Variant report

Variant	nsv1204
Chromosome Location	chr14:21343404-21417608
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	ATF1	chr14:21349520-21349644	K562	blood:	n/a	n/a
2	CEBPB	chr14:21390780-21390974	K562	blood:	n/a	n/a
3	CEBPB	chr14:21387301-21387487	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
4	CEBPB	chr14:21387278-21387542	IMR90	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
5	CEBPB	chr14:21344519-21344558	HepG2	liver:	n/a	chr14:21344532-21344543
6	CEBPB	chr14:21359339-21359538	K562	blood:	n/a	chr14:21359447-21359460
7	CEBPB	chr14:21387184-21387565	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
8	CEBPB	chr14:21404892-21405089	MCF-7	breast:	n/a	n/a
9	CEBPB	chr14:21362153-21362361	IMR90	lung:	n/a	chr14:21362250-21362261
10	CEBPB	chr14:21404946-21405126	K562	blood:	n/a	n/a
11	CEBPB	chr14:21390663-21390987	HepG2	liver:	n/a	n/a
12	CEBPB	chr14:21387296-21387479	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
13	CEBPB	chr14:21362091-21362409	HepG2	liver:	n/a	chr14:21362250-21362261
14	CEBPB	chr14:21387189-21387569	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
15	CEBPB	chr14:21372661-21372946	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr14:21390806-21390847	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr14:21362247-21362271	H1-hESC	embryonic stem cell:	n/a	chr14:21362250-21362261
18	CEBPB	chr14:21387183-21387567	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
19	CEBPB	chr14:21390712-21390883	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr14:21373948-21374221	HepG2	liver:	n/a	chr14:21374057-21374070
21	CEBPB	chr14:21362201-21362274	K562	blood:	n/a	chr14:21362250-21362261
22	CEBPB	chr14:21390675-21390974	A549	lung:	n/a	n/a
23	CEBPB	chr14:21387196-21387557	Hela-S3	cervix:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
24	CEBPB	chr14:21387199-21387544	A549	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
25	CEBPB	chr14:21362168-21362307	Hela-S3	cervix:	n/a	chr14:21362250-21362261
26	CEBPB	chr14:21387197-21387553	H1-hESC	embryonic stem cell:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
27	CEBPB	chr14:21387140-21387598	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
28	CEBPB	chr14:21387233-21387541	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
29	CEBPB	chr14:21390705-21391054	MCF-7	breast:	n/a	n/a
30	CEBPB	chr14:21387328-21387608	MCF-7	breast:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
31	CEBPB	chr14:21362130-21362293	A549	lung:	n/a	chr14:21362250-21362261
32	CEBPB	chr14:21404959-21405123	Hela-S3	cervix:	n/a	n/a
33	CEBPD	chr14:21387228-21387447	HepG2	liver:	n/a	chr14:21387366-21387377 chr14:21387368-21387377
34	CTCF	chr14:21402453-21402600	GM10248	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
35	CTCF	chr14:21372644-21372825	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr14:21402460-21402610	HBMEC	blood vessel:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
37	CTCF	chr14:21402440-21402590	HRPEpiC	eye:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
38	CTCF	chr14:21402400-21402550	GM12874	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
39	CTCF	chr14:21402360-21402510	A549	lung:	n/a	n/a
40	CTCF	chr14:21402400-21402550	GM12872	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
41	CTCF	chr14:21372521-21372923	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr14:21372720-21372870	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr14:21402260-21402410	AG04450	lung:	n/a	n/a
44	CTCF	chr14:21372640-21372790	HL-60	blood:	n/a	n/a
45	CTCF	chr14:21359369-21359415	GM10266	blood:	n/a	n/a
46	CTCF	chr14:21402460-21402610	GM12866	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
47	CTCF	chr14:21402257-21402617	MCF-7	breast:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
48	CTCF	chr14:21402400-21402550	HCT-116	colon:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
49	CTCF	chr14:21402380-21402530	HFF-Myc	foreskin:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
50	CTCF	chr14:21402308-21402616	K562	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21359737-21359787	HRPEpiC	eye:	n/a
2	chr14:21359737-21359787	HRPEpiC	eye:	n/a
3	chr14:21359295-21359345	NT2-D1	testis:	n/a
4	chr14:21359737-21359787	HCF	heart:	n/a
5	chr14:21359295-21359345	MCF10A-Er-Src	breast:	n/a
6	chr14:21359737-21359787	SKMC	muscle:	n/a
7	chr14:21359295-21359345	BJ	skin:	n/a
8	chr14:21358233-21358283	AoSMC	blood vessel:	n/a
9	chr14:21358233-21358283	T-47D	breast:	n/a
10	chr14:21359943-21359993	AG10803	skin:	n/a
11	chr14:21358099-21358149	NHBE	bronchial:	n/a
12	chr14:21359295-21359345	AG10803	skin:	n/a
13	chr14:21358099-21358149	Jurkat	blood:	n/a
14	chr14:21359295-21359345	ovcar-3	ovarian:	n/a
15	chr14:21359295-21359345	PANC-1	pancreas:	n/a
16	chr14:21386453-21386503	CMK	blood:	n/a
17	chr14:21358099-21358149	HAEpiC	amniotic membrane:	n/a
18	chr14:21359737-21359787	AG09319	gingival:	n/a
19	chr14:21359295-21359345	AG04450	lung:	fetal
20	chr14:21359295-21359345	CMK	blood:	n/a
21	chr14:21359943-21359993	Hepatocyte	liver:	n/a
22	chr14:21359295-21359345	GM19239	blood:	n/a
23	chr14:21358233-21358283	GM19239	blood:	n/a
24	chr14:21358233-21358283	SKMC	muscle:	n/a
25	chr14:21386453-21386503	HEEpiC	esophagus:	n/a
26	chr14:21359737-21359787	AG04450	lung:	fetal
27	chr14:21359295-21359345	AG04449	skin:	fetal
28	chr14:21359943-21359993	GM19239	blood:	n/a
29	chr14:21359295-21359345	T-47D	breast:	n/a
30	chr14:21359737-21359787	HL-60	blood:	n/a
31	chr14:21359737-21359787	GM12892	blood:	n/a
32	chr14:21359943-21359993	HL-60	blood:	n/a
33	chr14:21358099-21358149	LNCaP	prostate:	n/a
34	chr14:21386453-21386503	NHBE	bronchial:	n/a
35	chr14:21359295-21359345	NHDF-neo	bronchial:	n/a
36	chr14:21358099-21358149	HepG2	liver:	n/a
37	chr14:21359737-21359787	NHBE	bronchial:	n/a
38	chr14:21359943-21359993	A549	lung:	n/a
39	chr14:21359943-21359993	HUVEC	blood vessel:	n/a
40	chr14:21386453-21386503	U87	brain:	n/a
41	chr14:21358233-21358283	CMK	blood:	n/a
42	chr14:21386453-21386503	PANC-1	pancreas:	n/a
43	chr14:21358099-21358149	ProgFib	skin:	n/a
44	chr14:21386453-21386503	Hepatocyte	liver:	n/a
45	chr14:21358233-21358283	LNCaP	prostate:	n/a
46	chr14:21359737-21359787	ECC-1	luminal epithelium:	n/a
47	chr14:21358233-21358283	Caco-2	colon:	n/a
48	chr14:21359295-21359345	HCPEpiC	choroid plexus:	n/a
49	chr14:21359295-21359345	H1-hESC	embryonic stem cell:	embryo
50	chr14:21358099-21358149	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:21345187..21348103-chr14:21455224..21457829,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDRG2-2	chr14:21384925-21385029	ENSG00000258772
2	lnc-RNASE3-1	chr14:21387795-21388335	ENSG00000136315
3	lnc-NDRG2-3	chr14:21366144-21366340	ENSG00000258918
4	lnc-RNASE3-1	chr14:21387500-21387563	ENSG00000136315
5	lnc-RNASE1-1	chr14:21343696-21343904	XLOC_010966
6	lnc-NDRG2-3	chr14:21404261-21404414	ENSG00000258918
7	lnc-RNASE1-1	chr14:21343696-21343927	ENSG00000258642.1
8	lnc-NDRG2-2	chr14:21396396-21396739	ENSG00000258772

Variant related genes	Relation type
ENSG00000258772	TF binding region
ENSG00000136315	TF binding region
ENSG00000258642	TF binding region
RNASE3	TF binding region
ENSG00000258918	TF binding region
ENSG00000259130	TF binding region
ENSG00000258772	CpG island
ENSG00000136315	CpG island
ENSG00000258642	CpG island
RNASE3	CpG island
ENSG00000258918	CpG island
ENSG00000259130	CpG island

Extended variants
information (count: 2305 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2305 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145497292	chr14:21343404-21343405	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs111767175	chr14:21343482-21343483	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs111391792	chr14:21343487-21343488	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs529003726	chr14:21343496-21343497	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs544983301	chr14:21343586-21343587	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs565889757	chr14:21343594-21343595	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs148934343	chr14:21343667-21343668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181622670	chr14:21343671-21343672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184398608	chr14:21343692-21343693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs527562173	chr14:21343701-21343702	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs537035858	chr14:21343754-21343755	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs557353669	chr14:21343756-21343757	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs567627863	chr14:21343757-21343758	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs536768021	chr14:21343773-21343774	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs188389368	chr14:21343781-21343782	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs372446851	chr14:21343838-21343839	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs11852222	chr14:21343852-21343853	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs538895841	chr14:21343872-21343873	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs181213333	chr14:21343873-21343874	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs575558183	chr14:21343880-21343881	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs377190539	chr14:21343896-21343897	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs185662698	chr14:21343925-21343926	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs563310278	chr14:21343926-21343927	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs28544189	chr14:21343957-21343958	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs55738263	chr14:21343959-21343960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559536131	chr14:21343976-21343977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528286407	chr14:21343981-21343982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7144670	chr14:21344043-21344044	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs549816939	chr14:21344066-21344067	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs565155293	chr14:21344076-21344077	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs571624154	chr14:21344124-21344125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12435849	chr14:21344168-21344169	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs550667717	chr14:21344192-21344193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114369892	chr14:21344212-21344213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548121333	chr14:21344222-21344223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536304553	chr14:21344255-21344256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190747908	chr14:21344263-21344264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566666834	chr14:21344286-21344287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538824224	chr14:21344295-21344296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181026650	chr14:21344310-21344311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575812106	chr14:21344322-21344323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369307789	chr14:21344324-21344325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140823035	chr14:21344357-21344358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144824778	chr14:21344396-21344397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573576715	chr14:21344397-21344398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542298642	chr14:21344427-21344428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560621065	chr14:21344486-21344487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138745452	chr14:21344487-21344488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7492769	chr14:21344531-21344532	Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs545196128	chr14:21344535-21344536	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:182 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21342200-21344800	Weak transcription	Duodenum Mucosa	Duodenum
2	chr14:21342400-21343800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr14:21342400-21347600	Weak transcription	Right Atrium	heart
4	chr14:21342600-21343800	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr14:21342600-21346800	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr14:21343200-21345200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr14:21343800-21346600	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr14:21343800-21346800	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr14:21344800-21345400	Enhancers	Duodenum Mucosa	Duodenum
10	chr14:21344800-21345800	Enhancers	Fetal Intestine Large	intestine
11	chr14:21344800-21345800	Enhancers	Fetal Intestine Small	intestine
12	chr14:21345200-21345400	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr14:21345400-21345800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr14:21345800-21346400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr14:21346600-21350200	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr14:21346800-21347600	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr14:21346800-21348800	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr14:21347000-21347600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr14:21347600-21347800	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr14:21347600-21347800	Enhancers	Right Atrium	heart
21	chr14:21347600-21348200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr14:21347600-21350200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr14:21347800-21348600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr14:21348000-21348800	Weak transcription	Primary T cells from cord blood	blood
25	chr14:21348000-21350000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr14:21348200-21349400	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr14:21348600-21350000	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr14:21348800-21349000	Enhancers	Primary T cells from cord blood	blood
29	chr14:21348800-21349200	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr14:21349000-21349800	Weak transcription	Primary T cells from cord blood	blood
31	chr14:21349200-21350200	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr14:21349400-21350000	Enhancers	Fetal Thymus	thymus
33	chr14:21349400-21350000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
34	chr14:21349800-21350200	Enhancers	Primary T cells from cord blood	blood
35	chr14:21350000-21350200	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr14:21350000-21354200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr14:21350200-21352800	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr14:21350200-21352800	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr14:21350200-21354000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr14:21350200-21354200	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr14:21352800-21353200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr14:21352800-21353400	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr14:21352800-21355600	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr14:21353400-21353800	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr14:21353800-21355000	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr14:21354000-21354200	Weak transcription	Thymus	Thymus
47	chr14:21354000-21355000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr14:21354200-21354400	Enhancers	Thymus	Thymus
49	chr14:21354200-21354800	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr14:21354200-21354800	Enhancers	Primary hematopoietic stem cells	blood

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