Variant report

Variant	rs61597562
Chromosome Location	chr4:75243590-75243591
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:12)
CpG islands
(count:0)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:12 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr4:75243440-75243590	A549	lung:	n/a	n/a
2	POLR2A	chr4:75239405-75245347	U87	brain:	n/a	n/a
3	POLR2A	chr4:75243427-75247382	U87	brain:	n/a	n/a
4	POLR2A	chr4:75239411-75245187	U87	brain:	n/a	n/a
5	POLR2A	chr4:75241178-75245344	K562	blood:	n/a	n/a
6	POLR2A	chr4:75241190-75254074	HCT-116	colon:	n/a	n/a
7	POLR2A	chr4:75241188-75247382	U87	brain:	n/a	n/a
8	POLR2A	chr4:75238558-75255627	K562	blood:	n/a	n/a
9	BCLAF1	chr4:75243377-75245211	K562	blood:	n/a	n/a
10	POLR2A	chr4:75241290-75245913	A549	lung:	n/a	n/a
11	POLR2A	chr4:75243272-75244217	HCT-116	colon:	n/a	n/a
12	RAD21	chr4:75243395-75243610	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:75237376..75245686-chr4:75542486..75553167,38	MCF-7	breast:
2	chr4:75242903..75245454-chr4:75261986..75264008,2	MCF-7	breast:
3	chr4:75238775..75245761-chr4:75502353..75511633,27	MCF-7	breast:
4	chr4:75242050..75244304-chr4:75395919..75398280,2	K562	blood:
5	chr4:75243039..75246605-chr4:75251008..75254702,4	MCF-7	breast:
6	chr4:75239500..75243798-chr4:75584318..75589677,7	MCF-7	breast:
7	chr4:75237356..75240485-chr4:75242482..75245521,3	MCF-7	breast:
8	chr4:75243054..75246948-chr4:75395050..75399502,5	MCF-7	breast:
9	chr4:75242686..75244334-chr4:75394035..75395662,2	K562	blood:
10	chr4:75241409..75245016-chr4:75381716..75384369,3	MCF-7	breast:
11	chr4:75195893..75197465-chr4:75242238..75243930,2	K562	blood:
12	chr4:75237783..75245297-chr4:75502226..75511466,15	MCF-7	breast:
13	chr4:75240046..75244737-chr4:75409045..75413612,10	MCF-7	breast:
14	chr4:75239348..75243782-chr4:75542387..75546294,5	MCF-7	breast:
15	chr4:75242697..75245320-chr4:75245789..75249062,3	MCF-7	breast:
16	chr4:75241383..75245809-chr4:75253127..75255983,4	MCF-7	breast:
17	chr4:75240256..75244968-chr4:75576649..75579766,6	MCF-7	breast:
18	chr4:75234462..75244182-chr4:75405315..75413749,23	MCF-7	breast:
19	chr4:75241245..75244515-chr4:75557688..75560674,3	MCF-7	breast:
20	chr4:75234009..75245794-chr4:75391033..75405138,38	MCF-7	breast:

No data

Variant related genes	Relation type
EREG	TF binding region
ENSG00000124882	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10518126	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1460015	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57346142	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57839099	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57933408	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59107719	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59690065	0.89[EUR][1000 genomes]
rs60611827	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60972393	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61476105	0.89[EUR][1000 genomes]
rs61549491	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs61684000	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6831666	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6836436	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6837909	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72859325	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72859327	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72859333	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72859334	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72859338	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72859361	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72859363	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72859366	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7668475	0.89[EUR][1000 genomes]
rs7669104	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7669542	0.89[EUR][1000 genomes]
rs7669666	0.89[EUR][1000 genomes]
rs7674887	0.89[EUR][1000 genomes]
rs7675690	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7690224	0.89[EUR][1000 genomes]
rs7690629	0.89[EUR][1000 genomes]
rs7691008	0.89[EUR][1000 genomes]
rs7696072	0.89[EUR][1000 genomes]
rs7697009	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525980	chr4:74731526-75382209	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1009099	chr4:75089233-75726206	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:75239800-75243600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:75240600-75255200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr4:75240800-75244200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:75240800-75244800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:75241400-75260200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr4:75241600-75243600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr4:75242000-75244000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr4:75242200-75243600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:75242400-75248200	Weak transcription	Fetal Intestine Large	intestine
10	chr4:75242600-75244000	Weak transcription	Osteobl	bone
11	chr4:75242600-75244600	Genic enhancers	NHEK	skin
12	chr4:75242600-75252600	Weak transcription	Fetal Intestine Small	intestine
13	chr4:75242800-75244400	Genic enhancers	A549	lung
14	chr4:75242800-75244800	Enhancers	HMEC	breast
15	chr4:75243200-75248400	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr4:75243400-75244200	Weak transcription	HSMM	muscle
17	chr4:75243400-75244600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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