Variant report

Variant	rs4147782
Chromosome Location	chr11:67805563-67805564
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	NR2F2	chr11:67805554-67806651	K562	blood:	n/a	n/a
2	YY1	chr11:67805420-67806783	HepG2	liver:	n/a	chr11:67805655-67805666 chr11:67806427-67806436 chr11:67806424-67806438
3	MBD4	chr11:67805378-67806066	HepG2	liver:	n/a	n/a
4	ZBTB7A	chr11:67805541-67806000	HepG2	liver:	n/a	n/a
5	POLR2A	chr11:67805531-67806728	HepG2	liver:	n/a	n/a
6	SMARCB1	chr11:67805474-67806918	Hela-S3	cervix:	n/a	chr11:67805613-67805622
7	HEY1	chr11:67805439-67805958	HepG2	liver:	n/a	n/a
8	TBP	chr11:67805513-67806669	HepG2	liver:	n/a	n/a
9	POLR2A	chr11:67805544-67806101	A549	lung:	n/a	n/a
10	HNF4A	chr11:67805517-67806016	HepG2	liver:	n/a	chr11:67805976-67805984 chr11:67805901-67805913 chr11:67805752-67805767 chr11:67805900-67805913 chr11:67805754-67805767 chr11:67805901-67805913 chr11:67805754-67805766 chr11:67805901-67805913 chr11:67805901-67805913
11	ESR1	chr11:67805518-67806031	ECC-1	luminal epithelium:	n/a	chr11:67805840-67805855 chr11:67805839-67805856 chr11:67805840-67805857
12	SIX5	chr11:67804813-67805637	A549	lung:	n/a	n/a
13	POLR2A	chr11:67805509-67806844	A549	lung:	n/a	n/a
14	POLR2A	chr11:67804507-67808204	HepG2	liver:	n/a	n/a
15	GATA3	chr11:67805528-67806259	MCF-7	breast:	n/a	n/a
16	POLR2A	chr11:67804142-67806889	GM12892	blood:	n/a	n/a
17	POLR2A	chr11:67804126-67807123	GM12878	blood:	n/a	n/a
18	FOSL1	chr11:67805534-67806035	K562	blood:	n/a	chr11:67805614-67805622
19	SMC3	chr11:67805559-67805920	HepG2	liver:	n/a	n/a
20	NFIC	chr11:67805511-67806058	HepG2	liver:	n/a	n/a
21	POLR2A	chr11:67805432-67806023	HepG2	liver:	n/a	n/a
22	TAF1	chr11:67805528-67806703	HepG2	liver:	n/a	n/a
23	CEBPD	chr11:67805455-67806690	HepG2	liver:	n/a	n/a
24	POLR2A	chr11:67805432-67806880	GM12878	blood:	n/a	n/a
25	FOXA1	chr11:67805547-67806128	HepG2	liver:	n/a	n/a
26	POLR2A	chr11:67805393-67805812	HCT-116	colon:	n/a	n/a
27	POLR2A	chr11:67804959-67805686	HUVEC	blood vessel:	n/a	n/a
28	POLR2A	chr11:67804335-67807010	U87	brain:	n/a	n/a
29	POLR2A	chr11:67804010-67806704	HepG2	liver:	n/a	n/a
30	POLR2A	chr11:67804218-67806047	HCT-116	colon:	n/a	n/a
31	POLR2A	chr11:67804150-67807001	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr11:67804941-67806745	HepG2	liver:	n/a	n/a
33	TCF12	chr11:67805504-67807229	A549	lung:	n/a	chr11:67805897-67805904 chr11:67807204-67807212 chr11:67805928-67805938
34	MXI1	chr11:67805483-67806715	HepG2	liver:	n/a	n/a
35	JUND	chr11:67804829-67805851	A549	lung:	n/a	chr11:67805614-67805622
36	POLR2A	chr11:67803451-67807095	PANC-1	pancreas:	n/a	n/a
37	GATA3	chr11:67804453-67806034	A549	lung:	n/a	chr11:67804664-67804674
38	RXRA	chr11:67805475-67806147	HepG2	liver:	n/a	n/a
39	HNF4G	chr11:67805473-67806093	HepG2	liver:	n/a	chr11:67805976-67805984 chr11:67805901-67805913 chr11:67805900-67805913 chr11:67805754-67805767 chr11:67805901-67805913 chr11:67805754-67805766 chr11:67805901-67805913 chr11:67805901-67805913
40	POLR2A	chr11:67805427-67806750	HepG2	liver:	n/a	n/a
41	POLR2A	chr11:67802860-67805955	K562	blood:	n/a	n/a
42	POLR2A	chr11:67805501-67808649	HL-60	blood:	n/a	n/a
43	MYBL2	chr11:67805333-67806895	HepG2	liver:	n/a	n/a
44	BCL3	chr11:67804432-67806447	A549	lung:	n/a	chr11:67805867-67805880 chr11:67805657-67805670 chr11:67804665-67804674 chr11:67806423-67806436 chr11:67804697-67804706
45	ARID3A	chr11:67805561-67806005	HepG2	liver:	n/a	n/a
46	POLR2A	chr11:67804085-67805943	U87	brain:	n/a	n/a
47	POLR2A	chr11:67805411-67806824	HUVEC	blood vessel:	n/a	n/a
48	MTA3	chr11:67804296-67808730	GM12878	blood:	n/a	n/a
49	POLR2A	chr11:67803556-67806713	Hela-S3	cervix:	n/a	n/a
50	HCFC1	chr11:67805278-67807291	Hela-S3	cervix:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:67770583..67773138-chr11:67804309..67805810,2	K562	blood:
2	chr11:67805173..67809189-chr11:67886289..67889765,4	K562	blood:
3	chr11:67803641..67806455-chr11:67892940..67895598,3	MCF-7	breast:
4	chr1:115323245..115324929-chr11:67804198..67805795,2	MCF-7	breast:
5	chr11:67803003..67807692-chr11:67979461..67982180,5	MCF-7	breast:
6	chr11:67804584..67806148-chr11:67919212..67921767,2	MCF-7	breast:
7	chr11:67770218..67773172-chr11:67805064..67808057,3	K562	blood:
8	chr11:67785578..67786397-chr11:67805432..67806299,2	MCF-7	breast:
9	chr11:67803608..67807840-chr11:67979633..67982182,3	K562	blood:
10	chr11:67805532..67808187-chr11:67887312..67890096,4	MCF-7	breast:
11	chr11:67805173..67807792-chr11:67887405..67889765,3	K562	blood:
12	chr11:67776070..67778120-chr11:67803675..67805660,2	K562	blood:
13	chr11:67791829..67792701-chr11:67805432..67806435,3	MCF-7	breast:
14	chr11:67785486..67786541-chr11:67805426..67806312,6	MCF-7	breast:
15	chr11:67785486..67786448-chr11:67805426..67806286,4	MCF-7	breast:

Variant related genes	Relation type
TCIRG1	TF binding region
ENSG00000110057	Chromatin interaction
ENSG00000255236	Chromatin interaction
ENSG00000110721	Chromatin interaction
ENSG00000006534	Chromatin interaction
ENSG00000110066	Chromatin interaction
ENSG00000052723	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs11228127	0.82[ASN][1000 genomes]
rs11481	0.83[ASN][1000 genomes]
rs2075609	0.81[ASN][1000 genomes]
rs4147780	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs884826	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:37 , 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	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	nsv555279	chr11:67789553-67816936	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
27	nsv897848	chr11:67789837-67816936	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
28	nsv897849	chr11:67789837-67821036	Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
29	nsv555280	chr11:67793014-67816936	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
30	nsv897851	chr11:67793448-67821036	Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
31	nsv897852	chr11:67795066-67833543	Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
32	nsv555281	chr11:67796691-67821036	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
33	nsv555282	chr11:67798567-67818325	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
34	nsv555283	chr11:67804074-67816936	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	10 gene(s)	inside rSNPs	diseases
35	nsv897853	chr11:67804074-67817876	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
36	nsv897854	chr11:67805476-67818325	Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
37	nsv897855	chr11:67805563-67842369	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67799000-67806000	Weak transcription	Fetal Kidney	kidney
2	chr11:67799200-67805800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:67799200-67806200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr11:67799800-67806000	Weak transcription	Fetal Brain Male	brain
5	chr11:67799800-67806400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:67801600-67806000	Weak transcription	Aorta	Aorta
7	chr11:67802000-67805600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:67802000-67805600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr11:67802000-67805600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr11:67802000-67805600	Weak transcription	Brain Angular Gyrus	brain
11	chr11:67802000-67805600	Weak transcription	HSMM	muscle
12	chr11:67802000-67805600	Weak transcription	NHDF-Ad	bronchial
13	chr11:67802000-67805800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr11:67802000-67806000	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr11:67802000-67807400	Weak transcription	Dnd41	blood
16	chr11:67802200-67805600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr11:67802200-67805600	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr11:67802200-67805800	Weak transcription	Primary T cells from cord blood	blood
19	chr11:67802200-67805800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr11:67802200-67805800	Weak transcription	HMEC	breast
21	chr11:67802600-67805800	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr11:67803000-67805800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr11:67803000-67806000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr11:67803200-67805800	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr11:67803200-67805800	Weak transcription	Fetal Brain Female	brain
26	chr11:67803200-67806000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr11:67803400-67805600	Weak transcription	Fetal Lung	lung
28	chr11:67803400-67806000	Enhancers	Primary T cells fromperipheralblood	blood
29	chr11:67803400-67806200	Enhancers	Primary hematopoietic stem cells	blood
30	chr11:67803600-67805600	Enhancers	Adipose Nuclei	Adipose
31	chr11:67803600-67805800	Enhancers	Right Ventricle	heart
32	chr11:67803600-67805800	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr11:67803600-67806000	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr11:67803600-67806000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
35	chr11:67803600-67806000	Enhancers	Left Ventricle	heart
36	chr11:67803600-67806200	Enhancers	Primary B cells from cord blood	blood
37	chr11:67803600-67806200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr11:67803600-67806400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
39	chr11:67803600-67806400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr11:67803800-67805800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr11:67803800-67805800	Enhancers	Colonic Mucosa	Colon
42	chr11:67803800-67805800	Enhancers	Lung	lung
43	chr11:67803800-67806000	Enhancers	Primary B cells from peripheral blood	blood
44	chr11:67803800-67806000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr11:67803800-67806000	Enhancers	Spleen	Spleen
46	chr11:67803800-67806200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr11:67804000-67806000	Enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr11:67804000-67806000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
49	chr11:67804000-67806000	Enhancers	Fetal Thymus	thymus
50	chr11:67804000-67806000	Enhancers	Right Atrium	heart

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