Variant report

Variant	esv1840955
Chromosome Location	chr8:58115815-58130784
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:597)
CpG islands
(count:1222)
Chromatin interactive
region (count:13)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:597 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:58122168-58122783	HepG2	liver:	n/a	n/a
2	ATF1	chr8:58122169-58123010	K562	blood:	n/a	n/a
3	BACH1	chr8:58122347-58122997	K562	blood:	n/a	n/a
4	BHLHE40	chr8:58127590-58127948	K562	blood:	n/a	n/a
5	BHLHE40	chr8:58118159-58118698	K562	blood:	n/a	n/a
6	BHLHE40	chr8:58122112-58123036	K562	blood:	n/a	n/a
7	BRCA1	chr8:58127438-58127751	HepG2	liver:	n/a	n/a
8	BRCA1	chr8:58122208-58123016	GM12878	blood:	n/a	n/a
9	BRCA1	chr8:58122170-58122971	HepG2	liver:	n/a	n/a
10	BRCA1	chr8:58127563-58127875	GM12878	blood:	n/a	n/a
11	BRCA1	chr8:58118301-58118654	GM12878	blood:	n/a	n/a
12	CEBPB	chr8:58118292-58118614	HepG2	liver:	n/a	chr8:58118437-58118448
13	CEBPB	chr8:58118253-58118637	K562	blood:	n/a	chr8:58118437-58118448
14	CEBPB	chr8:58122125-58123045	K562	blood:	n/a	n/a
15	CEBPZ	chr8:58118279-58118527	HepG2	liver:	n/a	n/a
16	CHD1	chr8:58118485-58118679	GM12878	blood:	n/a	n/a
17	CHD1	chr8:58122169-58123189	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr8:58122268-58123011	HepG2	liver:	n/a	n/a
19	CHD2	chr8:58122614-58122989	GM12878	blood:	n/a	n/a
20	CHD2	chr8:58127562-58127861	HepG2	liver:	n/a	n/a
21	CHD2	chr8:58118259-58118697	HepG2	liver:	n/a	n/a
22	CHD2	chr8:58116729-58116763	K562	blood:	n/a	n/a
23	CHD2	chr8:58122153-58122987	K562	blood:	n/a	n/a
24	CTCF	chr8:58123544-58123642	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr8:58122200-58122350	NHEK	skin:	n/a	n/a
26	CTCF	chr8:58118520-58118670	HEK293	kidney:	n/a	n/a
27	CTCF	chr8:58122660-58122810	AG10803	skin:	n/a	n/a
28	CTCF	chr8:58118280-58118430	MCF-7	breast:	n/a	n/a
29	CTCF	chr8:58126535-58126668	K562	blood:	n/a	n/a
30	CTCF	chr8:58122260-58122410	AG04450	lung:	n/a	n/a
31	CTCF	chr8:58122500-58122650	GM12875	blood:	n/a	n/a
32	CTCF	chr8:58122200-58122350	GM12873	blood:	n/a	n/a
33	CTCF	chr8:58118240-58118390	HEK293	kidney:	n/a	n/a
34	CTCF	chr8:58126261-58126832	K562	blood:	n/a	n/a
35	CTCF	chr8:58122150-58122436	MCF-7	breast:	n/a	n/a
36	CTCF	chr8:58122240-58122390	GM12868	blood:	n/a	n/a
37	CTCF	chr8:58125520-58125670	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr8:58125184-58125217	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr8:58122740-58122890	HL-60	blood:	n/a	n/a
40	CTCF	chr8:58122220-58122370	NHEK	skin:	n/a	n/a
41	CTCF	chr8:58126424-58126500	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr8:58125660-58125810	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr8:58122220-58122370	HCT-116	colon:	n/a	n/a
44	CTCF	chr8:58122200-58122350	GM12866	blood:	n/a	n/a
45	CTCF	chr8:58122193-58122287	MCF-7	breast:	n/a	n/a
46	CTCF	chr8:58122106-58122590	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr8:58122180-58122330	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:58118300-58118450	GM12870	blood:	n/a	n/a
49	CTCF	chr8:58122640-58122790	GM12864	blood:	n/a	n/a
50	CTCF	chr8:58122180-58122330	GM12865	blood:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:58117541-58117591	HCT-116	colon:	n/a
2	chr8:58117125-58117175	GM12891	blood:	n/a
3	chr8:58117541-58117591	HCT-116	colon:	n/a
4	chr8:58117125-58117175	GM12891	blood:	n/a
5	chr8:58130467-58130517	HCF	heart:	n/a
6	chr8:58126962-58127012	K562	blood:	n/a
7	chr8:58119141-58119191	CMK	blood:	n/a
8	chr8:58122850-58122900	HIPEpiC	eye:	n/a
9	chr8:58130041-58130091	PANC-1	pancreas:	n/a
10	chr8:58119141-58119191	NB4	blood:	n/a
11	chr8:58130467-58130517	HNPCEpiC	eye:	n/a
12	chr8:58130467-58130517	HRCEpiC	kidney:	n/a
13	chr8:58126962-58127012	RPTEC	kidney:	n/a
14	chr8:58122850-58122900	GM06990	blood:	n/a
15	chr8:58126962-58127012	HRCEpiC	kidney:	n/a
16	chr8:58116908-58116958	SAEC	small airway:	n/a
17	chr8:58118711-58118761	Hepatocyte	liver:	n/a
18	chr8:58117687-58117737	K562	blood:	n/a
19	chr8:58126962-58127012	AG10803	skin:	n/a
20	chr8:58126962-58127012	HMEC	breast:	n/a
21	chr8:58117687-58117737	ProgFib	skin:	n/a
22	chr8:58128466-58128516	CMK	blood:	n/a
23	chr8:58119141-58119191	HL-60	blood:	n/a
24	chr8:58124249-58124299	Hepatocyte	liver:	n/a
25	chr8:58120465-58120515	NB4	blood:	n/a
26	chr8:58120465-58120515	SK-N-MC	brain:	n/a
27	chr8:58130041-58130091	T-47D	breast:	n/a
28	chr8:58126962-58127012	SKMC	muscle:	n/a
29	chr8:58130323-58130373	HEK293	kidney:	embryo
30	chr8:58118711-58118761	HCF	heart:	n/a
31	chr8:58128466-58128516	PFSK-1	brain:	n/a
32	chr8:58122215-58122265	AG04449	skin:	fetal
33	chr8:58130467-58130517	GM06990	blood:	n/a
34	chr8:58116908-58116958	HEEpiC	esophagus:	n/a
35	chr8:58130041-58130091	GM12878	blood:	n/a
36	chr8:58122215-58122265	T-47D	breast:	n/a
37	chr8:58117125-58117175	T-47D	breast:	n/a
38	chr8:58128724-58128774	SK-N-SH_RA	brain:	n/a
39	chr8:58122850-58122900	RPTEC	kidney:	n/a
40	chr8:58121215-58121265	HL-60	blood:	n/a
41	chr8:58121215-58121265	HCM	heart:	n/a
42	chr8:58119141-58119191	NH-A	brain:	n/a
43	chr8:58117687-58117737	HNPCEpiC	eye:	n/a
44	chr8:58122850-58122900	SK-N-MC	brain:	n/a
45	chr8:58121215-58121265	HRE	kidney:	n/a
46	chr8:58122850-58122900	AG04450	lung:	fetal
47	chr8:58116908-58116958	HNPCEpiC	eye:	n/a
48	chr8:58124249-58124299	Caco-2	colon:	n/a
49	chr8:58116908-58116958	NHBE	bronchial:	n/a
50	chr8:58117687-58117737	NB4	blood:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:58116966..58119487-chr8:58121967..58124287,2	MCF-7	breast:
2	chr8:58111629..58114368-chr8:58116589..58119919,3	K562	blood:
3	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
4	chr8:58117787..58118343-chr8:58127587..58128273,3	K562	blood:
5	chr8:58111742..58114368-chr8:58116589..58118815,2	K562	blood:
6	chr8:58116966..58119487-chr8:58121967..58124287,2	MCF-7	breast:
7	chr8:58121826..58122902-chr8:58255580..58256503,3	MCF-7	breast:
8	chr8:58117787..58118343-chr8:58127587..58128273,3	K562	blood:
9	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:
10	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:
11	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
12	chr8:58127588..58129747-chr8:58135062..58137669,2	K562	blood:
13	chr8:58122191..58122786-chr8:58255142..58256110,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM110B-8	chr8:58121058-58121191	ENSG00000253301.1
2	lnc-FAM110B-8	chr8:58120568-58120763	ENSG00000253301.1

No data

Variant related genes	Relation type
ENSG00000253301	TF binding region
ENSG00000253301	CpG island
ENSG00000253871	chromatin interactions

Extended variants
information (count: 1084 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1084 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10092332	chr8:58115815-58115816	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554777701	chr8:58115848-58115849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs68079439	chr8:58115857-58115858	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs192012813	chr8:58115863-58115864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs77753517	chr8:58115897-58115898	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
6	rs112266073	chr8:58115913-58115914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577637803	chr8:58115915-58115916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112168705	chr8:58115921-58115922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546541835	chr8:58115944-58115945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147997579	chr8:58115960-58115961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576718962	chr8:58115961-58115962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140773550	chr8:58115969-58115970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145907632	chr8:58115970-58115971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113986644	chr8:58115989-58115990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527271627	chr8:58116001-58116002	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547112650	chr8:58116015-58116016	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183141805	chr8:58116019-58116020	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375363981	chr8:58116023-58116024	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546381383	chr8:58116026-58116027	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112422637	chr8:58116029-58116030	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549683526	chr8:58116030-58116031	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73603902	chr8:58116045-58116046	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs77051226	chr8:58116056-58116057	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs199659725	chr8:58116059-58116060	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs59854264	chr8:58116086-58116087	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200226604	chr8:58116087-58116088	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201150808	chr8:58116096-58116097	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549110060	chr8:58116099-58116100	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs76523219	chr8:58116104-58116105	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139222198	chr8:58116105-58116106	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs386725761	chr8:58116145-58116146	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs74907546	chr8:58116147-58116148	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs143249442	chr8:58116150-58116151	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540096383	chr8:58116163-58116164	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556898033	chr8:58116168-58116169	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187658440	chr8:58116170-58116171	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542099964	chr8:58116184-58116185	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192265645	chr8:58116258-58116259	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs386725762	chr8:58116263-58116264	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541145718	chr8:58116264-58116265	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs56289889	chr8:58116276-58116277	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs184326089	chr8:58116283-58116284	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200217937	chr8:58116325-58116326	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549620289	chr8:58116334-58116335	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs386725764	chr8:58116340-58116341	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369567332	chr8:58116341-58116342	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199777346	chr8:58116342-58116343	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs56168253	chr8:58116344-58116345	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529067836	chr8:58116361-58116362	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs56266649	chr8:58116364-58116365	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	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	20729466	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
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	22183965	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58115400-58118200	Weak transcription	Right Atrium	heart
2	chr8:58116000-58117400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:58116200-58117000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:58116200-58117200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr8:58116400-58117000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:58116400-58117000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr8:58116400-58117000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
8	chr8:58116400-58117200	ZNF genes & repeats	Spleen	Spleen
9	chr8:58116400-58117400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
10	chr8:58116400-58118000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr8:58116600-58116800	ZNF genes & repeats	Brain Hippocampus Middle	brain
12	chr8:58116600-58117000	Enhancers	Gastric	stomach
13	chr8:58116600-58117200	ZNF genes & repeats	Fetal Kidney	kidney
14	chr8:58116600-58117200	ZNF genes & repeats	Pancreas	Pancrea
15	chr8:58116600-58117600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr8:58116600-58118800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr8:58116800-58118200	Weak transcription	Brain Hippocampus Middle	brain
18	chr8:58117000-58118200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr8:58117000-58118200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:58117000-58118200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr8:58117000-58118200	Weak transcription	Gastric	stomach
22	chr8:58117000-58119000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr8:58117200-58118200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr8:58117200-58118200	Weak transcription	Fetal Kidney	kidney
25	chr8:58117400-58118200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr8:58117800-58118800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
27	chr8:58118000-58118800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
28	chr8:58118000-58118800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr8:58118000-58118800	ZNF genes & repeats	Brain Germinal Matrix	brain
30	chr8:58118000-58118800	ZNF genes & repeats	Pancreas	Pancrea
31	chr8:58118200-58118400	Bivalent/Poised TSS	Primary T killer memory cells from peripheral blood	blood
32	chr8:58118200-58118600	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
33	chr8:58118200-58118600	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
34	chr8:58118200-58118600	ZNF genes & repeats	Fetal Intestine Large	intestine
35	chr8:58118200-58118600	ZNF genes & repeats	Fetal Intestine Small	intestine
36	chr8:58118200-58118600	ZNF genes & repeats	Fetal Muscle Trunk	muscle
37	chr8:58118200-58118600	ZNF genes & repeats	Placenta	Placenta
38	chr8:58118200-58118600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
39	chr8:58118200-58118600	ZNF genes & repeats	NHEK	skin
40	chr8:58118200-58118800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
41	chr8:58118200-58118800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr8:58118200-58118800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr8:58118200-58118800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr8:58118200-58118800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr8:58118200-58118800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
46	chr8:58118200-58118800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
47	chr8:58118200-58118800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
48	chr8:58118200-58118800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
49	chr8:58118200-58118800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr8:58118200-58118800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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