Variant report

Variant rs4437620
Chromosome Location chr8:107446939-107446940
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:107404400-107447000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr8:107441000-107447200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr8:107441600-107447000 Weak transcription Primary hematopoietic stem cells short term culture blood
4 chr8:107443600-107447200 Weak transcription Esophagus oesophagus
5 chr8:107443800-107447000 Weak transcription NHLF lung
6 chr8:107444800-107451400 Weak transcription Aorta Aorta
7 chr8:107445400-107447200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr8:107446400-107447000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr8:107446400-107447400 Enhancers Muscle Satellite Cultured Cells --
10 chr8:107446400-107447400 Enhancers NH-A brain
11 chr8:107446400-107447400 Enhancers Osteobl bone
12 chr8:107446400-107447600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
13 chr8:107446600-107447000 Enhancers HUVEC blood vessel
14 chr8:107446800-107447200 Weak transcription Breast Myoepithelial Primary Cells Breast
15 chr8:107446800-107447400 Enhancers Fetal Heart heart
16 chr8:107446800-107447800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
17 chr8:107446800-107450200 Enhancers Primary T cells from cord blood blood

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