Variant report

Variant	rs210126
Chromosome Location	chr6:33532585-33532586
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs169738	0.82[AMR][1000 genomes]
rs169740	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs183300	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs210133	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs210156	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs210158	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs210160	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs210161	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs210170	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6910233	0.94[ASN][1000 genomes]
rs9380369	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33516800-33537600	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr6:33521200-33533800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr6:33530400-33533000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr6:33530400-33534400	Weak transcription	HMEC	breast
5	chr6:33530400-33534600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:33530400-33536800	Weak transcription	K562	blood
7	chr6:33530400-33537600	Weak transcription	GM12878-XiMat	blood
8	chr6:33530400-33538800	Weak transcription	Esophagus	oesophagus
9	chr6:33531000-33538200	Weak transcription	Primary T cells from cord blood	blood
10	chr6:33531400-33538400	Weak transcription	Osteobl	bone
11	chr6:33532200-33533000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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