Variant report

Variant rs561257801
Chromosome Location chr7:17546052-17546053
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17537600-17546400 Weak transcription Ovary ovary
2 chr7:17542200-17547400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr7:17542800-17547400 Enhancers Liver Liver
4 chr7:17543200-17548000 Enhancers HepG2 liver
5 chr7:17543600-17550600 Weak transcription NHDF-Ad bronchial
6 chr7:17544600-17546800 Enhancers GM12878-XiMat blood
7 chr7:17544600-17547800 Enhancers Fetal Intestine Large intestine
8 chr7:17544800-17546400 Weak transcription Pancreas Pancrea
9 chr7:17544800-17547600 Enhancers Stomach Mucosa stomach
10 chr7:17545000-17546600 Enhancers Small Intestine intestine
11 chr7:17545600-17547800 Enhancers Fetal Intestine Small intestine
12 chr7:17545800-17546200 Enhancers Esophagus oesophagus
13 chr7:17545800-17546200 Active TSS Rectal Mucosa Donor 29 rectum
14 chr7:17545800-17546200 Enhancers Sigmoid Colon Sigmoid Colon
15 chr7:17545800-17546200 Enhancers NHLF lung
16 chr7:17545800-17546600 Enhancers Fetal Stomach stomach
17 chr7:17545800-17546600 Enhancers Gastric stomach
18 chr7:17545800-17546600 Enhancers A549 lung
19 chr7:17545800-17546800 Enhancers Rectal Mucosa Donor 31 rectum
20 chr7:17546000-17546200 Active TSS Pancreatic Islets Pancreatic Islet
21 chr7:17546000-17546400 Enhancers Fetal Lung lung

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