Variant report

Variant rs6948537
Chromosome Location chr7:137371830-137371831
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:137368000-137372400 Weak transcription HMEC breast
2 chr7:137369600-137372400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr7:137369600-137372800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
4 chr7:137369800-137372000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr7:137369800-137372000 Enhancers Muscle Satellite Cultured Cells --
6 chr7:137369800-137374800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
7 chr7:137370000-137374000 Enhancers Osteobl bone
8 chr7:137370200-137373600 Enhancers HSMMtube muscle
9 chr7:137370400-137380600 Weak transcription Brain Angular Gyrus brain
10 chr7:137370600-137374000 Enhancers Aorta Aorta
11 chr7:137370800-137372400 Weak transcription NHDF-Ad bronchial
12 chr7:137370800-137373400 Enhancers NH-A brain
13 chr7:137370800-137374800 Weak transcription Brain Germinal Matrix brain
14 chr7:137370800-137384600 Weak transcription Fetal Brain Female brain
15 chr7:137371600-137373400 Genic enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr7:137371800-137372400 Flanking Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
17 chr7:137371800-137372800 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
18 chr7:137371800-137372800 Flanking Active TSS HSMM muscle

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