Variant report

Variant rs531907937
Chromosome Location chr1:77331767-77331768
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:77319800-77333200 Weak transcription Gastric stomach
2 chr1:77320400-77333000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr1:77329600-77332800 Enhancers HSMMtube muscle
4 chr1:77330200-77332800 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr1:77330600-77332800 Weak transcription NH-A brain
6 chr1:77330800-77332200 Enhancers Cortex derived primary cultured neurospheres brain
7 chr1:77330800-77332200 Enhancers Pancreatic Islets Pancreatic Islet
8 chr1:77330800-77332800 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr1:77331000-77332800 Weak transcription ES-I3 Cell Line embryonic stem cell
10 chr1:77331400-77332000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
11 chr1:77331400-77332400 Bivalent Enhancer Brain Cingulate Gyrus brain
12 chr1:77331400-77332800 Enhancers Fetal Brain Female brain
13 chr1:77331600-77331800 Enhancers Duodenum Smooth Muscle Duodenum
14 chr1:77331600-77332000 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
15 chr1:77331600-77332000 Enhancers Aorta Aorta
16 chr1:77331600-77332000 Enhancers Ovary ovary
17 chr1:77331600-77332000 Enhancers HSMM muscle
18 chr1:77331600-77332200 Enhancers Rectal Smooth Muscle rectum

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