Variant report

Variant	nsv995049
Chromosome Location	chr9:26162115-26760535
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	chr9:26562360-26562554	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:26746655-26746928	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:26744401-26744755	HepG2	liver:	n/a	n/a
4	ATF2	chr9:26637055-26637518	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr9:26746311-26747148	GM12878	blood:	n/a	n/a
6	ATF2	chr9:26637101-26637510	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr9:26261860-26262340	A549	lung:	n/a	n/a
8	BACH1	chr9:26466284-26466388	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr9:26746447-26747018	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:26217484-26217659	H1-hESC	embryonic stem cell:	n/a	chr9:26217549-26217563
11	BATF	chr9:26234964-26235147	GM12878	blood:	n/a	chr9:26235038-26235049 chr9:26235039-26235049
12	BATF	chr9:26234932-26235150	GM12878	blood:	n/a	chr9:26235038-26235049 chr9:26235039-26235049
13	BCL3	chr9:26261760-26262350	A549	lung:	n/a	n/a
14	BHLHE40	chr9:26326577-26326743	HepG2	liver:	n/a	n/a
15	BHLHE40	chr9:26398178-26398243	A549	lung:	n/a	n/a
16	BHLHE40	chr9:26326640-26326828	GM12878	blood:	n/a	n/a
17	BHLHE40	chr9:26561963-26562264	GM12878	blood:	n/a	n/a
18	BHLHE40	chr9:26746185-26747145	GM12878	blood:	n/a	n/a
19	BRCA1	chr9:26245594-26245856	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr9:26261524-26262299	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr9:26326386-26326867	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr9:26242897-26244299	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr9:26207504-26207553	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr9:26746383-26747096	HCT-116	colon:	n/a	n/a
25	CBX3	chr9:26746522-26747086	HCT-116	colon:	n/a	n/a
26	CEBPB	chr9:26510218-26510495	A549	lung:	n/a	chr9:26510350-26510359 chr9:26510348-26510359 chr9:26510350-26510359 chr9:26510350-26510359 chr9:26510348-26510361
27	CEBPB	chr9:26533884-26534333	HepG2	liver:	n/a	chr9:26534241-26534252
28	CEBPB	chr9:26399635-26399877	A549	lung:	n/a	chr9:26399708-26399719
29	CEBPB	chr9:26292874-26293557	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr9:26364412-26364581	A549	lung:	n/a	n/a
31	CEBPB	chr9:26746742-26746968	MCF-7	breast:	n/a	n/a
32	CEBPB	chr9:26727788-26728098	A549	lung:	n/a	chr9:26727923-26727936 chr9:26727923-26727934 chr9:26727923-26727936
33	CEBPB	chr9:26727899-26727940	H1-hESC	embryonic stem cell:	n/a	chr9:26727923-26727936 chr9:26727923-26727934 chr9:26727923-26727936
34	CEBPB	chr9:26356473-26356831	ECC-1	luminal epithelium:	n/a	chr9:26356616-26356629 chr9:26356616-26356629 chr9:26356618-26356629
35	CEBPB	chr9:26562339-26562734	Hela-S3	cervix:	n/a	chr9:26562535-26562548
36	CEBPB	chr9:26667005-26667349	HepG2	liver:	n/a	chr9:26667180-26667191 chr9:26667178-26667191 chr9:26667178-26667189 chr9:26667178-26667191
37	CEBPB	chr9:26307069-26307347	A549	lung:	n/a	chr9:26307226-26307237 chr9:26307227-26307238 chr9:26307228-26307237
38	CEBPB	chr9:26262794-26263038	A549	lung:	n/a	chr9:26262878-26262889 chr9:26262925-26262936 chr9:26262877-26262890
39	CEBPB	chr9:26540177-26540384	HepG2	liver:	n/a	n/a
40	CEBPB	chr9:26326123-26326815	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr9:26737005-26737170	A549	lung:	n/a	n/a
42	CEBPB	chr9:26571262-26571469	HepG2	liver:	n/a	chr9:26571303-26571314
43	CEBPB	chr9:26531008-26531123	A549	lung:	n/a	n/a
44	CEBPB	chr9:26685947-26686220	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr9:26356606-26356647	A549	lung:	n/a	chr9:26356616-26356629 chr9:26356616-26356629 chr9:26356618-26356629
46	CEBPB	chr9:26261892-26262338	A549	lung:	n/a	n/a
47	CEBPB	chr9:26225106-26225409	A549	lung:	n/a	chr9:26225251-26225260 chr9:26225251-26225260 chr9:26225249-26225260 chr9:26225249-26225262 chr9:26225249-26225262 chr9:26225251-26225260 chr9:26225250-26225261 chr9:26225249-26225260 chr9:26225251-26225260 chr9:26225249-26225262
48	CEBPB	chr9:26727749-26728064	K562	blood:	n/a	chr9:26727923-26727936 chr9:26727923-26727934 chr9:26727923-26727936
49	CEBPB	chr9:26466190-26466376	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr9:26265171-26265679	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:26293669-26293719	HRE	kidney:	n/a
2	chr9:26293669-26293719	GM12878	blood:	n/a
3	chr9:26722560-26722610	PANC-1	pancreas:	n/a
4	chr9:26293669-26293719	HCPEpiC	choroid plexus:	n/a
5	chr9:26293669-26293719	ProgFib	skin:	n/a
6	chr9:26293669-26293719	T-47D	breast:	n/a
7	chr9:26293669-26293719	HRPEpiC	eye:	n/a
8	chr9:26722560-26722610	HRPEpiC	eye:	n/a
9	chr9:26722560-26722610	PrEC	prostate:	n/a
10	chr9:26293669-26293719	AG09309	skin:	n/a
11	chr9:26293669-26293719	SK-N-SH_RA	brain:	n/a
12	chr9:26293669-26293719	PANC-1	pancreas:	n/a
13	chr9:26722560-26722610	HRE	kidney:	n/a
14	chr9:26722560-26722610	NB4	blood:	n/a
15	chr9:26293669-26293719	AoSMC	blood vessel:	n/a
16	chr9:26722560-26722610	AG09319	gingival:	n/a
17	chr9:26722560-26722610	LNCaP	prostate:	n/a
18	chr9:26722560-26722610	SKMC	muscle:	n/a
19	chr9:26293669-26293719	NH-A	brain:	n/a
20	chr9:26293669-26293719	HPAEpiC	pulmonary alveolar:	n/a
21	chr9:26722560-26722610	PFSK-1	brain:	n/a
22	chr9:26293669-26293719	HCM	heart:	n/a
23	chr9:26722560-26722610	K562	blood:	n/a
24	chr9:26293669-26293719	SK-N-SH	brain:	n/a
25	chr9:26722560-26722610	HCM	heart:	n/a
26	chr9:26293669-26293719	GM12892	blood:	n/a
27	chr9:26293669-26293719	SKMC	muscle:	n/a
28	chr9:26722560-26722610	HIPEpiC	eye:	n/a
29	chr9:26722560-26722610	NH-A	brain:	n/a
30	chr9:26293669-26293719	IMR90	lung:	fetal
31	chr9:26293669-26293719	K562	blood:	n/a
32	chr9:26722560-26722610	HMEC	breast:	n/a
33	chr9:26293669-26293719	HIPEpiC	eye:	n/a
34	chr9:26293669-26293719	GM12891	blood:	n/a
35	chr9:26722560-26722610	ECC-1	luminal epithelium:	n/a
36	chr9:26293669-26293719	SK-N-MC	brain:	n/a
37	chr9:26722560-26722610	HNPCEpiC	eye:	n/a
38	chr9:26722560-26722610	BE2_C	brain:	n/a
39	chr9:26293669-26293719	Jurkat	blood:	n/a
40	chr9:26722560-26722610	SK-N-SH	brain:	n/a
41	chr9:26293669-26293719	BE2_C	brain:	n/a
42	chr9:26293669-26293719	BJ	skin:	n/a
43	chr9:26293669-26293719	H1-hESC	embryonic stem cell:	embryo
44	chr9:26722560-26722610	Jurkat	blood:	n/a
45	chr9:26722560-26722610	HCPEpiC	choroid plexus:	n/a
46	chr9:26722560-26722610	BJ	skin:	n/a
47	chr9:26722560-26722610	CMK	blood:	n/a
48	chr9:26293669-26293719	HAEpiC	amniotic membrane:	n/a
49	chr9:26293669-26293719	AG04450	lung:	fetal
50	chr9:26293669-26293719	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:26758275..26760056-chr9:26761242..26763572,2	K562	blood:
2	chr9:26744400..26745094-chr9:26856160..26856966,3	MCF-7	breast:
3	chr9:25964124..25964728-chr9:26326171..26327079,3	MCF-7	breast:
4	chr9:26697199..26699954-chr9:26703852..26705743,2	K562	blood:
5	chr2:208730009..208732803-chr9:26161574..26164201,2	MCF-7	breast:
6	chr9:26237527..26239681-chr9:26241580..26243699,2	MCF-7	breast:
7	chr9:26744169..26744992-chr9:26856156..26857045,4	MCF-7	breast:
8	chr9:26326443..26327103-chr9:26862889..26863559,2	MCF-7	breast:
9	chr9:25963971..25964744-chr9:26326247..26327016,2	MCF-7	breast:
10	chr9:26723206..26723920-chr9:26975181..26975897,2	K562	blood:
11	chr9:26751819..26753348-chr9:26754776..26757194,2	MCF-7	breast:
12	chr9:26744400..26745007-chr9:26975049..26975918,2	MCF-7	breast:
13	chr9:26237527..26239681-chr9:26241580..26243699,2	MCF-7	breast:
14	chr9:26722378..26723174-chr9:26856170..26856819,2	MCF-7	breast:
15	chr9:26744529..26745078-chr9:26976174..26976879,2	K562	blood:
16	chr9:26745009..26745599-chr9:26856133..26856633,2	MCF-7	breast:
17	chr9:26751819..26753348-chr9:26754776..26757194,2	MCF-7	breast:
18	chr9:26697199..26699954-chr9:26703852..26705743,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf82-1	chr9:26718906-26718917	XLOC_007661
2	lnc-C9orf82-1	chr9:26716406-26716605	XLOC_007661
3	lnc-C9orf82-3	chr9:26642695-26644593	NONHSAT130585

Variant related genes	Relation type
ENSG00000266429	TF binding region
ENSG00000254261	TF binding region
ENSG00000266429	CpG island
ENSG00000254261	CpG island
ENSG00000096872	chromatin interactions

Extended variants
information (count: 12917 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:12917 , 50 per page) page: 1 2 3 4 5 6 7 ... 259

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147108945	chr9:26162116-26162117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs180724562	chr9:26162117-26162118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548433926	chr9:26162129-26162130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185115162	chr9:26162140-26162141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs117269318	chr9:26162148-26162149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114676932	chr9:26162160-26162161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571061560	chr9:26162241-26162242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538717690	chr9:26162248-26162249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557116326	chr9:26162277-26162278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575268576	chr9:26162340-26162341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536254307	chr9:26162384-26162385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536558868	chr9:26162397-26162398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189924164	chr9:26162408-26162409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369812468	chr9:26162438-26162439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs147758006	chr9:26162483-26162484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540555174	chr9:26162525-26162526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76340513	chr9:26162526-26162527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115627134	chr9:26162549-26162550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73441636	chr9:26162562-26162563	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs544264441	chr9:26162587-26162588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562653779	chr9:26162610-26162611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35404869	chr9:26162663-26162664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs398087219	chr9:26162668-26162669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs397707198	chr9:26162669-26162670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73645314	chr9:26162706-26162707	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs181591448	chr9:26162727-26162728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560575960	chr9:26162743-26162744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186713455	chr9:26162759-26162760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79733515	chr9:26162778-26162779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs74848432	chr9:26162794-26162795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552864984	chr9:26162843-26162844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192013885	chr9:26162946-26162947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577288460	chr9:26163040-26163041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369324003	chr9:26163050-26163051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141040147	chr9:26163111-26163112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543274407	chr9:26163112-26163113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183781624	chr9:26163159-26163160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113681212	chr9:26163175-26163176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541502261	chr9:26163283-26163284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs36013673	chr9:26163284-26163285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561876843	chr9:26163296-26163297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568967385	chr9:26163304-26163305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536390400	chr9:26163307-26163308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537462029	chr9:26163309-26163310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556473154	chr9:26163310-26163311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528991479	chr9:26163394-26163395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533816682	chr9:26163409-26163410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558828086	chr9:26163442-26163443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576589564	chr9:26163443-26163444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544006441	chr9:26163444-26163445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:123)

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
Pancreatic cancer	21811587	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
polycythaemia	22829968	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioblastoma multiforme	21525872	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1275 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:26160600-26164400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr9:26161600-26163600	Weak transcription	NHDF-Ad	bronchial
3	chr9:26161800-26163600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr9:26163600-26164400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr9:26163600-26165000	Enhancers	NHDF-Ad	bronchial
6	chr9:26163800-26164600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr9:26164000-26164600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr9:26164200-26164800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr9:26164400-26164600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr9:26164400-26164800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr9:26164400-26165200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr9:26164600-26164800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:26164600-26169200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr9:26164600-26169200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr9:26164800-26165000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr9:26164800-26169800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr9:26165000-26165400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr9:26165400-26167800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr9:26166000-26166200	Enhancers	H9 Cell Line	embryonic stem cell
20	chr9:26166400-26169800	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr9:26167800-26168200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr9:26168000-26168200	Enhancers	HMEC	breast
23	chr9:26168200-26168400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr9:26168200-26169600	Enhancers	NHDF-Ad	bronchial
25	chr9:26168400-26168600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr9:26168400-26169600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr9:26168600-26172200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr9:26169000-26171600	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr9:26169200-26170000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr9:26169200-26170000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr9:26169200-26170200	Enhancers	A549	lung
32	chr9:26169200-26175600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr9:26169400-26171000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr9:26169600-26169800	Flanking Active TSS	NHDF-Ad	bronchial
35	chr9:26169600-26170000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr9:26169600-26170600	Enhancers	NHEK	skin
37	chr9:26169600-26170800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr9:26169600-26170800	Enhancers	Hela-S3	cervix
39	chr9:26169600-26170800	Enhancers	HSMMtube	muscle
40	chr9:26169600-26170800	Enhancers	NH-A	brain
41	chr9:26169600-26171000	Enhancers	HSMM	muscle
42	chr9:26169800-26170000	Enhancers	H9 Cell Line	embryonic stem cell
43	chr9:26169800-26170000	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr9:26169800-26170000	Enhancers	NHDF-Ad	bronchial
45	chr9:26169800-26170200	Enhancers	Adipose Nuclei	Adipose
46	chr9:26169800-26170800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr9:26169800-26170800	Enhancers	Muscle Satellite Cultured Cells	--
48	chr9:26169800-26170800	Enhancers	HMEC	breast
49	chr9:26169800-26172400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr9:26170000-26170200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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