Variant report

Variant	nsv1027919
Chromosome Location	chr9:44136778-44855725
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2855)
CpG islands
(count:732)
Chromatin interactive
region (count:1)
LncRNA
region (count:33)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2855 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:44781098-44781371	K562	blood:	n/a	n/a
2	ARID3A	chr9:44799676-44800004	HepG2	liver:	n/a	n/a
3	ATF1	chr9:44781241-44781724	K562	blood:	n/a	n/a
4	BACH1	chr9:44227184-44227631	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr9:44227257-44227630	K562	blood:	n/a	n/a
6	BATF	chr9:44342315-44342531	GM12878	blood:	n/a	n/a
7	BATF	chr9:44556907-44557469	GM12878	blood:	n/a	n/a
8	BATF	chr9:44528122-44528281	GM12878	blood:	n/a	n/a
9	BATF	chr9:44280534-44280732	GM12878	blood:	n/a	n/a
10	BATF	chr9:44645280-44645491	GM12878	blood:	n/a	chr9:44645403-44645414
11	BATF	chr9:44605070-44605809	GM12878	blood:	n/a	n/a
12	BATF	chr9:44605098-44605838	GM12878	blood:	n/a	n/a
13	BATF	chr9:44306841-44307126	GM12878	blood:	n/a	n/a
14	BATF	chr9:44212515-44212942	GM12878	blood:	n/a	chr9:44212712-44212723
15	BATF	chr9:44552225-44552444	GM12878	blood:	n/a	n/a
16	BATF	chr9:44280452-44280759	GM12878	blood:	n/a	n/a
17	BATF	chr9:44292314-44292554	GM12878	blood:	n/a	n/a
18	BATF	chr9:44145517-44145676	GM12878	blood:	n/a	n/a
19	BATF	chr9:44342310-44342546	GM12878	blood:	n/a	n/a
20	BATF	chr9:44401329-44401837	GM12878	blood:	n/a	n/a
21	BATF	chr9:44533431-44533653	GM12878	blood:	n/a	n/a
22	BATF	chr9:44245873-44246195	GM12878	blood:	n/a	n/a
23	BATF	chr9:44341546-44341772	GM12878	blood:	n/a	chr9:44341638-44341649
24	BATF	chr9:44836556-44836749	GM12878	blood:	n/a	n/a
25	BATF	chr9:44401959-44402428	GM12878	blood:	n/a	n/a
26	BATF	chr9:44245139-44246113	GM12878	blood:	n/a	n/a
27	BATF	chr9:44265544-44265770	GM12878	blood:	n/a	n/a
28	BATF	chr9:44539620-44540220	GM12878	blood:	n/a	n/a
29	BATF	chr9:44577860-44578259	GM12878	blood:	n/a	chr9:44577967-44577975
30	BATF	chr9:44552199-44552435	GM12878	blood:	n/a	n/a
31	BATF	chr9:44382132-44382329	GM12878	blood:	n/a	n/a
32	BATF	chr9:44340761-44341046	GM12878	blood:	n/a	n/a
33	BATF	chr9:44212521-44212907	GM12878	blood:	n/a	chr9:44212712-44212723
34	BATF	chr9:44403838-44404118	GM12878	blood:	n/a	n/a
35	BATF	chr9:44551132-44551329	GM12878	blood:	n/a	n/a
36	BATF	chr9:44355328-44355568	GM12878	blood:	n/a	n/a
37	BATF	chr9:44434645-44435048	GM12878	blood:	n/a	n/a
38	BATF	chr9:44550459-44550750	GM12878	blood:	n/a	n/a
39	BATF	chr9:44176537-44176725	GM12878	blood:	n/a	n/a
40	BATF	chr9:44402919-44403250	GM12878	blood:	n/a	n/a
41	BATF	chr9:44355408-44355626	GM12878	blood:	n/a	n/a
42	BATF	chr9:44556841-44557602	GM12878	blood:	n/a	n/a
43	BATF	chr9:44245375-44245745	GM12878	blood:	n/a	n/a
44	BATF	chr9:44645234-44645529	GM12878	blood:	n/a	chr9:44645403-44645414
45	BATF	chr9:44306098-44306362	GM12878	blood:	n/a	n/a
46	BATF	chr9:44550562-44550766	GM12878	blood:	n/a	n/a
47	BATF	chr9:44539661-44540230	GM12878	blood:	n/a	n/a
48	BATF	chr9:44419769-44419966	GM12878	blood:	n/a	n/a
49	BATF	chr9:44469306-44469638	GM12878	blood:	n/a	n/a
50	BATF	chr9:44306115-44306341	GM12878	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:44842398-44842448	AG10803	skin:	n/a
2	chr9:44745070-44745120	HAEpiC	amniotic membrane:	n/a
3	chr9:44841495-44841545	GM12892	blood:	n/a
4	chr9:44841495-44841545	AG10803	skin:	n/a
5	chr9:44742086-44742136	HPAEpiC	pulmonary alveolar:	n/a
6	chr9:44227339-44227389	HCM	heart:	n/a
7	chr9:44227210-44227260	PFSK-1	brain:	n/a
8	chr9:44841495-44841545	NHDF-neo	bronchial:	n/a
9	chr9:44313114-44313164	HRCEpiC	kidney:	n/a
10	chr9:44745070-44745120	NHDF-neo	bronchial:	n/a
11	chr9:44842398-44842448	NB4	blood:	n/a
12	chr9:44841495-44841545	BE2_C	brain:	n/a
13	chr9:44744257-44744307	NHBE	bronchial:	n/a
14	chr9:44420179-44420229	GM12891	blood:	n/a
15	chr9:44742086-44742136	SK-N-SH	brain:	n/a
16	chr9:44420179-44420229	NT2-D1	testis:	n/a
17	chr9:44422602-44422652	ECC-1	luminal epithelium:	n/a
18	chr9:44313114-44313164	HRPEpiC	eye:	n/a
19	chr9:44227339-44227389	NH-A	brain:	n/a
20	chr9:44227210-44227260	SK-N-MC	brain:	n/a
21	chr9:44420179-44420229	AG04450	lung:	fetal
22	chr9:44422602-44422652	AG09319	gingival:	n/a
23	chr9:44841495-44841545	SAEC	small airway:	n/a
24	chr9:44420179-44420229	PrEC	prostate:	n/a
25	chr9:44841495-44841545	ovcar-3	ovarian:	n/a
26	chr9:44841495-44841545	GM12878	blood:	n/a
27	chr9:44401998-44402048	ECC-1	luminal epithelium:	n/a
28	chr9:44742086-44742136	PrEC	prostate:	n/a
29	chr9:44841495-44841545	HRCEpiC	kidney:	n/a
30	chr9:44227210-44227260	HMEC	breast:	n/a
31	chr9:44743856-44743906	HMEC	breast:	n/a
32	chr9:44227210-44227260	Hepatocyte	liver:	n/a
33	chr9:44742086-44742136	NHDF-neo	bronchial:	n/a
34	chr9:44744257-44744307	BJ	skin:	n/a
35	chr9:44842398-44842448	HRCEpiC	kidney:	n/a
36	chr9:44743856-44743906	ProgFib	skin:	n/a
37	chr9:44744257-44744307	HCM	heart:	n/a
38	chr9:44227210-44227260	IMR90	lung:	fetal
39	chr9:44227339-44227389	SK-N-MC	brain:	n/a
40	chr9:44227339-44227389	U87	brain:	n/a
41	chr9:44743856-44743906	BJ	skin:	n/a
42	chr9:44313114-44313164	AG09319	gingival:	n/a
43	chr9:44841495-44841545	NB4	blood:	n/a
44	chr9:44227210-44227260	AG09319	gingival:	n/a
45	chr9:44743856-44743906	HUVEC	blood vessel:	n/a
46	chr9:44401998-44402048	HCPEpiC	choroid plexus:	n/a
47	chr9:44227210-44227260	GM12891	blood:	n/a
48	chr9:44742086-44742136	K562	blood:	n/a
49	chr9:44841495-44841545	ECC-1	luminal epithelium:	n/a
50	chr9:44745070-44745120	SK-N-SH	brain:	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:33 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM75A6-2	chr9:44182692-44183417	XLOC_007697
2	lnc-FAM75A6-3	chr9:44256189-44256817	ENSG00000233424
3	lnc-FAM75A6-2	chr9:44181550-44181732	XLOC_007697
4	lnc-FAM75A6-1	chr9:44144869-44145101	XLOC_007696
5	lnc-CNTNAP3B-1	chr9:44384585-44387483	ENSG00000229311
6	lnc-CNTNAP3B-1	chr9:44387768-44387853	NR_046203
7	lnc-RP11-160N1.10.1-1	chr9:44828088-44828239	ENSG00000231248.2
8	lnc-FAM75A6-14	chr9:44676388-44676450	NONHSAT131392
9	lnc-RP11-160N1.10.1-1	chr9:44823714-44823845	ENSG00000231248.2
10	lnc-RP11-160N1.10.1-1	chr9:44834508-44834806	ENSG00000231248.2
11	lnc-RP11-160N1.10.1-4	chr9:44775383-44775517	NONHSAT131393
12	lnc-RP11-160N1.10.1-1	chr9:44835387-44835521	ENSG00000231248.2
13	lnc-CNTNAP3B-1	chr9:44391077-44391705	ENSG00000229311
14	lnc-FAM75A6-14	chr9:44673720-44673889	NONHSAT131392
15	lnc-FAM75A6-14	chr9:44674678-44674747	NONHSAT131392
16	lnc-FAM75A6-13	chr9:44478194-44478456	NONHSAT131390
17	lnc-RP11-160N1.10.1-4	chr9:44774504-44774802	NONHSAT131393
18	lnc-FAM75A6-3	chr9:44256580-44256817	ENSG00000233424.2
19	lnc-RP11-160N1.10.1-2	chr9:44403060-44403260	ENSG00000237357
20	lnc-FAM75A6-3	chr9:44260422-44263319	ENSG00000233424.2
21	lnc-RP11-160N1.10.1-4	chr9:44768084-44768235	NONHSAT131393
22	lnc-FAM75A6-1	chr9:44136621-44137011	XLOC_007696
23	lnc-CNTNAP3B-1	chr9:44391077-44391416	NR_046203
24	lnc-CNTNAP3B-1	chr9:44387387-44387483	NR_046203
25	lnc-RP11-160N1.10.1-4	chr9:44763709-44763841	NONHSAT131393
26	lnc-FAM75A6-13	chr9:44477549-44477882	NONHSAT131390
27	lnc-RP11-160N1.10.1-2	chr9:44402460-44402515	ENSG00000237357
28	lnc-FAM75A6-3	chr9:44260052-44260139	ENSG00000233424
29	lnc-CNTNAP3B-1	chr9:44387768-44387853	ENSG00000229311
30	lnc-RP11-160N1.10.1-5	chr9:44562093-44562588	NONHSAT131391
31	lnc-FAM75A6-14	chr9:44672800-44672959	NONHSAT131392
32	lnc-FAM75A6-3	chr9:44260052-44260139	ENSG00000233424.2
33	lnc-FAM75A6-3	chr9:44260422-44263319	ENSG00000233424

No data

Variant related genes	Relation type
ENSG00000223664	TF binding region
ATP5A1P6	TF binding region
ENSG00000231248	TF binding region
ENSG00000228920	TF binding region
ENSG00000230245	TF binding region
MEP1AP4	TF binding region
ENSG00000227353	TF binding region
ENSG00000216829	TF binding region
ENSG00000268708	TF binding region
ENSG00000212952	TF binding region
ENSG00000238933	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
ENSG00000268234	TF binding region
ENSG00000223664	CpG island
ATP5A1P6	CpG island
ENSG00000231248	CpG island
ENSG00000228920	CpG island
ENSG00000230245	CpG island
MEP1AP4	CpG island
ENSG00000227353	CpG island
ENSG00000216829	CpG island
ENSG00000268708	CpG island
ENSG00000212952	CpG island
ENSG00000238933	CpG island
ENSG00000204818	CpG island
ENSG00000237357	CpG island
RBPJP6	CpG island
ENSG00000204816	CpG island
ENSG00000233424	CpG island
ENSG00000229311	CpG island
ENSG00000268234	CpG island
ZBTB39	miRNA target sites

Extended variants
information (count: 3640 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:3640 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143444840	chr9:44136779-44136780	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs568965460	chr9:44136793-44136794	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs539591798	chr9:44136878-44136879	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs558364210	chr9:44136901-44136902	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs573508507	chr9:44136917-44136918	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs28685579	chr9:44136950-44136951	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs188657227	chr9:44136951-44136952	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs192311648	chr9:44136958-44136959	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs544289315	chr9:44136959-44136960	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs556178836	chr9:44136961-44136962	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs577712835	chr9:44136993-44136994	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs572943902	chr9:44137004-44137005	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs563974519	chr9:44140611-44140612	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs187572884	chr9:44140620-44140621	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs138329898	chr9:44140632-44140633	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs375465425	chr9:44140636-44140637	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs564499132	chr9:44140676-44140677	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs143036392	chr9:44140679-44140680	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs555105056	chr9:44140687-44140688	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs575278477	chr9:44140699-44140700	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs546792016	chr9:44140704-44140705	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs142768814	chr9:44140756-44140757	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs193030158	chr9:44140825-44140826	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs529848390	chr9:44140849-44140850	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs71364291	chr9:44140856-44140857	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs398113482	chr9:44140869-44140870	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs138146692	chr9:44140911-44140912	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs569607276	chr9:44140954-44140955	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs536998591	chr9:44140982-44140983	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs185570323	chr9:44140993-44140994	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs190628885	chr9:44140997-44140998	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs112856245	chr9:44144869-44144870	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs538730265	chr9:44144879-44144880	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs370940720	chr9:44144880-44144881	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs572908570	chr9:44144890-44144891	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs533978405	chr9:44144913-44144914	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs200100209	chr9:44144919-44144920	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs555645167	chr9:44144928-44144929	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs143903958	chr9:44144931-44144932	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs62539327	chr9:44144935-44144936	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs139412333	chr9:44144938-44144939	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs62539328	chr9:44144964-44144965	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs576180616	chr9:44145034-44145035	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs556163502	chr9:44145046-44145047	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs60487881	chr9:44145050-44145051	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs577590662	chr9:44145052-44145053	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs187379027	chr9:44145058-44145059	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs192217325	chr9:44145062-44145063	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs544733688	chr9:44145065-44145066	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs560202766	chr9:44145068-44145069	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Lung cancer	17086460	CNVD
Rhabdomyosarcoma	16790082	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	23813976	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:44140600-44140800	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr9:44140600-44141000	Active TSS	K562	blood
3	chr9:44153800-44154200	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr9:44162000-44162200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
5	chr9:44163600-44163800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
6	chr9:44163600-44163800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
7	chr9:44163600-44163800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
8	chr9:44163800-44164000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
9	chr9:44163800-44164400	Active TSS	Brain Anterior Caudate	brain
10	chr9:44164200-44164600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr9:44164400-44164600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
12	chr9:44164600-44165000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr9:44165000-44165400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr9:44165200-44165400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
15	chr9:44165200-44165800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
16	chr9:44165400-44166800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr9:44165600-44165800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr9:44165600-44166000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
19	chr9:44165600-44166200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
20	chr9:44165800-44166200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
21	chr9:44165800-44180000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr9:44166200-44166600	Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr9:44166600-44166800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr9:44166600-44167000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
25	chr9:44166800-44167000	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr9:44166800-44167000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr9:44166800-44168400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
28	chr9:44167000-44167200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
29	chr9:44167000-44167200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
30	chr9:44167000-44168600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
31	chr9:44167200-44167400	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr9:44167200-44168200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr9:44168000-44169200	Enhancers	Adipose Nuclei	Adipose
34	chr9:44168200-44168400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
35	chr9:44168200-44168400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr9:44169200-44170000	Weak transcription	Adipose Nuclei	Adipose
37	chr9:44170000-44170800	Enhancers	Adipose Nuclei	Adipose
38	chr9:44170400-44170800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
39	chr9:44176200-44176400	Enhancers	Adipose Nuclei	Adipose
40	chr9:44176200-44176800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
41	chr9:44176800-44177000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
42	chr9:44176800-44177000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
43	chr9:44177000-44177200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
44	chr9:44180000-44180200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr9:44180200-44187800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr9:44183400-44183600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
47	chr9:44183400-44183600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
48	chr9:44187400-44187800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr9:44187800-44188000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr9:44187800-44188000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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