Variant report

Variant	nsv531339
Chromosome Location	chr6:162654091-163000320
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	chr6:162794306-162794665	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:162671087-162671724	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:162910482-162910786	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:162857639-162857816	HepG2	liver:	n/a	n/a
5	ATF1	chr6:162812215-162812339	K562	blood:	n/a	n/a
6	ATF1	chr6:162782228-162782581	K562	blood:	n/a	n/a
7	ATF1	chr6:162784797-162785113	K562	blood:	n/a	n/a
8	ATF1	chr6:162812647-162812847	K562	blood:	n/a	n/a
9	ATF3	chr6:162784742-162785052	K562	blood:	n/a	n/a
10	BACH1	chr6:162975725-162976098	K562	blood:	n/a	n/a
11	BHLHE40	chr6:162899266-162899534	GM12878	blood:	n/a	n/a
12	BRCA1	chr6:162658617-162658742	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr6:162871740-162871751	H1-hESC	embryonic stem cell:	n/a	n/a
14	CBX3	chr6:162784775-162785143	K562	blood:	n/a	n/a
15	CBX3	chr6:162785538-162785848	K562	blood:	n/a	n/a
16	CEBPB	chr6:162794250-162794499	HepG2	liver:	n/a	chr6:162794312-162794323
17	CEBPB	chr6:162671584-162671889	IMR90	lung:	n/a	n/a
18	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
19	CEBPB	chr6:162671564-162671902	A549	lung:	n/a	n/a
20	CEBPB	chr6:162775249-162775526	HepG2	liver:	n/a	chr6:162775385-162775396
21	CEBPB	chr6:162672448-162672478	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:162784839-162785153	HepG2	liver:	n/a	chr6:162785029-162785040
23	CEBPB	chr6:162910493-162910789	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:162961979-162962215	HepG2	liver:	n/a	chr6:162962080-162962091
25	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
26	CEBPB	chr6:162825981-162826255	HepG2	liver:	n/a	chr6:162826093-162826104
27	CEBPB	chr6:162910422-162910805	HepG2	liver:	n/a	n/a
28	CEBPB	chr6:162675613-162675797	A549	lung:	n/a	chr6:162675652-162675661 chr6:162675652-162675661 chr6:162675652-162675663 chr6:162675650-162675661 chr6:162675652-162675661 chr6:162675650-162675663 chr6:162675652-162675661
29	CEBPB	chr6:162784873-162785124	H1-hESC	embryonic stem cell:	n/a	chr6:162785029-162785040
30	CEBPB	chr6:162745722-162745922	HepG2	liver:	n/a	chr6:162745751-162745762
31	CEBPB	chr6:162871443-162871750	MCF-7	breast:	n/a	chr6:162871605-162871616
32	CEBPB	chr6:162857299-162857541	HepG2	liver:	n/a	chr6:162857420-162857431
33	CEBPB	chr6:162656289-162656489	A549	lung:	n/a	n/a
34	CEBPB	chr6:162944101-162944302	HepG2	liver:	n/a	n/a
35	CEBPB	chr6:162726891-162727117	HepG2	liver:	n/a	chr6:162726998-162727009 chr6:162726998-162727011 chr6:162727074-162727083 chr6:162727018-162727029 chr6:162727072-162727085
36	CEBPB	chr6:162784733-162785018	K562	blood:	n/a	n/a
37	CEBPB	chr6:162939387-162939585	HepG2	liver:	n/a	chr6:162939453-162939464
38	CEBPB	chr6:162871405-162871712	H1-hESC	embryonic stem cell:	n/a	chr6:162871605-162871616
39	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
40	CEBPB	chr6:162910460-162910714	HepG2	liver:	n/a	n/a
41	CEBPB	chr6:162670249-162670473	HepG2	liver:	n/a	chr6:162670378-162670389
42	CEBPB	chr6:162656180-162656471	HepG2	liver:	n/a	chr6:162656287-162656298 chr6:162656286-162656299
43	CEBPB	chr6:162779025-162779284	HepG2	liver:	n/a	chr6:162779118-162779129
44	CEBPB	chr6:162868765-162868950	HepG2	liver:	n/a	chr6:162868884-162868895
45	CEBPB	chr6:162675529-162675821	HepG2	liver:	n/a	chr6:162675652-162675661 chr6:162675652-162675661 chr6:162675652-162675663 chr6:162675650-162675661 chr6:162675652-162675661 chr6:162675650-162675663 chr6:162675652-162675661
46	CEBPB	chr6:162857291-162857590	HepG2	liver:	n/a	chr6:162857420-162857431
47	CEBPB	chr6:162876249-162876534	IMR90	lung:	n/a	n/a
48	CEBPB	chr6:162671554-162671904	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:162784761-162785142	K562	blood:	n/a	chr6:162785029-162785040
50	CEBPB	chr6:162871496-162871684	HepG2	liver:	n/a	chr6:162871605-162871616

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:162865258-162865308	GM12878	blood:	n/a
2	chr6:162865258-162865308	GM12878	blood:	n/a
3	chr6:162684441-162684491	IMR90	lung:	fetal
4	chr6:162864586-162864636	BJ	skin:	n/a
5	chr6:162863505-162863555	K562	blood:	n/a
6	chr6:162863505-162863555	A549	lung:	n/a
7	chr6:162831837-162831887	MCF10A-Er-Src	breast:	n/a
8	chr6:162831837-162831887	PrEC	prostate:	n/a
9	chr6:162684526-162684576	SKMC	muscle:	n/a
10	chr6:162865171-162865221	LNCaP	prostate:	n/a
11	chr6:162684441-162684491	PFSK-1	brain:	n/a
12	chr6:162831837-162831887	HCF	heart:	n/a
13	chr6:162683961-162684011	AG09309	skin:	n/a
14	chr6:162865258-162865308	Hela-S3	cervix:	n/a
15	chr6:162684441-162684491	AG09319	gingival:	n/a
16	chr6:162865171-162865221	ProgFib	skin:	n/a
17	chr6:162964378-162964428	NHBE	bronchial:	n/a
18	chr6:162863505-162863555	HUVEC	blood vessel:	n/a
19	chr6:162683881-162683931	GM12891	blood:	n/a
20	chr6:162865171-162865221	H1-hESC	embryonic stem cell:	embryo
21	chr6:162865258-162865308	RPTEC	kidney:	n/a
22	chr6:162865258-162865308	HCPEpiC	choroid plexus:	n/a
23	chr6:162684526-162684576	SK-N-SH	brain:	n/a
24	chr6:162683961-162684011	HCT-116	colon:	n/a
25	chr6:162964378-162964428	ProgFib	skin:	n/a
26	chr6:162865258-162865308	PrEC	prostate:	n/a
27	chr6:162684526-162684576	GM12891	blood:	n/a
28	chr6:162683961-162684011	H1-hESC	embryonic stem cell:	embryo
29	chr6:162864586-162864636	CMK	blood:	n/a
30	chr6:162831837-162831887	RPTEC	kidney:	n/a
31	chr6:162684526-162684576	SK-N-SH_RA	brain:	n/a
32	chr6:162864586-162864636	Hela-S3	cervix:	n/a
33	chr6:162684526-162684576	HUVEC	blood vessel:	n/a
34	chr6:162831837-162831887	HEEpiC	esophagus:	n/a
35	chr6:162684441-162684491	PrEC	prostate:	n/a
36	chr6:162683881-162683931	HRE	kidney:	n/a
37	chr6:162865171-162865221	NHDF-neo	bronchial:	n/a
38	chr6:162865258-162865308	Jurkat	blood:	n/a
39	chr6:162863505-162863555	GM12891	blood:	n/a
40	chr6:162865171-162865221	HPAEpiC	pulmonary alveolar:	n/a
41	chr6:162863505-162863555	HEK293	kidney:	embryo
42	chr6:162964378-162964428	BJ	skin:	n/a
43	chr6:162684526-162684576	PFSK-1	brain:	n/a
44	chr6:162865171-162865221	HEK293	kidney:	embryo
45	chr6:162683961-162684011	SK-N-SH	brain:	n/a
46	chr6:162683857-162683907	Hela-S3	cervix:	n/a
47	chr6:162684526-162684576	HMEC	breast:	n/a
48	chr6:162684526-162684576	HRCEpiC	kidney:	n/a
49	chr6:162865258-162865308	HIPEpiC	eye:	n/a
50	chr6:162683961-162684011	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:162661286..162663139-chr6:162673530..162675376,2	K562	blood:
2	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
3	chr6:162721411..162723925-chr6:162726328..162729326,2	K562	blood:
4	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
5	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
6	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:
7	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
8	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
9	chr6:162666890..162668464-chr6:162670216..162671922,2	K562	blood:
10	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
11	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
12	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
13	chr6:162721411..162723925-chr6:162726328..162729326,2	K562	blood:
14	chr6:162666890..162668464-chr6:162670216..162671922,2	K562	blood:
15	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:
16	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
17	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
18	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
19	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:
20	chr6:162661286..162663139-chr6:162673530..162675376,2	K562	blood:
21	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
22	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:

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

Extended variants
information (count: 14616 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:14616 , 50 per page) page: 1 2 3 4 5 6 7 ... 293

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs36053942	chr6:162654104-162654105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs577167235	chr6:162654145-162654146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181206052	chr6:162654236-162654237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76899302	chr6:162654239-162654240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537430009	chr6:162654246-162654247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575915441	chr6:162654320-162654321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs578121607	chr6:162654325-162654326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555703367	chr6:162654329-162654330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540080547	chr6:162654344-162654345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6455803	chr6:162654346-162654347	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs6455804	chr6:162654356-162654357	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs114118379	chr6:162654398-162654399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372909678	chr6:162654407-162654408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564268381	chr6:162654437-162654438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs533283727	chr6:162654448-162654449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549791067	chr6:162654449-162654450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs6930012	chr6:162654450-162654451	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs531561394	chr6:162654491-162654492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187122395	chr6:162654509-162654510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568256190	chr6:162654520-162654521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs75166571	chr6:162654524-162654525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547614188	chr6:162654528-162654529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs74357398	chr6:162654541-162654542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377150743	chr6:162654578-162654579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570943977	chr6:162654598-162654599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs60497046	chr6:162654643-162654644	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs556549360	chr6:162654645-162654646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375298960	chr6:162654701-162654702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373791105	chr6:162654706-162654707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs61033853	chr6:162654712-162654713	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs535238335	chr6:162654713-162654714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555390199	chr6:162654877-162654878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191660599	chr6:162654906-162654907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372513591	chr6:162654911-162654912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12663868	chr6:162654925-162654926	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs77260842	chr6:162654926-162654927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564055393	chr6:162654929-162654930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575998028	chr6:162654965-162654966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114656786	chr6:162654968-162654969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs115202701	chr6:162654972-162654973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181698180	chr6:162654995-162654996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186449889	chr6:162655046-162655047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541869372	chr6:162655048-162655049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6935521	chr6:162655089-162655090	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs527816084	chr6:162655093-162655094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547454265	chr6:162655112-162655113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571048710	chr6:162655117-162655118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113519971	chr6:162655118-162655119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs118071731	chr6:162655129-162655130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112033253	chr6:162655131-162655132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Parkinson disease	21829596	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	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	17122850	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:1141 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162653600-162655800	Weak transcription	Right Atrium	heart
2	chr6:162654000-162655800	Weak transcription	Fetal Heart	heart
3	chr6:162655200-162688200	Weak transcription	Ovary	ovary
4	chr6:162655800-162656000	Enhancers	Brain Hippocampus Middle	brain
5	chr6:162655800-162656400	Enhancers	Fetal Heart	heart
6	chr6:162655800-162656400	Active TSS	Right Atrium	heart
7	chr6:162656200-162659800	Weak transcription	Aorta	Aorta
8	chr6:162656400-162658000	Weak transcription	Fetal Heart	heart
9	chr6:162657800-162659200	Enhancers	Brain Germinal Matrix	brain
10	chr6:162657800-162659200	Enhancers	Fetal Kidney	kidney
11	chr6:162658000-162659200	Enhancers	Fetal Heart	heart
12	chr6:162658200-162658600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr6:162658600-162659000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:162658600-162663000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:162659000-162666600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:162659200-162663600	Weak transcription	Brain Germinal Matrix	brain
17	chr6:162659800-162660000	ZNF genes & repeats	Aorta	Aorta
18	chr6:162660000-162660200	Weak transcription	Aorta	Aorta
19	chr6:162663000-162663400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr6:162663600-162664400	Enhancers	Brain Germinal Matrix	brain
21	chr6:162666600-162667000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:162666600-162667200	Enhancers	HepG2	liver
23	chr6:162666800-162667400	Enhancers	Liver	Liver
24	chr6:162667200-162670400	Weak transcription	HepG2	liver
25	chr6:162667400-162670600	Weak transcription	Liver	Liver
26	chr6:162670400-162670800	Enhancers	HepG2	liver
27	chr6:162670600-162670800	Enhancers	Liver	Liver
28	chr6:162670800-162671400	Flanking Active TSS	Liver	Liver
29	chr6:162670800-162671400	Flanking Active TSS	HepG2	liver
30	chr6:162671400-162672400	Enhancers	Liver	Liver
31	chr6:162671400-162672400	Enhancers	HepG2	liver
32	chr6:162674000-162694600	Weak transcription	Aorta	Aorta
33	chr6:162675400-162675800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr6:162675600-162675800	Enhancers	Brain Anterior Caudate	brain
35	chr6:162675800-162681000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr6:162676600-162676800	Enhancers	Brain Anterior Caudate	brain
37	chr6:162676600-162676800	Enhancers	Left Ventricle	heart
38	chr6:162676800-162677600	Weak transcription	Left Ventricle	heart
39	chr6:162677600-162677800	Enhancers	Left Ventricle	heart
40	chr6:162677600-162677800	Enhancers	Pancreas	Pancrea
41	chr6:162677600-162678000	Enhancers	Fetal Lung	lung
42	chr6:162677800-162679600	Weak transcription	Left Ventricle	heart
43	chr6:162677800-162705400	Weak transcription	Pancreas	Pancrea
44	chr6:162679600-162679800	Enhancers	Left Ventricle	heart
45	chr6:162680800-162682200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr6:162681000-162681400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:162681000-162683800	Weak transcription	Psoas Muscle	Psoas
48	chr6:162681400-162685400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr6:162682000-162682200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:162682400-162685600	Weak transcription	Brain Anterior Caudate	brain

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