Variant report

Variant rs1393564
Chromosome Location chr9:85612428-85612429
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:85594800-85628200 Weak transcription Sigmoid Colon Sigmoid Colon
2 chr9:85597200-85627000 Weak transcription A549 lung
3 chr9:85603000-85615800 Weak transcription Fetal Intestine Small intestine
4 chr9:85603000-85628200 Weak transcription Fetal Stomach stomach
5 chr9:85603200-85621600 Weak transcription Esophagus oesophagus
6 chr9:85603200-85643800 Weak transcription Duodenum Mucosa Duodenum
7 chr9:85603800-85613200 Weak transcription Colonic Mucosa Colon
8 chr9:85608800-85628000 Weak transcription Fetal Kidney kidney
9 chr9:85609200-85616200 Strong transcription Pancreas Pancrea
10 chr9:85609400-85612600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr9:85609400-85616600 Weak transcription Stomach Mucosa stomach
12 chr9:85609400-85620800 Weak transcription Gastric stomach
13 chr9:85610800-85642000 Weak transcription Fetal Intestine Large intestine
14 chr9:85611600-85612600 Enhancers Fetal Thymus thymus
15 chr9:85611800-85613400 Enhancers HMEC breast
16 chr9:85611800-85614000 Strong transcription Cortex derived primary cultured neurospheres brain
17 chr9:85611800-85615600 Strong transcription Rectal Mucosa Donor 31 rectum
18 chr9:85612000-85617000 Weak transcription Fetal Lung lung
19 chr9:85612200-85612800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
20 chr9:85612200-85613400 Weak transcription Fetal Brain Male brain
21 chr9:85612400-85612800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
22 chr9:85612400-85616200 Strong transcription Rectal Mucosa Donor 29 rectum

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