Variant report

Variant	esv3324566
Chromosome Location	chr14:104393824-104396372
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:26)
CpG islands
(count:428)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:26 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr14:104394557-104395284	Hela-S3	cervix:	n/a	n/a
2	CTCF	chr14:104394223-104394259	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr14:104394521-104394607	Hela-S3	cervix:	n/a	n/a
4	CTCF	chr14:104394000-104394210	HRE	kidney:	n/a	n/a
5	E2F6	chr14:104394552-104395015	H1-hESC	embryonic stem cell:	n/a	chr14:104394715-104394729 chr14:104394792-104394804 chr14:104394617-104394627 chr14:104394755-104394764
6	E2F6	chr14:104394607-104394991	H1-hESC	embryonic stem cell:	n/a	chr14:104394715-104394729 chr14:104394792-104394804 chr14:104394617-104394627 chr14:104394755-104394764
7	E2F6	chr14:104394490-104395125	Hela-S3	cervix:	n/a	chr14:104394715-104394729 chr14:104394792-104394804 chr14:104394617-104394627 chr14:104394755-104394764 chr14:104395069-104395078
8	HCFC1	chr14:104394314-104395181	Hela-S3	cervix:	n/a	n/a
9	MAX	chr14:104394475-104394955	Hela-S3	cervix:	n/a	chr14:104394523-104394532
10	MAX	chr14:104393709-104393964	K562	blood:	n/a	chr14:104393901-104393910
11	MAZ	chr14:104394844-104394952	Hela-S3	cervix:	n/a	n/a
12	MXI1	chr14:104394650-104394907	Hela-S3	cervix:	n/a	n/a
13	NFYA	chr14:104394551-104394899	Hela-S3	cervix:	n/a	n/a
14	NFYB	chr14:104394601-104395027	Hela-S3	cervix:	n/a	n/a
15	NFYB	chr14:104394575-104394849	K562	blood:	n/a	n/a
16	POLR2A	chr14:104394475-104395117	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr14:104395427-104395434	MCF-7	breast:	n/a	n/a
18	POLR2A	chr14:104395512-104395515	MCF-7	breast:	n/a	n/a
19	POLR2A	chr14:104395435-104395510	MCF-7	breast:	n/a	n/a
20	POLR2A	chr14:104394696-104395045	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr14:104394646-104395016	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr14:104394707-104395045	Hela-S3	cervix:	n/a	n/a
23	RFX5	chr14:104394471-104394852	Hela-S3	cervix:	n/a	n/a
24	SMC3	chr14:104394569-104394608	Hela-S3	cervix:	n/a	n/a
25	TBP	chr14:104394805-104394871	Hela-S3	cervix:	n/a	n/a
26	ZNF143	chr14:104394457-104394805	Hela-S3	cervix:	n/a	chr14:104394620-104394638

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104394621-104394671	HIPEpiC	eye:	n/a
2	chr14:104394621-104394671	HIPEpiC	eye:	n/a
3	chr14:104394430-104394480	NH-A	brain:	n/a
4	chr14:104395485-104395535	GM19239	blood:	n/a
5	chr14:104394430-104394480	AoSMC	blood vessel:	n/a
6	chr14:104394621-104394671	GM19239	blood:	n/a
7	chr14:104395165-104395215	HRCEpiC	kidney:	n/a
8	chr14:104394831-104394881	AoSMC	blood vessel:	n/a
9	chr14:104395165-104395215	SKMC	muscle:	n/a
10	chr14:104394621-104394671	AoSMC	blood vessel:	n/a
11	chr14:104394621-104394671	HEEpiC	esophagus:	n/a
12	chr14:104395429-104395479	HPAEpiC	pulmonary alveolar:	n/a
13	chr14:104394831-104394881	HepG2	liver:	n/a
14	chr14:104394621-104394671	HCF	heart:	n/a
15	chr14:104394430-104394480	A549	lung:	n/a
16	chr14:104395485-104395535	T-47D	breast:	n/a
17	chr14:104395485-104395535	LNCaP	prostate:	n/a
18	chr14:104395485-104395535	AG04449	skin:	fetal
19	chr14:104394530-104394580	PrEC	prostate:	n/a
20	chr14:104395165-104395215	HRPEpiC	eye:	n/a
21	chr14:104395429-104395479	AG04450	lung:	fetal
22	chr14:104395165-104395215	BJ	skin:	n/a
23	chr14:104395485-104395535	HMEC	breast:	n/a
24	chr14:104394621-104394671	SKMC	muscle:	n/a
25	chr14:104394530-104394580	HPAEpiC	pulmonary alveolar:	n/a
26	chr14:104395165-104395215	HNPCEpiC	eye:	n/a
27	chr14:104394430-104394480	ECC-1	luminal epithelium:	n/a
28	chr14:104395429-104395479	HRPEpiC	eye:	n/a
29	chr14:104394831-104394881	HL-60	blood:	n/a
30	chr14:104394831-104394881	IMR90	lung:	fetal
31	chr14:104394430-104394480	AG09309	skin:	n/a
32	chr14:104394831-104394881	Hepatocyte	liver:	n/a
33	chr14:104394621-104394671	AG10803	skin:	n/a
34	chr14:104395429-104395479	AG09309	skin:	n/a
35	chr14:104394621-104394671	PFSK-1	brain:	n/a
36	chr14:104395165-104395215	LNCaP	prostate:	n/a
37	chr14:104394530-104394580	PFSK-1	brain:	n/a
38	chr14:104394831-104394881	ProgFib	skin:	n/a
39	chr14:104394621-104394671	Hepatocyte	liver:	n/a
40	chr14:104394621-104394671	NHBE	bronchial:	n/a
41	chr14:104395165-104395215	PANC-1	pancreas:	n/a
42	chr14:104394831-104394881	H1-hESC	embryonic stem cell:	embryo
43	chr14:104395485-104395535	U87	brain:	n/a
44	chr14:104394430-104394480	HEK293	kidney:	embryo
45	chr14:104394530-104394580	U87	brain:	n/a
46	chr14:104394831-104394881	HNPCEpiC	eye:	n/a
47	chr14:104395165-104395215	AG04450	lung:	fetal
48	chr14:104395485-104395535	GM12878	blood:	n/a
49	chr14:104395165-104395215	HepG2	liver:	n/a
50	chr14:104395485-104395535	NHBE	bronchial:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:104393603..104397064-chr14:104407702..104410726,3	K562	blood:
2	chr14:104391863..104393842-chr14:104396870..104399828,2	K562	blood:
3	chr14:104395726..104398249-chr14:104421446..104423004,2	K562	blood:
4	chr14:104387638..104390416-chr14:104390451..104394175,4	K562	blood:
5	chr14:104385710..104388983-chr14:104393675..104397966,4	MCF-7	breast:
6	chr14:104159423..104160385-chr14:104396350..104397254,2	MCF-7	breast:
7	chr14:104393603..104396242-chr14:104407114..104410000,4	K562	blood:
8	chr14:104379142..104381534-chr14:104393675..104395664,2	K562	blood:

No data

Variant related genes	Relation type
TDRD9	TF binding region
C14orf2	TF binding region
TDRD9	CpG island
C14orf2	CpG island
ENSG00000227729	chromatin interactions
ENSG00000156411	chromatin interactions

Extended variants
information (count: 104 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:104 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72712871	chr14:104393891-104393892	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs74548289	chr14:104393903-104393904	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs190449168	chr14:104393905-104393906	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs1040812	chr14:104393932-104393933	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs8014519	chr14:104393947-104393948	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs183391985	chr14:104393990-104393991	ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs561611715	chr14:104394000-104394001	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs545893481	chr14:104394004-104394005	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs73352428	chr14:104394035-104394036	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs540273417	chr14:104394049-104394050	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs560604425	chr14:104394092-104394093	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs140677218	chr14:104394094-104394095	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs145748280	chr14:104394102-104394103	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs115365255	chr14:104394144-104394145	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs536267147	chr14:104394199-104394200	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs74086759	chr14:104394210-104394211	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs28563863	chr14:104394230-104394231	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs533733891	chr14:104394238-104394239	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs562796190	chr14:104394270-104394271	ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs547094478	chr14:104394317-104394318	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs374528698	chr14:104394340-104394341	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs375698382	chr14:104394386-104394387	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs370067446	chr14:104394424-104394425	ZNF genes & repeats Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs187850754	chr14:104394432-104394433	ZNF genes & repeats Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs10149651	chr14:104394440-104394441	ZNF genes & repeats Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs372311010	chr14:104394459-104394460	ZNF genes & repeats Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs144284991	chr14:104394468-104394469	ZNF genes & repeats Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs555257081	chr14:104394548-104394549	ZNF genes & repeats Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs148307886	chr14:104394556-104394557	ZNF genes & repeats Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs141396018	chr14:104394572-104394573	ZNF genes & repeats Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs560269207	chr14:104394590-104394591	ZNF genes & repeats Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs192364024	chr14:104394599-104394600	ZNF genes & repeats Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs545887384	chr14:104394634-104394635	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs113602507	chr14:104394638-104394639	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs562682555	chr14:104394667-104394668	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs531362452	chr14:104394699-104394700	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs530246903	chr14:104394754-104394755	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs113496080	chr14:104394774-104394775	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs9324065	chr14:104394835-104394836	Weak transcription Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs9324066	chr14:104394850-104394851	Weak transcription Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs184390484	chr14:104394879-104394880	Weak transcription Active TSS Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs187691561	chr14:104394894-104394895	Weak transcription Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs539463501	chr14:104394897-104394898	Weak transcription Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs549865389	chr14:104394911-104394912	Weak transcription Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs569772232	chr14:104394944-104394945	Weak transcription Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs538416055	chr14:104394982-104394983	Weak transcription Active TSS Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs112776471	chr14:104395048-104395049	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs376931720	chr14:104395108-104395109	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs555214454	chr14:104395154-104395155	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs368783260	chr14:104395156-104395157	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
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
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
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104390200-104395400	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr14:104392200-104395200	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr14:104392400-104395600	Weak transcription	HepG2	liver
4	chr14:104393800-104394600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr14:104394400-104395800	Active TSS	Hela-S3	cervix
6	chr14:104394600-104395000	Enhancers	Spleen	Spleen
7	chr14:104394600-104398200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr14:104394800-104395000	Enhancers	Pancreas	Pancrea
9	chr14:104394800-104395200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr14:104394800-104395200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr14:104394800-104395200	Bivalent/Poised TSS	Fetal Brain Female	brain
12	chr14:104394800-104395200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
13	chr14:104395000-104401200	Weak transcription	Spleen	Spleen
14	chr14:104395200-104395600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr14:104395200-104395600	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr14:104395200-104395600	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr14:104395400-104396200	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr14:104395400-104399400	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr14:104395600-104395800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr14:104395600-104397200	Enhancers	HepG2	liver
21	chr14:104395600-104398200	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr14:104395800-104396000	Flanking Active TSS	Hela-S3	cervix
23	chr14:104395800-104396200	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr14:104396000-104396200	Active TSS	Hela-S3	cervix
25	chr14:104396200-104396600	Flanking Active TSS	Hela-S3	cervix
26	chr14:104396200-104397000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
27	chr14:104396200-104397200	Enhancers	Primary B cells from cord blood	blood
28	chr14:104396200-104399800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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