Variant report

Variant	rs73964975
Chromosome Location	chr2:145045951-145045952
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:145045908..145048354-chr2:145051759..145054020,2	MCF-7	breast:
2	chr2:145025434..145028287-chr2:145045134..145047501,2	K562	blood:

Variant related genes	Relation type
ENSG00000121964	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs55637225	1.00[AMR][1000 genomes]
rs55775060	0.95[AFR][1000 genomes]
rs55915218	1.00[AMR][1000 genomes]
rs56001970	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56258437	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57183340	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57398691	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57410426	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57677579	1.00[AMR][1000 genomes]
rs57783534	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58722310	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59290279	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59430219	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59505116	1.00[AMR][1000 genomes]
rs60225630	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60644335	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60696610	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61639522	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73962193	1.00[AMR][1000 genomes]
rs73962196	1.00[AMR][1000 genomes]
rs73964914	1.00[AMR][1000 genomes]
rs73964919	1.00[AMR][1000 genomes]
rs73964925	1.00[AMR][1000 genomes]
rs73964931	1.00[AMR][1000 genomes]
rs73964932	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964942	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964943	0.85[AFR][1000 genomes]
rs73964944	0.90[AFR][1000 genomes]
rs73964945	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964947	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964949	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964951	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964952	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964953	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964955	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964956	0.90[AFR][1000 genomes]
rs73964957	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964962	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964964	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964965	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964969	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964970	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964972	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964973	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964974	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964976	0.95[AFR][1000 genomes]
rs73964977	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73964979	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532755	chr2:144631279-145270874	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv1006344	chr2:144657716-145334899	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv535951	chr2:144657716-145334899	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv1067624	chr2:144657717-145425705	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv531413	chr2:144657717-145425705	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
6	nsv532756	chr2:144746353-145315596	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
7	nsv1008032	chr2:144840552-145234229	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
8	nsv997624	chr2:144906679-145294503	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
9	nsv535952	chr2:144906679-145294503	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
10	nsv532757	chr2:144922143-145263446	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
11	nsv916172	chr2:144970681-145425713	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
12	nsv948474	chr2:145035890-145436665	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
13	esv3380397	chr2:145035938-145056247	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 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	chr2:145015000-145066800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:145032400-145057000	Weak transcription	Primary B cells from cord blood	blood
3	chr2:145035800-145048800	Weak transcription	Aorta	Aorta
4	chr2:145037200-145046000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr2:145042000-145046000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr2:145045000-145046200	Weak transcription	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links