Variant report
Variant | rs12664024 |
---|---|
Chromosome Location | chr6:110405151-110405152 |
allele | A/G |
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:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr6:110400293..110402395-chr6:110404111..110406019,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs12660108 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12662027 | 0.87[EUR][1000 genomes] |
rs12662099 | 0.87[EUR][1000 genomes] |
rs12662559 | 0.87[EUR][1000 genomes] |
rs12662965 | 0.85[ASN][1000 genomes] |
rs12664697 | 0.87[EUR][1000 genomes] |
rs12665152 | 0.87[EUR][1000 genomes] |
rs12665178 | 0.87[EUR][1000 genomes] |
rs12665650 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs1350943 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1350944 | 1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1381688 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1462491 | 0.96[ASN][1000 genomes] |
rs2002631 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs2361500 | 0.87[EUR][1000 genomes] |
rs2885293 | 0.87[EUR][1000 genomes] |
rs3806158 | 0.86[EUR][1000 genomes] |
rs3828928 | 1.00[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs41288574 | 0.87[EUR][1000 genomes] |
rs41288576 | 0.87[EUR][1000 genomes] |
rs56662730 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs57771959 | 0.87[EUR][1000 genomes] |
rs58100980 | 1.00[EUR][1000 genomes] |
rs58965432 | 0.85[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs59181827 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs60105161 | 0.87[EUR][1000 genomes] |
rs61494781 | 0.87[EUR][1000 genomes] |
rs6568630 | 0.89[ASN][1000 genomes] |
rs6922245 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs6922536 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6926993 | 0.94[EUR][1000 genomes] |
rs6927304 | 0.89[ASN][1000 genomes] |
rs6935544 | 0.87[EUR][1000 genomes] |
rs6937364 | 0.87[EUR][1000 genomes] |
rs6940347 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6941101 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs73533811 | 0.89[ASN][1000 genomes] |
rs73765657 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs73765660 | 1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs73765665 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs7752069 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7770634 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7771649 | 0.87[EUR][1000 genomes] |
rs7771909 | 0.87[EUR][1000 genomes] |
rs9374149 | 0.90[ASN][1000 genomes] |
rs9374151 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9374152 | 0.96[ASN][1000 genomes] |
rs9374153 | 1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9374154 | 1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs9374155 | 1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs9374157 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs9384733 | 0.89[ASN][1000 genomes] |
rs9386871 | 0.85[ASN][1000 genomes] |
rs9386873 | 0.90[ASN][1000 genomes] |
rs9386874 | 0.90[ASN][1000 genomes] |
rs9386875 | 0.90[ASN][1000 genomes] |
rs9386877 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9386878 | 0.99[ASN][1000 genomes] |
rs9386879 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs9398230 | 0.89[ASN][1000 genomes] |
rs9400356 | 0.86[ASN][1000 genomes] |
rs9400357 | 0.86[ASN][1000 genomes] |
rs9400358 | 0.89[ASN][1000 genomes] |
rs9400361 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs9400362 | 0.86[EUR][1000 genomes];0.99[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv886535 | chr6:110377006-110551463 | Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 3 gene(s) | inside rSNPs | diseases |
2 | nsv1017551 | chr6:110385054-110413225 | Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | nsv1023185 | chr6:110386197-110416868 | Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
4 | nsv1029169 | chr6:110389869-110413225 | Weak transcription Enhancers Strong transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | esv2757188 | chr6:110389926-110504680 | Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 3 gene(s) | inside rSNPs | diseases |
6 | esv2759462 | chr6:110389926-110504680 | Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 3 gene(s) | inside rSNPs | diseases |
7 | esv2763956 | chr6:110394513-110413237 | Weak transcription Enhancers Strong transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
8 | esv2761056 | chr6:110394513-110415428 | Enhancers Weak transcription ZNF genes & repeats Strong transcription | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
9 | nsv1017890 | chr6:110394894-110416868 | Enhancers Weak transcription Strong transcription ZNF genes & repeats | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
10 | nsv7954 | chr6:110395986-110413365 | Enhancers Strong transcription Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
11 | esv33686 | chr6:110396119-110413310 | Weak transcription Enhancers Strong transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
12 | nsv604487 | chr6:110396540-110406212 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
13 | nsv604488 | chr6:110396540-110406426 | Weak transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
14 | nsv604489 | chr6:110396540-110408904 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
15 | nsv604490 | chr6:110396540-110411065 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
16 | nsv604491 | chr6:110396540-110412259 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
17 | nsv1026085 | chr6:110396676-110420721 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
18 | nsv604492 | chr6:110398923-110411065 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
19 | nsv604493 | chr6:110398923-110412259 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
20 | nsv604494 | chr6:110399223-110412259 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
21 | nsv604495 | chr6:110399873-110412259 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
22 | nsv604496 | chr6:110400783-110411065 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
23 | nsv604497 | chr6:110401183-110411065 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
24 | nsv604498 | chr6:110401183-110412259 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
25 | nsv604499 | chr6:110401183-110420374 | Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
26 | nsv604500 | chr6:110402895-110412259 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
27 | esv2829867 | chr6:110404180-110414749 | Weak transcription Enhancers Strong transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:110390000-110405200 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
2 | chr6:110397000-110412800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr6:110397000-110415400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
4 | chr6:110401200-110405200 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
5 | chr6:110402800-110414400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
6 | chr6:110402800-110419800 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
7 | chr6:110404600-110406800 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
8 | chr6:110405000-110405400 | Enhancers | NHDF-Ad | bronchial |
9 | chr6:110405000-110405600 | Enhancers | HUES6 Cell Line | embryonic stem cell |
10 | chr6:110405000-110405600 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
11 | chr6:110405000-110405800 | Enhancers | Ovary | ovary |
12 | chr6:110405000-110405800 | Enhancers | HepG2 | liver |
13 | chr6:110405000-110406000 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |