Variant report

Variant	esv2829896
Chromosome Location	chr8:46896972-47287147
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1440)
CpG islands
(count:3665)
Chromatin interactive
region (count:30)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1440 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:46957931-46958134	K562	blood:	n/a	n/a
2	ATF1	chr8:47049142-47049269	K562	blood:	n/a	n/a
3	ATF1	chr8:47263663-47264034	K562	blood:	n/a	n/a
4	BACH1	chr8:46941041-46941571	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:46947654-46948010	K562	blood:	n/a	n/a
6	BACH1	chr8:46941197-46941413	K562	blood:	n/a	n/a
7	BATF	chr8:46901802-46902038	GM12878	blood:	n/a	n/a
8	BATF	chr8:46901795-46902254	GM12878	blood:	n/a	n/a
9	BATF	chr8:46902039-46902259	GM12878	blood:	n/a	n/a
10	BATF	chr8:46900715-46900876	GM12878	blood:	n/a	n/a
11	BATF	chr8:46905994-46906308	GM12878	blood:	n/a	n/a
12	BATF	chr8:46898528-46898824	GM12878	blood:	n/a	n/a
13	BATF	chr8:46906372-46906659	GM12878	blood:	n/a	n/a
14	BATF	chr8:46898531-46898820	GM12878	blood:	n/a	n/a
15	BATF	chr8:46906370-46906776	GM12878	blood:	n/a	n/a
16	BCL11A	chr8:46906364-46906971	GM12878	blood:	n/a	n/a
17	BCL11A	chr8:46906458-46906651	GM12878	blood:	n/a	n/a
18	BCL11A	chr8:46901785-46902162	GM12878	blood:	n/a	n/a
19	BCL11A	chr8:46898534-46898764	GM12878	blood:	n/a	n/a
20	BCL11A	chr8:46906018-46906340	GM12878	blood:	n/a	n/a
21	BCL11A	chr8:46898463-46898855	GM12878	blood:	n/a	n/a
22	BCL11A	chr8:46901800-46902043	GM12878	blood:	n/a	n/a
23	BCL11A	chr8:46951900-46952080	GM12878	blood:	n/a	n/a
24	BHLHE40	chr8:46901710-46902131	HepG2	liver:	n/a	n/a
25	BHLHE40	chr8:47010522-47010548	GM12878	blood:	n/a	n/a
26	BHLHE40	chr8:46903018-46903391	HepG2	liver:	n/a	n/a
27	BHLHE40	chr8:46943192-46943391	K562	blood:	n/a	n/a
28	BHLHE40	chr8:46947643-46947854	K562	blood:	n/a	n/a
29	BHLHE40	chr8:47047525-47047640	K562	blood:	n/a	n/a
30	BHLHE40	chr8:46941196-46941455	GM12878	blood:	n/a	n/a
31	BHLHE40	chr8:46906352-46906671	HepG2	liver:	n/a	n/a
32	BHLHE40	chr8:46898475-46898784	HepG2	liver:	n/a	n/a
33	BHLHE40	chr8:46900710-46900891	HepG2	liver:	n/a	n/a
34	BHLHE40	chr8:46941082-46941569	K562	blood:	n/a	n/a
35	BRCA1	chr8:46947645-46948018	GM12878	blood:	n/a	n/a
36	BRCA1	chr8:47128832-47128850	HepG2	liver:	n/a	n/a
37	BRCA1	chr8:46947751-46947982	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr8:46941122-46941455	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr8:47213331-47213535	GM12878	blood:	n/a	n/a
40	BRCA1	chr8:46941198-46941413	GM12878	blood:	n/a	n/a
41	BRCA1	chr8:46943363-46943388	GM12878	blood:	n/a	n/a
42	BRCA1	chr8:46947817-46948017	HepG2	liver:	n/a	n/a
43	BRCA1	chr8:46941195-46941450	HepG2	liver:	n/a	n/a
44	BRCA1	chr8:46941199-46941397	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr8:46943192-46943497	Hela-S3	cervix:	n/a	n/a
46	CBX3	chr8:46950708-46950925	K562	blood:	n/a	n/a
47	CCNT2	chr8:46941041-46941424	K562	blood:	n/a	n/a
48	CEBPB	chr8:46942488-46942647	HepG2	liver:	n/a	chr8:46942556-46942567
49	CEBPB	chr8:46933173-46933376	A549	lung:	n/a	n/a
50	CEBPB	chr8:46941199-46941418	K562	blood:	n/a	n/a

(count:3665 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:47160830-47160880	NHBE	bronchial:	n/a
2	chr8:47130777-47130827	AG09319	gingival:	n/a
3	chr8:46951335-46951385	HAEpiC	amniotic membrane:	n/a
4	chr8:47171826-47171876	Caco-2	colon:	n/a
5	chr8:46951335-46951385	HepG2	liver:	n/a
6	chr8:47160830-47160880	NHBE	bronchial:	n/a
7	chr8:47130777-47130827	AG09319	gingival:	n/a
8	chr8:46951335-46951385	HAEpiC	amniotic membrane:	n/a
9	chr8:47171826-47171876	Caco-2	colon:	n/a
10	chr8:46951335-46951385	HepG2	liver:	n/a
11	chr8:47015829-47015879	RPTEC	kidney:	n/a
12	chr8:46951335-46951385	GM12891	blood:	n/a
13	chr8:46941151-46941201	HMEC	breast:	n/a
14	chr8:47120700-47120750	HEK293	kidney:	embryo
15	chr8:47174026-47174076	GM19239	blood:	n/a
16	chr8:46950927-46950977	PANC-1	pancreas:	n/a
17	chr8:47165292-47165342	RPTEC	kidney:	n/a
18	chr8:47130777-47130827	CMK	blood:	n/a
19	chr8:47040066-47040116	PFSK-1	brain:	n/a
20	chr8:47109311-47109361	SKMC	muscle:	n/a
21	chr8:47171826-47171876	HIPEpiC	eye:	n/a
22	chr8:47160997-47161047	HEK293	kidney:	embryo
23	chr8:47108770-47108820	HPAEpiC	pulmonary alveolar:	n/a
24	chr8:47016783-47016833	HepG2	liver:	n/a
25	chr8:47165292-47165342	GM12892	blood:	n/a
26	chr8:47112438-47112488	SK-N-MC	brain:	n/a
27	chr8:47130822-47130872	HEEpiC	esophagus:	n/a
28	chr8:47108992-47109042	SAEC	small airway:	n/a
29	chr8:47120700-47120750	BJ	skin:	n/a
30	chr8:47092995-47093045	HAEpiC	amniotic membrane:	n/a
31	chr8:47045963-47046013	MCF10A-Er-Src	breast:	n/a
32	chr8:47112438-47112488	GM12892	blood:	n/a
33	chr8:47165292-47165342	HCPEpiC	choroid plexus:	n/a
34	chr8:47119035-47119085	PANC-1	pancreas:	n/a
35	chr8:47045969-47046019	LNCaP	prostate:	n/a
36	chr8:47092995-47093045	NH-A	brain:	n/a
37	chr8:47119319-47119369	IMR90	lung:	fetal
38	chr8:47109229-47109279	AG10803	skin:	n/a
39	chr8:47108770-47108820	IMR90	lung:	fetal
40	chr8:47015665-47015715	SAEC	small airway:	n/a
41	chr8:47016783-47016833	SK-N-MC	brain:	n/a
42	chr8:46950927-46950977	HEK293	kidney:	embryo
43	chr8:47174026-47174076	GM12878	blood:	n/a
44	chr8:47165292-47165342	GM19239	blood:	n/a
45	chr8:46951897-46951947	SK-N-SH	brain:	n/a
46	chr8:47140781-47140831	NH-A	brain:	n/a
47	chr8:46941151-46941201	GM12892	blood:	n/a
48	chr8:47120476-47120526	HEEpiC	esophagus:	n/a
49	chr8:47174026-47174076	GM06990	blood:	n/a
50	chr8:47112230-47112280	Hepatocyte	liver:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:47059851..47061946-chr8:47064644..47066356,2	MCF-7	breast:
2	chr8:46940855..46941726-chr8:47130252..47130754,2	K562	blood:
3	chr8:47168205..47168775-chr8:47479656..47480472,2	MCF-7	breast:
4	chr22:25265936..25266456-chr8:46940874..46941393,2	MCF-7	breast:
5	chr8:47059851..47061946-chr8:47064644..47066356,2	MCF-7	breast:
6	chr10:42530427..42532590-chr8:46977725..46979226,2	MCF-7	breast:
7	chr8:46940678..46941746-chr8:47130003..47131748,8	MCF-7	breast:
8	chr19:23254197..23254711-chr8:46940755..46941394,2	K562	blood:
9	chr1:112439856..112440376-chr8:46940777..46941392,3	MCF-7	breast:
10	chr19:21665376..21665988-chr8:46940890..46941394,3	MCF-7	breast:
11	chr8:46940678..46941746-chr8:47130003..47131748,8	MCF-7	breast:
12	chr8:47152207..47152786-chr8:47399264..47399945,2	MCF-7	breast:
13	chr8:46948914..46951388-chr8:46959571..46961840,2	K562	blood:
14	chr8:46940855..46941726-chr8:47130252..47130754,2	K562	blood:
15	chr1:156185756..156186427-chr8:46940757..46941368,2	K562	blood:
16	chr3:19097583..19098083-chr8:46940757..46941373,3	MCF-7	breast:
17	chr8:46940536..46941325-chr8:47868294..47869211,2	K562	blood:
18	chr20:26190442..26190988-chr8:46940868..46941390,2	MCF-7	breast:
19	chr19:21665377..21666008-chr8:46940755..46941391,3	MCF-7	breast:
20	chr16:1494211..1494730-chr8:46940868..46941388,2	MCF-7	breast:
21	chr8:46948914..46951388-chr8:46959571..46961840,2	K562	blood:
22	chr22:28194390..28194890-chr8:46940890..46941394,2	MCF-7	breast:
23	chr4:107699957..107700477-chr8:46940755..46941372,3	MCF-7	breast:
24	chr11:10829784..10830763-chr8:46940754..46941373,2	MCF-7	breast:
25	chr8:47144016..47144925-chr8:47484500..47485152,3	MCF-7	breast:
26	chr19:23254194..23254711-chr8:46940869..46941389,2	MCF-7	breast:
27	chr8:47103663..47106274-chr8:47108285..47110930,2	K562	blood:
28	chr2:133016687..133017416-chr8:46947342..46948320,4	MCF-7	breast:
29	chr2:86830620..86831120-chr8:47284541..47285069,2	MCF-7	breast:
30	chr8:47103663..47106274-chr8:47108285..47110930,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000255915	TF binding region
ENSG00000255915	CpG island
ENSG00000227195	chromatin interactions
ENSG00000110321	chromatin interactions
ENSG00000197599	chromatin interactions
ENSG00000269543	chromatin interactions

Extended variants
information (count: 19779 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:19779 , 50 per page) page: 1 2 3 4 5 6 7 ... 396

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4612356	chr8:46896972-46896973	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs145456683	chr8:46896983-46896984	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs529140316	chr8:46897011-46897012	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs549193113	chr8:46897014-46897015	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs190174962	chr8:46897031-46897032	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs181288184	chr8:46897035-46897036	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs186494060	chr8:46897054-46897055	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs111835703	chr8:46897069-46897070	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs571126445	chr8:46897080-46897081	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs533762281	chr8:46897081-46897082	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs184251883	chr8:46897085-46897086	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs553620943	chr8:46897093-46897094	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs112677021	chr8:46897096-46897097	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs567014130	chr8:46897106-46897107	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs535698253	chr8:46897114-46897115	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs4872740	chr8:46897119-46897120	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs4509329	chr8:46897123-46897124	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs115115180	chr8:46897126-46897127	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs555994870	chr8:46897148-46897149	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs201793520	chr8:46897176-46897177	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs558155773	chr8:46897184-46897185	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs200245428	chr8:46897193-46897194	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs368259712	chr8:46897198-46897199	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs535358806	chr8:46897200-46897201	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs372356817	chr8:46897202-46897203	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs201270735	chr8:46897207-46897208	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs529358792	chr8:46897208-46897209	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs542853577	chr8:46897210-46897211	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs199765156	chr8:46897233-46897234	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs200471117	chr8:46897243-46897244	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs577378199	chr8:46897263-46897264	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs201381467	chr8:46897269-46897270	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs543234457	chr8:46897275-46897276	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs190943119	chr8:46897282-46897283	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs531659347	chr8:46897288-46897289	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs199507049	chr8:46897299-46897300	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs551415136	chr8:46897309-46897310	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs563170613	chr8:46897339-46897340	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs13253311	chr8:46897341-46897342	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs143078884	chr8:46897349-46897350	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs182108075	chr8:46897352-46897353	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs567028441	chr8:46897363-46897364	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs111826503	chr8:46897365-46897366	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs535907407	chr8:46897386-46897387	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs555557830	chr8:46897397-46897398	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs569083675	chr8:46897411-46897412	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs13257202	chr8:46897414-46897415	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs558206103	chr8:46897428-46897429	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs578192170	chr8:46897429-46897430	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs148201776	chr8:46897433-46897434	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:450 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:46896800-46911200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
2	chr8:46897400-46899000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
3	chr8:46897600-46898800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
4	chr8:46897800-46898200	Active TSS	Primary T helper naive cells from peripheral blood	blood
5	chr8:46898000-46899400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr8:46898600-46899200	ZNF genes & repeats	HUVEC	blood vessel
7	chr8:46899200-46900400	Weak transcription	HUVEC	blood vessel
8	chr8:46900400-46900600	ZNF genes & repeats	HUVEC	blood vessel
9	chr8:46900600-46902000	Weak transcription	NH-A	brain
10	chr8:46900600-46903000	Weak transcription	HUVEC	blood vessel
11	chr8:46901400-46908200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
12	chr8:46901600-46901800	Active TSS	Primary T killer memory cells from peripheral blood	blood
13	chr8:46901600-46903800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
14	chr8:46901800-46903000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr8:46901800-46911400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr8:46902000-46902200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
17	chr8:46902000-46902400	Strong transcription	NH-A	brain
18	chr8:46902200-46903000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr8:46902400-46903000	Weak transcription	NH-A	brain
20	chr8:46902400-46908200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
21	chr8:46902600-46903400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr8:46902800-46903600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
23	chr8:46903000-46903400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
24	chr8:46903000-46903400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr8:46903000-46903400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr8:46903000-46903400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr8:46903000-46903400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
28	chr8:46903000-46903400	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood
29	chr8:46903000-46903400	Flanking Bivalent TSS/Enh	Primary T helper naive cells from peripheral blood	blood
30	chr8:46903000-46903400	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
31	chr8:46903000-46903400	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
32	chr8:46903000-46903400	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
33	chr8:46903000-46903400	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
34	chr8:46903000-46903400	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr8:46903000-46903400	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
36	chr8:46903000-46903400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr8:46903000-46903400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr8:46903000-46903400	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
39	chr8:46903000-46903400	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
40	chr8:46903000-46903400	ZNF genes & repeats	Colon Smooth Muscle	Colon
41	chr8:46903000-46903400	ZNF genes & repeats	Fetal Heart	heart
42	chr8:46903000-46903400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
43	chr8:46903000-46903400	ZNF genes & repeats	Left Ventricle	heart
44	chr8:46903000-46903400	Active TSS	Ovary	ovary
45	chr8:46903000-46903400	Active TSS	Psoas Muscle	Psoas
46	chr8:46903000-46903400	ZNF genes & repeats	Stomach Mucosa	stomach
47	chr8:46903000-46903400	ZNF genes & repeats	HepG2	liver
48	chr8:46903000-46903400	ZNF genes & repeats	K562	blood
49	chr8:46903000-46903400	ZNF genes & repeats	NH-A	brain
50	chr8:46903000-46903600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell

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