Variant report

Variant	nsv603239
Chromosome Location	chr6:58285920-58770624
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1340)
CpG islands
(count:918)
Chromatin interactive
region (count:3)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1340 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:58312840-58313086	GM12878	blood:	n/a	n/a
2	ATF2	chr6:58287667-58287899	GM12878	blood:	n/a	n/a
3	ATF2	chr6:58287566-58287962	GM12878	blood:	n/a	n/a
4	BATF	chr6:58312874-58313176	GM12878	blood:	n/a	chr6:58313100-58313108
5	BATF	chr6:58287533-58287892	GM12878	blood:	n/a	n/a
6	BATF	chr6:58764416-58764615	GM12878	blood:	n/a	n/a
7	BATF	chr6:58737236-58737386	GM12878	blood:	n/a	n/a
8	BATF	chr6:58326544-58326859	GM12878	blood:	n/a	n/a
9	BATF	chr6:58312874-58313181	GM12878	blood:	n/a	chr6:58313100-58313108
10	BCL11A	chr6:58312939-58313153	GM12878	blood:	n/a	chr6:58313103-58313112
11	BCL11A	chr6:58737244-58737378	GM12878	blood:	n/a	n/a
12	BCL11A	chr6:58287319-58287843	GM12878	blood:	n/a	n/a
13	BCL11A	chr6:58287570-58287800	GM12878	blood:	n/a	n/a
14	BCL11A	chr6:58312858-58313167	GM12878	blood:	n/a	chr6:58313103-58313112
15	BCLAF1	chr6:58287548-58287910	GM12878	blood:	n/a	n/a
16	BCLAF1	chr6:58287452-58288025	GM12878	blood:	n/a	n/a
17	BCLAF1	chr6:58312816-58313161	GM12878	blood:	n/a	chr6:58313103-58313112
18	BHLHE40	chr6:58737228-58737405	HepG2	liver:	n/a	n/a
19	BHLHE40	chr6:58312965-58313069	GM12878	blood:	n/a	n/a
20	CBX3	chr6:58287498-58287998	K562	blood:	n/a	n/a
21	CBX3	chr6:58287493-58287955	K562	blood:	n/a	n/a
22	CCNT2	chr6:58287622-58287859	K562	blood:	n/a	n/a
23	CEBPB	chr6:58385936-58386118	IMR90	lung:	n/a	n/a
24	CEBPB	chr6:58287720-58287958	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr6:58441968-58442111	HepG2	liver:	n/a	chr6:58442072-58442083 chr6:58442073-58442084
26	CEBPB	chr6:58287831-58287968	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:58334093-58334264	HepG2	liver:	n/a	chr6:58334239-58334250 chr6:58334239-58334248 chr6:58334237-58334250 chr6:58334239-58334248 chr6:58334239-58334248 chr6:58334237-58334250 chr6:58334239-58334250 chr6:58334239-58334248 chr6:58334237-58334250 chr6:58334237-58334248
28	CEBPB	chr6:58357831-58357857	HepG2	liver:	n/a	chr6:58357833-58357844 chr6:58357834-58357845
29	CEBPB	chr6:58302675-58303028	K562	blood:	n/a	n/a
30	CEBPB	chr6:58506303-58506382	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:58576509-58576728	HepG2	liver:	n/a	n/a
32	CEBPB	chr6:58524581-58524685	IMR90	lung:	n/a	n/a
33	CEBPB	chr6:58287573-58287962	K562	blood:	n/a	n/a
34	CEBPB	chr6:58524736-58524936	Hela-S3	cervix:	n/a	n/a
35	CEBPD	chr6:58300940-58301286	K562	blood:	n/a	n/a
36	CEBPD	chr6:58302568-58303070	K562	blood:	n/a	n/a
37	CEBPD	chr6:58287449-58287865	HepG2	liver:	n/a	n/a
38	CEBPD	chr6:58287424-58287881	K562	blood:	n/a	n/a
39	CHD2	chr6:58312973-58313106	GM12878	blood:	n/a	n/a
40	CHD2	chr6:58287662-58287760	GM12878	blood:	n/a	n/a
41	CHD2	chr6:58364578-58364789	K562	blood:	n/a	n/a
42	CHD2	chr6:58287615-58287825	Hela-S3	cervix:	n/a	n/a
43	CREB1	chr6:58287533-58287896	A549	lung:	n/a	n/a
44	CTCF	chr6:58287619-58287895	SK-N-SH_RA	brain:	n/a	chr6:58287791-58287807 chr6:58287792-58287805 chr6:58287790-58287808 chr6:58287792-58287805
45	CTCF	chr6:58329860-58330010	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:58329720-58330010	WI-38	lung:	n/a	n/a
47	CTCF	chr6:58287600-58287939	MCF-7	breast:	n/a	chr6:58287791-58287807 chr6:58287792-58287805 chr6:58287790-58287808 chr6:58287792-58287805
48	CTCF	chr6:58329820-58329970	RPTEC	kidney:	n/a	n/a
49	CTCF	chr6:58418361-58418384	K562	blood:	n/a	n/a
50	CTCF	chr6:58361598-58361769	GM12878	blood:	n/a	n/a

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:58287827-58287877	HPAEpiC	pulmonary alveolar:	n/a
2	chr6:58290947-58290997	ovcar-3	ovarian:	n/a
3	chr6:58287827-58287877	SAEC	small airway:	n/a
4	chr6:58287827-58287877	HPAEpiC	pulmonary alveolar:	n/a
5	chr6:58290947-58290997	ovcar-3	ovarian:	n/a
6	chr6:58287827-58287877	SAEC	small airway:	n/a
7	chr6:58399599-58399649	AG04449	skin:	fetal
8	chr6:58286735-58286785	GM06990	blood:	n/a
9	chr6:58399599-58399649	SK-N-SH_RA	brain:	n/a
10	chr6:58287430-58287480	MCF10A-Er-Src	breast:	n/a
11	chr6:58399599-58399649	Hela-S3	cervix:	n/a
12	chr6:58287822-58287872	ECC-1	luminal epithelium:	n/a
13	chr6:58289118-58289168	AG09319	gingival:	n/a
14	chr6:58399599-58399649	SKMC	muscle:	n/a
15	chr6:58584053-58584103	AG04449	skin:	fetal
16	chr6:58399664-58399714	Hepatocyte	liver:	n/a
17	chr6:58287822-58287872	GM12878	blood:	n/a
18	chr6:58287758-58287808	HCM	heart:	n/a
19	chr6:58289118-58289168	AG04449	skin:	fetal
20	chr6:58287822-58287872	PrEC	prostate:	n/a
21	chr6:58287430-58287480	GM12878	blood:	n/a
22	chr6:58286735-58286785	GM12878	blood:	n/a
23	chr6:58399664-58399714	SKMC	muscle:	n/a
24	chr6:58399664-58399714	HNPCEpiC	eye:	n/a
25	chr6:58290947-58290997	Caco-2	colon:	n/a
26	chr6:58399664-58399714	Caco-2	colon:	n/a
27	chr6:58399664-58399714	AoSMC	blood vessel:	n/a
28	chr6:58287822-58287872	AG04450	lung:	fetal
29	chr6:58287825-58287875	CMK	blood:	n/a
30	chr6:58290947-58290997	HCF	heart:	n/a
31	chr6:58289131-58289181	GM12891	blood:	n/a
32	chr6:58584053-58584103	Hela-S3	cervix:	n/a
33	chr6:58289118-58289168	GM12878	blood:	n/a
34	chr6:58287827-58287877	ovcar-3	ovarian:	n/a
35	chr6:58287827-58287877	HCT-116	colon:	n/a
36	chr6:58399664-58399714	H1-hESC	embryonic stem cell:	embryo
37	chr6:58287825-58287875	AG04449	skin:	fetal
38	chr6:58287827-58287877	HNPCEpiC	eye:	n/a
39	chr6:58399599-58399649	HCM	heart:	n/a
40	chr6:58286735-58286785	AG09319	gingival:	n/a
41	chr6:58289131-58289181	SK-N-SH_RA	brain:	n/a
42	chr6:58287758-58287808	AG04449	skin:	fetal
43	chr6:58287938-58287988	HL-60	blood:	n/a
44	chr6:58289118-58289168	MCF10A-Er-Src	breast:	n/a
45	chr6:58399664-58399714	NT2-D1	testis:	n/a
46	chr6:58287822-58287872	AoSMC	blood vessel:	n/a
47	chr6:58290947-58290997	BE2_C	brain:	n/a
48	chr6:58287758-58287808	AG10803	skin:	n/a
49	chr6:58287825-58287875	SK-N-MC	brain:	n/a
50	chr6:58287430-58287480	PANC-1	pancreas:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:58293670..58295896-chr6:58296442..58300027,3	K562	blood:
2	chr5:37379216..37379885-chr6:58287233..58287739,2	Hela-S3	cervix:
3	chr6:58293670..58295896-chr6:58296442..58298545,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAG2-7	chr6:58513504-58513860	ENSG00000223633.2
2	lnc-RAB23-3	chr6:58287430-58287502	NONHSAT113319
3	lnc-BAG2-12	chr6:58294832-58295048	l_3195_chr6:58290605-58295048_testes
4	lnc-BAG2-6	chr6:58291908-58292021	ENSG00000225096
5	lnc-RAB23-3	chr6:58287599-58287654	NONHSAT113319
6	lnc-BAG2-6	chr6:58297873-58297934	ENSG00000225096
7	lnc-BAG2-7	chr6:58488888-58489027	ENSG00000223633.2
8	lnc-RAB23-19	chr6:58397998-58399412	NONHSAT113321
9	lnc-RAB23-3	chr6:58287430-58287502	NONHSAT113317
10	lnc-BAG2-7	chr6:58488888-58489027	ENSG00000223633.1
11	lnc-BAG2-12	chr6:58290606-58290988	l_3195_chr6:58290605-58295048_testes
12	lnc-RAB23-3	chr6:58287599-58287654	NONHSAT113317
13	lnc-BAG2-6	chr6:58298372-58298496	ENSG00000225096

No data

Variant related genes	Relation type
LINC00680	TF binding region
GAPDHP15	TF binding region
ENSG00000225096	TF binding region
ENSG00000223633	TF binding region
ENSG00000216687	TF binding region
RBBP4P4	TF binding region
LINC00680	CpG island
GAPDHP15	CpG island
ENSG00000225096	CpG island
ENSG00000223633	CpG island
ENSG00000216687	CpG island
RBBP4P4	CpG island
ENSG00000082068	chromatin interactions
ENSG00000214563	chromatin interactions

Extended variants
information (count: 3466 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3466 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4469327	chr6:58285920-58285921	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561005963	chr6:58285941-58285942	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs547751092	chr6:58285957-58285958	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs576706835	chr6:58285971-58285972	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs543985279	chr6:58285991-58285992	Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs565482133	chr6:58286018-58286019	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs532659291	chr6:58286060-58286061	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs372926570	chr6:58286079-58286080	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs548089837	chr6:58286099-58286100	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs559474492	chr6:58286102-58286103	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs530078924	chr6:58286202-58286203	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs548275596	chr6:58286216-58286217	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs373916269	chr6:58286270-58286271	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs200015816	chr6:58286309-58286310	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs369823321	chr6:58286313-58286314	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs75174700	chr6:58286330-58286331	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs569770533	chr6:58286350-58286351	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs181938660	chr6:58286356-58286357	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs578077770	chr6:58286363-58286364	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs377521562	chr6:58286453-58286454	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs111356813	chr6:58286484-58286485	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs571443353	chr6:58286495-58286496	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs567527670	chr6:58286537-58286538	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs186933705	chr6:58286540-58286541	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs370764224	chr6:58286549-58286550	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs373191115	chr6:58286552-58286553	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs565669163	chr6:58286559-58286560	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs536299255	chr6:58286576-58286577	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs554608073	chr6:58286587-58286588	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs71549776	chr6:58286627-58286628	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs191352944	chr6:58286634-58286635	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs70993114	chr6:58286637-58286638	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs181358272	chr6:58286727-58286728	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs377469630	chr6:58286840-58286841	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs543516577	chr6:58286849-58286850	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs558854560	chr6:58286857-58286858	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs536348510	chr6:58286882-58286883	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs577394573	chr6:58286922-58286923	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs541354199	chr6:58286924-58286925	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs559668515	chr6:58286938-58286939	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs71550553	chr6:58286981-58286982	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs377140745	chr6:58287019-58287020	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541783588	chr6:58287073-58287074	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs370268613	chr6:58287091-58287092	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563358486	chr6:58287124-58287125	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs200381870	chr6:58287238-58287239	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs373679395	chr6:58287239-58287240	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs146555904	chr6:58287243-58287244	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs113766643	chr6:58287248-58287249	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs530885708	chr6:58287249-58287250	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Neuroblastoma	16790693	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
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:413 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:58244200-58287200	Weak transcription	Right Ventricle	heart
2	chr6:58250800-58287200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:58261400-58286600	Weak transcription	Brain Germinal Matrix	brain
4	chr6:58270200-58287200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr6:58270600-58287000	Weak transcription	Brain Anterior Caudate	brain
6	chr6:58270800-58286600	Weak transcription	Osteobl	bone
7	chr6:58271000-58286600	Weak transcription	NHDF-Ad	bronchial
8	chr6:58271000-58287000	Weak transcription	NHEK	skin
9	chr6:58271000-58287000	Weak transcription	NHLF	lung
10	chr6:58271000-58287200	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr6:58271200-58286600	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr6:58271200-58287000	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr6:58271400-58286600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr6:58271400-58287200	Weak transcription	Pancreas	Pancrea
15	chr6:58271600-58287000	Weak transcription	Colonic Mucosa	Colon
16	chr6:58271600-58287200	Weak transcription	Small Intestine	intestine
17	chr6:58272000-58287200	Weak transcription	HSMM	muscle
18	chr6:58272400-58287000	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr6:58272400-58287200	Weak transcription	Primary B cells from cord blood	blood
20	chr6:58272600-58287000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr6:58273200-58287000	Weak transcription	HUVEC	blood vessel
22	chr6:58273200-58287200	Weak transcription	Placenta	Placenta
23	chr6:58273400-58286600	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr6:58273400-58286600	Weak transcription	GM12878-XiMat	blood
25	chr6:58273400-58287200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr6:58273600-58286600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr6:58273600-58287200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr6:58273600-58287200	Weak transcription	Brain Substantia Nigra	brain
29	chr6:58273800-58286600	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr6:58273800-58287000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr6:58274000-58286600	Weak transcription	Fetal Kidney	kidney
32	chr6:58274000-58287000	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr6:58274000-58287000	Weak transcription	Rectal Smooth Muscle	rectum
34	chr6:58274200-58286600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr6:58275200-58286600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr6:58275400-58286400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr6:58275400-58286600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr6:58275400-58286600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr6:58275400-58286600	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr6:58275400-58287000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr6:58275400-58287000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr6:58275400-58287000	Weak transcription	Duodenum Mucosa	Duodenum
43	chr6:58275400-58287000	Weak transcription	Fetal Muscle Leg	muscle
44	chr6:58275400-58287200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr6:58275400-58287200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr6:58275400-58287200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr6:58275400-58287200	Weak transcription	Aorta	Aorta
48	chr6:58275400-58287200	Weak transcription	Esophagus	oesophagus
49	chr6:58275400-58287200	Weak transcription	Gastric	stomach
50	chr6:58275400-58287200	Weak transcription	Sigmoid Colon	Sigmoid Colon

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