Variant report

Variant	rs4261112
Chromosome Location	chr1:159413460-159413461
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10908720	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11265191	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11265196	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11265204	0.93[ASN][1000 genomes]
rs11265205	0.90[ASN][1000 genomes]
rs11811256	0.89[ASN][1000 genomes]
rs12023055	0.96[ASN][1000 genomes]
rs12034243	0.93[ASN][1000 genomes]
rs12047230	0.85[ASN][1000 genomes]
rs12048482	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12133577	0.93[ASN][1000 genomes]
rs12145079	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12734524	0.91[ASN][1000 genomes]
rs34388918	0.93[ASN][1000 genomes]
rs4656235	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61821535	0.88[ASN][1000 genomes]
rs7521220	0.91[ASN][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:159410200-159414600	Enhancers	Fetal Intestine Small	intestine
2	chr1:159410600-159415400	Enhancers	Fetal Intestine Large	intestine
3	chr1:159411600-159414200	Enhancers	Liver	Liver
4	chr1:159412200-159416800	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr1:159412400-159416600	Weak transcription	Primary monocytes fromperipheralblood	blood

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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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