Variant report

Variant	nsv1029750
Chromosome Location	chr9:24531007-24657061
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	BRCA1	chr9:24608414-24608450	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr9:24635554-24635668	A549	lung:	n/a	n/a
3	CEBPB	chr9:24601485-24601846	A549	lung:	n/a	chr9:24601658-24601669 chr9:24601659-24601670
4	CEBPB	chr9:24556332-24556354	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr9:24601476-24601834	IMR90	lung:	n/a	chr9:24601658-24601669 chr9:24601659-24601670
6	CEBPB	chr9:24556226-24556465	HepG2	liver:	n/a	chr9:24556345-24556356
7	CEBPB	chr9:24542908-24543131	HepG2	liver:	n/a	chr9:24542993-24543004
8	CEBPB	chr9:24573070-24573358	A549	lung:	n/a	chr9:24573224-24573235
9	CEBPB	chr9:24582769-24583084	HepG2	liver:	n/a	chr9:24582926-24582935 chr9:24582926-24582935 chr9:24582924-24582937 chr9:24582926-24582935 chr9:24582925-24582936 chr9:24582924-24582935 chr9:24582926-24582935
10	CEBPB	chr9:24601485-24601836	HepG2	liver:	n/a	chr9:24601658-24601669 chr9:24601659-24601670
11	CEBPB	chr9:24601522-24601759	Hela-S3	cervix:	n/a	chr9:24601658-24601669 chr9:24601659-24601670
12	CEBPB	chr9:24565572-24565772	A549	lung:	n/a	n/a
13	CEBPB	chr9:24562320-24562452	A549	lung:	n/a	n/a
14	CEBPB	chr9:24573116-24573355	HepG2	liver:	n/a	chr9:24573224-24573235
15	CTCF	chr9:24614220-24614370	BE2_C	brain:	n/a	chr9:24614271-24614279
16	CTCF	chr9:24614160-24614310	AoAF	blood vessel:	n/a	chr9:24614271-24614279
17	CTCF	chr9:24614159-24614338	SK-N-SH_RA	brain:	n/a	chr9:24614271-24614279
18	CTCF	chr9:24614220-24614370	HA-sp	spinal cord:	n/a	chr9:24614271-24614279
19	CTCF	chr9:24614180-24614330	WERI-Rb-1	eye:	n/a	chr9:24614271-24614279
20	CTCF	chr9:24614220-24614370	RPTEC	kidney:	n/a	chr9:24614271-24614279
21	CTCF	chr9:24616980-24617130	HMEC	breast:	n/a	n/a
22	CTCF	chr9:24614160-24614310	HEEpiC	esophagus:	n/a	chr9:24614271-24614279
23	CTCF	chr9:24614200-24614350	HRPEpiC	eye:	n/a	chr9:24614271-24614279
24	CTCF	chr9:24616993-24617074	Gliobla	brain:	n/a	n/a
25	CTCF	chr9:24617020-24617170	RPTEC	kidney:	n/a	n/a
26	CTCF	chr9:24614200-24614350	HPAF	blood vessel:	n/a	chr9:24614271-24614279
27	CTCF	chr9:24614240-24614390	HEEpiC	esophagus:	n/a	chr9:24614271-24614279
28	CTCF	chr9:24628280-24628430	NHDF-neo	bronchial:	n/a	n/a
29	CTCF	chr9:24614220-24614370	NHEK	skin:	n/a	chr9:24614271-24614279
30	CTCF	chr9:24616940-24617090	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr9:24614180-24614330	HMF	breast:	n/a	chr9:24614271-24614279
32	CTCF	chr9:24617022-24617121	Pancreas_OC	pancreas:	n/a	n/a
33	CTCF	chr9:24614180-24614330	HMEC	breast:	n/a	chr9:24614271-24614279
34	CTCF	chr9:24614140-24614290	WERI-Rb-1	eye:	n/a	chr9:24614271-24614279
35	CTCF	chr9:24613951-24614483	SK-N-SH	brain:	n/a	chr9:24614271-24614279
36	CTCF	chr9:24617000-24617150	RPTEC	kidney:	n/a	n/a
37	CTCF	chr9:24614180-24614330	HA-sp	spinal cord:	n/a	chr9:24614271-24614279
38	CTCF	chr9:24614177-24614370	LNCaP	prostate:	n/a	chr9:24614271-24614279
39	CTCF	chr9:24617009-24617011	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr9:24614100-24614250	HAc	cerebellar:	n/a	n/a
41	CTCF	chr9:24614170-24614367	LNCaP	prostate:	n/a	chr9:24614271-24614279
42	CTCF	chr9:24614140-24614290	HCPEpiC	choroid plexus:	n/a	chr9:24614271-24614279
43	CTCF	chr9:24614300-24614450	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr9:24616992-24617136	LNCaP	prostate:	n/a	n/a
45	CTCF	chr9:24614080-24614230	HAc	cerebellar:	n/a	n/a
46	CTCF	chr9:24616940-24617090	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr9:24614220-24614370	MCF-7	breast:	n/a	chr9:24614271-24614279
48	CTCF	chr9:24614160-24614310	HMF	breast:	n/a	chr9:24614271-24614279
49	CTCF	chr9:24614160-24614310	HRPEpiC	eye:	n/a	chr9:24614271-24614279
50	CTCF	chr9:24614240-24614390	HRE	kidney:	n/a	chr9:24614271-24614279

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:24613953..24614528-chr9:25350122..25350850,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMRTA1-7	chr9:24561754-24561848	XLOC_007304
2	lnc-DMRTA1-7	chr9:24590269-24590449	XLOC_007304
3	lnc-DMRTA1-7	chr9:24590269-24590449	XLOC_007304
4	lnc-DMRTA1-7	chr9:24551961-24552127	ENSG00000269957.1
5	lnc-DMRTA1-7	chr9:24545996-24546127	ENSG00000269957.1
6	lnc-DMRTA1-7	chr9:24561325-24561428	XLOC_007304
7	lnc-DMRTA1-7	chr9:24561754-24561848	XLOC_007304
8	lnc-DMRTA1-7	chr9:24545856-24546127	XLOC_007304
9	lnc-DMRTA1-7	chr9:24545856-24546127	XLOC_007304
10	lnc-DMRTA1-7	chr9:24561754-24561848	ENSG00000269957.1
11	lnc-DMRTA1-7	chr9:24590269-24590449	XLOC_007304
12	lnc-DMRTA1-7	chr9:24561754-24561848	XLOC_007304
13	lnc-DMRTA1-7	chr9:24591877-24592081	XLOC_007304
14	lnc-DMRTA1-7	chr9:24591877-24591991	ENSG00000269957.1
15	lnc-DMRTA1-7	chr9:24545950-24546127	ENSG00000269957.1
16	lnc-DMRTA1-7	chr9:24552919-24553237	ENSG00000269957.1
17	lnc-DMRTA1-7	chr9:24545400-24545526	XLOC_007304
18	lnc-DMRTA1-7	chr9:24551961-24552156	XLOC_007304
19	lnc-DMRTA1-7	chr9:24590269-24590449	ENSG00000269957.1
20	lnc-DMRTA1-7	chr9:24551961-24552127	XLOC_007304
21	lnc-DMRTA1-7	chr9:24545423-24545526	XLOC_007304
22	lnc-DMRTA1-7	chr9:24551961-24552127	ENSG00000269957.1
23	lnc-DMRTA1-7	chr9:24591877-24592081	XLOC_007304
24	lnc-DMRTA1-7	chr9:24552919-24553082	XLOC_007304
25	lnc-DMRTA1-7	chr9:24545422-24546127	XLOC_007304
26	lnc-DMRTA1-7	chr9:24545422-24546127	XLOC_007304
27	lnc-DMRTA1-7	chr9:24591877-24592305	XLOC_007304

Variant related genes	Relation type
IZUMO3	TF binding region
ENSG00000269957	TF binding region
MAP3K4	miRNA target sites
ZDHHC17	miRNA target sites
MAP3K3	miRNA target sites
LEPROTL1	miRNA target sites
MAP3K7	miRNA target sites
FRS2	miRNA target sites

Extended variants
information (count: 2474 )
Associated
traits (count: 146 )

Variant overlapped rSNPs/rCNVs (count:2474 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189768701	chr9:24542221-24542222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs116291908	chr9:24542227-24542228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574210298	chr9:24542256-24542257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181193669	chr9:24542279-24542280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184499568	chr9:24542359-24542360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188357425	chr9:24542420-24542421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139318231	chr9:24542433-24542434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543122741	chr9:24542444-24542445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs180768360	chr9:24542452-24542453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115333704	chr9:24542468-24542469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150003950	chr9:24542484-24542485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186453363	chr9:24542548-24542549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190875399	chr9:24542550-24542551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564666360	chr9:24542555-24542556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565042373	chr9:24542557-24542558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527610696	chr9:24542605-24542606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531965077	chr9:24542612-24542613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561148538	chr9:24542633-24542634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs145371948	chr9:24542665-24542666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs549796147	chr9:24542672-24542673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536120324	chr9:24542676-24542677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs142529329	chr9:24542686-24542687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556952296	chr9:24542687-24542688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551705291	chr9:24542729-24542730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs146917602	chr9:24542739-24542740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550515526	chr9:24542746-24542747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs140442698	chr9:24542770-24542771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563973115	chr9:24542774-24542775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534115596	chr9:24542779-24542780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563019656	chr9:24542786-24542787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181885259	chr9:24542930-24542931	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs186956657	chr9:24542937-24542938	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs556097069	chr9:24542952-24542953	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs117408698	chr9:24542956-24542957	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs191299021	chr9:24542979-24542980	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs73652281	chr9:24542993-24542994	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs557827153	chr9:24543027-24543028	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs16908482	chr9:24543044-24543045	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs183323376	chr9:24543045-24543046	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs561209869	chr9:24543049-24543050	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs79904354	chr9:24543050-24543051	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs543447091	chr9:24543059-24543060	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs574659147	chr9:24543070-24543071	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs537221730	chr9:24543961-24543962	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs557270365	chr9:24543973-24543974	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs192470680	chr9:24543999-24544000	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs577053638	chr9:24544035-24544036	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs545792103	chr9:24544049-24544050	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs545964426	chr9:24544082-24544083	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs559038930	chr9:24544104-24544105	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:146)

Disease	PMID	Source
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
Oral squamous cell carcinoma	17134496	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
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
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Myelofibrosis	22110671	CNVD
Ewing''s sarcoma	22429812	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	19435819	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung cancer	21911935	CNVD
Primary central nervous system lymphoma	21088137	CNVD
head and neck squamous cell carcinoma	21798897	CNVD
Cancer	21253487	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Urothelial cell carcinoma	18451213	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Leukemia	19602459	CNVD
Acute monocytic leukemia	16498392	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Leukemia	18688285	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Acute myeloid leukemia	19651601	CNVD
Coronary Disease	20032323	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21732550	CNVD
Gastric cancer	22539939	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Metastatic melanoma	18483359	CNVD
Non-small cell lung cancer	20864512	CNVD
Cervical cancer	21062161	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioblastoma	17090523	CNVD
Lung cancer	16773561	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16774939	CNVD
Bladder cancer	19088036	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	16977458	CNVD
Glioblastoma multiforme	17369134	CNVD
Chagasic megaesophagus	20163722	CNVD
Melanoma	19566914	CNVD
Squamous cell cancer	19047905	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Melanoma	17363583	CNVD
Glioblastoma multiforme	19115005	CNVD
Adenoid cystic carcinoma	18332873	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Esophageal adenocarcinoma	18519675	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:24542200-24542800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr9:24545200-24545600	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr9:24545200-24546200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:24546200-24547200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr9:24547400-24547600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr9:24552600-24553000	Enhancers	Fetal Kidney	kidney
7	chr9:24553000-24553200	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr9:24571600-24571800	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr9:24571800-24572200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr9:24571800-24580000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr9:24572200-24572600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr9:24572200-24573200	Enhancers	Adipose Nuclei	Adipose
13	chr9:24572600-24573400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr9:24580000-24580200	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr9:24580000-24580400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr9:24580000-24580400	Active TSS	HUES48 Cell Line	embryonic stem cell
17	chr9:24580000-24580400	Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr9:24580000-24580400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr9:24580000-24580600	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr9:24580000-24580600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr9:24580000-24580600	Active TSS	H9 Cell Line	embryonic stem cell
22	chr9:24580000-24580600	Active TSS	HUES64 Cell Line	embryonic stem cell
23	chr9:24580000-24580600	Active TSS	iPS-15b Cell Line	embryonic stem cell
24	chr9:24580200-24580600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
25	chr9:24580200-24580600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr9:24580400-24580600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr9:24580600-24580800	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr9:24580600-24580800	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr9:24580600-24581400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr9:24582200-24582800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr9:24582200-24582800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr9:24582400-24582600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr9:24582600-24583000	Active TSS	Rectal Mucosa Donor 29	rectum
34	chr9:24582800-24585400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr9:24585600-24585800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr9:24585800-24592200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr9:24590400-24591400	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr9:24590600-24590800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr9:24590600-24591000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr9:24590600-24592600	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr9:24590600-24592800	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr9:24590600-24593000	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr9:24590800-24591400	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr9:24590800-24591400	Enhancers	HMEC	breast
45	chr9:24591400-24592200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr9:24591400-24593000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr9:24591600-24592400	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr9:24591800-24592600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr9:24592200-24592400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr9:24592200-24592600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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