Variant report

Variant	esv1833488
Chromosome Location	chr9:44046700-44821943
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3733)
CpG islands
(count:979)
Chromatin interactive
region (count:1)
LncRNA
region (count:31)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3733 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

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	ARID3A	chr9:44118677-44118886	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:44108136-44108696	HepG2	liver:	n/a	n/a
5	ATF1	chr9:44781241-44781724	K562	blood:	n/a	n/a
6	BACH1	chr9:44227257-44227630	K562	blood:	n/a	n/a
7	BACH1	chr9:44227184-44227631	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr9:44245873-44246195	GM12878	blood:	n/a	n/a
9	BATF	chr9:44645280-44645491	GM12878	blood:	n/a	chr9:44645403-44645414
10	BATF	chr9:44145517-44145676	GM12878	blood:	n/a	n/a
11	BATF	chr9:44556907-44557469	GM12878	blood:	n/a	n/a
12	BATF	chr9:44108799-44108996	GM12878	blood:	n/a	n/a
13	BATF	chr9:44552199-44552435	GM12878	blood:	n/a	n/a
14	BATF	chr9:44292314-44292554	GM12878	blood:	n/a	n/a
15	BATF	chr9:44107334-44107970	GM12878	blood:	n/a	n/a
16	BATF	chr9:44245375-44245745	GM12878	blood:	n/a	n/a
17	BATF	chr9:44243686-44243967	GM12878	blood:	n/a	n/a
18	BATF	chr9:44108339-44108646	GM12878	blood:	n/a	chr9:44108541-44108552
19	BATF	chr9:44379817-44379994	GM12878	blood:	n/a	chr9:44379913-44379924
20	BATF	chr9:44086267-44086535	GM12878	blood:	n/a	n/a
21	BATF	chr9:44125369-44125590	GM12878	blood:	n/a	n/a
22	BATF	chr9:44401959-44402428	GM12878	blood:	n/a	n/a
23	BATF	chr9:44403838-44404118	GM12878	blood:	n/a	n/a
24	BATF	chr9:44605098-44605838	GM12878	blood:	n/a	n/a
25	BATF	chr9:44606159-44606345	GM12878	blood:	n/a	n/a
26	BATF	chr9:44401104-44402763	GM12878	blood:	n/a	n/a
27	BATF	chr9:44063096-44063309	GM12878	blood:	n/a	n/a
28	BATF	chr9:44133305-44133513	GM12878	blood:	n/a	chr9:44133433-44133441
29	BATF	chr9:44552225-44552444	GM12878	blood:	n/a	n/a
30	BATF	chr9:44065395-44065684	GM12878	blood:	n/a	n/a
31	BATF	chr9:44577860-44578259	GM12878	blood:	n/a	chr9:44577967-44577975
32	BATF	chr9:44305341-44305592	GM12878	blood:	n/a	n/a
33	BATF	chr9:44124132-44124352	GM12878	blood:	n/a	n/a
34	BATF	chr9:44088871-44089267	GM12878	blood:	n/a	chr9:44088983-44088991
35	BATF	chr9:44533431-44533653	GM12878	blood:	n/a	n/a
36	BATF	chr9:44107144-44107983	GM12878	blood:	n/a	n/a
37	BATF	chr9:44118541-44118761	GM12878	blood:	n/a	n/a
38	BATF	chr9:44341546-44341772	GM12878	blood:	n/a	chr9:44341638-44341649
39	BATF	chr9:44100518-44100936	GM12878	blood:	n/a	chr9:44100637-44100647
40	BATF	chr9:44054788-44055026	GM12878	blood:	n/a	n/a
41	BATF	chr9:44402875-44403302	GM12878	blood:	n/a	n/a
42	BATF	chr9:44355408-44355626	GM12878	blood:	n/a	n/a
43	BATF	chr9:44088928-44089261	GM12878	blood:	n/a	chr9:44088983-44088991
44	BATF	chr9:44355328-44355568	GM12878	blood:	n/a	n/a
45	BATF	chr9:44095589-44095794	GM12878	blood:	n/a	n/a
46	BATF	chr9:44245139-44246113	GM12878	blood:	n/a	n/a
47	BATF	chr9:44072537-44072807	GM12878	blood:	n/a	chr9:44072668-44072679
48	BATF	chr9:44539661-44540230	GM12878	blood:	n/a	n/a
49	BATF	chr9:44434613-44435054	GM12878	blood:	n/a	n/a
50	BATF	chr9:44108035-44108219	GM12878	blood:	n/a	n/a

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:44743856-44743906	HMEC	breast:	n/a
2	chr9:44227210-44227260	HEK293	kidney:	embryo
3	chr9:44119413-44119463	LNCaP	prostate:	n/a
4	chr9:44743856-44743906	HMEC	breast:	n/a
5	chr9:44227210-44227260	HEK293	kidney:	embryo
6	chr9:44119413-44119463	LNCaP	prostate:	n/a
7	chr9:44119823-44119873	HRPEpiC	eye:	n/a
8	chr9:44227339-44227389	BE2_C	brain:	n/a
9	chr9:44420179-44420229	A549	lung:	n/a
10	chr9:44422602-44422652	NHDF-neo	bronchial:	n/a
11	chr9:44118915-44118965	MCF-7	breast:	n/a
12	chr9:44745070-44745120	GM12878	blood:	n/a
13	chr9:44744257-44744307	A549	lung:	n/a
14	chr9:44313114-44313164	A549	lung:	n/a
15	chr9:44401998-44402048	NH-A	brain:	n/a
16	chr9:44120147-44120197	MCF-7	breast:	n/a
17	chr9:44227339-44227389	SK-N-SH	brain:	n/a
18	chr9:44401998-44402048	AG09319	gingival:	n/a
19	chr9:44744257-44744307	HUVEC	blood vessel:	n/a
20	chr9:44743856-44743906	SK-N-MC	brain:	n/a
21	chr9:44119823-44119873	GM12891	blood:	n/a
22	chr9:44118236-44118286	GM06990	blood:	n/a
23	chr9:44422602-44422652	ovcar-3	ovarian:	n/a
24	chr9:44744257-44744307	GM06990	blood:	n/a
25	chr9:44743856-44743906	U87	brain:	n/a
26	chr9:44119413-44119463	HRE	kidney:	n/a
27	chr9:44227210-44227260	AG09309	skin:	n/a
28	chr9:44401998-44402048	SK-N-MC	brain:	n/a
29	chr9:44401998-44402048	ovcar-3	ovarian:	n/a
30	chr9:44118236-44118286	AG04449	skin:	fetal
31	chr9:44420179-44420229	SKMC	muscle:	n/a
32	chr9:44743856-44743906	HUVEC	blood vessel:	n/a
33	chr9:44119413-44119463	SK-N-SH	brain:	n/a
34	chr9:44743856-44743906	CMK	blood:	n/a
35	chr9:44420179-44420229	MCF-7	breast:	n/a
36	chr9:44118236-44118286	MCF-7	breast:	n/a
37	chr9:44118236-44118286	SK-N-MC	brain:	n/a
38	chr9:44745070-44745120	IMR90	lung:	fetal
39	chr9:44745070-44745120	AoSMC	blood vessel:	n/a
40	chr9:44119823-44119873	AG09319	gingival:	n/a
41	chr9:44118915-44118965	BE2_C	brain:	n/a
42	chr9:44119413-44119463	HPAEpiC	pulmonary alveolar:	n/a
43	chr9:44118014-44118064	ovcar-3	ovarian:	n/a
44	chr9:44119823-44119873	AG04450	lung:	fetal
45	chr9:44420179-44420229	HCF	heart:	n/a
46	chr9:44743856-44743906	MCF10A-Er-Src	breast:	n/a
47	chr9:44118915-44118965	HCT-116	colon:	n/a
48	chr9:44227339-44227389	Caco-2	colon:	n/a
49	chr9:44742086-44742136	GM06990	blood:	n/a
50	chr9:44118236-44118286	T-47D	breast:	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:31 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNTNAP3B-1	chr9:44384585-44387483	ENSG00000229311
2	lnc-FAM75A6-1	chr9:44136621-44137011	XLOC_007696
3	lnc-FAM75A6-3	chr9:44260052-44260139	ENSG00000233424
4	lnc-RP11-160N1.10.1-2	chr9:44403060-44403260	ENSG00000237357
5	lnc-CNTNAP3B-1	chr9:44391077-44391416	NR_046203
6	lnc-RP11-160N1.10.1-2	chr9:44402460-44402515	ENSG00000237357
7	lnc-FAM75A6-3	chr9:44260052-44260139	ENSG00000233424.2
8	lnc-CNTNAP3B-1	chr9:44387768-44387853	NR_046203
9	lnc-FAM75A6-1	chr9:44144869-44145101	XLOC_007696
10	lnc-FAM75A6-14	chr9:44672800-44672959	NONHSAT131392
11	lnc-FAM75A6-7	chr9:44046989-44047817	NONHSAT131371
12	lnc-RP11-160N1.10.1-4	chr9:44763709-44763841	NONHSAT131393
13	lnc-CNTNAP3B-1	chr9:44387387-44387483	NR_046203
14	lnc-FAM75A6-3	chr9:44260422-44263319	ENSG00000233424.2
15	lnc-FAM75A6-8	chr9:44075932-44076173	NONHSAT131372
16	lnc-FAM75A6-13	chr9:44477549-44477882	NONHSAT131390
17	lnc-FAM75A6-14	chr9:44676388-44676450	NONHSAT131392
18	lnc-RP11-160N1.10.1-4	chr9:44775383-44775517	NONHSAT131393
19	lnc-FAM75A6-14	chr9:44674678-44674747	NONHSAT131392
20	lnc-CNTNAP3B-1	chr9:44391077-44391705	ENSG00000229311
21	lnc-FAM75A6-13	chr9:44478194-44478456	NONHSAT131390
22	lnc-RP11-160N1.10.1-4	chr9:44774504-44774802	NONHSAT131393
23	lnc-FAM75A6-3	chr9:44256189-44256817	ENSG00000233424
24	lnc-FAM75A6-2	chr9:44182692-44183417	XLOC_007697
25	lnc-FAM75A6-2	chr9:44181550-44181732	XLOC_007697
26	lnc-RP11-160N1.10.1-4	chr9:44768084-44768235	NONHSAT131393
27	lnc-FAM75A6-14	chr9:44673720-44673889	NONHSAT131392
28	lnc-FAM75A6-3	chr9:44256580-44256817	ENSG00000233424.2
29	lnc-RP11-160N1.10.1-5	chr9:44562093-44562588	NONHSAT131391
30	lnc-FAM75A6-3	chr9:44260422-44263319	ENSG00000233424
31	lnc-CNTNAP3B-1	chr9:44387768-44387853	ENSG00000229311

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
ENSG00000170165	TF binding region
ENSG00000216829	TF binding region
ENSG00000268708	TF binding region
ENSG00000212952	TF binding region
ANKRD20A7P	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
ENSG00000223664	CpG island
ATP5A1P6	CpG island
ENSG00000231248	CpG island
ENSG00000228920	CpG island
ENSG00000230245	CpG island
MEP1AP4	CpG island
ENSG00000227353	CpG island
ENSG00000170165	CpG island
ENSG00000216829	CpG island
ENSG00000268708	CpG island
ENSG00000212952	CpG island
ANKRD20A7P	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
ZBTB39	miRNA target sites

Extended variants
information (count: 6897 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:6897 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62536267	chr9:44047497-44047498	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs62536270	chr9:44049031-44049032	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs62536273	chr9:44050270-44050271	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs62536274	chr9:44050282-44050283	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs62536275	chr9:44050448-44050449	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs549530150	chr9:44057234-44057235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200277147	chr9:44057244-44057245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201054468	chr9:44057262-44057263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538723266	chr9:44057273-44057274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553782065	chr9:44057302-44057303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs4031759	chr9:44057312-44057313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4031760	chr9:44057313-44057314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572766073	chr9:44057333-44057334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187292841	chr9:44057352-44057353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372225075	chr9:44057365-44057366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146243940	chr9:44057408-44057409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138099558	chr9:44057409-44057410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142676408	chr9:44057416-44057417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs4031761	chr9:44057431-44057432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537322994	chr9:44057460-44057461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146296338	chr9:44057462-44057463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559168424	chr9:44057478-44057479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77523686	chr9:44057479-44057480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577841468	chr9:44057605-44057606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545110328	chr9:44057613-44057614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559933820	chr9:44057650-44057651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191969952	chr9:44057660-44057661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377223332	chr9:44057690-44057691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542217119	chr9:44057759-44057760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148521027	chr9:44057822-44057823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575911116	chr9:44057866-44057867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531473162	chr9:44057873-44057874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549591531	chr9:44057886-44057887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571092424	chr9:44057912-44057913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532507773	chr9:44057915-44057916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538253330	chr9:44057916-44057917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547863991	chr9:44057933-44057934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62536295	chr9:44057943-44057944	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs62536296	chr9:44058050-44058051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548256462	chr9:44058057-44058058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570350784	chr9:44058058-44058059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571800846	chr9:44058078-44058079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs62536297	chr9:44058088-44058089	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs559231036	chr9:44058139-44058140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146881459	chr9:44058140-44058141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577504160	chr9:44058141-44058142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538786121	chr9:44058149-44058150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553839802	chr9:44058151-44058152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572011282	chr9:44058161-44058162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs542629739	chr9:44058168-44058169	Weak transcription	n/a	n/a	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
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:492 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:44057200-44070600	Weak transcription	Liver	Liver
2	chr9:44070200-44070600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr9:44070600-44070800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr9:44070600-44070800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
5	chr9:44070600-44070800	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
6	chr9:44070600-44070800	ZNF genes & repeats	Primary T cells from cord blood	blood
7	chr9:44070600-44070800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
8	chr9:44070600-44070800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
9	chr9:44070600-44070800	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
10	chr9:44070600-44070800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
11	chr9:44070600-44070800	Flanking Bivalent TSS/Enh	Primary T killer naive cells fromperipheralblood	blood
12	chr9:44070600-44070800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr9:44070600-44070800	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
14	chr9:44070600-44070800	Enhancers	Adipose Nuclei	Adipose
15	chr9:44070600-44070800	Bivalent Enhancer	Aorta	Aorta
16	chr9:44070600-44070800	Active TSS	Brain Anterior Caudate	brain
17	chr9:44070600-44070800	ZNF genes & repeats	Colonic Mucosa	Colon
18	chr9:44070600-44070800	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
19	chr9:44070600-44070800	Enhancers	Right Ventricle	heart
20	chr9:44070600-44071000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
21	chr9:44070600-44071000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
22	chr9:44070600-44071000	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr9:44070600-44071000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr9:44070600-44071000	Flanking Bivalent TSS/Enh	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr9:44070600-44071000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr9:44070600-44071000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
27	chr9:44070600-44071000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
28	chr9:44070600-44071000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
29	chr9:44070600-44071000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
30	chr9:44070600-44071000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
31	chr9:44070600-44071000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr9:44070600-44071000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr9:44070600-44071000	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr9:44070600-44071000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
35	chr9:44070600-44071000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
36	chr9:44070600-44071000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
37	chr9:44070600-44071000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
38	chr9:44070600-44071000	Flanking Bivalent TSS/Enh	Primary T helper naive cells from peripheral blood	blood
39	chr9:44070600-44071000	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
40	chr9:44070600-44071000	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
41	chr9:44070600-44071000	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
42	chr9:44070600-44071000	Flanking Bivalent TSS/Enh	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr9:44070600-44071000	Flanking Bivalent TSS/Enh	Primary T killer memory cells from peripheral blood	blood
44	chr9:44070600-44071000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr9:44070600-44071000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr9:44070600-44071000	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
47	chr9:44070600-44071000	Flanking Bivalent TSS/Enh	Liver	Liver
48	chr9:44070600-44071000	ZNF genes & repeats	Brain Hippocampus Middle	brain
49	chr9:44070600-44071000	Flanking Bivalent TSS/Enh	Brain Substantia Nigra	brain
50	chr9:44070600-44071000	ZNF genes & repeats	Colon Smooth Muscle	Colon

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