Variant report
Variant | rs7157931 |
---|---|
Chromosome Location | chr14:37781926-37781927 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr14:37781292..37783643-chr14:37787358..37789012,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1005539 | 1.00[EUR][1000 genomes] |
rs1005540 | 1.00[EUR][1000 genomes] |
rs10129341 | 1.00[EUR][1000 genomes] |
rs10132652 | 1.00[EUR][1000 genomes] |
rs10132727 | 1.00[ASW][hapmap];1.00[MEX][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10134469 | 1.00[ASW][hapmap] |
rs10134672 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10135014 | 0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10136240 | 1.00[ASW][hapmap];0.82[LWK][hapmap];1.00[EUR][1000 genomes] |
rs10137554 | 1.00[EUR][1000 genomes] |
rs10140854 | 0.87[YRI][hapmap] |
rs10141822 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10143648 | 1.00[ASW][hapmap] |
rs10144237 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10144304 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10145246 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10146919 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10148472 | 1.00[ASW][hapmap];0.87[YRI][hapmap] |
rs1014880 | 0.82[LWK][hapmap];1.00[EUR][1000 genomes] |
rs10150559 | 1.00[ASW][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10782385 | 1.00[ASW][hapmap] |
rs10782386 | 1.00[EUR][1000 genomes] |
rs11845464 | 0.87[EUR][1000 genomes] |
rs11846576 | 0.87[EUR][1000 genomes] |
rs11848827 | 1.00[EUR][1000 genomes] |
rs11849999 | 1.00[EUR][1000 genomes] |
rs12434053 | 1.00[EUR][1000 genomes] |
rs12437318 | 1.00[EUR][1000 genomes] |
rs12586942 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12717263 | 1.00[EUR][1000 genomes] |
rs12879622 | 1.00[CEU][hapmap] |
rs1474885 | 0.87[YRI][hapmap] |
rs1474887 | 0.88[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1474888 | 0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1546973 | 1.00[EUR][1000 genomes] |
rs1884406 | 1.00[ASW][hapmap];0.82[LWK][hapmap] |
rs1950516 | 0.87[YRI][hapmap] |
rs1950518 | 1.00[EUR][1000 genomes] |
rs1950525 | 1.00[EUR][1000 genomes] |
rs1950528 | 1.00[EUR][1000 genomes] |
rs1950535 | 1.00[EUR][1000 genomes] |
rs1950888 | 0.82[YRI][hapmap] |
rs1955931 | 1.00[ASW][hapmap];0.87[YRI][hapmap] |
rs1955932 | 1.00[EUR][1000 genomes] |
rs1955933 | 1.00[EUR][1000 genomes] |
rs1955935 | 1.00[EUR][1000 genomes] |
rs1955937 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1955941 | 1.00[ASW][hapmap] |
rs1955948 | 1.00[ASW][hapmap];0.87[YRI][hapmap] |
rs1955953 | 0.82[LWK][hapmap];1.00[EUR][1000 genomes] |
rs1955954 | 1.00[EUR][1000 genomes] |
rs1955955 | 0.87[YRI][hapmap] |
rs1955956 | 1.00[EUR][1000 genomes] |
rs1956517 | 1.00[EUR][1000 genomes] |
rs1998019 | 1.00[EUR][1000 genomes] |
rs2103891 | 0.87[YRI][hapmap] |
rs2103893 | 1.00[ASW][hapmap];0.82[LWK][hapmap] |
rs2144582 | 1.00[EUR][1000 genomes] |
rs2180252 | 1.00[EUR][1000 genomes] |
rs2180253 | 1.00[EUR][1000 genomes] |
rs2207861 | 1.00[EUR][1000 genomes] |
rs2207863 | 1.00[EUR][1000 genomes] |
rs2224155 | 1.00[EUR][1000 genomes] |
rs2224157 | 1.00[EUR][1000 genomes] |
rs2224344 | 1.00[ASW][hapmap] |
rs2415390 | 0.87[EUR][1000 genomes] |
rs2415392 | 1.00[EUR][1000 genomes] |
rs2415394 | 1.00[EUR][1000 genomes] |
rs2415395 | 1.00[EUR][1000 genomes] |
rs2899856 | 1.00[EUR][1000 genomes] |
rs2899858 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs34172996 | 1.00[EUR][1000 genomes] |
rs41307090 | 1.00[EUR][1000 genomes] |
rs4522332 | 1.00[EUR][1000 genomes] |
rs4898593 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4900779 | 1.00[EUR][1000 genomes] |
rs4900823 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4900834 | 1.00[ASW][hapmap];0.82[LWK][hapmap];1.00[EUR][1000 genomes] |
rs4900867 | 0.87[YRI][hapmap] |
rs57167835 | 0.87[EUR][1000 genomes] |
rs57900485 | 0.87[EUR][1000 genomes] |
rs58520096 | 1.00[EUR][1000 genomes] |
rs59258105 | 1.00[EUR][1000 genomes] |
rs59542560 | 0.87[EUR][1000 genomes] |
rs59544181 | 0.87[EUR][1000 genomes] |
rs60287404 | 1.00[EUR][1000 genomes] |
rs6420826 | 0.95[AFR][1000 genomes] |
rs6571804 | 1.00[EUR][1000 genomes] |
rs6571805 | 1.00[EUR][1000 genomes] |
rs6571809 | 1.00[EUR][1000 genomes] |
rs7142072 | 1.00[ASW][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];0.88[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7142933 | 1.00[EUR][1000 genomes] |
rs7143412 | 1.00[EUR][1000 genomes] |
rs7145905 | 1.00[ASW][hapmap] |
rs7146631 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7150214 | 1.00[ASW][hapmap];0.87[LWK][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7150986 | 0.87[EUR][1000 genomes] |
rs7153565 | 1.00[ASW][hapmap];0.87[YRI][hapmap] |
rs7154479 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7154977 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7158473 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7159514 | 1.00[CEU][hapmap] |
rs7160824 | 1.00[EUR][1000 genomes] |
rs7161464 | 1.00[EUR][1000 genomes] |
rs719135 | 1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[EUR][1000 genomes] |
rs761818 | 0.87[YRI][hapmap] |
rs8013329 | 0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs8013599 | 0.87[YRI][hapmap] |
rs8014311 | 1.00[EUR][1000 genomes] |
rs8015886 | 1.00[EUR][1000 genomes] |
rs8016268 | 1.00[ASW][hapmap] |
rs8016309 | 1.00[EUR][1000 genomes] |
rs8017263 | 1.00[ASW][hapmap] |
rs8019167 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs8019673 | 1.00[EUR][1000 genomes] |
rs8019983 | 1.00[ASW][hapmap] |
rs8020631 | 1.00[EUR][1000 genomes] |
rs8020687 | 1.00[ASW][hapmap];0.87[YRI][hapmap] |
rs8022961 | 1.00[EUR][1000 genomes] |
rs987859 | 1.00[ASW][hapmap];1.00[EUR][1000 genomes] |
rs9989228 | 1.00[ASW][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.88[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv530038 | chr14:37590543-38336191 | Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 58 gene(s) | inside rSNPs | diseases |
2 | nsv915783 | chr14:37607836-38002966 | Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
3 | nsv1036854 | chr14:37609535-38013533 | Active TSS ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
4 | nsv542045 | chr14:37609535-38013533 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
5 | nsv901635 | chr14:37623177-37782273 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
6 | nsv901638 | chr14:37702799-37814824 | Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
7 | esv1797813 | chr14:37738197-37846877 | Weak transcription Active TSS ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
8 | esv1820642 | chr14:37738197-37846877 | Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
9 | esv1822817 | chr14:37738197-37846877 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
10 | esv1851834 | chr14:37738197-37846877 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
11 | nsv901639 | chr14:37743583-38038468 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
12 | esv1813852 | chr14:37768769-37810699 | Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:37752400-37796200 | Weak transcription | Skeletal Muscle Female | skeletal muscle |
2 | chr14:37759000-37810600 | Weak transcription | Psoas Muscle | Psoas |
3 | chr14:37762600-37812400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
4 | chr14:37763200-37797400 | Weak transcription | Left Ventricle | heart |
5 | chr14:37769400-37800000 | Weak transcription | Duodenum Smooth Muscle | Duodenum |
6 | chr14:37774200-37785600 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
7 | chr14:37775200-37817000 | Weak transcription | Aorta | Aorta |
8 | chr14:37776200-37792400 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
9 | chr14:37778800-37785200 | Weak transcription | Adipose Nuclei | Adipose |
10 | chr14:37780400-37786200 | Weak transcription | HUVEC | blood vessel |
11 | chr14:37780400-37795000 | Weak transcription | Ovary | ovary |
12 | chr14:37780600-37796800 | Weak transcription | HepG2 | liver |