Variant report

Variant rs1868358
Chromosome Location chr7:17544993-17544994
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17537600-17546400 Weak transcription Ovary ovary
2 chr7:17542200-17545800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
3 chr7:17542200-17547400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr7:17542800-17545800 Weak transcription NHLF lung
5 chr7:17542800-17547400 Enhancers Liver Liver
6 chr7:17543200-17548000 Enhancers HepG2 liver
7 chr7:17543600-17545000 Weak transcription Fetal Intestine Small intestine
8 chr7:17543600-17550600 Weak transcription NHDF-Ad bronchial
9 chr7:17544600-17545600 Enhancers Pancreatic Islets Pancreatic Islet
10 chr7:17544600-17545800 Enhancers Fetal Lung lung
11 chr7:17544600-17545800 Weak transcription Sigmoid Colon Sigmoid Colon
12 chr7:17544600-17546800 Enhancers GM12878-XiMat blood
13 chr7:17544600-17547800 Enhancers Fetal Intestine Large intestine
14 chr7:17544800-17545800 Weak transcription Esophagus oesophagus
15 chr7:17544800-17545800 Weak transcription Gastric stomach
16 chr7:17544800-17546400 Weak transcription Pancreas Pancrea
17 chr7:17544800-17547600 Enhancers Stomach Mucosa stomach

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