The 2.0 version of rSNPBase

Variant report

Variant rs111793871
Chromosome Location chr7:4302836-4302837
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:4287600-4304200 Weak transcription Gastric stomach
2 chr7:4289200-4304000 Weak transcription Pancreas Pancrea
3 chr7:4291400-4304200 Weak transcription Aorta Aorta
4 chr7:4294800-4311800 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr7:4298200-4307400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
6 chr7:4301400-4304200 Weak transcription Fetal Intestine Small intestine
7 chr7:4301400-4304600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr7:4301400-4306600 Weak transcription HSMMtube muscle
9 chr7:4301600-4304000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr7:4301600-4304400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr7:4301600-4304600 Weak transcription Cortex derived primary cultured neurospheres brain
12 chr7:4301600-4306600 Weak transcription Colon Smooth Muscle Colon
13 chr7:4301600-4306600 Weak transcription Rectal Smooth Muscle rectum
14 chr7:4301600-4307000 Weak transcription Stomach Smooth Muscle stomach
15 chr7:4301600-4309800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
16 chr7:4302600-4303000 Enhancers HSMM muscle
17 chr7:4302800-4303000 Bivalent Enhancer Fetal Stomach stomach

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Last update: Aug 31, 2015