Variant report

Variant	nsv468568
Chromosome Location	chr11:55682795-55819544
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	ATF1	chr11:55749566-55749730	K562	blood:	n/a	n/a
2	BRCA1	chr11:55684123-55684321	GM12878	blood:	n/a	n/a
3	CEBPB	chr11:55704335-55704572	HepG2	liver:	n/a	chr11:55704400-55704413 chr11:55704401-55704412
4	CEBPB	chr11:55710296-55710606	HepG2	liver:	n/a	n/a
5	CEBPB	chr11:55698713-55698910	A549	lung:	n/a	n/a
6	CEBPB	chr11:55730191-55730507	HepG2	liver:	n/a	chr11:55730352-55730363
7	CEBPB	chr11:55807323-55807629	HepG2	liver:	n/a	chr11:55807438-55807449
8	CEBPB	chr11:55741577-55741777	HepG2	liver:	n/a	chr11:55741709-55741720
9	CEBPB	chr11:55684084-55684322	K562	blood:	n/a	n/a
10	CEBPB	chr11:55730195-55730482	IMR90	lung:	n/a	chr11:55730352-55730363
11	CTCF	chr11:55710400-55710550	WI-38	lung:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
12	CTCF	chr11:55710340-55710538	Gliobla	brain:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
13	CTCF	chr11:55716920-55717067	A549	lung:	n/a	n/a
14	CTCF	chr11:55710320-55710470	SAEC	small airway:	n/a	chr11:55710457-55710465 chr11:55710452-55710470 chr11:55710453-55710469
15	CTCF	chr11:55710351-55710527	HepG2	liver:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
16	CTCF	chr11:55710340-55710490	GM12868	blood:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
17	CTCF	chr11:55710400-55710550	HepG2	liver:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
18	CTCF	chr11:55710380-55710530	BE2_C	brain:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
19	CTCF	chr11:55710340-55710490	HCT-116	colon:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
20	CTCF	chr11:55716918-55717061	MCF-7	breast:	n/a	n/a
21	CTCF	chr11:55710360-55710510	BJ	skin:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
22	CTCF	chr11:55710420-55710570	GM12867	blood:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
23	CTCF	chr11:55710320-55710470	AG09309	skin:	n/a	chr11:55710457-55710465 chr11:55710452-55710470 chr11:55710453-55710469
24	CTCF	chr11:55710300-55710450	BE2_C	brain:	n/a	n/a
25	CTCF	chr11:55710360-55710510	Hela-S3	cervix:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
26	CTCF	chr11:55710284-55710595	A549	lung:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
27	CTCF	chr11:55710400-55710550	NHEK	skin:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
28	CTCF	chr11:55717015-55717022	GM12892	blood:	n/a	n/a
29	CTCF	chr11:55710377-55710519	MCF-7	breast:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
30	CTCF	chr11:55710320-55710470	HRPEpiC	eye:	n/a	chr11:55710457-55710465 chr11:55710452-55710470 chr11:55710453-55710469
31	CTCF	chr11:55710282-55710658	K562	blood:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
32	CTCF	chr11:55768300-55768450	HFF-Myc	foreskin:	n/a	n/a
33	CTCF	chr11:55710360-55710510	GM12865	blood:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
34	CTCF	chr11:55710440-55710590	AG09319	gingival:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
35	CTCF	chr11:55710280-55710430	HCT-116	colon:	n/a	n/a
36	CTCF	chr11:55710333-55710524	A549	lung:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
37	CTCF	chr11:55710280-55710430	BJ	skin:	n/a	n/a
38	CTCF	chr11:55807160-55807183	GM10248	blood:	n/a	n/a
39	CTCF	chr11:55710400-55710550	MCF-7	breast:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
40	CTCF	chr11:55710360-55710510	SK-N-SH_RA	brain:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
41	CTCF	chr11:55694723-55694780	LNCaP	prostate:	n/a	n/a
42	CTCF	chr11:55710360-55710510	AoAF	blood vessel:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
43	CTCF	chr11:55710340-55710490	GM12864	blood:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
44	CTCF	chr11:55710400-55710550	HL-60	blood:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
45	CTCF	chr11:55710363-55710529	Spleen_OC	spleen:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
46	CTCF	chr11:55710640-55710790	HMEC	breast:	n/a	n/a
47	CTCF	chr11:55710340-55710490	HA-sp	spinal cord:	n/a	chr11:55710457-55710465 chr11:55710454-55710475 chr11:55710452-55710470 chr11:55710453-55710469
48	CTCF	chr11:55716951-55717039	GM12878	blood:	n/a	n/a
49	CTCF	chr11:55764276-55764363	Lung_OC	lung:	n/a	n/a
50	CTCF	chr11:55710280-55710430	HCM	heart:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:55749739-55749789	T-47D	breast:	n/a
2	chr11:55796572-55796622	Hepatocyte	liver:	n/a
3	chr11:55796572-55796622	IMR90	lung:	fetal
4	chr11:55797628-55797678	GM06990	blood:	n/a
5	chr11:55749739-55749789	NH-A	brain:	n/a
6	chr11:55797628-55797678	BE2_C	brain:	n/a
7	chr11:55704601-55704651	ovcar-3	ovarian:	n/a
8	chr11:55749739-55749789	LNCaP	prostate:	n/a
9	chr11:55798206-55798256	GM06990	blood:	n/a
10	chr11:55736968-55737018	NHDF-neo	bronchial:	n/a
11	chr11:55704364-55704414	HL-60	blood:	n/a
12	chr11:55735459-55735509	IMR90	lung:	fetal
13	chr11:55797626-55797676	SK-N-MC	brain:	n/a
14	chr11:55737045-55737095	BE2_C	brain:	n/a
15	chr11:55704601-55704651	AG09309	skin:	n/a
16	chr11:55753849-55753899	SK-N-SH_RA	brain:	n/a
17	chr11:55749739-55749789	AG04449	skin:	fetal
18	chr11:55797628-55797678	GM19239	blood:	n/a
19	chr11:55737045-55737095	Caco-2	colon:	n/a
20	chr11:55705284-55705334	AG04449	skin:	fetal
21	chr11:55749739-55749789	HL-60	blood:	n/a
22	chr11:55737045-55737095	Hepatocyte	liver:	n/a
23	chr11:55704364-55704414	SKMC	muscle:	n/a
24	chr11:55704601-55704651	NT2-D1	testis:	n/a
25	chr11:55737045-55737095	NT2-D1	testis:	n/a
26	chr11:55753849-55753899	MCF10A-Er-Src	breast:	n/a
27	chr11:55737072-55737122	PrEC	prostate:	n/a
28	chr11:55798206-55798256	HL-60	blood:	n/a
29	chr11:55798206-55798256	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:55735459-55735509	GM12878	blood:	n/a
31	chr11:55735459-55735509	MCF-7	breast:	n/a
32	chr11:55704364-55704414	IMR90	lung:	fetal
33	chr11:55737072-55737122	HUVEC	blood vessel:	n/a
34	chr11:55736968-55737018	HAEpiC	amniotic membrane:	n/a
35	chr11:55735459-55735509	HRE	kidney:	n/a
36	chr11:55737072-55737122	HRCEpiC	kidney:	n/a
37	chr11:55797628-55797678	Caco-2	colon:	n/a
38	chr11:55797628-55797678	MCF-7	breast:	n/a
39	chr11:55704364-55704414	A549	lung:	n/a
40	chr11:55736968-55737018	AG04449	skin:	fetal
41	chr11:55753849-55753899	AoSMC	blood vessel:	n/a
42	chr11:55796572-55796622	HCPEpiC	choroid plexus:	n/a
43	chr11:55705284-55705334	HRPEpiC	eye:	n/a
44	chr11:55735459-55735509	SKMC	muscle:	n/a
45	chr11:55796572-55796622	GM12878	blood:	n/a
46	chr11:55736968-55737018	U87	brain:	n/a
47	chr11:55797628-55797678	AG04449	skin:	fetal
48	chr11:55796572-55796622	SK-N-MC	brain:	n/a
49	chr11:55796572-55796622	AG09309	skin:	n/a
50	chr11:55798206-55798256	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:55726290..55727933-chr11:55735253..55737882,2	K562	blood:
2	chr11:55702690..55706471-chr11:55707075..55709513,3	MCF-7	breast:
3	chr11:55698028..55700897-chr11:55714005..55716618,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR10AG1-1	chr11:55724692-55725106	NONHSAT021375

Variant related genes	Relation type
OR10AF1P	TF binding region
OR7E5P	TF binding region
OR5AQ1P	TF binding region
OR10AK1P	TF binding region
OR5I1	TF binding region
OR5AS1	TF binding region
OR5F2P	TF binding region
OR10AG1	TF binding region
OR5W2	TF binding region
OR5F1	TF binding region
OR10AF1P	CpG island
OR7E5P	CpG island
OR5AQ1P	CpG island
OR10AK1P	CpG island
OR5I1	CpG island
OR5AS1	CpG island
OR5F2P	CpG island
OR10AG1	CpG island
OR5W2	CpG island
OR5F1	CpG island
ENSG00000167825	chromatin interactions
ENSG00000255416	chromatin interactions
ENSG00000174970	chromatin interactions

Extended variants
information (count: 1590 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574339132	chr11:55684114-55684115	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs541954018	chr11:55684129-55684130	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs184542223	chr11:55684146-55684147	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs575466206	chr11:55684169-55684170	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs372682745	chr11:55684174-55684175	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs112221306	chr11:55684181-55684182	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs12575825	chr11:55684190-55684191	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs566535065	chr11:55684222-55684223	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs528738209	chr11:55684265-55684266	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs147865558	chr11:55684276-55684277	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs566317108	chr11:55684289-55684290	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs71490410	chr11:55684291-55684292	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs529271379	chr11:55684312-55684313	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs2512729	chr11:55684320-55684321	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs529324633	chr11:55684868-55684869	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs544585318	chr11:55684875-55684876	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs184532672	chr11:55684912-55684913	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs562994402	chr11:55684956-55684957	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs372922035	chr11:55684973-55684974	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs533421867	chr11:55685025-55685026	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs554623417	chr11:55686849-55686850	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs191951987	chr11:55686851-55686852	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs114825178	chr11:55686867-55686868	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs182007249	chr11:55686892-55686893	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs148016962	chr11:55686896-55686897	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs545001681	chr11:55686952-55686953	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs559936124	chr11:55686957-55686958	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs373575683	chr11:55686977-55686978	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs527255685	chr11:55686979-55686980	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs577017087	chr11:55698033-55698034	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs570542629	chr11:55698040-55698041	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs539514588	chr11:55698041-55698042	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs140177020	chr11:55698042-55698043	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs7941718	chr11:55698048-55698049	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs559576107	chr11:55698076-55698077	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs138222239	chr11:55698099-55698100	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs36088468	chr11:55698107-55698108	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs192574287	chr11:55698126-55698127	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs61894170	chr11:55698164-55698165	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs546319335	chr11:55698235-55698236	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs565117221	chr11:55698258-55698259	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs532306918	chr11:55698268-55698269	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs149579300	chr11:55698284-55698285	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs77113517	chr11:55698352-55698353	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs574809667	chr11:55698354-55698355	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs529706762	chr11:55698358-55698359	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs9667319	chr11:55698444-55698445	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs74780821	chr11:55698494-55698495	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs536792311	chr11:55698499-55698500	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs558217894	chr11:55698519-55698520	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21990379	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Multiple myeloma	16616336	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:55698800-55699000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:55717000-55717400	Enhancers	Pancreas	Pancrea
3	chr11:55730000-55734000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:55733400-55734800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr11:55734000-55734200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr11:55734000-55734400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr11:55741000-55741400	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr11:55741200-55742000	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr11:55741400-55746000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr11:55742000-55742400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr11:55742400-55742600	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr11:55742600-55745600	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr11:55745600-55747000	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr11:55745800-55747000	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr11:55746000-55746800	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr11:55746000-55746800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr11:55746000-55746800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr11:55746200-55747200	Enhancers	H9 Cell Line	embryonic stem cell
19	chr11:55746200-55747400	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr11:55746600-55747400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr11:55746800-55747400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr11:55747400-55753000	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr11:55753000-55754000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
24	chr11:55753400-55753600	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr11:55753400-55753800	Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr11:55753600-55754000	Active TSS	HUES64 Cell Line	embryonic stem cell
27	chr11:55761200-55761400	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr11:55761400-55762600	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr11:55762600-55763600	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr11:55762800-55764200	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr11:55798200-55798800	Enhancers	Pancreas	Pancrea
32	chr11:55800400-55800600	Enhancers	Pancreas	Pancrea

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