Variant report

Variant rs555662705
Chromosome Location chr4:147971695-147971696
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:147967800-147971800 Weak transcription Fetal Kidney kidney
2 chr4:147968400-147971800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr4:147970600-147972800 Enhancers Psoas Muscle Psoas
4 chr4:147970600-147972800 Enhancers Hela-S3 cervix
5 chr4:147970800-147972200 Enhancers Fetal Heart heart
6 chr4:147970800-147972600 Enhancers Fetal Lung lung
7 chr4:147971000-147971800 Enhancers Fetal Muscle Leg muscle
8 chr4:147971000-147972000 Enhancers Colon Smooth Muscle Colon
9 chr4:147971000-147972200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr4:147971000-147972200 Enhancers NHLF lung
11 chr4:147971000-147972400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr4:147971200-147971800 Flanking Active TSS Muscle Satellite Cultured Cells --
13 chr4:147971200-147971800 Enhancers Fetal Stomach stomach
14 chr4:147971200-147971800 Enhancers Rectal Smooth Muscle rectum
15 chr4:147971200-147972000 Enhancers iPS-20b Cell Line embryonic stem cell
16 chr4:147971400-147971800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr4:147971400-147971800 Active TSS NHDF-Ad bronchial
18 chr4:147971400-147972000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
19 chr4:147971600-147971800 Active TSS Stomach Smooth Muscle stomach
20 chr4:147971600-147972000 Enhancers HMEC breast
21 chr4:147971600-147972800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
22 chr4:147971600-147978400 Weak transcription Aorta Aorta
23 chr4:147971600-147978400 Weak transcription Placenta Amnion Placenta Amnion

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