Variant report

Variant	rs71421871
Chromosome Location	chr14:105018836-105018837
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:105017888..105020132-chr14:105106949..105108571,2	MCF-7	breast:
2	chr14:105017735..105019335-chr6:28831183..28833671,2	MCF-7	breast:
3	chr14:105017921..105022172-chr14:105022189..105024897,5	MCF-7	breast:
4	chr14:105018505..105021042-chr14:105030444..105032502,2	MCF-7	breast:
5	chr14:105016071..105018557-chr14:105018817..105021096,3	K562	blood:

Variant related genes	Relation type
ENSG00000225595	Chromatin interaction

Extended variants
information (count: 81 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs11849460	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12435213	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12435241	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12894325	0.83[ASN][1000 genomes]
rs28406509	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28419025	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28434197	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28538818	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28559773	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28658432	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs28756902	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34115973	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34220962	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34344768	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34453164	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34600691	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34677118	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34686607	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34785484	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34793922	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34925347	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34967457	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35164057	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35374053	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35816659	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs36048730	0.90[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs36050392	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs36051245	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs36116500	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3936136	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3936137	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4341690	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4407001	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4465541	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4983405	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4983428	0.83[ASN][1000 genomes]
rs4983429	0.83[ASN][1000 genomes]
rs4983430	0.83[ASN][1000 genomes]
rs4983597	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4983599	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4983604	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4983605	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4983606	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4983607	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4983609	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs5027824	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs5027826	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs58381709	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs58869604	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs59862477	0.83[ASN][1000 genomes]
rs59952466	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs60629623	0.83[ASN][1000 genomes]
rs66488742	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs67776435	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs68185009	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72713804	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1826669	chr14:104554461-105065941	Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv1049810	chr14:104577600-105060539	Bivalent Enhancer Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv530812	chr14:104775571-105364883	Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
4	esv2761599	chr14:104789113-105067734	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv1054482	chr14:104961016-105037016	Enhancers Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1035993	chr14:104965025-105037016	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1053751	chr14:104968968-105036524	Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv542221	chr14:104968968-105036524	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv1042527	chr14:104968968-105052401	Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv542222	chr14:104968968-105052401	Bivalent Enhancer Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv1051647	chr14:104983302-105153720	Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	30 gene(s)	inside rSNPs	diseases
12	nsv542223	chr14:104983302-105153720	Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	30 gene(s)	inside rSNPs	diseases
13	nsv566045	chr14:104983655-105037425	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
14	esv1821679	chr14:104991128-105037557	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
15	esv1816766	chr14:105007585-105126354	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
16	esv1828013	chr14:105007815-105037425	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
17	esv1831875	chr14:105007815-105037425	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
18	nsv902371	chr14:105011436-105057102	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
19	nsv902372	chr14:105011436-105200377	Genic enhancers Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
20	esv1831726	chr14:105011590-105037425	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
21	esv1818095	chr14:105011617-105037425	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
22	esv1817661	chr14:105011775-105040988	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
23	nsv566046	chr14:105012010-105019386	Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
24	esv1823950	chr14:105012253-105023512	Genic enhancers Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
25	nsv902373	chr14:105012858-105078153	Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105015800-105020600	Weak transcription	Fetal Brain Female	brain
2	chr14:105016400-105019600	Weak transcription	Brain Germinal Matrix	brain
3	chr14:105018000-105019200	Weak transcription	Fetal Brain Male	brain
4	chr14:105018200-105019600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr14:105018800-105019000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin

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