Variant report

Variant	nsv1034869
Chromosome Location	chr9:43757334-44739032
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3763)
CpG islands
(count:916)
Chromatin interactive
region (count:1)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3763 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:44108136-44108696	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:44118677-44118886	HepG2	liver:	n/a	n/a
3	ATF1	chr9:43939526-43939892	K562	blood:	n/a	n/a
4	ATF3	chr9:43939586-43939712	K562	blood:	n/a	n/a
5	BACH1	chr9:44227184-44227631	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr9:44227257-44227630	K562	blood:	n/a	n/a
7	BATF	chr9:44063096-44063309	GM12878	blood:	n/a	n/a
8	BATF	chr9:44108035-44108219	GM12878	blood:	n/a	n/a
9	BATF	chr9:44645280-44645491	GM12878	blood:	n/a	chr9:44645403-44645414
10	BATF	chr9:44552225-44552444	GM12878	blood:	n/a	n/a
11	BATF	chr9:44577860-44578259	GM12878	blood:	n/a	chr9:44577967-44577975
12	BATF	chr9:44280534-44280732	GM12878	blood:	n/a	n/a
13	BATF	chr9:44367127-44367454	GM12878	blood:	n/a	n/a
14	BATF	chr9:44054788-44055026	GM12878	blood:	n/a	n/a
15	BATF	chr9:44030553-44030791	GM12878	blood:	n/a	n/a
16	BATF	chr9:44108319-44108733	GM12878	blood:	n/a	chr9:44108541-44108552
17	BATF	chr9:44245873-44246195	GM12878	blood:	n/a	n/a
18	BATF	chr9:44065378-44065708	GM12878	blood:	n/a	n/a
19	BATF	chr9:44340761-44341046	GM12878	blood:	n/a	n/a
20	BATF	chr9:44118541-44118761	GM12878	blood:	n/a	n/a
21	BATF	chr9:44124043-44124400	GM12878	blood:	n/a	n/a
22	BATF	chr9:44245375-44245745	GM12878	blood:	n/a	n/a
23	BATF	chr9:44112676-44113049	GM12878	blood:	n/a	n/a
24	BATF	chr9:44107144-44107983	GM12878	blood:	n/a	n/a
25	BATF	chr9:44125369-44125590	GM12878	blood:	n/a	n/a
26	BATF	chr9:44552199-44552435	GM12878	blood:	n/a	n/a
27	BATF	chr9:44550459-44550750	GM12878	blood:	n/a	n/a
28	BATF	chr9:43837850-43838056	GM12878	blood:	n/a	n/a
29	BATF	chr9:44076866-44077089	GM12878	blood:	n/a	n/a
30	BATF	chr9:44306841-44307126	GM12878	blood:	n/a	n/a
31	BATF	chr9:44145517-44145676	GM12878	blood:	n/a	n/a
32	BATF	chr9:44124132-44124352	GM12878	blood:	n/a	n/a
33	BATF	chr9:44605098-44605838	GM12878	blood:	n/a	n/a
34	BATF	chr9:44401329-44401837	GM12878	blood:	n/a	n/a
35	BATF	chr9:44086267-44086535	GM12878	blood:	n/a	n/a
36	BATF	chr9:44379817-44379994	GM12878	blood:	n/a	chr9:44379913-44379924
37	BATF	chr9:44082194-44082452	GM12878	blood:	n/a	n/a
38	BATF	chr9:44539661-44540230	GM12878	blood:	n/a	n/a
39	BATF	chr9:44030517-44030875	GM12878	blood:	n/a	n/a
40	BATF	chr9:44176537-44176725	GM12878	blood:	n/a	n/a
41	BATF	chr9:44355408-44355626	GM12878	blood:	n/a	n/a
42	BATF	chr9:44606159-44606345	GM12878	blood:	n/a	n/a
43	BATF	chr9:44401104-44402763	GM12878	blood:	n/a	n/a
44	BATF	chr9:43925013-43925176	GM12878	blood:	n/a	n/a
45	BATF	chr9:44107334-44107970	GM12878	blood:	n/a	n/a
46	BATF	chr9:44088871-44089267	GM12878	blood:	n/a	chr9:44088983-44088991
47	BATF	chr9:44133305-44133513	GM12878	blood:	n/a	chr9:44133433-44133441
48	BATF	chr9:44265544-44265770	GM12878	blood:	n/a	n/a
49	BATF	chr9:44401959-44402428	GM12878	blood:	n/a	n/a
50	BATF	chr9:44086306-44086516	GM12878	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:44120147-44120197	ProgFib	skin:	n/a
2	chr9:44120147-44120197	ProgFib	skin:	n/a
3	chr9:44118915-44118965	GM12878	blood:	n/a
4	chr9:43860027-43860077	AG04450	lung:	fetal
5	chr9:44119823-44119873	BE2_C	brain:	n/a
6	chr9:44119823-44119873	GM19239	blood:	n/a
7	chr9:44120147-44120197	SKMC	muscle:	n/a
8	chr9:44118236-44118286	HEK293	kidney:	embryo
9	chr9:43860965-43861015	HRCEpiC	kidney:	n/a
10	chr9:44227339-44227389	HCF	heart:	n/a
11	chr9:44119823-44119873	Jurkat	blood:	n/a
12	chr9:43860027-43860077	NT2-D1	testis:	n/a
13	chr9:44118014-44118064	NH-A	brain:	n/a
14	chr9:43915234-43915284	BE2_C	brain:	n/a
15	chr9:44420179-44420229	HNPCEpiC	eye:	n/a
16	chr9:44119823-44119873	SAEC	small airway:	n/a
17	chr9:44119823-44119873	AG09319	gingival:	n/a
18	chr9:44227339-44227389	K562	blood:	n/a
19	chr9:44118915-44118965	SK-N-SH_RA	brain:	n/a
20	chr9:44401998-44402048	U87	brain:	n/a
21	chr9:44422602-44422652	HIPEpiC	eye:	n/a
22	chr9:44119413-44119463	ECC-1	luminal epithelium:	n/a
23	chr9:44118915-44118965	HCF	heart:	n/a
24	chr9:44118236-44118286	Hepatocyte	liver:	n/a
25	chr9:44120147-44120197	GM06990	blood:	n/a
26	chr9:44118915-44118965	HEK293	kidney:	embryo
27	chr9:44118236-44118286	ECC-1	luminal epithelium:	n/a
28	chr9:44118236-44118286	NH-A	brain:	n/a
29	chr9:44401998-44402048	HNPCEpiC	eye:	n/a
30	chr9:43860965-43861015	GM12878	blood:	n/a
31	chr9:44227210-44227260	NHDF-neo	bronchial:	n/a
32	chr9:44120147-44120197	HCM	heart:	n/a
33	chr9:44118915-44118965	NH-A	brain:	n/a
34	chr9:44313114-44313164	BJ	skin:	n/a
35	chr9:43860965-43861015	AG09319	gingival:	n/a
36	chr9:44313114-44313164	HEK293	kidney:	embryo
37	chr9:44119823-44119873	HAEpiC	amniotic membrane:	n/a
38	chr9:44119823-44119873	HRCEpiC	kidney:	n/a
39	chr9:44401998-44402048	AoSMC	blood vessel:	n/a
40	chr9:44119413-44119463	AG09309	skin:	n/a
41	chr9:44119413-44119463	A549	lung:	n/a
42	chr9:44118014-44118064	SK-N-SH	brain:	n/a
43	chr9:44118014-44118064	NT2-D1	testis:	n/a
44	chr9:44227339-44227389	HIPEpiC	eye:	n/a
45	chr9:44120147-44120197	GM12892	blood:	n/a
46	chr9:43915234-43915284	GM12878	blood:	n/a
47	chr9:44118236-44118286	SK-N-SH_RA	brain:	n/a
48	chr9:44401998-44402048	GM12892	blood:	n/a
49	chr9:44422602-44422652	NH-A	brain:	n/a
50	chr9:44227210-44227260	CMK	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:107699957..107700478-chr9:44227430..44227950,2	MCF-7	breast:

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-160N1.10.1-8	chr9:43822729-43822779	NONHSAT131364
2	lnc-FAM75A6-7	chr9:44046989-44047817	NONHSAT131371
3	lnc-CNTNAP3B-1	chr9:44391077-44391705	ENSG00000229311
4	lnc-RP11-160N1.10.1-8	chr9:43844144-43844200	NONHSAT131364
5	lnc-FAM75A6-14	chr9:44676388-44676450	NONHSAT131392
6	lnc-CNTNAP3B-1	chr9:44387387-44387483	NR_046203
7	lnc-FAM75A6-3	chr9:44256189-44256817	ENSG00000233424
8	lnc-RP11-160N1.10.1-8	chr9:43853497-43853563	NONHSAT131364
9	lnc-RP11-160N1.10.1-8	chr9:43822613-43822699	NONHSAT131364
10	lnc-FAM75A6-2	chr9:44182692-44183417	XLOC_007697
11	lnc-CNTNAP3B-1	chr9:44384585-44387483	ENSG00000229311
12	lnc-RP11-160N1.10.1-8	chr9:43861003-43861206	NONHSAT131364
13	lnc-FAM75A6-2	chr9:44181550-44181732	XLOC_007697
14	lnc-CNTNAP3B-1	chr9:44387768-44387853	ENSG00000229311
15	lnc-FAM75A6-3	chr9:44260052-44260139	ENSG00000233424
16	lnc-FAM75A6-14	chr9:44672800-44672959	NONHSAT131392
17	lnc-RP11-160N1.10.1-2	chr9:44403060-44403260	ENSG00000237357
18	lnc-RP11-160N1.10.1-8	chr9:43875989-43876034	NONHSAT131364
19	lnc-FAM75A6-3	chr9:44256580-44256817	ENSG00000233424.2
20	lnc-FAM75A6-3	chr9:44260052-44260139	ENSG00000233424.2
21	lnc-FAM75A6-8	chr9:44075932-44076173	NONHSAT131372
22	lnc-FAM75A6-1	chr9:44144869-44145101	XLOC_007696
23	lnc-FAM75A6-14	chr9:44674678-44674747	NONHSAT131392
24	lnc-RP11-160N1.10.1-5	chr9:44562093-44562588	NONHSAT131391
25	lnc-FAM75A6-6	chr9:43830636-43831108	NONHSAT131365
26	lnc-RP11-160N1.10.1-2	chr9:44402460-44402515	ENSG00000237357
27	lnc-FAM75A6-3	chr9:44260422-44263319	ENSG00000233424.2
28	lnc-CNTNAP3B-1	chr9:44387768-44387853	NR_046203
29	lnc-FAM75A6-13	chr9:44478194-44478456	NONHSAT131390
30	lnc-FAM75A6-1	chr9:44136621-44137011	XLOC_007696
31	lnc-CNTNAP3B-3	chr9:44011053-44011839	NONHSAT131369
32	lnc-FAM75A6-5	chr9:43802781-43803039	NONHSAT131363
33	lnc-FAM75A6-14	chr9:44673720-44673889	NONHSAT131392
34	lnc-FAM75A6-6	chr9:43833702-43835037	NONHSAT131365
35	lnc-CNTNAP3B-1	chr9:44391077-44391416	NR_046203
36	lnc-FAM75A6-3	chr9:44260422-44263319	ENSG00000233424
37	lnc-FAM75A6-13	chr9:44477549-44477882	NONHSAT131390
38	lnc-RP11-160N1.10.1-8	chr9:43828157-43828221	NONHSAT131364

No data

Variant related genes	Relation type
ENSG00000223664	TF binding region
ATP5A1P6	TF binding region
ENSG00000228920	TF binding region
ENSG00000230245	TF binding region
ENSG00000237207	TF binding region
ENSG00000229079	TF binding region
MEP1AP4	TF binding region
ENSG00000227353	TF binding region
CYP4F60P	TF binding region
ENSG00000170165	TF binding region
ENSG00000216829	TF binding region
ENSG00000268708	TF binding region
ENSG00000270909	TF binding region
ENSG00000212952	TF binding region
ANKRD20A7P	TF binding region
RN7SL343P	TF binding region
ENSG00000204818	TF binding region
ENSG00000237357	TF binding region
RBPJP6	TF binding region
ENSG00000204816	TF binding region
ENSG00000233424	TF binding region
ENSG00000229311	TF binding region
SNX18P5	TF binding region
RNU6-599P	TF binding region
ENSG00000268234	TF binding region
CNN2P4	TF binding region
CNTNAP3B	TF binding region
ENSG00000223664	CpG island
ATP5A1P6	CpG island
ENSG00000228920	CpG island
ENSG00000230245	CpG island
ENSG00000237207	CpG island
ENSG00000229079	CpG island
MEP1AP4	CpG island
ENSG00000227353	CpG island
CYP4F60P	CpG island
ENSG00000170165	CpG island
ENSG00000216829	CpG island
ENSG00000268708	CpG island
ENSG00000270909	CpG island
ENSG00000212952	CpG island
ANKRD20A7P	CpG island
RN7SL343P	CpG island
ENSG00000204818	CpG island
ENSG00000237357	CpG island
RBPJP6	CpG island
ENSG00000204816	CpG island
ENSG00000233424	CpG island
ENSG00000229311	CpG island
SNX18P5	CpG island
RNU6-599P	CpG island
ENSG00000268234	CpG island
CNN2P4	CpG island
CNTNAP3B	CpG island
ZBTB39	miRNA target sites

Extended variants
information (count: 7586 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:7586 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576657748	chr9:43783403-43783404	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs200466084	chr9:43783404-43783405	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs192622832	chr9:43783426-43783427	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs71258127	chr9:43783458-43783459	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs201075038	chr9:43783473-43783474	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs71274672	chr9:43783541-43783542	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs199693629	chr9:43783575-43783576	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs199721419	chr9:43783576-43783577	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs200916750	chr9:43783577-43783578	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs375533967	chr9:43783582-43783583	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs369913704	chr9:43783586-43783587	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs373385474	chr9:43783595-43783596	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs372447509	chr9:43783597-43783598	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs368041454	chr9:43783604-43783605	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs148450386	chr9:43795508-43795509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs62554972	chr9:43795515-43795516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527707116	chr9:43795524-43795525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543007136	chr9:43795544-43795545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561601806	chr9:43795556-43795557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532021428	chr9:43795562-43795563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550390457	chr9:43795619-43795620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571758665	chr9:43795646-43795647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532694264	chr9:43795655-43795656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551210756	chr9:43795727-43795728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566198116	chr9:43795738-43795739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs533579832	chr9:43795756-43795757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554923925	chr9:43795768-43795769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs146543546	chr9:43795941-43795942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs200880168	chr9:43804284-43804285	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs576129278	chr9:43822635-43822636	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs537144932	chr9:43822643-43822644	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs558656659	chr9:43822646-43822647	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs3739623	chr9:43822668-43822669	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs576928822	chr9:43822673-43822674	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs541010648	chr9:43822674-43822675	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs559624696	chr9:43822676-43822677	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs574639542	chr9:43822677-43822678	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs542045919	chr9:43822685-43822686	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs62555055	chr9:43822686-43822687	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs563348983	chr9:43822687-43822688	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs530574260	chr9:43822689-43822690	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs552278160	chr9:43822690-43822691	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs1755755	chr9:43822749-43822750	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs528502511	chr9:43822758-43822759	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs3739620	chr9:43822762-43822763	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs199834686	chr9:43823617-43823618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs62556360	chr9:43823625-43823626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563571801	chr9:43823647-43823648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192105182	chr9:43823660-43823661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575115152	chr9:43823688-43823689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
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
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	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
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Sezary syndrome	18413736	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Lung adenocarcinoma	17086460	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
Lung cancer	17086460	CNVD
Rhabdomyosarcoma	16790082	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	23813976	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:43783400-43783800	Active TSS	Breast Myoepithelial Primary Cells	Breast
2	chr9:43795400-43795800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:43795400-43795800	Enhancers	HUVEC	blood vessel
4	chr9:43795600-43795800	Enhancers	NH-A	brain
5	chr9:43795600-43796000	Enhancers	HMEC	breast
6	chr9:43823600-43828400	Weak transcription	A549	lung
7	chr9:43824200-43828600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr9:43827800-43850400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr9:43838400-43863800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr9:43844400-43856400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr9:43845200-43863600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr9:43845600-43856400	Weak transcription	HUVEC	blood vessel
13	chr9:43858400-43863600	Weak transcription	Adipose Nuclei	Adipose
14	chr9:44057200-44070600	Weak transcription	Liver	Liver
15	chr9:44070200-44070600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr9:44070600-44070800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr9:44070600-44070800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
18	chr9:44070600-44070800	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
19	chr9:44070600-44070800	ZNF genes & repeats	Primary T cells from cord blood	blood
20	chr9:44070600-44070800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
21	chr9:44070600-44070800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
22	chr9:44070600-44070800	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
23	chr9:44070600-44070800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
24	chr9:44070600-44070800	Flanking Bivalent TSS/Enh	Primary T killer naive cells fromperipheralblood	blood
25	chr9:44070600-44070800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr9:44070600-44070800	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
27	chr9:44070600-44070800	Enhancers	Adipose Nuclei	Adipose
28	chr9:44070600-44070800	Bivalent Enhancer	Aorta	Aorta
29	chr9:44070600-44070800	Active TSS	Brain Anterior Caudate	brain
30	chr9:44070600-44070800	ZNF genes & repeats	Colonic Mucosa	Colon
31	chr9:44070600-44070800	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
32	chr9:44070600-44070800	Enhancers	Right Ventricle	heart
33	chr9:44070600-44071000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
34	chr9:44070600-44071000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
35	chr9:44070600-44071000	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr9:44070600-44071000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr9:44070600-44071000	Flanking Bivalent TSS/Enh	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr9:44070600-44071000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr9:44070600-44071000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
40	chr9:44070600-44071000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
41	chr9:44070600-44071000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
42	chr9:44070600-44071000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
43	chr9:44070600-44071000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
44	chr9:44070600-44071000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr9:44070600-44071000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr9:44070600-44071000	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr9:44070600-44071000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
48	chr9:44070600-44071000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
49	chr9:44070600-44071000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
50	chr9:44070600-44071000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood

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