Variant report

Variant	esv3447003
Chromosome Location	chr14:21346068-21409779
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	chr14:21362247-21362271	H1-hESC	embryonic stem cell:	n/a	chr14:21362250-21362261
4	CEBPB	chr14:21387199-21387544	A549	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
5	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
6	CEBPB	chr14:21390806-21390847	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr14:21387189-21387569	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
8	CEBPB	chr14:21390675-21390974	A549	lung:	n/a	n/a
9	CEBPB	chr14:21362153-21362361	IMR90	lung:	n/a	chr14:21362250-21362261
10	CEBPB	chr14:21362168-21362307	Hela-S3	cervix:	n/a	chr14:21362250-21362261
11	CEBPB	chr14:21404959-21405123	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr14:21362130-21362293	A549	lung:	n/a	chr14:21362250-21362261
13	CEBPB	chr14:21387233-21387541	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
14	CEBPB	chr14:21372661-21372946	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr14:21404946-21405126	K562	blood:	n/a	n/a
16	CEBPB	chr14:21387328-21387608	MCF-7	breast:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
17	CEBPB	chr14:21387301-21387487	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
18	CEBPB	chr14:21387140-21387598	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
19	CEBPB	chr14:21359339-21359538	K562	blood:	n/a	chr14:21359447-21359460
20	CEBPB	chr14:21362091-21362409	HepG2	liver:	n/a	chr14:21362250-21362261
21	CEBPB	chr14:21387196-21387557	Hela-S3	cervix:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
22	CEBPB	chr14:21373948-21374221	HepG2	liver:	n/a	chr14:21374057-21374070
23	CEBPB	chr14:21387183-21387567	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
24	CEBPB	chr14:21362201-21362274	K562	blood:	n/a	chr14:21362250-21362261
25	CEBPB	chr14:21387278-21387542	IMR90	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
26	CEBPB	chr14:21390712-21390883	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr14:21390663-21390987	HepG2	liver:	n/a	n/a
28	CEBPB	chr14:21387296-21387479	HepG2	liver:	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	chr14:21404892-21405089	MCF-7	breast:	n/a	n/a
31	CEBPB	chr14:21387184-21387565	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
32	CEBPD	chr14:21387228-21387447	HepG2	liver:	n/a	chr14:21387366-21387377 chr14:21387368-21387377
33	CTCF	chr14:21402414-21402609	MCF-7	breast:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
34	CTCF	chr14:21402320-21402470	HAc	cerebellar:	n/a	n/a
35	CTCF	chr14:21402440-21402590	HVMF	connective:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
36	CTCF	chr14:21372680-21372830	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr14:21402400-21402550	HMEC	breast:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
38	CTCF	chr14:21372660-21372810	HepG2	liver:	n/a	n/a
39	CTCF	chr14:21402426-21402599	MCF-7	breast:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
40	CTCF	chr14:21402439-21402586	GM20000	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
41	CTCF	chr14:21402480-21402630	GM12801	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
42	CTCF	chr14:21402360-21402510	BE2_C	brain:	n/a	n/a
43	CTCF	chr14:21385976-21386064	GM13976	blood:	n/a	n/a
44	CTCF	chr14:21402040-21402190	HCT-116	colon:	n/a	n/a
45	CTCF	chr14:21402420-21402570	NHEK	skin:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
46	CTCF	chr14:21402404-21402628	HUVEC	blood vessel:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
47	CTCF	chr14:21402640-21402790	A549	lung:	n/a	n/a
48	CTCF	chr14:21372660-21372810	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr14:21402400-21402550	HepG2	liver:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
50	CTCF	chr14:21402440-21402590	GM12864	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	chr14:21358099-21358149	BJ	skin:	n/a
2	chr14:21358099-21358149	BJ	skin:	n/a
3	chr14:21359943-21359993	HL-60	blood:	n/a
4	chr14:21359737-21359787	HL-60	blood:	n/a
5	chr14:21386453-21386503	HPAEpiC	pulmonary alveolar:	n/a
6	chr14:21358233-21358283	HCF	heart:	n/a
7	chr14:21359943-21359993	HRCEpiC	kidney:	n/a
8	chr14:21358099-21358149	ovcar-3	ovarian:	n/a
9	chr14:21358099-21358149	SAEC	small airway:	n/a
10	chr14:21359943-21359993	HAEpiC	amniotic membrane:	n/a
11	chr14:21386453-21386503	NT2-D1	testis:	n/a
12	chr14:21358099-21358149	LNCaP	prostate:	n/a
13	chr14:21359295-21359345	GM12878	blood:	n/a
14	chr14:21359943-21359993	BE2_C	brain:	n/a
15	chr14:21386453-21386503	Hepatocyte	liver:	n/a
16	chr14:21386453-21386503	HRE	kidney:	n/a
17	chr14:21359295-21359345	A549	lung:	n/a
18	chr14:21359737-21359787	LNCaP	prostate:	n/a
19	chr14:21359943-21359993	HCPEpiC	choroid plexus:	n/a
20	chr14:21358233-21358283	BJ	skin:	n/a
21	chr14:21359943-21359993	RPTEC	kidney:	n/a
22	chr14:21358233-21358283	NHBE	bronchial:	n/a
23	chr14:21358099-21358149	U87	brain:	n/a
24	chr14:21359737-21359787	PFSK-1	brain:	n/a
25	chr14:21359295-21359345	NHBE	bronchial:	n/a
26	chr14:21359295-21359345	T-47D	breast:	n/a
27	chr14:21359295-21359345	HCF	heart:	n/a
28	chr14:21359295-21359345	K562	blood:	n/a
29	chr14:21359943-21359993	LNCaP	prostate:	n/a
30	chr14:21359295-21359345	HMEC	breast:	n/a
31	chr14:21359295-21359345	GM12891	blood:	n/a
32	chr14:21358099-21358149	AG04450	lung:	fetal
33	chr14:21359943-21359993	HRPEpiC	eye:	n/a
34	chr14:21359943-21359993	SKMC	muscle:	n/a
35	chr14:21358099-21358149	T-47D	breast:	n/a
36	chr14:21386453-21386503	HUVEC	blood vessel:	n/a
37	chr14:21359943-21359993	A549	lung:	n/a
38	chr14:21359943-21359993	AG09309	skin:	n/a
39	chr14:21359737-21359787	SK-N-SH_RA	brain:	n/a
40	chr14:21358233-21358283	CMK	blood:	n/a
41	chr14:21358099-21358149	K562	blood:	n/a
42	chr14:21358233-21358283	Caco-2	colon:	n/a
43	chr14:21358233-21358283	NB4	blood:	n/a
44	chr14:21358099-21358149	AG09309	skin:	n/a
45	chr14:21359943-21359993	HUVEC	blood vessel:	n/a
46	chr14:21358233-21358283	GM06990	blood:	n/a
47	chr14:21359295-21359345	U87	brain:	n/a
48	chr14:21358233-21358283	AG04449	skin:	fetal
49	chr14:21359295-21359345	IMR90	lung:	fetal
50	chr14:21359295-21359345	GM12892	blood:	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-RNASE3-1	chr14:21387795-21388335	ENSG00000136315
2	lnc-NDRG2-3	chr14:21404261-21404414	ENSG00000258918
3	lnc-NDRG2-2	chr14:21396396-21396739	ENSG00000258772
4	lnc-NDRG2-2	chr14:21384925-21385029	ENSG00000258772
5	lnc-RNASE3-1	chr14:21387500-21387563	ENSG00000136315
6	lnc-NDRG2-3	chr14:21366144-21366340	ENSG00000258918

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

Extended variants
information (count: 1937 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1937 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532361786	chr14:21346071-21346072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs139231536	chr14:21346079-21346080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562977415	chr14:21346081-21346082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531734282	chr14:21346083-21346084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548729538	chr14:21346095-21346096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562153327	chr14:21346098-21346099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs190048858	chr14:21346122-21346123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548108625	chr14:21346165-21346166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571204140	chr14:21346222-21346223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558059350	chr14:21346229-21346230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182663478	chr14:21346276-21346277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188419537	chr14:21346299-21346300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192240860	chr14:21346347-21346348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537551023	chr14:21346353-21346354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149993503	chr14:21346372-21346373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145244984	chr14:21346396-21346397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533777152	chr14:21346398-21346399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149171649	chr14:21346415-21346416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34049131	chr14:21346460-21346461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553634592	chr14:21346562-21346563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576755281	chr14:21346567-21346568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546151076	chr14:21346578-21346579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562757388	chr14:21346608-21346609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144759041	chr14:21346611-21346612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146716328	chr14:21346629-21346630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562211902	chr14:21346649-21346650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573035074	chr14:21346669-21346670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140354419	chr14:21346675-21346676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145513019	chr14:21346716-21346717	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs533691651	chr14:21346761-21346762	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs552107033	chr14:21346771-21346772	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs111308354	chr14:21346791-21346792	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs34640651	chr14:21346831-21346832	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs537891005	chr14:21346848-21346849	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs561446422	chr14:21346870-21346871	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs572266940	chr14:21346873-21346874	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs116707251	chr14:21346876-21346877	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs188649116	chr14:21346877-21346878	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs533715546	chr14:21346910-21346911	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs192547967	chr14:21346971-21346972	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs184179358	chr14:21346987-21346988	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs539361942	chr14:21346992-21346993	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs4981342	chr14:21346993-21346994	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs576356585	chr14:21347026-21347027	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs542251146	chr14:21347060-21347061	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs544286279	chr14:21347079-21347080	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs572603053	chr14:21347156-21347157	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs148063104	chr14:21347224-21347225	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs11156734	chr14:21347232-21347233	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs373924936	chr14:21347268-21347269	Enhancers Weak transcription	n/a	n/a	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:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21342400-21347600	Weak transcription	Right Atrium	heart
2	chr14:21342600-21346800	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr14:21343800-21346600	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr14:21343800-21346800	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr14:21345800-21346400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr14:21346600-21350200	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr14:21346800-21347600	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr14:21346800-21348800	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr14:21347000-21347600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr14:21347600-21347800	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr14:21347600-21347800	Enhancers	Right Atrium	heart
12	chr14:21347600-21348200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
13	chr14:21347600-21350200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr14:21347800-21348600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr14:21348000-21348800	Weak transcription	Primary T cells from cord blood	blood
16	chr14:21348000-21350000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr14:21348200-21349400	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr14:21348600-21350000	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr14:21348800-21349000	Enhancers	Primary T cells from cord blood	blood
20	chr14:21348800-21349200	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr14:21349000-21349800	Weak transcription	Primary T cells from cord blood	blood
22	chr14:21349200-21350200	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr14:21349400-21350000	Enhancers	Fetal Thymus	thymus
24	chr14:21349400-21350000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
25	chr14:21349800-21350200	Enhancers	Primary T cells from cord blood	blood
26	chr14:21350000-21350200	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr14:21350000-21354200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr14:21350200-21352800	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr14:21350200-21352800	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr14:21350200-21354000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr14:21350200-21354200	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr14:21352800-21353200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr14:21352800-21353400	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr14:21352800-21355600	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr14:21353400-21353800	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr14:21353800-21355000	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr14:21354000-21354200	Weak transcription	Thymus	Thymus
38	chr14:21354000-21355000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr14:21354200-21354400	Enhancers	Thymus	Thymus
40	chr14:21354200-21354800	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr14:21354200-21354800	Enhancers	Primary hematopoietic stem cells	blood
42	chr14:21354200-21355200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr14:21354400-21357200	Weak transcription	Thymus	Thymus
44	chr14:21354800-21355800	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr14:21355000-21356000	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr14:21355200-21356200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr14:21355600-21356000	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr14:21355800-21358200	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr14:21356000-21359200	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr14:21356000-21362200	Enhancers	Primary monocytes fromperipheralblood	blood

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