Variant report

Variant	rs10945148
Chromosome Location	chr6:69632576-69632577
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	chr6:69631911..69634740-chr6:69647956..69650887,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10806607	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10945147	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12174093	0.82[ASN][1000 genomes]
rs13193787	0.84[ASN][1000 genomes]
rs1403926	0.82[ASN][1000 genomes]
rs1523936	0.82[ASN][1000 genomes]
rs1523938	0.90[ASN][1000 genomes]
rs1932616	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2184724	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2184725	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2224011	0.81[ASN][1000 genomes]
rs2342763	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3798966	0.89[ASN][1000 genomes]
rs3798967	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4706061	0.82[ASN][1000 genomes]
rs4706712	0.82[ASN][1000 genomes]
rs478789	0.82[ASN][1000 genomes]
rs491833	0.82[ASN][1000 genomes]
rs497728	0.81[ASN][1000 genomes]
rs504160	0.82[ASN][1000 genomes]
rs509304	0.82[ASN][1000 genomes]
rs512094	0.81[ASN][1000 genomes]
rs522513	0.81[ASN][1000 genomes]
rs525342	0.81[ASN][1000 genomes]
rs527932	0.81[ASN][1000 genomes]
rs530244	0.82[ASN][1000 genomes]
rs550348	0.82[ASN][1000 genomes]
rs550695	0.82[ASN][1000 genomes]
rs553613	0.81[ASN][1000 genomes]
rs558452	0.82[ASN][1000 genomes]
rs6906092	0.80[ASN][1000 genomes]
rs6912997	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6920061	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6920573	0.81[ASN][1000 genomes]
rs6922823	0.82[ASN][1000 genomes]
rs6927848	0.82[ASN][1000 genomes]
rs6939663	0.89[ASN][1000 genomes]
rs6941602	0.81[ASN][1000 genomes]
rs9342736	0.81[ASN][1000 genomes]
rs9346252	0.81[ASN][1000 genomes]
rs9351741	0.80[ASN][1000 genomes]
rs9446070	0.92[ASN][1000 genomes]
rs9454636	0.82[ASN][1000 genomes]
rs9454639	0.81[ASN][1000 genomes]
rs9454655	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9689807	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470831	chr6:69581991-69654650	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv886136	chr6:69598297-69654650	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv525968	chr6:69618480-69638504	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv519494	chr6:69619007-69638504	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:69632000-69632800	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr6:69632200-69632600	Enhancers	H9 Cell Line	embryonic stem cell
3	chr6:69632200-69632800	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr6:69632200-69632800	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr6:69632200-69633000	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr6:69632400-69632800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr6:69632400-69633000	Enhancers	HUES48 Cell Line	embryonic stem cell

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