Variant report

Variant	rs1374752
Chromosome Location	chr11:45637375-45637376
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1488679	0.82[EUR][1000 genomes]
rs1488681	0.83[EUR][1000 genomes]
rs275586	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs275587	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs275588	0.83[EUR][1000 genomes]
rs275589	0.83[EUR][1000 genomes]
rs275590	0.82[EUR][1000 genomes]
rs275591	0.84[EUR][1000 genomes]
rs275592	0.84[EUR][1000 genomes]
rs275593	0.84[EUR][1000 genomes]
rs275594	0.84[EUR][1000 genomes]
rs275595	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs275599	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7396878	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7930664	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs901906	0.85[CHB][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45628400-45639000	Weak transcription	Fetal Muscle Leg	muscle
2	chr11:45628600-45641600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:45630000-45638800	Weak transcription	Left Ventricle	heart
4	chr11:45633800-45641800	Weak transcription	Gastric	stomach

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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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