Variant report

Variant rs2785608
Chromosome Location chr1:93461481-93461482
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:93451800-93466000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr1:93459200-93462000 Enhancers Fetal Intestine Large intestine
3 chr1:93459200-93462200 Enhancers Fetal Intestine Small intestine
4 chr1:93459800-93466000 Weak transcription Brain Anterior Caudate brain
5 chr1:93459800-93466000 Weak transcription GM12878-XiMat blood
6 chr1:93460800-93461600 Enhancers A549 lung
7 chr1:93460800-93461800 Enhancers HepG2 liver
8 chr1:93460800-93461800 Enhancers Monocytes-CD14+_RO01746 blood
9 chr1:93460800-93462000 Flanking Active TSS Rectal Mucosa Donor 31 rectum
10 chr1:93461000-93461600 Weak transcription Sigmoid Colon Sigmoid Colon
11 chr1:93461000-93461800 Enhancers Primary monocytes fromperipheralblood blood
12 chr1:93461000-93461800 Enhancers Pancreas Pancrea
13 chr1:93461000-93462000 Enhancers Fetal Adrenal Gland Adrenal Gland
14 chr1:93461200-93461600 Flanking Active TSS Stomach Mucosa stomach
15 chr1:93461200-93462200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr1:93461400-93461600 Bivalent Enhancer Osteobl bone
17 chr1:93461400-93461800 Flanking Active TSS Duodenum Mucosa Duodenum
18 chr1:93461400-93461800 Flanking Active TSS Rectal Mucosa Donor 29 rectum

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