Variant report

Variant	esv34252
Chromosome Location	chr6:167621589-167812498
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2978)
CpG islands
(count:5683)
Chromatin interactive
region (count:32)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2978 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167629887-167630151	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167652605-167653007	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167637599-167638030	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167629415-167629646	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167628930-167629130	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167809998-167810531	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:167624462-167624811	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:167699867-167700232	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
13	ARID3A	chr6:167651727-167651738	HepG2	liver:	n/a	n/a
14	ARID3A	chr6:167655013-167655211	HepG2	liver:	n/a	n/a
15	ARID3A	chr6:167645950-167646149	HepG2	liver:	n/a	n/a
16	ARID3A	chr6:167632046-167632420	HepG2	liver:	n/a	n/a
17	ARID3A	chr6:167702230-167702578	HepG2	liver:	n/a	n/a
18	ARID3A	chr6:167811767-167812223	HepG2	liver:	n/a	n/a
19	ARID3A	chr6:167682223-167682912	HepG2	liver:	n/a	n/a
20	ARID3A	chr6:167633428-167633974	HepG2	liver:	n/a	n/a
21	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
22	ATF1	chr6:167702337-167702425	K562	blood:	n/a	n/a
23	ATF1	chr6:167727339-167727444	K562	blood:	n/a	n/a
24	ATF2	chr6:167626020-167626431	GM12878	blood:	n/a	n/a
25	ATF2	chr6:167625939-167626508	GM12878	blood:	n/a	n/a
26	ATF2	chr6:167651500-167652487	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr6:167641333-167641936	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr6:167641353-167641826	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr6:167754224-167754403	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr6:167702257-167702472	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr6:167641591-167641850	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr6:167631950-167632087	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr6:167637370-167637829	H1-hESC	embryonic stem cell:	n/a	n/a
37	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a
38	BATF	chr6:167801477-167801674	GM12878	blood:	n/a	n/a
39	BATF	chr6:167785311-167785621	GM12878	blood:	n/a	n/a
40	BATF	chr6:167726056-167726329	GM12878	blood:	n/a	n/a
41	BATF	chr6:167631870-167632155	GM12878	blood:	n/a	n/a
42	BATF	chr6:167625959-167626402	GM12878	blood:	n/a	n/a
43	BATF	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
44	BATF	chr6:167702166-167702414	GM12878	blood:	n/a	n/a
45	BATF	chr6:167726053-167726251	GM12878	blood:	n/a	n/a
46	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
47	BATF	chr6:167625794-167626502	GM12878	blood:	n/a	n/a
48	BCL11A	chr6:167801472-167801775	GM12878	blood:	n/a	n/a
49	BCL11A	chr6:167801474-167801790	GM12878	blood:	n/a	n/a
50	BCL11A	chr6:167800632-167800815	GM12878	blood:	n/a	n/a

(count:5683 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167633955-167634005	GM12892	blood:	n/a
2	chr6:167786592-167786642	PANC-1	pancreas:	n/a
3	chr6:167770239-167770289	SKMC	muscle:	n/a
4	chr6:167661905-167661955	CMK	blood:	n/a
5	chr6:167634139-167634189	HRPEpiC	eye:	n/a
6	chr6:167789539-167789589	MCF10A-Er-Src	breast:	n/a
7	chr6:167653982-167654032	AG10803	skin:	n/a
8	chr6:167764523-167764573	SK-N-SH_RA	brain:	n/a
9	chr6:167734054-167734104	Hepatocyte	liver:	n/a
10	chr6:167786592-167786642	HCM	heart:	n/a
11	chr6:167633955-167634005	GM12892	blood:	n/a
12	chr6:167786592-167786642	PANC-1	pancreas:	n/a
13	chr6:167770239-167770289	SKMC	muscle:	n/a
14	chr6:167661905-167661955	CMK	blood:	n/a
15	chr6:167634139-167634189	HRPEpiC	eye:	n/a
16	chr6:167789539-167789589	MCF10A-Er-Src	breast:	n/a
17	chr6:167653982-167654032	AG10803	skin:	n/a
18	chr6:167764523-167764573	SK-N-SH_RA	brain:	n/a
19	chr6:167734054-167734104	Hepatocyte	liver:	n/a
20	chr6:167786592-167786642	HCM	heart:	n/a
21	chr6:167738425-167738475	U87	brain:	n/a
22	chr6:167703591-167703641	PrEC	prostate:	n/a
23	chr6:167798410-167798460	U87	brain:	n/a
24	chr6:167789539-167789589	HRPEpiC	eye:	n/a
25	chr6:167810395-167810445	GM12892	blood:	n/a
26	chr6:167797877-167797927	PrEC	prostate:	n/a
27	chr6:167705253-167705303	MCF10A-Er-Src	breast:	n/a
28	chr6:167763819-167763869	HPAEpiC	pulmonary alveolar:	n/a
29	chr6:167718461-167718511	HCT-116	colon:	n/a
30	chr6:167632873-167632923	HCT-116	colon:	n/a
31	chr6:167680455-167680505	GM12878	blood:	n/a
32	chr6:167810343-167810393	HCPEpiC	choroid plexus:	n/a
33	chr6:167704673-167704723	HCM	heart:	n/a
34	chr6:167763758-167763808	RPTEC	kidney:	n/a
35	chr6:167654977-167655027	GM06990	blood:	n/a
36	chr6:167738592-167738642	Caco-2	colon:	n/a
37	chr6:167763320-167763370	T-47D	breast:	n/a
38	chr6:167792741-167792791	Caco-2	colon:	n/a
39	chr6:167810395-167810445	LNCaP	prostate:	n/a
40	chr6:167700000-167700050	GM06990	blood:	n/a
41	chr6:167756099-167756149	HIPEpiC	eye:	n/a
42	chr6:167763758-167763808	SK-N-SH_RA	brain:	n/a
43	chr6:167792741-167792791	SKMC	muscle:	n/a
44	chr6:167764620-167764670	LNCaP	prostate:	n/a
45	chr6:167786592-167786642	RPTEC	kidney:	n/a
46	chr6:167808551-167808601	BJ	skin:	n/a
47	chr6:167810343-167810393	HL-60	blood:	n/a
48	chr6:167808551-167808601	LNCaP	prostate:	n/a
49	chr6:167655053-167655103	AoSMC	blood vessel:	n/a
50	chr6:167786642-167786692	ovcar-3	ovarian:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:28836187..28837925-chr6:167694572..167696254,2	K562	blood:
2	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
3	chr6:167620399..167623068-chr6:167623897..167626646,2	K562	blood:
4	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
5	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
6	chr6:167699179..167702166-chr6:167703091..167705361,2	K562	blood:
7	chr6:167669951..167671777-chr6:167683631..167687000,3	K562	blood:
8	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
9	chr6:167668192..167671777-chr6:167684157..167687082,3	K562	blood:
10	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
11	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
12	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
13	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
14	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
15	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
16	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
17	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
18	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
19	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
20	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
21	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
22	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
23	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
24	chr6:167187967..167188932-chr6:167764453..167765086,2	K562	blood:
25	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
26	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
27	chr6:167623945..167626187-chr6:168297648..168300373,2	K562	blood:
28	chr6:167703616..167705764-chr6:167717598..167719278,2	MCF-7	breast:
29	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
30	chr6:167662732..167663315-chr6:167819023..167819880,2	K562	blood:
31	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
32	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC93A-3	chr6:167764293-167764966	NONHSAT116095
2	lnc-GPR31-1	chr6:167653636-167653833	XLOC_005921
3	lnc-TTLL2-1	chr6:167804760-167804979	XLOC_005541
4	lnc-TCP10-2	chr6:167810373-167814438	ucscGeneNc_uc003qvx_1
5	lnc-GPR31-1	chr6:167650996-167651293	XLOC_005921
6	lnc-TCP10-1	chr6:167787839-167789289	NONHSAT116097
7	lnc-UNC93A-2	chr6:167760960-167761541	NONHSAT116094
8	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095
9	lnc-TTLL2-1	chr6:167803650-167803969	XLOC_005541
10	lnc-GPR31-1	chr6:167651156-167651293	XLOC_005921
11	lnc-TCP10-1	chr6:167786578-167786848	NONHSAT116097
12	lnc-UNC93A-1	chr6:167655379-167655453	XLOC_005540
13	lnc-UNC93A-1	chr6:167659275-167659404	XLOC_005540
14	lnc-GPR31-1	chr6:167653688-167653968	XLOC_005921

No data

Variant related genes	Relation type
UNC93A	TF binding region
TCP10	TF binding region
TTLL2	TF binding region
ENSG00000231720	TF binding region
ENSG00000228648	TF binding region
ENSG00000216966	TF binding region
ENSG00000217447	TF binding region
UNC93A	CpG island
TCP10	CpG island
TTLL2	CpG island
ENSG00000231720	CpG island
ENSG00000228648	CpG island
ENSG00000216966	CpG island
ENSG00000217447	CpG island
ENSG00000180198	chromatin interactions
ENSG00000216966	chromatin interactions
ENSG00000112494	chromatin interactions
CYBASC3	miRNA target sites
CYB5R4	miRNA target sites

Extended variants
information (count: 9027 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:9027 , 50 per page) page: 1 2 3 4 5 6 7 ... 181

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539353891	chr6:167621589-167621590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs557901649	chr6:167621593-167621594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532186853	chr6:167621607-167621608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs376615475	chr6:167621659-167621660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199626367	chr6:167621703-167621704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533767404	chr6:167621791-167621792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201500114	chr6:167621854-167621855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573445693	chr6:167621857-167621858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571813748	chr6:167621861-167621862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566223460	chr6:167621864-167621865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139961955	chr6:167621880-167621881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372872083	chr6:167621895-167621896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375835003	chr6:167621899-167621900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs578176913	chr6:167621913-167621914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567232847	chr6:167621929-167621930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369581479	chr6:167621944-167621945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545391624	chr6:167621948-167621949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs57931385	chr6:167621950-167621951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572006753	chr6:167621962-167621963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531550566	chr6:167621963-167621964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527862807	chr6:167621964-167621965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565427351	chr6:167621968-167621969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532772618	chr6:167621975-167621976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs441907	chr6:167621989-167621990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145666762	chr6:167622002-167622003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs59177026	chr6:167622036-167622037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531720132	chr6:167622049-167622050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs671511	chr6:167622070-167622071	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs28661326	chr6:167622105-167622106	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs201306396	chr6:167622136-167622137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181506854	chr6:167622139-167622140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200471567	chr6:167622146-167622147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1213108	chr6:167622156-167622157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533731890	chr6:167622158-167622159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548778592	chr6:167622159-167622160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370214052	chr6:167622185-167622186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566977974	chr6:167622203-167622204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs28588506	chr6:167622205-167622206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556087659	chr6:167622221-167622222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577548196	chr6:167622266-167622267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377156535	chr6:167622268-167622269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs199926465	chr6:167622283-167622284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35304076	chr6:167622284-167622285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572815833	chr6:167622285-167622286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184109591	chr6:167622295-167622296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138781434	chr6:167622318-167622319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111371115	chr6:167622334-167622335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576452585	chr6:167622344-167622345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs9459922	chr6:167622347-167622348	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs199790398	chr6:167622370-167622371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
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
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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1828 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167613800-167622200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:167614400-167623200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr6:167615800-167628800	Weak transcription	Right Atrium	heart
4	chr6:167617400-167622400	Weak transcription	Fetal Intestine Large	intestine
5	chr6:167618400-167624400	Weak transcription	Colon Smooth Muscle	Colon
6	chr6:167619000-167622400	Weak transcription	Fetal Intestine Small	intestine
7	chr6:167619000-167624200	Weak transcription	Rectal Smooth Muscle	rectum
8	chr6:167620200-167621600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:167620800-167622400	Weak transcription	HepG2	liver
10	chr6:167621000-167622400	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr6:167621000-167623600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr6:167621200-167623000	Weak transcription	Fetal Brain Male	brain
13	chr6:167621600-167624400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:167622200-167623000	Enhancers	H1 Cell Line	embryonic stem cell
15	chr6:167622200-167623000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr6:167622200-167624600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr6:167622200-167624600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:167622400-167622800	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr6:167622400-167622800	Enhancers	Fetal Intestine Large	intestine
20	chr6:167622400-167623200	Enhancers	Fetal Intestine Small	intestine
21	chr6:167622400-167626600	Enhancers	Placenta Amnion	Placenta Amnion
22	chr6:167622400-167627200	Enhancers	HepG2	liver
23	chr6:167622600-167623000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
24	chr6:167622800-167623000	Enhancers	H9 Cell Line	embryonic stem cell
25	chr6:167622800-167624200	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr6:167623000-167623400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:167623000-167623800	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr6:167623000-167629200	Enhancers	Fetal Brain Male	brain
29	chr6:167623200-167623800	Weak transcription	Fetal Intestine Small	intestine
30	chr6:167623200-167624600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr6:167623400-167624200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr6:167623600-167623800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr6:167623600-167628200	Enhancers	Fetal Brain Female	brain
34	chr6:167623800-167624400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr6:167623800-167624600	Enhancers	H1 Cell Line	embryonic stem cell
36	chr6:167624000-167624600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr6:167624000-167624800	Enhancers	Brain Germinal Matrix	brain
38	chr6:167624200-167624600	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr6:167624200-167624600	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr6:167624200-167624600	Bivalent Enhancer	Brain Cingulate Gyrus	brain
41	chr6:167624200-167624600	Enhancers	Lung	lung
42	chr6:167624200-167624800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
43	chr6:167624200-167625600	Enhancers	Rectal Smooth Muscle	rectum
44	chr6:167624400-167624600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr6:167624400-167624600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr6:167624400-167625800	Enhancers	Colon Smooth Muscle	Colon
47	chr6:167624600-167625200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr6:167624600-167632800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr6:167624800-167627800	Weak transcription	Brain Germinal Matrix	brain
50	chr6:167625000-167625200	Bivalent Enhancer	Stomach Smooth Muscle	stomach

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