Variant report

Variant	nsv886916
Chromosome Location	chr6:163312845-163410185
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	CBX3	chr6:163385655-163386353	HCT-116	colon:	n/a	n/a
2	CBX3	chr6:163385583-163386388	HCT-116	colon:	n/a	n/a
3	CCNT2	chr6:163315115-163315237	K562	blood:	n/a	n/a
4	CCNT2	chr6:163334181-163334374	K562	blood:	n/a	n/a
5	CEBPB	chr6:163384837-163385142	IMR90	lung:	n/a	n/a
6	CEBPB	chr6:163325154-163325392	K562	blood:	n/a	chr6:163325287-163325298
7	CEBPB	chr6:163385746-163386445	HCT-116	colon:	n/a	n/a
8	CEBPB	chr6:163325809-163326020	HepG2	liver:	n/a	chr6:163325933-163325944
9	CEBPB	chr6:163325147-163325444	A549	lung:	n/a	chr6:163325287-163325298
10	CEBPB	chr6:163385672-163386327	HCT-116	colon:	n/a	n/a
11	CEBPB	chr6:163325129-163325412	IMR90	lung:	n/a	chr6:163325287-163325298
12	CEBPB	chr6:163325142-163325406	H1-hESC	embryonic stem cell:	n/a	chr6:163325287-163325298
13	CEBPB	chr6:163315544-163315822	HepG2	liver:	n/a	chr6:163315679-163315690 chr6:163315678-163315691 chr6:163315678-163315689
14	CEBPB	chr6:163385817-163386320	IMR90	lung:	n/a	n/a
15	CEBPB	chr6:163325122-163325456	HepG2	liver:	n/a	chr6:163325287-163325298
16	CHD2	chr6:163342515-163342650	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr6:163320283-163320453	Fibrobl	skin:	n/a	n/a
18	CTCF	chr6:163329000-163329150	AG09319	gingival:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
19	CTCF	chr6:163329040-163329190	HRE	kidney:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
20	CTCF	chr6:163329040-163329190	HMEC	breast:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
21	CTCF	chr6:163328920-163329070	HCT-116	colon:	n/a	n/a
22	CTCF	chr6:163364764-163364779	Fibrobl	skin:	n/a	n/a
23	CTCF	chr6:163328900-163329050	GM12878	blood:	n/a	n/a
24	CTCF	chr6:163329040-163329190	GM12875	blood:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
25	CTCF	chr6:163328986-163329172	Kidney_OC	kidney:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
26	CTCF	chr6:163329020-163329170	SK-N-SH_RA	brain:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
27	CTCF	chr6:163320329-163320420	GM12891	blood:	n/a	n/a
28	CTCF	chr6:163329020-163329170	NHDF-neo	bronchial:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
29	CTCF	chr6:163329020-163329170	NHEK	skin:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
30	CTCF	chr6:163329060-163329210	HRPEpiC	eye:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
31	CTCF	chr6:163329060-163329210	GM12866	blood:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
32	CTCF	chr6:163329007-163329189	LNCaP	prostate:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
33	CTCF	chr6:163329020-163329170	GM12865	blood:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
34	CTCF	chr6:163329022-163329202	Pancreas_OC	pancreas:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
35	CTCF	chr6:163328980-163329130	HepG2	liver:	n/a	chr6:163329108-163329126 chr6:163329109-163329125
36	CTCF	chr6:163329006-163329186	LNCaP	prostate:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
37	CTCF	chr6:163342220-163342370	GM12871	blood:	n/a	chr6:163342324-163342337
38	CTCF	chr6:163320274-163320482	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:163364560-163364710	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr6:163320300-163320450	AG09309	skin:	n/a	n/a
41	CTCF	chr6:163328972-163329228	K562	blood:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
42	CTCF	chr6:163329016-163329328	HCT-116	colon:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
43	CTCF	chr6:163329001-163329203	GM13977	blood:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
44	CTCF	chr6:163329020-163329170	WERI-Rb-1	eye:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
45	CTCF	chr6:163329120-163329270	GM06990	blood:	n/a	n/a
46	CTCF	chr6:163328940-163329090	HCM	heart:	n/a	n/a
47	CTCF	chr6:163328920-163329266	IMR90	lung:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
48	CTCF	chr6:163329020-163329170	GM12872	blood:	n/a	chr6:163329108-163329126 chr6:163329110-163329131 chr6:163329109-163329125
49	CTCF	chr6:163320358-163320371	HepG2	liver:	n/a	n/a
50	CTCF	chr6:163329340-163329490	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163321435-163321485	SKMC	muscle:	n/a
2	chr6:163321435-163321485	AG04449	skin:	fetal
3	chr6:163321435-163321485	SKMC	muscle:	n/a
4	chr6:163321435-163321485	AG04449	skin:	fetal
5	chr6:163321435-163321485	MCF10A-Er-Src	breast:	n/a
6	chr6:163321157-163321207	NHDF-neo	bronchial:	n/a
7	chr6:163321305-163321355	SAEC	small airway:	n/a
8	chr6:163321305-163321355	AG09309	skin:	n/a
9	chr6:163362155-163362205	GM19239	blood:	n/a
10	chr6:163321435-163321485	HEK293	kidney:	embryo
11	chr6:163362155-163362205	Caco-2	colon:	n/a
12	chr6:163321305-163321355	HRE	kidney:	n/a
13	chr6:163321157-163321207	GM19239	blood:	n/a
14	chr6:163362155-163362205	HCPEpiC	choroid plexus:	n/a
15	chr6:163321305-163321355	HCF	heart:	n/a
16	chr6:163321305-163321355	NT2-D1	testis:	n/a
17	chr6:163321305-163321355	HUVEC	blood vessel:	n/a
18	chr6:163362155-163362205	AG09309	skin:	n/a
19	chr6:163321157-163321207	IMR90	lung:	fetal
20	chr6:163321435-163321485	HepG2	liver:	n/a
21	chr6:163362155-163362205	NB4	blood:	n/a
22	chr6:163321157-163321207	SK-N-SH	brain:	n/a
23	chr6:163321305-163321355	ProgFib	skin:	n/a
24	chr6:163321157-163321207	SK-N-SH_RA	brain:	n/a
25	chr6:163321157-163321207	ECC-1	luminal epithelium:	n/a
26	chr6:163321305-163321355	HEEpiC	esophagus:	n/a
27	chr6:163321305-163321355	BE2_C	brain:	n/a
28	chr6:163321435-163321485	AoSMC	blood vessel:	n/a
29	chr6:163321305-163321355	HEK293	kidney:	embryo
30	chr6:163321305-163321355	MCF10A-Er-Src	breast:	n/a
31	chr6:163321435-163321485	NT2-D1	testis:	n/a
32	chr6:163321305-163321355	SKMC	muscle:	n/a
33	chr6:163321305-163321355	LNCaP	prostate:	n/a
34	chr6:163321305-163321355	HL-60	blood:	n/a
35	chr6:163321157-163321207	PrEC	prostate:	n/a
36	chr6:163321157-163321207	T-47D	breast:	n/a
37	chr6:163321305-163321355	SK-N-SH_RA	brain:	n/a
38	chr6:163321305-163321355	NHDF-neo	bronchial:	n/a
39	chr6:163362155-163362205	H1-hESC	embryonic stem cell:	embryo
40	chr6:163362155-163362205	AG09319	gingival:	n/a
41	chr6:163362155-163362205	BJ	skin:	n/a
42	chr6:163321435-163321485	A549	lung:	n/a
43	chr6:163321157-163321207	HUVEC	blood vessel:	n/a
44	chr6:163362155-163362205	HNPCEpiC	eye:	n/a
45	chr6:163321435-163321485	CMK	blood:	n/a
46	chr6:163362155-163362205	RPTEC	kidney:	n/a
47	chr6:163362155-163362205	Hepatocyte	liver:	n/a
48	chr6:163321157-163321207	HNPCEpiC	eye:	n/a
49	chr6:163321305-163321355	ECC-1	luminal epithelium:	n/a
50	chr6:163321157-163321207	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:163332495..163335026-chr6:163337698..163339412,2	K562	blood:
2	chr6:163320477..163321997-chr6:163470936..163472773,2	K562	blood:
3	chr6:163383289..163384996-chr6:163389712..163391752,2	MCF-7	breast:
4	chr6:163312379..163314050-chr6:163315693..163317902,2	K562	blood:
5	chr6:163332495..163335026-chr6:163337698..163339412,2	K562	blood:
6	chr6:163312379..163314050-chr6:163315693..163317902,2	K562	blood:
7	chr6:163321321..163323965-chr6:163834423..163836018,2	MCF-7	breast:
8	chr6:163316641..163319996-chr6:163320032..163324686,4	K562	blood:
9	chr6:163383289..163384996-chr6:163389712..163391752,2	MCF-7	breast:
10	chr6:163316641..163319996-chr6:163320032..163324686,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL078585.1-13	chr6:163387606-163387705	ucscGeneNc_uc003qud_1
2	lnc-AL078585.1-13	chr6:163392282-163393054	ucscGeneNc_uc003qud_1
3	lnc-AL078585.1-13	chr6:163384002-163384191	ucscGeneNc_uc003qud_1
4	lnc-AL078585.1-14	chr6:163378290-163378580	NONHSAT115947
5	lnc-AL078585.1-13	chr6:163394947-163395183	ucscGeneNc_uc003qud_1

Variant related genes	Relation type
ENSG00000217557	TF binding region
ENSG00000217557	CpG island
ENSG00000112531	chromatin interactions
ENSG00000270419	chromatin interactions
ENSG00000225437	chromatin interactions

Extended variants
information (count: 2242 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2242 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9365505	chr6:163312845-163312846	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553217461	chr6:163312850-163312851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573479859	chr6:163312875-163312876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545560879	chr6:163312912-163312913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565372051	chr6:163312952-163312953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575288232	chr6:163312995-163312996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369836355	chr6:163313014-163313015	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs572000008	chr6:163313016-163313017	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs560965184	chr6:163313022-163313023	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs529672233	chr6:163313050-163313051	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs540247846	chr6:163313058-163313059	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs144337192	chr6:163313067-163313068	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs532340743	chr6:163313069-163313070	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs77459500	chr6:163313078-163313079	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs377638229	chr6:163313093-163313094	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs146572373	chr6:163313094-163313095	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs191132889	chr6:163313136-163313137	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs550620402	chr6:163313168-163313169	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs78290128	chr6:163313183-163313184	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs539426726	chr6:163313188-163313189	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs557507330	chr6:163313190-163313191	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs139332090	chr6:163313278-163313279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144107447	chr6:163313279-163313280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182508684	chr6:163313284-163313285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186717277	chr6:163313345-163313346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191159923	chr6:163313368-163313369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs144981218	chr6:163313378-163313379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554668146	chr6:163313421-163313422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35828657	chr6:163313433-163313434	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs547850643	chr6:163313490-163313491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540219993	chr6:163313505-163313506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559935964	chr6:163313532-163313533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576099187	chr6:163313568-163313569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545733148	chr6:163313578-163313579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs149113558	chr6:163313601-163313602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73605830	chr6:163313624-163313625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143161499	chr6:163313637-163313638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555448928	chr6:163313658-163313659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567398691	chr6:163313697-163313698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11966615	chr6:163313708-163313709	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs540846393	chr6:163313719-163313720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546580285	chr6:163313743-163313744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566798699	chr6:163313753-163313754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539024208	chr6:163313862-163313863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559199301	chr6:163313904-163313905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182502377	chr6:163313915-163313916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569547868	chr6:163313923-163313924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568149209	chr6:163313936-163313937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs137919156	chr6:163313937-163313938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34227883	chr6:163313940-163313941	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
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
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
abnormal development	18461090	CNVD

Chromatin state (count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163309800-163313000	Weak transcription	Pancreas	Pancrea
2	chr6:163310800-163315200	Weak transcription	Brain Angular Gyrus	brain
3	chr6:163313000-163313200	ZNF genes & repeats	Pancreas	Pancrea
4	chr6:163313200-163318800	Weak transcription	Pancreas	Pancrea
5	chr6:163313600-163322800	Weak transcription	Gastric	stomach
6	chr6:163314800-163316000	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr6:163315000-163315200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:163315200-163315400	Enhancers	Brain Cingulate Gyrus	brain
9	chr6:163315200-163315600	Enhancers	Brain Angular Gyrus	brain
10	chr6:163315400-163316000	Enhancers	Brain Hippocampus Middle	brain
11	chr6:163316000-163322800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr6:163318800-163319000	ZNF genes & repeats	Pancreas	Pancrea
13	chr6:163318800-163329800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:163319000-163320400	Weak transcription	Pancreas	Pancrea
15	chr6:163320400-163320600	ZNF genes & repeats	Pancreas	Pancrea
16	chr6:163320400-163320800	Active TSS	Skeletal Muscle Female	skeletal muscle
17	chr6:163320600-163329400	Weak transcription	Pancreas	Pancrea
18	chr6:163320800-163321000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr6:163325800-163326000	Enhancers	Brain Anterior Caudate	brain
20	chr6:163326000-163326200	Enhancers	Brain Hippocampus Middle	brain
21	chr6:163326000-163326400	Enhancers	Brain Angular Gyrus	brain
22	chr6:163326000-163326400	Flanking Active TSS	Brain Anterior Caudate	brain
23	chr6:163326200-163326400	Flanking Active TSS	Brain Hippocampus Middle	brain
24	chr6:163326200-163326800	Active TSS	Brain Inferior Temporal Lobe	brain
25	chr6:163326200-163327000	Active TSS	Brain Cingulate Gyrus	brain
26	chr6:163326400-163326600	Active TSS	Brain Anterior Caudate	brain
27	chr6:163326400-163326800	Active TSS	Brain Angular Gyrus	brain
28	chr6:163326400-163327000	Active TSS	Brain Hippocampus Middle	brain
29	chr6:163326600-163326800	Flanking Active TSS	Brain Anterior Caudate	brain
30	chr6:163326800-163327000	Active TSS	Brain Anterior Caudate	brain
31	chr6:163329400-163330000	ZNF genes & repeats	Pancreas	Pancrea
32	chr6:163329800-163330000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr6:163331200-163331600	Enhancers	Fetal Heart	heart
34	chr6:163331600-163332800	Weak transcription	Fetal Heart	heart
35	chr6:163337800-163339800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr6:163338200-163338400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr6:163338200-163339600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr6:163338200-163340200	Enhancers	Muscle Satellite Cultured Cells	--
39	chr6:163338200-163340200	Enhancers	NHDF-Ad	bronchial
40	chr6:163338400-163339200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr6:163339200-163339400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr6:163339200-163339800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr6:163339400-163342200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr6:163339800-163340200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr6:163340200-163340400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr6:163340400-163342200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr6:163341400-163343400	Enhancers	Fetal Stomach	stomach
48	chr6:163342200-163343000	Enhancers	Fetal Muscle Trunk	muscle
49	chr6:163342200-163343200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr6:163342200-163343400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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