Variant report

Variant	nsv508619
Chromosome Location	chr11:27028494-27110734
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	ARID3A	chr11:27046863-27047194	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:27076369-27077106	HepG2	liver:	n/a	n/a
3	BHLHE40	chr11:27076685-27077064	HepG2	liver:	n/a	n/a
4	CEBPB	chr11:27069501-27069701	HepG2	liver:	n/a	chr11:27069586-27069597
5	CEBPB	chr11:27062330-27062641	A549	lung:	n/a	chr11:27062468-27062481 chr11:27062470-27062479 chr11:27062469-27062480 chr11:27062468-27062479
6	CEBPB	chr11:27062323-27062641	Hela-S3	cervix:	n/a	chr11:27062468-27062481 chr11:27062470-27062479 chr11:27062469-27062480 chr11:27062468-27062479
7	CEBPB	chr11:27063948-27063974	Hela-S3	cervix:	n/a	chr11:27063955-27063966
8	CEBPB	chr11:27046927-27047231	HepG2	liver:	n/a	n/a
9	CEBPB	chr11:27062301-27062649	H1-hESC	embryonic stem cell:	n/a	chr11:27062468-27062481 chr11:27062470-27062479 chr11:27062469-27062480 chr11:27062468-27062479
10	CEBPB	chr11:27105338-27105516	HepG2	liver:	n/a	n/a
11	CEBPB	chr11:27062292-27062594	ECC-1	luminal epithelium:	n/a	chr11:27062468-27062481 chr11:27062470-27062479 chr11:27062469-27062480 chr11:27062468-27062479
12	CEBPB	chr11:27076627-27077013	HepG2	liver:	n/a	n/a
13	CEBPB	chr11:27063838-27064094	IMR90	lung:	n/a	chr11:27063955-27063966
14	CEBPB	chr11:27076591-27076974	HepG2	liver:	n/a	n/a
15	CEBPB	chr11:27063843-27064056	H1-hESC	embryonic stem cell:	n/a	chr11:27063955-27063966
16	CEBPB	chr11:27096835-27097038	IMR90	lung:	n/a	n/a
17	CEBPB	chr11:27062199-27062721	MCF-7	breast:	n/a	chr11:27062468-27062481 chr11:27062470-27062479 chr11:27062469-27062480 chr11:27062468-27062479
18	CEBPB	chr11:27062204-27062731	MCF-7	breast:	n/a	chr11:27062468-27062481 chr11:27062470-27062479 chr11:27062469-27062480 chr11:27062468-27062479
19	CEBPB	chr11:27062318-27062621	IMR90	lung:	n/a	chr11:27062468-27062481 chr11:27062470-27062479 chr11:27062469-27062480 chr11:27062468-27062479
20	CEBPB	chr11:27063813-27064037	A549	lung:	n/a	chr11:27063955-27063966
21	CEBPB	chr11:27063824-27064086	HepG2	liver:	n/a	chr11:27063955-27063966
22	CEBPB	chr11:27109863-27110153	HepG2	liver:	n/a	chr11:27110008-27110019 chr11:27110009-27110020 chr11:27110008-27110021 chr11:27110010-27110019
23	CEBPB	chr11:27062301-27062658	HepG2	liver:	n/a	chr11:27062468-27062481 chr11:27062470-27062479 chr11:27062469-27062480 chr11:27062468-27062479
24	CEBPB	chr11:27109893-27110076	A549	lung:	n/a	chr11:27110008-27110019 chr11:27110009-27110020 chr11:27110008-27110021 chr11:27110010-27110019
25	CHD2	chr11:27076760-27076919	HepG2	liver:	n/a	n/a
26	CTCF	chr11:27061520-27061670	HRPEpiC	eye:	n/a	chr11:27061627-27061645 chr11:27061609-27061617
27	CTCF	chr11:27061612-27061658	GM12878	blood:	n/a	chr11:27061627-27061645
28	CTCF	chr11:27060856-27060964	GM20000	blood:	n/a	n/a
29	CTCF	chr11:27061580-27061730	BJ	skin:	n/a	chr11:27061627-27061645 chr11:27061609-27061617
30	CTCF	chr11:27061537-27061657	SK-N-SH_RA	brain:	n/a	chr11:27061627-27061645 chr11:27061609-27061617
31	CTCF	chr11:27061540-27061690	MCF-7	breast:	n/a	chr11:27061627-27061645 chr11:27061609-27061617
32	CTCF	chr11:27061540-27061690	AoAF	blood vessel:	n/a	chr11:27061627-27061645 chr11:27061609-27061617
33	CTCF	chr11:27061520-27061670	HRE	kidney:	n/a	chr11:27061627-27061645 chr11:27061609-27061617
34	CTCF	chr11:27061580-27061730	AG04449	skin:	n/a	chr11:27061627-27061645 chr11:27061609-27061617
35	CTCF	chr11:27097580-27097730	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr11:27061620-27061770	K562	blood:	n/a	chr11:27061627-27061645
37	CTCF	chr11:27097580-27097730	HepG2	liver:	n/a	n/a
38	CTCF	chr11:27061540-27061690	WERI-Rb-1	eye:	n/a	chr11:27061627-27061645 chr11:27061609-27061617
39	CTCF	chr11:27061640-27061790	HAc	cerebellar:	n/a	n/a
40	CTCF	chr11:27061520-27061670	HEEpiC	esophagus:	n/a	chr11:27061627-27061645 chr11:27061609-27061617
41	CTCF	chr11:27061500-27061650	HepG2	liver:	n/a	chr11:27061627-27061645 chr11:27061609-27061617
42	CTCF	chr11:27061441-27061785	H1-hESC	embryonic stem cell:	n/a	chr11:27061627-27061645 chr11:27061609-27061617
43	CTCF	chr11:27061600-27061750	HFF	foreskin:	n/a	chr11:27061627-27061645 chr11:27061609-27061617
44	CTCF	chr11:27061557-27061694	LNCaP	prostate:	n/a	chr11:27061627-27061645 chr11:27061609-27061617
45	CTCF	chr11:27068680-27068830	GM12872	blood:	n/a	n/a
46	CTCF	chr11:27061560-27061710	HRE	kidney:	n/a	chr11:27061627-27061645 chr11:27061609-27061617
47	CTCF	chr11:27098240-27098390	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr11:27061545-27061692	LNCaP	prostate:	n/a	chr11:27061627-27061645 chr11:27061609-27061617
49	CTCF	chr11:27062640-27062790	AG04450	lung:	n/a	n/a
50	CTCF	chr11:27061552-27061668	Gliobla	brain:	n/a	chr11:27061627-27061645 chr11:27061609-27061617

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:27061756-27061806	MCF-7	breast:	n/a
2	chr11:27105814-27105864	ECC-1	luminal epithelium:	n/a
3	chr11:27061756-27061806	MCF-7	breast:	n/a
4	chr11:27105814-27105864	ECC-1	luminal epithelium:	n/a
5	chr11:27061756-27061806	HCPEpiC	choroid plexus:	n/a
6	chr11:27062416-27062466	HEK293	kidney:	embryo
7	chr11:27097023-27097073	BJ	skin:	n/a
8	chr11:27097023-27097073	NT2-D1	testis:	n/a
9	chr11:27061756-27061806	HCF	heart:	n/a
10	chr11:27105814-27105864	Hela-S3	cervix:	n/a
11	chr11:27034225-27034275	K562	blood:	n/a
12	chr11:27105814-27105864	LNCaP	prostate:	n/a
13	chr11:27062416-27062466	HPAEpiC	pulmonary alveolar:	n/a
14	chr11:27062963-27063013	K562	blood:	n/a
15	chr11:27061899-27061949	Jurkat	blood:	n/a
16	chr11:27062416-27062466	HRPEpiC	eye:	n/a
17	chr11:27061756-27061806	NT2-D1	testis:	n/a
18	chr11:27097023-27097073	HUVEC	blood vessel:	n/a
19	chr11:27061756-27061806	SK-N-MC	brain:	n/a
20	chr11:27061899-27061949	GM12891	blood:	n/a
21	chr11:27097023-27097073	Hepatocyte	liver:	n/a
22	chr11:27034225-27034275	GM06990	blood:	n/a
23	chr11:27105814-27105864	GM12891	blood:	n/a
24	chr11:27061899-27061949	A549	lung:	n/a
25	chr11:27061899-27061949	IMR90	lung:	fetal
26	chr11:27062963-27063013	NT2-D1	testis:	n/a
27	chr11:27061756-27061806	HCM	heart:	n/a
28	chr11:27061533-27061583	HIPEpiC	eye:	n/a
29	chr11:27062416-27062466	HepG2	liver:	n/a
30	chr11:27062963-27063013	BJ	skin:	n/a
31	chr11:27105814-27105864	SKMC	muscle:	n/a
32	chr11:27061533-27061583	HUVEC	blood vessel:	n/a
33	chr11:27061899-27061949	H1-hESC	embryonic stem cell:	embryo
34	chr11:27105814-27105864	PrEC	prostate:	n/a
35	chr11:27061533-27061583	H1-hESC	embryonic stem cell:	embryo
36	chr11:27034225-27034275	SKMC	muscle:	n/a
37	chr11:27062963-27063013	HPAEpiC	pulmonary alveolar:	n/a
38	chr11:27062963-27063013	AoSMC	blood vessel:	n/a
39	chr11:27061899-27061949	GM06990	blood:	n/a
40	chr11:27105814-27105864	Jurkat	blood:	n/a
41	chr11:27034225-27034275	AG04449	skin:	fetal
42	chr11:27061533-27061583	IMR90	lung:	fetal
43	chr11:27061533-27061583	SAEC	small airway:	n/a
44	chr11:27105814-27105864	SAEC	small airway:	n/a
45	chr11:27061756-27061806	NH-A	brain:	n/a
46	chr11:27062416-27062466	HL-60	blood:	n/a
47	chr11:27062416-27062466	BJ	skin:	n/a
48	chr11:27061756-27061806	T-47D	breast:	n/a
49	chr11:27062416-27062466	HRCEpiC	kidney:	n/a
50	chr11:27105814-27105864	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:27050228..27052948-chr11:27053328..27055109,2	MCF-7	breast:
2	chr11:27046527..27047233-chr8:129115547..129116417,2	MCF-7	breast:
3	chr11:27015097..27016903-chr11:27033368..27035440,2	K562	blood:
4	chr11:27050228..27052948-chr11:27053328..27055109,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC34-1	chr11:27088039-27088209	ENSG00000254560.1
2	lnc-FIBIN-1	chr11:27062418-27062566	NONHSAT018464
3	lnc-FIBIN-1	chr11:27062763-27063025	NONHSAT018464
4	lnc-CCDC34-1	chr11:27068733-27068859	ENSG00000254560.1
5	lnc-FIBIN-1	chr11:27067789-27067833	NONHSAT018464
6	lnc-CCDC34-1	chr11:27084530-27084607	ENSG00000254560.1

Variant related genes	Relation type
BBOX1	TF binding region
BBOX1	CpG island
ENSG00000176971	chromatin interactions

Extended variants
information (count: 3147 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3147 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs202182867	chr11:27028498-27028499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs558163482	chr11:27028512-27028513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573229712	chr11:27028537-27028538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371931977	chr11:27028567-27028568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572427412	chr11:27028663-27028664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376814115	chr11:27028685-27028686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143848862	chr11:27028688-27028689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559550292	chr11:27028702-27028703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538586513	chr11:27028755-27028756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs16916429	chr11:27028807-27028808	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs563427523	chr11:27028821-27028822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530870505	chr11:27028827-27028828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148618270	chr11:27028835-27028836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186324108	chr11:27028836-27028837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528134696	chr11:27028838-27028839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369233555	chr11:27028890-27028891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116477608	chr11:27028916-27028917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144894101	chr11:27028982-27028983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546740600	chr11:27029011-27029012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs117584880	chr11:27029029-27029030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs147953308	chr11:27029045-27029046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569429869	chr11:27029057-27029058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540149120	chr11:27029077-27029078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs72874782	chr11:27029122-27029123	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs140223539	chr11:27029215-27029216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573544851	chr11:27029306-27029307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534238813	chr11:27029341-27029342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540689783	chr11:27029451-27029452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10835098	chr11:27029459-27029460	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs10767591	chr11:27029464-27029465	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs551550789	chr11:27029470-27029471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563518686	chr11:27029532-27029533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145552914	chr11:27029553-27029554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11029778	chr11:27029560-27029561	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs563879262	chr11:27029607-27029608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147730027	chr11:27029634-27029635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546226820	chr11:27029639-27029640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140969036	chr11:27029678-27029679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528980219	chr11:27029692-27029693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577177915	chr11:27029737-27029738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150224826	chr11:27029783-27029784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567471285	chr11:27029801-27029802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539707033	chr11:27029815-27029816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534946093	chr11:27029835-27029836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544546284	chr11:27029864-27029865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567099400	chr11:27029926-27029927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534176138	chr11:27029950-27029951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372580479	chr11:27029962-27029963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556683850	chr11:27030027-27030028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10835099	chr11:27030056-27030057	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:60)

Disease	PMID	Source
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
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Neuroticism	17667963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:27019200-27033200	Weak transcription	NHDF-Ad	bronchial
2	chr11:27024800-27033200	Weak transcription	Colon Smooth Muscle	Colon
3	chr11:27028400-27038600	Weak transcription	Pancreas	Pancrea
4	chr11:27030800-27031000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr11:27030800-27031600	Enhancers	HMEC	breast
6	chr11:27031000-27031400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr11:27031000-27033400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr11:27031200-27031400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr11:27031200-27031400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:27031400-27033400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr11:27031400-27033600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr11:27031600-27033200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr11:27031600-27035600	Weak transcription	HMEC	breast
14	chr11:27032200-27033000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr11:27032200-27033200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr11:27032200-27036400	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr11:27032200-27036600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr11:27033000-27034200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr11:27033200-27033600	Enhancers	Placenta	Placenta
20	chr11:27033200-27033800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr11:27033200-27034000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr11:27033200-27034000	Enhancers	Fetal Lung	lung
23	chr11:27033200-27034200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr11:27033200-27034200	Enhancers	Rectal Smooth Muscle	rectum
25	chr11:27033200-27034400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr11:27033200-27034400	Enhancers	NHDF-Ad	bronchial
27	chr11:27033200-27035000	Enhancers	Brain Anterior Caudate	brain
28	chr11:27033200-27035000	Enhancers	Fetal Stomach	stomach
29	chr11:27033200-27035600	Enhancers	HSMMtube	muscle
30	chr11:27033200-27035800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr11:27033200-27036200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr11:27033200-27036600	Enhancers	Colon Smooth Muscle	Colon
33	chr11:27033400-27033600	Enhancers	Muscle Satellite Cultured Cells	--
34	chr11:27033400-27033800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr11:27033400-27033800	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr11:27033400-27033800	Enhancers	Aorta	Aorta
37	chr11:27033400-27034000	Active TSS	Brain Cingulate Gyrus	brain
38	chr11:27033400-27034400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr11:27033400-27034400	Enhancers	Brain Angular Gyrus	brain
40	chr11:27033400-27034400	Enhancers	HSMM	muscle
41	chr11:27033400-27034400	Enhancers	NH-A	brain
42	chr11:27033400-27034800	Enhancers	Brain Hippocampus Middle	brain
43	chr11:27033400-27034800	Enhancers	Fetal Intestine Small	intestine
44	chr11:27033400-27035000	Enhancers	Fetal Intestine Large	intestine
45	chr11:27033400-27035000	Enhancers	Fetal Muscle Leg	muscle
46	chr11:27033400-27035000	Enhancers	Ovary	ovary
47	chr11:27033400-27035200	Enhancers	Stomach Smooth Muscle	stomach
48	chr11:27033400-27035600	Enhancers	NHLF	lung
49	chr11:27033400-27035800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr11:27033400-27036000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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