Variant report

Variant	rs10197054
Chromosome Location	chr2:34402456-34402457
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	chr2:34401156..34402823-chr2:34426410..34428532,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10170231	0.82[ASN][1000 genomes]
rs10174698	0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10176113	0.82[ASN][1000 genomes]
rs10210068	0.83[ASN][1000 genomes]
rs10210837	0.82[ASN][1000 genomes]
rs11690457	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13421243	0.82[ASN][1000 genomes]
rs17014921	0.81[ASN][1000 genomes]
rs17432481	0.82[ASN][1000 genomes]
rs1990838	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2193805	0.82[ASN][1000 genomes]
rs2371924	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2371930	0.90[ASN][1000 genomes]
rs2888194	0.82[ASN][1000 genomes]
rs2888196	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4316922	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4670076	0.82[ASN][1000 genomes]
rs4670077	0.82[ASN][1000 genomes]
rs4670078	0.82[ASN][1000 genomes]
rs4670079	0.82[ASN][1000 genomes]
rs4670080	0.82[ASN][1000 genomes]
rs4670333	0.86[ASN][1000 genomes]
rs4670339	0.82[ASN][1000 genomes]
rs4670340	0.82[ASN][1000 genomes]
rs4670341	0.82[ASN][1000 genomes]
rs5023564	0.82[ASN][1000 genomes]
rs5023565	0.82[ASN][1000 genomes]
rs5023566	0.82[ASN][1000 genomes]
rs5023567	0.82[ASN][1000 genomes]
rs6719943	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6725420	0.84[ASN][1000 genomes]
rs6751907	0.84[ASN][1000 genomes]
rs7557064	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7595827	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006001	chr2:33991364-34858721	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv535628	chr2:33991364-34858721	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv873798	chr2:33996983-34410240	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv873799	chr2:33996983-34821990	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv999091	chr2:34154486-34993188	ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv535629	chr2:34154486-34993188	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv873804	chr2:34156867-35047107	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
8	nsv873808	chr2:34275757-34703057	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv1012401	chr2:34302403-34468097	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv833714	chr2:34348193-34504892	Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv522079	chr2:34398738-34403344	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:34402000-34402800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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