Variant report

Variant	rs538365564
Chromosome Location	chr7:136280008-136280009
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv518439	chr7:136134265-136452082	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv3476807	chr7:136279874-136280383	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3476809	chr7:136279874-136280383	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3359078	chr7:136279931-136280321	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136278600-136280800	Enhancers	Colon Smooth Muscle	Colon
2	chr7:136279200-136280800	Enhancers	Rectal Smooth Muscle	rectum
3	chr7:136279600-136280200	Enhancers	Fetal Brain Male	brain
4	chr7:136279600-136280600	Weak transcription	Fetal Stomach	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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