Variant report

Variant rs1007170
Chromosome Location chr1:154881461-154881462
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:154879200-154893200 Weak transcription Stomach Smooth Muscle stomach
2 chr1:154879400-154882400 Weak transcription Spleen Spleen
3 chr1:154879800-154894800 Weak transcription Aorta Aorta
4 chr1:154880400-154881800 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr1:154880400-154894400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
6 chr1:154880800-154881800 Enhancers HepG2 liver
7 chr1:154881000-154882200 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
8 chr1:154881000-154883800 Weak transcription Right Ventricle heart
9 chr1:154881200-154881800 Enhancers Esophagus oesophagus
10 chr1:154881400-154881600 ZNF genes & repeats Cortex derived primary cultured neurospheres brain
11 chr1:154881400-154881800 Enhancers K562 blood
12 chr1:154881400-154894800 Weak transcription Brain Inferior Temporal Lobe brain

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