Variant report

Variant	rs12660150
Chromosome Location	chr6:34448434-34448435
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:34441851..34443719-chr6:34445470..34448449,2	K562	blood:
2	chr6:34439648..34441569-chr6:34446146..34448661,2	K562	blood:

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs12660470	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12661696	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12663061	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1409284	0.83[EUR][1000 genomes]
rs1886980	0.83[EUR][1000 genomes]
rs1889733	1.00[AFR][1000 genomes]
rs205271	1.00[AFR][1000 genomes]
rs206938	1.00[AFR][1000 genomes]
rs2395563	1.00[AFR][1000 genomes]
rs2395565	1.00[AFR][1000 genomes]
rs2395596	0.83[EUR][1000 genomes]
rs2840286	1.00[AFR][1000 genomes]
rs2894399	1.00[AFR][1000 genomes]
rs34603400	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3778069	0.83[EUR][1000 genomes]
rs3778071	0.83[EUR][1000 genomes]
rs3778075	0.83[EUR][1000 genomes]
rs3798546	0.83[EUR][1000 genomes]
rs3798549	0.83[EUR][1000 genomes]
rs3822986	0.83[EUR][1000 genomes]
rs3846870	1.00[AFR][1000 genomes]
rs3857561	1.00[AFR][1000 genomes]
rs3945698	0.83[EUR][1000 genomes]
rs443351	1.00[AFR][1000 genomes]
rs453919	1.00[AFR][1000 genomes]
rs4713778	1.00[AFR][1000 genomes]
rs4713814	1.00[AFR][1000 genomes]
rs55660517	0.83[EUR][1000 genomes]
rs56781192	0.83[EUR][1000 genomes]
rs58067963	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58218720	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs58741004	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs59738570	0.83[EUR][1000 genomes]
rs60793757	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61453687	0.83[EUR][1000 genomes]
rs6457780	1.00[AFR][1000 genomes]
rs6457782	1.00[AFR][1000 genomes]
rs6908420	1.00[AFR][1000 genomes]
rs7760590	1.00[AFR][1000 genomes]
rs7763757	0.83[EUR][1000 genomes]
rs913017	0.83[EUR][1000 genomes]
rs9461986	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022844	chr6:34317219-35060519	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv538195	chr6:34317219-35060519	Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	esv2758046	chr6:34382492-34714677	Genic enhancers Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	esv2759418	chr6:34382492-34714677	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv885785	chr6:34404636-34874002	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	nsv462904	chr6:34416388-34493012	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
7	nsv602903	chr6:34416388-34493012	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
8	nsv885786	chr6:34426884-34542662	Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34441400-34494000	Weak transcription	Right Atrium	heart
2	chr6:34444600-34468200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr6:34444800-34452400	Weak transcription	Fetal Thymus	thymus
4	chr6:34444800-34452600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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