Variant report

Variant	nsv1034119
Chromosome Location	chr8:19115084-19164833
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:872)
CpG islands
(count:122)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:872 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:19124872-19125433	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:19137599-19138311	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:19128678-19129043	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:19149146-19149417	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:19125250-19125277	K562	blood:	n/a	n/a
6	BCL3	chr8:19148800-19149410	A549	lung:	n/a	n/a
7	BRCA1	chr8:19148949-19149382	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr8:19125027-19125674	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr8:19148884-19149453	HCT-116	colon:	n/a	n/a
10	CEBPB	chr8:19137227-19137431	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr8:19128736-19129013	MCF-7	breast:	n/a	n/a
12	CEBPB	chr8:19128745-19129090	HCT-116	colon:	n/a	n/a
13	CEBPB	chr8:19128684-19129051	HepG2	liver:	n/a	n/a
14	CEBPB	chr8:19148912-19149467	HCT-116	colon:	n/a	chr8:19148933-19148946
15	CEBPB	chr8:19128747-19129011	K562	blood:	n/a	n/a
16	CEBPB	chr8:19149138-19149329	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr8:19153183-19153441	IMR90	lung:	n/a	chr8:19153309-19153320 chr8:19153309-19153322
18	CEBPB	chr8:19137796-19138239	HepG2	liver:	n/a	n/a
19	CEBPB	chr8:19163278-19163543	IMR90	lung:	n/a	n/a
20	CEBPB	chr8:19128787-19129003	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:19148697-19149552	A549	lung:	n/a	chr8:19148933-19148946
22	CEBPB	chr8:19148893-19149493	MCF-7	breast:	n/a	chr8:19148933-19148946
23	CEBPB	chr8:19129554-19129721	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr8:19128702-19129031	HCT-116	colon:	n/a	n/a
25	CEBPB	chr8:19128679-19129059	HepG2	liver:	n/a	n/a
26	CEBPB	chr8:19148817-19149547	MCF-7	breast:	n/a	chr8:19148933-19148946
27	CEBPB	chr8:19128709-19129034	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr8:19128692-19129039	A549	lung:	n/a	n/a
29	CEBPB	chr8:19149055-19149255	K562	blood:	n/a	n/a
30	CEBPB	chr8:19132687-19132958	HepG2	liver:	n/a	n/a
31	CEBPB	chr8:19148824-19149440	ECC-1	luminal epithelium:	n/a	chr8:19148933-19148946
32	CEBPB	chr8:19128695-19129021	HepG2	liver:	n/a	n/a
33	CEBPB	chr8:19122576-19122892	HepG2	liver:	n/a	chr8:19122725-19122742
34	CEBPB	chr8:19122611-19122869	A549	lung:	n/a	chr8:19122725-19122742
35	CEBPB	chr8:19132662-19132800	K562	blood:	n/a	n/a
36	CEBPB	chr8:19148873-19149418	A549	lung:	n/a	chr8:19148933-19148946
37	CEBPB	chr8:19148764-19149466	IMR90	lung:	n/a	chr8:19148933-19148946
38	CEBPB	chr8:19156052-19156603	IMR90	lung:	n/a	n/a
39	CEBPB	chr8:19153165-19153379	HepG2	liver:	n/a	chr8:19153309-19153320 chr8:19153309-19153322
40	CEBPB	chr8:19128734-19129031	A549	lung:	n/a	n/a
41	CEBPB	chr8:19124929-19125474	Hela-S3	cervix:	n/a	chr8:19125053-19125064
42	CEBPB	chr8:19148939-19149431	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr8:19132686-19132921	A549	lung:	n/a	n/a
44	CEBPB	chr8:19148777-19149483	Hela-S3	cervix:	n/a	chr8:19148933-19148946
45	CEBPB	chr8:19121978-19122340	HepG2	liver:	n/a	n/a
46	CEBPB	chr8:19128654-19129089	A549	lung:	n/a	n/a
47	CEBPB	chr8:19128767-19129064	ECC-1	luminal epithelium:	n/a	n/a
48	CEBPB	chr8:19129441-19129898	ECC-1	luminal epithelium:	n/a	n/a
49	CEBPB	chr8:19148959-19149407	HepG2	liver:	n/a	n/a
50	CEBPB	chr8:19128773-19129043	MCF-7	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:19156146-19156196	AG04450	lung:	fetal
2	chr8:19125368-19125418	HPAEpiC	pulmonary alveolar:	n/a
3	chr8:19156146-19156196	SKMC	muscle:	n/a
4	chr8:19125368-19125418	NB4	blood:	n/a
5	chr8:19125368-19125418	NT2-D1	testis:	n/a
6	chr8:19156146-19156196	HepG2	liver:	n/a
7	chr8:19156146-19156196	HCF	heart:	n/a
8	chr8:19156146-19156196	HIPEpiC	eye:	n/a
9	chr8:19156146-19156196	HMEC	breast:	n/a
10	chr8:19125368-19125418	PFSK-1	brain:	n/a
11	chr8:19125368-19125418	GM12878	blood:	n/a
12	chr8:19156146-19156196	PANC-1	pancreas:	n/a
13	chr8:19125368-19125418	NHDF-neo	bronchial:	n/a
14	chr8:19125368-19125418	Hepatocyte	liver:	n/a
15	chr8:19156146-19156196	Hela-S3	cervix:	n/a
16	chr8:19125368-19125418	SK-N-MC	brain:	n/a
17	chr8:19125368-19125418	AG04449	skin:	fetal
18	chr8:19156146-19156196	SK-N-MC	brain:	n/a
19	chr8:19156146-19156196	GM06990	blood:	n/a
20	chr8:19125368-19125418	AG04450	lung:	fetal
21	chr8:19125368-19125418	HCF	heart:	n/a
22	chr8:19125368-19125418	Jurkat	blood:	n/a
23	chr8:19125368-19125418	PrEC	prostate:	n/a
24	chr8:19156146-19156196	HUVEC	blood vessel:	n/a
25	chr8:19156146-19156196	AG10803	skin:	n/a
26	chr8:19125368-19125418	GM12891	blood:	n/a
27	chr8:19125368-19125418	HUVEC	blood vessel:	n/a
28	chr8:19156146-19156196	K562	blood:	n/a
29	chr8:19125368-19125418	HCM	heart:	n/a
30	chr8:19125368-19125418	SAEC	small airway:	n/a
31	chr8:19156146-19156196	SK-N-SH	brain:	n/a
32	chr8:19156146-19156196	AG04449	skin:	fetal
33	chr8:19156146-19156196	HRE	kidney:	n/a
34	chr8:19125368-19125418	HCT-116	colon:	n/a
35	chr8:19156146-19156196	MCF-7	breast:	n/a
36	chr8:19156146-19156196	HRCEpiC	kidney:	n/a
37	chr8:19156146-19156196	IMR90	lung:	fetal
38	chr8:19125368-19125418	K562	blood:	n/a
39	chr8:19125368-19125418	T-47D	breast:	n/a
40	chr8:19156146-19156196	NHBE	bronchial:	n/a
41	chr8:19125368-19125418	HepG2	liver:	n/a
42	chr8:19125368-19125418	A549	lung:	n/a
43	chr8:19125368-19125418	HL-60	blood:	n/a
44	chr8:19156146-19156196	HPAEpiC	pulmonary alveolar:	n/a
45	chr8:19125368-19125418	BJ	skin:	n/a
46	chr8:19125368-19125418	HNPCEpiC	eye:	n/a
47	chr8:19156146-19156196	GM12878	blood:	n/a
48	chr8:19125368-19125418	PANC-1	pancreas:	n/a
49	chr8:19156146-19156196	Caco-2	colon:	n/a
50	chr8:19156146-19156196	SAEC	small airway:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:19156532..19159524-chr8:19170148..19172446,2	MCF-7	breast:
2	chr8:19034788..19035554-chr8:19124800..19125342,2	MCF-7	breast:
3	chr8:19123737..19126710-chr8:19170516..19173345,2	MCF-7	breast:
4	chr8:19120168..19121747-chr8:19134338..19135929,2	K562	blood:
5	chr8:19147589..19149540-chr8:19523160..19524664,2	MCF-7	breast:
6	chr8:19147926..19150795-chr8:19170285..19172249,2	MCF-7	breast:
7	chr8:19152770..19154882-chr8:19158766..19160464,2	K562	blood:
8	chr8:19120168..19121747-chr8:19134338..19135929,2	K562	blood:
9	chr8:19148156..19152459-chr8:19169128..19172088,7	MCF-7	breast:
10	chr8:19144461..19147739-chr8:19170304..19172981,3	MCF-7	breast:
11	chr8:19148177..19150555-chr8:19150746..19153628,2	K562	blood:
12	chr8:19125143..19125678-chr8:19171239..19172025,2	MCF-7	breast:
13	chr8:19146966..19149051-chr8:19185409..19187470,2	MCF-7	breast:
14	chr8:19126347..19128223-chr8:19186550..19188769,2	K562	blood:
15	chr8:19155044..19157820-chr8:19172820..19174971,2	MCF-7	breast:
16	chr8:19142668..19144947-chr8:19171540..19174164,2	MCF-7	breast:
17	chr8:19128887..19134305-chr8:19169094..19173373,6	MCF-7	breast:
18	chr8:19148177..19150555-chr8:19150746..19153628,2	K562	blood:
19	chr8:18769464..18770410-chr8:19124856..19125711,4	K562	blood:
20	chr8:19152770..19154882-chr8:19158766..19160464,2	K562	blood:
21	chr8:19149962..19152072-chr8:19173164..19175700,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000253557	TF binding region
ENSG00000253280	TF binding region
ENSG00000253557	CpG island
ENSG00000253280	CpG island
ENSG00000104611	chromatin interactions

Extended variants
information (count: 2642 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:2642 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185627171	chr8:19115084-19115085	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs188890173	chr8:19115117-19115118	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs547803277	chr8:19115135-19115136	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs7010888	chr8:19115136-19115137	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs368625738	chr8:19115140-19115141	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs79611771	chr8:19115183-19115184	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs192631033	chr8:19115199-19115200	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs578099699	chr8:19115206-19115207	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs184420465	chr8:19115274-19115275	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs570216915	chr8:19115281-19115282	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs189695278	chr8:19115284-19115285	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs529287127	chr8:19115303-19115304	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs372894958	chr8:19115319-19115320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141182585	chr8:19115321-19115322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs6986433	chr8:19115326-19115327	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs551817548	chr8:19115348-19115349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7836792	chr8:19115398-19115399	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs376892022	chr8:19115475-19115476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527458300	chr8:19115477-19115478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547762341	chr8:19115491-19115492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144117938	chr8:19115513-19115514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536510987	chr8:19115544-19115545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs28492702	chr8:19115549-19115550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201371092	chr8:19115576-19115577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199579617	chr8:19115577-19115578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs397892441	chr8:19115586-19115587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2683313	chr8:19115604-19115605	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs559993057	chr8:19115635-19115636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10088618	chr8:19115680-19115681	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs578131540	chr8:19115682-19115683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181218692	chr8:19115717-19115718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553905897	chr8:19115744-19115745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573995485	chr8:19115762-19115763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542882718	chr8:19115769-19115770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6586818	chr8:19115772-19115773	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs572170425	chr8:19115777-19115778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs111305420	chr8:19115854-19115855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531715068	chr8:19115856-19115857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545198671	chr8:19115857-19115858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9644621	chr8:19115882-19115883	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs148374796	chr8:19115897-19115898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534738109	chr8:19115899-19115900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547623020	chr8:19115913-19115914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2672227	chr8:19115947-19115948	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs530039606	chr8:19115998-19115999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550017585	chr8:19116021-19116022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569587203	chr8:19116029-19116030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs17128053	chr8:19116030-19116031	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs558416625	chr8:19116032-19116033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141441490	chr8:19116055-19116056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
Prostate cancer	21965145	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
Colorectal cancer	16272173	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
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Epilepsy	22083797	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17603634	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cancer	18840272	CNVD
Breast cancer	19602461	CNVD
Osteosarcoma	19286668	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	19258508	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
small cell lung cancer	20016488	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Gastric adenocarcinoma	19115996	CNVD
Colorectal cancer	19455253	CNVD

Chromatin state (count:536 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19113400-19119600	Weak transcription	Ovary	ovary
2	chr8:19118400-19119000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr8:19118600-19118800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr8:19119000-19121800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr8:19119000-19122000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr8:19119600-19119800	Enhancers	HepG2	liver
7	chr8:19119600-19120400	Enhancers	Ovary	ovary
8	chr8:19119600-19120400	Enhancers	A549	lung
9	chr8:19119600-19120400	Enhancers	Osteobl	bone
10	chr8:19119600-19120600	Enhancers	NH-A	brain
11	chr8:19119600-19123800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr8:19119600-19124600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr8:19119800-19121000	Weak transcription	HepG2	liver
14	chr8:19120400-19121200	Weak transcription	Ovary	ovary
15	chr8:19120400-19124600	Weak transcription	Osteobl	bone
16	chr8:19120400-19124800	Weak transcription	A549	lung
17	chr8:19120600-19124600	Weak transcription	NH-A	brain
18	chr8:19121000-19121600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr8:19121000-19123000	Enhancers	Fetal Heart	heart
20	chr8:19121000-19123600	Enhancers	HepG2	liver
21	chr8:19121200-19121800	Enhancers	Brain Anterior Caudate	brain
22	chr8:19121200-19122200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr8:19121200-19123800	Enhancers	Ovary	ovary
24	chr8:19121400-19121600	Enhancers	Spleen	Spleen
25	chr8:19121400-19123600	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr8:19121600-19124000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr8:19121600-19129400	Weak transcription	Spleen	Spleen
28	chr8:19121800-19122000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr8:19121800-19122200	Weak transcription	Brain Anterior Caudate	brain
30	chr8:19121800-19123000	Enhancers	Stomach Mucosa	stomach
31	chr8:19122000-19122400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr8:19122000-19122400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr8:19122000-19122400	Enhancers	Pancreas	Pancrea
34	chr8:19122000-19122800	Enhancers	Fetal Muscle Leg	muscle
35	chr8:19122000-19123200	Enhancers	Fetal Intestine Small	intestine
36	chr8:19122000-19123200	Enhancers	Gastric	stomach
37	chr8:19122000-19123800	Enhancers	Duodenum Mucosa	Duodenum
38	chr8:19122000-19124800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr8:19122200-19122400	Enhancers	Brain Anterior Caudate	brain
40	chr8:19122200-19123600	Enhancers	Fetal Intestine Large	intestine
41	chr8:19122200-19123800	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr8:19122200-19124600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr8:19122400-19124600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr8:19122400-19125000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr8:19122400-19125000	Weak transcription	Brain Anterior Caudate	brain
46	chr8:19122400-19129800	Weak transcription	Pancreas	Pancrea
47	chr8:19122600-19123000	Enhancers	Small Intestine	intestine
48	chr8:19122800-19125000	Weak transcription	Fetal Muscle Leg	muscle
49	chr8:19123000-19123600	Weak transcription	Stomach Mucosa	stomach
50	chr8:19123000-19124800	Weak transcription	Fetal Heart	heart

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