Variant report

Variant	nsv896951
Chromosome Location	chr11:5773981-5832191
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:411)
CpG islands
(count:488)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:411 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:5831584-5831916	K562	blood:	n/a	n/a
2	ATF1	chr11:5831302-5831989	K562	blood:	n/a	n/a
3	BACH1	chr11:5829711-5830281	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr11:5829596-5830093	GM12878	blood:	n/a	n/a
5	BHLHE40	chr11:5830544-5830763	GM12878	blood:	n/a	n/a
6	BRCA1	chr11:5829767-5829891	HepG2	liver:	n/a	n/a
7	CBX3	chr11:5825288-5825535	K562	blood:	n/a	n/a
8	CBX3	chr11:5825224-5825619	K562	blood:	n/a	n/a
9	CBX3	chr11:5831651-5832009	K562	blood:	n/a	n/a
10	CBX3	chr11:5831070-5832111	K562	blood:	n/a	n/a
11	CCNT2	chr11:5831446-5832015	K562	blood:	n/a	n/a
12	CEBPB	chr11:5775147-5775155	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr11:5818464-5818701	HepG2	liver:	n/a	chr11:5818599-5818608 chr11:5818599-5818608 chr11:5818598-5818609 chr11:5818599-5818608 chr11:5818597-5818608 chr11:5818599-5818608
14	CEBPB	chr11:5788246-5788520	HepG2	liver:	n/a	n/a
15	CEBPB	chr11:5789130-5789308	HepG2	liver:	n/a	chr11:5789200-5789211
16	CEBPB	chr11:5789182-5789250	A549	lung:	n/a	chr11:5789200-5789211
17	CEBPB	chr11:5788174-5788674	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr11:5818545-5818706	A549	lung:	n/a	chr11:5818599-5818608 chr11:5818599-5818608 chr11:5818598-5818609 chr11:5818599-5818608 chr11:5818597-5818608 chr11:5818599-5818608
19	CHD2	chr11:5831707-5832014	K562	blood:	n/a	n/a
20	CREB1	chr11:5829862-5830357	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr11:5829661-5830342	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr11:5828760-5828910	GM06990	blood:	n/a	n/a
23	CTCF	chr11:5829780-5829930	HVMF	connective:	n/a	n/a
24	CTCF	chr11:5829657-5830076	T-47D	breast:	n/a	n/a
25	CTCF	chr11:5829780-5829930	HPF	lung:	n/a	n/a
26	CTCF	chr11:5829780-5829930	GM12874	blood:	n/a	n/a
27	CTCF	chr11:5829820-5829970	WI-38	lung:	n/a	n/a
28	CTCF	chr11:5829780-5829930	HEK293	kidney:	n/a	n/a
29	CTCF	chr11:5829645-5829982	A549	lung:	n/a	n/a
30	CTCF	chr11:5829820-5829970	AG04450	lung:	n/a	n/a
31	CTCF	chr11:5829800-5829950	NB4	blood:	n/a	n/a
32	CTCF	chr11:5828866-5829184	HepG2	liver:	n/a	n/a
33	CTCF	chr11:5828874-5829135	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr11:5828940-5829090	HepG2	liver:	n/a	n/a
35	CTCF	chr11:5829780-5829930	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr11:5829613-5830068	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr11:5829800-5829950	HepG2	liver:	n/a	n/a
38	CTCF	chr11:5829740-5829890	BJ	skin:	n/a	n/a
39	CTCF	chr11:5829740-5829890	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr11:5829712-5830003	MCF-7	breast:	n/a	n/a
41	CTCF	chr11:5829695-5830001	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr11:5829800-5829950	RPTEC	kidney:	n/a	n/a
43	CTCF	chr11:5829800-5829950	GM12873	blood:	n/a	n/a
44	CTCF	chr11:5829820-5829970	HCT-116	colon:	n/a	n/a
45	CTCF	chr11:5828860-5829010	HepG2	liver:	n/a	n/a
46	CTCF	chr11:5829717-5830036	Fibrobl	skin:	n/a	n/a
47	CTCF	chr11:5829800-5829950	GM12874	blood:	n/a	n/a
48	CTCF	chr11:5829760-5829910	MCF-7	breast:	n/a	n/a
49	CTCF	chr11:5829760-5829910	HRE	kidney:	n/a	n/a
50	CTCF	chr11:5829780-5829930	BE2_C	brain:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:5830162-5830212	HEK293	kidney:	embryo
2	chr11:5800287-5800337	BJ	skin:	n/a
3	chr11:5811184-5811234	GM12878	blood:	n/a
4	chr11:5809911-5809961	HPAEpiC	pulmonary alveolar:	n/a
5	chr11:5801244-5801294	HCF	heart:	n/a
6	chr11:5800287-5800337	AG09309	skin:	n/a
7	chr11:5811184-5811234	NH-A	brain:	n/a
8	chr11:5809911-5809961	ECC-1	luminal epithelium:	n/a
9	chr11:5800287-5800337	A549	lung:	n/a
10	chr11:5830119-5830169	HIPEpiC	eye:	n/a
11	chr11:5801244-5801294	AG09319	gingival:	n/a
12	chr11:5830119-5830169	HCF	heart:	n/a
13	chr11:5800287-5800337	ovcar-3	ovarian:	n/a
14	chr11:5799446-5799496	SK-N-SH	brain:	n/a
15	chr11:5830030-5830080	HRE	kidney:	n/a
16	chr11:5830030-5830080	PANC-1	pancreas:	n/a
17	chr11:5799446-5799496	HNPCEpiC	eye:	n/a
18	chr11:5811184-5811234	HepG2	liver:	n/a
19	chr11:5830119-5830169	Hepatocyte	liver:	n/a
20	chr11:5830030-5830080	HMEC	breast:	n/a
21	chr11:5811184-5811234	K562	blood:	n/a
22	chr11:5830162-5830212	GM19239	blood:	n/a
23	chr11:5830119-5830169	PrEC	prostate:	n/a
24	chr11:5799446-5799496	Jurkat	blood:	n/a
25	chr11:5811184-5811234	U87	brain:	n/a
26	chr11:5800287-5800337	RPTEC	kidney:	n/a
27	chr11:5830030-5830080	GM12891	blood:	n/a
28	chr11:5830030-5830080	SK-N-SH_RA	brain:	n/a
29	chr11:5801244-5801294	HEK293	kidney:	embryo
30	chr11:5830119-5830169	HL-60	blood:	n/a
31	chr11:5830162-5830212	SKMC	muscle:	n/a
32	chr11:5830119-5830169	ECC-1	luminal epithelium:	n/a
33	chr11:5799446-5799496	PANC-1	pancreas:	n/a
34	chr11:5830030-5830080	Jurkat	blood:	n/a
35	chr11:5811184-5811234	IMR90	lung:	fetal
36	chr11:5801244-5801294	U87	brain:	n/a
37	chr11:5830162-5830212	K562	blood:	n/a
38	chr11:5799446-5799496	Caco-2	colon:	n/a
39	chr11:5830162-5830212	HEEpiC	esophagus:	n/a
40	chr11:5801244-5801294	K562	blood:	n/a
41	chr11:5830030-5830080	NH-A	brain:	n/a
42	chr11:5811184-5811234	HL-60	blood:	n/a
43	chr11:5830030-5830080	A549	lung:	n/a
44	chr11:5830030-5830080	HCM	heart:	n/a
45	chr11:5801244-5801294	NB4	blood:	n/a
46	chr11:5809911-5809961	RPTEC	kidney:	n/a
47	chr11:5830162-5830212	LNCaP	prostate:	n/a
48	chr11:5830162-5830212	AG04449	skin:	fetal
49	chr11:5811184-5811234	HRE	kidney:	n/a
50	chr11:5830030-5830080	AG04449	skin:	fetal

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	11:5076469-5081549..11:5767550-5775401	K562	blood:
2	chr11:5823269..5825988-chr11:5829238..5831177,2	K562	blood:
3	chr11:5831234..5833906-chr11:5837299..5840310,3	K562	blood:
4	chr11:5831415..5833368-chr11:5835410..5837074,2	K562	blood:
5	chr11:5811775..5813823-chr11:5815438..5817025,2	K562	blood:
6	chr11:5830212..5830820-chr3:156846082..156846678,2	HCT-116	colon:
7	chr11:5823269..5825988-chr11:5829238..5831177,2	K562	blood:
8	chr11:5811775..5813823-chr11:5815438..5817025,2	K562	blood:
9	chr11:5621238..5622269-chr11:5829297..5830332,4	MCF-7	breast:
10	chr11:5497451..5498014-chr11:5829478..5830015,2	MCF-7	breast:
11	chr11:5830455..5833171-chr11:5843435..5846091,2	K562	blood:
12	chr11:5831234..5833906-chr11:5837299..5840310,4	K562	blood:
13	chr11:5829421..5830302-chr11:5912492..5913020,2	MCF-7	breast:

No data

Variant related genes	Relation type
OR52N1	TF binding region
OR56B2P	TF binding region
OR52N5	TF binding region
OR52N4	TF binding region
OR52N3P	TF binding region
OR52N1	CpG island
OR56B2P	CpG island
OR52N5	CpG island
OR52N4	CpG island
OR52N3P	CpG island
ENSG00000176787	chromatin interactions

Extended variants
information (count: 736 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:736 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7394716	chr11:5773981-5773982	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs540119328	chr11:5773990-5773991	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs12793267	chr11:5774025-5774026	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs573472119	chr11:5774071-5774072	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs577094815	chr11:5774117-5774118	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs371302123	chr11:5774172-5774173	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs562560045	chr11:5774191-5774192	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs12364223	chr11:5774253-5774254	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs551497384	chr11:5774281-5774282	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs559880570	chr11:5774283-5774284	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs187526498	chr11:5774294-5774295	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs191161348	chr11:5774326-5774327	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs559341824	chr11:5774379-5774380	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs536016723	chr11:5774402-5774403	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs367807554	chr11:5774428-5774429	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs12364563	chr11:5774429-5774430	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs12365564	chr11:5774436-5774437	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs12365568	chr11:5774455-5774456	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs183336689	chr11:5774495-5774496	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs558683975	chr11:5774497-5774498	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs114287197	chr11:5774535-5774536	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs143429553	chr11:5774569-5774570	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs555206559	chr11:5774570-5774571	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs150931619	chr11:5774605-5774606	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs188065186	chr11:5774635-5774636	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs544204693	chr11:5774640-5774641	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs567404999	chr11:5774646-5774647	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs12364265	chr11:5774653-5774654	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs141811947	chr11:5774674-5774675	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs377653042	chr11:5774676-5774677	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs556099477	chr11:5774689-5774690	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs192520345	chr11:5774719-5774720	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs12362742	chr11:5774732-5774733	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs375810874	chr11:5774758-5774759	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs147111513	chr11:5774760-5774761	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs12362750	chr11:5774765-5774766	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs537973827	chr11:5774783-5774784	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs529610104	chr11:5774811-5774812	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs4414254	chr11:5774814-5774815	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs138593881	chr11:5774816-5774817	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs184371836	chr11:5774821-5774822	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs4636704	chr11:5774841-5774842	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs4636705	chr11:5774842-5774843	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs4561239	chr11:5774853-5774854	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs555341932	chr11:5774865-5774866	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs567367602	chr11:5774885-5774886	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs187556253	chr11:5774892-5774893	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs374698960	chr11:5774897-5774898	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs1566280	chr11:5774907-5774908	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs113490978	chr11:5774933-5774934	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Esophageal adenocarcinoma	18519675	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
Breast cancer	22522925	CNVD
Pancreatic cancer	23613489	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD
Type 2 diabetes	21526130	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5809200-5809600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr11:5812200-5812600	Enhancers	Fetal Brain Male	brain
3	chr11:5818400-5819000	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr11:5821000-5821800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr11:5821000-5824400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr11:5821600-5821800	Enhancers	Left Ventricle	heart
7	chr11:5821600-5822000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr11:5823200-5829600	Weak transcription	Fetal Heart	heart
9	chr11:5824400-5826200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr11:5825800-5829400	Weak transcription	Primary hematopoietic stem cells	blood
11	chr11:5826200-5828600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr11:5828600-5828800	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr11:5828600-5828800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr11:5828800-5829000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr11:5828800-5829200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr11:5828800-5829200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
17	chr11:5828800-5829600	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr11:5828800-5829800	Enhancers	H1 Cell Line	embryonic stem cell
19	chr11:5828800-5829800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr11:5828800-5829800	Enhancers	Placenta	Placenta
21	chr11:5828800-5832200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr11:5829000-5829200	Enhancers	Right Atrium	heart
23	chr11:5829000-5829200	Active TSS	Right Ventricle	heart
24	chr11:5829000-5829600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr11:5829200-5829600	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr11:5829200-5829800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr11:5829200-5829800	Enhancers	Right Ventricle	heart
28	chr11:5829400-5829800	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr11:5829400-5829800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr11:5829400-5830200	Active TSS	Primary hematopoietic stem cells	blood
31	chr11:5829600-5829800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr11:5829600-5829800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr11:5829600-5829800	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr11:5829600-5829800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr11:5829600-5829800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr11:5829600-5829800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
37	chr11:5829600-5829800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr11:5829600-5829800	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr11:5829600-5829800	Enhancers	Primary B cells from peripheral blood	blood
40	chr11:5829600-5829800	Bivalent/Poised TSS	Primary T cells fromperipheralblood	blood
41	chr11:5829600-5829800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
42	chr11:5829600-5829800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr11:5829600-5829800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
44	chr11:5829600-5829800	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
45	chr11:5829600-5829800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr11:5829600-5829800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
47	chr11:5829600-5829800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr11:5829600-5829800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr11:5829600-5829800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr11:5829600-5829800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin

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