Variant report

Variant	nsv539590
Chromosome Location	chr8:47459550-47698142
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:909)
CpG islands
(count:305)
Chromatin interactive
region (count:26)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:909 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:47529231-47529761	K562	blood:	n/a	n/a
2	ATF1	chr8:47551373-47551428	K562	blood:	n/a	n/a
3	ATF1	chr8:47548283-47548344	K562	blood:	n/a	n/a
4	ATF3	chr8:47529101-47529363	K562	blood:	n/a	n/a
5	BACH1	chr8:47536608-47536724	K562	blood:	n/a	n/a
6	BHLHE40	chr8:47570504-47570636	K562	blood:	n/a	n/a
7	BHLHE40	chr8:47484595-47485045	K562	blood:	n/a	n/a
8	BHLHE40	chr8:47528443-47529576	K562	blood:	n/a	chr8:47528874-47528890 chr8:47529336-47529352
9	CBX3	chr8:47529072-47529420	K562	blood:	n/a	n/a
10	CCNT2	chr8:47528797-47529481	K562	blood:	n/a	n/a
11	CEBPB	chr8:47691009-47691710	A549	lung:	n/a	n/a
12	CEBPB	chr8:47610006-47610207	IMR90	lung:	n/a	chr8:47610104-47610115
13	CEBPB	chr8:47506841-47507041	K562	blood:	n/a	chr8:47506900-47506917
14	CEBPB	chr8:47546529-47547110	HepG2	liver:	n/a	chr8:47546682-47546693
15	CEBPB	chr8:47530129-47530132	K562	blood:	n/a	n/a
16	CEBPB	chr8:47546537-47546824	A549	lung:	n/a	chr8:47546682-47546693
17	CEBPB	chr8:47646735-47647020	MCF-7	breast:	n/a	chr8:47646871-47646882
18	CEBPB	chr8:47610035-47610215	HepG2	liver:	n/a	chr8:47610104-47610115
19	CEBPB	chr8:47662835-47663134	MCF-7	breast:	n/a	chr8:47662934-47662945
20	CEBPB	chr8:47529068-47529484	K562	blood:	n/a	n/a
21	CEBPB	chr8:47548607-47548874	A549	lung:	n/a	chr8:47548763-47548774
22	CEBPB	chr8:47587299-47587532	A549	lung:	n/a	n/a
23	CEBPB	chr8:47689369-47689570	HepG2	liver:	n/a	n/a
24	CEBPB	chr8:47529073-47529534	MCF-7	breast:	n/a	n/a
25	CEBPB	chr8:47562910-47563178	MCF-7	breast:	n/a	n/a
26	CEBPB	chr8:47491088-47491218	IMR90	lung:	n/a	chr8:47491158-47491169
27	CEBPB	chr8:47480858-47480864	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:47491067-47491227	A549	lung:	n/a	chr8:47491158-47491169
29	CEBPB	chr8:47597167-47597429	A549	lung:	n/a	chr8:47597321-47597332 chr8:47597291-47597302
30	CEBPB	chr8:47534171-47534437	A549	lung:	n/a	n/a
31	CEBPB	chr8:47662869-47663115	HepG2	liver:	n/a	chr8:47662934-47662945
32	CEBPB	chr8:47557998-47558160	K562	blood:	n/a	chr8:47558092-47558103
33	CEBPB	chr8:47491043-47491262	K562	blood:	n/a	chr8:47491158-47491169
34	CEBPB	chr8:47678009-47678239	A549	lung:	n/a	chr8:47678131-47678142
35	CEBPB	chr8:47540841-47541021	HepG2	liver:	n/a	chr8:47540937-47540948
36	CEBPB	chr8:47678002-47678303	IMR90	lung:	n/a	chr8:47678131-47678142
37	CEBPB	chr8:47557938-47558285	IMR90	lung:	n/a	chr8:47558092-47558103
38	CEBPB	chr8:47548637-47548787	HepG2	liver:	n/a	chr8:47548763-47548774
39	CEBPB	chr8:47554606-47555182	A549	lung:	n/a	n/a
40	CEBPB	chr8:47587262-47587581	IMR90	lung:	n/a	n/a
41	CEBPB	chr8:47547945-47548304	A549	lung:	n/a	n/a
42	CEBPB	chr8:47560585-47560829	HepG2	liver:	n/a	n/a
43	CEBPB	chr8:47579903-47580243	HepG2	liver:	n/a	n/a
44	CEBPB	chr8:47493915-47494006	K562	blood:	n/a	n/a
45	CEBPB	chr8:47565561-47565644	A549	lung:	n/a	chr8:47565589-47565600
46	CEBPB	chr8:47550037-47550193	K562	blood:	n/a	n/a
47	CEBPB	chr8:47587362-47587504	K562	blood:	n/a	n/a
48	CEBPB	chr8:47579829-47580162	K562	blood:	n/a	n/a
49	CEBPB	chr8:47554891-47555151	K562	blood:	n/a	n/a
50	CEBPB	chr8:47562301-47562634	A549	lung:	n/a	chr8:47562536-47562547

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:47529280-47529330	AoSMC	blood vessel:	n/a
2	chr8:47529545-47529595	SAEC	small airway:	n/a
3	chr8:47527657-47527707	BE2_C	brain:	n/a
4	chr8:47526309-47526359	H1-hESC	embryonic stem cell:	embryo
5	chr8:47529280-47529330	Caco-2	colon:	n/a
6	chr8:47529015-47529065	NB4	blood:	n/a
7	chr8:47527657-47527707	PFSK-1	brain:	n/a
8	chr8:47529545-47529595	IMR90	lung:	fetal
9	chr8:47526309-47526359	Caco-2	colon:	n/a
10	chr8:47529015-47529065	AG04450	lung:	fetal
11	chr8:47527657-47527707	H1-hESC	embryonic stem cell:	embryo
12	chr8:47526309-47526359	NHBE	bronchial:	n/a
13	chr8:47529015-47529065	Hela-S3	cervix:	n/a
14	chr8:47529280-47529330	NHBE	bronchial:	n/a
15	chr8:47527657-47527707	K562	blood:	n/a
16	chr8:47529015-47529065	AoSMC	blood vessel:	n/a
17	chr8:47529280-47529330	SK-N-MC	brain:	n/a
18	chr8:47529545-47529595	HAEpiC	amniotic membrane:	n/a
19	chr8:47527657-47527707	HAEpiC	amniotic membrane:	n/a
20	chr8:47529545-47529595	NHBE	bronchial:	n/a
21	chr8:47529280-47529330	IMR90	lung:	fetal
22	chr8:47527657-47527707	IMR90	lung:	fetal
23	chr8:47529015-47529065	SAEC	small airway:	n/a
24	chr8:47526309-47526359	ProgFib	skin:	n/a
25	chr8:47529015-47529065	GM12878	blood:	n/a
26	chr8:47529280-47529330	AG09319	gingival:	n/a
27	chr8:47527657-47527707	HCF	heart:	n/a
28	chr8:47529015-47529065	HPAEpiC	pulmonary alveolar:	n/a
29	chr8:47529280-47529330	HUVEC	blood vessel:	n/a
30	chr8:47527657-47527707	HNPCEpiC	eye:	n/a
31	chr8:47529545-47529595	HCF	heart:	n/a
32	chr8:47529015-47529065	NT2-D1	testis:	n/a
33	chr8:47529280-47529330	NB4	blood:	n/a
34	chr8:47527657-47527707	HCT-116	colon:	n/a
35	chr8:47529015-47529065	NHDF-neo	bronchial:	n/a
36	chr8:47526309-47526359	HEEpiC	esophagus:	n/a
37	chr8:47529545-47529595	HMEC	breast:	n/a
38	chr8:47529545-47529595	HIPEpiC	eye:	n/a
39	chr8:47527657-47527707	HEK293	kidney:	embryo
40	chr8:47529280-47529330	PFSK-1	brain:	n/a
41	chr8:47526309-47526359	HIPEpiC	eye:	n/a
42	chr8:47529545-47529595	CMK	blood:	n/a
43	chr8:47529280-47529330	PANC-1	pancreas:	n/a
44	chr8:47529280-47529330	HL-60	blood:	n/a
45	chr8:47527657-47527707	PrEC	prostate:	n/a
46	chr8:47529015-47529065	HUVEC	blood vessel:	n/a
47	chr8:47529280-47529330	HEEpiC	esophagus:	n/a
48	chr8:47526309-47526359	AG04450	lung:	fetal
49	chr8:47529015-47529065	Caco-2	colon:	n/a
50	chr8:47529280-47529330	HRE	kidney:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:97501587..97502366-chr8:47529051..47529557,3	HCT-116	colon:
2	chr8:47512649..47514644-chr8:47529072..47530746,2	K562	blood:
3	chr8:47491632..47493538-chr8:47505350..47507971,2	K562	blood:
4	chr8:47619331..47620431-chr8:47868217..47869326,4	MCF-7	breast:
5	chr8:47524927..47529861-chr8:47530508..47536088,6	K562	blood:
6	chr8:47517410..47521817-chr8:47524226..47528650,6	K562	blood:
7	chr8:47618307..47619237-chr8:47916938..47917469,2	MCF-7	breast:
8	chr8:47619541..47620262-chr8:47868295..47869178,3	MCF-7	breast:
9	chr8:47619682..47620259-chr8:47831736..47832439,2	MCF-7	breast:
10	chr8:47519082..47521588-chr8:47524616..47530066,4	K562	blood:
11	chr8:47487702..47490248-chr8:47515594..47517867,2	K562	blood:
12	chr8:47506585..47508657-chr8:47510206..47513067,2	K562	blood:
13	chr7:97495363..97496869-chr8:47517938..47519464,2	K562	blood:
14	chr8:47144016..47144925-chr8:47484500..47485152,3	MCF-7	breast:
15	chr8:47528106..47530039-chr8:47536064..47537656,2	MCF-7	breast:
16	chr8:47512649..47514644-chr8:47529072..47530746,2	K562	blood:
17	chr8:47484279..47485112-chr8:47579488..47580411,3	MCF-7	breast:
18	chr8:47528106..47530039-chr8:47536064..47537656,2	MCF-7	breast:
19	chr8:47515437..47518605-chr8:47528973..47530959,3	K562	blood:
20	chr8:47487702..47490248-chr8:47515594..47517867,2	K562	blood:
21	chr8:47484279..47485112-chr8:47579488..47580411,3	MCF-7	breast:
22	chr8:47506585..47508657-chr8:47510206..47513067,2	K562	blood:
23	chr8:47618289..47619061-chr8:47868266..47869014,2	MCF-7	breast:
24	chr8:47168205..47168775-chr8:47479656..47480472,2	MCF-7	breast:
25	chr8:47491632..47493538-chr8:47505350..47507971,2	K562	blood:
26	chr8:47515437..47518605-chr8:47528973..47530959,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LINC00293-4	chr8:47460711-47460990	NONHSAT126406
2	lnc-LINC00293-4	chr8:47462233-47462424	NONHSAT126406

No data

Variant related genes	Relation type
HSPA8P13	TF binding region
ENSG00000254070	TF binding region
ASNSP1	TF binding region
ENSG00000228984	TF binding region
ASNSP4	TF binding region
HSPA8P13	CpG island
ENSG00000254070	CpG island
ASNSP1	CpG island
ENSG00000228984	CpG island
ASNSP4	CpG island
ENSG00000070669	chromatin interactions
ENSG00000248498	chromatin interactions

Extended variants
information (count: 2784 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2784 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114107293	chr8:47460722-47460723	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs138725639	chr8:47460753-47460754	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs546128317	chr8:47460810-47460811	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs559879839	chr8:47460813-47460814	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs543207825	chr8:47460818-47460819	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs528643016	chr8:47460833-47460834	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs548684169	chr8:47460834-47460835	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs568519674	chr8:47460849-47460850	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs182290728	chr8:47460934-47460935	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs530934171	chr8:47460965-47460966	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs189849632	chr8:47462251-47462252	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs200702677	chr8:47462252-47462253	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs529172553	chr8:47462265-47462266	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs548794619	chr8:47462269-47462270	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs181646606	chr8:47462270-47462271	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs531373525	chr8:47462285-47462286	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs73571015	chr8:47462286-47462287	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs571213369	chr8:47462331-47462332	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs533821800	chr8:47462341-47462342	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs553482189	chr8:47462371-47462372	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs567180150	chr8:47462397-47462398	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs554209197	chr8:47463031-47463032	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs573700621	chr8:47463055-47463056	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs570871881	chr8:47463093-47463094	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs542571675	chr8:47463096-47463097	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs180799994	chr8:47463100-47463101	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs207469109	chr8:47463116-47463117	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs185779426	chr8:47463120-47463121	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs536666863	chr8:47463135-47463136	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs556811094	chr8:47463137-47463138	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs375773673	chr8:47463152-47463153	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs564914696	chr8:47463164-47463165	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs149677293	chr8:47463176-47463177	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs4535748	chr8:47463201-47463202	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs547198628	chr8:47463205-47463206	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs373179075	chr8:47463211-47463212	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs560919900	chr8:47463300-47463301	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs529724065	chr8:47463325-47463326	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs549793955	chr8:47463341-47463342	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs536047544	chr8:47463348-47463349	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs34914939	chr8:47463395-47463396	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs569620373	chr8:47463397-47463398	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs553177849	chr8:47463410-47463411	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs572952642	chr8:47463435-47463436	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs538519522	chr8:47463436-47463437	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs551987647	chr8:47463438-47463439	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs571765070	chr8:47463446-47463447	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs376915009	chr8:47463452-47463453	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs545440913	chr8:47463459-47463460	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs115926898	chr8:47463482-47463483	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Oral cancer	21386901	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
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	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
Acute myeloid leukemia	21251322	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
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	20607354	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
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	20409316	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
Tetralogy of Fallot	22912587	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:47463000-47463600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:47477600-47477800	Active TSS	Monocytes-CD14+_RO01746	blood
3	chr8:47477800-47478000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr8:47484400-47484600	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr8:47486400-47486800	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr8:47486400-47488800	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr8:47486800-47487800	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr8:47487800-47488600	Enhancers	Skeletal Muscle Female	skeletal muscle
9	chr8:47488000-47488800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
10	chr8:47488600-47490200	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr8:47488800-47489800	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr8:47489800-47491200	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr8:47490200-47490800	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr8:47498200-47498600	Enhancers	Placenta	Placenta
15	chr8:47514200-47518600	Weak transcription	K562	blood
16	chr8:47518600-47520200	Strong transcription	K562	blood
17	chr8:47520200-47525800	Weak transcription	K562	blood
18	chr8:47525800-47526000	Genic enhancers	K562	blood
19	chr8:47526000-47526200	Enhancers	K562	blood
20	chr8:47526200-47527000	Weak transcription	K562	blood
21	chr8:47527000-47529400	Active TSS	K562	blood
22	chr8:47528200-47529200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr8:47528200-47529200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr8:47528600-47528800	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
25	chr8:47528600-47529400	Active TSS	Pancreas	Pancrea
26	chr8:47528800-47529200	ZNF genes & repeats	Placenta	Placenta
27	chr8:47529000-47529200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
28	chr8:47529200-47529600	Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr8:47529400-47529800	Flanking Active TSS	K562	blood
30	chr8:47529400-47531400	Weak transcription	Pancreas	Pancrea
31	chr8:47529800-47531000	Enhancers	K562	blood
32	chr8:47531600-47535200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr8:47531800-47532200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr8:47534800-47535200	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr8:47539400-47539800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr8:47547400-47549400	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr8:47547400-47549600	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr8:47548000-47549200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
39	chr8:47549400-47554800	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr8:47549600-47555000	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr8:47554800-47555600	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr8:47555000-47556600	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr8:47555600-47560600	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr8:47556600-47560600	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr8:47560600-47564400	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr8:47560600-47564400	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr8:47567200-47567600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
48	chr8:47578800-47579200	Active TSS	Fetal Heart	heart
49	chr8:47596600-47596800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr8:47596800-47597800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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