Variant report

Variant	rs6798252
Chromosome Location	chr3:151166422-151166423
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:151165718..151167387-chr3:151169116..151170709,2	K562	blood:

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs13088575	0.84[CEU][hapmap];0.82[EUR][1000 genomes]
rs2172248	0.93[ASW][hapmap];0.93[CHB][hapmap];0.83[JPT][hapmap];0.89[YRI][hapmap];0.82[AFR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4234322	0.93[CHB][hapmap];0.83[JPT][hapmap];0.86[ASN][1000 genomes]
rs4435614	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];0.95[MEX][hapmap];0.96[TSI][hapmap];0.81[YRI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4680440	0.84[CEU][hapmap];0.93[CHB][hapmap];0.83[JPT][hapmap];0.86[LWK][hapmap];0.81[TSI][hapmap];0.92[YRI][hapmap];0.85[AFR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4680442	0.84[CEU][hapmap];0.93[CHB][hapmap];0.83[JPT][hapmap];0.81[TSI][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4680443	0.84[CEU][hapmap];0.93[CHB][hapmap];0.83[JPT][hapmap];0.86[LWK][hapmap];0.81[TSI][hapmap];0.92[YRI][hapmap];0.82[AFR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6769246	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7610769	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7619322	0.93[ASW][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap];0.82[LWK][hapmap];0.98[MKK][hapmap];0.92[TSI][hapmap];0.85[YRI][hapmap];0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7621591	0.84[CEU][hapmap];0.93[CHB][hapmap];0.83[JPT][hapmap];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9289838	0.84[CEU][hapmap];0.93[CHB][hapmap];0.83[JPT][hapmap];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9812989	0.93[CHB][hapmap];0.83[JPT][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9817904	0.93[CHB][hapmap];0.83[JPT][hapmap];0.85[ASN][1000 genomes]
rs9824609	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9825817	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9843590	1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs9863400	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9871952	0.83[CEU][hapmap];0.93[CHB][hapmap];0.83[JPT][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9873499	0.83[EUR][1000 genomes]
rs9877298	0.84[CEU][hapmap];0.93[CHB][hapmap];0.82[JPT][hapmap];0.86[EUR][1000 genomes];0.88[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	nsv829757	chr3:151044880-151226442	Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1000355	chr3:151108859-151243835	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv995048	chr3:151114074-151560019	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv877649	chr3:151147968-151236562	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:151161600-151178600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:151163800-151168200	ZNF genes & repeats	Fetal Lung	lung
3	chr3:151163800-151170200	Weak transcription	Fetal Brain Male	brain
4	chr3:151166000-151166600	Active TSS	Brain Substantia Nigra	brain
5	chr3:151166200-151167200	Strong transcription	Ovary	ovary
6	chr3:151166400-151167800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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