Variant report

Variant rs2645375
Chromosome Location chr4:101912362-101912363
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:101907800-101912800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr4:101908000-101912800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr4:101908800-101912800 Weak transcription ES-I3 Cell Line embryonic stem cell
4 chr4:101909600-101913000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr4:101911600-101912600 Weak transcription HSMMtube muscle
6 chr4:101911600-101912600 Weak transcription NHDF-Ad bronchial
7 chr4:101911600-101913000 Enhancers Osteobl bone
8 chr4:101911800-101913000 Enhancers NH-A brain
9 chr4:101912000-101912400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr4:101912000-101912600 Enhancers HUES6 Cell Line embryonic stem cell
11 chr4:101912000-101913000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr4:101912000-101913000 Enhancers Muscle Satellite Cultured Cells --
13 chr4:101912200-101912800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
14 chr4:101912200-101913000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr4:101912200-101913200 Enhancers HSMM muscle

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