Variant report

Variant rs12648414
Chromosome Location chr4:26841969-26841970
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:26839200-26843200 Enhancers Fetal Heart heart
2 chr4:26839600-26842400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
3 chr4:26839600-26842400 Enhancers Fetal Muscle Leg muscle
4 chr4:26840000-26842200 Weak transcription Fetal Thymus thymus
5 chr4:26840000-26842400 Enhancers Fetal Lung lung
6 chr4:26840000-26858800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr4:26840600-26844200 Weak transcription Primary monocytes fromperipheralblood blood
8 chr4:26841000-26842800 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr4:26841200-26842000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr4:26841200-26843400 Enhancers Thymus Thymus
11 chr4:26841400-26842200 Weak transcription Fetal Intestine Large intestine
12 chr4:26841400-26845400 Weak transcription Gastric stomach
13 chr4:26841400-26858600 Weak transcription Aorta Aorta
14 chr4:26841600-26842000 Weak transcription Skeletal Muscle Female skeletal muscle
15 chr4:26841600-26842200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
16 chr4:26841600-26842400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
17 chr4:26841600-26843600 Weak transcription Right Atrium heart
18 chr4:26841600-26858600 Weak transcription Muscle Satellite Cultured Cells --
19 chr4:26841800-26842200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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