Variant report

Variant	rs1871039
Chromosome Location	chr11:67417427-67417428
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	MTA3	chr11:67415135-67418528	GM12878	blood:	n/a	n/a
2	POLR2A	chr11:67417321-67418505	GM12892	blood:	n/a	n/a
3	RUNX3	chr11:67416514-67418425	GM12878	blood:	n/a	n/a
4	CTCF	chr11:67417013-67417460	GM12892	blood:	n/a	n/a
5	TCF3	chr11:67416222-67417686	GM12878	blood:	n/a	chr11:67417530-67417544
6	ZBTB33	chr11:67416914-67417481	GM12878	blood:	n/a	n/a
7	TCF3	chr11:67416964-67417455	GM12878	blood:	n/a	n/a
8	BCL3	chr11:67416602-67417626	GM12878	blood:	n/a	chr11:67416891-67416900
9	RCOR1	chr11:67417319-67417504	K562	blood:	n/a	n/a
10	SUZ12	chr11:67416985-67417481	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr11:67417360-67417510	GM12872	blood:	n/a	n/a
12	ZNF143	chr11:67417365-67417507	K562	blood:	n/a	n/a
13	POLR2A	chr11:67417001-67417541	Gliobla	brain:	n/a	n/a
14	CTCF	chr11:67416979-67417454	GM19239	blood:	n/a	n/a
15	POLR2A	chr11:67416994-67417641	HepG2	liver:	n/a	n/a
16	ATF2	chr11:67416556-67417488	GM12878	blood:	n/a	n/a
17	NFIC	chr11:67416385-67417509	GM12878	blood:	n/a	chr11:67416900-67416917 chr11:67416900-67416916
18	POU2F2	chr11:67416699-67417580	GM12891	blood:	n/a	n/a
19	NFIC	chr11:67416475-67417471	GM12878	blood:	n/a	chr11:67416900-67416917 chr11:67416900-67416916
20	MAX	chr11:67416997-67417431	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL3	chr11:67416629-67417679	GM12878	blood:	n/a	chr11:67416891-67416900
22	POLR2A	chr11:67416913-67417568	MCF-7	breast:	n/a	n/a
23	KAP1	chr11:67417003-67417455	HEK293	kidney:	n/a	n/a
24	ELF1	chr11:67415566-67417716	GM12878	blood:	n/a	n/a
25	POLR2A	chr11:67416299-67418548	GM12892	blood:	n/a	n/a
26	NFATC1	chr11:67416675-67417719	GM12878	blood:	n/a	n/a
27	STAT5A	chr11:67416915-67417546	GM12878	blood:	n/a	n/a
28	CBX3	chr11:67417207-67417601	K562	blood:	n/a	n/a
29	POU2F2	chr11:67416710-67417598	GM12891	blood:	n/a	n/a
30	POLR2A	chr11:67416607-67417475	HL-60	blood:	n/a	n/a
31	MAX	chr11:67417100-67417473	GM12878	blood:	n/a	n/a
32	CEBPB	chr11:67416678-67417514	GM12878	blood:	n/a	n/a
33	MYC	chr11:67416985-67417473	MCF-7	breast:	n/a	n/a
34	STAT5A	chr11:67416586-67417891	GM12878	blood:	n/a	chr11:67416889-67416900
35	BRCA1	chr11:67417041-67417787	GM12878	blood:	n/a	n/a
36	MAX	chr11:67416933-67417488	HUVEC	blood vessel:	n/a	n/a
37	ZBTB33	chr11:67416761-67417568	GM12878	blood:	n/a	n/a
38	MAX	chr11:67416951-67417464	K562	blood:	n/a	n/a
39	POLR2A	chr11:67416974-67417495	MCF-7	breast:	n/a	n/a
40	PBX3	chr11:67416900-67417535	GM12878	blood:	n/a	n/a
41	MYC	chr11:67416903-67417498	GM12878	blood:	n/a	n/a
42	MAX	chr11:67416932-67417485	NB4	blood:	n/a	n/a
43	POLR2A	chr11:67416645-67418491	GM12892	blood:	n/a	n/a
44	IRF4	chr11:67416591-67417494	GM12878	blood:	n/a	n/a
45	CTCF	chr11:67417280-67417430	GM12870	blood:	n/a	n/a
46	RUNX3	chr11:67416433-67417782	GM12878	blood:	n/a	n/a
47	PML	chr11:67416726-67418413	GM12878	blood:	n/a	n/a
48	NFATC1	chr11:67416637-67417634	GM12878	blood:	n/a	n/a
49	NR2C2	chr11:67416981-67417570	GM12878	blood:	n/a	n/a
50	MAX	chr11:67416902-67418372	A549	lung:	n/a	chr11:67418053-67418063 chr11:67418052-67418062 chr11:67418053-67418062 chr11:67418052-67418063 chr11:67418053-67418062 chr11:67418052-67418063 chr11:67418053-67418062

No.	Distal block	Cell Line	Cell type
1	chr11:67396543..67400484-chr11:67414425..67419634,5	MCF-7	breast:
2	chr11:67412966..67415782-chr11:67417103..67418705,2	K562	blood:
3	chr11:67275644..67277559-chr11:67415737..67417580,2	K562	blood:

Variant related genes	Relation type
ACY3	TF binding region
ENSG00000132744	Chromatin interaction
ENSG00000167799	Chromatin interaction
ENSG00000167797	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1111928	0.89[AMR][1000 genomes]
rs1551885	0.87[AMR][1000 genomes]
rs1871038	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1871040	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2252727	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2361139	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2361140	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2361143	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2447582	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2514033	0.89[AMR][1000 genomes]
rs2514041	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2514042	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2514043	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2514044	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs34428407	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs3928535	0.87[AMR][1000 genomes]
rs4244825	0.87[AMR][1000 genomes]
rs4930463	0.87[AMR][1000 genomes]
rs4930464	0.87[AMR][1000 genomes]
rs6591269	0.87[AMR][1000 genomes]
rs7947754	0.87[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:41 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers 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	271 gene(s)	inside rSNPs	diseases
2	nsv897801	chr11:67033076-67432479	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
3	nsv897808	chr11:67155210-67419855	Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
4	esv2422195	chr11:67234322-67626901	Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh 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	146 gene(s)	inside rSNPs	diseases
5	nsv1041988	chr11:67319916-67749246	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
6	nsv897814	chr11:67339949-67460529	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
7	nsv1050463	chr11:67343421-67717338	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
8	nsv1038189	chr11:67345320-67749246	Transcr. at gene 5' and 3' Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
9	nsv1047236	chr11:67345320-67764068	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
10	nsv555268	chr11:67346743-67752972	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers 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 target site	81 gene(s)	inside rSNPs	diseases
11	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
12	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
13	nsv1053811	chr11:67349444-67749246	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
14	esv1817852	chr11:67349899-67626567	Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Weak 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 target site	69 gene(s)	inside rSNPs	diseases
15	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
16	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
17	nsv897816	chr11:67353579-67460529	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
18	nsv1041887	chr11:67357365-67464893	Flanking Active TSS Genic enhancers Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
19	nsv541080	chr11:67357365-67464893	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers 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
20	nsv529452	chr11:67358204-67465721	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking 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	49 gene(s)	inside rSNPs	diseases
21	nsv492253	chr11:67358204-67574402	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
22	nsv1043487	chr11:67360899-67662476	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
23	nsv897818	chr11:67372477-67419855	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
24	nsv468607	chr11:67372477-67423892	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Strong transcription 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	46 gene(s)	inside rSNPs	diseases
25	nsv555270	chr11:67372477-67423892	Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription 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	46 gene(s)	inside rSNPs	diseases
26	nsv897819	chr11:67372477-67426797	Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
27	nsv468608	chr11:67372477-67433869	Genic enhancers Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription 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	48 gene(s)	inside rSNPs	diseases
28	nsv555271	chr11:67372477-67433869	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active 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	48 gene(s)	inside rSNPs	diseases
29	nsv897820	chr11:67372477-67460529	Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
30	nsv897821	chr11:67378594-67430762	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
31	nsv897822	chr11:67378594-67441553	Genic enhancers Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
32	nsv897823	chr11:67378594-67460529	Enhancers Bivalent Enhancer Active TSS Genic enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
33	nsv897824	chr11:67379575-67418202	Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	40 gene(s)	inside rSNPs	diseases
34	nsv897825	chr11:67381110-67460529	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
35	nsv468609	chr11:67395714-67433869	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
36	nsv555273	chr11:67395714-67433869	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
37	nsv469963	chr11:67395714-67438195	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
38	nsv897826	chr11:67408791-67462549	Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
39	esv1812708	chr11:67414492-67441553	Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
40	esv3356225	chr11:67414976-67419374	Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
41	esv3334811	chr11:67415776-67418674	Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67398800-67418600	Weak transcription	Right Atrium	heart
2	chr11:67411800-67417600	Enhancers	Pancreas	Pancrea
3	chr11:67411800-67419600	Enhancers	Primary B cells from cord blood	blood
4	chr11:67412200-67420600	Enhancers	Primary hematopoietic stem cells	blood
5	chr11:67412400-67417800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr11:67412600-67417600	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr11:67412800-67418000	Enhancers	Spleen	Spleen
8	chr11:67413000-67417600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr11:67413400-67417800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr11:67413600-67417800	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr11:67413600-67417800	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr11:67413600-67418000	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr11:67413800-67418000	Enhancers	Thymus	Thymus
14	chr11:67414400-67417800	Enhancers	Placenta	Placenta
15	chr11:67414600-67417800	Enhancers	Primary T cells fromperipheralblood	blood
16	chr11:67414600-67417800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr11:67414600-67418000	Enhancers	Fetal Thymus	thymus
18	chr11:67414800-67417800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr11:67415600-67417600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
20	chr11:67416200-67417800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr11:67416200-67417800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr11:67416400-67417800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr11:67416400-67417800	Enhancers	Stomach Mucosa	stomach
24	chr11:67416400-67418400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr11:67416600-67417600	Enhancers	Primary T cells from cord blood	blood
26	chr11:67416600-67417800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
27	chr11:67416600-67417800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr11:67416600-67418400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr11:67416800-67417800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
30	chr11:67417000-67417600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr11:67417000-67417600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
32	chr11:67417000-67417600	Bivalent Enhancer	Fetal Brain Male	brain
33	chr11:67417000-67417600	ZNF genes & repeats	Fetal Kidney	kidney
34	chr11:67417000-67417600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
35	chr11:67417000-67417600	Enhancers	HepG2	liver
36	chr11:67417000-67417800	Enhancers	Liver	Liver
37	chr11:67417000-67417800	Enhancers	Brain Cingulate Gyrus	brain
38	chr11:67417000-67417800	Enhancers	Brain Hippocampus Middle	brain
39	chr11:67417000-67417800	Enhancers	Esophagus	oesophagus
40	chr11:67417000-67417800	Enhancers	Gastric	stomach
41	chr11:67417000-67418000	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr11:67417000-67418400	Flanking Active TSS	GM12878-XiMat	blood
43	chr11:67417000-67419200	Flanking Active TSS	Dnd41	blood
44	chr11:67417200-67417800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr11:67417200-67418000	Enhancers	Lung	lung
46	chr11:67417200-67418200	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr11:67417200-67418200	Flanking Active TSS	Colonic Mucosa	Colon
48	chr11:67417400-67417600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr11:67417400-67417600	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr11:67417400-67417600	Enhancers	A549	lung

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