Variant report

Variant	nsv970709
Chromosome Location	chr6:163342264-163409316
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	chr6:163385583-163386388	HCT-116	colon:	n/a	n/a
2	CBX3	chr6:163385655-163386353	HCT-116	colon:	n/a	n/a
3	CEBPB	chr6:163385672-163386327	HCT-116	colon:	n/a	n/a
4	CEBPB	chr6:163385746-163386445	HCT-116	colon:	n/a	n/a
5	CEBPB	chr6:163384837-163385142	IMR90	lung:	n/a	n/a
6	CEBPB	chr6:163385817-163386320	IMR90	lung:	n/a	n/a
7	CHD2	chr6:163342515-163342650	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr6:163398907-163398925	LNCaP	prostate:	n/a	n/a
9	CTCF	chr6:163364360-163364510	HBMEC	blood vessel:	n/a	n/a
10	CTCF	chr6:163405131-163405173	LNCaP	prostate:	n/a	n/a
11	CTCF	chr6:163342319-163342345	H1-hESC	embryonic stem cell:	n/a	chr6:163342324-163342337
12	CTCF	chr6:163357067-163357107	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr6:163364764-163364779	Fibrobl	skin:	n/a	n/a
14	CTCF	chr6:163364620-163364770	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr6:163364340-163364490	HBMEC	blood vessel:	n/a	n/a
16	CTCF	chr6:163385660-163385810	NHDF-neo	bronchial:	n/a	n/a
17	CTCF	chr6:163364560-163364710	GM12865	blood:	n/a	n/a
18	CTCF	chr6:163364560-163364710	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr6:163342260-163342410	WERI-Rb-1	eye:	n/a	chr6:163342324-163342337
20	CTCF	chr6:163342220-163342370	GM12871	blood:	n/a	chr6:163342324-163342337
21	CTCF	chr6:163364644-163364718	H1-hESC	embryonic stem cell:	n/a	n/a
22	E2F4	chr6:163355752-163355963	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr6:163385218-163385631	MCF10A-Er-Src	breast:	n/a	n/a
24	EP300	chr6:163373455-163373759	SK-N-SH_RA	brain:	n/a	chr6:163373516-163373529
25	EP300	chr6:163385755-163386147	SK-N-SH_RA	brain:	n/a	n/a
26	EP300	chr6:163373427-163373700	SK-N-SH_RA	brain:	n/a	chr6:163373516-163373529
27	EP300	chr6:163385478-163386462	SK-N-SH	brain:	n/a	n/a
28	EP300	chr6:163385446-163386483	SK-N-SH	brain:	n/a	n/a
29	EP300	chr6:163385625-163386215	SK-N-SH_RA	brain:	n/a	n/a
30	FOS	chr6:163383223-163383489	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr6:163395381-163395720	MCF10A-Er-Src	breast:	n/a	chr6:163395533-163395542 chr6:163395534-163395541 chr6:163395535-163395546 chr6:163395534-163395543 chr6:163395532-163395544 chr6:163395534-163395542
32	FOS	chr6:163385751-163386192	MCF10A-Er-Src	breast:	n/a	chr6:163385820-163385830 chr6:163385812-163385822 chr6:163385812-163385822 chr6:163385820-163385830 chr6:163385812-163385822
33	FOS	chr6:163395454-163396054	MCF10A-Er-Src	breast:	n/a	chr6:163395533-163395542 chr6:163395534-163395541 chr6:163395535-163395546 chr6:163395534-163395543 chr6:163395532-163395544 chr6:163395534-163395542
34	FOS	chr6:163395383-163396057	MCF10A-Er-Src	breast:	n/a	chr6:163395533-163395542 chr6:163395534-163395541 chr6:163395535-163395546 chr6:163395534-163395543 chr6:163395532-163395544 chr6:163395534-163395542
35	FOS	chr6:163399783-163400105	MCF10A-Er-Src	breast:	n/a	chr6:163399914-163399923 chr6:163399916-163399927 chr6:163399914-163399924 chr6:163399915-163399924 chr6:163399913-163399925
36	FOS	chr6:163383251-163383454	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr6:163384975-163385009	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr6:163399805-163400072	MCF10A-Er-Src	breast:	n/a	chr6:163399914-163399923 chr6:163399916-163399927 chr6:163399914-163399924 chr6:163399915-163399924 chr6:163399913-163399925
39	FOS	chr6:163383159-163383461	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr6:163395382-163396058	MCF10A-Er-Src	breast:	n/a	chr6:163395533-163395542 chr6:163395534-163395541 chr6:163395535-163395546 chr6:163395534-163395543 chr6:163395532-163395544 chr6:163395534-163395542
41	FOS	chr6:163385686-163386217	MCF10A-Er-Src	breast:	n/a	chr6:163385820-163385830 chr6:163385812-163385822 chr6:163385812-163385822 chr6:163385820-163385830 chr6:163385812-163385822
42	FOS	chr6:163363974-163364214	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr6:163363939-163364250	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr6:163385755-163386215	MCF10A-Er-Src	breast:	n/a	chr6:163385820-163385830 chr6:163385812-163385822 chr6:163385812-163385822 chr6:163385820-163385830 chr6:163385812-163385822
45	FOS	chr6:163399783-163400048	MCF10A-Er-Src	breast:	n/a	chr6:163399914-163399923 chr6:163399916-163399927 chr6:163399914-163399924 chr6:163399915-163399924 chr6:163399913-163399925
46	FOS	chr6:163385630-163386329	MCF10A-Er-Src	breast:	n/a	chr6:163385820-163385830 chr6:163385812-163385822 chr6:163385812-163385822 chr6:163385820-163385830 chr6:163385812-163385822
47	FOSL1	chr6:163385670-163386292	HCT-116	colon:	n/a	chr6:163385820-163385830 chr6:163385812-163385822 chr6:163385812-163385822 chr6:163385820-163385830 chr6:163385812-163385822
48	FOSL1	chr6:163385554-163386328	HCT-116	colon:	n/a	chr6:163385820-163385830 chr6:163385812-163385822 chr6:163385812-163385822 chr6:163385820-163385830 chr6:163385812-163385822
49	FOSL2	chr6:163385497-163386233	SK-N-SH	brain:	n/a	chr6:163385820-163385830 chr6:163385812-163385822 chr6:163385812-163385822 chr6:163385820-163385830 chr6:163385812-163385822
50	FOSL2	chr6:163385601-163386261	SK-N-SH	brain:	n/a	chr6:163385820-163385830 chr6:163385812-163385822 chr6:163385812-163385822 chr6:163385820-163385830 chr6:163385812-163385822

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163362155-163362205	HEK293	kidney:	embryo
2	chr6:163362155-163362205	BJ	skin:	n/a
3	chr6:163362155-163362205	HCT-116	colon:	n/a
4	chr6:163362155-163362205	AG04449	skin:	fetal
5	chr6:163362155-163362205	NH-A	brain:	n/a
6	chr6:163362155-163362205	LNCaP	prostate:	n/a
7	chr6:163362155-163362205	ovcar-3	ovarian:	n/a
8	chr6:163362155-163362205	BE2_C	brain:	n/a
9	chr6:163362155-163362205	Jurkat	blood:	n/a
10	chr6:163362155-163362205	Hela-S3	cervix:	n/a
11	chr6:163362155-163362205	HAEpiC	amniotic membrane:	n/a
12	chr6:163362155-163362205	HPAEpiC	pulmonary alveolar:	n/a
13	chr6:163362155-163362205	AG10803	skin:	n/a
14	chr6:163362155-163362205	SK-N-SH_RA	brain:	n/a
15	chr6:163362155-163362205	HMEC	breast:	n/a
16	chr6:163362155-163362205	HRCEpiC	kidney:	n/a
17	chr6:163362155-163362205	NHDF-neo	bronchial:	n/a
18	chr6:163362155-163362205	RPTEC	kidney:	n/a
19	chr6:163362155-163362205	HUVEC	blood vessel:	n/a
20	chr6:163362155-163362205	GM06990	blood:	n/a
21	chr6:163362155-163362205	U87	brain:	n/a
22	chr6:163362155-163362205	AG09319	gingival:	n/a
23	chr6:163362155-163362205	IMR90	lung:	fetal
24	chr6:163362155-163362205	AoSMC	blood vessel:	n/a
25	chr6:163362155-163362205	H1-hESC	embryonic stem cell:	embryo
26	chr6:163362155-163362205	PFSK-1	brain:	n/a
27	chr6:163362155-163362205	HIPEpiC	eye:	n/a
28	chr6:163362155-163362205	SAEC	small airway:	n/a
29	chr6:163362155-163362205	HL-60	blood:	n/a
30	chr6:163362155-163362205	HCPEpiC	choroid plexus:	n/a
31	chr6:163362155-163362205	HCF	heart:	n/a
32	chr6:163362155-163362205	Caco-2	colon:	n/a
33	chr6:163362155-163362205	PrEC	prostate:	n/a
34	chr6:163362155-163362205	ProgFib	skin:	n/a
35	chr6:163362155-163362205	K562	blood:	n/a
36	chr6:163362155-163362205	NHBE	bronchial:	n/a
37	chr6:163362155-163362205	T-47D	breast:	n/a
38	chr6:163362155-163362205	HRE	kidney:	n/a
39	chr6:163362155-163362205	MCF-7	breast:	n/a
40	chr6:163362155-163362205	HRPEpiC	eye:	n/a
41	chr6:163362155-163362205	HCM	heart:	n/a
42	chr6:163362155-163362205	ECC-1	luminal epithelium:	n/a
43	chr6:163362155-163362205	HNPCEpiC	eye:	n/a
44	chr6:163362155-163362205	PANC-1	pancreas:	n/a
45	chr6:163362155-163362205	SK-N-MC	brain:	n/a
46	chr6:163362155-163362205	NB4	blood:	n/a
47	chr6:163362155-163362205	GM12892	blood:	n/a
48	chr6:163362155-163362205	GM19239	blood:	n/a
49	chr6:163362155-163362205	SKMC	muscle:	n/a
50	chr6:163362155-163362205	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:163383289..163384996-chr6:163389712..163391752,2	MCF-7	breast:
2	chr6:163383289..163384996-chr6:163389712..163391752,2	MCF-7	breast:

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

Variant related genes	Relation type
ENSG00000217557	TF binding region
ENSG00000217557	CpG island

Extended variants
information (count: 1416 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1416 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568053035	chr6:163342296-163342297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs147211865	chr6:163342304-163342305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533733447	chr6:163342308-163342309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs117407201	chr6:163342325-163342326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570632608	chr6:163342326-163342327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538722035	chr6:163342334-163342335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138504997	chr6:163342364-163342365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575685917	chr6:163342393-163342394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs544653089	chr6:163342419-163342420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191721302	chr6:163342443-163342444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184611952	chr6:163342451-163342452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs141691100	chr6:163342476-163342477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs4565281	chr6:163342501-163342502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532757163	chr6:163342504-163342505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76671504	chr6:163342511-163342512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs150742921	chr6:163342518-163342519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs75594236	chr6:163342526-163342527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577929611	chr6:163342538-163342539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs115372296	chr6:163342541-163342542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs999467	chr6:163342547-163342548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs4557497	chr6:163342610-163342611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs367934356	chr6:163342677-163342678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs139372435	chr6:163342718-163342719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs539644815	chr6:163342719-163342720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs558764403	chr6:163342749-163342750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs373908916	chr6:163342753-163342754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188750512	chr6:163342824-163342825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547542727	chr6:163342831-163342832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538242255	chr6:163343022-163343023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs118126501	chr6:163343056-163343057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs574898070	chr6:163343062-163343063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150041223	chr6:163343145-163343146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554470721	chr6:163343187-163343188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531080929	chr6:163343206-163343207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577345273	chr6:163343279-163343280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546412496	chr6:163343315-163343316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562239471	chr6:163343322-163343323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575683588	chr6:163343354-163343355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs541533721	chr6:163343356-163343357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs144320182	chr6:163343387-163343388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192861444	chr6:163343430-163343431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs28863850	chr6:163343453-163343454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs564438188	chr6:163343464-163343465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs111572277	chr6:163343523-163343524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532975027	chr6:163343526-163343527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs527538276	chr6:163343531-163343532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185831833	chr6:163343544-163343545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569872548	chr6:163343575-163343576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141030624	chr6:163343671-163343672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs549149565	chr6:163343676-163343677	Enhancers	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:237 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163341400-163343400	Enhancers	Fetal Stomach	stomach
2	chr6:163342200-163343000	Enhancers	Fetal Muscle Trunk	muscle
3	chr6:163342200-163343200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr6:163342200-163343400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr6:163343000-163344400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr6:163343200-163344000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr6:163357200-163357400	ZNF genes & repeats	Brain Cingulate Gyrus	brain
8	chr6:163357200-163359200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:163357400-163358000	Weak transcription	Brain Cingulate Gyrus	brain
10	chr6:163358600-163358800	Weak transcription	Spleen	Spleen
11	chr6:163359200-163362000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr6:163361000-163361200	Enhancers	Brain Substantia Nigra	brain
13	chr6:163361000-163361400	Enhancers	Brain Anterior Caudate	brain
14	chr6:163361200-163361400	Enhancers	Brain Hippocampus Middle	brain
15	chr6:163361200-163361600	Flanking Active TSS	Brain Substantia Nigra	brain
16	chr6:163361200-163362400	Active TSS	Brain Angular Gyrus	brain
17	chr6:163361400-163361800	Flanking Active TSS	Brain Hippocampus Middle	brain
18	chr6:163361400-163362200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr6:163361400-163362200	Active TSS	Brain Inferior Temporal Lobe	brain
20	chr6:163361400-163362400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
21	chr6:163361400-163362400	Enhancers	Fetal Brain Male	brain
22	chr6:163361400-163362400	Enhancers	Fetal Lung	lung
23	chr6:163361400-163362600	Active TSS	Brain Anterior Caudate	brain
24	chr6:163361400-163362600	Enhancers	Fetal Heart	heart
25	chr6:163361600-163361800	Enhancers	NHDF-Ad	bronchial
26	chr6:163361600-163362000	Active TSS	Brain Cingulate Gyrus	brain
27	chr6:163361600-163362200	Active TSS	Brain Substantia Nigra	brain
28	chr6:163361600-163362400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr6:163361600-163362600	Enhancers	Left Ventricle	heart
30	chr6:163361600-163364400	Enhancers	Fetal Intestine Small	intestine
31	chr6:163361800-163362200	Active TSS	NHDF-Ad	bronchial
32	chr6:163361800-163362400	Active TSS	Brain Hippocampus Middle	brain
33	chr6:163362000-163362600	Enhancers	Brain Cingulate Gyrus	brain
34	chr6:163362000-163362600	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr6:163362000-163362800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr6:163362000-163363400	Enhancers	Fetal Intestine Large	intestine
37	chr6:163362200-163362600	Enhancers	H1 Cell Line	embryonic stem cell
38	chr6:163362200-163362600	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr6:163362200-163362600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
40	chr6:163362200-163362600	Flanking Active TSS	Brain Substantia Nigra	brain
41	chr6:163362200-163362600	Flanking Active TSS	NHDF-Ad	bronchial
42	chr6:163362200-163363000	Enhancers	Brain Germinal Matrix	brain
43	chr6:163362400-163362600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr6:163362400-163362600	Flanking Active TSS	Brain Angular Gyrus	brain
45	chr6:163362400-163362600	Flanking Active TSS	Brain Hippocampus Middle	brain
46	chr6:163362400-163362600	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr6:163362400-163362800	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr6:163362400-163362800	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr6:163362400-163363200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:163362400-163363200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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