Variant report

Variant rs4452771
Chromosome Location chr8:103988773-103988774
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:103974400-103989200 Weak transcription H9 Cell Line embryonic stem cell
2 chr8:103974400-103989200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr8:103977000-103989200 Weak transcription H1 Cell Line embryonic stem cell
4 chr8:103981200-103992600 Weak transcription Brain Substantia Nigra brain
5 chr8:103982000-103989600 Weak transcription Brain Hippocampus Middle brain
6 chr8:103983800-103989200 Weak transcription Pancreas Pancrea
7 chr8:103985800-103989000 Weak transcription Primary B cells from cord blood blood
8 chr8:103985800-103989200 Weak transcription ES-I3 Cell Line embryonic stem cell
9 chr8:103986200-103989200 Weak transcription HUES48 Cell Line embryonic stem cell
10 chr8:103987200-103989200 Enhancers Primary neutrophils fromperipheralblood blood
11 chr8:103988200-103991200 Enhancers Primary monocytes fromperipheralblood blood
12 chr8:103988400-103989200 Enhancers Monocytes-CD14+_RO01746 blood
13 chr8:103988400-103991200 Enhancers Breast Myoepithelial Primary Cells Breast
14 chr8:103988600-103989400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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