Variant report

Variant	nsv969455
Chromosome Location	chr6:149720845-149727255
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	chr6:149727101-149727335	K562	blood:	n/a	n/a
2	ATF3	chr6:149727009-149727485	K562	blood:	n/a	chr6:149727355-149727365
3	CEBPB	chr6:149727151-149727347	MCF-7	breast:	n/a	n/a
4	CEBPB	chr6:149727102-149727461	HepG2	liver:	n/a	n/a
5	CEBPB	chr6:149727143-149727356	K562	blood:	n/a	n/a
6	CEBPB	chr6:149727026-149727573	A549	lung:	n/a	n/a
7	CEBPB	chr6:149727112-149727471	IMR90	lung:	n/a	n/a
8	CEBPB	chr6:149727106-149727506	A549	lung:	n/a	n/a
9	CEBPB	chr6:149727046-149727522	K562	blood:	n/a	n/a
10	CEBPB	chr6:149727076-149727563	K562	blood:	n/a	n/a
11	CEBPB	chr6:149727151-149727402	HCT-116	colon:	n/a	n/a
12	CEBPB	chr6:149727097-149727635	Hela-S3	cervix:	n/a	n/a
13	E2F4	chr6:149727056-149727219	MCF10A-Er-Src	breast:	n/a	n/a
14	EP300	chr6:149727082-149727425	K562	blood:	n/a	n/a
15	FOS	chr6:149727099-149727574	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr6:149724810-149724998	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr6:149724796-149724945	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr6:149727073-149727723	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr6:149727089-149727605	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr6:149724704-149725015	MCF10A-Er-Src	breast:	n/a	n/a
21	IRF1	chr6:149726658-149726707	K562	blood:	n/a	n/a
22	JUN	chr6:149727121-149727413	HepG2	liver:	n/a	chr6:149727276-149727289
23	JUND	chr6:149727130-149727429	HepG2	liver:	n/a	n/a
24	JUND	chr6:149726695-149727442	K562	blood:	n/a	n/a
25	MAX	chr6:149727046-149727695	NB4	blood:	n/a	chr6:149727278-149727287 chr6:149727243-149727253 chr6:149727244-149727253 chr6:149727244-149727255 chr6:149727243-149727256 chr6:149727244-149727254 chr6:149727241-149727256 chr6:149727245-149727252 chr6:149727245-149727254
26	MAX	chr6:149727098-149727370	K562	blood:	n/a	chr6:149727278-149727287 chr6:149727243-149727253 chr6:149727244-149727253 chr6:149727244-149727255 chr6:149727243-149727256 chr6:149727244-149727254 chr6:149727241-149727256 chr6:149727245-149727252 chr6:149727245-149727254
27	MAX	chr6:149727099-149727344	K562	blood:	n/a	chr6:149727278-149727287 chr6:149727243-149727253 chr6:149727244-149727253 chr6:149727244-149727255 chr6:149727243-149727256 chr6:149727244-149727254 chr6:149727241-149727256 chr6:149727245-149727252 chr6:149727245-149727254
28	MAX	chr6:149727052-149727439	K562	blood:	n/a	chr6:149727278-149727287 chr6:149727243-149727253 chr6:149727244-149727253 chr6:149727244-149727255 chr6:149727243-149727256 chr6:149727244-149727254 chr6:149727241-149727256 chr6:149727245-149727252 chr6:149727245-149727254
29	MAX	chr6:149727104-149727362	Hela-S3	cervix:	n/a	chr6:149727278-149727287 chr6:149727243-149727253 chr6:149727244-149727253 chr6:149727244-149727255 chr6:149727243-149727256 chr6:149727244-149727254 chr6:149727241-149727256 chr6:149727245-149727252 chr6:149727245-149727254
30	MYC	chr6:149727155-149727327	K562	blood:	n/a	chr6:149727278-149727287 chr6:149727243-149727253 chr6:149727244-149727253 chr6:149727244-149727255 chr6:149727243-149727256 chr6:149727244-149727254 chr6:149727241-149727256 chr6:149727245-149727252 chr6:149727245-149727254
31	MYC	chr6:149727083-149727439	K562	blood:	n/a	chr6:149727278-149727287 chr6:149727243-149727253 chr6:149727244-149727253 chr6:149727244-149727255 chr6:149727243-149727256 chr6:149727244-149727254 chr6:149727241-149727256 chr6:149727245-149727252 chr6:149727245-149727254
32	MYC	chr6:149727015-149727450	MCF10A-Er-Src	breast:	n/a	chr6:149727278-149727287 chr6:149727243-149727253 chr6:149727244-149727253 chr6:149727244-149727255 chr6:149727243-149727256 chr6:149727244-149727254 chr6:149727241-149727256 chr6:149727245-149727252 chr6:149727245-149727254
33	MYC	chr6:149727025-149727650	NB4	blood:	n/a	chr6:149727278-149727287 chr6:149727243-149727253 chr6:149727244-149727253 chr6:149727244-149727255 chr6:149727243-149727256 chr6:149727244-149727254 chr6:149727241-149727256 chr6:149727245-149727252 chr6:149727245-149727254
34	MYC	chr6:149721330-149721490	MCF-7	breast:	n/a	n/a
35	MYC	chr6:149726705-149727459	MCF10A-Er-Src	breast:	n/a	chr6:149727278-149727287 chr6:149727243-149727253 chr6:149727244-149727253 chr6:149727244-149727255 chr6:149727243-149727256 chr6:149727244-149727254 chr6:149727241-149727256 chr6:149727245-149727252 chr6:149727245-149727254
36	MYC	chr6:149724681-149724823	MCF10A-Er-Src	breast:	n/a	n/a
37	MYC	chr6:149721324-149721468	H1-hESC	embryonic stem cell:	n/a	n/a
38	MYC	chr6:149726692-149727787	K562	blood:	n/a	chr6:149727278-149727287 chr6:149727243-149727253 chr6:149727244-149727253 chr6:149727244-149727255 chr6:149727243-149727256 chr6:149727244-149727254 chr6:149727241-149727256 chr6:149727245-149727252 chr6:149727245-149727254
39	MYC	chr6:149724740-149724967	MCF10A-Er-Src	breast:	n/a	n/a
40	MYC	chr6:149721330-149721493	MCF-7	breast:	n/a	n/a
41	POLR2A	chr6:149722735-149723449	K562	blood:	n/a	n/a
42	POLR2A	chr6:149725052-149725158	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr6:149723043-149723153	GM12878	blood:	n/a	n/a
44	POLR2A	chr6:149721378-149721478	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr6:149721367-149721514	MCF-7	breast:	n/a	n/a
46	POLR2A	chr6:149721343-149721536	MCF-7	breast:	n/a	n/a
47	POLR2A	chr6:149724639-149727754	K562	blood:	n/a	n/a
48	POLR2A	chr6:149726510-149726546	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr6:149722191-149722382	K562	blood:	n/a	n/a
50	POLR2A	chr6:149727000-149727212	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:149721425-149721475	GM12892	blood:	n/a
2	chr6:149721425-149721475	GM12892	blood:	n/a
3	chr6:149721457-149721507	Caco-2	colon:	n/a
4	chr6:149721359-149721409	GM12891	blood:	n/a
5	chr6:149721359-149721409	Jurkat	blood:	n/a
6	chr6:149721457-149721507	AG09319	gingival:	n/a
7	chr6:149721480-149721530	A549	lung:	n/a
8	chr6:149721376-149721426	HEK293	kidney:	embryo
9	chr6:149721145-149721195	NH-A	brain:	n/a
10	chr6:149721145-149721195	Hepatocyte	liver:	n/a
11	chr6:149721844-149721894	Hepatocyte	liver:	n/a
12	chr6:149721480-149721530	HCM	heart:	n/a
13	chr6:149721844-149721894	HepG2	liver:	n/a
14	chr6:149721145-149721195	K562	blood:	n/a
15	chr6:149721376-149721426	SK-N-MC	brain:	n/a
16	chr6:149721367-149721417	SK-N-SH_RA	brain:	n/a
17	chr6:149721457-149721507	AG09309	skin:	n/a
18	chr6:149721145-149721195	AG04450	lung:	fetal
19	chr6:149721367-149721417	HNPCEpiC	eye:	n/a
20	chr6:149721359-149721409	RPTEC	kidney:	n/a
21	chr6:149721425-149721475	MCF10A-Er-Src	breast:	n/a
22	chr6:149721844-149721894	SK-N-SH	brain:	n/a
23	chr6:149721145-149721195	SK-N-SH	brain:	n/a
24	chr6:149721367-149721417	A549	lung:	n/a
25	chr6:149721367-149721417	AoSMC	blood vessel:	n/a
26	chr6:149721376-149721426	AG10803	skin:	n/a
27	chr6:149721376-149721426	HCF	heart:	n/a
28	chr6:149721359-149721409	AG04450	lung:	fetal
29	chr6:149721359-149721409	Caco-2	colon:	n/a
30	chr6:149721359-149721409	HUVEC	blood vessel:	n/a
31	chr6:149721457-149721507	SK-N-SH_RA	brain:	n/a
32	chr6:149721480-149721530	SK-N-MC	brain:	n/a
33	chr6:149721376-149721426	BE2_C	brain:	n/a
34	chr6:149721480-149721530	SKMC	muscle:	n/a
35	chr6:149721457-149721507	GM06990	blood:	n/a
36	chr6:149721457-149721507	AG04450	lung:	fetal
37	chr6:149721145-149721195	HMEC	breast:	n/a
38	chr6:149721367-149721417	AG10803	skin:	n/a
39	chr6:149721359-149721409	CMK	blood:	n/a
40	chr6:149721425-149721475	AG10803	skin:	n/a
41	chr6:149721145-149721195	HNPCEpiC	eye:	n/a
42	chr6:149721457-149721507	K562	blood:	n/a
43	chr6:149721376-149721426	ovcar-3	ovarian:	n/a
44	chr6:149721359-149721409	HEK293	kidney:	embryo
45	chr6:149721376-149721426	AoSMC	blood vessel:	n/a
46	chr6:149721367-149721417	PFSK-1	brain:	n/a
47	chr6:149721367-149721417	RPTEC	kidney:	n/a
48	chr6:149721480-149721530	AG04449	skin:	fetal
49	chr6:149721457-149721507	NHBE	bronchial:	n/a
50	chr6:149721425-149721475	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:149637077..149638837-chr6:149727129..149729209,2	K562	blood:
2	chr6:149499792..149502412-chr6:149727216..149730047,2	K562	blood:

Variant related genes	Relation type
SUMO4	TF binding region
SUMO4	CpG island

Extended variants
information (count: 273 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:273 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17506789	chr6:149720846-149720847	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs541817485	chr6:149720888-149720889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561682914	chr6:149720901-149720902	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34097428	chr6:149720958-149720959	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs600739	chr6:149721024-149721025	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs13219372	chr6:149721049-149721050	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143026688	chr6:149721076-149721077	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs13203208	chr6:149721079-149721080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370573714	chr6:149721094-149721095	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs35598212	chr6:149721123-149721124	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140160276	chr6:149721134-149721135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs13203242	chr6:149721144-149721145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs193050139	chr6:149721146-149721147	Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs559989879	chr6:149721154-149721155	Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs147452423	chr6:149721160-149721161	Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs36010723	chr6:149721189-149721190	Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs142697068	chr6:149721207-149721208	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537145331	chr6:149721231-149721232	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185716896	chr6:149721275-149721276	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559643560	chr6:149721287-149721288	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs373734196	chr6:149721293-149721294	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs570868018	chr6:149721359-149721360	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs573295701	chr6:149721368-149721369	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs367925523	chr6:149721381-149721382	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs553311748	chr6:149721432-149721433	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs567134069	chr6:149721456-149721457	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs536188960	chr6:149721465-149721466	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs150999965	chr6:149721466-149721467	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs575355265	chr6:149721475-149721476	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs139591747	chr6:149721481-149721482	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs376636840	chr6:149721484-149721485	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs368757912	chr6:149721487-149721488	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs557792484	chr6:149721491-149721492	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs577687718	chr6:149721496-149721497	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs373938642	chr6:149721517-149721518	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200269880	chr6:149721518-149721519	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs78701690	chr6:149721528-149721529	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs17875292	chr6:149721529-149721530	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs141254994	chr6:149721536-149721537	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542559551	chr6:149721545-149721546	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200700577	chr6:149721554-149721555	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147083506	chr6:149721571-149721572	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530895667	chr6:149721589-149721590	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs377412354	chr6:149721649-149721650	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs527357500	chr6:149721668-149721669	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569573383	chr6:149721678-149721679	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs57327874	chr6:149721679-149721680	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs237025	chr6:149721690-149721691	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs371155775	chr6:149721701-149721702	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547199824	chr6:149721722-149721723	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
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
Follicular lymphoma	20505157	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
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149687800-149726400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:149700400-149728400	Weak transcription	Hela-S3	cervix
3	chr6:149700400-149732400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:149700600-149721200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr6:149700600-149721200	Weak transcription	Colonic Mucosa	Colon
6	chr6:149700600-149721200	Weak transcription	Right Ventricle	heart
7	chr6:149700600-149730800	Weak transcription	Fetal Brain Male	brain
8	chr6:149700800-149721000	Weak transcription	K562	blood
9	chr6:149700800-149721200	Weak transcription	Aorta	Aorta
10	chr6:149700800-149732800	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr6:149701200-149721200	Weak transcription	Brain Cingulate Gyrus	brain
12	chr6:149701400-149721200	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr6:149701400-149730800	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr6:149701400-149734200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr6:149701600-149733600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr6:149702400-149721200	Weak transcription	Fetal Brain Female	brain
17	chr6:149703200-149721200	Weak transcription	Spleen	Spleen
18	chr6:149703400-149721000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr6:149703400-149721200	Weak transcription	HSMMtube	muscle
20	chr6:149703400-149730600	Weak transcription	Brain Germinal Matrix	brain
21	chr6:149703600-149730400	Weak transcription	NHLF	lung
22	chr6:149705200-149721200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr6:149705200-149721200	Weak transcription	Stomach Smooth Muscle	stomach
24	chr6:149705200-149734600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr6:149707400-149721200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr6:149709400-149733000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr6:149709600-149721200	Weak transcription	Brain Hippocampus Middle	brain
28	chr6:149709600-149721200	Weak transcription	Gastric	stomach
29	chr6:149709600-149721200	Weak transcription	Left Ventricle	heart
30	chr6:149709600-149721200	Weak transcription	Lung	lung
31	chr6:149709600-149721200	Weak transcription	Ovary	ovary
32	chr6:149709600-149721200	Weak transcription	Pancreas	Pancrea
33	chr6:149709600-149721200	Weak transcription	NHEK	skin
34	chr6:149709600-149729800	Weak transcription	Fetal Heart	heart
35	chr6:149709600-149750200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr6:149709800-149721200	Weak transcription	Fetal Intestine Small	intestine
37	chr6:149710000-149721000	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr6:149710400-149721200	Weak transcription	Esophagus	oesophagus
39	chr6:149710600-149721200	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr6:149711000-149721000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr6:149711400-149721200	Weak transcription	Colon Smooth Muscle	Colon
42	chr6:149711400-149726000	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr6:149711400-149726600	Strong transcription	Monocytes-CD14+_RO01746	blood
44	chr6:149712000-149727200	Strong transcription	Primary hematopoietic stem cells	blood
45	chr6:149712200-149721200	Weak transcription	Rectal Smooth Muscle	rectum
46	chr6:149713000-149721200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr6:149713000-149721200	Weak transcription	Fetal Stomach	stomach
48	chr6:149713800-149721000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr6:149713800-149721200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr6:149713800-149721200	Weak transcription	Psoas Muscle	Psoas

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