Variant report

Variant	nsv1052156
Chromosome Location	chr11:6003428-6107778
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	CBX3	chr11:6097747-6098010	K562	blood:	n/a	n/a
4	CBX3	chr11:6097757-6098009	K562	blood:	n/a	n/a
5	CEBPB	chr11:6033323-6033607	HepG2	liver:	n/a	chr11:6033456-6033467
6	CEBPB	chr11:6063225-6063240	K562	blood:	n/a	n/a
7	CEBPB	chr11:6017836-6017846	A549	lung:	n/a	n/a
8	CEBPB	chr11:6076851-6077255	HepG2	liver:	n/a	chr11:6076938-6076951 chr11:6077005-6077016
9	CEBPB	chr11:6044337-6044593	HepG2	liver:	n/a	n/a
10	CEBPB	chr11:6033395-6033567	K562	blood:	n/a	chr11:6033456-6033467
11	CEBPB	chr11:6076861-6077195	IMR90	lung:	n/a	chr11:6076938-6076951 chr11:6077005-6077016
12	CEBPB	chr11:6063192-6063391	HepG2	liver:	n/a	chr11:6063231-6063242
13	CEBPB	chr11:6033365-6033570	A549	lung:	n/a	chr11:6033456-6033467
14	CEBPB	chr11:6076913-6077239	H1-hESC	embryonic stem cell:	n/a	chr11:6076938-6076951 chr11:6077005-6077016
15	CEBPB	chr11:6076869-6077315	A549	lung:	n/a	chr11:6076938-6076951 chr11:6077005-6077016
16	CEBPB	chr11:6084882-6084898	A549	lung:	n/a	n/a
17	CEBPB	chr11:6044250-6044569	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr11:6044265-6044551	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr11:6088579-6088770	HepG2	liver:	n/a	chr11:6088617-6088628
20	CEBPB	chr11:6061447-6061492	A549	lung:	n/a	chr11:6061465-6061476 chr11:6061476-6061487
21	CEBPB	chr11:6028331-6028529	HepG2	liver:	n/a	chr11:6028446-6028457
22	CEBPB	chr11:6061408-6061572	HepG2	liver:	n/a	chr11:6061465-6061476 chr11:6061476-6061487
23	CEBPB	chr11:6076871-6077114	K562	blood:	n/a	chr11:6076938-6076951 chr11:6077005-6077016
24	CEBPB	chr11:6097859-6098067	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr11:6083960-6084110	GM12870	blood:	n/a	chr11:6084098-6084107 chr11:6084100-6084110
26	CTCF	chr11:6044240-6044390	A549	lung:	n/a	n/a
27	CTCF	chr11:6044260-6044410	HRE	kidney:	n/a	n/a
28	CTCF	chr11:6013980-6014130	Caco-2	colon:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
29	CTCF	chr11:6044280-6044430	NHDF-neo	bronchial:	n/a	chr11:6044390-6044411
30	CTCF	chr11:6051075-6051115	Pancreas_OC	pancreas:	n/a	n/a
31	CTCF	chr11:6083980-6084130	GM12872	blood:	n/a	chr11:6084095-6084113 chr11:6084098-6084107 chr11:6084100-6084110 chr11:6084096-6084112
32	CTCF	chr11:6013930-6014159	MCF-7	breast:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
33	CTCF	chr11:6004823-6004921	K562	blood:	n/a	n/a
34	CTCF	chr11:6013831-6014186	A549	lung:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
35	CTCF	chr11:6084004-6084191	GM12878	blood:	n/a	chr11:6084095-6084113 chr11:6084098-6084107 chr11:6084100-6084110 chr11:6084096-6084112
36	CTCF	chr11:6044199-6044584	H1-hESC	embryonic stem cell:	n/a	chr11:6044390-6044411
37	CTCF	chr11:6014000-6014150	BJ	skin:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
38	CTCF	chr11:6044340-6044490	GM12878	blood:	n/a	chr11:6044390-6044411
39	CTCF	chr11:6004800-6004950	GM12873	blood:	n/a	n/a
40	CTCF	chr11:6084088-6084182	Fibrobl	skin:	n/a	chr11:6084095-6084113 chr11:6084098-6084107 chr11:6084100-6084110 chr11:6084096-6084112
41	CTCF	chr11:6084056-6084161	GM13977	blood:	n/a	chr11:6084095-6084113 chr11:6084098-6084107 chr11:6084100-6084110 chr11:6084096-6084112
42	CTCF	chr11:6013940-6014090	HCT-116	colon:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
43	CTCF	chr11:6044320-6044470	K562	blood:	n/a	chr11:6044390-6044411
44	CTCF	chr11:6044257-6044536	Gliobla	brain:	n/a	chr11:6044390-6044411
45	CTCF	chr11:6013993-6014116	GM13976	blood:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
46	CTCF	chr11:6013940-6014090	SK-N-SH_RA	brain:	n/a	chr11:6014044-6014065 chr11:6014046-6014053 chr11:6014045-6014058 chr11:6014043-6014059 chr11:6014042-6014060
47	CTCF	chr11:6044320-6044470	HCT-116	colon:	n/a	chr11:6044390-6044411
48	CTCF	chr11:6099485-6099627	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr11:6044320-6044470	HPF	lung:	n/a	chr11:6044390-6044411
50	CTCF	chr11:6004820-6004970	AoAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:6025553-6025603	HUVEC	blood vessel:	n/a
2	chr11:6024966-6025016	HIPEpiC	eye:	n/a
3	chr11:6049729-6049779	Caco-2	colon:	n/a
4	chr11:6024754-6024804	BE2_C	brain:	n/a
5	chr11:6024266-6024316	A549	lung:	n/a
6	chr11:6008246-6008296	CMK	blood:	n/a
7	chr11:6024754-6024804	AoSMC	blood vessel:	n/a
8	chr11:6047917-6047967	Hela-S3	cervix:	n/a
9	chr11:6024966-6025016	SAEC	small airway:	n/a
10	chr11:6007128-6007178	HMEC	breast:	n/a
11	chr11:6007128-6007178	GM12891	blood:	n/a
12	chr11:6024966-6025016	BJ	skin:	n/a
13	chr11:6047917-6047967	U87	brain:	n/a
14	chr11:6007249-6007299	HRPEpiC	eye:	n/a
15	chr11:6024754-6024804	SK-N-SH	brain:	n/a
16	chr11:6007249-6007299	RPTEC	kidney:	n/a
17	chr11:6008246-6008296	HRE	kidney:	n/a
18	chr11:6007128-6007178	HRCEpiC	kidney:	n/a
19	chr11:6007128-6007178	NH-A	brain:	n/a
20	chr11:6025553-6025603	GM12892	blood:	n/a
21	chr11:6008246-6008296	NHBE	bronchial:	n/a
22	chr11:6007128-6007178	AG10803	skin:	n/a
23	chr11:6024266-6024316	Hepatocyte	liver:	n/a
24	chr11:6024266-6024316	HCM	heart:	n/a
25	chr11:6024966-6025016	AG04450	lung:	fetal
26	chr11:6024966-6025016	GM06990	blood:	n/a
27	chr11:6047917-6047967	HRCEpiC	kidney:	n/a
28	chr11:6049729-6049779	MCF-7	breast:	n/a
29	chr11:6007249-6007299	AG09309	skin:	n/a
30	chr11:6024966-6025016	HCM	heart:	n/a
31	chr11:6024754-6024804	A549	lung:	n/a
32	chr11:6048685-6048735	Hela-S3	cervix:	n/a
33	chr11:6024266-6024316	GM12878	blood:	n/a
34	chr11:6049729-6049779	NHBE	bronchial:	n/a
35	chr11:6048685-6048735	HL-60	blood:	n/a
36	chr11:6024754-6024804	AG09309	skin:	n/a
37	chr11:6024754-6024804	BJ	skin:	n/a
38	chr11:6047917-6047967	HRE	kidney:	n/a
39	chr11:6007249-6007299	HCPEpiC	choroid plexus:	n/a
40	chr11:6008246-6008296	AG04450	lung:	fetal
41	chr11:6048685-6048735	HRPEpiC	eye:	n/a
42	chr11:6049729-6049779	SK-N-MC	brain:	n/a
43	chr11:6024266-6024316	HMEC	breast:	n/a
44	chr11:6024266-6024316	T-47D	breast:	n/a
45	chr11:6049729-6049779	Hela-S3	cervix:	n/a
46	chr11:6007249-6007299	U87	brain:	n/a
47	chr11:6048685-6048735	K562	blood:	n/a
48	chr11:6048685-6048735	AoSMC	blood vessel:	n/a
49	chr11:6024266-6024316	HCT-116	colon:	n/a
50	chr11:6049729-6049779	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:6066450..6068610-chr11:6073886..6076316,2	K562	blood:
2	chr11:6043910..6044862-chr11:6319531..6320460,4	MCF-7	breast:
3	chr11:6043916..6044925-chr11:6374369..6375324,6	K562	blood:
4	chr11:6044164..6044871-chr11:6383964..6384538,2	MCF-7	breast:
5	chr11:6076616..6078585-chr11:6085137..6086663,2	K562	blood:
6	chr11:6004815..6007784-chr11:6008495..6010982,2	K562	blood:
7	chr11:6053200..6056022-chr11:6059517..6061036,2	K562	blood:
8	chr11:6043976..6044671-chr11:6319784..6320496,2	MCF-7	breast:
9	chr11:6044002..6044856-chr11:6336753..6337323,5	K562	blood:
10	chr11:6076616..6078585-chr11:6085137..6086663,2	K562	blood:
11	chr11:6024226..6025750-chr11:6027975..6030359,2	K562	blood:
12	chr11:4756725..4758910-chr11:6017875..6020369,2	K562	blood:
13	chr11:6018411..6021348-chr11:6022621..6024806,3	K562	blood:
14	chr11:6043946..6044830-chr11:6374351..6375089,3	MCF-7	breast:
15	chr11:6019848..6022456-chr11:6022621..6025038,2	K562	blood:
16	chr11:6053200..6056022-chr11:6059517..6061036,2	K562	blood:
17	chr11:6044103..6044910-chr11:6290904..6291724,2	K562	blood:
18	chr11:6004815..6007784-chr11:6008495..6010982,2	K562	blood:

Variant related genes	Relation type
OR56A7P	TF binding region
OR52X1P	TF binding region
OR56A1	TF binding region
OR52L2P	TF binding region
OR52L1	TF binding region
RNA5SP329	TF binding region
OR56A4	TF binding region
KRT18P58	TF binding region
OR56A7P	CpG island
OR52X1P	CpG island
OR56A1	CpG island
OR52L2P	CpG island
OR52L1	CpG island
RNA5SP329	CpG island
OR56A4	CpG island
KRT18P58	CpG island
ENSG00000255481	chromatin interactions
ENSG00000272559	chromatin interactions
ENSG00000254443	chromatin interactions
ENSG00000270435	chromatin interactions
ENSG00000183389	chromatin interactions

Extended variants
information (count: 2400 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2400 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528166600	chr11:6003476-6003477	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs541769114	chr11:6003482-6003483	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs568038674	chr11:6003511-6003512	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs10839170	chr11:6003512-6003513	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs550608937	chr11:6003515-6003516	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs140591461	chr11:6003531-6003532	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs537751973	chr11:6003543-6003544	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs4385881	chr11:6003549-6003550	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs564923676	chr11:6003596-6003597	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs577406135	chr11:6003598-6003599	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs536814780	chr11:6008246-6008247	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs370783232	chr11:6008263-6008264	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs576851641	chr11:6008774-6008775	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs192758322	chr11:6008797-6008798	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs535110771	chr11:6008819-6008820	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs184897118	chr11:6010284-6010285	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs563605247	chr11:6010289-6010290	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs574521284	chr11:6010302-6010303	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs541744271	chr11:6010307-6010308	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs138073977	chr11:6010321-6010322	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs35541041	chr11:6010338-6010339	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs190393754	chr11:6010414-6010415	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs546114676	chr11:6010438-6010439	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs181667747	chr11:6010444-6010445	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs116119719	chr11:6010454-6010455	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs111930657	chr11:6010484-6010485	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs142444876	chr11:6010499-6010500	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs528915978	chr11:6010516-6010517	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs550318570	chr11:6010593-6010594	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs545304120	chr11:6010644-6010645	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs143856977	chr11:6010646-6010647	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs34091641	chr11:6010647-6010648	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs139717846	chr11:6010651-6010652	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs397785362	chr11:6010654-6010655	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs199979819	chr11:6010655-6010656	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs200748178	chr11:6010656-6010657	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs202227234	chr11:6010659-6010660	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs4758320	chr11:6010679-6010680	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs376203445	chr11:6010701-6010702	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs10769544	chr11:6010718-6010719	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs35730497	chr11:6010760-6010761	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs139438492	chr11:6010802-6010803	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs186663508	chr11:6010818-6010819	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs35484966	chr11:6013069-6013070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553362505	chr11:6013079-6013080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573194098	chr11:6013087-6013088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs540618791	chr11:6013127-6013128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562289165	chr11:6013131-6013132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs548673489	chr11:6013141-6013142	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs117264936	chr11:6013182-6013183	Enhancers	TF binding region	1 gene(s)	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:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:6003200-6003600	ZNF genes & repeats	Pancreas	Pancrea
2	chr11:6013000-6013800	Enhancers	Adipose Nuclei	Adipose
3	chr11:6013000-6014000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr11:6013000-6014400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr11:6022800-6024000	Enhancers	Left Ventricle	heart
6	chr11:6029000-6029200	Enhancers	Left Ventricle	heart
7	chr11:6029400-6031600	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr11:6030400-6030600	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr11:6030400-6030600	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr11:6030600-6032800	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr11:6031600-6032800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr11:6032800-6034400	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr11:6032800-6034600	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
14	chr11:6032800-6034600	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr11:6034000-6034600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr11:6034200-6034600	Enhancers	Pancreas	Pancrea
17	chr11:6034600-6036400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr11:6034600-6036400	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr11:6035400-6035800	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr11:6036200-6037000	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr11:6036400-6036800	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr11:6036400-6037000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr11:6043400-6044800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr11:6044000-6044200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
25	chr11:6044200-6045000	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr11:6044400-6044600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
27	chr11:6044400-6044800	Enhancers	Fetal Heart	heart
28	chr11:6044800-6045600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr11:6048600-6049400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr11:6051600-6052000	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr11:6051600-6052000	Enhancers	Fetal Brain Male	brain
32	chr11:6060600-6060800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
33	chr11:6060800-6061000	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr11:6061000-6061400	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr11:6061000-6061400	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr11:6061000-6062200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr11:6061200-6062000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr11:6061400-6061800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
39	chr11:6061400-6061800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
40	chr11:6061600-6061800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
41	chr11:6061600-6062200	Active TSS	Primary B cells from cord blood	blood
42	chr11:6061800-6062000	Active TSS	Primary monocytes fromperipheralblood	blood
43	chr11:6061800-6062000	Active TSS	Primary neutrophils fromperipheralblood	blood
44	chr11:6061800-6062000	Enhancers	Adipose Nuclei	Adipose
45	chr11:6062000-6062200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
46	chr11:6062000-6062200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
47	chr11:6062000-6062400	Flanking Active TSS	Adipose Nuclei	Adipose
48	chr11:6062000-6062400	Enhancers	HUVEC	blood vessel
49	chr11:6062200-6062600	Active TSS	Primary neutrophils fromperipheralblood	blood
50	chr11:6062200-6063000	Active TSS	Primary monocytes fromperipheralblood	blood

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