Item | Value |
---|---|
geneid | 4092 |
ensemblid | ENSG00000101665.10 |
hgncid | 6773 |
symbol | SMAD7 |
name | SMAD family member 7 |
refseq_nuc | NM_005904.4 |
refseq_prot | NP_005895.1 |
ensembl_nuc | ENST00000262158.8 |
ensembl_prot | ENSP00000262158.2 |
mane_status | MANE Select |
chr | chr18 |
start | 48919853 |
end | 48950965 |
strand | - |
ver | v1.2 |
region | chr18:48919853-48950965 |
region5000 | chr18:48914853-48955965 |
regionname0 | SMAD7_chr18_48919853_48950965 |
regionname5000 | SMAD7_chr18_48914853_48955965 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 426 | 395 | 96 | 72 | 161 | 18 | 46 | 120 | SMAD7_chr18_48914853_48955965 | SMAD7 | MFRTK others(421): Show |
chr18 | 48914853 | 48955965 |
a0002 | 0/0 | 426 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | MFRTK others(421): Show |
chr18 | 48914853 | 48955965 |
a0003 | 0/0 | 426 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | MFRTK others(421): Show |
chr18 | 48914853 | 48955965 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1278 | 362 | 91 | 66 | 141 | 18 | 44 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATGTT others(1273): Show |
chr18 | 48914853 | 48955965 | ||
a0001c0002 | 0/0 | 1278 | 19 | 1 | 4 | 13 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATGTT others(1273): Show |
chr18 | 48914853 | 48955965 | ||
a0001c0003 | 0/0 | 1278 | 4 | 0 | 0 | 4 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATGTT others(1273): Show |
chr18 | 48914853 | 48955965 | ||
a0001c0005 | 0/0 | 1278 | 2 | 0 | 1 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATGTT others(1273): Show |
chr18 | 48914853 | 48955965 | ||
a0001c0006 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATGTT others(1273): Show |
chr18 | 48914853 | 48955965 | ||
a0001c0007 | 0/0 | 1278 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATGTT others(1273): Show |
chr18 | 48914853 | 48955965 | ||
a0001c0008 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATGTT others(1273): Show |
chr18 | 48914853 | 48955965 | ||
a0001c0009 | 0/0 | 1278 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATGTT others(1273): Show |
chr18 | 48914853 | 48955965 | ||
a0001c0010 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATGTT others(1273): Show |
chr18 | 48914853 | 48955965 | ||
a0001c0011 | 0/0 | 1278 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATGTT others(1273): Show |
chr18 | 48914853 | 48955965 | ||
a0001c0012 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATGTT others(1273): Show |
chr18 | 48914853 | 48955965 | ||
a0001c0014 | 0/0 | 1278 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATGTT others(1273): Show |
chr18 | 48914853 | 48955965 | ||
a0002c0004 | 0/0 | 1278 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATGTT others(1273): Show |
chr18 | 48914853 | 48955965 | ||
a0003c0013 | 0/0 | 1278 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATGTT others(1273): Show |
chr18 | 48914853 | 48955965 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3341 | 234 | 44 | 46 | 98 | 14 | 31 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0002 | 0/0 | 3341 | 34 | 1 | 2 | 27 | 1 | 3 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0003 | 0/0 | 3341 | 24 | 22 | 2 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0004 | 0/1 | 3341 | 21 | 0 | 7 | 7 | 3 | 3 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0005 | 0/0 | 3341 | 7 | 7 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0006 | 0/0 | 3341 | 6 | 1 | 5 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0007 | 0/0 | 3341 | 5 | 0 | 0 | 1 | 0 | 4 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0008 | 0/0 | 3341 | 4 | 4 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0009 | 0/0 | 3342 | 3 | 1 | 1 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3337): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0010 | 0/0 | 3341 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0011 | 0/0 | 3341 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0012 | 0/0 | 3341 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0013 | 0/0 | 3342 | 2 | 0 | 0 | 1 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3337): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0014 | 0/0 | 3341 | 2 | 1 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0015 | 0/0 | 3341 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0016 | 0/0 | 3341 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0017 | 0/0 | 3341 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0019 | 0/0 | 3341 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0020 | 0/0 | 3341 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0021 | 0/0 | 3341 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0022 | 0/0 | 3341 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0023 | 0/0 | 3341 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0025 | 0/0 | 3342 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3337): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0026 | 0/0 | 3342 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3337): Show |
chr18 | 48914853 | 48955965 |
a0001c0001t0027 | 0/0 | 3341 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0002t0001 | 0/0 | 3341 | 15 | 1 | 4 | 9 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0002t0002 | 0/0 | 3341 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0002t0004 | 0/0 | 3341 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0003t0001 | 0/0 | 3341 | 4 | 0 | 0 | 4 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0005t0001 | 0/0 | 3341 | 2 | 0 | 1 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0006t0003 | 0/0 | 3341 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0007t0009 | 0/0 | 3342 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3337): Show |
chr18 | 48914853 | 48955965 |
a0001c0008t0003 | 0/0 | 3341 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0009t0001 | 0/0 | 3341 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0010t0028 | 0/0 | 3341 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0011t0001 | 0/0 | 3341 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0012t0024 | 0/0 | 3341 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0001c0014t0018 | 0/0 | 3341 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0002c0004t0001 | 0/0 | 3341 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
a0003c0013t0001 | 0/0 | 3341 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | ATTGC others(3336): Show |
chr18 | 48914853 | 48955965 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0276 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0002g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0003g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0006g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0006g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0006g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0006g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0007g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0007g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0007g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0007g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0007g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0009g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0009g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0009g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0010g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0010g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0010g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0011g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0011g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0011g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0012g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0012g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0013g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0013g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0014g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0014g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0015g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0015g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0016g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0017g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0019g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0020g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0021g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0022g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0023g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0025g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0026g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0001t0027g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0005t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0005t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0006t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0007t0009g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0008t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0009t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0010t0028g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0011t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0012t0024g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0001c0014t0018g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0002c0004t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0002c0004t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
a0003c0013t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0239 | EUR | GBR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | GBR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0030 | EUR | GBR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | FIN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | FIN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | FIN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | CHS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00423 | hp2 | a0003 | c0013 | t0001 | g0369 | EAS | CHS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | CHS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | CHS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | CHS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00544 | hp2 | a0001 | c0007 | t0009 | g0231 | EAS | CHS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | CHS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00597 | hp1 | a0001 | c0001 | t0012 | g0042 | EAS | CHS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | CHS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00735 | hp1 | a0001 | c0001 | t0009 | g0347 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0346 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00741 | hp1 | a0001 | c0001 | t0017 | g0031 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0348 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0343 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0359 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0040 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0034 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01109 | hp2 | a0001 | c0001 | t0014 | g0214 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01168 | hp2 | a0002 | c0004 | t0001 | g0061 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01169 | hp1 | a0002 | c0004 | t0001 | g0060 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01175 | hp2 | a0001 | c0005 | t0001 | g0062 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01192 | hp1 | a0001 | c0001 | t0006 | g0015 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0056 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01243 | hp2 | a0001 | c0014 | t0018 | g0057 | AMR | PUR | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0366 | AMR | CLM | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | CLM | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0242 | AMR | CLM | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0050 | AMR | CLM | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | CLM | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | CLM | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01358 | hp2 | a0001 | c0001 | t0006 | g0246 | AMR | CLM | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0151 | AMR | CLM | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01433 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | CLM | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0036 | AMR | CLM | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0160 | EUR | IBS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0048 | EUR | IBS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0047 | EUR | IBS | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01884 | hp2 | a0001 | c0001 | t0009 | g0356 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0329 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0357 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01978 | hp2 | a0001 | c0001 | t0006 | g0243 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0051 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0360 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02004 | hp2 | a0001 | c0001 | t0020 | g0059 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02055 | hp2 | a0001 | c0008 | t0003 | g0321 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0364 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02080 | hp1 | a0001 | c0001 | t0023 | g0123 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02080 | hp2 | a0001 | c0001 | t0012 | g0041 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0148 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CDX | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | CDX | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0213 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02258 | hp1 | a0001 | c0001 | t0015 | g0371 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02293 | hp1 | a0001 | c0001 | t0006 | g0194 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02451 | hp1 | a0001 | c0001 | t0008 | g0095 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02572 | hp2 | a0001 | c0001 | t0011 | g0302 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0305 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02630 | hp2 | a0001 | c0001 | t0014 | g0319 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0358 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02738 | hp1 | a0001 | c0001 | t0013 | g0038 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02738 | hp2 | a0001 | c0001 | t0009 | g0248 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0334 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0323 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0218 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0283 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0294 | AFR | ESN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0340 | AFR | ESN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0331 | AFR | ESN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | ESN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0341 | AFR | ESN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | ESN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0335 | AFR | ESN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | ESN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ESN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03209 | hp1 | a0001 | c0001 | t0010 | g0284 | AFR | MSL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0333 | AFR | MSL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03225 | hp1 | a0001 | c0001 | t0008 | g0168 | AFR | MSL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03453 | hp1 | a0001 | c0006 | t0003 | g0064 | AFR | MSL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0217 | AFR | MSL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03491 | hp2 | a0001 | c0001 | t0007 | g0046 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03492 | hp1 | a0001 | c0001 | t0007 | g0032 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03516 | hp1 | a0001 | c0001 | t0025 | g0132 | AFR | ESN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03516 | hp2 | a0001 | c0001 | t0011 | g0289 | AFR | ESN | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | GWD | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0181 | AFR | MSL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03579 | hp2 | a0001 | c0001 | t0008 | g0170 | AFR | MSL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | STU | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03704 | hp2 | a0001 | c0001 | t0007 | g0043 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0327 | SAS | PJL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0091 | SAS | BEB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0037 | SAS | BEB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03942 | hp1 | a0001 | c0001 | t0026 | g0310 | SAS | BEB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | STU | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0045 | SAS | STU | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0241 | SAS | BEB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | BEB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0035 | SAS | STU | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG04204 | hp2 | a0001 | c0005 | t0001 | g0063 | SAS | STU | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG04228 | hp2 | a0001 | c0001 | t0007 | g0044 | SAS | STU | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | YRI | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | CHB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18747 | hp2 | a0001 | c0001 | t0019 | g0058 | EAS | CHB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18906 | hp1 | a0001 | c0001 | t0010 | g0303 | AFR | YRI | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | YRI | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18950 | hp1 | a0001 | c0011 | t0001 | g0235 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18951 | hp1 | a0001 | c0003 | t0001 | g0082 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0353 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18959 | hp1 | a0001 | c0001 | t0013 | g0028 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18960 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18965 | hp1 | a0001 | c0003 | t0001 | g0083 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18979 | hp1 | a0001 | c0001 | t0016 | g0023 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18990 | hp1 | a0001 | c0009 | t0001 | g0115 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18993 | hp1 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18997 | hp1 | a0001 | c0003 | t0001 | g0080 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19001 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19005 | hp1 | a0001 | c0001 | t0022 | g0271 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19010 | hp1 | a0001 | c0003 | t0001 | g0081 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0367 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | LWK | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19030 | hp2 | a0001 | c0010 | t0028 | g0373 | AFR | LWK | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19043 | hp1 | a0001 | c0001 | t0021 | g0210 | AFR | LWK | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | LWK | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19055 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19062 | hp1 | a0001 | c0002 | t0004 | g0054 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19081 | hp2 | a0001 | c0002 | t0004 | g0053 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19085 | hp2 | a0001 | c0001 | t0027 | g0372 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0352 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | YRI | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | ASW | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0314 | AFR | ASW | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0345 | EUR | TSI | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | TSI | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | TSI | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0275 | EUR | TSI | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | GIH | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | GIH | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | CLM | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0316 | AMR | CLM | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0129 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02559 | hp1 | a0001 | c0001 | t0010 | g0130 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0355 | AFR | ACB | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03471 | hp1 | a0001 | c0001 | t0008 | g0169 | AFR | MSL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | MSL | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG06807 | hp1 | a0001 | c0012 | t0024 | g0368 | AFR | USA | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | USA | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA20300 | hp1 | a0001 | c0001 | t0015 | g0370 | AFR | USA | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0245 | AFR | USA | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0215 | AFR | LWK | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
NA21309 | hp2 | a0001 | c0001 | t0011 | g0365 | AFR | LWK | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0049 | REF | REF | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0276 | REF | REF | SMAD7_chr18_48914853_48955965 | SMAD7 | chr18 | 48914853 | 48955965 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:48950022 | T | C | 1 | a0003 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.403A>G | p.Arg135Gly | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/4 | 944/3341 | 403/1281 | 135/426 | chr18 | 48950022 | |||
chr18:48950310 | C | T | 1 | a0002 | 2 | HG01168.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.115G>A | p.Gly39Arg | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/4 | 656/3341 | 115/1281 | 39/426 | chr18 | 48950310 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:48921447 | G | C | 1 | a0001c0002 | 19 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(16): Show |
synonymous_variant | LOW | c.1206C>G | p.Gly402Gly | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 1747/3341 | 1206/1281 | 402/426 | chr18 | 48921447 | |||
chr18:48921531 | C | T | 1 | a0001c0008 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.1122G>A | p.Ala374Ala | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 1663/3341 | 1122/1281 | 374/426 | chr18 | 48921531 | |||
chr18:48921546 | G | A | 1 | a0001c0009 | 1 | NA18990.hp1 | synonymous_variant | LOW | c.1107C>T | p.Phe369Phe | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 1648/3341 | 1107/1281 | 369/426 | chr18 | 48921546 | |||
chr18:48921567 | G | A | 1 | a0001c0010 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1086C>T | p.Pro362Pro | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 1627/3341 | 1086/1281 | 362/426 | chr18 | 48921567 | |||
chr18:48921603 | C | T | 1 | a0001c0007 | 1 | HG00544.hp2 | synonymous_variant | LOW | c.1050G>A | p.Pro350Pro | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 1591/3341 | 1050/1281 | 350/426 | chr18 | 48921603 | |||
chr18:48921759 | G | A | 2 | a0001c0002 a0001c0011 |
20 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(17): Show |
synonymous_variant | LOW | c.894C>T | p.Leu298Leu | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 1435/3341 | 894/1281 | 298/426 | chr18 | 48921759 | |||
chr18:48948427 | G | T | 1 | a0001c0003 | 4 | NA18951.hp1 NA18965.hp1 NA18997.hp1 others(1): Show |
synonymous_variant | LOW | c.624C>A | p.Pro208Pro | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/4 | 1165/3341 | 624/1281 | 208/426 | chr18 | 48948427 | |||
chr18:48949957 | G | A | 1 | a0001c0012 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.468C>T | p.Pro156Pro | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/4 | 1009/3341 | 468/1281 | 156/426 | chr18 | 48949957 | |||
chr18:48949963 | C | T | 1 | a0001c0006 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.462G>A | p.Ser154Ser | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/4 | 1003/3341 | 462/1281 | 154/426 | chr18 | 48949963 | |||
chr18:48950191 | T | C | 1 | a0001c0014 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.234A>G | p.Pro78Pro | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/4 | 775/3341 | 234/1281 | 78/426 | chr18 | 48950191 | |||
chr18:48950278 | C | T | 1 | a0001c0005 | 2 | HG01175.hp2 HG04204.hp2 |
synonymous_variant | LOW | c.147G>A | p.Gly49Gly | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/4 | 688/3341 | 147/1281 | 49/426 | chr18 | 48950278 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:48920144 | G | C | 1 | a0001c0012t0024 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1228C>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 1228 | chr18 | 48920144 | ||||||
chr18:48920145 | T | G | 3 | a0001c0001t0010 a0001c0001t0011 a0001c0010t0028 |
7 | HG02559.hp1 HG02572.hp2 HG03209.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1227A>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 1227 | chr18 | 48920145 | ||||||
chr18:48920219 | T | C | 7 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(4): Show |
51 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1153A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 1153 | chr18 | 48920219 | ||||||
chr18:48920470 | A | C | 9 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0010 others(6): Show |
41 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*902T>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 902 | chr18 | 48920470 | ||||||
chr18:48920655 | G | A | 1 | a0001c0001t0012 | 2 | HG00597.hp1 HG02080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*717C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 717 | chr18 | 48920655 | ||||||
chr18:48920671 | C | T | 1 | a0001c0001t0023 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*701G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 701 | chr18 | 48920671 | ||||||
chr18:48920761 | C | T | 1 | a0001c0001t0022 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*611G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 611 | chr18 | 48920761 | ||||||
chr18:48920778 | A | G | 1 | a0001c0001t0021 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*594T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 594 | chr18 | 48920778 | ||||||
chr18:48921054 | G | C | 1 | a0001c0001t0006 | 6 | HG01192.hp1 HG01358.hp2 HG01433.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*318C>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 318 | chr18 | 48921054 | ||||||
chr18:48921060 | C | T | 1 | a0001c0001t0017 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*312G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 312 | chr18 | 48921060 | ||||||
chr18:48921253 | C | CA | 5 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0025 others(2): Show |
8 | HG00544.hp2 HG00735.hp1 HG01884.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*118dupT | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 118 | chr18 | 48921253 | ||||||
chr18:48921263 | A | C | 1 | a0001c0010t0028 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*109T>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 109 | chr18 | 48921263 | ||||||
chr18:48921264 | C | T | 2 | a0001c0001t0008 a0001c0001t0014 |
6 | HG01109.hp2 HG02451.hp1 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*108G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 4/4 | 108 | chr18 | 48921264 | ||||||
chr18:48950454 | T | C | 1 | a0001c0001t0015 | 2 | HG02258.hp1 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-30A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/4 | 30 | chr18 | 48950454 | ||||||
chr18:48950496 | G | T | 1 | a0001c0001t0020 | 1 | HG02004.hp2 | 5_prime_UTR_variant | MODIFIER | c.-72C>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/4 | 72 | chr18 | 48950496 | ||||||
chr18:48950720 | G | C | 1 | a0001c0001t0019 | 1 | NA18747.hp2 | 5_prime_UTR_variant | MODIFIER | c.-296C>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/4 | 296 | chr18 | 48950720 | ||||||
chr18:48950736 | C | G | 8 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0012 others(5): Show |
34 | HG00140.hp2 HG00597.hp1 HG00741.hp1 others(31): Show |
5_prime_UTR_variant | MODIFIER | c.-312G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/4 | 312 | chr18 | 48950736 | ||||||
chr18:48950762 | G | A | 1 | a0001c0001t0027 | 1 | NA19085.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-338C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/4 | chr18 | 48950762 | |||||||
chr18:48950837 | C | T | 1 | a0001c0001t0016 | 1 | NA18979.hp1 | 5_prime_UTR_variant | MODIFIER | c.-413G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/4 | 413 | chr18 | 48950837 | ||||||
chr18:48950920 | C | G | 1 | a0001c0010t0028 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-496G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/4 | 496 | chr18 | 48950920 | ||||||
chr18:48950926 | G | C | 1 | a0001c0010t0028 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-502C>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/4 | 502 | chr18 | 48950926 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:48921952 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.743-42A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48921952 | |||||||
chr18:48922016 | G | A | 20 | a0001c0002t0001g0078 a0001c0002t0001g0101 a0001c0002t0001g0125 others(17): Show |
20 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.743-106C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48922016 | |||||||
chr18:48922279 | C | T | 1 | a0001c0001t0003g0216 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.743-369G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48922279 | |||||||
chr18:48922435 | T | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(255): Show |
275 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.743-525A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48922435 | |||||||
chr18:48922449 | C | G | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(226): Show |
244 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.743-539G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48922449 | |||||||
chr18:48922505 | A | G | 363 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(360): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.743-595T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48922505 | |||||||
chr18:48922507 | C | CCTCT | 258 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(255): Show |
275 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.743-598_743-597ins others(4): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48922507 | |||||||
chr18:48922662 | G | A | 25 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0071 others(22): Show |
27 | HG00639.hp1 HG00642.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.743-752C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48922662 | |||||||
chr18:48922724 | T | A | 1 | a0001c0001t0002g0089 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.743-814A>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48922724 | |||||||
chr18:48922741 | T | C | 89 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0013 others(86): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.743-831A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48922741 | |||||||
chr18:48922825 | C | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0017 others(48): Show |
55 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.743-915G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48922825 | |||||||
chr18:48922889 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.743-979C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48922889 | |||||||
chr18:48922911 | A | C | 3 | a0001c0001t0003g0282 a0001c0001t0003g0283 a0001c0014t0018g0057 |
3 | HG01243.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.743-1001T>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48922911 | |||||||
chr18:48923195 | C | G | 98 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0013 others(95): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.743-1285G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48923195 | |||||||
chr18:48923262 | A | G | 7 | a0001c0001t0001g0332 a0001c0001t0003g0128 a0001c0001t0003g0129 others(4): Show |
7 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.743-1352T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48923262 | |||||||
chr18:48923348 | C | T | 2 | a0001c0005t0001g0062 a0001c0005t0001g0063 |
2 | HG01175.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.743-1438G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48923348 | |||||||
chr18:48923349 | G | A | 1 | a0001c0003t0001g0080 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.743-1439C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48923349 | |||||||
chr18:48923389 | A | G | 3 | a0001c0001t0003g0282 a0001c0001t0003g0283 a0001c0014t0018g0057 |
3 | HG01243.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.743-1479T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48923389 | |||||||
chr18:48923467 | A | AGTT | 5 | a0001c0001t0008g0168 a0001c0001t0008g0169 a0001c0001t0008g0170 others(2): Show |
5 | HG01109.hp2 HG02630.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-1560_743-1558d others(5): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48923467 | |||||||
chr18:48923467 | AGTT | A | 27 | a0001c0001t0001g0201 a0001c0001t0001g0351 a0001c0001t0003g0331 others(24): Show |
27 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.743-1560_743-1558d others(5): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48923467 | |||||||
chr18:48923555 | C | T | 27 | a0001c0001t0001g0201 a0001c0001t0001g0351 a0001c0001t0003g0331 others(24): Show |
27 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.743-1645G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48923555 | |||||||
chr18:48923589 | A | T | 27 | a0001c0001t0001g0201 a0001c0001t0001g0351 a0001c0001t0003g0331 others(24): Show |
27 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.743-1679T>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48923589 | |||||||
chr18:48923605 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.743-1695T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48923605 | |||||||
chr18:48923745 | A | G | 7 | a0001c0001t0001g0096 a0001c0001t0001g0202 a0001c0001t0001g0204 others(4): Show |
7 | HG02055.hp2 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.743-1835T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48923745 | |||||||
chr18:48923779 | G | A | 6 | a0001c0001t0001g0201 a0001c0001t0003g0331 a0001c0001t0005g0213 others(3): Show |
6 | HG02257.hp1 HG02559.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.743-1869C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48923779 | |||||||
chr18:48923826 | T | C | 1 | a0001c0001t0005g0215 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.743-1916A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48923826 | |||||||
chr18:48923903 | C | T | 5 | a0001c0001t0008g0168 a0001c0001t0008g0169 a0001c0001t0008g0170 others(2): Show |
5 | HG01109.hp2 HG02630.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-1993G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48923903 | |||||||
chr18:48923934 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.743-2024G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48923934 | |||||||
chr18:48924306 | C | CAGG | 3 | a0001c0001t0003g0216 a0001c0001t0009g0356 a0001c0006t0003g0064 |
3 | HG01884.hp2 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.743-2399_743-2397d others(5): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48924306 | |||||||
chr18:48924355 | G | T | 1 | a0001c0014t0018g0057 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.743-2445C>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48924355 | |||||||
chr18:48924378 | C | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0195 a0001c0001t0001g0279 |
4 | HG02523.hp1 NA18944.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-2468G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48924378 | |||||||
chr18:48924606 | A | G | 316 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(313): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.743-2696T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48924606 | |||||||
chr18:48924677 | G | T | 7 | a0001c0001t0001g0019 a0001c0001t0001g0191 a0001c0001t0001g0249 others(4): Show |
8 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.743-2767C>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48924677 | |||||||
chr18:48924703 | C | G | 109 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0013 others(106): Show |
117 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.743-2793G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48924703 | |||||||
chr18:48924713 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0244 |
6 | HG02735.hp1 NA18982.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.743-2803G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48924713 | |||||||
chr18:48924726 | C | A | 1 | a0001c0001t0002g0089 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.743-2816G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48924726 | |||||||
chr18:48924776 | G | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
131 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.743-2866C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48924776 | |||||||
chr18:48924847 | G | A | 5 | a0001c0001t0001g0187 a0001c0001t0002g0188 a0001c0001t0002g0238 others(2): Show |
5 | NA18947.hp2 NA18969.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.743-2937C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48924847 | |||||||
chr18:48924850 | C | T | 4 | a0001c0001t0005g0181 a0001c0001t0005g0217 a0001c0001t0005g0218 others(1): Show |
4 | HG02886.hp1 HG02895.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-2940G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48924850 | |||||||
chr18:48924913 | A | G | 1 | a0001c0001t0002g0124 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.743-3003T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48924913 | |||||||
chr18:48924924 | C | T | 2 | a0001c0001t0003g0282 a0001c0001t0003g0283 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.743-3014G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48924924 | |||||||
chr18:48925075 | G | A | 1 | a0001c0001t0001g0360 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.743-3165C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925075 | |||||||
chr18:48925211 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.743-3301G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925211 | |||||||
chr18:48925272 | A | C | 1 | a0001c0001t0002g0089 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.743-3362T>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925272 | |||||||
chr18:48925275 | A | G | 5 | a0001c0001t0001g0201 a0001c0001t0003g0331 a0001c0001t0010g0130 others(2): Show |
5 | HG02559.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.743-3365T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925275 | |||||||
chr18:48925280 | T | C | 1 | a0001c0001t0004g0037 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.743-3370A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925280 | |||||||
chr18:48925431 | T | TG | 4 | a0001c0001t0001g0088 a0001c0001t0001g0097 a0001c0001t0001g0176 others(1): Show |
4 | HG02451.hp1 HG02723.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.743-3522dupC | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925431 | |||||||
chr18:48925432 | G | GC | 111 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0013 others(108): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.743-3523dupG | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925432 | |||||||
chr18:48925432 | G | GCC | 18 | a0001c0001t0001g0180 a0001c0001t0001g0185 a0001c0001t0001g0193 others(15): Show |
18 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.743-3524_743-3523d others(4): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925432 | |||||||
chr18:48925435 | C | CG | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(194): Show |
214 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.743-3526_743-3525i others(3): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925435 | |||||||
chr18:48925442 | A | C | 365 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(362): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.743-3532T>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925442 | |||||||
chr18:48925453 | T | C | 5 | a0001c0001t0001g0201 a0001c0001t0003g0331 a0001c0001t0010g0130 others(2): Show |
5 | HG02559.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.743-3543A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925453 | |||||||
chr18:48925474 | C | A | 1 | a0001c0001t0001g0336 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.743-3564G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925474 | |||||||
chr18:48925503 | G | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(209): Show |
229 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.743-3593C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925503 | |||||||
chr18:48925513 | G | A | 14 | a0001c0001t0001g0111 a0001c0001t0001g0288 a0001c0001t0001g0328 others(11): Show |
14 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.743-3603C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925513 | |||||||
chr18:48925650 | G | A | 6 | a0001c0001t0005g0213 a0001c0001t0008g0168 a0001c0001t0008g0169 others(3): Show |
6 | HG01109.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.743-3740C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925650 | |||||||
chr18:48925752 | C | CT | 6 | a0001c0001t0005g0213 a0001c0001t0008g0168 a0001c0001t0008g0169 others(3): Show |
6 | HG01109.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.743-3843dupA | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925752 | |||||||
chr18:48925752 | CT | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(206): Show |
226 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.743-3843delA | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925752 | |||||||
chr18:48925770 | G | A | 6 | a0001c0001t0005g0213 a0001c0001t0008g0168 a0001c0001t0008g0169 others(3): Show |
6 | HG01109.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.743-3860C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925770 | |||||||
chr18:48925777 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.743-3867G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925777 | |||||||
chr18:48925778 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0109 |
2 | NA18998.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.743-3868C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925778 | |||||||
chr18:48925785 | C | T | 4 | a0001c0001t0005g0181 a0001c0001t0005g0217 a0001c0001t0005g0218 others(1): Show |
4 | HG02886.hp1 HG02895.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-3875G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925785 | |||||||
chr18:48925804 | T | C | 9 | a0001c0001t0001g0096 a0001c0001t0001g0202 a0001c0001t0001g0204 others(6): Show |
9 | HG01884.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.743-3894A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925804 | |||||||
chr18:48925830 | T | C | 9 | a0001c0001t0001g0096 a0001c0001t0001g0202 a0001c0001t0001g0204 others(6): Show |
9 | HG01884.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.743-3920A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925830 | |||||||
chr18:48925892 | A | G | 6 | a0001c0001t0005g0213 a0001c0001t0008g0168 a0001c0001t0008g0169 others(3): Show |
6 | HG01109.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.743-3982T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925892 | |||||||
chr18:48925896 | G | A | 6 | a0001c0001t0005g0213 a0001c0001t0008g0168 a0001c0001t0008g0169 others(3): Show |
6 | HG01109.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.743-3986C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925896 | |||||||
chr18:48925907 | T | C | 6 | a0001c0001t0005g0213 a0001c0001t0008g0168 a0001c0001t0008g0169 others(3): Show |
6 | HG01109.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.743-3997A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925907 | |||||||
chr18:48925957 | A | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(205): Show |
225 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.743-4047T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925957 | |||||||
chr18:48925967 | C | T | 1 | a0001c0001t0003g0294 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.743-4057G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925967 | |||||||
chr18:48925988 | C | T | 8 | a0001c0001t0001g0096 a0001c0001t0001g0202 a0001c0001t0001g0204 others(5): Show |
8 | HG01884.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.743-4078G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925988 | |||||||
chr18:48925993 | G | A | 5 | a0001c0001t0001g0201 a0001c0001t0003g0331 a0001c0001t0010g0130 others(2): Show |
5 | HG02559.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.743-4083C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48925993 | |||||||
chr18:48926036 | G | A | 1 | a0001c0012t0024g0368 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.743-4126C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48926036 | |||||||
chr18:48926039 | C | T | 2 | a0001c0001t0001g0293 a0001c0001t0004g0050 |
2 | HG01099.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.743-4129G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48926039 | |||||||
chr18:48926267 | A | G | 360 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(357): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.743-4357T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48926267 | |||||||
chr18:48926269 | C | T | 2 | a0001c0001t0003g0167 a0001c0001t0003g0221 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.743-4359G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48926269 | |||||||
chr18:48926331 | A | AAAG | 113 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0013 others(110): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.743-4424_743-4422d others(5): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48926331 | |||||||
chr18:48926366 | A | C | 21 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0201 others(18): Show |
21 | HG01884.hp1 HG02055.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.743-4456T>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48926366 | |||||||
chr18:48926484 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.743-4574G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48926484 | |||||||
chr18:48926559 | C | T | 1 | a0001c0001t0005g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743-4649G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48926559 | |||||||
chr18:48926596 | G | A | 3 | a0001c0001t0001g0332 a0001c0001t0003g0334 a0001c0001t0003g0335 |
3 | HG02818.hp2 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.743-4686C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48926596 | |||||||
chr18:48926734 | C | T | 6 | a0001c0001t0001g0096 a0001c0001t0001g0202 a0001c0001t0001g0204 others(3): Show |
6 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.743-4824G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48926734 | |||||||
chr18:48926756 | C | T | 7 | a0001c0001t0001g0332 a0001c0001t0003g0128 a0001c0001t0003g0129 others(4): Show |
7 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.743-4846G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48926756 | |||||||
chr18:48926786 | A | T | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(215): Show |
235 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.743-4876T>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48926786 | |||||||
chr18:48926796 | C | T | 1 | a0001c0001t0022g0271 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.743-4886G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48926796 | |||||||
chr18:48926836 | A | G | 3 | a0001c0001t0003g0282 a0001c0001t0003g0283 a0001c0014t0018g0057 |
3 | HG01243.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.743-4926T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48926836 | |||||||
chr18:48927007 | C | T | 6 | a0001c0001t0005g0213 a0001c0001t0008g0168 a0001c0001t0008g0169 others(3): Show |
6 | HG01109.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.743-5097G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48927007 | |||||||
chr18:48927008 | G | A | 1 | a0001c0001t0006g0246 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.743-5098C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48927008 | |||||||
chr18:48927036 | A | C | 341 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(338): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.743-5126T>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48927036 | |||||||
chr18:48927093 | T | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(255): Show |
276 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.743-5183A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48927093 | |||||||
chr18:48927199 | G | A | 5 | a0001c0001t0006g0015 a0001c0001t0006g0194 a0001c0001t0006g0243 others(2): Show |
6 | HG01192.hp1 HG01358.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.743-5289C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48927199 | |||||||
chr18:48927311 | A | AT | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(209): Show |
228 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.743-5402dupA | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48927311 | |||||||
chr18:48927384 | C | T | 73 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(70): Show |
81 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.743-5474G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48927384 | |||||||
chr18:48927485 | C | G | 16 | a0001c0001t0001g0098 a0001c0001t0001g0133 a0001c0001t0001g0171 others(13): Show |
17 | HG00735.hp2 HG00738.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.743-5575G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48927485 | |||||||
chr18:48927511 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.743-5601C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48927511 | |||||||
chr18:48927559 | C | T | 90 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0013 others(87): Show |
98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.743-5649G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48927559 | |||||||
chr18:48927564 | C | G | 8 | a0001c0001t0001g0201 a0001c0001t0003g0282 a0001c0001t0003g0283 others(5): Show |
8 | HG01243.hp2 HG02559.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.743-5654G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48927564 | |||||||
chr18:48927678 | A | G | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(244): Show |
264 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.743-5768T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48927678 | |||||||
chr18:48927699 | C | T | 1 | a0001c0001t0001g0336 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.743-5789G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48927699 | |||||||
chr18:48927769 | A | G | 352 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(349): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.743-5859T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48927769 | |||||||
chr18:48927842 | G | A | 2 | a0001c0001t0003g0216 a0001c0001t0009g0356 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.743-5932C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48927842 | |||||||
chr18:48927888 | A | T | 5 | a0001c0001t0001g0201 a0001c0001t0003g0331 a0001c0001t0010g0130 others(2): Show |
5 | HG02559.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.743-5978T>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48927888 | |||||||
chr18:48928113 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0244 |
4 | NA18982.hp1 NA18983.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-6203C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48928113 | |||||||
chr18:48928455 | TTTC | T | 17 | a0001c0001t0001g0088 a0001c0001t0001g0097 a0001c0001t0001g0176 others(14): Show |
17 | HG01109.hp2 HG02257.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.743-6548_743-6546d others(5): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48928455 | |||||||
chr18:48928457 | TC | T | 3 | a0001c0001t0003g0216 a0001c0001t0009g0356 a0001c0006t0003g0064 |
3 | HG01884.hp2 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.743-6548delG | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48928457 | |||||||
chr18:48928520 | C | A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0079 a0001c0001t0001g0087 others(14): Show |
18 | HG01496.hp1 HG02083.hp1 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.743-6610G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48928520 | |||||||
chr18:48928521 | G | A | 1 | a0001c0001t0005g0215 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.743-6611C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48928521 | |||||||
chr18:48928581 | T | G | 15 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0202 others(12): Show |
15 | HG01884.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.743-6671A>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48928581 | |||||||
chr18:48928595 | T | C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0104 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.743-6685A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48928595 | |||||||
chr18:48928647 | C | T | 2 | a0001c0001t0001g0349 a0001c0001t0001g0354 |
2 | NA19067.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.743-6737G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48928647 | |||||||
chr18:48928730 | G | A | 3 | a0001c0001t0003g0216 a0001c0001t0009g0356 a0001c0006t0003g0064 |
3 | HG01884.hp2 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.743-6820C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48928730 | |||||||
chr18:48928867 | C | T | 1 | a0001c0001t0001g0020 | 2 | NA18950.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.743-6957G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48928867 | |||||||
chr18:48928953 | C | T | 1 | a0001c0010t0028g0373 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.743-7043G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48928953 | |||||||
chr18:48929066 | G | A | 3 | a0001c0001t0003g0216 a0001c0001t0009g0356 a0001c0006t0003g0064 |
3 | HG01884.hp2 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.743-7156C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929066 | |||||||
chr18:48929098 | TA | T | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(248): Show |
268 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.743-7189delT | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929098 | |||||||
chr18:48929310 | C | A | 10 | a0001c0001t0001g0166 a0001c0001t0003g0282 a0001c0001t0003g0283 others(7): Show |
10 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.743-7400G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929310 | |||||||
chr18:48929364 | T | C | 1 | a0001c0001t0005g0305 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.743-7454A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929364 | |||||||
chr18:48929381 | C | T | 3 | a0001c0001t0001g0201 a0001c0001t0010g0130 a0001c0001t0010g0284 |
3 | HG02559.hp1 HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.743-7471G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929381 | |||||||
chr18:48929516 | TTCTC | T | 6 | a0001c0001t0001g0070 a0001c0001t0001g0351 a0001c0002t0001g0125 others(3): Show |
6 | HG01257.hp1 HG02083.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.743-7610_743-7607d others(6): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929516 | |||||||
chr18:48929530 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0195 a0001c0001t0001g0279 |
4 | HG02523.hp1 NA18944.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-7620G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929530 | |||||||
chr18:48929550 | T | C | 3 | a0001c0001t0003g0216 a0001c0001t0009g0356 a0001c0006t0003g0064 |
3 | HG01884.hp2 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.743-7640A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929550 | |||||||
chr18:48929550 | TTC | T | 31 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0071 others(28): Show |
33 | HG00639.hp1 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.743-7642_743-7641d others(4): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929550 | |||||||
chr18:48929565 | T | TCA | 5 | a0001c0001t0001g0175 a0001c0001t0001g0308 a0001c0001t0001g0325 others(2): Show |
5 | HG02145.hp2 HG03225.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-7656_743-7655i others(4): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929565 | |||||||
chr18:48929567 | T | A | 7 | a0001c0001t0001g0113 a0001c0001t0001g0158 a0001c0001t0001g0175 others(4): Show |
7 | HG02145.hp2 HG02165.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.743-7657A>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929567 | |||||||
chr18:48929567 | T | TCACACAC others(9): Show |
1 | a0001c0001t0001g0322 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.743-7658_743-7657i others(18): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929567 | |||||||
chr18:48929567 | T | TCACACAC others(11): Show |
1 | a0001c0001t0001g0111 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.743-7658_743-7657i others(20): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929567 | |||||||
chr18:48929567 | T | TCACACAC others(13): Show |
1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.743-7658_743-7657i others(22): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929567 | |||||||
chr18:48929569 | T | A | 11 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0126 others(8): Show |
11 | HG02145.hp2 HG02165.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.743-7659A>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCACACAC others(9): Show |
1 | a0001c0001t0001g0344 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.743-7660_743-7659i others(18): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCACACAC others(11): Show |
2 | a0001c0001t0001g0330 a0001c0010t0028g0373 |
2 | HG00738.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.743-7660_743-7659i others(20): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCACACAC others(13): Show |
5 | a0001c0001t0001g0162 a0001c0001t0001g0177 a0001c0001t0001g0200 others(2): Show |
5 | HG02970.hp2 HG03098.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(22): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCACACAC others(15): Show |
3 | a0001c0001t0001g0203 a0001c0001t0002g0089 a0001c0001t0003g0294 |
3 | HG02717.hp1 HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.743-7660_743-7659i others(24): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCACACAC others(17): Show |
2 | a0001c0001t0001g0207 a0001c0001t0001g0295 |
2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.743-7660_743-7659i others(26): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCACAC others(3): Show |
1 | a0001c0001t0001g0136 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.743-7660_743-7659i others(12): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCACAC others(5): Show |
5 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0274 others(2): Show |
7 | HG00323.hp1 HG00408.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(14): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCACAC others(7): Show |
15 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0076 others(12): Show |
17 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(16): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCACAC others(9): Show |
31 | a0001c0001t0001g0066 a0001c0001t0001g0074 a0001c0001t0001g0133 others(28): Show |
31 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(18): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCACAC others(11): Show |
12 | a0001c0001t0001g0093 a0001c0001t0001g0103 a0001c0001t0001g0163 others(9): Show |
12 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(20): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCACAC others(13): Show |
9 | a0001c0001t0001g0067 a0001c0001t0001g0180 a0001c0001t0001g0224 others(6): Show |
9 | HG00438.hp1 HG01243.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(22): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCACAC others(15): Show |
5 | a0001c0001t0001g0100 a0001c0001t0001g0336 a0001c0001t0002g0237 others(2): Show |
5 | HG03195.hp2 NA18952.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(24): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCACAC others(17): Show |
4 | a0001c0001t0001g0267 a0001c0001t0002g0255 a0001c0001t0003g0167 others(1): Show |
4 | HG00438.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(26): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCAC others(1): Show |
8 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0065 others(5): Show |
10 | HG00609.hp2 HG02523.hp1 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(10): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCAC others(3): Show |
5 | a0001c0001t0001g0007 a0001c0001t0001g0094 a0001c0001t0001g0156 others(2): Show |
6 | HG01175.hp2 HG02132.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(12): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCAC others(5): Show |
69 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(66): Show |
79 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(14): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCAC others(7): Show |
22 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0001g0087 others(19): Show |
22 | HG01167.hp1 HG01169.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(16): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCAC others(9): Show |
4 | a0001c0001t0001g0006 a0001c0001t0001g0119 a0001c0001t0001g0234 others(1): Show |
5 | HG00140.hp1 HG01496.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(18): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCAC others(11): Show |
7 | a0001c0001t0001g0121 a0001c0001t0001g0137 a0001c0001t0001g0138 others(4): Show |
7 | HG01074.hp1 HG01123.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(20): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCAC others(13): Show |
21 | a0001c0001t0001g0070 a0001c0001t0001g0088 a0001c0001t0001g0097 others(18): Show |
21 | HG00597.hp1 HG00597.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(22): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCAC others(15): Show |
6 | a0001c0001t0001g0351 a0001c0001t0002g0146 a0001c0002t0001g0125 others(3): Show |
6 | HG01257.hp1 HG02083.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(24): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCAC others(17): Show |
3 | a0001c0001t0001g0202 a0001c0001t0002g0240 a0001c0001t0002g0254 |
3 | HG02717.hp2 NA18957.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.743-7660_743-7659i others(26): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCAC others(19): Show |
1 | a0001c0001t0002g0188 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.743-7660_743-7659i others(28): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCAC others(14): Show |
1 | a0001c0001t0001g0184 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.743-7660_743-7659i others(23): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCTC others(3): Show |
1 | a0001c0001t0014g0319 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.743-7660_743-7659i others(12): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCTC others(5): Show |
3 | a0001c0001t0001g0153 a0001c0001t0001g0337 a0001c0001t0006g0243 |
3 | HG00733.hp2 HG01346.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.743-7660_743-7659i others(14): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCTC others(9): Show |
8 | a0001c0001t0001g0003 a0001c0001t0001g0068 a0001c0001t0001g0165 others(5): Show |
10 | HG02040.hp1 HG02083.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(18): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCTC others(11): Show |
5 | a0001c0001t0001g0120 a0001c0001t0001g0204 a0001c0001t0001g0205 others(2): Show |
5 | HG02572.hp1 HG02683.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(20): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCTC others(13): Show |
8 | a0001c0001t0001g0096 a0001c0001t0001g0363 a0001c0001t0002g0001 others(5): Show |
10 | HG02040.hp2 HG02622.hp2 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.743-7660_743-7659i others(22): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCTC others(15): Show |
1 | a0001c0001t0001g0197 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.743-7660_743-7659i others(24): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCTC others(17): Show |
2 | a0001c0001t0001g0187 a0001c0001t0001g0220 |
2 | HG03688.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.743-7660_743-7659i others(26): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCTC others(19): Show |
2 | a0001c0001t0001g0362 a0001c0001t0004g0055 |
2 | NA18951.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.743-7660_743-7659i others(28): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCTC others(23): Show |
1 | a0001c0001t0002g0268 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.743-7660_743-7659i others(32): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCTC others(13): Show |
1 | a0001c0001t0002g0102 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.743-7660_743-7659i others(22): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929569 | T | TCTCTCTC others(19): Show |
1 | a0001c0001t0002g0238 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.743-7660_743-7659i others(28): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929569 | |||||||
chr18:48929571 | A | T | 1 | a0001c0001t0005g0215 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.743-7661T>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929571 | |||||||
chr18:48929573 | T | A | 294 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(291): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.743-7663A>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929573 | |||||||
chr18:48929573 | T | TCA | 7 | a0001c0001t0001g0131 a0001c0001t0001g0201 a0001c0001t0003g0172 others(4): Show |
7 | HG02258.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.743-7665_743-7664d others(4): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929573 | |||||||
chr18:48929573 | TCA | T | 31 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0071 others(28): Show |
33 | HG00639.hp1 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.743-7665_743-7664d others(4): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929573 | |||||||
chr18:48929718 | C | A | 1 | a0001c0001t0001g0265 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.743-7808G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929718 | |||||||
chr18:48929760 | C | T | 7 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0152 others(4): Show |
9 | HG00642.hp2 HG00733.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.743-7850G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929760 | |||||||
chr18:48929855 | A | G | 369 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(366): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.743-7945T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929855 | |||||||
chr18:48929860 | ACTCCACT others(74): Show |
A | 1 | a0001c0001t0001g0304 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.743-8031_743-7951d others(83): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48929860 | |||||||
chr18:48930024 | C | T | 6 | a0001c0001t0001g0070 a0001c0001t0001g0351 a0001c0002t0001g0125 others(3): Show |
6 | HG01257.hp1 HG02083.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.743-8114G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930024 | |||||||
chr18:48930091 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.743-8181C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930091 | |||||||
chr18:48930103 | G | T | 1 | a0001c0001t0001g0197 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.743-8193C>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930103 | |||||||
chr18:48930351 | C | T | 19 | a0001c0001t0001g0140 a0001c0001t0001g0145 a0001c0001t0001g0149 others(16): Show |
19 | HG00423.hp1 HG01433.hp1 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.743-8441G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930351 | |||||||
chr18:48930367 | C | G | 1 | a0001c0007t0009g0231 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.743-8457G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930367 | |||||||
chr18:48930368 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743-8458C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930368 | |||||||
chr18:48930378 | A | T | 1 | a0001c0001t0001g0277 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.743-8468T>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930378 | |||||||
chr18:48930531 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.743-8621A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930531 | |||||||
chr18:48930681 | T | C | 26 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(23): Show |
27 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.743-8771A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930681 | |||||||
chr18:48930717 | GC | G | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.743-8808delG | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930717 | |||||||
chr18:48930726 | T | C | 306 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(303): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.743-8816A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930726 | |||||||
chr18:48930758 | C | T | 7 | a0001c0001t0001g0308 a0001c0001t0001g0330 a0001c0001t0001g0336 others(4): Show |
7 | HG00738.hp2 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.743-8848G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930758 | |||||||
chr18:48930778 | C | T | 5 | a0001c0001t0001g0330 a0001c0001t0003g0329 a0001c0001t0008g0168 others(2): Show |
5 | HG00738.hp2 HG01891.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.743-8868G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930778 | |||||||
chr18:48930804 | T | C | 112 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0016 others(109): Show |
117 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.743-8894A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930804 | |||||||
chr18:48930841 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.743-8931C>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930841 | |||||||
chr18:48930843 | C | T | 1 | a0001c0001t0001g0313 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.743-8933G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930843 | |||||||
chr18:48930862 | A | T | 1 | a0001c0001t0001g0325 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.743-8952T>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930862 | |||||||
chr18:48930888 | C | T | 9 | a0001c0001t0001g0066 a0001c0001t0001g0111 a0001c0001t0001g0163 others(6): Show |
9 | HG01884.hp1 HG02258.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.743-8978G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930888 | |||||||
chr18:48930935 | A | C | 7 | a0001c0001t0001g0209 a0001c0001t0001g0332 a0001c0001t0003g0333 others(4): Show |
7 | HG02559.hp2 HG02647.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.743-9025T>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930935 | |||||||
chr18:48930988 | A | G | 22 | a0001c0001t0001g0065 a0001c0001t0001g0140 a0001c0001t0001g0145 others(19): Show |
22 | HG00280.hp2 HG00423.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.743-9078T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48930988 | |||||||
chr18:48931007 | C | A | 131 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0021 others(128): Show |
137 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.743-9097G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48931007 | |||||||
chr18:48931008 | G | A | 10 | a0001c0001t0001g0209 a0001c0001t0001g0332 a0001c0001t0003g0282 others(7): Show |
10 | HG02559.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.743-9098C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48931008 | |||||||
chr18:48931093 | T | C | 22 | a0001c0001t0001g0007 a0001c0001t0001g0126 a0001c0001t0001g0137 others(19): Show |
23 | HG01099.hp2 HG02055.hp1 HG02132.hp1 others(20): Show |
intron_variant | MODIFIER | c.743-9183A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48931093 | |||||||
chr18:48931132 | G | C | 10 | a0001c0001t0001g0066 a0001c0001t0001g0111 a0001c0001t0001g0163 others(7): Show |
10 | HG01884.hp1 HG02258.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.743-9222C>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48931132 | |||||||
chr18:48931484 | G | A | 3 | a0001c0001t0001g0171 a0001c0001t0003g0172 a0001c0001t0003g0173 |
3 | HG00735.hp2 HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.743-9574C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48931484 | |||||||
chr18:48931645 | C | A | 15 | a0001c0001t0001g0209 a0001c0001t0001g0301 a0001c0001t0001g0304 others(12): Show |
16 | HG01109.hp2 HG01255.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.743-9735G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48931645 | |||||||
chr18:48931681 | G | A | 1 | a0001c0001t0003g0355 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.743-9771C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48931681 | |||||||
chr18:48931743 | C | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0070 others(14): Show |
19 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.743-9833G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48931743 | |||||||
chr18:48931857 | A | C | 44 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0133 others(41): Show |
46 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.743-9947T>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48931857 | |||||||
chr18:48931927 | G | T | 1 | a0001c0001t0007g0044 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.743-10017C>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48931927 | |||||||
chr18:48931928 | G | C | 1 | a0001c0001t0002g0089 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.743-10018C>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48931928 | |||||||
chr18:48931967 | C | A | 1 | a0001c0001t0001g0280 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.743-10057G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48931967 | |||||||
chr18:48931979 | G | GC | 157 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0022 others(154): Show |
163 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.743-10070dupG | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48931979 | |||||||
chr18:48931980 | C | CT | 24 | a0001c0001t0001g0065 a0001c0001t0001g0140 a0001c0001t0001g0145 others(21): Show |
24 | HG00280.hp2 HG00423.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.743-10071_743-1007 others(5): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48931980 | |||||||
chr18:48932551 | T | G | 144 | a0001c0001t0001g0007 a0001c0001t0001g0065 a0001c0001t0001g0066 others(141): Show |
148 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.742+9930A>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48932551 | |||||||
chr18:48932580 | G | A | 184 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0022 others(181): Show |
190 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.742+9901C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48932580 | |||||||
chr18:48932662 | T | C | 44 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0133 others(41): Show |
46 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.742+9819A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48932662 | |||||||
chr18:48932671 | G | T | 1 | a0001c0014t0018g0057 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.742+9810C>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48932671 | |||||||
chr18:48932809 | A | C | 23 | a0001c0001t0001g0065 a0001c0001t0001g0140 a0001c0001t0001g0145 others(20): Show |
23 | HG00280.hp2 HG00423.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.742+9672T>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48932809 | |||||||
chr18:48932892 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.742+9589A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48932892 | |||||||
chr18:48932894 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.742+9587G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48932894 | |||||||
chr18:48932921 | C | A | 1 | a0001c0001t0001g0230 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.742+9560G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48932921 | |||||||
chr18:48932953 | C | T | 185 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0022 others(182): Show |
191 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.742+9528G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48932953 | |||||||
chr18:48933103 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.742+9378G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48933103 | |||||||
chr18:48933174 | A | G | 1 | a0001c0001t0002g0089 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.742+9307T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48933174 | |||||||
chr18:48933333 | C | T | 2 | a0001c0001t0003g0167 a0001c0001t0003g0221 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.742+9148G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48933333 | |||||||
chr18:48933539 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.742+8942G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48933539 | |||||||
chr18:48933630 | A | G | 19 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00738.hp2 HG01243.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.742+8851T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48933630 | |||||||
chr18:48933645 | C | G | 19 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00738.hp2 HG01243.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.742+8836G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48933645 | |||||||
chr18:48933754 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.742+8727C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48933754 | |||||||
chr18:48933789 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.742+8692G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48933789 | |||||||
chr18:48933807 | T | C | 1 | a0001c0001t0022g0271 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.742+8674A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48933807 | |||||||
chr18:48934015 | A | G | 112 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0066 others(109): Show |
116 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.742+8466T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48934015 | |||||||
chr18:48934121 | C | T | 1 | a0001c0001t0003g0221 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.742+8360G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48934121 | |||||||
chr18:48934148 | C | T | 1 | a0001c0001t0004g0035 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.742+8333G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48934148 | |||||||
chr18:48934176 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.742+8305T>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48934176 | |||||||
chr18:48934286 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0070 a0001c0001t0001g0071 others(14): Show |
18 | HG00323.hp2 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.742+8195C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48934286 | |||||||
chr18:48934335 | C | T | 44 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0093 others(41): Show |
46 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.742+8146G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48934335 | |||||||
chr18:48934338 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0068 a0001c0001t0001g0180 others(7): Show |
11 | HG02055.hp1 HG02132.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.742+8143C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48934338 | |||||||
chr18:48934362 | G | A | 24 | a0001c0001t0001g0007 a0001c0001t0001g0068 a0001c0001t0001g0180 others(21): Show |
26 | HG01109.hp2 HG01255.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.742+8119C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48934362 | |||||||
chr18:48934412 | A | G | 2 | a0001c0001t0015g0370 a0001c0001t0015g0371 |
2 | HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.742+8069T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48934412 | |||||||
chr18:48934453 | C | CA | 224 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(221): Show |
233 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.742+8027dupT | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48934453 | |||||||
chr18:48934506 | T | C | 1 | a0001c0001t0002g0089 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.742+7975A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48934506 | |||||||
chr18:48934533 | C | G | 247 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(244): Show |
257 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.742+7948G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48934533 | |||||||
chr18:48934642 | G | A | 44 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0093 others(41): Show |
46 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.742+7839C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48934642 | |||||||
chr18:48934859 | C | A | 1 | a0001c0001t0001g0337 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.742+7622G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48934859 | |||||||
chr18:48935113 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.742+7368A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48935113 | |||||||
chr18:48935117 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0070 a0001c0001t0001g0071 others(7): Show |
11 | HG00323.hp2 HG00642.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.742+7364G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48935117 | |||||||
chr18:48935380 | G | A | 1 | a0001c0001t0004g0051 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.742+7101C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48935380 | |||||||
chr18:48935416 | T | C | 236 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(233): Show |
245 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.742+7065A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48935416 | |||||||
chr18:48935589 | T | C | 17 | a0001c0001t0001g0131 a0001c0001t0001g0171 a0001c0001t0003g0128 others(14): Show |
17 | HG00735.hp2 HG01243.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.742+6892A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48935589 | |||||||
chr18:48935722 | G | A | 9 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0097 others(6): Show |
9 | HG00738.hp2 HG01891.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.742+6759C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48935722 | |||||||
chr18:48935813 | A | G | 78 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0022 others(75): Show |
82 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.742+6668T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48935813 | |||||||
chr18:48935933 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.742+6548C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48935933 | |||||||
chr18:48935947 | C | T | 4 | a0001c0001t0001g0093 a0001c0001t0002g0124 a0001c0001t0004g0039 others(1): Show |
4 | HG02056.hp1 HG02080.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+6534G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48935947 | |||||||
chr18:48936032 | G | A | 1 | a0001c0001t0001g0318 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.742+6449C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936032 | |||||||
chr18:48936039 | C | A | 2 | a0001c0001t0001g0325 a0001c0001t0001g0327 |
2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.742+6442G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936039 | |||||||
chr18:48936076 | AAACAC | A | 6 | a0001c0001t0001g0068 a0001c0001t0001g0144 a0001c0001t0001g0159 others(3): Show |
6 | HG01993.hp2 HG03927.hp2 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.742+6400_742+6404d others(7): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936076 | |||||||
chr18:48936076 | AAACACAC others(2): Show |
A | 3 | a0001c0001t0001g0267 a0001c0001t0002g0150 a0001c0001t0002g0281 |
3 | HG00597.hp2 HG00673.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.742+6396_742+6404d others(11): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936076 | |||||||
chr18:48936077 | A | AC | 3 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0120 |
3 | NA18944.hp2 NA18983.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.742+6403_742+6404i others(3): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936077 | |||||||
chr18:48936094 | ACACACAC others(16): Show |
A | 3 | a0001c0001t0001g0226 a0001c0001t0009g0356 a0001c0006t0003g0064 |
3 | HG01884.hp2 HG03453.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.742+6364_742+6386d others(25): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936094 | |||||||
chr18:48936096 | ACACACAC others(14): Show |
A | 1 | a0001c0001t0014g0319 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.742+6364_742+6384d others(23): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936096 | |||||||
chr18:48936098 | ACACACAC others(12): Show |
A | 4 | a0001c0001t0001g0067 a0001c0001t0001g0330 a0001c0001t0003g0329 others(1): Show |
4 | HG00738.hp2 HG01891.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+6364_742+6382d others(21): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936098 | |||||||
chr18:48936100 | ACACACAC others(10): Show |
A | 4 | a0001c0001t0001g0096 a0001c0001t0001g0126 a0001c0001t0001g0262 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+6364_742+6380d others(19): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936100 | |||||||
chr18:48936102 | ACACACAC others(8): Show |
A | 9 | a0001c0001t0001g0088 a0001c0001t0001g0131 a0001c0001t0004g0050 others(6): Show |
9 | HG01243.hp2 HG01258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.742+6364_742+6378d others(17): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936102 | |||||||
chr18:48936104 | ACACACAC others(6): Show |
A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0097 a0001c0001t0001g0147 others(14): Show |
18 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.742+6364_742+6376d others(15): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936104 | |||||||
chr18:48936106 | ACACACAC others(4): Show |
A | 35 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0071 others(32): Show |
35 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.742+6364_742+6374d others(13): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936106 | |||||||
chr18:48936108 | ACACACAC others(2): Show |
A | 66 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0065 others(63): Show |
67 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.742+6364_742+6372d others(11): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936108 | |||||||
chr18:48936110 | ACACACAC | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(91): Show |
102 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.742+6364_742+6370d others(9): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936110 | |||||||
chr18:48936112 | ACACAC | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0069 others(36): Show |
41 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.742+6364_742+6368d others(7): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936112 | |||||||
chr18:48936114 | ACAC | A | 17 | a0001c0001t0001g0087 a0001c0001t0001g0112 a0001c0001t0001g0156 others(14): Show |
18 | HG00438.hp2 HG00673.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.742+6364_742+6366d others(5): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936114 | |||||||
chr18:48936116 | AC | A | 32 | a0001c0001t0001g0068 a0001c0001t0001g0079 a0001c0001t0001g0084 others(29): Show |
32 | HG00597.hp2 HG00673.hp2 HG01993.hp2 others(29): Show |
intron_variant | MODIFIER | c.742+6364delG | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936116 | |||||||
chr18:48936117 | C | CA | 24 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(21): Show |
27 | HG00544.hp2 HG02083.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.742+6363_742+6364i others(3): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936117 | |||||||
chr18:48936117 | C | CACA | 12 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0104 others(9): Show |
12 | HG00408.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.742+6363_742+6364i others(5): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936117 | |||||||
chr18:48936175 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.742+6306T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936175 | |||||||
chr18:48936283 | T | C | 1 | a0001c0001t0021g0210 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.742+6198A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936283 | |||||||
chr18:48936405 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.742+6076C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936405 | |||||||
chr18:48936406 | G | A | 1 | a0001c0001t0003g0179 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.742+6075C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936406 | |||||||
chr18:48936471 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.742+6010C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936471 | |||||||
chr18:48936525 | A | G | 9 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0097 others(6): Show |
9 | HG00738.hp2 HG01891.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.742+5956T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936525 | |||||||
chr18:48936582 | T | C | 72 | a0001c0001t0001g0066 a0001c0001t0001g0126 a0001c0001t0001g0131 others(69): Show |
74 | HG00597.hp1 HG00735.hp2 HG01099.hp2 others(71): Show |
intron_variant | MODIFIER | c.742+5899A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936582 | |||||||
chr18:48936619 | C | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0144 a0001c0001t0001g0183 others(4): Show |
8 | NA18945.hp2 NA18946.hp1 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.742+5862G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936619 | |||||||
chr18:48936675 | C | G | 1 | a0001c0001t0001g0163 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.742+5806G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936675 | |||||||
chr18:48936688 | A | G | 363 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(360): Show |
387 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(384): Show |
intron_variant | MODIFIER | c.742+5793T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936688 | |||||||
chr18:48936766 | A | G | 236 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(233): Show |
245 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.742+5715T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936766 | |||||||
chr18:48936777 | A | G | 29 | a0001c0001t0001g0007 a0001c0001t0001g0068 a0001c0001t0001g0180 others(26): Show |
31 | HG01109.hp2 HG01255.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.742+5704T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936777 | |||||||
chr18:48936853 | G | A | 5 | a0001c0001t0001g0288 a0001c0001t0001g0328 a0001c0001t0001g0342 others(2): Show |
5 | HG02818.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+5628C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936853 | |||||||
chr18:48936854 | C | T | 8 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
8 | HG00738.hp2 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.742+5627G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936854 | |||||||
chr18:48936916 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.742+5565G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936916 | |||||||
chr18:48936928 | C | A | 1 | a0001c0001t0001g0192 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.742+5553G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936928 | |||||||
chr18:48936948 | G | A | 2 | a0001c0001t0009g0356 a0001c0006t0003g0064 |
2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.742+5533C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48936948 | |||||||
chr18:48937083 | TA | T | 19 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0137 others(16): Show |
19 | HG00544.hp1 HG00733.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.742+5397delT | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937083 | |||||||
chr18:48937084 | A | T | 17 | a0001c0001t0001g0131 a0001c0001t0001g0171 a0001c0001t0003g0128 others(14): Show |
17 | HG00735.hp2 HG01243.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.742+5397T>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937084 | |||||||
chr18:48937123 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.742+5358C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937123 | |||||||
chr18:48937158 | C | A | 1 | a0001c0001t0001g0307 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.742+5323G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937158 | |||||||
chr18:48937204 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.742+5277G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937204 | |||||||
chr18:48937232 | G | A | 1 | a0001c0001t0002g0268 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.742+5249C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937232 | |||||||
chr18:48937242 | T | G | 20 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0097 others(17): Show |
20 | HG00738.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.742+5239A>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937242 | |||||||
chr18:48937263 | C | CGTGTGTG others(3): Show |
2 | a0001c0001t0003g0129 a0001c0001t0003g0340 |
2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.742+5217_742+5218i others(12): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937263 | |||||||
chr18:48937263 | C | CGTGTGTG others(5): Show |
1 | a0001c0001t0003g0128 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.742+5217_742+5218i others(14): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937263 | |||||||
chr18:48937264 | A | ATG | 44 | a0001c0001t0001g0156 a0001c0001t0001g0183 a0001c0001t0001g0184 others(41): Show |
46 | HG00609.hp1 HG00609.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.742+5215_742+5216d others(4): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937264 | |||||||
chr18:48937264 | A | ATGTG | 28 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0086 others(25): Show |
28 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.742+5213_742+5216d others(6): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937264 | |||||||
chr18:48937264 | A | ATGTGTG | 39 | a0001c0001t0001g0006 a0001c0001t0001g0065 a0001c0001t0001g0069 others(36): Show |
40 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.742+5211_742+5216d others(8): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937264 | |||||||
chr18:48937264 | A | ATGTGTGT others(1): Show |
56 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0073 others(53): Show |
58 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.742+5209_742+5216d others(10): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937264 | |||||||
chr18:48937264 | A | ATGTGTGT others(3): Show |
29 | a0001c0001t0001g0022 a0001c0001t0001g0072 a0001c0001t0001g0092 others(26): Show |
30 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.742+5207_742+5216d others(12): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937264 | |||||||
chr18:48937264 | A | ATGTGTGT others(5): Show |
25 | a0001c0001t0001g0020 a0001c0001t0001g0071 a0001c0001t0001g0085 others(22): Show |
26 | HG00642.hp1 HG01081.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.742+5205_742+5216d others(14): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937264 | |||||||
chr18:48937264 | A | ATGTGTGT others(7): Show |
16 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0070 others(13): Show |
18 | HG01243.hp1 HG01515.hp1 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.742+5203_742+5216d others(16): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937264 | |||||||
chr18:48937264 | A | ATGTGTGT others(9): Show |
9 | a0001c0001t0001g0068 a0001c0001t0001g0107 a0001c0001t0001g0288 others(6): Show |
9 | HG00544.hp2 HG02965.hp2 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.742+5201_742+5216d others(18): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937264 | |||||||
chr18:48937264 | A | ATGTGTGT others(11): Show |
2 | a0001c0001t0001g0066 a0001c0002t0001g0125 |
2 | HG02698.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.742+5199_742+5216d others(20): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937264 | |||||||
chr18:48937264 | A | ATGTGTGT others(13): Show |
3 | a0001c0001t0001g0106 a0001c0001t0001g0311 a0001c0001t0008g0169 |
3 | HG03017.hp1 HG03471.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.742+5197_742+5216d others(22): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937264 | |||||||
chr18:48937264 | A | ATGTGTGT others(15): Show |
1 | a0001c0001t0008g0168 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.742+5195_742+5216d others(24): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937264 | |||||||
chr18:48937264 | A | G | 7 | a0001c0001t0001g0133 a0001c0001t0001g0162 a0001c0001t0001g0307 others(4): Show |
7 | HG01884.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.742+5217T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937264 | |||||||
chr18:48937264 | ATG | A | 9 | a0001c0001t0001g0067 a0001c0001t0001g0208 a0001c0001t0001g0270 others(6): Show |
9 | HG00673.hp1 HG01515.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.742+5215_742+5216d others(4): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937264 | |||||||
chr18:48937264 | ATGTG | A | 5 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0002g0272 others(2): Show |
5 | HG00408.hp2 HG00423.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+5213_742+5216d others(6): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937264 | |||||||
chr18:48937264 | ATGTGTGT others(1): Show |
A | 3 | a0001c0001t0001g0171 a0001c0001t0003g0172 a0001c0001t0003g0173 |
3 | HG00735.hp2 HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.742+5209_742+5216d others(10): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937264 | |||||||
chr18:48937294 | G | A | 9 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0097 others(6): Show |
9 | HG00738.hp2 HG01891.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.742+5187C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937294 | |||||||
chr18:48937349 | G | A | 1 | a0001c0001t0014g0319 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.742+5132C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937349 | |||||||
chr18:48937386 | T | C | 233 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(230): Show |
240 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.742+5095A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937386 | |||||||
chr18:48937426 | G | T | 2 | a0001c0001t0015g0370 a0001c0001t0015g0371 |
2 | HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.742+5055C>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937426 | |||||||
chr18:48937435 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0158 |
2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.742+5046C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937435 | |||||||
chr18:48937647 | G | A | 1 | a0001c0002t0001g0125 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.742+4834C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937647 | |||||||
chr18:48937687 | G | T | 2 | a0001c0001t0015g0370 a0001c0001t0015g0371 |
2 | HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.742+4794C>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937687 | |||||||
chr18:48937730 | G | A | 3 | a0001c0001t0014g0319 a0001c0001t0015g0370 a0001c0001t0015g0371 |
3 | HG02258.hp1 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.742+4751C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937730 | |||||||
chr18:48937853 | A | G | 26 | a0001c0001t0001g0065 a0001c0001t0001g0140 a0001c0001t0001g0141 others(23): Show |
26 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.742+4628T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937853 | |||||||
chr18:48937897 | C | A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0068 a0001c0001t0001g0180 others(11): Show |
15 | HG02055.hp1 HG02132.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.742+4584G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48937897 | |||||||
chr18:48938222 | A | C | 2 | a0001c0001t0001g0342 a0001c0001t0003g0341 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.742+4259T>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48938222 | |||||||
chr18:48938294 | A | C | 17 | a0001c0001t0001g0131 a0001c0001t0001g0171 a0001c0001t0003g0128 others(14): Show |
17 | HG00735.hp2 HG01243.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.742+4187T>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48938294 | |||||||
chr18:48938403 | T | G | 3 | a0001c0001t0005g0181 a0001c0001t0005g0217 a0001c0001t0005g0218 |
3 | HG02895.hp1 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.742+4078A>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48938403 | |||||||
chr18:48938557 | C | T | 8 | a0001c0001t0001g0332 a0001c0001t0003g0331 a0001c0001t0003g0333 others(5): Show |
8 | HG02258.hp1 HG02630.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.742+3924G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48938557 | |||||||
chr18:48938558 | C | G | 6 | a0001c0001t0001g0332 a0001c0001t0003g0331 a0001c0001t0003g0333 others(3): Show |
6 | HG02630.hp2 HG02818.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.742+3923G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48938558 | |||||||
chr18:48938753 | C | T | 1 | a0001c0010t0028g0373 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.742+3728G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48938753 | |||||||
chr18:48938978 | A | C | 39 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0085 others(36): Show |
41 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.742+3503T>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48938978 | |||||||
chr18:48939094 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.742+3387C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48939094 | |||||||
chr18:48939102 | G | A | 1 | a0001c0014t0018g0057 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.742+3379C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48939102 | |||||||
chr18:48939114 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.742+3367C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48939114 | |||||||
chr18:48939170 | A | C | 240 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(237): Show |
248 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.742+3311T>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48939170 | |||||||
chr18:48939185 | G | A | 8 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
8 | HG00738.hp2 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.742+3296C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48939185 | |||||||
chr18:48939295 | A | G | 153 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(150): Show |
157 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.742+3186T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48939295 | |||||||
chr18:48939347 | C | A | 1 | a0001c0001t0001g0348 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.742+3134G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48939347 | |||||||
chr18:48939367 | G | A | 57 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(54): Show |
60 | HG00408.hp1 HG00544.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.742+3114C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48939367 | |||||||
chr18:48939547 | C | G | 367 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(364): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.742+2934G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48939547 | |||||||
chr18:48939660 | G | A | 1 | a0001c0001t0004g0039 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.742+2821C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48939660 | |||||||
chr18:48939851 | T | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0070 a0001c0001t0001g0071 others(7): Show |
11 | HG00323.hp2 HG00642.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.742+2630A>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48939851 | |||||||
chr18:48939894 | T | G | 1 | a0001c0012t0024g0368 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.742+2587A>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48939894 | |||||||
chr18:48939906 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0311 |
2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.742+2575A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48939906 | |||||||
chr18:48939917 | G | A | 1 | a0001c0001t0004g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.742+2564C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48939917 | |||||||
chr18:48940102 | C | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0070 a0001c0001t0001g0071 others(8): Show |
12 | HG00323.hp2 HG00642.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.742+2379G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48940102 | |||||||
chr18:48940114 | G | A | 150 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(147): Show |
154 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.742+2367C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48940114 | |||||||
chr18:48940142 | C | T | 82 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(79): Show |
85 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.742+2339G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48940142 | |||||||
chr18:48940188 | G | A | 2 | a0001c0001t0001g0193 a0001c0002t0001g0161 |
2 | HG00609.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.742+2293C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48940188 | |||||||
chr18:48940603 | T | C | 1 | a0001c0001t0001g0004 | 2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.742+1878A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48940603 | |||||||
chr18:48940737 | C | T | 25 | a0001c0001t0001g0065 a0001c0001t0001g0140 a0001c0001t0001g0141 others(22): Show |
25 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.742+1744G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48940737 | |||||||
chr18:48940766 | C | T | 12 | a0001c0001t0001g0171 a0001c0001t0001g0332 a0001c0001t0003g0172 others(9): Show |
12 | HG00735.hp2 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.742+1715G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48940766 | |||||||
chr18:48940869 | G | A | 4 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0176 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+1612C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48940869 | |||||||
chr18:48940925 | G | A | 82 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(79): Show |
85 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.742+1556C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48940925 | |||||||
chr18:48940939 | A | T | 4 | a0001c0001t0001g0332 a0001c0001t0003g0333 a0001c0001t0003g0334 others(1): Show |
4 | HG02818.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.742+1542T>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48940939 | |||||||
chr18:48941003 | C | T | 1 | a0001c0001t0023g0123 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.742+1478G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48941003 | |||||||
chr18:48941122 | G | C | 19 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG00738.hp2 HG01243.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.742+1359C>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48941122 | |||||||
chr18:48941287 | A | C | 1 | a0001c0001t0001g0299 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.742+1194T>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48941287 | |||||||
chr18:48941339 | T | C | 2 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
2 | HG02698.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.742+1142A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48941339 | |||||||
chr18:48941421 | G | A | 2 | a0001c0001t0001g0277 a0001c0001t0020g0059 |
2 | HG01978.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.742+1060C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48941421 | |||||||
chr18:48941590 | T | C | 80 | a0001c0001t0001g0066 a0001c0001t0001g0088 a0001c0001t0001g0096 others(77): Show |
80 | HG00597.hp1 HG00738.hp2 HG01099.hp2 others(77): Show |
intron_variant | MODIFIER | c.742+891A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48941590 | |||||||
chr18:48941627 | G | A | 1 | a0001c0001t0005g0305 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.742+854C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48941627 | |||||||
chr18:48941666 | T | C | 75 | a0001c0001t0001g0066 a0001c0001t0001g0088 a0001c0001t0001g0096 others(72): Show |
75 | HG00597.hp1 HG00738.hp2 HG01099.hp2 others(72): Show |
intron_variant | MODIFIER | c.742+815A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48941666 | |||||||
chr18:48941730 | G | T | 1 | a0001c0001t0003g0331 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.742+751C>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48941730 | |||||||
chr18:48941843 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.742+638G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48941843 | |||||||
chr18:48941863 | A | ACGCATAC others(8): Show |
5 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0029 others(2): Show |
5 | NA18959.hp1 NA18960.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.742+603_742+617dup others(15): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48941863 | |||||||
chr18:48941881 | T | C | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(109): Show |
117 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.742+600A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48941881 | |||||||
chr18:48941986 | G | A | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(109): Show |
117 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.742+495C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48941986 | |||||||
chr18:48941989 | T | C | 50 | a0001c0001t0001g0066 a0001c0001t0001g0126 a0001c0001t0001g0137 others(47): Show |
50 | HG00597.hp1 HG01099.hp2 HG01891.hp1 others(47): Show |
intron_variant | MODIFIER | c.742+492A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48941989 | |||||||
chr18:48942103 | C | CGTGTAA | 4 | a0001c0001t0009g0356 a0001c0001t0015g0370 a0001c0001t0015g0371 others(1): Show |
4 | HG01884.hp2 HG02258.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+377_742+378ins others(6): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48942103 | |||||||
chr18:48942119 | G | C | 1 | a0001c0001t0014g0214 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.742+362C>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48942119 | |||||||
chr18:48942132 | A | G | 13 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0097 others(10): Show |
13 | HG00738.hp2 HG01891.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.742+349T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48942132 | |||||||
chr18:48942212 | G | A | 1 | a0001c0001t0003g0173 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.742+269C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48942212 | |||||||
chr18:48942273 | G | C | 1 | a0001c0001t0001g0358 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.742+208C>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48942273 | |||||||
chr18:48942348 | C | T | 20 | a0001c0001t0001g0013 a0001c0001t0001g0093 a0001c0001t0002g0124 others(17): Show |
21 | HG00140.hp2 HG00741.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.742+133G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48942348 | |||||||
chr18:48942389 | C | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0070 a0001c0001t0001g0071 others(7): Show |
11 | HG00323.hp2 HG00642.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.742+92G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 3/3 | chr18 | 48942389 | |||||||
chr18:48942576 | G | A | 30 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0070 others(27): Show |
32 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.668-21C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48942576 | |||||||
chr18:48942678 | G | A | 1 | a0001c0001t0006g0194 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.668-123C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48942678 | |||||||
chr18:48942679 | C | A | 1 | a0001c0001t0006g0194 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.668-124G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48942679 | |||||||
chr18:48942845 | G | A | 1 | a0001c0001t0014g0319 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.668-290C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48942845 | |||||||
chr18:48942941 | C | T | 90 | a0001c0001t0001g0007 a0001c0001t0001g0066 a0001c0001t0001g0068 others(87): Show |
91 | HG00597.hp1 HG00738.hp2 HG01099.hp2 others(88): Show |
intron_variant | MODIFIER | c.668-386G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48942941 | |||||||
chr18:48943046 | T | C | 6 | a0001c0001t0001g0171 a0001c0001t0003g0172 a0001c0001t0003g0173 others(3): Show |
6 | HG00735.hp2 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.668-491A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48943046 | |||||||
chr18:48943178 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.668-623C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48943178 | |||||||
chr18:48943208 | A | G | 129 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0066 others(126): Show |
132 | HG00323.hp1 HG00597.hp1 HG00735.hp1 others(129): Show |
intron_variant | MODIFIER | c.668-653T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48943208 | |||||||
chr18:48943280 | A | G | 86 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0014 others(83): Show |
90 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.668-725T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48943280 | |||||||
chr18:48943294 | A | G | 241 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
249 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.668-739T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48943294 | |||||||
chr18:48943311 | C | T | 1 | a0001c0001t0026g0310 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.668-756G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48943311 | |||||||
chr18:48943319 | C | T | 5 | a0001c0001t0001g0280 a0001c0001t0001g0290 a0001c0001t0001g0291 others(2): Show |
5 | HG02055.hp2 HG02683.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.668-764G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48943319 | |||||||
chr18:48943508 | C | A | 1 | a0001c0001t0014g0319 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.668-953G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48943508 | |||||||
chr18:48943549 | T | C | 1 | a0001c0012t0024g0368 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.668-994A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48943549 | |||||||
chr18:48943592 | C | G | 240 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(237): Show |
248 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.668-1037G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48943592 | |||||||
chr18:48943628 | C | T | 1 | a0001c0001t0003g0221 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.668-1073G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48943628 | |||||||
chr18:48943631 | A | G | 24 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0069 others(21): Show |
26 | HG00408.hp1 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.668-1076T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48943631 | |||||||
chr18:48943765 | C | T | 67 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(64): Show |
70 | HG00408.hp1 HG00735.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.668-1210G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48943765 | |||||||
chr18:48943773 | T | C | 66 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(63): Show |
69 | HG00408.hp1 HG00735.hp2 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.668-1218A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48943773 | |||||||
chr18:48943838 | G | GC | 143 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0065 others(140): Show |
145 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.668-1284dupG | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48943838 | |||||||
chr18:48943843 | C | G | 8 | a0001c0001t0001g0171 a0001c0001t0001g0338 a0001c0001t0003g0167 others(5): Show |
8 | HG00735.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.668-1288G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48943843 | |||||||
chr18:48944227 | A | G | 11 | a0001c0001t0001g0098 a0001c0001t0001g0131 a0001c0001t0001g0133 others(8): Show |
11 | HG01243.hp2 HG02109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.668-1672T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48944227 | |||||||
chr18:48944374 | T | C | 1 | a0001c0001t0003g0216 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.668-1819A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48944374 | |||||||
chr18:48944508 | T | A | 2 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
2 | HG02698.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.668-1953A>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48944508 | |||||||
chr18:48944514 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.668-1959T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48944514 | |||||||
chr18:48944672 | A | G | 1 | a0001c0001t0011g0365 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.668-2117T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48944672 | |||||||
chr18:48944747 | G | A | 1 | a0001c0001t0004g0024 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.668-2192C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48944747 | |||||||
chr18:48944873 | A | T | 1 | a0001c0001t0001g0005 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.668-2318T>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48944873 | |||||||
chr18:48944972 | CA | C | 30 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0065 others(27): Show |
32 | HG00280.hp2 HG00597.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.668-2418delT | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48944972 | |||||||
chr18:48945247 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0155 |
3 | HG01074.hp2 HG01167.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.668-2692C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48945247 | |||||||
chr18:48945259 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.668-2704C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48945259 | |||||||
chr18:48945290 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.668-2735C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48945290 | |||||||
chr18:48945297 | C | T | 1 | a0001c0001t0001g0337 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.668-2742G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48945297 | |||||||
chr18:48945359 | G | A | 1 | a0001c0010t0028g0373 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.668-2804C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48945359 | |||||||
chr18:48945409 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0002g0102 a0001c0002t0001g0101 |
3 | NA18612.hp1 NA18960.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.668-2854G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48945409 | |||||||
chr18:48945536 | T | A | 1 | a0001c0001t0001g0166 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.667+2848A>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48945536 | |||||||
chr18:48945630 | G | A | 7 | a0001c0001t0001g0068 a0001c0001t0001g0349 a0001c0001t0001g0350 others(4): Show |
7 | NA18957.hp1 NA18981.hp1 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.667+2754C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48945630 | |||||||
chr18:48945680 | C | T | 1 | a0001c0001t0003g0167 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.667+2704G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48945680 | |||||||
chr18:48945681 | G | A | 1 | a0001c0002t0001g0148 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.667+2703C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48945681 | |||||||
chr18:48945772 | C | T | 83 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0079 others(80): Show |
86 | HG00408.hp1 HG00673.hp1 HG00738.hp2 others(83): Show |
intron_variant | MODIFIER | c.667+2612G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48945772 | |||||||
chr18:48945808 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.667+2576C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48945808 | |||||||
chr18:48945836 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.667+2548C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48945836 | |||||||
chr18:48945876 | A | G | 1 | a0001c0001t0001g0229 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.667+2508T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48945876 | |||||||
chr18:48946116 | C | A | 1 | a0001c0001t0001g0313 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.667+2268G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48946116 | |||||||
chr18:48946187 | A | G | 1 | a0001c0010t0028g0373 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.667+2197T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48946187 | |||||||
chr18:48946188 | G | C | 31 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(28): Show |
34 | HG00280.hp2 HG00597.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.667+2196C>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48946188 | |||||||
chr18:48946251 | A | C | 41 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(38): Show |
45 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.667+2133T>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48946251 | |||||||
chr18:48946306 | G | A | 58 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0066 others(55): Show |
60 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.667+2078C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48946306 | |||||||
chr18:48946429 | G | C | 1 | a0001c0001t0001g0099 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.667+1955C>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48946429 | |||||||
chr18:48946430 | C | CGGG | 24 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(21): Show |
27 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.667+1951_667+1953d others(5): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48946430 | |||||||
chr18:48946430 | C | G | 1 | a0001c0001t0001g0099 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.667+1954G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48946430 | |||||||
chr18:48946438 | G | T | 13 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(10): Show |
13 | HG00423.hp2 HG00558.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.667+1946C>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48946438 | |||||||
chr18:48946517 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.667+1867C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48946517 | |||||||
chr18:48946538 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.667+1846C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48946538 | |||||||
chr18:48946713 | T | C | 1 | a0001c0001t0001g0298 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.667+1671A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48946713 | |||||||
chr18:48946930 | G | A | 2 | a0001c0001t0001g0330 a0001c0001t0003g0329 |
2 | HG00738.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.667+1454C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48946930 | |||||||
chr18:48947125 | C | G | 1 | a0001c0001t0003g0221 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.667+1259G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947125 | |||||||
chr18:48947157 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.667+1227A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947157 | |||||||
chr18:48947171 | T | C | 1 | a0001c0001t0011g0365 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.667+1213A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947171 | |||||||
chr18:48947223 | C | G | 1 | a0001c0001t0001g0084 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.667+1161G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947223 | |||||||
chr18:48947240 | C | A | 2 | a0001c0001t0001g0299 a0001c0002t0001g0300 |
2 | HG00544.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.667+1144G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947240 | |||||||
chr18:48947241 | G | A | 2 | a0001c0001t0003g0355 a0001c0001t0009g0356 |
2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.667+1143C>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947241 | |||||||
chr18:48947364 | G | C | 93 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0079 others(90): Show |
96 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(93): Show |
intron_variant | MODIFIER | c.667+1020C>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947364 | |||||||
chr18:48947364 | G | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0069 others(11): Show |
15 | HG00323.hp2 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.667+1020C>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947364 | |||||||
chr18:48947531 | C | T | 26 | a0001c0001t0001g0013 a0001c0001t0001g0220 a0001c0001t0004g0026 others(23): Show |
27 | HG00140.hp2 HG00597.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.667+853G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947531 | |||||||
chr18:48947542 | T | A | 6 | a0001c0001t0001g0332 a0001c0001t0001g0336 a0001c0001t0003g0331 others(3): Show |
6 | HG02818.hp2 HG02970.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.667+842A>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947542 | |||||||
chr18:48947600 | A | T | 1 | a0001c0001t0001g0140 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.667+784T>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947600 | |||||||
chr18:48947603 | T | G | 1 | a0001c0001t0001g0140 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.667+781A>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947603 | |||||||
chr18:48947606 | G | T | 1 | a0001c0001t0001g0140 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.667+778C>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947606 | |||||||
chr18:48947808 | T | C | 157 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(154): Show |
165 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.667+576A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947808 | |||||||
chr18:48947822 | T | C | 239 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(236): Show |
249 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.667+562A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947822 | |||||||
chr18:48947847 | C | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0219 |
2 | NA18986.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.667+537G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947847 | |||||||
chr18:48947875 | T | C | 1 | a0001c0001t0001g0309 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.667+509A>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947875 | |||||||
chr18:48947891 | T | TC | 8 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0144 others(5): Show |
8 | HG02004.hp1 NA18947.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.667+492_667+493ins others(1): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947891 | |||||||
chr18:48947891 | T | TCC | 8 | a0001c0001t0001g0147 a0001c0001t0001g0149 a0001c0001t0002g0146 others(5): Show |
8 | HG00597.hp2 HG01109.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.667+492_667+493ins others(2): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947891 | |||||||
chr18:48947892 | A | AC | 66 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0065 others(63): Show |
69 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.667+491dupG | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947892 | |||||||
chr18:48947892 | A | ACC | 18 | a0001c0001t0001g0008 a0001c0001t0001g0085 a0001c0001t0001g0086 others(15): Show |
19 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.667+490_667+491dup others(2): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947892 | |||||||
chr18:48947892 | A | C | 16 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0144 others(13): Show |
16 | HG00597.hp2 HG01109.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.667+492T>G | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947892 | |||||||
chr18:48947892 | AC | A | 74 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(71): Show |
77 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.667+491delG | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947892 | |||||||
chr18:48947895 | C | CT | 6 | a0001c0001t0001g0171 a0001c0001t0003g0172 a0001c0001t0003g0173 others(3): Show |
6 | HG00735.hp2 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.667+488_667+489ins others(1): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947895 | |||||||
chr18:48947897 | C | G | 1 | a0001c0001t0003g0167 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.667+487G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947897 | |||||||
chr18:48947898 | C | G | 1 | a0001c0001t0001g0166 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.667+486G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947898 | |||||||
chr18:48947901 | C | G | 1 | a0001c0001t0001g0165 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.667+483G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947901 | |||||||
chr18:48947902 | C | G | 1 | a0001c0001t0001g0164 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.667+482G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947902 | |||||||
chr18:48947902 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.667+482G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947902 | |||||||
chr18:48947903 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.667+481G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947903 | |||||||
chr18:48947918 | T | G | 42 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(39): Show |
46 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.667+466A>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947918 | |||||||
chr18:48947958 | A | G | 1 | a0001c0001t0011g0365 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.667+426T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48947958 | |||||||
chr18:48948291 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.667+93G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48948291 | |||||||
chr18:48948367 | A | T | 1 | a0001c0002t0001g0161 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.667+17T>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48948367 | |||||||
chr18:48948376 | C | T | 93 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
98 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(95): Show |
splice_region_variant&intron_variant | LOW | c.667+8G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 2/3 | chr18 | 48948376 | |||||||
chr18:48948445 | T | A | 1 | a0001c0001t0001g0361 | 1 | NA18978.hp1 | splice_region_variant&intron_variant | LOW | c.614-8A>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/3 | chr18 | 48948445 | |||||||
chr18:48948490 | A | G | 2 | a0001c0001t0001g0079 a0001c0002t0001g0078 |
2 | NA18952.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.614-53T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/3 | chr18 | 48948490 | |||||||
chr18:48948613 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.614-176G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/3 | chr18 | 48948613 | |||||||
chr18:48948704 | C | G | 1 | a0001c0001t0007g0025 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.614-267G>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/3 | chr18 | 48948704 | |||||||
chr18:48948966 | A | T | 1 | a0001c0001t0011g0365 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.614-529T>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/3 | chr18 | 48948966 | |||||||
chr18:48949280 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0366 |
2 | HG00639.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.613+532G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/3 | chr18 | 48949280 | |||||||
chr18:48949363 | T | G | 2 | a0001c0001t0001g0362 a0001c0001t0001g0363 |
2 | NA18951.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.613+449A>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/3 | chr18 | 48949363 | |||||||
chr18:48949429 | C | A | 1 | a0001c0001t0001g0364 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.613+383G>T | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/3 | chr18 | 48949429 | |||||||
chr18:48949458 | A | AC | 10 | a0001c0001t0001g0005 a0001c0001t0001g0067 a0001c0001t0001g0068 others(7): Show |
11 | HG00323.hp2 HG00642.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.613+353dupG | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/3 | chr18 | 48949458 | |||||||
chr18:48949513 | T | G | 1 | a0001c0001t0011g0365 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.613+299A>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/3 | chr18 | 48949513 | |||||||
chr18:48949521 | G | T | 1 | a0001c0010t0028g0373 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.613+291C>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/3 | chr18 | 48949521 | |||||||
chr18:48949570 | A | G | 1 | a0001c0001t0004g0024 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.613+242T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/3 | chr18 | 48949570 | |||||||
chr18:48949639 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.613+173G>A | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/3 | chr18 | 48949639 | |||||||
chr18:48949647 | T | TTCCCAGG others(15): Show |
2 | a0001c0001t0001g0366 a0001c0001t0002g0367 |
2 | HG01255.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.613+143_613+164dup others(22): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/3 | chr18 | 48949647 | |||||||
chr18:48949647 | TTCCCAGG others(15): Show |
T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0065 a0001c0010t0028g0373 |
4 | HG03041.hp1 NA18999.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+143_613+164del others(22): Show |
SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/3 | chr18 | 48949647 | |||||||
chr18:48949704 | A | G | 1 | a0001c0006t0003g0064 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.613+108T>C | SMAD7 | ENSG00000101665.10 | transcript | ENST00000262158.8 | protein_coding | 1/3 | chr18 | 48949704 |