Variant report

Variant rs1910252
Chromosome Location chr8:49407362-49407363
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49404400-49407600 Enhancers Fetal Adrenal Gland Adrenal Gland
2 chr8:49405600-49407400 Enhancers HMEC breast
3 chr8:49406000-49407400 Enhancers Muscle Satellite Cultured Cells --
4 chr8:49406000-49407400 Enhancers Osteobl bone
5 chr8:49406200-49407400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr8:49406400-49407400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr8:49406400-49407400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr8:49407000-49409200 Weak transcription ES-I3 Cell Line embryonic stem cell
9 chr8:49407000-49413800 Weak transcription NH-A brain
10 chr8:49407200-49408200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr8:49407200-49413400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
12 chr8:49407200-49413400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr8:49407200-49413400 Weak transcription A549 lung

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