Variant report

Variant	nsv611841
Chromosome Location	chr8:107048059-107090500
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:553)
CpG islands
(count:183)
Chromatin interactive
region (count:22)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:553 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:107072154-107072271	K562	blood:	n/a	n/a
2	ARID3A	chr8:107067353-107067359	K562	blood:	n/a	n/a
3	ATF1	chr8:107058179-107058512	K562	blood:	n/a	n/a
4	ATF1	chr8:107072604-107072988	K562	blood:	n/a	n/a
5	ATF1	chr8:107072018-107072389	K562	blood:	n/a	n/a
6	ATF3	chr8:107058211-107058479	K562	blood:	n/a	n/a
7	ATF3	chr8:107072658-107072977	K562	blood:	n/a	n/a
8	ATF3	chr8:107072561-107072963	K562	blood:	n/a	n/a
9	ATF3	chr8:107072484-107073066	A549	lung:	n/a	n/a
10	ATF3	chr8:107072077-107072433	K562	blood:	n/a	n/a
11	BACH1	chr8:107072152-107072328	K562	blood:	n/a	n/a
12	BCL3	chr8:107071980-107073024	A549	lung:	n/a	n/a
13	BHLHE40	chr8:107072676-107073002	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:107055029-107055050	A549	lung:	n/a	n/a
15	BHLHE40	chr8:107072299-107073050	A549	lung:	n/a	n/a
16	BHLHE40	chr8:107072605-107073075	HepG2	liver:	n/a	n/a
17	BHLHE40	chr8:107072099-107073241	K562	blood:	n/a	n/a
18	BHLHE40	chr8:107088754-107088803	K562	blood:	n/a	n/a
19	BRCA1	chr8:107072522-107072963	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr8:107071833-107072250	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr8:107072508-107073114	K562	blood:	n/a	n/a
22	CBX3	chr8:107089412-107089774	K562	blood:	n/a	n/a
23	CBX3	chr8:107089317-107089881	HCT-116	colon:	n/a	n/a
24	CBX3	chr8:107089487-107089864	HCT-116	colon:	n/a	n/a
25	CBX3	chr8:107071874-107073234	K562	blood:	n/a	n/a
26	CBX3	chr8:107057765-107058775	HCT-116	colon:	n/a	chr8:107058743-107058754
27	CBX3	chr8:107089452-107089755	K562	blood:	n/a	n/a
28	CBX3	chr8:107071889-107073308	HCT-116	colon:	n/a	n/a
29	CBX3	chr8:107057803-107058675	HCT-116	colon:	n/a	n/a
30	CBX3	chr8:107059497-107060201	HCT-116	colon:	n/a	n/a
31	CEBPB	chr8:107071852-107073313	HCT-116	colon:	n/a	n/a
32	CEBPB	chr8:107071912-107073002	IMR90	lung:	n/a	n/a
33	CEBPB	chr8:107057813-107058664	HCT-116	colon:	n/a	chr8:107058222-107058234
34	CEBPB	chr8:107071945-107073070	A549	lung:	n/a	n/a
35	CEBPB	chr8:107072065-107073011	K562	blood:	n/a	n/a
36	CEBPB	chr8:107058134-107058568	MCF-7	breast:	n/a	chr8:107058222-107058234
37	CEBPB	chr8:107057842-107058821	HCT-116	colon:	n/a	chr8:107058222-107058234
38	CEBPB	chr8:107071945-107073205	HCT-116	colon:	n/a	n/a
39	CEBPB	chr8:107059405-107060328	HCT-116	colon:	n/a	chr8:107059683-107059691
40	CEBPB	chr8:107059742-107059959	A549	lung:	n/a	n/a
41	CEBPB	chr8:107071772-107073057	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr8:107072037-107073011	A549	lung:	n/a	n/a
43	CEBPB	chr8:107072577-107073044	A549	lung:	n/a	n/a
44	CEBPB	chr8:107072693-107072882	K562	blood:	n/a	n/a
45	CEBPB	chr8:107074237-107074439	HepG2	liver:	n/a	chr8:107074331-107074342
46	CEBPB	chr8:107072118-107072291	K562	blood:	n/a	n/a
47	CEBPB	chr8:107072709-107072985	HepG2	liver:	n/a	n/a
48	CEBPB	chr8:107071998-107073020	K562	blood:	n/a	n/a
49	CEBPB	chr8:107059738-107060071	IMR90	lung:	n/a	n/a
50	CHD2	chr8:107072635-107072960	Hela-S3	cervix:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:107057242-107057292	NT2-D1	testis:	n/a
2	chr8:107072690-107072740	HEK293	kidney:	embryo
3	chr8:107058373-107058423	AoSMC	blood vessel:	n/a
4	chr8:107058373-107058423	K562	blood:	n/a
5	chr8:107058373-107058423	IMR90	lung:	fetal
6	chr8:107058373-107058423	HL-60	blood:	n/a
7	chr8:107072690-107072740	NHDF-neo	bronchial:	n/a
8	chr8:107058373-107058423	AG10803	skin:	n/a
9	chr8:107057242-107057292	IMR90	lung:	fetal
10	chr8:107072690-107072740	HPAEpiC	pulmonary alveolar:	n/a
11	chr8:107072690-107072740	MCF10A-Er-Src	breast:	n/a
12	chr8:107058373-107058423	NB4	blood:	n/a
13	chr8:107072690-107072740	SAEC	small airway:	n/a
14	chr8:107058373-107058423	PFSK-1	brain:	n/a
15	chr8:107072690-107072740	PFSK-1	brain:	n/a
16	chr8:107057242-107057292	AG09319	gingival:	n/a
17	chr8:107058373-107058423	RPTEC	kidney:	n/a
18	chr8:107057242-107057292	LNCaP	prostate:	n/a
19	chr8:107057242-107057292	ovcar-3	ovarian:	n/a
20	chr8:107072690-107072740	U87	brain:	n/a
21	chr8:107057242-107057292	HEK293	kidney:	embryo
22	chr8:107072690-107072740	NHBE	bronchial:	n/a
23	chr8:107072690-107072740	HEEpiC	esophagus:	n/a
24	chr8:107057242-107057292	Hela-S3	cervix:	n/a
25	chr8:107072690-107072740	ECC-1	luminal epithelium:	n/a
26	chr8:107057242-107057292	PANC-1	pancreas:	n/a
27	chr8:107058373-107058423	HCT-116	colon:	n/a
28	chr8:107057242-107057292	SK-N-SH	brain:	n/a
29	chr8:107072690-107072740	GM12891	blood:	n/a
30	chr8:107058373-107058423	SAEC	small airway:	n/a
31	chr8:107058373-107058423	ECC-1	luminal epithelium:	n/a
32	chr8:107058373-107058423	GM12878	blood:	n/a
33	chr8:107058373-107058423	AG04450	lung:	fetal
34	chr8:107072690-107072740	AG09319	gingival:	n/a
35	chr8:107057242-107057292	NHDF-neo	bronchial:	n/a
36	chr8:107058373-107058423	GM06990	blood:	n/a
37	chr8:107072690-107072740	AG04449	skin:	fetal
38	chr8:107058373-107058423	NHBE	bronchial:	n/a
39	chr8:107058373-107058423	A549	lung:	n/a
40	chr8:107058373-107058423	HNPCEpiC	eye:	n/a
41	chr8:107072690-107072740	PrEC	prostate:	n/a
42	chr8:107057242-107057292	AG09309	skin:	n/a
43	chr8:107057242-107057292	NB4	blood:	n/a
44	chr8:107057242-107057292	PFSK-1	brain:	n/a
45	chr8:107072690-107072740	H1-hESC	embryonic stem cell:	embryo
46	chr8:107058373-107058423	AG09309	skin:	n/a
47	chr8:107058373-107058423	SK-N-MC	brain:	n/a
48	chr8:107057242-107057292	HL-60	blood:	n/a
49	chr8:107057242-107057292	BJ	skin:	n/a
50	chr8:107072690-107072740	PANC-1	pancreas:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:106953058..106955739-chr8:107063560..107065111,2	K562	blood:
2	chr8:107046034..107047733-chr8:107070265..107072124,2	K562	blood:
3	chr8:107041900..107044728-chr8:107046317..107048149,2	K562	blood:
4	chr8:107014553..107016972-chr8:107063903..107066317,2	K562	blood:
5	chr8:107043250..107045560-chr8:107060894..107062848,2	K562	blood:
6	chr8:107045005..107047534-chr8:107070265..107071984,2	K562	blood:
7	chr8:107054893..107058550-chr8:107060735..107063239,3	K562	blood:
8	chr8:107065574..107067380-chr8:107096296..107097895,2	K562	blood:
9	chr8:107071254..107072899-chr8:107075666..107077404,2	K562	blood:
10	chr8:107055539..107058466-chr8:107069487..107071012,2	K562	blood:
11	chr8:107047054..107052420-chr8:107054763..107060033,4	K562	blood:
12	chr8:107085770..107087985-chr8:107092764..107094318,2	MCF-7	breast:
13	chr8:107054893..107058550-chr8:107060735..107063239,3	K562	blood:
14	chr8:107045809..107048572-chr8:107053112..107054871,2	K562	blood:
15	chr8:107047054..107052420-chr8:107054763..107060033,4	K562	blood:
16	chr8:107044060..107046114-chr8:107059954..107062848,2	K562	blood:
17	chr8:107059219..107060866-chr8:107093801..107095788,2	K562	blood:
18	chr8:107069077..107070630-chr8:107070667..107072859,2	K562	blood:
19	chr8:107055539..107058466-chr8:107069487..107071012,2	K562	blood:
20	chr8:107071316..107072942-chr8:107075565..107078465,2	MCF-7	breast:
21	chr8:107057702..107058412-chr8:107636030..107636553,2	MCF-7	breast:
22	chr8:107045809..107048572-chr8:107053112..107054871,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-778D12.2.1-4	chr8:107072609-107072752	ENSG00000251003.2
2	lnc-RP11-778D12.2.1-4	chr8:107071309-107071364	ENSG00000251003.2
3	lnc-RP11-778D12.2.1-4	chr8:107072609-107072671	ENSG00000251003.2
4	lnc-RP11-778D12.2.1-4	chr8:107072609-107072695	ENSG00000251003.2
5	lnc-RP11-778D12.2.1-4	chr8:107072609-107072719	ENSG00000251003.2
6	lnc-RP11-778D12.2.1-4	chr8:107072363-107072462	ENSG00000251003.2
7	lnc-RP11-778D12.2.1-4	chr8:107072609-107072689	ENSG00000251003.2
8	lnc-RP11-778D12.2.1-4	chr8:107072609-107072705	ENSG00000251003.2

No data

Variant related genes	Relation type
ENSG00000251003	TF binding region
ENSG00000251003	CpG island
ENSG00000251003	chromatin interactions

Extended variants
information (count: 1277 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1277 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7829062	chr8:107048059-107048060	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538924249	chr8:107048088-107048089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543033141	chr8:107048089-107048090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs6469031	chr8:107048095-107048096	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs571598624	chr8:107048109-107048110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572242907	chr8:107048120-107048121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528547034	chr8:107048133-107048134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148150935	chr8:107048137-107048138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192858966	chr8:107048166-107048167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs143989221	chr8:107048180-107048181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370704510	chr8:107048218-107048219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375214076	chr8:107048278-107048279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552854375	chr8:107048294-107048295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566295272	chr8:107048303-107048304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569105114	chr8:107048327-107048328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535872436	chr8:107048338-107048339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116477757	chr8:107048419-107048420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554507622	chr8:107048479-107048480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs1429680	chr8:107048542-107048543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539984238	chr8:107048571-107048572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115215586	chr8:107048598-107048599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs75518372	chr8:107048604-107048605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182636958	chr8:107048613-107048614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562191257	chr8:107048649-107048650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147333589	chr8:107048657-107048658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187973985	chr8:107048689-107048690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542667101	chr8:107048690-107048691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs16874064	chr8:107048792-107048793	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs191264096	chr8:107048795-107048796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs1429681	chr8:107048808-107048809	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs7830351	chr8:107048825-107048826	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs557075763	chr8:107048848-107048849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550748040	chr8:107048852-107048853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs73295362	chr8:107048861-107048862	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs570779177	chr8:107048884-107048885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536588110	chr8:107048922-107048923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs554561837	chr8:107048927-107048928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566489246	chr8:107048962-107048963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533526773	chr8:107048974-107048975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs558248677	chr8:107049007-107049008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs76753278	chr8:107049018-107049019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576504074	chr8:107049061-107049062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs538852521	chr8:107049152-107049153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs184842805	chr8:107049217-107049218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575741516	chr8:107049220-107049221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538566771	chr8:107049236-107049237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558396254	chr8:107049289-107049290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543353036	chr8:107049372-107049373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189168292	chr8:107049401-107049402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571931109	chr8:107049406-107049407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	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
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
small cell lung cancer	20016488	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
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Multiple myeloma	16461302	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	22539939	CNVD
Non-small cell lung cancer	19010865	CNVD

Chromatin state (count:254 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:107036400-107052000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:107044800-107057200	Weak transcription	Aorta	Aorta
3	chr8:107045000-107057400	Weak transcription	Hela-S3	cervix
4	chr8:107046000-107048600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr8:107046000-107057200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr8:107046400-107048800	Weak transcription	Osteobl	bone
7	chr8:107047200-107049000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr8:107048600-107049000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr8:107048800-107049000	Enhancers	Osteobl	bone
10	chr8:107048800-107049200	Enhancers	Dnd41	blood
11	chr8:107049000-107049200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr8:107052000-107052200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr8:107052200-107069200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr8:107053800-107058200	Weak transcription	K562	blood
15	chr8:107055200-107055400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr8:107055400-107056400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr8:107056000-107056200	Enhancers	NH-A	brain
18	chr8:107056000-107056400	Enhancers	Colon Smooth Muscle	Colon
19	chr8:107056000-107058800	Enhancers	Fetal Kidney	kidney
20	chr8:107056200-107056400	Enhancers	Pancreas	Pancrea
21	chr8:107056200-107057200	Weak transcription	NH-A	brain
22	chr8:107056400-107056600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr8:107056400-107057800	Enhancers	HUVEC	blood vessel
24	chr8:107056400-107059000	Weak transcription	Colon Smooth Muscle	Colon
25	chr8:107056400-107060800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr8:107056600-107057400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr8:107057000-107060600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr8:107057200-107057400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr8:107057200-107057400	Enhancers	Aorta	Aorta
30	chr8:107057200-107057400	Enhancers	Pancreas	Pancrea
31	chr8:107057200-107058000	Enhancers	NH-A	brain
32	chr8:107057200-107058600	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr8:107057200-107058600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr8:107057200-107059800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr8:107057200-107060600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr8:107057200-107060800	Enhancers	NHDF-Ad	bronchial
37	chr8:107057200-107060800	Enhancers	Osteobl	bone
38	chr8:107057400-107057800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr8:107057400-107057800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr8:107057400-107057800	Weak transcription	Aorta	Aorta
41	chr8:107057400-107058600	Enhancers	Stomach Mucosa	stomach
42	chr8:107057400-107060000	Enhancers	Hela-S3	cervix
43	chr8:107057800-107058000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr8:107057800-107058200	Enhancers	A549	lung
45	chr8:107057800-107058400	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr8:107057800-107058600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr8:107057800-107058600	Enhancers	Aorta	Aorta
48	chr8:107057800-107058600	Flanking Active TSS	HUVEC	blood vessel
49	chr8:107057800-107059200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:107057800-107059400	Enhancers	NHEK	skin

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