Variant report

Variant	rs56352322
Chromosome Location	chr19:51407293-51407294
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:51405117..51408111-chr19:51411398..51414932,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000167749	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs1139132	0.88[ASN][1000 genomes]
rs11881354	0.89[ASN][1000 genomes]
rs1701925	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2235091	0.87[ASN][1000 genomes]
rs2569531	0.89[ASN][1000 genomes]
rs3875143	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1060760	chr19:50883425-51463712	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
2	nsv1058177	chr19:50984774-51463712	Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
3	nsv511623	chr19:51400775-51408842	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
4	esv3322316	chr19:51404940-51410038	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
5	esv3373904	chr19:51405340-51409338	Weak transcription Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
6	esv3318619	chr19:51406376-51408809	Enhancers Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
7	esv18371	chr19:51406607-51408006	Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
8	nsv821568	chr19:51406607-51408006	Bivalent/Poised TSS Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
9	nsv512588	chr19:51406618-51408346	Bivalent/Poised TSS Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
10	esv3318617	chr19:51406707-51408403	Bivalent/Poised TSS Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
11	esv1709160	chr19:51406777-51408353	Bivalent/Poised TSS Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
12	esv3318620	chr19:51406803-51408414	Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
13	nsv138426	chr19:51406850-51408425	Bivalent/Poised TSS Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
14	esv989477	chr19:51406942-51408006	Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
15	nsv579952	chr19:51406972-51407302	Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
16	nsv579953	chr19:51406972-51407357	Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
17	nsv579954	chr19:51406972-51407408	Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
18	nsv579955	chr19:51406972-51407721	Bivalent/Poised TSS Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
19	nsv579956	chr19:51406972-51407935	Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
20	nsv579957	chr19:51407200-51407721	Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:51407200-51408000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell

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