Variant report

Variant	nsv901469
Chromosome Location	chr14:21043283-21070264
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:143)
CpG islands
(count:795)
Chromatin interactive
region (count:29)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:143 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr14:21047261-21047719	K562	blood:	n/a	n/a
2	ATF1	chr14:21058674-21058931	K562	blood:	n/a	n/a
3	ATF2	chr14:21046450-21047006	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr14:21046491-21046921	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr14:21046521-21046725	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr14:21046514-21046771	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr14:21047256-21047424	K562	blood:	n/a	n/a
8	BHLHE40	chr14:21062708-21062978	HepG2	liver:	n/a	n/a
9	BRCA1	chr14:21046462-21046941	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr14:21069783-21069820	K562	blood:	n/a	chr14:21069799-21069810
11	CEBPB	chr14:21069782-21069837	HepG2	liver:	n/a	chr14:21069799-21069810
12	CEBPB	chr14:21052263-21052409	HepG2	liver:	n/a	n/a
13	CEBPB	chr14:21046484-21046779	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr14:21061218-21061373	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:21052257-21052469	K562	blood:	n/a	n/a
16	CEBPB	chr14:21069671-21069886	H1-hESC	embryonic stem cell:	n/a	chr14:21069799-21069810
17	CEBPB	chr14:21061232-21061270	A549	lung:	n/a	n/a
18	CEBPB	chr14:21062873-21062940	HepG2	liver:	n/a	chr14:21062877-21062888
19	CREB1	chr14:21046514-21046868	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr14:21046437-21047026	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr14:21067320-21067470	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr14:21067260-21067410	HepG2	liver:	n/a	n/a
23	CTCF	chr14:21067220-21067370	GM12873	blood:	n/a	n/a
24	CTCF	chr14:21067320-21067470	NB4	blood:	n/a	n/a
25	CTCF	chr14:21067300-21067450	HEK293	kidney:	n/a	n/a
26	CTCF	chr14:21067640-21067790	GM12868	blood:	n/a	n/a
27	CTCF	chr14:21066920-21067070	GM12873	blood:	n/a	n/a
28	CTCF	chr14:21067120-21067270	GM12864	blood:	n/a	n/a
29	CTCF	chr14:21067280-21067430	GM12872	blood:	n/a	n/a
30	CTCF	chr14:21067240-21067390	GM12875	blood:	n/a	n/a
31	CTCF	chr14:21067300-21067450	K562	blood:	n/a	n/a
32	CTCF	chr14:21067300-21067450	HCT-116	colon:	n/a	n/a
33	CTCF	chr14:21067290-21067353	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr14:21067140-21067290	BE2_C	brain:	n/a	n/a
35	CTCF	chr14:21067280-21067430	GM12864	blood:	n/a	n/a
36	CTCF	chr14:21067320-21067470	GM12871	blood:	n/a	n/a
37	CTCF	chr14:21067240-21067390	GM12868	blood:	n/a	n/a
38	CTCF	chr14:21067240-21067390	GM12870	blood:	n/a	n/a
39	CTCF	chr14:21067300-21067450	GM12868	blood:	n/a	n/a
40	CTCF	chr14:21067300-21067450	GM12873	blood:	n/a	n/a
41	CTCF	chr14:21067260-21067410	GM12866	blood:	n/a	n/a
42	CTCF	chr14:21067280-21067430	GM12874	blood:	n/a	n/a
43	CTCF	chr14:21067260-21067410	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr14:21069100-21069250	NHEK	skin:	n/a	n/a
45	CUX1	chr14:21045968-21045969	K562	blood:	n/a	n/a
46	E2F4	chr14:21054256-21054284	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F6	chr14:21047376-21047561	K562	blood:	n/a	n/a
48	EGR1	chr14:21047191-21047504	K562	blood:	n/a	n/a
49	ELF1	chr14:21047262-21047715	K562	blood:	n/a	chr14:21047506-21047519
50	EP300	chr14:21046351-21046845	H1-hESC	embryonic stem cell:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21051204-21051254	HIPEpiC	eye:	n/a
2	chr14:21060349-21060399	H1-hESC	embryonic stem cell:	embryo
3	chr14:21051204-21051254	HIPEpiC	eye:	n/a
4	chr14:21060349-21060399	H1-hESC	embryonic stem cell:	embryo
5	chr14:21046712-21046762	GM06990	blood:	n/a
6	chr14:21058422-21058472	K562	blood:	n/a
7	chr14:21058422-21058472	Hepatocyte	liver:	n/a
8	chr14:21051204-21051254	HAEpiC	amniotic membrane:	n/a
9	chr14:21051204-21051254	Hepatocyte	liver:	n/a
10	chr14:21058360-21058410	HAEpiC	amniotic membrane:	n/a
11	chr14:21060022-21060072	MCF-7	breast:	n/a
12	chr14:21060022-21060072	GM12892	blood:	n/a
13	chr14:21058422-21058472	HepG2	liver:	n/a
14	chr14:21046712-21046762	BJ	skin:	n/a
15	chr14:21058360-21058410	HCPEpiC	choroid plexus:	n/a
16	chr14:21059287-21059337	H1-hESC	embryonic stem cell:	embryo
17	chr14:21058901-21058951	T-47D	breast:	n/a
18	chr14:21060349-21060399	IMR90	lung:	fetal
19	chr14:21060349-21060399	HRPEpiC	eye:	n/a
20	chr14:21046712-21046762	SK-N-SH_RA	brain:	n/a
21	chr14:21058901-21058951	HMEC	breast:	n/a
22	chr14:21046712-21046762	ECC-1	luminal epithelium:	n/a
23	chr14:21058422-21058472	NH-A	brain:	n/a
24	chr14:21060349-21060399	AG09319	gingival:	n/a
25	chr14:21053613-21053663	HAEpiC	amniotic membrane:	n/a
26	chr14:21058422-21058472	T-47D	breast:	n/a
27	chr14:21046712-21046762	HPAEpiC	pulmonary alveolar:	n/a
28	chr14:21051204-21051254	Caco-2	colon:	n/a
29	chr14:21053613-21053663	ECC-1	luminal epithelium:	n/a
30	chr14:21057691-21057741	AG04450	lung:	fetal
31	chr14:21058360-21058410	NT2-D1	testis:	n/a
32	chr14:21055941-21055991	Hepatocyte	liver:	n/a
33	chr14:21058901-21058951	AG09319	gingival:	n/a
34	chr14:21059287-21059337	HCM	heart:	n/a
35	chr14:21046712-21046762	CMK	blood:	n/a
36	chr14:21053613-21053663	SK-N-SH	brain:	n/a
37	chr14:21058901-21058951	H1-hESC	embryonic stem cell:	embryo
38	chr14:21059287-21059337	MCF10A-Er-Src	breast:	n/a
39	chr14:21060292-21060342	A549	lung:	n/a
40	chr14:21053613-21053663	ovcar-3	ovarian:	n/a
41	chr14:21058422-21058472	HRCEpiC	kidney:	n/a
42	chr14:21051204-21051254	HUVEC	blood vessel:	n/a
43	chr14:21052361-21052411	U87	brain:	n/a
44	chr14:21057691-21057741	NHBE	bronchial:	n/a
45	chr14:21060292-21060342	HMEC	breast:	n/a
46	chr14:21058422-21058472	U87	brain:	n/a
47	chr14:21052361-21052411	HIPEpiC	eye:	n/a
48	chr14:21060349-21060399	HCF	heart:	n/a
49	chr14:21060022-21060072	HCM	heart:	n/a
50	chr14:21060022-21060072	HCPEpiC	choroid plexus:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:20978423..20980940-chr14:21069047..21071756,2	MCF-7	breast:
2	chr14:20809995..20812316-chr14:21065759..21069408,3	MCF-7	breast:
3	chr14:21043291..21046271-chr14:21048584..21050829,2	K562	blood:
4	chr14:21046680..21048657-chr14:21053189..21055861,2	K562	blood:
5	chr14:20950018..20952777-chr14:21061740..21063709,2	K562	blood:
6	chr14:20937739..20939896-chr14:21068888..21071182,2	K562	blood:
7	chr14:21059833..21061804-chr14:21063655..21065292,3	K562	blood:
8	chr14:21049235..21051954-chr14:21055969..21057496,2	K562	blood:
9	chr14:21061985..21064587-chr14:21067797..21070259,2	K562	blood:
10	chr14:21059501..21061333-chr14:21062790..21065178,2	K562	blood:
11	chr14:20927556..20929500-chr14:21059360..21061622,2	K562	blood:
12	chr14:20927922..20930747-chr14:21065703..21067468,2	MCF-7	breast:
13	chr14:21042120..21044791-chr14:21048447..21050084,2	K562	blood:
14	chr14:21058419..21061270-chr14:21065664..21067355,2	K562	blood:
15	chr14:21065540..21068039-chr14:21068996..21071664,4	MCF-7	breast:
16	chr14:21035422..21037672-chr14:21048431..21050378,2	K562	blood:
17	chr14:20879979..20881731-chr14:21063409..21065951,2	MCF-7	breast:
18	chr14:21061985..21064587-chr14:21067797..21070259,2	K562	blood:
19	chr14:21059833..21061804-chr14:21063655..21065292,3	K562	blood:
20	chr14:21049700..21052691-chr14:21053305..21054830,2	K562	blood:
21	chr14:20943575..20945745-chr14:21061611..21063951,2	K562	blood:
22	chr14:21065540..21068039-chr14:21068996..21071664,4	MCF-7	breast:
23	chr14:21059501..21061333-chr14:21062790..21065178,2	K562	blood:
24	chr14:20922233..20924621-chr14:21051519..21054114,2	K562	blood:
25	chr14:21049700..21052691-chr14:21053305..21054830,2	K562	blood:
26	chr14:21043291..21046271-chr14:21048584..21050829,2	K562	blood:
27	chr14:20936477..20939001-chr14:21050782..21053613,2	MCF-7	breast:
28	chr14:20928768..20931716-chr14:21059130..21062025,2	MCF-7	breast:
29	chr14:21042120..21044791-chr14:21048447..21050084,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNASE10-2	chr14:21055851-21056008	ENSG00000258573.1
2	lnc-RNASE10-2	chr14:21058596-21058887	ENSG00000258573.1
3	lnc-RNASE12.1-1	chr14:21058752-21058920	ENSG00000259060.1
4	lnc-RNASE10-2	chr14:21058561-21058887	ENSG00000258573.1
5	lnc-RNASE10-2	chr14:21058749-21058887	ENSG00000258573.1
6	lnc-RNASE10-2	chr14:21055844-21056008	ENSG00000258573.1
7	lnc-RNASE10-2	chr14:21058343-21058417	ENSG00000258573.1
8	lnc-RNASE10-2	chr14:21055818-21056008	ENSG00000258573.1
9	lnc-RNASE10-2	chr14:21064830-21064978	ENSG00000258573.1
10	lnc-RNASE10-2	chr14:21064830-21064978	ENSG00000258573.1
11	lnc-RNASE12.1-1	chr14:21052499-21052655	ENSG00000259060.1
12	lnc-RNASE10-2	chr14:21055803-21056520	ENSG00000258573.1
13	lnc-RNASE10-2	chr14:21064835-21064950	ENSG00000258573.1
14	lnc-RNASE10-2	chr14:21058749-21058887	ENSG00000258573.1

No data

Variant related genes	Relation type
RNASE12	TF binding region
ENSG00000259060	TF binding region
RNASE11	TF binding region
ENSG00000258573	TF binding region
RNASE12	CpG island
ENSG00000259060	CpG island
RNASE11	CpG island
ENSG00000258573	CpG island
ENSG00000258908	chromatin interactions
ENSG00000259060	chromatin interactions
ENSG00000092094	chromatin interactions
ENSG00000182545	chromatin interactions
ENSG00000173464	chromatin interactions
ENSG00000258436	chromatin interactions
ENSG00000165782	chromatin interactions
ENSG00000129484	chromatin interactions
ENSG00000129566	chromatin interactions
ENSG00000259001	chromatin interactions
ENSG00000258573	chromatin interactions
ENSG00000198805	chromatin interactions
ENSG00000100823	chromatin interactions

Extended variants
information (count: 1121 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1121 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1243631	chr14:21043283-21043284	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533272684	chr14:21043297-21043298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141047767	chr14:21043373-21043374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144946759	chr14:21043379-21043380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537278552	chr14:21043380-21043381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs147867260	chr14:21043412-21043413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201182651	chr14:21043437-21043438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567036827	chr14:21043448-21043449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371978237	chr14:21043471-21043472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552552537	chr14:21043550-21043551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181605250	chr14:21043593-21043594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577179397	chr14:21043595-21043596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185778421	chr14:21043623-21043624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs79032601	chr14:21043647-21043648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536548157	chr14:21043694-21043695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372546851	chr14:21043695-21043696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576641613	chr14:21043705-21043706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528311226	chr14:21043778-21043779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375992492	chr14:21043804-21043805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs58586086	chr14:21043829-21043830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142845939	chr14:21043863-21043864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs1243630	chr14:21043894-21043895	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs541493905	chr14:21043967-21043968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559875082	chr14:21043976-21043977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192072077	chr14:21043991-21043992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551463391	chr14:21044050-21044051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs367661947	chr14:21044056-21044057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562240284	chr14:21044069-21044070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371829307	chr14:21044146-21044147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569967080	chr14:21044236-21044237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530681325	chr14:21044242-21044243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs34778826	chr14:21044277-21044278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375446431	chr14:21044278-21044279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1243629	chr14:21044363-21044364	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs1261803	chr14:21044376-21044377	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs533414627	chr14:21044381-21044382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1243628	chr14:21044418-21044419	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs184007153	chr14:21044422-21044423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571008490	chr14:21044445-21044446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538658055	chr14:21044447-21044448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35566700	chr14:21044492-21044493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1756399	chr14:21044493-21044494	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs187760832	chr14:21044522-21044523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556004057	chr14:21044527-21044528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191033326	chr14:21044532-21044533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568188053	chr14:21044533-21044534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376442118	chr14:21044573-21044574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201002911	chr14:21044591-21044592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201617489	chr14:21044592-21044593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs28881850	chr14:21044594-21044595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	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
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	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
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:171 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21026800-21047000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr14:21037800-21046000	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr14:21040600-21046800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr14:21041400-21045600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr14:21041400-21045800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr14:21041600-21045800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr14:21045200-21046200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr14:21045400-21046000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr14:21045400-21046200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr14:21045600-21045800	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr14:21045600-21046400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr14:21045600-21046800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr14:21045800-21046000	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr14:21045800-21047000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr14:21045800-21047800	Enhancers	H9 Cell Line	embryonic stem cell
16	chr14:21045800-21049000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr14:21045800-21049200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr14:21045800-21049600	Enhancers	K562	blood
19	chr14:21046000-21046200	Enhancers	H1 Cell Line	embryonic stem cell
20	chr14:21046000-21046200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
21	chr14:21046000-21046200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
22	chr14:21046000-21048400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr14:21046200-21046400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr14:21046200-21046600	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr14:21046200-21046600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
26	chr14:21046200-21047000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr14:21046200-21049600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr14:21046400-21046600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr14:21046400-21046600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
30	chr14:21046400-21048000	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr14:21046600-21046800	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr14:21046600-21046800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr14:21046600-21046800	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr14:21046600-21046800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr14:21046600-21047200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr14:21046600-21047800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr14:21046600-21048600	Enhancers	H1 Cell Line	embryonic stem cell
38	chr14:21046600-21049200	Enhancers	Primary hematopoietic stem cells	blood
39	chr14:21046600-21049400	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr14:21046600-21049600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr14:21046800-21047000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr14:21046800-21047000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
43	chr14:21046800-21047000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
44	chr14:21046800-21047000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
45	chr14:21046800-21047800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr14:21047000-21047800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr14:21047000-21047800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr14:21047000-21048800	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr14:21047000-21048800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr14:21047000-21048800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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