Variant report

Variant	rs574033856
Chromosome Location	chr6:64200276-64200277
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019831	chr6:63279677-64230736	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv970135	chr6:64200126-64215926	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:64197600-64202400	Weak transcription	Stomach Mucosa	stomach
2	chr6:64197600-64202400	Weak transcription	HepG2	liver
3	chr6:64197600-64203400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:64198000-64202200	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr6:64198400-64200600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr6:64198400-64200800	Weak transcription	A549	lung
7	chr6:64198400-64201000	Weak transcription	Liver	Liver
8	chr6:64200000-64201000	Enhancers	Hela-S3	cervix

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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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