Variant report

Variant	nsv91
Chromosome Location	chr14:24469668-24504712
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	chr14:24483172-24483507	K562	blood:	n/a	n/a
2	ARID3A	chr14:24483175-24483522	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:24502290-24502595	HepG2	liver:	n/a	n/a
4	BACH1	chr14:24476252-24476312	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr14:24502093-24502738	A549	lung:	n/a	n/a
6	BHLHE40	chr14:24475943-24476541	HepG2	liver:	n/a	n/a
7	BHLHE40	chr14:24483227-24483438	K562	blood:	n/a	n/a
8	BHLHE40	chr14:24483187-24483465	GM12878	blood:	n/a	n/a
9	BRCA1	chr14:24483351-24483423	GM12878	blood:	n/a	n/a
10	CBX3	chr14:24476155-24476416	K562	blood:	n/a	n/a
11	CBX3	chr14:24483218-24483539	K562	blood:	n/a	n/a
12	CBX3	chr14:24501866-24502194	K562	blood:	n/a	n/a
13	CBX3	chr14:24501883-24502114	K562	blood:	n/a	n/a
14	CBX3	chr14:24483227-24483553	K562	blood:	n/a	n/a
15	CEBPB	chr14:24503875-24503956	A549	lung:	n/a	n/a
16	CEBPB	chr14:24504095-24504242	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:24502174-24502650	HepG2	liver:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
18	CEBPB	chr14:24482978-24483461	A549	lung:	n/a	n/a
19	CEBPB	chr14:24502254-24502670	IMR90	lung:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
20	CEBPB	chr14:24502095-24502733	A549	lung:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
21	CEBPB	chr14:24502235-24502633	MCF-7	breast:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
22	CEBPB	chr14:24503705-24503975	MCF-7	breast:	n/a	n/a
23	CEBPB	chr14:24503786-24503943	HepG2	liver:	n/a	n/a
24	CEBPB	chr14:24502325-24502567	HepG2	liver:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
25	CEBPB	chr14:24504202-24504207	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr14:24502292-24502624	K562	blood:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
27	CEBPB	chr14:24502259-24502654	HepG2	liver:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
28	CEBPB	chr14:24502257-24502651	A549	lung:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
29	CEBPB	chr14:24502240-24502694	Hela-S3	cervix:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
30	CEBPB	chr14:24502240-24502596	A549	lung:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
31	CEBPB	chr14:24502247-24502669	HepG2	liver:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
32	CEBPB	chr14:24502288-24502568	K562	blood:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
33	CEBPB	chr14:24503873-24504233	HepG2	liver:	n/a	n/a
34	CEBPD	chr14:24502317-24502638	HepG2	liver:	n/a	chr14:24502435-24502446
35	CEBPD	chr14:24475992-24476248	HepG2	liver:	n/a	n/a
36	CEBPD	chr14:24502325-24502575	HepG2	liver:	n/a	chr14:24502435-24502446
37	CHD1	chr14:24483316-24483498	GM12878	blood:	n/a	n/a
38	CHD2	chr14:24502364-24502617	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr14:24483281-24483447	GM12878	blood:	n/a	n/a
40	CREB1	chr14:24502329-24502597	A549	lung:	n/a	n/a
41	CTCF	chr14:24483100-24483250	A549	lung:	n/a	n/a
42	CTCF	chr14:24483280-24483430	RPTEC	kidney:	n/a	n/a
43	CTCF	chr14:24489820-24489970	GM12870	blood:	n/a	n/a
44	CTCF	chr14:24483260-24483410	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr14:24503720-24503870	NHLF	lung:	n/a	n/a
46	CTCF	chr14:24489260-24489410	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr14:24503720-24503870	HepG2	liver:	n/a	n/a
48	CTCF	chr14:24489360-24489510	AG10803	skin:	n/a	n/a
49	CTCF	chr14:24483280-24483430	GM12868	blood:	n/a	n/a
50	CTCF	chr14:24503440-24503590	GM12872	blood:	n/a	chr14:24503511-24503527 chr14:24503510-24503528

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24478620-24478670	T-47D	breast:	n/a
2	chr14:24503311-24503361	Caco-2	colon:	n/a
3	chr14:24476559-24476609	HRPEpiC	eye:	n/a
4	chr14:24476478-24476528	BJ	skin:	n/a
5	chr14:24503311-24503361	K562	blood:	n/a
6	chr14:24476082-24476132	GM12891	blood:	n/a
7	chr14:24476478-24476528	NB4	blood:	n/a
8	chr14:24475906-24475956	HL-60	blood:	n/a
9	chr14:24478620-24478670	HPAEpiC	pulmonary alveolar:	n/a
10	chr14:24475906-24475956	AG09309	skin:	n/a
11	chr14:24475053-24475103	NHBE	bronchial:	n/a
12	chr14:24503311-24503361	H1-hESC	embryonic stem cell:	embryo
13	chr14:24476478-24476528	HEEpiC	esophagus:	n/a
14	chr14:24476478-24476528	K562	blood:	n/a
15	chr14:24473832-24473882	HCM	heart:	n/a
16	chr14:24476559-24476609	U87	brain:	n/a
17	chr14:24476559-24476609	HCF	heart:	n/a
18	chr14:24475053-24475103	BE2_C	brain:	n/a
19	chr14:24478620-24478670	NT2-D1	testis:	n/a
20	chr14:24473832-24473882	HIPEpiC	eye:	n/a
21	chr14:24476478-24476528	SK-N-MC	brain:	n/a
22	chr14:24475053-24475103	K562	blood:	n/a
23	chr14:24475053-24475103	AG09309	skin:	n/a
24	chr14:24476082-24476132	MCF10A-Er-Src	breast:	n/a
25	chr14:24478620-24478670	AG10803	skin:	n/a
26	chr14:24476559-24476609	ovcar-3	ovarian:	n/a
27	chr14:24475906-24475956	GM12891	blood:	n/a
28	chr14:24503311-24503361	MCF-7	breast:	n/a
29	chr14:24503311-24503361	GM12878	blood:	n/a
30	chr14:24476478-24476528	GM19239	blood:	n/a
31	chr14:24475906-24475956	T-47D	breast:	n/a
32	chr14:24503311-24503361	GM12891	blood:	n/a
33	chr14:24476559-24476609	GM06990	blood:	n/a
34	chr14:24475906-24475956	GM12892	blood:	n/a
35	chr14:24503311-24503361	HEEpiC	esophagus:	n/a
36	chr14:24503311-24503361	U87	brain:	n/a
37	chr14:24476478-24476528	H1-hESC	embryonic stem cell:	embryo
38	chr14:24473832-24473882	AG04450	lung:	fetal
39	chr14:24476082-24476132	HepG2	liver:	n/a
40	chr14:24503311-24503361	NH-A	brain:	n/a
41	chr14:24473832-24473882	HRE	kidney:	n/a
42	chr14:24473832-24473882	AG10803	skin:	n/a
43	chr14:24476478-24476528	AoSMC	blood vessel:	n/a
44	chr14:24473832-24473882	HPAEpiC	pulmonary alveolar:	n/a
45	chr14:24475906-24475956	AG09319	gingival:	n/a
46	chr14:24475053-24475103	SAEC	small airway:	n/a
47	chr14:24475906-24475956	U87	brain:	n/a
48	chr14:24475906-24475956	SKMC	muscle:	n/a
49	chr14:24475906-24475956	HRE	kidney:	n/a
50	chr14:24473832-24473882	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:24482946..24483934-chr14:24503845..24504435,3	MCF-7	breast:
2	chr14:24482659..24484974-chr14:24503307..24504865,2	MCF-7	breast:
3	chr14:24482840..24483718-chr14:24710880..24711620,2	MCF-7	breast:
4	chr14:24422701..24424551-chr14:24504249..24506129,2	MCF-7	breast:
5	chr14:24483262..24483795-chr14:24906005..24906586,2	K562	blood:
6	chr14:24482858..24483785-chr14:24559502..24560237,2	K562	blood:
7	chr14:24503791..24508058-chr14:24562194..24566408,5	MCF-7	breast:
8	chr14:24504490..24506127-chr14:24583788..24585514,2	MCF-7	breast:
9	chr14:24482659..24484974-chr14:24503307..24504865,2	MCF-7	breast:
10	chr14:24476695..24479385-chr14:24563251..24564763,2	MCF-7	breast:
11	chr14:24421533..24423333-chr14:24480435..24482151,2	K562	blood:
12	chr14:24504090..24505966-chr14:24768791..24770568,2	MCF-7	breast:
13	chr14:24482946..24483934-chr14:24503845..24504435,3	MCF-7	breast:
14	chr14:24483165..24483827-chr14:24559565..24560642,4	MCF-7	breast:
15	chr14:24482802..24483800-chr14:24505642..24506553,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000225766	TF binding region
ENSG00000225766	CpG island
ENSG00000196943	chromatin interactions
ENSG00000215256	chromatin interactions
ENSG00000100897	chromatin interactions
ENSG00000157379	chromatin interactions
ENSG00000129535	chromatin interactions
ENSG00000100889	chromatin interactions
ENSG00000225766	chromatin interactions
ENSG00000157326	chromatin interactions
ENSG00000092330	chromatin interactions

Extended variants
information (count: 1420 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1420 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533636646	chr14:24469715-24469716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs550053470	chr14:24469719-24469720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs3832937	chr14:24469720-24469721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs59027712	chr14:24469876-24469877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570063294	chr14:24469892-24469893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528838051	chr14:24469946-24469947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368156723	chr14:24470029-24470030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565736401	chr14:24470056-24470057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372465757	chr14:24470058-24470059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376746348	chr14:24470063-24470064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369323650	chr14:24470073-24470074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371326305	chr14:24470087-24470088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375966037	chr14:24470088-24470089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571342578	chr14:24470098-24470099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537286969	chr14:24470106-24470107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369877396	chr14:24470113-24470114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557269720	chr14:24470130-24470131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs1811890	chr14:24470138-24470139	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs372826656	chr14:24470139-24470140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375757538	chr14:24470144-24470145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376969886	chr14:24470150-24470151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201378287	chr14:24470156-24470157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144805644	chr14:24470167-24470168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572457229	chr14:24470168-24470169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs28535492	chr14:24470180-24470181	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs564645090	chr14:24470186-24470187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs76909974	chr14:24470187-24470188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370529426	chr14:24470192-24470193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs61334310	chr14:24470199-24470200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563626521	chr14:24470202-24470203	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376879565	chr14:24470204-24470205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200895612	chr14:24470207-24470208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs55700022	chr14:24470209-24470210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148108526	chr14:24470218-24470219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs199946299	chr14:24470219-24470220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79847141	chr14:24470231-24470232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
37	rs372329309	chr14:24470243-24470244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs375756199	chr14:24470245-24470246	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369752605	chr14:24470246-24470247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141120035	chr14:24470260-24470261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146938082	chr14:24470261-24470262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551182555	chr14:24470269-24470270	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571346834	chr14:24470274-24470275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138190990	chr14:24470277-24470278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs367972568	chr14:24470285-24470286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372253775	chr14:24470292-24470293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10130249	chr14:24470352-24470353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532242395	chr14:24470397-24470398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567537725	chr14:24470401-24470402	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs536553696	chr14:24470408-24470409	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
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
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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21390271	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:511 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24458800-24476000	Weak transcription	Fetal Intestine Small	intestine
2	chr14:24459000-24475200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:24459200-24470400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr14:24459200-24476000	Weak transcription	Liver	Liver
5	chr14:24459400-24475800	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr14:24459600-24474800	Weak transcription	Dnd41	blood
7	chr14:24470200-24470400	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr14:24470200-24470800	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr14:24470200-24471200	Enhancers	Primary B cells from peripheral blood	blood
10	chr14:24470400-24470800	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr14:24470400-24470800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr14:24470800-24471200	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr14:24470800-24475000	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr14:24471200-24475000	Weak transcription	Primary B cells from peripheral blood	blood
15	chr14:24471200-24475000	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr14:24472800-24476000	Weak transcription	Pancreas	Pancrea
17	chr14:24474000-24475800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr14:24474800-24475000	Enhancers	Primary B cells from cord blood	blood
19	chr14:24474800-24475000	Enhancers	Fetal Brain Female	brain
20	chr14:24474800-24475200	Enhancers	Primary T helper naive cells from peripheral blood	blood
21	chr14:24474800-24475400	Enhancers	Dnd41	blood
22	chr14:24475000-24475200	Enhancers	H1 Cell Line	embryonic stem cell
23	chr14:24475000-24475200	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr14:24475000-24475200	Enhancers	Brain Hippocampus Middle	brain
25	chr14:24475000-24475200	Enhancers	GM12878-XiMat	blood
26	chr14:24475000-24475200	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr14:24475000-24475800	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr14:24475000-24475800	Enhancers	Primary B cells from peripheral blood	blood
29	chr14:24475000-24475800	Enhancers	Primary T cells fromperipheralblood	blood
30	chr14:24475000-24475800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr14:24475000-24475800	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr14:24475000-24475800	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr14:24475000-24475800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr14:24475000-24475800	Enhancers	Fetal Muscle Leg	muscle
35	chr14:24475000-24475800	Enhancers	Stomach Smooth Muscle	stomach
36	chr14:24475000-24476000	Weak transcription	Primary B cells from cord blood	blood
37	chr14:24475200-24475600	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr14:24475200-24475800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr14:24475200-24475800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr14:24475200-24480000	Weak transcription	GM12878-XiMat	blood
41	chr14:24475400-24475600	Enhancers	Fetal Brain Male	brain
42	chr14:24475400-24475600	Flanking Active TSS	Dnd41	blood
43	chr14:24475400-24475800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr14:24475400-24475800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
45	chr14:24475400-24475800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr14:24475400-24475800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr14:24475400-24475800	Enhancers	Adipose Nuclei	Adipose
48	chr14:24475400-24475800	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr14:24475400-24475800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
50	chr14:24475400-24475800	Enhancers	Duodenum Mucosa	Duodenum

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