Variant report

Variant rs61981591
Chromosome Location chr14:69456217-69456218
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:69447000-69471400 Weak transcription Esophagus oesophagus
2 chr14:69449200-69458400 Weak transcription HUVEC blood vessel
3 chr14:69453200-69456400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
4 chr14:69453400-69460600 Weak transcription Primary T helper naive cells fromperipheralblood blood
5 chr14:69454400-69456400 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr14:69454800-69457400 Weak transcription HUES6 Cell Line embryonic stem cell
7 chr14:69454800-69461200 Weak transcription Primary T killer naive cells fromperipheralblood blood
8 chr14:69455400-69456400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
9 chr14:69455400-69456600 Enhancers HUES64 Cell Line embryonic stem cell
10 chr14:69455600-69465200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr14:69456000-69464400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
12 chr14:69456000-69471200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr14:69456200-69456400 Enhancers iPS-15b Cell Line embryonic stem cell
14 chr14:69456200-69456800 Enhancers iPS-20b Cell Line embryonic stem cell

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