Variant report

Variant	esv2761219
Chromosome Location	chr8:6494655-6505115
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:174)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:174 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:6498370-6498595	HepG2	liver:	n/a	n/a
2	ATF2	chr8:6502283-6502814	GM12878	blood:	n/a	n/a
3	ATF2	chr8:6502240-6502826	GM12878	blood:	n/a	n/a
4	BACH1	chr8:6502437-6502793	K562	blood:	n/a	n/a
5	BACH1	chr8:6502386-6502829	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr8:6502324-6502817	GM12878	blood:	n/a	n/a
7	BATF	chr8:6502391-6502630	GM12878	blood:	n/a	n/a
8	BCL11A	chr8:6502407-6502751	GM12878	blood:	n/a	n/a
9	BCL3	chr8:6502319-6502765	GM12878	blood:	n/a	n/a
10	BCLAF1	chr8:6502395-6502820	GM12878	blood:	n/a	n/a
11	CBX3	chr8:6502276-6502961	HCT-116	colon:	n/a	n/a
12	CEBPB	chr8:6502288-6502757	IMR90	lung:	n/a	n/a
13	CHD2	chr8:6502515-6502784	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr8:6504200-6504350	HAc	cerebellar:	n/a	n/a
15	CUX1	chr8:6502466-6502805	GM12878	blood:	n/a	n/a
16	E2F4	chr8:6500141-6500374	MCF10A-Er-Src	breast:	n/a	n/a
17	EBF1	chr8:6502405-6502816	GM12878	blood:	n/a	n/a
18	EBF1	chr8:6502418-6502824	GM12878	blood:	n/a	n/a
19	EBF1	chr8:6502402-6502756	GM12878	blood:	n/a	n/a
20	EP300	chr8:6498306-6498614	HepG2	liver:	n/a	n/a
21	EP300	chr8:6502309-6502831	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chr8:6502431-6502826	HepG2	liver:	n/a	n/a
23	EP300	chr8:6502344-6502880	Hela-S3	cervix:	n/a	n/a
24	EP300	chr8:6502394-6502788	SK-N-SH_RA	brain:	n/a	n/a
25	EP300	chr8:6499860-6500557	SK-N-SH	brain:	n/a	n/a
26	EP300	chr8:6502464-6502933	K562	blood:	n/a	n/a
27	EP300	chr8:6502167-6503047	SK-N-SH	brain:	n/a	n/a
28	EP300	chr8:6502075-6503041	SK-N-SH	brain:	n/a	n/a
29	FOS	chr8:6502326-6502837	HUVEC	blood vessel:	n/a	n/a
30	FOS	chr8:6502325-6502910	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr8:6502292-6502825	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr8:6500070-6500317	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr8:6498315-6498596	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr8:6502353-6502811	Hela-S3	cervix:	n/a	n/a
35	FOS	chr8:6502328-6502801	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr8:6502292-6503030	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr8:6500063-6500329	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr8:6500129-6500251	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr8:6500053-6500351	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr8:6499196-6499259	MCF10A-Er-Src	breast:	n/a	n/a
41	FOSL1	chr8:6498214-6498569	HCT-116	colon:	n/a	n/a
42	FOSL1	chr8:6498193-6498770	HCT-116	colon:	n/a	n/a
43	FOSL1	chr8:6502140-6502987	HCT-116	colon:	n/a	n/a
44	FOSL1	chr8:6498870-6499490	HCT-116	colon:	n/a	n/a
45	FOSL1	chr8:6502235-6502879	HCT-116	colon:	n/a	n/a
46	FOSL2	chr8:6498354-6498539	HepG2	liver:	n/a	n/a
47	FOSL2	chr8:6502414-6502726	A549	lung:	n/a	n/a
48	FOSL2	chr8:6502268-6502862	A549	lung:	n/a	n/a
49	FOSL2	chr8:6502364-6502773	MCF-7	breast:	n/a	n/a
50	FOSL2	chr8:6502271-6502834	SK-N-SH	brain:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6501499-6501549	Caco-2	colon:	n/a
2	chr8:6501499-6501549	HCPEpiC	choroid plexus:	n/a
3	chr8:6501499-6501549	Jurkat	blood:	n/a
4	chr8:6501499-6501549	T-47D	breast:	n/a
5	chr8:6501499-6501549	HEEpiC	esophagus:	n/a
6	chr8:6501499-6501549	ovcar-3	ovarian:	n/a
7	chr8:6501499-6501549	NH-A	brain:	n/a
8	chr8:6501499-6501549	AG09309	skin:	n/a
9	chr8:6501499-6501549	ECC-1	luminal epithelium:	n/a
10	chr8:6501499-6501549	LNCaP	prostate:	n/a
11	chr8:6501499-6501549	AG09319	gingival:	n/a
12	chr8:6501499-6501549	AG04449	skin:	fetal
13	chr8:6501499-6501549	HNPCEpiC	eye:	n/a
14	chr8:6501499-6501549	RPTEC	kidney:	n/a
15	chr8:6501499-6501549	PrEC	prostate:	n/a
16	chr8:6501499-6501549	ProgFib	skin:	n/a
17	chr8:6501499-6501549	NHBE	bronchial:	n/a
18	chr8:6501499-6501549	A549	lung:	n/a
19	chr8:6501499-6501549	SK-N-SH	brain:	n/a
20	chr8:6501499-6501549	SK-N-SH_RA	brain:	n/a
21	chr8:6501499-6501549	AG10803	skin:	n/a
22	chr8:6501499-6501549	GM06990	blood:	n/a
23	chr8:6501499-6501549	IMR90	lung:	fetal
24	chr8:6501499-6501549	AoSMC	blood vessel:	n/a
25	chr8:6501499-6501549	SKMC	muscle:	n/a
26	chr8:6501499-6501549	GM12878	blood:	n/a
27	chr8:6501499-6501549	CMK	blood:	n/a
28	chr8:6501499-6501549	Hepatocyte	liver:	n/a
29	chr8:6501499-6501549	MCF-7	breast:	n/a
30	chr8:6501499-6501549	PANC-1	pancreas:	n/a
31	chr8:6501499-6501549	HUVEC	blood vessel:	n/a
32	chr8:6501499-6501549	BE2_C	brain:	n/a
33	chr8:6501499-6501549	HCT-116	colon:	n/a
34	chr8:6501499-6501549	HEK293	kidney:	embryo
35	chr8:6501499-6501549	HCM	heart:	n/a
36	chr8:6501499-6501549	HAEpiC	amniotic membrane:	n/a
37	chr8:6501499-6501549	Hela-S3	cervix:	n/a
38	chr8:6501499-6501549	U87	brain:	n/a
39	chr8:6501499-6501549	NHDF-neo	bronchial:	n/a
40	chr8:6501499-6501549	H1-hESC	embryonic stem cell:	embryo
41	chr8:6501499-6501549	HPAEpiC	pulmonary alveolar:	n/a
42	chr8:6501499-6501549	GM12892	blood:	n/a
43	chr8:6501499-6501549	HRCEpiC	kidney:	n/a
44	chr8:6501499-6501549	HRPEpiC	eye:	n/a
45	chr8:6501499-6501549	NT2-D1	testis:	n/a
46	chr8:6501499-6501549	BJ	skin:	n/a
47	chr8:6501499-6501549	NB4	blood:	n/a
48	chr8:6501499-6501549	GM19239	blood:	n/a
49	chr8:6501499-6501549	GM12891	blood:	n/a
50	chr8:6501499-6501549	HRE	kidney:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:6498880..6501314-chr8:6501971..6503524,2	K562	blood:
2	chr8:6498880..6501314-chr8:6501971..6503524,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MCPH1-1	chr8:6503576-6506025	ENSG00000271927.1

No data

Variant related genes	Relation type
ENSG00000271927	TF binding region
ENSG00000271927	CpG island

Extended variants
information (count: 652 )
Associated
traits (count: 136 )

Variant overlapped rSNPs/rCNVs (count:652 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2911991	chr8:6494655-6494656	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs550538967	chr8:6494659-6494660	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189177855	chr8:6494663-6494664	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs151191215	chr8:6494686-6494687	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140325483	chr8:6494697-6494698	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150355230	chr8:6494718-6494719	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372538903	chr8:6494731-6494732	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539037463	chr8:6494733-6494734	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144872944	chr8:6494752-6494753	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559176348	chr8:6494755-6494756	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs180703921	chr8:6494769-6494770	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184299249	chr8:6494774-6494775	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2911993	chr8:6494777-6494778	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs145504115	chr8:6494809-6494810	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs75051129	chr8:6494812-6494813	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113300786	chr8:6494821-6494822	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188858915	chr8:6494833-6494834	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2515563	chr8:6494850-6494851	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs559026477	chr8:6494861-6494862	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533705064	chr8:6494869-6494870	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73515128	chr8:6494888-6494889	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs181180440	chr8:6494901-6494902	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186222650	chr8:6494903-6494904	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74807890	chr8:6494935-6494936	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190507511	chr8:6494972-6494973	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567507671	chr8:6495013-6495014	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182213328	chr8:6495031-6495032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547066805	chr8:6495064-6495065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566993107	chr8:6495073-6495074	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs137963699	chr8:6495121-6495122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368171389	chr8:6495131-6495132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140910517	chr8:6495146-6495147	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187202553	chr8:6495152-6495153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372143724	chr8:6495154-6495155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144561524	chr8:6495156-6495157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574646007	chr8:6495166-6495167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540450310	chr8:6495214-6495215	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190818145	chr8:6495222-6495223	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114204403	chr8:6495224-6495225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11784339	chr8:6495245-6495246	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs564772533	chr8:6495252-6495253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369285244	chr8:6495279-6495280	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544136179	chr8:6495289-6495290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183021802	chr8:6495299-6495300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7836799	chr8:6495300-6495301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116667535	chr8:6495307-6495308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2433146	chr8:6495316-6495317	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs532526743	chr8:6495320-6495321	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552534640	chr8:6495321-6495322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371348077	chr8:6495322-6495323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:136)

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
Pancreatic cancer	17952125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Osteosarcoma	21215367	CNVD
Cognitive impairment	21505072	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6458000-6498400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:6474200-6505200	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr8:6474800-6498400	Weak transcription	HSMM	muscle
4	chr8:6476400-6499000	Weak transcription	Brain Angular Gyrus	brain
5	chr8:6476400-6502800	Weak transcription	Colonic Mucosa	Colon
6	chr8:6478400-6498400	Weak transcription	HMEC	breast
7	chr8:6479600-6499800	Weak transcription	Aorta	Aorta
8	chr8:6480000-6502000	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr8:6480200-6501800	Weak transcription	NHEK	skin
10	chr8:6480200-6502000	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr8:6480200-6502600	Weak transcription	Gastric	stomach
12	chr8:6480200-6523800	Weak transcription	Fetal Brain Female	brain
13	chr8:6480400-6498400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr8:6480400-6499600	Weak transcription	Brain Anterior Caudate	brain
15	chr8:6480400-6499800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr8:6480400-6499800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr8:6480400-6499800	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr8:6480400-6502200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr8:6480400-6505400	Weak transcription	Lung	lung
20	chr8:6480800-6499600	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr8:6481800-6501800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr8:6482000-6501800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr8:6482000-6503600	Weak transcription	Esophagus	oesophagus
24	chr8:6482200-6501200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr8:6483200-6496200	Weak transcription	Pancreas	Pancrea
26	chr8:6483800-6504400	Weak transcription	Liver	Liver
27	chr8:6484000-6500200	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr8:6484000-6502000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr8:6484000-6502200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr8:6484400-6499800	Weak transcription	Brain Hippocampus Middle	brain
31	chr8:6484400-6502400	Weak transcription	Stomach Smooth Muscle	stomach
32	chr8:6484400-6503000	Weak transcription	Spleen	Spleen
33	chr8:6484400-6503400	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr8:6484800-6496400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr8:6484800-6505200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr8:6485000-6499800	Weak transcription	Fetal Muscle Leg	muscle
37	chr8:6485000-6500400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr8:6485000-6502800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr8:6485000-6504400	Weak transcription	Fetal Intestine Large	intestine
40	chr8:6485200-6502000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr8:6485400-6494800	Weak transcription	Dnd41	blood
42	chr8:6485400-6499000	Weak transcription	Placenta	Placenta
43	chr8:6485400-6499800	Weak transcription	Fetal Muscle Trunk	muscle
44	chr8:6485400-6501400	Weak transcription	Fetal Intestine Small	intestine
45	chr8:6485400-6503800	Weak transcription	Fetal Stomach	stomach
46	chr8:6487200-6498600	Weak transcription	Primary hematopoietic stem cells	blood
47	chr8:6487400-6502000	Weak transcription	Primary B cells from cord blood	blood
48	chr8:6487400-6502000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr8:6487600-6501000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr8:6487800-6502000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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