Variant report

Variant	rs7766091
Chromosome Location	chr6:143967030-143967031
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:143965764..143968046-chr6:144327940..144330274,2	K562	blood:
2	chr6:143966000..143968139-chr6:143973368..143975325,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000118495	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11155318	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11155320	0.96[CEU][hapmap];0.88[JPT][hapmap];0.86[EUR][1000 genomes]
rs11962519	0.96[CEU][hapmap];0.91[CHB][hapmap];0.88[JPT][hapmap];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12530310	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13190772	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13191259	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13204954	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13220613	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2024693	0.87[CHB][hapmap];0.84[ASN][1000 genomes]
rs2051008	1.00[JPT][hapmap]
rs2092762	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2474150	1.00[JPT][hapmap]
rs3924968	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4299843	0.96[CHB][hapmap];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4523103	0.96[CEU][hapmap];0.91[JPT][hapmap];0.93[EUR][1000 genomes]
rs6570571	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6570572	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6570573	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6913687	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6914940	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6916245	0.87[CHB][hapmap];0.81[EUR][1000 genomes]
rs6931556	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7450663	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7738179	0.96[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7739094	0.86[JPT][hapmap]
rs7741628	1.00[CHB][hapmap];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7741901	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7741998	0.92[CEU][hapmap];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7747182	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7758298	0.96[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7760178	0.87[CHB][hapmap]
rs7762598	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7764549	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7770812	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7771214	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap]
rs7772898	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7773502	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap]
rs910419	0.96[CEU][hapmap];0.91[CHB][hapmap];0.87[JPT][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9321933	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9321934	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9376773	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9376774	1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9376775	1.00[CHB][hapmap];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9376777	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9390127	0.87[CHB][hapmap]
rs9399454	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9399456	0.87[CHB][hapmap]
rs9399459	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs9403520	0.86[CEU][hapmap];0.87[CHB][hapmap];0.83[JPT][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9403522	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9484785	0.91[JPT][hapmap]
rs9484794	0.93[CEU][hapmap];0.87[CHB][hapmap];0.88[JPT][hapmap];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9496712	0.86[JPT][hapmap]
rs9496718	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9496721	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9496729	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9496733	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap]
rs9496734	0.87[CHB][hapmap]
rs9496735	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758084	chr6:143916621-144079976	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv2759476	chr6:143916621-144079976	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1032369	chr6:143925374-144007513	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv604805	chr6:143930404-144005949	Weak transcription Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv517253	chr6:143953672-143975157	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:143917000-143973600	Weak transcription	Fetal Intestine Small	intestine
2	chr6:143955800-143967200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr6:143956000-143967600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr6:143956000-143973800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr6:143959000-143968800	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr6:143959000-143978400	Weak transcription	Left Ventricle	heart
7	chr6:143959200-143973800	Weak transcription	Right Atrium	heart
8	chr6:143961600-143969800	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr6:143962600-143968600	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr6:143964000-143974000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr6:143964600-143969000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr6:143965400-143968600	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr6:143965400-143969600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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