Variant report

Variant rs545086929
Chromosome Location chr10:4708168-4708169
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:4703600-4708200 Enhancers NHDF-Ad bronchial
2 chr10:4703600-4708400 Enhancers Fetal Intestine Small intestine
3 chr10:4704200-4708600 Enhancers Stomach Mucosa stomach
4 chr10:4705200-4708600 Enhancers HUVEC blood vessel
5 chr10:4705800-4708400 Enhancers Fetal Heart heart
6 chr10:4706200-4708400 Enhancers NHEK skin
7 chr10:4707000-4710000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr10:4707000-4710800 Weak transcription Rectal Mucosa Donor 31 rectum
9 chr10:4707000-4713000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
10 chr10:4707400-4712600 Weak transcription Osteobl bone
11 chr10:4707600-4712200 Weak transcription HMEC breast
12 chr10:4707600-4712800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr10:4707800-4708600 Enhancers A549 lung
14 chr10:4707800-4709200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr10:4707800-4712800 Weak transcription Muscle Satellite Cultured Cells --
16 chr10:4707800-4713200 Weak transcription Skeletal Muscle Female skeletal muscle
17 chr10:4708000-4712800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr10:4708000-4713000 Weak transcription HSMM muscle

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