Variant report

Variant	nsv1025517
Chromosome Location	chr8:43327179-43824036
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4055)
CpG islands
(count:976)
Chromatin interactive
region (count:6)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4055 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:43785555-43785668	K562	blood:	n/a	n/a
2	ATF1	chr8:43786577-43787136	K562	blood:	n/a	n/a
3	ATF1	chr8:43819080-43819187	K562	blood:	n/a	n/a
4	ATF1	chr8:43792645-43793396	K562	blood:	n/a	n/a
5	BACH1	chr8:43654724-43654750	K562	blood:	n/a	n/a
6	BACH1	chr8:43717526-43717725	K562	blood:	n/a	n/a
7	BACH1	chr8:43818947-43819136	K562	blood:	n/a	n/a
8	BACH1	chr8:43820379-43820751	K562	blood:	n/a	n/a
9	BACH1	chr8:43779446-43779599	K562	blood:	n/a	n/a
10	BACH1	chr8:43572418-43572443	K562	blood:	n/a	n/a
11	BACH1	chr8:43790059-43790248	K562	blood:	n/a	n/a
12	BATF	chr8:43805641-43805845	GM12878	blood:	n/a	n/a
13	BATF	chr8:43813396-43813769	GM12878	blood:	n/a	n/a
14	BATF	chr8:43803086-43803339	GM12878	blood:	n/a	n/a
15	BATF	chr8:43760193-43760718	GM12878	blood:	n/a	n/a
16	BATF	chr8:43783535-43783800	GM12878	blood:	n/a	n/a
17	BATF	chr8:43801942-43802323	GM12878	blood:	n/a	n/a
18	BATF	chr8:43790975-43791219	GM12878	blood:	n/a	n/a
19	BATF	chr8:43811590-43811948	GM12878	blood:	n/a	n/a
20	BATF	chr8:43817245-43817428	GM12878	blood:	n/a	n/a
21	BATF	chr8:43803567-43803962	GM12878	blood:	n/a	n/a
22	BATF	chr8:43795406-43795581	GM12878	blood:	n/a	n/a
23	BATF	chr8:43795705-43796262	GM12878	blood:	n/a	n/a
24	BATF	chr8:43813428-43813791	GM12878	blood:	n/a	n/a
25	BATF	chr8:43816102-43816270	GM12878	blood:	n/a	n/a
26	BATF	chr8:43797239-43797997	GM12878	blood:	n/a	n/a
27	BATF	chr8:43822263-43823134	GM12878	blood:	n/a	n/a
28	BATF	chr8:43796330-43796659	GM12878	blood:	n/a	n/a
29	BATF	chr8:43793545-43795103	GM12878	blood:	n/a	n/a
30	BATF	chr8:43793089-43793493	GM12878	blood:	n/a	n/a
31	BATF	chr8:43810569-43810876	GM12878	blood:	n/a	n/a
32	BATF	chr8:43789506-43789769	GM12878	blood:	n/a	n/a
33	BATF	chr8:43809217-43809758	GM12878	blood:	n/a	n/a
34	BATF	chr8:43761295-43761752	GM12878	blood:	n/a	n/a
35	BATF	chr8:43796850-43797049	GM12878	blood:	n/a	n/a
36	BATF	chr8:43818959-43819224	GM12878	blood:	n/a	n/a
37	BATF	chr8:43812453-43812698	GM12878	blood:	n/a	n/a
38	BATF	chr8:43795629-43796232	GM12878	blood:	n/a	n/a
39	BATF	chr8:43798448-43798632	GM12878	blood:	n/a	n/a
40	BATF	chr8:43790147-43790722	GM12878	blood:	n/a	n/a
41	BATF	chr8:43800371-43800565	GM12878	blood:	n/a	n/a
42	BATF	chr8:43771245-43771622	GM12878	blood:	n/a	n/a
43	BATF	chr8:43771808-43772466	GM12878	blood:	n/a	n/a
44	BATF	chr8:43776273-43776586	GM12878	blood:	n/a	n/a
45	BATF	chr8:43778905-43779151	GM12878	blood:	n/a	n/a
46	BATF	chr8:43800956-43801154	GM12878	blood:	n/a	n/a
47	BATF	chr8:43822327-43823068	GM12878	blood:	n/a	n/a
48	BATF	chr8:43789506-43789826	GM12878	blood:	n/a	n/a
49	BATF	chr8:43805047-43805337	GM12878	blood:	n/a	n/a
50	BATF	chr8:43798729-43799230	GM12878	blood:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:43404458-43404508	HL-60	blood:	n/a
2	chr8:43401874-43401924	HPAEpiC	pulmonary alveolar:	n/a
3	chr8:43417291-43417341	Hepatocyte	liver:	n/a
4	chr8:43405687-43405737	HUVEC	blood vessel:	n/a
5	chr8:43405739-43405789	HUVEC	blood vessel:	n/a
6	chr8:43417050-43417100	AG04450	lung:	fetal
7	chr8:43794595-43794645	ovcar-3	ovarian:	n/a
8	chr8:43418406-43418456	NT2-D1	testis:	n/a
9	chr8:43794595-43794645	SKMC	muscle:	n/a
10	chr8:43405739-43405789	HCPEpiC	choroid plexus:	n/a
11	chr8:43402930-43402980	H1-hESC	embryonic stem cell:	embryo
12	chr8:43406411-43406461	Jurkat	blood:	n/a
13	chr8:43405687-43405737	Hela-S3	cervix:	n/a
14	chr8:43418721-43418771	HCPEpiC	choroid plexus:	n/a
15	chr8:43417050-43417100	SKMC	muscle:	n/a
16	chr8:43406314-43406364	HL-60	blood:	n/a
17	chr8:43404458-43404508	IMR90	lung:	fetal
18	chr8:43405687-43405737	AG04450	lung:	fetal
19	chr8:43406144-43406194	NHBE	bronchial:	n/a
20	chr8:43405687-43405737	HEK293	kidney:	embryo
21	chr8:43794595-43794645	NH-A	brain:	n/a
22	chr8:43406144-43406194	SK-N-MC	brain:	n/a
23	chr8:43418406-43418456	NH-A	brain:	n/a
24	chr8:43402630-43402680	HCPEpiC	choroid plexus:	n/a
25	chr8:43418721-43418771	ECC-1	luminal epithelium:	n/a
26	chr8:43418406-43418456	PrEC	prostate:	n/a
27	chr8:43405739-43405789	IMR90	lung:	fetal
28	chr8:43794595-43794645	HAEpiC	amniotic membrane:	n/a
29	chr8:43418721-43418771	NB4	blood:	n/a
30	chr8:43404458-43404508	GM12892	blood:	n/a
31	chr8:43403277-43403327	HL-60	blood:	n/a
32	chr8:43794595-43794645	LNCaP	prostate:	n/a
33	chr8:43405687-43405737	Jurkat	blood:	n/a
34	chr8:43418406-43418456	PFSK-1	brain:	n/a
35	chr8:43417291-43417341	GM12891	blood:	n/a
36	chr8:43406144-43406194	AG09309	skin:	n/a
37	chr8:43402630-43402680	H1-hESC	embryonic stem cell:	embryo
38	chr8:43401874-43401924	SKMC	muscle:	n/a
39	chr8:43406144-43406194	Hepatocyte	liver:	n/a
40	chr8:43401874-43401924	MCF-7	breast:	n/a
41	chr8:43418406-43418456	AG09309	skin:	n/a
42	chr8:43404458-43404508	HCM	heart:	n/a
43	chr8:43404214-43404264	HRE	kidney:	n/a
44	chr8:43406314-43406364	H1-hESC	embryonic stem cell:	embryo
45	chr8:43406144-43406194	IMR90	lung:	fetal
46	chr8:43418721-43418771	BJ	skin:	n/a
47	chr8:43401874-43401924	Hepatocyte	liver:	n/a
48	chr8:43401874-43401924	AG09309	skin:	n/a
49	chr8:43418406-43418456	LNCaP	prostate:	n/a
50	chr8:43417050-43417100	SAEC	small airway:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:43092429..43093269-chr8:43823893..43824414,2	MCF-7	breast:
2	chr8:43394978..43396738-chr8:43399115..43401110,2	K562	blood:
3	chr15:63385860..63386443-chr8:43553599..43554374,2	MCF-7	breast:
4	chr8:43395245..43397661-chr8:43402500..43405220,3	K562	blood:
5	chr8:43370024..43372377-chr8:43374871..43376951,2	K562	blood:
6	chr8:43370024..43372377-chr8:43374871..43376951,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HGSNAT-9	chr8:43368786-43369564	NONHSAT126361
2	lnc-RNF170-8	chr8:43366963-43367176	NONHSAT126358
3	lnc-HGSNAT-8	chr8:43349080-43349905	NONHSAT126357
4	lnc-HGSNAT-10	chr8:43394280-43394615	NONHSAT126362
5	lnc-HGSNAT-12	chr8:43527966-43528218	NONHSAT126367
6	lnc-RNF170-9	chr8:43529413-43529734	NONHSAT126368

No data

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

Extended variants
information (count: 28737 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:28737 , 50 per page) page: 1 2 3 4 5 6 7 ... 575

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183903434	chr8:43333014-43333015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs187740100	chr8:43333045-43333046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs115918605	chr8:43333088-43333089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574936546	chr8:43333092-43333093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374913102	chr8:43333128-43333129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs145128039	chr8:43333129-43333130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563980591	chr8:43333172-43333173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148345594	chr8:43333214-43333215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs546103554	chr8:43333217-43333218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs141476102	chr8:43333269-43333270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150840147	chr8:43333297-43333298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577276151	chr8:43333299-43333300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs139255259	chr8:43333308-43333309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562739705	chr8:43333334-43333335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs550117052	chr8:43333344-43333345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192594443	chr8:43333362-43333363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs184367621	chr8:43333400-43333401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534491657	chr8:43333407-43333408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs190282894	chr8:43333417-43333418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535290860	chr8:43333457-43333458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs147242184	chr8:43333469-43333470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75850328	chr8:43333526-43333527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537445802	chr8:43333581-43333582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545401781	chr8:43333585-43333586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140642358	chr8:43333591-43333592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73675578	chr8:43333600-43333601	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs570175884	chr8:43346852-43346853	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs542980098	chr8:43346856-43346857	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs552963187	chr8:43346875-43346876	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs188016824	chr8:43346888-43346889	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs542150044	chr8:43346909-43346910	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs555663226	chr8:43346915-43346916	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs575513966	chr8:43346922-43346923	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs377172682	chr8:43346958-43346959	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs376033289	chr8:43346979-43346980	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs563789332	chr8:43346990-43346991	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs532675841	chr8:43346993-43346994	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs545976501	chr8:43346996-43346997	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs559738033	chr8:43347050-43347051	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs528433091	chr8:43347056-43347057	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs548473890	chr8:43347059-43347060	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs568387082	chr8:43347062-43347063	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs531024932	chr8:43347096-43347097	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs550795976	chr8:43347100-43347101	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs190516939	chr8:43347118-43347119	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs541021273	chr8:43347134-43347135	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs563695104	chr8:43347136-43347137	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs546369016	chr8:43347154-43347155	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs181489693	chr8:43347165-43347166	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs532877254	chr8:43347175-43347176	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
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:1336 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:43333000-43333600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr8:43352000-43352600	Enhancers	A549	lung
3	chr8:43352000-43353600	Enhancers	Muscle Satellite Cultured Cells	--
4	chr8:43352200-43353000	Enhancers	Hela-S3	cervix
5	chr8:43352600-43352800	Active TSS	A549	lung
6	chr8:43352800-43353000	Flanking Active TSS	A549	lung
7	chr8:43355400-43355600	Enhancers	Muscle Satellite Cultured Cells	--
8	chr8:43355600-43355800	Weak transcription	Aorta	Aorta
9	chr8:43359800-43360200	Enhancers	Hela-S3	cervix
10	chr8:43360000-43362600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
11	chr8:43362400-43362600	Active TSS	Spleen	Spleen
12	chr8:43362600-43367800	Weak transcription	Spleen	Spleen
13	chr8:43363800-43364000	Enhancers	Gastric	stomach
14	chr8:43364000-43368000	Weak transcription	Gastric	stomach
15	chr8:43366400-43369200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr8:43366600-43368600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:43367000-43368400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
18	chr8:43367800-43368200	ZNF genes & repeats	Spleen	Spleen
19	chr8:43368000-43369000	ZNF genes & repeats	Gastric	stomach
20	chr8:43368200-43369400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr8:43368200-43373000	Weak transcription	Spleen	Spleen
22	chr8:43371800-43373600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr8:43373000-43373600	Enhancers	Spleen	Spleen
24	chr8:43375200-43376400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr8:43377200-43380000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr8:43378400-43379600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr8:43378600-43379600	Enhancers	HepG2	liver
28	chr8:43378800-43379200	Enhancers	HMEC	breast
29	chr8:43378800-43380000	Enhancers	Left Ventricle	heart
30	chr8:43379000-43379400	Enhancers	NHEK	skin
31	chr8:43379400-43380000	Enhancers	Spleen	Spleen
32	chr8:43379600-43382200	Weak transcription	HepG2	liver
33	chr8:43379800-43380000	Enhancers	Lung	lung
34	chr8:43381400-43383200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr8:43382200-43382600	Enhancers	HepG2	liver
36	chr8:43384000-43389600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
37	chr8:43388600-43391400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr8:43388800-43389200	Active TSS	Fetal Heart	heart
39	chr8:43388800-43393000	Weak transcription	Spleen	Spleen
40	chr8:43390200-43390400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
41	chr8:43390400-43391600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
42	chr8:43392400-43392600	Enhancers	Right Ventricle	heart
43	chr8:43392400-43412600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr8:43392600-43393400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr8:43392600-43394000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr8:43392600-43394000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
47	chr8:43393000-43393400	Enhancers	Spleen	Spleen
48	chr8:43393400-43396000	Weak transcription	Spleen	Spleen
49	chr8:43394800-43396000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr8:43395600-43399400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell

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