Variant report

Variant	nsv564933
Chromosome Location	chr14:65667546-65710580
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1579)
CpG islands
(count:306)
Chromatin interactive
region (count:74)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1579 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:65693405-65694433	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:65705871-65705878	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:65696786-65696882	K562	blood:	n/a	n/a
4	ARID3A	chr14:65710400-65710925	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:65709002-65709879	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:65706131-65706466	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:65696583-65697677	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:65678125-65678490	K562	blood:	n/a	n/a
9	ARID3A	chr14:65698249-65698596	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:65704844-65705411	HepG2	liver:	n/a	n/a
11	ATF1	chr14:65706101-65706348	K562	blood:	n/a	n/a
12	ATF1	chr14:65674949-65675149	K562	blood:	n/a	n/a
13	ATF1	chr14:65676877-65677224	K562	blood:	n/a	n/a
14	ATF1	chr14:65678101-65678411	K562	blood:	n/a	n/a
15	ATF1	chr14:65672237-65672405	K562	blood:	n/a	n/a
16	ATF1	chr14:65704691-65705078	K562	blood:	n/a	n/a
17	ATF1	chr14:65695273-65695449	K562	blood:	n/a	n/a
18	ATF2	chr14:65674669-65675610	GM12878	blood:	n/a	n/a
19	ATF2	chr14:65671966-65672572	GM12878	blood:	n/a	n/a
20	ATF2	chr14:65671841-65674132	GM12878	blood:	n/a	n/a
21	ATF2	chr14:65676588-65677170	GM12878	blood:	n/a	n/a
22	ATF2	chr14:65672774-65673886	GM12878	blood:	n/a	n/a
23	ATF2	chr14:65695027-65695763	GM12878	blood:	n/a	n/a
24	ATF2	chr14:65695005-65695758	GM12878	blood:	n/a	n/a
25	ATF2	chr14:65676522-65677325	GM12878	blood:	n/a	n/a
26	ATF2	chr14:65692024-65692684	GM12878	blood:	n/a	n/a
27	ATF3	chr14:65678113-65678420	K562	blood:	n/a	n/a
28	BACH1	chr14:65696360-65696709	H1-hESC	embryonic stem cell:	n/a	n/a
29	BATF	chr14:65672658-65674315	GM12878	blood:	n/a	n/a
30	BATF	chr14:65692206-65692615	GM12878	blood:	n/a	n/a
31	BATF	chr14:65675229-65675482	GM12878	blood:	n/a	chr14:65675361-65675372
32	BATF	chr14:65676813-65677146	GM12878	blood:	n/a	n/a
33	BATF	chr14:65672135-65672469	GM12878	blood:	n/a	n/a
34	BATF	chr14:65672149-65672545	GM12878	blood:	n/a	n/a
35	BATF	chr14:65672936-65673837	GM12878	blood:	n/a	n/a
36	BATF	chr14:65695081-65695545	GM12878	blood:	n/a	n/a
37	BATF	chr14:65676779-65677168	GM12878	blood:	n/a	n/a
38	BATF	chr14:65692027-65692648	GM12878	blood:	n/a	n/a
39	BATF	chr14:65695093-65695515	GM12878	blood:	n/a	n/a
40	BCL11A	chr14:65695196-65695540	GM12878	blood:	n/a	n/a
41	BCL11A	chr14:65692239-65692563	GM12878	blood:	n/a	n/a
42	BCL11A	chr14:65676725-65677215	GM12878	blood:	n/a	n/a
43	BCL11A	chr14:65692188-65692602	GM12878	blood:	n/a	n/a
44	BCL11A	chr14:65672134-65672464	GM12878	blood:	n/a	n/a
45	BCL11A	chr14:65695074-65695576	GM12878	blood:	n/a	n/a
46	BCL11A	chr14:65673514-65674055	GM12878	blood:	n/a	n/a
47	BCL11A	chr14:65672061-65672527	GM12878	blood:	n/a	n/a
48	BCL11A	chr14:65676815-65677169	GM12878	blood:	n/a	n/a
49	BCL11A	chr14:65672937-65674148	GM12878	blood:	n/a	chr14:65673142-65673151
50	BCL3	chr14:65673002-65674310	GM12878	blood:	n/a	chr14:65673142-65673151

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:65696480-65696530	GM12891	blood:	n/a
2	chr14:65696480-65696530	GM12891	blood:	n/a
3	chr14:65673646-65673696	ECC-1	luminal epithelium:	n/a
4	chr14:65681230-65681280	PFSK-1	brain:	n/a
5	chr14:65704960-65705010	A549	lung:	n/a
6	chr14:65681230-65681280	SK-N-MC	brain:	n/a
7	chr14:65704156-65704206	A549	lung:	n/a
8	chr14:65704960-65705010	HRE	kidney:	n/a
9	chr14:65704156-65704206	PrEC	prostate:	n/a
10	chr14:65681230-65681280	MCF-7	breast:	n/a
11	chr14:65696480-65696530	A549	lung:	n/a
12	chr14:65704960-65705010	HL-60	blood:	n/a
13	chr14:65704960-65705010	SK-N-MC	brain:	n/a
14	chr14:65696480-65696530	Hela-S3	cervix:	n/a
15	chr14:65681230-65681280	CMK	blood:	n/a
16	chr14:65704156-65704206	Hepatocyte	liver:	n/a
17	chr14:65696480-65696530	AG09319	gingival:	n/a
18	chr14:65704156-65704206	HRCEpiC	kidney:	n/a
19	chr14:65704156-65704206	RPTEC	kidney:	n/a
20	chr14:65704960-65705010	ovcar-3	ovarian:	n/a
21	chr14:65704960-65705010	PANC-1	pancreas:	n/a
22	chr14:65681230-65681280	AG04449	skin:	fetal
23	chr14:65704960-65705010	PFSK-1	brain:	n/a
24	chr14:65681230-65681280	NHDF-neo	bronchial:	n/a
25	chr14:65704960-65705010	AG09319	gingival:	n/a
26	chr14:65704156-65704206	SK-N-MC	brain:	n/a
27	chr14:65696480-65696530	HPAEpiC	pulmonary alveolar:	n/a
28	chr14:65704156-65704206	GM12891	blood:	n/a
29	chr14:65704960-65705010	MCF10A-Er-Src	breast:	n/a
30	chr14:65673646-65673696	K562	blood:	n/a
31	chr14:65681230-65681280	GM06990	blood:	n/a
32	chr14:65704960-65705010	U87	brain:	n/a
33	chr14:65704960-65705010	AG04449	skin:	fetal
34	chr14:65681230-65681280	HCF	heart:	n/a
35	chr14:65681230-65681280	SKMC	muscle:	n/a
36	chr14:65704960-65705010	T-47D	breast:	n/a
37	chr14:65704960-65705010	GM12878	blood:	n/a
38	chr14:65696480-65696530	HAEpiC	amniotic membrane:	n/a
39	chr14:65704156-65704206	HCF	heart:	n/a
40	chr14:65681230-65681280	ovcar-3	ovarian:	n/a
41	chr14:65696480-65696530	HCM	heart:	n/a
42	chr14:65696480-65696530	HEEpiC	esophagus:	n/a
43	chr14:65696480-65696530	ECC-1	luminal epithelium:	n/a
44	chr14:65673646-65673696	NHBE	bronchial:	n/a
45	chr14:65704960-65705010	HepG2	liver:	n/a
46	chr14:65681230-65681280	NB4	blood:	n/a
47	chr14:65696480-65696530	PFSK-1	brain:	n/a
48	chr14:65681230-65681280	Jurkat	blood:	n/a
49	chr14:65704960-65705010	HCM	heart:	n/a
50	chr14:65681230-65681280	HRPEpiC	eye:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:65689122..65691456-chr14:65806206..65809002,2	MCF-7	breast:
2	chr14:65696039..65697546-chr14:65753255..65754853,2	MCF-7	breast:
3	chr14:65703266..65707350-chr14:65709369..65712516,3	K562	blood:
4	chr14:65631189..65632726-chr14:65692735..65694396,2	MCF-7	breast:
5	chr14:65689494..65692237-chr14:65695472..65698101,2	K562	blood:
6	chr14:65696604..65698657-chr14:65706204..65708336,3	K562	blood:
7	chr14:65709528..65711067-chr14:65712244..65714160,2	MCF-7	breast:
8	chr14:65685385..65700060-chr14:65874568..65884730,76	MCF-7	breast:
9	chr14:65583338..65585299-chr14:65708352..65712057,3	MCF-7	breast:
10	chr14:65703752..65707201-chr14:65707603..65710596,4	MCF-7	breast:
11	chr10:24512569..24513529-chr14:65673481..65674224,2	MCF-7	breast:
12	chr14:65692463..65695041-chr14:65818683..65822827,3	MCF-7	breast:
13	chr14:65695112..65697010-chr14:65821133..65822947,2	MCF-7	breast:
14	chr14:65703192..65707325-chr14:65876761..65880324,6	MCF-7	breast:
15	chr14:65583557..65585174-chr14:65692284..65694348,2	MCF-7	breast:
16	chr14:65687275..65689393-chr14:65708965..65710587,2	MCF-7	breast:
17	chr14:65693679..65698667-chr14:65701405..65705460,7	MCF-7	breast:
18	chr14:65696604..65698657-chr14:65706204..65708336,3	K562	blood:
19	chr14:65670192..65672045-chr14:65675137..65676974,2	K562	blood:
20	chr14:65692867..65695461-chr14:65904405..65906189,2	MCF-7	breast:
21	chr14:65691185..65703550-chr14:65706694..65715001,23	MCF-7	breast:
22	chr14:65630625..65634047-chr14:65708648..65711135,3	MCF-7	breast:
23	chr14:65694260..65697862-chr14:65826001..65829124,3	MCF-7	breast:
24	chr14:65708249..65716123-chr14:65876687..65882798,15	MCF-7	breast:
25	chr14:65689494..65692237-chr14:65695472..65698101,2	K562	blood:
26	chr14:65708389..65714331-chr14:65715596..65724154,17	MCF-7	breast:
27	chr14:65684066..65685787-chr14:65691739..65693406,2	MCF-7	breast:
28	chr14:65700230..65702841-chr14:65877569..65880268,3	MCF-7	breast:
29	chr14:65703346..65706250-chr14:65727582..65729755,2	MCF-7	breast:
30	chr14:65687538..65689210-chr14:65800729..65803430,2	MCF-7	breast:
31	chr14:65698766..65701527-chr14:65799891..65802325,2	MCF-7	breast:
32	chr14:65681195..65684359-chr14:65877909..65881383,4	MCF-7	breast:
33	chr14:65681059..65683272-chr14:65691597..65694149,3	MCF-7	breast:
34	chr14:65687978..65690881-chr14:65733392..65735746,2	MCF-7	breast:
35	chr14:65665649..65668443-chr14:65670507..65672924,2	K562	blood:
36	chr14:65665649..65668443-chr14:65670507..65672924,2	K562	blood:
37	chr14:65677692..65679763-chr14:65878183..65880174,3	MCF-7	breast:
38	chr14:64969629..64971559-chr14:65694755..65697380,2	MCF-7	breast:
39	chr14:65707878..65709895-chr14:65801423..65803291,2	MCF-7	breast:
40	chr14:65700105..65703075-chr14:65877781..65880441,2	MCF-7	breast:
41	chr14:65674009..65676655-chr14:65879335..65881090,2	MCF-7	breast:
42	chr14:65657472..65658987-chr14:65692347..65693955,2	MCF-7	breast:
43	chr14:65670192..65672045-chr14:65675137..65676974,2	K562	blood:
44	chr14:65631009..65633878-chr14:65689261..65691263,2	MCF-7	breast:
45	chr14:65684066..65685787-chr14:65691739..65693406,2	MCF-7	breast:
46	chr14:65694009..65696273-chr14:65703311..65706029,2	K562	blood:
47	chr14:65630590..65631461-chr14:65667717..65668463,3	MCF-7	breast:
48	chr14:65693998..65695540-chr14:65823003..65824928,3	MCF-7	breast:
49	chr14:65681059..65683272-chr14:65691597..65694149,3	MCF-7	breast:
50	chr14:65665995..65668443-chr14:65670507..65672680,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAX-2	chr14:65708499-65709934	XLOC_011054
2	lnc-MAX-5	chr14:65670172-65670684	NONHSAT037375
3	lnc-MAX-1	chr14:65688937-65689065	XLOC_011053
4	lnc-MAX-1	chr14:65684419-65684508	ENSG00000255002
5	lnc-MAX-1	chr14:65679611-65680644	ENSG00000255002
6	lnc-MAX-6	chr14:65701233-65701819	NONHSAT037377
7	lnc-MAX-1	chr14:65685225-65685413	XLOC_011053
8	lnc-MAX-1	chr14:65688937-65689065	ENSG00000255002
9	lnc-MAX-1	chr14:65684419-65684508	XLOC_011053
10	lnc-MAX-1	chr14:65679612-65680644	XLOC_011053
11	lnc-MAX-1	chr14:65685225-65685413	ENSG00000255002

No data

Variant related genes	Relation type
ENSG00000258878	TF binding region
ENSG00000255002	TF binding region
ENSG00000258878	CpG island
ENSG00000255002	CpG island
ENSG00000126804	chromatin interactions
ENSG00000266740	chromatin interactions
ENSG00000033170	chromatin interactions
ENSG00000258878	chromatin interactions
ENSG00000089775	chromatin interactions
ENSG00000214759	chromatin interactions
ENSG00000255002	chromatin interactions
ENSG00000258613	chromatin interactions
EIF2C1	miRNA target sites

Extended variants
information (count: 1692 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1692 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1123493	chr14:65667546-65667547	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs145659704	chr14:65667553-65667554	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373566756	chr14:65667641-65667642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376457962	chr14:65667706-65667707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370479421	chr14:65667707-65667708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs578175027	chr14:65667713-65667714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs534977341	chr14:65667734-65667735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374149241	chr14:65667876-65667877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574734798	chr14:65667892-65667893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs193070114	chr14:65667908-65667909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554918567	chr14:65667925-65667926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563411658	chr14:65667927-65667928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576937795	chr14:65668031-65668032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs138125301	chr14:65668075-65668076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559479780	chr14:65668078-65668079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112713673	chr14:65668178-65668179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142617179	chr14:65668340-65668341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs75694648	chr14:65668347-65668348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs77186339	chr14:65668407-65668408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188547899	chr14:65668445-65668446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191467009	chr14:65668449-65668450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs183612818	chr14:65668495-65668496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs374707548	chr14:65668500-65668501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1679874	chr14:65668504-65668505	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs566253116	chr14:65668509-65668510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs77421777	chr14:65668513-65668514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373161630	chr14:65668514-65668515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs61989794	chr14:65668516-65668517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79285631	chr14:65668532-65668533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369110667	chr14:65668534-65668535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs56116751	chr14:65668561-65668562	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs557104802	chr14:65668562-65668563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs149302888	chr14:65668571-65668572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370579922	chr14:65668574-65668575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs142593497	chr14:65668580-65668581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs148438690	chr14:65668606-65668607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545885776	chr14:65668623-65668624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556919257	chr14:65668648-65668649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576857527	chr14:65668661-65668662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188247898	chr14:65668703-65668704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553234019	chr14:65668729-65668730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572955477	chr14:65668813-65668814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182253242	chr14:65668814-65668815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561989321	chr14:65668852-65668853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374735668	chr14:65668873-65668874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530842604	chr14:65668880-65668881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368376852	chr14:65668881-65668882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185594670	chr14:65668887-65668888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564068180	chr14:65669025-65669026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs190072151	chr14:65669042-65669043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Bipolar disorder	19114987	CNVD

Chromatin state (count:1504 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65665000-65667600	Weak transcription	Primary B cells from peripheral blood	blood
2	chr14:65665600-65667600	Weak transcription	Fetal Intestine Large	intestine
3	chr14:65665600-65667800	Weak transcription	Fetal Intestine Small	intestine
4	chr14:65665600-65668000	Weak transcription	GM12878-XiMat	blood
5	chr14:65665600-65671000	Weak transcription	HepG2	liver
6	chr14:65667200-65667600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr14:65667400-65667600	Enhancers	Fetal Muscle Leg	muscle
8	chr14:65667600-65668000	Enhancers	Fetal Intestine Large	intestine
9	chr14:65667600-65668600	Enhancers	Primary B cells from peripheral blood	blood
10	chr14:65667600-65670400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr14:65667800-65668200	Enhancers	Fetal Intestine Small	intestine
12	chr14:65668000-65668200	Enhancers	GM12878-XiMat	blood
13	chr14:65668000-65671200	Weak transcription	Fetal Intestine Large	intestine
14	chr14:65668600-65669000	Weak transcription	Primary B cells from peripheral blood	blood
15	chr14:65668600-65669000	Weak transcription	GM12878-XiMat	blood
16	chr14:65669000-65673400	Enhancers	Primary B cells from peripheral blood	blood
17	chr14:65669400-65669800	Weak transcription	GM12878-XiMat	blood
18	chr14:65670000-65670400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr14:65670200-65671000	Enhancers	GM12878-XiMat	blood
20	chr14:65670200-65672800	Enhancers	Primary B cells from cord blood	blood
21	chr14:65670200-65678400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr14:65670400-65670800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr14:65670400-65670800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr14:65670400-65673200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr14:65670800-65671000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr14:65670800-65671000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr14:65670800-65671800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr14:65671000-65671200	Flanking Active TSS	GM12878-XiMat	blood
29	chr14:65671000-65671400	Enhancers	HepG2	liver
30	chr14:65671000-65672200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr14:65671000-65672600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr14:65671000-65672600	Enhancers	Dnd41	blood
33	chr14:65671000-65672800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr14:65671000-65677400	Enhancers	Fetal Thymus	thymus
35	chr14:65671200-65671600	Enhancers	GM12878-XiMat	blood
36	chr14:65671200-65672000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr14:65671200-65672800	Enhancers	Fetal Intestine Large	intestine
38	chr14:65671200-65672800	Enhancers	Fetal Intestine Small	intestine
39	chr14:65671200-65672800	Enhancers	Spleen	Spleen
40	chr14:65671200-65675800	Enhancers	Primary T cells fromperipheralblood	blood
41	chr14:65671400-65671600	Enhancers	Thymus	Thymus
42	chr14:65671400-65672000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr14:65671400-65672000	Flanking Active TSS	HepG2	liver
44	chr14:65671400-65672200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr14:65671400-65672600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr14:65671400-65672800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr14:65671400-65673400	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr14:65671400-65673600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr14:65671400-65675800	Enhancers	Primary hematopoietic stem cells	blood
50	chr14:65671600-65671800	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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