Variant report

Variant	nsv892810
Chromosome Location	chr9:24985964-25392322
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	chr9:25196208-25196218	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr9:25326438-25326445	GM12878	blood:	n/a	n/a
3	CEBPB	chr9:25295529-25295869	HepG2	liver:	n/a	chr9:25295792-25295803
4	CEBPB	chr9:25061742-25062230	HepG2	liver:	n/a	chr9:25061891-25061902
5	CEBPB	chr9:25016586-25016879	IMR90	lung:	n/a	chr9:25016717-25016728
6	CEBPB	chr9:25295738-25295836	H1-hESC	embryonic stem cell:	n/a	chr9:25295792-25295803
7	CEBPB	chr9:25113820-25114148	IMR90	lung:	n/a	chr9:25113981-25113994 chr9:25113981-25113994 chr9:25113982-25113993 chr9:25113981-25113994 chr9:25113981-25113992
8	CEBPB	chr9:25061791-25062224	A549	lung:	n/a	chr9:25061891-25061902
9	CEBPB	chr9:25184538-25184836	HepG2	liver:	n/a	chr9:25184693-25184704
10	CEBPB	chr9:25184536-25184742	IMR90	lung:	n/a	chr9:25184693-25184704
11	CEBPB	chr9:25295585-25295836	IMR90	lung:	n/a	chr9:25295792-25295803
12	CEBPB	chr9:25164371-25164613	HepG2	liver:	n/a	chr9:25164483-25164496
13	CEBPB	chr9:25132436-25132726	HepG2	liver:	n/a	chr9:25132558-25132571 chr9:25132558-25132571 chr9:25132558-25132569
14	CEBPB	chr9:25259215-25259447	A549	lung:	n/a	chr9:25259325-25259336
15	CEBPB	chr9:25080282-25080607	HepG2	liver:	n/a	chr9:25080435-25080446
16	CEBPB	chr9:25259212-25259436	HepG2	liver:	n/a	chr9:25259325-25259336
17	CEBPB	chr9:25016672-25016872	H1-hESC	embryonic stem cell:	n/a	chr9:25016717-25016728
18	CEBPB	chr9:25080310-25080602	A549	lung:	n/a	chr9:25080435-25080446
19	CEBPB	chr9:25016591-25016872	Hela-S3	cervix:	n/a	chr9:25016717-25016728
20	CEBPB	chr9:25184541-25184806	A549	lung:	n/a	chr9:25184693-25184704
21	CEBPB	chr9:25076912-25077160	HepG2	liver:	n/a	chr9:25077037-25077048
22	CEBPB	chr9:25113879-25114154	A549	lung:	n/a	chr9:25113981-25113994 chr9:25113981-25113994 chr9:25113982-25113993 chr9:25113981-25113994 chr9:25113981-25113992
23	CEBPB	chr9:25175043-25175302	HepG2	liver:	n/a	chr9:25175179-25175190
24	CEBPB	chr9:25197108-25197307	HepG2	liver:	n/a	chr9:25197184-25197195
25	CEBPB	chr9:25149576-25149833	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr9:25016549-25016871	HepG2	liver:	n/a	chr9:25016717-25016728
27	CEBPB	chr9:25209441-25209662	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr9:25195131-25195416	A549	lung:	n/a	chr9:25195249-25195260
29	CEBPB	chr9:25113838-25114177	HepG2	liver:	n/a	chr9:25113981-25113994 chr9:25113981-25113994 chr9:25113982-25113993 chr9:25113981-25113994 chr9:25113981-25113992
30	CEBPB	chr9:25195122-25195409	IMR90	lung:	n/a	chr9:25195249-25195260
31	CEBPB	chr9:25191472-25191672	HepG2	liver:	n/a	n/a
32	CEBPB	chr9:25328436-25328691	HepG2	liver:	n/a	chr9:25328557-25328570 chr9:25328557-25328568 chr9:25328559-25328568 chr9:25328558-25328569
33	CEBPB	chr9:25246228-25246529	A549	lung:	n/a	n/a
34	CEBPB	chr9:25328439-25328664	A549	lung:	n/a	chr9:25328557-25328570 chr9:25328557-25328568 chr9:25328559-25328568 chr9:25328558-25328569
35	CEBPB	chr9:24997515-24997658	A549	lung:	n/a	chr9:24997567-24997580 chr9:24997567-24997578 chr9:24997567-24997580 chr9:24997567-24997580
36	CEBPB	chr9:25040306-25040459	IMR90	lung:	n/a	n/a
37	CEBPB	chr9:24997436-24997715	HepG2	liver:	n/a	chr9:24997567-24997580 chr9:24997567-24997578 chr9:24997567-24997580 chr9:24997567-24997580
38	CEBPB	chr9:25080318-25080550	Hela-S3	cervix:	n/a	chr9:25080435-25080446
39	CEBPB	chr9:25174966-25175239	A549	lung:	n/a	chr9:25175179-25175190
40	CEBPB	chr9:25032987-25033173	A549	lung:	n/a	n/a
41	CEBPB	chr9:25012655-25012930	HepG2	liver:	n/a	chr9:25012799-25012808 chr9:25012799-25012808 chr9:25012797-25012810 chr9:25012799-25012808 chr9:25012798-25012809 chr9:25012797-25012810 chr9:25012799-25012808 chr9:25012797-25012808
42	CEBPB	chr9:25132402-25132676	A549	lung:	n/a	chr9:25132558-25132571 chr9:25132558-25132571 chr9:25132558-25132569
43	CEBPB	chr9:25295517-25295831	A549	lung:	n/a	chr9:25295792-25295803
44	CEBPB	chr9:25263243-25263382	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr9:25012702-25012900	A549	lung:	n/a	chr9:25012799-25012808 chr9:25012799-25012808 chr9:25012797-25012810 chr9:25012799-25012808 chr9:25012798-25012809 chr9:25012797-25012810 chr9:25012799-25012808 chr9:25012797-25012808
46	CEBPB	chr9:25195102-25195400	HepG2	liver:	n/a	chr9:25195249-25195260
47	CEBPB	chr9:25197074-25197259	A549	lung:	n/a	chr9:25197184-25197195
48	CEBPB	chr9:25030939-25031206	A549	lung:	n/a	chr9:25031104-25031115 chr9:25031051-25031062
49	CEBPB	chr9:24997422-24997735	IMR90	lung:	n/a	chr9:24997567-24997580 chr9:24997567-24997578 chr9:24997567-24997580 chr9:24997567-24997580
50	CEBPB	chr9:25093460-25093660	HepG2	liver:	n/a	chr9:25093560-25093571

No.	Distal block	Cell Line	Cell type
1	chr9:25267661..25270080-chr9:25677540..25679201,2	MCF-7	breast:
2	chr9:25135319..25136895-chr9:25139782..25142029,2	MCF-7	breast:
3	chr9:25292451..25293431-chr9:25673511..25674229,2	MCF-7	breast:
4	chr9:25096345..25098093-chr9:25100107..25101850,2	MCF-7	breast:
5	chr9:25261310..25262090-chr9:25716255..25716920,2	MCF-7	breast:
6	chr9:25321931..25322446-chr9:25349957..25350559,2	MCF-7	breast:
7	chr9:25135319..25136895-chr9:25139782..25142029,2	MCF-7	breast:
8	chr9:25175084..25177209-chr9:25178097..25179794,2	MCF-7	breast:
9	chr9:25346387..25349185-chr9:25351167..25353046,2	MCF-7	breast:
10	chr9:24613953..24614528-chr9:25350122..25350850,2	MCF-7	breast:
11	chr9:25349920..25350511-chr9:25716130..25716944,2	MCF-7	breast:
12	chr9:25350133..25352434-chr9:25677647..25679713,3	MCF-7	breast:
13	chr9:25321931..25322446-chr9:25349957..25350559,2	MCF-7	breast:
14	chr9:25175084..25177209-chr9:25178097..25179794,2	MCF-7	breast:
15	chr9:25096345..25098093-chr9:25100107..25101850,2	MCF-7	breast:
16	chr9:25352690..25354379-chr9:25676635..25678931,2	MCF-7	breast:
17	chr9:25346387..25349185-chr9:25351167..25353046,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TUSC1-1	chr9:25290336-25290489	NONHSAT130499
2	lnc-TUSC1-1	chr9:25288488-25288555	NONHSAT130499
3	lnc-IZUMO3-1	chr9:25088809-25089149	NONHSAT130498

Variant related genes	Relation type
RN7SKP120	TF binding region
ENSG00000198680	chromatin interactions

Extended variants
information (count: 3285 )
Associated
traits (count: 152 )

Variant overlapped rSNPs/rCNVs (count:3285 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527443698	chr9:24995822-24995823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs143298358	chr9:24995835-24995836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147539524	chr9:24995842-24995843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567330214	chr9:24995846-24995847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188065246	chr9:24995857-24995858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375339858	chr9:24995862-24995863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs1889776	chr9:24995870-24995871	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs60886386	chr9:24995930-24995931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538250841	chr9:24995933-24995934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558389170	chr9:24995955-24995956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs578215757	chr9:24995969-24995970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540816870	chr9:24996019-24996020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs193097567	chr9:24996023-24996024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76064061	chr9:24996043-24996044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574166914	chr9:24996046-24996047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs116379622	chr9:24996053-24996054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs73469737	chr9:24996071-24996072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs553535625	chr9:24996116-24996117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185535522	chr9:24996118-24996119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545085325	chr9:24996135-24996136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs565177831	chr9:24996145-24996146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188448895	chr9:24996195-24996196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs578236766	chr9:24996232-24996233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs193057032	chr9:24996234-24996235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547552742	chr9:24996241-24996242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545609263	chr9:24996283-24996284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563805920	chr9:24996286-24996287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs554223385	chr9:24996301-24996302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs184101375	chr9:24996328-24996329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs566840451	chr9:24996337-24996338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188488152	chr9:24996346-24996347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191442371	chr9:24996383-24996384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569421870	chr9:24996410-24996411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs10966626	chr9:24996417-24996418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1461331	chr9:24996421-24996422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189293901	chr9:24996447-24996448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs559300174	chr9:24996475-24996476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373770149	chr9:24996482-24996483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs113108195	chr9:24996547-24996548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534260151	chr9:24996600-24996601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554464698	chr9:24996605-24996606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182184250	chr9:24996607-24996608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs187258208	chr9:24996625-24996626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190096321	chr9:24996648-24996649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs138255223	chr9:24996651-24996652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs111681456	chr9:24996678-24996679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs117721452	chr9:24996716-24996717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs369292709	chr9:24996744-24996745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538130687	chr9:24996749-24996750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs527698528	chr9:24996804-24996805	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:152)

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
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
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	21811587	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	21215367	CNVD
Chordoma	21215367	CNVD
Bipolar disorder	19114987	CNVD
Non-small cell lung cancer	16651412	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:24995800-24997000	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr9:25003000-25004200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr9:25003200-25003800	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr9:25003400-25003600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
5	chr9:25003400-25003800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr9:25003400-25004200	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr9:25003400-25004200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr9:25003400-25004400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr9:25003600-25003800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
10	chr9:25003600-25004400	Enhancers	H1 Cell Line	embryonic stem cell
11	chr9:25004000-25004400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr9:25004000-25004600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr9:25021800-25022000	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
14	chr9:25048400-25048800	Enhancers	Adipose Nuclei	Adipose
15	chr9:25050400-25050600	Enhancers	Adipose Nuclei	Adipose
16	chr9:25076800-25077200	Enhancers	Hela-S3	cervix
17	chr9:25090600-25091000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr9:25090600-25091000	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr9:25091000-25091400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr9:25115000-25115600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr9:25115600-25117400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr9:25117400-25118000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr9:25118000-25119600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr9:25118400-25120200	Enhancers	Fetal Lung	lung
25	chr9:25119600-25120000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr9:25177800-25178200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr9:25178000-25179000	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr9:25201600-25204600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr9:25204400-25205000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr9:25204400-25205200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr9:25204600-25205200	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr9:25204600-25205600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr9:25204600-25205800	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr9:25204800-25206400	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr9:25205000-25205600	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr9:25205000-25206000	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr9:25205000-25206200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr9:25205000-25206400	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr9:25205200-25205400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr9:25205200-25205600	Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr9:25205400-25205600	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr9:25205600-25205800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr9:25205600-25206000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr9:25205600-25206000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr9:25205600-25206000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr9:25205600-25206000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
47	chr9:25205800-25206400	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr9:25206000-25206400	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr9:25206000-25206400	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr9:25206000-25206400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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