Variant report

Variant	rs3751084
Chromosome Location	chr11:67784278-67784279
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	RAD21	chr11:67784213-67784530	HepG2	liver:	n/a	n/a
2	USF1	chr11:67784231-67784710	A549	lung:	n/a	chr11:67784483-67784494
3	CTCF	chr11:67784200-67784350	MCF-7	breast:	n/a	chr11:67784274-67784287
4	MAX	chr11:67783561-67785297	A549	lung:	n/a	chr11:67784748-67784758
5	EP300	chr11:67784132-67786005	A549	lung:	n/a	n/a
6	ZBTB33	chr11:67784173-67784913	A549	lung:	n/a	n/a
7	CTCF	chr11:67784200-67784350	BE2_C	brain:	n/a	chr11:67784274-67784287
8	POLR2A	chr11:67783647-67785244	A549	lung:	n/a	n/a
9	POLR2A	chr11:67783701-67785292	HepG2	liver:	n/a	n/a
10	POLR2A	chr11:67784220-67784635	HepG2	liver:	n/a	n/a
11	MAX	chr11:67783460-67786676	A549	lung:	n/a	chr11:67784748-67784758
12	CTCF	chr11:67784123-67784332	K562	blood:	n/a	chr11:67784274-67784287
13	CTCF	chr11:67784235-67784318	K562	blood:	n/a	chr11:67784274-67784287
14	CTCF	chr11:67784220-67784370	Hela-S3	cervix:	n/a	chr11:67784274-67784287
15	CTCF	chr11:67784200-67784350	HBMEC	blood vessel:	n/a	chr11:67784274-67784287
16	USF1	chr11:67784112-67784914	HCT-116	colon:	n/a	chr11:67784483-67784494
17	POLR2A	chr11:67784198-67785237	A549	lung:	n/a	n/a
18	POLR2A	chr11:67784187-67785272	HepG2	liver:	n/a	n/a
19	USF1	chr11:67784253-67784585	K562	blood:	n/a	chr11:67784483-67784494
20	POLR2A	chr11:67784197-67784573	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr11:67784047-67785237	HepG2	liver:	n/a	n/a
22	SMC3	chr11:67784084-67784813	Hela-S3	cervix:	n/a	chr11:67784688-67784695
23	CTCF	chr11:67784240-67784390	HVMF	connective:	n/a	chr11:67784274-67784287
24	SIN3AK20	chr11:67784210-67784918	A549	lung:	n/a	n/a
25	USF1	chr11:67784203-67784754	ECC-1	luminal epithelium:	n/a	chr11:67784483-67784494
26	POLR2A	chr11:67784183-67784804	HCT-116	colon:	n/a	n/a
27	MAX	chr11:67784142-67784685	NB4	blood:	n/a	n/a
28	NFYA	chr11:67784275-67784764	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr11:67784180-67784330	MCF-7	breast:	n/a	chr11:67784274-67784287
30	MYC	chr11:67784253-67784873	Hela-S3	cervix:	n/a	chr11:67784748-67784758
31	EBF1	chr11:67784138-67784363	GM12878	blood:	n/a	chr11:67784231-67784240 chr11:67784230-67784241 chr11:67784229-67784242 chr11:67784231-67784240 chr11:67784231-67784241
32	CTCF	chr11:67784240-67784390	K562	blood:	n/a	chr11:67784274-67784287
33	YY1	chr11:67783910-67784290	A549	lung:	n/a	chr11:67783932-67783951
34	CTCF	chr11:67784140-67784290	HPAF	blood vessel:	n/a	chr11:67784274-67784287
35	CTCF	chr11:67784260-67784410	NB4	blood:	n/a	chr11:67784274-67784287
36	ELF1	chr11:67784152-67786100	A549	lung:	n/a	n/a
37	TCF12	chr11:67783390-67787243	A549	lung:	n/a	chr11:67786974-67786981 chr11:67786944-67786954
38	USF2	chr11:67784275-67784789	Hela-S3	cervix:	n/a	n/a
39	CREB1	chr11:67783956-67785043	A549	lung:	n/a	n/a
40	USF1	chr11:67784019-67784825	A549	lung:	n/a	chr11:67784483-67784494
41	POLR2A	chr11:67783663-67786839	Hela-S3	cervix:	n/a	n/a
42	POLR2A	chr11:67783535-67785046	HL-60	blood:	n/a	n/a
43	POLR2A	chr11:67784056-67785272	U87	brain:	n/a	n/a
44	USF1	chr11:67784245-67784726	A549	lung:	n/a	chr11:67784483-67784494
45	RFX5	chr11:67784175-67784740	Hela-S3	cervix:	n/a	n/a
46	MYBL2	chr11:67784118-67785417	HepG2	liver:	n/a	n/a
47	USF1	chr11:67784206-67784875	A549	lung:	n/a	chr11:67784483-67784494
48	TCF12	chr11:67784217-67784978	A549	lung:	n/a	n/a
49	ZKSCAN1	chr11:67784085-67784769	Hela-S3	cervix:	n/a	n/a
50	PBX3	chr11:67783504-67785430	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:67783695..67784431-chr12:6960221..6961043,2	Hela-S3	cervix:
2	chr11:67779784..67784526-chr11:67980026..67983056,5	MCF-7	breast:
3	chr11:67783919..67784466-chr7:35734315..35735218,2	Hela-S3	cervix:
4	chr11:67783063..67785124-chr11:67886491..67888333,2	K562	blood:
5	chr11:67783191..67785391-chr11:67975759..67978285,2	K562	blood:

Variant related genes	Relation type
ALDH3B1	TF binding region
ENSG00000111665	Chromatin interaction
ENSG00000110721	Chromatin interaction
ENSG00000271122	Chromatin interaction
ENSG00000110066	Chromatin interaction
ENSG00000122557	Chromatin interaction

Extended variants
information (count: 63 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1003777	1.00[CEU][hapmap];0.93[CHB][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1122731	0.93[CEU][hapmap];0.91[GIH][hapmap];0.86[MEX][hapmap];0.94[TSI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12277180	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12284146	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs15518	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2075626	0.93[CEU][hapmap];0.82[GIH][hapmap];0.94[TSI][hapmap];0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2286163	1.00[CEU][hapmap];0.93[CHB][hapmap];0.86[MEX][hapmap];0.97[TSI][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2286164	1.00[CEU][hapmap];0.93[CHB][hapmap];0.93[MEX][hapmap];0.97[TSI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2286165	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2286166	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2286168	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2286169	1.00[CEU][hapmap];0.93[CHB][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3115547	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3133268	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3764816	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3764817	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3764819	0.93[CHB][hapmap];0.93[MEX][hapmap];0.97[TSI][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3764821	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.80[MEX][hapmap];0.97[TSI][hapmap];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3794177	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4147777	0.93[CEU][hapmap]
rs4244839	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4646808	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4646812	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4646813	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72926415	0.84[ASN][1000 genomes]
rs7952122	0.85[CHB][hapmap];0.92[JPT][hapmap]
rs886701	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs886702	1.00[CEU][hapmap];0.93[CHB][hapmap];0.93[MEX][hapmap];0.97[TSI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1036101	chr11:67346813-67828351	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription 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	139 gene(s)	inside rSNPs	diseases
2	nsv541079	chr11:67346813-67828351	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
3	nsv468606	chr11:67352689-67816936	Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
4	nsv555269	chr11:67352689-67816936	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Active TSS 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	136 gene(s)	inside rSNPs	diseases
5	nsv427892	chr11:67451649-67926562	Bivalent Enhancer Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
6	esv2757450	chr11:67472905-67891289	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	112 gene(s)	inside rSNPs	diseases
7	esv2759835	chr11:67472905-67891289	Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	112 gene(s)	inside rSNPs	diseases
8	nsv428260	chr11:67524937-67797669	Enhancers Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	80 gene(s)	inside rSNPs	diseases
9	esv2758275	chr11:67524937-67859490	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	87 gene(s)	inside rSNPs	diseases
10	nsv469856	chr11:67639037-67859490	Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
11	nsv482760	chr11:67639037-67859490	Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
12	nsv1038960	chr11:67727827-67785555	Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
13	nsv1047567	chr11:67747160-67819790	Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
14	nsv8836	chr11:67752879-67819799	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
15	nsv897836	chr11:67757350-67816936	Enhancers Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
16	nsv897837	chr11:67757350-67821036	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
17	nsv897838	chr11:67757350-67833543	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
18	nsv825963	chr11:67763676-68197054	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	149 gene(s)	inside rSNPs	diseases
19	nsv1050471	chr11:67764068-67821610	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
20	nsv897839	chr11:67765056-67793014	Genic enhancers Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
21	nsv468613	chr11:67765056-67794643	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
22	nsv555277	chr11:67765056-67794643	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
23	nsv468614	chr11:67765056-67799926	ZNF genes & repeats Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
24	nsv897840	chr11:67765056-67804605	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS 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 miRNA	58 gene(s)	inside rSNPs	diseases
25	nsv468615	chr11:67765056-67816936	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
26	nsv555278	chr11:67765056-67816936	Enhancers Genic enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
27	nsv897841	chr11:67765056-67816936	Bivalent Enhancer Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
28	nsv469964	chr11:67765056-67821036	Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
29	nsv897842	chr11:67765056-67821036	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
30	nsv897843	chr11:67765056-67833543	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
31	nsv1046054	chr11:67768796-67819790	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	60 gene(s)	inside rSNPs	diseases
32	nsv897844	chr11:67772729-67793014	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
33	nsv897845	chr11:67774231-67821036	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
34	nsv897846	chr11:67776465-67794643	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
35	nsv897847	chr11:67776465-67804605	Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription 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	55 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs3751084	SPDYC	cis	parietal	SCAN
rs3751084	NDUFS8	Cis_1M	lymphoblastoid	RTeQTL
rs3751084	NDUFS8	cis	parietal	SCAN
rs3751084	RP5-901A4.1	cis	Thyroid	GTEx
rs3751084	KCNK4	cis	cerebellum	SCAN

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67771600-67797600	Weak transcription	Small Intestine	intestine
2	chr11:67772600-67792400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr11:67778400-67787400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr11:67778600-67784400	Weak transcription	Right Atrium	heart
5	chr11:67778600-67788000	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr11:67778800-67784400	Weak transcription	Brain Angular Gyrus	brain
7	chr11:67779400-67784400	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr11:67779600-67784400	Weak transcription	Liver	Liver
9	chr11:67779800-67785600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr11:67780200-67784600	Weak transcription	Right Ventricle	heart
11	chr11:67781400-67786800	Enhancers	Esophagus	oesophagus
12	chr11:67781600-67784600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr11:67781800-67784400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr11:67782000-67784400	Weak transcription	Brain Cingulate Gyrus	brain
15	chr11:67782000-67784400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr11:67782200-67784400	Weak transcription	Brain Anterior Caudate	brain
17	chr11:67782400-67784400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr11:67782400-67784400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr11:67782400-67785200	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr11:67782400-67785400	Flanking Active TSS	Hela-S3	cervix
21	chr11:67782400-67788200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr11:67782400-67791400	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr11:67782400-67794800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr11:67782400-67794800	Strong transcription	Primary neutrophils fromperipheralblood	blood
25	chr11:67782400-67796800	Weak transcription	Colon Smooth Muscle	Colon
26	chr11:67782600-67789000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr11:67782600-67791400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr11:67782600-67791600	Weak transcription	Ovary	ovary
29	chr11:67782600-67791600	Weak transcription	Stomach Smooth Muscle	stomach
30	chr11:67782600-67792200	Weak transcription	HSMMtube	muscle
31	chr11:67782600-67792600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr11:67782600-67794000	Weak transcription	NH-A	brain
33	chr11:67782600-67797000	Weak transcription	Rectal Smooth Muscle	rectum
34	chr11:67782800-67784400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr11:67782800-67784400	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr11:67782800-67784400	Weak transcription	NHEK	skin
37	chr11:67782800-67795800	Strong transcription	Primary monocytes fromperipheralblood	blood
38	chr11:67782800-67797200	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr11:67783400-67784800	Enhancers	Placenta Amnion	Placenta Amnion
40	chr11:67783400-67786000	Enhancers	Adipose Nuclei	Adipose
41	chr11:67783600-67785000	Enhancers	Lung	lung
42	chr11:67783600-67786200	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr11:67783800-67784800	Enhancers	Stomach Mucosa	stomach
44	chr11:67783800-67785000	Enhancers	Muscle Satellite Cultured Cells	--
45	chr11:67783800-67785000	Enhancers	Fetal Intestine Large	intestine
46	chr11:67783800-67785000	Genic enhancers	Fetal Intestine Small	intestine
47	chr11:67783800-67785200	Flanking Active TSS	A549	lung
48	chr11:67783800-67785400	Enhancers	Placenta	Placenta
49	chr11:67783800-67785400	Flanking Active TSS	HepG2	liver
50	chr11:67783800-67785400	Weak transcription	Monocytes-CD14+_RO01746	blood

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