Variant report

Variant rs11617982
Chromosome Location chr13:95650792-95650793
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:95646600-95654400 Weak transcription Osteobl bone
2 chr13:95648400-95650800 Enhancers ES-WA7 Cell Line embryonic stem cell
3 chr13:95648400-95650800 Enhancers HUES48 Cell Line embryonic stem cell
4 chr13:95648400-95650800 Enhancers iPS-18 Cell Line embryonic stem cell
5 chr13:95648400-95651000 Enhancers iPS-20b Cell Line embryonic stem cell
6 chr13:95649200-95655600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr13:95649800-95651000 Enhancers ES-I3 Cell Line embryonic stem cell
8 chr13:95649800-95651000 Enhancers HUES6 Cell Line embryonic stem cell
9 chr13:95649800-95651000 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr13:95650400-95651200 Enhancers H1 Cell Line embryonic stem cell
11 chr13:95650600-95650800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr13:95650600-95651200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
13 chr13:95650600-95654200 Weak transcription H9 Cell Line embryonic stem cell
14 chr13:95650600-95654600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell

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