Variant report

Variant	nsv1035355
Chromosome Location	chr11:4805922-4907672
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:324)
CpG islands
(count:978)
Chromatin interactive
region (count:27)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:4903288-4903949	K562	blood:	n/a	n/a
2	BACH1	chr11:4903312-4903361	K562	blood:	n/a	n/a
3	BHLHE40	chr11:4903370-4903912	K562	blood:	n/a	n/a
4	CBX3	chr11:4903266-4903716	K562	blood:	n/a	n/a
5	CCNT2	chr11:4903333-4904063	K562	blood:	n/a	n/a
6	CEBPB	chr11:4848087-4848331	A549	lung:	n/a	n/a
7	CEBPB	chr11:4884836-4885140	H1-hESC	embryonic stem cell:	n/a	chr11:4884971-4884982 chr11:4884971-4884984
8	CEBPB	chr11:4847987-4848334	HepG2	liver:	n/a	chr11:4848050-4848061
9	CEBPB	chr11:4884835-4885128	A549	lung:	n/a	chr11:4884971-4884982 chr11:4884971-4884984
10	CEBPB	chr11:4845401-4845737	IMR90	lung:	n/a	chr11:4845553-4845564
11	CEBPB	chr11:4845429-4845720	HepG2	liver:	n/a	chr11:4845553-4845564
12	CEBPB	chr11:4903071-4903449	IMR90	lung:	n/a	n/a
13	CEBPB	chr11:4903325-4903673	K562	blood:	n/a	n/a
14	CEBPB	chr11:4815769-4815953	K562	blood:	n/a	n/a
15	CEBPB	chr11:4884811-4885319	HepG2	liver:	n/a	chr11:4884971-4884982 chr11:4884971-4884984
16	CEBPB	chr11:4845391-4845677	A549	lung:	n/a	chr11:4845553-4845564
17	CEBPB	chr11:4845499-4845699	K562	blood:	n/a	chr11:4845553-4845564
18	CEBPB	chr11:4847965-4848232	K562	blood:	n/a	chr11:4848050-4848061
19	CEBPB	chr11:4903137-4903989	K562	blood:	n/a	n/a
20	CEBPB	chr11:4811479-4811616	K562	blood:	n/a	n/a
21	CEBPD	chr11:4903295-4903815	K562	blood:	n/a	n/a
22	CEBPD	chr11:4903302-4904220	K562	blood:	n/a	n/a
23	CHD2	chr11:4846254-4846282	K562	blood:	n/a	n/a
24	CTCF	chr11:4904546-4904730	K562	blood:	n/a	n/a
25	CTCF	chr11:4847831-4848009	MCF-7	breast:	n/a	n/a
26	CTCF	chr11:4898270-4898420	K562	blood:	n/a	n/a
27	CTCF	chr11:4847880-4848030	WI-38	lung:	n/a	n/a
28	CTCF	chr11:4847803-4847951	HepG2	liver:	n/a	n/a
29	CTCF	chr11:4870203-4870432	K562	blood:	n/a	n/a
30	CTCF	chr11:4847760-4847910	HMEC	breast:	n/a	n/a
31	CTCF	chr11:4847860-4848010	HCFaa	heart:	n/a	n/a
32	CTCF	chr11:4847840-4847990	Caco-2	colon:	n/a	n/a
33	CTCF	chr11:4847879-4848000	GM13977	blood:	n/a	n/a
34	CTCF	chr11:4847840-4847990	HVMF	connective:	n/a	n/a
35	CTCF	chr11:4861220-4861370	HCFaa	heart:	n/a	n/a
36	CTCF	chr11:4861140-4861290	GM12873	blood:	n/a	n/a
37	CTCF	chr11:4898300-4898450	HepG2	liver:	n/a	n/a
38	CTCF	chr11:4847866-4847960	HepG2	liver:	n/a	n/a
39	CTCF	chr11:4847820-4847970	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr11:4847840-4847990	NB4	blood:	n/a	n/a
41	CTCF	chr11:4847860-4848010	GM12871	blood:	n/a	n/a
42	CTCF	chr11:4847800-4847950	AG09319	gingival:	n/a	n/a
43	CTCF	chr11:4861260-4861410	HCT-116	colon:	n/a	n/a
44	CTCF	chr11:4847800-4847950	GM12875	blood:	n/a	n/a
45	CTCF	chr11:4847702-4848108	IMR90	lung:	n/a	n/a
46	CTCF	chr11:4847742-4848063	K562	blood:	n/a	n/a
47	CTCF	chr11:4847683-4848150	HCT-116	colon:	n/a	n/a
48	CTCF	chr11:4847823-4847989	GM12878	blood:	n/a	n/a
49	CTCF	chr11:4847840-4847990	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr11:4847840-4847990	HA-sp	spinal cord:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4824704-4824754	Caco-2	colon:	n/a
2	chr11:4843021-4843071	HPAEpiC	pulmonary alveolar:	n/a
3	chr11:4824704-4824754	Caco-2	colon:	n/a
4	chr11:4843021-4843071	HPAEpiC	pulmonary alveolar:	n/a
5	chr11:4841204-4841254	HRE	kidney:	n/a
6	chr11:4824704-4824754	NT2-D1	testis:	n/a
7	chr11:4903155-4903205	HCF	heart:	n/a
8	chr11:4870255-4870305	HCF	heart:	n/a
9	chr11:4903155-4903205	HNPCEpiC	eye:	n/a
10	chr11:4902464-4902514	HEK293	kidney:	embryo
11	chr11:4869963-4870013	MCF10A-Er-Src	breast:	n/a
12	chr11:4841204-4841254	HIPEpiC	eye:	n/a
13	chr11:4870255-4870305	BE2_C	brain:	n/a
14	chr11:4869963-4870013	HEK293	kidney:	embryo
15	chr11:4902583-4902633	CMK	blood:	n/a
16	chr11:4902583-4902633	BE2_C	brain:	n/a
17	chr11:4843021-4843071	U87	brain:	n/a
18	chr11:4870255-4870305	H1-hESC	embryonic stem cell:	embryo
19	chr11:4871813-4871863	GM12878	blood:	n/a
20	chr11:4869963-4870013	H1-hESC	embryonic stem cell:	embryo
21	chr11:4843021-4843071	GM19239	blood:	n/a
22	chr11:4902491-4902541	GM12878	blood:	n/a
23	chr11:4824704-4824754	HL-60	blood:	n/a
24	chr11:4825815-4825865	AG09309	skin:	n/a
25	chr11:4841204-4841254	Caco-2	colon:	n/a
26	chr11:4824704-4824754	NH-A	brain:	n/a
27	chr11:4825640-4825690	MCF10A-Er-Src	breast:	n/a
28	chr11:4843021-4843071	BJ	skin:	n/a
29	chr11:4824704-4824754	NHDF-neo	bronchial:	n/a
30	chr11:4841204-4841254	AG09319	gingival:	n/a
31	chr11:4870453-4870503	A549	lung:	n/a
32	chr11:4825815-4825865	IMR90	lung:	fetal
33	chr11:4871813-4871863	HRE	kidney:	n/a
34	chr11:4902583-4902633	BJ	skin:	n/a
35	chr11:4871813-4871863	AG09309	skin:	n/a
36	chr11:4825232-4825282	U87	brain:	n/a
37	chr11:4870255-4870305	AG09319	gingival:	n/a
38	chr11:4903155-4903205	IMR90	lung:	fetal
39	chr11:4870453-4870503	HUVEC	blood vessel:	n/a
40	chr11:4902583-4902633	PrEC	prostate:	n/a
41	chr11:4902491-4902541	HCM	heart:	n/a
42	chr11:4902464-4902514	IMR90	lung:	fetal
43	chr11:4903155-4903205	BJ	skin:	n/a
44	chr11:4841204-4841254	GM12891	blood:	n/a
45	chr11:4902464-4902514	GM12878	blood:	n/a
46	chr11:4870255-4870305	SK-N-SH	brain:	n/a
47	chr11:4870255-4870305	GM06990	blood:	n/a
48	chr11:4902583-4902633	GM06990	blood:	n/a
49	chr11:4869963-4870013	NHDF-neo	bronchial:	n/a
50	chr11:4902464-4902514	HCT-116	colon:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:4855919..4858881-chr11:4862668..4864924,2	MCF-7	breast:
2	chr11:4806483..4808284-chr11:4810226..4812694,2	K562	blood:
3	chr11:4884965..4887784-chr11:4890382..4892090,2	K562	blood:
4	chr11:4657833..4658473-chr11:4847439..4848013,2	MCF-7	breast:
5	11:4869840-4870943..11:4870943-4872364	Hela-S3	cervix:
6	chr11:4822926..4825696-chr11:4829994..4831787,2	K562	blood:
7	chr11:4822926..4825841-chr11:4830287..4832476,2	K562	blood:
8	chr11:4855919..4858881-chr11:4862668..4864924,2	MCF-7	breast:
9	11:4820112-4824892..11:5018576-5020673	H1-hESC	embryonic stem cell:	embryo
10	11:4820112-4824892..11:5527719-5533869	H1-hESC	embryonic stem cell:	embryo
11	chr11:4817686..4819750-chr11:4821906..4823690,2	K562	blood:
12	chr11:4817686..4819750-chr11:4821906..4823690,2	K562	blood:
13	11:4820112-4824892..11:5700314-5707362	K562	blood:
14	11:4886992-4893242..11:5714465-5718134	K562	blood:
15	11:4801044-4820112..11:5700314-5707362	H1-hESC	embryonic stem cell:	embryo
16	chr11:4884965..4887784-chr11:4890382..4892090,2	K562	blood:
17	chr11:4899835..4902548-chr11:4904411..4907145,2	K562	blood:
18	11:4849537-4851766..11:5527719-5533869	H1-hESC	embryonic stem cell:	embryo
19	11:4886992-4893242..11:5721056-5732713	K562	blood:
20	chr11:4887759..4889897-chr11:4893466..4895197,2	K562	blood:
21	chr11:4894111..4896171-chr11:4899276..4901453,2	K562	blood:
22	11:4886992-4893242..11:5700314-5707362	Hela-S3	cervix:
23	chr11:4887759..4889897-chr11:4893466..4895197,2	K562	blood:
24	chr11:4789671..4792092-chr11:4812812..4815235,2	K562	blood:
25	chr11:4894111..4896171-chr11:4899276..4901453,2	K562	blood:
26	11:4820112-4824892..11:5721056-5732713	H1-hESC	embryonic stem cell:	embryo
27	chr11:4899835..4902548-chr11:4904411..4907145,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR52R1-1	chr11:4815008-4815466	NONHSAT017656
2	lnc-OR52R1-1	chr11:4816146-4816514	NONHSAT017656

No data

Variant related genes	Relation type
OR51S1	TF binding region
OR51N1P	TF binding region
OR52R1	TF binding region
OR51A8P	TF binding region
OR52Y1P	TF binding region
OR51T1	TF binding region
OR51H1P	TF binding region
OR51F2	TF binding region
OR51H2P	TF binding region
OR51S1	CpG island
OR51N1P	CpG island
OR52R1	CpG island
OR51A8P	CpG island
OR52Y1P	CpG island
OR51T1	CpG island
OR51H1P	CpG island
OR51F2	CpG island
OR51H2P	CpG island
ENSG00000176922	chromatin interactions
ENSG00000176798	chromatin interactions
ENSG00000176951	chromatin interactions
ENSG00000188069	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000176937	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000175520	chromatin interactions

Extended variants
information (count: 2366 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2366 , 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	rs144441791	chr11:4805978-4805979	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs552670728	chr11:4805988-4805989	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs66473029	chr11:4806004-4806005	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs117191896	chr11:4806058-4806059	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs546987949	chr11:4806067-4806068	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs71480720	chr11:4806073-4806074	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs183386411	chr11:4806136-4806137	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs148440645	chr11:4806137-4806138	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs76415953	chr11:4806166-4806167	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs76490169	chr11:4806167-4806168	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs557803157	chr11:4806170-4806171	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs572751106	chr11:4806186-4806187	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs1433910	chr11:4806200-4806201	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs141688716	chr11:4806211-4806212	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs35324703	chr11:4806248-4806249	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs544495393	chr11:4806249-4806250	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs35956756	chr11:4806262-4806263	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs35788626	chr11:4806270-4806271	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs11033870	chr11:4806282-4806283	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs552707458	chr11:4806318-4806319	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs35212944	chr11:4806325-4806326	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs563307446	chr11:4806326-4806327	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs56295748	chr11:4806342-4806343	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs76440360	chr11:4806344-4806345	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs547021757	chr11:4806363-4806364	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs78596644	chr11:4806365-4806366	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs563773939	chr11:4806375-4806376	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs552181717	chr11:4806376-4806377	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs550826662	chr11:4806382-4806383	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs569128575	chr11:4806391-4806392	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs539595487	chr11:4806445-4806446	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs557577884	chr11:4806462-4806463	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs201113091	chr11:4806469-4806470	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs192995066	chr11:4806505-4806506	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs375625809	chr11:4806506-4806507	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs140103956	chr11:4806514-4806515	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs34414646	chr11:4806531-4806532	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs201441972	chr11:4806541-4806542	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs113392418	chr11:4806547-4806548	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs145516030	chr11:4806565-4806566	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs548491370	chr11:4806581-4806582	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs544540530	chr11:4806586-4806587	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs556450891	chr11:4806604-4806605	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs375392657	chr11:4806610-4806611	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs184694909	chr11:4806621-4806622	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs545231962	chr11:4806625-4806626	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs370872132	chr11:4806673-4806674	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs78092605	chr11:4806674-4806675	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs1433909	chr11:4806706-4806707	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs562127578	chr11:4806723-4806724	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Bipolar disorder	19114987	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4808000-4808400	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr11:4815400-4816200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:4815800-4816000	Enhancers	Small Intestine	intestine
4	chr11:4816200-4820200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:4816400-4816600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr11:4816400-4816800	Enhancers	Gastric	stomach
7	chr11:4816800-4817000	Weak transcription	Gastric	stomach
8	chr11:4817000-4817400	Enhancers	Gastric	stomach
9	chr11:4817200-4817400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr11:4817400-4821200	Weak transcription	Gastric	stomach
11	chr11:4817600-4817800	Enhancers	Stomach Mucosa	stomach
12	chr11:4818000-4818800	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr11:4818600-4818800	Enhancers	Stomach Mucosa	stomach
14	chr11:4820200-4820400	Enhancers	Stomach Mucosa	stomach
15	chr11:4820200-4821000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr11:4821200-4821600	Enhancers	Gastric	stomach
17	chr11:4821600-4825000	Weak transcription	Gastric	stomach
18	chr11:4824000-4826600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr11:4825000-4825200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr11:4825000-4825200	Enhancers	Spleen	Spleen
21	chr11:4825000-4825400	Bivalent/Poised TSS	Brain Substantia Nigra	brain
22	chr11:4825000-4825400	Active TSS	Gastric	stomach
23	chr11:4840200-4842000	Enhancers	NHDF-Ad	bronchial
24	chr11:4840400-4842400	Enhancers	Muscle Satellite Cultured Cells	--
25	chr11:4840600-4842000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr11:4840600-4842000	Enhancers	NHEK	skin
27	chr11:4841000-4842000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr11:4841000-4842000	Enhancers	HMEC	breast
29	chr11:4841000-4842200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr11:4842600-4843000	Active TSS	Brain Substantia Nigra	brain
31	chr11:4843000-4843200	Bivalent/Poised TSS	Brain Substantia Nigra	brain
32	chr11:4844800-4846200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr11:4845200-4846400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr11:4852000-4852600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr11:4856600-4857000	Enhancers	Rectal Smooth Muscle	rectum
36	chr11:4861400-4861800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr11:4863600-4863800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr11:4870000-4870400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr11:4870000-4870600	Enhancers	Gastric	stomach
40	chr11:4870200-4870800	Enhancers	Liver	Liver
41	chr11:4870400-4871600	Enhancers	Fetal Heart	heart
42	chr11:4870800-4872200	Weak transcription	Liver	Liver
43	chr11:4871600-4872400	Weak transcription	Fetal Heart	heart
44	chr11:4872200-4872600	Enhancers	Liver	Liver
45	chr11:4872200-4872600	Enhancers	Right Ventricle	heart
46	chr11:4872400-4872600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr11:4872400-4872600	Enhancers	Esophagus	oesophagus
48	chr11:4872400-4872600	Enhancers	Fetal Heart	heart
49	chr11:4872400-4872600	Enhancers	Gastric	stomach
50	chr11:4872400-4872600	Enhancers	Lung	lung

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