Variant report

Variant	rs2691535
Chromosome Location	chr7:77961417-77961418
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:77928905..77931883-chr7:77960086..77962563,2	K562	blood:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10254017	0.93[ASN][1000 genomes]
rs12154641	0.95[CHB][hapmap];0.93[JPT][hapmap];0.86[YRI][hapmap];0.85[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs12705409	0.94[CHB][hapmap];0.93[JPT][hapmap];0.88[YRI][hapmap];0.82[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs1860538	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1990370	0.90[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2075013	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2075014	0.84[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2159511	0.96[YRI][hapmap];0.97[ASN][1000 genomes]
rs2534646	0.83[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs2534647	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2534648	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2534649	0.83[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.84[ASN][1000 genomes]
rs2691513	1.00[CHB][hapmap];0.93[JPT][hapmap];0.93[YRI][hapmap];0.86[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs2691530	0.80[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2691531	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2691532	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2691533	0.83[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.97[YRI][hapmap];0.97[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs2691538	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2691539	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2691540	1.00[CHB][hapmap];0.93[JPT][hapmap];0.97[YRI][hapmap];0.93[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs2691544	0.94[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs2691545	0.81[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs2691546	0.90[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs4371942	0.89[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs4374924	1.00[CHB][hapmap];0.93[JPT][hapmap];0.82[YRI][hapmap];0.88[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs4556031	0.90[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs6976483	0.95[CHB][hapmap];0.93[JPT][hapmap];0.90[YRI][hapmap];0.80[ASN][1000 genomes]
rs798308	0.82[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.93[YRI][hapmap];0.84[ASN][1000 genomes]
rs798309	0.81[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.93[YRI][hapmap];0.84[ASN][1000 genomes]
rs798310	0.86[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.96[YRI][hapmap]
rs798314	0.82[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.83[YRI][hapmap];0.93[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs798317	0.93[AFR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv607654	chr7:77537964-78014329	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1022764	chr7:77911072-78316607	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:77946200-77976000	Weak transcription	Aorta	Aorta
2	chr7:77953600-77986600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:77955200-77963000	Weak transcription	Esophagus	oesophagus
4	chr7:77956800-77964400	Weak transcription	Ovary	ovary
5	chr7:77957000-77975800	Weak transcription	Brain Angular Gyrus	brain
6	chr7:77957200-77973200	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr7:77957200-77975800	Weak transcription	Brain Substantia Nigra	brain
8	chr7:77957600-77974800	Weak transcription	Brain Hippocampus Middle	brain
9	chr7:77957600-77976000	Weak transcription	Brain Cingulate Gyrus	brain
10	chr7:77957600-77978600	Weak transcription	Brain Anterior Caudate	brain
11	chr7:77958000-77979800	Weak transcription	Fetal Brain Female	brain
12	chr7:77961400-77964200	Enhancers	Fetal Intestine Small	intestine

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