Variant report

Variant	esv1816189
Chromosome Location	chr8:58093977-58126589
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:754)
CpG islands
(count:1220)
Chromatin interactive
region (count:19)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:754 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

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	chr8:58118159-58118698	K562	blood:	n/a	n/a
5	BHLHE40	chr8:58122112-58123036	K562	blood:	n/a	n/a
6	BHLHE40	chr8:58105853-58106191	K562	blood:	n/a	n/a
7	BRCA1	chr8:58118301-58118654	GM12878	blood:	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	CBX3	chr8:58105849-58106177	K562	blood:	n/a	n/a
11	CCNT2	chr8:58105900-58106102	K562	blood:	n/a	n/a
12	CEBPB	chr8:58122125-58123045	K562	blood:	n/a	n/a
13	CEBPB	chr8:58118292-58118614	HepG2	liver:	n/a	chr8:58118437-58118448
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	chr8:58122169-58123189	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr8:58118485-58118679	GM12878	blood:	n/a	n/a
18	CHD2	chr8:58105531-58106370	K562	blood:	n/a	n/a
19	CHD2	chr8:58118259-58118697	HepG2	liver:	n/a	n/a
20	CHD2	chr8:58122614-58122989	GM12878	blood:	n/a	n/a
21	CHD2	chr8:58122153-58122987	K562	blood:	n/a	n/a
22	CHD2	chr8:58116729-58116763	K562	blood:	n/a	n/a
23	CHD2	chr8:58122268-58123011	HepG2	liver:	n/a	n/a
24	CTCF	chr8:58095000-58095150	BE2_C	brain:	n/a	n/a
25	CTCF	chr8:58118320-58118470	GM12872	blood:	n/a	n/a
26	CTCF	chr8:58100977-58101320	K562	blood:	n/a	n/a
27	CTCF	chr8:58126296-58126324	GM19239	blood:	n/a	n/a
28	CTCF	chr8:58094840-58094990	AoAF	blood vessel:	n/a	n/a
29	CTCF	chr8:58094865-58095007	Lung_OC	lung:	n/a	n/a
30	CTCF	chr8:58118280-58118430	GM12872	blood:	n/a	n/a
31	CTCF	chr8:58118280-58118430	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr8:58094820-58094970	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr8:58122260-58122410	HVMF	connective:	n/a	n/a
34	CTCF	chr8:58122740-58122890	HL-60	blood:	n/a	n/a
35	CTCF	chr8:58094880-58095030	HEK293	kidney:	n/a	n/a
36	CTCF	chr8:58094800-58094950	HL-60	blood:	n/a	n/a
37	CTCF	chr8:58122200-58122350	K562	blood:	n/a	n/a
38	CTCF	chr8:58122200-58122350	AG04449	skin:	n/a	n/a
39	CTCF	chr8:58122138-58122351	HepG2	liver:	n/a	n/a
40	CTCF	chr8:58123340-58123490	HPF	lung:	n/a	n/a
41	CTCF	chr8:58126534-58126613	HepG2	liver:	n/a	n/a
42	CTCF	chr8:58122200-58122350	HFF	foreskin:	n/a	n/a
43	CTCF	chr8:58123240-58123390	GM12866	blood:	n/a	n/a
44	CTCF	chr8:58094820-58094970	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr8:58118260-58118410	NHLF	lung:	n/a	n/a
46	CTCF	chr8:58122180-58122330	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr8:58122620-58122770	GM12865	blood:	n/a	n/a
48	CTCF	chr8:58101095-58101113	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr8:58125620-58125770	NB4	blood:	n/a	n/a
50	CTCF	chr8:58122200-58122350	HEEpiC	esophagus:	n/a	n/a

(count:1220 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:58114915-58114965	BJ	skin:	n/a
2	chr8:58122850-58122900	Hela-S3	cervix:	n/a
3	chr8:58117541-58117591	GM12878	blood:	n/a
4	chr8:58106520-58106570	NT2-D1	testis:	n/a
5	chr8:58122215-58122265	HNPCEpiC	eye:	n/a
6	chr8:58123513-58123563	HPAEpiC	pulmonary alveolar:	n/a
7	chr8:58106520-58106570	SK-N-SH	brain:	n/a
8	chr8:58106094-58106144	PFSK-1	brain:	n/a
9	chr8:58122215-58122265	SK-N-SH_RA	brain:	n/a
10	chr8:58114950-58115000	CMK	blood:	n/a
11	chr8:58119141-58119191	IMR90	lung:	fetal
12	chr8:58106155-58106205	SK-N-SH_RA	brain:	n/a
13	chr8:58122215-58122265	HMEC	breast:	n/a
14	chr8:58117125-58117175	HCM	heart:	n/a
15	chr8:58120465-58120515	GM06990	blood:	n/a
16	chr8:58123513-58123563	Hela-S3	cervix:	n/a
17	chr8:58121215-58121265	AG04449	skin:	fetal
18	chr8:58116908-58116958	PFSK-1	brain:	n/a
19	chr8:58123513-58123563	PANC-1	pancreas:	n/a
20	chr8:58121215-58121265	HRE	kidney:	n/a
21	chr8:58118711-58118761	HCT-116	colon:	n/a
22	chr8:58124249-58124299	ovcar-3	ovarian:	n/a
23	chr8:58117687-58117737	A549	lung:	n/a
24	chr8:58121215-58121265	PANC-1	pancreas:	n/a
25	chr8:58118711-58118761	HCM	heart:	n/a
26	chr8:58117794-58117844	GM12892	blood:	n/a
27	chr8:58120465-58120515	A549	lung:	n/a
28	chr8:58106155-58106205	HRPEpiC	eye:	n/a
29	chr8:58119141-58119191	GM12892	blood:	n/a
30	chr8:58119141-58119191	AG10803	skin:	n/a
31	chr8:58117541-58117591	A549	lung:	n/a
32	chr8:58117794-58117844	AG04450	lung:	fetal
33	chr8:58106598-58106648	HepG2	liver:	n/a
34	chr8:58124249-58124299	SK-N-SH	brain:	n/a
35	chr8:58106598-58106648	HUVEC	blood vessel:	n/a
36	chr8:58119141-58119191	ovcar-3	ovarian:	n/a
37	chr8:58106155-58106205	PrEC	prostate:	n/a
38	chr8:58114950-58115000	HCM	heart:	n/a
39	chr8:58106598-58106648	Jurkat	blood:	n/a
40	chr8:58106598-58106648	PrEC	prostate:	n/a
41	chr8:58115012-58115062	Hepatocyte	liver:	n/a
42	chr8:58117687-58117737	MCF-7	breast:	n/a
43	chr8:58106155-58106205	AG10803	skin:	n/a
44	chr8:58114915-58114965	HAEpiC	amniotic membrane:	n/a
45	chr8:58121215-58121265	HCT-116	colon:	n/a
46	chr8:58119141-58119191	H1-hESC	embryonic stem cell:	embryo
47	chr8:58121215-58121265	GM19239	blood:	n/a
48	chr8:58117794-58117844	Hepatocyte	liver:	n/a
49	chr8:58117541-58117591	ProgFib	skin:	n/a
50	chr8:58124249-58124299	HRCEpiC	kidney:	n/a

(count:19 , 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	chr8:58098067..58099836-chr8:58101928..58103636,2	K562	blood:
4	chr8:58121826..58122902-chr8:58255580..58256503,3	MCF-7	breast:
5	chr8:58117787..58118343-chr8:58127587..58128273,3	K562	blood:
6	chr8:58116966..58119487-chr8:58121967..58124287,2	MCF-7	breast:
7	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
8	chr8:58094799..58095495-chr8:58255642..58256690,5	MCF-7	breast:
9	chr8:58098067..58099836-chr8:58101928..58103636,2	K562	blood:
10	chr8:58122191..58122786-chr8:58255142..58256110,2	K562	blood:
11	chr8:58094506..58095013-chr8:58135741..58136318,2	MCF-7	breast:
12	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:
13	chr8:58094338..58095391-chr8:58255624..58256416,4	MCF-7	breast:
14	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
15	chr8:58111742..58114368-chr8:58116589..58118815,2	K562	blood:
16	chr8:58111742..58114368-chr8:58116589..58118815,2	K562	blood:
17	chr8:58104914..58107604-chr8:58109994..58112221,3	K562	blood:
18	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:
19	chr8:58111629..58114368-chr8:58116589..58119919,3	K562	blood:

(count:6 , 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	chr8:58106179-58106275	ENSG00000253301.1
3	lnc-FAM110B-8	chr8:58106444-58106570	ENSG00000253301.1
4	lnc-FAM110B-8	chr8:58106149-58106248	ENSG00000253301.1
5	lnc-FAM110B-8	chr8:58121058-58121191	ENSG00000253301.1
6	lnc-FAM110B-8	chr8:58106444-58106570	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: 1194 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1194 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542172980	chr8:58094354-58094355	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs561854317	chr8:58094355-58094356	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs372954588	chr8:58094435-58094436	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs57238808	chr8:58094450-58094451	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs75857502	chr8:58094451-58094452	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs367974648	chr8:58094452-58094453	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs527446058	chr8:58094463-58094464	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs561071556	chr8:58094473-58094474	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs185811346	chr8:58094476-58094477	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs190324695	chr8:58094526-58094527	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs193195710	chr8:58094533-58094534	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs371061814	chr8:58094564-58094565	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs552137204	chr8:58094590-58094591	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs568941235	chr8:58094594-58094595	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs150861969	chr8:58094613-58094614	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs373109401	chr8:58094658-58094659	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs548441813	chr8:58094673-58094674	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs184326201	chr8:58094685-58094686	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs200218277	chr8:58094715-58094716	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs534353265	chr8:58094718-58094719	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs554116050	chr8:58094729-58094730	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs188563457	chr8:58094768-58094769	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs539574131	chr8:58094798-58094799	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs139560975	chr8:58094823-58094824	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs576078680	chr8:58094868-58094869	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs541860468	chr8:58094894-58094895	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs561971371	chr8:58094896-58094897	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs181051210	chr8:58094957-58094958	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs555024859	chr8:58094989-58094990	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs564161290	chr8:58094998-58094999	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs56406973	chr8:58095069-58095070	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs185136732	chr8:58095091-58095092	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs562660014	chr8:58095122-58095123	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs531560166	chr8:58095136-58095137	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs548292905	chr8:58095152-58095153	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs55868332	chr8:58095165-58095166	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs189343588	chr8:58095289-58095290	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs547953332	chr8:58095337-58095338	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs570984644	chr8:58095358-58095359	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs540059235	chr8:58095395-58095396	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs114031072	chr8:58095468-58095469	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs575466136	chr8:58101149-58101150	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs570563158	chr8:58101165-58101166	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs541673629	chr8:58101189-58101190	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs181552851	chr8:58101216-58101217	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs186726433	chr8:58101309-58101310	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs540831946	chr8:58101550-58101551	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs182869636	chr8:58101560-58101561	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs532512058	chr8:58101594-58101595	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs111956349	chr8:58103648-58103649	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

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

Chromatin state (count:231 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58105400-58105600	Enhancers	K562	blood
2	chr8:58105600-58106000	Flanking Active TSS	K562	blood
3	chr8:58105800-58106000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:58106000-58106200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:58106000-58107200	Active TSS	K562	blood
6	chr8:58106200-58114800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:58111800-58112200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr8:58114800-58115400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr8:58115400-58118200	Weak transcription	Right Atrium	heart
10	chr8:58116000-58117400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:58116200-58117000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:58116200-58117200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr8:58116400-58117000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr8:58116400-58117000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:58116400-58117000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
16	chr8:58116400-58117200	ZNF genes & repeats	Spleen	Spleen
17	chr8:58116400-58117400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
18	chr8:58116400-58118000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr8:58116600-58116800	ZNF genes & repeats	Brain Hippocampus Middle	brain
20	chr8:58116600-58117000	Enhancers	Gastric	stomach
21	chr8:58116600-58117200	ZNF genes & repeats	Fetal Kidney	kidney
22	chr8:58116600-58117200	ZNF genes & repeats	Pancreas	Pancrea
23	chr8:58116600-58117600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr8:58116600-58118800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr8:58116800-58118200	Weak transcription	Brain Hippocampus Middle	brain
26	chr8:58117000-58118200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr8:58117000-58118200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:58117000-58118200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr8:58117000-58118200	Weak transcription	Gastric	stomach
30	chr8:58117000-58119000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr8:58117200-58118200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr8:58117200-58118200	Weak transcription	Fetal Kidney	kidney
33	chr8:58117400-58118200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr8:58117800-58118800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
35	chr8:58118000-58118800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
36	chr8:58118000-58118800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr8:58118000-58118800	ZNF genes & repeats	Brain Germinal Matrix	brain
38	chr8:58118000-58118800	ZNF genes & repeats	Pancreas	Pancrea
39	chr8:58118200-58118400	Bivalent/Poised TSS	Primary T killer memory cells from peripheral blood	blood
40	chr8:58118200-58118600	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
41	chr8:58118200-58118600	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
42	chr8:58118200-58118600	ZNF genes & repeats	Fetal Intestine Large	intestine
43	chr8:58118200-58118600	ZNF genes & repeats	Fetal Intestine Small	intestine
44	chr8:58118200-58118600	ZNF genes & repeats	Fetal Muscle Trunk	muscle
45	chr8:58118200-58118600	ZNF genes & repeats	Placenta	Placenta
46	chr8:58118200-58118600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
47	chr8:58118200-58118600	ZNF genes & repeats	NHEK	skin
48	chr8:58118200-58118800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
49	chr8:58118200-58118800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr8:58118200-58118800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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