Variant report

Variant rs13175335
Chromosome Location chr5:180096234-180096235
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:180086200-180100400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr5:180092000-180097200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr5:180095400-180096400 Bivalent Enhancer HepG2 liver
4 chr5:180095600-180097800 Enhancers K562 blood
5 chr5:180096000-180096800 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
6 chr5:180096000-180097200 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
7 chr5:180096000-180097400 Enhancers Brain Cingulate Gyrus brain
8 chr5:180096000-180097400 Enhancers Brain Hippocampus Middle brain
9 chr5:180096000-180097400 Enhancers Brain Substantia Nigra brain
10 chr5:180096200-180097400 Enhancers Brain Angular Gyrus brain
11 chr5:180096200-180097800 Enhancers HSMM muscle
12 chr5:180096200-180097800 Enhancers HSMMtube muscle

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