Variant report

Variant	nsv430995
Chromosome Location	chr14:42952536-43140276
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	BACH1	chr14:43088748-43088782	K562	blood:	n/a	n/a
2	BATF	chr14:42992903-42993204	GM12878	blood:	n/a	n/a
3	BCL11A	chr14:42992865-42993250	GM12878	blood:	n/a	n/a
4	BRCA1	chr14:43010506-43011087	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr14:43112026-43112359	IMR90	lung:	n/a	chr14:43112172-43112183
6	CEBPB	chr14:43006799-43007063	IMR90	lung:	n/a	chr14:43006914-43006925 chr14:43006916-43006925
7	CEBPB	chr14:43112050-43112355	A549	lung:	n/a	chr14:43112172-43112183
8	CEBPB	chr14:43112063-43112289	H1-hESC	embryonic stem cell:	n/a	chr14:43112172-43112183
9	CEBPB	chr14:42973693-42973995	A549	lung:	n/a	chr14:42973833-42973846 chr14:42973851-42973862 chr14:42973834-42973845 chr14:42973849-42973860 chr14:42973851-42973860
10	CEBPB	chr14:42995827-42996065	HepG2	liver:	n/a	chr14:42995926-42995937 chr14:42995924-42995935
11	CEBPB	chr14:42973793-42973878	K562	blood:	n/a	chr14:42973833-42973846 chr14:42973851-42973862 chr14:42973834-42973845 chr14:42973849-42973860 chr14:42973851-42973860
12	CEBPB	chr14:43098476-43098668	HepG2	liver:	n/a	n/a
13	CEBPB	chr14:42973675-42974008	IMR90	lung:	n/a	chr14:42973833-42973846 chr14:42973851-42973862 chr14:42973834-42973845 chr14:42973849-42973860 chr14:42973851-42973860
14	CEBPB	chr14:43058937-43059272	HepG2	liver:	n/a	chr14:43059110-43059121
15	CEBPB	chr14:43057650-43057809	HepG2	liver:	n/a	chr14:43057739-43057750
16	CEBPB	chr14:43006767-43007104	HepG2	liver:	n/a	chr14:43006914-43006925 chr14:43006916-43006925
17	CEBPB	chr14:43112013-43112367	HepG2	liver:	n/a	chr14:43112172-43112183
18	CEBPB	chr14:43112092-43112319	MCF-7	breast:	n/a	chr14:43112172-43112183
19	CEBPB	chr14:43020465-43020677	HepG2	liver:	n/a	chr14:43020529-43020540
20	CEBPB	chr14:43058980-43059253	A549	lung:	n/a	chr14:43059110-43059121
21	CEBPB	chr14:42968792-42969062	IMR90	lung:	n/a	chr14:42968894-42968905 chr14:42968918-42968929
22	CEBPB	chr14:43112055-43112323	Hela-S3	cervix:	n/a	chr14:43112172-43112183
23	CEBPB	chr14:42968790-42969062	A549	lung:	n/a	chr14:42968894-42968905 chr14:42968918-42968929
24	CEBPB	chr14:42973667-42974028	HepG2	liver:	n/a	chr14:42973833-42973846 chr14:42973851-42973862 chr14:42973834-42973845 chr14:42973849-42973860 chr14:42973851-42973860
25	CEBPB	chr14:42970807-42970999	HepG2	liver:	n/a	chr14:42970856-42970867
26	CEBPB	chr14:43094448-43094984	HepG2	liver:	n/a	chr14:43094870-43094883 chr14:43094573-43094586 chr14:43094870-43094881
27	CEBPB	chr14:43104496-43104820	HepG2	liver:	n/a	chr14:43104691-43104702 chr14:43104647-43104658
28	CEBPB	chr14:42968773-42969081	HepG2	liver:	n/a	chr14:42968894-42968905 chr14:42968918-42968929
29	CEBPB	chr14:43112099-43112243	K562	blood:	n/a	chr14:43112172-43112183
30	CEBPB	chr14:42973656-42974004	Hela-S3	cervix:	n/a	chr14:42973833-42973846 chr14:42973851-42973862 chr14:42973834-42973845 chr14:42973849-42973860 chr14:42973851-42973860
31	CEBPB	chr14:43071917-43072221	HepG2	liver:	n/a	n/a
32	CEBPB	chr14:43045458-43045742	HepG2	liver:	n/a	chr14:43045602-43045613
33	CEBPB	chr14:43006817-43007048	A549	lung:	n/a	chr14:43006914-43006925 chr14:43006916-43006925
34	CEBPB	chr14:43010664-43011294	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr14:43098443-43098643	A549	lung:	n/a	n/a
36	CEBPB	chr14:43081131-43081221	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr14:43009532-43009798	HepG2	liver:	n/a	n/a
38	CEBPB	chr14:43088861-43089038	A549	lung:	n/a	n/a
39	CEBPB	chr14:43088915-43089065	HepG2	liver:	n/a	n/a
40	CHD2	chr14:43040531-43040693	HepG2	liver:	n/a	n/a
41	CTCF	chr14:43033920-43034070	MCF-7	breast:	n/a	n/a
42	CTCF	chr14:43004778-43004868	MCF-7	breast:	n/a	n/a
43	CTCF	chr14:43004773-43004858	MCF-7	breast:	n/a	n/a
44	CTCF	chr14:43032180-43032330	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr14:43046579-43046616	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr14:43004760-43004910	GM12874	blood:	n/a	n/a
47	CTCF	chr14:43033740-43033890	HCT-116	colon:	n/a	n/a
48	CTCF	chr14:43041340-43041490	A549	lung:	n/a	n/a
49	CTCF	chr14:43041371-43041426	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr14:43026528-43026584	GM10248	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:43123081-43123131	K562	blood:	n/a
2	chr14:43123081-43123131	CMK	blood:	n/a
3	chr14:43123081-43123131	AoSMC	blood vessel:	n/a
4	chr14:43123081-43123131	GM06990	blood:	n/a
5	chr14:43123081-43123131	SK-N-SH	brain:	n/a
6	chr14:43123081-43123131	GM19239	blood:	n/a
7	chr14:43123081-43123131	LNCaP	prostate:	n/a
8	chr14:43123081-43123131	SAEC	small airway:	n/a
9	chr14:43123081-43123131	U87	brain:	n/a
10	chr14:43123081-43123131	GM12892	blood:	n/a
11	chr14:43123081-43123131	BE2_C	brain:	n/a
12	chr14:43123081-43123131	AG04449	skin:	fetal
13	chr14:43123081-43123131	HepG2	liver:	n/a
14	chr14:43123081-43123131	HRPEpiC	eye:	n/a
15	chr14:43123081-43123131	HCT-116	colon:	n/a
16	chr14:43123081-43123131	MCF-7	breast:	n/a
17	chr14:43123081-43123131	SK-N-SH_RA	brain:	n/a
18	chr14:43123081-43123131	NT2-D1	testis:	n/a
19	chr14:43123081-43123131	ECC-1	luminal epithelium:	n/a
20	chr14:43123081-43123131	HAEpiC	amniotic membrane:	n/a
21	chr14:43123081-43123131	Hepatocyte	liver:	n/a
22	chr14:43123081-43123131	HIPEpiC	eye:	n/a
23	chr14:43123081-43123131	HPAEpiC	pulmonary alveolar:	n/a
24	chr14:43123081-43123131	HRCEpiC	kidney:	n/a
25	chr14:43123081-43123131	PANC-1	pancreas:	n/a
26	chr14:43123081-43123131	A549	lung:	n/a
27	chr14:43123081-43123131	Caco-2	colon:	n/a
28	chr14:43123081-43123131	HL-60	blood:	n/a
29	chr14:43123081-43123131	GM12878	blood:	n/a
30	chr14:43123081-43123131	PFSK-1	brain:	n/a
31	chr14:43123081-43123131	PrEC	prostate:	n/a
32	chr14:43123081-43123131	AG04450	lung:	fetal
33	chr14:43123081-43123131	Hela-S3	cervix:	n/a
34	chr14:43123081-43123131	NH-A	brain:	n/a
35	chr14:43123081-43123131	GM12891	blood:	n/a
36	chr14:43123081-43123131	SK-N-MC	brain:	n/a
37	chr14:43123081-43123131	AG09319	gingival:	n/a
38	chr14:43123081-43123131	Jurkat	blood:	n/a
39	chr14:43123081-43123131	BJ	skin:	n/a
40	chr14:43123081-43123131	AG10803	skin:	n/a
41	chr14:43123081-43123131	NHDF-neo	bronchial:	n/a
42	chr14:43123081-43123131	ProgFib	skin:	n/a
43	chr14:43123081-43123131	T-47D	breast:	n/a
44	chr14:43123081-43123131	HRE	kidney:	n/a
45	chr14:43123081-43123131	HEEpiC	esophagus:	n/a
46	chr14:43123081-43123131	HCM	heart:	n/a
47	chr14:43123081-43123131	HNPCEpiC	eye:	n/a
48	chr14:43123081-43123131	RPTEC	kidney:	n/a
49	chr14:43123081-43123131	HCPEpiC	choroid plexus:	n/a
50	chr14:43123081-43123131	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:43078769..43080628-chr14:43081211..43084199,2	MCF-7	breast:
2	chr14:43078769..43080628-chr14:43081211..43084199,2	MCF-7	breast:
3	chr14:42579463..42579970-chr14:43055430..43056355,2	MCF-7	breast:
4	chr14:42955061..42956041-chr18:32446617..32447280,2	MCF-7	breast:
5	chr14:43030553..43031053-chr17:8338863..8339416,2	Hela-S3	cervix:
6	chr14:43134052..43134776-chr3:181029654..181030646,2	MCF-7	breast:
7	chr14:43090850..43092635-chr14:43095537..43098102,2	K562	blood:
8	chr14:42995581..42997108-chr14:42999086..43001857,2	K562	blood:
9	chr14:43090850..43092635-chr14:43095537..43098102,2	K562	blood:
10	chr14:42995581..42997108-chr14:42999086..43001857,2	K562	blood:
11	chr14:43055616..43058571-chr14:43062767..43065185,2	MCF-7	breast:
12	chr14:43055616..43058571-chr14:43062767..43065185,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-214N1.1.1-3	chr14:43078071-43078780	NONHSAT036591
2	lnc-RP11-214N1.1.1-2	chr14:42997872-42998091	ENSG00000258850.1
3	lnc-RP11-214N1.1.1-2	chr14:42972301-42972709	NONHSAT036588
4	lnc-RP11-214N1.1.1-2	chr14:42997872-42998001	NONHSAT036588
5	lnc-RP11-214N1.1.1-2	chr14:42998014-42998060	NONHSAT036588

Variant related genes	Relation type
ENSG00000258622	TF binding region
ENSG00000258505	TF binding region
ENSG00000258622	CpG island
ENSG00000258505	CpG island
ENSG00000166579	chromatin interactions

Extended variants
information (count: 3058 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:3058 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11157293	chr14:42952536-42952537	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs527581847	chr14:42952559-42952560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567239092	chr14:42952646-42952647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534625195	chr14:42952679-42952680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs74047187	chr14:42952693-42952694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571261809	chr14:42952719-42952720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78681432	chr14:42952725-42952726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557315611	chr14:42952740-42952741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544338499	chr14:42952743-42952744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113204623	chr14:42952746-42952747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575869813	chr14:42952747-42952748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556188254	chr14:42952784-42952785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561080275	chr14:42952795-42952796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542948174	chr14:42952799-42952800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141234154	chr14:42952821-42952822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554858481	chr14:42952825-42952826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs74047188	chr14:42952848-42952849	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs187885631	chr14:42952855-42952856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs1499393	chr14:42952885-42952886	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs1499392	chr14:42952898-42952899	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs532546538	chr14:42952902-42952903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373757427	chr14:42952946-42952947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558104000	chr14:42952986-42952987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35807748	chr14:42953023-42953024	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs370440303	chr14:42953044-42953045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549273023	chr14:42953050-42953051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs141393856	chr14:42953212-42953213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540424725	chr14:42953215-42953216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528053046	chr14:42953227-42953228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1499391	chr14:42953319-42953320	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs150863307	chr14:42953322-42953323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538380516	chr14:42953327-42953328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192661380	chr14:42953371-42953372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569318293	chr14:42953466-42953467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76828609	chr14:42953496-42953497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554793404	chr14:42953513-42953514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184384069	chr14:42953584-42953585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540230624	chr14:42953585-42953586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566406170	chr14:42953707-42953708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535246742	chr14:42953754-42953755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs116821125	chr14:42953758-42953759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs368294706	chr14:42953760-42953761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577252656	chr14:42953791-42953792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544347028	chr14:42953855-42953856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189088849	chr14:42953866-42953867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575465669	chr14:42953868-42953869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77629421	chr14:42953869-42953870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs74047191	chr14:42953891-42953892	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs139300909	chr14:42953907-42953908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184941499	chr14:42953917-42953918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	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
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Glioblastoma multiforme	21569311	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:42948600-42958200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr14:42952200-42952600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:42957600-42958400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr14:42958200-42958400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr14:42959600-42960200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr14:42968000-42968200	Enhancers	H9 Cell Line	embryonic stem cell
7	chr14:42977000-42977200	Enhancers	H1 Cell Line	embryonic stem cell
8	chr14:42977000-42977200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr14:42977200-42977400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr14:42977200-42977800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr14:42977400-42977600	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr14:42977400-42978000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr14:42977400-42978000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr14:42977400-42978000	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr14:42977600-42978200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr14:42977800-42978400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr14:42978000-42978600	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr14:42978000-42982200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr14:42978000-42983000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr14:42978200-42978400	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr14:42978200-42981400	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr14:42978400-42979200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr14:42981400-42981600	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr14:42981600-42982000	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr14:42982000-42984600	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr14:42982200-42984200	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr14:42982400-42984000	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr14:42982400-42984200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr14:42982600-42983000	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr14:42982600-42983600	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr14:42982600-42984000	Enhancers	H1 Cell Line	embryonic stem cell
32	chr14:42982800-42983400	Enhancers	Primary B cells from peripheral blood	blood
33	chr14:42982800-42984800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr14:42983000-42983400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr14:42983000-42983400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr14:42983000-42984200	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr14:42983400-42984000	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr14:42983400-42987200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr14:42984200-42987800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr14:42987200-42987600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr14:42987200-42987600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr14:42987200-42987800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr14:42987600-42992800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr14:42987800-42988000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
45	chr14:42988000-42991400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr14:42992200-42994800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr14:42992800-42993200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr14:42992800-42993200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr14:42992800-42993200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr14:42992800-42993200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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