Variant report

Variant	esv3693378
Chromosome Location	chr8:58051501-58128557
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:878)
CpG islands
(count:2138)
Chromatin interactive
region (count:27)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:878 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

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	chr8:58105853-58106191	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	BHLHE40	chr8:58127590-58127948	K562	blood:	n/a	n/a
8	BRCA1	chr8:58127563-58127875	GM12878	blood:	n/a	n/a
9	BRCA1	chr8:58122170-58122971	HepG2	liver:	n/a	n/a
10	BRCA1	chr8:58122208-58123016	GM12878	blood:	n/a	n/a
11	BRCA1	chr8:58127438-58127751	HepG2	liver:	n/a	n/a
12	BRCA1	chr8:58118301-58118654	GM12878	blood:	n/a	n/a
13	CBX3	chr8:58105849-58106177	K562	blood:	n/a	n/a
14	CCNT2	chr8:58105900-58106102	K562	blood:	n/a	n/a
15	CEBPB	chr8:58053930-58054161	K562	blood:	n/a	n/a
16	CEBPB	chr8:58061157-58061275	K562	blood:	n/a	n/a
17	CEBPB	chr8:58059648-58059906	MCF-7	breast:	n/a	chr8:58059752-58059765 chr8:58059752-58059763
18	CEBPB	chr8:58061084-58061385	IMR90	lung:	n/a	chr8:58061133-58061146
19	CEBPB	chr8:58061093-58061371	HepG2	liver:	n/a	chr8:58061133-58061146
20	CEBPB	chr8:58053895-58054196	IMR90	lung:	n/a	n/a
21	CEBPB	chr8:58118253-58118637	K562	blood:	n/a	chr8:58118437-58118448
22	CEBPB	chr8:58053845-58054196	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:58122125-58123045	K562	blood:	n/a	n/a
24	CEBPB	chr8:58053850-58054200	A549	lung:	n/a	n/a
25	CEBPB	chr8:58053880-58054182	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr8:58118292-58118614	HepG2	liver:	n/a	chr8:58118437-58118448
27	CEBPZ	chr8:58118279-58118527	HepG2	liver:	n/a	n/a
28	CHD1	chr8:58122169-58123189	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr8:58118485-58118679	GM12878	blood:	n/a	n/a
30	CHD2	chr8:58116729-58116763	K562	blood:	n/a	n/a
31	CHD2	chr8:58122153-58122987	K562	blood:	n/a	n/a
32	CHD2	chr8:58122614-58122989	GM12878	blood:	n/a	n/a
33	CHD2	chr8:58127562-58127861	HepG2	liver:	n/a	n/a
34	CHD2	chr8:58105531-58106370	K562	blood:	n/a	n/a
35	CHD2	chr8:58122268-58123011	HepG2	liver:	n/a	n/a
36	CHD2	chr8:58118259-58118697	HepG2	liver:	n/a	n/a
37	CTCF	chr8:58118280-58118430	MCF-7	breast:	n/a	n/a
38	CTCF	chr8:58094760-58094910	HMEC	breast:	n/a	n/a
39	CTCF	chr8:58118420-58118570	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr8:58122180-58122330	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr8:58123340-58123490	HPF	lung:	n/a	n/a
42	CTCF	chr8:58118460-58118610	GM12867	blood:	n/a	n/a
43	CTCF	chr8:58126296-58126324	GM19239	blood:	n/a	n/a
44	CTCF	chr8:58122200-58122350	GM12873	blood:	n/a	n/a
45	CTCF	chr8:58122200-58122350	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr8:58094882-58094957	HepG2	liver:	n/a	n/a
47	CTCF	chr8:58094880-58095030	BJ	skin:	n/a	n/a
48	CTCF	chr8:58094741-58095107	GM12878	blood:	n/a	n/a
49	CTCF	chr8:58094780-58094930	AG09309	skin:	n/a	n/a
50	CTCF	chr8:58122200-58122350	HPAF	blood vessel:	n/a	n/a

(count:2138 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:58055168-58055218	CMK	blood:	n/a
2	chr8:58128466-58128516	RPTEC	kidney:	n/a
3	chr8:58124249-58124299	H1-hESC	embryonic stem cell:	embryo
4	chr8:58055168-58055218	CMK	blood:	n/a
5	chr8:58128466-58128516	RPTEC	kidney:	n/a
6	chr8:58124249-58124299	H1-hESC	embryonic stem cell:	embryo
7	chr8:58106155-58106205	HL-60	blood:	n/a
8	chr8:58056501-58056551	U87	brain:	n/a
9	chr8:58056026-58056076	GM19239	blood:	n/a
10	chr8:58122215-58122265	SAEC	small airway:	n/a
11	chr8:58106094-58106144	AG04450	lung:	fetal
12	chr8:58056113-58056163	U87	brain:	n/a
13	chr8:58106520-58106570	HMEC	breast:	n/a
14	chr8:58054756-58054806	MCF10A-Er-Src	breast:	n/a
15	chr8:58056026-58056076	HMEC	breast:	n/a
16	chr8:58106520-58106570	HCPEpiC	choroid plexus:	n/a
17	chr8:58124249-58124299	LNCaP	prostate:	n/a
18	chr8:58117125-58117175	Hepatocyte	liver:	n/a
19	chr8:58117687-58117737	MCF10A-Er-Src	breast:	n/a
20	chr8:58115012-58115062	BE2_C	brain:	n/a
21	chr8:58053663-58053713	A549	lung:	n/a
22	chr8:58053663-58053713	GM12892	blood:	n/a
23	chr8:58055876-58055926	AG09319	gingival:	n/a
24	chr8:58117541-58117591	Jurkat	blood:	n/a
25	chr8:58118711-58118761	HIPEpiC	eye:	n/a
26	chr8:58055876-58055926	AG04449	skin:	fetal
27	chr8:58053663-58053713	AG04450	lung:	fetal
28	chr8:58057665-58057715	HIPEpiC	eye:	n/a
29	chr8:58055876-58055926	HRCEpiC	kidney:	n/a
30	chr8:58118711-58118761	HepG2	liver:	n/a
31	chr8:58056501-58056551	HAEpiC	amniotic membrane:	n/a
32	chr8:58114950-58115000	HEK293	kidney:	embryo
33	chr8:58055876-58055926	NHBE	bronchial:	n/a
34	chr8:58122850-58122900	GM06990	blood:	n/a
35	chr8:58117687-58117737	Hela-S3	cervix:	n/a
36	chr8:58117687-58117737	HRCEpiC	kidney:	n/a
37	chr8:58123513-58123563	NT2-D1	testis:	n/a
38	chr8:58116908-58116958	HUVEC	blood vessel:	n/a
39	chr8:58106155-58106205	U87	brain:	n/a
40	chr8:58120465-58120515	CMK	blood:	n/a
41	chr8:58055591-58055641	PANC-1	pancreas:	n/a
42	chr8:58128466-58128516	HCT-116	colon:	n/a
43	chr8:58106598-58106648	GM12878	blood:	n/a
44	chr8:58106520-58106570	Hepatocyte	liver:	n/a
45	chr8:58122850-58122900	SAEC	small airway:	n/a
46	chr8:58055024-58055074	GM12891	blood:	n/a
47	chr8:58124249-58124299	AG04449	skin:	fetal
48	chr8:58117687-58117737	NHBE	bronchial:	n/a
49	chr8:58106094-58106144	SK-N-SH	brain:	n/a
50	chr8:58055024-58055074	HCPEpiC	choroid plexus:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:58111742..58114368-chr8:58116589..58118815,2	K562	blood:
2	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:
3	chr8:58111629..58114368-chr8:58116589..58119919,3	K562	blood:
4	chr8:58076519..58079288-chr8:58083789..58085655,2	K562	blood:
5	chr8:58094338..58095391-chr8:58255624..58256416,4	MCF-7	breast:
6	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
7	chr8:58127588..58129747-chr8:58135062..58137669,2	K562	blood:
8	chr8:58094799..58095495-chr8:58255642..58256690,5	MCF-7	breast:
9	chr8:58116966..58119487-chr8:58121967..58124287,2	MCF-7	breast:
10	chr8:58098067..58099836-chr8:58101928..58103636,2	K562	blood:
11	chr8:58117787..58118343-chr8:58127587..58128273,3	K562	blood:
12	chr8:58117787..58118343-chr8:58127587..58128273,3	K562	blood:
13	chr8:58122191..58122786-chr8:58255142..58256110,2	K562	blood:
14	chr8:58083900..58086328-chr8:58091891..58093782,2	K562	blood:
15	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
16	chr8:58111742..58114368-chr8:58116589..58118815,2	K562	blood:
17	chr8:58111629..58114368-chr8:58116589..58119919,3	K562	blood:
18	chr8:58098067..58099836-chr8:58101928..58103636,2	K562	blood:
19	chr8:58057960..58058531-chr8:58255912..58256499,2	MCF-7	breast:
20	chr8:58048196..58050433-chr8:58051015..58053775,2	K562	blood:
21	chr8:58094506..58095013-chr8:58135741..58136318,2	MCF-7	breast:
22	chr8:58121826..58122902-chr8:58255580..58256503,3	MCF-7	breast:
23	chr8:58083900..58086328-chr8:58091891..58093782,2	K562	blood:
24	chr8:58104914..58107604-chr8:58109994..58112221,3	K562	blood:
25	chr8:58076519..58079288-chr8:58083789..58085655,2	K562	blood:
26	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:
27	chr8:58116966..58119487-chr8:58121967..58124287,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM110B-8	chr8:58106444-58106570	ENSG00000253301.1
2	lnc-FAM110B-8	chr8:58106444-58106570	ENSG00000253301.1
3	lnc-FAM110B-8	chr8:58063159-58063293	NONHSAT126727
4	lnc-FAM110B-8	chr8:58121058-58121191	ENSG00000253301.1
5	lnc-FAM110B-8	chr8:58106149-58106248	ENSG00000253301.1
6	lnc-FAM110B-8	chr8:58120568-58120763	ENSG00000253301.1
7	lnc-FAM110B-8	chr8:58055271-58055444	NONHSAT126727
8	lnc-FAM110B-8	chr8:58106179-58106275	ENSG00000253301.1

No data

Variant related genes	Relation type
ENSG00000220984	TF binding region
ENSG00000253301	TF binding region
ENSG00000220984	CpG island
ENSG00000253301	CpG island
ENSG00000253871	chromatin interactions
ENSG00000253301	chromatin interactions

Extended variants
information (count: 1857 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1857 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10958523	chr8:58051501-58051502	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10958524	chr8:58051521-58051522	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs34120669	chr8:58051523-58051524	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs10958525	chr8:58051528-58051529	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs16921675	chr8:58052082-58052083	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs78941440	chr8:58052095-58052096	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs146166438	chr8:58052223-58052224	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs565782291	chr8:58052235-58052236	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs16921677	chr8:58052431-58052432	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs76745945	chr8:58052432-58052433	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs573715836	chr8:58052434-58052435	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs116904737	chr8:58052443-58052444	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs2218271	chr8:58052446-58052447	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs191778725	chr8:58052449-58052450	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs541159093	chr8:58052464-58052465	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs564127245	chr8:58052472-58052473	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs577659584	chr8:58052533-58052534	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs10086384	chr8:58052559-58052560	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs564016380	chr8:58052614-58052615	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs5891642	chr8:58052647-58052648	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs34668494	chr8:58052648-58052649	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs200547167	chr8:58052649-58052650	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs200003324	chr8:58052650-58052651	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs529431637	chr8:58052675-58052676	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs549574927	chr8:58052699-58052700	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs559725135	chr8:58052728-58052729	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs561028940	chr8:58052729-58052730	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs182313120	chr8:58052737-58052738	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs73680613	chr8:58052858-58052859	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs371057886	chr8:58052864-58052865	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs34652409	chr8:58052867-58052868	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs571216131	chr8:58052895-58052896	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs374269543	chr8:58052912-58052913	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs373659476	chr8:58053863-58053864	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs148469571	chr8:58053937-58053938	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs543258358	chr8:58053945-58053946	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs553398389	chr8:58053956-58053957	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs573439927	chr8:58053978-58053979	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs545637976	chr8:58053985-58053986	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs565505601	chr8:58054029-58054030	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs530603882	chr8:58054030-58054031	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs73603849	chr8:58054031-58054032	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs560938992	chr8:58054042-58054043	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs529662763	chr8:58054057-58054058	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs145295750	chr8:58054071-58054072	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs113929714	chr8:58054076-58054077	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs532148342	chr8:58054200-58054201	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs72649132	chr8:58054615-58054616	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs543366176	chr8:58054632-58054633	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs539871395	chr8:58054642-58054643	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58054600-58055000	Bivalent Enhancer	Fetal Muscle Leg	muscle
2	chr8:58054800-58055000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr8:58054800-58055000	Bivalent/Poised TSS	Brain Angular Gyrus	brain
4	chr8:58054800-58055000	Bivalent Enhancer	Fetal Thymus	thymus
5	chr8:58054800-58055000	Enhancers	Pancreas	Pancrea
6	chr8:58054800-58055200	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
7	chr8:58054800-58055200	Bivalent Enhancer	Fetal Stomach	stomach
8	chr8:58054800-58055400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
9	chr8:58054800-58055600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr8:58054800-58055600	Active TSS	Brain Anterior Caudate	brain
11	chr8:58054800-58055600	Bivalent Enhancer	Placenta	Placenta
12	chr8:58054800-58055800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
13	chr8:58054800-58055800	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
14	chr8:58054800-58056000	Enhancers	Lung	lung
15	chr8:58054800-58056200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr8:58054800-58056400	Active TSS	Brain Germinal Matrix	brain
17	chr8:58054800-58057000	Active TSS	Fetal Brain Female	brain
18	chr8:58055000-58055200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
19	chr8:58055000-58055200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr8:58055000-58055200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr8:58055000-58055200	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
22	chr8:58055000-58055200	Flanking Active TSS	Brain Angular Gyrus	brain
23	chr8:58055000-58055200	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
24	chr8:58055000-58055200	Flanking Bivalent TSS/Enh	Right Ventricle	heart
25	chr8:58055000-58055200	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
26	chr8:58055000-58055400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr8:58055000-58055400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr8:58055000-58055400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr8:58055000-58055400	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
30	chr8:58055000-58055400	Flanking Active TSS	Pancreas	Pancrea
31	chr8:58055000-58055400	Enhancers	Spleen	Spleen
32	chr8:58055000-58055400	Bivalent Enhancer	HMEC	breast
33	chr8:58055000-58055600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
34	chr8:58055000-58055600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
35	chr8:58055000-58055600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
36	chr8:58055000-58055600	Bivalent Enhancer	Left Ventricle	heart
37	chr8:58055000-58055600	Active TSS	Right Atrium	heart
38	chr8:58055000-58055600	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
39	chr8:58055000-58055600	Bivalent Enhancer	Thymus	Thymus
40	chr8:58055000-58055800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr8:58055000-58056000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr8:58055000-58056000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
43	chr8:58055000-58056000	Bivalent Enhancer	Ovary	ovary
44	chr8:58055200-58055400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr8:58055200-58055400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
46	chr8:58055200-58055400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr8:58055200-58055400	Active TSS	Brain Angular Gyrus	brain
48	chr8:58055200-58055400	Bivalent/Poised TSS	Placenta Amnion	Placenta Amnion
49	chr8:58055200-58055400	Bivalent/Poised TSS	Right Ventricle	heart
50	chr8:58055200-58055600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived

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