Variant report

Variant	rs13312839
Chromosome Location	chr8:90998017-90998018
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:90995516..90998828-chr8:91010778..91014105,5	K562	blood:
2	chr8:90788699..90792573-chr8:90996217..90998925,4	MCF-7	breast:
3	chr8:90766360..90773428-chr8:90991217..91000142,22	MCF-7	breast:
4	chr8:90735002..90740593-chr8:90994599..90998168,11	MCF-7	breast:
5	chr8:90766719..90773256-chr8:90991979..90999179,19	MCF-7	breast:
6	chr8:90735826..90740064-chr8:90995306..90998250,3	MCF-7	breast:
7	chr8:90913353..90915903-chr8:90994626..90998419,6	K562	blood:
8	chr8:90994579..90998162-chr8:91656500..91661270,5	K562	blood:
9	chr8:90912595..90916756-chr8:90994852..90998205,9	K562	blood:
10	chr8:90718183..90720246-chr8:90997582..90999794,2	MCF-7	breast:
11	chr8:90995523..90999017-chr8:91656346..91659175,4	K562	blood:
12	chr8:90790967..90797055-chr8:90994383..90998113,5	MCF-7	breast:
13	chr8:90993651..90998172-chr8:91012740..91014695,4	MCF-7	breast:
14	chr8:90911185..90916499-chr8:90992960..90998209,20	MCF-7	breast:
15	chr8:90996289..90998136-chr8:91010778..91015164,5	K562	blood:

No data

Variant related genes	Relation type
ENSG00000251136	Chromatin interaction
ENSG00000164823	Chromatin interaction
ENSG00000246792	Chromatin interaction
ENSG00000207359	Chromatin interaction
ENSG00000104325	Chromatin interaction
ENSG00000180694	Chromatin interaction
ENSG00000104312	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10098170	1.00[ASN][1000 genomes]
rs10099102	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10282890	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10504886	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10504887	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1076559	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10956407	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11986818	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11989543	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11989795	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11991697	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11992856	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11995294	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11998021	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12114835	1.00[ASN][1000 genomes]
rs13312846	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805785	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1805805	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805820	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805829	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805866	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805879	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28376519	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28654557	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58332188	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6470521	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6985667	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6992671	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6998280	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7005583	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7009268	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7013140	0.87[ASN][1000 genomes]
rs7017304	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs717873	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72550706	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs741779	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7812899	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7813356	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7818989	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7821822	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7823833	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7831876	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7834469	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7837423	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7840431	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs972376	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933502	chr8:90702392-91049100	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	62 gene(s)	inside rSNPs	diseases
2	nsv934114	chr8:90720182-90999106	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
3	nsv891183	chr8:90975550-91111193	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90997000-90999400	Weak transcription	HMEC	breast
2	chr8:90997000-91004600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:90997200-90999000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr8:90997200-90999600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:90997200-91005600	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr8:90997400-90999000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:90997400-90999200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr8:90997600-90998800	Weak transcription	K562	blood
9	chr8:90997600-90999200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr8:90997600-90999200	Weak transcription	NHEK	skin
11	chr8:90997600-91005200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr8:90997800-90999400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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