Variant report

Variant	nsv971718
Chromosome Location	chr8:58121099-58130658
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:427)
CpG islands
(count:735)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	BRCA1	chr8:58122208-58123016	GM12878	blood:	n/a	n/a
7	BRCA1	chr8:58122170-58122971	HepG2	liver:	n/a	n/a
8	BRCA1	chr8:58127438-58127751	HepG2	liver:	n/a	n/a
9	BRCA1	chr8:58127563-58127875	GM12878	blood:	n/a	n/a
10	CEBPB	chr8:58122125-58123045	K562	blood:	n/a	n/a
11	CHD1	chr8:58122169-58123189	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr8:58122268-58123011	HepG2	liver:	n/a	n/a
13	CHD2	chr8:58122153-58122987	K562	blood:	n/a	n/a
14	CHD2	chr8:58127562-58127861	HepG2	liver:	n/a	n/a
15	CHD2	chr8:58122614-58122989	GM12878	blood:	n/a	n/a
16	CTCF	chr8:58122760-58122910	WERI-Rb-1	eye:	n/a	n/a
17	CTCF	chr8:58122122-58122463	T-47D	breast:	n/a	n/a
18	CTCF	chr8:58122600-58122750	GM12869	blood:	n/a	n/a
19	CTCF	chr8:58122170-58122320	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr8:58122120-58122270	NHDF-neo	bronchial:	n/a	n/a
21	CTCF	chr8:58122200-58122350	HCM	heart:	n/a	n/a
22	CTCF	chr8:58124140-58124290	GM12866	blood:	n/a	n/a
23	CTCF	chr8:58122200-58122350	HMEC	breast:	n/a	n/a
24	CTCF	chr8:58125600-58125750	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr8:58126396-58126724	K562	blood:	n/a	n/a
26	CTCF	chr8:58121947-58122573	K562	blood:	n/a	n/a
27	CTCF	chr8:58122500-58122650	GM12875	blood:	n/a	n/a
28	CTCF	chr8:58122142-58122337	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr8:58122220-58122370	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr8:58122640-58122790	GM12866	blood:	n/a	n/a
31	CTCF	chr8:58122800-58122950	GM12878	blood:	n/a	n/a
32	CTCF	chr8:58122660-58122810	HEK293	kidney:	n/a	n/a
33	CTCF	chr8:58122099-58122369	LNCaP	prostate:	n/a	n/a
34	CTCF	chr8:58122480-58122630	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr8:58122740-58122890	HL-60	blood:	n/a	n/a
36	CTCF	chr8:58122160-58122310	GM12874	blood:	n/a	n/a
37	CTCF	chr8:58122660-58122810	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr8:58122190-58122304	GM12878	blood:	n/a	n/a
39	CTCF	chr8:58122680-58122830	HPF	lung:	n/a	n/a
40	CTCF	chr8:58122122-58122368	K562	blood:	n/a	n/a
41	CTCF	chr8:58122200-58122350	A549	lung:	n/a	n/a
42	CTCF	chr8:58122840-58122990	WI-38	lung:	n/a	n/a
43	CTCF	chr8:58124180-58124330	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr8:58122200-58122350	HPF	lung:	n/a	n/a
45	CTCF	chr8:58122180-58122330	Caco-2	colon:	n/a	n/a
46	CTCF	chr8:58122129-58122348	LNCaP	prostate:	n/a	n/a
47	CTCF	chr8:58122180-58122330	BE2_C	brain:	n/a	n/a
48	CTCF	chr8:58122860-58123010	GM12865	blood:	n/a	n/a
49	CTCF	chr8:58122640-58122790	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr8:58122520-58122670	GM12868	blood:	n/a	n/a

(count:735 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:58130323-58130373	NHBE	bronchial:	n/a
2	chr8:58123513-58123563	CMK	blood:	n/a
3	chr8:58124249-58124299	AG09319	gingival:	n/a
4	chr8:58130323-58130373	NHBE	bronchial:	n/a
5	chr8:58123513-58123563	CMK	blood:	n/a
6	chr8:58124249-58124299	AG09319	gingival:	n/a
7	chr8:58126962-58127012	AG04449	skin:	fetal
8	chr8:58122850-58122900	PFSK-1	brain:	n/a
9	chr8:58128724-58128774	AG04450	lung:	fetal
10	chr8:58123513-58123563	HUVEC	blood vessel:	n/a
11	chr8:58128466-58128516	GM12892	blood:	n/a
12	chr8:58126962-58127012	HepG2	liver:	n/a
13	chr8:58130467-58130517	HepG2	liver:	n/a
14	chr8:58122850-58122900	NB4	blood:	n/a
15	chr8:58130041-58130091	T-47D	breast:	n/a
16	chr8:58130467-58130517	NH-A	brain:	n/a
17	chr8:58122215-58122265	SK-N-SH_RA	brain:	n/a
18	chr8:58122215-58122265	MCF-7	breast:	n/a
19	chr8:58130041-58130091	GM06990	blood:	n/a
20	chr8:58128466-58128516	GM12891	blood:	n/a
21	chr8:58126962-58127012	Hela-S3	cervix:	n/a
22	chr8:58130323-58130373	NH-A	brain:	n/a
23	chr8:58128466-58128516	ECC-1	luminal epithelium:	n/a
24	chr8:58130041-58130091	MCF-7	breast:	n/a
25	chr8:58128466-58128516	GM19239	blood:	n/a
26	chr8:58123513-58123563	H1-hESC	embryonic stem cell:	embryo
27	chr8:58129604-58129654	PANC-1	pancreas:	n/a
28	chr8:58124249-58124299	NHDF-neo	bronchial:	n/a
29	chr8:58123513-58123563	AG09319	gingival:	n/a
30	chr8:58126962-58127012	GM12878	blood:	n/a
31	chr8:58122215-58122265	AG09309	skin:	n/a
32	chr8:58122215-58122265	AG10803	skin:	n/a
33	chr8:58121215-58121265	SK-N-MC	brain:	n/a
34	chr8:58130323-58130373	HIPEpiC	eye:	n/a
35	chr8:58121215-58121265	H1-hESC	embryonic stem cell:	embryo
36	chr8:58122215-58122265	SAEC	small airway:	n/a
37	chr8:58130467-58130517	A549	lung:	n/a
38	chr8:58121215-58121265	A549	lung:	n/a
39	chr8:58130467-58130517	NHBE	bronchial:	n/a
40	chr8:58121215-58121265	HIPEpiC	eye:	n/a
41	chr8:58122215-58122265	NB4	blood:	n/a
42	chr8:58128466-58128516	NHBE	bronchial:	n/a
43	chr8:58126962-58127012	Jurkat	blood:	n/a
44	chr8:58130323-58130373	HRPEpiC	eye:	n/a
45	chr8:58130323-58130373	Hela-S3	cervix:	n/a
46	chr8:58128724-58128774	H1-hESC	embryonic stem cell:	embryo
47	chr8:58130041-58130091	NH-A	brain:	n/a
48	chr8:58126962-58127012	NT2-D1	testis:	n/a
49	chr8:58123513-58123563	AG04450	lung:	fetal
50	chr8:58128466-58128516	K562	blood:	n/a

(count:7 , 50 per page) page: 1

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

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

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

No data

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

Extended variants
information (count: 679 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:679 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2005307	chr8:58121221-58121222	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs201666422	chr8:58121252-58121253	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs137886159	chr8:58121321-58121322	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs535655135	chr8:58121333-58121334	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs370358877	chr8:58121349-58121350	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs2002255	chr8:58121368-58121369	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs150593055	chr8:58121501-58121502	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs549130140	chr8:58121513-58121514	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs2019510	chr8:58121577-58121578	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs149727196	chr8:58121578-58121579	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs370611325	chr8:58121607-58121608	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs374319411	chr8:58121608-58121609	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs2019511	chr8:58121609-58121610	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs140861252	chr8:58121617-58121618	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs565952826	chr8:58121622-58121623	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs1805305	chr8:58121653-58121654	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs147863655	chr8:58121737-58121738	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs147010349	chr8:58121766-58121767	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs147650441	chr8:58121767-58121768	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs141551667	chr8:58121787-58121788	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs142955646	chr8:58121799-58121800	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs142252824	chr8:58121810-58121811	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs28425196	chr8:58121831-58121832	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs145395805	chr8:58121842-58121843	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs28638327	chr8:58121853-58121854	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs4079364	chr8:58121925-58121926	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs60281970	chr8:58121954-58121955	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs557473948	chr8:58121973-58121974	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs577566191	chr8:58121991-58121992	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs150253849	chr8:58122029-58122030	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs3884441	chr8:58122048-58122049	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs61676223	chr8:58122085-58122086	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs60928677	chr8:58122087-58122088	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs4077859	chr8:58122137-58122138	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs10094883	chr8:58122192-58122193	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs78914538	chr8:58122210-58122211	ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs3884439	chr8:58122215-58122216	ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs3884353	chr8:58122221-58122222	ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs140263692	chr8:58122222-58122223	ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs145189441	chr8:58122230-58122231	ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs3884354	chr8:58122235-58122236	ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs537080370	chr8:58122242-58122243	ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs2005486	chr8:58122243-58122244	ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs2318082	chr8:58122246-58122247	ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs78459311	chr8:58122250-58122251	ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs2318084	chr8:58122257-58122258	ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs74213435	chr8:58122273-58122274	ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs4060565	chr8:58122274-58122275	ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs4060566	chr8:58122280-58122281	ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs386725775	chr8:58122310-58122311	ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	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:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58118800-58121400	Weak transcription	Pancreas	Pancrea
2	chr8:58118800-58122000	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr8:58118800-58122200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr8:58118800-58122200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr8:58118800-58122200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr8:58118800-58122200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr8:58118800-58122200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr8:58118800-58122200	Weak transcription	Brain Angular Gyrus	brain
9	chr8:58118800-58122200	Weak transcription	Brain Anterior Caudate	brain
10	chr8:58118800-58122200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr8:58118800-58122200	Weak transcription	Brain Substantia Nigra	brain
12	chr8:58118800-58122200	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr8:58118800-58122200	Weak transcription	Fetal Brain Male	brain
14	chr8:58118800-58122200	Weak transcription	Fetal Heart	heart
15	chr8:58118800-58122200	Weak transcription	Gastric	stomach
16	chr8:58118800-58122200	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr8:58118800-58122200	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr8:58118800-58122200	Weak transcription	Rectal Smooth Muscle	rectum
19	chr8:58118800-58122200	Weak transcription	Right Atrium	heart
20	chr8:58118800-58122200	Weak transcription	Right Ventricle	heart
21	chr8:58118800-58122200	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr8:58118800-58122200	Weak transcription	Stomach Mucosa	stomach
23	chr8:58119000-58122200	Weak transcription	Duodenum Mucosa	Duodenum
24	chr8:58119000-58122200	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr8:58119000-58122200	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr8:58119000-58122200	Weak transcription	NHDF-Ad	bronchial
27	chr8:58120200-58123400	ZNF genes & repeats	Brain Germinal Matrix	brain
28	chr8:58121000-58121400	Weak transcription	Spleen	Spleen
29	chr8:58121000-58122200	Weak transcription	Fetal Kidney	kidney
30	chr8:58122000-58123200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr8:58122000-58123200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
32	chr8:58122000-58123200	ZNF genes & repeats	Fetal Brain Female	brain
33	chr8:58122000-58123200	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
34	chr8:58122000-58123400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr8:58122000-58123400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr8:58122000-58123400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
37	chr8:58122000-58123400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr8:58122000-58123400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr8:58122200-58122400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
40	chr8:58122200-58122600	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
41	chr8:58122200-58122800	ZNF genes & repeats	Brain Angular Gyrus	brain
42	chr8:58122200-58122800	ZNF genes & repeats	Fetal Heart	heart
43	chr8:58122200-58123000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
44	chr8:58122200-58123000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr8:58122200-58123000	ZNF genes & repeats	Adipose Nuclei	Adipose
46	chr8:58122200-58123000	ZNF genes & repeats	Aorta	Aorta
47	chr8:58122200-58123000	ZNF genes & repeats	Brain Anterior Caudate	brain
48	chr8:58122200-58123000	ZNF genes & repeats	Brain Hippocampus Middle	brain
49	chr8:58122200-58123000	ZNF genes & repeats	Brain Substantia Nigra	brain
50	chr8:58122200-58123000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum

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