Variant report

Variant rs17007868
Chromosome Location chr1:220685580-220685581
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr1:220684000-220685800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:220684000-220685800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr1:220684400-220686000 Enhancers HMEC breast
5 chr1:220684600-220685600 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr1:220684600-220685600 Enhancers HUES6 Cell Line embryonic stem cell
7 chr1:220684600-220685600 Enhancers iPS-15b Cell Line embryonic stem cell
8 chr1:220684600-220685800 Enhancers Hela-S3 cervix
9 chr1:220684600-220686000 Enhancers Fetal Heart heart
10 chr1:220684800-220685600 Enhancers ES-WA7 Cell Line embryonic stem cell
11 chr1:220685000-220685800 Enhancers iPS-18 Cell Line embryonic stem cell
12 chr1:220685200-220685600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr1:220685200-220685800 Enhancers Left Ventricle heart
14 chr1:220685200-220689400 Weak transcription iPS-20b Cell Line embryonic stem cell
15 chr1:220685400-220685800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
16 chr1:220685400-220686200 Enhancers NHEK skin
17 chr1:220685400-220687000 Weak transcription Placenta Placenta

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