Variant report

Variant	esv1846255
Chromosome Location	chr8:58106529-58127901
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:604)
CpG islands
(count:1160)
Chromatin interactive
region (count:16)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:604 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

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	chr8:58122112-58123036	K562	blood:	n/a	n/a
6	BHLHE40	chr8:58118159-58118698	K562	blood:	n/a	n/a
7	BRCA1	chr8:58127438-58127751	HepG2	liver:	n/a	n/a
8	BRCA1	chr8:58122170-58122971	HepG2	liver:	n/a	n/a
9	BRCA1	chr8:58127563-58127875	GM12878	blood:	n/a	n/a
10	BRCA1	chr8:58122208-58123016	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	chr8:58122125-58123045	K562	blood:	n/a	n/a
14	CEBPB	chr8:58118253-58118637	K562	blood:	n/a	chr8:58118437-58118448
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	chr8:58122153-58122987	K562	blood:	n/a	n/a
19	CHD2	chr8:58116729-58116763	K562	blood:	n/a	n/a
20	CHD2	chr8:58122614-58122989	GM12878	blood:	n/a	n/a
21	CHD2	chr8:58122268-58123011	HepG2	liver:	n/a	n/a
22	CHD2	chr8:58127562-58127861	HepG2	liver:	n/a	n/a
23	CHD2	chr8:58118259-58118697	HepG2	liver:	n/a	n/a
24	CTCF	chr8:58118420-58118570	NHDF-neo	bronchial:	n/a	n/a
25	CTCF	chr8:58118560-58118710	GM12870	blood:	n/a	n/a
26	CTCF	chr8:58125620-58125770	NB4	blood:	n/a	n/a
27	CTCF	chr8:58122220-58122370	HCT-116	colon:	n/a	n/a
28	CTCF	chr8:58122700-58122850	AG10803	skin:	n/a	n/a
29	CTCF	chr8:58118340-58118490	GM12871	blood:	n/a	n/a
30	CTCF	chr8:58122860-58123010	HCT-116	colon:	n/a	n/a
31	CTCF	chr8:58122740-58122890	HL-60	blood:	n/a	n/a
32	CTCF	chr8:58118300-58118450	GM12870	blood:	n/a	n/a
33	CTCF	chr8:58118280-58118430	HepG2	liver:	n/a	n/a
34	CTCF	chr8:58122880-58123030	GM12867	blood:	n/a	n/a
35	CTCF	chr8:58122160-58122310	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr8:58122640-58122790	GM12864	blood:	n/a	n/a
37	CTCF	chr8:58122200-58122350	HCFaa	heart:	n/a	n/a
38	CTCF	chr8:58122180-58122330	GM12870	blood:	n/a	n/a
39	CTCF	chr8:58122520-58122670	AG04449	skin:	n/a	n/a
40	CTCF	chr8:58123200-58123350	NHLF	lung:	n/a	n/a
41	CTCF	chr8:58122200-58122350	NHEK	skin:	n/a	n/a
42	CTCF	chr8:58118320-58118470	GM12872	blood:	n/a	n/a
43	CTCF	chr8:58118300-58118590	AG04449	skin:	n/a	n/a
44	CTCF	chr8:58122220-58122510	HPF	lung:	n/a	n/a
45	CTCF	chr8:58122540-58122690	GM12867	blood:	n/a	n/a
46	CTCF	chr8:58122220-58122370	GM12872	blood:	n/a	n/a
47	CTCF	chr8:58118280-58118430	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:58122880-58123030	GM12869	blood:	n/a	n/a
49	CTCF	chr8:58122129-58122348	LNCaP	prostate:	n/a	n/a
50	CTCF	chr8:58126534-58126613	HepG2	liver:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:58114950-58115000	HNPCEpiC	eye:	n/a
2	chr8:58114950-58115000	HNPCEpiC	eye:	n/a
3	chr8:58114915-58114965	BJ	skin:	n/a
4	chr8:58114915-58114965	GM19239	blood:	n/a
5	chr8:58116908-58116958	MCF10A-Er-Src	breast:	n/a
6	chr8:58117541-58117591	AG09319	gingival:	n/a
7	chr8:58117687-58117737	SAEC	small airway:	n/a
8	chr8:58117541-58117591	AG09309	skin:	n/a
9	chr8:58121215-58121265	HRPEpiC	eye:	n/a
10	chr8:58114915-58114965	NH-A	brain:	n/a
11	chr8:58106598-58106648	IMR90	lung:	fetal
12	chr8:58117125-58117175	HUVEC	blood vessel:	n/a
13	chr8:58122850-58122900	HCT-116	colon:	n/a
14	chr8:58117794-58117844	HCM	heart:	n/a
15	chr8:58117125-58117175	GM12878	blood:	n/a
16	chr8:58106598-58106648	ovcar-3	ovarian:	n/a
17	chr8:58120465-58120515	HPAEpiC	pulmonary alveolar:	n/a
18	chr8:58114950-58115000	A549	lung:	n/a
19	chr8:58106520-58106570	Jurkat	blood:	n/a
20	chr8:58117541-58117591	NHDF-neo	bronchial:	n/a
21	chr8:58117794-58117844	GM12892	blood:	n/a
22	chr8:58117541-58117591	HepG2	liver:	n/a
23	chr8:58117125-58117175	HNPCEpiC	eye:	n/a
24	chr8:58114915-58114965	MCF10A-Er-Src	breast:	n/a
25	chr8:58116908-58116958	AG10803	skin:	n/a
26	chr8:58106598-58106648	NHDF-neo	bronchial:	n/a
27	chr8:58106598-58106648	MCF-7	breast:	n/a
28	chr8:58106520-58106570	LNCaP	prostate:	n/a
29	chr8:58122215-58122265	U87	brain:	n/a
30	chr8:58124249-58124299	HMEC	breast:	n/a
31	chr8:58114950-58115000	GM12891	blood:	n/a
32	chr8:58116908-58116958	NHBE	bronchial:	n/a
33	chr8:58126962-58127012	CMK	blood:	n/a
34	chr8:58117125-58117175	Hela-S3	cervix:	n/a
35	chr8:58117687-58117737	HCPEpiC	choroid plexus:	n/a
36	chr8:58117541-58117591	HNPCEpiC	eye:	n/a
37	chr8:58117687-58117737	BJ	skin:	n/a
38	chr8:58120465-58120515	SKMC	muscle:	n/a
39	chr8:58117687-58117737	NHBE	bronchial:	n/a
40	chr8:58122215-58122265	AG09309	skin:	n/a
41	chr8:58121215-58121265	HPAEpiC	pulmonary alveolar:	n/a
42	chr8:58106520-58106570	AG09319	gingival:	n/a
43	chr8:58106598-58106648	HRPEpiC	eye:	n/a
44	chr8:58114915-58114965	HMEC	breast:	n/a
45	chr8:58106598-58106648	A549	lung:	n/a
46	chr8:58106598-58106648	AG09319	gingival:	n/a
47	chr8:58117125-58117175	Hepatocyte	liver:	n/a
48	chr8:58106520-58106570	SK-N-SH_RA	brain:	n/a
49	chr8:58106520-58106570	A549	lung:	n/a
50	chr8:58122850-58122900	HUVEC	blood vessel:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:58116966..58119487-chr8:58121967..58124287,2	MCF-7	breast:
2	chr8:58111742..58114368-chr8:58116589..58118815,2	K562	blood:
3	chr8:58121826..58122902-chr8:58255580..58256503,3	MCF-7	breast:
4	chr8:58116966..58119487-chr8:58121967..58124287,2	MCF-7	breast:
5	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
6	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
7	chr8:58111629..58114368-chr8:58116589..58119919,3	K562	blood:
8	chr8:58127588..58129747-chr8:58135062..58137669,2	K562	blood:
9	chr8:58117787..58118343-chr8:58127587..58128273,3	K562	blood:
10	chr8:58111629..58114368-chr8:58116589..58119919,3	K562	blood:
11	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:
12	chr8:58104914..58107604-chr8:58109994..58112221,3	K562	blood:
13	chr8:58117787..58118343-chr8:58127587..58128273,3	K562	blood:
14	chr8:58111742..58114368-chr8:58116589..58118815,2	K562	blood:
15	chr8:58122191..58122786-chr8:58255142..58256110,2	K562	blood:
16	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM110B-8	chr8:58120568-58120763	ENSG00000253301.1
2	lnc-FAM110B-8	chr8:58106444-58106570	ENSG00000253301.1
3	lnc-FAM110B-8	chr8:58106444-58106570	ENSG00000253301.1
4	lnc-FAM110B-8	chr8:58121058-58121191	ENSG00000253301.1

No data

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

Extended variants
information (count: 1285 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1285 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575203694	chr8:58106579-58106580	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs61241336	chr8:58106585-58106586	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs570430068	chr8:58106586-58106587	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs139173646	chr8:58106658-58106659	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs556137812	chr8:58106691-58106692	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs16921812	chr8:58106737-58106738	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs562035357	chr8:58106750-58106751	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs555177887	chr8:58106804-58106805	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs2005392	chr8:58106896-58106897	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs556032337	chr8:58106926-58106927	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs540295876	chr8:58106932-58106933	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs560220999	chr8:58106966-58106967	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs186425360	chr8:58106991-58106992	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs190868046	chr8:58107010-58107011	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs575598421	chr8:58107030-58107031	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs183685611	chr8:58107046-58107047	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs371591117	chr8:58107050-58107051	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs532062049	chr8:58107071-58107072	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs142143576	chr8:58107078-58107079	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs562240976	chr8:58107102-58107103	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs527906148	chr8:58107129-58107130	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs150142025	chr8:58107153-58107154	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs570531401	chr8:58107168-58107169	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs17194792	chr8:58107195-58107196	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs549789294	chr8:58107198-58107199	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs561083554	chr8:58107222-58107223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569835894	chr8:58107263-58107264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529284100	chr8:58107299-58107300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535711591	chr8:58107320-58107321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558082533	chr8:58107351-58107352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555257686	chr8:58107419-58107420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs16921814	chr8:58107421-58107422	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs16921817	chr8:58107563-58107564	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs138624372	chr8:58107587-58107588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376358987	chr8:58107592-58107593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201162672	chr8:58107610-58107611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs386725759	chr8:58107611-58107612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73603871	chr8:58107612-58107613	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs562926292	chr8:58107653-58107654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140243935	chr8:58107675-58107676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576382659	chr8:58107676-58107677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542509797	chr8:58107733-58107734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550929481	chr8:58107758-58107759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201705548	chr8:58107767-58107768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192940583	chr8:58107798-58107799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs370886827	chr8:58107801-58107802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149322004	chr8:58107818-58107819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144650904	chr8:58107819-58107820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533082477	chr8:58107855-58107856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536295932	chr8:58107888-58107889	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:254 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58106000-58107200	Active TSS	K562	blood
2	chr8:58106200-58114800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:58111800-58112200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr8:58114800-58115400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:58115400-58118200	Weak transcription	Right Atrium	heart
6	chr8:58116000-58117400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr8:58116200-58117000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr8:58116200-58117200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr8:58116400-58117000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr8:58116400-58117000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr8:58116400-58117000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
12	chr8:58116400-58117200	ZNF genes & repeats	Spleen	Spleen
13	chr8:58116400-58117400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr8:58116400-58118000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr8:58116600-58116800	ZNF genes & repeats	Brain Hippocampus Middle	brain
16	chr8:58116600-58117000	Enhancers	Gastric	stomach
17	chr8:58116600-58117200	ZNF genes & repeats	Fetal Kidney	kidney
18	chr8:58116600-58117200	ZNF genes & repeats	Pancreas	Pancrea
19	chr8:58116600-58117600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr8:58116600-58118800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr8:58116800-58118200	Weak transcription	Brain Hippocampus Middle	brain
22	chr8:58117000-58118200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr8:58117000-58118200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr8:58117000-58118200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr8:58117000-58118200	Weak transcription	Gastric	stomach
26	chr8:58117000-58119000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr8:58117200-58118200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr8:58117200-58118200	Weak transcription	Fetal Kidney	kidney
29	chr8:58117400-58118200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr8:58117800-58118800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
31	chr8:58118000-58118800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
32	chr8:58118000-58118800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr8:58118000-58118800	ZNF genes & repeats	Brain Germinal Matrix	brain
34	chr8:58118000-58118800	ZNF genes & repeats	Pancreas	Pancrea
35	chr8:58118200-58118400	Bivalent/Poised TSS	Primary T killer memory cells from peripheral blood	blood
36	chr8:58118200-58118600	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
37	chr8:58118200-58118600	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
38	chr8:58118200-58118600	ZNF genes & repeats	Fetal Intestine Large	intestine
39	chr8:58118200-58118600	ZNF genes & repeats	Fetal Intestine Small	intestine
40	chr8:58118200-58118600	ZNF genes & repeats	Fetal Muscle Trunk	muscle
41	chr8:58118200-58118600	ZNF genes & repeats	Placenta	Placenta
42	chr8:58118200-58118600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
43	chr8:58118200-58118600	ZNF genes & repeats	NHEK	skin
44	chr8:58118200-58118800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
45	chr8:58118200-58118800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr8:58118200-58118800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr8:58118200-58118800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr8:58118200-58118800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr8:58118200-58118800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
50	chr8:58118200-58118800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell

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