Variant report

Variant	nsv611844
Chromosome Location	chr8:107440038-107494918
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	BATF	chr8:107441048-107441442	GM12878	blood:	n/a	n/a
2	BCL11A	chr8:107441081-107441314	GM12878	blood:	n/a	n/a
3	CBX3	chr8:107439476-107440053	HCT-116	colon:	n/a	n/a
4	CBX3	chr8:107468207-107468776	HCT-116	colon:	n/a	n/a
5	CBX3	chr8:107439576-107440042	HCT-116	colon:	n/a	n/a
6	CBX3	chr8:107473833-107474256	HCT-116	colon:	n/a	n/a
7	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
8	CEBPB	chr8:107476849-107477229	K562	blood:	n/a	chr8:107477032-107477041 chr8:107477032-107477041 chr8:107477031-107477042 chr8:107477030-107477043 chr8:107477032-107477041
9	CEBPB	chr8:107473873-107474212	HCT-116	colon:	n/a	n/a
10	CEBPB	chr8:107476848-107477218	HepG2	liver:	n/a	chr8:107477032-107477041 chr8:107477032-107477041 chr8:107477031-107477042 chr8:107477030-107477043 chr8:107477032-107477041
11	CEBPB	chr8:107467574-107468789	HCT-116	colon:	n/a	n/a
12	CEBPB	chr8:107476776-107477259	A549	lung:	n/a	chr8:107477032-107477041 chr8:107477032-107477041 chr8:107477031-107477042 chr8:107477030-107477043 chr8:107477032-107477041
13	CEBPB	chr8:107491586-107491906	HepG2	liver:	n/a	chr8:107491745-107491756
14	CEBPB	chr8:107478839-107479085	A549	lung:	n/a	chr8:107478966-107478977
15	CEBPB	chr8:107476852-107477225	IMR90	lung:	n/a	chr8:107477032-107477041 chr8:107477032-107477041 chr8:107477031-107477042 chr8:107477030-107477043 chr8:107477032-107477041
16	CEBPB	chr8:107465721-107466045	IMR90	lung:	n/a	chr8:107465878-107465889
17	CEBPB	chr8:107465750-107466053	A549	lung:	n/a	chr8:107465878-107465889
18	CEBPB	chr8:107465735-107466018	HepG2	liver:	n/a	chr8:107465878-107465889
19	CEBPB	chr8:107476840-107477240	A549	lung:	n/a	chr8:107477032-107477041 chr8:107477032-107477041 chr8:107477031-107477042 chr8:107477030-107477043 chr8:107477032-107477041
20	CEBPB	chr8:107476864-107477204	Hela-S3	cervix:	n/a	chr8:107477032-107477041 chr8:107477032-107477041 chr8:107477031-107477042 chr8:107477030-107477043 chr8:107477032-107477041
21	CEBPB	chr8:107491692-107491907	H1-hESC	embryonic stem cell:	n/a	chr8:107491745-107491756
22	CEBPB	chr8:107491638-107491922	Hela-S3	cervix:	n/a	chr8:107491745-107491756
23	CEBPB	chr8:107478827-107479115	HepG2	liver:	n/a	chr8:107478966-107478977
24	CEBPB	chr8:107478853-107479101	K562	blood:	n/a	chr8:107478966-107478977
25	CEBPB	chr8:107476854-107477218	A549	lung:	n/a	chr8:107477032-107477041 chr8:107477032-107477041 chr8:107477031-107477042 chr8:107477030-107477043 chr8:107477032-107477041
26	CEBPB	chr8:107491579-107491918	IMR90	lung:	n/a	chr8:107491745-107491756
27	CEBPB	chr8:107473787-107474375	HCT-116	colon:	n/a	n/a
28	CEBPB	chr8:107447973-107448173	A549	lung:	n/a	n/a
29	CEBPB	chr8:107491640-107491899	A549	lung:	n/a	chr8:107491745-107491756
30	CEBPB	chr8:107478787-107479147	IMR90	lung:	n/a	chr8:107478966-107478977
31	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
32	CHD2	chr8:107460096-107460304	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr8:107469640-107469790	A549	lung:	n/a	n/a
34	CTCF	chr8:107448880-107449030	HPF	lung:	n/a	n/a
35	CTCF	chr8:107439920-107440070	SAEC	small airway:	n/a	chr8:107440040-107440053
36	CTCF	chr8:107459080-107459230	HMF	breast:	n/a	chr8:107459209-107459218 chr8:107459198-107459219 chr8:107459203-107459221
37	CTCF	chr8:107459160-107459310	HPAF	blood vessel:	n/a	chr8:107459209-107459218 chr8:107459198-107459219 chr8:107459203-107459221
38	CTCF	chr8:107459020-107459170	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr8:107459100-107459250	HVMF	connective:	n/a	chr8:107459209-107459218 chr8:107459198-107459219 chr8:107459203-107459221
40	CTCF	chr8:107439390-107440223	A549	lung:	n/a	chr8:107440040-107440053 chr8:107439735-107439744
41	CTCF	chr8:107459020-107459170	AG04450	lung:	n/a	n/a
42	CTCF	chr8:107465348-107465433	Fibrobl	skin:	n/a	n/a
43	CTCF	chr8:107459060-107459210	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr8:107473180-107473330	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr8:107459020-107459170	HCFaa	heart:	n/a	n/a
46	CTCF	chr8:107459140-107459290	AG04449	skin:	n/a	chr8:107459209-107459218 chr8:107459198-107459219 chr8:107459203-107459221
47	CTCF	chr8:107459140-107459290	HPAF	blood vessel:	n/a	chr8:107459209-107459218 chr8:107459198-107459219 chr8:107459203-107459221
48	CTCF	chr8:107459023-107459455	HCT-116	colon:	n/a	chr8:107459209-107459218 chr8:107459198-107459219 chr8:107459203-107459221
49	CTCF	chr8:107459120-107459270	AG04450	lung:	n/a	chr8:107459209-107459218 chr8:107459198-107459219 chr8:107459203-107459221
50	CTCF	chr8:107439472-107440127	HCT-116	colon:	n/a	chr8:107440040-107440053 chr8:107439735-107439744

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:107460168-107460218	IMR90	lung:	fetal
2	chr8:107462460-107462510	GM12891	blood:	n/a
3	chr8:107460168-107460218	HepG2	liver:	n/a
4	chr8:107460168-107460218	SK-N-SH_RA	brain:	n/a
5	chr8:107462460-107462510	HNPCEpiC	eye:	n/a
6	chr8:107462460-107462510	Hela-S3	cervix:	n/a
7	chr8:107460168-107460218	MCF10A-Er-Src	breast:	n/a
8	chr8:107462460-107462510	SK-N-SH_RA	brain:	n/a
9	chr8:107462460-107462510	HMEC	breast:	n/a
10	chr8:107460168-107460218	HMEC	breast:	n/a
11	chr8:107462460-107462510	U87	brain:	n/a
12	chr8:107462460-107462510	PFSK-1	brain:	n/a
13	chr8:107462460-107462510	ovcar-3	ovarian:	n/a
14	chr8:107462460-107462510	AG04450	lung:	fetal
15	chr8:107460168-107460218	PANC-1	pancreas:	n/a
16	chr8:107462460-107462510	HCM	heart:	n/a
17	chr8:107460168-107460218	GM06990	blood:	n/a
18	chr8:107462460-107462510	T-47D	breast:	n/a
19	chr8:107462460-107462510	K562	blood:	n/a
20	chr8:107462460-107462510	NB4	blood:	n/a
21	chr8:107460168-107460218	HEK293	kidney:	embryo
22	chr8:107460168-107460218	HCF	heart:	n/a
23	chr8:107460168-107460218	AG09309	skin:	n/a
24	chr8:107460168-107460218	H1-hESC	embryonic stem cell:	embryo
25	chr8:107462460-107462510	AG10803	skin:	n/a
26	chr8:107462460-107462510	GM19239	blood:	n/a
27	chr8:107462460-107462510	HepG2	liver:	n/a
28	chr8:107462460-107462510	SK-N-MC	brain:	n/a
29	chr8:107460168-107460218	MCF-7	breast:	n/a
30	chr8:107462460-107462510	AoSMC	blood vessel:	n/a
31	chr8:107462460-107462510	HRE	kidney:	n/a
32	chr8:107462460-107462510	H1-hESC	embryonic stem cell:	embryo
33	chr8:107460168-107460218	CMK	blood:	n/a
34	chr8:107460168-107460218	PFSK-1	brain:	n/a
35	chr8:107460168-107460218	SAEC	small airway:	n/a
36	chr8:107460168-107460218	NHDF-neo	bronchial:	n/a
37	chr8:107462460-107462510	HUVEC	blood vessel:	n/a
38	chr8:107460168-107460218	HNPCEpiC	eye:	n/a
39	chr8:107462460-107462510	ECC-1	luminal epithelium:	n/a
40	chr8:107460168-107460218	SKMC	muscle:	n/a
41	chr8:107460168-107460218	T-47D	breast:	n/a
42	chr8:107462460-107462510	GM06990	blood:	n/a
43	chr8:107460168-107460218	HUVEC	blood vessel:	n/a
44	chr8:107462460-107462510	AG09319	gingival:	n/a
45	chr8:107462460-107462510	A549	lung:	n/a
46	chr8:107460168-107460218	HCM	heart:	n/a
47	chr8:107460168-107460218	Jurkat	blood:	n/a
48	chr8:107462460-107462510	Jurkat	blood:	n/a
49	chr8:107462460-107462510	MCF-7	breast:	n/a
50	chr8:107462460-107462510	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:107434524..107437041-chr8:107438558..107440145,2	K562	blood:
2	chr8:107426897..107429687-chr8:107442914..107445145,2	K562	blood:
3	chr8:107282403..107283907-chr8:107484126..107486179,2	K562	blood:
4	chr7:84922126..84922846-chr8:107469062..107469738,2	HCT-116	colon:
5	chr8:107428187..107430398-chr8:107443082..107445145,2	K562	blood:
6	chr8:107473925..107475852-chr8:107477064..107479538,2	K562	blood:
7	chr8:107473925..107475852-chr8:107477064..107479538,2	K562	blood:
8	chr8:107479862..107482476-chr8:107487797..107489316,2	K562	blood:
9	chr8:107479862..107482476-chr8:107487797..107489316,2	K562	blood:
10	chr8:107466184..107467709-chr8:107494491..107496529,2	MCF-7	breast:
11	chr8:107466184..107467709-chr8:107494491..107496529,2	MCF-7	breast:
12	chr8:107480149..107482279-chr8:107497864..107500285,3	MCF-7	breast:
13	chr8:107195796..107197608-chr8:107475772..107478613,2	K562	blood:

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

Extended variants
information (count: 1933 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1933 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7015711	chr8:107440038-107440039	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189163948	chr8:107440050-107440051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530256862	chr8:107440051-107440052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542494011	chr8:107440075-107440076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181557370	chr8:107440102-107440103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10110262	chr8:107440144-107440145	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs540064832	chr8:107440198-107440199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565131846	chr8:107440305-107440306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532096929	chr8:107440372-107440373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185147262	chr8:107440381-107440382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544326332	chr8:107440654-107440655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563081832	chr8:107440677-107440678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530517692	chr8:107440687-107440688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571122777	chr8:107440699-107440700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377202571	chr8:107440712-107440713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562445468	chr8:107440720-107440721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529736617	chr8:107440762-107440763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs202087982	chr8:107440836-107440837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs58317157	chr8:107440852-107440853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs142258337	chr8:107440879-107440880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189994193	chr8:107440907-107440908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540146122	chr8:107440936-107440937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs117788108	chr8:107440946-107440947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528650468	chr8:107441032-107441033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566472354	chr8:107441094-107441095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181209478	chr8:107441125-107441126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186414809	chr8:107441169-107441170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538742173	chr8:107441170-107441171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190850609	chr8:107441239-107441240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568886506	chr8:107441298-107441299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs115101750	chr8:107441319-107441320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554404818	chr8:107441329-107441330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572795726	chr8:107441356-107441357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540559311	chr8:107441399-107441400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558454167	chr8:107441403-107441404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78307930	chr8:107441416-107441417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs535474263	chr8:107441426-107441427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373050549	chr8:107441459-107441460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs180707741	chr8:107441467-107441468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562585637	chr8:107441496-107441497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529672326	chr8:107441625-107441626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186451867	chr8:107441641-107441642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs13250208	chr8:107441695-107441696	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs191028614	chr8:107441708-107441709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146824912	chr8:107441787-107441788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10100064	chr8:107441818-107441819	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs565316528	chr8:107441851-107441852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs28657963	chr8:107441856-107441857	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs550630334	chr8:107441866-107441867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376928060	chr8:107441881-107441882	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:227 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:107404400-107447000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:107414600-107446400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr8:107441000-107447200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr8:107441200-107441600	Enhancers	Primary hematopoietic stem cells	blood
5	chr8:107441200-107441600	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr8:107441600-107447000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr8:107442000-107446800	Weak transcription	Primary T cells from cord blood	blood
8	chr8:107442400-107446400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr8:107442600-107444400	Weak transcription	Aorta	Aorta
10	chr8:107443400-107446400	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr8:107443600-107447200	Weak transcription	Esophagus	oesophagus
12	chr8:107443800-107446400	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr8:107443800-107447000	Weak transcription	NHLF	lung
14	chr8:107444400-107444800	ZNF genes & repeats	Aorta	Aorta
15	chr8:107444600-107445400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:107444800-107451400	Weak transcription	Aorta	Aorta
17	chr8:107445400-107447200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr8:107445800-107446400	Enhancers	HUVEC	blood vessel
19	chr8:107446400-107446600	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr8:107446400-107446600	Flanking Active TSS	HUVEC	blood vessel
21	chr8:107446400-107446800	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr8:107446400-107447000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr8:107446400-107447400	Enhancers	Muscle Satellite Cultured Cells	--
24	chr8:107446400-107447400	Enhancers	NH-A	brain
25	chr8:107446400-107447400	Enhancers	Osteobl	bone
26	chr8:107446400-107447600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr8:107446600-107447000	Enhancers	HUVEC	blood vessel
28	chr8:107446800-107447200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr8:107446800-107447400	Enhancers	Fetal Heart	heart
30	chr8:107446800-107447800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr8:107446800-107450200	Enhancers	Primary T cells from cord blood	blood
32	chr8:107447000-107447200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr8:107447000-107447200	Enhancers	Duodenum Mucosa	Duodenum
34	chr8:107447000-107447200	Enhancers	Thymus	Thymus
35	chr8:107447000-107447200	Enhancers	NHLF	lung
36	chr8:107447000-107447400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr8:107447000-107447400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr8:107447000-107447600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr8:107447000-107447600	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr8:107447000-107447600	Enhancers	Stomach Mucosa	stomach
41	chr8:107447000-107447800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr8:107447000-107447800	Enhancers	Fetal Thymus	thymus
43	chr8:107447000-107447800	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr8:107447000-107447800	Flanking Active TSS	HUVEC	blood vessel
45	chr8:107447000-107448400	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr8:107447000-107451400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr8:107447200-107447400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr8:107447200-107447400	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr8:107447200-107447400	Bivalent Enhancer	Small Intestine	intestine
50	chr8:107447200-107447600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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