Variant report

Variant rs375669178
Chromosome Location chr7:103021028-103021029
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:102989800-103021200 Weak transcription Fetal Heart heart
2 chr7:103009000-103021200 Weak transcription Fetal Lung lung
3 chr7:103009000-103029200 Weak transcription Spleen Spleen
4 chr7:103020600-103021600 Enhancers K562 blood
5 chr7:103020800-103021600 Enhancers HepG2 liver
6 chr7:103021000-103021200 Enhancers Fetal Intestine Large intestine
7 chr7:103021000-103021200 Enhancers Ovary ovary
8 chr7:103021000-103021200 Enhancers Pancreas Pancrea
9 chr7:103021000-103021400 Enhancers Stomach Mucosa stomach
10 chr7:103021000-103022600 Enhancers Gastric stomach

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