Variant report

Variant	esv3511206
Chromosome Location	chr14:21350813-21414167
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	CEBPB	chr14:21387328-21387608	MCF-7	breast:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
2	CEBPB	chr14:21362091-21362409	HepG2	liver:	n/a	chr14:21362250-21362261
3	CEBPB	chr14:21362153-21362361	IMR90	lung:	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	chr14:21390712-21390883	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	chr14:21387233-21387541	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
8	CEBPB	chr14:21387189-21387569	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
9	CEBPB	chr14:21390675-21390974	A549	lung:	n/a	n/a
10	CEBPB	chr14:21362168-21362307	Hela-S3	cervix:	n/a	chr14:21362250-21362261
11	CEBPB	chr14:21387196-21387557	Hela-S3	cervix:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
12	CEBPB	chr14:21387301-21387487	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
13	CEBPB	chr14:21359339-21359538	K562	blood:	n/a	chr14:21359447-21359460
14	CEBPB	chr14:21390663-21390987	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:21390705-21391054	MCF-7	breast:	n/a	n/a
16	CEBPB	chr14:21404959-21405123	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr14:21362130-21362293	A549	lung:	n/a	chr14:21362250-21362261
18	CEBPB	chr14:21390806-21390847	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr14:21404892-21405089	MCF-7	breast:	n/a	n/a
20	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
21	CEBPB	chr14:21387183-21387567	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
22	CEBPB	chr14:21362247-21362271	H1-hESC	embryonic stem cell:	n/a	chr14:21362250-21362261
23	CEBPB	chr14:21387140-21387598	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
24	CEBPB	chr14:21387184-21387565	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
25	CEBPB	chr14:21373948-21374221	HepG2	liver:	n/a	chr14:21374057-21374070
26	CEBPB	chr14:21362201-21362274	K562	blood:	n/a	chr14:21362250-21362261
27	CEBPB	chr14:21390780-21390974	K562	blood:	n/a	n/a
28	CEBPB	chr14:21372661-21372946	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr14:21404946-21405126	K562	blood:	n/a	n/a
30	CEBPB	chr14:21387296-21387479	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
31	CEBPD	chr14:21387228-21387447	HepG2	liver:	n/a	chr14:21387366-21387377 chr14:21387368-21387377
32	CTCF	chr14:21402475-21402553	GM19239	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
33	CTCF	chr14:21402400-21402550	K562	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
34	CTCF	chr14:21401920-21402070	AG09319	gingival:	n/a	n/a
35	CTCF	chr14:21402385-21402641	A549	lung:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
36	CTCF	chr14:21402440-21402590	HVMF	connective:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
37	CTCF	chr14:21402460-21402610	AoAF	blood vessel:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
38	CTCF	chr14:21402440-21402590	HPAF	blood vessel:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
39	CTCF	chr14:21387762-21387795	Lung_OC	lung:	n/a	n/a
40	CTCF	chr14:21402420-21402570	NHLF	lung:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
41	CTCF	chr14:21402380-21402530	Caco-2	colon:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
42	CTCF	chr14:21402700-21402850	BE2_C	brain:	n/a	n/a
43	CTCF	chr14:21372617-21372879	K562	blood:	n/a	n/a
44	CTCF	chr14:21402400-21402550	HCFaa	heart:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
45	CTCF	chr14:21372644-21372825	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr14:21402440-21402590	GM12870	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
47	CTCF	chr14:21372680-21372830	HCT-116	colon:	n/a	n/a
48	CTCF	chr14:21372602-21372857	K562	blood:	n/a	n/a
49	CTCF	chr14:21372601-21372892	K562	blood:	n/a	n/a
50	CTCF	chr14:21372680-21372830	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21358233-21358283	SAEC	small airway:	n/a
2	chr14:21358233-21358283	AG04450	lung:	fetal
3	chr14:21358099-21358149	Hepatocyte	liver:	n/a
4	chr14:21359943-21359993	LNCaP	prostate:	n/a
5	chr14:21359943-21359993	PrEC	prostate:	n/a
6	chr14:21386453-21386503	AG10803	skin:	n/a
7	chr14:21386453-21386503	HepG2	liver:	n/a
8	chr14:21358099-21358149	HepG2	liver:	n/a
9	chr14:21359295-21359345	MCF10A-Er-Src	breast:	n/a
10	chr14:21358099-21358149	LNCaP	prostate:	n/a
11	chr14:21359737-21359787	HUVEC	blood vessel:	n/a
12	chr14:21359737-21359787	GM19239	blood:	n/a
13	chr14:21358099-21358149	AG09309	skin:	n/a
14	chr14:21358099-21358149	SK-N-SH_RA	brain:	n/a
15	chr14:21386453-21386503	U87	brain:	n/a
16	chr14:21359295-21359345	HCF	heart:	n/a
17	chr14:21358233-21358283	GM19239	blood:	n/a
18	chr14:21359943-21359993	RPTEC	kidney:	n/a
19	chr14:21359295-21359345	AG09309	skin:	n/a
20	chr14:21358233-21358283	U87	brain:	n/a
21	chr14:21359943-21359993	SAEC	small airway:	n/a
22	chr14:21358099-21358149	HAEpiC	amniotic membrane:	n/a
23	chr14:21358099-21358149	HIPEpiC	eye:	n/a
24	chr14:21359295-21359345	HRPEpiC	eye:	n/a
25	chr14:21358233-21358283	BJ	skin:	n/a
26	chr14:21358233-21358283	HCM	heart:	n/a
27	chr14:21386453-21386503	GM12878	blood:	n/a
28	chr14:21358099-21358149	SK-N-MC	brain:	n/a
29	chr14:21358233-21358283	ProgFib	skin:	n/a
30	chr14:21359295-21359345	BJ	skin:	n/a
31	chr14:21358099-21358149	PrEC	prostate:	n/a
32	chr14:21359737-21359787	SK-N-SH_RA	brain:	n/a
33	chr14:21359295-21359345	PFSK-1	brain:	n/a
34	chr14:21359943-21359993	GM19239	blood:	n/a
35	chr14:21358099-21358149	HEK293	kidney:	embryo
36	chr14:21359295-21359345	SK-N-MC	brain:	n/a
37	chr14:21358233-21358283	MCF-7	breast:	n/a
38	chr14:21359295-21359345	Caco-2	colon:	n/a
39	chr14:21386453-21386503	AG09309	skin:	n/a
40	chr14:21359295-21359345	PrEC	prostate:	n/a
41	chr14:21358233-21358283	HRPEpiC	eye:	n/a
42	chr14:21386453-21386503	HUVEC	blood vessel:	n/a
43	chr14:21359295-21359345	A549	lung:	n/a
44	chr14:21358099-21358149	IMR90	lung:	fetal
45	chr14:21358233-21358283	NHDF-neo	bronchial:	n/a
46	chr14:21359943-21359993	NB4	blood:	n/a
47	chr14:21386453-21386503	HEK293	kidney:	embryo
48	chr14:21359295-21359345	AG10803	skin:	n/a
49	chr14:21358233-21358283	IMR90	lung:	fetal
50	chr14:21359943-21359993	Jurkat	blood:	n/a

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

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

Extended variants
information (count: 1912 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1912 , 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	rs142391976	chr14:21350909-21350910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs56150642	chr14:21351124-21351125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs56227189	chr14:21351184-21351185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs55653606	chr14:21351196-21351197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs55667097	chr14:21351223-21351224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs56039998	chr14:21351227-21351228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs56348910	chr14:21351244-21351245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs56109210	chr14:21351246-21351247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs56073255	chr14:21351317-21351318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1743058	chr14:21351408-21351409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144594396	chr14:21351609-21351610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532727424	chr14:21351622-21351623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377696491	chr14:21351645-21351646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs55647138	chr14:21351647-21351648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538161587	chr14:21351737-21351738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548603219	chr14:21351776-21351777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs55987805	chr14:21351786-21351787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374754701	chr14:21351799-21351800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549842890	chr14:21351969-21351970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77835194	chr14:21351978-21351979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149435878	chr14:21351993-21351994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs1612407	chr14:21352006-21352007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556957210	chr14:21352046-21352047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567261726	chr14:21352047-21352048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536300884	chr14:21352070-21352071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs61980361	chr14:21352088-21352089	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs572886484	chr14:21352090-21352091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552514902	chr14:21352103-21352104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570997535	chr14:21352159-21352160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186249382	chr14:21352268-21352269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538359689	chr14:21352269-21352270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575446888	chr14:21352290-21352291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544185989	chr14:21352321-21352322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560886262	chr14:21352417-21352418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191494104	chr14:21352437-21352438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs34341736	chr14:21352456-21352457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112700740	chr14:21352459-21352460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78948696	chr14:21352460-21352461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2984144	chr14:21352465-21352466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143797459	chr14:21352471-21352472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs398056919	chr14:21352478-21352479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs398024501	chr14:21352480-21352481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143247800	chr14:21352482-21352483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs55680252	chr14:21352484-21352485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560180796	chr14:21352485-21352486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532522818	chr14:21352487-21352488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113164123	chr14:21352488-21352489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552693422	chr14:21352489-21352490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112115770	chr14:21352491-21352492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs80153059	chr14:21352492-21352493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:141 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21350000-21354200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr14:21350200-21352800	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr14:21350200-21352800	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr14:21350200-21354000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr14:21350200-21354200	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr14:21352800-21353200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr14:21352800-21353400	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr14:21352800-21355600	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr14:21353400-21353800	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr14:21353800-21355000	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr14:21354000-21354200	Weak transcription	Thymus	Thymus
12	chr14:21354000-21355000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr14:21354200-21354400	Enhancers	Thymus	Thymus
14	chr14:21354200-21354800	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr14:21354200-21354800	Enhancers	Primary hematopoietic stem cells	blood
16	chr14:21354200-21355200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr14:21354400-21357200	Weak transcription	Thymus	Thymus
18	chr14:21354800-21355800	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr14:21355000-21356000	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr14:21355200-21356200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr14:21355600-21356000	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr14:21355800-21358200	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr14:21356000-21359200	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr14:21356000-21362200	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr14:21356200-21356800	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr14:21356200-21357200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr14:21356800-21359400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr14:21357200-21357400	Enhancers	Thymus	Thymus
29	chr14:21358200-21358600	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr14:21358600-21359600	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr14:21359200-21360400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
32	chr14:21359400-21359800	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr14:21359600-21359800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
34	chr14:21359800-21360000	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr14:21360000-21360200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
36	chr14:21360200-21360800	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr14:21360400-21362400	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr14:21360800-21361200	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr14:21361200-21362200	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr14:21362200-21363200	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr14:21362200-21364600	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr14:21362400-21363400	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr14:21363200-21363800	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr14:21363400-21364200	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr14:21363800-21364600	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr14:21364200-21364400	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr14:21364400-21364800	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr14:21364600-21365600	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr14:21364600-21365600	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr14:21364800-21365400	Weak transcription	Monocytes-CD14+_RO01746	blood

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