Variant report

Variant	nsv892837
Chromosome Location	chr9:25713816-25825595
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:303)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:43)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr9:25761278-25761303	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr9:25783890-25784164	HepG2	liver:	n/a	chr9:25784053-25784064 chr9:25784055-25784064
3	CEBPB	chr9:25739358-25739637	A549	lung:	n/a	chr9:25739524-25739537 chr9:25739524-25739537 chr9:25739524-25739535 chr9:25739524-25739537 chr9:25739524-25739535
4	CEBPB	chr9:25742343-25742555	HepG2	liver:	n/a	chr9:25742446-25742459 chr9:25742447-25742458
5	CEBPB	chr9:25742271-25742634	HepG2	liver:	n/a	chr9:25742446-25742459 chr9:25742447-25742458
6	CEBPB	chr9:25742380-25742601	H1-hESC	embryonic stem cell:	n/a	chr9:25742446-25742459 chr9:25742447-25742458
7	CEBPB	chr9:25763598-25763944	HepG2	liver:	n/a	chr9:25763776-25763787
8	CEBPB	chr9:25761129-25761425	HepG2	liver:	n/a	chr9:25761277-25761288
9	CEBPB	chr9:25763654-25763950	A549	lung:	n/a	chr9:25763776-25763787
10	CEBPB	chr9:25748958-25749217	ECC-1	luminal epithelium:	n/a	chr9:25749030-25749041
11	CEBPB	chr9:25742264-25742634	HepG2	liver:	n/a	chr9:25742446-25742459 chr9:25742447-25742458
12	CEBPB	chr9:25724495-25724789	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr9:25763645-25763886	H1-hESC	embryonic stem cell:	n/a	chr9:25763776-25763787
14	CEBPB	chr9:25783879-25784164	IMR90	lung:	n/a	chr9:25784053-25784064 chr9:25784055-25784064
15	CEBPB	chr9:25724429-25724877	IMR90	lung:	n/a	n/a
16	CEBPB	chr9:25763626-25763962	IMR90	lung:	n/a	chr9:25763776-25763787
17	CEBPB	chr9:25742346-25742582	HepG2	liver:	n/a	chr9:25742446-25742459 chr9:25742447-25742458
18	CEBPD	chr9:25742337-25742570	HepG2	liver:	n/a	n/a
19	CTCF	chr9:25727900-25728050	HEK293	kidney:	n/a	n/a
20	CTCF	chr9:25716260-25716510	GM12866	blood:	n/a	n/a
21	CTCF	chr9:25716360-25716510	AG04450	lung:	n/a	n/a
22	CTCF	chr9:25716380-25716530	AG04450	lung:	n/a	n/a
23	CTCF	chr9:25716360-25716510	SAEC	small airway:	n/a	n/a
24	CTCF	chr9:25716259-25716659	MCF-7	breast:	n/a	n/a
25	CTCF	chr9:25716380-25716530	AG09319	gingival:	n/a	n/a
26	CTCF	chr9:25716380-25716530	SAEC	small airway:	n/a	n/a
27	CTCF	chr9:25716348-25716583	LNCaP	prostate:	n/a	n/a
28	CTCF	chr9:25716380-25716530	AoAF	blood vessel:	n/a	n/a
29	CTCF	chr9:25716360-25716510	NHLF	lung:	n/a	n/a
30	CTCF	chr9:25716100-25716250	HFF	foreskin:	n/a	n/a
31	CTCF	chr9:25716336-25716593	MCF-7	breast:	n/a	n/a
32	CTCF	chr9:25716380-25716530	NHEK	skin:	n/a	n/a
33	CTCF	chr9:25716400-25716550	HVMF	connective:	n/a	n/a
34	CTCF	chr9:25716420-25716570	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr9:25716400-25716550	GM12872	blood:	n/a	n/a
36	CTCF	chr9:25716360-25716510	MCF-7	breast:	n/a	n/a
37	CTCF	chr9:25716400-25716550	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr9:25734263-25734303	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr9:25716360-25716510	HPF	lung:	n/a	n/a
40	CTCF	chr9:25716360-25716510	NHEK	skin:	n/a	n/a
41	CTCF	chr9:25716317-25716622	ProgFib	skin:	n/a	n/a
42	CTCF	chr9:25716604-25716605	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr9:25716400-25716550	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr9:25769883-25769937	GM13976	blood:	n/a	n/a
45	CTCF	chr9:25716400-25716550	HepG2	liver:	n/a	n/a
46	CTCF	chr9:25716310-25716611	MCF-7	breast:	n/a	n/a
47	CTCF	chr9:25716380-25716530	HCM	heart:	n/a	n/a
48	CTCF	chr9:25716340-25716603	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr9:25716448-25716454	MCF-7	breast:	n/a	n/a
50	CTCF	chr9:25716400-25716550	HA-sp	spinal cord:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:25677137..25679533-chr9:25758553..25761140,2	MCF-7	breast:
2	chr9:25349920..25350511-chr9:25716130..25716944,2	MCF-7	breast:
3	chr9:25736248..25739126-chr9:25740036..25742643,2	MCF-7	breast:
4	chr9:25676380..25678945-chr9:25713748..25715266,2	MCF-7	breast:
5	chr9:25736248..25739126-chr9:25740036..25742643,2	MCF-7	breast:
6	chr9:25261310..25262090-chr9:25716255..25716920,2	MCF-7	breast:
7	chr9:25612676..25613650-chr9:25715920..25716890,2	MCF-7	breast:

(count:43 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFT74-3	chr9:25780054-25780166	XLOC_007306
2	lnc-IFT74-3	chr9:25784413-25784614	XLOC_007306
3	lnc-IFT74-8	chr9:25774413-25774614	ucscGeneNc_uc003zpy_2
4	lnc-IFT74-3	chr9:25798743-25798941	NONHSAT130503
5	lnc-IFT74-3	chr9:25798032-25798204	XLOC_007306
6	lnc-IFT74-3	chr9:25812619-25812963	XLOC_007306
7	lnc-IFT74-8	chr9:25770054-25770166	NONHSAT130502
8	lnc-IFT74-3	chr9:25812619-25812942	XLOC_007306
9	lnc-IFT74-3	chr9:25780414-25780615	XLOC_007306
10	lnc-IFT74-3	chr9:25798743-25798941	XLOC_007306
11	lnc-IFT74-8	chr9:25802619-25802963	ucscGeneNc_uc003zpy_2
12	lnc-IFT74-3	chr9:25798032-25798204	NONHSAT130503
13	lnc-IFT74-3	chr9:25780075-25780166	XLOC_007306
14	lnc-IFT74-3	chr9:25780414-25780615	XLOC_007306
15	lnc-IFT74-3	chr9:25798743-25798941	XLOC_007306
16	lnc-IFT74-3	chr9:25784413-25784614	XLOC_007306
17	lnc-IFT74-3	chr9:25780414-25780615	NONHSAT130503
18	lnc-IFT74-3	chr9:25784413-25784614	NONHSAT130503
19	lnc-IFT74-3	chr9:25780075-25780166	XLOC_007306
20	lnc-IFT74-8	chr9:25788743-25788941	ucscGeneNc_uc003zpy_2
21	lnc-IFT74-3	chr9:25780054-25780166	XLOC_007306
22	lnc-IFT74-3	chr9:25798743-25798941	XLOC_007306
23	lnc-IFT74-3	chr9:25802427-25802517	XLOC_007306
24	lnc-IFT74-3	chr9:25812619-25812966	NONHSAT130503
25	lnc-IFT74-3	chr9:25804154-25804257	XLOC_007306
26	lnc-IFT74-8	chr9:25788032-25788204	ucscGeneNc_uc003zpy_2
27	lnc-IFT74-3	chr9:25784413-25784560	XLOC_007306
28	lnc-IFT74-3	chr9:25780414-25780615	XLOC_007306
29	lnc-IFT74-3	chr9:25798032-25798205	XLOC_007306
30	lnc-IFT74-3	chr9:25806693-25806736	XLOC_007306
31	lnc-IFT74-3	chr9:25804154-25804257	XLOC_007306
32	lnc-IFT74-3	chr9:25798032-25798204	XLOC_007306
33	lnc-IFT74-3	chr9:25802427-25802517	XLOC_007306
34	lnc-IFT74-8	chr9:25770414-25770615	ucscGeneNc_uc003zpy_2
35	lnc-IFT74-3	chr9:25806594-25806736	XLOC_007306
36	lnc-IFT74-8	chr9:25774413-25774560	NONHSAT130502
37	lnc-IFT74-8	chr9:25770414-25770615	NONHSAT130502
38	lnc-IFT74-3	chr9:25780414-25780615	XLOC_007306
39	lnc-IFT74-3	chr9:25784413-25784614	XLOC_007306
40	lnc-IFT74-8	chr9:25770054-25770166	ucscGeneNc_uc003zpy_2
41	lnc-IFT74-3	chr9:25806594-25806736	XLOC_007306
42	lnc-IFT74-3	chr9:25780054-25780166	NONHSAT130503
43	lnc-IFT74-3	chr9:25812619-25812942	XLOC_007306

No data

Variant related genes	Relation type
ENSG00000236306	TF binding region
ENSG00000198680	chromatin interactions
FBXW7	miRNA target sites
ARID5B	miRNA target sites
PDE4D	miRNA target sites
DEPDC1	miRNA target sites
RNF182	miRNA target sites
PRPF38B	miRNA target sites
FAM49B	miRNA target sites

Extended variants
information (count: 1529 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:1529 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12005755	chr9:25713816-25713817	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568848382	chr9:25713851-25713852	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs572532986	chr9:25713857-25713858	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs546323554	chr9:25713862-25713863	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs564642651	chr9:25713870-25713871	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs531958562	chr9:25713992-25713993	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs541637321	chr9:25714018-25714019	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs16909632	chr9:25714096-25714097	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs562292399	chr9:25714129-25714130	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs529682021	chr9:25714246-25714247	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs576656428	chr9:25714273-25714274	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs140229951	chr9:25714294-25714295	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs563027056	chr9:25714328-25714329	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs143972713	chr9:25714339-25714340	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs545473976	chr9:25714370-25714371	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs201651515	chr9:25714371-25714372	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs189054798	chr9:25714396-25714397	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs564069493	chr9:25714421-25714422	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs16909634	chr9:25714478-25714479	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs528077318	chr9:25714483-25714484	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs556423151	chr9:25714519-25714520	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs539006340	chr9:25714537-25714538	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs574685926	chr9:25714579-25714580	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs535752573	chr9:25714580-25714581	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs553836374	chr9:25714678-25714679	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs572494435	chr9:25714726-25714727	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs368630616	chr9:25714729-25714730	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs372675488	chr9:25714758-25714759	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs147292247	chr9:25714771-25714772	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs140940905	chr9:25714802-25714803	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs180967178	chr9:25714811-25714812	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs114632777	chr9:25714814-25714815	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs2074259	chr9:25714851-25714852	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs149894160	chr9:25714855-25714856	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs548089943	chr9:25714954-25714955	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs559682768	chr9:25715014-25715015	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs559106263	chr9:25715016-25715017	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs371024527	chr9:25715030-25715031	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs7021492	chr9:25715070-25715071	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs186068130	chr9:25715072-25715073	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs7021695	chr9:25715128-25715129	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs375262104	chr9:25715130-25715131	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs76937379	chr9:25715132-25715133	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs568250308	chr9:25715164-25715165	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs535360031	chr9:25715209-25715210	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs181413624	chr9:25715602-25715603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs199610921	chr9:25715603-25715604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539751941	chr9:25715622-25715623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185939059	chr9:25715654-25715655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570051659	chr9:25715692-25715693	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Medulloblastoma	21979893	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
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
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Hodgkin''s lymphoma	18179710	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
Esophageal adenocarcinoma	18519675	CNVD
Pancreatic cancer	21811587	CNVD
Bipolar disorder	19114987	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
polycythaemia	22829968	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:25715600-25716400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:25715600-25716400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr9:25715600-25716400	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr9:25715800-25716200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr9:25715800-25716400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr9:25715800-25716400	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr9:25715800-25716400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr9:25715800-25716400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr9:25715800-25716600	Enhancers	Fetal Heart	heart
10	chr9:25716000-25716400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr9:25716000-25716400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr9:25716000-25716400	Enhancers	Fetal Intestine Small	intestine
13	chr9:25716000-25716400	Enhancers	Hela-S3	cervix
14	chr9:25716000-25716600	Enhancers	Colon Smooth Muscle	Colon
15	chr9:25716000-25716800	Enhancers	Fetal Kidney	kidney
16	chr9:25716200-25716400	Enhancers	Adipose Nuclei	Adipose
17	chr9:25716200-25716400	Enhancers	Pancreas	Pancrea
18	chr9:25716200-25716600	Enhancers	H1 Cell Line	embryonic stem cell
19	chr9:25716200-25716600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr9:25716400-25721200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr9:25716400-25721800	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr9:25716800-25724400	Weak transcription	Fetal Kidney	kidney
23	chr9:25721000-25721600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr9:25721000-25721800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr9:25721000-25721800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr9:25721200-25721800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr9:25721600-25724000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr9:25721800-25722400	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr9:25721800-25724000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr9:25721800-25724200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr9:25721800-25724400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr9:25724000-25724600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr9:25724000-25724600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr9:25724200-25724600	Enhancers	Muscle Satellite Cultured Cells	--
35	chr9:25724200-25724600	Enhancers	Hela-S3	cervix
36	chr9:25724200-25724600	Active TSS	HMEC	breast
37	chr9:25724200-25724600	Active TSS	NHEK	skin
38	chr9:25724200-25725600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr9:25724400-25724600	Enhancers	Fetal Kidney	kidney
40	chr9:25724400-25725000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr9:25724600-25727200	Weak transcription	Fetal Kidney	kidney
42	chr9:25726800-25727200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr9:25726800-25727400	Enhancers	Rectal Smooth Muscle	rectum
44	chr9:25727000-25727800	Enhancers	Fetal Stomach	stomach
45	chr9:25727200-25728400	Enhancers	Fetal Kidney	kidney
46	chr9:25731200-25731800	Enhancers	Gastric	stomach
47	chr9:25731200-25732800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr9:25740200-25742400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr9:25740400-25740800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr9:25740800-25741200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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