Variant report

Variant	nsv539910
Chromosome Location	chr9:1096993-1189143
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	chr9:1165172-1165199	HepG2	liver:	n/a	n/a
2	BHLHE40	chr9:1184742-1184955	GM12878	blood:	n/a	n/a
3	BHLHE40	chr9:1157837-1158199	GM12878	blood:	n/a	n/a
4	CEBPB	chr9:1110151-1110411	HepG2	liver:	n/a	chr9:1110272-1110283
5	CEBPB	chr9:1098609-1098809	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr9:1173097-1173543	MCF-7	breast:	n/a	n/a
7	CEBPB	chr9:1110139-1110339	A549	lung:	n/a	chr9:1110272-1110283
8	CEBPB	chr9:1115880-1116108	HepG2	liver:	n/a	chr9:1116009-1116020
9	CTCF	chr9:1101000-1101150	Hela-S3	cervix:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
10	CTCF	chr9:1101060-1101210	GM12872	blood:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
11	CTCF	chr9:1100948-1101265	MCF-7	breast:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
12	CTCF	chr9:1101038-1101221	SK-N-SH_RA	brain:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
13	CTCF	chr9:1101080-1101230	NHDF-neo	bronchial:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
14	CTCF	chr9:1101000-1101150	AG04450	lung:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
15	CTCF	chr9:1101040-1101190	AG04449	skin:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
16	CTCF	chr9:1101080-1101230	HL-60	blood:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
17	CTCF	chr9:1100859-1101390	MCF-7	breast:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
18	CTCF	chr9:1101060-1101210	MCF-7	breast:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
19	CTCF	chr9:1101020-1101170	GM12868	blood:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
20	CTCF	chr9:1101040-1101190	SAEC	small airway:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
21	CTCF	chr9:1101060-1101210	NHLF	lung:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
22	CTCF	chr9:1160180-1160330	GM12873	blood:	n/a	n/a
23	CTCF	chr9:1100962-1101279	MCF-7	breast:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
24	CTCF	chr9:1120080-1120230	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr9:1101027-1101229	GM13977	blood:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
26	CTCF	chr9:1101100-1101250	HEEpiC	esophagus:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
27	CTCF	chr9:1101061-1101199	Spleen_OC	spleen:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
28	CTCF	chr9:1101060-1101210	SAEC	small airway:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
29	CTCF	chr9:1100960-1101110	GM12869	blood:	n/a	n/a
30	CTCF	chr9:1101080-1101230	GM12867	blood:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
31	CTCF	chr9:1101020-1101170	HFF	foreskin:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
32	CTCF	chr9:1151940-1152090	NB4	blood:	n/a	n/a
33	CTCF	chr9:1101020-1101170	Caco-2	colon:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
34	CTCF	chr9:1101100-1101250	GM12868	blood:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
35	CTCF	chr9:1101008-1101253	HepG2	liver:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
36	CTCF	chr9:1101080-1101230	GM12866	blood:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
37	CTCF	chr9:1101045-1101171	GM13976	blood:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
38	CTCF	chr9:1101080-1101230	GM12872	blood:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
39	CTCF	chr9:1101031-1101193	SK-N-SH_RA	brain:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
40	CTCF	chr9:1101020-1101170	GM12873	blood:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
41	CTCF	chr9:1101020-1101170	HFF-Myc	foreskin:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
42	CTCF	chr9:1101040-1101190	HRPEpiC	eye:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
43	CTCF	chr9:1101007-1101218	GM12892	blood:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
44	CTCF	chr9:1100980-1101304	T-47D	breast:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
45	CTCF	chr9:1101040-1101190	HRE	kidney:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
46	CTCF	chr9:1101040-1101190	WERI-Rb-1	eye:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
47	CTCF	chr9:1100996-1101234	LNCaP	prostate:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
48	CTCF	chr9:1100974-1101266	Gliobla	brain:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
49	CTCF	chr9:1101026-1101212	Hela-S3	cervix:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136
50	CTCF	chr9:1101060-1101210	HCPEpiC	choroid plexus:	n/a	chr9:1101123-1101130 chr9:1101119-1101137 chr9:1101121-1101142 chr9:1101120-1101136

No.	Distal block	Cell Line	Cell type
1	chr9:1100620..1101481-chr9:1337009..1337893,4	MCF-7	breast:
2	chr9:1100954..1101519-chr9:1619985..1620571,2	MCF-7	breast:
3	chr9:1100638..1101499-chr9:1337048..1337780,3	MCF-7	breast:
4	chr9:1156562..1162179-chr9:1163960..1167701,5	MCF-7	breast:
5	chr9:1167206..1169983-chr9:1171593..1173584,2	MCF-7	breast:
6	chr9:1155504..1158028-chr9:1171284..1172916,2	MCF-7	breast:
7	chr9:1017784..1019327-chr9:1158625..1160475,2	MCF-7	breast:
8	chr9:1167206..1169983-chr9:1171593..1173584,2	MCF-7	breast:
9	chr9:1155504..1158028-chr9:1171284..1172916,2	MCF-7	breast:
10	chr9:1124326..1126756-chr9:1130042..1131544,2	MCF-7	breast:
11	chr9:1100633..1101579-chr9:1428962..1429946,8	MCF-7	breast:
12	chr9:1120059..1122097-chr9:1123938..1125710,2	K562	blood:
13	chr9:1100898..1101474-chr9:1619645..1620185,2	MCF-7	breast:
14	chr9:1156903..1158809-chr9:1163538..1165114,2	MCF-7	breast:
15	chr9:1163342..1166297-chr9:1170947..1173135,2	MCF-7	breast:
16	chr9:1048644..1051362-chr9:1182528..1184402,2	MCF-7	breast:
17	chr9:1172064..1174566-chr9:1177825..1179718,2	MCF-7	breast:
18	chr4:183090047..183090870-chr9:1152117..1153038,2	MCF-7	breast:
19	chr9:1124326..1126756-chr9:1130042..1131544,2	MCF-7	breast:
20	chr9:1172064..1174566-chr9:1177825..1179718,2	MCF-7	breast:
21	chr9:1048965..1051949-chr9:1170856..1173228,2	MCF-7	breast:
22	chr9:1120059..1122097-chr9:1123938..1125710,2	K562	blood:
23	chr9:1036905..1039413-chr9:1128661..1130161,2	MCF-7	breast:
24	chr9:1101941..1102561-chr9:1429407..1430134,2	MCF-7	breast:
25	chr9:613569..614095-chr9:1100690..1101615,2	MCF-7	breast:

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

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

Extended variants
information (count: 1782 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:1782 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558666169	chr9:1097011-1097012	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs565643870	chr9:1097032-1097033	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534574307	chr9:1097046-1097047	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76852540	chr9:1097060-1097061	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs60568067	chr9:1097068-1097069	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1355140	chr9:1097069-1097070	Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs1355141	chr9:1097089-1097090	Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs576671011	chr9:1097133-1097134	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545680098	chr9:1097190-1097191	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186994205	chr9:1098616-1098617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554128276	chr9:1098622-1098623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574288526	chr9:1098649-1098650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542782858	chr9:1098694-1098695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs77344430	chr9:1098708-1098709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs562769170	chr9:1098735-1098736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143570649	chr9:1098747-1098748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs116226793	chr9:1098774-1098775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs73639862	chr9:1098790-1098791	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs532745669	chr9:1098834-1098835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546585975	chr9:1098838-1098839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs566616622	chr9:1098870-1098871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540140243	chr9:1098879-1098880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369543645	chr9:1098880-1098881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs75857685	chr9:1098901-1098902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs552062276	chr9:1098939-1098940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs202236958	chr9:1098940-1098941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs199549799	chr9:1098948-1098949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs549178821	chr9:1098953-1098954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543640867	chr9:1098954-1098955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs146829659	chr9:1098968-1098969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535667579	chr9:1099008-1099009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs7025718	chr9:1099019-1099020	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs555954016	chr9:1099053-1099054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7040663	chr9:1099073-1099074	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs533904683	chr9:1099101-1099102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191435910	chr9:1099154-1099155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs533606400	chr9:1099162-1099163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553470568	chr9:1099202-1099203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs545848752	chr9:1099203-1099204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs148533587	chr9:1099252-1099253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs373761108	chr9:1099259-1099260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs142169325	chr9:1099267-1099268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs556328402	chr9:1099269-1099270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs77520177	chr9:1099294-1099295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183644540	chr9:1099347-1099348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563986939	chr9:1099378-1099379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs188983240	chr9:1099409-1099410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12685238	chr9:1099418-1099419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539821758	chr9:1099435-1099436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs560124375	chr9:1099505-1099506	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Esophageal cancer	21851588	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:1096200-1097000	Enhancers	NHEK	skin
2	chr9:1096600-1097000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr9:1096600-1097200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr9:1097000-1097200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr9:1098600-1099600	Enhancers	Fetal Muscle Leg	muscle
6	chr9:1099600-1100600	Weak transcription	Fetal Muscle Leg	muscle
7	chr9:1100200-1101000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr9:1100600-1101200	Enhancers	Fetal Muscle Leg	muscle
9	chr9:1100800-1101000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
10	chr9:1102400-1102600	Enhancers	Right Atrium	heart
11	chr9:1102400-1102800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr9:1102400-1103000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr9:1102600-1103000	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr9:1102800-1103000	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr9:1102800-1103200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr9:1119800-1120000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr9:1120000-1120200	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr9:1120000-1120200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr9:1120200-1125600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr9:1120400-1120800	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr9:1120400-1121000	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr9:1120600-1121200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr9:1125600-1125800	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr9:1125600-1125800	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr9:1125600-1126200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr9:1125800-1128800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr9:1127800-1129600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr9:1127800-1129800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr9:1128200-1129600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
30	chr9:1128400-1129400	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr9:1128800-1129400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr9:1128800-1129800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr9:1128800-1130200	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr9:1129200-1129600	Enhancers	H9 Cell Line	embryonic stem cell
35	chr9:1129200-1129800	Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr9:1129200-1130200	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr9:1129200-1130200	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr9:1129400-1129600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr9:1129400-1129600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
40	chr9:1129600-1129800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr9:1129600-1130000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr9:1129600-1130200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
43	chr9:1129600-1130400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
44	chr9:1129800-1130000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr9:1129800-1130400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
46	chr9:1130000-1130400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
47	chr9:1130200-1130400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
48	chr9:1140800-1141000	ZNF genes & repeats	Pancreas	Pancrea
49	chr9:1154600-1155800	Enhancers	Muscle Satellite Cultured Cells	--
50	chr9:1156800-1157200	Enhancers	Fetal Muscle Leg	muscle

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