Variant report

Variant	nsv824701
Chromosome Location	chr8:107378298-107520063
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	chr8:107497865-107497994	K562	blood:	n/a	n/a
2	BACH1	chr8:107431314-107431625	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr8:107512495-107512857	GM12878	blood:	n/a	n/a
4	BATF	chr8:107512571-107512851	GM12878	blood:	n/a	n/a
5	BATF	chr8:107441048-107441442	GM12878	blood:	n/a	n/a
6	BATF	chr8:107378819-107379079	GM12878	blood:	n/a	n/a
7	BCL11A	chr8:107512572-107512797	GM12878	blood:	n/a	n/a
8	BCL11A	chr8:107441081-107441314	GM12878	blood:	n/a	n/a
9	BCL11A	chr8:107378828-107379071	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:107512501-107512846	GM12878	blood:	n/a	n/a
11	CBX3	chr8:107468207-107468776	HCT-116	colon:	n/a	n/a
12	CBX3	chr8:107439576-107440042	HCT-116	colon:	n/a	n/a
13	CBX3	chr8:107473833-107474256	HCT-116	colon:	n/a	n/a
14	CBX3	chr8:107439476-107440053	HCT-116	colon:	n/a	n/a
15	CEBPB	chr8:107491638-107491922	Hela-S3	cervix:	n/a	chr8:107491745-107491756
16	CEBPB	chr8:107465735-107466018	HepG2	liver:	n/a	chr8:107465878-107465889
17	CEBPB	chr8:107478827-107479115	HepG2	liver:	n/a	chr8:107478966-107478977
18	CEBPB	chr8:107498335-107498419	HepG2	liver:	n/a	n/a
19	CEBPB	chr8:107478853-107479101	K562	blood:	n/a	chr8:107478966-107478977
20	CEBPB	chr8:107476871-107477220	H1-hESC	embryonic stem cell:	n/a	chr8:107477032-107477041 chr8:107477032-107477041 chr8:107477031-107477042 chr8:107477030-107477043 chr8:107477032-107477041
21	CEBPB	chr8:107491586-107491906	HepG2	liver:	n/a	chr8:107491745-107491756
22	CEBPB	chr8:107476852-107477225	IMR90	lung:	n/a	chr8:107477032-107477041 chr8:107477032-107477041 chr8:107477031-107477042 chr8:107477030-107477043 chr8:107477032-107477041
23	CEBPB	chr8:107478787-107479147	IMR90	lung:	n/a	chr8:107478966-107478977
24	CEBPB	chr8:107396631-107396939	IMR90	lung:	n/a	chr8:107396751-107396759
25	CEBPB	chr8:107517242-107517556	IMR90	lung:	n/a	n/a
26	CEBPB	chr8:107387760-107388013	H1-hESC	embryonic stem cell:	n/a	chr8:107387853-107387866
27	CEBPB	chr8:107395538-107395786	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:107410533-107410823	IMR90	lung:	n/a	n/a
29	CEBPB	chr8:107473873-107474212	HCT-116	colon:	n/a	n/a
30	CEBPB	chr8:107465750-107466053	A549	lung:	n/a	chr8:107465878-107465889
31	CEBPB	chr8:107411494-107411663	HepG2	liver:	n/a	n/a
32	CEBPB	chr8:107476848-107477218	HepG2	liver:	n/a	chr8:107477032-107477041 chr8:107477032-107477041 chr8:107477031-107477042 chr8:107477030-107477043 chr8:107477032-107477041
33	CEBPB	chr8:107467574-107468789	HCT-116	colon:	n/a	n/a
34	CEBPB	chr8:107476854-107477218	A549	lung:	n/a	chr8:107477032-107477041 chr8:107477032-107477041 chr8:107477031-107477042 chr8:107477030-107477043 chr8:107477032-107477041
35	CEBPB	chr8:107476947-107477145	ECC-1	luminal epithelium:	n/a	chr8:107477031-107477042 chr8:107477030-107477043 chr8:107477032-107477041 chr8:107477032-107477041 chr8:107477032-107477041
36	CEBPB	chr8:107476849-107477229	K562	blood:	n/a	chr8:107477032-107477041 chr8:107477032-107477041 chr8:107477031-107477042 chr8:107477030-107477043 chr8:107477032-107477041
37	CEBPB	chr8:107476840-107477240	A549	lung:	n/a	chr8:107477032-107477041 chr8:107477032-107477041 chr8:107477031-107477042 chr8:107477030-107477043 chr8:107477032-107477041
38	CEBPB	chr8:107394265-107394488	HepG2	liver:	n/a	chr8:107394429-107394440
39	CEBPB	chr8:107447973-107448173	A549	lung:	n/a	n/a
40	CEBPB	chr8:107411518-107411677	A549	lung:	n/a	n/a
41	CEBPB	chr8:107491692-107491907	H1-hESC	embryonic stem cell:	n/a	chr8:107491745-107491756
42	CEBPB	chr8:107394327-107394577	IMR90	lung:	n/a	chr8:107394429-107394440
43	CEBPB	chr8:107396734-107396825	A549	lung:	n/a	chr8:107396751-107396759
44	CEBPB	chr8:107465721-107466045	IMR90	lung:	n/a	chr8:107465878-107465889
45	CEBPB	chr8:107476776-107477259	A549	lung:	n/a	chr8:107477032-107477041 chr8:107477032-107477041 chr8:107477031-107477042 chr8:107477030-107477043 chr8:107477032-107477041
46	CEBPB	chr8:107473787-107474375	HCT-116	colon:	n/a	n/a
47	CEBPB	chr8:107476864-107477204	Hela-S3	cervix:	n/a	chr8:107477032-107477041 chr8:107477032-107477041 chr8:107477031-107477042 chr8:107477030-107477043 chr8:107477032-107477041
48	CEBPB	chr8:107491579-107491918	IMR90	lung:	n/a	chr8:107491745-107491756
49	CEBPB	chr8:107491640-107491899	A549	lung:	n/a	chr8:107491745-107491756
50	CEBPB	chr8:107439684-107439884	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:107462460-107462510	H1-hESC	embryonic stem cell:	embryo
2	chr8:107462460-107462510	H1-hESC	embryonic stem cell:	embryo
3	chr8:107460168-107460218	HRPEpiC	eye:	n/a
4	chr8:107460168-107460218	AG09319	gingival:	n/a
5	chr8:107460168-107460218	HRCEpiC	kidney:	n/a
6	chr8:107460168-107460218	AG04449	skin:	fetal
7	chr8:107460168-107460218	HMEC	breast:	n/a
8	chr8:107460168-107460218	SK-N-SH_RA	brain:	n/a
9	chr8:107460168-107460218	Hepatocyte	liver:	n/a
10	chr8:107462460-107462510	NHDF-neo	bronchial:	n/a
11	chr8:107460168-107460218	Jurkat	blood:	n/a
12	chr8:107460168-107460218	K562	blood:	n/a
13	chr8:107462460-107462510	HCF	heart:	n/a
14	chr8:107462460-107462510	BE2_C	brain:	n/a
15	chr8:107460168-107460218	SK-N-MC	brain:	n/a
16	chr8:107460168-107460218	AG10803	skin:	n/a
17	chr8:107462460-107462510	A549	lung:	n/a
18	chr8:107462460-107462510	SK-N-SH_RA	brain:	n/a
19	chr8:107460168-107460218	BE2_C	brain:	n/a
20	chr8:107462460-107462510	CMK	blood:	n/a
21	chr8:107460168-107460218	SK-N-SH	brain:	n/a
22	chr8:107462460-107462510	SAEC	small airway:	n/a
23	chr8:107460168-107460218	AG04450	lung:	fetal
24	chr8:107460168-107460218	U87	brain:	n/a
25	chr8:107460168-107460218	SKMC	muscle:	n/a
26	chr8:107460168-107460218	H1-hESC	embryonic stem cell:	embryo
27	chr8:107462460-107462510	HRPEpiC	eye:	n/a
28	chr8:107462460-107462510	HL-60	blood:	n/a
29	chr8:107460168-107460218	PANC-1	pancreas:	n/a
30	chr8:107462460-107462510	RPTEC	kidney:	n/a
31	chr8:107462460-107462510	ECC-1	luminal epithelium:	n/a
32	chr8:107460168-107460218	HNPCEpiC	eye:	n/a
33	chr8:107460168-107460218	Hela-S3	cervix:	n/a
34	chr8:107462460-107462510	HCPEpiC	choroid plexus:	n/a
35	chr8:107462460-107462510	IMR90	lung:	fetal
36	chr8:107460168-107460218	LNCaP	prostate:	n/a
37	chr8:107460168-107460218	HCF	heart:	n/a
38	chr8:107460168-107460218	Caco-2	colon:	n/a
39	chr8:107462460-107462510	U87	brain:	n/a
40	chr8:107462460-107462510	SKMC	muscle:	n/a
41	chr8:107460168-107460218	NT2-D1	testis:	n/a
42	chr8:107460168-107460218	GM19239	blood:	n/a
43	chr8:107460168-107460218	GM06990	blood:	n/a
44	chr8:107462460-107462510	PANC-1	pancreas:	n/a
45	chr8:107460168-107460218	MCF-7	breast:	n/a
46	chr8:107460168-107460218	HCM	heart:	n/a
47	chr8:107460168-107460218	A549	lung:	n/a
48	chr8:107460168-107460218	CMK	blood:	n/a
49	chr8:107462460-107462510	HMEC	breast:	n/a
50	chr8:107462460-107462510	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:107466184..107467709-chr8:107494491..107496529,2	MCF-7	breast:
2	chr8:107426897..107429687-chr8:107442914..107445145,2	K562	blood:
3	chr8:107434524..107437041-chr8:107438558..107440145,2	K562	blood:
4	chr8:107479862..107482476-chr8:107487797..107489316,2	K562	blood:
5	chr8:107425582..107427133-chr8:107435679..107438329,2	K562	blood:
6	chr8:107389009..107391752-chr8:107392605..107394490,2	MCF-7	breast:
7	chr8:107195796..107197608-chr8:107475772..107478613,2	K562	blood:
8	chr8:107221506..107223299-chr8:107416923..107419855,2	K562	blood:
9	chr8:107480149..107482279-chr8:107497864..107500285,3	MCF-7	breast:
10	chr8:107282403..107283907-chr8:107484126..107486179,2	K562	blood:
11	chr8:107515040..107517376-chr8:107517992..107519843,2	K562	blood:
12	chr8:107473925..107475852-chr8:107477064..107479538,2	K562	blood:
13	chr8:107428187..107430398-chr8:107443082..107445145,2	K562	blood:
14	chr8:107434524..107437041-chr8:107438558..107440145,2	K562	blood:
15	chr8:107426897..107429687-chr8:107442914..107445145,2	K562	blood:
16	chr8:107480149..107482279-chr8:107497864..107500285,3	MCF-7	breast:
17	chr8:107473925..107475852-chr8:107477064..107479538,2	K562	blood:
18	chr8:107515040..107517376-chr8:107517992..107519843,2	K562	blood:
19	chr8:107479862..107482476-chr8:107487797..107489316,2	K562	blood:
20	chr16:89626976..89627502-chr8:107414504..107415468,2	MCF-7	breast:
21	chr8:107425582..107427133-chr8:107435679..107438329,2	K562	blood:
22	chr7:84922126..84922846-chr8:107469062..107469738,2	HCT-116	colon:
23	chr8:107511052..107513324-chr8:107531040..107533004,2	K562	blood:
24	chr8:107389009..107391752-chr8:107392605..107394490,2	MCF-7	breast:
25	chr8:107428187..107430398-chr8:107443082..107445145,2	K562	blood:
26	chr8:107466184..107467709-chr8:107494491..107496529,2	MCF-7	breast:

Variant related genes	Relation type
OXR1	TF binding region
OXR1	CpG island
ENSG00000167526	chromatin interactions
ENSG00000254615	chromatin interactions
ENSG00000164830	chromatin interactions

Extended variants
information (count: 5017 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:5017 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577401466	chr8:107378339-107378340	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs544437540	chr8:107378354-107378355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112594742	chr8:107378355-107378356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574532769	chr8:107378376-107378377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150136279	chr8:107378385-107378386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559986169	chr8:107378422-107378423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368563737	chr8:107378471-107378472	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548046708	chr8:107378538-107378539	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527318043	chr8:107378564-107378565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138774770	chr8:107378568-107378569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563876721	chr8:107378590-107378591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190855853	chr8:107378641-107378642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549799644	chr8:107378659-107378660	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569362351	chr8:107378660-107378661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536823243	chr8:107378665-107378666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181690997	chr8:107378681-107378682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568271589	chr8:107378705-107378706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567152530	chr8:107378722-107378723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534220225	chr8:107378734-107378735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141848201	chr8:107378772-107378773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571005653	chr8:107378773-107378774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532554659	chr8:107378825-107378826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs116251878	chr8:107378851-107378852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539027890	chr8:107378852-107378853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185677872	chr8:107378877-107378878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574567776	chr8:107378880-107378881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372810066	chr8:107378905-107378906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553681755	chr8:107378911-107378912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376474553	chr8:107378934-107378935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571996668	chr8:107378958-107378959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190144969	chr8:107379012-107379013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565407946	chr8:107379059-107379060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557287767	chr8:107379061-107379062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563740310	chr8:107379062-107379063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182834543	chr8:107379081-107379082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543170152	chr8:107379084-107379085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539608391	chr8:107379105-107379106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561796111	chr8:107379162-107379163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530262488	chr8:107379174-107379175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548784898	chr8:107379238-107379239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141005067	chr8:107379293-107379294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs398009244	chr8:107379308-107379309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs117556932	chr8:107379313-107379314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527988723	chr8:107379314-107379315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539017180	chr8:107379344-107379345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558939594	chr8:107379353-107379354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552858526	chr8:107379359-107379360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs6469063	chr8:107379371-107379372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538210509	chr8:107379376-107379377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187955239	chr8:107379382-107379383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Prostate cancer	22341455	CNVD
Colorectal cancer	21645411	CNVD
Multiple myeloma	17550852	CNVD

Chromatin state (count:640 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:107362400-107427000	Weak transcription	Aorta	Aorta
2	chr8:107362800-107397000	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr8:107372000-107384400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr8:107372400-107382400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr8:107372600-107378600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr8:107374000-107384000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr8:107374400-107409800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr8:107375600-107378800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr8:107378800-107379800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr8:107379800-107381200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr8:107381200-107403400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr8:107382000-107390400	Weak transcription	Gastric	stomach
13	chr8:107383800-107384400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr8:107383800-107384400	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr8:107383800-107384600	Enhancers	H1 Cell Line	embryonic stem cell
16	chr8:107383800-107384600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr8:107383800-107384600	Enhancers	Placenta Amnion	Placenta Amnion
18	chr8:107384000-107384200	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr8:107384000-107384400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr8:107384000-107384400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr8:107384000-107384400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr8:107384000-107384400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr8:107384000-107384400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr8:107384000-107384400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr8:107384000-107384600	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr8:107384000-107384600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr8:107384000-107384600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr8:107384000-107384600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr8:107384000-107384600	Enhancers	Esophagus	oesophagus
30	chr8:107384000-107384600	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr8:107384000-107384800	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr8:107384200-107386600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr8:107384400-107387800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr8:107384400-107396600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr8:107384600-107404000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr8:107387800-107388200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr8:107388600-107389000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
38	chr8:107389600-107390200	Enhancers	HUVEC	blood vessel
39	chr8:107390000-107390400	Enhancers	Fetal Heart	heart
40	chr8:107390400-107390800	Enhancers	Gastric	stomach
41	chr8:107390800-107396600	Weak transcription	Gastric	stomach
42	chr8:107396200-107399000	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr8:107396600-107396800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr8:107396600-107396800	Enhancers	Gastric	stomach
45	chr8:107396600-107398400	Enhancers	Fetal Intestine Large	intestine
46	chr8:107396800-107399600	Weak transcription	Gastric	stomach
47	chr8:107397000-107398200	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr8:107397200-107398400	Enhancers	Fetal Intestine Small	intestine
49	chr8:107398200-107398400	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr8:107398200-107409400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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