Variant report

Variant	rs6907024
Chromosome Location	chr6:119786848-119786849
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:119784285..119787164-chr6:119791659..119794640,2	K562	blood:
2	chr6:119775117..119777566-chr6:119786329..119787981,2	K562	blood:
3	chr6:119784955..119788555-chr6:119797336..119801146,3	K562	blood:
4	chr6:119773729..119776617-chr6:119785441..119787829,2	K562	blood:

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10484999	1.00[AFR][1000 genomes]
rs10485000	1.00[AFR][1000 genomes]
rs10485002	1.00[AFR][1000 genomes]
rs1342312	1.00[AFR][1000 genomes]
rs17052761	1.00[AFR][1000 genomes]
rs17080956	1.00[AFR][1000 genomes]
rs17080961	1.00[AFR][1000 genomes]
rs17080974	1.00[AFR][1000 genomes]
rs17080980	1.00[AFR][1000 genomes]
rs17080995	1.00[ASW][hapmap];1.00[AFR][1000 genomes]
rs17081016	1.00[AFR][1000 genomes]
rs17081019	1.00[AFR][1000 genomes]
rs17081022	1.00[AFR][1000 genomes]
rs17081026	1.00[AFR][1000 genomes]
rs17081029	1.00[AFR][1000 genomes]
rs17081031	1.00[AFR][1000 genomes]
rs17081044	1.00[AFR][1000 genomes]
rs2299885	1.00[AFR][1000 genomes]
rs28364695	1.00[AFR][1000 genomes]
rs3778105	1.00[AFR][1000 genomes]
rs3778106	1.00[AFR][1000 genomes]
rs3778108	1.00[AFR][1000 genomes]
rs3778109	1.00[AFR][1000 genomes]
rs3798625	1.00[AFR][1000 genomes]
rs3798626	1.00[AFR][1000 genomes]
rs3798627	1.00[AFR][1000 genomes]
rs3798628	1.00[AFR][1000 genomes]
rs3798629	1.00[AFR][1000 genomes]
rs3798630	1.00[AFR][1000 genomes]
rs3798633	1.00[AFR][1000 genomes]
rs3798634	1.00[AFR][1000 genomes]
rs3798635	1.00[AFR][1000 genomes]
rs3798637	1.00[AFR][1000 genomes]
rs3798638	1.00[AFR][1000 genomes]
rs3798639	1.00[AFR][1000 genomes]
rs3798640	1.00[AFR][1000 genomes]
rs3798641	1.00[AFR][1000 genomes]
rs3798642	1.00[AFR][1000 genomes]
rs3798643	1.00[AFR][1000 genomes]
rs3798645	1.00[AFR][1000 genomes]
rs3798646	1.00[AFR][1000 genomes]
rs3798647	1.00[AFR][1000 genomes]
rs3798656	1.00[AFR][1000 genomes]
rs3823001	1.00[AFR][1000 genomes]
rs3823004	1.00[AFR][1000 genomes]
rs3823005	1.00[AFR][1000 genomes]
rs57114522	1.00[AFR][1000 genomes]
rs57560532	1.00[AFR][1000 genomes]
rs57606082	1.00[AFR][1000 genomes]
rs57900721	1.00[AFR][1000 genomes]
rs58263645	1.00[AFR][1000 genomes]
rs59771009	1.00[AFR][1000 genomes]
rs60944461	1.00[AFR][1000 genomes]
rs6918093	1.00[AFR][1000 genomes]
rs6922532	1.00[AFR][1000 genomes]
rs6922683	1.00[AFR][1000 genomes]
rs6922722	1.00[AFR][1000 genomes]
rs6922867	1.00[AFR][1000 genomes]
rs6923320	1.00[AFR][1000 genomes]
rs6923365	1.00[AFR][1000 genomes]
rs6923755	1.00[AFR][1000 genomes]
rs6929286	1.00[AFR][1000 genomes]
rs6935561	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7745631	1.00[AFR][1000 genomes]
rs7746844	1.00[AFR][1000 genomes]
rs947589	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3447598	chr6:119558591-120119384	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	esv3389526	chr6:119558598-120190087	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1027904	chr6:119709488-120001986	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv533518	chr6:119712186-119998618	ZNF genes & repeats Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	esv3442553	chr6:119742069-120076777	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119776200-119789200	Weak transcription	Fetal Heart	heart
2	chr6:119785200-119788600	Weak transcription	Primary hematopoietic stem cells	blood
3	chr6:119785600-119787600	Weak transcription	Dnd41	blood

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