Variant report

Variant	nsv901696
Chromosome Location	chr14:41350392-41437680
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:187)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:187 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr14:41407165-41407367	K562	blood:	n/a	n/a
2	BHLHE40	chr14:41407166-41407365	K562	blood:	n/a	n/a
3	CCNT2	chr14:41407166-41407534	K562	blood:	n/a	n/a
4	CEBPB	chr14:41375618-41375858	A549	lung:	n/a	chr14:41375728-41375739
5	CEBPB	chr14:41398166-41398394	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr14:41398163-41398409	A549	lung:	n/a	n/a
7	CEBPB	chr14:41431432-41431774	HepG2	liver:	n/a	chr14:41431587-41431598 chr14:41431719-41431730 chr14:41431440-41431451
8	CEBPB	chr14:41383697-41384072	A549	lung:	n/a	chr14:41383938-41383951 chr14:41383983-41383994 chr14:41383985-41383996
9	CEBPB	chr14:41383813-41384128	HepG2	liver:	n/a	chr14:41383938-41383951 chr14:41383983-41383994 chr14:41383985-41383996
10	CEBPB	chr14:41402655-41402752	HepG2	liver:	n/a	n/a
11	CEBPB	chr14:41370218-41370432	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr14:41416310-41416495	HepG2	liver:	n/a	n/a
13	CEBPB	chr14:41379195-41379395	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr14:41398162-41398406	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:41395584-41395765	HepG2	liver:	n/a	chr14:41395663-41395674
16	CEBPB	chr14:41375603-41375912	HepG2	liver:	n/a	chr14:41375728-41375739
17	CEBPB	chr14:41398158-41398368	IMR90	lung:	n/a	n/a
18	CEBPB	chr14:41410937-41411137	HepG2	liver:	n/a	n/a
19	CHD1	chr14:41424252-41424603	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr14:41387938-41388019	HepG2	liver:	n/a	n/a
21	CTCF	chr14:41370270-41370359	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr14:41394296-41394322	MCF-7	breast:	n/a	n/a
23	CTCF	chr14:41407165-41407535	K562	blood:	n/a	n/a
24	CTCF	chr14:41360259-41360382	MCF-7	breast:	n/a	n/a
25	CTCF	chr14:41360911-41360944	ProgFib	skin:	n/a	n/a
26	CTCF	chr14:41423959-41424077	Fibrobl	skin:	n/a	n/a
27	CTCF	chr14:41360180-41360330	MCF-7	breast:	n/a	n/a
28	CTCF	chr14:41360245-41360379	MCF-7	breast:	n/a	n/a
29	CTCF	chr14:41360275-41360364	MCF-7	breast:	n/a	n/a
30	CTCF	chr14:41360905-41360908	ProgFib	skin:	n/a	n/a
31	CTCF	chr14:41360247-41360398	MCF-7	breast:	n/a	n/a
32	CTCF	chr14:41394324-41394326	MCF-7	breast:	n/a	n/a
33	CTCF	chr14:41360240-41360390	MCF-7	breast:	n/a	n/a
34	E2F4	chr14:41371235-41371450	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr14:41408071-41408178	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr14:41407167-41407535	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr14:41388272-41388589	MCF10A-Er-Src	breast:	n/a	n/a
38	EBF1	chr14:41414787-41414807	GM12878	blood:	n/a	n/a
39	ELK1	chr14:41407166-41407365	K562	blood:	n/a	n/a
40	EP300	chr14:41417395-41417401	HepG2	liver:	n/a	n/a
41	EP300	chr14:41405527-41406623	SK-N-SH	brain:	n/a	chr14:41406478-41406492 chr14:41406434-41406441
42	EP300	chr14:41407161-41407367	K562	blood:	n/a	n/a
43	FOXA1	chr14:41423566-41423707	T-47D	breast:	n/a	n/a
44	FOXA1	chr14:41424373-41424764	T-47D	breast:	n/a	n/a
45	FOXA1	chr14:41424445-41424637	T-47D	breast:	n/a	n/a
46	FOXA2	chr14:41423554-41423873	A549	lung:	n/a	n/a
47	FOXA2	chr14:41423326-41424027	A549	lung:	n/a	n/a
48	GATA2	chr14:41379043-41379466	SH-SY5Y	brain:	n/a	n/a
49	GATA2	chr14:41406107-41406457	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr14:41378987-41379493	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:41423839-41423889	HRPEpiC	eye:	n/a
2	chr14:41423839-41423889	HPAEpiC	pulmonary alveolar:	n/a
3	chr14:41423839-41423889	BE2_C	brain:	n/a
4	chr14:41423839-41423889	PFSK-1	brain:	n/a
5	chr14:41423839-41423889	A549	lung:	n/a
6	chr14:41423839-41423889	AG10803	skin:	n/a
7	chr14:41423839-41423889	LNCaP	prostate:	n/a
8	chr14:41423839-41423889	BJ	skin:	n/a
9	chr14:41423839-41423889	HNPCEpiC	eye:	n/a
10	chr14:41423839-41423889	HIPEpiC	eye:	n/a
11	chr14:41423839-41423889	Jurkat	blood:	n/a
12	chr14:41423839-41423889	HepG2	liver:	n/a
13	chr14:41423839-41423889	HCM	heart:	n/a
14	chr14:41423839-41423889	HRCEpiC	kidney:	n/a
15	chr14:41423839-41423889	NHDF-neo	bronchial:	n/a
16	chr14:41423839-41423889	HL-60	blood:	n/a
17	chr14:41423839-41423889	SK-N-SH	brain:	n/a
18	chr14:41423839-41423889	H1-hESC	embryonic stem cell:	embryo
19	chr14:41423839-41423889	GM19239	blood:	n/a
20	chr14:41423839-41423889	SK-N-MC	brain:	n/a
21	chr14:41423839-41423889	NHBE	bronchial:	n/a
22	chr14:41423839-41423889	RPTEC	kidney:	n/a
23	chr14:41423839-41423889	ovcar-3	ovarian:	n/a
24	chr14:41423839-41423889	HUVEC	blood vessel:	n/a
25	chr14:41423839-41423889	SAEC	small airway:	n/a
26	chr14:41423839-41423889	AG04450	lung:	fetal
27	chr14:41423839-41423889	K562	blood:	n/a
28	chr14:41423839-41423889	Hela-S3	cervix:	n/a
29	chr14:41423839-41423889	MCF10A-Er-Src	breast:	n/a
30	chr14:41423839-41423889	U87	brain:	n/a
31	chr14:41423839-41423889	SK-N-SH_RA	brain:	n/a
32	chr14:41423839-41423889	NT2-D1	testis:	n/a
33	chr14:41423839-41423889	HCF	heart:	n/a
34	chr14:41423839-41423889	AG09319	gingival:	n/a
35	chr14:41423839-41423889	NH-A	brain:	n/a
36	chr14:41423839-41423889	HCPEpiC	choroid plexus:	n/a
37	chr14:41423839-41423889	MCF-7	breast:	n/a
38	chr14:41423839-41423889	NB4	blood:	n/a
39	chr14:41423839-41423889	HEK293	kidney:	embryo
40	chr14:41423839-41423889	HCT-116	colon:	n/a
41	chr14:41423839-41423889	GM12891	blood:	n/a
42	chr14:41423839-41423889	AG09309	skin:	n/a
43	chr14:41423839-41423889	IMR90	lung:	fetal
44	chr14:41423839-41423889	HMEC	breast:	n/a
45	chr14:41423839-41423889	CMK	blood:	n/a
46	chr14:41423839-41423889	HRE	kidney:	n/a
47	chr14:41423839-41423889	AoSMC	blood vessel:	n/a
48	chr14:41423839-41423889	ProgFib	skin:	n/a
49	chr14:41423839-41423889	GM12878	blood:	n/a
50	chr14:41423839-41423889	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr14:41383629..41385317-chr14:41390343..41392614,2	K562	blood:
2	chr14:41377936..41380382-chr14:41413256..41415527,2	MCF-7	breast:
3	chr14:41383629..41385317-chr14:41390343..41392614,2	K562	blood:
4	chr14:41377936..41380382-chr14:41413256..41415527,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRFN5-1	chr14:41424123-41424157	XLOC_010813
2	lnc-LRFN5-1	chr14:41431994-41432047	ENSG00000251363
3	lnc-LRFN5-1	chr14:41431995-41432047	XLOC_010813
4	lnc-LRFN5-1	chr14:41423916-41424157	XLOC_010813
5	lnc-LRFN5-1	chr14:41431995-41432047	XLOC_010813
6	lnc-LRFN5-1	chr14:41423916-41424157	NR_109757
7	lnc-LRFN5-1	chr14:41431995-41432047	NR_109757
8	lnc-LRFN5-1	chr14:41423916-41424157	ENSG00000251363
9	lnc-LRFN5-1	chr14:41423822-41424157	XLOC_010813
10	lnc-LRFN5-1	chr14:41431995-41432050	XLOC_010813
11	lnc-LRFN5-1	chr14:41424103-41424157	ENSG00000251363
12	lnc-LRFN5-1	chr14:41431995-41432047	NR_109758
13	lnc-LRFN5-1	chr14:41423916-41424157	NR_109758
14	lnc-LRFN5-1	chr14:41431995-41432047	ENSG00000251363

No data

Variant related genes	Relation type
ENSG00000251363	TF binding region
ENSG00000251363	CpG island
KLHL28	miRNA target sites
SLC25A15	miRNA target sites
SLC25A1	miRNA target sites
APBB2	miRNA target sites

Extended variants
information (count: 742 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:742 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532799395	chr14:41379217-41379218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs551030639	chr14:41379220-41379221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540764250	chr14:41379235-41379236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561065630	chr14:41379248-41379249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs182589766	chr14:41379264-41379265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs186905542	chr14:41379292-41379293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs192114021	chr14:41379307-41379308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549082624	chr14:41379320-41379321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567332770	chr14:41379323-41379324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534731532	chr14:41379326-41379327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs117712594	chr14:41379395-41379396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs66463734	chr14:41379397-41379398	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs544443241	chr14:41380212-41380213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs143142034	chr14:41380269-41380270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545691323	chr14:41380274-41380275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375655499	chr14:41380284-41380285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs146676146	chr14:41380286-41380287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs542551999	chr14:41380294-41380295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560860692	chr14:41380298-41380299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115862006	chr14:41380307-41380308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs565558530	chr14:41380326-41380327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564865358	chr14:41380366-41380367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532250049	chr14:41380381-41380382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78057151	chr14:41380398-41380399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140188698	chr14:41380429-41380430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs568719073	chr14:41380466-41380467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150310735	chr14:41380529-41380530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548124275	chr14:41380543-41380544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569247705	chr14:41387811-41387812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558117761	chr14:41387830-41387831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570157212	chr14:41387838-41387839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144909820	chr14:41387950-41387951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373536897	chr14:41387987-41387988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190212832	chr14:41388016-41388017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574461779	chr14:41388046-41388047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541978481	chr14:41388047-41388048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553689317	chr14:41388066-41388067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572265292	chr14:41388106-41388107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1530697	chr14:41388129-41388130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574926175	chr14:41388140-41388141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183205063	chr14:41388166-41388167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530162910	chr14:41388196-41388197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556540099	chr14:41388248-41388249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531770406	chr14:41388276-41388277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543920195	chr14:41388284-41388285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562180263	chr14:41388296-41388297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35106976	chr14:41388309-41388310	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs140389643	chr14:41388333-41388334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565483530	chr14:41388337-41388338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566180161	chr14:41388341-41388342	Weak transcription	n/a	n/a	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
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
Pancreatic ductal adenocarcinoma	19077451	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 cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:41379200-41379400	Enhancers	Gastric	stomach
2	chr14:41380200-41380600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr14:41387800-41390600	Weak transcription	Psoas Muscle	Psoas
4	chr14:41413600-41414000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr14:41423600-41425000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr14:41423600-41426000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr14:41423800-41425600	Active TSS	H1 Cell Line	embryonic stem cell
8	chr14:41423800-41426000	Active TSS	HUES6 Cell Line	embryonic stem cell
9	chr14:41424000-41424400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr14:41424000-41425000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
11	chr14:41424000-41425000	Active TSS	iPS-15b Cell Line	embryonic stem cell
12	chr14:41424000-41425200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr14:41424000-41425200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
14	chr14:41424000-41425400	Active TSS	H9 Cell Line	embryonic stem cell
15	chr14:41424000-41425400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr14:41424000-41425400	Active TSS	Breast Myoepithelial Primary Cells	Breast
17	chr14:41424000-41425600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr14:41424000-41425800	Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr14:41424000-41425800	Active TSS	iPS-20b Cell Line	embryonic stem cell
20	chr14:41424000-41426200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr14:41424000-41426400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr14:41424000-41426400	Active TSS	HUES48 Cell Line	embryonic stem cell
23	chr14:41424000-41426400	Active TSS	HUES64 Cell Line	embryonic stem cell
24	chr14:41424000-41426600	Active TSS	iPS-18 Cell Line	embryonic stem cell
25	chr14:41424200-41424600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr14:41424200-41424600	Active TSS	Right Ventricle	heart
27	chr14:41424200-41424800	Active TSS	Pancreatic Islets	Pancreatic Islet
28	chr14:41424200-41424800	Active TSS	Placenta	Placenta
29	chr14:41424200-41424800	Active TSS	HUVEC	blood vessel
30	chr14:41424200-41424800	Active TSS	K562	blood
31	chr14:41424400-41428400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr14:41425000-41425400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
33	chr14:41425000-41425600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr14:41425200-41425400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr14:41425200-41428400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr14:41425400-41425600	Active TSS	iPS-15b Cell Line	embryonic stem cell
37	chr14:41425400-41427600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr14:41425400-41427800	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr14:41425400-41428400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr14:41425600-41425800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr14:41425600-41426400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr14:41425600-41427800	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr14:41425600-41427800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr14:41425800-41426000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr14:41425800-41427800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr14:41426000-41426200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr14:41426000-41426400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr14:41426000-41426400	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr14:41426200-41426600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr14:41426200-41426600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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