Variant report

Variant	rs246826
Chromosome Location	chr7:12983174-12983175
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:12982252..12985209-chr7:12989086..12991470,2	MCF-7	breast:
2	chr7:12982597..12985238-chr7:12986749..12990745,4	K562	blood:
3	chr7:12980961..12983258-chr7:13154370..13156023,2	MCF-7	breast:
4	chr7:12725676..12727718-chr7:12981615..12985353,4	MCF-7	breast:
5	chr7:12961395..12963715-chr7:12983088..12984785,2	K562	blood:

Variant related genes	Relation type
ENSG00000122644	Chromatin interaction
ENSG00000230879	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10254523	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10479912	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11765383	0.94[ASN][1000 genomes]
rs13236466	0.80[ASN][1000 genomes]
rs2024402	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs246828	1.00[ASN][1000 genomes]
rs28478673	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34044	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34048	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34049	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34055	0.93[ASN][1000 genomes]
rs34061	0.81[ASN][1000 genomes]
rs34066	0.93[ASN][1000 genomes]
rs34067	0.92[ASN][1000 genomes]
rs34068	0.93[ASN][1000 genomes]
rs34076	0.88[ASN][1000 genomes]
rs34078	0.82[ASN][1000 genomes]
rs4721165	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs58455143	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6969615	0.89[ASN][1000 genomes]
rs73301278	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932020	chr7:12676890-13239551	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv868830	chr7:12712753-13517417	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv606235	chr7:12781381-13205950	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1020568	chr7:12802640-13183737	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv464384	chr7:12907178-13077065	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv606238	chr7:12907178-13077065	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1029771	chr7:12927648-13153855	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv538736	chr7:12927648-13153855	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1026624	chr7:12963907-13123408	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv981786	chr7:12968068-12991292	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv887642	chr7:12973609-13067198	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12979800-12991000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:12980400-12983800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr7:12980600-12984000	Enhancers	NHEK	skin
4	chr7:12980800-12983200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr7:12981400-12983600	Enhancers	Fetal Intestine Large	intestine
6	chr7:12981400-12983800	Enhancers	Fetal Intestine Small	intestine
7	chr7:12981600-12983800	Enhancers	HMEC	breast
8	chr7:12981800-12991000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr7:12982200-12983800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr7:12982400-12983400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr7:12982600-12983200	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr7:12982600-12983200	Enhancers	Pancreas	Pancrea
13	chr7:12982600-12983600	Enhancers	A549	lung
14	chr7:12982600-12985400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr7:12982600-12991000	Weak transcription	Osteobl	bone
16	chr7:12982800-12983600	Enhancers	Liver	Liver
17	chr7:12982800-12985200	Enhancers	HepG2	liver
18	chr7:12983000-12988000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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