Variant report

Variant rs1533891
Chromosome Location chr8:8464032-8464033
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:8458200-8467000 Weak transcription Small Intestine intestine
2 chr8:8458800-8466800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr8:8459000-8467600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr8:8459000-8467800 Weak transcription HUES64 Cell Line embryonic stem cell
5 chr8:8459400-8468000 Weak transcription Placenta Placenta
6 chr8:8459600-8467800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr8:8459600-8468000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr8:8459600-8468200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr8:8459600-8468800 Weak transcription Pancreas Pancrea
10 chr8:8459800-8467400 Weak transcription HUVEC blood vessel
11 chr8:8460000-8469200 Weak transcription Right Atrium heart
12 chr8:8460000-8470200 Weak transcription Left Ventricle heart
13 chr8:8463400-8464200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr8:8463400-8464400 Enhancers Hela-S3 cervix
15 chr8:8463600-8464200 Enhancers HMEC breast
16 chr8:8463600-8464400 Flanking Active TSS A549 lung
17 chr8:8464000-8464400 Enhancers Breast Myoepithelial Primary Cells Breast
18 chr8:8464000-8464400 Enhancers NHEK skin

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