Variant report

Variant	rs967370
Chromosome Location	chr15:35467096-35467097
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:35466538..35468319-chr15:35479018..35480889,2	K562	blood:
2	chr15:35466950..35469719-chr15:35470407..35472296,2	K562	blood:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10152519	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10152995	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1017553	0.88[ASN][1000 genomes]
rs10444813	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11073086	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11854262	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11854457	0.92[EUR][1000 genomes]
rs11855339	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11857698	0.88[EUR][1000 genomes]
rs12232307	0.87[EUR][1000 genomes]
rs12906317	0.87[YRI][hapmap]
rs13313465	0.87[EUR][1000 genomes]
rs1380089	0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1458885	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16960534	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16960582	0.86[EUR][1000 genomes]
rs16960587	0.94[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16960605	0.93[ASN][1000 genomes]
rs1903077	0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2168959	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55662900	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55763113	0.85[ASN][1000 genomes]
rs56225597	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62006770	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62006771	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6495758	0.94[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs67156387	0.88[EUR][1000 genomes]
rs73389201	0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8026065	0.83[YRI][hapmap]
rs8027994	0.85[YRI][hapmap]
rs8031065	0.85[YRI][hapmap]
rs8038846	0.88[ASN][1000 genomes]
rs9944276	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9972525	0.88[CEU][hapmap];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3350109	chr15:34668106-35534229	Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv904073	chr15:35467096-35686267	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:35458800-35473200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr15:35459200-35467800	Weak transcription	Fetal Kidney	kidney
3	chr15:35463400-35467600	Weak transcription	Brain Anterior Caudate	brain
4	chr15:35466000-35473400	Weak transcription	NHLF	lung
5	chr15:35466200-35468600	Enhancers	K562	blood

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