Variant report

Variant	rs17357253
Chromosome Location	chr7:16113964-16113965
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	chr7:16101293..16103976-chr7:16112163..16114440,2	K562	blood:
2	chr7:16113784..16116426-chr7:16125295..16127374,2	K562	blood:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1527220	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs1528136	0.87[ASN][1000 genomes]
rs1528147	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1528149	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17285792	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17286418	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17357511	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17358277	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs17359183	0.87[ASN][1000 genomes]
rs17359294	0.87[ASN][1000 genomes]
rs1918259	1.00[CHB][hapmap]
rs2389581	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28422957	0.85[EUR][1000 genomes]
rs3857708	0.83[ASN][1000 genomes]
rs3857709	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4621696	0.83[ASN][1000 genomes]
rs56290213	0.95[ASN][1000 genomes]
rs60333130	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62439474	0.87[ASN][1000 genomes]
rs62440849	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62440852	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62440855	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62442360	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs62442361	0.81[AMR][1000 genomes]
rs6952865	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73056339	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs740823	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7778438	1.00[CHB][hapmap]
rs987932	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016642	chr7:15884061-16799788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv949309	chr7:15986709-16236162	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv949555	chr7:16078412-16279290	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 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	chr7:16103600-16114800	Weak transcription	Fetal Heart	heart
2	chr7:16113600-16117400	Weak transcription	Fetal Lung	lung

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