Variant report

Variant rs4938012
Chromosome Location chr11:113259654-113259655
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:113257000-113260200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
2 chr11:113258000-113272200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr11:113258600-113260800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
4 chr11:113258800-113260000 Weak transcription H9 Cell Line embryonic stem cell
5 chr11:113258800-113260600 Enhancers HUES48 Cell Line embryonic stem cell
6 chr11:113258800-113287400 Weak transcription Gastric stomach
7 chr11:113259000-113260600 Enhancers HUES6 Cell Line embryonic stem cell
8 chr11:113259200-113260200 Bivalent Enhancer Fetal Brain Female brain
9 chr11:113259200-113276000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr11:113259400-113260600 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr11:113259400-113261800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr11:113259400-113268600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr11:113259400-113272000 Weak transcription HMEC breast
14 chr11:113259600-113259800 Bivalent Enhancer Fetal Brain Male brain
15 chr11:113259600-113260200 Enhancers iPS-18 Cell Line embryonic stem cell

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