Variant report

Variant	rs12699786
Chromosome Location	chr7:16406272-16406273
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:16406024..16408482-chr7:16460009..16462034,2	K562	blood:
2	chr7:16394955..16400745-chr7:16401367..16408404,9	K562	blood:
3	chr7:16404045..16407640-chr7:16460095..16463015,3	MCF-7	breast:
4	chr7:16404670..16406505-chr7:16408648..16410407,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000214960	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10261188	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10486789	0.87[EUR][1000 genomes]
rs12667765	0.85[CEU][hapmap];0.93[JPT][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12699780	0.87[EUR][1000 genomes]
rs12699781	0.87[EUR][1000 genomes]
rs12699782	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12699783	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12699787	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1295146	0.83[JPT][hapmap]
rs13226547	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13232066	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13233751	0.87[EUR][1000 genomes]
rs13237371	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2189732	0.87[EUR][1000 genomes]
rs2389594	0.87[CHD][hapmap];0.87[JPT][hapmap];0.86[TSI][hapmap]
rs34992551	0.81[ASN][1000 genomes]
rs4349896	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4529354	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4602788	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6948602	0.81[GIH][hapmap]
rs6956615	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6968139	0.87[EUR][1000 genomes]
rs6977050	0.87[EUR][1000 genomes]
rs6980295	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016642	chr7:15884061-16799788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	esv2759514	chr7:16236162-16527390	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv1022388	chr7:16251992-16431864	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	esv2758105	chr7:16272822-16527390	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	esv2757215	chr7:16346139-16458474	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	esv34392	chr7:16351845-16412625	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv508447	chr7:16360614-16446053	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv1031019	chr7:16377519-16458474	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Genic enhancers	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
9	nsv1028556	chr7:16404615-16440024	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16386600-16409400	Weak transcription	Ovary	ovary
2	chr7:16396000-16416000	Weak transcription	HSMMtube	muscle
3	chr7:16397600-16409600	Weak transcription	Fetal Stomach	stomach
4	chr7:16398000-16409600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr7:16398000-16409800	Weak transcription	Esophagus	oesophagus
6	chr7:16398000-16415400	Weak transcription	Left Ventricle	heart
7	chr7:16398000-16417400	Weak transcription	Gastric	stomach
8	chr7:16402000-16409600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr7:16402200-16416000	Weak transcription	Liver	Liver
10	chr7:16403600-16415200	Weak transcription	Psoas Muscle	Psoas
11	chr7:16405000-16409400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr7:16405000-16417400	Weak transcription	Right Ventricle	heart
13	chr7:16406000-16413600	Weak transcription	K562	blood
14	chr7:16406200-16407800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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