Variant report

Variant rs74063385
Chromosome Location chr14:77966859-77966860
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:77965600-77977600 Weak transcription Aorta Aorta
2 chr14:77965800-77967200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr14:77965800-77974600 Weak transcription A549 lung
4 chr14:77966000-77973400 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr14:77966000-77977400 Weak transcription HMEC breast
6 chr14:77966200-77970600 Weak transcription HSMM muscle
7 chr14:77966400-77972800 Weak transcription Esophagus oesophagus
8 chr14:77966400-77974000 Weak transcription Primary T helper cells fromperipheralblood blood
9 chr14:77966400-77976800 Weak transcription Spleen Spleen
10 chr14:77966400-77977000 Weak transcription Pancreas Pancrea
11 chr14:77966400-77977600 Weak transcription Gastric stomach
12 chr14:77966600-77967200 Flanking Active TSS HepG2 liver
13 chr14:77966600-77977000 Weak transcription Sigmoid Colon Sigmoid Colon
14 chr14:77966600-77977600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
15 chr14:77966600-77977800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
16 chr14:77966800-77972600 Weak transcription Osteobl bone
17 chr14:77966800-77972800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
18 chr14:77966800-77973200 Weak transcription Placenta Placenta

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