Variant report

Variant	nsv510639
Chromosome Location	chr14:65853883-65884315
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	chr14:65882360-65882842	K562	blood:	n/a	n/a
2	ARID3A	chr14:65879048-65879428	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:65881803-65882062	K562	blood:	n/a	chr14:65881991-65882007 chr14:65881992-65882008
4	ATF2	chr14:65878149-65878731	GM12878	blood:	n/a	n/a
5	ATF2	chr14:65879101-65879487	GM12878	blood:	n/a	n/a
6	ATF2	chr14:65878954-65879590	GM12878	blood:	n/a	n/a
7	ATF2	chr14:65878935-65879439	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr14:65879086-65879534	A549	lung:	n/a	chr14:65879340-65879349
9	ATF3	chr14:65878972-65879545	A549	lung:	n/a	chr14:65879340-65879349
10	BACH1	chr14:65879013-65879315	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr14:65878938-65879500	A549	lung:	n/a	chr14:65879384-65879397 chr14:65879279-65879292
12	BCL3	chr14:65878352-65880086	GM12878	blood:	n/a	chr14:65879708-65879721 chr14:65879384-65879397 chr14:65878599-65878608 chr14:65879763-65879772 chr14:65879279-65879292 chr14:65879586-65879595 chr14:65879766-65879775 chr14:65879587-65879600
13	BCLAF1	chr14:65878372-65879479	GM12878	blood:	n/a	chr14:65879384-65879397 chr14:65878599-65878608 chr14:65879279-65879292
14	BCLAF1	chr14:65878451-65880046	GM12878	blood:	n/a	chr14:65879708-65879721 chr14:65879384-65879397 chr14:65878599-65878608 chr14:65879763-65879772 chr14:65879279-65879292 chr14:65879586-65879595 chr14:65879766-65879775 chr14:65879587-65879600
15	BCLAF1	chr14:65880254-65881026	GM12878	blood:	n/a	chr14:65880264-65880273
16	BHLHE40	chr14:65879155-65879530	K562	blood:	n/a	chr14:65879506-65879522 chr14:65879455-65879471
17	BHLHE40	chr14:65878942-65879567	HepG2	liver:	n/a	chr14:65879506-65879522 chr14:65879455-65879471
18	BHLHE40	chr14:65880419-65880464	K562	blood:	n/a	n/a
19	BHLHE40	chr14:65878424-65879949	GM12878	blood:	n/a	chr14:65879506-65879522 chr14:65879455-65879471
20	BHLHE40	chr14:65879038-65879515	A549	lung:	n/a	chr14:65879455-65879471
21	BHLHE40	chr14:65878495-65878716	K562	blood:	n/a	n/a
22	BRCA1	chr14:65879150-65879791	HepG2	liver:	n/a	n/a
23	BRCA1	chr14:65879150-65879366	GM12878	blood:	n/a	n/a
24	BRCA1	chr14:65878973-65879829	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr14:65878961-65879399	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr14:65878571-65878681	GM12878	blood:	n/a	n/a
27	BRCA1	chr14:65878359-65878532	HepG2	liver:	n/a	n/a
28	CBX3	chr14:65861943-65862436	K562	blood:	n/a	n/a
29	CCNT2	chr14:65879008-65880028	K562	blood:	n/a	chr14:65879340-65879349
30	CEBPB	chr14:65878862-65879393	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr14:65879070-65879447	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr14:65880539-65880739	Hela-S3	cervix:	n/a	n/a
33	CEBPD	chr14:65878507-65878869	HepG2	liver:	n/a	n/a
34	CHD1	chr14:65879023-65879292	H1-hESC	embryonic stem cell:	n/a	chr14:65879160-65879170
35	CHD1	chr14:65877984-65880997	IMR90	lung:	n/a	chr14:65879341-65879351 chr14:65879708-65879718 chr14:65879918-65879928 chr14:65879160-65879170
36	CHD1	chr14:65878234-65878415	GM12878	blood:	n/a	n/a
37	CHD1	chr14:65879768-65879974	H1-hESC	embryonic stem cell:	n/a	chr14:65879918-65879928
38	CHD1	chr14:65878732-65879412	GM12878	blood:	n/a	chr14:65879341-65879351 chr14:65879160-65879170
39	CHD2	chr14:65878344-65879876	H1-hESC	embryonic stem cell:	n/a	chr14:65879341-65879351 chr14:65879708-65879718 chr14:65879160-65879170
40	CHD2	chr14:65879536-65879843	K562	blood:	n/a	chr14:65879708-65879718
41	CHD2	chr14:65878387-65880282	GM12878	blood:	n/a	chr14:65879341-65879351 chr14:65879708-65879718 chr14:65879918-65879928 chr14:65879160-65879170
42	CHD2	chr14:65878406-65878693	HepG2	liver:	n/a	n/a
43	CHD2	chr14:65878325-65880371	Hela-S3	cervix:	n/a	chr14:65879341-65879351 chr14:65879708-65879718 chr14:65879918-65879928 chr14:65879160-65879170
44	CHD2	chr14:65878955-65879944	HepG2	liver:	n/a	chr14:65879341-65879351 chr14:65879708-65879718 chr14:65879918-65879928 chr14:65879160-65879170
45	CHD2	chr14:65878389-65878692	K562	blood:	n/a	n/a
46	CHD2	chr14:65880138-65880328	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr14:65878276-65878842	A549	lung:	n/a	n/a
48	CREB1	chr14:65878213-65879959	HepG2	liver:	n/a	n/a
49	CREB1	chr14:65878298-65880034	GM12878	blood:	n/a	n/a
50	CREB1	chr14:65878939-65879571	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:65876437-65876487	HRCEpiC	kidney:	n/a
2	chr14:65876437-65876487	HRCEpiC	kidney:	n/a
3	chr14:65876476-65876526	RPTEC	kidney:	n/a
4	chr14:65881787-65881837	A549	lung:	n/a
5	chr14:65880036-65880086	ovcar-3	ovarian:	n/a
6	chr14:65876476-65876526	CMK	blood:	n/a
7	chr14:65879007-65879057	LNCaP	prostate:	n/a
8	chr14:65880369-65880419	HCPEpiC	choroid plexus:	n/a
9	chr14:65879007-65879057	Caco-2	colon:	n/a
10	chr14:65881787-65881837	HEEpiC	esophagus:	n/a
11	chr14:65878633-65878683	AG04450	lung:	fetal
12	chr14:65881787-65881837	ECC-1	luminal epithelium:	n/a
13	chr14:65876865-65876915	AG04449	skin:	fetal
14	chr14:65880369-65880419	HCT-116	colon:	n/a
15	chr14:65881787-65881837	Hela-S3	cervix:	n/a
16	chr14:65880369-65880419	AoSMC	blood vessel:	n/a
17	chr14:65878866-65878916	GM12878	blood:	n/a
18	chr14:65879906-65879956	Hepatocyte	liver:	n/a
19	chr14:65876737-65876787	NHDF-neo	bronchial:	n/a
20	chr14:65876437-65876487	GM19239	blood:	n/a
21	chr14:65879396-65879446	MCF-7	breast:	n/a
22	chr14:65879396-65879446	NT2-D1	testis:	n/a
23	chr14:65876476-65876526	HCF	heart:	n/a
24	chr14:65876737-65876787	H1-hESC	embryonic stem cell:	embryo
25	chr14:65878866-65878916	AoSMC	blood vessel:	n/a
26	chr14:65879893-65879943	ECC-1	luminal epithelium:	n/a
27	chr14:65876476-65876526	SK-N-MC	brain:	n/a
28	chr14:65878633-65878683	HCT-116	colon:	n/a
29	chr14:65878633-65878683	MCF-7	breast:	n/a
30	chr14:65876476-65876526	AG09309	skin:	n/a
31	chr14:65881787-65881837	HIPEpiC	eye:	n/a
32	chr14:65876737-65876787	CMK	blood:	n/a
33	chr14:65878866-65878916	Caco-2	colon:	n/a
34	chr14:65879393-65879443	HCPEpiC	choroid plexus:	n/a
35	chr14:65876476-65876526	HEK293	kidney:	embryo
36	chr14:65876865-65876915	RPTEC	kidney:	n/a
37	chr14:65879893-65879943	HNPCEpiC	eye:	n/a
38	chr14:65879393-65879443	Hela-S3	cervix:	n/a
39	chr14:65880369-65880419	SK-N-SH	brain:	n/a
40	chr14:65878866-65878916	GM19239	blood:	n/a
41	chr14:65876865-65876915	NHDF-neo	bronchial:	n/a
42	chr14:65879393-65879443	HIPEpiC	eye:	n/a
43	chr14:65879007-65879057	AG09319	gingival:	n/a
44	chr14:65878866-65878916	AG04450	lung:	fetal
45	chr14:65879393-65879443	PANC-1	pancreas:	n/a
46	chr14:65876476-65876526	MCF10A-Er-Src	breast:	n/a
47	chr14:65876865-65876915	BJ	skin:	n/a
48	chr14:65878633-65878683	SK-N-SH	brain:	n/a
49	chr14:65876865-65876915	HNPCEpiC	eye:	n/a
50	chr14:65880369-65880419	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:65876760..65881066-chr14:65882756..65887312,10	MCF-7	breast:
2	chr14:65879676..65881204-chr14:65933662..65936142,2	MCF-7	breast:
3	chr14:65881391..65882373-chr14:66299222..66299740,2	MCF-7	breast:
4	chr14:65881498..65882398-chr14:66291188..66291694,2	K562	blood:
5	chr14:65876592..65878564-chr6:54710365..54711981,2	MCF-7	breast:
6	chr14:65878879..65879745-chr16:87350756..87351618,2	Hela-S3	cervix:
7	chr14:65799114..65802639-chr14:65877920..65880470,4	MCF-7	breast:
8	chr14:65882552..65883151-chr14:66291137..66291691,2	MCF-7	breast:
9	chr14:65569137..65571197-chr14:65878383..65880649,2	MCF-7	breast:
10	chr14:65864996..65866526-chr14:65868395..65870395,2	K562	blood:
11	chr14:65864996..65866526-chr14:65868395..65870395,2	K562	blood:
12	chr14:65682951..65699539-chr14:65874873..65882779,51	MCF-7	breast:
13	chr14:65745595..65748280-chr14:65878483..65880878,2	MCF-7	breast:
14	chr14:65854015..65856643-chr14:65859496..65861468,2	K562	blood:
15	chr14:65862260..65865116-chr14:65877901..65880398,3	MCF-7	breast:
16	chr14:65685385..65700060-chr14:65874568..65884730,76	MCF-7	breast:
17	chr14:65879206..65879893-chr17:58603152..58603849,2	MCF-7	breast:
18	chr14:65769045..65770910-chr14:65878599..65880667,2	MCF-7	breast:
19	chr14:65700105..65703075-chr14:65877781..65880441,2	MCF-7	breast:
20	chr14:65854015..65856643-chr14:65859496..65861468,2	K562	blood:
21	chr14:65868206..65869815-chr14:65870159..65873099,2	K562	blood:
22	chr14:65880088..65881939-chr14:66282983..66284508,2	MCF-7	breast:
23	chr14:65710525..65712418-chr14:65882853..65884868,2	MCF-7	breast:
24	chr14:65877301..65879579-chr20:36761978..36764479,2	MCF-7	breast:
25	chr14:65870073..65871791-chr14:65877472..65880048,2	K562	blood:
26	chr14:65877799..65879344-chr20:52823519..52825312,2	MCF-7	breast:
27	chr14:65880600..65882625-chr14:65890707..65892397,2	MCF-7	breast:
28	chr14:65881120..65883411-chr14:65884854..65887991,3	MCF-7	breast:
29	chr14:65868206..65869815-chr14:65870159..65873099,2	K562	blood:
30	chr14:65858309..65860376-chr14:65878138..65880007,2	MCF-7	breast:
31	chr14:65881389..65882114-chr14:66425535..66426219,3	MCF-7	breast:
32	chr14:65879358..65881230-chr14:65883604..65885446,2	K562	blood:
33	chr14:65721681..65725033-chr14:65872611..65875727,3	MCF-7	breast:
34	chr14:65688460..65689522-chr14:65878564..65879464,3	MCF-7	breast:
35	chr14:65700230..65702841-chr14:65877569..65880268,3	MCF-7	breast:
36	chr14:65688822..65689388-chr14:65878671..65879347,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAX-11	chr14:65877311-65879335	NONHSAT037389
2	lnc-MAX-10	chr14:65857081-65857420	NONHSAT037388

Variant related genes	Relation type
FUT8	TF binding region
FUT8	CpG island
ENSG00000259349	chromatin interactions
ENSG00000258878	chromatin interactions
ENSG00000260456	chromatin interactions
ENSG00000033170	chromatin interactions
ENSG00000062725	chromatin interactions
ENSG00000198959	chromatin interactions
ENSG00000255002	chromatin interactions
ENSG00000266740	chromatin interactions
ENSG00000101132	chromatin interactions
ENSG00000258760	chromatin interactions
ENSG00000270006	chromatin interactions
ENSG00000168143	chromatin interactions
ENSG00000125952	chromatin interactions
ENSG00000180662	chromatin interactions
ENSG00000259078	chromatin interactions

Extended variants
information (count: 1081 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1081 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575411080	chr14:65853924-65853925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs545638918	chr14:65853975-65853976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376911252	chr14:65854029-65854030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572773194	chr14:65854030-65854031	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116631909	chr14:65854047-65854048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561329454	chr14:65854061-65854062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs190845851	chr14:65854092-65854093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182991631	chr14:65854093-65854094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188609425	chr14:65854099-65854100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561661678	chr14:65854108-65854109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369145748	chr14:65854119-65854120	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552778795	chr14:65854157-65854158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192740012	chr14:65854174-65854175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12433416	chr14:65854175-65854176	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs548927556	chr14:65854195-65854196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371764587	chr14:65854204-65854205	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs79390727	chr14:65854227-65854228	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs12433423	chr14:65854237-65854238	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs117475483	chr14:65854260-65854261	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs77964848	chr14:65854262-65854263	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs140912928	chr14:65854263-65854264	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs552714611	chr14:65854320-65854321	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs115548080	chr14:65854326-65854327	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs541697633	chr14:65854345-65854346	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs183168097	chr14:65854365-65854366	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs534188823	chr14:65854421-65854422	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs373458284	chr14:65854429-65854430	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs543816432	chr14:65854536-65854537	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs73282223	chr14:65854555-65854556	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs149745466	chr14:65854608-65854609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs10136947	chr14:65854611-65854612	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs10136953	chr14:65854676-65854677	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs528744699	chr14:65854876-65854877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549176385	chr14:65854890-65854891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs145672291	chr14:65854902-65854903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562202304	chr14:65854907-65854908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs531238195	chr14:65854950-65854951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs8017202	chr14:65854958-65854959	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs187607344	chr14:65855026-65855027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570840650	chr14:65855074-65855075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs539527760	chr14:65855076-65855077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs4899177	chr14:65855103-65855104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528390545	chr14:65855111-65855112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546529206	chr14:65855119-65855120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs546715175	chr14:65855135-65855136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs12437394	chr14:65855214-65855215	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs1815654	chr14:65855232-65855233	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs555542377	chr14:65855247-65855248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538674306	chr14:65855250-65855251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550805485	chr14:65855270-65855271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Hypoplastic left heart syndrome	22349727	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65849400-65861800	Weak transcription	Brain Substantia Nigra	brain
2	chr14:65852800-65854000	Weak transcription	GM12878-XiMat	blood
3	chr14:65854000-65854200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr14:65854000-65854200	Enhancers	GM12878-XiMat	blood
5	chr14:65854000-65854400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr14:65854000-65854400	Enhancers	Fetal Thymus	thymus
7	chr14:65854200-65854600	Flanking Active TSS	GM12878-XiMat	blood
8	chr14:65854600-65855200	Enhancers	GM12878-XiMat	blood
9	chr14:65858200-65860000	Enhancers	Placenta	Placenta
10	chr14:65858800-65859000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr14:65859000-65859400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr14:65859000-65860000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr14:65859400-65859600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr14:65860200-65874600	Weak transcription	Stomach Mucosa	stomach
15	chr14:65861800-65862000	ZNF genes & repeats	Brain Substantia Nigra	brain
16	chr14:65861800-65862400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr14:65862600-65863600	ZNF genes & repeats	Primary B cells from peripheral blood	blood
18	chr14:65863600-65864600	Enhancers	Primary B cells from peripheral blood	blood
19	chr14:65864200-65864400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr14:65864400-65878400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr14:65864800-65865200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr14:65868000-65869600	Enhancers	Placenta	Placenta
23	chr14:65868800-65869000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr14:65869000-65877800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr14:65869400-65871600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr14:65869600-65870200	Enhancers	Duodenum Mucosa	Duodenum
27	chr14:65869600-65870400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr14:65869600-65870400	Enhancers	Muscle Satellite Cultured Cells	--
29	chr14:65869600-65870400	Enhancers	NHDF-Ad	bronchial
30	chr14:65869600-65870600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr14:65869600-65870600	Enhancers	Osteobl	bone
32	chr14:65869800-65870400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr14:65870000-65870400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr14:65870200-65870800	Enhancers	Ovary	ovary
35	chr14:65870200-65871600	Weak transcription	Duodenum Mucosa	Duodenum
36	chr14:65870400-65877600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr14:65870400-65877600	Weak transcription	NHDF-Ad	bronchial
38	chr14:65870600-65877800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr14:65870800-65878200	Weak transcription	Ovary	ovary
40	chr14:65871000-65877400	Weak transcription	Primary B cells from cord blood	blood
41	chr14:65873000-65877800	Weak transcription	Primary T cells from cord blood	blood
42	chr14:65874200-65876400	Weak transcription	Duodenum Mucosa	Duodenum
43	chr14:65874400-65877600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr14:65874600-65875200	Enhancers	Stomach Mucosa	stomach
45	chr14:65874800-65875000	Enhancers	Brain Substantia Nigra	brain
46	chr14:65875000-65875600	Weak transcription	Brain Substantia Nigra	brain
47	chr14:65875000-65877200	Enhancers	Brain Hippocampus Middle	brain
48	chr14:65875200-65877800	Weak transcription	Stomach Mucosa	stomach
49	chr14:65875600-65878000	Enhancers	Brain Substantia Nigra	brain
50	chr14:65875800-65877400	Enhancers	Brain Cingulate Gyrus	brain

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