Variant report

Variant	rs12255894
Chromosome Location	chr10:91429429-91429430
allele	C/T
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:10)

rs_ID	r²[population]
rs10047318	1.00[AMR][1000 genomes]
rs12246132	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12246192	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12247535	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12249849	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12250250	1.00[AFR][1000 genomes]
rs12253906	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs12258258	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12259477	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12260995	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91425400-91430000	Weak transcription	HSMMtube	muscle
2	chr10:91427800-91429600	Enhancers	Fetal Intestine Large	intestine
3	chr10:91427800-91431400	Enhancers	HepG2	liver
4	chr10:91428200-91429600	Enhancers	Fetal Intestine Small	intestine
5	chr10:91428400-91431800	Enhancers	Fetal Muscle Leg	muscle
6	chr10:91429000-91430200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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