Variant report

Variant	nsv886011
Chromosome Location	chr6:65873577-66237309
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:698)
CpG islands
(count:366)
Chromatin interactive
region (count:14)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:698 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:66049641-66049730	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:66120388-66120433	HepG2	liver:	n/a	n/a
3	ATF1	chr6:66171007-66171493	K562	blood:	n/a	n/a
4	ATF1	chr6:66160376-66160599	K562	blood:	n/a	n/a
5	BACH1	chr6:66066175-66066268	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:65934747-65934766	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr6:65970555-65970750	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr6:66193565-66193851	K562	blood:	n/a	n/a
9	CCNT2	chr6:66171045-66171349	K562	blood:	n/a	n/a
10	CCNT2	chr6:66100608-66100682	K562	blood:	n/a	n/a
11	CCNT2	chr6:66139022-66139218	K562	blood:	n/a	n/a
12	CEBPB	chr6:66064262-66064425	K562	blood:	n/a	chr6:66064368-66064379 chr6:66064370-66064381 chr6:66064370-66064379
13	CEBPB	chr6:65895196-65895497	A549	lung:	n/a	chr6:65895346-65895357
14	CEBPB	chr6:66192989-66193263	HepG2	liver:	n/a	chr6:66193166-66193179 chr6:66193107-66193120 chr6:66193107-66193118
15	CEBPB	chr6:66109620-66109995	HepG2	liver:	n/a	chr6:66109790-66109801 chr6:66109810-66109821
16	CEBPB	chr6:65909589-65909973	MCF-7	breast:	n/a	n/a
17	CEBPB	chr6:66064204-66064473	IMR90	lung:	n/a	chr6:66064368-66064379 chr6:66064370-66064381 chr6:66064370-66064379
18	CEBPB	chr6:66010691-66010956	K562	blood:	n/a	chr6:66010782-66010793
19	CEBPB	chr6:65877133-65877402	HepG2	liver:	n/a	chr6:65877288-65877299
20	CEBPB	chr6:66037858-66038164	HepG2	liver:	n/a	chr6:66037990-66038001
21	CEBPB	chr6:66138219-66138426	HepG2	liver:	n/a	chr6:66138267-66138278
22	CEBPB	chr6:66010679-66010939	K562	blood:	n/a	chr6:66010782-66010793
23	CEBPB	chr6:66064192-66064538	HepG2	liver:	n/a	chr6:66064368-66064379 chr6:66064370-66064381 chr6:66064370-66064379
24	CEBPB	chr6:65969974-65970326	H1-hESC	embryonic stem cell:	n/a	chr6:65970271-65970283
25	CEBPB	chr6:66010665-66010970	HepG2	liver:	n/a	chr6:66010782-66010793
26	CEBPB	chr6:66064245-66064517	Hela-S3	cervix:	n/a	chr6:66064368-66064379 chr6:66064370-66064381 chr6:66064370-66064379
27	CEBPB	chr6:66156810-66157084	K562	blood:	n/a	n/a
28	CEBPB	chr6:65969128-65969281	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr6:65989228-65989353	HepG2	liver:	n/a	chr6:65989300-65989311 chr6:65989339-65989350
30	CEBPB	chr6:66143961-66144277	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:66037840-66038160	IMR90	lung:	n/a	chr6:66037990-66038001
32	CEBPB	chr6:66230294-66230581	IMR90	lung:	n/a	n/a
33	CEBPB	chr6:65895166-65895539	HepG2	liver:	n/a	chr6:65895346-65895357
34	CEBPB	chr6:66156754-66157125	HepG2	liver:	n/a	chr6:66157101-66157114
35	CEBPB	chr6:66127902-66128153	HepG2	liver:	n/a	chr6:66128011-66128022 chr6:66128012-66128021
36	CEBPB	chr6:66230260-66230571	HepG2	liver:	n/a	n/a
37	CEBPB	chr6:66037851-66038095	A549	lung:	n/a	chr6:66037990-66038001
38	CEBPB	chr6:65968981-65969345	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr6:66120214-66120512	HepG2	liver:	n/a	n/a
40	CEBPB	chr6:66066493-66066779	HepG2	liver:	n/a	chr6:66066621-66066632
41	CEBPB	chr6:66064226-66064435	H1-hESC	embryonic stem cell:	n/a	chr6:66064368-66064379 chr6:66064370-66064381 chr6:66064370-66064379
42	CEBPB	chr6:66195051-66195251	IMR90	lung:	n/a	n/a
43	CEBPB	chr6:66064211-66064491	A549	lung:	n/a	chr6:66064368-66064379 chr6:66064370-66064381 chr6:66064370-66064379
44	CEBPB	chr6:65909779-65909892	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPD	chr6:66171023-66171458	K562	blood:	n/a	n/a
46	CEBPD	chr6:66076790-66077115	K562	blood:	n/a	n/a
47	CHD2	chr6:65969943-65970228	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr6:65969080-65969230	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr6:65969080-65969230	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr6:66201727-66201746	GM13977	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:66010172-66010222	AG04449	skin:	fetal
2	chr6:66011288-66011338	SKMC	muscle:	n/a
3	chr6:66013901-66013951	SK-N-SH	brain:	n/a
4	chr6:66010172-66010222	HUVEC	blood vessel:	n/a
5	chr6:66010172-66010222	H1-hESC	embryonic stem cell:	embryo
6	chr6:66011288-66011338	NHDF-neo	bronchial:	n/a
7	chr6:66011626-66011676	HRCEpiC	kidney:	n/a
8	chr6:66011288-66011338	ECC-1	luminal epithelium:	n/a
9	chr6:66207286-66207336	HCF	heart:	n/a
10	chr6:66011288-66011338	SK-N-SH_RA	brain:	n/a
11	chr6:66207286-66207336	HCM	heart:	n/a
12	chr6:66207286-66207336	Jurkat	blood:	n/a
13	chr6:66010172-66010222	SK-N-MC	brain:	n/a
14	chr6:66011626-66011676	AG09319	gingival:	n/a
15	chr6:66205227-66205277	NHDF-neo	bronchial:	n/a
16	chr6:66010172-66010222	GM12878	blood:	n/a
17	chr6:66205227-66205277	Caco-2	colon:	n/a
18	chr6:66010172-66010222	NHBE	bronchial:	n/a
19	chr6:66010172-66010222	AG10803	skin:	n/a
20	chr6:66207286-66207336	NT2-D1	testis:	n/a
21	chr6:66011626-66011676	AoSMC	blood vessel:	n/a
22	chr6:66205227-66205277	HEEpiC	esophagus:	n/a
23	chr6:66011626-66011676	SAEC	small airway:	n/a
24	chr6:66207286-66207336	ProgFib	skin:	n/a
25	chr6:66011626-66011676	T-47D	breast:	n/a
26	chr6:66013901-66013951	AG10803	skin:	n/a
27	chr6:66011626-66011676	Jurkat	blood:	n/a
28	chr6:66207286-66207336	HMEC	breast:	n/a
29	chr6:66013901-66013951	HMEC	breast:	n/a
30	chr6:66010172-66010222	SKMC	muscle:	n/a
31	chr6:66011626-66011676	ovcar-3	ovarian:	n/a
32	chr6:66013901-66013951	NB4	blood:	n/a
33	chr6:66011288-66011338	HAEpiC	amniotic membrane:	n/a
34	chr6:66207286-66207336	NH-A	brain:	n/a
35	chr6:66011288-66011338	NT2-D1	testis:	n/a
36	chr6:66207286-66207336	SK-N-SH	brain:	n/a
37	chr6:66013901-66013951	Hela-S3	cervix:	n/a
38	chr6:66011288-66011338	HRE	kidney:	n/a
39	chr6:66011626-66011676	NHBE	bronchial:	n/a
40	chr6:66205227-66205277	T-47D	breast:	n/a
41	chr6:66205227-66205277	AG09319	gingival:	n/a
42	chr6:66013901-66013951	HAEpiC	amniotic membrane:	n/a
43	chr6:66207286-66207336	HCPEpiC	choroid plexus:	n/a
44	chr6:66010172-66010222	HAEpiC	amniotic membrane:	n/a
45	chr6:66013901-66013951	Caco-2	colon:	n/a
46	chr6:66010172-66010222	HNPCEpiC	eye:	n/a
47	chr6:66013901-66013951	NHDF-neo	bronchial:	n/a
48	chr6:66010172-66010222	HRCEpiC	kidney:	n/a
49	chr6:66205227-66205277	HNPCEpiC	eye:	n/a
50	chr6:66010172-66010222	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:66078369..66080351-chr6:66082016..66084974,2	K562	blood:
2	chr6:66060579..66062154-chr6:66063684..66065572,2	MCF-7	breast:
3	chr6:66051771..66054306-chr6:66063446..66065850,2	K562	blood:
4	chr6:66097248..66097748-chr7:48217360..48217884,2	MCF-7	breast:
5	chr6:66158867..66160946-chr6:66172650..66174788,2	K562	blood:
6	chr6:66228230..66230523-chr6:66231359..66233821,2	MCF-7	breast:
7	chr6:66060579..66062154-chr6:66063684..66065572,2	MCF-7	breast:
8	chr6:66051771..66054306-chr6:66063446..66065850,2	K562	blood:
9	chr6:66158867..66160946-chr6:66172650..66174788,2	K562	blood:
10	chr6:65879743..65881792-chr6:65884642..65887053,2	MCF-7	breast:
11	chr6:66205424..66207848-chr6:66208785..66211406,2	K562	blood:
12	chr6:66078369..66080351-chr6:66082016..66084974,2	K562	blood:
13	chr6:66228230..66230523-chr6:66231359..66233821,2	MCF-7	breast:
14	chr6:65879743..65881792-chr6:65884642..65887053,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHF3-3	chr6:66191208-66191429	ENSG00000230672.1
2	lnc-LGSN-6	chr6:66010740-66010831	NONHSAT113370
3	lnc-LGSN-7	chr6:66199254-66200600	NONHSAT113373
4	lnc-LGSN-7	chr6:66205752-66205886	NONHSAT113373
5	lnc-LGSN-6	chr6:66005650-66006012	NONHSAT113369
6	lnc-LGSN-6	chr6:66012701-66012904	NONHSAT113369
7	lnc-LGSN-6	chr6:66005718-66006012	NONHSAT113370
8	lnc-LGSN-7	chr6:66204556-66205500	NONHSAT113373
9	lnc-LGSN-6	chr6:66012701-66012830	NONHSAT113370
10	lnc-PHF3-3	chr6:66191784-66191981	ENSG00000230672.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	EYS	hsa-miR-124-3p	chr6:66040931-66040951

Variant related genes	Relation type
ENSG00000265187	TF binding region
EYS	TF binding region
ENSG00000214558	TF binding region
ENSG00000265187	CpG island
EYS	CpG island
ENSG00000214558	CpG island
ENSG00000188107	chromatin interactions

Extended variants
information (count: 2451 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2451 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9453211	chr6:65873577-65873578	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369543474	chr6:65873662-65873663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs371949235	chr6:65873761-65873762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572315647	chr6:65873792-65873793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541010036	chr6:65873817-65873818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200763042	chr6:65873850-65873851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564424560	chr6:65873916-65873917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532952842	chr6:65873937-65873938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569151760	chr6:65873946-65873947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549009539	chr6:65873973-65873974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187685675	chr6:65874042-65874043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs150062108	chr6:65874075-65874076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563684223	chr6:65874083-65874084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568013439	chr6:65874126-65874127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532863603	chr6:65874163-65874164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552561977	chr6:65874169-65874170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566349136	chr6:65874212-65874213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533801647	chr6:65874244-65874245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs140939211	chr6:65874253-65874254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547416736	chr6:65874258-65874259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567406379	chr6:65874303-65874304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536596708	chr6:65874307-65874308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs66997223	chr6:65874311-65874312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556325088	chr6:65874312-65874313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576126423	chr6:65874319-65874320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572951460	chr6:65874357-65874358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540056534	chr6:65874395-65874396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538938406	chr6:65874464-65874465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs62407233	chr6:65874466-65874467	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs77707778	chr6:65874474-65874475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs541073268	chr6:65874491-65874492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs147911736	chr6:65874495-65874496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs556848079	chr6:65874499-65874500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191309751	chr6:65874532-65874533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs148928905	chr6:65874628-65874629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563922904	chr6:65874637-65874638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532633034	chr6:65874665-65874666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs546358930	chr6:65874698-65874699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559844425	chr6:65874720-65874721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs143678578	chr6:65874721-65874722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369910544	chr6:65874727-65874728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs183797768	chr6:65874731-65874732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs374488024	chr6:65874744-65874745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539191633	chr6:65887813-65887814	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs191029450	chr6:65887857-65887858	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs9345597	chr6:65887937-65887938	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs557443212	chr6:65887945-65887946	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs181125881	chr6:65887954-65887955	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs185666169	chr6:65887999-65888000	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs571088930	chr6:65888000-65888001	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Endometrioid adenocarcinoma	16974079	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	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	21364760	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Epilepsy	20502679	CNVD
Dyslexia	22102821	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Retinitis pigmentosa	21519034	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:65871800-65874800	Enhancers	Fetal Brain Male	brain
2	chr6:65873400-65874400	Enhancers	Fetal Brain Female	brain
3	chr6:65887800-65888200	Active TSS	Aorta	Aorta
4	chr6:65888000-65888400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:65896400-65897200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr6:65899600-65900000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr6:65899800-65901800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr6:65900000-65900400	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr6:65900400-65901800	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr6:65900400-65902000	Enhancers	Brain Germinal Matrix	brain
11	chr6:65900600-65901800	Enhancers	H1 Cell Line	embryonic stem cell
12	chr6:65900600-65901800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr6:65900600-65901800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr6:65900600-65902000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr6:65900600-65902000	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr6:65900800-65901800	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr6:65900800-65901800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:65901200-65902000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr6:65901400-65901800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr6:65901800-65905200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr6:65902000-65910200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr6:65909200-65909600	Enhancers	HUVEC	blood vessel
23	chr6:65910200-65910400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr6:65911600-65913000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr6:65913000-65913400	ZNF genes & repeats	Fetal Lung	lung
26	chr6:65939000-65940400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr6:65939200-65940000	Enhancers	Fetal Lung	lung
28	chr6:65939200-65940400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr6:65939200-65940400	Enhancers	HUVEC	blood vessel
30	chr6:65939600-65940000	Enhancers	Colon Smooth Muscle	Colon
31	chr6:65939600-65940000	Enhancers	Duodenum Smooth Muscle	Duodenum
32	chr6:65940400-65941800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr6:65941600-65941800	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr6:65941800-65942200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr6:65961600-65962000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr6:65969000-65969800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr6:65969200-65969400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:65969200-65970600	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr6:65969400-65970400	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr6:65969400-65970800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr6:65969600-65969800	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr6:65969600-65970400	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr6:65969600-65971000	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr6:65969800-65970000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr6:65970000-65970400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr6:65970000-65970400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr6:65970800-65971800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr6:65999000-66000200	Enhancers	HUVEC	blood vessel
49	chr6:66007600-66009400	Enhancers	HUVEC	blood vessel
50	chr6:66028600-66028800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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