Variant report

Variant	rs11211176
Chromosome Location	chr1:46223086-46223087
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:46221868..46223615-chr1:46227697..46230065,2	K562	blood:
2	chr1:46222162..46224088-chr1:46263999..46266661,2	K562	blood:

Extended variants
information (count: 212 )
Associated
traits (count: 17 )

rSNPs within LD-proxies of this variant (count:179)

rs_ID	r²[population]
rs10157795	0.96[ASN][1000 genomes]
rs10430105	0.90[CHD][hapmap]
rs10430123	0.95[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs10430124	0.95[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs10749856	0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs10789467	0.86[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs10789468	0.88[ASN][1000 genomes]
rs10789470	0.86[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs10789471	0.85[CHD][hapmap]
rs1084086	0.83[CHD][hapmap]
rs10890333	0.86[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs10890336	0.89[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs10890337	0.88[ASN][1000 genomes]
rs10890343	0.88[ASN][1000 genomes]
rs10890344	0.91[ASN][1000 genomes]
rs10890346	0.91[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10890361	0.83[LWK][hapmap];0.86[MEX][hapmap];0.88[MKK][hapmap]
rs10890363	0.83[LWK][hapmap];0.81[MKK][hapmap]
rs11211145	0.86[CHD][hapmap]
rs11211149	0.80[CHB][hapmap]
rs11211151	0.87[ASN][1000 genomes]
rs11211152	0.86[CHD][hapmap]
rs11211157	0.86[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs11211158	0.88[ASN][1000 genomes]
rs11211159	0.88[ASN][1000 genomes]
rs11211161	0.90[CHD][hapmap]
rs11211163	0.86[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs11211165	0.88[ASN][1000 genomes]
rs11211166	0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs11211168	0.86[CHD][hapmap]
rs11211169	0.82[CHB][hapmap];0.90[CHD][hapmap]
rs11211171	0.85[CHD][hapmap]
rs11211173	0.86[CHD][hapmap]
rs11211174	0.96[ASN][1000 genomes]
rs11211175	0.96[ASN][1000 genomes]
rs11211177	0.86[CHD][hapmap]
rs11211178	0.91[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs11211179	0.96[ASN][1000 genomes]
rs11211181	0.91[CHB][hapmap];0.88[CHD][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs11211188	0.81[ASN][1000 genomes]
rs12022141	0.87[ASN][1000 genomes]
rs12024590	0.86[CHD][hapmap]
rs12025621	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12031182	0.96[ASN][1000 genomes]
rs12037803	0.88[ASN][1000 genomes]
rs12043945	0.86[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs12045096	0.87[ASN][1000 genomes]
rs12045165	0.81[ASN][1000 genomes]
rs12049027	0.83[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs12069121	0.91[ASN][1000 genomes]
rs12091503	0.86[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs12404197	0.96[ASN][1000 genomes]
rs1250	0.86[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs12564201	0.95[ASN][1000 genomes]
rs1541131	0.83[ASN][1000 genomes]
rs1547924	0.86[CHB][hapmap];0.90[CHD][hapmap];0.95[JPT][hapmap];0.80[ASN][1000 genomes]
rs1547925	0.90[CHD][hapmap]
rs1972410	0.85[CHD][hapmap]
rs2050376	0.86[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.80[ASN][1000 genomes]
rs2088102	0.90[CHB][hapmap];0.82[CHD][hapmap];0.84[JPT][hapmap];0.90[MEX][hapmap]
rs2152078	0.86[CHD][hapmap]
rs2230657	0.87[CHB][hapmap];0.90[JPT][hapmap]
rs2230658	0.86[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.80[ASN][1000 genomes]
rs2230659	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs2253862	0.90[CHD][hapmap]
rs2275085	0.86[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs2275086	0.90[CHD][hapmap]
rs28361459	0.90[ASN][1000 genomes]
rs28370457	0.86[CHD][hapmap]
rs28375469	0.82[CHB][hapmap];0.90[CHD][hapmap]
rs28376548	0.86[ASN][1000 genomes]
rs28378621	0.99[ASN][1000 genomes]
rs28406914	0.96[ASN][1000 genomes]
rs28432365	0.96[ASN][1000 genomes]
rs28438704	0.91[ASN][1000 genomes]
rs28442079	0.91[ASN][1000 genomes]
rs28456069	0.88[ASN][1000 genomes]
rs28474773	0.96[ASN][1000 genomes]
rs28490344	0.96[ASN][1000 genomes]
rs28495425	0.96[ASN][1000 genomes]
rs28498557	0.93[ASN][1000 genomes]
rs28501477	0.95[ASN][1000 genomes]
rs28508523	0.82[ASN][1000 genomes]
rs28528139	0.88[ASN][1000 genomes]
rs28550303	0.82[CHB][hapmap];0.90[CHD][hapmap]
rs28564319	0.96[ASN][1000 genomes]
rs28617418	0.89[ASN][1000 genomes]
rs28635845	0.93[ASN][1000 genomes]
rs28641748	0.96[ASN][1000 genomes]
rs28647556	1.00[CHB][hapmap];0.92[CHD][hapmap];0.95[JPT][hapmap];0.89[LWK][hapmap];0.91[MEX][hapmap];0.88[MKK][hapmap];0.83[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs28683093	0.88[ASN][1000 genomes]
rs28719889	0.86[CHD][hapmap]
rs28789495	0.96[ASN][1000 genomes]
rs28817701	0.90[CHB][hapmap];0.93[CHD][hapmap];0.90[JPT][hapmap];0.96[ASN][1000 genomes]
rs28844317	0.99[ASN][1000 genomes]
rs28890893	0.85[CHD][hapmap]
rs2934857	0.91[CHB][hapmap];0.93[CHD][hapmap];0.90[MEX][hapmap]
rs2991979	0.85[CHD][hapmap]
rs2991985	0.84[ASN][1000 genomes]
rs2991986	0.86[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs2991987	0.86[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs2991988	0.90[CHD][hapmap]
rs3013594	0.85[ASN][1000 genomes]
rs3013595	0.91[CHB][hapmap];0.90[CHD][hapmap];0.95[JPT][hapmap];0.91[LWK][hapmap];0.91[MEX][hapmap];0.88[MKK][hapmap];0.91[ASN][1000 genomes]
rs3013596	0.91[ASN][1000 genomes]
rs3013597	0.90[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs3014210	0.86[CHB][hapmap];0.93[CHD][hapmap];0.85[JPT][hapmap]
rs3014216	0.91[CHB][hapmap];0.93[CHD][hapmap];0.85[JPT][hapmap];0.89[LWK][hapmap];0.91[MEX][hapmap];0.83[MKK][hapmap]
rs3014218	0.83[CHB][hapmap];0.93[CHD][hapmap];0.85[JPT][hapmap];0.81[LWK][hapmap];0.86[MEX][hapmap]
rs3014236	0.83[ASN][1000 genomes]
rs3014237	0.86[CHD][hapmap]
rs3014238	0.91[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.89[LWK][hapmap];0.91[MEX][hapmap];0.84[MKK][hapmap];0.85[ASN][1000 genomes]
rs3014239	0.86[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs3014241	0.86[CHD][hapmap]
rs3014242	0.86[CHB][hapmap];0.93[CHD][hapmap];0.85[JPT][hapmap]
rs3014243	0.94[ASN][1000 genomes]
rs3014245	0.90[CHD][hapmap]
rs3014247	0.88[ASN][1000 genomes]
rs3014251	0.80[ASN][1000 genomes]
rs34895634	0.94[ASN][1000 genomes]
rs3811435	0.88[ASN][1000 genomes]
rs3811436	0.90[CHD][hapmap]
rs3935296	0.96[ASN][1000 genomes]
rs4274104	1.00[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.91[LWK][hapmap];0.95[MEX][hapmap];0.88[MKK][hapmap];0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4330955	0.93[ASN][1000 genomes]
rs4391704	0.84[CHB][hapmap]
rs4423054	0.96[ASN][1000 genomes]
rs4431884	0.82[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs4439382	0.90[CHD][hapmap]
rs4468203	0.94[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs4545281	0.88[MKK][hapmap]
rs4559551	0.95[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs4564187	0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs4609469	0.86[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs4626927	0.83[ASW][hapmap];0.84[JPT][hapmap];0.83[LWK][hapmap];0.86[MEX][hapmap];0.85[MKK][hapmap]
rs4660312	0.95[CHB][hapmap];0.90[CHD][hapmap];0.80[GIH][hapmap];0.84[JPT][hapmap];0.91[LWK][hapmap];0.86[MEX][hapmap];0.87[MKK][hapmap];0.90[ASN][1000 genomes]
rs4660313	0.86[CHD][hapmap]
rs4660314	0.96[ASN][1000 genomes]
rs4660319	0.81[LWK][hapmap];0.86[MEX][hapmap];0.83[MKK][hapmap]
rs4660879	0.81[ASN][1000 genomes]
rs4660880	0.86[CHD][hapmap]
rs4660882	0.95[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.91[LWK][hapmap];0.91[MEX][hapmap];0.86[MKK][hapmap];0.90[ASN][1000 genomes]
rs4660883	0.91[CHB][hapmap];0.90[CHD][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs4660885	0.91[MEX][hapmap];0.81[ASN][1000 genomes]
rs5021934	0.91[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.91[LWK][hapmap];0.91[MEX][hapmap];0.86[MKK][hapmap];0.90[ASN][1000 genomes]
rs518216	0.90[CHB][hapmap];0.90[CHD][hapmap];0.85[JPT][hapmap]
rs56177313	0.96[ASN][1000 genomes]
rs56255771	0.96[ASN][1000 genomes]
rs59916372	0.96[ASN][1000 genomes]
rs61784796	0.90[ASN][1000 genomes]
rs61784800	0.94[ASN][1000 genomes]
rs61784803	0.96[ASN][1000 genomes]
rs61784824	0.88[ASN][1000 genomes]
rs61784833	0.94[ASN][1000 genomes]
rs6429574	0.88[ASN][1000 genomes]
rs6429575	0.88[ASN][1000 genomes]
rs6429576	1.00[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.91[LWK][hapmap];0.95[MEX][hapmap];0.86[MKK][hapmap];0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6429582	0.80[LWK][hapmap];0.86[MEX][hapmap];0.83[MKK][hapmap]
rs6656279	0.91[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs6658700	0.90[CHD][hapmap]
rs6661163	0.81[ASN][1000 genomes]
rs6665808	0.90[ASN][1000 genomes]
rs6666743	0.86[MEX][hapmap]
rs6671802	0.91[ASN][1000 genomes]
rs6686134	0.83[LWK][hapmap];0.88[MKK][hapmap]
rs6686944	0.85[ASN][1000 genomes]
rs6690926	0.88[ASN][1000 genomes]
rs6694340	0.86[MEX][hapmap]
rs6697821	0.95[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs6699418	0.84[ASN][1000 genomes]
rs6703960	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs72688483	0.91[ASN][1000 genomes]
rs7519900	0.96[ASN][1000 genomes]
rs7520123	0.96[ASN][1000 genomes]
rs7524495	0.83[LWK][hapmap];0.86[MEX][hapmap];0.86[MKK][hapmap]
rs7556436	0.83[LWK][hapmap];0.86[MKK][hapmap]
rs8179296	0.88[ASN][1000 genomes]
rs8179402	0.88[ASN][1000 genomes]
rs9793568	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:33 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529631	chr1:45905936-46335246	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	207 gene(s)	inside rSNPs	diseases
2	nsv932680	chr1:45935520-46686477	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	232 gene(s)	inside rSNPs	diseases
3	nsv868828	chr1:45953923-46686477	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	232 gene(s)	inside rSNPs	diseases
4	nsv871928	chr1:46024701-46609736	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking 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 target site	123 gene(s)	inside rSNPs	diseases
5	nsv1011587	chr1:46051672-46244492	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
6	nsv1014128	chr1:46097670-46394540	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
7	nsv1010054	chr1:46144479-46320493	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers 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	75 gene(s)	inside rSNPs	diseases
8	nsv1006861	chr1:46144479-46417621	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers 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 target site	76 gene(s)	inside rSNPs	diseases
9	nsv1003049	chr1:46144479-46476149	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
10	nsv870511	chr1:46148138-46245423	Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
11	nsv871233	chr1:46153203-46311275	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
12	nsv1008219	chr1:46160098-46493958	Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
13	nsv534943	chr1:46160098-46493958	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
14	nsv1000498	chr1:46171836-46438252	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
15	nsv870791	chr1:46182916-46398415	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
16	nsv871023	chr1:46184300-46301182	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
17	nsv998925	chr1:46184925-46353041	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
18	nsv1003986	chr1:46184925-46417621	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
19	nsv1007501	chr1:46184925-46439533	Enhancers Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
20	nsv534944	chr1:46184925-46439533	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
21	nsv871763	chr1:46186576-46236098	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
22	nsv1006891	chr1:46189258-46408032	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
23	nsv1009355	chr1:46189258-46463012	Active TSS Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
24	nsv870626	chr1:46196813-46314170	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
25	nsv871312	chr1:46196813-46353332	Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
26	esv2830426	chr1:46202361-46347367	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
27	nsv546158	chr1:46216575-46495434	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
28	nsv870911	chr1:46216575-46498375	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
29	nsv1013628	chr1:46221617-46356565	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
30	nsv431268	chr1:46223080-46495480	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
31	nsv546159	chr1:46223086-46398415	Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
32	nsv461417	chr1:46223086-46416348	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
33	nsv546160	chr1:46223086-46416348	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:17)

SNP	Gene	Cis/trans	Tissue	Source
rs11211176	NSUN4	cis	cerebellum	SCAN
rs11211176	IPP	Cis_1M	lymphoblastoid	RTeQTL
rs11211176	MAST2	cis	Artery Aorta	GTEx
rs11211176	IPP	cis	lymphoblastoid	seeQTL
rs11211176	CYP4Z2P	cis	parietal	SCAN
rs11211176	SNORD38A	cis	cerebellum	SCAN
rs11211176	GPBP1L1	cis	Muscle Skeletal	GTEx
rs11211176	BEND5	cis	cerebellum	SCAN
rs11211176	GPBP1L1	cis	Lymphoblastoid	GTEx
rs11211176	LOC126661	Cis_1M	lymphoblastoid	RTeQTL
rs11211176	IPP	trans	brain	seeQTL
rs11211176	UROD	cis	multi-tissue	Pritchard
rs11211176	IPP	cis	brain	seeQTL
rs11211176	Hs.396207	cis	multi-tissue	Pritchard
rs11211176	CYP4Z2P	cis	cerebellum	SCAN
rs11211176	CCDC163P	cis	Skin Sun Exposed Lower leg	GTEx
rs11211176	MAST2	cis	Artery Tibial	GTEx

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:46222400-46224400	Enhancers	Gastric	stomach
2	chr1:46222800-46223600	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr1:46223000-46223400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:46223000-46224600	Enhancers	Stomach Mucosa	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links