Variant report

Variant	rs35637601
Chromosome Location	chr7:117278528-117278529
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs34018535	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34518775	0.83[AFR][1000 genomes]
rs34623047	0.83[AFR][1000 genomes]
rs35730624	0.83[AFR][1000 genomes]
rs35746597	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73477477	1.00[AMR][1000 genomes]
rs73477483	1.00[AMR][1000 genomes]
rs73477495	1.00[AMR][1000 genomes]
rs73479305	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3384260	chr7:117277612-117278579	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:117245200-117294000	Weak transcription	Pancreas	Pancrea
2	chr7:117258200-117286600	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr7:117269400-117283000	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr7:117270800-117285600	Weak transcription	Stomach Mucosa	stomach
5	chr7:117271600-117285600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr7:117271800-117281600	Weak transcription	Duodenum Mucosa	Duodenum
7	chr7:117271800-117285600	Weak transcription	Fetal Intestine Large	intestine
8	chr7:117272600-117286600	Weak transcription	Fetal Intestine Small	intestine
9	chr7:117274600-117287400	Weak transcription	Sigmoid Colon	Sigmoid Colon

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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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