Variant report

Variant	nsv1025355
Chromosome Location	chr8:43286480-43683349
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:712)
CpG islands
(count:917)
Chromatin interactive
region (count:7)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:712 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:43654724-43654750	K562	blood:	n/a	n/a
2	BACH1	chr8:43572418-43572443	K562	blood:	n/a	n/a
3	BHLHE40	chr8:43572418-43572443	K562	blood:	n/a	n/a
4	BHLHE40	chr8:43654723-43654750	K562	blood:	n/a	n/a
5	BRCA1	chr8:43519669-43520216	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr8:43420572-43420906	K562	blood:	n/a	n/a
7	CEBPB	chr8:43317774-43318025	HepG2	liver:	n/a	chr8:43317903-43317914 chr8:43317902-43317915
8	CEBPB	chr8:43352248-43352856	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr8:43359811-43360200	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr8:43306476-43306804	HepG2	liver:	n/a	chr8:43306646-43306657 chr8:43306657-43306668
11	CEBPB	chr8:43572435-43572642	A549	lung:	n/a	n/a
12	CEBPB	chr8:43306612-43306676	K562	blood:	n/a	chr8:43306646-43306657 chr8:43306657-43306668
13	CEBPB	chr8:43373683-43374020	IMR90	lung:	n/a	chr8:43373832-43373843
14	CEBPB	chr8:43352224-43352840	A549	lung:	n/a	n/a
15	CEBPB	chr8:43373700-43374000	HepG2	liver:	n/a	chr8:43373832-43373843
16	CEBPB	chr8:43414546-43414811	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr8:43306491-43306829	A549	lung:	n/a	chr8:43306646-43306657 chr8:43306657-43306668
18	CEBPB	chr8:43302895-43303465	A549	lung:	n/a	chr8:43303409-43303422 chr8:43303410-43303421
19	CEBPB	chr8:43303234-43303525	HepG2	liver:	n/a	chr8:43303409-43303422 chr8:43303410-43303421
20	CEBPB	chr8:43317791-43318030	A549	lung:	n/a	chr8:43317903-43317914 chr8:43317902-43317915
21	CEBPB	chr8:43373772-43373988	A549	lung:	n/a	chr8:43373832-43373843
22	CEBPB	chr8:43306501-43306786	IMR90	lung:	n/a	chr8:43306646-43306657 chr8:43306657-43306668
23	CEBPB	chr8:43414610-43414720	HepG2	liver:	n/a	n/a
24	CEBPB	chr8:43572344-43572445	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr8:43519669-43520389	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr8:43573553-43573580	K562	blood:	n/a	n/a
27	CTCF	chr8:43554000-43554150	AG09309	skin:	n/a	n/a
28	CTCF	chr8:43556380-43556530	GM12870	blood:	n/a	n/a
29	CTCF	chr8:43556460-43556610	AG09309	skin:	n/a	n/a
30	CTCF	chr8:43554080-43554230	HepG2	liver:	n/a	n/a
31	CTCF	chr8:43291145-43291400	LNCaP	prostate:	n/a	n/a
32	CTCF	chr8:43554020-43554170	HMF	breast:	n/a	n/a
33	CTCF	chr8:43554000-43554150	MCF-7	breast:	n/a	n/a
34	CTCF	chr8:43291280-43291430	A549	lung:	n/a	n/a
35	CTCF	chr8:43556423-43556510	MCF-7	breast:	n/a	n/a
36	CTCF	chr8:43554040-43554190	HepG2	liver:	n/a	n/a
37	CTCF	chr8:43303012-43303058	GM10266	blood:	n/a	n/a
38	CTCF	chr8:43554020-43554170	A549	lung:	n/a	n/a
39	CTCF	chr8:43291280-43291430	HepG2	liver:	n/a	n/a
40	CTCF	chr8:43303220-43303370	AG10803	skin:	n/a	n/a
41	CTCF	chr8:43391968-43392105	MCF-7	breast:	n/a	n/a
42	CTCF	chr8:43291180-43291330	HCT-116	colon:	n/a	n/a
43	CTCF	chr8:43391975-43392099	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:43556480-43556630	SAEC	small airway:	n/a	n/a
45	CTCF	chr8:43556420-43556570	Caco-2	colon:	n/a	n/a
46	CTCF	chr8:43303259-43303375	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr8:43556400-43556550	Caco-2	colon:	n/a	n/a
48	CTCF	chr8:43391998-43392066	A549	lung:	n/a	n/a
49	CTCF	chr8:43556460-43556610	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr8:43291213-43291352	Spleen_OC	spleen:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:43405687-43405737	PFSK-1	brain:	n/a
2	chr8:43405739-43405789	Hepatocyte	liver:	n/a
3	chr8:43405687-43405737	PFSK-1	brain:	n/a
4	chr8:43405739-43405789	Hepatocyte	liver:	n/a
5	chr8:43417050-43417100	RPTEC	kidney:	n/a
6	chr8:43417291-43417341	SKMC	muscle:	n/a
7	chr8:43406314-43406364	U87	brain:	n/a
8	chr8:43404458-43404508	SK-N-SH_RA	brain:	n/a
9	chr8:43418406-43418456	PFSK-1	brain:	n/a
10	chr8:43404214-43404264	ProgFib	skin:	n/a
11	chr8:43402630-43402680	SK-N-SH	brain:	n/a
12	chr8:43403277-43403327	GM12892	blood:	n/a
13	chr8:43405739-43405789	HRPEpiC	eye:	n/a
14	chr8:43404214-43404264	HRE	kidney:	n/a
15	chr8:43417050-43417100	SAEC	small airway:	n/a
16	chr8:43406314-43406364	LNCaP	prostate:	n/a
17	chr8:43418721-43418771	GM06990	blood:	n/a
18	chr8:43406411-43406461	IMR90	lung:	fetal
19	chr8:43418721-43418771	NT2-D1	testis:	n/a
20	chr8:43405687-43405737	ProgFib	skin:	n/a
21	chr8:43406144-43406194	Jurkat	blood:	n/a
22	chr8:43404458-43404508	HNPCEpiC	eye:	n/a
23	chr8:43404458-43404508	HMEC	breast:	n/a
24	chr8:43403277-43403327	NHDF-neo	bronchial:	n/a
25	chr8:43405687-43405737	H1-hESC	embryonic stem cell:	embryo
26	chr8:43403277-43403327	AG09309	skin:	n/a
27	chr8:43401874-43401924	AG04449	skin:	fetal
28	chr8:43418721-43418771	HIPEpiC	eye:	n/a
29	chr8:43417050-43417100	MCF10A-Er-Src	breast:	n/a
30	chr8:43402630-43402680	HepG2	liver:	n/a
31	chr8:43418406-43418456	HCPEpiC	choroid plexus:	n/a
32	chr8:43406314-43406364	HL-60	blood:	n/a
33	chr8:43406411-43406461	AoSMC	blood vessel:	n/a
34	chr8:43405739-43405789	K562	blood:	n/a
35	chr8:43404458-43404508	LNCaP	prostate:	n/a
36	chr8:43405687-43405737	PrEC	prostate:	n/a
37	chr8:43403277-43403327	HRPEpiC	eye:	n/a
38	chr8:43402930-43402980	HRPEpiC	eye:	n/a
39	chr8:43406314-43406364	Hepatocyte	liver:	n/a
40	chr8:43403277-43403327	MCF10A-Er-Src	breast:	n/a
41	chr8:43403277-43403327	NH-A	brain:	n/a
42	chr8:43417050-43417100	NH-A	brain:	n/a
43	chr8:43401874-43401924	Hela-S3	cervix:	n/a
44	chr8:43418721-43418771	HCM	heart:	n/a
45	chr8:43403277-43403327	GM06990	blood:	n/a
46	chr8:43404458-43404508	HepG2	liver:	n/a
47	chr8:43405687-43405737	BE2_C	brain:	n/a
48	chr8:43417291-43417341	Jurkat	blood:	n/a
49	chr8:43405687-43405737	SKMC	muscle:	n/a
50	chr8:43406144-43406194	MCF-7	breast:	n/a

(count:7 , 50 per page) page: 1

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

(count:11 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 18072 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:18072 , 50 per page) page: 1 2 3 4 5 6 7 ... 362

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148312493	chr8:43295156-43295157	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs114734745	chr8:43295159-43295160	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs554632105	chr8:43295160-43295161	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs574363306	chr8:43295164-43295165	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs557304185	chr8:43295219-43295220	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs140495894	chr8:43295225-43295226	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs546119379	chr8:43295233-43295234	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs559616030	chr8:43295244-43295245	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs573059789	chr8:43295255-43295256	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs150412893	chr8:43295277-43295278	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs561406257	chr8:43295287-43295288	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs138134802	chr8:43295295-43295296	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs544461827	chr8:43295301-43295302	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs142687842	chr8:43295304-43295305	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs371868773	chr8:43295308-43295309	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs571736688	chr8:43295349-43295350	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs146023431	chr8:43295353-43295354	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs138690571	chr8:43295362-43295363	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs565965227	chr8:43295365-43295366	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs375380638	chr8:43295506-43295507	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs369285364	chr8:43295520-43295521	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs547985932	chr8:43295533-43295534	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs372787980	chr8:43295544-43295545	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs561663794	chr8:43295545-43295546	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs539145614	chr8:43295584-43295585	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs182765883	chr8:43295591-43295592	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs141703762	chr8:43295597-43295598	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs78158847	chr8:43295600-43295601	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs553271280	chr8:43295652-43295653	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs144498543	chr8:43295671-43295672	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs148441767	chr8:43295675-43295676	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs561234700	chr8:43295723-43295724	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs574917666	chr8:43295727-43295728	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs543549500	chr8:43295760-43295761	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs115854850	chr8:43295769-43295770	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs554092397	chr8:43295781-43295782	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs552464638	chr8:43295790-43295791	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs547318155	chr8:43298070-43298071	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs567450510	chr8:43298094-43298095	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs529394074	chr8:43298101-43298102	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs10089191	chr8:43298155-43298156	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs149491342	chr8:43298162-43298163	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs538213930	chr8:43298171-43298172	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs116022298	chr8:43298188-43298189	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs543726871	chr8:43300475-43300476	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs540418511	chr8:43300492-43300493	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs533706108	chr8:43300495-43300496	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs141713957	chr8:43300511-43300512	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs552775977	chr8:43300544-43300545	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs188644329	chr8:43300562-43300563	Inactive region	Chromatin interactive region	1 gene(s)	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:228 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:43295200-43295800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:43303200-43303800	Enhancers	Liver	Liver
3	chr8:43321800-43324400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
4	chr8:43322000-43322800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr8:43333000-43333600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr8:43352000-43352600	Enhancers	A549	lung
7	chr8:43352000-43353600	Enhancers	Muscle Satellite Cultured Cells	--
8	chr8:43352200-43353000	Enhancers	Hela-S3	cervix
9	chr8:43352600-43352800	Active TSS	A549	lung
10	chr8:43352800-43353000	Flanking Active TSS	A549	lung
11	chr8:43355400-43355600	Enhancers	Muscle Satellite Cultured Cells	--
12	chr8:43355600-43355800	Weak transcription	Aorta	Aorta
13	chr8:43359800-43360200	Enhancers	Hela-S3	cervix
14	chr8:43360000-43362600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
15	chr8:43362400-43362600	Active TSS	Spleen	Spleen
16	chr8:43362600-43367800	Weak transcription	Spleen	Spleen
17	chr8:43363800-43364000	Enhancers	Gastric	stomach
18	chr8:43364000-43368000	Weak transcription	Gastric	stomach
19	chr8:43366400-43369200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chr8:43366600-43368600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr8:43367000-43368400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
22	chr8:43367800-43368200	ZNF genes & repeats	Spleen	Spleen
23	chr8:43368000-43369000	ZNF genes & repeats	Gastric	stomach
24	chr8:43368200-43369400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr8:43368200-43373000	Weak transcription	Spleen	Spleen
26	chr8:43371800-43373600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr8:43373000-43373600	Enhancers	Spleen	Spleen
28	chr8:43375200-43376400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr8:43377200-43380000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr8:43378400-43379600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr8:43378600-43379600	Enhancers	HepG2	liver
32	chr8:43378800-43379200	Enhancers	HMEC	breast
33	chr8:43378800-43380000	Enhancers	Left Ventricle	heart
34	chr8:43379000-43379400	Enhancers	NHEK	skin
35	chr8:43379400-43380000	Enhancers	Spleen	Spleen
36	chr8:43379600-43382200	Weak transcription	HepG2	liver
37	chr8:43379800-43380000	Enhancers	Lung	lung
38	chr8:43381400-43383200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr8:43382200-43382600	Enhancers	HepG2	liver
40	chr8:43384000-43389600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
41	chr8:43388600-43391400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr8:43388800-43389200	Active TSS	Fetal Heart	heart
43	chr8:43388800-43393000	Weak transcription	Spleen	Spleen
44	chr8:43390200-43390400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
45	chr8:43390400-43391600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
46	chr8:43392400-43392600	Enhancers	Right Ventricle	heart
47	chr8:43392400-43412600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
48	chr8:43392600-43393400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr8:43392600-43394000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr8:43392600-43394000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell

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