Variant report
Variant | rs66672772 |
---|---|
Chromosome Location | chr6:34705937-34705938 |
allele | C/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 | chr6:34696691..34699544-chr6:34703628..34706154,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1018622 | 0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs1051115 | 0.88[EUR][1000 genomes] |
rs11961041 | 0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11963234 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs11966100 | 0.89[EUR][1000 genomes] |
rs11967912 | 0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11968954 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11968972 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12111129 | 0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs13193526 | 0.80[ASN][1000 genomes] |
rs13195029 | 0.85[EUR][1000 genomes] |
rs13195361 | 0.89[EUR][1000 genomes] |
rs13195490 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13196785 | 0.89[EUR][1000 genomes] |
rs13196983 | 0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs13200792 | 0.85[EUR][1000 genomes] |
rs13205210 | 0.89[EUR][1000 genomes] |
rs13206245 | 0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs13208149 | 0.89[EUR][1000 genomes] |
rs13210470 | 0.89[EUR][1000 genomes] |
rs13212699 | 0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs13213239 | 0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs13213288 | 0.89[EUR][1000 genomes] |
rs13213604 | 0.89[EUR][1000 genomes] |
rs13214596 | 0.92[EUR][1000 genomes] |
rs16895659 | 0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs2296361 | 0.89[EUR][1000 genomes] |
rs2296362 | 0.89[EUR][1000 genomes] |
rs2395603 | 0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs2395605 | 0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs28360525 | 0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs34261333 | 0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs34355573 | 0.89[EUR][1000 genomes] |
rs34377413 | 0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs34463942 | 0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs34480956 | 0.89[EUR][1000 genomes] |
rs34681295 | 0.92[EUR][1000 genomes] |
rs34840245 | 0.89[EUR][1000 genomes] |
rs35081279 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs35103554 | 0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs35143960 | 0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs35186650 | 0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs35195182 | 0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs35203657 | 0.89[EUR][1000 genomes] |
rs35285054 | 0.80[ASN][1000 genomes] |
rs35369977 | 0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs35444671 | 0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs35684630 | 0.83[ASN][1000 genomes] |
rs35744142 | 0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35940001 | 0.89[EUR][1000 genomes] |
rs36026951 | 0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4438945 | 0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4646933 | 0.88[EUR][1000 genomes] |
rs6457792 | 0.90[ASN][1000 genomes] |
rs6457797 | 0.84[EUR][1000 genomes] |
rs6457798 | 0.84[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs66926909 | 0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs67622212 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs67895864 | 0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs6904996 | 0.88[EUR][1000 genomes] |
rs6908462 | 0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6909393 | 0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6910824 | 0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6914031 | 0.80[EUR][1000 genomes] |
rs6914351 | 0.86[EUR][1000 genomes] |
rs6925175 | 0.89[EUR][1000 genomes] |
rs6926373 | 0.89[EUR][1000 genomes] |
rs6934741 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6941453 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs71567467 | 0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs72892238 | 0.94[ASN][1000 genomes] |
rs72892286 | 0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs72910111 | 0.92[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs72910167 | 0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs7739385 | 0.88[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs7743724 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7743949 | 0.87[EUR][1000 genomes] |
rs7749750 | 0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs7755354 | 0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs7758743 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs7759412 | 0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs7759985 | 0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs7761391 | 0.87[EUR][1000 genomes] |
rs7763989 | 0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs7764126 | 0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs7775947 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7776439 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs912717 | 0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs9462001 | 0.88[ASN][1000 genomes] |
rs9462002 | 0.88[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9462003 | 0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9469847 | 0.86[ASN][1000 genomes] |
rs9469852 | 0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs9968782 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1022844 | chr6:34317219-35060519 | Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 67 gene(s) | inside rSNPs | diseases |
2 | nsv538195 | chr6:34317219-35060519 | Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 67 gene(s) | inside rSNPs | diseases |
3 | esv2758046 | chr6:34382492-34714677 | Genic enhancers Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 37 gene(s) | inside rSNPs | diseases |
4 | esv2759418 | chr6:34382492-34714677 | Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 37 gene(s) | inside rSNPs | diseases |
5 | nsv885785 | chr6:34404636-34874002 | Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 49 gene(s) | inside rSNPs | diseases |
6 | nsv1033583 | chr6:34471572-34828372 | Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
7 | nsv885793 | chr6:34520267-34886436 | Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
8 | nsv830640 | chr6:34542489-34714677 | Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 24 gene(s) | inside rSNPs | diseases |
9 | nsv1032557 | chr6:34565802-34802008 | Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 33 gene(s) | inside rSNPs | diseases |
10 | nsv538196 | chr6:34565802-34802008 | Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 33 gene(s) | inside rSNPs | diseases |
11 | esv2763967 | chr6:34566255-34925463 | Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 42 gene(s) | inside rSNPs | diseases |
12 | nsv1020710 | chr6:34607214-34890143 | Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
13 | nsv508401 | chr6:34669708-34710302 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
14 | nsv885795 | chr6:34704613-34823187 | Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 24 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:34698000-34714000 | Weak transcription | Esophagus | oesophagus |
2 | chr6:34699400-34707000 | Weak transcription | K562 | blood |
3 | chr6:34699800-34712200 | Weak transcription | Stomach Mucosa | stomach |
4 | chr6:34705800-34706000 | Flanking Active TSS | HepG2 | liver |