Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2017 |
| ensemblid | ENSG00000085733.16 |
| hgncid | 3338 |
| symbol | CTTN |
| name | cortactin |
| refseq_nuc | NM_005231.4 |
| refseq_prot | NP_005222.2 |
| ensembl_nuc | ENST00000301843.13 |
| ensembl_prot | ENSP00000301843.8 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 70398529 |
| end | 70436575 |
| strand | + |
| ver | v1.2 |
| region | chr11:70398529-70436575 |
| region5000 | chr11:70393529-70441575 |
| regionname0 | CTTN_chr11_70398529_70436575 |
| regionname5000 | CTTN_chr11_70393529_70441575 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 550 | 300 | 77 | 60 | 111 | 16 | 34 | 74 | CTTN_chr11_70393529_70441575 | CTTN | MWKAS others(545): Show |
chr11 | 70393529 | 70441575 |
| a0002 | 0/0 | 550 | 18 | 18 | 0 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | MWKAS others(545): Show |
chr11 | 70393529 | 70441575 |
| a0003 | 0/0 | 550 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CTTN_chr11_70393529_70441575 | CTTN | MWKAS others(545): Show |
chr11 | 70393529 | 70441575 |
| a0004 | 0/0 | 550 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | MWKAS others(545): Show |
chr11 | 70393529 | 70441575 |
| a0005 | 0/0 | 550 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | MWKAS others(545): Show |
chr11 | 70393529 | 70441575 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1650 | 189 | 43 | 33 | 90 | 6 | 15 | CTTN_chr11_70393529_70441575 | CTTN | ATGTG others(1645): Show |
chr11 | 70393529 | 70441575 | ||
| a0001c0002 | 0/0 | 1650 | 56 | 24 | 13 | 5 | 3 | 11 | CTTN_chr11_70393529_70441575 | CTTN | ATGTG others(1645): Show |
chr11 | 70393529 | 70441575 | ||
| a0001c0003 | 0/0 | 1650 | 42 | 3 | 12 | 15 | 6 | 6 | CTTN_chr11_70393529_70441575 | CTTN | ATGTG others(1645): Show |
chr11 | 70393529 | 70441575 | ||
| a0001c0005 | 0/0 | 1650 | 4 | 0 | 2 | 0 | 0 | 2 | CTTN_chr11_70393529_70441575 | CTTN | ATGTG others(1645): Show |
chr11 | 70393529 | 70441575 | ||
| a0001c0006 | 0/0 | 1650 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | ATGTG others(1645): Show |
chr11 | 70393529 | 70441575 | ||
| a0001c0009 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | ATGTG others(1645): Show |
chr11 | 70393529 | 70441575 | ||
| a0001c0010 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | ATGTG others(1645): Show |
chr11 | 70393529 | 70441575 | ||
| a0001c0011 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | ATGTG others(1645): Show |
chr11 | 70393529 | 70441575 | ||
| a0001c0013 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | ATGTG others(1645): Show |
chr11 | 70393529 | 70441575 | ||
| a0001c0014 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | ATGTG others(1645): Show |
chr11 | 70393529 | 70441575 | ||
| a0001c0015 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | ATGTG others(1645): Show |
chr11 | 70393529 | 70441575 | ||
| a0001c0016 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | ATGTG others(1645): Show |
chr11 | 70393529 | 70441575 | ||
| a0002c0004 | 0/0 | 1650 | 18 | 18 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | ATGTG others(1645): Show |
chr11 | 70393529 | 70441575 | ||
| a0003c0007 | 0/0 | 1650 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | ATGTG others(1645): Show |
chr11 | 70393529 | 70441575 | ||
| a0004c0008 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | ATGTG others(1645): Show |
chr11 | 70393529 | 70441575 | ||
| a0005c0012 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | ATGTG others(1645): Show |
chr11 | 70393529 | 70441575 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3249 | 137 | 9 | 29 | 79 | 5 | 13 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0001c0001t0002 | 0/0 | 3250 | 10 | 1 | 2 | 7 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3245): Show |
chr11 | 70393529 | 70441575 |
| a0001c0001t0003 | 0/0 | 3248 | 14 | 14 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3243): Show |
chr11 | 70393529 | 70441575 |
| a0001c0001t0007 | 0/0 | 3248 | 10 | 8 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3243): Show |
chr11 | 70393529 | 70441575 |
| a0001c0001t0013 | 0/0 | 3247 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3242): Show |
chr11 | 70393529 | 70441575 |
| a0001c0001t0014 | 0/0 | 3248 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3243): Show |
chr11 | 70393529 | 70441575 |
| a0001c0001t0015 | 0/0 | 3247 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3242): Show |
chr11 | 70393529 | 70441575 |
| a0001c0001t0016 | 0/0 | 3249 | 2 | 0 | 1 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0001c0001t0017 | 0/0 | 3247 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3242): Show |
chr11 | 70393529 | 70441575 |
| a0001c0001t0021 | 0/0 | 3247 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3242): Show |
chr11 | 70393529 | 70441575 |
| a0001c0001t0022 | 0/0 | 3247 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3242): Show |
chr11 | 70393529 | 70441575 |
| a0001c0001t0023 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0001c0001t0024 | 0/0 | 3249 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0001c0001t0025 | 0/0 | 3249 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0001c0001t0026 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0001c0001t0030 | 0/0 | 3249 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0001c0001t0031 | 0/0 | 3249 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0001c0001t0034 | 0/0 | 3248 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3243): Show |
chr11 | 70393529 | 70441575 |
| a0001c0001t0035 | 0/0 | 3249 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0001c0002t0001 | 0/0 | 3249 | 10 | 8 | 1 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0001c0002t0002 | 0/0 | 3250 | 34 | 14 | 9 | 2 | 1 | 8 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3245): Show |
chr11 | 70393529 | 70441575 |
| a0001c0002t0009 | 0/0 | 3251 | 7 | 2 | 2 | 1 | 1 | 1 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3246): Show |
chr11 | 70393529 | 70441575 |
| a0001c0002t0010 | 0/0 | 3250 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3245): Show |
chr11 | 70393529 | 70441575 |
| a0001c0002t0020 | 0/0 | 3251 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3246): Show |
chr11 | 70393529 | 70441575 |
| a0001c0002t0032 | 0/0 | 3251 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3246): Show |
chr11 | 70393529 | 70441575 |
| a0001c0002t0033 | 0/0 | 3249 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0001c0003t0001 | 0/0 | 3249 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0001c0003t0005 | 0/0 | 3246 | 12 | 3 | 2 | 1 | 2 | 4 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3241): Show |
chr11 | 70393529 | 70441575 |
| a0001c0003t0006 | 0/0 | 3246 | 12 | 0 | 1 | 9 | 1 | 1 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3241): Show |
chr11 | 70393529 | 70441575 |
| a0001c0003t0008 | 0/0 | 3247 | 9 | 0 | 9 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3242): Show |
chr11 | 70393529 | 70441575 |
| a0001c0003t0011 | 0/0 | 3246 | 3 | 0 | 0 | 3 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3241): Show |
chr11 | 70393529 | 70441575 |
| a0001c0003t0019 | 0/0 | 3249 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0001c0003t0027 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3241): Show |
chr11 | 70393529 | 70441575 |
| a0001c0003t0028 | 0/0 | 3247 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3242): Show |
chr11 | 70393529 | 70441575 |
| a0001c0003t0029 | 0/0 | 3249 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0001c0003t0036 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3241): Show |
chr11 | 70393529 | 70441575 |
| a0001c0005t0002 | 0/0 | 3250 | 4 | 0 | 2 | 0 | 0 | 2 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3245): Show |
chr11 | 70393529 | 70441575 |
| a0001c0006t0012 | 0/0 | 3249 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0001c0009t0001 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0001c0010t0002 | 0/0 | 3250 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3245): Show |
chr11 | 70393529 | 70441575 |
| a0001c0011t0012 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0001c0013t0013 | 0/0 | 3247 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3242): Show |
chr11 | 70393529 | 70441575 |
| a0001c0014t0007 | 0/0 | 3248 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3243): Show |
chr11 | 70393529 | 70441575 |
| a0001c0015t0003 | 0/0 | 3248 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3243): Show |
chr11 | 70393529 | 70441575 |
| a0001c0016t0010 | 0/0 | 3250 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3245): Show |
chr11 | 70393529 | 70441575 |
| a0002c0004t0001 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0002c0004t0002 | 0/0 | 3250 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3245): Show |
chr11 | 70393529 | 70441575 |
| a0002c0004t0004 | 0/0 | 3249 | 14 | 14 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0002c0004t0010 | 0/0 | 3250 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3245): Show |
chr11 | 70393529 | 70441575 |
| a0002c0004t0018 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0003c0007t0001 | 0/0 | 3249 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0004c0008t0004 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| a0005c0012t0001 | 0/0 | 3249 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | GGAAC others(3244): Show |
chr11 | 70393529 | 70441575 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 12 | 0 | 3 | 6 | 2 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 5 | 3 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0011 | 1/0 | 3 | 0 | 0 | 0 | 1 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0176 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0003g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0007g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0007g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0007g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0014g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0014g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0015g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0015g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0016g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0016g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0017g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0021g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0022g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0023g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0024g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0025g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0026g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0030g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0031g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0034g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0001t0035g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0004 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0008 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0009g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0009g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0009g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0009g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0009g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0009g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0010g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0010g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0020g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0032g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0002t0033g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0005g0006 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0005g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0005g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0006g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0006g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0006g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0006g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0006g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0008g0005 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0008g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0008g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0008g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0011g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0011g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0011g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0019g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0027g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0028g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0029g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0003t0036g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0005t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0005t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0005t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0006t0012g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0006t0012g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0009t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0010t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0011t0012g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0013t0013g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0014t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0015t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0001c0016t0010g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0002c0004t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0002c0004t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0002c0004t0004g0003 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0002c0004t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0002c0004t0004g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0002c0004t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0002c0004t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0002c0004t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0002c0004t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0002c0004t0010g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0002c0004t0018g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0003c0007t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0003c0007t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0004c0008t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| a0005c0012t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0005 | g0016 | EUR | GBR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00099 | hp2 | a0001 | c0016 | t0010 | g0067 | EUR | GBR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00280 | hp1 | a0001 | c0002 | t0009 | g0224 | EUR | FIN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00323 | hp1 | a0001 | c0003 | t0028 | g0143 | EUR | FIN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | FIN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00558 | hp1 | a0001 | c0002 | t0010 | g0059 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00733 | hp1 | a0001 | c0002 | t0009 | g0222 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00735 | hp1 | a0001 | c0003 | t0008 | g0062 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00735 | hp2 | a0001 | c0001 | t0024 | g0213 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0020 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0020 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01074 | hp1 | a0001 | c0003 | t0006 | g0130 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01074 | hp2 | a0001 | c0002 | t0032 | g0092 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01106 | hp1 | a0001 | c0003 | t0005 | g0006 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01175 | hp1 | a0001 | c0003 | t0008 | g0066 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0090 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01243 | hp2 | a0001 | c0005 | t0002 | g0027 | AMR | PUR | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01256 | hp1 | a0001 | c0003 | t0008 | g0006 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01257 | hp1 | a0001 | c0002 | t0009 | g0004 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01346 | hp2 | a0001 | c0005 | t0002 | g0027 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0119 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0019 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01496 | hp1 | a0001 | c0001 | t0016 | g0165 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01515 | hp1 | a0001 | c0001 | t0025 | g0168 | EUR | IBS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0039 | EUR | IBS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01516 | hp2 | a0001 | c0003 | t0029 | g0140 | EUR | IBS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01517 | hp1 | a0001 | c0003 | t0027 | g0138 | EUR | IBS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0039 | EUR | IBS | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01884 | hp2 | a0002 | c0004 | t0004 | g0100 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01891 | hp1 | a0001 | c0003 | t0005 | g0006 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01934 | hp2 | a0001 | c0003 | t0008 | g0005 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01943 | hp2 | a0001 | c0003 | t0008 | g0005 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01981 | hp2 | a0001 | c0003 | t0008 | g0005 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01993 | hp1 | a0001 | c0003 | t0008 | g0005 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02027 | hp2 | a0001 | c0003 | t0006 | g0026 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0097 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02080 | hp1 | a0001 | c0003 | t0006 | g0135 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02083 | hp2 | a0001 | c0003 | t0006 | g0024 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02132 | hp1 | a0001 | c0003 | t0005 | g0068 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02135 | hp1 | a0001 | c0001 | t0007 | g0111 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02148 | hp2 | a0001 | c0003 | t0005 | g0006 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CDX | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CDX | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02257 | hp2 | a0001 | c0003 | t0005 | g0060 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02258 | hp2 | a0002 | c0004 | t0004 | g0099 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02273 | hp1 | a0001 | c0003 | t0008 | g0005 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02280 | hp1 | a0001 | c0015 | t0003 | g0049 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02300 | hp2 | a0001 | c0003 | t0008 | g0005 | AMR | PEL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0083 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02451 | hp2 | a0001 | c0001 | t0017 | g0232 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02523 | hp2 | a0001 | c0003 | t0006 | g0137 | EAS | KHV | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02572 | hp2 | a0002 | c0004 | t0004 | g0003 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0008 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0080 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02630 | hp1 | a0004 | c0008 | t0004 | g0231 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0079 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02647 | hp1 | a0002 | c0004 | t0004 | g0022 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0216 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0126 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02717 | hp2 | a0001 | c0001 | t0026 | g0117 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0215 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0078 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02735 | hp1 | a0001 | c0003 | t0005 | g0065 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02735 | hp2 | a0001 | c0005 | t0002 | g0070 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02809 | hp1 | a0001 | c0001 | t0014 | g0233 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02809 | hp2 | a0002 | c0004 | t0004 | g0003 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02895 | hp1 | a0002 | c0004 | t0004 | g0230 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0116 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02896 | hp2 | a0001 | c0014 | t0007 | g0085 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02897 | hp2 | a0002 | c0004 | t0004 | g0003 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02922 | hp2 | a0002 | c0004 | t0004 | g0003 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02965 | hp1 | a0001 | c0001 | t0015 | g0017 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0124 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03041 | hp1 | a0001 | c0009 | t0001 | g0104 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0223 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03098 | hp1 | a0002 | c0004 | t0010 | g0003 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03098 | hp2 | a0001 | c0002 | t0009 | g0019 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03130 | hp1 | a0002 | c0004 | t0004 | g0003 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03130 | hp2 | a0002 | c0004 | t0018 | g0022 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0084 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0095 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0081 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03209 | hp1 | a0002 | c0004 | t0004 | g0236 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0082 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03225 | hp1 | a0001 | c0001 | t0022 | g0234 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03239 | hp2 | a0001 | c0003 | t0005 | g0063 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0089 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03453 | hp2 | a0001 | c0006 | t0012 | g0075 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03486 | hp1 | a0001 | c0001 | t0015 | g0096 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03486 | hp2 | a0002 | c0004 | t0004 | g0003 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0125 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03516 | hp1 | a0001 | c0001 | t0021 | g0229 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0235 | AFR | ESN | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03540 | hp1 | a0002 | c0004 | t0001 | g0077 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | GWD | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03579 | hp2 | a0001 | c0001 | t0013 | g0048 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03654 | hp1 | a0001 | c0002 | t0033 | g0122 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03654 | hp2 | a0001 | c0001 | t0016 | g0030 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03688 | hp1 | a0001 | c0003 | t0005 | g0061 | SAS | STU | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | STU | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03710 | hp1 | a0001 | c0005 | t0002 | g0148 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03710 | hp2 | a0001 | c0001 | t0035 | g0147 | SAS | PJL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0121 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0225 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03927 | hp1 | a0001 | c0002 | t0020 | g0058 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03927 | hp2 | a0001 | c0002 | t0009 | g0120 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0123 | SAS | STU | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG04115 | hp2 | a0001 | c0003 | t0006 | g0026 | SAS | STU | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG04184 | hp2 | a0001 | c0003 | t0005 | g0016 | SAS | BEB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG04228 | hp1 | a0001 | c0003 | t0019 | g0057 | SAS | STU | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | STU | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0072 | AFR | YRI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | YRI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18612 | hp1 | a0005 | c0012 | t0001 | g0185 | EAS | CHB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18906 | hp2 | a0001 | c0002 | t0009 | g0086 | AFR | YRI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18942 | hp2 | a0001 | c0001 | t0007 | g0180 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18946 | hp2 | a0001 | c0002 | t0010 | g0069 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18948 | hp1 | a0001 | c0003 | t0006 | g0227 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18953 | hp1 | a0001 | c0003 | t0006 | g0024 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18966 | hp1 | a0003 | c0007 | t0001 | g0112 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18977 | hp1 | a0001 | c0002 | t0009 | g0118 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18979 | hp1 | a0003 | c0007 | t0001 | g0113 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18995 | hp1 | a0001 | c0003 | t0036 | g0129 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18997 | hp2 | a0001 | c0003 | t0011 | g0056 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19001 | hp2 | a0001 | c0001 | t0030 | g0209 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19004 | hp1 | a0001 | c0003 | t0006 | g0136 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19011 | hp1 | a0001 | c0003 | t0006 | g0141 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | LWK | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19043 | hp1 | a0002 | c0004 | t0004 | g0041 | AFR | LWK | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | LWK | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19057 | hp2 | a0001 | c0003 | t0011 | g0071 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19062 | hp1 | a0001 | c0003 | t0006 | g0128 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19066 | hp2 | a0001 | c0003 | t0011 | g0064 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19077 | hp2 | a0001 | c0001 | t0031 | g0023 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19084 | hp2 | a0001 | c0010 | t0002 | g0202 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19089 | hp1 | a0001 | c0003 | t0001 | g0139 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | YRI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA19240 | hp2 | a0001 | c0006 | t0012 | g0074 | AFR | YRI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ASW | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA20129 | hp2 | a0001 | c0001 | t0034 | g0217 | AFR | ASW | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | TSI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA20752 | hp2 | a0001 | c0003 | t0006 | g0142 | EUR | TSI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA20805 | hp2 | a0001 | c0003 | t0005 | g0006 | EUR | TSI | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02109 | hp1 | a0002 | c0004 | t0004 | g0041 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02486 | hp1 | a0001 | c0001 | t0023 | g0149 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0042 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02559 | hp1 | a0001 | c0003 | t0005 | g0055 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0094 | AFR | ACB | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03471 | hp1 | a0001 | c0013 | t0013 | g0043 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0076 | AFR | MSL | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | USA | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| HG06807 | hp2 | a0002 | c0004 | t0004 | g0003 | AFR | USA | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA20300 | hp1 | a0002 | c0004 | t0002 | g0103 | AFR | USA | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | USA | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA21309 | hp1 | a0001 | c0011 | t0012 | g0073 | AFR | LWK | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0088 | AFR | LWK | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0176 | REF | REF | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0011 | REF | REF | CTTN_chr11_70393529_70441575 | CTTN | chr11 | 70393529 | 70441575 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:70405267 | G | A | 1 | a0001 | 1 | HG00735.hp2 | splice_region_variant | LOW | c.-95G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/18 | chr11 | 70405267 | |||||||
| chr11:70407334 | G | A | 1 | a0004 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.37G>A | p.Ala13Thr | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 3/18 | 220/3249 | 37/1653 | 13/550 | chr11 | 70407334 | |||
| chr11:70431228 | C | T | 1 | a0003 | 2 | NA18966.hp1 NA18979.hp1 |
missense_variant | MODERATE | c.1214C>T | p.Ser405Leu | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/18 | 1397/3249 | 1214/1653 | 405/550 | chr11 | 70431228 | |||
| chr11:70433653 | G | A | 2 | a0002 a0004 |
19 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(16): Show |
missense_variant | MODERATE | c.1451G>A | p.Ser484Asn | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/18 | 1634/3249 | 1451/1653 | 484/550 | chr11 | 70433653 | |||
| chr11:70433661 | G | A | 1 | a0005 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.1459G>A | p.Asp487Asn | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/18 | 1642/3249 | 1459/1653 | 487/550 | chr11 | 70433661 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:70407369 | C | T | 2 | a0001c0003 a0001c0016 |
43 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(40): Show |
synonymous_variant | LOW | c.72C>T | p.Thr24Thr | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 3/18 | 255/3249 | 72/1653 | 24/550 | chr11 | 70407369 | |||
| chr11:70419774 | C | T | 1 | a0001c0005 | 4 | HG01243.hp2 HG01346.hp2 HG02735.hp2 others(1): Show |
synonymous_variant | LOW | c.597C>T | p.Tyr199Tyr | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/18 | 780/3249 | 597/1653 | 199/550 | chr11 | 70419774 | |||
| chr11:70422974 | G | A | 1 | a0001c0009 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.936G>A | p.Val312Val | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/18 | 1119/3249 | 936/1653 | 312/550 | chr11 | 70422974 | |||
| chr11:70425337 | G | A | 1 | a0001c0010 | 1 | NA19084.hp2 | synonymous_variant | LOW | c.963G>A | p.Ala321Ala | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/18 | 1146/3249 | 963/1653 | 321/550 | chr11 | 70425337 | |||
| chr11:70425352 | T | C | 1 | a0001c0011 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.978T>C | p.Asp326Asp | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/18 | 1161/3249 | 978/1653 | 326/550 | chr11 | 70425352 | |||
| chr11:70429172 | G | A | 1 | a0004c0008 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.1149G>A | p.Glu383Glu | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/18 | 1332/3249 | 1149/1653 | 383/550 | chr11 | 70429172 | |||
| chr11:70433133 | C | T | 1 | a0001c0015 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.1299C>T | p.Tyr433Tyr | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 16/18 | 1482/3249 | 1299/1653 | 433/550 | chr11 | 70433133 | |||
| chr11:70433166 | C | T | 1 | a0001c0006 | 2 | HG03453.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.1332C>T | p.Pro444Pro | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 16/18 | 1515/3249 | 1332/1653 | 444/550 | chr11 | 70433166 | |||
| chr11:70433660 | C | T | 4 | a0001c0002 a0001c0005 a0001c0014 others(1): Show |
62 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(59): Show |
synonymous_variant | LOW | c.1458C>T | p.Tyr486Tyr | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/18 | 1641/3249 | 1458/1653 | 486/550 | chr11 | 70433660 | |||
| chr11:70433669 | C | T | 1 | a0001c0014 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.1467C>T | p.Tyr489Tyr | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/18 | 1650/3249 | 1467/1653 | 489/550 | chr11 | 70433669 | |||
| chr11:70433705 | C | T | 1 | a0001c0013 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.1503C>T | p.Tyr501Tyr | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/18 | 1686/3249 | 1503/1653 | 501/550 | chr11 | 70433705 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:70398550 | T | C | 21 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0014 others(18): Show |
71 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(68): Show |
5_prime_UTR_variant | MODIFIER | c.-162T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/18 | 8748 | chr11 | 70398550 | ||||||
| chr11:70398555 | G | A | 1 | a0001c0001t0023 | 1 | HG02486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-157G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/18 | 8743 | chr11 | 70398555 | ||||||
| chr11:70405299 | T | C | 1 | a0001c0001t0025 | 1 | HG01515.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/18 | chr11 | 70405299 | |||||||
| chr11:70405327 | C | T | 4 | a0001c0001t0021 a0001c0001t0022 a0001c0006t0012 others(1): Show |
5 | HG03225.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-35C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/18 | chr11 | 70405327 | |||||||
| chr11:70435173 | C | G | 1 | a0001c0003t0036 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 11 | chr11 | 70435173 | ||||||
| chr11:70435177 | C | G | 1 | a0001c0001t0035 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 15 | chr11 | 70435177 | ||||||
| chr11:70435178 | C | A | 1 | a0001c0001t0026 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 16 | chr11 | 70435178 | ||||||
| chr11:70435178 | C | G | 2 | a0001c0001t0034 a0001c0003t0011 |
4 | NA18997.hp2 NA19057.hp2 NA19066.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*16C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 16 | chr11 | 70435178 | ||||||
| chr11:70435253 | G | GT | 8 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0010 others(5): Show |
54 | HG00099.hp2 HG00558.hp1 HG01070.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*116dupT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 117 | INFO_REALIGN_3_PRIME | chr11 | 70435253 | |||||
| chr11:70435253 | G | GTT | 3 | a0001c0002t0009 a0001c0002t0020 a0001c0002t0032 |
9 | HG00280.hp1 HG00733.hp1 HG01074.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*115_*116dupTT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 117 | INFO_REALIGN_3_PRIME | chr11 | 70435253 | |||||
| chr11:70435253 | G | T | 1 | a0001c0002t0033 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 91 | chr11 | 70435253 | ||||||
| chr11:70435253 | GT | G | 6 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0014 others(3): Show |
29 | HG01891.hp2 HG02055.hp2 HG02135.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*116delT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 116 | INFO_REALIGN_3_PRIME | chr11 | 70435253 | |||||
| chr11:70435253 | GTT | G | 8 | a0001c0001t0013 a0001c0001t0015 a0001c0001t0017 others(5): Show |
17 | HG00323.hp1 HG00735.hp1 HG01175.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*115_*116delTT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 115 | INFO_REALIGN_3_PRIME | chr11 | 70435253 | |||||
| chr11:70435253 | GTTT | G | 5 | a0001c0003t0005 a0001c0003t0006 a0001c0003t0011 others(2): Show |
29 | HG00099.hp1 HG01074.hp1 HG01106.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*114_*116delTTT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 114 | INFO_REALIGN_3_PRIME | chr11 | 70435253 | |||||
| chr11:70435739 | G | A | 1 | a0001c0001t0016 | 2 | HG01496.hp1 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*577G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 577 | chr11 | 70435739 | ||||||
| chr11:70435832 | G | A | 2 | a0001c0003t0027 a0001c0003t0029 |
2 | HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*670G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 670 | chr11 | 70435832 | ||||||
| chr11:70435995 | T | C | 1 | a0002c0004t0018 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*833T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 833 | chr11 | 70435995 | ||||||
| chr11:70436001 | C | T | 2 | a0001c0001t0014 a0001c0001t0017 |
3 | HG02451.hp2 HG02809.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*839C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 839 | chr11 | 70436001 | ||||||
| chr11:70436057 | G | A | 1 | a0001c0001t0030 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*895G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 895 | chr11 | 70436057 | ||||||
| chr11:70436099 | C | T | 1 | a0001c0001t0031 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*937C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 937 | chr11 | 70436099 | ||||||
| chr11:70436119 | A | G | 1 | a0001c0001t0026 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*957A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 957 | chr11 | 70436119 | ||||||
| chr11:70436227 | C | T | 1 | a0001c0001t0022 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1065C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 1065 | chr11 | 70436227 | ||||||
| chr11:70436288 | C | T | 1 | a0001c0002t0032 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1126C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 1126 | chr11 | 70436288 | ||||||
| chr11:70436523 | A | C | 9 | a0001c0003t0005 a0001c0003t0006 a0001c0003t0008 others(6): Show |
41 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1361A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 18/18 | 1361 | chr11 | 70436523 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:70398808 | G | A | 1 | a0001c0002t0002g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-98+194G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70398808 | |||||||
| chr11:70398875 | G | A | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-98+261G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70398875 | |||||||
| chr11:70398940 | G | A | 34 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(31): Show |
46 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.-98+326G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70398940 | |||||||
| chr11:70398955 | G | T | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-98+341G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70398955 | |||||||
| chr11:70399020 | G | C | 2 | a0001c0001t0003g0044 a0001c0001t0003g0045 |
2 | HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-98+406G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70399020 | |||||||
| chr11:70399051 | A | G | 11 | a0001c0001t0014g0233 a0001c0001t0014g0235 a0001c0001t0017g0232 others(8): Show |
18 | HG02109.hp1 HG02451.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.-98+437A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70399051 | |||||||
| chr11:70399056 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-98+442C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70399056 | |||||||
| chr11:70399169 | G | T | 10 | a0001c0001t0014g0233 a0001c0001t0014g0235 a0001c0001t0017g0232 others(7): Show |
16 | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-98+555G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70399169 | |||||||
| chr11:70399361 | G | A | 3 | a0001c0001t0007g0017 a0001c0001t0007g0072 a0001c0001t0015g0017 |
3 | HG02055.hp2 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-98+747G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70399361 | |||||||
| chr11:70399590 | A | G | 1 | a0002c0004t0004g0236 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-98+976A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70399590 | |||||||
| chr11:70399641 | A | G | 1 | a0001c0003t0011g0071 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-98+1027A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70399641 | |||||||
| chr11:70399664 | G | A | 3 | a0001c0006t0012g0074 a0001c0006t0012g0075 a0001c0011t0012g0073 |
3 | HG03453.hp2 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-98+1050G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70399664 | |||||||
| chr11:70399718 | TGGACGTT others(12): Show |
T | 1 | a0001c0003t0006g0227 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-98+1107_-98+1125d others(21): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 70399718 | ||||||
| chr11:70399912 | A | T | 1 | a0001c0003t0006g0227 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-98+1298A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70399912 | |||||||
| chr11:70400095 | G | A | 3 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0013g0048 |
3 | HG02717.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-98+1481G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400095 | |||||||
| chr11:70400134 | A | C | 1 | a0001c0001t0001g0226 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-98+1520A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400134 | |||||||
| chr11:70400148 | T | C | 34 | a0001c0001t0001g0098 a0001c0001t0003g0046 a0001c0001t0003g0047 others(31): Show |
37 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.-98+1534T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400148 | |||||||
| chr11:70400262 | A | T | 1 | a0001c0003t0006g0227 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-98+1648A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400262 | |||||||
| chr11:70400307 | A | G | 13 | a0001c0001t0014g0233 a0001c0001t0014g0235 a0001c0001t0017g0232 others(10): Show |
20 | HG02109.hp1 HG02451.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.-98+1693A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400307 | |||||||
| chr11:70400613 | G | A | 7 | a0001c0001t0021g0229 a0002c0004t0004g0003 a0002c0004t0004g0041 others(4): Show |
14 | HG02109.hp1 HG02572.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.-98+1999G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400613 | |||||||
| chr11:70400656 | G | C | 1 | a0001c0011t0012g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-98+2042G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400656 | |||||||
| chr11:70400830 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0002g0040 |
6 | HG01928.hp2 HG01943.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-98+2216A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400830 | |||||||
| chr11:70400850 | C | A | 37 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(34): Show |
49 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-98+2236C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400850 | |||||||
| chr11:70400855 | T | A | 1 | a0001c0003t0006g0227 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-98+2241T>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400855 | |||||||
| chr11:70400886 | C | T | 9 | a0001c0002t0001g0004 a0001c0002t0001g0039 a0001c0002t0002g0004 others(6): Show |
13 | HG00280.hp1 HG00733.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.-98+2272C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400886 | |||||||
| chr11:70400895 | C | A | 2 | a0001c0001t0003g0010 a0001c0001t0003g0015 |
5 | HG02145.hp1 HG02258.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-98+2281C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400895 | |||||||
| chr11:70400967 | T | A | 1 | a0001c0002t0002g0101 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-98+2353T>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70400967 | |||||||
| chr11:70401171 | G | A | 14 | a0001c0001t0014g0233 a0001c0001t0014g0235 a0001c0001t0017g0232 others(11): Show |
21 | HG02109.hp1 HG02451.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.-98+2557G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401171 | |||||||
| chr11:70401302 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-98+2688C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401302 | |||||||
| chr11:70401306 | T | TA | 66 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(63): Show |
81 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-98+2703dupA | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 70401306 | ||||||
| chr11:70401314 | A | C | 1 | a0001c0011t0012g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-98+2700A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401314 | |||||||
| chr11:70401317 | A | T | 1 | a0001c0001t0001g0220 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-98+2703A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401317 | |||||||
| chr11:70401332 | C | T | 12 | a0001c0001t0014g0233 a0001c0001t0014g0235 a0001c0001t0017g0232 others(9): Show |
19 | HG02109.hp1 HG02451.hp2 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.-98+2718C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401332 | |||||||
| chr11:70401336 | C | T | 2 | a0001c0001t0001g0219 a0001c0011t0012g0073 |
2 | HG00544.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-98+2722C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401336 | |||||||
| chr11:70401565 | T | C | 8 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0003g0050 others(5): Show |
8 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-98+2951T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401565 | |||||||
| chr11:70401625 | G | A | 1 | a0001c0003t0006g0227 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-98+3011G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401625 | |||||||
| chr11:70401660 | A | C | 1 | a0001c0001t0002g0218 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-98+3046A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401660 | |||||||
| chr11:70401660 | A | T | 1 | a0001c0003t0006g0227 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-98+3046A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401660 | |||||||
| chr11:70401661 | C | A | 1 | a0001c0001t0002g0218 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-98+3047C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401661 | |||||||
| chr11:70401819 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-98+3205G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401819 | |||||||
| chr11:70401864 | G | A | 39 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(36): Show |
51 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.-98+3250G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401864 | |||||||
| chr11:70401967 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-97-3298C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70401967 | |||||||
| chr11:70402007 | G | C | 31 | a0001c0001t0007g0017 a0001c0001t0007g0018 a0001c0001t0007g0072 others(28): Show |
34 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.-97-3258G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402007 | |||||||
| chr11:70402022 | G | A | 2 | a0001c0003t0005g0016 a0001c0003t0005g0055 |
3 | HG00099.hp1 HG02559.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-97-3243G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402022 | |||||||
| chr11:70402050 | A | T | 1 | a0001c0001t0015g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-97-3215A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402050 | |||||||
| chr11:70402080 | G | T | 1 | a0001c0003t0006g0227 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-97-3185G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402080 | |||||||
| chr11:70402162 | A | C | 1 | a0001c0003t0006g0227 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-97-3103A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402162 | |||||||
| chr11:70402179 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-97-3086G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402179 | |||||||
| chr11:70402187 | T | C | 1 | a0001c0003t0006g0227 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-97-3078T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402187 | |||||||
| chr11:70402188 | C | A | 1 | a0001c0003t0006g0227 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-97-3077C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402188 | |||||||
| chr11:70402274 | A | T | 14 | a0001c0001t0014g0233 a0001c0001t0014g0235 a0001c0001t0017g0232 others(11): Show |
21 | HG02109.hp1 HG02451.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.-97-2991A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402274 | |||||||
| chr11:70402339 | A | G | 2 | a0001c0006t0012g0074 a0001c0006t0012g0075 |
2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-97-2926A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402339 | |||||||
| chr11:70402371 | C | T | 1 | a0001c0003t0006g0227 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-97-2894C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402371 | |||||||
| chr11:70402377 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-97-2888G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402377 | |||||||
| chr11:70402569 | A | T | 1 | a0001c0003t0006g0227 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-97-2696A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402569 | |||||||
| chr11:70402794 | C | T | 83 | a0001c0001t0001g0098 a0001c0001t0003g0010 a0001c0001t0003g0015 others(80): Show |
104 | HG00099.hp2 HG00558.hp1 HG00735.hp1 others(101): Show |
intron_variant | MODIFIER | c.-97-2471C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70402794 | |||||||
| chr11:70403036 | T | A | 1 | a0001c0003t0011g0056 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-97-2229T>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403036 | |||||||
| chr11:70403186 | C | CT | 34 | a0001c0001t0001g0014 a0001c0001t0001g0098 a0001c0001t0001g0208 others(31): Show |
45 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.-97-2058dupT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 70403186 | ||||||
| chr11:70403186 | C | CTT | 7 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0052 others(4): Show |
7 | HG01891.hp2 HG02257.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-97-2059_-97-2058d others(4): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 70403186 | ||||||
| chr11:70403186 | CT | C | 18 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0106 others(15): Show |
20 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.-97-2058delT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 70403186 | ||||||
| chr11:70403228 | C | T | 1 | a0001c0001t0022g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-97-2037C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403228 | |||||||
| chr11:70403249 | C | T | 1 | a0001c0001t0022g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-97-2016C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403249 | |||||||
| chr11:70403257 | C | T | 4 | a0001c0001t0013g0048 a0001c0002t0002g0076 a0001c0002t0002g0215 others(1): Show |
4 | HG02647.hp2 HG02723.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-97-2008C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403257 | |||||||
| chr11:70403293 | G | A | 37 | a0001c0001t0013g0048 a0001c0001t0014g0235 a0001c0001t0022g0234 others(34): Show |
53 | HG00099.hp1 HG00735.hp1 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.-97-1972G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403293 | |||||||
| chr11:70403305 | C | CAGCCTCC others(2): Show |
88 | a0001c0001t0001g0098 a0001c0001t0001g0127 a0001c0001t0003g0010 others(85): Show |
117 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(114): Show |
intron_variant | MODIFIER | c.-97-1957_-97-1949d others(11): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr11 | 70403305 | ||||||
| chr11:70403429 | C | T | 12 | a0001c0001t0013g0048 a0002c0004t0001g0077 a0002c0004t0004g0003 others(9): Show |
19 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-97-1836C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403429 | |||||||
| chr11:70403434 | G | A | 2 | a0001c0001t0021g0229 a0001c0011t0012g0073 |
2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-97-1831G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403434 | |||||||
| chr11:70403749 | C | T | 3 | a0001c0001t0022g0234 a0001c0006t0012g0074 a0001c0006t0012g0075 |
3 | HG03225.hp1 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-97-1516C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403749 | |||||||
| chr11:70403763 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-97-1502A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403763 | |||||||
| chr11:70403771 | C | T | 5 | a0001c0001t0021g0229 a0001c0001t0022g0234 a0001c0006t0012g0074 others(2): Show |
5 | HG03225.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-97-1494C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70403771 | |||||||
| chr11:70404039 | C | T | 1 | a0001c0001t0021g0229 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-97-1226C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404039 | |||||||
| chr11:70404070 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-97-1195A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404070 | |||||||
| chr11:70404206 | T | A | 1 | a0001c0003t0006g0227 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-97-1059T>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404206 | |||||||
| chr11:70404293 | A | C | 1 | a0001c0003t0006g0227 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-97-972A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404293 | |||||||
| chr11:70404419 | C | G | 1 | a0001c0003t0006g0227 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-97-846C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404419 | |||||||
| chr11:70404651 | G | A | 5 | a0001c0001t0021g0229 a0001c0001t0022g0234 a0001c0006t0012g0074 others(2): Show |
5 | HG03225.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-97-614G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404651 | |||||||
| chr11:70404784 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-97-481C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404784 | |||||||
| chr11:70404831 | C | T | 3 | a0001c0001t0001g0203 a0001c0001t0001g0221 a0001c0001t0007g0116 |
3 | HG02615.hp1 HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-97-434C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404831 | |||||||
| chr11:70404942 | C | T | 1 | a0001c0001t0003g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-97-323C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404942 | |||||||
| chr11:70404951 | G | A | 3 | a0001c0003t0006g0024 a0001c0003t0006g0128 a0001c0003t0036g0129 |
4 | HG02083.hp2 NA18953.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.-97-314G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404951 | |||||||
| chr11:70404954 | A | C | 1 | a0001c0005t0002g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-97-311A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70404954 | |||||||
| chr11:70405071 | A | C | 1 | a0001c0001t0026g0117 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-97-194A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70405071 | |||||||
| chr11:70405076 | C | T | 2 | a0001c0001t0001g0201 a0001c0010t0002g0202 |
2 | HG02015.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-97-189C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70405076 | |||||||
| chr11:70405140 | C | G | 3 | a0002c0004t0004g0022 a0002c0004t0004g0100 a0002c0004t0018g0022 |
3 | HG01884.hp2 HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-97-125C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70405140 | |||||||
| chr11:70405154 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-97-111G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70405154 | |||||||
| chr11:70405231 | C | G | 3 | a0001c0001t0022g0234 a0001c0006t0012g0074 a0001c0006t0012g0075 |
3 | HG03225.hp1 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-97-34C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70405231 | |||||||
| chr11:70405255 | C | G | 1 | a0002c0004t0001g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-97-10C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 1/17 | chr11 | 70405255 | |||||||
| chr11:70405529 | T | A | 1 | a0001c0003t0006g0227 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-1+168T>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70405529 | |||||||
| chr11:70405552 | C | G | 4 | a0002c0004t0004g0022 a0002c0004t0004g0099 a0002c0004t0004g0100 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+191C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70405552 | |||||||
| chr11:70405615 | G | T | 1 | a0001c0003t0011g0056 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-1+254G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70405615 | |||||||
| chr11:70405706 | T | C | 89 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0025 others(86): Show |
112 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.-1+345T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70405706 | |||||||
| chr11:70405861 | A | T | 1 | a0001c0003t0006g0227 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-1+500A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70405861 | |||||||
| chr11:70405906 | G | A | 1 | a0001c0003t0006g0130 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-1+545G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70405906 | |||||||
| chr11:70405945 | G | A | 8 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0007g0017 others(5): Show |
9 | HG02055.hp2 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1+584G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70405945 | |||||||
| chr11:70405984 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-1+623G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70405984 | |||||||
| chr11:70406103 | C | A | 1 | a0001c0001t0021g0229 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-1+742C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70406103 | |||||||
| chr11:70406173 | G | T | 2 | a0001c0001t0021g0229 a0001c0011t0012g0073 |
2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-1+812G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70406173 | |||||||
| chr11:70406201 | C | T | 3 | a0001c0001t0022g0234 a0001c0006t0012g0074 a0001c0006t0012g0075 |
3 | HG03225.hp1 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-1+840C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70406201 | |||||||
| chr11:70406293 | A | G | 8 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0007g0017 others(5): Show |
9 | HG02055.hp2 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1+932A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70406293 | |||||||
| chr11:70406345 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1-953C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70406345 | |||||||
| chr11:70406514 | A | G | 2 | a0001c0001t0021g0229 a0001c0011t0012g0073 |
2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1-784A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70406514 | |||||||
| chr11:70406521 | GA | G | 13 | a0001c0001t0001g0115 a0001c0001t0001g0198 a0001c0001t0001g0199 others(10): Show |
16 | HG02145.hp1 HG02258.hp1 HG03225.hp1 others(13): Show |
intron_variant | MODIFIER | c.1-762delA | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr11 | 70406521 | ||||||
| chr11:70406682 | G | C | 1 | a0001c0001t0001g0145 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1-616G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70406682 | |||||||
| chr11:70406839 | C | T | 3 | a0001c0001t0022g0234 a0001c0006t0012g0074 a0001c0006t0012g0075 |
3 | HG03225.hp1 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1-459C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70406839 | |||||||
| chr11:70406947 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1-351G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70406947 | |||||||
| chr11:70407004 | T | C | 1 | a0001c0011t0012g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1-294T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70407004 | |||||||
| chr11:70407015 | CT | C | 3 | a0001c0001t0014g0233 a0001c0001t0014g0235 a0001c0001t0017g0232 |
3 | HG02451.hp2 HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1-277delT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr11 | 70407015 | ||||||
| chr11:70407084 | G | T | 1 | a0001c0001t0001g0038 | 2 | HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1-214G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70407084 | |||||||
| chr11:70407283 | C | T | 36 | a0001c0001t0014g0233 a0001c0001t0014g0235 a0001c0001t0017g0232 others(33): Show |
47 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.1-15C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 2/17 | chr11 | 70407283 | |||||||
| chr11:70407394 | G | A | 1 | a0001c0001t0035g0147 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.87+10G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 3/17 | chr11 | 70407394 | |||||||
| chr11:70407480 | T | C | 131 | a0001c0001t0001g0098 a0001c0001t0001g0127 a0001c0001t0003g0010 others(128): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.88-38T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 3/17 | chr11 | 70407480 | |||||||
| chr11:70407482 | C | A | 1 | a0001c0001t0017g0232 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.88-36C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 3/17 | chr11 | 70407482 | |||||||
| chr11:70407660 | A | G | 2 | a0001c0001t0021g0229 a0001c0011t0012g0073 |
2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.161+69A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70407660 | |||||||
| chr11:70407805 | G | T | 1 | a0001c0001t0021g0229 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.161+214G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70407805 | |||||||
| chr11:70407851 | A | C | 1 | a0001c0009t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.161+260A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70407851 | |||||||
| chr11:70407868 | G | A | 1 | a0001c0001t0003g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.161+277G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70407868 | |||||||
| chr11:70407884 | G | T | 1 | a0001c0001t0001g0197 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.161+293G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70407884 | |||||||
| chr11:70407950 | T | C | 1 | a0001c0009t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.161+359T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70407950 | |||||||
| chr11:70408050 | G | A | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.161+459G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408050 | |||||||
| chr11:70408082 | G | C | 1 | a0001c0009t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.161+491G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408082 | |||||||
| chr11:70408264 | C | G | 1 | a0002c0004t0004g0099 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.161+673C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408264 | |||||||
| chr11:70408278 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.161+687G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408278 | |||||||
| chr11:70408380 | G | T | 5 | a0001c0001t0021g0229 a0001c0001t0022g0234 a0001c0006t0012g0074 others(2): Show |
5 | HG03225.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.161+789G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408380 | |||||||
| chr11:70408457 | G | C | 1 | a0001c0001t0003g0046 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.161+866G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408457 | |||||||
| chr11:70408462 | A | G | 2 | a0001c0001t0003g0044 a0001c0001t0003g0045 |
2 | HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.161+871A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408462 | |||||||
| chr11:70408690 | G | A | 3 | a0001c0001t0022g0234 a0001c0006t0012g0074 a0001c0006t0012g0075 |
3 | HG03225.hp1 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.161+1099G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408690 | |||||||
| chr11:70408775 | C | T | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.162-1056C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408775 | |||||||
| chr11:70408784 | G | A | 128 | a0001c0001t0001g0098 a0001c0001t0003g0010 a0001c0001t0003g0015 others(125): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.162-1047G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70408784 | |||||||
| chr11:70409069 | G | T | 23 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(20): Show |
33 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.162-762G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70409069 | |||||||
| chr11:70409217 | G | T | 2 | a0001c0001t0001g0037 a0001c0001t0002g0196 |
3 | NA18994.hp2 NA18999.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.162-614G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70409217 | |||||||
| chr11:70409624 | C | T | 1 | a0001c0003t0008g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.162-207C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 4/17 | chr11 | 70409624 | |||||||
| chr11:70410029 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.291+69C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410029 | |||||||
| chr11:70410078 | G | A | 1 | a0001c0001t0022g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.291+118G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410078 | |||||||
| chr11:70410371 | C | T | 1 | a0001c0011t0012g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.291+411C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410371 | |||||||
| chr11:70410437 | C | T | 1 | a0001c0009t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.291+477C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410437 | |||||||
| chr11:70410451 | G | A | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291+491G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410451 | |||||||
| chr11:70410539 | C | T | 4 | a0001c0002t0001g0021 a0001c0002t0001g0087 a0001c0002t0001g0097 others(1): Show |
5 | HG01884.hp1 HG02055.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.291+579C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410539 | |||||||
| chr11:70410545 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.291+585C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410545 | |||||||
| chr11:70410840 | C | T | 2 | a0001c0006t0012g0074 a0001c0006t0012g0075 |
2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.291+880C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410840 | |||||||
| chr11:70410882 | G | A | 3 | a0001c0001t0022g0234 a0001c0006t0012g0074 a0001c0006t0012g0075 |
3 | HG03225.hp1 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.291+922G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410882 | |||||||
| chr11:70410913 | A | C | 45 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0025 others(42): Show |
58 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.291+953A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70410913 | |||||||
| chr11:70411004 | T | C | 1 | a0001c0001t0034g0217 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.291+1044T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411004 | |||||||
| chr11:70411184 | A | G | 25 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(22): Show |
35 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.291+1224A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411184 | |||||||
| chr11:70411185 | A | AGTGCACA others(143): Show |
1 | a0001c0001t0022g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.291+1273_291+1274i others(152): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 70411185 | ||||||
| chr11:70411185 | A | T | 25 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(22): Show |
35 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.291+1225A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411185 | |||||||
| chr11:70411185 | AGTGCACA others(43): Show |
A | 1 | a0001c0001t0001g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.291+1399_291+1448d others(52): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 70411185 | ||||||
| chr11:70411234 | G | A | 53 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0025 others(50): Show |
66 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.291+1274G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411234 | |||||||
| chr11:70411274 | C | T | 1 | a0001c0002t0002g0126 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.291+1314C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411274 | |||||||
| chr11:70411279 | G | A | 4 | a0001c0002t0002g0101 a0001c0002t0002g0207 a0001c0002t0009g0118 others(1): Show |
4 | HG02080.hp1 NA18950.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.291+1319G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411279 | |||||||
| chr11:70411328 | C | T | 2 | a0001c0001t0007g0079 a0001c0001t0007g0080 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.291+1368C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411328 | |||||||
| chr11:70411360 | TGTGTTCA others(41): Show |
T | 1 | a0001c0001t0001g0127 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.291+1449_291+1496d others(50): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 70411360 | ||||||
| chr11:70411408 | C | CATGTGTT others(95): Show |
1 | a0001c0001t0034g0217 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.291+1448_291+1449i others(104): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411408 | |||||||
| chr11:70411408 | C | CATGTGTT others(195): Show |
1 | a0002c0004t0002g0103 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.291+1448_291+1449i others(204): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411408 | |||||||
| chr11:70411408 | C | CATGTGTT others(145): Show |
4 | a0001c0001t0021g0229 a0001c0006t0012g0074 a0001c0006t0012g0075 others(1): Show |
4 | HG03453.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.291+1448_291+1449i others(154): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411408 | |||||||
| chr11:70411408 | C | CATGTGTT others(195): Show |
24 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(21): Show |
33 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.291+1448_291+1449i others(204): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411408 | |||||||
| chr11:70411441 | C | T | 1 | a0001c0010t0002g0202 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.291+1481C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411441 | |||||||
| chr11:70411503 | A | T | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.291+1543A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411503 | |||||||
| chr11:70411563 | A | G | 141 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0025 others(138): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.291+1603A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411563 | |||||||
| chr11:70411632 | G | A | 2 | a0001c0006t0012g0074 a0001c0006t0012g0075 |
2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.291+1672G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411632 | |||||||
| chr11:70411669 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.291+1709C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411669 | |||||||
| chr11:70411689 | C | T | 1 | a0001c0003t0019g0057 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.291+1729C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411689 | |||||||
| chr11:70411770 | C | T | 1 | a0001c0002t0002g0020 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.291+1810C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411770 | |||||||
| chr11:70411799 | C | A | 4 | a0002c0004t0004g0022 a0002c0004t0004g0099 a0002c0004t0004g0100 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.291+1839C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411799 | |||||||
| chr11:70411890 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.291+1930G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411890 | |||||||
| chr11:70411907 | C | G | 1 | a0001c0001t0001g0200 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.291+1947C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411907 | |||||||
| chr11:70411942 | C | G | 1 | a0001c0001t0023g0149 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.291+1982C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411942 | |||||||
| chr11:70411942 | C | T | 1 | a0001c0003t0005g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.291+1982C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411942 | |||||||
| chr11:70411943 | C | A | 1 | a0001c0001t0034g0217 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.291+1983C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411943 | |||||||
| chr11:70411944 | C | G | 2 | a0001c0001t0021g0229 a0001c0001t0022g0234 |
2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.291+1984C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70411944 | |||||||
| chr11:70412005 | C | T | 1 | a0001c0011t0012g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.291+2045C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412005 | |||||||
| chr11:70412035 | G | A | 1 | a0001c0002t0002g0215 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.291+2075G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412035 | |||||||
| chr11:70412038 | TC | T | 2 | a0001c0001t0003g0010 a0001c0001t0003g0015 |
5 | HG02145.hp1 HG02258.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.291+2080delC | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 70412038 | ||||||
| chr11:70412073 | T | C | 32 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(29): Show |
42 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.291+2113T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412073 | |||||||
| chr11:70412126 | C | T | 31 | a0001c0001t0001g0102 a0001c0001t0003g0010 a0001c0001t0003g0015 others(28): Show |
41 | HG00438.hp1 HG01884.hp2 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.291+2166C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412126 | |||||||
| chr11:70412162 | G | C | 31 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(28): Show |
41 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.291+2202G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412162 | |||||||
| chr11:70412340 | C | T | 1 | a0001c0011t0012g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.292-2202C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412340 | |||||||
| chr11:70412430 | A | T | 1 | a0001c0002t0001g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.292-2112A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412430 | |||||||
| chr11:70412432 | A | T | 1 | a0001c0002t0001g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.292-2110A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412432 | |||||||
| chr11:70412436 | A | C | 1 | a0002c0004t0002g0103 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.292-2106A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412436 | |||||||
| chr11:70412503 | CTA | C | 3 | a0001c0001t0001g0105 a0001c0001t0001g0152 a0001c0001t0001g0195 |
3 | HG02165.hp2 NA18977.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.292-2038_292-2037d others(4): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412503 | |||||||
| chr11:70412904 | T | C | 1 | a0001c0002t0002g0119 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.292-1638T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412904 | |||||||
| chr11:70412923 | C | T | 1 | a0001c0009t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.292-1619C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70412923 | |||||||
| chr11:70413011 | C | T | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(1): Show |
4 | HG00609.hp1 NA18942.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-1531C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70413011 | |||||||
| chr11:70413102 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.292-1440G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70413102 | |||||||
| chr11:70413176 | C | T | 1 | a0001c0003t0005g0065 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.292-1366C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70413176 | |||||||
| chr11:70413207 | G | A | 1 | a0001c0009t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.292-1335G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70413207 | |||||||
| chr11:70413914 | G | A | 1 | a0001c0001t0023g0149 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.292-628G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70413914 | |||||||
| chr11:70413922 | C | CCA | 5 | a0001c0001t0021g0229 a0001c0001t0022g0234 a0001c0006t0012g0074 others(2): Show |
5 | HG03225.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.292-617_292-616dup others(2): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr11 | 70413922 | ||||||
| chr11:70414198 | A | C | 1 | a0001c0003t0028g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.292-344A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70414198 | |||||||
| chr11:70414291 | G | A | 1 | a0001c0003t0006g0136 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.292-251G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70414291 | |||||||
| chr11:70414339 | T | C | 145 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0025 others(142): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.292-203T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70414339 | |||||||
| chr11:70414395 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.292-147G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70414395 | |||||||
| chr11:70414437 | C | G | 1 | a0001c0011t0012g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.292-105C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70414437 | |||||||
| chr11:70414466 | C | T | 1 | a0001c0001t0013g0048 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.292-76C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70414466 | |||||||
| chr11:70414492 | C | T | 17 | a0001c0003t0005g0006 a0001c0003t0005g0016 a0001c0003t0005g0055 others(14): Show |
26 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.292-50C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70414492 | |||||||
| chr11:70414503 | T | C | 50 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0025 others(47): Show |
63 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.292-39T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 5/17 | chr11 | 70414503 | |||||||
| chr11:70414664 | G | A | 1 | a0001c0003t0005g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.402+12G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70414664 | |||||||
| chr11:70414727 | G | T | 5 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(2): Show |
5 | HG00597.hp2 HG00609.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+75G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70414727 | |||||||
| chr11:70414839 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.402+187C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70414839 | |||||||
| chr11:70414878 | C | T | 1 | a0001c0003t0006g0136 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.402+226C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70414878 | |||||||
| chr11:70414955 | A | G | 11 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0037 others(8): Show |
22 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.402+303A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70414955 | |||||||
| chr11:70415037 | T | C | 24 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(21): Show |
34 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.402+385T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70415037 | |||||||
| chr11:70415149 | G | C | 1 | a0001c0001t0022g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.402+497G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70415149 | |||||||
| chr11:70415227 | T | G | 1 | a0001c0003t0005g0060 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.403-436T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70415227 | |||||||
| chr11:70415298 | G | C | 24 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(21): Show |
34 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.403-365G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70415298 | |||||||
| chr11:70415430 | A | G | 50 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0025 others(47): Show |
63 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.403-233A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70415430 | |||||||
| chr11:70415487 | T | G | 1 | a0001c0001t0014g0235 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.403-176T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70415487 | |||||||
| chr11:70415619 | A | G | 1 | a0005c0012t0001g0185 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.403-44A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70415619 | |||||||
| chr11:70415622 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.403-41G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 6/17 | chr11 | 70415622 | |||||||
| chr11:70415725 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03688.hp2 | splice_region_variant&intron_variant | LOW | c.457+8G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70415725 | |||||||
| chr11:70415727 | G | A | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.457+10G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70415727 | |||||||
| chr11:70415793 | T | TC | 5 | a0001c0001t0001g0157 a0001c0001t0003g0050 a0001c0001t0007g0111 others(2): Show |
5 | HG00733.hp1 HG02135.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.457+80dupC | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr11 | 70415793 | ||||||
| chr11:70415999 | C | T | 1 | a0001c0009t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.457+282C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70415999 | |||||||
| chr11:70416109 | ATTC | A | 62 | a0001c0001t0001g0098 a0001c0001t0003g0046 a0001c0001t0003g0047 others(59): Show |
73 | HG00280.hp1 HG00558.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.457+395_457+397del others(3): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr11 | 70416109 | ||||||
| chr11:70416203 | G | T | 1 | a0001c0001t0001g0189 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.457+486G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70416203 | |||||||
| chr11:70416229 | T | G | 1 | a0001c0001t0001g0189 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.457+512T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70416229 | |||||||
| chr11:70416245 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.457+528G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70416245 | |||||||
| chr11:70416273 | T | G | 53 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0025 others(50): Show |
70 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.457+556T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70416273 | |||||||
| chr11:70416545 | C | A | 24 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(21): Show |
34 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.458-468C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70416545 | |||||||
| chr11:70416635 | G | A | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.458-378G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70416635 | |||||||
| chr11:70416827 | G | A | 1 | a0001c0003t0005g0061 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.458-186G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70416827 | |||||||
| chr11:70416868 | C | A | 4 | a0001c0001t0021g0229 a0001c0001t0022g0234 a0001c0006t0012g0074 others(1): Show |
4 | HG03225.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.458-145C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70416868 | |||||||
| chr11:70416882 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.458-131T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 7/17 | chr11 | 70416882 | |||||||
| chr11:70417245 | G | A | 61 | a0001c0001t0001g0098 a0001c0001t0003g0046 a0001c0001t0003g0047 others(58): Show |
72 | HG00280.hp1 HG00558.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.568+122G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417245 | |||||||
| chr11:70417409 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.568+286C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417409 | |||||||
| chr11:70417428 | G | A | 3 | a0001c0001t0007g0017 a0001c0001t0007g0072 a0001c0001t0015g0017 |
3 | HG02055.hp2 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.568+305G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417428 | |||||||
| chr11:70417491 | G | A | 8 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0003g0050 others(5): Show |
8 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.568+368G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417491 | |||||||
| chr11:70417610 | T | C | 34 | a0001c0001t0001g0154 a0001c0003t0001g0139 a0001c0003t0005g0006 others(31): Show |
45 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.568+487T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417610 | |||||||
| chr11:70417620 | C | T | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.568+497C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417620 | |||||||
| chr11:70417684 | C | T | 1 | a0002c0004t0001g0077 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.568+561C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417684 | |||||||
| chr11:70417685 | G | A | 1 | a0001c0006t0012g0074 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.568+562G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417685 | |||||||
| chr11:70417716 | G | T | 7 | a0002c0004t0001g0077 a0002c0004t0004g0003 a0002c0004t0004g0041 others(4): Show |
14 | HG02109.hp1 HG02572.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.568+593G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417716 | |||||||
| chr11:70417736 | T | TCGCCCTG others(10): Show |
1 | a0001c0001t0001g0189 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.568+615_568+631dup others(17): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr11 | 70417736 | ||||||
| chr11:70417801 | T | C | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.568+678T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70417801 | |||||||
| chr11:70418121 | CA | C | 42 | a0001c0001t0001g0036 a0001c0001t0001g0154 a0001c0001t0001g0181 others(39): Show |
53 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.568+1012delA | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr11 | 70418121 | ||||||
| chr11:70418259 | T | G | 131 | a0001c0001t0001g0098 a0001c0001t0001g0127 a0001c0001t0001g0154 others(128): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.568+1136T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418259 | |||||||
| chr11:70418289 | G | A | 1 | a0001c0003t0006g0137 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.568+1166G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418289 | |||||||
| chr11:70418355 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.568+1232C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418355 | |||||||
| chr11:70418507 | C | T | 1 | a0001c0001t0017g0232 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.569-1239C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418507 | |||||||
| chr11:70418560 | A | G | 2 | a0001c0006t0012g0074 a0001c0006t0012g0075 |
2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.569-1186A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418560 | |||||||
| chr11:70418584 | A | G | 35 | a0001c0001t0001g0154 a0001c0003t0001g0139 a0001c0003t0005g0006 others(32): Show |
46 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.569-1162A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418584 | |||||||
| chr11:70418714 | C | T | 1 | a0001c0003t0006g0142 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.569-1032C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418714 | |||||||
| chr11:70418736 | G | A | 8 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0003g0050 others(5): Show |
8 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.569-1010G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418736 | |||||||
| chr11:70418779 | C | CT | 11 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0003g0050 others(8): Show |
11 | HG02257.hp1 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.569-951dupT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr11 | 70418779 | ||||||
| chr11:70418779 | CT | C | 9 | a0001c0001t0001g0108 a0001c0001t0001g0158 a0001c0001t0001g0159 others(6): Show |
9 | HG00639.hp2 HG01517.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.569-951delT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr11 | 70418779 | ||||||
| chr11:70418801 | G | A | 1 | a0001c0005t0002g0148 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.569-945G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418801 | |||||||
| chr11:70418840 | G | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0151 a0001c0001t0001g0160 others(3): Show |
6 | HG00639.hp1 HG01106.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.569-906G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418840 | |||||||
| chr11:70418869 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.569-877C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418869 | |||||||
| chr11:70418908 | C | T | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.569-838C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70418908 | |||||||
| chr11:70419053 | G | A | 1 | a0001c0002t0002g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.569-693G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70419053 | |||||||
| chr11:70419114 | CT | C | 119 | a0001c0001t0001g0107 a0001c0001t0001g0154 a0001c0001t0001g0157 others(116): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.569-619delT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr11 | 70419114 | ||||||
| chr11:70419132 | T | C | 4 | a0001c0001t0007g0018 a0001c0001t0007g0079 a0001c0001t0007g0080 others(1): Show |
5 | HG02559.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-614T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70419132 | |||||||
| chr11:70419146 | T | G | 13 | a0001c0002t0001g0089 a0001c0002t0001g0091 a0001c0002t0001g0093 others(10): Show |
14 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.569-600T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70419146 | |||||||
| chr11:70419330 | A | G | 33 | a0001c0001t0001g0154 a0001c0003t0001g0139 a0001c0003t0005g0006 others(30): Show |
44 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.569-416A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70419330 | |||||||
| chr11:70419361 | C | A | 2 | a0001c0006t0012g0074 a0001c0006t0012g0075 |
2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.569-385C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70419361 | |||||||
| chr11:70419488 | C | A | 34 | a0001c0001t0001g0154 a0001c0003t0001g0139 a0001c0003t0005g0006 others(31): Show |
45 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.569-258C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70419488 | |||||||
| chr11:70419572 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.569-174T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 8/17 | chr11 | 70419572 | |||||||
| chr11:70419938 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.679+82G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/17 | chr11 | 70419938 | |||||||
| chr11:70420012 | C | A | 1 | a0001c0001t0001g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.679+156C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/17 | chr11 | 70420012 | |||||||
| chr11:70420100 | G | A | 1 | a0001c0002t0002g0081 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.679+244G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/17 | chr11 | 70420100 | |||||||
| chr11:70420140 | G | A | 33 | a0001c0001t0001g0154 a0001c0003t0001g0139 a0001c0003t0005g0006 others(30): Show |
44 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.680-260G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/17 | chr11 | 70420140 | |||||||
| chr11:70420151 | G | T | 1 | a0001c0009t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.680-249G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/17 | chr11 | 70420151 | |||||||
| chr11:70420157 | G | A | 1 | a0001c0001t0001g0029 | 2 | NA19066.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.680-243G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/17 | chr11 | 70420157 | |||||||
| chr11:70420221 | T | G | 1 | a0001c0001t0013g0048 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.680-179T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/17 | chr11 | 70420221 | |||||||
| chr11:70420235 | A | G | 10 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0007g0017 others(7): Show |
11 | HG02055.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.680-165A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/17 | chr11 | 70420235 | |||||||
| chr11:70420336 | A | G | 22 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0003g0050 others(19): Show |
29 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.680-64A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 9/17 | chr11 | 70420336 | |||||||
| chr11:70420520 | C | T | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.790+10C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70420520 | |||||||
| chr11:70420621 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.790+111C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70420621 | |||||||
| chr11:70420736 | C | T | 1 | a0001c0002t0002g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.790+226C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70420736 | |||||||
| chr11:70420752 | C | T | 3 | a0001c0001t0001g0178 a0001c0001t0001g0183 a0001c0001t0024g0213 |
3 | HG00735.hp2 HG01070.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.790+242C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70420752 | |||||||
| chr11:70420772 | G | A | 1 | a0001c0002t0002g0082 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.790+262G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70420772 | |||||||
| chr11:70420817 | G | C | 1 | a0001c0011t0012g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.790+307G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70420817 | |||||||
| chr11:70420835 | G | A | 1 | a0001c0002t0002g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.790+325G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70420835 | |||||||
| chr11:70420920 | A | G | 34 | a0001c0001t0001g0154 a0001c0003t0001g0139 a0001c0003t0005g0006 others(31): Show |
45 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.790+410A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70420920 | |||||||
| chr11:70420987 | G | A | 1 | a0001c0002t0001g0087 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.790+477G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70420987 | |||||||
| chr11:70421063 | C | T | 3 | a0001c0002t0002g0076 a0001c0002t0002g0215 a0001c0002t0002g0216 |
3 | HG02647.hp2 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.791-407C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70421063 | |||||||
| chr11:70421113 | A | G | 25 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(22): Show |
35 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.791-357A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70421113 | |||||||
| chr11:70421141 | A | T | 1 | a0001c0001t0001g0204 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.791-329A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70421141 | |||||||
| chr11:70421164 | G | T | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.791-306G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | chr11 | 70421164 | |||||||
| chr11:70421242 | G | GT | 34 | a0001c0001t0001g0154 a0001c0003t0001g0139 a0001c0003t0005g0006 others(31): Show |
45 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.791-226dupT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr11 | 70421242 | ||||||
| chr11:70421748 | C | G | 1 | a0001c0001t0001g0159 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.901+168C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70421748 | |||||||
| chr11:70421823 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.901+243G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70421823 | |||||||
| chr11:70421877 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.901+297G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70421877 | |||||||
| chr11:70422035 | C | T | 1 | a0001c0001t0007g0080 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.901+455C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70422035 | |||||||
| chr11:70422086 | G | A | 1 | a0001c0003t0005g0065 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.901+506G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70422086 | |||||||
| chr11:70422368 | G | A | 7 | a0001c0002t0001g0004 a0001c0002t0002g0004 a0001c0002t0002g0223 others(4): Show |
11 | HG00280.hp1 HG00733.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.902-572G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70422368 | |||||||
| chr11:70422704 | C | T | 1 | a0001c0001t0007g0080 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.902-236C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70422704 | |||||||
| chr11:70422716 | A | T | 1 | a0001c0001t0007g0080 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.902-224A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70422716 | |||||||
| chr11:70422724 | GC | G | 3 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0013g0048 |
6 | HG02145.hp1 HG02258.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.902-212delC | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr11 | 70422724 | ||||||
| chr11:70422804 | C | T | 32 | a0001c0003t0001g0139 a0001c0003t0005g0006 a0001c0003t0005g0016 others(29): Show |
43 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.902-136C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70422804 | |||||||
| chr11:70422882 | G | A | 1 | a0001c0003t0005g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.902-58G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 11/17 | chr11 | 70422882 | |||||||
| chr11:70423051 | G | T | 1 | a0001c0001t0007g0080 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.957+56G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423051 | |||||||
| chr11:70423080 | C | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0208 a0001c0001t0001g0211 others(2): Show |
7 | HG00438.hp2 HG00544.hp1 HG00621.hp1 others(4): Show |
intron_variant | MODIFIER | c.957+85C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423080 | |||||||
| chr11:70423109 | G | A | 1 | a0001c0002t0002g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.957+114G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423109 | |||||||
| chr11:70423128 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.957+133T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423128 | |||||||
| chr11:70423209 | T | A | 2 | a0001c0006t0012g0074 a0001c0006t0012g0075 |
2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.957+214T>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423209 | |||||||
| chr11:70423370 | T | C | 2 | a0001c0001t0001g0164 a0001c0001t0030g0209 |
2 | NA19001.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.957+375T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423370 | |||||||
| chr11:70423372 | C | G | 2 | a0001c0001t0001g0164 a0001c0001t0030g0209 |
2 | NA19001.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.957+377C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423372 | |||||||
| chr11:70423451 | A | G | 1 | a0001c0003t0006g0142 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.957+456A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423451 | |||||||
| chr11:70423538 | G | A | 1 | a0001c0001t0022g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.957+543G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423538 | |||||||
| chr11:70423670 | G | A | 3 | a0001c0002t0002g0101 a0001c0002t0002g0207 a0001c0002t0009g0118 |
3 | NA18950.hp1 NA18977.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.957+675G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423670 | |||||||
| chr11:70423671 | T | G | 62 | a0001c0001t0001g0098 a0001c0001t0003g0046 a0001c0001t0003g0047 others(59): Show |
73 | HG00280.hp1 HG00558.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.957+676T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423671 | |||||||
| chr11:70423781 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0169 others(3): Show |
7 | HG00738.hp1 HG01346.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.957+786G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423781 | |||||||
| chr11:70423783 | C | T | 3 | a0001c0003t0006g0024 a0001c0003t0006g0128 a0001c0003t0036g0129 |
4 | HG02083.hp2 NA18953.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.957+788C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423783 | |||||||
| chr11:70423816 | C | T | 1 | a0001c0002t0002g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.957+821C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70423816 | |||||||
| chr11:70424037 | G | A | 3 | a0001c0001t0007g0017 a0001c0001t0007g0072 a0001c0001t0015g0017 |
3 | HG02055.hp2 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.957+1042G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424037 | |||||||
| chr11:70424114 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0016g0030 a0001c0001t0016g0165 |
3 | HG01496.hp1 HG02109.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.957+1119G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424114 | |||||||
| chr11:70424121 | T | G | 5 | a0001c0001t0021g0229 a0001c0001t0022g0234 a0001c0006t0012g0074 others(2): Show |
5 | HG03225.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.957+1126T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424121 | |||||||
| chr11:70424356 | G | A | 1 | a0001c0003t0019g0057 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.958-976G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424356 | |||||||
| chr11:70424360 | G | A | 1 | a0001c0009t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.958-972G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424360 | |||||||
| chr11:70424496 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(246): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.958-836A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424496 | |||||||
| chr11:70424538 | A | G | 34 | a0001c0001t0001g0154 a0001c0003t0001g0139 a0001c0003t0005g0006 others(31): Show |
45 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.958-794A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424538 | |||||||
| chr11:70424737 | G | T | 2 | a0001c0001t0021g0229 a0001c0001t0022g0234 |
2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.958-595G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424737 | |||||||
| chr11:70424859 | C | A | 1 | a0002c0004t0004g0100 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.958-473C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424859 | |||||||
| chr11:70424892 | G | A | 1 | a0001c0001t0003g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.958-440G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70424892 | |||||||
| chr11:70425175 | T | G | 1 | a0001c0011t0012g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.958-157T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 12/17 | chr11 | 70425175 | |||||||
| chr11:70425522 | G | A | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1027+121G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70425522 | |||||||
| chr11:70425590 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1027+189C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70425590 | |||||||
| chr11:70425598 | C | T | 3 | a0001c0002t0002g0076 a0001c0002t0002g0215 a0001c0002t0002g0216 |
3 | HG02647.hp2 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1027+197C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70425598 | |||||||
| chr11:70425614 | C | T | 4 | a0002c0004t0004g0022 a0002c0004t0004g0099 a0002c0004t0004g0100 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027+213C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70425614 | |||||||
| chr11:70425821 | G | A | 33 | a0001c0001t0001g0154 a0001c0003t0001g0139 a0001c0003t0005g0006 others(30): Show |
44 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.1027+420G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70425821 | |||||||
| chr11:70425936 | A | G | 37 | a0001c0001t0001g0154 a0001c0001t0001g0177 a0001c0001t0001g0220 others(34): Show |
48 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.1027+535A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70425936 | |||||||
| chr11:70426164 | T | C | 2 | a0001c0006t0012g0074 a0001c0006t0012g0075 |
2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1027+763T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426164 | |||||||
| chr11:70426223 | C | T | 31 | a0001c0001t0001g0154 a0001c0003t0005g0006 a0001c0003t0005g0016 others(28): Show |
42 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1027+822C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426223 | |||||||
| chr11:70426302 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1027+901T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426302 | |||||||
| chr11:70426392 | C | T | 1 | a0001c0003t0006g0024 | 2 | HG02083.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1027+991C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426392 | |||||||
| chr11:70426406 | G | A | 1 | a0001c0002t0002g0121 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1027+1005G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426406 | |||||||
| chr11:70426410 | C | CA | 14 | a0001c0001t0001g0109 a0001c0001t0001g0189 a0001c0001t0003g0050 others(11): Show |
14 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.1027+1025dupA | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr11 | 70426410 | ||||||
| chr11:70426413 | A | G | 1 | a0001c0001t0013g0048 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1027+1012A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426413 | |||||||
| chr11:70426646 | G | A | 1 | a0001c0009t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1027+1245G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426646 | |||||||
| chr11:70426668 | C | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0034 others(7): Show |
15 | HG00544.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.1027+1267C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426668 | |||||||
| chr11:70426781 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1027+1380T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426781 | |||||||
| chr11:70426785 | A | G | 1 | a0001c0002t0002g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1027+1384A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426785 | |||||||
| chr11:70426801 | C | T | 1 | a0001c0001t0023g0149 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1027+1400C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426801 | |||||||
| chr11:70426822 | G | T | 2 | a0001c0001t0003g0046 a0001c0001t0003g0047 |
2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1027+1421G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426822 | |||||||
| chr11:70426895 | C | T | 34 | a0001c0001t0001g0154 a0001c0001t0001g0177 a0001c0001t0001g0220 others(31): Show |
45 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1027+1494C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70426895 | |||||||
| chr11:70427030 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1027+1629A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427030 | |||||||
| chr11:70427065 | C | T | 5 | a0001c0001t0021g0229 a0001c0001t0022g0234 a0001c0006t0012g0074 others(2): Show |
5 | HG03225.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027+1664C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427065 | |||||||
| chr11:70427087 | T | C | 132 | a0001c0001t0001g0098 a0001c0001t0001g0154 a0001c0001t0001g0177 others(129): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1027+1686T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427087 | |||||||
| chr11:70427090 | C | T | 1 | a0001c0003t0005g0065 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1027+1689C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427090 | |||||||
| chr11:70427150 | G | C | 1 | a0001c0001t0003g0046 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1027+1749G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427150 | |||||||
| chr11:70427195 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0030g0209 |
2 | NA19001.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1027+1794C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427195 | |||||||
| chr11:70427342 | T | G | 2 | a0001c0001t0001g0169 a0001c0001t0025g0168 |
2 | HG01515.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1028-1709T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427342 | |||||||
| chr11:70427395 | T | G | 1 | a0001c0001t0003g0015 | 2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1028-1656T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427395 | |||||||
| chr11:70427436 | T | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0175 |
3 | HG01981.hp1 NA19066.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1028-1615T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427436 | |||||||
| chr11:70427484 | C | T | 1 | a0001c0001t0013g0048 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1028-1567C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427484 | |||||||
| chr11:70427506 | G | A | 7 | a0002c0004t0001g0077 a0002c0004t0004g0003 a0002c0004t0004g0041 others(4): Show |
14 | HG02109.hp1 HG02572.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1028-1545G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427506 | |||||||
| chr11:70427524 | G | T | 5 | a0001c0001t0021g0229 a0001c0001t0022g0234 a0001c0006t0012g0074 others(2): Show |
5 | HG03225.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1028-1527G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427524 | |||||||
| chr11:70427654 | C | T | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1028-1397C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427654 | |||||||
| chr11:70427665 | C | T | 3 | a0001c0002t0001g0091 a0001c0002t0001g0093 a0001c0002t0032g0092 |
3 | HG01074.hp2 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1028-1386C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427665 | |||||||
| chr11:70427800 | A | T | 1 | a0002c0004t0002g0103 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1028-1251A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70427800 | |||||||
| chr11:70427893 | AT | A | 35 | a0001c0001t0001g0154 a0001c0001t0001g0177 a0001c0001t0001g0220 others(32): Show |
46 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1028-1154delT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr11 | 70427893 | ||||||
| chr11:70428042 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1028-1009A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428042 | |||||||
| chr11:70428085 | G | T | 41 | a0001c0001t0001g0154 a0001c0001t0001g0177 a0001c0001t0001g0220 others(38): Show |
52 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1028-966G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428085 | |||||||
| chr11:70428120 | G | A | 1 | a0002c0004t0002g0103 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1028-931G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428120 | |||||||
| chr11:70428153 | C | CT | 4 | a0001c0001t0001g0013 a0001c0001t0001g0226 a0001c0001t0002g0196 others(1): Show |
6 | HG00733.hp2 HG01952.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1028-867dupT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr11 | 70428153 | ||||||
| chr11:70428153 | CT | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(80): Show |
104 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1028-867delT | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr11 | 70428153 | ||||||
| chr11:70428153 | CTT | C | 48 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0131 others(45): Show |
61 | HG00280.hp1 HG00558.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.1028-868_1028-867d others(4): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr11 | 70428153 | ||||||
| chr11:70428153 | CTTT | C | 38 | a0001c0001t0001g0127 a0001c0001t0001g0154 a0001c0001t0001g0177 others(35): Show |
45 | HG00099.hp1 HG00735.hp1 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.1028-869_1028-867d others(5): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr11 | 70428153 | ||||||
| chr11:70428153 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0003g0052 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1028-876_1028-867d others(12): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr11 | 70428153 | ||||||
| chr11:70428153 | CTTTTTTT others(4): Show |
C | 24 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(21): Show |
34 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1028-877_1028-867d others(13): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr11 | 70428153 | ||||||
| chr11:70428184 | T | G | 1 | a0001c0009t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1028-867T>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428184 | |||||||
| chr11:70428290 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1028-761C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428290 | |||||||
| chr11:70428293 | G | C | 2 | a0001c0006t0012g0074 a0001c0006t0012g0075 |
2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1028-758G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428293 | |||||||
| chr11:70428385 | T | C | 35 | a0001c0001t0001g0154 a0001c0001t0001g0177 a0001c0001t0001g0220 others(32): Show |
46 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1028-666T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428385 | |||||||
| chr11:70428406 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1028-645C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428406 | |||||||
| chr11:70428468 | T | C | 1 | a0001c0001t0022g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1028-583T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428468 | |||||||
| chr11:70428636 | A | T | 35 | a0001c0001t0001g0154 a0001c0001t0001g0177 a0001c0001t0001g0220 others(32): Show |
46 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1028-415A>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428636 | |||||||
| chr11:70428660 | G | A | 1 | a0001c0001t0014g0235 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1028-391G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428660 | |||||||
| chr11:70428794 | C | T | 1 | a0001c0009t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1028-257C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428794 | |||||||
| chr11:70428795 | G | A | 1 | a0001c0001t0022g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1028-256G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428795 | |||||||
| chr11:70428847 | C | T | 1 | a0001c0001t0002g0172 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1028-204C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428847 | |||||||
| chr11:70428873 | T | C | 36 | a0001c0001t0001g0154 a0001c0001t0001g0177 a0001c0001t0001g0220 others(33): Show |
47 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1028-178T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 13/17 | chr11 | 70428873 | |||||||
| chr11:70429203 | A | G | 7 | a0002c0004t0001g0077 a0002c0004t0004g0003 a0002c0004t0004g0041 others(4): Show |
14 | HG02109.hp1 HG02572.hp2 HG02630.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.1176+4A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429203 | |||||||
| chr11:70429409 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1176+210C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429409 | |||||||
| chr11:70429410 | G | A | 1 | a0001c0001t0026g0117 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1176+211G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429410 | |||||||
| chr11:70429417 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1176+218G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429417 | |||||||
| chr11:70429438 | C | T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0025 others(10): Show |
15 | HG00408.hp2 HG00673.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1176+239C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429438 | |||||||
| chr11:70429528 | A | G | 1 | a0001c0002t0032g0092 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1176+329A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429528 | |||||||
| chr11:70429532 | G | A | 7 | a0002c0004t0001g0077 a0002c0004t0004g0003 a0002c0004t0004g0041 others(4): Show |
14 | HG02109.hp1 HG02572.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1176+333G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429532 | |||||||
| chr11:70429538 | C | T | 1 | a0001c0001t0015g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1176+339C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429538 | |||||||
| chr11:70429668 | G | A | 63 | a0001c0001t0001g0098 a0001c0001t0003g0046 a0001c0001t0003g0047 others(60): Show |
74 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1176+469G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429668 | |||||||
| chr11:70429702 | C | T | 1 | a0001c0002t0009g0224 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1176+503C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429702 | |||||||
| chr11:70429793 | C | T | 52 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0039 others(49): Show |
62 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1176+594C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429793 | |||||||
| chr11:70429826 | A | AC | 6 | a0001c0001t0001g0028 a0001c0001t0001g0151 a0001c0001t0001g0160 others(3): Show |
6 | HG00639.hp1 HG01106.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1176+627_1176+628i others(3): Show |
CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429826 | |||||||
| chr11:70429869 | G | T | 34 | a0001c0001t0001g0154 a0001c0001t0001g0177 a0001c0001t0001g0220 others(31): Show |
45 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1176+670G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429869 | |||||||
| chr11:70429874 | G | A | 1 | a0002c0004t0004g0100 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1176+675G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429874 | |||||||
| chr11:70429903 | A | G | 41 | a0001c0001t0001g0154 a0001c0001t0001g0177 a0001c0001t0001g0220 others(38): Show |
52 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1176+704A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70429903 | |||||||
| chr11:70430089 | C | T | 2 | a0001c0001t0021g0229 a0001c0001t0022g0234 |
2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1176+890C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430089 | |||||||
| chr11:70430090 | G | A | 1 | a0001c0001t0007g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1176+891G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430090 | |||||||
| chr11:70430157 | C | T | 7 | a0002c0004t0001g0077 a0002c0004t0004g0003 a0002c0004t0004g0041 others(4): Show |
14 | HG02109.hp1 HG02572.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1176+958C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430157 | |||||||
| chr11:70430171 | C | T | 1 | a0001c0009t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1176+972C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430171 | |||||||
| chr11:70430240 | T | C | 40 | a0001c0001t0001g0177 a0001c0001t0001g0220 a0001c0001t0021g0229 others(37): Show |
51 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1177-951T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430240 | |||||||
| chr11:70430373 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1177-818T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430373 | |||||||
| chr11:70430390 | G | A | 36 | a0001c0001t0001g0177 a0001c0001t0001g0220 a0001c0001t0021g0229 others(33): Show |
47 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1177-801G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430390 | |||||||
| chr11:70430609 | C | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0226 |
2 | HG02074.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.1177-582C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430609 | |||||||
| chr11:70430629 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1177-562G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430629 | |||||||
| chr11:70430667 | T | A | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1177-524T>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430667 | |||||||
| chr11:70430712 | C | T | 52 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0039 others(49): Show |
62 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1177-479C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430712 | |||||||
| chr11:70430723 | C | T | 13 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0144 others(10): Show |
15 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.1177-468C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430723 | |||||||
| chr11:70430789 | A | G | 4 | a0001c0002t0002g0019 a0001c0002t0002g0020 a0001c0002t0002g0082 others(1): Show |
5 | HG01070.hp1 HG01071.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1177-402A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430789 | |||||||
| chr11:70430880 | C | T | 1 | a0001c0002t0001g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1177-311C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430880 | |||||||
| chr11:70430885 | C | T | 1 | a0001c0001t0014g0235 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1177-306C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430885 | |||||||
| chr11:70430911 | G | A | 1 | a0001c0001t0016g0165 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1177-280G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430911 | |||||||
| chr11:70430948 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1177-243G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 14/17 | chr11 | 70430948 | |||||||
| chr11:70431312 | G | C | 1 | a0001c0001t0001g0208 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1266+32G>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70431312 | |||||||
| chr11:70431366 | G | A | 1 | a0001c0002t0020g0058 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1266+86G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70431366 | |||||||
| chr11:70431377 | T | C | 1 | a0001c0002t0033g0122 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1266+97T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70431377 | |||||||
| chr11:70431411 | G | A | 1 | a0001c0011t0012g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1266+131G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70431411 | |||||||
| chr11:70431536 | C | G | 9 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0003g0050 others(6): Show |
9 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1266+256C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70431536 | |||||||
| chr11:70431681 | C | T | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1266+401C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70431681 | |||||||
| chr11:70431793 | C | T | 3 | a0001c0002t0002g0101 a0001c0002t0002g0207 a0001c0002t0009g0118 |
3 | NA18950.hp1 NA18977.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1266+513C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70431793 | |||||||
| chr11:70431983 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1266+703T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70431983 | |||||||
| chr11:70432081 | G | A | 1 | a0001c0009t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1266+801G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432081 | |||||||
| chr11:70432144 | A | G | 29 | a0001c0003t0005g0006 a0001c0003t0005g0016 a0001c0003t0005g0055 others(26): Show |
40 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1266+864A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432144 | |||||||
| chr11:70432145 | C | T | 127 | a0001c0001t0001g0098 a0001c0001t0003g0010 a0001c0001t0003g0015 others(124): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1266+865C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432145 | |||||||
| chr11:70432271 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1267-830A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432271 | |||||||
| chr11:70432280 | C | T | 2 | a0001c0006t0012g0074 a0001c0006t0012g0075 |
2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1267-821C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432280 | |||||||
| chr11:70432304 | C | A | 1 | a0001c0009t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1267-797C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432304 | |||||||
| chr11:70432369 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1267-732C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432369 | |||||||
| chr11:70432459 | C | A | 64 | a0001c0001t0001g0098 a0001c0001t0003g0046 a0001c0001t0003g0047 others(61): Show |
75 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1267-642C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432459 | |||||||
| chr11:70432461 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1267-640G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432461 | |||||||
| chr11:70432467 | A | G | 31 | a0001c0003t0005g0006 a0001c0003t0005g0016 a0001c0003t0005g0055 others(28): Show |
42 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1267-634A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432467 | |||||||
| chr11:70432510 | G | T | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1267-591G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432510 | |||||||
| chr11:70432557 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0160 a0001c0001t0002g0028 |
3 | HG02145.hp2 HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1267-544G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432557 | |||||||
| chr11:70432565 | T | A | 1 | a0001c0003t0008g0062 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1267-536T>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432565 | |||||||
| chr11:70432651 | C | T | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1267-450C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432651 | |||||||
| chr11:70432689 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1267-412A>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432689 | |||||||
| chr11:70432729 | T | C | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1267-372T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432729 | |||||||
| chr11:70432732 | G | A | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1267-369G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432732 | |||||||
| chr11:70432786 | G | A | 1 | a0001c0003t0005g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1267-315G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432786 | |||||||
| chr11:70432799 | C | G | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1267-302C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432799 | |||||||
| chr11:70432873 | C | A | 1 | a0004c0008t0004g0231 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1267-228C>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432873 | |||||||
| chr11:70432982 | G | A | 22 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0003g0050 others(19): Show |
29 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1267-119G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432982 | |||||||
| chr11:70432995 | C | G | 1 | a0001c0001t0001g0188 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1267-106C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70432995 | |||||||
| chr11:70433012 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1267-89C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 15/17 | chr11 | 70433012 | |||||||
| chr11:70433359 | G | T | 25 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(22): Show |
35 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1444+81G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 16/17 | chr11 | 70433359 | |||||||
| chr11:70433365 | C | T | 1 | a0001c0009t0001g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1444+87C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 16/17 | chr11 | 70433365 | |||||||
| chr11:70433366 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1444+88G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 16/17 | chr11 | 70433366 | |||||||
| chr11:70433521 | G | A | 25 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(22): Show |
35 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1445-126G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 16/17 | chr11 | 70433521 | |||||||
| chr11:70433821 | G | A | 60 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(57): Show |
81 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.1516+103G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70433821 | |||||||
| chr11:70433832 | T | C | 10 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0007g0017 others(7): Show |
11 | HG02055.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1516+114T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70433832 | |||||||
| chr11:70433883 | C | G | 1 | a0001c0002t0002g0225 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1516+165C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70433883 | |||||||
| chr11:70433890 | C | G | 1 | a0001c0006t0012g0074 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1516+172C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70433890 | |||||||
| chr11:70434136 | A | G | 35 | a0001c0001t0021g0229 a0001c0001t0022g0234 a0001c0003t0005g0006 others(32): Show |
46 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1516+418A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434136 | |||||||
| chr11:70434168 | A | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0174 |
2 | HG02027.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1516+450A>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434168 | |||||||
| chr11:70434206 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1516+488C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434206 | |||||||
| chr11:70434216 | G | A | 1 | a0001c0002t0002g0123 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1516+498G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434216 | |||||||
| chr11:70434255 | G | A | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1516+537G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434255 | |||||||
| chr11:70434297 | C | T | 7 | a0001c0001t0001g0164 a0001c0001t0001g0171 a0001c0001t0001g0191 others(4): Show |
7 | HG00597.hp2 HG00609.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1516+579C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434297 | |||||||
| chr11:70434430 | G | A | 1 | a0001c0002t0009g0086 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1517-596G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434430 | |||||||
| chr11:70434630 | G | A | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1517-396G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434630 | |||||||
| chr11:70434696 | C | G | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1517-330C>G | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434696 | |||||||
| chr11:70434706 | C | T | 10 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0003g0050 others(7): Show |
10 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1517-320C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434706 | |||||||
| chr11:70434708 | C | T | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1517-318C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434708 | |||||||
| chr11:70434787 | G | A | 30 | a0001c0003t0005g0006 a0001c0003t0005g0016 a0001c0003t0005g0055 others(27): Show |
41 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1517-239G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434787 | |||||||
| chr11:70434886 | G | A | 63 | a0001c0001t0001g0098 a0001c0001t0003g0046 a0001c0001t0003g0047 others(60): Show |
74 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1517-140G>A | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434886 | |||||||
| chr11:70434895 | C | T | 1 | a0001c0002t0002g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1517-131C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434895 | |||||||
| chr11:70434900 | G | T | 1 | a0001c0013t0013g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1517-126G>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434900 | |||||||
| chr11:70434901 | T | C | 62 | a0001c0001t0003g0010 a0001c0001t0003g0015 a0001c0001t0003g0044 others(59): Show |
83 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.1517-125T>C | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434901 | |||||||
| chr11:70434977 | C | T | 3 | a0001c0001t0014g0233 a0001c0001t0014g0235 a0001c0001t0017g0232 |
3 | HG02451.hp2 HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1517-49C>T | CTTN | ENSG00000085733.16 | transcript | ENST00000301843.13 | protein_coding | 17/17 | chr11 | 70434977 |