Variant report

Variant	nsv892670
Chromosome Location	chr9:17378776-17507277
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	BACH1	chr9:17469243-17469263	K562	blood:	n/a	n/a
2	BHLHE40	chr9:17462961-17463213	GM12878	blood:	n/a	n/a
3	BHLHE40	chr9:17493831-17493973	K562	blood:	n/a	n/a
4	BRCA1	chr9:17396862-17396940	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr9:17458820-17458969	HepG2	liver:	n/a	chr9:17458858-17458869 chr9:17458860-17458869 chr9:17458858-17458871 chr9:17458859-17458870
6	CEBPB	chr9:17398373-17398650	IMR90	lung:	n/a	n/a
7	CEBPB	chr9:17464897-17465248	IMR90	lung:	n/a	n/a
8	CEBPB	chr9:17423031-17423372	IMR90	lung:	n/a	n/a
9	CEBPB	chr9:17464916-17465245	HepG2	liver:	n/a	n/a
10	CEBPB	chr9:17440917-17441132	HepG2	liver:	n/a	chr9:17441002-17441013
11	CEBPB	chr9:17437376-17437608	A549	lung:	n/a	chr9:17437440-17437453 chr9:17437442-17437451 chr9:17437442-17437451 chr9:17437440-17437453 chr9:17437442-17437453 chr9:17437442-17437451 chr9:17437442-17437453 chr9:17437440-17437453 chr9:17437442-17437451
12	CEBPB	chr9:17397451-17397769	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr9:17484945-17485204	IMR90	lung:	n/a	n/a
14	CEBPB	chr9:17464930-17465234	A549	lung:	n/a	n/a
15	CEBPB	chr9:17457566-17457746	HepG2	liver:	n/a	chr9:17457686-17457697
16	CEBPB	chr9:17397502-17397682	IMR90	lung:	n/a	n/a
17	CEBPB	chr9:17406793-17407054	IMR90	lung:	n/a	chr9:17406919-17406930 chr9:17406918-17406931
18	CEBPB	chr9:17406868-17407046	HepG2	liver:	n/a	chr9:17406919-17406930 chr9:17406918-17406931
19	CEBPB	chr9:17458729-17459037	IMR90	lung:	n/a	chr9:17458858-17458869 chr9:17458860-17458869 chr9:17458858-17458871 chr9:17458859-17458870
20	CEBPB	chr9:17437391-17437559	H1-hESC	embryonic stem cell:	n/a	chr9:17437440-17437453 chr9:17437442-17437451 chr9:17437442-17437451 chr9:17437440-17437453 chr9:17437442-17437453 chr9:17437442-17437451 chr9:17437442-17437453 chr9:17437440-17437453 chr9:17437442-17437451
21	CEBPB	chr9:17398398-17398610	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr9:17419882-17420104	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr9:17406822-17407056	A549	lung:	n/a	chr9:17406919-17406930 chr9:17406918-17406931
24	CEBPB	chr9:17440906-17441152	IMR90	lung:	n/a	chr9:17441002-17441013
25	CEBPB	chr9:17464984-17465188	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr9:17440948-17441127	A549	lung:	n/a	chr9:17441002-17441013
27	CEBPB	chr9:17494858-17494998	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr9:17464977-17465153	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr9:17396955-17397053	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr9:17462940-17463090	GM12875	blood:	n/a	chr9:17463044-17463060 chr9:17463038-17463059 chr9:17463045-17463058 chr9:17463050-17463057 chr9:17463043-17463061
31	CTCF	chr9:17402540-17402690	A549	lung:	n/a	n/a
32	CTCF	chr9:17462960-17463110	GM12865	blood:	n/a	chr9:17463044-17463060 chr9:17463038-17463059 chr9:17463045-17463058 chr9:17463050-17463057 chr9:17463043-17463061
33	CTCF	chr9:17402346-17402662	SK-N-SH	brain:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
34	CTCF	chr9:17402397-17402611	Hela-S3	cervix:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
35	CTCF	chr9:17462980-17463130	HRPEpiC	eye:	n/a	chr9:17463044-17463060 chr9:17463038-17463059 chr9:17463045-17463058 chr9:17463050-17463057 chr9:17463043-17463061
36	CTCF	chr9:17477210-17477231	GM13976	blood:	n/a	n/a
37	CTCF	chr9:17462869-17463246	K562	blood:	n/a	chr9:17463044-17463060 chr9:17463038-17463059 chr9:17463045-17463058 chr9:17463050-17463057 chr9:17463043-17463061
38	CTCF	chr9:17462860-17463010	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr9:17402466-17402572	GM13977	blood:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
40	CTCF	chr9:17462980-17463130	GM12873	blood:	n/a	chr9:17463044-17463060 chr9:17463038-17463059 chr9:17463045-17463058 chr9:17463050-17463057 chr9:17463043-17463061
41	CTCF	chr9:17402440-17402590	NB4	blood:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
42	CTCF	chr9:17402444-17402584	HepG2	liver:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
43	CTCF	chr9:17462940-17463090	HVMF	connective:	n/a	chr9:17463044-17463060 chr9:17463038-17463059 chr9:17463045-17463058 chr9:17463050-17463057 chr9:17463043-17463061
44	CTCF	chr9:17402364-17402560	HepG2	liver:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
45	CTCF	chr9:17402620-17402770	AG09309	skin:	n/a	n/a
46	CTCF	chr9:17402480-17402630	GM12874	blood:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
47	CTCF	chr9:17462692-17463705	A549	lung:	n/a	chr9:17463044-17463060 chr9:17463038-17463059 chr9:17463045-17463058 chr9:17463050-17463057 chr9:17463043-17463061
48	CTCF	chr9:17402447-17402553	Gliobla	brain:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
49	CTCF	chr9:17402460-17402610	AG04449	skin:	n/a	chr9:17402495-17402516 chr9:17402500-17402518
50	CTCF	chr9:17402434-17402556	MCF-7	breast:	n/a	chr9:17402495-17402516 chr9:17402500-17402518

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:17503269-17503319	ovcar-3	ovarian:	n/a
2	chr9:17503269-17503319	GM19239	blood:	n/a
3	chr9:17503269-17503319	AoSMC	blood vessel:	n/a
4	chr9:17503269-17503319	A549	lung:	n/a
5	chr9:17503269-17503319	ProgFib	skin:	n/a
6	chr9:17503269-17503319	RPTEC	kidney:	n/a
7	chr9:17503269-17503319	K562	blood:	n/a
8	chr9:17503269-17503319	HEK293	kidney:	embryo
9	chr9:17503269-17503319	HCT-116	colon:	n/a
10	chr9:17503269-17503319	HCF	heart:	n/a
11	chr9:17503269-17503319	AG09309	skin:	n/a
12	chr9:17503269-17503319	HCPEpiC	choroid plexus:	n/a
13	chr9:17503269-17503319	HUVEC	blood vessel:	n/a
14	chr9:17503269-17503319	HIPEpiC	eye:	n/a
15	chr9:17503269-17503319	NT2-D1	testis:	n/a
16	chr9:17503269-17503319	HRCEpiC	kidney:	n/a
17	chr9:17503269-17503319	AG09319	gingival:	n/a
18	chr9:17503269-17503319	MCF10A-Er-Src	breast:	n/a
19	chr9:17503269-17503319	ECC-1	luminal epithelium:	n/a
20	chr9:17503269-17503319	PANC-1	pancreas:	n/a
21	chr9:17503269-17503319	NB4	blood:	n/a
22	chr9:17503269-17503319	BJ	skin:	n/a
23	chr9:17503269-17503319	HMEC	breast:	n/a
24	chr9:17503269-17503319	HNPCEpiC	eye:	n/a
25	chr9:17503269-17503319	AG04449	skin:	fetal
26	chr9:17503269-17503319	HCM	heart:	n/a
27	chr9:17503269-17503319	AG10803	skin:	n/a
28	chr9:17503269-17503319	T-47D	breast:	n/a
29	chr9:17503269-17503319	GM12891	blood:	n/a
30	chr9:17503269-17503319	SKMC	muscle:	n/a
31	chr9:17503269-17503319	SK-N-MC	brain:	n/a
32	chr9:17503269-17503319	U87	brain:	n/a
33	chr9:17503269-17503319	LNCaP	prostate:	n/a
34	chr9:17503269-17503319	HRE	kidney:	n/a
35	chr9:17503269-17503319	PFSK-1	brain:	n/a
36	chr9:17503269-17503319	HepG2	liver:	n/a
37	chr9:17503269-17503319	Hepatocyte	liver:	n/a
38	chr9:17503269-17503319	MCF-7	breast:	n/a
39	chr9:17503269-17503319	Caco-2	colon:	n/a
40	chr9:17503269-17503319	HAEpiC	amniotic membrane:	n/a
41	chr9:17503269-17503319	GM12892	blood:	n/a
42	chr9:17503269-17503319	H1-hESC	embryonic stem cell:	embryo
43	chr9:17503269-17503319	HEEpiC	esophagus:	n/a
44	chr9:17503269-17503319	SK-N-SH	brain:	n/a
45	chr9:17503269-17503319	BE2_C	brain:	n/a
46	chr9:17503269-17503319	Jurkat	blood:	n/a
47	chr9:17503269-17503319	SAEC	small airway:	n/a
48	chr9:17503269-17503319	CMK	blood:	n/a
49	chr9:17503269-17503319	NHDF-neo	bronchial:	n/a
50	chr9:17503269-17503319	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr9:17219155..17220052-chr9:17401883..17402825,5	MCF-7	breast:
2	chr9:17063303..17064146-chr9:17462547..17463504,3	MCF-7	breast:
3	chr9:17116081..17117141-chr9:17402172..17402905,3	MCF-7	breast:
4	chr9:17219375..17219930-chr9:17402045..17403347,3	MCF-7	breast:
5	chr9:17116046..17116795-chr9:17462771..17463533,2	MCF-7	breast:
6	chr9:17219048..17219921-chr9:17462587..17463121,2	MCF-7	breast:
7	chr9:17116233..17116835-chr9:17462927..17463473,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH3GL2-2	chr9:17415964-17416187	NONHSAT130301
2	lnc-SH3GL2-2	chr9:17415816-17415879	NONHSAT130301
3	lnc-BNC2-4	chr9:17447143-17448541	NONHSAT130303
4	lnc-SH3GL2-2	chr9:17457522-17457626	NONHSAT130301
5	lnc-SH3GL2-2	chr9:17462914-17462982	NONHSAT130301
6	lnc-SH3GL2-1	chr9:17435732-17437445	NONHSAT130302
7	lnc-SH3GL2-2	chr9:17444195-17444244	NONHSAT130301

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CNTLN	hsa-miR-26b-5p	chr9:17503103-17503123

Variant related genes	Relation type
ENSG00000224488	TF binding region
CNTLN	TF binding region
ENSG00000224488	CpG island
CNTLN	CpG island

Extended variants
information (count: 5625 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:5625 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10963072	chr9:17378776-17378777	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs550387303	chr9:17378791-17378792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535762711	chr9:17378825-17378826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534503764	chr9:17378871-17378872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556876910	chr9:17378882-17378883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111793879	chr9:17378929-17378930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547522158	chr9:17378954-17378955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553178103	chr9:17378958-17378959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528973093	chr9:17378995-17378996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs151260386	chr9:17378999-17379000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369223623	chr9:17379001-17379002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111321191	chr9:17379015-17379016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75875378	chr9:17379051-17379052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140351994	chr9:17379075-17379076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112888743	chr9:17379080-17379081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs150378615	chr9:17379103-17379104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs1442533	chr9:17379146-17379147	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs78479470	chr9:17379147-17379148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544186058	chr9:17379153-17379154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563651187	chr9:17379154-17379155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1023778	chr9:17379161-17379162	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs184062501	chr9:17379174-17379175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564221735	chr9:17379201-17379202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528586686	chr9:17379203-17379204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186565794	chr9:17379204-17379205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546757886	chr9:17379255-17379256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532880131	chr9:17379257-17379258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189777804	chr9:17379261-17379262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529545338	chr9:17379280-17379281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182307691	chr9:17379296-17379297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs36057268	chr9:17379340-17379341	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs186924528	chr9:17379380-17379381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573330230	chr9:17379386-17379387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551384793	chr9:17379388-17379389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566544440	chr9:17379394-17379395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533888157	chr9:17379503-17379504	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs371485083	chr9:17379565-17379566	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs555558973	chr9:17379598-17379599	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs193004720	chr9:17379609-17379610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10963073	chr9:17379615-17379616	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs556172510	chr9:17379663-17379664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562313385	chr9:17379717-17379718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577899516	chr9:17379753-17379754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529522413	chr9:17379758-17379759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545853559	chr9:17379827-17379828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4554574	chr9:17379849-17379850	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs185122214	chr9:17379854-17379855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550377906	chr9:17379910-17379911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112641368	chr9:17379911-17379912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372126345	chr9:17379930-17379931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
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
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
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:539 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17362000-17394600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr9:17368400-17394600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:17368400-17457800	Weak transcription	Pancreas	Pancrea
4	chr9:17368600-17394800	Weak transcription	Adipose Nuclei	Adipose
5	chr9:17368600-17411200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr9:17368600-17411400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr9:17368600-17411400	Weak transcription	Aorta	Aorta
8	chr9:17368800-17380400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr9:17368800-17411400	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr9:17369000-17380600	Weak transcription	Fetal Lung	lung
11	chr9:17369000-17395000	Weak transcription	Stomach Smooth Muscle	stomach
12	chr9:17369200-17380000	Weak transcription	Left Ventricle	heart
13	chr9:17369200-17380200	Weak transcription	Fetal Muscle Leg	muscle
14	chr9:17369400-17411200	Weak transcription	Fetal Muscle Trunk	muscle
15	chr9:17370000-17380200	Weak transcription	Ovary	ovary
16	chr9:17370600-17386600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr9:17371400-17394800	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr9:17371600-17380200	Weak transcription	Liver	Liver
19	chr9:17377600-17403000	Weak transcription	Fetal Stomach	stomach
20	chr9:17377800-17383800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr9:17379400-17379600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr9:17379400-17381400	Weak transcription	Primary hematopoietic stem cells	blood
23	chr9:17379400-17404200	Weak transcription	Psoas Muscle	Psoas
24	chr9:17379600-17394800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr9:17379800-17394600	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr9:17380000-17380400	Enhancers	HMEC	breast
27	chr9:17380000-17380600	Strong transcription	Left Ventricle	heart
28	chr9:17380000-17381800	Enhancers	NHEK	skin
29	chr9:17380200-17381000	Strong transcription	Fetal Muscle Leg	muscle
30	chr9:17380200-17381400	Strong transcription	Ovary	ovary
31	chr9:17380200-17381800	Strong transcription	Liver	Liver
32	chr9:17380400-17380800	Enhancers	Colon Smooth Muscle	Colon
33	chr9:17380400-17381200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
34	chr9:17380600-17381000	Strong transcription	Fetal Lung	lung
35	chr9:17380600-17411000	Weak transcription	Left Ventricle	heart
36	chr9:17380800-17381200	Weak transcription	Colon Smooth Muscle	Colon
37	chr9:17381000-17389400	Weak transcription	Fetal Lung	lung
38	chr9:17381000-17411200	Weak transcription	Fetal Muscle Leg	muscle
39	chr9:17381200-17381400	Enhancers	Colon Smooth Muscle	Colon
40	chr9:17381200-17411200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr9:17381400-17382000	Strong transcription	Primary hematopoietic stem cells	blood
42	chr9:17381400-17397400	Weak transcription	Ovary	ovary
43	chr9:17381400-17422800	Weak transcription	Colon Smooth Muscle	Colon
44	chr9:17381800-17396000	Weak transcription	Liver	Liver
45	chr9:17382000-17394800	Weak transcription	Primary hematopoietic stem cells	blood
46	chr9:17385200-17385400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr9:17385200-17396400	Weak transcription	Right Ventricle	heart
48	chr9:17385400-17411400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr9:17386600-17386800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr9:17386600-17386800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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