Variant report

Variant	nsv892214
Chromosome Location	chr9:7774180-7822486
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:611)
CpG islands
(count:306)
Chromatin interactive
region (count:34)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:611 , 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	ATF1	chr9:7799673-7799970	K562	blood:	n/a	n/a
2	ATF3	chr9:7799704-7799917	GM12878	blood:	n/a	n/a
3	ATF3	chr9:7799216-7799916	GM12878	blood:	n/a	chr9:7799429-7799437
4	ATF3	chr9:7799628-7799981	HepG2	liver:	n/a	n/a
5	ATF3	chr9:7799280-7799457	K562	blood:	n/a	chr9:7799429-7799437
6	ATF3	chr9:7799647-7799949	K562	blood:	n/a	n/a
7	ATF3	chr9:7799547-7799974	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr9:7799559-7799954	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr9:7799872-7800146	GM12878	blood:	n/a	chr9:7800040-7800051
10	BATF	chr9:7799677-7799960	GM12878	blood:	n/a	n/a
11	BATF	chr9:7799963-7800195	GM12878	blood:	n/a	chr9:7800040-7800051
12	BCL11A	chr9:7784487-7784797	GM12878	blood:	n/a	n/a
13	BCL11A	chr9:7783624-7783901	GM12878	blood:	n/a	n/a
14	BCLAF1	chr9:7799525-7800090	GM12878	blood:	n/a	n/a
15	BCLAF1	chr9:7799298-7799961	GM12878	blood:	n/a	n/a
16	BHLHE40	chr9:7800146-7800155	K562	blood:	n/a	n/a
17	BHLHE40	chr9:7799605-7799952	HepG2	liver:	n/a	n/a
18	BHLHE40	chr9:7799210-7800252	GM12878	blood:	n/a	n/a
19	BHLHE40	chr9:7799316-7799827	K562	blood:	n/a	n/a
20	BHLHE40	chr9:7784514-7784716	GM12878	blood:	n/a	n/a
21	BRCA1	chr9:7798922-7799185	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr9:7799429-7799943	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr9:7820003-7820320	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr9:7802666-7802893	HepG2	liver:	n/a	n/a
25	CEBPB	chr9:7786693-7786871	HepG2	liver:	n/a	chr9:7786745-7786756
26	CEBPB	chr9:7819991-7820354	K562	blood:	n/a	n/a
27	CEBPB	chr9:7820026-7820292	A549	lung:	n/a	n/a
28	CEBPB	chr9:7821653-7821782	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr9:7819997-7820319	A549	lung:	n/a	n/a
30	CEBPB	chr9:7819955-7820368	A549	lung:	n/a	n/a
31	CEBPB	chr9:7820000-7820344	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr9:7784415-7784457	GM12878	blood:	n/a	n/a
33	CHD2	chr9:7799225-7800044	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr9:7799612-7800002	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr9:7799297-7799978	GM12878	blood:	n/a	n/a
36	CHD2	chr9:7799674-7799972	K562	blood:	n/a	n/a
37	CHD2	chr9:7784508-7784769	GM12878	blood:	n/a	n/a
38	CHD2	chr9:7799387-7799994	HepG2	liver:	n/a	n/a
39	CREB1	chr9:7799338-7800063	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr9:7799617-7799947	A549	lung:	n/a	n/a
41	CREB1	chr9:7799238-7800023	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr9:7799294-7800003	A549	lung:	n/a	n/a
43	CREB1	chr9:7799132-7800008	GM12878	blood:	n/a	n/a
44	CREB1	chr9:7799557-7799986	HepG2	liver:	n/a	n/a
45	CREB1	chr9:7799579-7800011	K562	blood:	n/a	n/a
46	CREB1	chr9:7799499-7799993	K562	blood:	n/a	n/a
47	CREB1	chr9:7799304-7800004	HepG2	liver:	n/a	n/a
48	CTCF	chr9:7786980-7787130	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr9:7799772-7799802	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr9:7799289-7799405	K562	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:7797524-7797574	AG10803	skin:	n/a
2	chr9:7797524-7797574	AG10803	skin:	n/a
3	chr9:7800256-7800306	HL-60	blood:	n/a
4	chr9:7797446-7797496	AG04450	lung:	fetal
5	chr9:7799690-7799740	AoSMC	blood vessel:	n/a
6	chr9:7797446-7797496	HIPEpiC	eye:	n/a
7	chr9:7797446-7797496	GM19239	blood:	n/a
8	chr9:7799961-7800011	GM12878	blood:	n/a
9	chr9:7797524-7797574	AG04450	lung:	fetal
10	chr9:7797446-7797496	A549	lung:	n/a
11	chr9:7797524-7797574	HRCEpiC	kidney:	n/a
12	chr9:7799961-7800011	HAEpiC	amniotic membrane:	n/a
13	chr9:7797446-7797496	NHBE	bronchial:	n/a
14	chr9:7799961-7800011	HepG2	liver:	n/a
15	chr9:7797524-7797574	ProgFib	skin:	n/a
16	chr9:7797524-7797574	GM12878	blood:	n/a
17	chr9:7797524-7797574	AG09309	skin:	n/a
18	chr9:7797446-7797496	HCF	heart:	n/a
19	chr9:7799690-7799740	HEK293	kidney:	embryo
20	chr9:7799690-7799740	AG10803	skin:	n/a
21	chr9:7800256-7800306	HPAEpiC	pulmonary alveolar:	n/a
22	chr9:7800256-7800306	AG04449	skin:	fetal
23	chr9:7797446-7797496	CMK	blood:	n/a
24	chr9:7797524-7797574	PrEC	prostate:	n/a
25	chr9:7799961-7800011	AoSMC	blood vessel:	n/a
26	chr9:7799961-7800011	HEEpiC	esophagus:	n/a
27	chr9:7797446-7797496	ovcar-3	ovarian:	n/a
28	chr9:7799690-7799740	HUVEC	blood vessel:	n/a
29	chr9:7800256-7800306	HNPCEpiC	eye:	n/a
30	chr9:7800256-7800306	HRCEpiC	kidney:	n/a
31	chr9:7799961-7800011	HPAEpiC	pulmonary alveolar:	n/a
32	chr9:7799961-7800011	HRCEpiC	kidney:	n/a
33	chr9:7797524-7797574	HUVEC	blood vessel:	n/a
34	chr9:7800256-7800306	LNCaP	prostate:	n/a
35	chr9:7799690-7799740	HMEC	breast:	n/a
36	chr9:7800256-7800306	AG04450	lung:	fetal
37	chr9:7799690-7799740	AG09319	gingival:	n/a
38	chr9:7800256-7800306	AG10803	skin:	n/a
39	chr9:7800256-7800306	U87	brain:	n/a
40	chr9:7799690-7799740	HIPEpiC	eye:	n/a
41	chr9:7797446-7797496	AG09309	skin:	n/a
42	chr9:7800256-7800306	H1-hESC	embryonic stem cell:	embryo
43	chr9:7797446-7797496	AG09319	gingival:	n/a
44	chr9:7797446-7797496	HPAEpiC	pulmonary alveolar:	n/a
45	chr9:7799690-7799740	HRE	kidney:	n/a
46	chr9:7797524-7797574	HCPEpiC	choroid plexus:	n/a
47	chr9:7797446-7797496	GM12892	blood:	n/a
48	chr9:7797446-7797496	U87	brain:	n/a
49	chr9:7797524-7797574	SK-N-MC	brain:	n/a
50	chr9:7799961-7800011	AG04450	lung:	fetal

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:7790070..7792908-chr9:7794043..7796147,3	MCF-7	breast:
2	chr9:7788086..7790950-chr9:7795081..7797619,2	K562	blood:
3	chr15:25414756..25415321-chr9:7799310..7799908,2	Hela-S3	cervix:
4	chr9:7782983..7784835-chr9:7794614..7797331,2	K562	blood:
5	chr9:7790070..7792908-chr9:7794043..7796147,3	MCF-7	breast:
6	chr9:7767607..7770435-chr9:7773162..7775185,2	K562	blood:
7	chr9:7785236..7788053-chr9:7798343..7800585,2	K562	blood:
8	chr9:7785236..7787094-chr9:7798343..7800559,2	K562	blood:
9	chr9:7770682..7773341-chr9:7794081..7796235,2	MCF-7	breast:
10	chr9:7775868..7780963-chr9:7782182..7785023,5	K562	blood:
11	chr9:7793288..7795096-chr9:7798393..7801013,3	MCF-7	breast:
12	chr9:7782983..7784835-chr9:7794614..7797331,2	K562	blood:
13	chr9:7799400..7802394-chr9:7804203..7806303,2	K562	blood:
14	chr9:7787126..7791154-chr9:7791178..7794501,4	K562	blood:
15	chr9:7772004..7774920-chr9:7780666..7782709,2	K562	blood:
16	chr9:7775868..7780963-chr9:7782182..7785023,5	K562	blood:
17	chr9:7764096..7766786-chr9:7797842..7799916,2	MCF-7	breast:
18	chr9:7798904..7801575-chr9:7807644..7809978,3	K562	blood:
19	chr9:7790664..7794706-chr9:7795945..7799232,5	K562	blood:
20	chr15:59981502..59982267-chr9:7799535..7800195,2	NB4	blood:
21	chr9:7526587..7529247-chr9:7794978..7796914,2	MCF-7	breast:
22	chr16:70408470..70409240-chr9:7799247..7799915,2	NB4	blood:
23	chr9:7785709..7788362-chr9:7790600..7793214,2	K562	blood:
24	chr4:148653204..148653996-chr9:7798836..7799339,2	Hela-S3	cervix:
25	chr9:7790664..7794706-chr9:7795945..7799232,5	K562	blood:
26	chr9:7799234..7801006-chr9:7803673..7806734,3	MCF-7	breast:
27	chr9:7785236..7788053-chr9:7798343..7800585,2	K562	blood:
28	chr17:56709050..56710030-chr9:7799215..7799951,2	NB4	blood:
29	chr9:7772004..7774920-chr9:7780666..7782709,2	K562	blood:
30	chr9:7781941..7784534-chr9:7791662..7794254,2	MCF-7	breast:
31	chr9:7781941..7784534-chr9:7791662..7794254,2	MCF-7	breast:
32	chr9:7785236..7787094-chr9:7798343..7800559,2	K562	blood:
33	chr9:7788086..7790950-chr9:7795081..7797619,2	K562	blood:
34	chr9:7787126..7791154-chr9:7791178..7794501,4	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf123-1	chr9:7787136-7787329	XLOC_007641
2	lnc-PTPRD-8	chr9:7800041-7800148	NONHSAT130178
3	lnc-PTPRD-8	chr9:7798199-7798637	NONHSAT130178
4	lnc-C9orf123-1	chr9:7788675-7788763	XLOC_007641
5	lnc-C9orf123-1	chr9:7788675-7788735	XLOC_007641
6	lnc-C9orf123-1	chr9:7782483-7782511	XLOC_007641
7	lnc-C9orf123-1	chr9:7785195-7787329	XLOC_007641
8	lnc-PTPRD-8	chr9:7798344-7798637	NONHSAT130179
9	lnc-C9orf123-1	chr9:7786105-7786688	ENSG00000273056.1

No data

Variant related genes	Relation type
TMEM261	TF binding region
ENSG00000273056	TF binding region
TMEM261	CpG island
ENSG00000273056	CpG island
ENSG00000212195	chromatin interactions
ENSG00000270814	chromatin interactions
ENSG00000140299	chromatin interactions
ENSG00000137038	chromatin interactions
ENSG00000071205	chromatin interactions
ENSG00000273056	chromatin interactions
SMARCC2	miRNA target sites
DLST	miRNA target sites
MMS19	miRNA target sites

Extended variants
information (count: 1989 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1989 , 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	rs533018962	chr9:7775204-7775205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs551928218	chr9:7775244-7775245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145899089	chr9:7775255-7775256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191774184	chr9:7775265-7775266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570797638	chr9:7775301-7775302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183941722	chr9:7775351-7775352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576706533	chr9:7775355-7775356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537971280	chr9:7775361-7775362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541771613	chr9:7775370-7775371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188131547	chr9:7775377-7775378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182412093	chr9:7775400-7775401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536104916	chr9:7775421-7775422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs187043388	chr9:7775429-7775430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562062416	chr9:7775431-7775432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs546470345	chr9:7775441-7775442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557488504	chr9:7775444-7775445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs10976568	chr9:7775472-7775473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs116193020	chr9:7775489-7775490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs190567427	chr9:7775493-7775494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs367896517	chr9:7775496-7775497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148213780	chr9:7775549-7775550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114874003	chr9:7775602-7775603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533079858	chr9:7775604-7775605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs9407384	chr9:7775651-7775652	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs181840753	chr9:7775663-7775664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140343725	chr9:7775745-7775746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543525242	chr9:7775794-7775795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563704097	chr9:7775797-7775798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549905649	chr9:7775810-7775811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs201887739	chr9:7775836-7775837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs529266629	chr9:7775838-7775839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs549391932	chr9:7775849-7775850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568606610	chr9:7775856-7775857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535909610	chr9:7775857-7775858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554407668	chr9:7775859-7775860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566424111	chr9:7775861-7775862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs566246263	chr9:7775868-7775869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539758709	chr9:7775909-7775910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558462872	chr9:7775933-7775934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185853283	chr9:7775939-7775940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576639210	chr9:7776021-7776022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs150347453	chr9:7776039-7776040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138092618	chr9:7776040-7776041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190256016	chr9:7776043-7776044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540696895	chr9:7776044-7776045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73417546	chr9:7776066-7776067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs532997785	chr9:7776084-7776085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs138955692	chr9:7776088-7776089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544857337	chr9:7776160-7776161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142616959	chr9:7776205-7776206	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
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
Disorders of sex development	21048976	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
Oral squamous cell carcinoma	17134496	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	21811587	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:959 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:7775200-7776600	Enhancers	HSMMtube	muscle
2	chr9:7776000-7776400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:7776200-7776800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:7776400-7780400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:7776600-7777000	Weak transcription	HSMMtube	muscle
6	chr9:7777000-7778000	Enhancers	Brain Germinal Matrix	brain
7	chr9:7777000-7778200	Enhancers	HSMMtube	muscle
8	chr9:7777600-7779200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr9:7777800-7778200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr9:7777800-7779600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr9:7778000-7778200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr9:7778000-7787000	Weak transcription	Brain Germinal Matrix	brain
13	chr9:7778000-7792400	Weak transcription	Psoas Muscle	Psoas
14	chr9:7778200-7778400	Enhancers	Fetal Muscle Leg	muscle
15	chr9:7778200-7779000	Weak transcription	HSMMtube	muscle
16	chr9:7778200-7780200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr9:7778200-7790200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr9:7778400-7780600	Weak transcription	Fetal Muscle Leg	muscle
19	chr9:7778600-7779600	Enhancers	Placenta Amnion	Placenta Amnion
20	chr9:7778600-7781000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr9:7778800-7779400	Enhancers	HMEC	breast
22	chr9:7778800-7779400	Enhancers	HSMM	muscle
23	chr9:7779000-7779400	Enhancers	Muscle Satellite Cultured Cells	--
24	chr9:7779000-7783800	Enhancers	HSMMtube	muscle
25	chr9:7779400-7779800	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr9:7779400-7779800	Weak transcription	HSMM	muscle
27	chr9:7779400-7780600	Weak transcription	HMEC	breast
28	chr9:7779600-7780400	Enhancers	NH-A	brain
29	chr9:7779600-7780600	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr9:7779600-7781000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr9:7779800-7780600	Enhancers	Muscle Satellite Cultured Cells	--
32	chr9:7779800-7781000	Enhancers	HSMM	muscle
33	chr9:7780000-7780200	Enhancers	H9 Cell Line	embryonic stem cell
34	chr9:7780000-7780400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr9:7780200-7780400	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr9:7780200-7780600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr9:7780200-7780800	Enhancers	Osteobl	bone
38	chr9:7780200-7782000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr9:7780200-7785000	Enhancers	Fetal Heart	heart
40	chr9:7780200-7786400	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr9:7780400-7780800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr9:7780400-7780800	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr9:7780400-7780800	Enhancers	Left Ventricle	heart
44	chr9:7780400-7780800	Enhancers	Thymus	Thymus
45	chr9:7780400-7781000	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr9:7780400-7781600	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr9:7780400-7786200	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr9:7780400-7792600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr9:7780600-7780800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr9:7780600-7780800	Enhancers	HMEC	breast

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