Variant report

Variant	rs13005937
Chromosome Location	chr2:52225258-52225259
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	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
2	chr2:50763606..50764181-chr2:52224822..52225393,2	MCF-7	breast:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10048713	0.81[ASN][1000 genomes]
rs11889433	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11890872	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12470258	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12473317	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12473567	0.82[AMR][1000 genomes]
rs12477454	0.84[EUR][1000 genomes]
rs13019533	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13389547	0.84[ASN][1000 genomes]
rs2883608	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34887541	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34973713	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35039215	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4246582	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4335986	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4441518	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4603799	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4971782	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62140027	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62140030	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6742260	0.83[ASN][1000 genomes]
rs6753994	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6754188	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009513	chr2:51890060-52821980	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv431047	chr2:51961737-52263543	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1013553	chr2:52010500-52471153	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv535712	chr2:52010500-52471153	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1004603	chr2:52083910-52265663	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv526141	chr2:52096257-52262932	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv999607	chr2:52096309-52263162	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv1013892	chr2:52102670-52263231	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv1014342	chr2:52114176-52378299	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv874097	chr2:52165998-52227824	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv581920	chr2:52182477-52227824	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv1009680	chr2:52185751-52307426	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv535713	chr2:52185751-52307426	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv581921	chr2:52188631-52236955	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv874098	chr2:52207361-52260752	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv1007633	chr2:52217555-52862389	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
17	nsv535714	chr2:52217555-52862389	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52218000-52225800	Weak transcription	Left Ventricle	heart
2	chr2:52222400-52225400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr2:52224200-52227000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr2:52224200-52227000	Weak transcription	NHLF	lung
5	chr2:52224400-52225800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr2:52224400-52227000	Weak transcription	NHDF-Ad	bronchial
7	chr2:52225000-52225400	Enhancers	Fetal Heart	heart

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