Variant report

Variant	rs4792715
Chromosome Location	chr17:15927223-15927224
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr17:15927179-15927544	HCT-116	colon:	n/a	n/a
2	POLR2A	chr17:15921428-15927637	K562	blood:	n/a	n/a
3	POLR2A	chr17:15926545-15927585	HepG2	liver:	n/a	n/a
4	POLR2A	chr17:15927107-15927505	Hela-S3	cervix:	n/a	n/a
5	POLR2A	chr17:15927123-15927400	HepG2	liver:	n/a	n/a

Variant related genes	Relation type
TTC19	TF binding region

Extended variants
information (count: 157 )
Associated
traits (count: 22 )

rSNPs within LD-proxies of this variant (count:137)

rs_ID	r²[population]
rs1045599	0.89[CEU][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];0.87[MEX][hapmap];0.93[TSI][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1065822	0.82[CEU][hapmap];0.81[EUR][1000 genomes]
rs1075901	0.92[CEU][hapmap];0.85[CHB][hapmap];0.84[CHD][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1079533	0.82[CEU][hapmap];0.82[EUR][1000 genomes]
rs11078320	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11078327	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11078328	0.82[EUR][1000 genomes]
rs11078330	0.81[EUR][1000 genomes]
rs11078331	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1125156	0.81[CEU][hapmap]
rs1160109	0.82[CEU][hapmap]
rs11650678	0.82[CEU][hapmap]
rs11651290	0.82[CEU][hapmap];0.82[EUR][1000 genomes]
rs11652025	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11654	0.89[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11655456	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11656046	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11657160	0.96[CEU][hapmap];0.85[CHB][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11657912	0.82[EUR][1000 genomes]
rs11869450	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11869563	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.96[MEX][hapmap];0.86[MKK][hapmap];0.98[TSI][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11872032	0.82[CEU][hapmap]
rs12451075	0.83[EUR][1000 genomes]
rs12942295	0.81[EUR][1000 genomes]
rs12945463	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12945546	0.82[EUR][1000 genomes]
rs178657	0.82[CEU][hapmap]
rs178791	0.85[CEU][hapmap]
rs178797	0.85[CEU][hapmap]
rs178798	0.82[CEU][hapmap]
rs178799	0.82[CEU][hapmap]
rs178802	0.81[CEU][hapmap]
rs178805	0.81[CEU][hapmap]
rs178809	0.82[CEU][hapmap]
rs178814	0.96[CEU][hapmap];0.85[CHB][hapmap]
rs178815	0.96[CEU][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap]
rs178816	0.82[CEU][hapmap]
rs178820	0.82[CEU][hapmap]
rs178822	0.96[CEU][hapmap];0.85[CHB][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap]
rs178838	0.96[CEU][hapmap];0.85[CHB][hapmap]
rs178839	0.96[CEU][hapmap]
rs1860643	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1860644	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1860645	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1989856	0.82[CEU][hapmap]
rs2015353	0.87[MEX][hapmap];0.84[TSI][hapmap]
rs2041459	0.80[EUR][1000 genomes]
rs2041460	0.80[EUR][1000 genomes]
rs2078050	0.96[CEU][hapmap];0.85[CHB][hapmap];0.82[CHD][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2109632	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2157990	0.93[CEU][hapmap];0.86[MEX][hapmap];0.93[TSI][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2157991	0.96[CEU][hapmap];0.85[CHB][hapmap];0.82[CHD][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2157992	0.82[CEU][hapmap];0.81[EUR][1000 genomes]
rs2159643	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2285580	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2285582	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2285583	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2286795	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2286796	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2302415	1.00[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];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs2324084	0.80[EUR][1000 genomes]
rs2324141	0.96[CEU][hapmap];0.85[CHB][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap]
rs2324142	0.96[CEU][hapmap];0.85[CHB][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap]
rs2535614	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2779207	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2779208	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2779210	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2779212	0.89[CEU][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.91[TSI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35168566	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3760297	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3760298	0.81[EUR][1000 genomes]
rs3785628	0.96[CEU][hapmap];0.85[CHB][hapmap];0.82[CHD][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3785629	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3785631	0.82[CEU][hapmap];0.82[EUR][1000 genomes]
rs3785632	0.85[CEU][hapmap];0.85[TSI][hapmap];0.85[EUR][1000 genomes]
rs3785633	0.82[CEU][hapmap];0.83[EUR][1000 genomes]
rs3815038	0.81[EUR][1000 genomes]
rs3815039	0.82[CEU][hapmap];0.82[EUR][1000 genomes]
rs3826360	0.82[CEU][hapmap];0.82[EUR][1000 genomes]
rs4435297	0.92[CEU][hapmap];0.85[CHB][hapmap];0.81[CHD][hapmap];0.96[MEX][hapmap];0.95[TSI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4791660	0.81[EUR][1000 genomes]
rs4791662	0.82[CEU][hapmap]
rs4792707	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4792708	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4792709	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4792711	0.80[EUR][1000 genomes]
rs4792712	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4792713	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4792716	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4792717	0.96[CEU][hapmap];0.85[CHB][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4792718	1.00[ASW][hapmap];1.00[CEU][hapmap];0.93[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4792719	0.82[EUR][1000 genomes]
rs4792721	0.81[CEU][hapmap];0.84[TSI][hapmap]
rs6416868	1.00[CEU][hapmap];1.00[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];0.98[ASN][1000 genomes]
rs6502479	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6502480	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6502482	0.96[CEU][hapmap];0.85[CHB][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6502488	0.96[CEU][hapmap];0.85[CHB][hapmap];0.85[CHD][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7207463	0.85[EUR][1000 genomes]
rs7209094	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7210655	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7214695	0.96[CEU][hapmap];0.85[CHB][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7214891	0.80[EUR][1000 genomes]
rs7216949	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7222886	0.81[EUR][1000 genomes]
rs7223346	0.96[CEU][hapmap];0.85[CHB][hapmap];0.81[CHD][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs758853	0.80[EUR][1000 genomes]
rs8064702	0.93[EUR][1000 genomes]
rs8065190	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs8066902	0.80[EUR][1000 genomes]
rs8070859	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.96[MEX][hapmap];0.86[MKK][hapmap];0.98[TSI][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8075345	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8076669	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs8076864	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs8079969	0.96[CEU][hapmap];0.85[CHB][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap]
rs8080221	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8081406	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs8081667	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9652827	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9652828	0.82[EUR][1000 genomes]
rs9709250	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9889822	0.82[EUR][1000 genomes]
rs9890012	0.82[CEU][hapmap];0.82[EUR][1000 genomes]
rs9891379	0.82[CEU][hapmap];0.81[EUR][1000 genomes]
rs9891938	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[TSI][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9896441	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9897542	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9898313	0.81[EUR][1000 genomes]
rs9899002	0.82[CEU][hapmap];0.83[EUR][1000 genomes]
rs9899995	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9902141	0.81[CEU][hapmap]
rs9905429	0.81[EUR][1000 genomes]
rs9907273	0.81[EUR][1000 genomes]
rs9908031	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs9909615	0.82[EUR][1000 genomes]
rs9909697	0.82[CEU][hapmap]
rs9916868	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934185	chr17:15552960-16551197	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	190 gene(s)	inside rSNPs	diseases
2	nsv1066023	chr17:15607267-16053512	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	esv3330182	chr17:15652014-16569534	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
4	esv3446844	chr17:15654843-16572246	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
5	nsv1061222	chr17:15672934-15999778	ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
6	nsv907706	chr17:15731923-16056442	ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
7	nsv1067555	chr17:15804228-16001117	Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
8	nsv1063459	chr17:15804228-16543593	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
9	nsv907707	chr17:15846535-15950751	Strong transcription Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
10	nsv907709	chr17:15851196-15937487	Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
11	nsv907708	chr17:15851196-15950751	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
12	nsv1057493	chr17:15852125-15930718	Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
13	nsv543215	chr17:15852125-15930718	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
14	nsv907710	chr17:15854257-15950751	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
15	nsv1062220	chr17:15869557-16093156	Genic enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
16	nsv1064878	chr17:15869557-16097241	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
17	nsv1055173	chr17:15875935-16097241	Flanking Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
18	nsv1056157	chr17:15890584-16088473	Strong transcription Genic enhancers Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
19	nsv833377	chr17:15912013-16104515	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
20	nsv522169	chr17:15923709-16147821	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases

mRNA abundance (count:22)

SNP	Gene	Cis/trans	Tissue	Source
rs4792715	ADORA2B	cis	Adipose Subcutaneous	GTEx
rs4792715	PRPSAP2	cis	parietal	SCAN
rs4792715	ADORA2B	cis	Artery Tibial	GTEx
rs4792715	CENPV	cis	Artery Tibial	GTEx
rs4792715	LOC125150	cis	normal skin	skin_eQTL
rs4792715	ADORA2B	cis	Muscle Skeletal	GTEx
rs4792715	ADORA2B	cis	Nerve Tibial	GTEx
rs4792715	ADORA2B	cis	Thyroid	GTEx
rs4792715	ADORA2B	cis	lung	GTEx
rs4792715	LOC125150	cis	lesional skin	skin_eQTL
rs4792715	CENPV	cis	parietal	SCAN
rs4792715	LOC125150	cis	uninvolved skin	skin_eQTL
rs4792715	NCOR1	Cis_1M	lymphoblastoid	RTeQTL
rs4792715	TTC19	cis	lymphoblastoid	seeQTL
rs4792715	ZSWIM7	Cis_1M	lymphoblastoid	RTeQTL
rs4792715	ELAC2	cis	parietal	SCAN
rs4792715	ZSWIM7	cis	Muscle Skeletal	GTEx
rs4792715	TTC19	Cis_1M	lymphoblastoid	RTeQTL
rs4792715	NCOR1	cis	parietal	SCAN
rs4792715	ADORA2B	cis	Esophagus Muscularis	GTEx
rs4792715	ADORA2B	cis	Heart Left Ventricle	GTEx
rs4792715	Hs.379903	cis	multi-tissue	Pritchard

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15905000-15939600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr17:15905000-15946400	Strong transcription	HUES48 Cell Line	embryonic stem cell
3	chr17:15905200-15986400	Strong transcription	Primary T helper cells fromperipheralblood	blood
4	chr17:15905400-15931000	Strong transcription	HUES64 Cell Line	embryonic stem cell
5	chr17:15905400-15946600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
6	chr17:15906400-15939400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr17:15907800-15935600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr17:15909000-15928000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr17:15909000-15928200	Weak transcription	Gastric	stomach
10	chr17:15909000-15929800	Weak transcription	Esophagus	oesophagus
11	chr17:15911000-15928200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr17:15912000-15929800	Weak transcription	Pancreas	Pancrea
13	chr17:15912200-15928200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr17:15912200-15928200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr17:15912200-15928200	Weak transcription	Colonic Mucosa	Colon
16	chr17:15912200-15928200	Weak transcription	Spleen	Spleen
17	chr17:15912200-15928800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr17:15912600-15928200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr17:15912600-15928200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr17:15912600-15928200	Weak transcription	Rectal Smooth Muscle	rectum
21	chr17:15913800-15990800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr17:15915200-15927800	Weak transcription	Fetal Kidney	kidney
23	chr17:15915200-15928400	Weak transcription	Stomach Mucosa	stomach
24	chr17:15915400-15998000	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr17:15917400-15952800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr17:15917800-15928000	Weak transcription	Brain Cingulate Gyrus	brain
27	chr17:15917800-15928200	Weak transcription	Fetal Brain Male	brain
28	chr17:15918000-15927400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr17:15918000-15927600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr17:15918000-15928200	Weak transcription	Ovary	ovary
31	chr17:15918200-15928000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr17:15918200-15930200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr17:15918400-15930400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr17:15918400-15930600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr17:15918600-15927800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr17:15919200-15930400	Strong transcription	A549	lung
37	chr17:15919400-15931000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr17:15919600-15930800	Strong transcription	Osteobl	bone
39	chr17:15920200-15930800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr17:15920200-15931000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr17:15921000-15930200	Strong transcription	HUVEC	blood vessel
42	chr17:15921000-15930800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr17:15921000-15946600	Strong transcription	HUES6 Cell Line	embryonic stem cell
44	chr17:15921000-15991000	Strong transcription	Primary monocytes fromperipheralblood	blood
45	chr17:15921000-15991200	Strong transcription	Primary B cells from peripheral blood	blood
46	chr17:15921400-15930400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr17:15921400-15930400	Strong transcription	NH-A	brain
48	chr17:15921400-15944400	Strong transcription	Duodenum Mucosa	Duodenum
49	chr17:15921400-15947000	Strong transcription	H1 Cell Line	embryonic stem cell
50	chr17:15921400-15955000	Strong transcription	Dnd41	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links