Variant report

Variant	nsv901755
Chromosome Location	chr14:43083557-43460115
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:843)
CpG islands
(count:184)
Chromatin interactive
region (count:39)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:843 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr14:43331466-43331661	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr14:43088748-43088782	K562	blood:	n/a	n/a
3	BACH1	chr14:43324407-43324692	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr14:43152884-43153470	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr14:43353343-43353620	ECC-1	luminal epithelium:	n/a	n/a
6	CEBPB	chr14:43408720-43409188	HepG2	liver:	n/a	chr14:43409058-43409069 chr14:43409057-43409070 chr14:43409057-43409070
7	CEBPB	chr14:43353267-43353697	IMR90	lung:	n/a	n/a
8	CEBPB	chr14:43200940-43201437	HepG2	liver:	n/a	n/a
9	CEBPB	chr14:43203747-43204000	HepG2	liver:	n/a	chr14:43203901-43203912 chr14:43203897-43203910 chr14:43203864-43203875 chr14:43203898-43203909
10	CEBPB	chr14:43104496-43104820	HepG2	liver:	n/a	chr14:43104691-43104702 chr14:43104647-43104658
11	CEBPB	chr14:43342276-43342436	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr14:43450264-43450500	HepG2	liver:	n/a	chr14:43450398-43450407 chr14:43450397-43450408
13	CEBPB	chr14:43353359-43353618	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr14:43245056-43245279	HepG2	liver:	n/a	chr14:43245175-43245186
15	CEBPB	chr14:43257346-43257491	HepG2	liver:	n/a	n/a
16	CEBPB	chr14:43220007-43220460	MCF-7	breast:	n/a	chr14:43220319-43220332 chr14:43220319-43220330
17	CEBPB	chr14:43342217-43342506	HepG2	liver:	n/a	n/a
18	CEBPB	chr14:43314011-43314256	A549	lung:	n/a	chr14:43314163-43314174
19	CEBPB	chr14:43276075-43276273	K562	blood:	n/a	chr14:43276132-43276143
20	CEBPB	chr14:43098443-43098643	A549	lung:	n/a	n/a
21	CEBPB	chr14:43341303-43341536	HepG2	liver:	n/a	chr14:43341407-43341418
22	CEBPB	chr14:43326483-43326809	IMR90	lung:	n/a	chr14:43326614-43326625
23	CEBPB	chr14:43112013-43112367	HepG2	liver:	n/a	chr14:43112172-43112183
24	CEBPB	chr14:43360942-43361442	HepG2	liver:	n/a	chr14:43361339-43361350
25	CEBPB	chr14:43326456-43326814	Hela-S3	cervix:	n/a	chr14:43326614-43326625
26	CEBPB	chr14:43326560-43326727	ECC-1	luminal epithelium:	n/a	chr14:43326614-43326625
27	CEBPB	chr14:43183727-43184112	A549	lung:	n/a	n/a
28	CEBPB	chr14:43434437-43434664	HepG2	liver:	n/a	n/a
29	CEBPB	chr14:43275951-43276432	IMR90	lung:	n/a	chr14:43276132-43276143
30	CEBPB	chr14:43396552-43396860	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr14:43183739-43184211	IMR90	lung:	n/a	n/a
32	CEBPB	chr14:43326514-43326823	A549	lung:	n/a	chr14:43326614-43326625
33	CEBPB	chr14:43353264-43353739	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr14:43152873-43153174	H1-hESC	embryonic stem cell:	n/a	chr14:43153045-43153058 chr14:43153045-43153056 chr14:43153047-43153056 chr14:43153045-43153058 chr14:43153058-43153071 chr14:43153046-43153057
35	CEBPB	chr14:43088915-43089065	HepG2	liver:	n/a	n/a
36	CEBPB	chr14:43112026-43112359	IMR90	lung:	n/a	chr14:43112172-43112183
37	CEBPB	chr14:43314175-43314216	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr14:43152905-43153236	A549	lung:	n/a	chr14:43153045-43153058 chr14:43153045-43153056 chr14:43153047-43153056 chr14:43153045-43153058 chr14:43153058-43153071 chr14:43153046-43153057
39	CEBPB	chr14:43301571-43301786	A549	lung:	n/a	n/a
40	CEBPB	chr14:43326458-43326808	HepG2	liver:	n/a	chr14:43326614-43326625
41	CEBPB	chr14:43220078-43220475	MCF-7	breast:	n/a	chr14:43220319-43220332 chr14:43220319-43220330
42	CEBPB	chr14:43183728-43184158	HepG2	liver:	n/a	n/a
43	CEBPB	chr14:43433139-43433257	HepG2	liver:	n/a	chr14:43433181-43433192
44	CEBPB	chr14:43453208-43453525	HepG2	liver:	n/a	chr14:43453354-43453365 chr14:43453356-43453367
45	CEBPB	chr14:43290599-43290911	A549	lung:	n/a	chr14:43290725-43290738 chr14:43290725-43290736 chr14:43290725-43290738
46	CEBPB	chr14:43155323-43155662	HepG2	liver:	n/a	chr14:43155494-43155505
47	CEBPB	chr14:43453278-43453537	IMR90	lung:	n/a	chr14:43453354-43453365 chr14:43453356-43453367
48	CEBPB	chr14:43112055-43112323	Hela-S3	cervix:	n/a	chr14:43112172-43112183
49	CEBPB	chr14:43281991-43282284	IMR90	lung:	n/a	n/a
50	CEBPB	chr14:43152636-43153526	Hela-S3	cervix:	n/a	chr14:43153045-43153058 chr14:43153045-43153056 chr14:43153047-43153056 chr14:43153045-43153058 chr14:43153058-43153071 chr14:43153046-43153057

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:43123081-43123131	GM12892	blood:	n/a
2	chr14:43123081-43123131	GM12892	blood:	n/a
3	chr14:43123081-43123131	PrEC	prostate:	n/a
4	chr14:43123081-43123131	RPTEC	kidney:	n/a
5	chr14:43277317-43277367	HAEpiC	amniotic membrane:	n/a
6	chr14:43428300-43428350	BJ	skin:	n/a
7	chr14:43277317-43277367	SK-N-SH_RA	brain:	n/a
8	chr14:43277317-43277367	AG04450	lung:	fetal
9	chr14:43123081-43123131	GM12878	blood:	n/a
10	chr14:43428300-43428350	HCF	heart:	n/a
11	chr14:43277317-43277367	AG10803	skin:	n/a
12	chr14:43277317-43277367	GM12878	blood:	n/a
13	chr14:43123081-43123131	IMR90	lung:	fetal
14	chr14:43123081-43123131	CMK	blood:	n/a
15	chr14:43123081-43123131	HL-60	blood:	n/a
16	chr14:43123081-43123131	ovcar-3	ovarian:	n/a
17	chr14:43277317-43277367	Hela-S3	cervix:	n/a
18	chr14:43123081-43123131	SK-N-MC	brain:	n/a
19	chr14:43277317-43277367	PANC-1	pancreas:	n/a
20	chr14:43123081-43123131	HCPEpiC	choroid plexus:	n/a
21	chr14:43277317-43277367	MCF-7	breast:	n/a
22	chr14:43123081-43123131	LNCaP	prostate:	n/a
23	chr14:43277317-43277367	ProgFib	skin:	n/a
24	chr14:43123081-43123131	BJ	skin:	n/a
25	chr14:43277317-43277367	NHBE	bronchial:	n/a
26	chr14:43123081-43123131	AG04450	lung:	fetal
27	chr14:43428300-43428350	HIPEpiC	eye:	n/a
28	chr14:43277317-43277367	NHDF-neo	bronchial:	n/a
29	chr14:43277317-43277367	HEEpiC	esophagus:	n/a
30	chr14:43123081-43123131	HCT-116	colon:	n/a
31	chr14:43277317-43277367	HCPEpiC	choroid plexus:	n/a
32	chr14:43277317-43277367	HCT-116	colon:	n/a
33	chr14:43277317-43277367	GM12892	blood:	n/a
34	chr14:43277317-43277367	AG09319	gingival:	n/a
35	chr14:43123081-43123131	NB4	blood:	n/a
36	chr14:43123081-43123131	HUVEC	blood vessel:	n/a
37	chr14:43428300-43428350	HCT-116	colon:	n/a
38	chr14:43123081-43123131	PANC-1	pancreas:	n/a
39	chr14:43277317-43277367	NH-A	brain:	n/a
40	chr14:43428300-43428350	A549	lung:	n/a
41	chr14:43428300-43428350	NHDF-neo	bronchial:	n/a
42	chr14:43428300-43428350	AG09309	skin:	n/a
43	chr14:43277317-43277367	SAEC	small airway:	n/a
44	chr14:43123081-43123131	PFSK-1	brain:	n/a
45	chr14:43277317-43277367	A549	lung:	n/a
46	chr14:43277317-43277367	CMK	blood:	n/a
47	chr14:43277317-43277367	HMEC	breast:	n/a
48	chr14:43277317-43277367	ovcar-3	ovarian:	n/a
49	chr14:43428300-43428350	Hela-S3	cervix:	n/a
50	chr14:43123081-43123131	HNPCEpiC	eye:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:43258257..43260320-chr6:32934540..32936791,2	MCF-7	breast:
2	chr14:43214694..43216920-chr14:43221221..43223715,2	MCF-7	breast:
3	chr14:43380269..43381028-chr14:44264574..44265376,2	MCF-7	breast:
4	chr14:43090850..43092635-chr14:43095537..43098102,2	K562	blood:
5	chr10:42398870..42399833-chr14:43322802..43323708,2	MCF-7	breast:
6	chr14:43400957..43403839-chr14:43411304..43413197,2	MCF-7	breast:
7	chr14:43401494..43403926-chr14:43416665..43419045,2	MCF-7	breast:
8	chr14:43227995..43229990-chr14:43231177..43232780,2	MCF-7	breast:
9	chr14:43301377..43304001-chr14:43306700..43308572,2	MCF-7	breast:
10	chr14:43400957..43403839-chr14:43411304..43413197,2	MCF-7	breast:
11	chr14:43214694..43216920-chr14:43221221..43223715,2	MCF-7	breast:
12	chr14:43169956..43172607-chr14:43173470..43175872,2	MCF-7	breast:
13	chr14:43401494..43403926-chr14:43416665..43419045,2	MCF-7	breast:
14	chr14:43429057..43431016-chr14:43435406..43438063,2	MCF-7	breast:
15	chr14:43390134..43392136-chr14:43396787..43398686,2	MCF-7	breast:
16	chr14:43134052..43134776-chr3:181029654..181030646,2	MCF-7	breast:
17	chr14:43199863..43201590-chr14:43205073..43207655,2	MCF-7	breast:
18	chr14:43302047..43305033-chr14:43305194..43307245,2	MCF-7	breast:
19	chr14:43140328..43142020-chr14:43153445..43155405,2	MCF-7	breast:
20	chr14:43429057..43431016-chr14:43435406..43438063,2	MCF-7	breast:
21	chr14:43363585..43364127-chr16:88972090..88972960,2	MCF-7	breast:
22	chr14:43180662..43182425-chr14:43185874..43188790,2	MCF-7	breast:
23	chr14:43414127..43415946-chr14:43415967..43417770,2	MCF-7	breast:
24	chr14:43180662..43182425-chr14:43185874..43188790,2	MCF-7	breast:
25	chr14:43301377..43304001-chr14:43306700..43308572,2	MCF-7	breast:
26	chr1:37940108..37941690-chr14:43314762..43317378,2	MCF-7	breast:
27	chr14:43199863..43201590-chr14:43205073..43207655,2	MCF-7	breast:
28	chr14:43415653..43418471-chr14:43420543..43423269,2	MCF-7	breast:
29	chr14:43390134..43392136-chr14:43396787..43398686,2	MCF-7	breast:
30	chr14:43410041..43412582-chr14:43414596..43418127,3	MCF-7	breast:
31	chr14:43090850..43092635-chr14:43095537..43098102,2	K562	blood:
32	chr14:43078769..43080628-chr14:43081211..43084199,2	MCF-7	breast:
33	chr14:43169956..43172607-chr14:43173470..43175872,2	MCF-7	breast:
34	chr14:43140328..43142020-chr14:43153445..43155405,2	MCF-7	breast:
35	chr14:43227995..43229990-chr14:43231177..43232780,2	MCF-7	breast:
36	chr14:43302047..43305033-chr14:43305194..43307245,2	MCF-7	breast:
37	chr14:43410041..43412582-chr14:43414596..43418127,3	MCF-7	breast:
38	chr14:43415653..43418471-chr14:43420543..43423269,2	MCF-7	breast:
39	chr14:43414127..43415946-chr14:43415967..43417770,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-214N1.1.1-2	chr14:43285583-43285888	NONHSAT036588
2	lnc-RP11-214N1.1.1-1	chr14:43172308-43172404	ENSG00000258394.1
3	lnc-RP11-214N1.1.1-1	chr14:43172607-43172858	ENSG00000258394.1

No data

Variant related genes	Relation type
ENSG00000258934	TF binding region
ENSG00000258622	TF binding region
ENSG00000259047	TF binding region
ENSG00000258934	CpG island
ENSG00000258622	CpG island
ENSG00000259047	CpG island
ENSG00000204257	chromatin interactions
ENSG00000163874	chromatin interactions
ENSG00000204256	chromatin interactions

Extended variants
information (count: 3268 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:3268 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576697935	chr14:43084847-43084848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs183312662	chr14:43084927-43084928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs562129230	chr14:43084931-43084932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574417400	chr14:43084984-43084985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572278579	chr14:43094820-43094821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534925251	chr14:43094865-43094866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs28711675	chr14:43094877-43094878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs192778787	chr14:43094939-43094940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1392028	chr14:43094962-43094963	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs141954882	chr14:43094973-43094974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs557088276	chr14:43094988-43094989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs144358552	chr14:43094997-43094998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545246218	chr14:43095205-43095206	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs563139405	chr14:43095223-43095224	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs141788679	chr14:43095234-43095235	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs548558505	chr14:43095253-43095254	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs543333716	chr14:43095275-43095276	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs560681445	chr14:43095284-43095285	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs570169276	chr14:43095303-43095304	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs528150598	chr14:43095309-43095310	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs57323481	chr14:43095319-43095320	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs74641037	chr14:43095348-43095349	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs558833563	chr14:43095398-43095399	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs143773438	chr14:43095433-43095434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs151082639	chr14:43095486-43095487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569442036	chr14:43095559-43095560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536685524	chr14:43095583-43095584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs554981181	chr14:43095609-43095610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141098964	chr14:43095619-43095620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537838156	chr14:43095642-43095643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369953013	chr14:43095646-43095647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534251440	chr14:43095651-43095652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs11850888	chr14:43095676-43095677	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs545893551	chr14:43095725-43095726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs79815992	chr14:43095815-43095816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535088918	chr14:43095871-43095872	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183758479	chr14:43095882-43095883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528678727	chr14:43095885-43095886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575431957	chr14:43095899-43095900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34157839	chr14:43095917-43095918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs202068208	chr14:43095927-43095928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189237924	chr14:43095955-43095956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150260471	chr14:43096006-43096007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548347977	chr14:43096033-43096034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528184061	chr14:43096074-43096075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562122454	chr14:43096119-43096120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539896741	chr14:43096152-43096153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138833945	chr14:43096158-43096159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532782730	chr14:43096195-43096196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531270923	chr14:43096346-43096347	Weak transcription	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
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
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	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
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Glioblastoma multiforme	21569311	CNVD
Schizophrenia	20967226	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:225 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:43084800-43085000	Enhancers	Fetal Heart	heart
2	chr14:43094800-43095000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr14:43095200-43095400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
4	chr14:43095400-43096000	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr14:43095600-43095800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr14:43095600-43095800	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr14:43095600-43095800	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr14:43095600-43096000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr14:43095800-43099200	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr14:43096000-43098800	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr14:43097400-43098600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr14:43097600-43099000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr14:43097800-43098800	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr14:43098800-43099200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr14:43098800-43102200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr14:43099200-43099400	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr14:43099200-43099600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr14:43099200-43100200	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr14:43099400-43100200	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr14:43100200-43100400	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr14:43100200-43100800	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr14:43100400-43101200	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr14:43100800-43101000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr14:43101200-43102200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr14:43102200-43103000	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr14:43102200-43104000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr14:43103400-43104000	Enhancers	Brain Anterior Caudate	brain
28	chr14:43121800-43122000	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr14:43121800-43123200	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
30	chr14:43121800-43123600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
31	chr14:43122200-43123200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
32	chr14:43122200-43123800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
33	chr14:43122400-43123200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr14:43122400-43123800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
35	chr14:43122400-43123800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
36	chr14:43122600-43122800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr14:43122600-43123200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
38	chr14:43122600-43123400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
39	chr14:43123000-43123200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
40	chr14:43123000-43123800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
41	chr14:43123000-43124800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr14:43123200-43123400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
43	chr14:43123200-43125000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr14:43123400-43123600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
45	chr14:43123400-43124600	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr14:43123400-43125200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr14:43123600-43123800	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
48	chr14:43123600-43124000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
49	chr14:43123600-43124000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
50	chr14:43123600-43124200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell

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