Variant report

Variant	nsv1053846
Chromosome Location	chr14:47465690-47636016
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	ATF2	chr14:47513971-47514339	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr14:47555354-47555385	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr14:47514116-47514346	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr14:47514066-47514301	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr14:47509696-47510005	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr14:47624242-47624527	A549	lung:	n/a	chr14:47624388-47624399
7	CEBPB	chr14:47485732-47485940	HepG2	liver:	n/a	chr14:47485846-47485857 chr14:47485886-47485898
8	CEBPB	chr14:47617899-47618250	IMR90	lung:	n/a	chr14:47618074-47618085
9	CEBPB	chr14:47617918-47618257	A549	lung:	n/a	chr14:47618074-47618085
10	CEBPB	chr14:47617920-47618180	H1-hESC	embryonic stem cell:	n/a	chr14:47618074-47618085
11	CEBPB	chr14:47510116-47510168	K562	blood:	n/a	n/a
12	CEBPB	chr14:47617889-47618242	HepG2	liver:	n/a	chr14:47618074-47618085
13	CEBPB	chr14:47550933-47551123	A549	lung:	n/a	chr14:47550992-47551005 chr14:47550994-47551005
14	CEBPB	chr14:47545880-47546163	HepG2	liver:	n/a	chr14:47546020-47546031 chr14:47546049-47546060 chr14:47546019-47546032
15	CEBPB	chr14:47520035-47520324	A549	lung:	n/a	n/a
16	CEBPB	chr14:47617931-47618193	K562	blood:	n/a	chr14:47618074-47618085
17	CEBPB	chr14:47514120-47514377	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr14:47485719-47485919	A549	lung:	n/a	chr14:47485846-47485857 chr14:47485886-47485898
19	CEBPB	chr14:47586722-47586989	HepG2	liver:	n/a	chr14:47586859-47586870
20	CEBPB	chr14:47586722-47587018	A549	lung:	n/a	chr14:47586859-47586870
21	CEBPB	chr14:47617893-47618243	ECC-1	luminal epithelium:	n/a	chr14:47618074-47618085
22	CEBPB	chr14:47624860-47625066	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:47624212-47624557	HepG2	liver:	n/a	chr14:47624388-47624399
24	CEBPB	chr14:47509711-47510131	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr14:47514070-47514415	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr14:47514132-47514339	LNCaP	prostate:	n/a	chr14:47514240-47514261 chr14:47514241-47514249 chr14:47514238-47514256
27	CTCF	chr14:47514140-47514290	HBMEC	blood vessel:	n/a	chr14:47514240-47514261 chr14:47514241-47514249 chr14:47514238-47514256
28	CTCF	chr14:47509750-47509998	MCF-7	breast:	n/a	n/a
29	CTCF	chr14:47509780-47509930	HEEpiC	esophagus:	n/a	n/a
30	CTCF	chr14:47514180-47514264	Pancreas_OC	pancreas:	n/a	chr14:47514240-47514261 chr14:47514241-47514249 chr14:47514238-47514256
31	CTCF	chr14:47525680-47525830	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr14:47514120-47514270	HAc	cerebellar:	n/a	chr14:47514240-47514261 chr14:47514241-47514249 chr14:47514238-47514256
33	CTCF	chr14:47525620-47525770	RPTEC	kidney:	n/a	n/a
34	CTCF	chr14:47509800-47509950	BE2_C	brain:	n/a	n/a
35	CTCF	chr14:47514200-47514350	SAEC	small airway:	n/a	chr14:47514240-47514261 chr14:47514241-47514249 chr14:47514238-47514256
36	CTCF	chr14:47514086-47514460	MCF-7	breast:	n/a	chr14:47514240-47514261 chr14:47514241-47514249 chr14:47514238-47514256
37	CTCF	chr14:47509740-47509890	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr14:47509681-47509942	HepG2	liver:	n/a	n/a
39	CTCF	chr14:47509847-47509908	GM19239	blood:	n/a	n/a
40	CTCF	chr14:47509786-47509946	GM12878	blood:	n/a	n/a
41	CTCF	chr14:47514163-47514287	A549	lung:	n/a	chr14:47514240-47514261 chr14:47514241-47514249 chr14:47514238-47514256
42	CTCF	chr14:47509780-47509930	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr14:47514038-47514440	T-47D	breast:	n/a	chr14:47514240-47514261 chr14:47514241-47514249 chr14:47514238-47514256
44	CTCF	chr14:47509844-47509900	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr14:47509776-47509985	MCF-7	breast:	n/a	n/a
46	CTCF	chr14:47514117-47514376	T-47D	breast:	n/a	chr14:47514240-47514261 chr14:47514241-47514249 chr14:47514238-47514256
47	CTCF	chr14:47509740-47509931	A549	lung:	n/a	n/a
48	CTCF	chr14:47597987-47598050	GM10248	blood:	n/a	n/a
49	CTCF	chr14:47509808-47509932	A549	lung:	n/a	n/a
50	CTCF	chr14:47509687-47510068	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:47544244-47544294	PANC-1	pancreas:	n/a
2	chr14:47513774-47513824	HEEpiC	esophagus:	n/a
3	chr14:47513774-47513824	SAEC	small airway:	n/a
4	chr14:47572921-47572971	NHBE	bronchial:	n/a
5	chr14:47513774-47513824	MCF10A-Er-Src	breast:	n/a
6	chr14:47572921-47572971	BJ	skin:	n/a
7	chr14:47513774-47513824	HMEC	breast:	n/a
8	chr14:47572921-47572971	GM06990	blood:	n/a
9	chr14:47544244-47544294	AG04450	lung:	fetal
10	chr14:47544244-47544294	HCPEpiC	choroid plexus:	n/a
11	chr14:47572921-47572971	NHDF-neo	bronchial:	n/a
12	chr14:47513774-47513824	GM12878	blood:	n/a
13	chr14:47513774-47513824	SK-N-SH_RA	brain:	n/a
14	chr14:47513774-47513824	ovcar-3	ovarian:	n/a
15	chr14:47513774-47513824	GM06990	blood:	n/a
16	chr14:47544244-47544294	NHDF-neo	bronchial:	n/a
17	chr14:47544244-47544294	IMR90	lung:	fetal
18	chr14:47544244-47544294	ovcar-3	ovarian:	n/a
19	chr14:47544244-47544294	ProgFib	skin:	n/a
20	chr14:47572921-47572971	HEEpiC	esophagus:	n/a
21	chr14:47572921-47572971	AG09319	gingival:	n/a
22	chr14:47513774-47513824	LNCaP	prostate:	n/a
23	chr14:47513774-47513824	NH-A	brain:	n/a
24	chr14:47544244-47544294	HRE	kidney:	n/a
25	chr14:47513774-47513824	Hela-S3	cervix:	n/a
26	chr14:47544244-47544294	HUVEC	blood vessel:	n/a
27	chr14:47513774-47513824	AG09319	gingival:	n/a
28	chr14:47572921-47572971	U87	brain:	n/a
29	chr14:47572921-47572971	CMK	blood:	n/a
30	chr14:47572921-47572971	Hela-S3	cervix:	n/a
31	chr14:47572921-47572971	GM12891	blood:	n/a
32	chr14:47572921-47572971	AoSMC	blood vessel:	n/a
33	chr14:47544244-47544294	AoSMC	blood vessel:	n/a
34	chr14:47513774-47513824	HAEpiC	amniotic membrane:	n/a
35	chr14:47513774-47513824	GM12892	blood:	n/a
36	chr14:47572921-47572971	HAEpiC	amniotic membrane:	n/a
37	chr14:47513774-47513824	NHDF-neo	bronchial:	n/a
38	chr14:47544244-47544294	GM12892	blood:	n/a
39	chr14:47513774-47513824	ProgFib	skin:	n/a
40	chr14:47544244-47544294	HCM	heart:	n/a
41	chr14:47513774-47513824	HCPEpiC	choroid plexus:	n/a
42	chr14:47513774-47513824	HRCEpiC	kidney:	n/a
43	chr14:47572921-47572971	SK-N-MC	brain:	n/a
44	chr14:47513774-47513824	HEK293	kidney:	embryo
45	chr14:47544244-47544294	HPAEpiC	pulmonary alveolar:	n/a
46	chr14:47572921-47572971	H1-hESC	embryonic stem cell:	embryo
47	chr14:47572921-47572971	ECC-1	luminal epithelium:	n/a
48	chr14:47572921-47572971	HCT-116	colon:	n/a
49	chr14:47544244-47544294	HL-60	blood:	n/a
50	chr14:47513774-47513824	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:47050056..47050875-chr14:47509400..47510237,2	MCF-7	breast:
2	chr14:47525262..47526210-chr14:47747163..47747902,2	MCF-7	breast:
3	chr12:54734855..54737428-chr14:47592677..47595618,2	MCF-7	breast:
4	chr14:47584419..47587324-chr14:47587496..47590029,2	MCF-7	breast:
5	chr14:47584419..47587324-chr14:47587496..47590029,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-11	chr14:47465657-47466377	NONHSAT036685

Variant related genes	Relation type
MDGA2	TF binding region
MDGA2	CpG island

Extended variants
information (count: 3418 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3418 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17117905	chr14:47465690-47465691	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553802443	chr14:47465696-47465697	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs111429067	chr14:47465704-47465705	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs373502249	chr14:47465706-47465707	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs552586803	chr14:47465727-47465728	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs560005617	chr14:47465745-47465746	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs552948288	chr14:47465748-47465749	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs564528748	chr14:47465751-47465752	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs375377239	chr14:47465763-47465764	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs9652331	chr14:47465783-47465784	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs530457141	chr14:47465896-47465897	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs550239639	chr14:47465949-47465950	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs115341110	chr14:47466000-47466001	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs372515225	chr14:47466003-47466004	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs546483498	chr14:47466015-47466016	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs141812386	chr14:47466052-47466053	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs538552323	chr14:47466070-47466071	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs558936227	chr14:47466071-47466072	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs575695972	chr14:47466088-47466089	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs146016036	chr14:47466134-47466135	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs555075214	chr14:47466155-47466156	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs17117907	chr14:47466159-47466160	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs186904996	chr14:47466176-47466177	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs9323124	chr14:47466177-47466178	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs77278518	chr14:47466217-47466218	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs546162982	chr14:47466252-47466253	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs562869223	chr14:47466255-47466256	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs190145283	chr14:47466318-47466319	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs139923641	chr14:47466341-47466342	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs560605931	chr14:47466377-47466378	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs529753345	chr14:47466379-47466380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546719074	chr14:47466388-47466389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566542013	chr14:47466390-47466391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183337942	chr14:47466401-47466402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188221514	chr14:47466428-47466429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376794023	chr14:47466450-47466451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569198893	chr14:47466538-47466539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73239249	chr14:47466579-47466580	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs143339024	chr14:47466589-47466590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574830164	chr14:47466612-47466613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs193128451	chr14:47466613-47466614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7142613	chr14:47466631-47466632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577343575	chr14:47466633-47466634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546008694	chr14:47466639-47466640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537129079	chr14:47466641-47466642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185322154	chr14:47466668-47466669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576335339	chr14:47466705-47466706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543755218	chr14:47466757-47466758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550686854	chr14:47466758-47466759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs146701931	chr14:47466759-47466760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21785460	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
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	19907438	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
Osteosarcoma	21215367	CNVD
Gastric cancer	18160780	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:47461400-47477400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr14:47471000-47473800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr14:47478800-47479200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr14:47478800-47479200	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr14:47478800-47479200	Enhancers	Fetal Kidney	kidney
6	chr14:47478800-47479400	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr14:47478800-47479400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr14:47479000-47479400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr14:47479000-47479400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr14:47486200-47486600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr14:47492400-47492600	Enhancers	Liver	Liver
12	chr14:47494400-47494800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr14:47494400-47495000	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr14:47495000-47495200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr14:47495200-47496800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr14:47503800-47504400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr14:47507800-47511200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr14:47508600-47508800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr14:47509000-47510000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr14:47509600-47510000	Enhancers	Fetal Kidney	kidney
21	chr14:47510000-47510200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr14:47510000-47510400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr14:47510200-47513000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr14:47512800-47513800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr14:47513000-47514200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr14:47513000-47514200	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr14:47513000-47514600	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr14:47513000-47514600	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr14:47513600-47514400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr14:47513600-47514600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr14:47513800-47514400	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr14:47513800-47514400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr14:47513800-47514400	Enhancers	Fetal Brain Male	brain
34	chr14:47513800-47514400	Enhancers	Fetal Lung	lung
35	chr14:47514000-47514400	Enhancers	Brain Anterior Caudate	brain
36	chr14:47514200-47514600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr14:47514200-47514600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
38	chr14:47514200-47514600	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr14:47523000-47523400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr14:47534000-47534600	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr14:47534000-47535000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr14:47534200-47535000	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr14:47534200-47535400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr14:47534400-47535200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr14:47535000-47538600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr14:47538600-47538800	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr14:47549800-47550000	Enhancers	H9 Cell Line	embryonic stem cell
48	chr14:47550000-47571600	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr14:47553800-47554000	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr14:47554000-47570600	Weak transcription	HUES6 Cell Line	embryonic stem cell

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