Variant report

Variant rs4141132
Chromosome Location chr7:84655167-84655168
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:84644600-84662600 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr7:84654000-84655400 Enhancers Fetal Heart heart
3 chr7:84654000-84655600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr7:84654000-84655600 Enhancers HUVEC blood vessel
5 chr7:84654200-84655400 Enhancers NHEK skin
6 chr7:84654400-84655600 Enhancers GM12878-XiMat blood
7 chr7:84654600-84655200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr7:84654600-84655200 Enhancers HUES6 Cell Line embryonic stem cell
9 chr7:84654600-84655400 Enhancers Cortex derived primary cultured neurospheres brain
10 chr7:84654600-84655400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
11 chr7:84654600-84655400 Enhancers Placenta Amnion Placenta Amnion
12 chr7:84654600-84655600 Enhancers HMEC breast
13 chr7:84654600-84655800 Enhancers NH-A brain
14 chr7:84654800-84655200 Enhancers Fetal Lung lung
15 chr7:84655000-84655200 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr7:84655000-84655600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr7:84655000-84655600 Enhancers Hela-S3 cervix
18 chr7:84655000-84661000 Weak transcription Aorta Aorta
19 chr7:84655000-84673600 Weak transcription Fetal Brain Male brain

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