Variant report

Variant	nsv1024279
Chromosome Location	chr8:47013353-47361594
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:680)
CpG islands
(count:4090)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:680 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:47049142-47049269	K562	blood:	n/a	n/a
2	ATF1	chr8:47263663-47264034	K562	blood:	n/a	n/a
3	BHLHE40	chr8:47047525-47047640	K562	blood:	n/a	n/a
4	BRCA1	chr8:47128832-47128850	HepG2	liver:	n/a	n/a
5	BRCA1	chr8:47213331-47213535	GM12878	blood:	n/a	n/a
6	CEBPB	chr8:47057114-47057285	K562	blood:	n/a	n/a
7	CEBPB	chr8:47214532-47214751	HepG2	liver:	n/a	chr8:47214612-47214623
8	CEBPB	chr8:47144487-47144545	K562	blood:	n/a	n/a
9	CEBPB	chr8:47333483-47333514	K562	blood:	n/a	n/a
10	CEBPB	chr8:47214503-47214753	A549	lung:	n/a	chr8:47214612-47214623
11	CEBPB	chr8:47323416-47323702	A549	lung:	n/a	n/a
12	CEBPB	chr8:47323477-47323711	MCF-7	breast:	n/a	n/a
13	CEBPB	chr8:47323407-47323734	HepG2	liver:	n/a	n/a
14	CEBPB	chr8:47214461-47214801	IMR90	lung:	n/a	chr8:47214612-47214623
15	CEBPB	chr8:47072394-47072659	HepG2	liver:	n/a	chr8:47072498-47072509
16	CTCF	chr8:47329535-47329800	T-47D	breast:	n/a	n/a
17	CTCF	chr8:47165160-47165306	K562	blood:	n/a	n/a
18	CTCF	chr8:47144343-47144614	HepG2	liver:	n/a	n/a
19	CTCF	chr8:47144305-47144642	T-47D	breast:	n/a	n/a
20	CTCF	chr8:47130641-47130845	HepG2	liver:	n/a	n/a
21	CTCF	chr8:47358715-47358760	GM20000	blood:	n/a	n/a
22	CTCF	chr8:47156886-47157118	T-47D	breast:	n/a	n/a
23	CTCF	chr8:47329587-47329799	HepG2	liver:	n/a	n/a
24	CTCF	chr8:47292134-47292136	K562	blood:	n/a	n/a
25	CTCF	chr8:47329634-47329824	MCF-7	breast:	n/a	n/a
26	CTCF	chr8:47168595-47168810	MCF-7	breast:	n/a	n/a
27	CTCF	chr8:47029924-47030029	Fibrobl	skin:	n/a	n/a
28	CTCF	chr8:47292095-47292291	MCF-7	breast:	n/a	n/a
29	CTCF	chr8:47292080-47292286	HepG2	liver:	n/a	n/a
30	CTCF	chr8:47019605-47019760	HepG2	liver:	n/a	n/a
31	CTCF	chr8:47171866-47171939	MCF-7	breast:	n/a	n/a
32	CTCF	chr8:47152185-47152213	K562	blood:	n/a	n/a
33	CTCF	chr8:47148155-47148199	GM13976	blood:	n/a	n/a
34	CTCF	chr8:47357595-47357736	MCF-7	breast:	n/a	n/a
35	CTCF	chr8:47019669-47019683	MCF-7	breast:	n/a	n/a
36	CTCF	chr8:47015452-47015479	GM20000	blood:	n/a	n/a
37	CTCF	chr8:47297922-47298021	MCF-7	breast:	n/a	n/a
38	CTCF	chr8:47144174-47144857	A549	lung:	n/a	n/a
39	CTCF	chr8:47177440-47177481	GM13976	blood:	n/a	n/a
40	CTCF	chr8:47353139-47353205	Gliobla	brain:	n/a	n/a
41	CTCF	chr8:47130606-47130874	MCF-7	breast:	n/a	n/a
42	CTCF	chr8:47320000-47320027	MCF-7	breast:	n/a	n/a
43	CTCF	chr8:47181893-47181897	ProgFib	skin:	n/a	n/a
44	CTCF	chr8:47130606-47130876	MCF-7	breast:	n/a	n/a
45	CTCF	chr8:47292090-47292302	MCF-7	breast:	n/a	n/a
46	CTCF	chr8:47130729-47130774	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr8:47131024-47131025	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:47319956-47320034	MCF-7	breast:	n/a	n/a
49	CTCF	chr8:47144330-47144718	K562	blood:	n/a	n/a
50	CTCF	chr8:47034695-47034776	MCF-7	breast:	n/a	n/a

(count:4090 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:47108992-47109042	HCPEpiC	choroid plexus:	n/a
2	chr8:47344178-47344228	HCM	heart:	n/a
3	chr8:47171722-47171772	Caco-2	colon:	n/a
4	chr8:47108992-47109042	HCPEpiC	choroid plexus:	n/a
5	chr8:47344178-47344228	HCM	heart:	n/a
6	chr8:47171722-47171772	Caco-2	colon:	n/a
7	chr8:47344178-47344228	HepG2	liver:	n/a
8	chr8:47142166-47142216	HMEC	breast:	n/a
9	chr8:47318698-47318748	SAEC	small airway:	n/a
10	chr8:47142166-47142216	Hepatocyte	liver:	n/a
11	chr8:47171722-47171772	NHBE	bronchial:	n/a
12	chr8:47119319-47119369	MCF-7	breast:	n/a
13	chr8:47144363-47144413	HRE	kidney:	n/a
14	chr8:47119319-47119369	ovcar-3	ovarian:	n/a
15	chr8:47093117-47093167	H1-hESC	embryonic stem cell:	embryo
16	chr8:47145527-47145577	NHBE	bronchial:	n/a
17	chr8:47160830-47160880	CMK	blood:	n/a
18	chr8:47109229-47109279	PrEC	prostate:	n/a
19	chr8:47344447-47344497	HRE	kidney:	n/a
20	chr8:47120476-47120526	IMR90	lung:	fetal
21	chr8:47109311-47109361	CMK	blood:	n/a
22	chr8:47108510-47108560	SK-N-SH_RA	brain:	n/a
23	chr8:47344447-47344497	HEEpiC	esophagus:	n/a
24	chr8:47156401-47156451	NT2-D1	testis:	n/a
25	chr8:47015665-47015715	SK-N-MC	brain:	n/a
26	chr8:47156401-47156451	NHBE	bronchial:	n/a
27	chr8:47119035-47119085	HMEC	breast:	n/a
28	chr8:47318698-47318748	T-47D	breast:	n/a
29	chr8:47046101-47046151	IMR90	lung:	fetal
30	chr8:47171826-47171876	HCF	heart:	n/a
31	chr8:47348070-47348120	AG04450	lung:	fetal
32	chr8:47040066-47040116	AG09319	gingival:	n/a
33	chr8:47165292-47165342	BJ	skin:	n/a
34	chr8:47130822-47130872	AG04449	skin:	fetal
35	chr8:47326950-47327000	NHBE	bronchial:	n/a
36	chr8:47120767-47120817	GM06990	blood:	n/a
37	chr8:47015868-47015918	GM12878	blood:	n/a
38	chr8:47025005-47025055	AG04449	skin:	fetal
39	chr8:47045963-47046013	MCF10A-Er-Src	breast:	n/a
40	chr8:47025005-47025055	H1-hESC	embryonic stem cell:	embryo
41	chr8:47318832-47318882	HNPCEpiC	eye:	n/a
42	chr8:47108770-47108820	GM12878	blood:	n/a
43	chr8:47093117-47093167	AG09319	gingival:	n/a
44	chr8:47108318-47108368	NHDF-neo	bronchial:	n/a
45	chr8:47344178-47344228	AG04449	skin:	fetal
46	chr8:47112230-47112280	HAEpiC	amniotic membrane:	n/a
47	chr8:47040066-47040116	BJ	skin:	n/a
48	chr8:47145556-47145606	NB4	blood:	n/a
49	chr8:47142166-47142216	HAEpiC	amniotic membrane:	n/a
50	chr8:47326950-47327000	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:47059851..47061946-chr8:47064644..47066356,2	MCF-7	breast:
2	chr8:47152207..47152786-chr8:47399264..47399945,2	MCF-7	breast:
3	chr19:35614212..35616054-chr8:47337776..47339296,2	MCF-7	breast:
4	chr8:47103663..47106274-chr8:47108285..47110930,2	K562	blood:
5	chr8:46940678..46941746-chr8:47130003..47131748,8	MCF-7	breast:
6	chr2:86830620..86831120-chr8:47284541..47285069,2	MCF-7	breast:
7	chr8:47168205..47168775-chr8:47479656..47480472,2	MCF-7	breast:
8	chr8:47059851..47061946-chr8:47064644..47066356,2	MCF-7	breast:
9	chr8:47144016..47144925-chr8:47484500..47485152,3	MCF-7	breast:
10	chr8:47103663..47106274-chr8:47108285..47110930,2	K562	blood:
11	chr8:46940855..46941726-chr8:47130252..47130754,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000255915	TF binding region
ENSG00000255915	CpG island

Extended variants
information (count: 18296 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:18296 , 50 per page) page: 1 2 3 4 5 6 7 ... 366

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572458486	chr8:47013412-47013413	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs530875977	chr8:47013440-47013441	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs76991260	chr8:47013460-47013461	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs188670172	chr8:47013511-47013512	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs554120969	chr8:47013540-47013541	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs570729332	chr8:47013555-47013556	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs555133660	chr8:47013560-47013561	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs543815792	chr8:47013649-47013650	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs539837135	chr8:47013656-47013657	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs556541109	chr8:47013667-47013668	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs181410016	chr8:47013702-47013703	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs564013121	chr8:47013722-47013723	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs563632331	chr8:47013735-47013736	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs546472808	chr8:47013753-47013754	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs559797522	chr8:47013758-47013759	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs186025041	chr8:47013784-47013785	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs548686413	chr8:47013815-47013816	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs562017993	chr8:47013836-47013837	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs530766719	chr8:47013890-47013891	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs550489990	chr8:47013926-47013927	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs570457787	chr8:47013929-47013930	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs73562715	chr8:47013933-47013934	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs546449310	chr8:47013961-47013962	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs566145110	chr8:47013963-47013964	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs141350117	chr8:47013985-47013986	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs555474718	chr8:47013986-47013987	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs7007847	chr8:47014009-47014010	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs576812342	chr8:47014024-47014025	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs137997631	chr8:47014036-47014037	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs557591601	chr8:47014037-47014038	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs368824438	chr8:47014043-47014044	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs546538038	chr8:47014069-47014070	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs560062179	chr8:47014070-47014071	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs189057116	chr8:47014106-47014107	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs180969683	chr8:47014115-47014116	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs562248702	chr8:47014149-47014150	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs149483152	chr8:47014168-47014169	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs531156330	chr8:47014182-47014183	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs143049273	chr8:47014188-47014189	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs563948635	chr8:47014189-47014190	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs57629643	chr8:47014200-47014201	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs372892027	chr8:47014205-47014206	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs148196020	chr8:47014228-47014229	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs546510855	chr8:47014244-47014245	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs566406715	chr8:47014251-47014252	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs574570552	chr8:47014252-47014253	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs547090871	chr8:47014253-47014254	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs187008398	chr8:47014274-47014275	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs35596671	chr8:47014286-47014287	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs540361306	chr8:47014363-47014364	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Oral cancer	21386901	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	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
Glioblastoma multiforme	21080181	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
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	20607354	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
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	20409316	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
Schizophrenia	20967226	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20841430	CNVD
Tetralogy of Fallot	22912587	CNVD

Chromatin state (count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:47009000-47035600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:47009400-47015600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr8:47009600-47033400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:47015000-47018200	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr8:47016200-47016800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr8:47016200-47017000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr8:47016400-47016600	Bivalent Enhancer	Right Ventricle	heart
8	chr8:47016400-47018200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
9	chr8:47018200-47019200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr8:47021600-47028400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr8:47022400-47025000	ZNF genes & repeats	Placenta	Placenta
12	chr8:47023400-47024000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr8:47030200-47030400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr8:47033400-47034000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr8:47033600-47035000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr8:47033800-47034000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr8:47034000-47034200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
18	chr8:47034000-47034600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr8:47034000-47035800	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr8:47034000-47038200	Enhancers	Ovary	ovary
21	chr8:47034200-47037600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr8:47034600-47034800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr8:47034800-47035200	Enhancers	Pancreas	Pancrea
24	chr8:47034800-47035200	Enhancers	Spleen	Spleen
25	chr8:47034800-47036800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr8:47034800-47037200	Enhancers	Skeletal Muscle Male	skeletal muscle
27	chr8:47034800-47037200	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr8:47035000-47036800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr8:47035200-47037000	Weak transcription	Spleen	Spleen
30	chr8:47035800-47036200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr8:47036200-47038600	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr8:47036800-47037800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr8:47036800-47037800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr8:47037000-47037200	Enhancers	Spleen	Spleen
35	chr8:47037000-47037400	Enhancers	Hela-S3	cervix
36	chr8:47037000-47037400	Enhancers	Osteobl	bone
37	chr8:47037000-47037600	Enhancers	Stomach Smooth Muscle	stomach
38	chr8:47037000-47038400	Enhancers	Stomach Mucosa	stomach
39	chr8:47037400-47037800	Active TSS	Hela-S3	cervix
40	chr8:47037600-47037800	Flanking Active TSS	Stomach Smooth Muscle	stomach
41	chr8:47038200-47038600	Active TSS	Ovary	ovary
42	chr8:47038600-47039200	Enhancers	Ovary	ovary
43	chr8:47039200-47064400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr8:47041200-47043800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr8:47041400-47041600	ZNF genes & repeats	Brain Germinal Matrix	brain
46	chr8:47042000-47043400	ZNF genes & repeats	Fetal Stomach	stomach
47	chr8:47046000-47063000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr8:47049200-47061200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr8:47050200-47050400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
50	chr8:47050400-47050600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin

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