Variant report

Variant	rs7745837
Chromosome Location	chr6:69460894-69460895
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:69451157..69453951-chr6:69460011..69462133,3	K562	blood:
2	chr6:69457273..69460915-chr6:69461599..69464794,3	K562	blood:
3	chr6:69452256..69454867-chr6:69459665..69461223,2	K562	blood:

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs1033520	0.84[JPT][hapmap]
rs10455674	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10455676	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10484791	0.95[CHB][hapmap];0.95[JPT][hapmap];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10945138	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10945139	0.81[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10945141	0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs10945142	0.85[CHB][hapmap];0.90[JPT][hapmap]
rs11752398	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11752837	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12154008	0.81[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12192235	0.98[ASN][1000 genomes]
rs12199251	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12200101	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12201488	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12206940	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12210045	1.00[CHB][hapmap];0.89[JPT][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12214149	0.85[CHB][hapmap];0.90[JPT][hapmap]
rs13218712	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2073135	0.81[CHB][hapmap];0.84[JPT][hapmap];0.88[ASN][1000 genomes]
rs2246104	0.91[CHB][hapmap];0.95[JPT][hapmap]
rs2253759	0.89[JPT][hapmap]
rs2253866	0.90[JPT][hapmap]
rs2254654	1.00[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs2585592	0.83[CEU][hapmap];0.85[JPT][hapmap];0.86[EUR][1000 genomes]
rs2585597	0.85[JPT][hapmap];0.82[EUR][1000 genomes]
rs2585598	0.83[CEU][hapmap];0.84[JPT][hapmap];0.88[EUR][1000 genomes]
rs2585599	0.90[JPT][hapmap];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2585600	0.88[CEU][hapmap];0.90[JPT][hapmap];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2585604	0.81[CEU][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2585621	1.00[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs2585622	1.00[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs2585626	0.81[JPT][hapmap]
rs2585627	0.81[JPT][hapmap]
rs2746125	0.90[JPT][hapmap];0.80[EUR][1000 genomes]
rs2746127	0.86[JPT][hapmap]
rs2746130	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2746131	0.82[EUR][1000 genomes]
rs2746132	0.88[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2746134	0.81[EUR][1000 genomes]
rs2746135	0.98[ASN][1000 genomes]
rs2746137	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2746140	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2746141	0.84[JPT][hapmap]
rs2802676	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2802677	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2802680	0.81[CEU][hapmap];0.91[JPT][hapmap];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2802683	0.91[JPT][hapmap];0.80[ASN][1000 genomes]
rs2802684	0.90[JPT][hapmap];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2802687	0.84[CEU][hapmap];0.86[JPT][hapmap];0.86[EUR][1000 genomes]
rs2802688	0.86[JPT][hapmap];0.80[EUR][1000 genomes]
rs2802689	0.89[JPT][hapmap]
rs2802691	0.84[JPT][hapmap]
rs2802693	0.89[JPT][hapmap]
rs2802694	0.85[JPT][hapmap]
rs2802701	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs3121775	0.84[CEU][hapmap];0.86[JPT][hapmap];0.85[EUR][1000 genomes]
rs41328149	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs4358587	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4507548	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6931354	0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs715294	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7768591	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886130	chr6:68950298-69531957	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:69452600-69464800	Weak transcription	Fetal Lung	lung
2	chr6:69457400-69466000	Weak transcription	Fetal Brain Female	brain
3	chr6:69457400-69466400	Weak transcription	Brain Anterior Caudate	brain
4	chr6:69457600-69464000	Weak transcription	Brain Substantia Nigra	brain
5	chr6:69460600-69461000	Enhancers	Brain Angular Gyrus	brain
6	chr6:69460600-69461000	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr6:69460800-69461200	Enhancers	Brain Cingulate Gyrus	brain

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