Variant report

Variant	esv1809118
Chromosome Location	chr11:4782207-4843426
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:111)
CpG islands
(count:549)
Chromatin interactive
region (count:27)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:111 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:4793218-4793283	K562	blood:	n/a	n/a
2	CEBPB	chr11:4815769-4815953	K562	blood:	n/a	n/a
3	CEBPB	chr11:4802820-4802858	K562	blood:	n/a	chr11:4802839-4802852 chr11:4802839-4802852 chr11:4802841-4802852
4	CEBPB	chr11:4811479-4811616	K562	blood:	n/a	n/a
5	CEBPB	chr11:4786195-4786260	HepG2	liver:	n/a	chr11:4786226-4786237
6	CTCF	chr11:4804240-4804390	GM12868	blood:	n/a	n/a
7	CTCF	chr11:4804240-4804390	GM06990	blood:	n/a	n/a
8	CTCF	chr11:4804240-4804390	GM12872	blood:	n/a	n/a
9	CTCF	chr11:4804260-4804410	GM12864	blood:	n/a	n/a
10	CTCF	chr11:4820319-4820345	GM10248	blood:	n/a	n/a
11	CTCF	chr11:4804280-4804430	GM12871	blood:	n/a	n/a
12	CTCF	chr11:4804200-4804350	AG04449	skin:	n/a	n/a
13	CTCF	chr11:4802760-4802868	K562	blood:	n/a	n/a
14	CTCF	chr11:4804220-4804370	GM12866	blood:	n/a	n/a
15	CTCF	chr11:4804259-4804393	GM12878	blood:	n/a	n/a
16	CTCF	chr11:4804254-4804393	K562	blood:	n/a	n/a
17	CTCF	chr11:4804220-4804370	GM06990	blood:	n/a	n/a
18	CTCF	chr11:4804240-4804390	HEK293	kidney:	n/a	n/a
19	CTCF	chr11:4804220-4804370	HBMEC	blood vessel:	n/a	n/a
20	CTCF	chr11:4804220-4804370	GM12865	blood:	n/a	n/a
21	CTCF	chr11:4836412-4836468	GM20000	blood:	n/a	n/a
22	CTCF	chr11:4804260-4804410	GM12872	blood:	n/a	n/a
23	CTCF	chr11:4804400-4804550	GM12878	blood:	n/a	n/a
24	CTCF	chr11:4804220-4804370	GM12864	blood:	n/a	n/a
25	CTCF	chr11:4804190-4804400	GM12878	blood:	n/a	n/a
26	CTCF	chr11:4804272-4804394	K562	blood:	n/a	n/a
27	CTCF	chr11:4804260-4804410	GM12871	blood:	n/a	n/a
28	CTCF	chr11:4804220-4804370	GM12870	blood:	n/a	n/a
29	CTCF	chr11:4804200-4804350	GM12874	blood:	n/a	n/a
30	CTCF	chr11:4804260-4804410	AG04449	skin:	n/a	n/a
31	CTCF	chr11:4804220-4804370	GM12878	blood:	n/a	n/a
32	CTCF	chr11:4804240-4804390	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr11:4804240-4804390	GM12873	blood:	n/a	n/a
34	CTCF	chr11:4804247-4804395	IMR90	lung:	n/a	n/a
35	CTCF	chr11:4802939-4802988	ProgFib	skin:	n/a	n/a
36	CTCF	chr11:4804278-4804380	GM19238	blood:	n/a	n/a
37	CTCF	chr11:4804220-4804370	GM12875	blood:	n/a	n/a
38	CTCF	chr11:4804340-4804490	WI-38	lung:	n/a	n/a
39	CTCF	chr11:4807280-4807430	HEK293	kidney:	n/a	n/a
40	CTCF	chr11:4804260-4804410	GM12874	blood:	n/a	n/a
41	CTCF	chr11:4804278-4804347	GM19239	blood:	n/a	n/a
42	CTCF	chr11:4804220-4804370	K562	blood:	n/a	n/a
43	CTCF	chr11:4804160-4804310	GM12867	blood:	n/a	n/a
44	CTCF	chr11:4804200-4804409	K562	blood:	n/a	n/a
45	CTCF	chr11:4804240-4804390	GM12869	blood:	n/a	n/a
46	CTCF	chr11:4804300-4804450	GM12864	blood:	n/a	n/a
47	CTCF	chr11:4804255-4804390	GM12891	blood:	n/a	n/a
48	CTCF	chr11:4804260-4804410	AG04450	lung:	n/a	n/a
49	CTCF	chr11:4804273-4804341	GM19240	blood:	n/a	n/a
50	CTCF	chr11:4804244-4804343	GM13977	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4825232-4825282	HRE	kidney:	n/a
2	chr11:4791012-4791062	HCPEpiC	choroid plexus:	n/a
3	chr11:4825232-4825282	CMK	blood:	n/a
4	chr11:4843021-4843071	BJ	skin:	n/a
5	chr11:4825815-4825865	SKMC	muscle:	n/a
6	chr11:4791012-4791062	Hepatocyte	liver:	n/a
7	chr11:4842355-4842405	HRCEpiC	kidney:	n/a
8	chr11:4792272-4792322	U87	brain:	n/a
9	chr11:4791012-4791062	HCM	heart:	n/a
10	chr11:4791012-4791062	NH-A	brain:	n/a
11	chr11:4824704-4824754	PANC-1	pancreas:	n/a
12	chr11:4841204-4841254	HRE	kidney:	n/a
13	chr11:4825232-4825282	A549	lung:	n/a
14	chr11:4842355-4842405	Hepatocyte	liver:	n/a
15	chr11:4842355-4842405	HCT-116	colon:	n/a
16	chr11:4824704-4824754	NHDF-neo	bronchial:	n/a
17	chr11:4843021-4843071	HAEpiC	amniotic membrane:	n/a
18	chr11:4825815-4825865	HCT-116	colon:	n/a
19	chr11:4824704-4824754	GM19239	blood:	n/a
20	chr11:4791012-4791062	HNPCEpiC	eye:	n/a
21	chr11:4842355-4842405	GM19239	blood:	n/a
22	chr11:4843021-4843071	Jurkat	blood:	n/a
23	chr11:4792272-4792322	CMK	blood:	n/a
24	chr11:4843021-4843071	HRCEpiC	kidney:	n/a
25	chr11:4842355-4842405	HPAEpiC	pulmonary alveolar:	n/a
26	chr11:4825640-4825690	AG10803	skin:	n/a
27	chr11:4825640-4825690	BE2_C	brain:	n/a
28	chr11:4792272-4792322	GM06990	blood:	n/a
29	chr11:4843021-4843071	NH-A	brain:	n/a
30	chr11:4825640-4825690	ECC-1	luminal epithelium:	n/a
31	chr11:4824704-4824754	LNCaP	prostate:	n/a
32	chr11:4792272-4792322	PFSK-1	brain:	n/a
33	chr11:4841204-4841254	HCF	heart:	n/a
34	chr11:4841204-4841254	AG10803	skin:	n/a
35	chr11:4825232-4825282	HPAEpiC	pulmonary alveolar:	n/a
36	chr11:4825815-4825865	GM12891	blood:	n/a
37	chr11:4841204-4841254	NB4	blood:	n/a
38	chr11:4842355-4842405	SK-N-MC	brain:	n/a
39	chr11:4791012-4791062	ovcar-3	ovarian:	n/a
40	chr11:4792272-4792322	ECC-1	luminal epithelium:	n/a
41	chr11:4792272-4792322	HepG2	liver:	n/a
42	chr11:4824704-4824754	AG09319	gingival:	n/a
43	chr11:4842355-4842405	T-47D	breast:	n/a
44	chr11:4842355-4842405	CMK	blood:	n/a
45	chr11:4841204-4841254	T-47D	breast:	n/a
46	chr11:4792272-4792322	HCM	heart:	n/a
47	chr11:4842355-4842405	SAEC	small airway:	n/a
48	chr11:4842355-4842405	NB4	blood:	n/a
49	chr11:4791012-4791062	AG09309	skin:	n/a
50	chr11:4825232-4825282	AoSMC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	11:4778081-4789138..11:5033143-5038367	K562	blood:
2	11:4801044-4820112..11:5700314-5707362	H1-hESC	embryonic stem cell:	embryo
3	11:4820112-4824892..11:5018576-5020673	H1-hESC	embryonic stem cell:	embryo
4	chr11:4783931..4787132-chr11:4790389..4793666,3	K562	blood:
5	11:4778081-4789138..11:5740069-5747001	K562	blood:
6	chr11:4822926..4825841-chr11:4830287..4832476,2	K562	blood:
7	chr11:4778466..4780961-chr11:4783951..4785593,2	K562	blood:
8	11:4794705-4799792..11:5527719-5533869	GM12878	blood:
9	11:4820112-4824892..11:5700314-5707362	K562	blood:
10	chr11:4785049..4787150-chr11:4787794..4789663,2	K562	blood:
11	11:4789513-4794705..11:4988858-5002113	Hela-S3	cervix:
12	11:4789513-4794705..11:5380014-5384338	H1-hESC	embryonic stem cell:	embryo
13	chr11:4822926..4825696-chr11:4829994..4831787,2	K562	blood:
14	11:4820112-4824892..11:5527719-5533869	H1-hESC	embryonic stem cell:	embryo
15	11:4820112-4824892..11:5721056-5732713	H1-hESC	embryonic stem cell:	embryo
16	11:4794705-4799792..11:5714465-5718134	H1-hESC	embryonic stem cell:	embryo
17	11:4778081-4789138..11:4988858-5002113	Hela-S3	cervix:
18	11:4794705-4799792..11:5721056-5732713	K562	blood:
19	chr11:4789671..4792092-chr11:4812812..4815235,2	K562	blood:
20	chr11:4806483..4808284-chr11:4810226..4812694,2	K562	blood:
21	11:4789513-4794705..11:5033143-5038367	K562	blood:
22	11:4794705-4799792..11:5700314-5707362	K562	blood:
23	chr11:4780407..4782336-chr11:4786292..4788948,2	K562	blood:
24	chr11:4817686..4819750-chr11:4821906..4823690,2	K562	blood:
25	chr11:4776926..4782057-chr11:4782402..4785593,4	K562	blood:
26	11:4789513-4794705..11:4799792-4801044	GM12878	blood:
27	chr11:4817686..4819750-chr11:4821906..4823690,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MMP26-1	chr11:4788500-4788571	NONHSAT017654
2	lnc-OR52R1-1	chr11:4816146-4816514	NONHSAT017656
3	lnc-OR52R1-1	chr11:4815008-4815466	NONHSAT017656

No data

Variant related genes	Relation type
OR51N1P	TF binding region
OR52R1	TF binding region
OR51F1	TF binding region
OR51F2	TF binding region
OR52Y1P	TF binding region
MMP26	TF binding region
OR51N1P	CpG island
OR52R1	CpG island
OR51F1	CpG island
OR51F2	CpG island
OR52Y1P	CpG island
MMP26	CpG island
ENSG00000176937	chromatin interactions
ENSG00000188069	chromatin interactions
ENSG00000175520	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000176951	chromatin interactions
ENSG00000232381	chromatin interactions
ENSG00000176798	chromatin interactions
ENSG00000225003	chromatin interactions
ENSG00000224300	chromatin interactions
ENSG00000236248	chromatin interactions
ENSG00000167346	chromatin interactions
ENSG00000201980	chromatin interactions
ENSG00000132256	chromatin interactions

Extended variants
information (count: 2445 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2445 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568879061	chr11:4782239-4782240	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs540904812	chr11:4782271-4782272	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs146300396	chr11:4782284-4782285	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs139645549	chr11:4782297-4782298	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs542832560	chr11:4782321-4782322	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs561061370	chr11:4782450-4782451	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs576022803	chr11:4782483-4782484	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs73393072	chr11:4782508-4782509	Inactive region	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs78425414	chr11:4782535-4782536	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs151050531	chr11:4782597-4782598	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs547747938	chr11:4782614-4782615	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs559362373	chr11:4782652-4782653	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs182112067	chr11:4782656-4782657	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs11033743	chr11:4782660-4782661	Inactive region	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs370125578	chr11:4782664-4782665	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs371384646	chr11:4782701-4782702	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs575058153	chr11:4782724-4782725	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs140841563	chr11:4782768-4782769	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs149709818	chr11:4782788-4782789	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs373954264	chr11:4782789-4782790	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs147859206	chr11:4782790-4782791	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs76172881	chr11:4782826-4782827	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs538634005	chr11:4782877-4782878	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs554071865	chr11:4782881-4782882	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs371264230	chr11:4782914-4782915	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs184998469	chr11:4782975-4782976	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs536869043	chr11:4783047-4783048	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs77699349	chr11:4783053-4783054	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs576575071	chr11:4783075-4783076	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs141435900	chr11:4783095-4783096	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs146942035	chr11:4783120-4783121	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs576941126	chr11:4783122-4783123	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs540996201	chr11:4783190-4783191	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs112964880	chr11:4783220-4783221	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs559611421	chr11:4783221-4783222	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs529904721	chr11:4783275-4783276	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs563385115	chr11:4783290-4783291	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs137917498	chr11:4783325-4783326	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs549898929	chr11:4783340-4783341	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs571388479	chr11:4783362-4783363	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs189854997	chr11:4783445-4783446	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs7122028	chr11:4783454-4783455	Inactive region	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs566373418	chr11:4783468-4783469	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs116463481	chr11:4783477-4783478	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs183211430	chr11:4783596-4783597	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs557760242	chr11:4783614-4783615	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs570187776	chr11:4783618-4783619	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs7125620	chr11:4783637-4783638	Inactive region	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs142362328	chr11:4783648-4783649	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs540360916	chr11:4783744-4783745	Inactive region	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4784000-4784800	Enhancers	GM12878-XiMat	blood
2	chr11:4797800-4798200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr11:4808000-4808400	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr11:4815400-4816200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:4815800-4816000	Enhancers	Small Intestine	intestine
6	chr11:4816200-4820200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr11:4816400-4816600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr11:4816400-4816800	Enhancers	Gastric	stomach
9	chr11:4816800-4817000	Weak transcription	Gastric	stomach
10	chr11:4817000-4817400	Enhancers	Gastric	stomach
11	chr11:4817200-4817400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr11:4817400-4821200	Weak transcription	Gastric	stomach
13	chr11:4817600-4817800	Enhancers	Stomach Mucosa	stomach
14	chr11:4818000-4818800	Enhancers	Sigmoid Colon	Sigmoid Colon
15	chr11:4818600-4818800	Enhancers	Stomach Mucosa	stomach
16	chr11:4820200-4820400	Enhancers	Stomach Mucosa	stomach
17	chr11:4820200-4821000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:4821200-4821600	Enhancers	Gastric	stomach
19	chr11:4821600-4825000	Weak transcription	Gastric	stomach
20	chr11:4824000-4826600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr11:4825000-4825200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr11:4825000-4825200	Enhancers	Spleen	Spleen
23	chr11:4825000-4825400	Bivalent/Poised TSS	Brain Substantia Nigra	brain
24	chr11:4825000-4825400	Active TSS	Gastric	stomach
25	chr11:4840200-4842000	Enhancers	NHDF-Ad	bronchial
26	chr11:4840400-4842400	Enhancers	Muscle Satellite Cultured Cells	--
27	chr11:4840600-4842000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr11:4840600-4842000	Enhancers	NHEK	skin
29	chr11:4841000-4842000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr11:4841000-4842000	Enhancers	HMEC	breast
31	chr11:4841000-4842200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr11:4842600-4843000	Active TSS	Brain Substantia Nigra	brain
33	chr11:4843000-4843200	Bivalent/Poised TSS	Brain Substantia Nigra	brain

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