Variant report

Variant	esv3405961
Chromosome Location	chr11:5991563-6069562
allele	n/a
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	BHLHE40	chr11:6044351-6044384	GM12878	blood:	n/a	n/a
2	BHLHE40	chr11:6013984-6014056	GM12878	blood:	n/a	n/a
3	CEBPB	chr11:6061408-6061572	HepG2	liver:	n/a	chr11:6061465-6061476 chr11:6061476-6061487
4	CEBPB	chr11:6044265-6044551	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr11:6044250-6044569	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr11:6028331-6028529	HepG2	liver:	n/a	chr11:6028446-6028457
7	CEBPB	chr11:6061447-6061492	A549	lung:	n/a	chr11:6061465-6061476 chr11:6061476-6061487
8	CEBPB	chr11:6044337-6044593	HepG2	liver:	n/a	n/a
9	CEBPB	chr11:6033365-6033570	A549	lung:	n/a	chr11:6033456-6033467
10	CEBPB	chr11:6063192-6063391	HepG2	liver:	n/a	chr11:6063231-6063242
11	CEBPB	chr11:6063225-6063240	K562	blood:	n/a	n/a
12	CEBPB	chr11:6033323-6033607	HepG2	liver:	n/a	chr11:6033456-6033467
13	CEBPB	chr11:6033395-6033567	K562	blood:	n/a	chr11:6033456-6033467
14	CEBPB	chr11:6017836-6017846	A549	lung:	n/a	n/a
15	CTCF	chr11:6044320-6044470	Hela-S3	cervix:	n/a	chr11:6044390-6044411
16	CTCF	chr11:6044300-6044450	AG10803	skin:	n/a	chr11:6044390-6044411
17	CTCF	chr11:6044280-6044430	HA-sp	spinal cord:	n/a	chr11:6044390-6044411
18	CTCF	chr11:6044291-6044476	Medullo	brain:	n/a	chr11:6044390-6044411
19	CTCF	chr11:6004746-6004923	K562	blood:	n/a	n/a
20	CTCF	chr11:6013940-6014090	GM12866	blood:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
21	CTCF	chr11:6013906-6014112	GM19238	blood:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
22	CTCF	chr11:6013920-6014070	AG04450	lung:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
23	CTCF	chr11:6044300-6044450	GM12871	blood:	n/a	chr11:6044390-6044411
24	CTCF	chr11:6013980-6014130	AG09319	gingival:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
25	CTCF	chr11:6044340-6044490	AG09309	skin:	n/a	chr11:6044390-6044411
26	CTCF	chr11:6013920-6014070	NHEK	skin:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
27	CTCF	chr11:6013960-6014110	AG10803	skin:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
28	CTCF	chr11:6004820-6004970	NHEK	skin:	n/a	n/a
29	CTCF	chr11:6004840-6004990	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr11:6044179-6044539	K562	blood:	n/a	chr11:6044390-6044411
31	CTCF	chr11:6013980-6014130	Caco-2	colon:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
32	CTCF	chr11:6004880-6005030	NHEK	skin:	n/a	n/a
33	CTCF	chr11:6015523-6015558	ProgFib	skin:	n/a	n/a
34	CTCF	chr11:6004820-6004970	GM12869	blood:	n/a	n/a
35	CTCF	chr11:6044320-6044470	GM12864	blood:	n/a	chr11:6044390-6044411
36	CTCF	chr11:6044260-6044410	GM12864	blood:	n/a	n/a
37	CTCF	chr11:6044277-6044506	MCF-7	breast:	n/a	chr11:6044390-6044411
38	CTCF	chr11:6051075-6051115	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr11:6013980-6014130	HCM	heart:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
40	CTCF	chr11:6044280-6044430	HCM	heart:	n/a	chr11:6044390-6044411
41	CTCF	chr11:6013940-6014090	A549	lung:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
42	CTCF	chr11:6013846-6014229	GM12878	blood:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
43	CTCF	chr11:6013917-6014209	K562	blood:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
44	CTCF	chr11:6014080-6014230	BE2_C	brain:	n/a	n/a
45	CTCF	chr11:6013400-6013550	GM12872	blood:	n/a	n/a
46	CTCF	chr11:6013980-6014130	HMEC	breast:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
47	CTCF	chr11:6044240-6044390	A549	lung:	n/a	n/a
48	CTCF	chr11:6013980-6014130	GM12868	blood:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
49	CTCF	chr11:6044320-6044470	AG09319	gingival:	n/a	chr11:6044390-6044411
50	CTCF	chr11:6044000-6044150	AoAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:6007899-6007949	A549	lung:	n/a
2	chr11:6048685-6048735	HEEpiC	esophagus:	n/a
3	chr11:6024266-6024316	SK-N-SH	brain:	n/a
4	chr11:6008246-6008296	NB4	blood:	n/a
5	chr11:6008246-6008296	GM06990	blood:	n/a
6	chr11:6048685-6048735	HCPEpiC	choroid plexus:	n/a
7	chr11:6025553-6025603	Jurkat	blood:	n/a
8	chr11:6024966-6025016	Caco-2	colon:	n/a
9	chr11:6025553-6025603	GM19239	blood:	n/a
10	chr11:6025553-6025603	PrEC	prostate:	n/a
11	chr11:6048685-6048735	SK-N-SH_RA	brain:	n/a
12	chr11:6007899-6007949	NHDF-neo	bronchial:	n/a
13	chr11:6008246-6008296	PrEC	prostate:	n/a
14	chr11:6025553-6025603	IMR90	lung:	fetal
15	chr11:6048685-6048735	SKMC	muscle:	n/a
16	chr11:6047917-6047967	A549	lung:	n/a
17	chr11:6024754-6024804	AG09309	skin:	n/a
18	chr11:6007128-6007178	AG04450	lung:	fetal
19	chr11:6048685-6048735	H1-hESC	embryonic stem cell:	embryo
20	chr11:6007899-6007949	HPAEpiC	pulmonary alveolar:	n/a
21	chr11:6048685-6048735	AG09319	gingival:	n/a
22	chr11:6047917-6047967	NHDF-neo	bronchial:	n/a
23	chr11:6047917-6047967	NHBE	bronchial:	n/a
24	chr11:6008246-6008296	SKMC	muscle:	n/a
25	chr11:6024754-6024804	GM12891	blood:	n/a
26	chr11:6024966-6025016	Jurkat	blood:	n/a
27	chr11:6008246-6008296	AG09319	gingival:	n/a
28	chr11:6024754-6024804	HNPCEpiC	eye:	n/a
29	chr11:6008246-6008296	IMR90	lung:	fetal
30	chr11:6024754-6024804	ovcar-3	ovarian:	n/a
31	chr11:6049729-6049779	HCPEpiC	choroid plexus:	n/a
32	chr11:6008246-6008296	HepG2	liver:	n/a
33	chr11:6025553-6025603	GM06990	blood:	n/a
34	chr11:6024266-6024316	AG09309	skin:	n/a
35	chr11:6048685-6048735	HIPEpiC	eye:	n/a
36	chr11:6025553-6025603	HEK293	kidney:	embryo
37	chr11:6007249-6007299	SK-N-SH_RA	brain:	n/a
38	chr11:6024754-6024804	HCPEpiC	choroid plexus:	n/a
39	chr11:6047917-6047967	NB4	blood:	n/a
40	chr11:6024966-6025016	HRPEpiC	eye:	n/a
41	chr11:6008246-6008296	GM12892	blood:	n/a
42	chr11:6049729-6049779	HCT-116	colon:	n/a
43	chr11:6007899-6007949	BE2_C	brain:	n/a
44	chr11:6025553-6025603	HRE	kidney:	n/a
45	chr11:6007249-6007299	K562	blood:	n/a
46	chr11:6008246-6008296	AG04450	lung:	fetal
47	chr11:6024966-6025016	LNCaP	prostate:	n/a
48	chr11:6024266-6024316	HCPEpiC	choroid plexus:	n/a
49	chr11:6008246-6008296	Jurkat	blood:	n/a
50	chr11:6007128-6007178	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:6053200..6056022-chr11:6059517..6061036,2	K562	blood:
2	chr11:6004815..6007784-chr11:6008495..6010982,2	K562	blood:
3	chr11:6044103..6044910-chr11:6290904..6291724,2	K562	blood:
4	chr11:6043976..6044671-chr11:6319784..6320496,2	MCF-7	breast:
5	chr11:6044002..6044856-chr11:6336753..6337323,5	K562	blood:
6	chr11:6044164..6044871-chr11:6383964..6384538,2	MCF-7	breast:
7	chr11:6019848..6022456-chr11:6022621..6025038,2	K562	blood:
8	chr11:4756725..4758910-chr11:6017875..6020369,2	K562	blood:
9	chr11:6053200..6056022-chr11:6059517..6061036,2	K562	blood:
10	chr11:6043910..6044862-chr11:6319531..6320460,4	MCF-7	breast:
11	chr11:6043916..6044925-chr11:6374369..6375324,6	K562	blood:
12	chr11:6043946..6044830-chr11:6374351..6375089,3	MCF-7	breast:
13	chr11:6018411..6021348-chr11:6022621..6024806,3	K562	blood:
14	chr11:6004815..6007784-chr11:6008495..6010982,2	K562	blood:
15	chr11:6024226..6025750-chr11:6027975..6030359,2	K562	blood:

Variant related genes	Relation type
ENSG00000188691	TF binding region
OR56A7P	TF binding region
OR56A1	TF binding region
OR52L1	TF binding region
RNA5SP329	TF binding region
OR56A4	TF binding region
KRT18P58	TF binding region
ENSG00000188691	CpG island
OR56A7P	CpG island
OR56A1	CpG island
OR52L1	CpG island
RNA5SP329	CpG island
OR56A4	CpG island
KRT18P58	CpG island
ENSG00000254443	chromatin interactions
ENSG00000270435	chromatin interactions
ENSG00000272559	chromatin interactions
ENSG00000183389	chromatin interactions

Extended variants
information (count: 1183 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1183 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147823757	chr11:5992204-5992205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs573883380	chr11:5992214-5992215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs4758290	chr11:5992215-5992216	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs562794271	chr11:5992277-5992278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575638115	chr11:5992279-5992280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539535467	chr11:5992338-5992339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs74053262	chr11:5992405-5992406	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs377618595	chr11:5992441-5992442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540300747	chr11:5992482-5992483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs562127398	chr11:5992511-5992512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573823611	chr11:5992524-5992525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544719720	chr11:5992535-5992536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562824709	chr11:5992544-5992545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544495028	chr11:5992576-5992577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs4237766	chr11:5992597-5992598	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs141379085	chr11:5992611-5992612	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs551481456	chr11:5992617-5992618	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs560325310	chr11:5992629-5992630	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs189730407	chr11:5992639-5992640	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs377509331	chr11:5992701-5992702	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs548674575	chr11:5992768-5992769	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs11040031	chr11:5992816-5992817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs180893423	chr11:5992817-5992818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs74792991	chr11:5992857-5992858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184912655	chr11:5992876-5992877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190895494	chr11:5992880-5992881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374286126	chr11:5992910-5992911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557812835	chr11:5992996-5992997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs77138277	chr11:5993000-5993001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs77309167	chr11:5993001-5993002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183436922	chr11:5993034-5993035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113668393	chr11:5993035-5993036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs12280826	chr11:5993088-5993089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76358417	chr11:5993089-5993090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560964709	chr11:5993119-5993120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs117831468	chr11:5993136-5993137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs149025898	chr11:5993145-5993146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs577898690	chr11:5993197-5993198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs545191924	chr11:5993204-5993205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560411276	chr11:5993246-5993247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs79760267	chr11:5993278-5993279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs138545560	chr11:5993317-5993318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560711758	chr11:5993334-5993335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs531382977	chr11:5993355-5993356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs72888819	chr11:5993361-5993362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569925502	chr11:5993392-5993393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569243757	chr11:5993430-5993431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs187338025	chr11:5993460-5993461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551529146	chr11:5993476-5993477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs567054320	chr11:5993502-5993503	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5992200-5996000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
2	chr11:5992600-5992800	Bivalent/Poised TSS	Brain Substantia Nigra	brain
3	chr11:6003200-6003600	ZNF genes & repeats	Pancreas	Pancrea
4	chr11:6013000-6013800	Enhancers	Adipose Nuclei	Adipose
5	chr11:6013000-6014000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:6013000-6014400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:6022800-6024000	Enhancers	Left Ventricle	heart
8	chr11:6029000-6029200	Enhancers	Left Ventricle	heart
9	chr11:6029400-6031600	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr11:6030400-6030600	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr11:6030400-6030600	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr11:6030600-6032800	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr11:6031600-6032800	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr11:6032800-6034400	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr11:6032800-6034600	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
16	chr11:6032800-6034600	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr11:6034000-6034600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr11:6034200-6034600	Enhancers	Pancreas	Pancrea
19	chr11:6034600-6036400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr11:6034600-6036400	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr11:6035400-6035800	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr11:6036200-6037000	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr11:6036400-6036800	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr11:6036400-6037000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr11:6043400-6044800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr11:6044000-6044200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
27	chr11:6044200-6045000	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr11:6044400-6044600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
29	chr11:6044400-6044800	Enhancers	Fetal Heart	heart
30	chr11:6044800-6045600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr11:6048600-6049400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr11:6051600-6052000	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr11:6051600-6052000	Enhancers	Fetal Brain Male	brain
34	chr11:6060600-6060800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
35	chr11:6060800-6061000	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr11:6061000-6061400	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr11:6061000-6061400	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr11:6061000-6062200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
39	chr11:6061200-6062000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr11:6061400-6061800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
41	chr11:6061400-6061800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
42	chr11:6061600-6061800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
43	chr11:6061600-6062200	Active TSS	Primary B cells from cord blood	blood
44	chr11:6061800-6062000	Active TSS	Primary monocytes fromperipheralblood	blood
45	chr11:6061800-6062000	Active TSS	Primary neutrophils fromperipheralblood	blood
46	chr11:6061800-6062000	Enhancers	Adipose Nuclei	Adipose
47	chr11:6062000-6062200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
48	chr11:6062000-6062200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
49	chr11:6062000-6062400	Flanking Active TSS	Adipose Nuclei	Adipose
50	chr11:6062000-6062400	Enhancers	HUVEC	blood vessel

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