Variant report

Variant	rs7179953
Chromosome Location	chr15:79121776-79121777
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:79112261..79115156-chr15:79120562..79122174,2	K562	blood:
2	chr15:79111381..79113761-chr15:79120562..79122732,2	K562	blood:

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10083696	0.83[EUR][1000 genomes]
rs10083697	0.83[EUR][1000 genomes]
rs11072807	0.83[EUR][1000 genomes]
rs11638020	0.83[EUR][1000 genomes]
rs11856953	0.82[EUR][1000 genomes]
rs12442476	0.82[EUR][1000 genomes]
rs12898292	0.81[EUR][1000 genomes]
rs12898392	0.81[EUR][1000 genomes]
rs12898452	0.81[EUR][1000 genomes]
rs12898712	0.81[EUR][1000 genomes]
rs12909317	0.83[EUR][1000 genomes]
rs28455815	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28505515	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs28513584	0.84[EUR][1000 genomes]
rs34372090	0.83[EUR][1000 genomes]
rs3890715	0.83[EUR][1000 genomes]
rs3971829	0.82[EUR][1000 genomes]
rs4073322	0.83[EUR][1000 genomes]
rs4380028	0.83[EUR][1000 genomes]
rs4387568	0.83[EUR][1000 genomes]
rs4389112	0.83[EUR][1000 genomes]
rs4389113	0.83[EUR][1000 genomes]
rs4433781	0.83[EUR][1000 genomes]
rs4468572	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55870734	0.82[EUR][1000 genomes]
rs56076311	0.80[EUR][1000 genomes]
rs56683682	0.83[EUR][1000 genomes]
rs58021857	0.83[EUR][1000 genomes]
rs61043060	0.83[EUR][1000 genomes]
rs62011002	0.83[EUR][1000 genomes]
rs6495333	0.83[EUR][1000 genomes]
rs6495335	0.82[EUR][1000 genomes]
rs66813213	0.85[EUR][1000 genomes]
rs66925868	0.82[EUR][1000 genomes]
rs67745769	0.83[EUR][1000 genomes]
rs7164479	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7165042	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7165075	0.82[EUR][1000 genomes]
rs7165081	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7165733	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7165902	0.82[EUR][1000 genomes]
rs7166764	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7167853	0.83[EUR][1000 genomes]
rs7176187	0.83[EUR][1000 genomes]
rs7178051	0.82[EUR][1000 genomes]
rs7181432	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7182103	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7182529	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7182716	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72749206	0.83[EUR][1000 genomes]
rs7403593	0.83[EUR][1000 genomes]
rs7403608	0.82[EUR][1000 genomes]
rs7403708	0.83[EUR][1000 genomes]
rs7403714	0.83[EUR][1000 genomes]
rs7403728	0.83[EUR][1000 genomes]
rs8026598	0.83[EUR][1000 genomes]
rs8027833	0.83[EUR][1000 genomes]
rs8032908	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs8035093	0.83[EUR][1000 genomes]
rs8041064	0.82[EUR][1000 genomes]
rs9806363	0.83[EUR][1000 genomes]
rs9920493	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917303	chr15:78491050-79205255	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	122 gene(s)	inside rSNPs	diseases
2	nsv904431	chr15:79006442-79155088	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	esv33573	chr15:79053484-79293881	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv904432	chr15:79066932-79175813	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:79110800-79122600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:79118400-79123200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr15:79118400-79138400	Weak transcription	Right Atrium	heart
4	chr15:79118600-79123000	Weak transcription	Pancreas	Pancrea
5	chr15:79118600-79123000	Weak transcription	GM12878-XiMat	blood
6	chr15:79118600-79123200	Weak transcription	Liver	Liver
7	chr15:79118600-79123200	Weak transcription	Fetal Lung	lung
8	chr15:79118800-79128400	Weak transcription	Ovary	ovary
9	chr15:79120800-79122200	Enhancers	Adipose Nuclei	Adipose
10	chr15:79121000-79121800	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr15:79121200-79121800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr15:79121200-79121800	Enhancers	Left Ventricle	heart
13	chr15:79121200-79121800	Enhancers	Lung	lung
14	chr15:79121200-79122000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr15:79121200-79122600	Enhancers	Spleen	Spleen
16	chr15:79121400-79122000	Enhancers	Right Ventricle	heart
17	chr15:79121400-79123600	Weak transcription	Fetal Heart	heart
18	chr15:79121600-79121800	Enhancers	Fetal Stomach	stomach
19	chr15:79121600-79123400	Weak transcription	Gastric	stomach

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