Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:167996633..167999387-chr2:168002848..168005501,2	K562	blood:

Variant related genes	Relation type
ENSG00000254552	Chromatin interaction

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10451542	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1155284	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11888230	0.90[EUR][1000 genomes]
rs11893404	0.87[EUR][1000 genomes]
rs11902653	0.88[EUR][1000 genomes]
rs1479592	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16853050	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16853057	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4000962	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55733637	0.86[EUR][1000 genomes]
rs58616240	0.86[EUR][1000 genomes]
rs6432979	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66701411	0.88[EUR][1000 genomes]
rs67074513	0.83[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs6711844	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6720352	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6720763	0.86[EUR][1000 genomes]
rs67386767	0.87[EUR][1000 genomes]
rs67726376	0.86[EUR][1000 genomes]
rs73017939	0.89[EUR][1000 genomes]
rs7569147	0.86[EUR][1000 genomes]
rs7575729	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs988445	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs998899	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875376	chr2:167844513-168037489	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:168000200-168005400	Weak transcription	Primary hematopoietic stem cells	blood
2	chr2:168000200-168009600	Weak transcription	Psoas Muscle	Psoas
3	chr2:168001000-168008600	Weak transcription	NHLF	lung
4	chr2:168001600-168005400	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr2:168002200-168005400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr2:168002400-168005200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr2:168003200-168004200	Enhancers	Fetal Intestine Large	intestine
8	chr2:168003200-168004400	Enhancers	Fetal Intestine Small	intestine

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