Variant report

Variant rs74145021
Chromosome Location chr1:222098000-222098001
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:222087600-222099200 Weak transcription Primary monocytes fromperipheralblood blood
2 chr1:222094800-222099200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr1:222095400-222117800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:222097000-222098200 Enhancers Muscle Satellite Cultured Cells --
5 chr1:222097400-222098000 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr1:222097400-222098000 Enhancers HSMM muscle
7 chr1:222097400-222098200 Enhancers NHDF-Ad bronchial
8 chr1:222097600-222098000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
9 chr1:222097600-222098000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr1:222097600-222098000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
11 chr1:222097600-222098000 Enhancers Left Ventricle heart
12 chr1:222097600-222098000 Enhancers Psoas Muscle Psoas
13 chr1:222097600-222098000 Enhancers Osteobl bone
14 chr1:222097600-222098200 Enhancers Skeletal Muscle Male skeletal muscle
15 chr1:222098000-222099000 Weak transcription ES-I3 Cell Line embryonic stem cell
16 chr1:222098000-222099200 Weak transcription HSMM muscle
17 chr1:222098000-222099200 Weak transcription Osteobl bone
18 chr1:222098000-222118800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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