Variant report

Variant	nsv901663
Chromosome Location	chr14:40640214-40879975
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:709)
CpG islands
(count:490)
Chromatin interactive
region (count:33)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:709 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr14:40787269-40787733	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr14:40808595-40808625	Hela-S3	cervix:	n/a	n/a
3	CBX3	chr14:40781497-40781964	HCT-116	colon:	n/a	n/a
4	CEBPB	chr14:40653195-40653313	A549	lung:	n/a	chr14:40653216-40653229 chr14:40653216-40653227 chr14:40653216-40653229 chr14:40653217-40653228
5	CEBPB	chr14:40777468-40777787	A549	lung:	n/a	chr14:40777637-40777648
6	CEBPB	chr14:40740360-40741168	MCF-7	breast:	n/a	n/a
7	CEBPB	chr14:40781436-40782040	HCT-116	colon:	n/a	n/a
8	CEBPB	chr14:40792398-40792568	HepG2	liver:	n/a	chr14:40792452-40792463 chr14:40792450-40792461
9	CEBPB	chr14:40670088-40670362	HepG2	liver:	n/a	chr14:40670202-40670213
10	CEBPB	chr14:40654411-40654669	HepG2	liver:	n/a	chr14:40654537-40654548
11	CEBPB	chr14:40766084-40766366	HepG2	liver:	n/a	chr14:40766236-40766247 chr14:40766236-40766249
12	CEBPB	chr14:40817387-40817417	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr14:40781562-40781987	HCT-116	colon:	n/a	n/a
14	CEBPB	chr14:40690565-40691096	MCF-7	breast:	n/a	chr14:40690859-40690870
15	CEBPB	chr14:40690711-40691007	HepG2	liver:	n/a	chr14:40690859-40690870
16	CEBPB	chr14:40691273-40691880	MCF-7	breast:	n/a	chr14:40691397-40691408 chr14:40691397-40691408
17	CEBPB	chr14:40868206-40868566	IMR90	lung:	n/a	chr14:40868377-40868388
18	CEBPB	chr14:40698864-40699284	MCF-7	breast:	n/a	n/a
19	CEBPB	chr14:40840922-40841392	HepG2	liver:	n/a	chr14:40841265-40841278 chr14:40841265-40841276 chr14:40841267-40841276
20	CEBPB	chr14:40868209-40868540	A549	lung:	n/a	chr14:40868377-40868388
21	CEBPB	chr14:40682874-40683323	MCF-7	breast:	n/a	n/a
22	CEBPB	chr14:40708473-40708701	HepG2	liver:	n/a	chr14:40708536-40708547
23	CEBPB	chr14:40777488-40777823	IMR90	lung:	n/a	chr14:40777637-40777648
24	CEBPB	chr14:40844308-40844652	HepG2	liver:	n/a	n/a
25	CEBPB	chr14:40864272-40864291	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr14:40683545-40684023	MCF-7	breast:	n/a	n/a
27	CEBPB	chr14:40844299-40844655	A549	lung:	n/a	n/a
28	CEBPB	chr14:40868231-40868559	Hela-S3	cervix:	n/a	chr14:40868377-40868388
29	CEBPB	chr14:40740652-40741098	MCF-7	breast:	n/a	n/a
30	CEBPB	chr14:40844357-40844564	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr14:40691533-40691789	HepG2	liver:	n/a	n/a
32	CEBPB	chr14:40868250-40868459	H1-hESC	embryonic stem cell:	n/a	chr14:40868377-40868388
33	CEBPB	chr14:40868225-40868461	K562	blood:	n/a	chr14:40868377-40868388
34	CEBPB	chr14:40649407-40649727	HepG2	liver:	n/a	chr14:40649589-40649600 chr14:40649541-40649552
35	CEBPB	chr14:40777455-40777816	HepG2	liver:	n/a	chr14:40777637-40777648
36	CEBPB	chr14:40690498-40691880	MCF-7	breast:	n/a	chr14:40690859-40690870 chr14:40691397-40691408 chr14:40691397-40691408
37	CEBPB	chr14:40714405-40714667	HepG2	liver:	n/a	chr14:40714501-40714512
38	CEBPB	chr14:40777495-40777808	H1-hESC	embryonic stem cell:	n/a	chr14:40777637-40777648
39	CEBPB	chr14:40787701-40787742	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr14:40840907-40841139	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr14:40683519-40683910	MCF-7	breast:	n/a	n/a
42	CEBPB	chr14:40844332-40844672	IMR90	lung:	n/a	n/a
43	CEBPB	chr14:40855306-40855459	HepG2	liver:	n/a	n/a
44	CEBPB	chr14:40653100-40653399	HepG2	liver:	n/a	chr14:40653216-40653229 chr14:40653216-40653227 chr14:40653216-40653229 chr14:40653217-40653228
45	CEBPB	chr14:40786957-40787099	HepG2	liver:	n/a	chr14:40787041-40787052
46	CEBPB	chr14:40739366-40739504	HepG2	liver:	n/a	chr14:40739434-40739447 chr14:40739436-40739445 chr14:40739434-40739445
47	CEBPB	chr14:40777458-40777834	MCF-7	breast:	n/a	chr14:40777637-40777648
48	CEBPB	chr14:40675844-40676060	HepG2	liver:	n/a	chr14:40675887-40675898
49	CEBPB	chr14:40868203-40868561	HepG2	liver:	n/a	chr14:40868377-40868388
50	CHD1	chr14:40817059-40817259	H1-hESC	embryonic stem cell:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:40817565-40817615	HCT-116	colon:	n/a
2	chr14:40809000-40809050	NHDF-neo	bronchial:	n/a
3	chr14:40817565-40817615	HCT-116	colon:	n/a
4	chr14:40809000-40809050	NHDF-neo	bronchial:	n/a
5	chr14:40685908-40685958	GM19239	blood:	n/a
6	chr14:40817565-40817615	Hepatocyte	liver:	n/a
7	chr14:40817444-40817494	SK-N-MC	brain:	n/a
8	chr14:40685771-40685821	RPTEC	kidney:	n/a
9	chr14:40809000-40809050	ECC-1	luminal epithelium:	n/a
10	chr14:40685908-40685958	HNPCEpiC	eye:	n/a
11	chr14:40686259-40686309	IMR90	lung:	fetal
12	chr14:40817444-40817494	HL-60	blood:	n/a
13	chr14:40685908-40685958	PFSK-1	brain:	n/a
14	chr14:40832309-40832359	AG04450	lung:	fetal
15	chr14:40686259-40686309	HRE	kidney:	n/a
16	chr14:40832309-40832359	BJ	skin:	n/a
17	chr14:40817565-40817615	U87	brain:	n/a
18	chr14:40685771-40685821	GM19239	blood:	n/a
19	chr14:40685771-40685821	AG09309	skin:	n/a
20	chr14:40685908-40685958	HCF	heart:	n/a
21	chr14:40685908-40685958	U87	brain:	n/a
22	chr14:40685908-40685958	A549	lung:	n/a
23	chr14:40809000-40809050	NH-A	brain:	n/a
24	chr14:40686259-40686309	HCF	heart:	n/a
25	chr14:40817565-40817615	GM19239	blood:	n/a
26	chr14:40809000-40809050	BE2_C	brain:	n/a
27	chr14:40686341-40686391	HMEC	breast:	n/a
28	chr14:40832309-40832359	U87	brain:	n/a
29	chr14:40685908-40685958	HIPEpiC	eye:	n/a
30	chr14:40685771-40685821	NHDF-neo	bronchial:	n/a
31	chr14:40685908-40685958	H1-hESC	embryonic stem cell:	embryo
32	chr14:40685771-40685821	HNPCEpiC	eye:	n/a
33	chr14:40832309-40832359	SKMC	muscle:	n/a
34	chr14:40809000-40809050	PrEC	prostate:	n/a
35	chr14:40832309-40832359	SK-N-MC	brain:	n/a
36	chr14:40817565-40817615	HL-60	blood:	n/a
37	chr14:40686341-40686391	AG10803	skin:	n/a
38	chr14:40685908-40685958	HepG2	liver:	n/a
39	chr14:40809000-40809050	AG09309	skin:	n/a
40	chr14:40832309-40832359	ovcar-3	ovarian:	n/a
41	chr14:40809000-40809050	GM19239	blood:	n/a
42	chr14:40817444-40817494	PANC-1	pancreas:	n/a
43	chr14:40686259-40686309	HEEpiC	esophagus:	n/a
44	chr14:40685908-40685958	SK-N-SH_RA	brain:	n/a
45	chr14:40686341-40686391	PANC-1	pancreas:	n/a
46	chr14:40809000-40809050	K562	blood:	n/a
47	chr14:40685771-40685821	Caco-2	colon:	n/a
48	chr14:40832309-40832359	GM12878	blood:	n/a
49	chr14:40832309-40832359	BE2_C	brain:	n/a
50	chr14:40685771-40685821	AG10803	skin:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:40860557..40863122-chr14:40865189..40868111,2	MCF-7	breast:
2	chr14:40672645..40675183-chr14:40686858..40690836,3	MCF-7	breast:
3	chr14:40669052..40670615-chr14:40680616..40683029,2	MCF-7	breast:
4	chr14:40665163..40668021-chr14:40668586..40671186,2	MCF-7	breast:
5	chr14:40676693..40679058-chr14:40690330..40692454,2	MCF-7	breast:
6	chr14:40669052..40670615-chr14:40680616..40683029,2	MCF-7	breast:
7	chr14:40852272..40855989-chr14:40856721..40860430,4	MCF-7	breast:
8	chr14:40676693..40679058-chr14:40690330..40692454,2	MCF-7	breast:
9	chr14:40762742..40765094-chr14:40766225..40768679,2	K562	blood:
10	chr14:40691066..40691614-chr14:40740770..40741278,2	MCF-7	breast:
11	chr14:40672645..40675183-chr14:40686858..40690836,3	MCF-7	breast:
12	chr14:40681513..40685602-chr14:40687253..40690509,3	MCF-7	breast:
13	chr14:40863521..40865803-chr14:40870395..40872089,2	MCF-7	breast:
14	chr14:40665163..40668021-chr14:40668586..40671186,2	MCF-7	breast:
15	chr14:40852272..40855989-chr14:40856721..40860430,4	MCF-7	breast:
16	chr14:40762742..40765094-chr14:40766225..40768679,2	K562	blood:
17	chr14:40857820..40860668-chr14:40862186..40864573,2	MCF-7	breast:
18	chr14:40457857..40458829-chr14:40749466..40750494,4	MCF-7	breast:
19	chr14:40653379..40656063-chr14:40662634..40665272,2	MCF-7	breast:
20	chr14:40879663..40882573-chr14:40893834..40895743,2	MCF-7	breast:
21	chr14:40839183..40841621-chr14:40841712..40843758,2	MCF-7	breast:
22	chr14:40862573..40865201-chr14:40865784..40867370,2	K562	blood:
23	chr14:40860557..40863122-chr14:40865189..40868111,2	MCF-7	breast:
24	chr14:40653379..40656063-chr14:40662634..40665272,2	MCF-7	breast:
25	chr14:40857820..40860668-chr14:40862186..40864573,2	MCF-7	breast:
26	chr14:40863521..40865803-chr14:40870395..40872089,2	MCF-7	breast:
27	chr14:40721840..40722668-chr15:81828412..81828932,3	MCF-7	breast:
28	chr14:40681513..40685602-chr14:40687253..40690509,3	MCF-7	breast:
29	chr14:40690264..40692278-chr14:40698670..40700192,2	MCF-7	breast:
30	chr14:40691066..40691614-chr14:40740770..40741278,2	MCF-7	breast:
31	chr14:40862573..40865201-chr14:40865784..40867370,2	K562	blood:
32	chr14:40690264..40692278-chr14:40698670..40700192,2	MCF-7	breast:
33	chr14:40839183..40841621-chr14:40841712..40843758,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTAGE5-2	chr14:40855738-40855998	ENSG00000258418
2	lnc-CTAGE5-3	chr14:40856762-40857244	ENSG00000258480
3	lnc-CTAGE5-3	chr14:40858281-40858344	ENSG00000258480
4	lnc-CTAGE5-2	chr14:40855456-40855647	ENSG00000258418

No data

Variant related genes	Relation type
ENSG00000258418	TF binding region
ENSG00000258480	TF binding region
ENSG00000258418	CpG island
ENSG00000258480	CpG island
ENSG00000258480	chromatin interactions
ENSG00000258418	chromatin interactions

Extended variants
information (count: 2990 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2990 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150290186	chr14:40672802-40672803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs537450521	chr14:40672803-40672804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373585137	chr14:40672808-40672809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs368856857	chr14:40672842-40672843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs137913369	chr14:40672853-40672854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs377138047	chr14:40672856-40672857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143480814	chr14:40672861-40672862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs145904249	chr14:40672875-40672876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34919515	chr14:40672885-40672886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181519851	chr14:40672898-40672899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs541995852	chr14:40672914-40672915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139240131	chr14:40672920-40672921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186490823	chr14:40672929-40672930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544628604	chr14:40672932-40672933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376942907	chr14:40672951-40672952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs34013092	chr14:40672956-40672957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564341464	chr14:40672966-40672967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs116168347	chr14:40673005-40673006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149411761	chr14:40673007-40673008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs538674778	chr14:40673053-40673054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs144794379	chr14:40673113-40673114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs551437446	chr14:40673130-40673131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560124711	chr14:40673138-40673139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs116849918	chr14:40673154-40673155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12881515	chr14:40673157-40673158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs568619841	chr14:40673197-40673198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs531173556	chr14:40673207-40673208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375798983	chr14:40673221-40673222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148578511	chr14:40673238-40673239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs8006378	chr14:40673256-40673257	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs142010007	chr14:40673290-40673291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536176750	chr14:40673311-40673312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566998268	chr14:40673367-40673368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189609519	chr14:40673384-40673385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146047998	chr14:40673390-40673391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575826014	chr14:40673438-40673439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140043484	chr14:40673441-40673442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181909808	chr14:40673449-40673450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs371854333	chr14:40673491-40673492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs577854983	chr14:40673506-40673507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540200810	chr14:40673511-40673512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560292071	chr14:40673516-40673517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529039602	chr14:40673523-40673524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs542428607	chr14:40673547-40673548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs76999768	chr14:40673612-40673613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531332065	chr14:40673629-40673630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs143689462	chr14:40673633-40673634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571192895	chr14:40673643-40673644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567449149	chr14:40673663-40673664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537976306	chr14:40673703-40673704	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Autism	22495311	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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21364760	CNVD
Intellectual disability	22102821	CNVD
Schizophrenia	23813976	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	19805367	CNVD

Chromatin state (count:163 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:40672800-40674000	Enhancers	Fetal Muscle Leg	muscle
2	chr14:40681600-40682200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr14:40687000-40688600	Enhancers	Primary B cells from peripheral blood	blood
4	chr14:40687400-40689000	Enhancers	Primary B cells from cord blood	blood
5	chr14:40717800-40718400	Enhancers	Fetal Kidney	kidney
6	chr14:40740600-40741000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr14:40740600-40741000	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr14:40753000-40753200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr14:40753200-40753800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr14:40753800-40754400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr14:40755200-40756000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr14:40756400-40756800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr14:40761000-40763600	Enhancers	Primary B cells from cord blood	blood
14	chr14:40761400-40761600	Enhancers	Primary B cells from peripheral blood	blood
15	chr14:40761600-40762200	Weak transcription	Primary B cells from peripheral blood	blood
16	chr14:40762200-40763400	Enhancers	Primary B cells from peripheral blood	blood
17	chr14:40763000-40763200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr14:40777000-40777200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr14:40777000-40777200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr14:40777000-40787400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr14:40782000-40782400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr14:40787400-40788000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr14:40787400-40788000	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr14:40787400-40788000	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr14:40787600-40788000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr14:40794600-40794800	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr14:40794600-40795400	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr14:40794800-40796200	Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr14:40795000-40795200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr14:40795000-40795800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
31	chr14:40795200-40795800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr14:40795200-40796000	Active TSS	iPS-15b Cell Line	embryonic stem cell
33	chr14:40795400-40795800	Active TSS	H1 Cell Line	embryonic stem cell
34	chr14:40795400-40795800	Enhancers	H9 Cell Line	embryonic stem cell
35	chr14:40795400-40796000	Active TSS	HUES6 Cell Line	embryonic stem cell
36	chr14:40795400-40796000	Active TSS	HUES64 Cell Line	embryonic stem cell
37	chr14:40795600-40796200	Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr14:40795800-40796200	Enhancers	H1 Cell Line	embryonic stem cell
39	chr14:40795800-40801600	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr14:40796000-40801600	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr14:40801600-40801800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
42	chr14:40801600-40802200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
43	chr14:40801800-40806000	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr14:40805000-40806600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr14:40805200-40806600	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr14:40805400-40806600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr14:40805400-40806800	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr14:40805600-40806200	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr14:40805600-40806600	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr14:40806000-40806400	Enhancers	HUES48 Cell Line	embryonic stem cell

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