Variant report

Variant rs75645575
Chromosome Location chr12:31357893-31357894
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:31355200-31362600 Enhancers HMEC breast
2 chr12:31356400-31358000 Enhancers iPS-20b Cell Line embryonic stem cell
3 chr12:31356400-31360800 Enhancers iPS-15b Cell Line embryonic stem cell
4 chr12:31356600-31358200 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr12:31356600-31360400 Enhancers iPS-18 Cell Line embryonic stem cell
6 chr12:31357000-31358200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr12:31357000-31360400 Enhancers HUES64 Cell Line embryonic stem cell
8 chr12:31357000-31360600 Enhancers HUES48 Cell Line embryonic stem cell
9 chr12:31357200-31359000 Weak transcription H1 Cell Line embryonic stem cell
10 chr12:31357200-31359000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr12:31357600-31358400 Enhancers Primary B cells from peripheral blood blood
12 chr12:31357600-31358400 Enhancers Primary T cells from cord blood blood
13 chr12:31357600-31358400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr12:31357600-31358600 Enhancers Primary B cells from cord blood blood
15 chr12:31357800-31358000 Active TSS GM12878-XiMat blood
16 chr12:31357800-31359400 Enhancers Cortex derived primary cultured neurospheres brain
17 chr12:31357800-31362000 Enhancers NHEK skin

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