Variant report
Variant | rs2460050 |
---|---|
Chromosome Location | chr11:93754227-93754228 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:9)
- CpG islands (count:61)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:9 , 50 per page) page:
1
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | STAT3 | chr11:93754178-93754570 | MCF10A-Er-Src | breast: | n/a | n/a |
2 | FOS | chr11:93754053-93754495 | MCF10A-Er-Src | breast: | n/a | n/a |
3 | FOS | chr11:93754169-93754442 | MCF10A-Er-Src | breast: | n/a | n/a |
4 | STAT3 | chr11:93754057-93754526 | MCF10A-Er-Src | breast: | n/a | n/a |
5 | SETDB1 | chr11:93753956-93754348 | U2OS | brain: | n/a | n/a |
6 | FOS | chr11:93753967-93754496 | MCF10A-Er-Src | breast: | n/a | n/a |
7 | KAP1 | chr11:93754006-93754272 | U2OS | brain: | n/a | n/a |
8 | MYC | chr11:93754199-93754466 | MCF10A-Er-Src | breast: | n/a | n/a |
9 | STAT3 | chr11:93754053-93754526 | MCF10A-Er-Src | breast: | n/a | n/a |
No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr11:93754223-93754273 | Caco-2 | colon: | n/a |
2 | chr11:93754223-93754273 | MCF-7 | breast: | n/a |
3 | chr11:93754223-93754273 | HRE | kidney: | n/a |
4 | chr11:93754223-93754273 | AG09309 | skin: | n/a |
5 | chr11:93754223-93754273 | NHBE | bronchial: | n/a |
6 | chr11:93754223-93754273 | Hepatocyte | liver: | n/a |
7 | chr11:93754223-93754273 | H1-hESC | embryonic stem cell: | embryo |
8 | chr11:93754223-93754273 | SKMC | muscle: | n/a |
9 | chr11:93754223-93754273 | HNPCEpiC | eye: | n/a |
10 | chr11:93754223-93754273 | ovcar-3 | ovarian: | n/a |
11 | chr11:93754223-93754273 | AG09319 | gingival: | n/a |
12 | chr11:93754223-93754273 | HCPEpiC | choroid plexus: | n/a |
13 | chr11:93754223-93754273 | GM12878 | blood: | n/a |
14 | chr11:93754223-93754273 | AG04449 | skin: | fetal |
15 | chr11:93754223-93754273 | HCT-116 | colon: | n/a |
16 | chr11:93754223-93754273 | GM12891 | blood: | n/a |
17 | chr11:93754223-93754273 | PANC-1 | pancreas: | n/a |
18 | chr11:93754223-93754273 | PFSK-1 | brain: | n/a |
19 | chr11:93754223-93754273 | SK-N-SH | brain: | n/a |
20 | chr11:93754223-93754273 | U87 | brain: | n/a |
21 | chr11:93754223-93754273 | HCF | heart: | n/a |
22 | chr11:93754223-93754273 | HIPEpiC | eye: | n/a |
23 | chr11:93754223-93754273 | HEK293 | kidney: | embryo |
24 | chr11:93754223-93754273 | NT2-D1 | testis: | n/a |
25 | chr11:93754223-93754273 | PrEC | prostate: | n/a |
26 | chr11:93754223-93754273 | HCM | heart: | n/a |
27 | chr11:93754223-93754273 | K562 | blood: | n/a |
28 | chr11:93754223-93754273 | HUVEC | blood vessel: | n/a |
29 | chr11:93754223-93754273 | NB4 | blood: | n/a |
30 | chr11:93754223-93754273 | BJ | skin: | n/a |
31 | chr11:93754223-93754273 | GM19239 | blood: | n/a |
32 | chr11:93754223-93754273 | ProgFib | skin: | n/a |
33 | chr11:93754223-93754273 | GM06990 | blood: | n/a |
34 | chr11:93754223-93754273 | AoSMC | blood vessel: | n/a |
35 | chr11:93754223-93754273 | MCF10A-Er-Src | breast: | n/a |
36 | chr11:93754223-93754273 | SAEC | small airway: | n/a |
37 | chr11:93754223-93754273 | HRPEpiC | eye: | n/a |
38 | chr11:93754223-93754273 | Jurkat | blood: | n/a |
39 | chr11:93754223-93754273 | IMR90 | lung: | fetal |
40 | chr11:93754223-93754273 | AG10803 | skin: | n/a |
41 | chr11:93754223-93754273 | GM12892 | blood: | n/a |
42 | chr11:93754223-93754273 | SK-N-SH_RA | brain: | n/a |
43 | chr11:93754223-93754273 | HAEpiC | amniotic membrane: | n/a |
44 | chr11:93754223-93754273 | HEEpiC | esophagus: | n/a |
45 | chr11:93754223-93754273 | NH-A | brain: | n/a |
46 | chr11:93754223-93754273 | A549 | lung: | n/a |
47 | chr11:93754223-93754273 | BE2_C | brain: | n/a |
48 | chr11:93754223-93754273 | CMK | blood: | n/a |
49 | chr11:93754223-93754273 | LNCaP | prostate: | n/a |
50 | chr11:93754223-93754273 | AG04450 | lung: | fetal |
No data |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
HEPHL1 | TF binding region |
HEPHL1 | CpG island |
rs_ID | r2[population] |
---|---|
rs10501813 | 0.95[ASN][1000 genomes] |
rs11820915 | 0.83[EUR][1000 genomes] |
rs11823303 | 0.85[EUR][1000 genomes] |
rs11825709 | 0.90[ASN][1000 genomes] |
rs11828737 | 0.83[EUR][1000 genomes] |
rs1401184 | 0.95[ASN][1000 genomes] |
rs1518560 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1518565 | 0.82[EUR][1000 genomes] |
rs1518566 | 0.82[EUR][1000 genomes] |
rs1568259 | 0.83[EUR][1000 genomes] |
rs1589166 | 0.95[ASN][1000 genomes] |
rs1607401 | 0.95[ASN][1000 genomes] |
rs16919810 | 0.85[EUR][1000 genomes] |
rs16919815 | 0.85[EUR][1000 genomes] |
rs16919858 | 0.81[EUR][1000 genomes] |
rs1850656 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1894165 | 0.95[ASN][1000 genomes] |
rs1894166 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1914723 | 0.83[EUR][1000 genomes] |
rs1945786 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1945787 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2020351 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2102857 | 0.95[ASN][1000 genomes] |
rs2139089 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2176563 | 0.95[ASN][1000 genomes] |
rs2203793 | 0.95[ASN][1000 genomes] |
rs2213108 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs2213110 | 0.93[ASN][1000 genomes] |
rs2399749 | 0.83[EUR][1000 genomes] |
rs2399750 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs2456556 | 0.89[EUR][1000 genomes] |
rs2460049 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs2460052 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs2460053 | 0.95[ASN][1000 genomes] |
rs2460064 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2460065 | 0.95[ASN][1000 genomes] |
rs2460069 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2460070 | 0.95[ASN][1000 genomes] |
rs2462733 | 0.95[ASN][1000 genomes] |
rs2462735 | 0.95[ASN][1000 genomes] |
rs2462756 | 0.94[ASN][1000 genomes] |
rs2462757 | 0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs2462758 | 0.95[ASN][1000 genomes] |
rs2462759 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2462760 | 0.94[ASN][1000 genomes] |
rs2462763 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2511380 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2511381 | 0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs2511403 | 0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs2511411 | 0.95[ASN][1000 genomes] |
rs4415716 | 0.83[EUR][1000 genomes] |
rs56355412 | 0.83[EUR][1000 genomes] |
rs56938392 | 0.94[ASN][1000 genomes] |
rs57106172 | 0.90[ASN][1000 genomes] |
rs57586533 | 0.90[ASN][1000 genomes] |
rs57953549 | 0.84[ASN][1000 genomes] |
rs59689949 | 0.90[ASN][1000 genomes] |
rs59793398 | 0.94[ASN][1000 genomes] |
rs66514329 | 0.95[ASN][1000 genomes] |
rs66523751 | 0.82[ASN][1000 genomes] |
rs66538341 | 0.90[ASN][1000 genomes] |
rs66977226 | 0.90[ASN][1000 genomes] |
rs67001808 | 0.94[ASN][1000 genomes] |
rs67243356 | 0.90[ASN][1000 genomes] |
rs67412659 | 0.94[ASN][1000 genomes] |
rs67988338 | 0.90[ASN][1000 genomes] |
rs7107851 | 0.85[EUR][1000 genomes] |
rs72964631 | 0.94[ASN][1000 genomes] |
rs72964645 | 0.94[ASN][1000 genomes] |
rs72964666 | 0.95[ASN][1000 genomes] |
rs72964672 | 0.81[EUR][1000 genomes] |
rs72964674 | 0.83[EUR][1000 genomes] |
rs72964683 | 0.83[EUR][1000 genomes] |
rs72964690 | 0.83[EUR][1000 genomes] |
rs72964693 | 0.83[EUR][1000 genomes] |
rs72966608 | 0.85[EUR][1000 genomes] |
rs72966612 | 0.83[EUR][1000 genomes] |
rs72966637 | 0.85[EUR][1000 genomes] |
rs73551180 | 0.82[ASN][1000 genomes] |
rs73564796 | 0.94[ASN][1000 genomes] |
rs73564799 | 0.94[ASN][1000 genomes] |
rs959342 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs959343 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs978777 | 0.94[ASN][1000 genomes] |
rs989088 | 0.95[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1049467 | chr11:93651025-93778717 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv898183 | chr11:93725384-93906735 | Strong transcription Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
3 | nsv898184 | chr11:93741612-93969726 | Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:93749600-93754400 | Enhancers | HMEC | breast |
2 | chr11:93750400-93754800 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr11:93752200-93758000 | Weak transcription | NH-A | brain |
4 | chr11:93753800-93755800 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
5 | chr11:93753800-93756200 | Flanking Active TSS | NHEK | skin |
6 | chr11:93754000-93756200 | Enhancers | Breast Myoepithelial Primary Cells | Breast |
7 | chr11:93754200-93754800 | Flanking Active TSS | Foreskin Keratinocyte Primary Cells skin02 | Skin |
8 | chr11:93754200-93754800 | Flanking Active TSS | Foreskin Keratinocyte Primary Cells skin03 | Skin |
9 | chr11:93754200-93754800 | Enhancers | Aorta | Aorta |