Variant report

Variant	nsv1024906
Chromosome Location	chr8:43233403-43635432
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:835)
CpG islands
(count:1038)
Chromatin interactive
region (count:9)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:835 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:43572418-43572443	K562	blood:	n/a	n/a
2	BHLHE40	chr8:43572418-43572443	K562	blood:	n/a	n/a
3	BRCA1	chr8:43519669-43520216	Hela-S3	cervix:	n/a	n/a
4	CBX3	chr8:43420572-43420906	K562	blood:	n/a	n/a
5	CEBPB	chr8:43373772-43373988	A549	lung:	n/a	chr8:43373832-43373843
6	CEBPB	chr8:43414546-43414811	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr8:43306476-43306804	HepG2	liver:	n/a	chr8:43306646-43306657 chr8:43306657-43306668
8	CEBPB	chr8:43303234-43303525	HepG2	liver:	n/a	chr8:43303409-43303422 chr8:43303410-43303421
9	CEBPB	chr8:43317774-43318025	HepG2	liver:	n/a	chr8:43317903-43317914 chr8:43317902-43317915
10	CEBPB	chr8:43302895-43303465	A549	lung:	n/a	chr8:43303409-43303422 chr8:43303410-43303421
11	CEBPB	chr8:43317791-43318030	A549	lung:	n/a	chr8:43317903-43317914 chr8:43317902-43317915
12	CEBPB	chr8:43572435-43572642	A549	lung:	n/a	n/a
13	CEBPB	chr8:43306501-43306786	IMR90	lung:	n/a	chr8:43306646-43306657 chr8:43306657-43306668
14	CEBPB	chr8:43373700-43374000	HepG2	liver:	n/a	chr8:43373832-43373843
15	CEBPB	chr8:43359811-43360200	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr8:43572344-43572445	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr8:43414610-43414720	HepG2	liver:	n/a	n/a
18	CEBPB	chr8:43352224-43352840	A549	lung:	n/a	n/a
19	CEBPB	chr8:43352248-43352856	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr8:43373683-43374020	IMR90	lung:	n/a	chr8:43373832-43373843
21	CEBPB	chr8:43306491-43306829	A549	lung:	n/a	chr8:43306646-43306657 chr8:43306657-43306668
22	CEBPB	chr8:43306612-43306676	K562	blood:	n/a	chr8:43306646-43306657 chr8:43306657-43306668
23	CHD2	chr8:43573553-43573580	K562	blood:	n/a	n/a
24	CHD2	chr8:43519669-43520389	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr8:43291160-43291310	AG09319	gingival:	n/a	n/a
26	CTCF	chr8:43554000-43554150	MCF-7	breast:	n/a	n/a
27	CTCF	chr8:43554022-43554159	GM12892	blood:	n/a	n/a
28	CTCF	chr8:43392004-43392051	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr8:43553932-43554433	SK-N-SH	brain:	n/a	n/a
30	CTCF	chr8:43553953-43554209	HepG2	liver:	n/a	n/a
31	CTCF	chr8:43303180-43303330	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr8:43550040-43550190	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr8:43303291-43303344	GM13976	blood:	n/a	n/a
34	CTCF	chr8:43265098-43265167	GM10266	blood:	n/a	n/a
35	CTCF	chr8:43556440-43556590	GM12866	blood:	n/a	n/a
36	CTCF	chr8:43291132-43291395	A549	lung:	n/a	n/a
37	CTCF	chr8:43291180-43291330	GM12874	blood:	n/a	n/a
38	CTCF	chr8:43265080-43265230	GM12873	blood:	n/a	n/a
39	CTCF	chr8:43303140-43303290	HFF	foreskin:	n/a	n/a
40	CTCF	chr8:43291220-43291370	HCFaa	heart:	n/a	n/a
41	CTCF	chr8:43286260-43286410	K562	blood:	n/a	n/a
42	CTCF	chr8:43556420-43556570	GM12873	blood:	n/a	n/a
43	CTCF	chr8:43556400-43556550	GM12873	blood:	n/a	n/a
44	CTCF	chr8:43265060-43265210	NHEK	skin:	n/a	n/a
45	CTCF	chr8:43303300-43303450	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr8:43554040-43554190	GM12874	blood:	n/a	n/a
47	CTCF	chr8:43554000-43554150	HMF	breast:	n/a	n/a
48	CTCF	chr8:43265020-43265170	GM12872	blood:	n/a	n/a
49	CTCF	chr8:43556422-43556589	K562	blood:	n/a	n/a
50	CTCF	chr8:43265080-43265230	Hela-S3	cervix:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:43418721-43418771	SK-N-MC	brain:	n/a
2	chr8:43418721-43418771	SK-N-MC	brain:	n/a
3	chr8:43406411-43406461	AoSMC	blood vessel:	n/a
4	chr8:43405739-43405789	SK-N-MC	brain:	n/a
5	chr8:43405739-43405789	HRPEpiC	eye:	n/a
6	chr8:43401874-43401924	LNCaP	prostate:	n/a
7	chr8:43403277-43403327	SAEC	small airway:	n/a
8	chr8:43404214-43404264	HUVEC	blood vessel:	n/a
9	chr8:43275453-43275503	H1-hESC	embryonic stem cell:	embryo
10	chr8:43402630-43402680	Hepatocyte	liver:	n/a
11	chr8:43278783-43278833	Jurkat	blood:	n/a
12	chr8:43402930-43402980	HMEC	breast:	n/a
13	chr8:43403277-43403327	Jurkat	blood:	n/a
14	chr8:43402930-43402980	IMR90	lung:	fetal
15	chr8:43404214-43404264	HepG2	liver:	n/a
16	chr8:43417050-43417100	SAEC	small airway:	n/a
17	chr8:43418721-43418771	GM12891	blood:	n/a
18	chr8:43402630-43402680	HL-60	blood:	n/a
19	chr8:43402930-43402980	HIPEpiC	eye:	n/a
20	chr8:43418721-43418771	NHBE	bronchial:	n/a
21	chr8:43405687-43405737	GM12878	blood:	n/a
22	chr8:43418406-43418456	MCF10A-Er-Src	breast:	n/a
23	chr8:43405739-43405789	HRE	kidney:	n/a
24	chr8:43406314-43406364	NHBE	bronchial:	n/a
25	chr8:43417050-43417100	K562	blood:	n/a
26	chr8:43405687-43405737	IMR90	lung:	fetal
27	chr8:43401874-43401924	GM12878	blood:	n/a
28	chr8:43403277-43403327	NH-A	brain:	n/a
29	chr8:43418721-43418771	HEK293	kidney:	embryo
30	chr8:43404458-43404508	Hela-S3	cervix:	n/a
31	chr8:43404214-43404264	GM06990	blood:	n/a
32	chr8:43405687-43405737	BJ	skin:	n/a
33	chr8:43402630-43402680	PFSK-1	brain:	n/a
34	chr8:43405687-43405737	H1-hESC	embryonic stem cell:	embryo
35	chr8:43404458-43404508	PFSK-1	brain:	n/a
36	chr8:43401874-43401924	HMEC	breast:	n/a
37	chr8:43418721-43418771	HEEpiC	esophagus:	n/a
38	chr8:43402630-43402680	HEEpiC	esophagus:	n/a
39	chr8:43402630-43402680	HAEpiC	amniotic membrane:	n/a
40	chr8:43406314-43406364	Caco-2	colon:	n/a
41	chr8:43403277-43403327	NHBE	bronchial:	n/a
42	chr8:43275453-43275503	ovcar-3	ovarian:	n/a
43	chr8:43401874-43401924	SK-N-SH	brain:	n/a
44	chr8:43403277-43403327	NB4	blood:	n/a
45	chr8:43417050-43417100	Jurkat	blood:	n/a
46	chr8:43417050-43417100	AG04450	lung:	fetal
47	chr8:43404214-43404264	NB4	blood:	n/a
48	chr8:43402930-43402980	NHBE	bronchial:	n/a
49	chr8:43275453-43275503	HNPCEpiC	eye:	n/a
50	chr8:43403277-43403327	HRE	kidney:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:42948083..42948640-chr8:43285913..43286769,2	MCF-7	breast:
2	chr8:43395245..43397661-chr8:43402500..43405220,3	K562	blood:
3	chr8:42947579..42949100-chr8:43300446..43303387,2	MCF-7	breast:
4	chr5:82184309..82184963-chr8:43234719..43235395,2	MCF-7	breast:
5	chr8:43370024..43372377-chr8:43374871..43376951,2	K562	blood:
6	chr8:43370024..43372377-chr8:43374871..43376951,2	K562	blood:
7	chr15:63385860..63386443-chr8:43553599..43554374,2	MCF-7	breast:
8	chr8:42948115..42950146-chr8:43255758..43258426,2	K562	blood:
9	chr8:43394978..43396738-chr8:43399115..43401110,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HGSNAT-12	chr8:43527966-43528218	NONHSAT126367
2	lnc-HGSNAT-7	chr8:43306599-43306780	NONHSAT126356
3	lnc-HGSNAT-9	chr8:43368786-43369564	NONHSAT126361
4	lnc-HGSNAT-7	chr8:43303948-43304047	NONHSAT126356
5	lnc-HGSNAT-10	chr8:43394280-43394615	NONHSAT126362
6	lnc-RNF170-9	chr8:43529413-43529734	NONHSAT126368
7	lnc-HGSNAT-7	chr8:43307943-43308055	NONHSAT126356
8	lnc-RNF170-8	chr8:43366963-43367176	NONHSAT126358
9	lnc-HGSNAT-7	chr8:43298045-43298224	NONHSAT126356
10	lnc-HGSNAT-5	chr8:43233441-43233652	NONHSAT126354
11	lnc-HGSNAT-6	chr8:43236787-43237091	NONHSAT126355
12	lnc-HGSNAT-8	chr8:43349080-43349905	NONHSAT126357
13	lnc-HGSNAT-7	chr8:43299491-43299558	NONHSAT126356

No data

Variant related genes	Relation type
CYP4F44P	TF binding region
ENSG00000253195	TF binding region
ENSG00000254145	TF binding region
ENSG00000250637	TF binding region
ENSG00000221295	TF binding region
ENSG00000253845	TF binding region
ENSG00000201329	TF binding region
ENSG00000253198	TF binding region
RN7SKP41	TF binding region
ENSG00000253319	TF binding region
SNX18P27	TF binding region
ENSG00000254069	TF binding region
CYP4F44P	CpG island
ENSG00000253195	CpG island
ENSG00000254145	CpG island
ENSG00000250637	CpG island
ENSG00000221295	CpG island
ENSG00000253845	CpG island
ENSG00000201329	CpG island
ENSG00000253198	CpG island
RN7SKP41	CpG island
ENSG00000253319	CpG island
SNX18P27	CpG island
ENSG00000254069	CpG island
ENSG00000253748	chromatin interactions
ENSG00000185900	chromatin interactions
ENSG00000253195	chromatin interactions

Extended variants
information (count: 15716 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:15716 , 50 per page) page: 1 2 3 4 5 6 7 ... 315

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565733432	chr8:43233447-43233448	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs548178045	chr8:43233453-43233454	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs568396114	chr8:43233455-43233456	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs530820154	chr8:43233505-43233506	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs551223293	chr8:43233519-43233520	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs543003810	chr8:43233520-43233521	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs139858868	chr8:43233521-43233522	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs553635895	chr8:43233546-43233547	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs566563127	chr8:43233557-43233558	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs537878344	chr8:43233563-43233564	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs555170485	chr8:43233569-43233570	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs575134357	chr8:43233574-43233575	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs182225423	chr8:43233577-43233578	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs558001795	chr8:43233597-43233598	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs577552596	chr8:43233604-43233605	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs540031559	chr8:43233608-43233609	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs186897387	chr8:43233610-43233611	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs573504384	chr8:43233613-43233614	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs541879924	chr8:43233616-43233617	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs149965433	chr8:43233641-43233642	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs576880960	chr8:43236878-43236879	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs185633183	chr8:43236880-43236881	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs559672433	chr8:43236916-43236917	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs528438780	chr8:43236934-43236935	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs541657604	chr8:43236941-43236942	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs561872711	chr8:43236951-43236952	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs530625376	chr8:43236976-43236977	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs7830474	chr8:43236981-43236982	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs190045827	chr8:43236993-43236994	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs532349716	chr8:43237000-43237001	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs140331173	chr8:43237011-43237012	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs566022872	chr8:43237026-43237027	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs557884349	chr8:43237029-43237030	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs181745422	chr8:43237042-43237043	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs186013730	chr8:43237055-43237056	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs537269506	chr8:43237075-43237076	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs535514122	chr8:43251807-43251808	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs549644333	chr8:43251829-43251830	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs569499399	chr8:43251835-43251836	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs538535866	chr8:43251838-43251839	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs557892545	chr8:43251842-43251843	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs533068392	chr8:43251849-43251850	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs189824078	chr8:43251850-43251851	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs200318848	chr8:43251857-43251858	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs376285500	chr8:43251860-43251861	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs575039203	chr8:43251864-43251865	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs553480763	chr8:43251878-43251879	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs573568221	chr8:43251882-43251883	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs542304608	chr8:43251887-43251888	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs562507057	chr8:43251888-43251889	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
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
Hepatocellular carcinoma	22174799	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
Melanoma	18172304	CNVD
Medulloblastoma	21979893	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
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Seminomas	18059402	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
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21785460	CNVD
Rhabdomyosarcoma	16790082	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	23813976	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19214233	CNVD

Chromatin state (count:214 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:43251800-43252200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
2	chr8:43259400-43260600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:43261800-43264000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
4	chr8:43263000-43263600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:43263200-43264800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr8:43265200-43266200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr8:43273200-43273600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr8:43273800-43274000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr8:43295200-43295800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr8:43303200-43303800	Enhancers	Liver	Liver
11	chr8:43321800-43324400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
12	chr8:43322000-43322800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr8:43333000-43333600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr8:43352000-43352600	Enhancers	A549	lung
15	chr8:43352000-43353600	Enhancers	Muscle Satellite Cultured Cells	--
16	chr8:43352200-43353000	Enhancers	Hela-S3	cervix
17	chr8:43352600-43352800	Active TSS	A549	lung
18	chr8:43352800-43353000	Flanking Active TSS	A549	lung
19	chr8:43355400-43355600	Enhancers	Muscle Satellite Cultured Cells	--
20	chr8:43355600-43355800	Weak transcription	Aorta	Aorta
21	chr8:43359800-43360200	Enhancers	Hela-S3	cervix
22	chr8:43360000-43362600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
23	chr8:43362400-43362600	Active TSS	Spleen	Spleen
24	chr8:43362600-43367800	Weak transcription	Spleen	Spleen
25	chr8:43363800-43364000	Enhancers	Gastric	stomach
26	chr8:43364000-43368000	Weak transcription	Gastric	stomach
27	chr8:43366400-43369200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
28	chr8:43366600-43368600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr8:43367000-43368400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
30	chr8:43367800-43368200	ZNF genes & repeats	Spleen	Spleen
31	chr8:43368000-43369000	ZNF genes & repeats	Gastric	stomach
32	chr8:43368200-43369400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr8:43368200-43373000	Weak transcription	Spleen	Spleen
34	chr8:43371800-43373600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr8:43373000-43373600	Enhancers	Spleen	Spleen
36	chr8:43375200-43376400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr8:43377200-43380000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr8:43378400-43379600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr8:43378600-43379600	Enhancers	HepG2	liver
40	chr8:43378800-43379200	Enhancers	HMEC	breast
41	chr8:43378800-43380000	Enhancers	Left Ventricle	heart
42	chr8:43379000-43379400	Enhancers	NHEK	skin
43	chr8:43379400-43380000	Enhancers	Spleen	Spleen
44	chr8:43379600-43382200	Weak transcription	HepG2	liver
45	chr8:43379800-43380000	Enhancers	Lung	lung
46	chr8:43381400-43383200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr8:43382200-43382600	Enhancers	HepG2	liver
48	chr8:43384000-43389600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
49	chr8:43388600-43391400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr8:43388800-43389200	Active TSS	Fetal Heart	heart

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