Variant report
Variant | rs4504642 |
---|---|
Chromosome Location | chr8:8448081-8448082 |
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 | chr8:8243125..8245371-chr8:8446587..8449167,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000182319 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10503378 | 0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10503379 | 1.00[CEU][hapmap];0.85[JPT][hapmap];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs11250208 | 0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs11250209 | 0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs11250210 | 0.83[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs11250211 | 0.83[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs11250213 | 0.88[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs11250214 | 1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12541355 | 1.00[CEU][hapmap];0.80[CHB][hapmap];0.90[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12541484 | 0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs12541658 | 0.89[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs12542803 | 0.87[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs12543456 | 1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12544432 | 0.87[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs12546276 | 1.00[CEU][hapmap];0.85[JPT][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12546296 | 1.00[CEU][hapmap];0.85[JPT][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12547034 | 0.84[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs12549726 | 1.00[CEU][hapmap];0.84[JPT][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12550737 | 0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs12675017 | 0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12675869 | 0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12676983 | 0.87[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12677476 | 0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs12677677 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12679599 | 0.83[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs12679906 | 0.87[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12680789 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs12681936 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs1522836 | 0.83[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs1533888 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs1533889 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs1533890 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs1533891 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1533893 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1533894 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs17154252 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs17154268 | 0.99[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs17154314 | 0.84[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs17154329 | 0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs17154369 | 0.83[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs17154375 | 0.80[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs17154379 | 0.83[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs17154440 | 1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs17154478 | 1.00[CEU][hapmap];0.84[JPT][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs2030566 | 0.87[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs2177253 | 0.87[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs2409020 | 0.87[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs2898082 | 0.87[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs3081466 | 0.98[EUR][1000 genomes] |
rs35016966 | 0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs35898686 | 0.89[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs4268132 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs4364633 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4367545 | 0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs4386982 | 0.87[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs4404922 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs4427178 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs4506213 | 1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs4515552 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4840994 | 0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs4840995 | 0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs4840996 | 0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4840997 | 0.83[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs4840998 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs4840999 | 0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs4841002 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs5019821 | 0.98[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs58059590 | 0.88[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs60510961 | 0.88[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs60906424 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs61052104 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs62492871 | 0.86[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs62492878 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs62492882 | 0.81[AMR][1000 genomes] |
rs62492883 | 0.81[AMR][1000 genomes] |
rs62494894 | 1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs62494895 | 0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs62494897 | 0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs62494916 | 0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs62494917 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs62494918 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs62494919 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs62494921 | 0.83[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs72494265 | 0.81[AMR][1000 genomes] |
rs73190549 | 0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs73190579 | 0.82[AMR][1000 genomes] |
rs73190600 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs73192404 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7357587 | 0.85[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs7464820 | 0.87[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7813359 | 1.00[CEU][hapmap];0.85[JPT][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7813381 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs7814697 | 0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7814889 | 0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7819718 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs7819733 | 0.87[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs7820321 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7824587 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7824895 | 0.82[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs7824908 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7825087 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7834575 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7838399 | 0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs7843691 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs870167 | 0.82[AMR][1000 genomes] |
rs873323 | 0.87[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs940027 | 0.87[AMR][1000 genomes];0.85[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv890331 | chr8:8093240-8971100 | Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 43 gene(s) | inside rSNPs | diseases |
2 | nsv610153 | chr8:8098079-8454531 | Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 21 gene(s) | inside rSNPs | diseases |
3 | nsv1025994 | chr8:8108863-8580201 | Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | diseases |
4 | nsv1030433 | chr8:8130629-8653691 | Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 26 gene(s) | inside rSNPs | diseases |
5 | nsv539447 | chr8:8130629-8653691 | Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 26 gene(s) | inside rSNPs | diseases |
6 | nsv1033463 | chr8:8221922-8674333 | Weak transcription Bivalent/Poised TSS Genic enhancers Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
7 | nsv539451 | chr8:8221922-8674333 | Weak transcription Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
8 | nsv1019613 | chr8:8239352-8636357 | Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
9 | nsv539452 | chr8:8239352-8636357 | Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
10 | nsv465452 | chr8:8313010-8450761 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
11 | nsv610173 | chr8:8313010-8450761 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
12 | nsv470182 | chr8:8318850-8448429 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
13 | nsv465454 | chr8:8318850-8448688 | Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
14 | nsv465455 | chr8:8318850-8448688 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
15 | nsv610175 | chr8:8318850-8448688 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
16 | nsv465456 | chr8:8318850-8450761 | Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
17 | nsv465457 | chr8:8318850-8450761 | Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
18 | nsv610176 | chr8:8318850-8450761 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
19 | nsv610177 | chr8:8318850-8454531 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
20 | nsv1026251 | chr8:8319925-8448688 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
21 | nsv1020159 | chr8:8324419-8450231 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
22 | nsv539455 | chr8:8324419-8450231 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
23 | nsv890333 | chr8:8328101-8456563 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
24 | nsv890334 | chr8:8328101-8471348 | Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
25 | nsv1019606 | chr8:8353661-8736992 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
26 | nsv539456 | chr8:8353661-8736992 | Strong transcription Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
27 | nsv995047 | chr8:8353662-8857913 | Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
28 | nsv890335 | chr8:8394297-8448429 | Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
29 | nsv890336 | chr8:8396676-8500562 | Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
30 | nsv1019794 | chr8:8419612-8454162 | Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
31 | nsv1016933 | chr8:8432279-8624770 | Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:8434200-8457400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr8:8441800-8458000 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
3 | chr8:8445800-8451000 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
4 | chr8:8446000-8455200 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
5 | chr8:8447600-8448200 | Enhancers | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
6 | chr8:8447800-8451600 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
7 | chr8:8448000-8448200 | Enhancers | Adipose Nuclei | Adipose |
8 | chr8:8448000-8452000 | Weak transcription | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |