Variant report

Variant	nsv891263
Chromosome Location	chr8:107210629-107239780
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:203)
CpG islands
(count:428)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:203 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:107219714-107219715	K562	blood:	n/a	n/a
2	CEBPB	chr8:107215733-107216028	ECC-1	luminal epithelium:	n/a	n/a
3	CEBPB	chr8:107210488-107210730	HepG2	liver:	n/a	chr8:107210614-107210623 chr8:107210614-107210625 chr8:107210612-107210623
4	CEBPB	chr8:107210509-107210741	IMR90	lung:	n/a	chr8:107210614-107210623 chr8:107210614-107210625 chr8:107210612-107210623
5	CEBPB	chr8:107215770-107216094	HepG2	liver:	n/a	n/a
6	CEBPB	chr8:107215756-107216152	A549	lung:	n/a	n/a
7	CEBPB	chr8:107215826-107216022	K562	blood:	n/a	n/a
8	CEBPB	chr8:107218599-107219013	IMR90	lung:	n/a	n/a
9	CEBPB	chr8:107215739-107216114	IMR90	lung:	n/a	n/a
10	CEBPB	chr8:107215618-107216141	A549	lung:	n/a	n/a
11	CEBPB	chr8:107215743-107216125	A549	lung:	n/a	n/a
12	CEBPB	chr8:107215778-107216065	MCF-7	breast:	n/a	n/a
13	CEBPB	chr8:107220975-107221422	IMR90	lung:	n/a	n/a
14	CEBPB	chr8:107215750-107216127	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr8:107221004-107221388	A549	lung:	n/a	n/a
16	CEBPB	chr8:107220993-107221403	A549	lung:	n/a	n/a
17	CEBPB	chr8:107215783-107216086	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr8:107227539-107227600	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr8:107227460-107227610	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr8:107227519-107227619	MCF-7	breast:	n/a	n/a
21	CTCF	chr8:107227500-107227650	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr8:107227500-107227650	MCF-7	breast:	n/a	n/a
23	CTCF	chr8:107227540-107227690	MCF-7	breast:	n/a	n/a
24	CTCF	chr8:107227480-107227630	HAc	cerebellar:	n/a	n/a
25	CTCF	chr8:107227500-107227650	HCM	heart:	n/a	n/a
26	CTCF	chr8:107227514-107227617	HepG2	liver:	n/a	n/a
27	CTCF	chr8:107227566-107227571	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:107211790-107211825	MCF-7	breast:	n/a	n/a
29	CTCF	chr8:107227542-107227612	K562	blood:	n/a	n/a
30	CTCF	chr8:107227532-107227599	LNCaP	prostate:	n/a	n/a
31	CTCF	chr8:107227562-107227598	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr8:107227460-107227610	HepG2	liver:	n/a	n/a
33	CTCF	chr8:107218720-107218870	WI-38	lung:	n/a	n/a
34	CTCF	chr8:107227517-107227608	Fibrobl	skin:	n/a	n/a
35	CTCF	chr8:107226640-107226790	GM12873	blood:	n/a	n/a
36	E2F4	chr8:107215804-107216057	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr8:107231703-107231769	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr8:107211242-107211396	MCF10A-Er-Src	breast:	n/a	chr8:107211364-107211373
39	E2F4	chr8:107218687-107218789	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr8:107234575-107234787	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr8:107221010-107221442	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr8:107238254-107238276	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F6	chr8:107227686-107227815	K562	blood:	n/a	n/a
44	EBF1	chr8:107218571-107218799	GM12878	blood:	n/a	chr8:107218697-107218707 chr8:107218696-107218707 chr8:107218696-107218709
45	EBF1	chr8:107218528-107218838	GM12878	blood:	n/a	chr8:107218697-107218707 chr8:107218696-107218707 chr8:107218550-107218563 chr8:107218696-107218709
46	ELF1	chr8:107218471-107219103	SK-N-SH	brain:	n/a	chr8:107218778-107218789
47	EP300	chr8:107231272-107231755	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr8:107221015-107221372	SK-N-SH_RA	brain:	n/a	n/a
49	EP300	chr8:107219534-107220167	SK-N-SH	brain:	n/a	n/a
50	EP300	chr8:107219733-107219957	SK-N-SH_RA	brain:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:107227990-107228040	GM12878	blood:	n/a
2	chr8:107227990-107228040	GM12878	blood:	n/a
3	chr8:107227990-107228040	NHDF-neo	bronchial:	n/a
4	chr8:107231654-107231704	HepG2	liver:	n/a
5	chr8:107227990-107228040	CMK	blood:	n/a
6	chr8:107231654-107231704	SK-N-MC	brain:	n/a
7	chr8:107228006-107228056	AG04449	skin:	fetal
8	chr8:107227878-107227928	SKMC	muscle:	n/a
9	chr8:107227878-107227928	BJ	skin:	n/a
10	chr8:107228203-107228253	HepG2	liver:	n/a
11	chr8:107228565-107228615	SK-N-SH	brain:	n/a
12	chr8:107227990-107228040	AoSMC	blood vessel:	n/a
13	chr8:107227878-107227928	HEEpiC	esophagus:	n/a
14	chr8:107228565-107228615	BJ	skin:	n/a
15	chr8:107228006-107228056	HCF	heart:	n/a
16	chr8:107231654-107231704	HEEpiC	esophagus:	n/a
17	chr8:107228006-107228056	IMR90	lung:	fetal
18	chr8:107231654-107231704	HRCEpiC	kidney:	n/a
19	chr8:107228006-107228056	HAEpiC	amniotic membrane:	n/a
20	chr8:107227878-107227928	HAEpiC	amniotic membrane:	n/a
21	chr8:107228203-107228253	NB4	blood:	n/a
22	chr8:107227878-107227928	HCF	heart:	n/a
23	chr8:107228203-107228253	U87	brain:	n/a
24	chr8:107228565-107228615	NT2-D1	testis:	n/a
25	chr8:107227990-107228040	HAEpiC	amniotic membrane:	n/a
26	chr8:107228006-107228056	RPTEC	kidney:	n/a
27	chr8:107218994-107219044	HRCEpiC	kidney:	n/a
28	chr8:107228006-107228056	HEEpiC	esophagus:	n/a
29	chr8:107228565-107228615	T-47D	breast:	n/a
30	chr8:107228565-107228615	PANC-1	pancreas:	n/a
31	chr8:107227878-107227928	ovcar-3	ovarian:	n/a
32	chr8:107218994-107219044	Hepatocyte	liver:	n/a
33	chr8:107228203-107228253	SK-N-MC	brain:	n/a
34	chr8:107228006-107228056	T-47D	breast:	n/a
35	chr8:107228565-107228615	GM12891	blood:	n/a
36	chr8:107227878-107227928	AG04450	lung:	fetal
37	chr8:107228203-107228253	HCT-116	colon:	n/a
38	chr8:107228203-107228253	SK-N-SH_RA	brain:	n/a
39	chr8:107218994-107219044	NHBE	bronchial:	n/a
40	chr8:107227990-107228040	HIPEpiC	eye:	n/a
41	chr8:107228565-107228615	Hepatocyte	liver:	n/a
42	chr8:107227878-107227928	GM06990	blood:	n/a
43	chr8:107227878-107227928	MCF10A-Er-Src	breast:	n/a
44	chr8:107227990-107228040	SK-N-SH_RA	brain:	n/a
45	chr8:107227990-107228040	HCT-116	colon:	n/a
46	chr8:107227878-107227928	H1-hESC	embryonic stem cell:	embryo
47	chr8:107227878-107227928	HEK293	kidney:	embryo
48	chr8:107218994-107219044	RPTEC	kidney:	n/a
49	chr8:107227878-107227928	AG09309	skin:	n/a
50	chr8:107227878-107227928	GM12878	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:107221506..107223299-chr8:107416923..107419855,2	K562	blood:

No data

Variant related genes	Relation type
SLC16A14P1	TF binding region
SLC16A14P1	CpG island

Extended variants
information (count: 1072 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1072 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1503565	chr8:107210629-107210630	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576778992	chr8:107210644-107210645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs35137868	chr8:107210646-107210647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs61381952	chr8:107210669-107210670	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs187906335	chr8:107210674-107210675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537313562	chr8:107210686-107210687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371656928	chr8:107210710-107210711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529799131	chr8:107210722-107210723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs115839267	chr8:107210748-107210749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs3905307	chr8:107210761-107210762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561489778	chr8:107210817-107210818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192194227	chr8:107210819-107210820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547273755	chr8:107210883-107210884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571844267	chr8:107210888-107210889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550780405	chr8:107210920-107210921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs116015383	chr8:107210948-107210949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550542833	chr8:107210991-107210992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76585210	chr8:107211035-107211036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6986205	chr8:107211101-107211102	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs554607238	chr8:107211112-107211113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566670039	chr8:107211201-107211202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373643388	chr8:107211225-107211226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11988559	chr8:107211233-107211234	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs558861816	chr8:107211249-107211250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552792414	chr8:107211271-107211272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185000121	chr8:107211272-107211273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572559883	chr8:107211340-107211341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114440114	chr8:107211341-107211342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544259948	chr8:107211402-107211403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556173932	chr8:107211425-107211426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs71305185	chr8:107211488-107211489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs189586917	chr8:107211533-107211534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375762057	chr8:107211551-107211552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs372394975	chr8:107211590-107211591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs370391845	chr8:107211594-107211595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs560242079	chr8:107211597-107211598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528729898	chr8:107211625-107211626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181886048	chr8:107211665-107211666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568511256	chr8:107211693-107211694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565606232	chr8:107211694-107211695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs184698091	chr8:107211741-107211742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550831004	chr8:107211764-107211765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs189967854	chr8:107211819-107211820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145796384	chr8:107211824-107211825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs548281492	chr8:107211843-107211844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554913147	chr8:107211870-107211871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566851550	chr8:107211939-107211940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534037275	chr8:107211954-107211955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs181373006	chr8:107212014-107212015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs73299601	chr8:107212028-107212029	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:96)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:210 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:107204200-107214400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:107206400-107219000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:107211400-107212400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:107211400-107212600	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr8:107211400-107212600	Enhancers	Osteobl	bone
6	chr8:107211400-107212800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:107211600-107212400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:107211600-107212400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr8:107211600-107212600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr8:107211600-107212600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr8:107211600-107212800	Enhancers	NHDF-Ad	bronchial
12	chr8:107211600-107213400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr8:107211800-107212400	Enhancers	Muscle Satellite Cultured Cells	--
14	chr8:107211800-107212400	Enhancers	NH-A	brain
15	chr8:107212000-107212200	Enhancers	HSMMtube	muscle
16	chr8:107212200-107212800	Enhancers	Fetal Heart	heart
17	chr8:107212400-107214200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr8:107212600-107218000	Weak transcription	Osteobl	bone
19	chr8:107212600-107218800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr8:107212800-107215200	Weak transcription	NHDF-Ad	bronchial
21	chr8:107212800-107215400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr8:107213000-107214600	Enhancers	Placenta Amnion	Placenta Amnion
23	chr8:107213400-107218600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr8:107214200-107214800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr8:107214200-107215600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr8:107214200-107216000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr8:107214400-107215000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr8:107214400-107215000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr8:107214600-107215800	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr8:107215000-107217000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr8:107215000-107218800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr8:107215200-107222200	Enhancers	NHDF-Ad	bronchial
33	chr8:107215400-107222200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr8:107215600-107216600	Enhancers	NHLF	lung
35	chr8:107215800-107216000	Enhancers	Placenta Amnion	Placenta Amnion
36	chr8:107215800-107216200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr8:107215800-107216200	Enhancers	A549	lung
38	chr8:107216000-107216400	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr8:107216000-107216600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr8:107216000-107218000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr8:107216200-107218200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr8:107216200-107218200	Weak transcription	A549	lung
43	chr8:107216400-107219400	Enhancers	Placenta Amnion	Placenta Amnion
44	chr8:107216600-107218200	Weak transcription	NHLF	lung
45	chr8:107216600-107218600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr8:107217000-107217200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr8:107217000-107217400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr8:107217200-107217800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr8:107217400-107218600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr8:107217800-107220000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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