Variant report

Variant	rs6697809
Chromosome Location	chr1:159410894-159410895
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:159410000-159412400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr1:159410200-159414600	Enhancers	Fetal Intestine Small	intestine
3	chr1:159410600-159415400	Enhancers	Fetal Intestine Large	intestine
4	chr1:159410800-159411600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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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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