Variant report

Variant rs17146756
Chromosome Location chr5:119876070-119876071
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:24 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:119839800-119879800 Weak transcription Psoas Muscle Psoas
2 chr5:119867200-119879800 Weak transcription Left Ventricle heart
3 chr5:119874000-119876400 Enhancers HMEC breast
4 chr5:119874400-119876200 Enhancers HUES48 Cell Line embryonic stem cell
5 chr5:119874400-119876600 Enhancers Fetal Heart heart
6 chr5:119874600-119876400 Enhancers NHDF-Ad bronchial
7 chr5:119874600-119877000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr5:119874800-119876400 Enhancers Muscle Satellite Cultured Cells --
9 chr5:119874800-119876400 Enhancers NHLF lung
10 chr5:119874800-119876400 Enhancers Osteobl bone
11 chr5:119874800-119876800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr5:119874800-119876800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr5:119874800-119877400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr5:119874800-119886000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr5:119875400-119876400 Enhancers iPS-20b Cell Line embryonic stem cell
16 chr5:119875400-119876600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
17 chr5:119875400-119878400 Weak transcription HSMM muscle
18 chr5:119875600-119876200 Enhancers HUES6 Cell Line embryonic stem cell
19 chr5:119875600-119876200 Enhancers iPS-18 Cell Line embryonic stem cell
20 chr5:119875800-119876200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
21 chr5:119876000-119876200 Enhancers Skeletal Muscle Male skeletal muscle
22 chr5:119876000-119876400 Enhancers Right Atrium heart
23 chr5:119876000-119879400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
24 chr5:119876000-119879600 Weak transcription NH-A brain

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