Variant report

Variant	nsv538523
Chromosome Location	chr6:162965483-163127021
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	chr6:163102512-163102850	HepG2	liver:	n/a	n/a
2	ATF1	chr6:163037119-163037243	K562	blood:	n/a	n/a
3	ATF2	chr6:163042363-163042635	GM12878	blood:	n/a	n/a
4	ATF3	chr6:163042298-163042684	HCT-116	colon:	n/a	n/a
5	BACH1	chr6:162975725-162976098	K562	blood:	n/a	n/a
6	BATF	chr6:163042347-163042655	GM12878	blood:	n/a	chr6:163042519-163042530
7	BATF	chr6:163042398-163042636	GM12878	blood:	n/a	chr6:163042519-163042530
8	BHLHE40	chr6:163042376-163042676	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:163102590-163102846	HepG2	liver:	n/a	n/a
10	CCNT2	chr6:163001825-163002025	K562	blood:	n/a	n/a
11	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
12	CEBPB	chr6:163095532-163095810	A549	lung:	n/a	chr6:163095668-163095677 chr6:163095667-163095678
13	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
14	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
15	CEBPB	chr6:163063873-163064127	IMR90	lung:	n/a	chr6:163063991-163064002
16	CEBPB	chr6:163042256-163042790	HCT-116	colon:	n/a	n/a
17	CEBPB	chr6:163067647-163067800	HepG2	liver:	n/a	chr6:163067696-163067707
18	CEBPB	chr6:163095583-163095738	HepG2	liver:	n/a	chr6:163095668-163095677 chr6:163095667-163095678
19	CEBPB	chr6:163121018-163121310	A549	lung:	n/a	chr6:163121209-163121220
20	CEBPB	chr6:163042384-163042569	H1-hESC	embryonic stem cell:	n/a	n/a
21	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
22	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
23	CEBPB	chr6:163102535-163102869	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:163121033-163121335	HepG2	liver:	n/a	chr6:163121209-163121220
25	CEBPB	chr6:163102596-163102728	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:163095503-163095821	HepG2	liver:	n/a	chr6:163095668-163095677 chr6:163095667-163095678
27	CEBPB	chr6:163063888-163064088	H1-hESC	embryonic stem cell:	n/a	chr6:163063991-163064002
28	CEBPB	chr6:163106060-163106305	HepG2	liver:	n/a	n/a
29	CEBPB	chr6:163122194-163122394	HepG2	liver:	n/a	chr6:163122352-163122363
30	CEBPB	chr6:163042252-163042579	MCF-7	breast:	n/a	n/a
31	CEBPB	chr6:163063853-163064152	HepG2	liver:	n/a	chr6:163063991-163064002
32	CHD1	chr6:163113285-163113303	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr6:162977821-162977975	MCF-7	breast:	n/a	chr6:162977884-162977902
34	CTCF	chr6:163033694-163033990	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr6:163085533-163085559	GM10266	blood:	n/a	n/a
36	CTCF	chr6:163001788-163001915	HepG2	liver:	n/a	n/a
37	CTCF	chr6:163092969-163093007	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr6:162977779-162978012	MCF-7	breast:	n/a	chr6:162977884-162977902
39	CTCF	chr6:162977840-162977990	BE2_C	brain:	n/a	chr6:162977884-162977902
40	CTCF	chr6:163041296-163041436	LNCaP	prostate:	n/a	chr6:163041356-163041369 chr6:163041349-163041370 chr6:163041354-163041372
41	CTCF	chr6:163033777-163033927	MCF-7	breast:	n/a	n/a
42	CTCF	chr6:162989674-162989762	GM20000	blood:	n/a	n/a
43	CTCF	chr6:163033780-163033930	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr6:162977820-162977970	WERI-Rb-1	eye:	n/a	chr6:162977884-162977902
45	CTCF	chr6:162977800-162977950	HRPEpiC	eye:	n/a	chr6:162977884-162977902
46	CTCF	chr6:162977800-162977950	SAEC	small airway:	n/a	chr6:162977884-162977902
47	CTCF	chr6:163033831-163033920	LNCaP	prostate:	n/a	n/a
48	CTCF	chr6:162977780-162978000	LNCaP	prostate:	n/a	chr6:162977884-162977902
49	CTCF	chr6:162977840-162977990	RPTEC	kidney:	n/a	chr6:162977884-162977902
50	CTCF	chr6:162977797-162977987	MCF-7	breast:	n/a	chr6:162977884-162977902

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163024624-163024674	GM12891	blood:	n/a
2	chr6:163024624-163024674	U87	brain:	n/a
3	chr6:163110854-163110904	T-47D	breast:	n/a
4	chr6:163024624-163024674	MCF10A-Er-Src	breast:	n/a
5	chr6:163024624-163024674	SKMC	muscle:	n/a
6	chr6:163024624-163024674	HRPEpiC	eye:	n/a
7	chr6:163110854-163110904	HNPCEpiC	eye:	n/a
8	chr6:163110854-163110904	HIPEpiC	eye:	n/a
9	chr6:163024624-163024674	AoSMC	blood vessel:	n/a
10	chr6:163024624-163024674	GM12892	blood:	n/a
11	chr6:163110854-163110904	AG04449	skin:	fetal
12	chr6:163110854-163110904	HUVEC	blood vessel:	n/a
13	chr6:163024624-163024674	GM06990	blood:	n/a
14	chr6:163110854-163110904	AG09319	gingival:	n/a
15	chr6:163024624-163024674	SK-N-SH	brain:	n/a
16	chr6:163024624-163024674	AG09309	skin:	n/a
17	chr6:163024624-163024674	A549	lung:	n/a
18	chr6:163110854-163110904	U87	brain:	n/a
19	chr6:163110854-163110904	HRPEpiC	eye:	n/a
20	chr6:163110854-163110904	IMR90	lung:	fetal
21	chr6:163024624-163024674	AG09319	gingival:	n/a
22	chr6:163110854-163110904	K562	blood:	n/a
23	chr6:163110854-163110904	AoSMC	blood vessel:	n/a
24	chr6:163110854-163110904	RPTEC	kidney:	n/a
25	chr6:163110854-163110904	ECC-1	luminal epithelium:	n/a
26	chr6:163024624-163024674	HIPEpiC	eye:	n/a
27	chr6:163110854-163110904	Jurkat	blood:	n/a
28	chr6:163110854-163110904	HAEpiC	amniotic membrane:	n/a
29	chr6:163110854-163110904	NB4	blood:	n/a
30	chr6:163110854-163110904	H1-hESC	embryonic stem cell:	embryo
31	chr6:163110854-163110904	HEEpiC	esophagus:	n/a
32	chr6:163024624-163024674	MCF-7	breast:	n/a
33	chr6:163110854-163110904	HCF	heart:	n/a
34	chr6:163110854-163110904	MCF10A-Er-Src	breast:	n/a
35	chr6:163024624-163024674	T-47D	breast:	n/a
36	chr6:163110854-163110904	HEK293	kidney:	embryo
37	chr6:163110854-163110904	AG10803	skin:	n/a
38	chr6:163024624-163024674	ProgFib	skin:	n/a
39	chr6:163024624-163024674	Caco-2	colon:	n/a
40	chr6:163024624-163024674	HNPCEpiC	eye:	n/a
41	chr6:163110854-163110904	LNCaP	prostate:	n/a
42	chr6:163024624-163024674	PANC-1	pancreas:	n/a
43	chr6:163024624-163024674	ECC-1	luminal epithelium:	n/a
44	chr6:163024624-163024674	HUVEC	blood vessel:	n/a
45	chr6:163110854-163110904	GM12892	blood:	n/a
46	chr6:163024624-163024674	CMK	blood:	n/a
47	chr6:163110854-163110904	HPAEpiC	pulmonary alveolar:	n/a
48	chr6:163024624-163024674	H1-hESC	embryonic stem cell:	embryo
49	chr6:163024624-163024674	AG10803	skin:	n/a
50	chr6:163110854-163110904	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
2	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
3	chr6:163103043..163104996-chr6:163109382..163111025,2	K562	blood:
4	chr6:163117200..163118947-chr6:163123211..163125034,2	K562	blood:
5	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
6	chr6:163117200..163118947-chr6:163123211..163125034,2	K562	blood:
7	chr6:163111769..163114753-chr6:163116374..163118174,2	K562	blood:
8	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
9	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
10	chr6:163100762..163102270-chr6:163108804..163111519,2	K562	blood:
11	chr6:163103043..163104996-chr6:163109382..163111025,2	K562	blood:
12	chr6:163111769..163114753-chr6:163116374..163118174,2	K562	blood:
13	chr6:163100762..163102270-chr6:163108804..163111519,2	K562	blood:
14	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:

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

Extended variants
information (count: 6324 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:6324 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191420472	chr6:162965514-162965515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185041292	chr6:162965515-162965516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189607038	chr6:162965545-162965546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs192820276	chr6:162965550-162965551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs36022778	chr6:162965555-162965556	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs185256313	chr6:162965562-162965563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34623056	chr6:162965619-162965620	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs562805849	chr6:162965629-162965630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs78913513	chr6:162965663-162965664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11296683	chr6:162965705-162965706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs71713082	chr6:162965726-162965727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs397752961	chr6:162965727-162965728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542000849	chr6:162965751-162965752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370828943	chr6:162965759-162965760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530109054	chr6:162965771-162965772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546709289	chr6:162965772-162965773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557771476	chr6:162965802-162965803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113573345	chr6:162965827-162965828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149095603	chr6:162965866-162965867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575915186	chr6:162965867-162965868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112052738	chr6:162965868-162965869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543426908	chr6:162965944-162965945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538196796	chr6:162965969-162965970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548742059	chr6:162965998-162965999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372656610	chr6:162966000-162966001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568583001	chr6:162966071-162966072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533839495	chr6:162966093-162966094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553915597	chr6:162966123-162966124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2803070	chr6:162966145-162966146	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs532962764	chr6:162966162-162966163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528993340	chr6:162966195-162966196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540815579	chr6:162966211-162966212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555929286	chr6:162966276-162966277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576273497	chr6:162966277-162966278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541784937	chr6:162966284-162966285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs56192477	chr6:162966314-162966315	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs549922458	chr6:162966321-162966322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577047959	chr6:162966333-162966334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2846463	chr6:162966431-162966432	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs540287744	chr6:162966432-162966433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114018599	chr6:162966462-162966463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532515898	chr6:162966483-162966484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552534427	chr6:162966539-162966540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370819124	chr6:162966544-162966545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551295260	chr6:162966598-162966599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188794585	chr6:162966599-162966600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548616876	chr6:162966647-162966648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568630166	chr6:162966656-162966657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138931091	chr6:162966660-162966661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548058876	chr6:162966703-162966704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:539 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162941200-162989400	Weak transcription	Aorta	Aorta
2	chr6:162955000-162973200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:162960200-162978200	Weak transcription	Psoas Muscle	Psoas
4	chr6:162960800-162977600	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr6:162962400-162975600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:162962600-162983400	Weak transcription	Left Ventricle	heart
7	chr6:162964400-162965600	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr6:162965000-162967000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr6:162965200-162965600	Enhancers	Brain Germinal Matrix	brain
10	chr6:162965200-162965600	Enhancers	Duodenum Smooth Muscle	Duodenum
11	chr6:162965400-162965600	Enhancers	Stomach Smooth Muscle	stomach
12	chr6:162965600-162966800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr6:162965600-162988800	Weak transcription	Stomach Smooth Muscle	stomach
14	chr6:162966800-162967000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr6:162966800-162967000	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr6:162967000-162967400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr6:162967600-162967800	Enhancers	Pancreas	Pancrea
18	chr6:162967800-162989400	Weak transcription	Pancreas	Pancrea
19	chr6:162968000-162968400	Enhancers	Fetal Brain Female	brain
20	chr6:162969200-162989400	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr6:162970800-162971000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr6:162971000-162975600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr6:162973200-162973400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr6:162975600-162975800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr6:162975600-162975800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr6:162975800-162986200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr6:162976000-162978600	Weak transcription	Right Atrium	heart
28	chr6:162978000-162978400	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr6:162978000-162978400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr6:162978200-162978400	Enhancers	Psoas Muscle	Psoas
31	chr6:162978200-162978600	Enhancers	Ovary	ovary
32	chr6:162978600-162989400	Weak transcription	Ovary	ovary
33	chr6:162983200-162983400	Enhancers	Right Ventricle	heart
34	chr6:162983400-162984000	Enhancers	Left Ventricle	heart
35	chr6:162983400-162989600	Weak transcription	Right Ventricle	heart
36	chr6:162983400-162991600	Weak transcription	Brain Substantia Nigra	brain
37	chr6:162984000-162986400	Weak transcription	Left Ventricle	heart
38	chr6:162986400-162986800	ZNF genes & repeats	Left Ventricle	heart
39	chr6:162986800-162989200	Weak transcription	Left Ventricle	heart
40	chr6:162988200-162989400	Weak transcription	Gastric	stomach
41	chr6:162988800-162989400	ZNF genes & repeats	Stomach Smooth Muscle	stomach
42	chr6:162988800-162990200	ZNF genes & repeats	Adipose Nuclei	Adipose
43	chr6:162989000-162989200	Weak transcription	Fetal Kidney	kidney
44	chr6:162989000-162989600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr6:162989000-162990000	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr6:162989200-162989800	Weak transcription	Brain Hippocampus Middle	brain
47	chr6:162989200-162990400	Strong transcription	Left Ventricle	heart
48	chr6:162989200-162990400	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
49	chr6:162989200-162992600	Weak transcription	Colon Smooth Muscle	Colon
50	chr6:162989400-162989800	Strong transcription	Gastric	stomach

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