Variant report

Variant	rs2701634
Chromosome Location	chr12:120860351-120860352
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11065103	0.84[ASN][1000 genomes]
rs11834189	0.81[ASN][1000 genomes]
rs12227457	0.84[ASN][1000 genomes]
rs12302952	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1732847	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1794741	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2701635	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2859282	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:120827200-120875200	Weak transcription	Right Atrium	heart
2	chr12:120852400-120875200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:120856400-120866400	Weak transcription	Fetal Intestine Small	intestine
4	chr12:120858000-120862400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:120860000-120863200	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr12:120860000-120863400	Weak transcription	HUES6 Cell Line	embryonic stem cell

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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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