Variant report

Variant rs10831064
Chromosome Location chr11:93324551-93324552
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:93323200-93329000 Weak transcription Fetal Intestine Small intestine
2 chr11:93324200-93325200 Enhancers Monocytes-CD14+_RO01746 blood
3 chr11:93324200-93325400 Enhancers HepG2 liver
4 chr11:93324400-93324600 Enhancers Rectal Mucosa Donor 29 rectum
5 chr11:93324400-93324600 Enhancers Rectal Mucosa Donor 31 rectum
6 chr11:93324400-93324600 Enhancers Small Intestine intestine
7 chr11:93324400-93324600 Enhancers Stomach Mucosa stomach
8 chr11:93324400-93325000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr11:93324400-93325000 Enhancers A549 lung
10 chr11:93324400-93325000 Enhancers HSMM muscle
11 chr11:93324400-93325000 Enhancers NH-A brain
12 chr11:93324400-93325200 Enhancers Primary hematopoietic stem cells short term culture blood
13 chr11:93324400-93325200 Enhancers Muscle Satellite Cultured Cells --
14 chr11:93324400-93325200 Enhancers Fetal Adrenal Gland Adrenal Gland
15 chr11:93324400-93325400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr11:93324400-93325400 Enhancers Primary monocytes fromperipheralblood blood
17 chr11:93324400-93325800 Enhancers GM12878-XiMat blood

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