Variant report

Variant rs423692
Chromosome Location chr1:153005681-153005682
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:153003200-153008200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr1:153003400-153006200 Flanking Active TSS NHEK skin
3 chr1:153004800-153007400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:153005200-153005800 Enhancers HUES48 Cell Line embryonic stem cell
5 chr1:153005200-153006000 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr1:153005400-153005800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
7 chr1:153005400-153006000 Enhancers iPS-20b Cell Line embryonic stem cell
8 chr1:153005400-153006000 Enhancers Placenta Placenta
9 chr1:153005400-153007800 Enhancers HMEC breast
10 chr1:153005600-153006000 Enhancers ES-WA7 Cell Line embryonic stem cell
11 chr1:153005600-153006000 Enhancers iPS-15b Cell Line embryonic stem cell
12 chr1:153005600-153006000 Enhancers Fetal Adrenal Gland Adrenal Gland
13 chr1:153005600-153007800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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