Variant report

Variant	esv1821221
Chromosome Location	chr9:99792208-99811206
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:430)
CpG islands
(count:428)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:99801525-99801543	K562	blood:	n/a	n/a
2	ATF2	chr9:99808522-99808882	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr9:99808542-99808951	H1-hESC	embryonic stem cell:	n/a	chr9:99808741-99808755
4	BACH1	chr9:99801351-99802104	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr9:99801251-99802030	K562	blood:	n/a	chr9:99801863-99801879 chr9:99801623-99801639
6	BRCA1	chr9:99801438-99801727	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr9:99801448-99801621	H1-hESC	embryonic stem cell:	n/a	n/a
8	CBX3	chr9:99808319-99809061	HCT-116	colon:	n/a	n/a
9	CBX3	chr9:99801286-99801621	K562	blood:	n/a	n/a
10	CBX3	chr9:99792799-99793133	K562	blood:	n/a	n/a
11	CBX3	chr9:99792858-99793126	K562	blood:	n/a	n/a
12	CCNT2	chr9:99801264-99801747	K562	blood:	n/a	chr9:99801467-99801476
13	CEBPB	chr9:99795135-99795191	A549	lung:	n/a	n/a
14	CEBPB	chr9:99804237-99804677	MCF-7	breast:	n/a	n/a
15	CEBPB	chr9:99804151-99804804	MCF-7	breast:	n/a	n/a
16	CEBPD	chr9:99801243-99801746	HepG2	liver:	n/a	n/a
17	CHD2	chr9:99801266-99801738	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr9:99808594-99808904	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr9:99808562-99808893	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr9:99801271-99802127	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr9:99801316-99801658	K562	blood:	n/a	n/a
22	CHD2	chr9:99801349-99801729	GM12878	blood:	n/a	n/a
23	CHD2	chr9:99801181-99802038	HepG2	liver:	n/a	n/a
24	CREB1	chr9:99801240-99801785	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr9:99801212-99801729	A549	lung:	n/a	n/a
26	CREB1	chr9:99801184-99801901	HepG2	liver:	n/a	n/a
27	CREB1	chr9:99801161-99802048	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr9:99801289-99801647	ECC-1	luminal epithelium:	n/a	n/a
29	CTBP2	chr9:99800892-99802098	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr9:99809231-99809240	K562	blood:	n/a	n/a
31	CTCF	chr9:99801480-99801630	Caco-2	colon:	n/a	chr9:99801510-99801523
32	CTCF	chr9:99801200-99801350	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr9:99801764-99801810	K562	blood:	n/a	n/a
34	CTCF	chr9:99801920-99802070	AG04450	lung:	n/a	n/a
35	CTCF	chr9:99794289-99794315	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr9:99801400-99801550	AG04449	skin:	n/a	chr9:99801510-99801523
37	CTCF	chr9:99794486-99794512	GM20000	blood:	n/a	n/a
38	CTCF	chr9:99809020-99809170	HCT-116	colon:	n/a	n/a
39	CTCF	chr9:99809144-99809339	K562	blood:	n/a	n/a
40	CTCF	chr9:99809160-99809310	SAEC	small airway:	n/a	n/a
41	CTCF	chr9:99801487-99801609	Spleen_OC	spleen:	n/a	chr9:99801510-99801523
42	CTCF	chr9:99809160-99809310	MCF-7	breast:	n/a	n/a
43	CTCF	chr9:99801800-99801950	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr9:99801300-99801450	Caco-2	colon:	n/a	n/a
45	CTCF	chr9:99809160-99809310	HMEC	breast:	n/a	n/a
46	CTCF	chr9:99801540-99801690	HMEC	breast:	n/a	n/a
47	CTCF	chr9:99808620-99808770	HMEC	breast:	n/a	n/a
48	CTCF	chr9:99801347-99801355	NHEK	skin:	n/a	n/a
49	CTCF	chr9:99801220-99801370	GM12865	blood:	n/a	n/a
50	CTCF	chr9:99801320-99801470	SK-N-SH_RA	brain:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:99801550-99801600	HRE	kidney:	n/a
2	chr9:99801550-99801600	HRE	kidney:	n/a
3	chr9:99801723-99801773	AG09319	gingival:	n/a
4	chr9:99800310-99800360	NB4	blood:	n/a
5	chr9:99801723-99801773	PANC-1	pancreas:	n/a
6	chr9:99801371-99801421	HL-60	blood:	n/a
7	chr9:99800310-99800360	T-47D	breast:	n/a
8	chr9:99800808-99800858	HIPEpiC	eye:	n/a
9	chr9:99801723-99801773	Caco-2	colon:	n/a
10	chr9:99801371-99801421	HRCEpiC	kidney:	n/a
11	chr9:99801410-99801460	ovcar-3	ovarian:	n/a
12	chr9:99801121-99801171	NT2-D1	testis:	n/a
13	chr9:99801371-99801421	HMEC	breast:	n/a
14	chr9:99801723-99801773	CMK	blood:	n/a
15	chr9:99801371-99801421	LNCaP	prostate:	n/a
16	chr9:99801371-99801421	MCF-7	breast:	n/a
17	chr9:99801723-99801773	NT2-D1	testis:	n/a
18	chr9:99800310-99800360	RPTEC	kidney:	n/a
19	chr9:99801550-99801600	HCM	heart:	n/a
20	chr9:99801410-99801460	GM06990	blood:	n/a
21	chr9:99801371-99801421	HEK293	kidney:	embryo
22	chr9:99801550-99801600	PFSK-1	brain:	n/a
23	chr9:99801723-99801773	SKMC	muscle:	n/a
24	chr9:99801121-99801171	PFSK-1	brain:	n/a
25	chr9:99801723-99801773	ProgFib	skin:	n/a
26	chr9:99801371-99801421	GM12892	blood:	n/a
27	chr9:99801121-99801171	PANC-1	pancreas:	n/a
28	chr9:99800310-99800360	HCPEpiC	choroid plexus:	n/a
29	chr9:99801371-99801421	HUVEC	blood vessel:	n/a
30	chr9:99801410-99801460	HEK293	kidney:	embryo
31	chr9:99801410-99801460	AoSMC	blood vessel:	n/a
32	chr9:99801550-99801600	AG04450	lung:	fetal
33	chr9:99801723-99801773	Hela-S3	cervix:	n/a
34	chr9:99800808-99800858	U87	brain:	n/a
35	chr9:99801723-99801773	SAEC	small airway:	n/a
36	chr9:99800310-99800360	HMEC	breast:	n/a
37	chr9:99800808-99800858	IMR90	lung:	fetal
38	chr9:99801371-99801421	SK-N-MC	brain:	n/a
39	chr9:99801371-99801421	HCT-116	colon:	n/a
40	chr9:99801550-99801600	HAEpiC	amniotic membrane:	n/a
41	chr9:99801723-99801773	AG04450	lung:	fetal
42	chr9:99800310-99800360	ProgFib	skin:	n/a
43	chr9:99801550-99801600	A549	lung:	n/a
44	chr9:99800808-99800858	NB4	blood:	n/a
45	chr9:99801723-99801773	HPAEpiC	pulmonary alveolar:	n/a
46	chr9:99801723-99801773	HCM	heart:	n/a
47	chr9:99801121-99801171	SKMC	muscle:	n/a
48	chr9:99801121-99801171	HPAEpiC	pulmonary alveolar:	n/a
49	chr9:99800808-99800858	AG04450	lung:	fetal
50	chr9:99801410-99801460	MCF10A-Er-Src	breast:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:99796298..99798736-chr9:99802625..99804401,2	MCF-7	breast:
2	chr9:99791951..99794165-chr9:99796736..99799706,2	K562	blood:
3	chr9:99792005..99793913-chr9:99798704..99801926,3	MCF-7	breast:
4	chr9:99636633..99638588-chr9:99800511..99803120,2	MCF-7	breast:
5	chr9:99791951..99794165-chr9:99796736..99799706,2	K562	blood:
6	chr9:99799829..99801401-chr9:99834490..99837117,2	MCF-7	breast:
7	chr9:99807016..99810374-chr9:99823217..99825198,3	MCF-7	breast:
8	chr9:99800041..99802433-chr9:99802740..99804578,2	MCF-7	breast:
9	chr9:99774341..99777390-chr9:99797289..99801643,6	MCF-7	breast:
10	chr9:99801883..99804719-chr9:99807015..99808695,2	MCF-7	breast:
11	chr9:99796298..99798736-chr9:99802625..99804401,2	MCF-7	breast:

No data

Variant related genes	Relation type
CTSV	TF binding region
CTSV	CpG island
ENSG00000196312	chromatin interactions
ENSG00000136943	chromatin interactions
ENSG00000196597	chromatin interactions

Extended variants
information (count: 730 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:730 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10123754	chr9:99792208-99792209	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569676712	chr9:99792220-99792221	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs537008949	chr9:99792245-99792246	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs10123757	chr9:99792249-99792250	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs58389479	chr9:99792311-99792312	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs538894735	chr9:99792320-99792321	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs527540466	chr9:99792343-99792344	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs10759389	chr9:99792419-99792420	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs10980209	chr9:99792494-99792495	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs190771124	chr9:99792530-99792531	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs546038495	chr9:99792600-99792601	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs371330804	chr9:99792628-99792629	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs10816926	chr9:99792636-99792637	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs76189259	chr9:99792697-99792698	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs543778762	chr9:99792729-99792730	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs79134422	chr9:99792743-99792744	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs577258940	chr9:99792754-99792755	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs35505250	chr9:99792787-99792788	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs540353589	chr9:99792793-99792794	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs540915244	chr9:99792816-99792817	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs559590632	chr9:99792846-99792847	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs531658641	chr9:99792906-99792907	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529873599	chr9:99792965-99792966	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs146353497	chr9:99793002-99793003	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs139368899	chr9:99793052-99793053	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530450465	chr9:99793067-99793068	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs552131562	chr9:99793111-99793112	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs149996893	chr9:99793117-99793118	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs144290153	chr9:99793123-99793124	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs112127902	chr9:99793144-99793145	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs565950799	chr9:99793194-99793195	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs371337838	chr9:99793218-99793219	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs536421814	chr9:99793225-99793226	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs554872657	chr9:99793302-99793303	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs573705269	chr9:99793333-99793334	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs200841230	chr9:99793346-99793347	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs374272999	chr9:99793369-99793370	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs537091118	chr9:99793401-99793402	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs558908701	chr9:99793414-99793415	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs75496954	chr9:99793421-99793422	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs16919034	chr9:99793583-99793584	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs568065363	chr9:99793610-99793611	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs541523652	chr9:99793637-99793638	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs541141229	chr9:99793652-99793653	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs371516339	chr9:99793677-99793678	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs574706304	chr9:99793678-99793679	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs35529217	chr9:99793714-99793715	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs187353351	chr9:99793742-99793743	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs190993337	chr9:99793755-99793756	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs547814752	chr9:99793764-99793765	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	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
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
overgrowth syndrome	16570072	CNVD
Neurodevelopmental disorder	22521361	CNVD
Nicotine dependence	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:595 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:99786400-99796000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr9:99789000-99792600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr9:99789000-99793000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr9:99790200-99792600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr9:99790800-99797200	Weak transcription	HMEC	breast
6	chr9:99791000-99792600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr9:99791000-99792800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr9:99791200-99792600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:99791400-99799400	Weak transcription	NHEK	skin
10	chr9:99791600-99797400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr9:99792000-99792800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr9:99792000-99794400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr9:99792000-99794400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
14	chr9:99792000-99794600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
15	chr9:99792000-99795200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
16	chr9:99792200-99794400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
17	chr9:99792200-99794400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
18	chr9:99792600-99793800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
19	chr9:99792600-99794200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr9:99792600-99796600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr9:99792600-99800000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr9:99792600-99800000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr9:99792800-99794200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
24	chr9:99792800-99799800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr9:99793000-99793200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr9:99793000-99794400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr9:99793200-99794200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr9:99793200-99796000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr9:99793200-99800600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr9:99793400-99799600	Weak transcription	Fetal Intestine Small	intestine
31	chr9:99793800-99799000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
32	chr9:99794000-99794200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
33	chr9:99794200-99795000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
34	chr9:99794200-99795400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr9:99794200-99795400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
36	chr9:99794200-99797600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
37	chr9:99794200-99800200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr9:99794400-99794800	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr9:99794400-99796400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr9:99794400-99799800	Strong transcription	H1 Cell Line	embryonic stem cell
41	chr9:99794400-99799800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr9:99794400-99799800	Strong transcription	HUES64 Cell Line	embryonic stem cell
43	chr9:99794600-99800000	Strong transcription	HUES48 Cell Line	embryonic stem cell
44	chr9:99794800-99800000	Strong transcription	H9 Cell Line	embryonic stem cell
45	chr9:99795000-99795600	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
46	chr9:99795000-99799000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr9:99795200-99799800	Strong transcription	HUES6 Cell Line	embryonic stem cell
48	chr9:99795400-99796400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr9:99795400-99799800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr9:99795600-99800000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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