Variant report

Variant	nsv1053205
Chromosome Location	chr9:95119195-95182612
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:276)
CpG islands
(count:244)
Chromatin interactive
region (count:30)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:276 , 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	chr9:95148207-95148373	K562	blood:	n/a	n/a
2	ARID3A	chr9:95169172-95169291	K562	blood:	n/a	n/a
3	ATF1	chr9:95155044-95155244	K562	blood:	n/a	n/a
4	ATF1	chr9:95175015-95175032	K562	blood:	n/a	n/a
5	ATF1	chr9:95168868-95169191	K562	blood:	n/a	n/a
6	ATF1	chr9:95173630-95173701	K562	blood:	n/a	n/a
7	BHLHE40	chr9:95160027-95160031	K562	blood:	n/a	n/a
8	BHLHE40	chr9:95168948-95169148	K562	blood:	n/a	n/a
9	BHLHE40	chr9:95168188-95168553	K562	blood:	n/a	n/a
10	BHLHE40	chr9:95121998-95122133	GM12878	blood:	n/a	n/a
11	BHLHE40	chr9:95122482-95122638	GM12878	blood:	n/a	n/a
12	CBX3	chr9:95137774-95138068	K562	blood:	n/a	n/a
13	CBX3	chr9:95135488-95135818	K562	blood:	n/a	n/a
14	CEBPB	chr9:95163391-95163420	HepG2	liver:	n/a	chr9:95163404-95163415
15	CEBPB	chr9:95166906-95167258	IMR90	lung:	n/a	chr9:95167075-95167086 chr9:95167077-95167086 chr9:95167076-95167087
16	CEBPB	chr9:95148300-95148607	IMR90	lung:	n/a	n/a
17	CEBPB	chr9:95166953-95167204	A549	lung:	n/a	chr9:95167075-95167086 chr9:95167077-95167086 chr9:95167076-95167087
18	CEBPB	chr9:95165101-95165284	HepG2	liver:	n/a	chr9:95165218-95165231
19	CEBPB	chr9:95146692-95146990	IMR90	lung:	n/a	n/a
20	CEBPB	chr9:95148145-95148732	HCT-116	colon:	n/a	n/a
21	CEBPB	chr9:95173408-95173841	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr9:95147807-95148647	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr9:95166932-95167201	HepG2	liver:	n/a	chr9:95167075-95167086 chr9:95167077-95167086 chr9:95167076-95167087
24	CTCF	chr9:95155480-95155630	AG04450	lung:	n/a	chr9:95155579-95155587
25	CTCF	chr9:95169020-95169170	GM12873	blood:	n/a	n/a
26	CTCF	chr9:95157780-95157930	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr9:95157900-95158050	NHLF	lung:	n/a	n/a
28	CTCF	chr9:95169069-95169097	K562	blood:	n/a	n/a
29	CTCF	chr9:95154781-95154878	GM10248	blood:	n/a	n/a
30	CTCF	chr9:95140320-95140470	WI-38	lung:	n/a	n/a
31	CTCF	chr9:95169080-95169230	NB4	blood:	n/a	n/a
32	CTCF	chr9:95169120-95169270	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr9:95157840-95157990	NHDF-neo	bronchial:	n/a	n/a
34	CTCF	chr9:95168935-95169185	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr9:95157840-95157990	HPF	lung:	n/a	n/a
36	CTCF	chr9:95159641-95159714	GM20000	blood:	n/a	n/a
37	CTCF	chr9:95148460-95148610	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr9:95182540-95182690	MCF-7	breast:	n/a	n/a
39	CTCF	chr9:95157860-95158010	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr9:95169068-95169161	Lung_OC	lung:	n/a	n/a
41	CTCF	chr9:95140580-95140730	GM12865	blood:	n/a	n/a
42	CTCF	chr9:95169060-95169210	NHLF	lung:	n/a	n/a
43	CUX1	chr9:95169339-95169697	K562	blood:	n/a	n/a
44	CUX1	chr9:95155807-95155828	GM12878	blood:	n/a	n/a
45	E2F4	chr9:95148194-95148605	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr9:95136850-95136958	MCF10A-Er-Src	breast:	n/a	n/a
47	ELK1	chr9:95169048-95169080	K562	blood:	n/a	n/a
48	EP300	chr9:95147917-95148715	Hela-S3	cervix:	n/a	chr9:95148707-95148715 chr9:95148418-95148427
49	EP300	chr9:95172708-95173138	SK-N-SH_RA	brain:	n/a	n/a
50	EP300	chr9:95172672-95173102	SK-N-SH_RA	brain:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:95140430-95140480	AG04450	lung:	fetal
2	chr9:95140430-95140480	T-47D	breast:	n/a
3	chr9:95140430-95140480	ovcar-3	ovarian:	n/a
4	chr9:95140430-95140480	HPAEpiC	pulmonary alveolar:	n/a
5	chr9:95181961-95182011	BJ	skin:	n/a
6	chr9:95153962-95154012	HEK293	kidney:	embryo
7	chr9:95181961-95182011	PFSK-1	brain:	n/a
8	chr9:95153962-95154012	GM06990	blood:	n/a
9	chr9:95140430-95140480	SK-N-MC	brain:	n/a
10	chr9:95181961-95182011	HMEC	breast:	n/a
11	chr9:95146356-95146406	HNPCEpiC	eye:	n/a
12	chr9:95140430-95140480	GM06990	blood:	n/a
13	chr9:95146356-95146406	NB4	blood:	n/a
14	chr9:95140430-95140480	NHBE	bronchial:	n/a
15	chr9:95146356-95146406	BE2_C	brain:	n/a
16	chr9:95181961-95182011	AG09319	gingival:	n/a
17	chr9:95153962-95154012	SAEC	small airway:	n/a
18	chr9:95140430-95140480	HRCEpiC	kidney:	n/a
19	chr9:95153962-95154012	HCT-116	colon:	n/a
20	chr9:95181961-95182011	HIPEpiC	eye:	n/a
21	chr9:95153962-95154012	HRCEpiC	kidney:	n/a
22	chr9:95181961-95182011	GM19239	blood:	n/a
23	chr9:95153962-95154012	MCF-7	breast:	n/a
24	chr9:95140430-95140480	K562	blood:	n/a
25	chr9:95146356-95146406	GM12878	blood:	n/a
26	chr9:95153962-95154012	SK-N-SH	brain:	n/a
27	chr9:95146356-95146406	GM12891	blood:	n/a
28	chr9:95181961-95182011	ovcar-3	ovarian:	n/a
29	chr9:95146356-95146406	HMEC	breast:	n/a
30	chr9:95140430-95140480	HAEpiC	amniotic membrane:	n/a
31	chr9:95140430-95140480	AG10803	skin:	n/a
32	chr9:95153962-95154012	K562	blood:	n/a
33	chr9:95181961-95182011	HCPEpiC	choroid plexus:	n/a
34	chr9:95181961-95182011	AG09309	skin:	n/a
35	chr9:95153962-95154012	HNPCEpiC	eye:	n/a
36	chr9:95181961-95182011	SAEC	small airway:	n/a
37	chr9:95146356-95146406	HEEpiC	esophagus:	n/a
38	chr9:95153962-95154012	NB4	blood:	n/a
39	chr9:95146356-95146406	HIPEpiC	eye:	n/a
40	chr9:95146356-95146406	NHDF-neo	bronchial:	n/a
41	chr9:95146356-95146406	SK-N-SH	brain:	n/a
42	chr9:95153962-95154012	GM12892	blood:	n/a
43	chr9:95153962-95154012	HMEC	breast:	n/a
44	chr9:95153962-95154012	HCPEpiC	choroid plexus:	n/a
45	chr9:95146356-95146406	GM19239	blood:	n/a
46	chr9:95146356-95146406	PFSK-1	brain:	n/a
47	chr9:95181961-95182011	HEK293	kidney:	embryo
48	chr9:95181961-95182011	ProgFib	skin:	n/a
49	chr9:95181961-95182011	BE2_C	brain:	n/a
50	chr9:95181961-95182011	T-47D	breast:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:95162747..95164508-chr9:95166825..95168545,2	MCF-7	breast:
2	chr9:95128615..95130359-chr9:95138980..95141028,2	MCF-7	breast:
3	chr9:95140461..95141981-chr9:107509705..107511221,2	MCF-7	breast:
4	chr9:95127021..95128965-chr9:95271997..95274273,2	K562	blood:
5	chr9:95121837..95124746-chr9:95134544..95136364,2	MCF-7	breast:
6	chr9:95086147..95089104-chr9:95166950..95169643,2	K562	blood:
7	chr9:95087119..95088886-chr9:95124074..95126235,2	MCF-7	breast:
8	chr9:95121837..95124746-chr9:95134544..95136364,2	MCF-7	breast:
9	chr9:95134609..95136461-chr9:95140478..95143032,2	K562	blood:
10	chr9:95134609..95136461-chr9:95140478..95143032,2	K562	blood:
11	chr9:95114363..95116588-chr9:95118609..95121490,2	K562	blood:
12	chr9:95180874..95182571-chr9:95184247..95186990,2	MCF-7	breast:
13	chr9:95176367..95178140-chr9:95181429..95184023,2	K562	blood:
14	chr9:95178951..95181323-chr9:95182899..95185671,2	K562	blood:
15	chr9:95175562..95177754-chr9:95179592..95182058,2	K562	blood:
16	chr9:95182280..95184197-chr9:95185829..95189194,3	K562	blood:
17	chr9:95123897..95125833-chr9:95129339..95132296,2	MCF-7	breast:
18	chr9:95179674..95182574-chr9:95182721..95184992,2	MCF-7	breast:
19	chr9:95138915..95141758-chr9:95143289..95145635,2	K562	blood:
20	chr9:95175562..95177754-chr9:95179592..95182058,2	K562	blood:
21	chr9:95056921..95058643-chr9:95144243..95146810,2	K562	blood:
22	chr9:95123897..95125833-chr9:95129339..95132296,2	MCF-7	breast:
23	chr9:95057188..95059914-chr9:95129364..95132359,2	K562	blood:
24	chr9:95111056..95113852-chr9:95145115..95147395,2	K562	blood:
25	chr2:240321650..240323210-chr9:95170170..95172647,2	MCF-7	breast:
26	chr9:95128615..95130359-chr9:95138980..95141028,2	MCF-7	breast:
27	chr9:95138915..95141758-chr9:95143289..95145635,2	K562	blood:
28	chr9:95155268..95158925-chr9:95160273..95163246,4	K562	blood:
29	chr9:95176367..95178140-chr9:95181429..95184023,2	K562	blood:
30	chr9:95179422..95181955-chr9:95199838..95202240,2	MCF-7	breast:

No data

Variant related genes	Relation type
OGN	TF binding region
OGN	CpG island
ENSG00000136783	chromatin interactions
ENSG00000188312	chromatin interactions
ENSG00000127083	chromatin interactions
ENSG00000222020	chromatin interactions
ENSG00000068024	chromatin interactions
ENSG00000106809	chromatin interactions
ENSG00000198000	chromatin interactions

Extended variants
information (count: 2155 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2155 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1152761	chr9:95119221-95119222	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs139335645	chr9:95119236-95119237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192577184	chr9:95119238-95119239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183783504	chr9:95119242-95119243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571759809	chr9:95119246-95119247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112975886	chr9:95119255-95119256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187939585	chr9:95119273-95119274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529324373	chr9:95119280-95119281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs117200024	chr9:95119356-95119357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543725191	chr9:95119363-95119364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567091851	chr9:95119474-95119475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111456792	chr9:95119484-95119485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372914488	chr9:95119485-95119486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558541261	chr9:95119547-95119548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576977258	chr9:95119587-95119588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs77922687	chr9:95119632-95119633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs199908738	chr9:95119683-95119684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200775356	chr9:95119701-95119702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559585359	chr9:95119735-95119736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370583447	chr9:95119743-95119744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs202067528	chr9:95119744-95119745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201176725	chr9:95119752-95119753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs202204349	chr9:95119774-95119775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146668722	chr9:95119776-95119777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542325882	chr9:95119798-95119799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563700732	chr9:95119837-95119838	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs530782550	chr9:95119869-95119870	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs552849499	chr9:95119894-95119895	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs571013364	chr9:95119904-95119905	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs528685295	chr9:95119910-95119911	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs546835287	chr9:95119933-95119934	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs568303612	chr9:95119952-95119953	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs192051649	chr9:95120000-95120001	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530781788	chr9:95120001-95120002	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs72752406	chr9:95120007-95120008	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs182737912	chr9:95120034-95120035	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577754855	chr9:95120066-95120067	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561089597	chr9:95120067-95120068	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577111957	chr9:95120068-95120069	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541324303	chr9:95120073-95120074	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541336350	chr9:95120081-95120082	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375169064	chr9:95120088-95120089	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553236793	chr9:95120098-95120099	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34445884	chr9:95120135-95120136	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376373524	chr9:95120136-95120137	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551847946	chr9:95120137-95120138	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs398011472	chr9:95120146-95120147	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs80287884	chr9:95120147-95120148	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs202162235	chr9:95120154-95120155	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574662784	chr9:95120155-95120156	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:778 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95089600-95121800	Weak transcription	Fetal Heart	heart
2	chr9:95091000-95120000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr9:95102000-95121000	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr9:95102200-95121400	Weak transcription	A549	lung
5	chr9:95102600-95120800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr9:95104200-95119800	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr9:95104200-95121200	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr9:95113400-95119400	Weak transcription	Fetal Lung	lung
9	chr9:95113400-95121800	Weak transcription	Rectal Smooth Muscle	rectum
10	chr9:95116600-95120000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr9:95116800-95119800	Weak transcription	Lung	lung
12	chr9:95116800-95119800	Weak transcription	Thymus	Thymus
13	chr9:95116800-95122200	Weak transcription	Primary T cells from cord blood	blood
14	chr9:95116800-95127600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr9:95116800-95128600	Weak transcription	Dnd41	blood
16	chr9:95117000-95121600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr9:95117000-95134800	Weak transcription	Ovary	ovary
18	chr9:95118000-95120000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr9:95118000-95135000	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr9:95118800-95119800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr9:95119800-95120000	ZNF genes & repeats	Lung	lung
22	chr9:95119800-95120000	ZNF genes & repeats	Thymus	Thymus
23	chr9:95119800-95120200	ZNF genes & repeats	Fetal Stomach	stomach
24	chr9:95119800-95120200	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
25	chr9:95119800-95120800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr9:95120000-95120200	ZNF genes & repeats	Fetal Intestine Small	intestine
27	chr9:95120000-95120200	ZNF genes & repeats	Fetal Lung	lung
28	chr9:95120000-95120400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr9:95120000-95120600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr9:95120000-95120600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr9:95120000-95120800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
32	chr9:95120000-95131400	Weak transcription	Thymus	Thymus
33	chr9:95120200-95121600	Weak transcription	Fetal Intestine Small	intestine
34	chr9:95120200-95121600	Weak transcription	Fetal Stomach	stomach
35	chr9:95120400-95130600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr9:95120600-95121800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr9:95120600-95128000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr9:95120600-95128600	Weak transcription	K562	blood
39	chr9:95120800-95121800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr9:95120800-95121800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr9:95121600-95122400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr9:95121600-95122400	Enhancers	Fetal Intestine Small	intestine
43	chr9:95121600-95122800	Enhancers	Fetal Stomach	stomach
44	chr9:95121800-95122000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr9:95121800-95122200	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr9:95121800-95122200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr9:95121800-95122200	Flanking Active TSS	Rectal Smooth Muscle	rectum
48	chr9:95121800-95122200	Enhancers	Stomach Smooth Muscle	stomach
49	chr9:95121800-95122400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr9:95121800-95122400	Enhancers	Primary monocytes fromperipheralblood	blood

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