Variant report

Variant	rs699990
Chromosome Location	chr6:49736665-49736666
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:49725544..49727159-chr6:49736149..49737766,2	K562	blood:
2	chr6:49725544..49727143-chr6:49736149..49738477,2	K562	blood:
3	chr6:49734608..49737152-chr6:49742477..49744023,2	K562	blood:
4	chr6:49730694..49733454-chr6:49734689..49738189,4	K562	blood:
5	chr6:49733982..49736710-chr6:49738623..49740973,2	K562	blood:
6	chr6:49735210..49737527-chr6:49738880..49740973,3	K562	blood:
7	chr6:49728930..49731188-chr6:49735644..49738540,2	MCF-7	breast:
8	chr6:49736274..49737979-chr6:49746785..49748919,2	K562	blood:

No data

Extended variants
information (count: 61 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs1621948	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs168623	0.94[ASN][1000 genomes]
rs183115	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs184857	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2068681	1.00[CEU][hapmap];0.85[CHB][hapmap];0.87[CHD][hapmap];0.94[GIH][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.87[AMR][1000 genomes]
rs2104029	1.00[CHB][hapmap]
rs360541	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs360542	0.98[ASN][1000 genomes]
rs360543	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs360544	0.98[ASN][1000 genomes]
rs360545	0.98[ASN][1000 genomes]
rs360546	0.98[ASN][1000 genomes]
rs360547	0.96[ASN][1000 genomes]
rs360548	0.98[ASN][1000 genomes]
rs360555	0.93[ASN][1000 genomes]
rs3799688	0.88[CEU][hapmap];0.85[CHB][hapmap];0.92[CHD][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap]
rs483914	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs488132	0.89[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.94[GIH][hapmap];0.80[LWK][hapmap];0.86[MKK][hapmap];0.88[TSI][hapmap];0.81[YRI][hapmap];0.98[ASN][1000 genomes]
rs500032	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs502256	0.81[ASN][1000 genomes]
rs512299	0.91[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.90[YRI][hapmap];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs513343	1.00[JPT][hapmap]
rs521489	0.98[ASN][1000 genomes]
rs521492	0.98[ASN][1000 genomes]
rs553584	0.98[ASN][1000 genomes]
rs555103	0.98[ASN][1000 genomes]
rs56085173	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56148648	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs571257	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.98[ASN][1000 genomes]
rs584490	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs584747	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs597544	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs614217	0.95[ASN][1000 genomes]
rs623996	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs626221	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs633319	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs643775	0.98[ASN][1000 genomes]
rs6458712	1.00[CHB][hapmap];0.83[CHD][hapmap]
rs659190	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs66909600	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs670624	0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6922618	1.00[CHB][hapmap]
rs6925452	0.92[CHB][hapmap]
rs693929	0.98[ASN][1000 genomes]
rs696717	0.98[ASN][1000 genomes]
rs699959	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs699960	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs699962	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs699972	0.95[ASN][1000 genomes]
rs699974	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.98[ASN][1000 genomes]
rs699977	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs699982	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs699991	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs699993	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs699994	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs699996	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7760595	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs780445	0.98[ASN][1000 genomes]
rs812969	0.98[ASN][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	nsv933942	chr6:49480550-50004231	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv933833	chr6:49515134-49961765	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs699990	TRAM2	cis	parietal	SCAN
rs699990	IL17F	cis	parietal	SCAN

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:49735800-49738400	Active TSS	Fetal Intestine Small	intestine
2	chr6:49735800-49738600	Active TSS	Fetal Intestine Large	intestine
3	chr6:49736000-49739400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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