Variant report

Variant rs6969052
Chromosome Location chr7:3902305-3902306
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:3900200-3902600 Enhancers iPS-18 Cell Line embryonic stem cell
2 chr7:3900600-3902400 Enhancers Colon Smooth Muscle Colon
3 chr7:3900600-3902800 Enhancers H9 Cell Line embryonic stem cell
4 chr7:3900600-3902800 Enhancers HUES48 Cell Line embryonic stem cell
5 chr7:3901000-3902400 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr7:3901000-3902400 Enhancers Adipose Nuclei Adipose
7 chr7:3901000-3902600 Enhancers HUES64 Cell Line embryonic stem cell
8 chr7:3901000-3902800 Enhancers H1 Cell Line embryonic stem cell
9 chr7:3901000-3902800 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr7:3901200-3902400 Weak transcription Lung lung
11 chr7:3901200-3902600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr7:3901200-3902600 Enhancers Breast Myoepithelial Primary Cells Breast
13 chr7:3901200-3902800 Enhancers HUES6 Cell Line embryonic stem cell
14 chr7:3901200-3902800 Enhancers iPS-20b Cell Line embryonic stem cell
15 chr7:3901200-3959600 Weak transcription Pancreas Pancrea
16 chr7:3902000-3907000 Weak transcription Fetal Stomach stomach
17 chr7:3902200-3902600 Enhancers Fetal Lung lung
18 chr7:3902200-3902800 Enhancers Stomach Smooth Muscle stomach
19 chr7:3902200-3907400 Weak transcription Muscle Satellite Cultured Cells --

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