Variant report

Variant	rs4756143
Chromosome Location	chr11:33219395-33219396
allele	A/G
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	CEBPB	chr11:33219304-33219484	Hela-S3	cervix:	n/a	n/a

Variant related genes	Relation type
ENSG00000200485	TF binding region

Extended variants
information (count: 200 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:161)

rs_ID	r²[population]
rs1026822	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1028564	0.88[ASN][1000 genomes]
rs1028663	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10734415	0.83[AMR][1000 genomes]
rs10767987	0.84[AMR][1000 genomes]
rs10767988	0.84[ASN][1000 genomes]
rs10767989	0.84[ASN][1000 genomes]
rs10767990	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10767992	0.88[ASN][1000 genomes]
rs10767994	0.90[ASN][1000 genomes]
rs10767995	0.90[ASN][1000 genomes]
rs10767998	0.90[ASN][1000 genomes]
rs10767999	0.90[ASN][1000 genomes]
rs10768001	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10836021	0.84[ASN][1000 genomes]
rs10836022	0.84[ASN][1000 genomes]
rs10836025	0.88[ASN][1000 genomes]
rs10836026	0.88[ASN][1000 genomes]
rs10836027	0.88[ASN][1000 genomes]
rs10836028	0.88[ASN][1000 genomes]
rs10836029	0.88[ASN][1000 genomes]
rs10836034	0.87[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10836035	0.90[ASN][1000 genomes]
rs10836036	0.90[ASN][1000 genomes]
rs10836038	0.91[ASN][1000 genomes]
rs10836039	0.90[ASN][1000 genomes]
rs10836041	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10836042	0.84[ASN][1000 genomes]
rs10836045	0.81[ASN][1000 genomes]
rs10836046	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10836049	0.83[AMR][1000 genomes]
rs11032190	0.90[ASN][1000 genomes]
rs11032191	0.90[ASN][1000 genomes]
rs11032193	0.90[ASN][1000 genomes]
rs11032200	0.90[ASN][1000 genomes]
rs11032201	0.90[ASN][1000 genomes]
rs11032213	0.84[ASN][1000 genomes]
rs11032214	0.83[ASN][1000 genomes]
rs11032222	0.82[AMR][1000 genomes]
rs11600589	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11602835	0.90[ASN][1000 genomes]
rs11605077	0.89[ASN][1000 genomes]
rs11823640	0.90[ASN][1000 genomes]
rs11825687	0.90[ASN][1000 genomes]
rs12360582	0.88[ASN][1000 genomes]
rs12418231	0.84[ASN][1000 genomes]
rs12798476	0.90[ASN][1000 genomes]
rs12798873	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12801128	0.88[ASN][1000 genomes]
rs12801140	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12801185	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs12805232	0.84[ASN][1000 genomes]
rs1386183	0.87[ASN][1000 genomes]
rs1407367	0.88[ASN][1000 genomes]
rs1471851	0.88[ASN][1000 genomes]
rs1610316	0.83[AMR][1000 genomes]
rs1679834	0.81[ASN][1000 genomes]
rs1967001	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1967061	0.88[ASN][1000 genomes]
rs1979543	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1994367	0.88[ASN][1000 genomes]
rs1994368	0.88[ASN][1000 genomes]
rs1994369	0.88[ASN][1000 genomes]
rs1998398	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2061996	0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2061997	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2065083	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2078321	0.83[AMR][1000 genomes]
rs2087087	0.88[ASN][1000 genomes]
rs2199917	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2199918	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2220287	0.87[ASN][1000 genomes]
rs2420021	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2474868	0.83[ASN][1000 genomes]
rs2474869	0.82[ASN][1000 genomes]
rs2474870	0.87[ASN][1000 genomes]
rs2475382	0.87[ASN][1000 genomes]
rs267428	0.82[ASN][1000 genomes]
rs267435	0.84[ASN][1000 genomes]
rs267437	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs267439	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs267440	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs267442	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs267445	0.80[AMR][1000 genomes]
rs267451	0.84[ASN][1000 genomes]
rs3117541	0.87[ASN][1000 genomes]
rs3117542	0.87[ASN][1000 genomes]
rs3117652	0.87[ASN][1000 genomes]
rs3117653	0.86[ASN][1000 genomes]
rs3117654	0.86[ASN][1000 genomes]
rs34143165	0.90[ASN][1000 genomes]
rs372754	0.86[ASN][1000 genomes]
rs373499	0.86[ASN][1000 genomes]
rs3736213	0.87[ASN][1000 genomes]
rs373705	0.84[ASN][1000 genomes]
rs375376	0.86[ASN][1000 genomes]
rs380540	0.87[ASN][1000 genomes]
rs385132	0.87[ASN][1000 genomes]
rs394634	0.86[ASN][1000 genomes]
rs396518	0.86[ASN][1000 genomes]
rs397935	0.86[ASN][1000 genomes]
rs409516	0.86[ASN][1000 genomes]
rs414940	0.86[ASN][1000 genomes]
rs416097	0.86[ASN][1000 genomes]
rs422493	0.85[ASN][1000 genomes]
rs4237680	0.82[AMR][1000 genomes]
rs425468	0.86[ASN][1000 genomes]
rs429439	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs441663	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs444575	0.86[ASN][1000 genomes]
rs446679	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs449444	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs450846	0.86[ASN][1000 genomes]
rs4755355	0.87[ASN][1000 genomes]
rs4755361	0.90[ASN][1000 genomes]
rs4756073	0.88[ASN][1000 genomes]
rs4756074	0.88[ASN][1000 genomes]
rs4756082	0.87[ASN][1000 genomes]
rs4756083	0.88[ASN][1000 genomes]
rs4756087	0.88[ASN][1000 genomes]
rs4756090	0.87[ASN][1000 genomes]
rs4756102	0.88[ASN][1000 genomes]
rs4756104	0.90[ASN][1000 genomes]
rs4756121	0.90[ASN][1000 genomes]
rs4756136	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4756141	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4756144	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs5018639	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs590224	0.80[AMR][1000 genomes]
rs603088	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs638759	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs639269	0.84[ASN][1000 genomes]
rs6484644	0.84[ASN][1000 genomes]
rs6484645	0.84[ASN][1000 genomes]
rs6484647	0.84[ASN][1000 genomes]
rs6484648	0.82[ASN][1000 genomes]
rs67433468	0.82[ASN][1000 genomes]
rs7104129	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7114770	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7117228	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7118056	0.90[ASN][1000 genomes]
rs7131287	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7395436	0.84[ASN][1000 genomes]
rs7482452	0.90[ASN][1000 genomes]
rs7928487	0.89[ASN][1000 genomes]
rs7929507	0.90[ASN][1000 genomes]
rs7932999	0.88[ASN][1000 genomes]
rs7933479	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7936132	0.88[ASN][1000 genomes]
rs7937448	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7938357	0.90[ASN][1000 genomes]
rs7942407	0.82[AMR][1000 genomes]
rs7946185	0.90[ASN][1000 genomes]
rs7946222	0.90[ASN][1000 genomes]
rs7950763	0.84[ASN][1000 genomes]
rs7951995	0.88[ASN][1000 genomes]
rs927177	0.84[ASN][1000 genomes]
rs927178	0.84[ASN][1000 genomes]
rs927179	0.84[ASN][1000 genomes]
rs932655	0.89[ASN][1000 genomes]
rs9667141	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:39 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2762904	chr11:32969258-33586535	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
2	nsv1041149	chr11:32981164-33496670	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
3	nsv1053823	chr11:32981164-33533356	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
4	nsv897194	chr11:32993887-33471804	Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
5	nsv1040572	chr11:33008191-33518964	Enhancers Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking 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 target site	64 gene(s)	inside rSNPs	diseases
6	nsv540989	chr11:33008191-33518964	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS 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	64 gene(s)	inside rSNPs	diseases
7	nsv1042860	chr11:33008191-33562490	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
8	nsv540990	chr11:33008191-33562490	Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
9	nsv533840	chr11:33008192-33595324	Bivalent Enhancer Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
10	nsv1051521	chr11:33008435-33239765	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
11	nsv540991	chr11:33008435-33239765	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
12	nsv1044478	chr11:33008435-33656273	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
13	nsv897195	chr11:33012493-33559186	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers 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 miRNA target site	65 gene(s)	inside rSNPs	diseases
14	nsv1053344	chr11:33028973-33499346	Bivalent Enhancer Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
15	nsv1046243	chr11:33043155-33439216	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
16	nsv540992	chr11:33043155-33439216	Genic enhancers Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
17	nsv1050944	chr11:33043155-33656273	Flanking Active TSS Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
18	nsv540993	chr11:33043155-33656273	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
19	nsv529212	chr11:33053073-33641691	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
20	nsv869418	chr11:33053073-33662479	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
21	nsv467786	chr11:33065394-33476703	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
22	nsv553994	chr11:33065394-33476703	Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Enhancers Genic enhancers 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	53 gene(s)	inside rSNPs	diseases
23	nsv521130	chr11:33068389-33602913	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
24	nsv1049756	chr11:33075082-33496670	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking 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 target site	52 gene(s)	inside rSNPs	diseases
25	nsv1053959	chr11:33075082-33565833	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers 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 target site	53 gene(s)	inside rSNPs	diseases
26	nsv540994	chr11:33075082-33565833	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
27	esv2761660	chr11:33114936-33486928	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
28	nsv1035618	chr11:33117833-33448457	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
29	nsv540995	chr11:33117833-33448457	Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats 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
30	nsv1047667	chr11:33119875-33301210	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
31	nsv897200	chr11:33132864-33383085	Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
32	nsv553995	chr11:33132864-33476703	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
33	nsv1038920	chr11:33142058-33482973	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers 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 target site	50 gene(s)	inside rSNPs	diseases
34	nsv897201	chr11:33154678-33370884	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
35	nsv1036238	chr11:33162914-33460303	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
36	nsv540996	chr11:33162914-33460303	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
37	nsv1037430	chr11:33183475-33341784	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription 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	34 gene(s)	inside rSNPs	diseases
38	nsv430370	chr11:33202614-33505494	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
39	nsv897202	chr11:33211190-33428255	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer 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 miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33210400-33219800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr11:33210800-33219800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr11:33213600-33219800	Weak transcription	HSMMtube	muscle
4	chr11:33214200-33219400	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr11:33217400-33219800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:33218000-33220200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr11:33219000-33220800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr11:33219200-33220400	Enhancers	Primary neutrophils fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links