Variant report

Variant	nsv605182
Chromosome Location	chr6:163166902-163280204
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	ATF1	chr6:163183429-163183540	K562	blood:	n/a	n/a
2	BACH1	chr6:163209996-163210055	K562	blood:	n/a	n/a
3	BACH1	chr6:163277893-163278240	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr6:163254840-163255091	HepG2	liver:	n/a	chr6:163254848-163254861 chr6:163254971-163254982
5	CEBPB	chr6:163171040-163171207	HepG2	liver:	n/a	n/a
6	CEBPB	chr6:163218815-163219032	A549	lung:	n/a	n/a
7	CEBPB	chr6:163206813-163207236	A549	lung:	n/a	n/a
8	CEBPB	chr6:163265498-163265698	K562	blood:	n/a	chr6:163265628-163265639
9	CEBPB	chr6:163265469-163265817	HepG2	liver:	n/a	chr6:163265628-163265639
10	CEBPB	chr6:163270461-163270490	HepG2	liver:	n/a	n/a
11	CEBPB	chr6:163254941-163255044	A549	lung:	n/a	chr6:163254971-163254982
12	CEBPB	chr6:163206936-163207086	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:163206844-163207228	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr6:163218870-163218983	HepG2	liver:	n/a	n/a
15	CEBPB	chr6:163192040-163192363	HepG2	liver:	n/a	chr6:163192194-163192205
16	CEBPB	chr6:163206834-163207227	MCF-7	breast:	n/a	n/a
17	CEBPB	chr6:163274043-163274199	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:163206961-163207175	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr6:163206848-163207222	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:163206905-163207198	IMR90	lung:	n/a	n/a
21	CEBPB	chr6:163192112-163192351	A549	lung:	n/a	chr6:163192194-163192205
22	CEBPB	chr6:163196390-163196524	A549	lung:	n/a	chr6:163196436-163196445 chr6:163196436-163196445 chr6:163196434-163196447 chr6:163196436-163196445
23	CEBPB	chr6:163206896-163207232	A549	lung:	n/a	n/a
24	CEBPB	chr6:163196280-163196606	HepG2	liver:	n/a	chr6:163196436-163196445 chr6:163196436-163196445 chr6:163196569-163196580 chr6:163196434-163196447 chr6:163196436-163196445
25	CEBPB	chr6:163206896-163207154	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr6:163206891-163207206	A549	lung:	n/a	n/a
27	CEBPB	chr6:163206824-163207160	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr6:163185436-163185658	HepG2	liver:	n/a	chr6:163185502-163185513 chr6:163185502-163185515 chr6:163185504-163185515 chr6:163185525-163185536
29	CEBPB	chr6:163206901-163207158	K562	blood:	n/a	n/a
30	CHD1	chr6:163222610-163222659	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr6:163235253-163235303	HepG2	liver:	n/a	n/a
32	CHD2	chr6:163277838-163278273	H1-hESC	embryonic stem cell:	n/a	n/a
33	CREB1	chr6:163277830-163278317	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr6:163277860-163278010	GM12865	blood:	n/a	n/a
35	CTCF	chr6:163277913-163278115	MCF-7	breast:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
36	CTCF	chr6:163171920-163172070	HCT-116	colon:	n/a	n/a
37	CTCF	chr6:163277997-163278092	GM12891	blood:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
38	CTCF	chr6:163277920-163278070	AG04450	lung:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
39	CTCF	chr6:163277960-163278110	HBMEC	blood vessel:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
40	CTCF	chr6:163277845-163278141	A549	lung:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
41	CTCF	chr6:163277940-163278090	GM12872	blood:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
42	CTCF	chr6:163277920-163278070	AG09319	gingival:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
43	CTCF	chr6:163277900-163278127	Gliobla	brain:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
44	CTCF	chr6:163277900-163278050	GM12878	blood:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
45	CTCF	chr6:163277834-163278220	IMR90	lung:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
46	CTCF	chr6:163199665-163199868	K562	blood:	n/a	chr6:163199789-163199807 chr6:163199792-163199805 chr6:163199790-163199806
47	CTCF	chr6:163277980-163278130	K562	blood:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
48	CTCF	chr6:163277977-163278090	MCF-7	breast:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
49	CTCF	chr6:163277900-163278050	GM12865	blood:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013
50	CTCF	chr6:163277940-163278090	HPAF	blood vessel:	n/a	chr6:163277999-163278020 chr6:163277998-163278014 chr6:163277997-163278015 chr6:163278000-163278013

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163199983-163200033	HAEpiC	amniotic membrane:	n/a
2	chr6:163199983-163200033	HAEpiC	amniotic membrane:	n/a
3	chr6:163275980-163276030	AG04450	lung:	fetal
4	chr6:163199983-163200033	T-47D	breast:	n/a
5	chr6:163200038-163200088	HRCEpiC	kidney:	n/a
6	chr6:163275980-163276030	PrEC	prostate:	n/a
7	chr6:163200038-163200088	IMR90	lung:	fetal
8	chr6:163275952-163276002	CMK	blood:	n/a
9	chr6:163276038-163276088	HCF	heart:	n/a
10	chr6:163276038-163276088	HEEpiC	esophagus:	n/a
11	chr6:163199983-163200033	HEEpiC	esophagus:	n/a
12	chr6:163273217-163273267	GM19239	blood:	n/a
13	chr6:163275980-163276030	AG09319	gingival:	n/a
14	chr6:163278126-163278176	HAEpiC	amniotic membrane:	n/a
15	chr6:163276038-163276088	HRE	kidney:	n/a
16	chr6:163200038-163200088	GM19239	blood:	n/a
17	chr6:163275952-163276002	HL-60	blood:	n/a
18	chr6:163278126-163278176	GM06990	blood:	n/a
19	chr6:163273217-163273267	AG09319	gingival:	n/a
20	chr6:163275952-163276002	HNPCEpiC	eye:	n/a
21	chr6:163275980-163276030	SK-N-SH_RA	brain:	n/a
22	chr6:163275980-163276030	HPAEpiC	pulmonary alveolar:	n/a
23	chr6:163275980-163276030	PANC-1	pancreas:	n/a
24	chr6:163276038-163276088	HCPEpiC	choroid plexus:	n/a
25	chr6:163276038-163276088	HRCEpiC	kidney:	n/a
26	chr6:163276038-163276088	HIPEpiC	eye:	n/a
27	chr6:163276038-163276088	K562	blood:	n/a
28	chr6:163200038-163200088	LNCaP	prostate:	n/a
29	chr6:163273217-163273267	HNPCEpiC	eye:	n/a
30	chr6:163273217-163273267	NH-A	brain:	n/a
31	chr6:163278126-163278176	HUVEC	blood vessel:	n/a
32	chr6:163275980-163276030	NHDF-neo	bronchial:	n/a
33	chr6:163278126-163278176	GM19239	blood:	n/a
34	chr6:163273217-163273267	HMEC	breast:	n/a
35	chr6:163278126-163278176	AoSMC	blood vessel:	n/a
36	chr6:163275952-163276002	ECC-1	luminal epithelium:	n/a
37	chr6:163199983-163200033	Hela-S3	cervix:	n/a
38	chr6:163199983-163200033	HPAEpiC	pulmonary alveolar:	n/a
39	chr6:163200038-163200088	HRE	kidney:	n/a
40	chr6:163275980-163276030	A549	lung:	n/a
41	chr6:163199983-163200033	HNPCEpiC	eye:	n/a
42	chr6:163278126-163278176	CMK	blood:	n/a
43	chr6:163199983-163200033	SKMC	muscle:	n/a
44	chr6:163275952-163276002	PANC-1	pancreas:	n/a
45	chr6:163275952-163276002	Hepatocyte	liver:	n/a
46	chr6:163200038-163200088	HUVEC	blood vessel:	n/a
47	chr6:163275980-163276030	HRE	kidney:	n/a
48	chr6:163199983-163200033	A549	lung:	n/a
49	chr6:163273217-163273267	HCF	heart:	n/a
50	chr6:163278126-163278176	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:163238180..163239692-chr6:163244197..163245718,2	K562	blood:
2	chr6:163258403..163260425-chr6:163266356..163268701,2	K562	blood:
3	chr6:163258403..163260425-chr6:163266356..163268701,2	K562	blood:
4	chr6:163238180..163239692-chr6:163244197..163245718,2	K562	blood:
5	chr4:72393798..72394589-chr6:163273105..163273631,2	MCF-7	breast:
6	chr6:163204105..163206331-chr6:163210537..163212839,2	K562	blood:
7	chr6:163204105..163206331-chr6:163210537..163212839,2	K562	blood:
8	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:

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

Extended variants
information (count: 1621 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1621 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536235651	chr6:163167645-163167646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370130790	chr6:163167677-163167678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553359912	chr6:163167691-163167692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572737752	chr6:163167736-163167737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs13213746	chr6:163167777-163167778	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs191379756	chr6:163167807-163167808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376347402	chr6:163167823-163167824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs183297867	chr6:163167830-163167831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs575431103	chr6:163167871-163167872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138680429	chr6:163167880-163167881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560636468	chr6:163167894-163167895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs529827322	chr6:163167940-163167941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540135085	chr6:163167969-163167970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs560057863	chr6:163168153-163168154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs141695194	chr6:163168183-163168184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552451240	chr6:163168184-163168185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145606101	chr6:163168197-163168198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556711007	chr6:163171218-163171219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573796732	chr6:163171245-163171246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150156709	chr6:163171268-163171269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs113496238	chr6:163171305-163171306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs112071729	chr6:163171306-163171307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs117812607	chr6:163171334-163171335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs189586980	chr6:163171343-163171344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs111542018	chr6:163171345-163171346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541471327	chr6:163171441-163171442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573942304	chr6:163171459-163171460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs572706929	chr6:163171591-163171592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539796410	chr6:163171613-163171614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs564917013	chr6:163171627-163171628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs533637758	chr6:163171655-163171656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550508937	chr6:163171669-163171670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532044736	chr6:163171688-163171689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181921907	chr6:163171706-163171707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs4568424	chr6:163171796-163171797	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs565810805	chr6:163171805-163171806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534309338	chr6:163171889-163171890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557361038	chr6:163171892-163171893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570933331	chr6:163171904-163171905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536913927	chr6:163171955-163171956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186297688	chr6:163171960-163171961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529880867	chr6:163171968-163171969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs9347686	chr6:163171970-163171971	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs536487547	chr6:163171977-163171978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs555562476	chr6:163171995-163171996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs572530304	chr6:163172070-163172071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs560143023	chr6:163172074-163172075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73601934	chr6:163172113-163172114	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs189457494	chr6:163172183-163172184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552257229	chr6:163172185-163172186	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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	22037309	CNVD

Chromatin state (count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163167600-163168200	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr6:163171200-163172800	Enhancers	A549	lung
3	chr6:163171600-163172200	Enhancers	Muscle Satellite Cultured Cells	--
4	chr6:163171600-163172400	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr6:163171800-163172200	Enhancers	NH-A	brain
6	chr6:163172200-163172600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr6:163172600-163173000	Enhancers	Muscle Satellite Cultured Cells	--
8	chr6:163181200-163181600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
9	chr6:163181200-163181800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr6:163183600-163184000	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr6:163186200-163186600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr6:163186200-163186600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr6:163192800-163194400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:163192800-163194400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:163206600-163207200	Enhancers	Left Ventricle	heart
16	chr6:163206800-163207000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr6:163206800-163207200	Enhancers	Right Atrium	heart
18	chr6:163219400-163219800	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr6:163219600-163219800	Enhancers	Brain Substantia Nigra	brain
20	chr6:163219600-163220000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr6:163219800-163220200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr6:163219800-163220200	Active TSS	Brain Substantia Nigra	brain
23	chr6:163220000-163220200	Enhancers	Brain Angular Gyrus	brain
24	chr6:163221000-163221200	Enhancers	Brain Substantia Nigra	brain
25	chr6:163230400-163230800	Weak transcription	Pancreas	Pancrea
26	chr6:163230800-163231200	ZNF genes & repeats	Pancreas	Pancrea
27	chr6:163230800-163238400	Weak transcription	Gastric	stomach
28	chr6:163231200-163237800	Weak transcription	Pancreas	Pancrea
29	chr6:163232600-163240000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr6:163235200-163235600	Weak transcription	Brain Anterior Caudate	brain
31	chr6:163235200-163236000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:163235600-163236000	Active TSS	Brain Anterior Caudate	brain
33	chr6:163235600-163236200	Enhancers	Brain Hippocampus Middle	brain
34	chr6:163236000-163242000	Weak transcription	Brain Anterior Caudate	brain
35	chr6:163236200-163241000	Weak transcription	Brain Hippocampus Middle	brain
36	chr6:163237800-163238600	ZNF genes & repeats	Pancreas	Pancrea
37	chr6:163238000-163238200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr6:163238000-163238600	Enhancers	NHDF-Ad	bronchial
39	chr6:163238200-163238400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr6:163238400-163238600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr6:163238400-163238600	Enhancers	Gastric	stomach
42	chr6:163240600-163243000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr6:163241000-163241800	Enhancers	Brain Hippocampus Middle	brain
44	chr6:163241400-163242200	Enhancers	Fetal Brain Female	brain
45	chr6:163241400-163242400	Enhancers	Brain Angular Gyrus	brain
46	chr6:163241800-163242200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr6:163241800-163242200	Weak transcription	Brain Hippocampus Middle	brain
48	chr6:163241800-163242600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr6:163241800-163242800	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr6:163241800-163242800	Enhancers	Fetal Brain Male	brain

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