Variant report

Variant	rs6753552
Chromosome Location	chr2:50713807-50713808
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	chr2:50712217..50714362-chr2:50715383..50718092,2	MCF-7	breast:

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1006138	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1014430	0.89[ASN][1000 genomes]
rs10168080	0.87[ASN][1000 genomes]
rs10176959	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10183541	0.98[ASN][1000 genomes]
rs10187846	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10190305	0.87[ASN][1000 genomes]
rs10191072	0.88[ASN][1000 genomes]
rs1019318	0.88[ASN][1000 genomes]
rs10199840	0.87[ASN][1000 genomes]
rs10207057	0.88[ASN][1000 genomes]
rs10210592	0.88[ASN][1000 genomes]
rs10211193	0.88[ASN][1000 genomes]
rs1030050	0.87[ASN][1000 genomes]
rs12713104	0.85[ASN][1000 genomes]
rs13012186	0.88[ASN][1000 genomes]
rs13034257	0.88[ASN][1000 genomes]
rs1984957	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2041868	0.86[ASN][1000 genomes]
rs2041869	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2058751	0.82[ASN][1000 genomes]
rs2058752	0.82[ASN][1000 genomes]
rs2066948	0.86[ASN][1000 genomes]
rs2111065	0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2111066	0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2111069	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2160448	0.86[ASN][1000 genomes]
rs2160449	0.87[ASN][1000 genomes]
rs2216171	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6545172	0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6545173	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6545174	0.93[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6545175	0.92[ASN][1000 genomes]
rs6545176	0.90[ASN][1000 genomes]
rs6545177	0.86[ASN][1000 genomes]
rs6545178	0.86[ASN][1000 genomes]
rs6713061	0.87[ASN][1000 genomes]
rs6722389	0.87[ASN][1000 genomes]
rs6732076	0.87[ASN][1000 genomes]
rs7564428	0.93[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7566514	0.88[ASN][1000 genomes]
rs759503	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7595040	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs759505	0.83[ASN][1000 genomes]
rs759506	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv492164	chr2:50399251-51029090	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1000653	chr2:50417660-51083470	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv535693	chr2:50417660-51083470	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv948361	chr2:50611076-50785178	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv933786	chr2:50628354-50780185	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1010510	chr2:50649641-51011565	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv535694	chr2:50649641-51011565	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv532650	chr2:50675808-51136752	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv491644	chr2:50680795-50892906	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv498102	chr2:50680795-50937503	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv2724	chr2:50688876-50734321	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv532651	chr2:50712339-50758351	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50691200-50716000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr2:50691600-50718600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr2:50699000-50742000	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr2:50704400-50718600	Weak transcription	Fetal Brain Male	brain
5	chr2:50706200-50719000	Weak transcription	Stomach Mucosa	stomach
6	chr2:50706600-50719400	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr2:50711600-50716600	Strong transcription	Fetal Brain Female	brain
8	chr2:50712400-50714600	Strong transcription	Brain Germinal Matrix	brain
9	chr2:50712600-50718800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr2:50713400-50718200	Weak transcription	Brain Angular Gyrus	brain

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