Variant report

Variant	nsv982079
Chromosome Location	chr8:46946757-47457829
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1307)
CpG islands
(count:4402)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1307 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

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	chr8:47368426-47368796	K562	blood:	n/a	n/a
3	ATF1	chr8:47263663-47264034	K562	blood:	n/a	n/a
4	ATF1	chr8:46957931-46958134	K562	blood:	n/a	n/a
5	BACH1	chr8:46947654-46948010	K562	blood:	n/a	n/a
6	BCL11A	chr8:46951900-46952080	GM12878	blood:	n/a	n/a
7	BHLHE40	chr8:47010522-47010548	GM12878	blood:	n/a	n/a
8	BHLHE40	chr8:47424515-47424559	GM12878	blood:	n/a	n/a
9	BHLHE40	chr8:47047525-47047640	K562	blood:	n/a	n/a
10	BHLHE40	chr8:46947643-46947854	K562	blood:	n/a	n/a
11	BRCA1	chr8:46947751-46947982	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr8:46947645-46948018	GM12878	blood:	n/a	n/a
13	BRCA1	chr8:47213331-47213535	GM12878	blood:	n/a	n/a
14	BRCA1	chr8:47128832-47128850	HepG2	liver:	n/a	n/a
15	BRCA1	chr8:46947817-46948017	HepG2	liver:	n/a	n/a
16	CBX3	chr8:47416966-47417169	K562	blood:	n/a	n/a
17	CBX3	chr8:46950708-46950925	K562	blood:	n/a	n/a
18	CCNT2	chr8:47432567-47432751	K562	blood:	n/a	n/a
19	CEBPB	chr8:47364262-47364621	H1-hESC	embryonic stem cell:	n/a	chr8:47364437-47364448
20	CEBPB	chr8:47374798-47374997	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:47323416-47323702	A549	lung:	n/a	n/a
22	CEBPB	chr8:47447545-47447780	A549	lung:	n/a	chr8:47447623-47447634
23	CEBPB	chr8:47364246-47364627	IMR90	lung:	n/a	chr8:47364437-47364448
24	CEBPB	chr8:47363583-47363906	IMR90	lung:	n/a	chr8:47363750-47363761
25	CEBPB	chr8:47374691-47375010	IMR90	lung:	n/a	n/a
26	CEBPB	chr8:47214503-47214753	A549	lung:	n/a	chr8:47214612-47214623
27	CEBPB	chr8:47363627-47363881	HepG2	liver:	n/a	chr8:47363750-47363761
28	CEBPB	chr8:47144487-47144545	K562	blood:	n/a	n/a
29	CEBPB	chr8:47368428-47368796	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr8:47214461-47214801	IMR90	lung:	n/a	chr8:47214612-47214623
31	CEBPB	chr8:47333483-47333514	K562	blood:	n/a	n/a
32	CEBPB	chr8:47363624-47363896	A549	lung:	n/a	chr8:47363750-47363761
33	CEBPB	chr8:47447503-47447785	HepG2	liver:	n/a	chr8:47447623-47447634
34	CEBPB	chr8:47364240-47364634	MCF-7	breast:	n/a	chr8:47364437-47364448
35	CEBPB	chr8:46957936-46958136	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr8:47433472-47433637	A549	lung:	n/a	chr8:47433563-47433574
37	CEBPB	chr8:47364256-47364632	A549	lung:	n/a	chr8:47364437-47364448
38	CEBPB	chr8:47364299-47364648	A549	lung:	n/a	chr8:47364437-47364448
39	CEBPB	chr8:47364259-47364626	MCF-7	breast:	n/a	chr8:47364437-47364448
40	CEBPB	chr8:47072394-47072659	HepG2	liver:	n/a	chr8:47072498-47072509
41	CEBPB	chr8:47364254-47364630	K562	blood:	n/a	chr8:47364437-47364448
42	CEBPB	chr8:46967731-46967781	K562	blood:	n/a	n/a
43	CEBPB	chr8:47214532-47214751	HepG2	liver:	n/a	chr8:47214612-47214623
44	CEBPB	chr8:47364252-47364625	HepG2	liver:	n/a	chr8:47364437-47364448
45	CEBPB	chr8:47323407-47323734	HepG2	liver:	n/a	n/a
46	CEBPB	chr8:47057114-47057285	K562	blood:	n/a	n/a
47	CEBPB	chr8:47364275-47364616	Hela-S3	cervix:	n/a	chr8:47364437-47364448
48	CEBPB	chr8:47433493-47433666	HepG2	liver:	n/a	chr8:47433563-47433574
49	CEBPB	chr8:47374682-47375049	MCF-7	breast:	n/a	n/a
50	CEBPB	chr8:47323477-47323711	MCF-7	breast:	n/a	n/a

(count:4402 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:47156687-47156737	SK-N-MC	brain:	n/a
2	chr8:47112438-47112488	HL-60	blood:	n/a
3	chr8:47156401-47156451	HEK293	kidney:	embryo
4	chr8:47112230-47112280	BE2_C	brain:	n/a
5	chr8:47045963-47046013	HUVEC	blood vessel:	n/a
6	chr8:47130777-47130827	HEK293	kidney:	embryo
7	chr8:47344447-47344497	HCM	heart:	n/a
8	chr8:47329505-47329555	HEK293	kidney:	embryo
9	chr8:47130777-47130827	SK-N-SH	brain:	n/a
10	chr8:47093117-47093167	SAEC	small airway:	n/a
11	chr8:47156687-47156737	SK-N-MC	brain:	n/a
12	chr8:47112438-47112488	HL-60	blood:	n/a
13	chr8:47156401-47156451	HEK293	kidney:	embryo
14	chr8:47112230-47112280	BE2_C	brain:	n/a
15	chr8:47045963-47046013	HUVEC	blood vessel:	n/a
16	chr8:47130777-47130827	HEK293	kidney:	embryo
17	chr8:47344447-47344497	HCM	heart:	n/a
18	chr8:47329505-47329555	HEK293	kidney:	embryo
19	chr8:47130777-47130827	SK-N-SH	brain:	n/a
20	chr8:47093117-47093167	SAEC	small airway:	n/a
21	chr8:47045963-47046013	SK-N-MC	brain:	n/a
22	chr8:47108953-47109003	AoSMC	blood vessel:	n/a
23	chr8:47015640-47015690	K562	blood:	n/a
24	chr8:47348070-47348120	BJ	skin:	n/a
25	chr8:47130822-47130872	HCM	heart:	n/a
26	chr8:47318698-47318748	NT2-D1	testis:	n/a
27	chr8:47108953-47109003	GM12892	blood:	n/a
28	chr8:47015665-47015715	AG04450	lung:	fetal
29	chr8:47160997-47161047	SAEC	small airway:	n/a
30	chr8:47318907-47318957	NT2-D1	testis:	n/a
31	chr8:47119035-47119085	AG09319	gingival:	n/a
32	chr8:47318907-47318957	GM12892	blood:	n/a
33	chr8:47142089-47142139	NHDF-neo	bronchial:	n/a
34	chr8:47015425-47015475	Caco-2	colon:	n/a
35	chr8:47171826-47171876	AG09319	gingival:	n/a
36	chr8:47108770-47108820	Hepatocyte	liver:	n/a
37	chr8:47344447-47344497	HEEpiC	esophagus:	n/a
38	chr8:47156401-47156451	RPTEC	kidney:	n/a
39	chr8:47120700-47120750	SK-N-MC	brain:	n/a
40	chr8:47040066-47040116	LNCaP	prostate:	n/a
41	chr8:46951755-46951805	IMR90	lung:	fetal
42	chr8:47045963-47046013	SK-N-SH_RA	brain:	n/a
43	chr8:47108770-47108820	SAEC	small airway:	n/a
44	chr8:47015640-47015690	ovcar-3	ovarian:	n/a
45	chr8:47040066-47040116	HEK293	kidney:	embryo
46	chr8:47015854-47015904	Jurkat	blood:	n/a
47	chr8:47318649-47318699	PrEC	prostate:	n/a
48	chr8:47348339-47348389	Hela-S3	cervix:	n/a
49	chr8:47112230-47112280	LNCaP	prostate:	n/a
50	chr8:47112438-47112488	HCT-116	colon:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:47152207..47152786-chr8:47399264..47399945,2	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	chr8:47059851..47061946-chr8:47064644..47066356,2	MCF-7	breast:
5	chr8:47103663..47106274-chr8:47108285..47110930,2	K562	blood:
6	chr8:47059851..47061946-chr8:47064644..47066356,2	MCF-7	breast:
7	chr2:86830620..86831120-chr8:47284541..47285069,2	MCF-7	breast:
8	chr8:46850638..46851140-chr8:47405865..47406365,2	MCF-7	breast:
9	chr8:46940678..46941746-chr8:47130003..47131748,8	MCF-7	breast:
10	chr8:46948914..46951388-chr8:46959571..46961840,2	K562	blood:
11	chr19:35614212..35616054-chr8:47337776..47339296,2	MCF-7	breast:
12	chr8:46948914..46951388-chr8:46959571..46961840,2	K562	blood:
13	chr2:133016687..133017416-chr8:46947342..46948320,4	MCF-7	breast:
14	chr8:47152207..47152786-chr8:47399264..47399945,2	MCF-7	breast:
15	chr10:42530427..42532590-chr8:46977725..46979226,2	MCF-7	breast:
16	chr8:47144016..47144925-chr8:47484500..47485152,3	MCF-7	breast:
17	chr8:47103663..47106274-chr8:47108285..47110930,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000255915	TF binding region
HSPA8P13	TF binding region
ENSG00000255915	CpG island
HSPA8P13	CpG island

Extended variants
information (count: 25831 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:25831 , 50 per page) page: 1 2 3 4 5 6 7 ... 517

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76706266	chr8:46946757-46946758	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs75763338	chr8:46946761-46946762	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs142805414	chr8:46946764-46946765	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs74428128	chr8:46946783-46946784	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs76334945	chr8:46946794-46946795	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs78588151	chr8:46946797-46946798	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs79434416	chr8:46946801-46946802	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs76136171	chr8:46946802-46946803	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs74431654	chr8:46946803-46946804	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs79310309	chr8:46946806-46946807	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs80177720	chr8:46946811-46946812	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs75188130	chr8:46946817-46946818	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs76043967	chr8:46946819-46946820	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs74837913	chr8:46946824-46946825	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs77833092	chr8:46946832-46946833	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs80209415	chr8:46946834-46946835	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs557578283	chr8:46946847-46946848	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs577804668	chr8:46946852-46946853	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs546468499	chr8:46946854-46946855	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs139024790	chr8:46946860-46946861	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs34177398	chr8:46946861-46946862	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs200239141	chr8:46946862-46946863	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs397686337	chr8:46946865-46946866	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs559967044	chr8:46946886-46946887	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs75097823	chr8:46946898-46946899	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs183433894	chr8:46946900-46946901	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs200532443	chr8:46946907-46946908	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs113280713	chr8:46946967-46946968	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs542171876	chr8:46946968-46946969	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs562376690	chr8:46946980-46946981	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs113529320	chr8:46946985-46946986	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs530811935	chr8:46946996-46946997	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs550909608	chr8:46947036-46947037	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs71527632	chr8:46947079-46947080	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs570651382	chr8:46947081-46947082	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs371892809	chr8:46947087-46947088	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs151033253	chr8:46947153-46947154	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs370365471	chr8:46947184-46947185	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs373367705	chr8:46947229-46947230	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs112468120	chr8:46947245-46947246	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs116094234	chr8:46947274-46947275	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs566345424	chr8:46947285-46947286	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs150035334	chr8:46947287-46947288	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs71239841	chr8:46947313-46947314	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs139662569	chr8:46947354-46947355	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs555378269	chr8:46947393-46947394	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs569094900	chr8:46947399-46947400	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs374798636	chr8:46947404-46947405	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs537485752	chr8:46947418-46947419	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs187322624	chr8:46947446-46947447	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:434 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:46946200-46949000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:46947000-46951000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
3	chr8:46947200-46951000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
4	chr8:46947400-46948000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr8:46947400-46948400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:46947600-46947800	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
7	chr8:46947600-46948000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr8:46947600-46948000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:46947600-46948000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:46947600-46948000	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr8:46947600-46948000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
12	chr8:46947600-46948000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:46947600-46948000	ZNF genes & repeats	Primary T cells from cord blood	blood
14	chr8:46947600-46948000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
15	chr8:46947600-46948000	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
16	chr8:46947600-46948000	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
17	chr8:46947600-46948000	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
18	chr8:46947600-46948000	ZNF genes & repeats	Colonic Mucosa	Colon
19	chr8:46947600-46948000	ZNF genes & repeats	Colon Smooth Muscle	Colon
20	chr8:46947600-46948000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
21	chr8:46947600-46948000	ZNF genes & repeats	Esophagus	oesophagus
22	chr8:46947600-46948000	ZNF genes & repeats	Fetal Lung	lung
23	chr8:46947600-46948000	Flanking Bivalent TSS/Enh	Gastric	stomach
24	chr8:46947600-46948000	Flanking Bivalent TSS/Enh	Pancreas	Pancrea
25	chr8:46947600-46948000	ZNF genes & repeats	Right Atrium	heart
26	chr8:46947600-46948000	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
27	chr8:46947600-46948000	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
28	chr8:46947600-46948000	ZNF genes & repeats	Spleen	Spleen
29	chr8:46947600-46948000	ZNF genes & repeats	Hela-S3	cervix
30	chr8:46947600-46948000	ZNF genes & repeats	NHEK	skin
31	chr8:46947600-46948200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
32	chr8:46947600-46948200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
33	chr8:46947600-46948200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
34	chr8:46947800-46948000	ZNF genes & repeats	Adipose Nuclei	Adipose
35	chr8:46947800-46948000	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
36	chr8:46947800-46948000	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
37	chr8:46947800-46948000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
38	chr8:46947800-46948000	ZNF genes & repeats	NHLF	lung
39	chr8:46948000-46949400	Weak transcription	Right Atrium	heart
40	chr8:46948000-46950200	Weak transcription	Primary T cells from cord blood	blood
41	chr8:46948000-46950400	Weak transcription	Primary T helper cells PMA-I stimulated	--
42	chr8:46948000-46950400	Weak transcription	Hela-S3	cervix
43	chr8:46948000-46950600	Weak transcription	Colon Smooth Muscle	Colon
44	chr8:46949400-46949600	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr8:46949600-46950400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr8:46950000-46952200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr8:46950000-46952200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
48	chr8:46950200-46950400	Flanking Active TSS	Primary hematopoietic stem cells	blood
49	chr8:46950200-46950400	Weak transcription	Right Atrium	heart
50	chr8:46950200-46950800	Active TSS	Primary T cells from cord blood	blood

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