Variant report

Variant	nsv601472
Chromosome Location	chr6:29922740-29937833
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:988)
CpG islands
(count:1525)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:988 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:29933748-29934309	K562	blood:	n/a	n/a
2	ARID3A	chr6:29935249-29935871	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:29932477-29933236	K562	blood:	n/a	n/a
4	ARID3A	chr6:29935252-29935904	K562	blood:	n/a	n/a
5	ARID3A	chr6:29931139-29931164	K562	blood:	n/a	n/a
6	ARID3A	chr6:29922852-29922901	K562	blood:	n/a	n/a
7	ARID3A	chr6:29932290-29932954	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:29937042-29937091	K562	blood:	n/a	n/a
9	ARID3A	chr6:29933775-29934240	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:29934522-29934914	K562	blood:	n/a	n/a
11	ATF1	chr6:29932584-29933076	K562	blood:	n/a	n/a
12	ATF1	chr6:29935286-29935585	K562	blood:	n/a	n/a
13	ATF2	chr6:29932433-29933091	GM12878	blood:	n/a	n/a
14	ATF2	chr6:29932488-29932978	GM12878	blood:	n/a	n/a
15	ATF3	chr6:29932615-29932943	K562	blood:	n/a	n/a
16	ATF3	chr6:29932539-29933023	K562	blood:	n/a	n/a
17	BACH1	chr6:29932453-29933278	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:29932608-29933062	K562	blood:	n/a	n/a
19	BATF	chr6:29932589-29933017	GM12878	blood:	n/a	chr6:29932797-29932808 chr6:29932798-29932808
20	BATF	chr6:29932612-29932987	GM12878	blood:	n/a	chr6:29932797-29932808 chr6:29932798-29932808
21	BCL11A	chr6:29932602-29932969	GM12878	blood:	n/a	chr6:29932797-29932806
22	BCL11A	chr6:29932639-29932881	GM12878	blood:	n/a	chr6:29932797-29932806
23	BCL3	chr6:29932533-29932943	GM12878	blood:	n/a	chr6:29932797-29932806
24	BCLAF1	chr6:29932428-29933119	GM12878	blood:	n/a	chr6:29932797-29932806
25	BCLAF1	chr6:29932494-29933203	GM12878	blood:	n/a	chr6:29932797-29932806
26	BHLHE40	chr6:29932548-29933279	GM12878	blood:	n/a	n/a
27	BHLHE40	chr6:29933714-29934091	HepG2	liver:	n/a	n/a
28	BHLHE40	chr6:29934607-29934610	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:29932569-29933159	K562	blood:	n/a	n/a
30	BHLHE40	chr6:29935166-29935758	K562	blood:	n/a	n/a
31	BHLHE40	chr6:29933866-29934118	GM12878	blood:	n/a	n/a
32	BHLHE40	chr6:29933686-29934301	K562	blood:	n/a	n/a
33	CBX3	chr6:29935109-29935665	K562	blood:	n/a	n/a
34	CBX3	chr6:29935905-29936437	HCT-116	colon:	n/a	n/a
35	CBX3	chr6:29933685-29934511	HCT-116	colon:	n/a	n/a
36	CBX3	chr6:29935860-29936460	HCT-116	colon:	n/a	n/a
37	CBX3	chr6:29932403-29933273	HCT-116	colon:	n/a	n/a
38	CBX3	chr6:29932504-29933475	K562	blood:	n/a	n/a
39	CBX3	chr6:29932608-29932997	K562	blood:	n/a	n/a
40	CCNT2	chr6:29935317-29935569	K562	blood:	n/a	n/a
41	CCNT2	chr6:29932623-29932970	K562	blood:	n/a	n/a
42	CEBPB	chr6:29929562-29929884	HepG2	liver:	n/a	n/a
43	CEBPB	chr6:29936002-29936359	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr6:29932409-29933285	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr6:29932577-29933269	K562	blood:	n/a	n/a
46	CEBPB	chr6:29934230-29934543	IMR90	lung:	n/a	n/a
47	CEBPB	chr6:29935073-29935816	K562	blood:	n/a	chr6:29935249-29935260 chr6:29935210-29935221
48	CEBPB	chr6:29935138-29935549	K562	blood:	n/a	chr6:29935249-29935260 chr6:29935210-29935221
49	CEBPB	chr6:29929504-29929848	K562	blood:	n/a	n/a
50	CEBPB	chr6:29932451-29933116	GM12878	blood:	n/a	n/a

(count:1525 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29933511-29933561	U87	brain:	n/a
2	chr6:29928362-29928412	HUVEC	blood vessel:	n/a
3	chr6:29924475-29924525	HIPEpiC	eye:	n/a
4	chr6:29928362-29928412	MCF-7	breast:	n/a
5	chr6:29923954-29924004	PFSK-1	brain:	n/a
6	chr6:29924299-29924349	HIPEpiC	eye:	n/a
7	chr6:29933971-29934021	HPAEpiC	pulmonary alveolar:	n/a
8	chr6:29924471-29924521	HAEpiC	amniotic membrane:	n/a
9	chr6:29924310-29924360	GM12892	blood:	n/a
10	chr6:29924310-29924360	NH-A	brain:	n/a
11	chr6:29924310-29924360	SK-N-SH_RA	brain:	n/a
12	chr6:29924407-29924457	IMR90	lung:	fetal
13	chr6:29924202-29924252	SKMC	muscle:	n/a
14	chr6:29924067-29924117	HCM	heart:	n/a
15	chr6:29933697-29933747	GM12892	blood:	n/a
16	chr6:29924404-29924454	AG09309	skin:	n/a
17	chr6:29933971-29934021	IMR90	lung:	fetal
18	chr6:29932743-29932793	AoSMC	blood vessel:	n/a
19	chr6:29924207-29924257	BJ	skin:	n/a
20	chr6:29924475-29924525	NHDF-neo	bronchial:	n/a
21	chr6:29923952-29924002	SK-N-SH	brain:	n/a
22	chr6:29924067-29924117	PrEC	prostate:	n/a
23	chr6:29932743-29932793	A549	lung:	n/a
24	chr6:29933915-29933965	NHDF-neo	bronchial:	n/a
25	chr6:29928362-29928412	GM06990	blood:	n/a
26	chr6:29923913-29923963	AG10803	skin:	n/a
27	chr6:29924310-29924360	AG04450	lung:	fetal
28	chr6:29932864-29932914	HL-60	blood:	n/a
29	chr6:29923954-29924004	HCPEpiC	choroid plexus:	n/a
30	chr6:29933971-29934021	HEEpiC	esophagus:	n/a
31	chr6:29933971-29934021	AoSMC	blood vessel:	n/a
32	chr6:29933925-29933975	GM12892	blood:	n/a
33	chr6:29923954-29924004	AG09319	gingival:	n/a
34	chr6:29932621-29932671	NT2-D1	testis:	n/a
35	chr6:29924202-29924252	BJ	skin:	n/a
36	chr6:29924404-29924454	HNPCEpiC	eye:	n/a
37	chr6:29933915-29933965	RPTEC	kidney:	n/a
38	chr6:29933915-29933965	NH-A	brain:	n/a
39	chr6:29933511-29933561	HRPEpiC	eye:	n/a
40	chr6:29933411-29933461	Hela-S3	cervix:	n/a
41	chr6:29928362-29928412	AG10803	skin:	n/a
42	chr6:29932621-29932671	GM06990	blood:	n/a
43	chr6:29932621-29932671	NHDF-neo	bronchial:	n/a
44	chr6:29933915-29933965	SKMC	muscle:	n/a
45	chr6:29928362-29928412	HPAEpiC	pulmonary alveolar:	n/a
46	chr6:29923695-29923745	MCF10A-Er-Src	breast:	n/a
47	chr6:29924207-29924257	SAEC	small airway:	n/a
48	chr6:29933925-29933975	Caco-2	colon:	n/a
49	chr6:29924475-29924525	AG04449	skin:	fetal
50	chr6:29924404-29924454	K562	blood:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:29892582..29894711-chr6:29932418..29935205,2	K562	blood:
2	chr6:29937399..29939324-chr6:29949163..29951713,2	K562	blood:
3	chr6:29926306..29930004-chr6:29943804..29947247,3	K562	blood:
4	chr6:29932263..29935141-chr6:29936079..29939709,3	K562	blood:
5	chr6:29927397..29931336-chr6:29932208..29936273,8	K562	blood:
6	chr6:29921960..29924230-chr6:29934596..29936833,2	K562	blood:
7	chr6:29815528..29816550-chr6:29935117..29936165,4	MCF-7	breast:
8	chr6:29927397..29931336-chr6:29932208..29936273,8	K562	blood:
9	chr14:77247003..77248532-chr6:29931290..29933642,2	K562	blood:
10	chr6:29921960..29924230-chr6:29934596..29936833,2	K562	blood:
11	chr6:29929604..29934270-chr6:29942846..29948120,6	K562	blood:
12	chr6:29931653..29934276-chr6:29943760..29946372,5	K562	blood:
13	chr6:29764926..29767618-chr6:29920990..29923179,3	MCF-7	breast:
14	chr6:29820931..29821695-chr6:29935492..29936150,2	MCF-7	breast:
15	chr6:29932263..29935141-chr6:29936079..29939709,3	K562	blood:
16	chr6:29937339..29939716-chr6:29942275..29944965,3	MCF-7	breast:
17	chr6:29917150..29919030-chr6:29920403..29922798,2	MCF-7	breast:
18	chr6:29937696..29939359-chr6:30032545..30034517,2	K562	blood:
19	chr6:29920547..29922811-chr6:29925895..29928597,2	MCF-7	breast:
20	chr6:29920527..29922060-chr6:29926055..29928693,2	K562	blood:
21	chr6:29820786..29821478-chr6:29935191..29935715,2	MCF-7	breast:
22	chr6:29920547..29922811-chr6:29925895..29928597,2	MCF-7	breast:
23	chr6:29933916..29936718-chr6:29943405..29945040,3	MCF-7	breast:
24	chr6:29917413..29919975-chr6:29932108..29934788,2	K562	blood:
25	chr6:29931492..29933251-chr6:30034694..30036479,2	K562	blood:
26	chr6:29931972..29934794-chr6:30027595..30029471,2	K562	blood:

No data

Variant related genes	Relation type
HLA-W	TF binding region
HLA-W	CpG island
ENSG00000204623	chromatin interactions
ENSG00000066379	chromatin interactions
ENSG00000204625	chromatin interactions
ENSG00000204619	chromatin interactions
ENSG00000259081	chromatin interactions
ENSG00000230795	chromatin interactions

Extended variants
information (count: 954 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:954 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16896742	chr6:29922740-29922741	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs367724541	chr6:29922741-29922742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs9260603	chr6:29922754-29922755	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs9260604	chr6:29922760-29922761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs114389840	chr6:29922763-29922764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs79506856	chr6:29922788-29922789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567476977	chr6:29922794-29922795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs77714616	chr6:29922806-29922807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114839838	chr6:29922810-29922811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs9260606	chr6:29922817-29922818	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs112970319	chr6:29922819-29922820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201103343	chr6:29922826-29922827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115494742	chr6:29922829-29922830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs116001094	chr6:29922849-29922850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs73725590	chr6:29922852-29922853	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs28780072	chr6:29922853-29922854	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs9260607	chr6:29922856-29922857	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs574436234	chr6:29922878-29922879	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs72848146	chr6:29922885-29922886	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs7763507	chr6:29922887-29922888	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
21	rs201096221	chr6:29922907-29922908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs9260608	chr6:29922913-29922914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9260609	chr6:29922926-29922927	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs9260610	chr6:29922932-29922933	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs1655915	chr6:29922934-29922935	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs386698616	chr6:29922944-29922945	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs386698617	chr6:29922962-29922963	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs200275650	chr6:29922963-29922964	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs200772546	chr6:29922981-29922982	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs9260614	chr6:29922995-29922996	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs7767914	chr6:29923000-29923001	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs2508036	chr6:29923008-29923009	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs9260615	chr6:29923020-29923021	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs7767668	chr6:29923023-29923024	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs9260616	chr6:29923032-29923033	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
36	rs536765394	chr6:29923057-29923058	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs9260617	chr6:29923060-29923061	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs73725593	chr6:29923063-29923064	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs371230687	chr6:29923077-29923078	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs9260618	chr6:29923079-29923080	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
41	rs9260619	chr6:29923086-29923087	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs114516961	chr6:29923090-29923091	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs9260620	chr6:29923091-29923092	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs4713267	chr6:29923116-29923117	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
45	rs554114183	chr6:29923119-29923120	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs9260621	chr6:29923126-29923127	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
47	rs9260622	chr6:29923128-29923129	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs75796752	chr6:29923136-29923137	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs7768084	chr6:29923137-29923138	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs9260623	chr6:29923140-29923141	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD

Chromatin state (count:713 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29912800-29924200	Weak transcription	Right Atrium	heart
2	chr6:29913000-29924000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr6:29913000-29924200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:29913400-29932200	Weak transcription	Brain Anterior Caudate	brain
5	chr6:29913400-29932600	Weak transcription	Brain Substantia Nigra	brain
6	chr6:29913600-29924400	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr6:29913600-29925400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr6:29913800-29932200	Weak transcription	Small Intestine	intestine
9	chr6:29914000-29923800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr6:29914000-29924200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr6:29914000-29932200	Weak transcription	Colon Smooth Muscle	Colon
12	chr6:29914600-29932200	Weak transcription	Colonic Mucosa	Colon
13	chr6:29914800-29932200	Weak transcription	Right Ventricle	heart
14	chr6:29915400-29931800	Weak transcription	Fetal Thymus	thymus
15	chr6:29915600-29932000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr6:29916400-29926400	Weak transcription	GM12878-XiMat	blood
17	chr6:29916800-29924400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:29916800-29928200	Weak transcription	HepG2	liver
19	chr6:29916800-29930000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr6:29916800-29932200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr6:29916800-29932200	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr6:29916800-29932200	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr6:29916800-29933000	Weak transcription	Esophagus	oesophagus
24	chr6:29916800-29933000	Weak transcription	Pancreas	Pancrea
25	chr6:29916800-29933200	Weak transcription	Lung	lung
26	chr6:29916800-29940200	Weak transcription	Gastric	stomach
27	chr6:29917000-29923400	Weak transcription	Stomach Smooth Muscle	stomach
28	chr6:29917000-29926800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr6:29917000-29931800	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr6:29917200-29926000	Weak transcription	Adipose Nuclei	Adipose
31	chr6:29917200-29926000	Weak transcription	Spleen	Spleen
32	chr6:29917200-29932000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr6:29917200-29932200	Weak transcription	Liver	Liver
34	chr6:29917200-29932200	Weak transcription	Brain Hippocampus Middle	brain
35	chr6:29917400-29927400	Weak transcription	Fetal Muscle Leg	muscle
36	chr6:29917800-29926400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr6:29917800-29932200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr6:29918000-29926000	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr6:29918000-29926600	Weak transcription	Primary B cells from peripheral blood	blood
40	chr6:29918000-29926600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr6:29918000-29932000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr6:29918000-29932200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr6:29918000-29932200	Weak transcription	Fetal Intestine Small	intestine
44	chr6:29918200-29925600	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr6:29918200-29926600	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr6:29918200-29931800	Weak transcription	Primary T cells from cord blood	blood
47	chr6:29918400-29925600	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr6:29918400-29927400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr6:29919000-29926800	Weak transcription	Primary B cells from cord blood	blood
50	chr6:29919800-29924200	Weak transcription	Left Ventricle	heart

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