Variant report

Variant rs11569162
Chromosome Location chr4:110935224-110935225
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:110920800-110935800 Strong transcription Skeletal Muscle Female skeletal muscle
2 chr4:110930000-110937200 Weak transcription Fetal Intestine Small intestine
3 chr4:110930400-110941600 Weak transcription Fetal Heart heart
4 chr4:110930800-110941600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr4:110931000-110937000 Weak transcription Skeletal Muscle Male skeletal muscle
6 chr4:110931000-110937600 Weak transcription iPS-20b Cell Line embryonic stem cell
7 chr4:110931000-110941600 Weak transcription HUES6 Cell Line embryonic stem cell
8 chr4:110934600-110935400 Enhancers HUES48 Cell Line embryonic stem cell
9 chr4:110935000-110935600 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr4:110935200-110935600 Enhancers Fetal Kidney kidney
11 chr4:110935200-110935800 Strong transcription Left Ventricle heart
12 chr4:110935200-110935800 Strong transcription Pancreas Pancrea

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