Variant report

Variant	rs903694
Chromosome Location	chr1:227733005-227733006
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:227724940..227726791-chr1:227731403..227734272,2	K562	blood:
2	chr1:227732140..227734388-chr1:227916123..227918168,2	MCF-7	breast:
3	chr1:227729010..227735281-chr1:227748522..227752811,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000181450	Chromatin interaction
ENSG00000202264	Chromatin interaction
ENSG00000143740	Chromatin interaction

Extended variants
information (count: 109 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs10047205	1.00[CEU][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1021553	0.91[JPT][hapmap]
rs1021554	0.91[JPT][hapmap]
rs10799432	0.87[JPT][hapmap]
rs10799435	0.87[JPT][hapmap]
rs10916165	0.87[JPT][hapmap]
rs10916178	1.00[CEU][hapmap];0.91[JPT][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10916182	0.87[JPT][hapmap]
rs10916187	0.83[JPT][hapmap]
rs10916192	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12025815	0.87[JPT][hapmap]
rs12059899	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12069550	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12070002	0.87[JPT][hapmap]
rs12070036	0.86[JPT][hapmap]
rs12070539	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12080321	0.87[JPT][hapmap]
rs12080590	1.00[CEU][hapmap];0.91[JPT][hapmap];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12082414	1.00[CEU][hapmap];0.91[JPT][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12092295	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12095502	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12096675	1.00[CEU][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12132444	0.95[JPT][hapmap]
rs1495846	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1495849	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16847966	1.00[CEU][hapmap];0.91[JPT][hapmap];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16847991	1.00[CEU][hapmap];0.91[JPT][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16847992	1.00[CEU][hapmap];0.91[JPT][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16848029	1.00[CEU][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1923821	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2012432	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2093609	0.87[JPT][hapmap]
rs2132366	1.00[CEU][hapmap];0.91[JPT][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2132367	0.87[JPT][hapmap]
rs2256599	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2453682	1.00[CEU][hapmap];0.80[CHB][hapmap];0.95[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2644143	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2644144	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2644146	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2644153	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2644161	1.00[CEU][hapmap];0.95[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2814059	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2814060	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2814061	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2814084	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2814085	1.00[CEU][hapmap];0.81[CHB][hapmap];0.84[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2819496	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2819498	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2819507	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2819511	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2935146	0.87[JPT][hapmap]
rs2935152	0.82[JPT][hapmap]
rs2935155	0.87[JPT][hapmap]
rs2999745	0.87[JPT][hapmap]
rs2999746	0.87[JPT][hapmap]
rs3010183	0.81[JPT][hapmap]
rs3010186	0.87[JPT][hapmap]
rs3010190	0.82[JPT][hapmap]
rs3010191	0.82[JPT][hapmap]
rs3010192	0.87[JPT][hapmap]
rs3010193	0.87[JPT][hapmap]
rs3010194	0.82[JPT][hapmap]
rs3748806	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4376731	1.00[CEU][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4589104	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4653514	0.87[JPT][hapmap]
rs4653849	0.91[JPT][hapmap]
rs4653853	0.83[JPT][hapmap]
rs58020705	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs59034043	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs59149651	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs59753688	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61343450	0.82[EUR][1000 genomes]
rs66471275	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs66491073	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6659745	0.92[AFR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs66736638	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6683151	0.87[JPT][hapmap]
rs6688145	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6693348	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs66938123	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6697867	0.91[JPT][hapmap]
rs67216605	0.82[EUR][1000 genomes]
rs67511833	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs67676707	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs68046179	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs68186506	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72632830	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72632831	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72632832	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72748074	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7413796	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7528094	0.91[JPT][hapmap]
rs753541	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7539151	1.00[CEU][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs903690	0.91[JPT][hapmap]
rs903692	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs903693	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs903695	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs965942	1.00[CEU][hapmap];0.91[JPT][hapmap];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][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	nsv534002	chr1:227315186-228047108	Bivalent/Poised TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
2	esv2753828	chr1:227670265-227791265	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv873244	chr1:227682414-227736363	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv873246	chr1:227694948-227884465	Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1007479	chr1:227695868-227984466	Genic enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
6	nsv873247	chr1:227697381-227736363	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv873248	chr1:227710381-227786033	ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
8	nsv947520	chr1:227724042-227750192	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
9	nsv947560	chr1:227726600-227750192	ZNF genes & repeats Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs903694	ZNF678	Cis_1M	lymphoblastoid	RTeQTL
rs903694	C1orf142	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227730400-227735000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:227730600-227734400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:227730800-227734000	Weak transcription	Spleen	Spleen
4	chr1:227730800-227736000	Enhancers	Fetal Muscle Trunk	muscle
5	chr1:227730800-227736000	Enhancers	Fetal Muscle Leg	muscle
6	chr1:227730800-227736000	Enhancers	Pancreas	Pancrea
7	chr1:227731000-227734600	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr1:227731000-227734600	Weak transcription	HepG2	liver
9	chr1:227731000-227735400	Weak transcription	Colonic Mucosa	Colon
10	chr1:227731000-227748400	Weak transcription	Right Atrium	heart
11	chr1:227731200-227735200	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr1:227731200-227735800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr1:227731200-227739000	Weak transcription	Fetal Intestine Small	intestine
14	chr1:227731400-227733600	Weak transcription	Fetal Lung	lung
15	chr1:227731400-227733800	Weak transcription	Placenta	Placenta
16	chr1:227731400-227733800	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr1:227731600-227736400	Weak transcription	Gastric	stomach
18	chr1:227732600-227734200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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