Variant report

Variant rs73101823
Chromosome Location chr1:220688218-220688219
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:220683200-220689800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr1:220685200-220689400 Weak transcription iPS-20b Cell Line embryonic stem cell
3 chr1:220685600-220689000 Weak transcription ES-WA7 Cell Line embryonic stem cell
4 chr1:220685600-220689000 Weak transcription HUES6 Cell Line embryonic stem cell
5 chr1:220685600-220689200 Weak transcription iPS-15b Cell Line embryonic stem cell
6 chr1:220685800-220689400 Weak transcription iPS-18 Cell Line embryonic stem cell
7 chr1:220686800-220689200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr1:220687200-220688800 Enhancers NHEK skin
9 chr1:220687200-220691000 Enhancers HMEC breast
10 chr1:220687400-220690400 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr1:220687400-220691000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr1:220688000-220688400 Weak transcription ES-I3 Cell Line embryonic stem cell

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