Variant report

Variant	nsv1034897
Chromosome Location	chr6:114454186-114555679
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:501)
CpG islands
(count:428)
Chromatin interactive
region (count:14)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:501 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:114488334-114488370	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:114491020-114492995	HepG2	liver:	n/a	chr6:114491965-114491981 chr6:114491966-114491982
3	ARID3A	chr6:114465847-114466767	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:114485413-114485841	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:114480739-114481242	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:114493457-114494086	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:114488706-114489732	HepG2	liver:	n/a	n/a
8	BACH1	chr6:114524772-114524969	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr6:114488791-114489676	HepG2	liver:	n/a	n/a
10	BHLHE40	chr6:114481000-114481212	HepG2	liver:	n/a	n/a
11	BRCA1	chr6:114544536-114544884	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr6:114483863-114484244	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr6:114466098-114466836	Hela-S3	cervix:	n/a	chr6:114466490-114466501 chr6:114466456-114466469 chr6:114466456-114466467
14	CEBPB	chr6:114488910-114489171	HepG2	liver:	n/a	n/a
15	CEBPB	chr6:114456516-114457165	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr6:114483935-114484103	K562	blood:	n/a	n/a
17	CEBPB	chr6:114483881-114484215	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr6:114483841-114484198	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr6:114483880-114484203	A549	lung:	n/a	n/a
20	CEBPB	chr6:114466184-114466705	HepG2	liver:	n/a	chr6:114466490-114466501 chr6:114466456-114466469 chr6:114466456-114466467
21	CEBPB	chr6:114475989-114476158	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr6:114488836-114489307	HepG2	liver:	n/a	n/a
23	CEBPB	chr6:114466178-114466800	HepG2	liver:	n/a	chr6:114466490-114466501 chr6:114466456-114466469 chr6:114466456-114466467
24	CEBPB	chr6:114523645-114523954	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr6:114488766-114489283	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:114488693-114489566	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:114495442-114495601	HepG2	liver:	n/a	chr6:114495493-114495504
28	CEBPB	chr6:114461175-114462013	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr6:114483874-114484231	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:114483867-114484228	IMR90	lung:	n/a	n/a
31	CEBPD	chr6:114488938-114489161	HepG2	liver:	n/a	n/a
32	CEBPZ	chr6:114488336-114488359	HepG2	liver:	n/a	n/a
33	CHD2	chr6:114476076-114476266	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr6:114488904-114489334	HepG2	liver:	n/a	n/a
35	CTCF	chr6:114489280-114489430	Caco-2	colon:	n/a	chr6:114489397-114489406
36	CTCF	chr6:114479220-114479236	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr6:114479196-114479270	HepG2	liver:	n/a	n/a
38	CTCF	chr6:114490860-114491010	HMEC	breast:	n/a	chr6:114490913-114490934 chr6:114490911-114490929
39	CTCF	chr6:114473164-114473204	GM13976	blood:	n/a	n/a
40	CTCF	chr6:114466840-114466990	HepG2	liver:	n/a	n/a
41	CTCF	chr6:114506522-114506565	GM20000	blood:	n/a	n/a
42	CTCF	chr6:114479142-114479270	HepG2	liver:	n/a	n/a
43	CTCF	chr6:114468075-114468113	LNCaP	prostate:	n/a	n/a
44	CTCF	chr6:114467680-114467830	HEK293	kidney:	n/a	n/a
45	CTCF	chr6:114497360-114497510	Caco-2	colon:	n/a	n/a
46	CTCF	chr6:114479160-114479310	BE2_C	brain:	n/a	n/a
47	CTCF	chr6:114479209-114479305	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:114465800-114465950	HRPEpiC	eye:	n/a	chr6:114465829-114465838
49	CTCF	chr6:114466720-114466870	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr6:114466854-114466940	H1-hESC	embryonic stem cell:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:114515500-114515550	ProgFib	skin:	n/a
2	chr6:114515500-114515550	ProgFib	skin:	n/a
3	chr6:114475951-114476001	K562	blood:	n/a
4	chr6:114515500-114515550	AG04450	lung:	fetal
5	chr6:114544140-114544190	HCT-116	colon:	n/a
6	chr6:114515500-114515550	Hela-S3	cervix:	n/a
7	chr6:114515500-114515550	AoSMC	blood vessel:	n/a
8	chr6:114466051-114466101	Hela-S3	cervix:	n/a
9	chr6:114466051-114466101	T-47D	breast:	n/a
10	chr6:114544140-114544190	SAEC	small airway:	n/a
11	chr6:114524946-114524996	AG09319	gingival:	n/a
12	chr6:114524946-114524996	CMK	blood:	n/a
13	chr6:114475951-114476001	SAEC	small airway:	n/a
14	chr6:114466051-114466101	HCT-116	colon:	n/a
15	chr6:114551190-114551240	HPAEpiC	pulmonary alveolar:	n/a
16	chr6:114524946-114524996	HRCEpiC	kidney:	n/a
17	chr6:114524946-114524996	HEEpiC	esophagus:	n/a
18	chr6:114549892-114549942	BE2_C	brain:	n/a
19	chr6:114515500-114515550	A549	lung:	n/a
20	chr6:114549892-114549942	PANC-1	pancreas:	n/a
21	chr6:114475951-114476001	HCPEpiC	choroid plexus:	n/a
22	chr6:114524946-114524996	SAEC	small airway:	n/a
23	chr6:114515500-114515550	CMK	blood:	n/a
24	chr6:114524946-114524996	IMR90	lung:	fetal
25	chr6:114475951-114476001	ProgFib	skin:	n/a
26	chr6:114466051-114466101	HRE	kidney:	n/a
27	chr6:114515500-114515550	HNPCEpiC	eye:	n/a
28	chr6:114544140-114544190	NH-A	brain:	n/a
29	chr6:114551190-114551240	HIPEpiC	eye:	n/a
30	chr6:114544140-114544190	CMK	blood:	n/a
31	chr6:114475951-114476001	GM06990	blood:	n/a
32	chr6:114551190-114551240	HepG2	liver:	n/a
33	chr6:114549892-114549942	SAEC	small airway:	n/a
34	chr6:114515500-114515550	SK-N-SH	brain:	n/a
35	chr6:114466051-114466101	Caco-2	colon:	n/a
36	chr6:114475951-114476001	HEK293	kidney:	embryo
37	chr6:114544140-114544190	AG04449	skin:	fetal
38	chr6:114475951-114476001	NHBE	bronchial:	n/a
39	chr6:114466051-114466101	HRCEpiC	kidney:	n/a
40	chr6:114515500-114515550	NHDF-neo	bronchial:	n/a
41	chr6:114475951-114476001	HEEpiC	esophagus:	n/a
42	chr6:114524946-114524996	HIPEpiC	eye:	n/a
43	chr6:114515500-114515550	BJ	skin:	n/a
44	chr6:114544140-114544190	PrEC	prostate:	n/a
45	chr6:114544140-114544190	HIPEpiC	eye:	n/a
46	chr6:114549892-114549942	HMEC	breast:	n/a
47	chr6:114475951-114476001	Caco-2	colon:	n/a
48	chr6:114544140-114544190	AoSMC	blood vessel:	n/a
49	chr6:114466051-114466101	NB4	blood:	n/a
50	chr6:114475951-114476001	HCM	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:114459085..114460810-chr6:114462793..114464611,2	MCF-7	breast:
2	chr6:114446450..114448117-chr6:114452314..114454263,2	K562	blood:
3	chr6:114548047..114550869-chr6:114555378..114557876,2	MCF-7	breast:
4	chr6:114459085..114460810-chr6:114462793..114464611,2	MCF-7	breast:
5	chr6:114554629..114558117-chr6:114558553..114561790,3	K562	blood:
6	chr6:114456567..114459418-chr6:114463134..114465528,2	K562	blood:
7	chr17:62502076..62503847-chr6:114506074..114508733,2	MCF-7	breast:
8	chr6:114474882..114478517-chr6:114482153..114484580,3	MCF-7	breast:
9	chr6:114490498..114491435-chr6:114625509..114626136,2	MCF-7	breast:
10	chr6:114456567..114459418-chr6:114463134..114465528,2	K562	blood:
11	chr6:114474882..114478517-chr6:114482153..114484580,3	MCF-7	breast:
12	chr6:114548047..114550869-chr6:114555378..114557876,2	MCF-7	breast:
13	chr6:114457639..114460635-chr6:114462244..114465623,4	K562	blood:
14	chr6:114457639..114460635-chr6:114462244..114465623,4	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HDAC2-7	chr6:114489519-114489614	NONHSAT114602
2	lnc-MARCKS-5	chr6:114543973-114544037	NONHSAT114604
3	lnc-MARCKS-5	chr6:114463951-114464185	ENSG00000228624
4	lnc-HDAC2-7	chr6:114488641-114488843	NONHSAT114602
5	lnc-MARCKS-5	chr6:114500189-114500321	ENSG00000228624
6	lnc-MARCKS-5	chr6:114464783-114465082	ENSG00000228624
7	lnc-MARCKS-5	chr6:114551321-114551487	ENSG00000228624
8	lnc-MARCKS-5	chr6:114552512-114552605	ENSG00000228624.3
9	lnc-MARCKS-5	chr6:114499817-114499884	ENSG00000228624
10	lnc-MARCKS-5	chr6:114500189-114500321	ENSG00000228624
11	lnc-MARCKS-5	chr6:114551305-114551510	ENSG00000228624

No data

Variant related genes	Relation type
ENSG00000228624	TF binding region
RNA5SP213	TF binding region
HS3ST5	TF binding region
ENSG00000228624	CpG island
RNA5SP213	CpG island
HS3ST5	CpG island
ENSG00000108654	chromatin interactions
ENSG00000258890	chromatin interactions
CXCL12	miRNA target sites
NFIB	miRNA target sites
RAD21	miRNA target sites
HSP90B1	miRNA target sites
LRRC59	miRNA target sites
CLIP4	miRNA target sites

Extended variants
information (count: 3236 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:3236 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373685185	chr6:114454197-114454198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs545797897	chr6:114454233-114454234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs144254715	chr6:114454285-114454286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183705370	chr6:114454310-114454311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531525344	chr6:114454350-114454351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs372660432	chr6:114454355-114454356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564749407	chr6:114454361-114454362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs75710978	chr6:114454391-114454392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562314658	chr6:114454405-114454406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs28583622	chr6:114454500-114454501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9387191	chr6:114454597-114454598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs147848334	chr6:114454609-114454610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148912529	chr6:114454725-114454726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187590626	chr6:114454773-114454774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192272847	chr6:114454830-114454831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73767010	chr6:114454840-114454841	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs60751360	chr6:114454911-114454912	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs559144826	chr6:114454936-114454937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542674337	chr6:114454998-114454999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73536655	chr6:114455030-114455031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561040100	chr6:114455031-114455032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553223700	chr6:114455106-114455107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574757288	chr6:114455112-114455113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs148216053	chr6:114455136-114455137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541832413	chr6:114455166-114455167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs58642146	chr6:114455175-114455176	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs369706601	chr6:114455176-114455177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112074450	chr6:114455206-114455207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374466101	chr6:114455220-114455221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200815825	chr6:114455234-114455235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575893590	chr6:114455273-114455274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182974177	chr6:114455290-114455291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs564735366	chr6:114455298-114455299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187317022	chr6:114455404-114455405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576176487	chr6:114455507-114455508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547454557	chr6:114455509-114455510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559155519	chr6:114455527-114455528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140972438	chr6:114455547-114455548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543390993	chr6:114455563-114455564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565315835	chr6:114455580-114455581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532661438	chr6:114455593-114455594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548071529	chr6:114455637-114455638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs57753254	chr6:114455722-114455723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569670577	chr6:114455732-114455733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531226636	chr6:114455749-114455750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145059936	chr6:114455756-114455757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138786982	chr6:114455772-114455773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559649491	chr6:114455776-114455777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534931340	chr6:114455791-114455792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11153466	chr6:114455821-114455822	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:120)

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
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:624 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:114430800-114477800	Weak transcription	Brain Anterior Caudate	brain
2	chr6:114444000-114465200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:114444000-114466000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr6:114445600-114457000	Weak transcription	Psoas Muscle	Psoas
5	chr6:114445600-114461200	Weak transcription	HSMMtube	muscle
6	chr6:114445600-114461600	Weak transcription	HSMM	muscle
7	chr6:114447400-114456200	Weak transcription	Brain Hippocampus Middle	brain
8	chr6:114447400-114466000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr6:114454200-114454400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:114454200-114454400	Enhancers	Brain Substantia Nigra	brain
11	chr6:114454400-114456400	Weak transcription	Brain Substantia Nigra	brain
12	chr6:114454400-114466000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:114455200-114455400	Enhancers	Pancreas	Pancrea
14	chr6:114455200-114457000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:114455400-114466800	Weak transcription	Pancreas	Pancrea
16	chr6:114456000-114457200	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr6:114456200-114457400	Enhancers	Hela-S3	cervix
18	chr6:114456400-114457000	Enhancers	Brain Substantia Nigra	brain
19	chr6:114456400-114466200	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr6:114456600-114457000	Enhancers	Brain Angular Gyrus	brain
21	chr6:114456600-114457200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr6:114456800-114457200	Enhancers	Muscle Satellite Cultured Cells	--
23	chr6:114456800-114457400	Enhancers	HepG2	liver
24	chr6:114457000-114457200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr6:114457000-114457200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr6:114457000-114457400	Enhancers	Psoas Muscle	Psoas
27	chr6:114457000-114463200	Weak transcription	Brain Substantia Nigra	brain
28	chr6:114457000-114466800	Weak transcription	Brain Angular Gyrus	brain
29	chr6:114457200-114457600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr6:114457200-114461000	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr6:114457200-114461800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr6:114457400-114460000	Weak transcription	HepG2	liver
33	chr6:114457400-114461200	Weak transcription	Hela-S3	cervix
34	chr6:114457400-114461800	Weak transcription	Psoas Muscle	Psoas
35	chr6:114458200-114465400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr6:114458800-114459000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:114460000-114460200	Enhancers	HepG2	liver
38	chr6:114460200-114460400	Weak transcription	HepG2	liver
39	chr6:114460400-114460600	Enhancers	HepG2	liver
40	chr6:114460600-114464000	Weak transcription	HepG2	liver
41	chr6:114461000-114461600	Enhancers	Muscle Satellite Cultured Cells	--
42	chr6:114461200-114461600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr6:114461200-114462400	Enhancers	Hela-S3	cervix
44	chr6:114461200-114462400	Enhancers	HSMMtube	muscle
45	chr6:114461400-114461600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr6:114461400-114461600	Enhancers	Osteobl	bone
47	chr6:114461600-114462000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr6:114461600-114462000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr6:114461600-114462000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr6:114461600-114462000	Flanking Active TSS	Muscle Satellite Cultured Cells	--

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