Variant report

Variant rs62174630
Chromosome Location chr2:173797840-173797841
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:173789200-173799400 Weak transcription Brain Angular Gyrus brain
2 chr2:173796000-173798600 Enhancers Liver Liver
3 chr2:173796400-173800400 Weak transcription Fetal Stomach stomach
4 chr2:173796400-173802600 Weak transcription Duodenum Mucosa Duodenum
5 chr2:173796600-173798000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr2:173796600-173798000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr2:173796600-173798000 Weak transcription Fetal Intestine Small intestine
8 chr2:173796600-173798000 Weak transcription Fetal Thymus thymus
9 chr2:173796600-173798200 Enhancers HUVEC blood vessel
10 chr2:173796600-173799000 Weak transcription Adipose Nuclei Adipose
11 chr2:173796600-173799600 Weak transcription Cortex derived primary cultured neurospheres brain
12 chr2:173796600-173799800 Weak transcription Fetal Adrenal Gland Adrenal Gland
13 chr2:173796600-173800200 Weak transcription Fetal Intestine Large intestine
14 chr2:173796600-173802800 Weak transcription Pancreas Pancrea
15 chr2:173796600-173809000 Weak transcription Fetal Heart heart
16 chr2:173797200-173800400 Weak transcription Brain Dorsolateral Prefrontal Cortex brain

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