Variant report

Variant	rs767374
Chromosome Location	chr1:220846703-220846704
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10495148	1.00[YRI][hapmap]
rs10495150	1.00[CEU][hapmap]
rs1073461	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs11803495	1.00[EUR][1000 genomes]
rs11806648	0.82[AFR][1000 genomes]
rs11811042	1.00[AFR][1000 genomes]
rs11811445	1.00[YRI][hapmap]
rs11811872	0.84[AFR][1000 genomes]
rs1193031	1.00[CEU][hapmap]
rs12070516	1.00[CEU][hapmap]
rs1337571	1.00[EUR][1000 genomes]
rs17007924	1.00[YRI][hapmap]
rs17008033	1.00[YRI][hapmap]
rs17008084	1.00[YRI][hapmap]
rs17008159	1.00[YRI][hapmap]
rs2786612	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs3849285	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs3897868	0.81[AFR][1000 genomes]
rs3897869	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs59609557	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6541152	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs6541153	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs6660022	1.00[CEU][hapmap]
rs6667072	1.00[EUR][1000 genomes]
rs6668644	1.00[EUR][1000 genomes]
rs6669644	1.00[EUR][1000 genomes]
rs6670387	1.00[YRI][hapmap]
rs6672055	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs6676051	1.00[CEU][hapmap]
rs6696723	0.87[EUR][1000 genomes]
rs6704108	0.82[AFR][1000 genomes]
rs73093505	1.00[EUR][1000 genomes]
rs73093521	1.00[EUR][1000 genomes]
rs73093530	1.00[EUR][1000 genomes]
rs73101842	0.87[EUR][1000 genomes]
rs73101870	1.00[EUR][1000 genomes]
rs73107667	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7512507	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs7518985	1.00[CEU][hapmap]
rs7523054	1.00[YRI][hapmap]
rs7530121	1.00[YRI][hapmap]
rs7547630	1.00[CEU][hapmap]
rs7547728	1.00[CEU][hapmap]
rs7556342	1.00[CEU][hapmap]

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	nsv468194	chr1:220845610-220885612	Bivalent Enhancer Strong transcription Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv549227	chr1:220845610-220885612	Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220829400-220847200	Weak transcription	Right Ventricle	heart
2	chr1:220845800-220848000	Enhancers	Fetal Heart	heart

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