Variant report

Variant	nsv892612
Chromosome Location	chr9:14654900-14694302
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:649)
CpG islands
(count:489)
Chromatin interactive
region (count:21)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:649 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:14661451-14661789	K562	blood:	n/a	n/a
2	ATF1	chr9:14661502-14661775	K562	blood:	n/a	n/a
3	ATF2	chr9:14688075-14688638	GM12878	blood:	n/a	n/a
4	ATF2	chr9:14693237-14693620	GM12878	blood:	n/a	n/a
5	BACH1	chr9:14693258-14693548	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr9:14693199-14693708	GM12878	blood:	n/a	n/a
7	BCLAF1	chr9:14693175-14693606	GM12878	blood:	n/a	n/a
8	BCLAF1	chr9:14688097-14688460	GM12878	blood:	n/a	chr9:14688341-14688350
9	BHLHE40	chr9:14688140-14688529	GM12878	blood:	n/a	n/a
10	BHLHE40	chr9:14692950-14693814	GM12878	blood:	n/a	chr9:14693117-14693133
11	BHLHE40	chr9:14689247-14689350	GM12878	blood:	n/a	n/a
12	CBX3	chr9:14654902-14655428	HCT-116	colon:	n/a	n/a
13	CBX3	chr9:14654942-14655330	K562	blood:	n/a	n/a
14	CBX3	chr9:14654909-14655424	HCT-116	colon:	n/a	n/a
15	CBX3	chr9:14654938-14655346	K562	blood:	n/a	n/a
16	CCNT2	chr9:14693300-14693572	K562	blood:	n/a	n/a
17	CEBPB	chr9:14687100-14687489	IMR90	lung:	n/a	n/a
18	CEBPB	chr9:14661506-14661801	K562	blood:	n/a	n/a
19	CHD1	chr9:14693268-14693369	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr9:14693269-14693945	GM12878	blood:	n/a	n/a
21	CHD1	chr9:14688156-14688623	GM12878	blood:	n/a	n/a
22	CHD2	chr9:14693310-14693896	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr9:14692865-14693793	GM12878	blood:	n/a	chr9:14693027-14693037
24	CHD2	chr9:14692666-14692698	HepG2	liver:	n/a	n/a
25	CREB1	chr9:14693169-14693584	A549	lung:	n/a	n/a
26	CREB1	chr9:14693141-14693720	HepG2	liver:	n/a	n/a
27	CTBP2	chr9:14693233-14693890	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr9:14661539-14661855	MCF-7	breast:	n/a	chr9:14661642-14661663
29	CTCF	chr9:14661620-14661770	HL-60	blood:	n/a	chr9:14661642-14661663
30	CTCF	chr9:14661372-14661853	IMR90	lung:	n/a	chr9:14661642-14661663
31	CTCF	chr9:14661540-14661690	GM12873	blood:	n/a	chr9:14661642-14661663
32	CTCF	chr9:14693040-14693190	HepG2	liver:	n/a	n/a
33	CTCF	chr9:14661560-14661710	HEK293	kidney:	n/a	chr9:14661642-14661663
34	CTCF	chr9:14661507-14661791	SK-N-SH_RA	brain:	n/a	chr9:14661642-14661663
35	CTCF	chr9:14661620-14661770	AG09309	skin:	n/a	chr9:14661642-14661663
36	CTCF	chr9:14661620-14661770	Caco-2	colon:	n/a	chr9:14661642-14661663
37	CTCF	chr9:14693035-14693112	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr9:14661560-14661710	HVMF	connective:	n/a	chr9:14661642-14661663
39	CTCF	chr9:14661640-14661790	GM12878	blood:	n/a	chr9:14661642-14661663
40	CTCF	chr9:14661606-14661751	GM10266	blood:	n/a	chr9:14661642-14661663
41	CTCF	chr9:14661480-14661630	HAc	cerebellar:	n/a	n/a
42	CTCF	chr9:14661600-14661750	HCPEpiC	choroid plexus:	n/a	chr9:14661642-14661663
43	CTCF	chr9:14661560-14661710	GM12874	blood:	n/a	chr9:14661642-14661663
44	CTCF	chr9:14693006-14693114	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr9:14661620-14661770	HFF-Myc	foreskin:	n/a	chr9:14661642-14661663
46	CTCF	chr9:14661453-14661803	H1-hESC	embryonic stem cell:	n/a	chr9:14661642-14661663
47	CTCF	chr9:14661620-14661770	HVMF	connective:	n/a	chr9:14661642-14661663
48	CTCF	chr9:14692960-14693110	GM12865	blood:	n/a	n/a
49	CTCF	chr9:14661660-14661810	GM12873	blood:	n/a	n/a
50	CTCF	chr9:14661640-14661790	GM12864	blood:	n/a	chr9:14661642-14661663

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14693648-14693698	A549	lung:	n/a
2	chr9:14693648-14693698	A549	lung:	n/a
3	chr9:14693538-14693588	LNCaP	prostate:	n/a
4	chr9:14692931-14692981	AG10803	skin:	n/a
5	chr9:14693504-14693554	AG04450	lung:	fetal
6	chr9:14692931-14692981	GM19239	blood:	n/a
7	chr9:14693888-14693938	HCF	heart:	n/a
8	chr9:14693082-14693132	HCPEpiC	choroid plexus:	n/a
9	chr9:14693082-14693132	PrEC	prostate:	n/a
10	chr9:14692931-14692981	Caco-2	colon:	n/a
11	chr9:14693538-14693588	AG09319	gingival:	n/a
12	chr9:14693538-14693588	HRCEpiC	kidney:	n/a
13	chr9:14693538-14693588	SK-N-SH_RA	brain:	n/a
14	chr9:14693888-14693938	HEK293	kidney:	embryo
15	chr9:14691289-14691339	K562	blood:	n/a
16	chr9:14690531-14690581	SK-N-SH	brain:	n/a
17	chr9:14693538-14693588	HPAEpiC	pulmonary alveolar:	n/a
18	chr9:14693888-14693938	HNPCEpiC	eye:	n/a
19	chr9:14690531-14690581	Hepatocyte	liver:	n/a
20	chr9:14693888-14693938	AG09309	skin:	n/a
21	chr9:14693648-14693698	Hepatocyte	liver:	n/a
22	chr9:14690531-14690581	HRE	kidney:	n/a
23	chr9:14693538-14693588	Hela-S3	cervix:	n/a
24	chr9:14693648-14693698	GM12878	blood:	n/a
25	chr9:14693648-14693698	ovcar-3	ovarian:	n/a
26	chr9:14691289-14691339	PFSK-1	brain:	n/a
27	chr9:14693538-14693588	NH-A	brain:	n/a
28	chr9:14690531-14690581	SKMC	muscle:	n/a
29	chr9:14691289-14691339	NB4	blood:	n/a
30	chr9:14693888-14693938	NHBE	bronchial:	n/a
31	chr9:14693648-14693698	HCF	heart:	n/a
32	chr9:14693082-14693132	U87	brain:	n/a
33	chr9:14693648-14693698	HMEC	breast:	n/a
34	chr9:14693082-14693132	SKMC	muscle:	n/a
35	chr9:14693648-14693698	PFSK-1	brain:	n/a
36	chr9:14693538-14693588	GM19239	blood:	n/a
37	chr9:14693504-14693554	HNPCEpiC	eye:	n/a
38	chr9:14693082-14693132	HPAEpiC	pulmonary alveolar:	n/a
39	chr9:14692931-14692981	Jurkat	blood:	n/a
40	chr9:14693082-14693132	GM06990	blood:	n/a
41	chr9:14691289-14691339	AG04449	skin:	fetal
42	chr9:14693504-14693554	GM12891	blood:	n/a
43	chr9:14693888-14693938	LNCaP	prostate:	n/a
44	chr9:14693504-14693554	AG09319	gingival:	n/a
45	chr9:14692931-14692981	SK-N-SH	brain:	n/a
46	chr9:14693538-14693588	GM12892	blood:	n/a
47	chr9:14693082-14693132	HCF	heart:	n/a
48	chr9:14693082-14693132	IMR90	lung:	fetal
49	chr9:14693504-14693554	NT2-D1	testis:	n/a
50	chr9:14690531-14690581	IMR90	lung:	fetal

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:14655200..14658776-chr9:14658922..14661546,4	K562	blood:
2	chr9:14671286..14673264-chr9:14676237..14678702,2	K562	blood:
3	chr9:14685829..14688724-chr9:14693473..14695940,2	K562	blood:
4	chr9:14677358..14679032-chr9:14729314..14731148,2	MCF-7	breast:
5	chr9:14655200..14658177-chr9:14659364..14661546,3	K562	blood:
6	chr9:14685829..14688724-chr9:14693473..14695940,2	K562	blood:
7	chr9:14676498..14678344-chr9:14692478..14694843,2	MCF-7	breast:
8	chr9:14652918..14654762-chr9:14661773..14663664,2	MCF-7	breast:
9	chr9:14655200..14658177-chr9:14659364..14661546,3	K562	blood:
10	chr9:14690708..14693231-chr9:14713433..14715842,2	MCF-7	breast:
11	chr9:14616153..14617361-chr9:14660905..14661912,4	MCF-7	breast:
12	chr9:14442256..14442845-chr9:14661275..14662107,4	K562	blood:
13	chr9:14464938..14465658-chr9:14661578..14662250,2	MCF-7	breast:
14	chr9:14678774..14681640-chr9:14758881..14761517,2	MCF-7	breast:
15	chr9:14671286..14673264-chr9:14676237..14678702,2	K562	blood:
16	chr9:14673551..14675387-chr9:14691158..14693433,2	MCF-7	breast:
17	chr9:14693520..14695525-chr9:14717829..14719510,2	MCF-7	breast:
18	chr9:14650294..14652492-chr9:14659969..14661655,2	K562	blood:
19	chr9:14686674..14691236-chr9:14691548..14694778,7	MCF-7	breast:
20	chr10:61799790..61802033-chr9:14680041..14681542,2	MCF-7	breast:
21	chr9:14655200..14658776-chr9:14658922..14661546,4	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CER1-1	chr9:14680031-14680160	NONHSAT130254
2	lnc-CER1-1	chr9:14690335-14690383	NONHSAT130254
3	lnc-CER1-1	chr9:14677364-14677470	NONHSAT130254
4	lnc-CER1-1	chr9:14693227-14693263	NONHSAT130254
5	lnc-CER1-1	chr9:14683569-14683727	NONHSAT130254

No data

Variant related genes	Relation type
ZDHHC21	TF binding region
ZDHHC21	CpG island
ENSG00000175893	chromatin interactions

Extended variants
information (count: 1979 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1979 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7853156	chr9:14654900-14654901	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576966743	chr9:14654915-14654916	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs35910177	chr9:14654940-14654941	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs139851180	chr9:14654952-14654953	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544326762	chr9:14654978-14654979	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561326665	chr9:14655020-14655021	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574426703	chr9:14655025-14655026	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368638118	chr9:14655030-14655031	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182606934	chr9:14655041-14655042	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186579880	chr9:14655044-14655045	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141220193	chr9:14655046-14655047	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs75077920	chr9:14655059-14655060	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562449059	chr9:14655060-14655061	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531434456	chr9:14655075-14655076	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553422337	chr9:14655090-14655091	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs150663470	chr9:14655100-14655101	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568036845	chr9:14655166-14655167	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372199288	chr9:14655190-14655191	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139928080	chr9:14655198-14655199	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376786753	chr9:14655206-14655207	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547331337	chr9:14655219-14655220	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs199890331	chr9:14655235-14655236	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10961638	chr9:14655280-14655281	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs35421808	chr9:14655295-14655296	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191414702	chr9:14655300-14655301	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559104287	chr9:14655306-14655307	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183198343	chr9:14655311-14655312	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538321661	chr9:14655324-14655325	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4542027	chr9:14655330-14655331	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs574515249	chr9:14655337-14655338	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189252384	chr9:14655338-14655339	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149851613	chr9:14655340-14655341	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576681458	chr9:14655346-14655347	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147945281	chr9:14655369-14655370	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567228958	chr9:14655410-14655411	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs193101743	chr9:14655418-14655419	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185121900	chr9:14655428-14655429	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548284729	chr9:14655434-14655435	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561729558	chr9:14655437-14655438	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10961639	chr9:14655458-14655459	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs140204209	chr9:14655465-14655466	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145333821	chr9:14655475-14655476	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147674180	chr9:14655476-14655477	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149160474	chr9:14655519-14655520	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143310963	chr9:14655522-14655523	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538028240	chr9:14655534-14655535	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190051438	chr9:14655557-14655558	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371592530	chr9:14655561-14655562	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs151194602	chr9:14655619-14655620	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533937646	chr9:14655627-14655628	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	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
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
early-passage human iPS cells	21368824	CNVD
Glioblastoma multiforme	18628472	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14597000-14655000	Weak transcription	Stomach Smooth Muscle	stomach
2	chr9:14626800-14655000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr9:14629400-14655000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr9:14631000-14692400	Weak transcription	HSMMtube	muscle
5	chr9:14634400-14686600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr9:14634600-14659000	Weak transcription	Fetal Stomach	stomach
7	chr9:14634600-14692400	Weak transcription	Gastric	stomach
8	chr9:14634600-14692600	Weak transcription	Aorta	Aorta
9	chr9:14635800-14659800	Weak transcription	Ovary	ovary
10	chr9:14648200-14663800	Weak transcription	Placenta	Placenta
11	chr9:14651400-14659400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr9:14652000-14687000	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr9:14652600-14658400	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr9:14652800-14655400	ZNF genes & repeats	A549	lung
15	chr9:14652800-14655600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr9:14653400-14655400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
17	chr9:14653400-14656200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr9:14653600-14655200	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
19	chr9:14653600-14655600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr9:14653600-14655600	ZNF genes & repeats	NHDF-Ad	bronchial
21	chr9:14653600-14655800	ZNF genes & repeats	Adipose Nuclei	Adipose
22	chr9:14653600-14656600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr9:14653600-14656600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr9:14653600-14657400	ZNF genes & repeats	GM12878-XiMat	blood
25	chr9:14653600-14661000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr9:14653800-14655200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr9:14653800-14657000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr9:14653800-14657800	ZNF genes & repeats	Primary B cells from cord blood	blood
29	chr9:14653800-14687200	Weak transcription	Left Ventricle	heart
30	chr9:14654000-14655200	ZNF genes & repeats	Primary T cells from cord blood	blood
31	chr9:14654000-14655400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr9:14654000-14655400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr9:14654000-14655600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr9:14654000-14655600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
35	chr9:14654000-14655600	ZNF genes & repeats	Liver	Liver
36	chr9:14654000-14655800	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
37	chr9:14654000-14663200	Weak transcription	Osteobl	bone
38	chr9:14654200-14655400	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
39	chr9:14654200-14655600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
40	chr9:14654200-14656600	Weak transcription	Fetal Heart	heart
41	chr9:14654200-14657200	ZNF genes & repeats	Primary B cells from peripheral blood	blood
42	chr9:14654200-14686200	Weak transcription	Fetal Brain Male	brain
43	chr9:14654200-14692600	Weak transcription	Pancreas	Pancrea
44	chr9:14654400-14655000	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
45	chr9:14654400-14655400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
46	chr9:14654400-14655400	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
47	chr9:14654400-14655600	ZNF genes & repeats	Fetal Lung	lung
48	chr9:14654400-14656400	ZNF genes & repeats	HUVEC	blood vessel
49	chr9:14654400-14657800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr9:14654600-14655400	ZNF genes & repeats	Muscle Satellite Cultured Cells	--

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