001c0001t0270g0272 a0001c0001t0271g0163 a0001c0001t0276g0162 |
3 | HG02145.hp2 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-77-7715T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2424848 | |||||||
chr7:2424932 | G | A | 1 | a0001c0001t0127g0260 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-77-7631G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2424932 | |||||||
chr7:2424978 | G | A | 1 | a0001c0001t0184g0139 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-77-7585G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2424978 | |||||||
chr7:2425008 | C | T | 1 | a0001c0001t0095g0256 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-77-7555C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425008 | |||||||
chr7:2425036 | T | A | 1 | a0005c0005t0002g0273 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-77-7527T>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425036 | |||||||
chr7:2425079 | G | A | 2 | a0001c0001t0288g0102 a0001c0001t0289g0103 |
2 | HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-77-7484G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425079 | |||||||
chr7:2425098 | C | T | 1 | a0003c0003t0044g0263 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-77-7465C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425098 | |||||||
chr7:2425153 | C | T | 3 | a0001c0001t0290g0104 a0001c0001t0291g0105 a0001c0001t0292g0261 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-77-7410C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425153 | |||||||
chr7:2425203 | C | CA | 15 | a0001c0001t0066g0016 a0001c0001t0094g0016 a0001c0001t0142g0226 others(12): Show |
16 | HG02027.hp2 HG02083.hp2 HG03834.hp1 others(13): Show |
intron_variant | MODIFIER | c.-77-7344dupA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2425203 | ||||||
chr7:2425203 | CAA | C | 9 | a0001c0001t0027g0094 a0001c0001t0273g0106 a0001c0001t0275g0108 others(6): Show |
9 | HG01891.hp2 HG01981.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-77-7345_-77-7344d others(4): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2425203 | ||||||
chr7:2425203 | CAAA | C | 82 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(79): Show |
84 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.-77-7346_-77-7344d others(5): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2425203 | ||||||
chr7:2425213 | A | C | 3 | a0001c0001t0270g0272 a0001c0001t0271g0163 a0001c0001t0276g0162 |
3 | HG02145.hp2 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-77-7350A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425213 | |||||||
chr7:2425217 | A | C | 1 | a0001c0001t0200g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-77-7346A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425217 | |||||||
chr7:2425220 | C | A | 7 | a0002c0002t0001g0283 a0002c0002t0001g0290 a0002c0002t0163g0284 others(4): Show |
7 | HG02056.hp2 HG02257.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.-77-7343C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425220 | |||||||
chr7:2425225 | A | C | 1 | a0001c0001t0200g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-77-7338A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425225 | |||||||
chr7:2425227 | C | A | 1 | a0001c0001t0200g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-77-7336C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425227 | |||||||
chr7:2425227 | C | CA | 293 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(290): Show |
300 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(297): Show |
intron_variant | MODIFIER | c.-77-7326dupA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2425227 | ||||||
chr7:2425231 | A | C | 3 | a0001c0001t0270g0272 a0001c0001t0271g0163 a0001c0001t0276g0162 |
3 | HG02145.hp2 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-77-7332A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425231 | |||||||
chr7:2425238 | C | A | 90 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(87): Show |
92 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.-77-7325C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425238 | |||||||
chr7:2425273 | G | A | 2 | a0001c0001t0288g0102 a0001c0001t0289g0103 |
2 | HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-77-7290G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425273 | |||||||
chr7:2425304 | G | A | 3 | a0001c0001t0270g0272 a0001c0001t0271g0163 a0001c0001t0276g0162 |
3 | HG02145.hp2 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-77-7259G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425304 | |||||||
chr7:2425452 | A | C | 88 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(85): Show |
90 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.-77-7111A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425452 | |||||||
chr7:2425468 | C | A | 2 | a0007c0008t0272g0269 a0007c0008t0274g0268 |
2 | HG03669.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-77-7095C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425468 | |||||||
chr7:2425538 | T | C | 3 | a0001c0001t0181g0035 a0001c0001t0182g0036 a0001c0001t0183g0101 |
3 | HG02615.hp1 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-77-7025T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425538 | |||||||
chr7:2425569 | G | A | 1 | a0002c0002t0165g0291 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-77-6994G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425569 | |||||||
chr7:2425623 | G | A | 1 | a0001c0001t0003g0128 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-77-6940G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425623 | |||||||
chr7:2425625 | G | A | 1 | a0001c0001t0275g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-77-6938G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425625 | |||||||
chr7:2425691 | C | CT | 18 | a0001c0001t0027g0093 a0001c0001t0029g0076 a0001c0001t0029g0089 others(15): Show |
18 | HG00438.hp2 HG02109.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.-77-6858dupT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2425691 | ||||||
chr7:2425691 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0270g0272 a0001c0001t0276g0162 |
2 | HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-77-6868_-77-6858d others(13): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2425691 | ||||||
chr7:2425691 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0271g0163 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-77-6869_-77-6858d others(14): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2425691 | ||||||
chr7:2425691 | C | CTTTTTTT others(6): Show |
2 | a0007c0008t0272g0269 a0007c0008t0274g0268 |
2 | HG03669.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-77-6870_-77-6858d others(15): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2425691 | ||||||
chr7:2425691 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0291g0105 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-77-6858_-77-6857i others(19): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2425691 | ||||||
chr7:2425691 | C | CTTTTTTT others(11): Show |
3 | a0001c0001t0196g0109 a0001c0001t0290g0104 a0001c0001t0292g0261 |
3 | HG01891.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-77-6858_-77-6857i others(20): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2425691 | ||||||
chr7:2425692 | T | G | 1 | a0001c0001t0068g0140 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-77-6871T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425692 | |||||||
chr7:2425859 | T | C | 1 | a0001c0001t0007g0135 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-77-6704T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2425859 | |||||||
chr7:2426011 | C | T | 3 | a0001c0001t0062g0145 a0001c0001t0096g0152 a0001c0001t0186g0144 |
3 | HG02523.hp1 NA18995.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-77-6552C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2426011 | |||||||
chr7:2426139 | T | A | 2 | a0002c0002t0023g0299 a0002c0002t0023g0303 |
2 | HG02523.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.-77-6424T>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2426139 | |||||||
chr7:2426155 | C | T | 1 | a0001c0001t0126g0234 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-77-6408C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2426155 | |||||||
chr7:2426279 | G | A | 3 | a0001c0001t0290g0104 a0001c0001t0291g0105 a0001c0001t0292g0261 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-77-6284G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2426279 | |||||||
chr7:2426281 | T | C | 1 | a0001c0001t0242g0097 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-77-6282T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2426281 | |||||||
chr7:2426349 | G | A | 7 | a0005c0005t0002g0028 a0005c0005t0002g0273 a0005c0005t0002g0275 others(4): Show |
8 | HG02055.hp2 HG02109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77-6214G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2426349 | |||||||
chr7:2426461 | G | A | 1 | a0001c0001t0087g0171 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-77-6102G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2426461 | |||||||
chr7:2426562 | C | A | 3 | a0001c0001t0290g0104 a0001c0001t0291g0105 a0001c0001t0292g0261 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-77-6001C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2426562 | |||||||
chr7:2426633 | T | G | 1 | a0001c0001t0112g0176 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-77-5930T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2426633 | |||||||
chr7:2426711 | T | G | 304 | a0001c0001t0003g0002 a0001c0001t0003g0128 a0001c0001t0003g0137 others(301): Show |
311 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.-77-5852T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2426711 | |||||||
chr7:2427028 | G | C | 1 | a0001c0001t0211g0052 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-77-5535G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2427028 | |||||||
chr7:2427109 | C | T | 2 | a0007c0008t0272g0269 a0007c0008t0274g0268 |
2 | HG03669.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-77-5454C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2427109 | |||||||
chr7:2427154 | C | T | 1 | a0001c0001t0236g0060 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-77-5409C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2427154 | |||||||
chr7:2427218 | A | C | 2 | a0007c0008t0272g0269 a0007c0008t0274g0268 |
2 | HG03669.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-77-5345A>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2427218 | |||||||
chr7:2427258 | C | T | 2 | a0001c0001t0031g0012 a0001c0001t0241g0012 |
2 | HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-77-5305C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2427258 | |||||||
chr7:2427264 | C | T | 1 | a0001c0001t0291g0105 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-77-5299C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2427264 | |||||||
chr7:2427265 | G | A | 13 | a0001c0001t0007g0034 a0001c0001t0007g0135 a0001c0001t0007g0148 others(10): Show |
13 | HG01261.hp2 HG01928.hp1 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.-77-5298G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2427265 | |||||||
chr7:2427268 | G | T | 2 | a0001c0001t0273g0106 a0001c0001t0275g0108 |
2 | HG02280.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-77-5295G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2427268 | |||||||
chr7:2427579 | C | G | 1 | a0001c0001t0287g0056 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-77-4984C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2427579 | |||||||
chr7:2427582 | C | G | 1 | a0001c0001t0264g0078 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-77-4981C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2427582 | |||||||
chr7:2427583 | CT | C | 4 | a0001c0001t0169g0172 a0001c0001t0270g0272 a0001c0001t0271g0163 others(1): Show |
4 | HG01243.hp1 HG02145.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77-4979delT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2427583 | |||||||
chr7:2427778 | C | T | 5 | a0001c0001t0273g0106 a0001c0001t0275g0108 a0001c0001t0290g0104 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-77-4785C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2427778 | |||||||
chr7:2427899 | C | T | 1 | a0001c0001t0249g0061 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-77-4664C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2427899 | |||||||
chr7:2427950 | GGGACTAC others(1959): Show |
G | 1 | a0001c0001t0146g0126 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-77-4602_-77-2637d others(2): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2427950 | ||||||
chr7:2427979 | G | C | 3 | a0001c0001t0290g0104 a0001c0001t0291g0105 a0001c0001t0292g0261 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-77-4584G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2427979 | |||||||
chr7:2428006 | C | T | 1 | a0001c0001t0106g0158 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-77-4557C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2428006 | |||||||
chr7:2428074 | G | A | 1 | a0001c0001t0093g0224 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-77-4489G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2428074 | |||||||
chr7:2428197 | CT | C | 96 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(93): Show |
98 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.-77-4351delT | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2428197 | ||||||
chr7:2428198 | T | TC | 3 | a0001c0001t0181g0035 a0001c0001t0182g0036 a0001c0001t0183g0101 |
3 | HG02615.hp1 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-77-4365_-77-4364i others(3): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2428198 | |||||||
chr7:2428231 | A | G | 2 | a0001c0001t0263g0107 a0001c0001t0264g0078 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-77-4332A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2428231 | |||||||
chr7:2428339 | C | T | 38 | a0002c0002t0001g0003 a0002c0002t0001g0029 a0002c0002t0001g0278 others(35): Show |
39 | HG00544.hp2 HG00609.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.-77-4224C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2428339 | |||||||
chr7:2428460 | C | T | 2 | a0001c0001t0263g0107 a0001c0001t0264g0078 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-77-4103C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2428460 | |||||||
chr7:2428485 | C | G | 2 | a0001c0001t0288g0102 a0001c0001t0289g0103 |
2 | HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-77-4078C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2428485 | |||||||
chr7:2428581 | C | T | 1 | a0001c0001t0069g0220 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-77-3982C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2428581 | |||||||
chr7:2428587 | T | C | 1 | a0001c0006t0035g0252 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-77-3976T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2428587 | |||||||
chr7:2428715 | A | G | 2 | a0001c0001t0277g0161 a0001c0001t0278g0160 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-77-3848A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2428715 | |||||||
chr7:2428765 | A | G | 5 | a0001c0001t0270g0272 a0001c0001t0271g0163 a0001c0001t0276g0162 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-77-3798A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2428765 | |||||||
chr7:2428846 | G | A | 3 | a0001c0001t0037g0204 a0001c0001t0038g0203 a0001c0001t0169g0172 |
3 | HG01243.hp1 HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-77-3717G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2428846 | |||||||
chr7:2428901 | C | T | 2 | a0001c0001t0263g0107 a0001c0001t0264g0078 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-77-3662C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2428901 | |||||||
chr7:2428950 | T | C | 2 | a0001c0001t0031g0096 a0001c0001t0250g0095 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-77-3613T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2428950 | |||||||
chr7:2429019 | T | C | 3 | a0001c0001t0029g0076 a0001c0001t0029g0089 a0001c0001t0204g0075 |
3 | HG02109.hp2 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-77-3544T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2429019 | |||||||
chr7:2429272 | G | A | 1 | a0001c0001t0051g0219 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-77-3291G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2429272 | |||||||
chr7:2429371 | C | T | 2 | a0007c0008t0272g0269 a0007c0008t0274g0268 |
2 | HG03669.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-77-3192C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2429371 | |||||||
chr7:2429555 | G | T | 2 | a0001c0001t0066g0016 a0003c0003t0125g0200 |
2 | HG02027.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.-77-3008G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2429555 | |||||||
chr7:2429639 | G | A | 6 | a0001c0001t0196g0109 a0001c0001t0290g0104 a0001c0001t0291g0105 others(3): Show |
6 | HG01891.hp2 HG03225.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-77-2924G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2429639 | |||||||
chr7:2429641 | T | A | 3 | a0001c0001t0290g0104 a0001c0001t0291g0105 a0001c0001t0292g0261 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-77-2922T>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2429641 | |||||||
chr7:2429657 | C | T | 1 | a0001c0001t0143g0231 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-77-2906C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2429657 | |||||||
chr7:2429874 | C | T | 6 | a0003c0003t0003g0156 a0003c0003t0013g0157 a0003c0003t0017g0119 others(3): Show |
6 | HG01256.hp1 HG01258.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-77-2689C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2429874 | |||||||
chr7:2429885 | C | T | 5 | a0001c0001t0043g0165 a0001c0001t0073g0166 a0001c0001t0074g0021 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.-77-2678C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2429885 | |||||||
chr7:2429917 | G | A | 31 | a0003c0003t0003g0156 a0003c0003t0009g0025 a0003c0003t0010g0025 others(28): Show |
32 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.-77-2646G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2429917 | |||||||
chr7:2430277 | A | G | 4 | a0001c0001t0277g0161 a0001c0001t0278g0160 a0001c0001t0288g0102 others(1): Show |
4 | HG02723.hp2 HG02809.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77-2286A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2430277 | |||||||
chr7:2430300 | T | G | 3 | a0001c0001t0290g0104 a0001c0001t0291g0105 a0001c0001t0292g0261 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-77-2263T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2430300 | |||||||
chr7:2430517 | C | T | 1 | a0002c0002t0165g0291 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-77-2046C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2430517 | |||||||
chr7:2430644 | G | T | 3 | a0001c0001t0090g0118 a0001c0001t0114g0206 a0001c0001t0252g0205 |
3 | HG02572.hp2 HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-77-1919G>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2430644 | |||||||
chr7:2430664 | C | A | 2 | a0007c0008t0272g0269 a0007c0008t0274g0268 |
2 | HG03669.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-77-1899C>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2430664 | |||||||
chr7:2430685 | C | G | 86 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(83): Show |
88 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-77-1878C>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2430685 | |||||||
chr7:2430703 | C | T | 2 | a0007c0008t0272g0269 a0007c0008t0274g0268 |
2 | HG03669.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-77-1860C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2430703 | |||||||
chr7:2430877 | C | T | 1 | a0001c0001t0021g0237 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-77-1686C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2430877 | |||||||
chr7:2430897 | A | G | 3 | a0001c0001t0263g0107 a0001c0001t0264g0078 a0001c0001t0287g0056 |
3 | HG02970.hp1 HG02976.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-77-1666A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2430897 | |||||||
chr7:2431328 | T | C | 1 | a0001c0001t0286g0146 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-77-1235T>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2431328 | |||||||
chr7:2431469 | G | A | 3 | a0001c0001t0290g0104 a0001c0001t0291g0105 a0001c0001t0292g0261 |
3 | HG01891.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-77-1094G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2431469 | |||||||
chr7:2431684 | G | C | 3 | a0001c0001t0196g0109 a0001c0001t0277g0161 a0001c0001t0278g0160 |
3 | HG02723.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-77-879G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2431684 | |||||||
chr7:2431719 | T | G | 1 | a0001c0001t0190g0194 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-77-844T>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2431719 | |||||||
chr7:2431865 | G | C | 2 | a0001c0001t0070g0017 a0001c0001t0071g0017 |
2 | HG00735.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.-77-698G>C | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2431865 | |||||||
chr7:2431916 | C | T | 2 | a0001c0001t0273g0106 a0001c0001t0275g0108 |
2 | HG02280.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-77-647C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2431916 | |||||||
chr7:2432016 | A | G | 2 | a0001c0001t0273g0106 a0001c0001t0275g0108 |
2 | HG02280.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-77-547A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2432016 | |||||||
chr7:2432025 | C | T | 1 | a0001c0001t0209g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-77-538C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2432025 | |||||||
chr7:2432054 | A | G | 2 | a0001c0001t0277g0161 a0001c0001t0278g0160 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-77-509A>G | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2432054 | |||||||
chr7:2432141 | C | CA | 61 | a0001c0001t0003g0128 a0001c0001t0006g0019 a0001c0001t0016g0019 others(58): Show |
61 | HG00099.hp1 HG00438.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.-77-386dupA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | C | CAA | 56 | a0001c0001t0003g0002 a0001c0001t0006g0002 a0001c0001t0014g0181 others(53): Show |
59 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.-77-387_-77-386dup others(2): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | C | CAAA | 36 | a0001c0001t0003g0137 a0001c0001t0007g0034 a0001c0001t0009g0122 others(33): Show |
36 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.-77-388_-77-386dup others(3): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | C | CAAAA | 20 | a0001c0001t0007g0135 a0001c0001t0007g0148 a0001c0001t0043g0165 others(17): Show |
20 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.-77-389_-77-386dup others(4): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | C | CAAAAA | 6 | a0001c0001t0062g0145 a0001c0001t0112g0176 a0001c0001t0126g0234 others(3): Show |
6 | HG02135.hp1 HG03453.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.-77-390_-77-386dup others(5): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | C | CAAAAAA | 6 | a0001c0001t0019g0113 a0001c0001t0059g0195 a0001c0001t0063g0117 others(3): Show |
6 | HG03491.hp1 NA18961.hp1 NA18997.hp1 others(3): Show |
intron_variant | MODIFIER | c.-77-391_-77-386dup others(6): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | C | CAAAAAAA | 7 | a0001c0001t0019g0112 a0001c0001t0042g0047 a0001c0001t0070g0017 others(4): Show |
7 | HG00733.hp1 HG00735.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.-77-392_-77-386dup others(7): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0280g0132 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-77-396_-77-386dup others(11): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | C | CAAAAAAA others(5): Show |
1 | a0005c0005t0002g0028 | 2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-77-397_-77-386dup others(12): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | C | CAAAAAAA others(6): Show |
1 | a0005c0005t0002g0275 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-77-398_-77-386dup others(13): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0106g0158 a0001c0001t0160g0271 |
2 | HG01099.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-77-399_-77-386dup others(14): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | C | CAAAAAAA others(9): Show |
1 | a0005c0005t0130g0037 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-77-401_-77-386dup others(16): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | C | CAAAAAAA others(16): Show |
1 | a0005c0005t0123g0274 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-77-408_-77-386dup others(23): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | CA | C | 28 | a0001c0001t0005g0069 a0001c0001t0029g0089 a0001c0001t0157g0241 others(25): Show |
28 | HG00639.hp1 HG01081.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.-77-386delA | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | CAA | C | 14 | a0001c0001t0005g0009 a0001c0001t0005g0011 a0001c0001t0005g0033 others(11): Show |
15 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-77-387_-77-386del others(2): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | CAAAAAAA | C | 7 | a0001c0001t0270g0272 a0001c0001t0271g0163 a0001c0001t0276g0162 others(4): Show |
7 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-77-392_-77-386del others(7): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | CAAAAAAA others(1): Show |
C | 16 | a0001c0001t0291g0105 a0001c0001t0292g0261 a0001c0006t0267g0251 others(13): Show |
17 | HG00609.hp2 HG01070.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-77-393_-77-386del others(8): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | CAAAAAAA others(2): Show |
C | 26 | a0001c0001t0211g0052 a0002c0002t0001g0029 a0002c0002t0001g0278 others(23): Show |
26 | HG00544.hp2 HG01361.hp1 HG02004.hp2 others(23): Show |
intron_variant | MODIFIER | c.-77-394_-77-386del others(9): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0190g0194 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-77-398_-77-386del others(13): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | CAAAAAAA others(9): Show |
C | 2 | a0003c0003t0110g0190 a0007c0008t0272g0269 |
2 | HG02129.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-77-401_-77-386del others(16): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432141 | CAAAAAAA others(10): Show |
C | 1 | a0007c0008t0274g0268 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-77-402_-77-386del others(17): Show |
CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr7 | 2432141 | ||||||
chr7:2432255 | G | A | 1 | a0001c0001t0289g0103 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-77-308G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2432255 | |||||||
chr7:2432300 | G | A | 1 | a0001c0001t0228g0059 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-77-263G>A | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2432300 | |||||||
chr7:2432344 | C | T | 1 | a0001c0001t0127g0260 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-77-219C>T | CHST12 | ENSG00000136213.10 | transcript | ENST00000618655.2 | protein_coding | 1/1 | chr7 | 2432344 |