Variant report

Variant	rs4721335
Chromosome Location	chr7:14505041-14505042
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:14503536..14506450-chr7:14511181..14513157,3	K562	blood:

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10235540	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs10247453	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10260659	0.81[CEU][hapmap]
rs10263131	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1030578	0.84[CEU][hapmap];0.81[EUR][1000 genomes]
rs10499441	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10499442	0.81[CEU][hapmap]
rs11762226	1.00[CEU][hapmap]
rs11767969	0.87[CEU][hapmap]
rs11771647	0.88[CEU][hapmap]
rs11771951	0.92[CEU][hapmap];0.90[EUR][1000 genomes]
rs11982590	0.89[CEU][hapmap]
rs12666867	0.81[CEU][hapmap]
rs12670458	0.88[CEU][hapmap];0.90[CHB][hapmap];0.82[JPT][hapmap]
rs12674261	0.80[CEU][hapmap]
rs12699617	0.96[CEU][hapmap]
rs12699618	1.00[CEU][hapmap];0.85[YRI][hapmap]
rs12699619	1.00[CEU][hapmap];0.86[JPT][hapmap];0.85[YRI][hapmap];0.85[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs12699621	0.92[CEU][hapmap];0.91[EUR][1000 genomes]
rs12699622	0.80[CEU][hapmap]
rs12699624	0.83[CEU][hapmap]
rs12699626	0.88[CEU][hapmap]
rs12699627	0.84[CEU][hapmap]
rs12699628	0.83[CEU][hapmap]
rs12699635	0.88[CEU][hapmap]
rs12699636	0.82[CEU][hapmap]
rs13223986	0.82[CEU][hapmap];1.00[YRI][hapmap]
rs13236153	0.86[CEU][hapmap]
rs13238777	0.86[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs13243691	1.00[CEU][hapmap]
rs13438642	0.80[CEU][hapmap]
rs1367780	0.87[CEU][hapmap];0.82[EUR][1000 genomes]
rs1367781	0.83[CEU][hapmap];0.95[CHB][hapmap]
rs1431520	0.96[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]
rs1431521	0.81[CEU][hapmap]
rs1431525	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1431526	1.00[CEU][hapmap];0.89[YRI][hapmap]
rs1431527	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1431532	1.00[CEU][hapmap];0.82[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs1541874	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1978671	0.95[CEU][hapmap];0.86[JPT][hapmap];0.94[EUR][1000 genomes]
rs1991685	0.80[CEU][hapmap]
rs2116314	0.83[CEU][hapmap]
rs2116315	0.89[CEU][hapmap]
rs2116319	0.88[CEU][hapmap]
rs2884348	1.00[CEU][hapmap];0.86[JPT][hapmap];0.94[EUR][1000 genomes]
rs3823843	0.80[CEU][hapmap]
rs4370419	0.81[CEU][hapmap]
rs4607508	0.91[EUR][1000 genomes]
rs4719405	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4719406	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4719407	0.84[CEU][hapmap];0.82[EUR][1000 genomes]
rs4719409	0.84[CEU][hapmap]
rs4721336	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4721337	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4721338	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs6461102	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6461104	0.80[CEU][hapmap]
rs6943928	1.00[CEU][hapmap];0.85[YRI][hapmap];0.83[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs6959924	0.81[CEU][hapmap]
rs7777868	0.91[EUR][1000 genomes]
rs7782805	1.00[CEU][hapmap];0.82[JPT][hapmap];0.92[EUR][1000 genomes]
rs7783911	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7793372	0.83[CEU][hapmap];1.00[CHB][hapmap];0.80[EUR][1000 genomes]
rs7794554	0.94[EUR][1000 genomes]
rs7807072	0.81[CEU][hapmap]
rs9639203	0.80[CEU][hapmap]
rs9690425	1.00[CEU][hapmap];0.86[YRI][hapmap];0.85[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs987449	0.80[CEU][hapmap]

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	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv915603	chr7:14443884-14624268	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv1848567	chr7:14464118-14579801	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv887707	chr7:14471682-14576163	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv887708	chr7:14494508-14617982	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14504800-14505800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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