Variant report

Variant rs7909314
Chromosome Location chr10:44347063-44347064
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:44339200-44349400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr10:44340800-44357600 Weak transcription Aorta Aorta
3 chr10:44341200-44347600 Weak transcription Gastric stomach
4 chr10:44342200-44347400 Weak transcription Fetal Heart heart
5 chr10:44342200-44347400 Weak transcription HSMMtube muscle
6 chr10:44342200-44350200 Weak transcription Right Atrium heart
7 chr10:44342400-44349200 Weak transcription HSMM muscle
8 chr10:44342800-44349000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
9 chr10:44342800-44349200 Weak transcription NHLF lung
10 chr10:44343000-44352400 Weak transcription HUVEC blood vessel
11 chr10:44343600-44349600 Weak transcription Left Ventricle heart
12 chr10:44346600-44350800 Enhancers Placenta Placenta
13 chr10:44346600-44353000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr10:44347000-44348000 Enhancers Pancreas Pancrea
15 chr10:44347000-44348200 Enhancers Fetal Muscle Leg muscle
16 chr10:44347000-44348600 Enhancers Fetal Brain Male brain
17 chr10:44347000-44350400 Enhancers Breast Myoepithelial Primary Cells Breast

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