Variant report

Variant	rs10882711
Chromosome Location	chr10:97776722-97776723
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97765400-97777200	Weak transcription	Brain Hippocampus Middle	brain
2	chr10:97767600-97786600	Weak transcription	Aorta	Aorta
3	chr10:97770600-97776800	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr10:97771200-97777200	Weak transcription	Left Ventricle	heart
5	chr10:97774600-97782200	Weak transcription	K562	blood
6	chr10:97775800-97777600	Enhancers	Fetal Stomach	stomach
7	chr10:97776400-97777400	Enhancers	Rectal Smooth Muscle	rectum
8	chr10:97776600-97777000	Enhancers	Stomach Smooth Muscle	stomach

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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