Variant report

Variant	nsv428536
Chromosome Location	chr9:18512807-18667760
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:18622195-18622391	HepG2	liver:	n/a	n/a
2	BACH1	chr9:18606813-18606827	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr9:18574188-18574199	GM12878	blood:	n/a	n/a
4	BRCA1	chr9:18658837-18659489	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr9:18638458-18639249	IMR90	lung:	n/a	n/a
6	CEBPB	chr9:18650195-18650502	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr9:18607360-18607559	HepG2	liver:	n/a	chr9:18607503-18607516 chr9:18607502-18607519 chr9:18607503-18607516 chr9:18607504-18607515 chr9:18607503-18607516 chr9:18607503-18607514
8	CEBPB	chr9:18658575-18659425	IMR90	lung:	n/a	chr9:18659245-18659262
9	CEBPB	chr9:18591917-18592017	Hela-S3	cervix:	n/a	chr9:18591978-18591989
10	CEBPB	chr9:18596985-18597185	HepG2	liver:	n/a	chr9:18597079-18597090
11	CEBPB	chr9:18632838-18633486	IMR90	lung:	n/a	n/a
12	CEBPB	chr9:18578617-18578692	HepG2	liver:	n/a	n/a
13	CEBPB	chr9:18666502-18666830	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr9:18544401-18544745	IMR90	lung:	n/a	chr9:18544557-18544570
15	CEBPB	chr9:18596902-18597284	Hela-S3	cervix:	n/a	chr9:18597079-18597090
16	CEBPB	chr9:18632787-18632970	HepG2	liver:	n/a	n/a
17	CEBPB	chr9:18578396-18578419	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr9:18607924-18608166	IMR90	lung:	n/a	chr9:18608045-18608056
19	CEBPB	chr9:18531238-18531526	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr9:18607894-18608148	A549	lung:	n/a	chr9:18608045-18608056
21	CEBPB	chr9:18658554-18659633	Hela-S3	cervix:	n/a	chr9:18659245-18659262
22	CEBPB	chr9:18597002-18597198	A549	lung:	n/a	chr9:18597079-18597090
23	CEBPB	chr9:18596902-18597290	IMR90	lung:	n/a	chr9:18597079-18597090
24	CEBPB	chr9:18526755-18527079	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr9:18631227-18631419	K562	blood:	n/a	chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631301-18631312 chr9:18631302-18631311
26	CEBPB	chr9:18580228-18580540	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr9:18544465-18544730	Hela-S3	cervix:	n/a	chr9:18544557-18544570
28	CEBPB	chr9:18631285-18631331	A549	lung:	n/a	chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631301-18631312 chr9:18631302-18631311
29	CEBPB	chr9:18532530-18532635	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr9:18591842-18592151	A549	lung:	n/a	chr9:18591978-18591989
31	CEBPB	chr9:18526754-18527079	IMR90	lung:	n/a	n/a
32	CEBPB	chr9:18607910-18608198	HepG2	liver:	n/a	chr9:18608045-18608056
33	CEBPB	chr9:18631140-18631424	IMR90	lung:	n/a	chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631301-18631312 chr9:18631302-18631311
34	CEBPB	chr9:18526773-18527003	A549	lung:	n/a	n/a
35	CEBPB	chr9:18526762-18527049	HepG2	liver:	n/a	n/a
36	CEBPB	chr9:18526744-18527111	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr9:18591830-18592160	HepG2	liver:	n/a	chr9:18591978-18591989
38	CEBPB	chr9:18631153-18631463	HepG2	liver:	n/a	chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631301-18631312 chr9:18631302-18631311
39	CEBPB	chr9:18591831-18592127	IMR90	lung:	n/a	chr9:18591978-18591989
40	CEBPB	chr9:18585070-18585095	A549	lung:	n/a	n/a
41	CHD1	chr9:18606430-18606432	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr9:18662583-18662584	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr9:18626205-18626366	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr9:18667080-18667230	NHLF	lung:	n/a	n/a
45	CTCF	chr9:18626214-18626391	LNCaP	prostate:	n/a	n/a
46	CTCF	chr9:18666200-18666350	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr9:18667080-18667230	AG09319	gingival:	n/a	n/a
48	CTCF	chr9:18622206-18622424	HepG2	liver:	n/a	n/a
49	CTCF	chr9:18617200-18617350	GM12867	blood:	n/a	n/a
50	CTCF	chr9:18619700-18619850	HFF-Myc	foreskin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:18514052-18514102	T-47D	breast:	n/a
2	chr9:18622331-18622381	MCF-7	breast:	n/a
3	chr9:18622331-18622381	U87	brain:	n/a
4	chr9:18622331-18622381	SK-N-MC	brain:	n/a
5	chr9:18622331-18622381	Hela-S3	cervix:	n/a
6	chr9:18605667-18605717	HEK293	kidney:	embryo
7	chr9:18605667-18605717	BJ	skin:	n/a
8	chr9:18622331-18622381	HCF	heart:	n/a
9	chr9:18514052-18514102	NHBE	bronchial:	n/a
10	chr9:18605667-18605717	GM06990	blood:	n/a
11	chr9:18514052-18514102	GM06990	blood:	n/a
12	chr9:18605667-18605717	ProgFib	skin:	n/a
13	chr9:18605667-18605717	SK-N-SH_RA	brain:	n/a
14	chr9:18514052-18514102	NHDF-neo	bronchial:	n/a
15	chr9:18622331-18622381	AoSMC	blood vessel:	n/a
16	chr9:18622331-18622381	Hepatocyte	liver:	n/a
17	chr9:18605667-18605717	HMEC	breast:	n/a
18	chr9:18605667-18605717	SAEC	small airway:	n/a
19	chr9:18622331-18622381	GM12891	blood:	n/a
20	chr9:18605667-18605717	SK-N-MC	brain:	n/a
21	chr9:18605667-18605717	AG10803	skin:	n/a
22	chr9:18622331-18622381	HMEC	breast:	n/a
23	chr9:18622331-18622381	ovcar-3	ovarian:	n/a
24	chr9:18605667-18605717	HCPEpiC	choroid plexus:	n/a
25	chr9:18514052-18514102	GM12891	blood:	n/a
26	chr9:18622331-18622381	HIPEpiC	eye:	n/a
27	chr9:18605667-18605717	HL-60	blood:	n/a
28	chr9:18514052-18514102	BJ	skin:	n/a
29	chr9:18622331-18622381	SK-N-SH_RA	brain:	n/a
30	chr9:18514052-18514102	GM12878	blood:	n/a
31	chr9:18622331-18622381	CMK	blood:	n/a
32	chr9:18514052-18514102	SK-N-SH_RA	brain:	n/a
33	chr9:18514052-18514102	HEK293	kidney:	embryo
34	chr9:18514052-18514102	HepG2	liver:	n/a
35	chr9:18622331-18622381	Jurkat	blood:	n/a
36	chr9:18622331-18622381	SAEC	small airway:	n/a
37	chr9:18605667-18605717	Hela-S3	cervix:	n/a
38	chr9:18605667-18605717	RPTEC	kidney:	n/a
39	chr9:18605667-18605717	Jurkat	blood:	n/a
40	chr9:18622331-18622381	BE2_C	brain:	n/a
41	chr9:18605667-18605717	SK-N-SH	brain:	n/a
42	chr9:18514052-18514102	SAEC	small airway:	n/a
43	chr9:18514052-18514102	SK-N-MC	brain:	n/a
44	chr9:18605667-18605717	ECC-1	luminal epithelium:	n/a
45	chr9:18514052-18514102	HNPCEpiC	eye:	n/a
46	chr9:18622331-18622381	A549	lung:	n/a
47	chr9:18605667-18605717	NHDF-neo	bronchial:	n/a
48	chr9:18514052-18514102	ovcar-3	ovarian:	n/a
49	chr9:18514052-18514102	HRE	kidney:	n/a
50	chr9:18514052-18514102	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:18662167..18665769-chr9:18669383..18672936,3	MCF-7	breast:
2	chr9:18377972..18379506-chr9:18518837..18521140,2	K562	blood:
3	chr1:149223595..149224343-chr9:18512967..18513487,3	Hela-S3	cervix:
4	chr2:126575127..126575844-chr9:18665491..18666183,2	MCF-7	breast:
5	chr1:149222514..149224923-chr9:18513487..18514987,2	K562	blood:
6	chr9:18552353..18554750-chr9:18819699..18822182,2	MCF-7	breast:
7	chr1:149223814..149224438-chr9:18512987..18513487,3	MCF-7	breast:
8	chr1:149223496..149224418-chr9:18512967..18513967,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RRAGA-3	chr9:18651145-18651448	NONHSAT130312

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

Variant related genes	Relation type
RN7SKP258	TF binding region
ADAMTSL1	TF binding region
MIR3152	TF binding region
RN7SKP258	CpG island
ADAMTSL1	CpG island
MIR3152	CpG island
ENSG00000206737	chromatin interactions

Extended variants
information (count: 7563 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:7563 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188427874	chr9:18512822-18512823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs145618718	chr9:18512838-18512839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568826268	chr9:18512865-18512866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539388520	chr9:18512881-18512882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369368707	chr9:18512888-18512889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs151089969	chr9:18512921-18512922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141068315	chr9:18512922-18512923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533755435	chr9:18512945-18512946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555100292	chr9:18512952-18512953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574594711	chr9:18512968-18512969	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs117424570	chr9:18512972-18512973	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs563570333	chr9:18513020-18513021	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs193240298	chr9:18513047-18513048	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs546205971	chr9:18513054-18513055	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs150242342	chr9:18513074-18513075	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs185031978	chr9:18513085-18513086	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs35518030	chr9:18513086-18513087	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs145778347	chr9:18513092-18513093	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs535335990	chr9:18513098-18513099	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs148948244	chr9:18513099-18513100	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs568790044	chr9:18513123-18513124	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs145647885	chr9:18513209-18513210	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs577285114	chr9:18513211-18513212	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs150064070	chr9:18513267-18513268	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs376368763	chr9:18513268-18513269	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs75073588	chr9:18513316-18513317	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs377592931	chr9:18513323-18513324	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs553578821	chr9:18513333-18513334	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs566765937	chr9:18513368-18513369	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs114329156	chr9:18513381-18513382	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs78979166	chr9:18513434-18513435	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs567112418	chr9:18513475-18513476	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs535587600	chr9:18513480-18513481	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs142667766	chr9:18513506-18513507	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs186794196	chr9:18513535-18513536	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546194083	chr9:18513542-18513543	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs144930219	chr9:18513544-18513545	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs573627393	chr9:18513551-18513552	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs191594092	chr9:18513557-18513558	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs373445831	chr9:18513588-18513589	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs576385747	chr9:18513615-18513616	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs183831973	chr9:18513630-18513631	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs529491390	chr9:18513637-18513638	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs36013602	chr9:18513645-18513646	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs377485976	chr9:18513688-18513689	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs189667670	chr9:18513705-18513706	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs117016252	chr9:18513723-18513724	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs181356928	chr9:18513736-18513737	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs533631677	chr9:18513741-18513742	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs566337407	chr9:18513761-18513762	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
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
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20841430	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1217 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18495400-18513200	Weak transcription	HUVEC	blood vessel
2	chr9:18501600-18520400	Weak transcription	Fetal Stomach	stomach
3	chr9:18502200-18518800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr9:18502800-18520400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr9:18506800-18519800	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr9:18509800-18513200	Weak transcription	NH-A	brain
7	chr9:18510000-18516600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr9:18510600-18533000	Weak transcription	NHDF-Ad	bronchial
9	chr9:18510800-18514600	Weak transcription	HSMM	muscle
10	chr9:18511400-18519200	Weak transcription	Osteobl	bone
11	chr9:18512400-18513000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr9:18513000-18516000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:18513200-18513400	Enhancers	HUVEC	blood vessel
14	chr9:18513200-18513800	Strong transcription	NH-A	brain
15	chr9:18513800-18520600	Weak transcription	NH-A	brain
16	chr9:18514600-18516800	Strong transcription	HSMM	muscle
17	chr9:18516000-18518800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr9:18516200-18517000	Enhancers	Liver	Liver
19	chr9:18516200-18517200	Enhancers	Fetal Heart	heart
20	chr9:18516600-18517400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr9:18516800-18519600	Weak transcription	HSMM	muscle
22	chr9:18517400-18519800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr9:18518800-18519200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr9:18518800-18519400	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr9:18519200-18521000	Enhancers	Osteobl	bone
26	chr9:18519200-18521400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr9:18519400-18533600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr9:18519600-18521200	Genic enhancers	HSMM	muscle
29	chr9:18519600-18521400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr9:18519800-18521000	Enhancers	Muscle Satellite Cultured Cells	--
31	chr9:18519800-18521400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr9:18520000-18520800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr9:18520000-18521000	Enhancers	Fetal Lung	lung
34	chr9:18520400-18520800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr9:18520400-18520800	Enhancers	Fetal Muscle Leg	muscle
36	chr9:18520400-18520800	Enhancers	HSMMtube	muscle
37	chr9:18520400-18521200	Enhancers	Fetal Stomach	stomach
38	chr9:18520600-18520800	Enhancers	NH-A	brain
39	chr9:18520800-18533200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr9:18521000-18521800	Weak transcription	Osteobl	bone
41	chr9:18521000-18529000	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr9:18521200-18522400	Strong transcription	HSMM	muscle
43	chr9:18521400-18521800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr9:18521800-18522200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr9:18521800-18522400	Strong transcription	Osteobl	bone
46	chr9:18522200-18530400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr9:18522400-18529200	Weak transcription	HSMM	muscle
48	chr9:18522400-18533200	Weak transcription	Osteobl	bone
49	chr9:18526200-18527400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr9:18526800-18527400	Enhancers	iPS-20b Cell Line	embryonic stem cell

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