Variant report

Variant rs17085988
Chromosome Location chr9:85657317-85657318
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:85644800-85670600 Weak transcription Rectal Mucosa Donor 29 rectum
2 chr9:85645600-85662800 Weak transcription Rectal Mucosa Donor 31 rectum
3 chr9:85655200-85671400 Weak transcription Fetal Intestine Small intestine
4 chr9:85656400-85657400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr9:85656400-85657400 Enhancers NH-A brain
6 chr9:85656400-85657400 Enhancers Osteobl bone
7 chr9:85656400-85659400 Enhancers Cortex derived primary cultured neurospheres brain
8 chr9:85656800-85657600 Enhancers A549 lung
9 chr9:85656800-85662800 Weak transcription Pancreas Pancrea
10 chr9:85657000-85657400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
11 chr9:85657000-85657800 Bivalent Enhancer Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr9:85657000-85657800 Weak transcription NHDF-Ad bronchial
13 chr9:85657000-85662400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
14 chr9:85657200-85660400 Weak transcription Stomach Mucosa stomach
15 chr9:85657200-85662400 Weak transcription Hela-S3 cervix

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