Variant report

Variant	nsv891324
Chromosome Location	chr8:113647451-113732965
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	chr8:113711892-113712099	K562	blood:	n/a	n/a
2	CEBPB	chr8:113675831-113676188	HepG2	liver:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
3	CEBPB	chr8:113675853-113676190	A549	lung:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
4	CEBPB	chr8:113675839-113676178	MCF-7	breast:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
5	CEBPB	chr8:113675869-113676172	K562	blood:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
6	CEBPB	chr8:113705928-113706157	HepG2	liver:	n/a	n/a
7	CEBPB	chr8:113695353-113695608	HepG2	liver:	n/a	n/a
8	CEBPB	chr8:113675839-113676180	Hela-S3	cervix:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
9	CEBPB	chr8:113682533-113683041	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr8:113675826-113676181	IMR90	lung:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
11	CEBPB	chr8:113680956-113681228	HepG2	liver:	n/a	n/a
12	CEBPB	chr8:113675862-113676155	H1-hESC	embryonic stem cell:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
13	CTCF	chr8:113697658-113697706	GM10248	blood:	n/a	n/a
14	CTCF	chr8:113649045-113649108	MCF-7	breast:	n/a	n/a
15	CTCF	chr8:113708148-113708187	GM20000	blood:	n/a	n/a
16	CTCF	chr8:113708092-113708207	Kidney_OC	kidney:	n/a	n/a
17	E2F4	chr8:113680266-113680439	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr8:113682728-113683040	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr8:113696988-113697270	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr8:113701602-113701908	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr8:113686741-113686999	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr8:113685558-113685640	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr8:113672535-113672733	MCF10A-Er-Src	breast:	n/a	n/a
24	EP300	chr8:113682683-113682986	Hela-S3	cervix:	n/a	n/a
25	EP300	chr8:113654305-113654316	K562	blood:	n/a	n/a
26	EP300	chr8:113690751-113690802	K562	blood:	n/a	n/a
27	EP300	chr8:113660100-113660633	MCF-7	breast:	n/a	n/a
28	FAM48A	chr8:113690656-113690715	GM12878	blood:	n/a	n/a
29	FOS	chr8:113686566-113687043	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr8:113685812-113686139	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr8:113672138-113672347	MCF10A-Er-Src	breast:	n/a	chr8:113672254-113672261
32	FOS	chr8:113680258-113680613	MCF10A-Er-Src	breast:	n/a	chr8:113680441-113680451 chr8:113680442-113680449 chr8:113680441-113680450 chr8:113680440-113680452 chr8:113680442-113680450 chr8:113680440-113680451 chr8:113680442-113680451
33	FOS	chr8:113682602-113683076	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr8:113685811-113686047	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr8:113680291-113680569	MCF10A-Er-Src	breast:	n/a	chr8:113680441-113680451 chr8:113680442-113680449 chr8:113680441-113680450 chr8:113680440-113680452 chr8:113680442-113680450 chr8:113680440-113680451 chr8:113680442-113680451
36	FOS	chr8:113686606-113687102	HUVEC	blood vessel:	n/a	n/a
37	FOS	chr8:113680275-113680765	MCF10A-Er-Src	breast:	n/a	chr8:113680441-113680451 chr8:113680442-113680449 chr8:113680441-113680450 chr8:113680440-113680452 chr8:113680442-113680450 chr8:113680440-113680451 chr8:113680442-113680451
38	FOS	chr8:113686615-113687028	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr8:113682564-113683084	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr8:113680274-113680604	HUVEC	blood vessel:	n/a	chr8:113680441-113680451 chr8:113680442-113680449 chr8:113680441-113680450 chr8:113680440-113680452 chr8:113680442-113680450 chr8:113680440-113680451 chr8:113680442-113680451
41	FOS	chr8:113687593-113687791	MCF10A-Er-Src	breast:	n/a	chr8:113687749-113687757
42	FOS	chr8:113662337-113662519	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr8:113686616-113686974	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr8:113685811-113686131	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr8:113662378-113662556	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr8:113682675-113683040	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr8:113682604-113683049	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr8:113680288-113680625	MCF10A-Er-Src	breast:	n/a	chr8:113680441-113680451 chr8:113680442-113680449 chr8:113680441-113680450 chr8:113680440-113680452 chr8:113680442-113680450 chr8:113680440-113680451 chr8:113680442-113680451
49	FOS	chr8:113686627-113686976	MCF10A-Er-Src	breast:	n/a	n/a
50	FOXA1	chr8:113679283-113679578	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:113656015-113656065	RPTEC	kidney:	n/a
2	chr8:113655436-113655486	T-47D	breast:	n/a
3	chr8:113703176-113703226	T-47D	breast:	n/a
4	chr8:113655436-113655486	SAEC	small airway:	n/a
5	chr8:113702707-113702757	MCF-7	breast:	n/a
6	chr8:113702707-113702757	HUVEC	blood vessel:	n/a
7	chr8:113656015-113656065	SK-N-SH	brain:	n/a
8	chr8:113656015-113656065	Hela-S3	cervix:	n/a
9	chr8:113655561-113655611	GM19239	blood:	n/a
10	chr8:113656015-113656065	AG09319	gingival:	n/a
11	chr8:113655561-113655611	NT2-D1	testis:	n/a
12	chr8:113655561-113655611	HCM	heart:	n/a
13	chr8:113702707-113702757	IMR90	lung:	fetal
14	chr8:113655436-113655486	PFSK-1	brain:	n/a
15	chr8:113655436-113655486	ProgFib	skin:	n/a
16	chr8:113702707-113702757	LNCaP	prostate:	n/a
17	chr8:113655561-113655611	HNPCEpiC	eye:	n/a
18	chr8:113655561-113655611	SK-N-SH_RA	brain:	n/a
19	chr8:113656015-113656065	PANC-1	pancreas:	n/a
20	chr8:113655436-113655486	IMR90	lung:	fetal
21	chr8:113702707-113702757	GM06990	blood:	n/a
22	chr8:113655436-113655486	BE2_C	brain:	n/a
23	chr8:113702707-113702757	HCM	heart:	n/a
24	chr8:113655561-113655611	HL-60	blood:	n/a
25	chr8:113655436-113655486	AG10803	skin:	n/a
26	chr8:113655436-113655486	MCF10A-Er-Src	breast:	n/a
27	chr8:113702707-113702757	HepG2	liver:	n/a
28	chr8:113656015-113656065	HRPEpiC	eye:	n/a
29	chr8:113702707-113702757	ECC-1	luminal epithelium:	n/a
30	chr8:113702707-113702757	Hela-S3	cervix:	n/a
31	chr8:113655561-113655611	AG04450	lung:	fetal
32	chr8:113656015-113656065	HL-60	blood:	n/a
33	chr8:113702707-113702757	GM19239	blood:	n/a
34	chr8:113703176-113703226	NT2-D1	testis:	n/a
35	chr8:113702707-113702757	NT2-D1	testis:	n/a
36	chr8:113656015-113656065	H1-hESC	embryonic stem cell:	embryo
37	chr8:113656015-113656065	Caco-2	colon:	n/a
38	chr8:113655561-113655611	PrEC	prostate:	n/a
39	chr8:113703176-113703226	HIPEpiC	eye:	n/a
40	chr8:113702707-113702757	HRE	kidney:	n/a
41	chr8:113656015-113656065	BE2_C	brain:	n/a
42	chr8:113702707-113702757	Caco-2	colon:	n/a
43	chr8:113703176-113703226	NB4	blood:	n/a
44	chr8:113655436-113655486	HEEpiC	esophagus:	n/a
45	chr8:113655436-113655486	H1-hESC	embryonic stem cell:	embryo
46	chr8:113655561-113655611	ECC-1	luminal epithelium:	n/a
47	chr8:113655436-113655486	HPAEpiC	pulmonary alveolar:	n/a
48	chr8:113702707-113702757	H1-hESC	embryonic stem cell:	embryo
49	chr8:113703176-113703226	HEEpiC	esophagus:	n/a
50	chr8:113702707-113702757	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:113659187..113660730-chr8:113666931..113668583,2	MCF-7	breast:
2	chr8:113656932..113658484-chr8:113659367..113661819,2	K562	blood:
3	chr8:113719443..113721302-chr8:113723054..113725365,2	K562	blood:
4	chr6:30778063..30780102-chr8:113652986..113654698,2	MCF-7	breast:
5	chr11:85195583..85198227-chr8:113682885..113684772,2	MCF-7	breast:
6	chr8:113648317..113650428-chr8:113651221..113653011,2	MCF-7	breast:
7	chr8:113730328..113732083-chr8:113748434..113750301,2	K562	blood:
8	chr8:113656932..113658484-chr8:113659367..113661819,2	K562	blood:
9	chr8:113719443..113721302-chr8:113723054..113725365,2	K562	blood:
10	chr8:113659187..113660730-chr8:113666931..113668583,2	MCF-7	breast:
11	chr8:113648317..113650428-chr8:113651221..113653011,2	MCF-7	breast:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-2053	chr8:113655782-113655804	MIMAT0009978

Variant related genes	Relation type
CSMD3	TF binding region
MIR2053	TF binding region
CSMD3	CpG island
MIR2053	CpG island

Extended variants
information (count: 2084 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:2084 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4876289	chr8:113647451-113647452	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs180766911	chr8:113647452-113647453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550158755	chr8:113647484-113647485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545942468	chr8:113647499-113647500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535917115	chr8:113647555-113647556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555595124	chr8:113647581-113647582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76114085	chr8:113647588-113647589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559115134	chr8:113647618-113647619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534497774	chr8:113647668-113647669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183696157	chr8:113647774-113647775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577508965	chr8:113647783-113647784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543325641	chr8:113647815-113647816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113070434	chr8:113647849-113647850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556495245	chr8:113647853-113647854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528307863	chr8:113647935-113647936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs149742760	chr8:113647943-113647944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542639817	chr8:113648014-113648015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559159902	chr8:113648041-113648042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528234594	chr8:113648090-113648091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541634253	chr8:113648122-113648123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111313780	chr8:113648144-113648145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564678742	chr8:113648190-113648191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533620274	chr8:113648209-113648210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550517019	chr8:113648271-113648272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190250521	chr8:113648297-113648298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146766114	chr8:113648326-113648327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549386899	chr8:113648368-113648369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566040544	chr8:113648372-113648373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374239873	chr8:113648373-113648374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568365854	chr8:113648426-113648427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs9643073	chr8:113648446-113648447	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs538857244	chr8:113648454-113648455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141195075	chr8:113648457-113648458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376163260	chr8:113648479-113648480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182428563	chr8:113648534-113648535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186545090	chr8:113648549-113648550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191824285	chr8:113648597-113648598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181725517	chr8:113648636-113648637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201728759	chr8:113648710-113648711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150077153	chr8:113648717-113648718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs5894093	chr8:113648718-113648719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139279990	chr8:113648723-113648724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs398009425	chr8:113648726-113648727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371171105	chr8:113648727-113648728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572809015	chr8:113648735-113648736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545128472	chr8:113648760-113648761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111942138	chr8:113648767-113648768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371845991	chr8:113648768-113648769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112686099	chr8:113648773-113648774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs377481851	chr8:113648782-113648783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Schizophrenia	20967226	CNVD
Prostate cancer	22341455	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:113629200-113680600	Weak transcription	NHEK	skin
2	chr8:113629400-113661800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:113636200-113663600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr8:113636800-113680400	Weak transcription	HMEC	breast
5	chr8:113645800-113649000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr8:113649000-113651200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr8:113655600-113656000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr8:113661800-113663400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr8:113663400-113676600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr8:113663600-113664400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr8:113664400-113666000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr8:113666000-113666400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr8:113666400-113675800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr8:113673600-113674000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr8:113675800-113678400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr8:113676600-113678000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr8:113678000-113678400	Enhancers	Fetal Lung	lung
18	chr8:113678000-113682400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr8:113678400-113682200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr8:113679400-113680000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr8:113679600-113679800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr8:113679800-113683200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr8:113680400-113681000	Enhancers	HMEC	breast
24	chr8:113680600-113681000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr8:113680600-113681000	Enhancers	NHEK	skin
26	chr8:113681000-113682200	Weak transcription	NHEK	skin
27	chr8:113681000-113682400	Weak transcription	HMEC	breast
28	chr8:113681000-113684400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr8:113682000-113682400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr8:113682000-113682800	Enhancers	Colon Smooth Muscle	Colon
31	chr8:113682200-113682400	Enhancers	NHEK	skin
32	chr8:113682200-113683000	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr8:113682200-113683200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr8:113682400-113682600	Flanking Active TSS	NHEK	skin
35	chr8:113682400-113683000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr8:113682400-113684400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr8:113682400-113685200	Enhancers	HMEC	breast
38	chr8:113682600-113682800	Enhancers	NHEK	skin
39	chr8:113682800-113683000	Flanking Active TSS	NHEK	skin
40	chr8:113683000-113684200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr8:113683000-113684200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr8:113683000-113684400	Enhancers	NHEK	skin
43	chr8:113683200-113683600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr8:113683200-113684600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr8:113683600-113684600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr8:113683800-113688600	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr8:113684200-113685400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr8:113684200-113686000	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr8:113684200-113688000	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr8:113684200-113688000	Enhancers	iPS-20b Cell Line	embryonic stem cell

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