Variant report

Variant	nsv564184
Chromosome Location	chr14:32688214-32734691
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1268)
CpG islands
(count:61)
Chromatin interactive
region (count:46)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1268 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:32721291-32721642	HepG2	liver:	n/a	chr14:32721574-32721590
2	ARID3A	chr14:32728811-32729269	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:32694417-32694578	K562	blood:	n/a	chr14:32694436-32694452 chr14:32694435-32694451
4	ARID3A	chr14:32694227-32694541	HepG2	liver:	n/a	chr14:32694436-32694452 chr14:32694435-32694451
5	ARID3A	chr14:32690131-32690331	HepG2	liver:	n/a	n/a
6	ATF1	chr14:32728882-32729227	K562	blood:	n/a	n/a
7	ATF2	chr14:32728594-32729315	GM12878	blood:	n/a	n/a
8	ATF2	chr14:32728492-32729284	GM12878	blood:	n/a	n/a
9	ATF3	chr14:32694292-32694475	K562	blood:	n/a	n/a
10	ATF3	chr14:32694218-32694573	K562	blood:	n/a	n/a
11	ATF3	chr14:32728847-32729205	K562	blood:	n/a	n/a
12	BACH1	chr14:32694402-32694433	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr14:32728917-32729152	H1-hESC	embryonic stem cell:	n/a	chr14:32729038-32729052
14	BACH1	chr14:32694327-32694425	K562	blood:	n/a	chr14:32694385-32694399
15	BATF	chr14:32728558-32729160	GM12878	blood:	n/a	chr14:32729042-32729052
16	BATF	chr14:32728582-32729224	GM12878	blood:	n/a	chr14:32729042-32729052
17	BCL11A	chr14:32728882-32729184	GM12878	blood:	n/a	chr14:32729040-32729049 chr14:32729041-32729050
18	BCL11A	chr14:32728557-32729299	GM12878	blood:	n/a	chr14:32729040-32729049 chr14:32729041-32729050
19	BCLAF1	chr14:32728842-32729317	GM12878	blood:	n/a	chr14:32729040-32729049 chr14:32729041-32729050
20	BCLAF1	chr14:32728890-32729256	GM12878	blood:	n/a	chr14:32729040-32729049 chr14:32729041-32729050
21	BHLHE40	chr14:32721268-32721645	HepG2	liver:	n/a	n/a
22	BHLHE40	chr14:32719532-32719580	K562	blood:	n/a	n/a
23	BHLHE40	chr14:32728457-32729168	GM12878	blood:	n/a	n/a
24	BHLHE40	chr14:32694209-32694417	K562	blood:	n/a	n/a
25	BHLHE40	chr14:32721359-32721558	K562	blood:	n/a	n/a
26	BRCA1	chr14:32721281-32721645	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr14:32733110-32733405	K562	blood:	n/a	n/a
28	CBX3	chr14:32728816-32729379	HCT-116	colon:	n/a	n/a
29	CBX3	chr14:32728831-32729249	K562	blood:	n/a	n/a
30	CBX3	chr14:32733187-32733393	K562	blood:	n/a	n/a
31	CBX3	chr14:32728875-32729112	K562	blood:	n/a	n/a
32	CEBPB	chr14:32724165-32724402	HepG2	liver:	n/a	n/a
33	CEBPB	chr14:32730156-32730366	IMR90	lung:	n/a	chr14:32730283-32730294
34	CEBPB	chr14:32702385-32702744	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr14:32730114-32730463	HepG2	liver:	n/a	chr14:32730283-32730294
36	CEBPB	chr14:32699299-32699878	A549	lung:	n/a	n/a
37	CEBPB	chr14:32700856-32700949	HepG2	liver:	n/a	n/a
38	CEBPB	chr14:32699305-32699793	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr14:32730131-32730366	A549	lung:	n/a	chr14:32730283-32730294
40	CEBPB	chr14:32702465-32702674	HepG2	liver:	n/a	n/a
41	CEBPB	chr14:32690327-32690369	A549	lung:	n/a	n/a
42	CEBPB	chr14:32724584-32724765	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr14:32692531-32692675	A549	lung:	n/a	chr14:32692647-32692658 chr14:32692649-32692658
44	CEBPB	chr14:32732362-32732637	HepG2	liver:	n/a	chr14:32732478-32732489
45	CEBPZ	chr14:32721294-32721692	HepG2	liver:	n/a	n/a
46	CHD1	chr14:32728818-32729406	IMR90	lung:	n/a	n/a
47	CHD1	chr14:32724104-32724574	IMR90	lung:	n/a	n/a
48	CHD2	chr14:32721344-32721550	K562	blood:	n/a	n/a
49	CHD2	chr14:32724442-32724492	HepG2	liver:	n/a	n/a
50	CREB1	chr14:32694281-32694451	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:32728466-32728516	HEK293	kidney:	embryo
2	chr14:32728466-32728516	HCF	heart:	n/a
3	chr14:32728466-32728516	HepG2	liver:	n/a
4	chr14:32728466-32728516	HCT-116	colon:	n/a
5	chr14:32728466-32728516	HRCEpiC	kidney:	n/a
6	chr14:32728466-32728516	ovcar-3	ovarian:	n/a
7	chr14:32728466-32728516	HAEpiC	amniotic membrane:	n/a
8	chr14:32728466-32728516	HRPEpiC	eye:	n/a
9	chr14:32728466-32728516	RPTEC	kidney:	n/a
10	chr14:32728466-32728516	SK-N-SH	brain:	n/a
11	chr14:32728466-32728516	Caco-2	colon:	n/a
12	chr14:32728466-32728516	GM12878	blood:	n/a
13	chr14:32728466-32728516	AG04449	skin:	fetal
14	chr14:32728466-32728516	SKMC	muscle:	n/a
15	chr14:32728466-32728516	H1-hESC	embryonic stem cell:	embryo
16	chr14:32728466-32728516	HNPCEpiC	eye:	n/a
17	chr14:32728466-32728516	HUVEC	blood vessel:	n/a
18	chr14:32728466-32728516	HCPEpiC	choroid plexus:	n/a
19	chr14:32728466-32728516	MCF10A-Er-Src	breast:	n/a
20	chr14:32728466-32728516	IMR90	lung:	fetal
21	chr14:32728466-32728516	MCF-7	breast:	n/a
22	chr14:32728466-32728516	LNCaP	prostate:	n/a
23	chr14:32728466-32728516	SK-N-SH_RA	brain:	n/a
24	chr14:32728466-32728516	ECC-1	luminal epithelium:	n/a
25	chr14:32728466-32728516	AG04450	lung:	fetal
26	chr14:32728466-32728516	AG09309	skin:	n/a
27	chr14:32728466-32728516	PFSK-1	brain:	n/a
28	chr14:32728466-32728516	HMEC	breast:	n/a
29	chr14:32728466-32728516	GM19239	blood:	n/a
30	chr14:32728466-32728516	HPAEpiC	pulmonary alveolar:	n/a
31	chr14:32728466-32728516	BE2_C	brain:	n/a
32	chr14:32728466-32728516	HRE	kidney:	n/a
33	chr14:32728466-32728516	AG10803	skin:	n/a
34	chr14:32728466-32728516	HCM	heart:	n/a
35	chr14:32728466-32728516	Hela-S3	cervix:	n/a
36	chr14:32728466-32728516	U87	brain:	n/a
37	chr14:32728466-32728516	K562	blood:	n/a
38	chr14:32728466-32728516	A549	lung:	n/a
39	chr14:32728466-32728516	CMK	blood:	n/a
40	chr14:32728466-32728516	NT2-D1	testis:	n/a
41	chr14:32728466-32728516	GM12891	blood:	n/a
42	chr14:32728466-32728516	SK-N-MC	brain:	n/a
43	chr14:32728466-32728516	SAEC	small airway:	n/a
44	chr14:32728466-32728516	AoSMC	blood vessel:	n/a
45	chr14:32728466-32728516	NH-A	brain:	n/a
46	chr14:32728466-32728516	HEEpiC	esophagus:	n/a
47	chr14:32728466-32728516	NHDF-neo	bronchial:	n/a
48	chr14:32728466-32728516	Hepatocyte	liver:	n/a
49	chr14:32728466-32728516	T-47D	breast:	n/a
50	chr14:32728466-32728516	GM12892	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:32542593..32543321-chr14:32699236..32699968,2	MCF-7	breast:
2	chr14:32413109..32414791-chr14:32721834..32724143,2	MCF-7	breast:
3	chr14:32403773..32404594-chr14:32713792..32714300,2	MCF-7	breast:
4	chr14:32673261..32674882-chr14:32699450..32701140,2	MCF-7	breast:
5	chr14:32727633..32729387-chr14:32733655..32736313,2	K562	blood:
6	chr14:32544361..32548285-chr14:32726893..32730492,3	MCF-7	breast:
7	chr14:32544703..32547760-chr14:32714259..32717739,4	MCF-7	breast:
8	chr14:32698519..32700470-chr14:32701311..32703904,2	K562	blood:
9	chr14:32542579..32543458-chr14:32720482..32722172,6	MCF-7	breast:
10	chr14:32547217..32549029-chr14:32699627..32701344,2	MCF-7	breast:
11	chr14:32693276..32694174-chr8:133368373..133369009,2	MCF-7	breast:
12	chr14:32723026..32725175-chr14:32851275..32852681,8	MCF-7	breast:
13	chr14:32394915..32396057-chr14:32721234..32722134,5	MCF-7	breast:
14	chr14:32687135..32688920-chr14:32690921..32692554,2	K562	blood:
15	chr14:32730953..32733918-chr14:32882288..32884788,2	MCF-7	breast:
16	chr14:32720658..32723115-chr14:32723813..32725711,2	K562	blood:
17	chr14:32723750..32724528-chr14:32851720..32852545,3	MCF-7	breast:
18	chr14:32544241..32545923-chr14:32709025..32711860,2	MCF-7	breast:
19	chr14:32714513..32717324-chr14:32719645..32722462,2	K562	blood:
20	chr14:32146895..32147481-chr14:32713372..32714254,2	MCF-7	breast:
21	chr14:32698519..32700470-chr14:32701311..32703904,2	K562	blood:
22	chr14:32691479..32693904-chr14:32695641..32697157,2	MCF-7	breast:
23	chr14:32676864..32680805-chr14:32686575..32689664,3	MCF-7	breast:
24	chr14:32404299..32405896-chr14:32722271..32724714,2	MCF-7	breast:
25	chr14:32542534..32543435-chr14:32713337..32714270,5	MCF-7	breast:
26	chr14:32542464..32543042-chr14:32723232..32724070,2	K562	blood:
27	chr14:32720658..32723115-chr14:32723813..32725711,2	K562	blood:
28	chr11:112568423..112569238-chr14:32721496..32722311,2	K562	blood:
29	chr14:32546346..32548378-chr14:32690479..32693406,2	K562	blood:
30	chr14:32542263..32548476-chr14:32718858..32724854,7	MCF-7	breast:
31	chr14:32714513..32717324-chr14:32719645..32722462,2	K562	blood:
32	chr14:32731562..32733975-chr14:32763214..32765356,2	MCF-7	breast:
33	chr14:32395062..32396238-chr14:32721028..32721952,3	MCF-7	breast:
34	chr14:32542547..32543455-chr14:32714700..32715234,2	MCF-7	breast:
35	chr14:32403221..32404535-chr14:32721037..32721949,6	MCF-7	breast:
36	chr14:32545977..32548666-chr14:32716017..32718304,2	MCF-7	breast:
37	chr14:32691479..32693904-chr14:32695641..32697157,2	MCF-7	breast:
38	chr14:32721143..32722141-chr14:32851679..32852591,2	MCF-7	breast:
39	chr14:32404021..32404551-chr14:32713638..32714218,2	MCF-7	breast:
40	chr14:32394989..32395944-chr14:32721409..32721963,3	K562	blood:
41	chr14:31925457..31927952-chr14:32721407..32723142,2	MCF-7	breast:
42	chr14:32723827..32724846-chr14:32835131..32836102,3	MCF-7	breast:
43	chr14:32542502..32543704-chr14:32720937..32721764,5	MCF-7	breast:
44	chr14:32542506..32543573-chr14:32720989..32721921,5	K562	blood:
45	chr14:32687135..32688920-chr14:32690921..32692554,2	K562	blood:
46	chr14:32727633..32729387-chr14:32733655..32736313,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C14orf126-10	chr14:32710730-32712299	NONHSAT036302

No data

Variant related genes	Relation type
ENSG00000258619	TF binding region
ENSG00000258619	CpG island
ENSG00000100852	chromatin interactions
ENSG00000258655	chromatin interactions
ENSG00000203546	chromatin interactions
ENSG00000258474	chromatin interactions
ENSG00000129480	chromatin interactions

Extended variants
information (count: 1918 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1918 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2149663	chr14:32688214-32688215	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113959903	chr14:32688225-32688226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs137908275	chr14:32688244-32688245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184847521	chr14:32688276-32688277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs538074605	chr14:32688280-32688281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs565211968	chr14:32688322-32688323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556703177	chr14:32688323-32688324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532319048	chr14:32688333-32688334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577693552	chr14:32688360-32688361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551718063	chr14:32688402-32688403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545086177	chr14:32688470-32688471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553844422	chr14:32688471-32688472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572071865	chr14:32688522-32688523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563109581	chr14:32688523-32688524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149446251	chr14:32688524-32688525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531617275	chr14:32688545-32688546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543278203	chr14:32688547-32688548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188790572	chr14:32688571-32688572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566745589	chr14:32688586-32688587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143959070	chr14:32688595-32688596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181742462	chr14:32688615-32688616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184786653	chr14:32688653-32688654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527741984	chr14:32688728-32688729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376098025	chr14:32688749-32688750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527703921	chr14:32688759-32688760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140368969	chr14:32688791-32688792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567901328	chr14:32688805-32688806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538508873	chr14:32688810-32688811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371502169	chr14:32688848-32688849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs117467695	chr14:32688860-32688861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142739118	chr14:32688893-32688894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553925955	chr14:32688904-32688905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548679463	chr14:32688922-32688923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147832161	chr14:32688926-32688927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs147416179	chr14:32688931-32688932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542678113	chr14:32688981-32688982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs8020915	chr14:32688986-32688987	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs139663458	chr14:32689060-32689061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543691470	chr14:32689121-32689122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564990569	chr14:32689136-32689137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532341668	chr14:32689162-32689163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35265337	chr14:32689167-32689168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111455189	chr14:32689184-32689185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556406701	chr14:32689195-32689196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577886929	chr14:32689230-32689231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531632922	chr14:32689262-32689263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34247177	chr14:32689312-32689313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142697140	chr14:32689325-32689326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527766872	chr14:32689347-32689348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373470802	chr14:32689350-32689351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	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
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32673600-32692800	Weak transcription	Psoas Muscle	Psoas
2	chr14:32675800-32694000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr14:32686800-32694000	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr14:32687000-32694000	Weak transcription	Duodenum Mucosa	Duodenum
5	chr14:32688200-32688400	Enhancers	Left Ventricle	heart
6	chr14:32688200-32691000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr14:32688400-32694000	Weak transcription	Brain Substantia Nigra	brain
8	chr14:32688400-32694200	Weak transcription	Left Ventricle	heart
9	chr14:32690000-32690200	ZNF genes & repeats	Fetal Intestine Small	intestine
10	chr14:32690000-32690400	Enhancers	HepG2	liver
11	chr14:32690000-32690600	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr14:32690200-32690800	Weak transcription	Fetal Intestine Small	intestine
13	chr14:32690400-32690600	Enhancers	Rectal Mucosa Donor 29	rectum
14	chr14:32690600-32693800	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr14:32690800-32691200	Enhancers	Fetal Intestine Small	intestine
16	chr14:32690800-32691400	Enhancers	Fetal Intestine Large	intestine
17	chr14:32691000-32691200	Enhancers	Sigmoid Colon	Sigmoid Colon
18	chr14:32691000-32691400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr14:32691000-32691400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr14:32691200-32694000	Weak transcription	Fetal Intestine Small	intestine
21	chr14:32691400-32693400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr14:32691400-32694400	Weak transcription	Fetal Intestine Large	intestine
23	chr14:32691400-32699800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr14:32693400-32694200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr14:32693600-32693800	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr14:32693800-32694400	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr14:32693800-32695800	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr14:32694000-32694400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr14:32694000-32694400	Enhancers	Aorta	Aorta
30	chr14:32694000-32694400	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr14:32694000-32694400	Enhancers	Ovary	ovary
32	chr14:32694000-32694600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr14:32694000-32694600	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr14:32694000-32694600	Enhancers	Duodenum Mucosa	Duodenum
35	chr14:32694000-32695000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr14:32694000-32695000	Enhancers	Brain Cingulate Gyrus	brain
37	chr14:32694000-32695000	Enhancers	Brain Substantia Nigra	brain
38	chr14:32694000-32695000	Enhancers	A549	lung
39	chr14:32694000-32695000	Enhancers	NH-A	brain
40	chr14:32694000-32695200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr14:32694000-32695200	Enhancers	Hela-S3	cervix
42	chr14:32694000-32695400	Enhancers	NHEK	skin
43	chr14:32694000-32695600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr14:32694000-32695600	Enhancers	Brain Hippocampus Middle	brain
45	chr14:32694000-32695600	Enhancers	Colon Smooth Muscle	Colon
46	chr14:32694000-32695600	Enhancers	Rectal Smooth Muscle	rectum
47	chr14:32694000-32695600	Enhancers	NHDF-Ad	bronchial
48	chr14:32694000-32695800	Enhancers	Fetal Intestine Small	intestine
49	chr14:32694000-32695800	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr14:32694000-32696000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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