Variant report

Variant	nsv1023443
Chromosome Location	chr8:6319260-6332157
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	ARID3A	chr8:6323049-6323486	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:6321256-6321847	HepG2	liver:	n/a	n/a
3	BHLHE40	chr8:6321381-6321736	HepG2	liver:	n/a	n/a
4	BHLHE40	chr8:6321392-6321688	HepG2	liver:	n/a	n/a
5	BHLHE40	chr8:6321267-6321818	HepG2	liver:	n/a	n/a
6	CEBPB	chr8:6321351-6321748	Hela-S3	cervix:	n/a	chr8:6321560-6321571
7	CEBPB	chr8:6321429-6321720	A549	lung:	n/a	chr8:6321560-6321571
8	CEBPB	chr8:6321383-6321746	HepG2	liver:	n/a	chr8:6321560-6321571
9	CEBPB	chr8:6321407-6321684	HepG2	liver:	n/a	chr8:6321560-6321571
10	CEBPB	chr8:6321392-6321716	HepG2	liver:	n/a	chr8:6321560-6321571
11	CEBPD	chr8:6321400-6321655	HepG2	liver:	n/a	n/a
12	CHD2	chr8:6323036-6323221	HepG2	liver:	n/a	n/a
13	CHD2	chr8:6321514-6321747	HepG2	liver:	n/a	n/a
14	CTCF	chr8:6321300-6321450	AG04449	skin:	n/a	chr8:6321395-6321416
15	CTCF	chr8:6321289-6321480	HepG2	liver:	n/a	chr8:6321395-6321416
16	CTCF	chr8:6329920-6330070	Caco-2	colon:	n/a	n/a
17	CTCF	chr8:6320640-6320790	HPAF	blood vessel:	n/a	chr8:6320737-6320750
18	CTCF	chr8:6321320-6321470	HEEpiC	esophagus:	n/a	chr8:6321395-6321416
19	CTCF	chr8:6320720-6320870	BE2_C	brain:	n/a	chr8:6320737-6320750
20	CTCF	chr8:6320641-6320846	H1-hESC	embryonic stem cell:	n/a	chr8:6320737-6320750
21	CTCF	chr8:6320640-6320905	K562	blood:	n/a	chr8:6320737-6320750
22	CTCF	chr8:6320738-6320788	K562	blood:	n/a	n/a
23	CTCF	chr8:6321280-6321430	SAEC	small airway:	n/a	chr8:6321395-6321416
24	CTCF	chr8:6321240-6321390	HMEC	breast:	n/a	n/a
25	CTCF	chr8:6321340-6321490	HEEpiC	esophagus:	n/a	chr8:6321395-6321416
26	CTCF	chr8:6320620-6320770	HBMEC	blood vessel:	n/a	chr8:6320737-6320750
27	CTCF	chr8:6321220-6321370	Caco-2	colon:	n/a	n/a
28	CTCF	chr8:6321260-6321410	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr8:6321307-6321456	Hela-S3	cervix:	n/a	chr8:6321395-6321416
30	CTCF	chr8:6320560-6320710	BE2_C	brain:	n/a	n/a
31	E2F4	chr8:6321453-6321628	MCF10A-Er-Src	breast:	n/a	n/a
32	EP300	chr8:6321310-6321810	HepG2	liver:	n/a	chr8:6321475-6321484
33	EP300	chr8:6321181-6321804	HepG2	liver:	n/a	chr8:6321475-6321484
34	EP300	chr8:6322909-6323477	HepG2	liver:	n/a	n/a
35	EP300	chr8:6321469-6321698	HepG2	liver:	n/a	chr8:6321475-6321484
36	EP300	chr8:6321063-6321485	SK-N-SH_RA	brain:	n/a	chr8:6321475-6321484
37	EP300	chr8:6323139-6323168	HepG2	liver:	n/a	n/a
38	EP300	chr8:6321062-6321481	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr8:6321577-6321932	SK-N-SH_RA	brain:	n/a	n/a
40	EP300	chr8:6320969-6321718	SK-N-SH	brain:	n/a	chr8:6321475-6321484
41	EP300	chr8:6320308-6322328	SK-N-SH	brain:	n/a	chr8:6320956-6320970 chr8:6321475-6321484
42	EP300	chr8:6321570-6321903	SK-N-SH_RA	brain:	n/a	n/a
43	FOS	chr8:6321321-6321626	MCF10A-Er-Src	breast:	n/a	chr8:6321475-6321484 chr8:6321474-6321483 chr8:6321473-6321485
44	FOS	chr8:6321303-6321663	MCF10A-Er-Src	breast:	n/a	chr8:6321475-6321484 chr8:6321474-6321483 chr8:6321473-6321485
45	FOS	chr8:6321336-6321653	MCF10A-Er-Src	breast:	n/a	chr8:6321475-6321484 chr8:6321474-6321483 chr8:6321473-6321485
46	FOS	chr8:6321299-6321713	MCF10A-Er-Src	breast:	n/a	chr8:6321475-6321484 chr8:6321474-6321483 chr8:6321473-6321485
47	FOSL2	chr8:6321070-6321831	SK-N-SH	brain:	n/a	chr8:6321475-6321484 chr8:6321474-6321485 chr8:6321474-6321483 chr8:6321473-6321485
48	FOSL2	chr8:6322989-6323481	HepG2	liver:	n/a	n/a
49	FOSL2	chr8:6322778-6323480	A549	lung:	n/a	n/a
50	FOSL2	chr8:6321281-6321846	HepG2	liver:	n/a	chr8:6321475-6321484 chr8:6321474-6321485 chr8:6321474-6321483 chr8:6321473-6321485

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6328807-6328857	BE2_C	brain:	n/a
2	chr8:6323131-6323181	HIPEpiC	eye:	n/a
3	chr8:6323131-6323181	GM19239	blood:	n/a
4	chr8:6323131-6323181	Caco-2	colon:	n/a
5	chr8:6321006-6321056	HepG2	liver:	n/a
6	chr8:6321006-6321056	HUVEC	blood vessel:	n/a
7	chr8:6321006-6321056	AG09309	skin:	n/a
8	chr8:6321006-6321056	HMEC	breast:	n/a
9	chr8:6321006-6321056	HRE	kidney:	n/a
10	chr8:6328807-6328857	HUVEC	blood vessel:	n/a
11	chr8:6328807-6328857	NH-A	brain:	n/a
12	chr8:6321006-6321056	LNCaP	prostate:	n/a
13	chr8:6321006-6321056	NT2-D1	testis:	n/a
14	chr8:6328807-6328857	HPAEpiC	pulmonary alveolar:	n/a
15	chr8:6323131-6323181	RPTEC	kidney:	n/a
16	chr8:6323131-6323181	HRPEpiC	eye:	n/a
17	chr8:6323131-6323181	NT2-D1	testis:	n/a
18	chr8:6323131-6323181	IMR90	lung:	fetal
19	chr8:6321006-6321056	H1-hESC	embryonic stem cell:	embryo
20	chr8:6328807-6328857	PANC-1	pancreas:	n/a
21	chr8:6321006-6321056	HRCEpiC	kidney:	n/a
22	chr8:6321006-6321056	NH-A	brain:	n/a
23	chr8:6328807-6328857	LNCaP	prostate:	n/a
24	chr8:6328807-6328857	SKMC	muscle:	n/a
25	chr8:6328807-6328857	GM06990	blood:	n/a
26	chr8:6328807-6328857	RPTEC	kidney:	n/a
27	chr8:6328807-6328857	HRCEpiC	kidney:	n/a
28	chr8:6323131-6323181	HPAEpiC	pulmonary alveolar:	n/a
29	chr8:6323131-6323181	LNCaP	prostate:	n/a
30	chr8:6321006-6321056	ECC-1	luminal epithelium:	n/a
31	chr8:6321006-6321056	Jurkat	blood:	n/a
32	chr8:6323131-6323181	BE2_C	brain:	n/a
33	chr8:6321006-6321056	MCF-7	breast:	n/a
34	chr8:6321006-6321056	HPAEpiC	pulmonary alveolar:	n/a
35	chr8:6321006-6321056	HCPEpiC	choroid plexus:	n/a
36	chr8:6323131-6323181	HL-60	blood:	n/a
37	chr8:6321006-6321056	PANC-1	pancreas:	n/a
38	chr8:6328807-6328857	NT2-D1	testis:	n/a
39	chr8:6321006-6321056	HCT-116	colon:	n/a
40	chr8:6328807-6328857	A549	lung:	n/a
41	chr8:6323131-6323181	HNPCEpiC	eye:	n/a
42	chr8:6321006-6321056	PrEC	prostate:	n/a
43	chr8:6328807-6328857	AG04449	skin:	fetal
44	chr8:6323131-6323181	SKMC	muscle:	n/a
45	chr8:6323131-6323181	HMEC	breast:	n/a
46	chr8:6328807-6328857	HCPEpiC	choroid plexus:	n/a
47	chr8:6328807-6328857	ProgFib	skin:	n/a
48	chr8:6321006-6321056	Hela-S3	cervix:	n/a
49	chr8:6321006-6321056	AG04450	lung:	fetal
50	chr8:6328807-6328857	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:6326969..6329620-chr8:6343917..6345900,2	K562	blood:
2	chr8:6286838..6288405-chr8:6317627..6319306,2	K562	blood:
3	chr8:6311610..6314385-chr8:6324095..6326791,2	K562	blood:
4	chr8:6308680..6311330-chr8:6317325..6320400,3	K562	blood:
5	chr8:6327001..6332096-chr8:6332476..6335725,6	K562	blood:

Variant related genes	Relation type
ENSG00000253550	TF binding region
MCPH1	TF binding region
ENSG00000253550	CpG island
MCPH1	CpG island
ENSG00000147316	chromatin interactions

Extended variants
information (count: 811 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:811 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7824209	chr8:6319260-6319261	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs2916743	chr8:6319284-6319285	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs537390348	chr8:6319290-6319291	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs11783794	chr8:6319330-6319331	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375587932	chr8:6319336-6319337	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2916742	chr8:6319337-6319338	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs118054038	chr8:6319360-6319361	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182848004	chr8:6319407-6319408	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs375527190	chr8:6319408-6319409	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147925060	chr8:6319411-6319412	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543661534	chr8:6319430-6319431	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs141789022	chr8:6319437-6319438	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532203574	chr8:6319504-6319505	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs2922818	chr8:6319522-6319523	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs73661748	chr8:6319546-6319547	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs561333561	chr8:6319567-6319568	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553016730	chr8:6319589-6319590	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187130758	chr8:6319607-6319608	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547263590	chr8:6319612-6319613	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2920660	chr8:6319647-6319648	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs147060365	chr8:6319673-6319674	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs527746595	chr8:6319678-6319679	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549713049	chr8:6319741-6319742	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138437831	chr8:6319750-6319751	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535560739	chr8:6319756-6319757	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2916741	chr8:6319763-6319764	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs572442312	chr8:6319768-6319769	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73661749	chr8:6319774-6319775	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs555527377	chr8:6319790-6319791	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115003275	chr8:6319791-6319792	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544140677	chr8:6319821-6319822	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192976954	chr8:6319846-6319847	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574211819	chr8:6319882-6319883	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574668195	chr8:6319911-6319912	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs561471682	chr8:6319964-6319965	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs527260770	chr8:6320035-6320036	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546998897	chr8:6320049-6320050	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35139232	chr8:6320081-6320082	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75068954	chr8:6320092-6320093	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146809760	chr8:6320132-6320133	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569200853	chr8:6320134-6320135	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2916740	chr8:6320172-6320173	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs550082734	chr8:6320180-6320181	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185157758	chr8:6320222-6320223	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577081356	chr8:6320236-6320237	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535668056	chr8:6320264-6320265	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188828028	chr8:6320265-6320266	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs55650285	chr8:6320296-6320297	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs566185222	chr8:6320304-6320305	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534966918	chr8:6320328-6320329	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:137)

Disease	PMID	Source
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	21364760	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20531469	CNVD

Chromatin state (count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6265000-6339200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr8:6287600-6344400	Weak transcription	Small Intestine	intestine
3	chr8:6301000-6338400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr8:6302800-6339800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr8:6303000-6319400	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr8:6303000-6321000	Weak transcription	Psoas Muscle	Psoas
7	chr8:6303000-6321000	Weak transcription	Hela-S3	cervix
8	chr8:6303000-6322800	Weak transcription	Ovary	ovary
9	chr8:6303000-6322800	Weak transcription	Spleen	Spleen
10	chr8:6303000-6325000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:6303000-6325200	Weak transcription	Pancreas	Pancrea
12	chr8:6303000-6338200	Weak transcription	Gastric	stomach
13	chr8:6303000-6338200	Weak transcription	Rectal Smooth Muscle	rectum
14	chr8:6303000-6338400	Weak transcription	Colonic Mucosa	Colon
15	chr8:6303000-6338400	Weak transcription	Right Ventricle	heart
16	chr8:6303000-6339400	Weak transcription	Placenta	Placenta
17	chr8:6303200-6320400	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr8:6303200-6321000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr8:6303200-6322600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr8:6303200-6322800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr8:6303200-6339400	Weak transcription	Primary hematopoietic stem cells	blood
22	chr8:6303200-6339400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr8:6303200-6340000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr8:6303400-6320600	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr8:6303400-6320800	Weak transcription	Colon Smooth Muscle	Colon
26	chr8:6303400-6321000	Weak transcription	Brain Anterior Caudate	brain
27	chr8:6303400-6321200	Weak transcription	HUVEC	blood vessel
28	chr8:6303600-6321600	Weak transcription	Brain Germinal Matrix	brain
29	chr8:6303800-6338400	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr8:6304000-6322600	Weak transcription	Fetal Brain Female	brain
31	chr8:6304000-6338000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr8:6304400-6360200	Weak transcription	Esophagus	oesophagus
33	chr8:6304600-6321200	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr8:6304800-6323000	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr8:6305200-6320000	Weak transcription	Fetal Muscle Leg	muscle
36	chr8:6305800-6319800	Weak transcription	Primary B cells from cord blood	blood
37	chr8:6305800-6322800	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr8:6306200-6322800	Weak transcription	Fetal Intestine Large	intestine
39	chr8:6306200-6325400	Weak transcription	K562	blood
40	chr8:6306200-6328200	Weak transcription	Fetal Lung	lung
41	chr8:6306600-6322800	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr8:6307600-6319600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr8:6308000-6320000	Weak transcription	Thymus	Thymus
44	chr8:6308000-6320600	Weak transcription	Fetal Thymus	thymus
45	chr8:6308000-6330000	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr8:6308000-6338400	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr8:6308000-6372600	Weak transcription	HMEC	breast
48	chr8:6308400-6321000	Weak transcription	Fetal Muscle Trunk	muscle
49	chr8:6308600-6320600	Weak transcription	Aorta	Aorta
50	chr8:6308800-6319400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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