Variant report

Variant	esv2760325
Chromosome Location	chr14:21345707-21425348
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	ARID3A	chr14:21423410-21423550	HepG2	liver:	n/a	n/a
2	ATF1	chr14:21349520-21349644	K562	blood:	n/a	n/a
3	CEBPB	chr14:21423391-21423541	Hela-S3	cervix:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
4	CEBPB	chr14:21387189-21387569	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
5	CEBPB	chr14:21390712-21390883	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr14:21387278-21387542	IMR90	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
7	CEBPB	chr14:21387196-21387557	Hela-S3	cervix:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
8	CEBPB	chr14:21362201-21362274	K562	blood:	n/a	chr14:21362250-21362261
9	CEBPB	chr14:21387183-21387567	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
10	CEBPB	chr14:21387301-21387487	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
11	CEBPB	chr14:21404946-21405126	K562	blood:	n/a	n/a
12	CEBPB	chr14:21387199-21387544	A549	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
13	CEBPB	chr14:21373948-21374221	HepG2	liver:	n/a	chr14:21374057-21374070
14	CEBPB	chr14:21387140-21387598	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
15	CEBPB	chr14:21362130-21362293	A549	lung:	n/a	chr14:21362250-21362261
16	CEBPB	chr14:21387296-21387479	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
17	CEBPB	chr14:21390663-21390987	HepG2	liver:	n/a	n/a
18	CEBPB	chr14:21390806-21390847	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr14:21362247-21362271	H1-hESC	embryonic stem cell:	n/a	chr14:21362250-21362261
20	CEBPB	chr14:21387233-21387541	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
21	CEBPB	chr14:21372661-21372946	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr14:21404892-21405089	MCF-7	breast:	n/a	n/a
23	CEBPB	chr14:21390780-21390974	K562	blood:	n/a	n/a
24	CEBPB	chr14:21362091-21362409	HepG2	liver:	n/a	chr14:21362250-21362261
25	CEBPB	chr14:21362153-21362361	IMR90	lung:	n/a	chr14:21362250-21362261
26	CEBPB	chr14:21404959-21405123	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr14:21423250-21423720	HepG2	liver:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
28	CEBPB	chr14:21423324-21423698	HepG2	liver:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
29	CEBPB	chr14:21423393-21423620	HepG2	liver:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
30	CEBPB	chr14:21362168-21362307	Hela-S3	cervix:	n/a	chr14:21362250-21362261
31	CEBPB	chr14:21423326-21423702	HepG2	liver:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
32	CEBPB	chr14:21387328-21387608	MCF-7	breast:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
33	CEBPB	chr14:21423483-21423531	A549	lung:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
34	CEBPB	chr14:21390705-21391054	MCF-7	breast:	n/a	n/a
35	CEBPB	chr14:21387184-21387565	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
36	CEBPB	chr14:21390675-21390974	A549	lung:	n/a	n/a
37	CEBPB	chr14:21359339-21359538	K562	blood:	n/a	chr14:21359447-21359460
38	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
39	CEBPD	chr14:21387228-21387447	HepG2	liver:	n/a	chr14:21387366-21387377 chr14:21387368-21387377
40	CEBPD	chr14:21423329-21423575	HepG2	liver:	n/a	chr14:21423499-21423510
41	CTCF	chr14:21402780-21402930	GM12868	blood:	n/a	n/a
42	CTCF	chr14:21402411-21402597	GM13976	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
43	CTCF	chr14:21402420-21402570	AG04449	skin:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
44	CTCF	chr14:21402422-21402574	LNCaP	prostate:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
45	CTCF	chr14:21402343-21402658	H1-hESC	embryonic stem cell:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
46	CTCF	chr14:21402640-21402790	A549	lung:	n/a	n/a
47	CTCF	chr14:21402420-21402570	GM12864	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
48	CTCF	chr14:21402360-21402510	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr14:21402420-21402570	NHLF	lung:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
50	CTCF	chr14:21372644-21372825	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21359295-21359345	Caco-2	colon:	n/a
2	chr14:21358099-21358149	AoSMC	blood vessel:	n/a
3	chr14:21359943-21359993	PFSK-1	brain:	n/a
4	chr14:21422205-21422255	HCPEpiC	choroid plexus:	n/a
5	chr14:21424117-21424167	SK-N-SH_RA	brain:	n/a
6	chr14:21359295-21359345	AG04450	lung:	fetal
7	chr14:21358233-21358283	AG04449	skin:	fetal
8	chr14:21422605-21422655	SK-N-SH_RA	brain:	n/a
9	chr14:21359737-21359787	PFSK-1	brain:	n/a
10	chr14:21423769-21423819	NB4	blood:	n/a
11	chr14:21359295-21359345	H1-hESC	embryonic stem cell:	embryo
12	chr14:21359295-21359345	HMEC	breast:	n/a
13	chr14:21423684-21423734	HIPEpiC	eye:	n/a
14	chr14:21359943-21359993	Jurkat	blood:	n/a
15	chr14:21422205-21422255	GM12878	blood:	n/a
16	chr14:21423684-21423734	SAEC	small airway:	n/a
17	chr14:21422605-21422655	HCF	heart:	n/a
18	chr14:21359737-21359787	BE2_C	brain:	n/a
19	chr14:21422605-21422655	HNPCEpiC	eye:	n/a
20	chr14:21422965-21423015	Jurkat	blood:	n/a
21	chr14:21423837-21423887	HEK293	kidney:	embryo
22	chr14:21423769-21423819	Caco-2	colon:	n/a
23	chr14:21359943-21359993	GM06990	blood:	n/a
24	chr14:21423837-21423887	HepG2	liver:	n/a
25	chr14:21359943-21359993	BE2_C	brain:	n/a
26	chr14:21358099-21358149	NB4	blood:	n/a
27	chr14:21423769-21423819	Jurkat	blood:	n/a
28	chr14:21422965-21423015	Hela-S3	cervix:	n/a
29	chr14:21422605-21422655	HepG2	liver:	n/a
30	chr14:21359737-21359787	GM12878	blood:	n/a
31	chr14:21358233-21358283	SK-N-MC	brain:	n/a
32	chr14:21359737-21359787	HCF	heart:	n/a
33	chr14:21423684-21423734	HNPCEpiC	eye:	n/a
34	chr14:21359295-21359345	ECC-1	luminal epithelium:	n/a
35	chr14:21422205-21422255	HCT-116	colon:	n/a
36	chr14:21386453-21386503	PrEC	prostate:	n/a
37	chr14:21422205-21422255	AG04449	skin:	fetal
38	chr14:21423684-21423734	HRE	kidney:	n/a
39	chr14:21359295-21359345	HRCEpiC	kidney:	n/a
40	chr14:21422205-21422255	HEK293	kidney:	embryo
41	chr14:21422205-21422255	HMEC	breast:	n/a
42	chr14:21423769-21423819	HUVEC	blood vessel:	n/a
43	chr14:21358233-21358283	Jurkat	blood:	n/a
44	chr14:21422605-21422655	HMEC	breast:	n/a
45	chr14:21358099-21358149	HMEC	breast:	n/a
46	chr14:21358099-21358149	NH-A	brain:	n/a
47	chr14:21423769-21423819	HEEpiC	esophagus:	n/a
48	chr14:21423684-21423734	K562	blood:	n/a
49	chr14:21359943-21359993	Hela-S3	cervix:	n/a
50	chr14:21358233-21358283	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:21417758..21420748-chr14:21423705..21426897,3	MCF-7	breast:
2	chr14:21417758..21420748-chr14:21423705..21426897,3	MCF-7	breast:
3	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	chr14:21366144-21366340	ENSG00000258918
3	lnc-RNASE2-1	chr14:21419045-21419476	NONHSAT035618
4	lnc-RNASE2-1	chr14:21418698-21418708	NONHSAT035618
5	lnc-NDRG2-2	chr14:21396396-21396739	ENSG00000258772
6	lnc-NDRG2-3	chr14:21404261-21404414	ENSG00000258918
7	lnc-NDRG2-2	chr14:21384925-21385029	ENSG00000258772
8	lnc-RNASE3-1	chr14:21387500-21387563	ENSG00000136315

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
RNASE2	TF binding region
ENSG00000258772	CpG island
ENSG00000136315	CpG island
ENSG00000258642	CpG island
RNASE3	CpG island
ENSG00000258918	CpG island
ENSG00000259130	CpG island
RNASE2	CpG island

Extended variants
information (count: 2565 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2565 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7152062	chr14:21345707-21345708	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566478935	chr14:21345713-21345714	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538685631	chr14:21345720-21345721	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374553261	chr14:21345770-21345771	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs111814151	chr14:21345795-21345796	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558612908	chr14:21345833-21345834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575280432	chr14:21345857-21345858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544376435	chr14:21345867-21345868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7140397	chr14:21345877-21345878	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs1743055	chr14:21345889-21345890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144898269	chr14:21345893-21345894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs151326579	chr14:21345932-21345933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556029111	chr14:21345961-21345962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532361786	chr14:21346071-21346072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139231536	chr14:21346079-21346080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562977415	chr14:21346081-21346082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531734282	chr14:21346083-21346084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548729538	chr14:21346095-21346096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562153327	chr14:21346098-21346099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190048858	chr14:21346122-21346123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548108625	chr14:21346165-21346166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571204140	chr14:21346222-21346223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558059350	chr14:21346229-21346230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182663478	chr14:21346276-21346277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188419537	chr14:21346299-21346300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192240860	chr14:21346347-21346348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537551023	chr14:21346353-21346354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149993503	chr14:21346372-21346373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145244984	chr14:21346396-21346397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533777152	chr14:21346398-21346399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149171649	chr14:21346415-21346416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs34049131	chr14:21346460-21346461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553634592	chr14:21346562-21346563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576755281	chr14:21346567-21346568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546151076	chr14:21346578-21346579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562757388	chr14:21346608-21346609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144759041	chr14:21346611-21346612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146716328	chr14:21346629-21346630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562211902	chr14:21346649-21346650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573035074	chr14:21346669-21346670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140354419	chr14:21346675-21346676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145513019	chr14:21346716-21346717	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs533691651	chr14:21346761-21346762	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs552107033	chr14:21346771-21346772	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs111308354	chr14:21346791-21346792	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs34640651	chr14:21346831-21346832	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs537891005	chr14:21346848-21346849	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs561446422	chr14:21346870-21346871	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs572266940	chr14:21346873-21346874	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs116707251	chr14:21346876-21346877	Enhancers Weak transcription	TF binding region	1 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:222 , 50 per page) page: 1 2 3 4 5

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	chr14:21344800-21345800	Enhancers	Fetal Intestine Large	intestine
6	chr14:21344800-21345800	Enhancers	Fetal Intestine Small	intestine
7	chr14:21345400-21345800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr14:21345800-21346400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr14:21346600-21350200	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr14:21346800-21347600	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr14:21346800-21348800	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr14:21347000-21347600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr14:21347600-21347800	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr14:21347600-21347800	Enhancers	Right Atrium	heart
15	chr14:21347600-21348200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr14:21347600-21350200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr14:21347800-21348600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr14:21348000-21348800	Weak transcription	Primary T cells from cord blood	blood
19	chr14:21348000-21350000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr14:21348200-21349400	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr14:21348600-21350000	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr14:21348800-21349000	Enhancers	Primary T cells from cord blood	blood
23	chr14:21348800-21349200	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr14:21349000-21349800	Weak transcription	Primary T cells from cord blood	blood
25	chr14:21349200-21350200	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr14:21349400-21350000	Enhancers	Fetal Thymus	thymus
27	chr14:21349400-21350000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
28	chr14:21349800-21350200	Enhancers	Primary T cells from cord blood	blood
29	chr14:21350000-21350200	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr14:21350000-21354200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr14:21350200-21352800	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr14:21350200-21352800	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr14:21350200-21354000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr14:21350200-21354200	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr14:21352800-21353200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr14:21352800-21353400	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr14:21352800-21355600	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr14:21353400-21353800	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr14:21353800-21355000	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr14:21354000-21354200	Weak transcription	Thymus	Thymus
41	chr14:21354000-21355000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr14:21354200-21354400	Enhancers	Thymus	Thymus
43	chr14:21354200-21354800	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr14:21354200-21354800	Enhancers	Primary hematopoietic stem cells	blood
45	chr14:21354200-21355200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr14:21354400-21357200	Weak transcription	Thymus	Thymus
47	chr14:21354800-21355800	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr14:21355000-21356000	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr14:21355200-21356200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr14:21355600-21356000	Weak transcription	Monocytes-CD14+_RO01746	blood

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