Variant report

Variant	rs61638226
Chromosome Location	chr6:145875898-145875899
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	chr6:145866896..145869158-chr6:145873363..145875899,2	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs17724951	0.88[ASN][1000 genomes]
rs17797768	0.95[ASN][1000 genomes]
rs17797774	0.95[ASN][1000 genomes]
rs1935614	1.00[EUR][1000 genomes]
rs2143065	0.91[ASN][1000 genomes]
rs28568954	1.00[EUR][1000 genomes]
rs4895676	1.00[EUR][1000 genomes]
rs4895677	1.00[EUR][1000 genomes]
rs4896819	1.00[EUR][1000 genomes]
rs4896823	1.00[EUR][1000 genomes]
rs4896825	1.00[EUR][1000 genomes]
rs4896845	0.84[AMR][1000 genomes]
rs4896847	0.84[AMR][1000 genomes]
rs56241331	0.84[AMR][1000 genomes]
rs58658594	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61041405	0.95[AMR][1000 genomes]
rs61358848	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6920248	0.84[AMR][1000 genomes]
rs6925385	0.82[ASN][1000 genomes]
rs73568138	0.84[AMR][1000 genomes]
rs73568402	0.88[AFR][1000 genomes]
rs73579478	0.84[AMR][1000 genomes]
rs9485005	1.00[EUR][1000 genomes]
rs9497351	0.91[ASN][1000 genomes]
rs9497352	1.00[EUR][1000 genomes]
rs9497355	1.00[EUR][1000 genomes]
rs9497366	0.88[EUR][1000 genomes]
rs9497368	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886746	chr6:145815949-145920894	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv886747	chr6:145815949-145922777	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1028290	chr6:145819982-145911857	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv886748	chr6:145835917-145911730	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1021041	chr6:145836942-145887333	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1016881	chr6:145840961-145887333	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv538465	chr6:145840961-145887333	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145870200-145881000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:145875800-145878000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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