Variant report

Variant rs58477989
Chromosome Location chr14:80893646-80893647
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:80891400-80893800 Enhancers NHEK skin
2 chr14:80891400-80894400 Enhancers Hela-S3 cervix
3 chr14:80891600-80893800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr14:80891600-80893800 Enhancers NH-A brain
5 chr14:80891800-80893800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr14:80892200-80893800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr14:80892200-80893800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr14:80893000-80893800 Enhancers Osteobl bone
9 chr14:80893000-80894200 Weak transcription Placenta Placenta
10 chr14:80893000-80900800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr14:80893400-80894200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
12 chr14:80893400-80894200 Weak transcription Skeletal Muscle Male skeletal muscle
13 chr14:80893400-80894600 Weak transcription NHLF lung
14 chr14:80893600-80893800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr14:80893600-80893800 Enhancers Rectal Smooth Muscle rectum
16 chr14:80893600-80893800 Enhancers HUVEC blood vessel
17 chr14:80893600-80895400 Enhancers Cortex derived primary cultured neurospheres brain

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