Variant report

Variant	nsv528830
Chromosome Location	chr14:40855032-40964161
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:439)
CpG islands
(count:62)
Chromatin interactive
region (count:18)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr14:40855306-40855459	HepG2	liver:	n/a	n/a
2	CEBPB	chr14:40890926-40891001	HepG2	liver:	n/a	n/a
3	CEBPB	chr14:40951668-40952003	HepG2	liver:	n/a	chr14:40951843-40951854 chr14:40951841-40951852 chr14:40951843-40951852
4	CEBPB	chr14:40921365-40921502	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr14:40864272-40864291	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr14:40947143-40947245	HepG2	liver:	n/a	chr14:40947184-40947195
7	CEBPB	chr14:40868206-40868566	IMR90	lung:	n/a	chr14:40868377-40868388
8	CEBPB	chr14:40929916-40930124	HepG2	liver:	n/a	n/a
9	CEBPB	chr14:40925582-40925755	A549	lung:	n/a	chr14:40925668-40925679
10	CEBPB	chr14:40951732-40951949	H1-hESC	embryonic stem cell:	n/a	chr14:40951843-40951854 chr14:40951841-40951852 chr14:40951843-40951852
11	CEBPB	chr14:40925538-40925827	HepG2	liver:	n/a	chr14:40925668-40925679
12	CEBPB	chr14:40883671-40884113	MCF-7	breast:	n/a	n/a
13	CEBPB	chr14:40868203-40868561	HepG2	liver:	n/a	chr14:40868377-40868388
14	CEBPB	chr14:40883524-40884236	MCF-7	breast:	n/a	n/a
15	CEBPB	chr14:40957075-40957435	HepG2	liver:	n/a	chr14:40957285-40957296 chr14:40957256-40957267 chr14:40957255-40957266 chr14:40957255-40957268
16	CEBPB	chr14:40942941-40943296	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:40883834-40884107	HepG2	liver:	n/a	n/a
18	CEBPB	chr14:40868209-40868540	A549	lung:	n/a	chr14:40868377-40868388
19	CEBPB	chr14:40868225-40868461	K562	blood:	n/a	chr14:40868377-40868388
20	CEBPB	chr14:40921214-40921478	HepG2	liver:	n/a	chr14:40921311-40921322 chr14:40921309-40921326
21	CEBPB	chr14:40868250-40868459	H1-hESC	embryonic stem cell:	n/a	chr14:40868377-40868388
22	CEBPB	chr14:40957082-40957421	A549	lung:	n/a	chr14:40957285-40957296 chr14:40957256-40957267 chr14:40957255-40957266 chr14:40957255-40957268
23	CEBPB	chr14:40868231-40868559	Hela-S3	cervix:	n/a	chr14:40868377-40868388
24	CTCF	chr14:40887042-40887301	GM12878	blood:	n/a	n/a
25	CTCF	chr14:40897278-40897325	LNCaP	prostate:	n/a	n/a
26	CTCF	chr14:40963823-40963931	LNCaP	prostate:	n/a	n/a
27	CTCF	chr14:40887068-40887239	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr14:40886941-40887421	HepG2	liver:	n/a	n/a
29	CTCF	chr14:40887140-40887290	GM12867	blood:	n/a	n/a
30	CTCF	chr14:40887100-40887250	HepG2	liver:	n/a	n/a
31	CTCF	chr14:40887094-40887292	MCF-7	breast:	n/a	n/a
32	CTCF	chr14:40887080-40887230	GM12869	blood:	n/a	n/a
33	CTCF	chr14:40887100-40887250	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr14:40887074-40887311	GM19238	blood:	n/a	n/a
35	CTCF	chr14:40887140-40887290	GM12873	blood:	n/a	n/a
36	CTCF	chr14:40887098-40887273	A549	lung:	n/a	n/a
37	CTCF	chr14:40887100-40887250	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr14:40894594-40894605	GM10248	blood:	n/a	n/a
39	CTCF	chr14:40887107-40887283	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr14:40887078-40887285	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr14:40887080-40887230	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr14:40887100-40887250	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr14:40887120-40887270	GM12872	blood:	n/a	n/a
44	CTCF	chr14:40887120-40887270	HMF	breast:	n/a	n/a
45	CTCF	chr14:40963900-40964050	MCF-7	breast:	n/a	n/a
46	CTCF	chr14:40887060-40887210	GM12867	blood:	n/a	n/a
47	CTCF	chr14:40887120-40887270	HepG2	liver:	n/a	n/a
48	CTCF	chr14:40887100-40887250	GM12865	blood:	n/a	n/a
49	CTCF	chr14:40963673-40964151	MCF-7	breast:	n/a	n/a
50	CTCF	chr14:40887200-40887350	A549	lung:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:40887312-40887362	HCT-116	colon:	n/a
2	chr14:40887312-40887362	HCT-116	colon:	n/a
3	chr14:40887312-40887362	SK-N-SH_RA	brain:	n/a
4	chr14:40887312-40887362	BJ	skin:	n/a
5	chr14:40887312-40887362	PrEC	prostate:	n/a
6	chr14:40887312-40887362	K562	blood:	n/a
7	chr14:40887312-40887362	HMEC	breast:	n/a
8	chr14:40887312-40887362	ProgFib	skin:	n/a
9	chr14:40887312-40887362	HCPEpiC	choroid plexus:	n/a
10	chr14:40887312-40887362	MCF10A-Er-Src	breast:	n/a
11	chr14:40887312-40887362	BE2_C	brain:	n/a
12	chr14:40887312-40887362	RPTEC	kidney:	n/a
13	chr14:40887312-40887362	IMR90	lung:	fetal
14	chr14:40887312-40887362	HepG2	liver:	n/a
15	chr14:40887312-40887362	Hela-S3	cervix:	n/a
16	chr14:40887312-40887362	Hepatocyte	liver:	n/a
17	chr14:40887312-40887362	GM12891	blood:	n/a
18	chr14:40887312-40887362	GM19239	blood:	n/a
19	chr14:40887312-40887362	T-47D	breast:	n/a
20	chr14:40887312-40887362	HEK293	kidney:	embryo
21	chr14:40887312-40887362	PFSK-1	brain:	n/a
22	chr14:40887312-40887362	GM12892	blood:	n/a
23	chr14:40887312-40887362	Jurkat	blood:	n/a
24	chr14:40887312-40887362	LNCaP	prostate:	n/a
25	chr14:40887312-40887362	SK-N-SH	brain:	n/a
26	chr14:40887312-40887362	NH-A	brain:	n/a
27	chr14:40887312-40887362	NHDF-neo	bronchial:	n/a
28	chr14:40887312-40887362	GM06990	blood:	n/a
29	chr14:40887312-40887362	HL-60	blood:	n/a
30	chr14:40887312-40887362	AG04449	skin:	fetal
31	chr14:40887312-40887362	SK-N-MC	brain:	n/a
32	chr14:40887312-40887362	SAEC	small airway:	n/a
33	chr14:40887312-40887362	HRCEpiC	kidney:	n/a
34	chr14:40887312-40887362	GM12878	blood:	n/a
35	chr14:40887312-40887362	ovcar-3	ovarian:	n/a
36	chr14:40887312-40887362	Caco-2	colon:	n/a
37	chr14:40887312-40887362	HEEpiC	esophagus:	n/a
38	chr14:40887312-40887362	AG09309	skin:	n/a
39	chr14:40887312-40887362	U87	brain:	n/a
40	chr14:40887312-40887362	HCM	heart:	n/a
41	chr14:40887312-40887362	H1-hESC	embryonic stem cell:	embryo
42	chr14:40887312-40887362	AG09319	gingival:	n/a
43	chr14:40887312-40887362	NT2-D1	testis:	n/a
44	chr14:40887312-40887362	HAEpiC	amniotic membrane:	n/a
45	chr14:40887312-40887362	SKMC	muscle:	n/a
46	chr14:40887312-40887362	ECC-1	luminal epithelium:	n/a
47	chr14:40887312-40887362	HRPEpiC	eye:	n/a
48	chr14:40887312-40887362	HNPCEpiC	eye:	n/a
49	chr14:40887312-40887362	CMK	blood:	n/a
50	chr14:40887312-40887362	AG10803	skin:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:40863521..40865803-chr14:40870395..40872089,2	MCF-7	breast:
2	chr14:40879663..40882573-chr14:40893834..40895743,2	MCF-7	breast:
3	chr14:40863521..40865803-chr14:40870395..40872089,2	MCF-7	breast:
4	chr14:40886743..40887636-chr14:41183711..41184631,4	MCF-7	breast:
5	chr14:40933785..40935420-chr14:40938659..40940644,2	K562	blood:
6	chr14:40860557..40863122-chr14:40865189..40868111,2	MCF-7	breast:
7	chr14:40933785..40935420-chr14:40938659..40940644,2	K562	blood:
8	chr14:40862573..40865201-chr14:40865784..40867370,2	K562	blood:
9	chr14:40852272..40855989-chr14:40856721..40860430,4	MCF-7	breast:
10	chr14:40857820..40860668-chr14:40862186..40864573,2	MCF-7	breast:
11	chr14:40852272..40855989-chr14:40856721..40860430,4	MCF-7	breast:
12	chr14:40905235..40906769-chr14:40907081..40909335,2	MCF-7	breast:
13	chr14:40879663..40882573-chr14:40893834..40895743,2	MCF-7	breast:
14	chr14:40886812..40887593-chr14:41183727..41184438,2	MCF-7	breast:
15	chr14:40862573..40865201-chr14:40865784..40867370,2	K562	blood:
16	chr14:40860557..40863122-chr14:40865189..40868111,2	MCF-7	breast:
17	chr14:40857820..40860668-chr14:40862186..40864573,2	MCF-7	breast:
18	chr14:40905235..40906769-chr14:40907081..40909335,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXO33-1	chr14:40882853-40882879	XLOC_011003
2	lnc-CTAGE5-3	chr14:40856762-40857244	ENSG00000258480
3	lnc-CTAGE5-4	chr14:40939239-40939586	XLOC_010812
4	lnc-CTAGE5-3	chr14:40858281-40858344	ENSG00000258480
5	lnc-CTAGE5-2	chr14:40855456-40855647	ENSG00000258418
6	lnc-FBXO33-1	chr14:40880506-40880728	XLOC_011003
7	lnc-CTAGE5-2	chr14:40855738-40855998	ENSG00000258418
8	lnc-CTAGE5-4	chr14:40938354-40938474	XLOC_010812

No data

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

Extended variants
information (count: 572 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:572 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1952933	chr14:40855032-40855033	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570058063	chr14:40855034-40855035	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs148632544	chr14:40855065-40855066	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs555644554	chr14:40855135-40855136	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs112121618	chr14:40855170-40855171	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs544417780	chr14:40855171-40855172	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs564153119	chr14:40855196-40855197	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs533144339	chr14:40855253-40855254	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs540367764	chr14:40855289-40855290	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs76859526	chr14:40855332-40855333	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs528895787	chr14:40855357-40855358	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs114907468	chr14:40855399-40855400	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs566174125	chr14:40855419-40855420	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs146360980	chr14:40855438-40855439	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs531139493	chr14:40855494-40855495	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs376232828	chr14:40855513-40855514	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs115579083	chr14:40855516-40855517	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs117277487	chr14:40855562-40855563	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs539643148	chr14:40855567-40855568	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs369360272	chr14:40855661-40855662	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs566587336	chr14:40855674-40855675	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs535856759	chr14:40855695-40855696	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs555447657	chr14:40855711-40855712	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs139656778	chr14:40855715-40855716	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs544213447	chr14:40855775-40855776	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs140248046	chr14:40855801-40855802	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs548325302	chr14:40855813-40855814	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs558020802	chr14:40855826-40855827	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs577957205	chr14:40855837-40855838	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs569807772	chr14:40855838-40855839	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs540379844	chr14:40855848-40855849	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs544419780	chr14:40855890-40855891	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs573754102	chr14:40855892-40855893	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs537108677	chr14:40855910-40855911	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs542688970	chr14:40855925-40855926	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs12881170	chr14:40856027-40856028	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs531330511	chr14:40856059-40856060	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs551038693	chr14:40856077-40856078	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs146143712	chr14:40856165-40856166	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs573865871	chr14:40856769-40856770	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs188082792	chr14:40856778-40856779	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs562600847	chr14:40856803-40856804	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs374722544	chr14:40856832-40856833	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs368744206	chr14:40856880-40856881	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs371049754	chr14:40856885-40856886	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs544950785	chr14:40856890-40856891	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs193011520	chr14:40856962-40856963	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs79804966	chr14:40856970-40856971	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs74442485	chr14:40856975-40856976	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs149767223	chr14:40857051-40857052	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:40861800-40862200	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr14:40862200-40863400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr14:40862800-40863600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr14:40863400-40864000	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr14:40875400-40875600	Enhancers	Aorta	Aorta
6	chr14:40875600-40875800	ZNF genes & repeats	Aorta	Aorta
7	chr14:40877200-40877800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr14:40882400-40883000	Enhancers	Fetal Heart	heart
9	chr14:40883000-40883400	Weak transcription	Fetal Heart	heart
10	chr14:40883400-40884000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr14:40883400-40884000	Enhancers	Fetal Heart	heart
12	chr14:40886600-40887400	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr14:40886800-40887000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr14:40886800-40887200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr14:40886800-40887200	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr14:40886800-40887400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr14:40933800-40934200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
18	chr14:40939000-40939800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr14:40944600-40945600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
20	chr14:40948000-40948400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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