Variant report

Variant	nsv892018
Chromosome Location	chr9:1124136-1235993
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:258)
CpG islands
(count:0)
Chromatin interactive
region (count:37)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:1232418-1233152	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:1165172-1165199	HepG2	liver:	n/a	n/a
3	BATF	chr9:1232670-1232943	GM12878	blood:	n/a	n/a
4	BHLHE40	chr9:1157837-1158199	GM12878	blood:	n/a	n/a
5	BHLHE40	chr9:1184742-1184955	GM12878	blood:	n/a	n/a
6	CEBPB	chr9:1233638-1233904	A549	lung:	n/a	n/a
7	CEBPB	chr9:1232528-1233024	HepG2	liver:	n/a	chr9:1232708-1232721 chr9:1232709-1232720 chr9:1232805-1232816
8	CEBPB	chr9:1232593-1232789	HepG2	liver:	n/a	chr9:1232708-1232721 chr9:1232709-1232720
9	CEBPB	chr9:1198121-1198664	MCF-7	breast:	n/a	n/a
10	CEBPB	chr9:1233604-1233963	HepG2	liver:	n/a	n/a
11	CEBPB	chr9:1233454-1233961	IMR90	lung:	n/a	n/a
12	CEBPB	chr9:1208265-1208585	IMR90	lung:	n/a	n/a
13	CEBPB	chr9:1232585-1232851	A549	lung:	n/a	chr9:1232708-1232721 chr9:1232709-1232720 chr9:1232805-1232816
14	CEBPB	chr9:1198107-1198494	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr9:1200905-1201341	HepG2	liver:	n/a	n/a
16	CEBPB	chr9:1173097-1173543	MCF-7	breast:	n/a	n/a
17	CEBPB	chr9:1232402-1232946	MCF-7	breast:	n/a	chr9:1232708-1232721 chr9:1232709-1232720 chr9:1232805-1232816
18	CEBPB	chr9:1198034-1198533	MCF-7	breast:	n/a	n/a
19	CEBPB	chr9:1198214-1198422	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr9:1232307-1233098	MCF-7	breast:	n/a	chr9:1233061-1233072 chr9:1232708-1232721 chr9:1232709-1232720 chr9:1232805-1232816
21	CEBPB	chr9:1232072-1232973	IMR90	lung:	n/a	chr9:1232708-1232721 chr9:1232709-1232720 chr9:1232805-1232816
22	CHD2	chr9:1200927-1201034	HepG2	liver:	n/a	n/a
23	CTCF	chr9:1173620-1173770	MCF-7	breast:	n/a	n/a
24	CTCF	chr9:1151940-1152090	NB4	blood:	n/a	n/a
25	CTCF	chr9:1222060-1222210	GM12867	blood:	n/a	n/a
26	CTCF	chr9:1156934-1157091	MCF-7	breast:	n/a	n/a
27	CTCF	chr9:1160180-1160330	GM12873	blood:	n/a	n/a
28	CTCF	chr9:1185120-1185270	GM12865	blood:	n/a	n/a
29	CTCF	chr9:1232000-1232150	NHDF-neo	bronchial:	n/a	n/a
30	CTCF	chr9:1211460-1211610	MCF-7	breast:	n/a	chr9:1211479-1211492 chr9:1211479-1211488 chr9:1211476-1211494 chr9:1211479-1211492
31	CTCF	chr9:1211440-1211784	MCF-7	breast:	n/a	chr9:1211479-1211492 chr9:1211479-1211488 chr9:1211476-1211494 chr9:1211479-1211492
32	CTCF	chr9:1211607-1211700	MCF-7	breast:	n/a	n/a
33	CTCF	chr9:1156939-1157087	MCF-7	breast:	n/a	n/a
34	CTCF	chr9:1211609-1211695	MCF-7	breast:	n/a	n/a
35	CTCF	chr9:1156920-1157070	MCF-7	breast:	n/a	n/a
36	CTCF	chr9:1211537-1211723	MCF-7	breast:	n/a	n/a
37	CTCF	chr9:1216472-1216482	Fibrobl	skin:	n/a	n/a
38	CTCF	chr9:1224000-1224045	NHEK	skin:	n/a	n/a
39	CTCF	chr9:1156940-1157090	MCF-7	breast:	n/a	n/a
40	CTCF	chr9:1232060-1232210	AG10803	skin:	n/a	n/a
41	CTCF	chr9:1211387-1211766	MCF-7	breast:	n/a	chr9:1211479-1211492 chr9:1211479-1211488 chr9:1211476-1211494 chr9:1211479-1211492
42	CTCF	chr9:1139523-1139567	GM20000	blood:	n/a	n/a
43	CTCF	chr9:1156994-1157045	MCF-7	breast:	n/a	n/a
44	CTCF	chr9:1211540-1211690	HEK293	kidney:	n/a	n/a
45	CTCF	chr9:1142328-1142394	GM10248	blood:	n/a	n/a
46	CTCF	chr9:1156926-1157033	GM12878	blood:	n/a	n/a
47	CTCF	chr9:1211496-1211741	MCF-7	breast:	n/a	n/a
48	CTCF	chr9:1211571-1211649	HepG2	liver:	n/a	n/a
49	CTCF	chr9:1211520-1211670	MCF-7	breast:	n/a	n/a
50	CTCF	chr9:1216920-1217070	GM06990	blood:	n/a	chr9:1217029-1217037

No data

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:1207734..1210015-chr9:1211203..1213257,2	MCF-7	breast:
2	chr9:1196784..1199122-chr9:1220785..1223370,2	MCF-7	breast:
3	chr9:1196174..1202144-chr9:1204882..1208508,8	MCF-7	breast:
4	chr9:1163342..1166297-chr9:1170947..1173135,2	MCF-7	breast:
5	chr9:1196174..1202144-chr9:1204882..1208508,8	MCF-7	breast:
6	chr9:1050050..1050882-chr9:1198084..1198894,4	MCF-7	breast:
7	chr9:1036905..1039413-chr9:1128661..1130161,2	MCF-7	breast:
8	chr9:1167206..1169983-chr9:1171593..1173584,2	MCF-7	breast:
9	chr9:1048965..1051949-chr9:1170856..1173228,2	MCF-7	breast:
10	chr9:1049962..1051601-chr9:1206448..1208602,2	MCF-7	breast:
11	chr9:1199075..1201039-chr9:1246978..1249972,2	K562	blood:
12	chr9:1155504..1158028-chr9:1171284..1172916,2	MCF-7	breast:
13	chr17:35897413..35898334-chr9:1234312..1235126,2	MCF-7	breast:
14	chr9:1207734..1210015-chr9:1211203..1213257,2	MCF-7	breast:
15	chr9:1048591..1051547-chr9:1195558..1198367,2	MCF-7	breast:
16	chr9:1050662..1052458-chr9:1210912..1212810,2	MCF-7	breast:
17	chr9:1050169..1051008-chr9:1198034..1198952,5	MCF-7	breast:
18	chr9:1050736..1051474-chr9:1211377..1212172,7	MCF-7	breast:
19	chr9:1048644..1051362-chr9:1182528..1184402,2	MCF-7	breast:
20	chr9:1050302..1051381-chr9:1211162..1212085,6	MCF-7	breast:
21	chr9:1156903..1158809-chr9:1163538..1165114,2	MCF-7	breast:
22	chr9:1124326..1126756-chr9:1130042..1131544,2	MCF-7	breast:
23	chr9:1050299..1051218-chr9:1211358..1212168,3	MCF-7	breast:
24	chr9:1017784..1019327-chr9:1158625..1160475,2	MCF-7	breast:
25	chr9:1196784..1199122-chr9:1220785..1223370,2	MCF-7	breast:
26	chr9:1048582..1050101-chr9:1206689..1209470,2	MCF-7	breast:
27	chr9:1167206..1169983-chr9:1171593..1173584,2	MCF-7	breast:
28	chr9:1120059..1122097-chr9:1123938..1125710,2	K562	blood:
29	chr9:1197110..1199229-chr9:1201325..1204281,3	MCF-7	breast:
30	chr9:1156562..1162179-chr9:1163960..1167701,5	MCF-7	breast:
31	chr4:183090047..183090870-chr9:1152117..1153038,2	MCF-7	breast:
32	chr9:1124326..1126756-chr9:1130042..1131544,2	MCF-7	breast:
33	chr9:1172064..1174566-chr9:1177825..1179718,2	MCF-7	breast:
34	chr9:1197110..1199229-chr9:1201325..1204281,3	MCF-7	breast:
35	chr9:1172064..1174566-chr9:1177825..1179718,2	MCF-7	breast:
36	chr9:1049307..1051830-chr9:1209993..1212929,2	MCF-7	breast:
37	chr9:1155504..1158028-chr9:1171284..1172916,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf66-12	chr9:1151807-1152140	NONHSAT129965
2	lnc-C9orf66-13	chr9:1164414-1164867	NONHSAT129966

No data

Variant related genes	Relation type
ENSG00000224836	TF binding region
RPS27AP14	TF binding region
ENSG00000236594	chromatin interactions
ENSG00000221227	chromatin interactions
ENSG00000173253	chromatin interactions
ENSG00000006114	chromatin interactions

Extended variants
information (count: 3170 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:3170 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17795397	chr9:1124136-1124137	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs545989056	chr9:1124149-1124150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138422359	chr9:1124172-1124173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528549735	chr9:1124173-1124174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs542306327	chr9:1124213-1124214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148982143	chr9:1124265-1124266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145793229	chr9:1124273-1124274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530912098	chr9:1124293-1124294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138498741	chr9:1124307-1124308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4740472	chr9:1124322-1124323	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs534437264	chr9:1124333-1124334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533357354	chr9:1124339-1124340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546740486	chr9:1124393-1124394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112856520	chr9:1124430-1124431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565898898	chr9:1124463-1124464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552790639	chr9:1124492-1124493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534458192	chr9:1124510-1124511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115167947	chr9:1124511-1124512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572923317	chr9:1124556-1124557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189350271	chr9:1124577-1124578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143044881	chr9:1124596-1124597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556992502	chr9:1124612-1124613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535036966	chr9:1124635-1124636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546025746	chr9:1124658-1124659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs68167478	chr9:1124675-1124676	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs573066023	chr9:1124686-1124687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541985583	chr9:1124736-1124737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562184084	chr9:1124745-1124746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530824397	chr9:1124756-1124757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544554034	chr9:1124780-1124781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181738312	chr9:1124805-1124806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs77009586	chr9:1124813-1124814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187068034	chr9:1124924-1124925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146068611	chr9:1124927-1124928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189862023	chr9:1124928-1124929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs375212678	chr9:1124937-1124938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554741224	chr9:1124958-1124959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529471013	chr9:1124993-1124994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10959574	chr9:1124996-1124997	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs568115045	chr9:1125067-1125068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369778935	chr9:1125102-1125103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536660097	chr9:1125107-1125108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181554954	chr9:1125113-1125114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs148304555	chr9:1125117-1125118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539786441	chr9:1125144-1125145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531696636	chr9:1125266-1125267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373545601	chr9:1125283-1125284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544057420	chr9:1125287-1125288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112483843	chr9:1125316-1125317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553289707	chr9:1125322-1125323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	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
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
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
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Cancer	21272361	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Esophageal cancer	21851588	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:321 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:1120200-1125600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr9:1125600-1125800	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr9:1125600-1125800	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr9:1125600-1126200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr9:1125800-1128800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr9:1127800-1129600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr9:1127800-1129800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr9:1128200-1129600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
9	chr9:1128400-1129400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr9:1128800-1129400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr9:1128800-1129800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr9:1128800-1130200	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr9:1129200-1129600	Enhancers	H9 Cell Line	embryonic stem cell
14	chr9:1129200-1129800	Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr9:1129200-1130200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr9:1129200-1130200	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr9:1129400-1129600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
18	chr9:1129400-1129600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
19	chr9:1129600-1129800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr9:1129600-1130000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr9:1129600-1130200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
22	chr9:1129600-1130400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
23	chr9:1129800-1130000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr9:1129800-1130400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
25	chr9:1130000-1130400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
26	chr9:1130200-1130400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
27	chr9:1140800-1141000	ZNF genes & repeats	Pancreas	Pancrea
28	chr9:1154600-1155800	Enhancers	Muscle Satellite Cultured Cells	--
29	chr9:1156800-1157200	Enhancers	Fetal Muscle Leg	muscle
30	chr9:1159200-1159400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr9:1159600-1162400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr9:1162400-1162800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr9:1169800-1170000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr9:1170000-1173000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr9:1170800-1171600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr9:1171000-1172200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr9:1171200-1171400	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr9:1171200-1172400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr9:1171400-1171600	Enhancers	Colonic Mucosa	Colon
40	chr9:1171400-1172200	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr9:1171600-1172000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr9:1171600-1172400	Weak transcription	Colonic Mucosa	Colon
43	chr9:1171600-1173000	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr9:1172000-1172400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr9:1172000-1172400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr9:1172200-1172600	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr9:1172400-1173800	Enhancers	Colonic Mucosa	Colon
48	chr9:1172600-1173400	Enhancers	Sigmoid Colon	Sigmoid Colon
49	chr9:1173000-1173400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr9:1173000-1173600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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