Variant report

Variant	nsv886012
Chromosome Location	chr6:65905998-66354809
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1125)
CpG islands
(count:489)
Chromatin interactive
region (count:21)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1125 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:66256936-66257108	K562	blood:	n/a	n/a
2	ARID3A	chr6:66120388-66120433	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:66049641-66049730	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:66257680-66257799	K562	blood:	n/a	n/a
5	ATF1	chr6:66171007-66171493	K562	blood:	n/a	n/a
6	ATF1	chr6:66160376-66160599	K562	blood:	n/a	n/a
7	BACH1	chr6:66256862-66257125	K562	blood:	n/a	n/a
8	BACH1	chr6:66284867-66284905	K562	blood:	n/a	n/a
9	BACH1	chr6:66066175-66066268	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr6:65934747-65934766	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr6:66297779-66297795	K562	blood:	n/a	n/a
12	BHLHE40	chr6:66255959-66256078	K562	blood:	n/a	n/a
13	BRCA1	chr6:65970555-65970750	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr6:66193565-66193851	K562	blood:	n/a	n/a
15	CCNT2	chr6:66139022-66139218	K562	blood:	n/a	n/a
16	CCNT2	chr6:66324927-66325066	K562	blood:	n/a	n/a
17	CCNT2	chr6:66171045-66171349	K562	blood:	n/a	n/a
18	CCNT2	chr6:66100608-66100682	K562	blood:	n/a	n/a
19	CEBPB	chr6:66138219-66138426	HepG2	liver:	n/a	chr6:66138267-66138278
20	CEBPB	chr6:66343281-66343819	MCF-7	breast:	n/a	chr6:66343568-66343579 chr6:66343530-66343541
21	CEBPB	chr6:66120214-66120512	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:66348020-66348319	HepG2	liver:	n/a	n/a
23	CEBPB	chr6:66230294-66230581	IMR90	lung:	n/a	n/a
24	CEBPB	chr6:66348034-66348300	K562	blood:	n/a	n/a
25	CEBPB	chr6:65968981-65969345	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr6:66230260-66230571	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:66335390-66335643	HepG2	liver:	n/a	chr6:66335405-66335422 chr6:66335484-66335495 chr6:66335483-66335496
28	CEBPB	chr6:66066493-66066779	HepG2	liver:	n/a	chr6:66066621-66066632
29	CEBPB	chr6:66336957-66337259	H1-hESC	embryonic stem cell:	n/a	chr6:66337098-66337109
30	CEBPB	chr6:66064226-66064435	H1-hESC	embryonic stem cell:	n/a	chr6:66064368-66064379 chr6:66064370-66064381 chr6:66064370-66064379
31	CEBPB	chr6:66248614-66248879	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr6:66336928-66337275	MCF-7	breast:	n/a	chr6:66337098-66337109
33	CEBPB	chr6:66064192-66064538	HepG2	liver:	n/a	chr6:66064368-66064379 chr6:66064370-66064381 chr6:66064370-66064379
34	CEBPB	chr6:66288426-66288597	HepG2	liver:	n/a	chr6:66288554-66288565
35	CEBPB	chr6:65909589-65909973	MCF-7	breast:	n/a	n/a
36	CEBPB	chr6:66037851-66038095	A549	lung:	n/a	chr6:66037990-66038001
37	CEBPB	chr6:66305442-66305793	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr6:66064211-66064491	A549	lung:	n/a	chr6:66064368-66064379 chr6:66064370-66064381 chr6:66064370-66064379
39	CEBPB	chr6:66255996-66256060	K562	blood:	n/a	n/a
40	CEBPB	chr6:66037858-66038164	HepG2	liver:	n/a	chr6:66037990-66038001
41	CEBPB	chr6:65989228-65989353	HepG2	liver:	n/a	chr6:65989300-65989311 chr6:65989339-65989350
42	CEBPB	chr6:66347922-66348400	MCF-7	breast:	n/a	n/a
43	CEBPB	chr6:65969974-65970326	H1-hESC	embryonic stem cell:	n/a	chr6:65970271-65970283
44	CEBPB	chr6:66348024-66348304	A549	lung:	n/a	n/a
45	CEBPB	chr6:66343413-66343709	HepG2	liver:	n/a	chr6:66343568-66343579 chr6:66343530-66343541
46	CEBPB	chr6:66337015-66337253	ECC-1	luminal epithelium:	n/a	chr6:66337098-66337109
47	CEBPB	chr6:66305450-66305808	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr6:66109620-66109995	HepG2	liver:	n/a	chr6:66109790-66109801 chr6:66109810-66109821
49	CEBPB	chr6:66336930-66337285	IMR90	lung:	n/a	chr6:66337098-66337109
50	CEBPB	chr6:66336963-66337249	ECC-1	luminal epithelium:	n/a	chr6:66337098-66337109

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:66337526-66337576	HIPEpiC	eye:	n/a
2	chr6:66337526-66337576	HIPEpiC	eye:	n/a
3	chr6:66207286-66207336	CMK	blood:	n/a
4	chr6:66013901-66013951	PrEC	prostate:	n/a
5	chr6:66207286-66207336	HCPEpiC	choroid plexus:	n/a
6	chr6:66011626-66011676	SK-N-SH_RA	brain:	n/a
7	chr6:66279436-66279486	CMK	blood:	n/a
8	chr6:66010172-66010222	CMK	blood:	n/a
9	chr6:66011288-66011338	HCM	heart:	n/a
10	chr6:66205227-66205277	Hepatocyte	liver:	n/a
11	chr6:66205227-66205277	HIPEpiC	eye:	n/a
12	chr6:66013901-66013951	HEK293	kidney:	embryo
13	chr6:66337526-66337576	HRPEpiC	eye:	n/a
14	chr6:66207286-66207336	HRE	kidney:	n/a
15	chr6:66205227-66205277	AG10803	skin:	n/a
16	chr6:66010172-66010222	AG04449	skin:	fetal
17	chr6:66279436-66279486	HRPEpiC	eye:	n/a
18	chr6:66205227-66205277	HEK293	kidney:	embryo
19	chr6:66207286-66207336	Hela-S3	cervix:	n/a
20	chr6:66205227-66205277	ECC-1	luminal epithelium:	n/a
21	chr6:66337526-66337576	HUVEC	blood vessel:	n/a
22	chr6:66337526-66337576	PANC-1	pancreas:	n/a
23	chr6:66207286-66207336	GM19239	blood:	n/a
24	chr6:66011626-66011676	AG10803	skin:	n/a
25	chr6:66337526-66337576	HEEpiC	esophagus:	n/a
26	chr6:66011288-66011338	PFSK-1	brain:	n/a
27	chr6:66337526-66337576	Hepatocyte	liver:	n/a
28	chr6:66013901-66013951	AG04450	lung:	fetal
29	chr6:66205227-66205277	HCPEpiC	choroid plexus:	n/a
30	chr6:66013901-66013951	HMEC	breast:	n/a
31	chr6:66011288-66011338	HIPEpiC	eye:	n/a
32	chr6:66010172-66010222	PrEC	prostate:	n/a
33	chr6:66011626-66011676	HIPEpiC	eye:	n/a
34	chr6:66207286-66207336	HCM	heart:	n/a
35	chr6:66013901-66013951	A549	lung:	n/a
36	chr6:66011626-66011676	HRE	kidney:	n/a
37	chr6:66205227-66205277	RPTEC	kidney:	n/a
38	chr6:66013901-66013951	U87	brain:	n/a
39	chr6:66011288-66011338	SK-N-MC	brain:	n/a
40	chr6:66205227-66205277	HNPCEpiC	eye:	n/a
41	chr6:66337526-66337576	ProgFib	skin:	n/a
42	chr6:66337526-66337576	AoSMC	blood vessel:	n/a
43	chr6:66011288-66011338	GM06990	blood:	n/a
44	chr6:66279436-66279486	HEK293	kidney:	embryo
45	chr6:66337526-66337576	GM19239	blood:	n/a
46	chr6:66011288-66011338	AoSMC	blood vessel:	n/a
47	chr6:66013901-66013951	HEEpiC	esophagus:	n/a
48	chr6:66011626-66011676	HNPCEpiC	eye:	n/a
49	chr6:66011288-66011338	HepG2	liver:	n/a
50	chr6:66011626-66011676	GM12892	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:66249610..66251834-chr6:66299808..66302442,2	K562	blood:
2	chr6:66060579..66062154-chr6:66063684..66065572,2	MCF-7	breast:
3	chr6:66228230..66230523-chr6:66231359..66233821,2	MCF-7	breast:
4	chr6:66291419..66293216-chr6:66300613..66302642,2	K562	blood:
5	chr6:66097248..66097748-chr7:48217360..48217884,2	MCF-7	breast:
6	chr6:66078369..66080351-chr6:66082016..66084974,2	K562	blood:
7	chr6:66078369..66080351-chr6:66082016..66084974,2	K562	blood:
8	chr6:66158867..66160946-chr6:66172650..66174788,2	K562	blood:
9	chr6:66291419..66293216-chr6:66300613..66302642,2	K562	blood:
10	chr6:66228230..66230523-chr6:66231359..66233821,2	MCF-7	breast:
11	chr6:66205424..66207848-chr6:66208785..66211406,2	K562	blood:
12	chr6:66344295..66347269-chr6:66347639..66350147,2	MCF-7	breast:
13	chr6:66298118..66300419-chr6:66305829..66308285,2	K562	blood:
14	chr6:66344295..66347269-chr6:66347639..66350147,2	MCF-7	breast:
15	chr6:66060579..66062154-chr6:66063684..66065572,2	MCF-7	breast:
16	chr6:66158867..66160946-chr6:66172650..66174788,2	K562	blood:
17	chr6:66298118..66300419-chr6:66305829..66308285,2	K562	blood:
18	chr6:66051771..66054306-chr6:66063446..66065850,2	K562	blood:
19	chr6:66249610..66251834-chr6:66299808..66302442,2	K562	blood:
20	chr6:66051771..66054306-chr6:66063446..66065850,2	K562	blood:
21	chr15:48090306..48091135-chr6:66342198..66342838,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHF3-3	chr6:66191784-66191981	ENSG00000230672.1
2	lnc-LGSN-7	chr6:66205752-66205886	NONHSAT113373
3	lnc-LGSN-6	chr6:66010740-66010831	NONHSAT113370
4	lnc-LGSN-6	chr6:66005718-66006012	NONHSAT113370
5	lnc-LGSN-7	chr6:66349671-66349785	NONHSAT113373
6	lnc-PHF3-3	chr6:66191208-66191429	ENSG00000230672.1
7	lnc-LGSN-6	chr6:66005650-66006012	NONHSAT113369
8	lnc-LGSN-7	chr6:66204556-66205500	NONHSAT113373
9	lnc-LGSN-6	chr6:66012701-66012830	NONHSAT113370
10	lnc-LGSN-6	chr6:66012701-66012904	NONHSAT113369
11	lnc-LGSN-7	chr6:66199254-66200600	NONHSAT113373

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
ENSG00000214558	TF binding region
ENSG00000265187	TF binding region
EYS	TF binding region
ENSG00000214558	CpG island
ENSG00000265187	CpG island
EYS	CpG island
ENSG00000188107	chromatin interactions

Extended variants
information (count: 3743 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:3743 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16896391	chr6:65905998-65905999	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113459778	chr6:65906042-65906043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs13210851	chr6:65906043-65906044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539780577	chr6:65906057-65906058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553295918	chr6:65906113-65906114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs16896392	chr6:65906179-65906180	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs550381892	chr6:65906218-65906219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535435177	chr6:65906263-65906264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555839514	chr6:65906311-65906312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs841531	chr6:65906330-65906331	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs544421649	chr6:65906334-65906335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559762105	chr6:65906395-65906396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557956355	chr6:65906432-65906433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183816611	chr6:65906440-65906441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540562788	chr6:65906464-65906465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187163452	chr6:65906497-65906498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568968401	chr6:65906528-65906529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115507448	chr6:65906547-65906548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192403588	chr6:65906603-65906604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561844905	chr6:65906604-65906605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs373831905	chr6:65906635-65906636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564428349	chr6:65906640-65906641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs686041	chr6:65906722-65906723	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs182145136	chr6:65906724-65906725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549986019	chr6:65906736-65906737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs78733506	chr6:65906745-65906746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs116746547	chr6:65906762-65906763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186702163	chr6:65906772-65906773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535856639	chr6:65906832-65906833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529457281	chr6:65906840-65906841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555445866	chr6:65906874-65906875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569212967	chr6:65906886-65906887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547804437	chr6:65906888-65906889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73741264	chr6:65906896-65906897	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs142337027	chr6:65906971-65906972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144577025	chr6:65906984-65906985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577860669	chr6:65907006-65907007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547772856	chr6:65907019-65907020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191564271	chr6:65907040-65907041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12207416	chr6:65907081-65907082	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs72881777	chr6:65907091-65907092	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs561566372	chr6:65907100-65907101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182534181	chr6:65907103-65907104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs151249272	chr6:65907104-65907105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376875405	chr6:65907120-65907121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188428779	chr6:65907152-65907153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373835173	chr6:65907166-65907167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12213645	chr6:65907167-65907168	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs573749005	chr6:65907179-65907180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140373726	chr6:65907190-65907191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Glioma	20126413	CNVD

Chromatin state (count:193 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:65902000-65910200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr6:65909200-65909600	Enhancers	HUVEC	blood vessel
3	chr6:65910200-65910400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr6:65911600-65913000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:65913000-65913400	ZNF genes & repeats	Fetal Lung	lung
6	chr6:65939000-65940400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr6:65939200-65940000	Enhancers	Fetal Lung	lung
8	chr6:65939200-65940400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr6:65939200-65940400	Enhancers	HUVEC	blood vessel
10	chr6:65939600-65940000	Enhancers	Colon Smooth Muscle	Colon
11	chr6:65939600-65940000	Enhancers	Duodenum Smooth Muscle	Duodenum
12	chr6:65940400-65941800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr6:65941600-65941800	Enhancers	Duodenum Smooth Muscle	Duodenum
14	chr6:65941800-65942200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr6:65961600-65962000	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr6:65969000-65969800	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr6:65969200-65969400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr6:65969200-65970600	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr6:65969400-65970400	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr6:65969400-65970800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr6:65969600-65969800	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr6:65969600-65970400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr6:65969600-65971000	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr6:65969800-65970000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
25	chr6:65970000-65970400	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr6:65970000-65970400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:65970800-65971800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr6:65999000-66000200	Enhancers	HUVEC	blood vessel
29	chr6:66007600-66009400	Enhancers	HUVEC	blood vessel
30	chr6:66028600-66028800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr6:66045000-66045800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr6:66061400-66062200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr6:66061600-66061800	Enhancers	Fetal Lung	lung
34	chr6:66076000-66077200	Enhancers	Fetal Stomach	stomach
35	chr6:66095800-66097200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr6:66096600-66097000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr6:66099200-66099600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr6:66108200-66109200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr6:66109200-66110000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr6:66110000-66110200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr6:66120200-66120600	Enhancers	HepG2	liver
42	chr6:66124200-66124400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr6:66124400-66125000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr6:66125000-66127800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr6:66125200-66127800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr6:66126000-66126200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr6:66126000-66127000	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr6:66126200-66133200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr6:66126400-66127400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr6:66133200-66135000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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