Variant report

Variant rs3766062
Chromosome Location chr1:169154328-169154329
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:169130400-169195200 Weak transcription Pancreas Pancrea
2 chr1:169137600-169158000 Weak transcription Primary T cells from cord blood blood
3 chr1:169150400-169162600 Weak transcription Psoas Muscle Psoas
4 chr1:169154000-169154400 Enhancers iPS-15b Cell Line embryonic stem cell
5 chr1:169154000-169154800 Enhancers iPS-18 Cell Line embryonic stem cell
6 chr1:169154200-169154400 Enhancers Pancreatic Islets Pancreatic Islet
7 chr1:169154200-169154600 Enhancers H9 Cell Line embryonic stem cell
8 chr1:169154200-169154800 Enhancers HUES64 Cell Line embryonic stem cell
9 chr1:169154200-169155600 Enhancers HUES48 Cell Line embryonic stem cell
10 chr1:169154200-169155600 Enhancers Skeletal Muscle Female skeletal muscle

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