Variant report

Variant	nsv901640
Chromosome Location	chr14:37782273-37963104
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:775)
CpG islands
(count:61)
Chromatin interactive
region (count:46)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:775 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:37798163-37799893	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:37935172-37936858	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:37854210-37854747	HepG2	liver:	n/a	chr14:37854604-37854612
4	ARID3A	chr14:37882908-37883266	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:37937245-37937930	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:37916975-37917561	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:37962806-37963218	HepG2	liver:	n/a	n/a
8	ATF1	chr14:37886466-37886666	K562	blood:	n/a	n/a
9	ATF1	chr14:37868829-37869057	K562	blood:	n/a	n/a
10	ATF3	chr14:37868759-37869025	K562	blood:	n/a	n/a
11	BHLHE40	chr14:37854614-37854788	HepG2	liver:	n/a	n/a
12	BHLHE40	chr14:37935661-37936300	HepG2	liver:	n/a	n/a
13	CEBPB	chr14:37962886-37963121	HepG2	liver:	n/a	n/a
14	CEBPB	chr14:37961519-37961800	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:37937293-37937508	IMR90	lung:	n/a	chr14:37937449-37937460
16	CEBPB	chr14:37867147-37867185	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr14:37961570-37961743	A549	lung:	n/a	n/a
18	CEBPB	chr14:37950147-37950352	HepG2	liver:	n/a	chr14:37950296-37950307
19	CEBPB	chr14:37868753-37869067	HepG2	liver:	n/a	chr14:37868895-37868906 chr14:37868894-37868907
20	CEBPB	chr14:37866985-37867271	HepG2	liver:	n/a	n/a
21	CEBPB	chr14:37868730-37869079	IMR90	lung:	n/a	chr14:37868895-37868906 chr14:37868894-37868907
22	CEBPB	chr14:37935878-37935967	K562	blood:	n/a	chr14:37935912-37935923 chr14:37935914-37935925
23	CEBPB	chr14:37868713-37869086	K562	blood:	n/a	chr14:37868895-37868906 chr14:37868894-37868907
24	CEBPB	chr14:37868840-37868959	Hela-S3	cervix:	n/a	chr14:37868895-37868906 chr14:37868894-37868907
25	CEBPB	chr14:37952890-37953331	MCF-7	breast:	n/a	n/a
26	CEBPB	chr14:37952857-37953222	K562	blood:	n/a	n/a
27	CEBPB	chr14:37792920-37793213	IMR90	lung:	n/a	n/a
28	CEBPB	chr14:37854490-37854791	MCF-7	breast:	n/a	chr14:37854544-37854557
29	CEBPB	chr14:37792902-37793196	HepG2	liver:	n/a	n/a
30	CEBPB	chr14:37935759-37936100	A549	lung:	n/a	chr14:37935912-37935923 chr14:37935914-37935925
31	CEBPB	chr14:37952866-37953238	HepG2	liver:	n/a	n/a
32	CEBPB	chr14:37952903-37953202	A549	lung:	n/a	n/a
33	CEBPB	chr14:37962189-37962375	HepG2	liver:	n/a	chr14:37962251-37962262 chr14:37962250-37962261
34	CEBPB	chr14:37880314-37880664	HepG2	liver:	n/a	n/a
35	CEBPB	chr14:37962862-37963192	IMR90	lung:	n/a	n/a
36	CEBPB	chr14:37875324-37875645	HepG2	liver:	n/a	chr14:37875492-37875505 chr14:37875492-37875503 chr14:37875494-37875505 chr14:37875492-37875505 chr14:37875397-37875408 chr14:37875494-37875505 chr14:37875492-37875505
37	CEBPB	chr14:37881059-37881505	HepG2	liver:	n/a	chr14:37881178-37881189
38	CEBPB	chr14:37881175-37881481	A549	lung:	n/a	chr14:37881178-37881189
39	CEBPB	chr14:37857277-37857321	HepG2	liver:	n/a	n/a
40	CEBPB	chr14:37793032-37793130	K562	blood:	n/a	n/a
41	CEBPB	chr14:37854470-37854783	HepG2	liver:	n/a	chr14:37854544-37854557
42	CEBPB	chr14:37882872-37883206	HepG2	liver:	n/a	n/a
43	CEBPB	chr14:37961531-37961805	IMR90	lung:	n/a	n/a
44	CEBPB	chr14:37952906-37953267	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr14:37935729-37936138	A549	lung:	n/a	chr14:37935912-37935923 chr14:37935914-37935925
46	CEBPB	chr14:37935591-37936194	HepG2	liver:	n/a	chr14:37935912-37935923 chr14:37935914-37935925
47	CEBPB	chr14:37868731-37869083	K562	blood:	n/a	chr14:37868895-37868906 chr14:37868894-37868907
48	CEBPB	chr14:37937274-37937545	HepG2	liver:	n/a	chr14:37937449-37937460
49	CEBPB	chr14:37866973-37867184	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr14:37935577-37936272	HepG2	liver:	n/a	chr14:37935912-37935923 chr14:37935914-37935925

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:37825967-37826017	ovcar-3	ovarian:	n/a
2	chr14:37825967-37826017	NB4	blood:	n/a
3	chr14:37825967-37826017	PFSK-1	brain:	n/a
4	chr14:37825967-37826017	HEK293	kidney:	embryo
5	chr14:37825967-37826017	PrEC	prostate:	n/a
6	chr14:37825967-37826017	HRCEpiC	kidney:	n/a
7	chr14:37825967-37826017	HRE	kidney:	n/a
8	chr14:37825967-37826017	GM12878	blood:	n/a
9	chr14:37825967-37826017	GM12891	blood:	n/a
10	chr14:37825967-37826017	HL-60	blood:	n/a
11	chr14:37825967-37826017	Hela-S3	cervix:	n/a
12	chr14:37825967-37826017	A549	lung:	n/a
13	chr14:37825967-37826017	U87	brain:	n/a
14	chr14:37825967-37826017	CMK	blood:	n/a
15	chr14:37825967-37826017	HNPCEpiC	eye:	n/a
16	chr14:37825967-37826017	SAEC	small airway:	n/a
17	chr14:37825967-37826017	GM19239	blood:	n/a
18	chr14:37825967-37826017	MCF-7	breast:	n/a
19	chr14:37825967-37826017	NHDF-neo	bronchial:	n/a
20	chr14:37825967-37826017	HEEpiC	esophagus:	n/a
21	chr14:37825967-37826017	GM06990	blood:	n/a
22	chr14:37825967-37826017	AoSMC	blood vessel:	n/a
23	chr14:37825967-37826017	K562	blood:	n/a
24	chr14:37825967-37826017	BJ	skin:	n/a
25	chr14:37825967-37826017	NHBE	bronchial:	n/a
26	chr14:37825967-37826017	HPAEpiC	pulmonary alveolar:	n/a
27	chr14:37825967-37826017	HCPEpiC	choroid plexus:	n/a
28	chr14:37825967-37826017	HUVEC	blood vessel:	n/a
29	chr14:37825967-37826017	RPTEC	kidney:	n/a
30	chr14:37825967-37826017	HCM	heart:	n/a
31	chr14:37825967-37826017	T-47D	breast:	n/a
32	chr14:37825967-37826017	Hepatocyte	liver:	n/a
33	chr14:37825967-37826017	NT2-D1	testis:	n/a
34	chr14:37825967-37826017	GM12892	blood:	n/a
35	chr14:37825967-37826017	HMEC	breast:	n/a
36	chr14:37825967-37826017	SK-N-SH	brain:	n/a
37	chr14:37825967-37826017	AG04449	skin:	fetal
38	chr14:37825967-37826017	IMR90	lung:	fetal
39	chr14:37825967-37826017	AG09319	gingival:	n/a
40	chr14:37825967-37826017	ProgFib	skin:	n/a
41	chr14:37825967-37826017	HIPEpiC	eye:	n/a
42	chr14:37825967-37826017	LNCaP	prostate:	n/a
43	chr14:37825967-37826017	HepG2	liver:	n/a
44	chr14:37825967-37826017	ECC-1	luminal epithelium:	n/a
45	chr14:37825967-37826017	HRPEpiC	eye:	n/a
46	chr14:37825967-37826017	SK-N-MC	brain:	n/a
47	chr14:37825967-37826017	MCF10A-Er-Src	breast:	n/a
48	chr14:37825967-37826017	AG09309	skin:	n/a
49	chr14:37825967-37826017	AG10803	skin:	n/a
50	chr14:37825967-37826017	SKMC	muscle:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:37923519..37926055-chr14:37998366..38001362,2	MCF-7	breast:
2	chr14:37904725..37909149-chr14:38061107..38065274,9	MCF-7	breast:
3	chr14:37899686..37902705-chr14:38064003..38066607,3	MCF-7	breast:
4	chr14:37814771..37816556-chr14:38063329..38065680,2	MCF-7	breast:
5	chr14:37903287..37907312-chr14:38059908..38064571,5	MCF-7	breast:
6	chr14:37922237..37924533-chr14:37931027..37932952,2	MCF-7	breast:
7	chr14:37895105..37897353-chr14:37902428..37905218,2	MCF-7	breast:
8	chr14:37868487..37870431-chr14:37872042..37874988,2	K562	blood:
9	chr14:37802283..37804083-chr14:38062449..38064880,2	MCF-7	breast:
10	chr14:37868487..37870431-chr14:37872042..37874988,2	K562	blood:
11	chr14:37845196..37847206-chr14:37851691..37853679,2	K562	blood:
12	chr14:37776717..37778378-chr14:37785144..37786956,2	MCF-7	breast:
13	chr14:37922172..37923880-chr14:37926758..37928419,2	MCF-7	breast:
14	chr14:37932975..37935866-chr14:38063340..38065304,3	MCF-7	breast:
15	chr14:37922172..37923880-chr14:37926758..37928419,2	MCF-7	breast:
16	chr14:37914831..37917471-chr14:37919271..37922132,2	MCF-7	breast:
17	chr14:37938461..37943364-chr14:38060246..38065845,4	MCF-7	breast:
18	chr14:37850388..37852120-chr14:38064172..38065752,2	MCF-7	breast:
19	chr14:37881541..37884067-chr14:38063012..38064941,2	MCF-7	breast:
20	chr14:37924566..37927073-chr14:38060566..38062784,2	MCF-7	breast:
21	chr14:37868011..37870667-chr14:37877895..37880422,2	K562	blood:
22	chr14:37884990..37886932-chr14:37888404..37890275,2	K562	blood:
23	chr14:37781292..37783643-chr14:37787358..37789012,2	MCF-7	breast:
24	chr14:37845196..37847206-chr14:37851691..37853679,2	K562	blood:
25	chr14:37922237..37924533-chr14:37931027..37932952,2	MCF-7	breast:
26	chr14:37840146..37842839-chr14:37843811..37846339,2	K562	blood:
27	chr14:37884990..37886932-chr14:37888404..37890275,2	K562	blood:
28	chr11:116508203..116508771-chr14:37786310..37786828,2	MCF-7	breast:
29	chr14:37789885..37792148-chr14:37882206..37884543,2	MCF-7	breast:
30	chr14:37789885..37792148-chr14:37882206..37884543,2	MCF-7	breast:
31	chr14:37797120..37799536-chr14:37801001..37803434,2	MCF-7	breast:
32	chr14:37923826..37925404-chr14:38041177..38044020,2	MCF-7	breast:
33	chr14:37781292..37783643-chr14:37787358..37789012,2	MCF-7	breast:
34	chr14:37868199..37870734-chr14:38056121..38058989,2	MCF-7	breast:
35	chr14:37858877..37861783-chr14:37988865..37991123,2	MCF-7	breast:
36	chr14:37914831..37917471-chr14:37919271..37922132,2	MCF-7	breast:
37	chr14:37868011..37870667-chr14:37877895..37880422,2	K562	blood:
38	chr14:37919150..37921478-chr14:38062353..38064686,2	MCF-7	breast:
39	chr14:37840146..37842839-chr14:37843811..37846339,2	K562	blood:
40	chr14:37897535..37899895-chr14:38063797..38065302,2	MCF-7	breast:
41	chr14:37905530..37906254-chr14:38016253..38017008,2	MCF-7	breast:
42	chr14:37793105..37794977-chr14:37796804..37798845,2	MCF-7	breast:
43	chr14:37797120..37799536-chr14:37801001..37803434,2	MCF-7	breast:
44	chr14:37793105..37794977-chr14:37796804..37798845,2	MCF-7	breast:
45	chr14:37811526..37813219-chr14:38057927..38059734,2	MCF-7	breast:
46	chr14:37889149..37891351-chr14:38062357..38065324,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTC6-2	chr14:37869005-37871105	NONHSAT036460
2	lnc-FOXA1-4	chr14:37853626-37855696	NONHSAT036459

No data

Variant related genes	Relation type
RNU6-886P	TF binding region
RNU6-886P	CpG island
ENSG00000207046	chromatin interactions
ENSG00000139865	chromatin interactions
ENSG00000129514	chromatin interactions
ENSG00000151338	chromatin interactions

Extended variants
information (count: 6369 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:6369 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10220291	chr14:37782273-37782274	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143889230	chr14:37782287-37782288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183560220	chr14:37782308-37782309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561187338	chr14:37782329-37782330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35584809	chr14:37782341-37782342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374508041	chr14:37782344-37782345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs398056994	chr14:37782345-37782346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs374850392	chr14:37782346-37782347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529994321	chr14:37782390-37782391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549743866	chr14:37782414-37782415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189051773	chr14:37782445-37782446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140322248	chr14:37782461-37782462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548420180	chr14:37782474-37782475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76986244	chr14:37782500-37782501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534334760	chr14:37782517-37782518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374937597	chr14:37782583-37782584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554118445	chr14:37782591-37782592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568446426	chr14:37782626-37782627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368478816	chr14:37782632-37782633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537335805	chr14:37782643-37782644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557315644	chr14:37782699-37782700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs193142729	chr14:37782767-37782768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372466900	chr14:37782804-37782805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142680364	chr14:37782811-37782812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113383153	chr14:37782846-37782847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553445718	chr14:37782865-37782866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569818496	chr14:37782880-37782881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573345703	chr14:37782885-37782886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115647471	chr14:37782891-37782892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139717683	chr14:37782942-37782943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182651343	chr14:37782956-37782957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186805666	chr14:37783018-37783019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142642555	chr14:37783024-37783025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532346007	chr14:37783047-37783048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552054555	chr14:37783078-37783079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565461334	chr14:37783085-37783086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs55995849	chr14:37783090-37783091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11156941	chr14:37783093-37783094	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs567714148	chr14:37783120-37783121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536593045	chr14:37783151-37783152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557641994	chr14:37783188-37783189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571019702	chr14:37783234-37783235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570612827	chr14:37783247-37783248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370150355	chr14:37783275-37783276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540043904	chr14:37783289-37783290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534320121	chr14:37783296-37783297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191683579	chr14:37783307-37783308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573409187	chr14:37783312-37783313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370822126	chr14:37783369-37783370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552523593	chr14:37783411-37783412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Osteosarcoma	21215367	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37752400-37796200	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr14:37759000-37810600	Weak transcription	Psoas Muscle	Psoas
3	chr14:37762600-37812400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr14:37763200-37797400	Weak transcription	Left Ventricle	heart
5	chr14:37769400-37800000	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr14:37774200-37785600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr14:37775200-37817000	Weak transcription	Aorta	Aorta
8	chr14:37776200-37792400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr14:37778800-37785200	Weak transcription	Adipose Nuclei	Adipose
10	chr14:37780400-37786200	Weak transcription	HUVEC	blood vessel
11	chr14:37780400-37795000	Weak transcription	Ovary	ovary
12	chr14:37780600-37796800	Weak transcription	HepG2	liver
13	chr14:37786200-37787400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr14:37786800-37787400	Enhancers	Primary hematopoietic stem cells	blood
15	chr14:37788200-37789000	Enhancers	NHEK	skin
16	chr14:37789000-37792200	Weak transcription	NHEK	skin
17	chr14:37789400-37789600	Enhancers	A549	lung
18	chr14:37789400-37790200	Enhancers	Hela-S3	cervix
19	chr14:37789600-37792800	Weak transcription	A549	lung
20	chr14:37791400-37791600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr14:37791600-37799600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr14:37792800-37799800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr14:37793200-37794000	Enhancers	Brain Germinal Matrix	brain
24	chr14:37795000-37796200	Strong transcription	Ovary	ovary
25	chr14:37795600-37795800	Enhancers	Gastric	stomach
26	chr14:37795600-37797800	Weak transcription	Fetal Intestine Small	intestine
27	chr14:37796200-37821400	Weak transcription	Ovary	ovary
28	chr14:37796800-37798200	Enhancers	HepG2	liver
29	chr14:37797800-37798000	Enhancers	A549	lung
30	chr14:37797800-37798200	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr14:37797800-37798200	Enhancers	Small Intestine	intestine
32	chr14:37797800-37798400	Enhancers	Duodenum Mucosa	Duodenum
33	chr14:37797800-37798600	Enhancers	HUVEC	blood vessel
34	chr14:37797800-37798800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr14:37797800-37799000	Enhancers	Fetal Intestine Large	intestine
36	chr14:37797800-37799000	Enhancers	Fetal Intestine Small	intestine
37	chr14:37797800-37799000	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr14:37797800-37800000	Enhancers	Liver	Liver
39	chr14:37798000-37798200	Flanking Active TSS	A549	lung
40	chr14:37798200-37798400	Enhancers	A549	lung
41	chr14:37798200-37799200	Flanking Active TSS	HepG2	liver
42	chr14:37798200-37801000	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr14:37798400-37798800	Weak transcription	Duodenum Mucosa	Duodenum
44	chr14:37798400-37799000	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr14:37798400-37799000	Flanking Active TSS	A549	lung
46	chr14:37798600-37811200	Weak transcription	HUVEC	blood vessel
47	chr14:37798800-37799200	Enhancers	Duodenum Mucosa	Duodenum
48	chr14:37799000-37799200	Active TSS	A549	lung
49	chr14:37799000-37801200	Weak transcription	Fetal Intestine Large	intestine
50	chr14:37799200-37799600	Enhancers	HepG2	liver

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