Variant report

Variant	nsv892690
Chromosome Location	chr9:18485434-18592374
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:508)
CpG islands
(count:123)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:508 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr9:18574188-18574199	GM12878	blood:	n/a	n/a
2	CEBPB	chr9:18578396-18578419	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr9:18544465-18544730	Hela-S3	cervix:	n/a	chr9:18544557-18544570
4	CEBPB	chr9:18490482-18491371	IMR90	lung:	n/a	n/a
5	CEBPB	chr9:18526754-18527079	IMR90	lung:	n/a	n/a
6	CEBPB	chr9:18532530-18532635	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr9:18544401-18544745	IMR90	lung:	n/a	chr9:18544557-18544570
8	CEBPB	chr9:18526744-18527111	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr9:18591830-18592160	HepG2	liver:	n/a	chr9:18591978-18591989
10	CEBPB	chr9:18526773-18527003	A549	lung:	n/a	n/a
11	CEBPB	chr9:18526762-18527049	HepG2	liver:	n/a	n/a
12	CEBPB	chr9:18591917-18592017	Hela-S3	cervix:	n/a	chr9:18591978-18591989
13	CEBPB	chr9:18585070-18585095	A549	lung:	n/a	n/a
14	CEBPB	chr9:18591842-18592151	A549	lung:	n/a	chr9:18591978-18591989
15	CEBPB	chr9:18591831-18592127	IMR90	lung:	n/a	chr9:18591978-18591989
16	CEBPB	chr9:18580228-18580540	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr9:18502612-18502871	IMR90	lung:	n/a	chr9:18502687-18502698
18	CEBPB	chr9:18531238-18531526	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr9:18578617-18578692	HepG2	liver:	n/a	n/a
20	CEBPB	chr9:18526755-18527079	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr9:18504800-18505016	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr9:18500454-18500578	GM12878	blood:	n/a	n/a
23	CTCF	chr9:18566277-18566314	Pancreas_OC	pancreas:	n/a	n/a
24	CTCF	chr9:18490620-18490770	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr9:18485600-18485750	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr9:18569940-18570090	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr9:18558416-18558461	LNCaP	prostate:	n/a	n/a
28	CTCF	chr9:18522681-18522736	GM13976	blood:	n/a	n/a
29	CTCF	chr9:18520100-18520250	NB4	blood:	n/a	n/a
30	CTCF	chr9:18539100-18539250	Caco-2	colon:	n/a	n/a
31	CTCF	chr9:18588040-18588190	AG10803	skin:	n/a	n/a
32	CTCF	chr9:18485560-18485710	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr9:18505460-18505610	AG10803	skin:	n/a	n/a
34	CTCF	chr9:18485580-18485730	HPF	lung:	n/a	n/a
35	CTCF	chr9:18485640-18485790	HA-sp	spinal cord:	n/a	n/a
36	CTCF	chr9:18485540-18485690	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr9:18588060-18588210	AG10803	skin:	n/a	n/a
38	CTCF	chr9:18536400-18536550	NB4	blood:	n/a	n/a
39	CTCF	chr9:18485860-18486010	HCPEpiC	choroid plexus:	n/a	n/a
40	E2F4	chr9:18495412-18495414	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr9:18566069-18566388	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr9:18531322-18531674	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr9:18490556-18490933	MCF10A-Er-Src	breast:	n/a	n/a
44	EP300	chr9:18588040-18588506	SK-N-SH	brain:	n/a	n/a
45	EP300	chr9:18544118-18544387	SK-N-SH_RA	brain:	n/a	chr9:18544377-18544385 chr9:18544203-18544217
46	EP300	chr9:18504712-18505061	H1-hESC	embryonic stem cell:	n/a	n/a
47	EP300	chr9:18568965-18569714	SK-N-SH_RA	brain:	n/a	chr9:18569464-18569471
48	EP300	chr9:18580008-18580719	SK-N-SH	brain:	n/a	n/a
49	EP300	chr9:18520109-18521277	SK-N-SH	brain:	n/a	chr9:18520738-18520746
50	EP300	chr9:18580185-18580513	SK-N-SH_RA	brain:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:18490009-18490059	Hepatocyte	liver:	n/a
2	chr9:18490009-18490059	Hepatocyte	liver:	n/a
3	chr9:18490009-18490059	T-47D	breast:	n/a
4	chr9:18514052-18514102	GM06990	blood:	n/a
5	chr9:18490009-18490059	LNCaP	prostate:	n/a
6	chr9:18514052-18514102	SKMC	muscle:	n/a
7	chr9:18514052-18514102	IMR90	lung:	fetal
8	chr9:18514052-18514102	NT2-D1	testis:	n/a
9	chr9:18490009-18490059	SKMC	muscle:	n/a
10	chr9:18514052-18514102	AoSMC	blood vessel:	n/a
11	chr9:18490009-18490059	SK-N-SH	brain:	n/a
12	chr9:18490009-18490059	Caco-2	colon:	n/a
13	chr9:18514052-18514102	PANC-1	pancreas:	n/a
14	chr9:18514052-18514102	AG09319	gingival:	n/a
15	chr9:18490009-18490059	NHDF-neo	bronchial:	n/a
16	chr9:18490009-18490059	HPAEpiC	pulmonary alveolar:	n/a
17	chr9:18514052-18514102	PrEC	prostate:	n/a
18	chr9:18490009-18490059	HNPCEpiC	eye:	n/a
19	chr9:18514052-18514102	HAEpiC	amniotic membrane:	n/a
20	chr9:18514052-18514102	HepG2	liver:	n/a
21	chr9:18514052-18514102	HEEpiC	esophagus:	n/a
22	chr9:18490009-18490059	Jurkat	blood:	n/a
23	chr9:18514052-18514102	SK-N-SH_RA	brain:	n/a
24	chr9:18490009-18490059	GM12878	blood:	n/a
25	chr9:18490009-18490059	K562	blood:	n/a
26	chr9:18490009-18490059	SAEC	small airway:	n/a
27	chr9:18490009-18490059	U87	brain:	n/a
28	chr9:18490009-18490059	IMR90	lung:	fetal
29	chr9:18514052-18514102	U87	brain:	n/a
30	chr9:18490009-18490059	BJ	skin:	n/a
31	chr9:18490009-18490059	SK-N-MC	brain:	n/a
32	chr9:18490009-18490059	ProgFib	skin:	n/a
33	chr9:18514052-18514102	HRCEpiC	kidney:	n/a
34	chr9:18514052-18514102	AG10803	skin:	n/a
35	chr9:18514052-18514102	HNPCEpiC	eye:	n/a
36	chr9:18490009-18490059	HL-60	blood:	n/a
37	chr9:18514052-18514102	Hepatocyte	liver:	n/a
38	chr9:18514052-18514102	HCF	heart:	n/a
39	chr9:18490009-18490059	NB4	blood:	n/a
40	chr9:18514052-18514102	AG09309	skin:	n/a
41	chr9:18514052-18514102	Caco-2	colon:	n/a
42	chr9:18514052-18514102	GM12878	blood:	n/a
43	chr9:18514052-18514102	HCPEpiC	choroid plexus:	n/a
44	chr9:18490009-18490059	RPTEC	kidney:	n/a
45	chr9:18490009-18490059	AG04449	skin:	fetal
46	chr9:18490009-18490059	PFSK-1	brain:	n/a
47	chr9:18490009-18490059	HMEC	breast:	n/a
48	chr9:18490009-18490059	PrEC	prostate:	n/a
49	chr9:18514052-18514102	K562	blood:	n/a
50	chr9:18514052-18514102	ECC-1	luminal epithelium:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:18377972..18379506-chr9:18518837..18521140,2	K562	blood:
2	chr1:149222514..149224923-chr9:18513487..18514987,2	K562	blood:
3	chr1:149223814..149224438-chr9:18512987..18513487,3	MCF-7	breast:
4	chr1:149223496..149224418-chr9:18512967..18513967,3	MCF-7	breast:
5	chr9:18552353..18554750-chr9:18819699..18822182,2	MCF-7	breast:
6	chr1:149223595..149224343-chr9:18512967..18513487,3	Hela-S3	cervix:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3152-5p	chr9:18573314-18573335	MIMAT0019207
hsa-miR-3152-3p	chr9:18573348-18573369	MIMAT0015025

No data

Variant related genes	Relation type
MIR3152	TF binding region
MIR3152	CpG island
ENSG00000206737	chromatin interactions

Extended variants
information (count: 5103 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:5103 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4961652	chr9:18485434-18485435	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553427396	chr9:18485439-18485440	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574742813	chr9:18485442-18485443	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535416788	chr9:18485454-18485455	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs76639717	chr9:18485513-18485514	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373606705	chr9:18485552-18485553	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189689921	chr9:18485560-18485561	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539184214	chr9:18485563-18485564	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142653918	chr9:18485591-18485592	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs564556855	chr9:18485638-18485639	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs180721794	chr9:18485651-18485652	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540002271	chr9:18485658-18485659	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs79977103	chr9:18485666-18485667	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528892834	chr9:18485670-18485671	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs114768954	chr9:18485681-18485682	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs113206637	chr9:18485682-18485683	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142437238	chr9:18485683-18485684	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540193543	chr9:18485686-18485687	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185976582	chr9:18485779-18485780	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs551687205	chr9:18485786-18485787	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs112018392	chr9:18485810-18485811	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540246157	chr9:18485824-18485825	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191319853	chr9:18485828-18485829	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546787688	chr9:18485868-18485869	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140576774	chr9:18485873-18485874	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs7019399	chr9:18485876-18485877	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs150454140	chr9:18485918-18485919	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138237861	chr9:18485960-18485961	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539782825	chr9:18485970-18485971	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558423627	chr9:18485990-18485991	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573656107	chr9:18486016-18486017	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534214664	chr9:18486037-18486038	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs75387763	chr9:18486038-18486039	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369035907	chr9:18486126-18486127	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183070989	chr9:18486159-18486160	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs373878488	chr9:18486167-18486168	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187470249	chr9:18486172-18486173	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7864622	chr9:18486176-18486177	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs544304990	chr9:18486185-18486186	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562504252	chr9:18486201-18486202	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532949993	chr9:18486206-18486207	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190748252	chr9:18486213-18486214	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs72688613	chr9:18486241-18486242	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs372679347	chr9:18486244-18486245	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs17207294	chr9:18486250-18486251	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs141286944	chr9:18486253-18486254	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs7864727	chr9:18486269-18486270	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs183359323	chr9:18486276-18486277	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145011669	chr9:18486292-18486293	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs539403705	chr9:18486300-18486301	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Ovarian cancer	19835627	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:945 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18476000-18485600	Weak transcription	Fetal Stomach	stomach
2	chr9:18477400-18489200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr9:18479200-18490000	Weak transcription	Aorta	Aorta
4	chr9:18480600-18485600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr9:18480800-18485600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr9:18482600-18492200	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr9:18482800-18485600	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr9:18484000-18486000	Genic enhancers	NHDF-Ad	bronchial
9	chr9:18484000-18486800	Genic enhancers	HSMM	muscle
10	chr9:18484400-18486200	Genic enhancers	Muscle Satellite Cultured Cells	--
11	chr9:18484400-18486200	Enhancers	Colon Smooth Muscle	Colon
12	chr9:18484600-18485600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr9:18484600-18486000	Enhancers	Fetal Muscle Leg	muscle
14	chr9:18484600-18486000	Enhancers	Stomach Smooth Muscle	stomach
15	chr9:18484800-18485600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr9:18485200-18486000	Genic enhancers	NH-A	brain
17	chr9:18485200-18486200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr9:18485200-18486400	Enhancers	Fetal Heart	heart
19	chr9:18485400-18486000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr9:18485400-18486000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr9:18485400-18486000	Genic enhancers	Osteobl	bone
22	chr9:18485400-18486400	Enhancers	HSMMtube	muscle
23	chr9:18485400-18488600	Weak transcription	HUVEC	blood vessel
24	chr9:18485600-18485800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr9:18485600-18485800	Enhancers	Fetal Brain Female	brain
26	chr9:18485600-18486000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr9:18485600-18486000	Enhancers	NHLF	lung
28	chr9:18485600-18486200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr9:18485600-18486200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr9:18485600-18486200	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr9:18485600-18486200	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr9:18485600-18486200	Enhancers	Fetal Stomach	stomach
33	chr9:18485800-18487200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr9:18485800-18490800	Weak transcription	Fetal Brain Female	brain
35	chr9:18486000-18486200	Enhancers	Fetal Lung	lung
36	chr9:18486000-18486600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr9:18486000-18487200	Weak transcription	Osteobl	bone
38	chr9:18486000-18487400	Enhancers	NHDF-Ad	bronchial
39	chr9:18486000-18488400	Weak transcription	NH-A	brain
40	chr9:18486000-18488800	Weak transcription	NHLF	lung
41	chr9:18486000-18490000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr9:18486000-18490000	Weak transcription	Fetal Muscle Leg	muscle
43	chr9:18486000-18490200	Weak transcription	Stomach Smooth Muscle	stomach
44	chr9:18486000-18490400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr9:18486200-18486600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr9:18486200-18487200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr9:18486200-18487400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr9:18486200-18487600	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr9:18486200-18487600	Weak transcription	Colon Smooth Muscle	Colon
50	chr9:18486200-18488600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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