Variant report

Variant	esv33752
Chromosome Location	chr6:114557760-114602482
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	ARID3A	chr6:114593702-114594112	HepG2	liver:	n/a	n/a
2	BRCA1	chr6:114600651-114600654	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr6:114559287-114559863	HepG2	liver:	n/a	chr6:114559446-114559457
4	CEBPB	chr6:114561965-114562339	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr6:114593930-114594151	HepG2	liver:	n/a	n/a
6	CEBPB	chr6:114593879-114594185	HepG2	liver:	n/a	n/a
7	CEBPZ	chr6:114593742-114594187	HepG2	liver:	n/a	n/a
8	CTCF	chr6:114577709-114577754	Pancreas_OC	pancreas:	n/a	n/a
9	CTCF	chr6:114574700-114574850	GM12875	blood:	n/a	chr6:114574788-114574795
10	CTCF	chr6:114577333-114577389	Kidney_OC	kidney:	n/a	n/a
11	CTCF	chr6:114560400-114560550	HEK293	kidney:	n/a	n/a
12	E2F4	chr6:114585681-114585881	MCF10A-Er-Src	breast:	n/a	n/a
13	E2F4	chr6:114581612-114581867	MCF10A-Er-Src	breast:	n/a	n/a
14	EP300	chr6:114593907-114594095	HepG2	liver:	n/a	n/a
15	EP300	chr6:114593688-114594261	HepG2	liver:	n/a	n/a
16	EP300	chr6:114562018-114562329	Hela-S3	cervix:	n/a	chr6:114562164-114562173
17	EP300	chr6:114597605-114598482	SK-N-SH	brain:	n/a	chr6:114597778-114597792 chr6:114597844-114597853 chr6:114598264-114598274 chr6:114598341-114598350
18	EP300	chr6:114590716-114591072	SK-N-SH_RA	brain:	n/a	n/a
19	EP300	chr6:114593699-114594201	HepG2	liver:	n/a	n/a
20	EP300	chr6:114597960-114598244	SK-N-SH_RA	brain:	n/a	n/a
21	EP300	chr6:114590069-114591923	SK-N-SH	brain:	n/a	n/a
22	FOS	chr6:114561984-114562391	MCF10A-Er-Src	breast:	n/a	chr6:114562164-114562173 chr6:114562164-114562171 chr6:114562163-114562173 chr6:114562163-114562173
23	FOS	chr6:114561985-114562393	MCF10A-Er-Src	breast:	n/a	chr6:114562164-114562173 chr6:114562164-114562171 chr6:114562163-114562173 chr6:114562163-114562173
24	FOS	chr6:114561978-114562429	MCF10A-Er-Src	breast:	n/a	chr6:114562164-114562173 chr6:114562164-114562171 chr6:114562163-114562173 chr6:114562163-114562173
25	FOS	chr6:114561982-114562379	MCF10A-Er-Src	breast:	n/a	chr6:114562164-114562173 chr6:114562164-114562171 chr6:114562163-114562173 chr6:114562163-114562173
26	FOXA1	chr6:114593651-114594248	HepG2	liver:	n/a	n/a
27	FOXA1	chr6:114593779-114594265	HepG2	liver:	n/a	n/a
28	FOXA1	chr6:114593747-114594137	HepG2	liver:	n/a	n/a
29	FOXA1	chr6:114593703-114594163	HepG2	liver:	n/a	n/a
30	FOXA2	chr6:114593767-114594193	HepG2	liver:	n/a	n/a
31	GATA2	chr6:114590732-114591416	SH-SY5Y	brain:	n/a	chr6:114590893-114590910 chr6:114590892-114590901
32	GATA3	chr6:114590656-114591231	SK-N-SH	brain:	n/a	chr6:114590893-114590910 chr6:114590892-114590901
33	GATA3	chr6:114590758-114591274	SH-SY5Y	brain:	n/a	chr6:114590893-114590910 chr6:114590892-114590901
34	GATA3	chr6:114597813-114598355	SH-SY5Y	brain:	n/a	chr6:114598138-114598148 chr6:114598339-114598349
35	GATA3	chr6:114593539-114593693	SH-SY5Y	brain:	n/a	n/a
36	GATA3	chr6:114584292-114584345	SH-SY5Y	brain:	n/a	n/a
37	GATA3	chr6:114590598-114591567	SK-N-SH	brain:	n/a	chr6:114590893-114590910 chr6:114590892-114590901
38	HDAC2	chr6:114593726-114594253	HepG2	liver:	n/a	n/a
39	HDAC2	chr6:114593696-114594256	HepG2	liver:	n/a	n/a
40	HNF4A	chr6:114593744-114594124	HepG2	liver:	n/a	chr6:114593988-114594003
41	HNF4A	chr6:114593866-114594156	HepG2	liver:	n/a	chr6:114593988-114594003
42	HNF4G	chr6:114593761-114594163	HepG2	liver:	n/a	chr6:114593987-114594002
43	JUN	chr6:114598407-114598423	H1-hESC	embryonic stem cell:	n/a	n/a
44	JUND	chr6:114562021-114562319	Hela-S3	cervix:	n/a	chr6:114562164-114562173 chr6:114562164-114562171 chr6:114562163-114562173 chr6:114562163-114562173
45	JUND	chr6:114593888-114594182	HepG2	liver:	n/a	n/a
46	JUND	chr6:114560626-114560669	HepG2	liver:	n/a	n/a
47	JUND	chr6:114593853-114594124	HepG2	liver:	n/a	n/a
48	KAP1	chr6:114568191-114568665	HEK293	kidney:	n/a	chr6:114568576-114568584
49	KAP1	chr6:114568060-114568698	U2OS	brain:	n/a	chr6:114568576-114568584
50	KAP1	chr6:114576790-114577016	HEK293	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:114567943-114567993	HPAEpiC	pulmonary alveolar:	n/a
2	chr6:114567943-114567993	IMR90	lung:	fetal
3	chr6:114567943-114567993	HCT-116	colon:	n/a
4	chr6:114567943-114567993	HRE	kidney:	n/a
5	chr6:114567943-114567993	AoSMC	blood vessel:	n/a
6	chr6:114567943-114567993	AG04449	skin:	fetal
7	chr6:114567943-114567993	HepG2	liver:	n/a
8	chr6:114567943-114567993	GM12892	blood:	n/a
9	chr6:114567943-114567993	GM12891	blood:	n/a
10	chr6:114567943-114567993	GM12878	blood:	n/a
11	chr6:114567943-114567993	HMEC	breast:	n/a
12	chr6:114567943-114567993	AG10803	skin:	n/a
13	chr6:114567943-114567993	AG09309	skin:	n/a
14	chr6:114567943-114567993	NHBE	bronchial:	n/a
15	chr6:114567943-114567993	A549	lung:	n/a
16	chr6:114567943-114567993	PFSK-1	brain:	n/a
17	chr6:114567943-114567993	LNCaP	prostate:	n/a
18	chr6:114567943-114567993	NH-A	brain:	n/a
19	chr6:114567943-114567993	HIPEpiC	eye:	n/a
20	chr6:114567943-114567993	HAEpiC	amniotic membrane:	n/a
21	chr6:114567943-114567993	SK-N-SH_RA	brain:	n/a
22	chr6:114567943-114567993	RPTEC	kidney:	n/a
23	chr6:114567943-114567993	Caco-2	colon:	n/a
24	chr6:114567943-114567993	GM19239	blood:	n/a
25	chr6:114567943-114567993	MCF10A-Er-Src	breast:	n/a
26	chr6:114567943-114567993	SAEC	small airway:	n/a
27	chr6:114567943-114567993	ProgFib	skin:	n/a
28	chr6:114567943-114567993	U87	brain:	n/a
29	chr6:114567943-114567993	HRCEpiC	kidney:	n/a
30	chr6:114567943-114567993	HCM	heart:	n/a
31	chr6:114567943-114567993	SK-N-SH	brain:	n/a
32	chr6:114567943-114567993	ovcar-3	ovarian:	n/a
33	chr6:114567943-114567993	CMK	blood:	n/a
34	chr6:114567943-114567993	BE2_C	brain:	n/a
35	chr6:114567943-114567993	PrEC	prostate:	n/a
36	chr6:114567943-114567993	HCPEpiC	choroid plexus:	n/a
37	chr6:114567943-114567993	Jurkat	blood:	n/a
38	chr6:114567943-114567993	HEEpiC	esophagus:	n/a
39	chr6:114567943-114567993	HUVEC	blood vessel:	n/a
40	chr6:114567943-114567993	SK-N-MC	brain:	n/a
41	chr6:114567943-114567993	HL-60	blood:	n/a
42	chr6:114567943-114567993	H1-hESC	embryonic stem cell:	embryo
43	chr6:114567943-114567993	AG04450	lung:	fetal
44	chr6:114567943-114567993	HNPCEpiC	eye:	n/a
45	chr6:114567943-114567993	BJ	skin:	n/a
46	chr6:114567943-114567993	AG09319	gingival:	n/a
47	chr6:114567943-114567993	SKMC	muscle:	n/a
48	chr6:114567943-114567993	MCF-7	breast:	n/a
49	chr6:114567943-114567993	K562	blood:	n/a
50	chr6:114567943-114567993	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:114582668..114584801-chr6:114587300..114589162,2	K562	blood:
2	chr6:114554629..114558117-chr6:114558553..114561790,3	K562	blood:
3	chr6:114582668..114584801-chr6:114587300..114589162,2	K562	blood:
4	chr6:114548047..114550869-chr6:114555378..114557876,2	MCF-7	breast:
5	chr6:114561580..114563702-chr6:114578615..114580670,2	K562	blood:
6	chr13:68241658..68242183-chr6:114561063..114561674,2	MCF-7	breast:
7	chr6:114554629..114558117-chr6:114558553..114561790,3	K562	blood:
8	chr6:114561580..114563702-chr6:114578615..114580670,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MARCKS-5	chr6:114560153-114560363	ENSG00000228624
2	lnc-MARCKS-5	chr6:114559937-114560160	NONHSAT114604
3	lnc-MARCKS-5	chr6:114572683-114573083	ENSG00000228624.3
4	lnc-HDAC2-9	chr6:114596212-114596297	NONHSAT114605
5	lnc-MARCKS-5	chr6:114559070-114559123	NONHSAT114604
6	lnc-HDAC2-9	chr6:114595334-114595536	NONHSAT114605

Variant related genes	Relation type
ENSG00000228624	TF binding region
ENSG00000221599	TF binding region
ENSG00000228624	CpG island
ENSG00000221599	CpG island
PBXIP1	miRNA target sites

Extended variants
information (count: 1514 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:1514 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542197447	chr6:114557781-114557782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs563722513	chr6:114557808-114557809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs12195272	chr6:114557813-114557814	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs543731572	chr6:114557814-114557815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184950397	chr6:114557822-114557823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373861896	chr6:114557845-114557846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532218825	chr6:114557849-114557850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs71553397	chr6:114557856-114557857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369374121	chr6:114557873-114557874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547079486	chr6:114557934-114557935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192035797	chr6:114557980-114557981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529763308	chr6:114557990-114557991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547752449	chr6:114558027-114558028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184165964	chr6:114558053-114558054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569670152	chr6:114558108-114558109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537323112	chr6:114558128-114558129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147932807	chr6:114558135-114558136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs367705445	chr6:114558142-114558143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535190445	chr6:114558206-114558207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553606202	chr6:114558211-114558212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574957290	chr6:114558213-114558214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111437183	chr6:114558271-114558272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569827421	chr6:114558290-114558291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371413478	chr6:114558357-114558358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149047241	chr6:114558387-114558388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375986282	chr6:114558427-114558428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536241701	chr6:114558463-114558464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs556636727	chr6:114558494-114558495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs397801185	chr6:114558506-114558507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs62415835	chr6:114558508-114558509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575619978	chr6:114558566-114558567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78187429	chr6:114558574-114558575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565222306	chr6:114558601-114558602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576730638	chr6:114558680-114558681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188724010	chr6:114558697-114558698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555010007	chr6:114558702-114558703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568358056	chr6:114558738-114558739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529728611	chr6:114558760-114558761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143078135	chr6:114558790-114558791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563135150	chr6:114558799-114558800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371576912	chr6:114558865-114558866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77624668	chr6:114558916-114558917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537760484	chr6:114558924-114558925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs72954564	chr6:114559067-114559068	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs571077513	chr6:114559072-114559073	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs535359254	chr6:114559081-114559082	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs148231449	chr6:114559083-114559084	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs200444173	chr6:114559105-114559106	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs568701709	chr6:114559111-114559112	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs529245936	chr6:114559145-114559146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:123)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Salivary gland tumor	18059337	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD

Chromatin state (count:157 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:114534400-114576000	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr6:114539000-114561200	Weak transcription	Brain Cingulate Gyrus	brain
3	chr6:114540800-114561000	Weak transcription	HSMMtube	muscle
4	chr6:114559400-114559600	Enhancers	Brain Angular Gyrus	brain
5	chr6:114560000-114561000	Weak transcription	Brain Angular Gyrus	brain
6	chr6:114560400-114560600	Enhancers	Brain Anterior Caudate	brain
7	chr6:114560600-114561400	Weak transcription	Brain Anterior Caudate	brain
8	chr6:114561000-114561600	Enhancers	Brain Angular Gyrus	brain
9	chr6:114561200-114561600	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr6:114561200-114561800	Enhancers	Brain Cingulate Gyrus	brain
11	chr6:114561400-114561600	Enhancers	Brain Anterior Caudate	brain
12	chr6:114561600-114562400	Weak transcription	Brain Anterior Caudate	brain
13	chr6:114561800-114562800	Enhancers	Hela-S3	cervix
14	chr6:114562400-114563200	Enhancers	Brain Anterior Caudate	brain
15	chr6:114563200-114566200	Weak transcription	Brain Anterior Caudate	brain
16	chr6:114563600-114593400	Weak transcription	HepG2	liver
17	chr6:114566000-114566200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr6:114566200-114566600	Enhancers	Brain Substantia Nigra	brain
19	chr6:114566200-114566800	Enhancers	Brain Anterior Caudate	brain
20	chr6:114566200-114568000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr6:114566400-114566600	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr6:114566600-114568200	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr6:114566800-114567200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr6:114567600-114568200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr6:114567800-114568600	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr6:114568000-114568800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr6:114568200-114568800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr6:114568200-114569000	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr6:114568800-114569000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr6:114568800-114574400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr6:114570000-114571000	Enhancers	HSMM	muscle
32	chr6:114570400-114570800	Enhancers	HSMMtube	muscle
33	chr6:114570600-114571000	Enhancers	Fetal Muscle Leg	muscle
34	chr6:114572600-114573200	Enhancers	H9 Cell Line	embryonic stem cell
35	chr6:114572800-114574600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr6:114573200-114576400	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr6:114573400-114574200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr6:114574200-114575400	Enhancers	HMEC	breast
39	chr6:114574200-114576200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr6:114574400-114574800	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr6:114574400-114575000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr6:114574600-114575000	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr6:114574600-114575400	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr6:114574600-114575400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr6:114574600-114575400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr6:114574600-114575400	Enhancers	NHEK	skin
47	chr6:114574800-114575400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr6:114574800-114576000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr6:114575000-114576400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr6:114575200-114575400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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