Variant report

Variant rs10787601
Chromosome Location chr10:117560604-117560605
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:117555800-117563800 Weak transcription Aorta Aorta
2 chr10:117555800-117574000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr10:117560000-117562000 Enhancers H1 Cell Line embryonic stem cell
4 chr10:117560000-117562400 Enhancers iPS-20b Cell Line embryonic stem cell
5 chr10:117560000-117562600 Enhancers HUES64 Cell Line embryonic stem cell
6 chr10:117560200-117560800 Enhancers ES-I3 Cell Line embryonic stem cell
7 chr10:117560200-117560800 Enhancers ES-WA7 Cell Line embryonic stem cell
8 chr10:117560200-117562000 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr10:117560200-117562200 Enhancers HUES48 Cell Line embryonic stem cell
10 chr10:117560400-117561000 Enhancers HUES6 Cell Line embryonic stem cell
11 chr10:117560400-117562000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr10:117560400-117562400 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr10:117560600-117561600 Weak transcription H9 Cell Line embryonic stem cell
14 chr10:117560600-117564000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell

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