Variant report

Variant	nsv892395
Chromosome Location	chr9:11817216-12370519
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	chr9:12328968-12329168	HepG2	liver:	n/a	n/a
2	BACH1	chr9:12170667-12170713	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr9:12292536-12292567	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr9:12230772-12231081	GM12878	blood:	n/a	n/a
5	BATF	chr9:12329455-12329670	GM12878	blood:	n/a	n/a
6	BCLAF1	chr9:12329426-12329668	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:12328995-12329158	K562	blood:	n/a	n/a
8	BHLHE40	chr9:12328884-12329725	HepG2	liver:	n/a	n/a
9	BHLHE40	chr9:12329021-12329257	GM12878	blood:	n/a	n/a
10	BRCA1	chr9:12368889-12368916	GM12878	blood:	n/a	n/a
11	BRCA1	chr9:12011400-12011402	GM12878	blood:	n/a	n/a
12	CBX3	chr9:12054451-12054644	K562	blood:	n/a	n/a
13	CEBPB	chr9:11933909-11934318	Hela-S3	cervix:	n/a	chr9:11934105-11934116 chr9:11934106-11934117 chr9:11934105-11934118
14	CEBPB	chr9:12012267-12012412	A549	lung:	n/a	n/a
15	CEBPB	chr9:12367335-12367535	HepG2	liver:	n/a	chr9:12367443-12367454
16	CEBPB	chr9:11933995-11934266	ECC-1	luminal epithelium:	n/a	chr9:11934105-11934116 chr9:11934106-11934117 chr9:11934105-11934118
17	CEBPB	chr9:12195470-12195708	H1-hESC	embryonic stem cell:	n/a	chr9:12195611-12195622
18	CEBPB	chr9:12288039-12288167	HepG2	liver:	n/a	n/a
19	CEBPB	chr9:11959566-11959766	K562	blood:	n/a	chr9:11959657-11959668
20	CEBPB	chr9:11968320-11968531	HepG2	liver:	n/a	chr9:11968445-11968456 chr9:11968447-11968456 chr9:11968446-11968457 chr9:11968445-11968458
21	CEBPB	chr9:12195456-12195797	HepG2	liver:	n/a	chr9:12195611-12195622
22	CEBPB	chr9:11934067-11934195	HepG2	liver:	n/a	chr9:11934105-11934116 chr9:11934106-11934117 chr9:11934105-11934118
23	CEBPB	chr9:11933929-11934303	IMR90	lung:	n/a	chr9:11934105-11934116 chr9:11934106-11934117 chr9:11934105-11934118
24	CEBPB	chr9:11946375-11946610	HepG2	liver:	n/a	chr9:11946481-11946492
25	CEBPB	chr9:12195471-12195788	IMR90	lung:	n/a	chr9:12195611-12195622
26	CEBPB	chr9:12193945-12194181	A549	lung:	n/a	chr9:12194071-12194082 chr9:12194071-12194084
27	CEBPB	chr9:11959593-11959818	IMR90	lung:	n/a	chr9:11959657-11959668
28	CEBPB	chr9:12129071-12129335	HepG2	liver:	n/a	n/a
29	CEBPB	chr9:11959508-11959839	HepG2	liver:	n/a	chr9:11959657-11959668
30	CEBPB	chr9:12208833-12209071	HepG2	liver:	n/a	chr9:12208898-12208909 chr9:12208899-12208908 chr9:12208897-12208910
31	CEBPB	chr9:11968269-11968582	A549	lung:	n/a	chr9:11968445-11968456 chr9:11968447-11968456 chr9:11968446-11968457 chr9:11968445-11968458
32	CEBPB	chr9:12180768-12180970	IMR90	lung:	n/a	n/a
33	CEBPB	chr9:12119993-12120079	A549	lung:	n/a	chr9:12120059-12120068 chr9:12120057-12120070 chr9:12120057-12120068
34	CEBPB	chr9:11899316-11899547	A549	lung:	n/a	n/a
35	CEBPB	chr9:12195488-12195695	K562	blood:	n/a	chr9:12195611-12195622
36	CEBPB	chr9:11946400-11946627	IMR90	lung:	n/a	chr9:11946481-11946492
37	CHD1	chr9:12314638-12314797	GM12878	blood:	n/a	n/a
38	CHD2	chr9:12314733-12314838	GM12878	blood:	n/a	n/a
39	CHD2	chr9:12319226-12319370	GM12878	blood:	n/a	n/a
40	CTCF	chr9:12329500-12329650	GM12866	blood:	n/a	n/a
41	CTCF	chr9:12329500-12329650	GM12875	blood:	n/a	n/a
42	CTCF	chr9:12329820-12329970	AG04450	lung:	n/a	n/a
43	CTCF	chr9:12329326-12329665	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr9:12101680-12101830	GM12869	blood:	n/a	n/a
45	CTCF	chr9:12329330-12329693	T-47D	breast:	n/a	n/a
46	CTCF	chr9:12329280-12329352	GM12892	blood:	n/a	n/a
47	CTCF	chr9:12329520-12329670	HPF	lung:	n/a	n/a
48	CTCF	chr9:12329500-12329650	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr9:12329520-12329670	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr9:12055107-12055140	GM13976	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:89002000..89004763-chr9:12244429..12246932,2	MCF-7	breast:
2	chr9:10855828..10856443-chr9:12329128..12329639,2	MCF-7	breast:
3	chr9:12268631..12271178-chr9:12273434..12276211,2	K562	blood:
4	chr9:10365979..10366914-chr9:12329143..12329893,2	MCF-7	breast:
5	chr9:12094328..12096426-chr9:12096756..12098736,2	K562	blood:
6	chr9:12182493..12185046-chr9:12186407..12189303,2	K562	blood:
7	chr9:12268631..12271178-chr9:12273434..12276211,2	K562	blood:
8	chr9:12182493..12185046-chr9:12186407..12189303,2	K562	blood:
9	chr9:12094328..12096426-chr9:12096756..12098736,2	K562	blood:
10	chr18:21570976..21573123-chr9:12145530..12147030,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTPRD-5	chr9:11829221-11829360	XLOC_007647
2	lnc-MPDZ-2	chr9:12116821-12116865	XLOC_007648
3	lnc-TYRP1-4	chr9:12287320-12288238	NONHSAT130222
4	lnc-PTPRD-5	chr9:11829210-11829360	XLOC_007647
5	lnc-PTPRD-10	chr9:11824674-11824988	l_3733_chr9:11816028-11824988_testes
6	lnc-PTPRD-10	chr9:11819221-11819360	l_3733_chr9:11816028-11824988_testes
7	lnc-PTPRD-5	chr9:11834674-11834988	XLOC_007647
8	lnc-MPDZ-2	chr9:12098660-12099015	XLOC_007648
9	lnc-PTPRD-5	chr9:11822678-11822704	XLOC_007647
10	lnc-MPDZ-2	chr9:12116821-12116865	XLOC_007648
11	lnc-MPDZ-2	chr9:12159117-12159147	XLOC_007648
12	lnc-PTPRD-5	chr9:11834674-11834959	XLOC_007647
13	lnc-MPDZ-9	chr9:12149117-12149147	NONHSAT130219
14	lnc-MPDZ-2	chr9:12098714-12099015	XLOC_007648
15	lnc-PTPRD-5	chr9:11826175-11826601	XLOC_007647
16	lnc-PTPRD-5	chr9:11834674-11834959	XLOC_007647
17	lnc-MPDZ-9	chr9:12136273-12136401	NONHSAT130219
18	lnc-MPDZ-2	chr9:12139007-12139044	XLOC_007648
19	lnc-MPDZ-9	chr9:12106821-12106865	NONHSAT130219
20	lnc-PTPRD-5	chr9:11829221-11829360	XLOC_007647
21	lnc-MPDZ-2	chr9:12146273-12146401	XLOC_007648
22	lnc-MPDZ-9	chr9:12088660-12089015	NONHSAT130219

Variant related genes	Relation type
ENSG00000231491	TF binding region
ENSG00000224935	TF binding region
RNU2-47P	TF binding region
ENSG00000168234	chromatin interactions
ENSG00000261226	chromatin interactions
CSF1	miRNA target sites
CUL5	miRNA target sites
FLOT2	miRNA target sites

Extended variants
information (count: 8250 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:8250 , 50 per page) page: 1 2 3 4 5 6 7 ... 165

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112037897	chr9:11819210-11819211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs533141558	chr9:11819227-11819228	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs531657	chr9:11819241-11819242	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs190204274	chr9:11819248-11819249	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs12237037	chr9:11819258-11819259	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs1684826	chr9:11819281-11819282	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs528933432	chr9:11819285-11819286	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs368015755	chr9:11819307-11819308	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs565301012	chr9:11819309-11819310	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs542213051	chr9:11819310-11819311	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs10960274	chr9:11819319-11819320	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs551635407	chr9:11819320-11819321	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs373163936	chr9:11819332-11819333	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs571640962	chr9:11819333-11819334	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs1300036	chr9:11819357-11819358	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs184626136	chr9:11819390-11819391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs114922875	chr9:11819400-11819401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10960275	chr9:11819429-11819430	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs536310805	chr9:11819451-11819452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553522087	chr9:11819456-11819457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573249083	chr9:11819469-11819470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12235141	chr9:11819477-11819478	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs564361951	chr9:11819486-11819487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1684824	chr9:11819488-11819489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146555359	chr9:11819529-11819530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189189780	chr9:11819551-11819552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561066453	chr9:11819576-11819577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs180871077	chr9:11819582-11819583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548638742	chr9:11819584-11819585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1300035	chr9:11819596-11819597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373959985	chr9:11819635-11819636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs75859965	chr9:11819645-11819646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185898004	chr9:11819651-11819652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs139135648	chr9:11819660-11819661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565000577	chr9:11819661-11819662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551002815	chr9:11819675-11819676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs10960276	chr9:11819686-11819687	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs10960277	chr9:11819691-11819692	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs551266364	chr9:11819709-11819710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111684125	chr9:11819759-11819760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181261285	chr9:11819854-11819855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186904493	chr9:11819875-11819876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553485375	chr9:11819890-11819891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570205974	chr9:11819935-11819936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372736745	chr9:11819936-11819937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78048317	chr9:11819959-11819960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373191994	chr9:11819963-11819964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539029312	chr9:11819970-11819971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558942137	chr9:11819977-11819978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190543524	chr9:11819979-11819980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Disorders of sex development	21048976	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Glioblastoma multiforme	21080181	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Cancer	20164920	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Schizophrenia	18511947	CNVD
Schizophrenia	23813976	CNVD
Type 2 diabetes	21526130	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:320 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:11819200-11820000	Weak transcription	Fetal Brain Male	brain
2	chr9:11820000-11820200	Enhancers	Fetal Brain Male	brain
3	chr9:11820000-11821400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr9:11820200-11821000	Weak transcription	Fetal Brain Male	brain
5	chr9:11820600-11822600	Enhancers	Fetal Heart	heart
6	chr9:11820800-11821800	Enhancers	Fetal Brain Female	brain
7	chr9:11820800-11822600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr9:11821000-11823400	Enhancers	Fetal Brain Male	brain
9	chr9:11821400-11821800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr9:11821400-11821800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr9:11821400-11821800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr9:11821400-11821800	Enhancers	Pancreas	Pancrea
13	chr9:11821600-11822000	Enhancers	Placenta Amnion	Placenta Amnion
14	chr9:11821800-11823000	Weak transcription	Fetal Brain Female	brain
15	chr9:11821800-11823200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr9:11823000-11823200	Enhancers	Fetal Brain Female	brain
17	chr9:11823400-11832200	Weak transcription	Fetal Brain Male	brain
18	chr9:11831800-11833000	Enhancers	Fetal Brain Female	brain
19	chr9:11832200-11832600	Enhancers	Fetal Brain Male	brain
20	chr9:11832600-11833600	Weak transcription	Fetal Brain Male	brain
21	chr9:11833600-11833800	Enhancers	Fetal Brain Male	brain
22	chr9:11867200-11868000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr9:11867200-11868000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr9:11867400-11867800	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr9:11868800-11869000	Enhancers	Fetal Brain Female	brain
26	chr9:11869000-11871800	Weak transcription	Fetal Brain Female	brain
27	chr9:11871600-11871800	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr9:11871800-11872400	Enhancers	Fetal Brain Male	brain
29	chr9:11871800-11872600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr9:11871800-11872800	Enhancers	Fetal Brain Female	brain
31	chr9:11874000-11874600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr9:11874000-11874600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr9:11874200-11874600	Enhancers	H1 Cell Line	embryonic stem cell
34	chr9:11874200-11874600	Enhancers	H9 Cell Line	embryonic stem cell
35	chr9:11874200-11874600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr9:11874200-11874600	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr9:11874200-11874600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr9:11874200-11874800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr9:11874200-11875000	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr9:11874200-11875400	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr9:11874600-11875800	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr9:11876000-11876200	Enhancers	H9 Cell Line	embryonic stem cell
43	chr9:11892600-11893200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr9:11892600-11893200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr9:11892800-11893600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr9:11892800-11894200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr9:11893000-11893400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr9:11893200-11894800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr9:11894600-11895000	Enhancers	K562	blood
50	chr9:11894800-11895400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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