Variant report

Variant	rs7762222
Chromosome Location	chr6:149765982-149765983
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:149757368..149759713-chr6:149765073..149766703,2	K562	blood:
2	chr6:149763379..149766103-chr6:149776553..149779366,2	MCF-7	breast:
3	chr6:149764839..149766396-chr6:149774052..149775951,2	MCF-7	breast:
4	chr6:149762143..149764363-chr6:149765543..149768268,2	K562	blood:
5	chr6:149763441..149766003-chr6:149768583..149771236,2	K562	blood:

Variant related genes	Relation type
ENSG00000178199	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1001305	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11155646	0.91[ASN][1000 genomes]
rs11155654	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12192159	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12192814	0.91[ASN][1000 genomes]
rs12195922	0.82[ASN][1000 genomes]
rs58747890	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62441727	1.00[ASN][1000 genomes]
rs6911411	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs6932778	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7741099	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7747354	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7747948	1.00[ASN][1000 genomes]
rs9485385	0.91[ASN][1000 genomes]
rs9485392	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9485394	0.91[ASN][1000 genomes]
rs9485397	1.00[ASN][1000 genomes]
rs9498349	0.91[ASN][1000 genomes]
rs9498351	0.91[ASN][1000 genomes]
rs9498352	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9498353	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9498354	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9498355	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9498356	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9498358	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530444	chr6:149654540-149848997	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv470866	chr6:149744632-149806552	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv5533	chr6:149748047-149793072	Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv464076	chr6:149755695-149798835	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv604846	chr6:149755695-149798835	ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	esv3406755	chr6:149763459-149768057	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv3368142	chr6:149764359-149767257	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	esv3358632	chr6:149764809-149767607	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149753400-149770000	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr6:149753600-149768400	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr6:149753600-149769600	Weak transcription	Primary B cells from peripheral blood	blood
4	chr6:149760600-149766600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr6:149761600-149769600	Weak transcription	Primary B cells from cord blood	blood
6	chr6:149762600-149770800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:149762800-149771000	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr6:149763200-149770000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr6:149763200-149771000	Weak transcription	Fetal Intestine Small	intestine
10	chr6:149763200-149771400	Weak transcription	Pancreas	Pancrea
11	chr6:149763400-149766000	Enhancers	HepG2	liver
12	chr6:149764600-149768600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
13	chr6:149764800-149771400	Weak transcription	Spleen	Spleen
14	chr6:149765000-149766400	Weak transcription	Left Ventricle	heart
15	chr6:149765200-149771400	Weak transcription	Brain Anterior Caudate	brain
16	chr6:149765600-149766000	Enhancers	Right Atrium	heart
17	chr6:149765800-149766000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr6:149765800-149766000	Enhancers	Right Ventricle	heart
19	chr6:149765800-149766200	Enhancers	GM12878-XiMat	blood
20	chr6:149765800-149766800	Enhancers	Fetal Heart	heart
21	chr6:149765800-149767600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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