Variant report

Variant	nsv886678
Chromosome Location	chr6:133550279-133631190
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	ATF3	chr6:133594012-133594132	K562	blood:	n/a	n/a
2	ATF3	chr6:133593811-133594231	A549	lung:	n/a	n/a
3	ATF3	chr6:133593875-133594187	A549	lung:	n/a	n/a
4	BACH1	chr6:133562969-133563328	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:133563677-133564366	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:133561788-133562724	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:133593897-133594281	K562	blood:	n/a	n/a
8	BATF	chr6:133575828-133576130	GM12878	blood:	n/a	n/a
9	BCL3	chr6:133593947-133594201	K562	blood:	n/a	n/a
10	BCLAF1	chr6:133593903-133594192	K562	blood:	n/a	n/a
11	BRCA1	chr6:133569086-133570297	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr6:133564377-133564805	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr6:133558051-133558488	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr6:133593847-133594281	GM12878	blood:	n/a	n/a
15	BRCA1	chr6:133561423-133562630	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr6:133593847-133594280	Hela-S3	cervix:	n/a	n/a
17	CCNT2	chr6:133593901-133594281	K562	blood:	n/a	n/a
18	CEBPB	chr6:133630769-133631097	HepG2	liver:	n/a	chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630922-133630933 chr6:133630922-133630931
19	CEBPB	chr6:133565725-133566378	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr6:133574131-133574827	ECC-1	luminal epithelium:	n/a	chr6:133574165-133574178
21	CEBPB	chr6:133575580-133576119	A549	lung:	n/a	n/a
22	CEBPB	chr6:133569575-133569985	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr6:133630758-133631086	IMR90	lung:	n/a	chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630922-133630933 chr6:133630922-133630931
24	CEBPB	chr6:133556456-133556767	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr6:133569692-133570006	A549	lung:	n/a	n/a
26	CEBPB	chr6:133611199-133611388	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr6:133575640-133576007	IMR90	lung:	n/a	n/a
28	CEBPB	chr6:133558048-133558480	A549	lung:	n/a	n/a
29	CEBPB	chr6:133608065-133608276	A549	lung:	n/a	n/a
30	CEBPB	chr6:133561904-133561970	A549	lung:	n/a	n/a
31	CEBPB	chr6:133575646-133575962	A549	lung:	n/a	n/a
32	CEBPB	chr6:133612150-133612485	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr6:133627113-133627388	HepG2	liver:	n/a	n/a
34	CEBPB	chr6:133569387-133570068	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr6:133569333-133570333	Hela-S3	cervix:	n/a	chr6:133570234-133570245 chr6:133570234-133570245
36	CEBPB	chr6:133630694-133631192	ECC-1	luminal epithelium:	n/a	chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630922-133630933 chr6:133630922-133630931
37	CEBPB	chr6:133569621-133570015	A549	lung:	n/a	n/a
38	CEBPB	chr6:133569610-133570048	IMR90	lung:	n/a	n/a
39	CEBPB	chr6:133568902-133569029	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr6:133557959-133558808	IMR90	lung:	n/a	n/a
41	CEBPB	chr6:133630750-133631095	Hela-S3	cervix:	n/a	chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630922-133630933 chr6:133630922-133630931
42	CEBPB	chr6:133566661-133566866	A549	lung:	n/a	n/a
43	CEBPB	chr6:133558034-133558590	A549	lung:	n/a	n/a
44	CEBPB	chr6:133557982-133558771	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr6:133630707-133631115	ECC-1	luminal epithelium:	n/a	chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630922-133630933 chr6:133630922-133630931
46	CEBPB	chr6:133607961-133608263	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr6:133566604-133566971	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr6:133575637-133575996	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr6:133558038-133558739	A549	lung:	n/a	n/a
50	CEBPB	chr6:133630813-133631078	A549	lung:	n/a	chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630920-133630931 chr6:133630920-133630933 chr6:133630922-133630931 chr6:133630922-133630933 chr6:133630922-133630931

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:133562196-133562246	Jurkat	blood:	n/a
2	chr6:133561719-133561769	SK-N-MC	brain:	n/a
3	chr6:133561614-133561664	ECC-1	luminal epithelium:	n/a
4	chr6:133564578-133564628	AoSMC	blood vessel:	n/a
5	chr6:133562196-133562246	Jurkat	blood:	n/a
6	chr6:133561719-133561769	SK-N-MC	brain:	n/a
7	chr6:133561614-133561664	ECC-1	luminal epithelium:	n/a
8	chr6:133564578-133564628	AoSMC	blood vessel:	n/a
9	chr6:133562267-133562317	HEEpiC	esophagus:	n/a
10	chr6:133561224-133561274	GM12892	blood:	n/a
11	chr6:133562035-133562085	HepG2	liver:	n/a
12	chr6:133562056-133562106	AG04450	lung:	fetal
13	chr6:133561224-133561274	Jurkat	blood:	n/a
14	chr6:133561716-133561766	NHDF-neo	bronchial:	n/a
15	chr6:133563868-133563918	U87	brain:	n/a
16	chr6:133561677-133561727	PrEC	prostate:	n/a
17	chr6:133561368-133561418	SK-N-MC	brain:	n/a
18	chr6:133562269-133562319	ProgFib	skin:	n/a
19	chr6:133561677-133561727	Hela-S3	cervix:	n/a
20	chr6:133562087-133562137	K562	blood:	n/a
21	chr6:133561368-133561418	SKMC	muscle:	n/a
22	chr6:133584189-133584239	LNCaP	prostate:	n/a
23	chr6:133561677-133561727	IMR90	lung:	fetal
24	chr6:133562336-133562386	GM06990	blood:	n/a
25	chr6:133559279-133559329	IMR90	lung:	fetal
26	chr6:133563868-133563918	HEEpiC	esophagus:	n/a
27	chr6:133562275-133562325	HCF	heart:	n/a
28	chr6:133561898-133561948	PrEC	prostate:	n/a
29	chr6:133563764-133563814	T-47D	breast:	n/a
30	chr6:133561886-133561936	HRCEpiC	kidney:	n/a
31	chr6:133561886-133561936	ovcar-3	ovarian:	n/a
32	chr6:133562267-133562317	AG04449	skin:	fetal
33	chr6:133561660-133561710	MCF-7	breast:	n/a
34	chr6:133561386-133561436	ProgFib	skin:	n/a
35	chr6:133562470-133562520	HMEC	breast:	n/a
36	chr6:133564466-133564516	GM06990	blood:	n/a
37	chr6:133561386-133561436	AG10803	skin:	n/a
38	chr6:133564066-133564116	GM06990	blood:	n/a
39	chr6:133563868-133563918	H1-hESC	embryonic stem cell:	embryo
40	chr6:133562494-133562544	GM12892	blood:	n/a
41	chr6:133562258-133562308	SK-N-SH_RA	brain:	n/a
42	chr6:133562485-133562535	NHDF-neo	bronchial:	n/a
43	chr6:133561719-133561769	Hela-S3	cervix:	n/a
44	chr6:133561814-133561864	U87	brain:	n/a
45	chr6:133563764-133563814	HCT-116	colon:	n/a
46	chr6:133561386-133561436	Caco-2	colon:	n/a
47	chr6:133561932-133561982	IMR90	lung:	fetal
48	chr6:133561886-133561936	ECC-1	luminal epithelium:	n/a
49	chr6:133562461-133562511	GM12891	blood:	n/a
50	chr6:133563532-133563582	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:133561719..133562540-chr9:100684595..100685146,2	Hela-S3	cervix:
2	chr6:133564949..133567622-chr6:133568456..133570501,2	MCF-7	breast:
3	chr19:24184300..24184982-chr6:133593600..133594102,2	MCF-7	breast:
4	chr19:24184476..24185016-chr6:133593470..133593971,2	MCF-7	breast:
5	chr6:133564949..133567622-chr6:133568456..133570501,2	MCF-7	breast:
6	chr6:133608197..133610275-chr6:133661303..133663477,2	MCF-7	breast:
7	chr6:133585301..133587177-chr6:133589198..133590844,2	K562	blood:
8	chr6:133607841..133608895-chr6:133689474..133690346,4	MCF-7	breast:
9	chr6:133585301..133587177-chr6:133589198..133590844,2	K562	blood:
10	chr6:133608130..133609733-chr6:133662657..133665396,2	K562	blood:
11	chr6:133607788..133608605-chr6:133833232..133834126,4	MCF-7	breast:
12	chr11:120081079..120081901-chr6:133563947..133564616,2	Hela-S3	cervix:
13	chr4:70296625..70297182-chr6:133594074..133594625,3	MCF-7	breast:
14	chr6:133134470..133136254-chr6:133566316..133568736,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPS12-6	chr6:133562511-133562887	NONHSAT114990
2	lnc-RPS12-6	chr6:133566236-133566367	NONHSAT114990
3	lnc-RPS12-6	chr6:133568002-133569991	NONHSAT114990

Variant related genes	Relation type
EYA4	TF binding region
EYA4	CpG island
ENSG00000184232	chromatin interactions
ENSG00000112306	chromatin interactions
ENSG00000136932	chromatin interactions

Extended variants
information (count: 2899 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2899 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551521626	chr6:133551216-133551217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs73773601	chr6:133551307-133551308	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs544136785	chr6:133551311-133551312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs7746298	chr6:133551344-133551345	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs574240195	chr6:133551361-133551362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113686757	chr6:133551393-133551394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs527558791	chr6:133551398-133551399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532515365	chr6:133554428-133554429	Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs370219651	chr6:133554443-133554444	Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs6569872	chr6:133554452-133554453	Bivalent/Poised TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs371303390	chr6:133554498-133554499	Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188427990	chr6:133554501-133554502	Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532541939	chr6:133554575-133554576	Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552553964	chr6:133554610-133554611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569223873	chr6:133554674-133554675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368669406	chr6:133554724-133554725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs73007659	chr6:133554726-133554727	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs548401055	chr6:133554729-133554730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548859986	chr6:133554785-133554786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs527705600	chr6:133556426-133556427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115778646	chr6:133556445-133556446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548000859	chr6:133556468-133556469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146340181	chr6:133556521-133556522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139641362	chr6:133556543-133556544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12211053	chr6:133556567-133556568	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs184819154	chr6:133556611-133556612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs568825645	chr6:133556633-133556634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537849536	chr6:133556701-133556702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142858686	chr6:133556708-133556709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537980094	chr6:133556728-133556729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs117747907	chr6:133556767-133556768	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs201024328	chr6:133556860-133556861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs151101770	chr6:133556886-133556887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187841724	chr6:133556888-133556889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570845758	chr6:133556960-133556961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539589541	chr6:133556986-133556987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113688193	chr6:133557004-133557005	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556240065	chr6:133557033-133557034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs28373668	chr6:133557079-133557080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575986744	chr6:133557126-133557127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373052349	chr6:133557142-133557143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113212096	chr6:133557152-133557153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs5880164	chr6:133557169-133557170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201766491	chr6:133557170-133557171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200881488	chr6:133557175-133557176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572735248	chr6:133557182-133557183	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541258335	chr6:133557225-133557226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs74502804	chr6:133557254-133557255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs370331637	chr6:133557268-133557269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs147944133	chr6:133557274-133557275	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Autism	21448237	CNVD
Autism	22495311	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
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	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
Ependymoma	16718352	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
Prostate cancer	18632612	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:823 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133551200-133551400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:133554400-133554600	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:133554400-133554800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:133556400-133556800	Enhancers	Hela-S3	cervix
5	chr6:133556800-133557200	Weak transcription	Hela-S3	cervix
6	chr6:133557000-133558000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr6:133557200-133559800	Enhancers	Hela-S3	cervix
8	chr6:133557400-133557600	Enhancers	Fetal Lung	lung
9	chr6:133557400-133558400	Enhancers	NHLF	lung
10	chr6:133557800-133559200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr6:133557800-133559400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:133557800-133559400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:133557800-133559400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr6:133557800-133559400	Enhancers	Muscle Satellite Cultured Cells	--
15	chr6:133557800-133559400	Enhancers	A549	lung
16	chr6:133558000-133558200	Enhancers	Fetal Stomach	stomach
17	chr6:133558000-133558200	Enhancers	Osteobl	bone
18	chr6:133558000-133558400	Enhancers	Adipose Nuclei	Adipose
19	chr6:133558000-133559000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr6:133558400-133558800	Weak transcription	NHLF	lung
21	chr6:133558800-133559400	Enhancers	NHLF	lung
22	chr6:133559000-133559400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr6:133559400-133560600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr6:133559400-133560800	Weak transcription	A549	lung
25	chr6:133559400-133561400	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr6:133559800-133560800	Weak transcription	Hela-S3	cervix
27	chr6:133560600-133560800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr6:133560800-133561000	Enhancers	Psoas Muscle	Psoas
29	chr6:133560800-133561000	Enhancers	A549	lung
30	chr6:133560800-133561200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr6:133560800-133561200	Enhancers	Hela-S3	cervix
32	chr6:133560800-133561400	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr6:133560800-133561400	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr6:133560800-133561600	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr6:133560800-133562000	Bivalent Enhancer	Fetal Heart	heart
36	chr6:133561000-133561400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
37	chr6:133561000-133561400	Flanking Active TSS	A549	lung
38	chr6:133561200-133561400	Bivalent Enhancer	Fetal Kidney	kidney
39	chr6:133561200-133561400	Flanking Active TSS	Hela-S3	cervix
40	chr6:133561200-133561600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr6:133561400-133561600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
42	chr6:133561400-133561600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
43	chr6:133561400-133561600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr6:133561400-133561600	Flanking Bivalent TSS/Enh	Fetal Kidney	kidney
45	chr6:133561400-133561600	Active TSS	Fetal Muscle Leg	muscle
46	chr6:133561400-133561800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
47	chr6:133561400-133561800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
48	chr6:133561400-133561800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
49	chr6:133561400-133561800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
50	chr6:133561400-133563400	Bivalent/Poised TSS	Fetal Lung	lung

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