Variant report

Variant rs147930949
Chromosome Location chr19:23881765-23881766
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:23880600-23882800 Enhancers HUES48 Cell Line embryonic stem cell
2 chr19:23881200-23882600 Enhancers iPS-15b Cell Line embryonic stem cell
3 chr19:23881400-23881800 Enhancers ES-I3 Cell Line embryonic stem cell
4 chr19:23881400-23881800 Enhancers HUES6 Cell Line embryonic stem cell
5 chr19:23881400-23881800 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr19:23881400-23881800 Flanking Active TSS Rectal Mucosa Donor 29 rectum
7 chr19:23881400-23882200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr19:23881400-23882600 Enhancers iPS-20b Cell Line embryonic stem cell
9 chr19:23881400-23882800 Enhancers HUES64 Cell Line embryonic stem cell
10 chr19:23881400-23882800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr19:23881400-23883000 Flanking Active TSS NHEK skin
12 chr19:23881400-23883400 Enhancers Placenta Placenta
13 chr19:23881600-23881800 Enhancers K562 blood
14 chr19:23881600-23882200 Active TSS Rectal Mucosa Donor 31 rectum
15 chr19:23881600-23882400 Enhancers H9 Cell Line embryonic stem cell
16 chr19:23881600-23882400 Enhancers Esophagus oesophagus
17 chr19:23881600-23882800 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin

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