Variant report

Variant rs17248456
Chromosome Location chr14:67688610-67688611
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:67687000-67689400 Enhancers HMEC breast
2 chr14:67687000-67689400 Enhancers NHEK skin
3 chr14:67687000-67697000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr14:67687600-67689400 Enhancers HSMMtube muscle
5 chr14:67687600-67689600 Enhancers Muscle Satellite Cultured Cells --
6 chr14:67687800-67689200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
7 chr14:67687800-67689200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr14:67687800-67689400 Enhancers HSMM muscle
9 chr14:67687800-67689400 Enhancers NH-A brain
10 chr14:67688000-67688800 Enhancers Fetal Intestine Small intestine
11 chr14:67688000-67688800 Enhancers Small Intestine intestine
12 chr14:67688000-67689000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr14:67688000-67689200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr14:67688000-67689200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr14:67688000-67689200 Enhancers Osteobl bone
16 chr14:67688000-67689400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr14:67688000-67689400 Enhancers Placenta Placenta
18 chr14:67688400-67688800 Flanking Active TSS Hela-S3 cervix

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