Variant report

Variant	rs36050742
Chromosome Location	chr4:110167688-110167689
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	chr4:110160872..110163368-chr4:110165331..110168777,3	K562	blood:
2	chr4:110166617..110169295-chr4:110175450..110177402,2	K562	blood:

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10007809	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10030903	0.92[AFR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10033402	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10488876	0.87[ASN][1000 genomes]
rs11932715	0.82[ASN][1000 genomes]
rs11934385	0.87[ASN][1000 genomes]
rs11939502	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11943443	0.87[ASN][1000 genomes]
rs11946089	0.87[ASN][1000 genomes]
rs12640529	0.87[AMR][1000 genomes]
rs12649586	0.87[AMR][1000 genomes]
rs17039896	0.87[AMR][1000 genomes]
rs17039914	0.87[AMR][1000 genomes]
rs17040025	0.87[AMR][1000 genomes]
rs17040052	0.87[AMR][1000 genomes]
rs17040077	0.87[ASN][1000 genomes]
rs17040080	0.87[ASN][1000 genomes]
rs17040084	0.87[ASN][1000 genomes]
rs17040089	0.87[ASN][1000 genomes]
rs17040091	0.87[ASN][1000 genomes]
rs17040094	0.87[ASN][1000 genomes]
rs17040097	0.87[ASN][1000 genomes]
rs2007788	0.87[ASN][1000 genomes]
rs2007789	0.87[ASN][1000 genomes]
rs2189705	0.87[ASN][1000 genomes]
rs2526439	0.87[AMR][1000 genomes]
rs2526446	0.87[AMR][1000 genomes]
rs2526448	0.87[AMR][1000 genomes]
rs2704105	0.87[AMR][1000 genomes]
rs2704111	0.87[AMR][1000 genomes]
rs28503704	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28698832	0.80[ASN][1000 genomes]
rs41395650	0.87[ASN][1000 genomes]
rs56844951	0.87[ASN][1000 genomes]
rs56946607	0.87[ASN][1000 genomes]
rs56982165	0.87[ASN][1000 genomes]
rs57810497	0.87[ASN][1000 genomes]
rs58194956	0.82[ASN][1000 genomes]
rs58325010	0.87[ASN][1000 genomes]
rs58848856	0.87[ASN][1000 genomes]
rs61659244	0.87[ASN][1000 genomes]
rs6533415	0.87[AMR][1000 genomes]
rs6825027	0.87[ASN][1000 genomes]
rs6825515	0.87[ASN][1000 genomes]
rs6825986	0.87[ASN][1000 genomes]
rs6842851	0.87[ASN][1000 genomes]
rs6843241	0.87[ASN][1000 genomes]
rs6843308	0.87[ASN][1000 genomes]
rs6849377	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7656748	0.87[ASN][1000 genomes]
rs7662008	0.87[ASN][1000 genomes]
rs7675810	0.87[ASN][1000 genomes]
rs7677934	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7681584	0.82[ASN][1000 genomes]
rs7692009	0.87[ASN][1000 genomes]
rs7692026	0.87[ASN][1000 genomes]
rs9999518	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv461613	chr4:109922064-110593460	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv595129	chr4:109922064-110593460	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv461614	chr4:110165434-110220384	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv595131	chr4:110165434-110220384	Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 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	chr4:110155200-110192200	Weak transcription	Hela-S3	cervix
2	chr4:110165200-110171400	Weak transcription	HSMM	muscle
3	chr4:110165400-110171200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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