Variant report

Variant	rs9902941
Chromosome Location	chr17:17733760-17733761
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:17732703..17734829-chr17:17808950..17811778,2	K562	blood:

Extended variants
information (count: 150 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:116)

rs_ID	r²[population]
rs10048206	0.85[GIH][hapmap];0.92[MEX][hapmap];0.81[TSI][hapmap]
rs1052299	0.95[CEU][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.93[TSI][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11078399	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11078400	0.86[CEU][hapmap];0.88[GIH][hapmap];0.91[MEX][hapmap];0.87[TSI][hapmap];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11078403	0.80[AMR][1000 genomes]
rs11078406	0.85[GIH][hapmap];0.92[MEX][hapmap];0.83[TSI][hapmap]
rs11078408	0.84[MEX][hapmap]
rs1108648	0.94[CEU][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11650649	0.82[GIH][hapmap];0.82[JPT][hapmap];0.91[MEX][hapmap]
rs11652144	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11652881	0.91[CEU][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap]
rs11654081	0.89[CEU][hapmap];0.84[JPT][hapmap]
rs11656665	0.95[CEU][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11657074	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11657130	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11657423	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.98[TSI][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11658309	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11870660	0.84[MEX][hapmap]
rs12450799	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12936037	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12936927	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12938501	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12941039	0.86[CEU][hapmap];0.85[GIH][hapmap];0.82[JPT][hapmap];0.91[MEX][hapmap];0.81[TSI][hapmap];0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12941550	0.80[AMR][1000 genomes]
rs12943500	0.82[JPT][hapmap];0.83[MEX][hapmap]
rs12946746	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12952723	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16960744	0.95[CEU][hapmap];0.91[GIH][hapmap];0.92[MEX][hapmap];0.95[TSI][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1889018	1.00[CEU][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2236513	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2297508	0.91[CEU][hapmap]
rs2350976	0.86[CEU][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap]
rs2350977	0.85[GIH][hapmap];0.92[MEX][hapmap];0.83[TSI][hapmap]
rs2955378	0.84[MEX][hapmap]
rs3183702	0.95[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35451946	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3744113	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3744115	0.91[CEU][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.93[TSI][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3818717	0.82[CEU][hapmap];1.00[JPT][hapmap]
rs4244602	0.82[JPT][hapmap]
rs4257260	0.85[GIH][hapmap];0.92[MEX][hapmap];0.81[TSI][hapmap]
rs4299203	0.84[MEX][hapmap]
rs4341796	0.82[GIH][hapmap];0.82[JPT][hapmap];0.91[MEX][hapmap]
rs4368210	0.84[MEX][hapmap]
rs4413022	0.82[CEU][hapmap]
rs4459604	0.88[MEX][hapmap]
rs4470201	0.85[GIH][hapmap];0.92[MEX][hapmap];0.83[TSI][hapmap]
rs4584886	0.83[MEX][hapmap]
rs4924821	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4924822	0.91[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.98[TSI][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4924823	0.86[CEU][hapmap];0.88[GIH][hapmap];0.92[MEX][hapmap];0.85[TSI][hapmap];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4924832	0.84[MEX][hapmap]
rs4925114	0.91[CEU][hapmap];0.82[TSI][hapmap]
rs4925115	0.95[CEU][hapmap];0.84[TSI][hapmap];0.82[EUR][1000 genomes]
rs4925116	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4925117	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4925119	0.95[CEU][hapmap];0.94[GIH][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4925120	0.95[CEU][hapmap];0.91[GIH][hapmap];0.92[MEX][hapmap];0.95[TSI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4925123	0.82[GIH][hapmap];0.82[JPT][hapmap];0.91[MEX][hapmap]
rs4925125	0.85[GIH][hapmap];0.92[MEX][hapmap];0.83[TSI][hapmap];0.87[AMR][1000 genomes]
rs4925126	0.85[GIH][hapmap];0.92[MEX][hapmap];0.83[TSI][hapmap];0.83[AMR][1000 genomes]
rs4925129	0.82[GIH][hapmap];0.82[JPT][hapmap];0.91[MEX][hapmap]
rs4925130	0.82[JPT][hapmap];0.87[MEX][hapmap]
rs5002487	0.82[GIH][hapmap];0.82[JPT][hapmap];0.91[MEX][hapmap]
rs58638639	0.84[EUR][1000 genomes]
rs6502618	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6502619	0.82[JPT][hapmap]
rs6502622	0.85[GIH][hapmap];0.92[MEX][hapmap];0.83[TSI][hapmap]
rs6502624	0.85[GIH][hapmap];0.92[MEX][hapmap];0.83[TSI][hapmap]
rs6502625	0.82[JPT][hapmap]
rs6502629	0.82[JPT][hapmap];0.83[MEX][hapmap]
rs6502632	0.84[MEX][hapmap]
rs7207395	0.82[JPT][hapmap]
rs7212167	0.84[MEX][hapmap]
rs7213225	0.85[GIH][hapmap];0.92[MEX][hapmap]
rs7214002	0.82[CEU][hapmap]
rs7219320	0.84[MEX][hapmap]
rs7222480	0.82[CEU][hapmap];0.81[GIH][hapmap];0.91[MEX][hapmap]
rs7224815	0.82[JPT][hapmap]
rs7359509	1.00[CEU][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7501812	0.91[CEU][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.89[TSI][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7503334	0.82[GIH][hapmap];0.82[JPT][hapmap];0.91[MEX][hapmap]
rs7503747	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs8065416	0.85[GIH][hapmap];0.92[MEX][hapmap];0.81[TSI][hapmap]
rs8065563	0.82[GIH][hapmap];0.82[JPT][hapmap];0.91[MEX][hapmap]
rs8066560	1.00[CEU][hapmap];1.00[GIH][hapmap];0.83[MEX][hapmap];0.91[TSI][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs8066982	0.85[GIH][hapmap];0.92[MEX][hapmap];0.81[TSI][hapmap]
rs8067439	0.81[TSI][hapmap]
rs8068175	0.82[CHB][hapmap];0.80[MEX][hapmap]
rs8070128	0.82[GIH][hapmap];0.82[JPT][hapmap];0.91[MEX][hapmap]
rs8070748	0.85[GIH][hapmap];0.92[MEX][hapmap];0.81[TSI][hapmap]
rs8073001	0.85[GIH][hapmap];0.92[MEX][hapmap];0.83[TSI][hapmap]
rs8078105	0.92[MEX][hapmap]
rs8078138	0.82[GIH][hapmap];0.82[JPT][hapmap];0.91[MEX][hapmap]
rs8078583	0.82[JPT][hapmap]
rs8078756	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs8079321	0.86[CEU][hapmap];0.88[GIH][hapmap];0.92[MEX][hapmap];0.87[TSI][hapmap];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs8080061	0.86[CEU][hapmap];0.88[GIH][hapmap];0.92[MEX][hapmap];0.87[TSI][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs8080823	0.82[GIH][hapmap];0.82[JPT][hapmap];0.91[MEX][hapmap]
rs950966	0.82[GIH][hapmap];0.82[JPT][hapmap];0.91[MEX][hapmap]
rs9891957	1.00[CEU][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9893690	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9894257	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9895335	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9895750	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9899634	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9906673	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9907246	0.86[CEU][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.83[TSI][hapmap];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9907287	0.86[CEU][hapmap];0.88[GIH][hapmap];0.92[MEX][hapmap];0.87[TSI][hapmap];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9908017	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9908299	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9911281	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9912895	0.85[GIH][hapmap];0.92[MEX][hapmap];0.83[TSI][hapmap]
rs9913277	0.88[MEX][hapmap]
rs9915248	0.95[CEU][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9915776	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:34 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv907748	chr17:17412032-17782404	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
2	nsv1065270	chr17:17430116-17823086	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
3	nsv543236	chr17:17430116-17823086	Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
4	nsv907752	chr17:17569012-17750907	Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
5	nsv531183	chr17:17571035-18205309	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
6	nsv907753	chr17:17573539-17747289	Genic enhancers Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
7	nsv907754	chr17:17573539-17782404	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
8	nsv1061126	chr17:17578826-17803194	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
9	nsv543238	chr17:17578826-17803194	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
10	nsv833385	chr17:17594037-17765578	Enhancers Genic enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
11	nsv1058884	chr17:17594370-17803194	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
12	nsv543240	chr17:17594370-17803194	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
13	nsv1064176	chr17:17596222-17803194	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
14	nsv543242	chr17:17596222-17803194	Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
15	nsv1062361	chr17:17598407-17746899	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
16	nsv543243	chr17:17598407-17746899	Genic enhancers Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
17	nsv907756	chr17:17619859-17747289	Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
18	nsv522668	chr17:17619859-17752809	Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
19	nsv907757	chr17:17619859-17752809	Flanking Bivalent TSS/Enh Active TSS Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
20	nsv907758	chr17:17619859-17782404	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
21	nsv907759	chr17:17619859-17802478	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
22	nsv1059949	chr17:17632590-17803194	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
23	nsv543244	chr17:17632590-17803194	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
24	nsv907760	chr17:17649423-17782404	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
25	nsv907761	chr17:17649423-17802478	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
26	nsv916653	chr17:17651916-18454952	Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
27	nsv907762	chr17:17668071-17802478	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
28	nsv907763	chr17:17673824-17749822	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
29	nsv907764	chr17:17673824-17754633	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
30	nsv907765	chr17:17682484-17802478	Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
31	nsv907766	chr17:17682484-17957348	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
32	nsv533142	chr17:17691726-18236686	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
33	nsv907767	chr17:17709136-17733760	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Strong transcription Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
34	nsv907768	chr17:17709136-17747289	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs9902941	TOM1L2	cis	cerebellum	SCAN
rs9902941	TOM1L2	cis	parietal	SCAN
rs9902941	SREBF1	cis	Whole Blood	GTEx

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17727600-17734400	Enhancers	Placenta	Placenta
2	chr17:17727600-17736400	Enhancers	Liver	Liver
3	chr17:17728600-17734200	Weak transcription	Brain Angular Gyrus	brain
4	chr17:17728600-17734200	Enhancers	Skeletal Muscle Female	skeletal muscle
5	chr17:17728600-17734600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr17:17728600-17734800	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr17:17728600-17737800	Weak transcription	NH-A	brain
8	chr17:17728600-17738400	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr17:17728600-17738400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr17:17728600-17738600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr17:17728600-17738600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr17:17728600-17738800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr17:17728600-17738800	Weak transcription	Fetal Kidney	kidney
14	chr17:17729000-17734000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr17:17729000-17734400	Weak transcription	Brain Germinal Matrix	brain
16	chr17:17729000-17738400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr17:17729200-17738400	Weak transcription	Aorta	Aorta
18	chr17:17729400-17733800	Weak transcription	Right Atrium	heart
19	chr17:17729400-17734000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr17:17729400-17734000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr17:17729400-17734400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr17:17729400-17734400	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr17:17729400-17734800	Weak transcription	NHDF-Ad	bronchial
24	chr17:17729400-17738400	Weak transcription	Small Intestine	intestine
25	chr17:17729400-17738400	Weak transcription	Osteobl	bone
26	chr17:17729600-17734200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr17:17729600-17734200	Strong transcription	Fetal Stomach	stomach
28	chr17:17729600-17734400	Weak transcription	Fetal Lung	lung
29	chr17:17729600-17737600	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr17:17729600-17738400	Weak transcription	HSMM	muscle
31	chr17:17729600-17738400	Weak transcription	HSMMtube	muscle
32	chr17:17729800-17734800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr17:17729800-17738800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr17:17730000-17734000	Weak transcription	Adipose Nuclei	Adipose
35	chr17:17730000-17734000	Weak transcription	Rectal Smooth Muscle	rectum
36	chr17:17730000-17734800	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr17:17730000-17735600	Genic enhancers	Fetal Thymus	thymus
38	chr17:17730000-17737800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr17:17730000-17738800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr17:17730200-17737800	Weak transcription	Dnd41	blood
41	chr17:17730400-17733800	Weak transcription	Left Ventricle	heart
42	chr17:17730400-17734800	Weak transcription	Primary B cells from cord blood	blood
43	chr17:17730400-17735800	Genic enhancers	Fetal Muscle Trunk	muscle
44	chr17:17730400-17737200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr17:17730400-17737600	Weak transcription	HUVEC	blood vessel
46	chr17:17730600-17734200	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr17:17730600-17734400	Weak transcription	Psoas Muscle	Psoas
48	chr17:17730600-17734600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr17:17730800-17733800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr17:17731000-17734800	Weak transcription	H1 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links