Variant report

Variant	esv2758091
Chromosome Location	chr6:162858322-163140375
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	chr6:162910482-162910786	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:163102512-163102850	HepG2	liver:	n/a	n/a
3	ATF1	chr6:163037119-163037243	K562	blood:	n/a	n/a
4	ATF2	chr6:163042363-163042635	GM12878	blood:	n/a	n/a
5	ATF3	chr6:163042298-163042684	HCT-116	colon:	n/a	n/a
6	BACH1	chr6:162975725-162976098	K562	blood:	n/a	n/a
7	BATF	chr6:163042398-163042636	GM12878	blood:	n/a	chr6:163042519-163042530
8	BATF	chr6:163042347-163042655	GM12878	blood:	n/a	chr6:163042519-163042530
9	BHLHE40	chr6:162899266-162899534	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:163102590-163102846	HepG2	liver:	n/a	n/a
11	BHLHE40	chr6:163042376-163042676	GM12878	blood:	n/a	n/a
12	BRCA1	chr6:162871740-162871751	H1-hESC	embryonic stem cell:	n/a	n/a
13	CCNT2	chr6:163001825-163002025	K562	blood:	n/a	n/a
14	CEBPB	chr6:162876192-162876578	MCF-7	breast:	n/a	n/a
15	CEBPB	chr6:163063873-163064127	IMR90	lung:	n/a	chr6:163063991-163064002
16	CEBPB	chr6:163036133-163036384	Hela-S3	cervix:	n/a	chr6:163036237-163036246 chr6:163036237-163036246 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036236-163036247
17	CEBPB	chr6:162944101-162944302	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:163122194-163122394	HepG2	liver:	n/a	chr6:163122352-163122363
19	CEBPB	chr6:162910422-162910805	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:163095583-163095738	HepG2	liver:	n/a	chr6:163095668-163095677 chr6:163095667-163095678
21	CEBPB	chr6:163036070-163036411	IMR90	lung:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
22	CEBPB	chr6:162961979-162962215	HepG2	liver:	n/a	chr6:162962080-162962091
23	CEBPB	chr6:163102596-163102728	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:163063888-163064088	H1-hESC	embryonic stem cell:	n/a	chr6:163063991-163064002
25	CEBPB	chr6:162910460-162910714	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:163042256-163042790	HCT-116	colon:	n/a	n/a
27	CEBPB	chr6:162871405-162871712	H1-hESC	embryonic stem cell:	n/a	chr6:162871605-162871616
28	CEBPB	chr6:163106060-163106305	HepG2	liver:	n/a	n/a
29	CEBPB	chr6:163102535-163102869	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:162939387-162939585	HepG2	liver:	n/a	chr6:162939453-162939464
31	CEBPB	chr6:162896813-162896974	HepG2	liver:	n/a	chr6:162896839-162896850
32	CEBPB	chr6:163095503-163095821	HepG2	liver:	n/a	chr6:163095668-163095677 chr6:163095667-163095678
33	CEBPB	chr6:162871429-162871791	HepG2	liver:	n/a	chr6:162871605-162871616
34	CEBPB	chr6:163121018-163121310	A549	lung:	n/a	chr6:163121209-163121220
35	CEBPB	chr6:163063853-163064152	HepG2	liver:	n/a	chr6:163063991-163064002
36	CEBPB	chr6:163036084-163036403	A549	lung:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
37	CEBPB	chr6:163121033-163121335	HepG2	liver:	n/a	chr6:163121209-163121220
38	CEBPB	chr6:162868765-162868950	HepG2	liver:	n/a	chr6:162868884-162868895
39	CEBPB	chr6:162943679-162943865	HepG2	liver:	n/a	n/a
40	CEBPB	chr6:163042252-163042579	MCF-7	breast:	n/a	n/a
41	CEBPB	chr6:163067647-163067800	HepG2	liver:	n/a	chr6:163067696-163067707
42	CEBPB	chr6:162876249-162876534	IMR90	lung:	n/a	n/a
43	CEBPB	chr6:162861366-162861450	H1-hESC	embryonic stem cell:	n/a	chr6:162861390-162861403
44	CEBPB	chr6:163042384-163042569	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr6:163036076-163036363	H1-hESC	embryonic stem cell:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
46	CEBPB	chr6:163036055-163036678	HepG2	liver:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036565-163036582 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
47	CEBPB	chr6:163095532-163095810	A549	lung:	n/a	chr6:163095668-163095677 chr6:163095667-163095678
48	CEBPB	chr6:162871496-162871684	HepG2	liver:	n/a	chr6:162871605-162871616
49	CEBPB	chr6:162910493-162910789	HepG2	liver:	n/a	n/a
50	CEBPB	chr6:162871443-162871750	MCF-7	breast:	n/a	chr6:162871605-162871616

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163024624-163024674	PFSK-1	brain:	n/a
2	chr6:163135177-163135227	AoSMC	blood vessel:	n/a
3	chr6:162865171-162865221	BJ	skin:	n/a
4	chr6:162863505-162863555	HMEC	breast:	n/a
5	chr6:162864586-162864636	HUVEC	blood vessel:	n/a
6	chr6:162865171-162865221	PANC-1	pancreas:	n/a
7	chr6:163110854-163110904	PANC-1	pancreas:	n/a
8	chr6:162964378-162964428	AG09319	gingival:	n/a
9	chr6:163135177-163135227	GM12878	blood:	n/a
10	chr6:163110854-163110904	Caco-2	colon:	n/a
11	chr6:163110854-163110904	HMEC	breast:	n/a
12	chr6:162865258-162865308	T-47D	breast:	n/a
13	chr6:163110854-163110904	HepG2	liver:	n/a
14	chr6:162964378-162964428	HepG2	liver:	n/a
15	chr6:162964378-162964428	LNCaP	prostate:	n/a
16	chr6:162865258-162865308	NH-A	brain:	n/a
17	chr6:162865171-162865221	HMEC	breast:	n/a
18	chr6:162863505-162863555	GM19239	blood:	n/a
19	chr6:162964378-162964428	HPAEpiC	pulmonary alveolar:	n/a
20	chr6:162964378-162964428	HCT-116	colon:	n/a
21	chr6:163135177-163135227	AG04449	skin:	fetal
22	chr6:162865171-162865221	A549	lung:	n/a
23	chr6:163135177-163135227	PFSK-1	brain:	n/a
24	chr6:162864586-162864636	HRPEpiC	eye:	n/a
25	chr6:162865258-162865308	HCM	heart:	n/a
26	chr6:163110854-163110904	NT2-D1	testis:	n/a
27	chr6:163135177-163135227	HCPEpiC	choroid plexus:	n/a
28	chr6:163024624-163024674	GM06990	blood:	n/a
29	chr6:162863505-162863555	HPAEpiC	pulmonary alveolar:	n/a
30	chr6:162863505-162863555	SK-N-MC	brain:	n/a
31	chr6:162863505-162863555	SK-N-SH_RA	brain:	n/a
32	chr6:163110854-163110904	NHDF-neo	bronchial:	n/a
33	chr6:163135177-163135227	ProgFib	skin:	n/a
34	chr6:162964378-162964428	GM06990	blood:	n/a
35	chr6:162863505-162863555	Caco-2	colon:	n/a
36	chr6:162865258-162865308	HUVEC	blood vessel:	n/a
37	chr6:162865171-162865221	HUVEC	blood vessel:	n/a
38	chr6:163110854-163110904	SAEC	small airway:	n/a
39	chr6:163110854-163110904	AG09309	skin:	n/a
40	chr6:163024624-163024674	HNPCEpiC	eye:	n/a
41	chr6:162864586-162864636	PrEC	prostate:	n/a
42	chr6:162863505-162863555	HCF	heart:	n/a
43	chr6:163135177-163135227	GM19239	blood:	n/a
44	chr6:162864586-162864636	SKMC	muscle:	n/a
45	chr6:162865171-162865221	ECC-1	luminal epithelium:	n/a
46	chr6:163135177-163135227	AG10803	skin:	n/a
47	chr6:162964378-162964428	AG10803	skin:	n/a
48	chr6:163024624-163024674	PANC-1	pancreas:	n/a
49	chr6:162863505-162863555	GM12878	blood:	n/a
50	chr6:162863505-162863555	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:163111769..163114753-chr6:163116374..163118174,2	K562	blood:
2	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
3	chr6:163103043..163104996-chr6:163109382..163111025,2	K562	blood:
4	chr6:163131701..163133797-chr6:163141922..163143768,2	K562	blood:
5	chr6:163130642..163133409-chr6:163136938..163139480,2	K562	blood:
6	chr6:163139294..163141851-chr6:163147296..163150092,3	MCF-7	breast:
7	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
8	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:
9	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
10	chr6:163138973..163143825-chr6:163144102..163148168,6	K562	blood:
11	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
12	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
13	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
14	chr6:163117200..163118947-chr6:163123211..163125034,2	K562	blood:
15	chr6:163111769..163114753-chr6:163116374..163118174,2	K562	blood:
16	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:
17	chr6:163100762..163102270-chr6:163108804..163111519,2	K562	blood:
18	chr6:163138657..163141393-chr6:163146602..163148183,2	MCF-7	breast:
19	chr6:163130642..163133409-chr6:163136938..163139480,2	K562	blood:
20	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
21	chr6:163100762..163102270-chr6:163108804..163111519,2	K562	blood:
22	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
23	chr6:163117200..163118947-chr6:163123211..163125034,2	K562	blood:
24	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
25	chr6:163135428..163138047-chr6:163139216..163143407,3	K562	blood:
26	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
27	chr6:163132663..163134210-chr6:163147086..163148664,2	K562	blood:
28	chr6:163135428..163138047-chr6:163139216..163143407,3	K562	blood:
29	chr6:163103043..163104996-chr6:163109382..163111025,2	K562	blood:
30	chr6:163136674..163141943-chr6:163143603..163148822,6	K562	blood:

Variant related genes	Relation type
KRT8P44	TF binding region
KRT8P44	CpG island
ENSG00000185345	chromatin interactions
ENSG00000112530	chromatin interactions

Extended variants
information (count: 11342 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:11342 , 50 per page) page: 1 2 3 4 5 6 7 ... 227

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147737823	chr6:162858325-162858326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs68053622	chr6:162858326-162858327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs35087580	chr6:162858327-162858328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs35223689	chr6:162858348-162858349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35266344	chr6:162858358-162858359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564509154	chr6:162858367-162858368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530544281	chr6:162858384-162858385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543860538	chr6:162858392-162858393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572272185	chr6:162858395-162858396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116470734	chr6:162858400-162858401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140385385	chr6:162858427-162858428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541343768	chr6:162858431-162858432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191555018	chr6:162858437-162858438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532413798	chr6:162858448-162858449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551820625	chr6:162858460-162858461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs140459737	chr6:162858469-162858470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs527281337	chr6:162858516-162858517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537551991	chr6:162858534-162858535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189050616	chr6:162858540-162858541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150307489	chr6:162858560-162858561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536834099	chr6:162858597-162858598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545575699	chr6:162858598-162858599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553426575	chr6:162858623-162858624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6927019	chr6:162858625-162858626	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs538921062	chr6:162858634-162858635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536509249	chr6:162858678-162858679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs137900805	chr6:162858716-162858717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531389290	chr6:162858733-162858734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142067854	chr6:162858767-162858768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs9346913	chr6:162858793-162858794	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs554942963	chr6:162858807-162858808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145828193	chr6:162858818-162858819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181376270	chr6:162858885-162858886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs139256051	chr6:162858886-162858887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552459557	chr6:162858913-162858914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565320206	chr6:162858949-162858950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs377653615	chr6:162859003-162859004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576502548	chr6:162859010-162859011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368798894	chr6:162859015-162859016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550824481	chr6:162859016-162859017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543826797	chr6:162859027-162859028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371326863	chr6:162859032-162859033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9365434	chr6:162859051-162859052	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs547196913	chr6:162859058-162859059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs78719731	chr6:162859084-162859085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538984749	chr6:162859107-162859108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs143178050	chr6:162859137-162859138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574919451	chr6:162859138-162859139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537831318	chr6:162859139-162859140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9347640	chr6:162859151-162859152	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:99)

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
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:1074 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162838000-162863600	Weak transcription	Aorta	Aorta
2	chr6:162838600-162868800	Weak transcription	Left Ventricle	heart
3	chr6:162839000-162860800	Weak transcription	Ovary	ovary
4	chr6:162844000-162859600	Weak transcription	Psoas Muscle	Psoas
5	chr6:162859000-162860400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:162859200-162860200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:162859400-162864800	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr6:162859600-162860400	ZNF genes & repeats	Psoas Muscle	Psoas
9	chr6:162859600-162863600	Weak transcription	Brain Angular Gyrus	brain
10	chr6:162860000-162860200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr6:162860000-162861000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr6:162860000-162861200	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr6:162860000-162861200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr6:162860000-162861200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr6:162860200-162860400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr6:162860200-162860600	Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr6:162860200-162861400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr6:162860400-162860600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr6:162860400-162861800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:162860400-162862200	Weak transcription	Psoas Muscle	Psoas
21	chr6:162860600-162860800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr6:162860600-162861200	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr6:162860600-162862600	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr6:162860800-162861200	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr6:162860800-162864000	Strong transcription	Ovary	ovary
26	chr6:162860800-162864600	Weak transcription	Adipose Nuclei	Adipose
27	chr6:162861000-162863400	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr6:162861200-162862600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr6:162861200-162862600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr6:162861200-162863200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr6:162861400-162865800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:162861800-162863200	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr6:162861800-162872600	Weak transcription	Stomach Smooth Muscle	stomach
34	chr6:162862200-162864200	Weak transcription	Right Ventricle	heart
35	chr6:162862600-162864200	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr6:162862600-162864200	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr6:162862600-162864600	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr6:162863000-162864000	Enhancers	Brain Germinal Matrix	brain
39	chr6:162863000-162864200	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr6:162863000-162864600	Enhancers	Fetal Brain Female	brain
41	chr6:162863000-162865000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr6:162863200-162863400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:162863200-162863400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr6:162863200-162863600	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr6:162863200-162863800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
46	chr6:162863200-162865200	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr6:162863400-162863600	Enhancers	Brain Anterior Caudate	brain
48	chr6:162863400-162863800	Weak transcription	Gastric	stomach
49	chr6:162863400-162864200	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr6:162863400-162864400	Enhancers	Fetal Brain Male	brain

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