Variant report

Variant	nsv464110
Chromosome Location	chr6:162729381-163015279
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	chr6:162857639-162857816	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:162910482-162910786	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:162794306-162794665	HepG2	liver:	n/a	n/a
4	ATF1	chr6:162784797-162785113	K562	blood:	n/a	n/a
5	ATF1	chr6:162812647-162812847	K562	blood:	n/a	n/a
6	ATF1	chr6:162812215-162812339	K562	blood:	n/a	n/a
7	ATF1	chr6:162782228-162782581	K562	blood:	n/a	n/a
8	ATF3	chr6:162784742-162785052	K562	blood:	n/a	n/a
9	BACH1	chr6:162975725-162976098	K562	blood:	n/a	n/a
10	BHLHE40	chr6:162899266-162899534	GM12878	blood:	n/a	n/a
11	BRCA1	chr6:162871740-162871751	H1-hESC	embryonic stem cell:	n/a	n/a
12	CBX3	chr6:162785538-162785848	K562	blood:	n/a	n/a
13	CBX3	chr6:162784775-162785143	K562	blood:	n/a	n/a
14	CCNT2	chr6:163001825-163002025	K562	blood:	n/a	n/a
15	CEBPB	chr6:162784761-162785142	K562	blood:	n/a	chr6:162785029-162785040
16	CEBPB	chr6:162871405-162871712	H1-hESC	embryonic stem cell:	n/a	chr6:162871605-162871616
17	CEBPB	chr6:162861366-162861450	H1-hESC	embryonic stem cell:	n/a	chr6:162861390-162861403
18	CEBPB	chr6:162766353-162766628	IMR90	lung:	n/a	chr6:162766482-162766491 chr6:162766482-162766491 chr6:162766481-162766492 chr6:162766482-162766491 chr6:162766480-162766491 chr6:162766482-162766491 chr6:162766480-162766493
19	CEBPB	chr6:162779025-162779284	HepG2	liver:	n/a	chr6:162779118-162779129
20	CEBPB	chr6:162910422-162910805	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:162857234-162857635	HepG2	liver:	n/a	chr6:162857420-162857431
22	CEBPB	chr6:162944101-162944302	HepG2	liver:	n/a	n/a
23	CEBPB	chr6:162766327-162766640	HepG2	liver:	n/a	chr6:162766482-162766491 chr6:162766482-162766491 chr6:162766481-162766492 chr6:162766482-162766491 chr6:162766480-162766491 chr6:162766482-162766491 chr6:162766480-162766493
24	CEBPB	chr6:162857291-162857590	HepG2	liver:	n/a	chr6:162857420-162857431
25	CEBPB	chr6:162910493-162910789	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:162876249-162876534	IMR90	lung:	n/a	n/a
27	CEBPB	chr6:162745722-162745922	HepG2	liver:	n/a	chr6:162745751-162745762
28	CEBPB	chr6:162868765-162868950	HepG2	liver:	n/a	chr6:162868884-162868895
29	CEBPB	chr6:162876192-162876578	MCF-7	breast:	n/a	n/a
30	CEBPB	chr6:162766332-162766577	H1-hESC	embryonic stem cell:	n/a	chr6:162766482-162766491 chr6:162766482-162766491 chr6:162766481-162766492 chr6:162766482-162766491 chr6:162766480-162766491 chr6:162766482-162766491 chr6:162766480-162766493
31	CEBPB	chr6:162766335-162766614	A549	lung:	n/a	chr6:162766482-162766491 chr6:162766482-162766491 chr6:162766481-162766492 chr6:162766482-162766491 chr6:162766480-162766491 chr6:162766482-162766491 chr6:162766480-162766493
32	CEBPB	chr6:162896813-162896974	HepG2	liver:	n/a	chr6:162896839-162896850
33	CEBPB	chr6:162825981-162826255	HepG2	liver:	n/a	chr6:162826093-162826104
34	CEBPB	chr6:162871496-162871684	HepG2	liver:	n/a	chr6:162871605-162871616
35	CEBPB	chr6:162784873-162785124	H1-hESC	embryonic stem cell:	n/a	chr6:162785029-162785040
36	CEBPB	chr6:162775249-162775526	HepG2	liver:	n/a	chr6:162775385-162775396
37	CEBPB	chr6:162839236-162839248	A549	lung:	n/a	n/a
38	CEBPB	chr6:162784839-162785153	HepG2	liver:	n/a	chr6:162785029-162785040
39	CEBPB	chr6:162857280-162857594	HepG2	liver:	n/a	chr6:162857420-162857431
40	CEBPB	chr6:162779076-162779247	A549	lung:	n/a	chr6:162779118-162779129
41	CEBPB	chr6:162939387-162939585	HepG2	liver:	n/a	chr6:162939453-162939464
42	CEBPB	chr6:162857299-162857541	HepG2	liver:	n/a	chr6:162857420-162857431
43	CEBPB	chr6:162943679-162943865	HepG2	liver:	n/a	n/a
44	CEBPB	chr6:162784733-162785018	K562	blood:	n/a	n/a
45	CEBPB	chr6:162794250-162794499	HepG2	liver:	n/a	chr6:162794312-162794323
46	CEBPB	chr6:162910460-162910714	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:162871443-162871750	MCF-7	breast:	n/a	chr6:162871605-162871616
48	CEBPB	chr6:162871429-162871791	HepG2	liver:	n/a	chr6:162871605-162871616
49	CEBPB	chr6:162961979-162962215	HepG2	liver:	n/a	chr6:162962080-162962091
50	CEBPD	chr6:162857313-162857505	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:162865171-162865221	ovcar-3	ovarian:	n/a
2	chr6:162863505-162863555	HRE	kidney:	n/a
3	chr6:162964378-162964428	MCF-7	breast:	n/a
4	chr6:162864586-162864636	ECC-1	luminal epithelium:	n/a
5	chr6:162865171-162865221	SK-N-SH	brain:	n/a
6	chr6:162863505-162863555	AG10803	skin:	n/a
7	chr6:162864586-162864636	SKMC	muscle:	n/a
8	chr6:162964378-162964428	HRE	kidney:	n/a
9	chr6:162864586-162864636	HCPEpiC	choroid plexus:	n/a
10	chr6:162831837-162831887	LNCaP	prostate:	n/a
11	chr6:162865171-162865221	GM12878	blood:	n/a
12	chr6:162863505-162863555	IMR90	lung:	fetal
13	chr6:162831837-162831887	PANC-1	pancreas:	n/a
14	chr6:162865171-162865221	HCT-116	colon:	n/a
15	chr6:162831837-162831887	GM12891	blood:	n/a
16	chr6:162964378-162964428	HUVEC	blood vessel:	n/a
17	chr6:162831837-162831887	RPTEC	kidney:	n/a
18	chr6:162863505-162863555	AG04450	lung:	fetal
19	chr6:162864586-162864636	MCF10A-Er-Src	breast:	n/a
20	chr6:162831837-162831887	HepG2	liver:	n/a
21	chr6:162865171-162865221	AoSMC	blood vessel:	n/a
22	chr6:162865171-162865221	HPAEpiC	pulmonary alveolar:	n/a
23	chr6:162864586-162864636	HL-60	blood:	n/a
24	chr6:162863505-162863555	NH-A	brain:	n/a
25	chr6:162863505-162863555	HCM	heart:	n/a
26	chr6:162964378-162964428	GM12892	blood:	n/a
27	chr6:162863505-162863555	AG09319	gingival:	n/a
28	chr6:162863505-162863555	PFSK-1	brain:	n/a
29	chr6:162964378-162964428	GM12891	blood:	n/a
30	chr6:162831837-162831887	AG04449	skin:	fetal
31	chr6:162864586-162864636	HCM	heart:	n/a
32	chr6:162865171-162865221	MCF-7	breast:	n/a
33	chr6:162831837-162831887	HL-60	blood:	n/a
34	chr6:162863505-162863555	AoSMC	blood vessel:	n/a
35	chr6:162865171-162865221	HEK293	kidney:	embryo
36	chr6:162964378-162964428	K562	blood:	n/a
37	chr6:162831837-162831887	BE2_C	brain:	n/a
38	chr6:162831837-162831887	AG09319	gingival:	n/a
39	chr6:162865258-162865308	PrEC	prostate:	n/a
40	chr6:162964378-162964428	NHDF-neo	bronchial:	n/a
41	chr6:162864586-162864636	GM12892	blood:	n/a
42	chr6:162831837-162831887	PrEC	prostate:	n/a
43	chr6:162865171-162865221	RPTEC	kidney:	n/a
44	chr6:162865171-162865221	BJ	skin:	n/a
45	chr6:162864586-162864636	T-47D	breast:	n/a
46	chr6:162831837-162831887	Hela-S3	cervix:	n/a
47	chr6:162865171-162865221	Hela-S3	cervix:	n/a
48	chr6:162964378-162964428	SAEC	small airway:	n/a
49	chr6:162865258-162865308	NT2-D1	testis:	n/a
50	chr6:162863505-162863555	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
2	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
3	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
4	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
5	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
6	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
7	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
8	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
9	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
10	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
11	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
12	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:
13	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:
14	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
15	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
16	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:

Variant related genes	Relation type
KRT8P44	TF binding region
KRT8P44	CpG island

Extended variants
information (count: 12037 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:12037 , 50 per page) page: 1 2 3 4 5 6 7 ... 241

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4709595	chr6:162729381-162729382	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs546373324	chr6:162729393-162729394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559690329	chr6:162729489-162729490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540519111	chr6:162729518-162729519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2156270	chr6:162729527-162729528	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs147108176	chr6:162729554-162729555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7769011	chr6:162729580-162729581	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs140932176	chr6:162729647-162729648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs4709596	chr6:162729719-162729720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576770474	chr6:162729721-162729722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567389227	chr6:162729751-162729752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535955785	chr6:162729763-162729764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546818179	chr6:162729771-162729772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs73598174	chr6:162729780-162729781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538553607	chr6:162729811-162729812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558394346	chr6:162729838-162729839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577634785	chr6:162729846-162729847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537073218	chr6:162729876-162729877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185303318	chr6:162729886-162729887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574127096	chr6:162729889-162729890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544145713	chr6:162729917-162729918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201687915	chr6:162729921-162729922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573336918	chr6:162729926-162729927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138760183	chr6:162729938-162729939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559908022	chr6:162729945-162729946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189159848	chr6:162729987-162729988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113093856	chr6:162730038-162730039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12215549	chr6:162730080-162730081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565605999	chr6:162730138-162730139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141033407	chr6:162730169-162730170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144741101	chr6:162730180-162730181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201159288	chr6:162730188-162730189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560717565	chr6:162730215-162730216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs62429435	chr6:162730224-162730225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181448429	chr6:162730256-162730257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546336051	chr6:162730273-162730274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112666012	chr6:162730275-162730276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138658399	chr6:162730282-162730283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141882858	chr6:162730283-162730284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189434979	chr6:162730313-162730314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181074851	chr6:162730322-162730323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371136134	chr6:162730347-162730348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs202081887	chr6:162730393-162730394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186006184	chr6:162730400-162730401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375662872	chr6:162730417-162730418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191331904	chr6:162730442-162730443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183343783	chr6:162730443-162730444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186229109	chr6:162730449-162730450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144598252	chr6:162730460-162730461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545652482	chr6:162730476-162730477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Renal cell carcinoma	18592004	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
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20838587	CNVD
Early-onset parkinson disease	21993715	CNVD
Glioblastoma	18772890	CNVD
Pancreatic cancer	20981101	CNVD
Autism	21360662	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Parkinson disease	0	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Schizophrenia	20967226	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Autism	22495309	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Schizophrenia	19805367	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:970 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162712600-162738200	Weak transcription	Psoas Muscle	Psoas
2	chr6:162720200-162732400	Weak transcription	Left Ventricle	heart
3	chr6:162728000-162765600	Weak transcription	Pancreas	Pancrea
4	chr6:162728400-162731400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:162731200-162731600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:162731400-162731600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:162735000-162735800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr6:162735400-162737800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:162735800-162737200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:162736200-162736800	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr6:162736200-162737200	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr6:162736400-162737000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr6:162736800-162737200	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr6:162738200-162738400	Enhancers	Psoas Muscle	Psoas
15	chr6:162744600-162745000	Active TSS	Primary T killer memory cells from peripheral blood	blood
16	chr6:162745800-162746600	Enhancers	Fetal Brain Male	brain
17	chr6:162746000-162746800	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr6:162746200-162746600	Enhancers	Fetal Lung	lung
19	chr6:162746400-162746800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr6:162746600-162747400	Weak transcription	Fetal Brain Male	brain
21	chr6:162747400-162747600	Enhancers	Fetal Brain Male	brain
22	chr6:162747400-162749800	Weak transcription	Ovary	ovary
23	chr6:162749600-162753000	Weak transcription	Aorta	Aorta
24	chr6:162749800-162750000	Strong transcription	Ovary	ovary
25	chr6:162750000-162753800	Weak transcription	Ovary	ovary
26	chr6:162753200-162753600	Enhancers	Adipose Nuclei	Adipose
27	chr6:162753600-162761000	Weak transcription	Adipose Nuclei	Adipose
28	chr6:162755000-162766200	Weak transcription	Ovary	ovary
29	chr6:162757800-162758000	Enhancers	Gastric	stomach
30	chr6:162757800-162758800	Enhancers	Fetal Heart	heart
31	chr6:162758600-162758800	Enhancers	Gastric	stomach
32	chr6:162761400-162761600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr6:162761600-162766000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr6:162762600-162763000	Weak transcription	Adipose Nuclei	Adipose
35	chr6:162763400-162763800	Enhancers	Fetal Lung	lung
36	chr6:162763600-162764200	Enhancers	Stomach Mucosa	stomach
37	chr6:162763800-162765200	Weak transcription	Fetal Lung	lung
38	chr6:162764000-162764600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr6:162764400-162764800	Enhancers	Brain Cingulate Gyrus	brain
40	chr6:162764400-162765400	Active TSS	Adipose Nuclei	Adipose
41	chr6:162764400-162766200	Enhancers	Fetal Muscle Leg	muscle
42	chr6:162764400-162766400	Enhancers	NHDF-Ad	bronchial
43	chr6:162764400-162766800	Enhancers	Brain Hippocampus Middle	brain
44	chr6:162764400-162767200	Enhancers	HMEC	breast
45	chr6:162764400-162767400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr6:162764400-162767600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr6:162764600-162765400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr6:162764600-162766400	Enhancers	Fetal Brain Male	brain
49	chr6:162764600-162767000	Enhancers	Fetal Heart	heart
50	chr6:162764800-162765400	Enhancers	Cortex derived primary cultured neurospheres	brain

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