Variant report

Variant rs7910021
Chromosome Location chr10:93545722-93545723
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:93539800-93547000 Weak transcription Esophagus oesophagus
2 chr10:93541000-93555800 Weak transcription Primary B cells from cord blood blood
3 chr10:93542600-93547000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr10:93543000-93548200 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr10:93543000-93548200 Weak transcription iPS-20b Cell Line embryonic stem cell
6 chr10:93543000-93548400 Weak transcription HUES64 Cell Line embryonic stem cell
7 chr10:93543200-93547000 Weak transcription iPS-15b Cell Line embryonic stem cell
8 chr10:93543400-93548200 Weak transcription iPS-18 Cell Line embryonic stem cell
9 chr10:93543400-93548400 Weak transcription HUES48 Cell Line embryonic stem cell
10 chr10:93543600-93548400 Weak transcription H1 Cell Line embryonic stem cell
11 chr10:93545400-93546000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr10:93545400-93546000 Enhancers NHEK skin
13 chr10:93545400-93546200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr10:93545600-93545800 Enhancers HMEC breast

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