Variant report

Variant	nsv1030815
Chromosome Location	chr9:44114860-44824251
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3162)
CpG islands
(count:977)
Chromatin interactive
region (count:1)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3162 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

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	chr9:44118677-44118886	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:44799676-44800004	HepG2	liver:	n/a	n/a
4	ATF1	chr9:44781241-44781724	K562	blood:	n/a	n/a
5	BACH1	chr9:44227257-44227630	K562	blood:	n/a	n/a
6	BACH1	chr9:44227184-44227631	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr9:44245873-44246195	GM12878	blood:	n/a	n/a
8	BATF	chr9:44539661-44540230	GM12878	blood:	n/a	n/a
9	BATF	chr9:44341525-44341789	GM12878	blood:	n/a	chr9:44341638-44341649
10	BATF	chr9:44265544-44265770	GM12878	blood:	n/a	n/a
11	BATF	chr9:44401959-44402428	GM12878	blood:	n/a	n/a
12	BATF	chr9:44245375-44245745	GM12878	blood:	n/a	n/a
13	BATF	chr9:44606159-44606345	GM12878	blood:	n/a	n/a
14	BATF	chr9:44125333-44125599	GM12878	blood:	n/a	n/a
15	BATF	chr9:44550459-44550750	GM12878	blood:	n/a	n/a
16	BATF	chr9:44367161-44367437	GM12878	blood:	n/a	n/a
17	BATF	chr9:44292314-44292554	GM12878	blood:	n/a	n/a
18	BATF	chr9:44556907-44557469	GM12878	blood:	n/a	n/a
19	BATF	chr9:44245139-44246113	GM12878	blood:	n/a	n/a
20	BATF	chr9:44212521-44212907	GM12878	blood:	n/a	chr9:44212712-44212723
21	BATF	chr9:44605098-44605838	GM12878	blood:	n/a	n/a
22	BATF	chr9:44124132-44124352	GM12878	blood:	n/a	n/a
23	BATF	chr9:44577860-44578259	GM12878	blood:	n/a	chr9:44577967-44577975
24	BATF	chr9:44355328-44355568	GM12878	blood:	n/a	n/a
25	BATF	chr9:44742136-44742432	GM12878	blood:	n/a	n/a
26	BATF	chr9:44367127-44367454	GM12878	blood:	n/a	n/a
27	BATF	chr9:44645280-44645491	GM12878	blood:	n/a	chr9:44645403-44645414
28	BATF	chr9:44401329-44401837	GM12878	blood:	n/a	n/a
29	BATF	chr9:44402875-44403302	GM12878	blood:	n/a	n/a
30	BATF	chr9:44340761-44341046	GM12878	blood:	n/a	n/a
31	BATF	chr9:44280452-44280759	GM12878	blood:	n/a	n/a
32	BATF	chr9:44577809-44578267	GM12878	blood:	n/a	chr9:44577967-44577975
33	BATF	chr9:44434645-44435048	GM12878	blood:	n/a	n/a
34	BATF	chr9:44605070-44605809	GM12878	blood:	n/a	n/a
35	BATF	chr9:44419769-44419966	GM12878	blood:	n/a	n/a
36	BATF	chr9:44342310-44342546	GM12878	blood:	n/a	n/a
37	BATF	chr9:44552225-44552444	GM12878	blood:	n/a	n/a
38	BATF	chr9:44124043-44124400	GM12878	blood:	n/a	n/a
39	BATF	chr9:44528122-44528281	GM12878	blood:	n/a	n/a
40	BATF	chr9:44306115-44306341	GM12878	blood:	n/a	n/a
41	BATF	chr9:44176537-44176725	GM12878	blood:	n/a	n/a
42	BATF	chr9:44403838-44404118	GM12878	blood:	n/a	n/a
43	BATF	chr9:44118541-44118761	GM12878	blood:	n/a	n/a
44	BATF	chr9:44305341-44305592	GM12878	blood:	n/a	n/a
45	BATF	chr9:44133305-44133513	GM12878	blood:	n/a	chr9:44133433-44133441
46	BATF	chr9:44145517-44145676	GM12878	blood:	n/a	n/a
47	BATF	chr9:44125369-44125590	GM12878	blood:	n/a	n/a
48	BATF	chr9:44556841-44557602	GM12878	blood:	n/a	n/a
49	BATF	chr9:44212515-44212942	GM12878	blood:	n/a	chr9:44212712-44212723
50	BATF	chr9:44550562-44550766	GM12878	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:44744257-44744307	SK-N-MC	brain:	n/a
2	chr9:44744257-44744307	SK-N-MC	brain:	n/a
3	chr9:44227339-44227389	MCF-7	breast:	n/a
4	chr9:44742086-44742136	HCF	heart:	n/a
5	chr9:44118236-44118286	ProgFib	skin:	n/a
6	chr9:44120147-44120197	U87	brain:	n/a
7	chr9:44313114-44313164	AG09319	gingival:	n/a
8	chr9:44118915-44118965	HMEC	breast:	n/a
9	chr9:44313114-44313164	Jurkat	blood:	n/a
10	chr9:44227210-44227260	AG09309	skin:	n/a
11	chr9:44120147-44120197	MCF10A-Er-Src	breast:	n/a
12	chr9:44745070-44745120	GM12891	blood:	n/a
13	chr9:44744257-44744307	PrEC	prostate:	n/a
14	chr9:44120147-44120197	SK-N-MC	brain:	n/a
15	chr9:44422602-44422652	SK-N-SH_RA	brain:	n/a
16	chr9:44227210-44227260	GM12891	blood:	n/a
17	chr9:44745070-44745120	Caco-2	colon:	n/a
18	chr9:44119823-44119873	SAEC	small airway:	n/a
19	chr9:44119413-44119463	PFSK-1	brain:	n/a
20	chr9:44742086-44742136	HEEpiC	esophagus:	n/a
21	chr9:44227210-44227260	HRCEpiC	kidney:	n/a
22	chr9:44744257-44744307	NB4	blood:	n/a
23	chr9:44119413-44119463	HEK293	kidney:	embryo
24	chr9:44313114-44313164	AG04449	skin:	fetal
25	chr9:44227339-44227389	HCM	heart:	n/a
26	chr9:44118915-44118965	Caco-2	colon:	n/a
27	chr9:44227210-44227260	U87	brain:	n/a
28	chr9:44742086-44742136	HUVEC	blood vessel:	n/a
29	chr9:44227210-44227260	GM12878	blood:	n/a
30	chr9:44118236-44118286	MCF-7	breast:	n/a
31	chr9:44118236-44118286	HPAEpiC	pulmonary alveolar:	n/a
32	chr9:44120147-44120197	NT2-D1	testis:	n/a
33	chr9:44743856-44743906	Hepatocyte	liver:	n/a
34	chr9:44119413-44119463	HEEpiC	esophagus:	n/a
35	chr9:44420179-44420229	ovcar-3	ovarian:	n/a
36	chr9:44744257-44744307	AG09319	gingival:	n/a
37	chr9:44118236-44118286	PrEC	prostate:	n/a
38	chr9:44118915-44118965	Hela-S3	cervix:	n/a
39	chr9:44313114-44313164	NHDF-neo	bronchial:	n/a
40	chr9:44422602-44422652	ovcar-3	ovarian:	n/a
41	chr9:44118014-44118064	HRCEpiC	kidney:	n/a
42	chr9:44119823-44119873	HepG2	liver:	n/a
43	chr9:44743856-44743906	GM06990	blood:	n/a
44	chr9:44742086-44742136	AoSMC	blood vessel:	n/a
45	chr9:44401998-44402048	A549	lung:	n/a
46	chr9:44118236-44118286	Hepatocyte	liver:	n/a
47	chr9:44743856-44743906	PFSK-1	brain:	n/a
48	chr9:44118014-44118064	LNCaP	prostate:	n/a
49	chr9:44118014-44118064	HRE	kidney:	n/a
50	chr9:44118014-44118064	ECC-1	luminal epithelium:	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:30 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
ENSG00000223664	TF binding region
ATP5A1P6	TF binding region
ENSG00000231248	TF binding region
ENSG00000204818	TF binding region
ENSG00000228920	TF binding region
ENSG00000230245	TF binding region
ENSG00000237357	TF binding region
MEP1AP4	TF binding region
ENSG00000227353	TF binding region
RBPJP6	TF binding region
ENSG00000204816	TF binding region
ENSG00000216829	TF binding region
ENSG00000233424	TF binding region
ENSG00000268708	TF binding region
ENSG00000229311	TF binding region
ENSG00000212952	TF binding region
ANKRD20A7P	TF binding region
ENSG00000268234	TF binding region
ENSG00000223664	CpG island
ATP5A1P6	CpG island
ENSG00000231248	CpG island
ENSG00000204818	CpG island
ENSG00000228920	CpG island
ENSG00000230245	CpG island
ENSG00000237357	CpG island
MEP1AP4	CpG island
ENSG00000227353	CpG island
RBPJP6	CpG island
ENSG00000204816	CpG island
ENSG00000216829	CpG island
ENSG00000233424	CpG island
ENSG00000268708	CpG island
ENSG00000229311	CpG island
ENSG00000212952	CpG island
ANKRD20A7P	CpG island
ENSG00000268234	CpG island
ZBTB39	miRNA target sites

Extended variants
information (count: 3855 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:3855 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140618852	chr9:44114864-44114865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs533775604	chr9:44114904-44114905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555222754	chr9:44114961-44114962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs573876566	chr9:44115007-44115008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565629568	chr9:44115052-44115053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534751673	chr9:44115084-44115085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371251407	chr9:44115137-44115138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555888171	chr9:44115145-44115146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577610928	chr9:44115179-44115180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545114063	chr9:44115204-44115205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs199503711	chr9:44115205-44115206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs560323076	chr9:44115256-44115257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527863206	chr9:44115260-44115261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182420228	chr9:44115261-44115262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113514358	chr9:44115299-44115300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs193155306	chr9:44115304-44115305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs144502214	chr9:44115308-44115309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs377540980	chr9:44115309-44115310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146615693	chr9:44115310-44115311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112567390	chr9:44115321-44115322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150282038	chr9:44115340-44115341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112146886	chr9:44115342-44115343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs111527469	chr9:44115347-44115348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113566810	chr9:44115349-44115350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568286039	chr9:44115365-44115366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs28731097	chr9:44115372-44115373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113834438	chr9:44115488-44115489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532413455	chr9:44115598-44115599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547472521	chr9:44115607-44115608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138948596	chr9:44115612-44115613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533713346	chr9:44115616-44115617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553966305	chr9:44115653-44115654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548912554	chr9:44115656-44115657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148810867	chr9:44115665-44115666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537744783	chr9:44115672-44115673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556460040	chr9:44115673-44115674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577549930	chr9:44115719-44115720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538665385	chr9:44115782-44115783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs28666423	chr9:44115808-44115809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553874833	chr9:44115821-44115822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187903247	chr9:44115829-44115830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs28612278	chr9:44115831-44115832	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs372541930	chr9:44115840-44115841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543204035	chr9:44115900-44115901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577118878	chr9:44115914-44115915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561327670	chr9:44116014-44116015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539443896	chr9:44116024-44116025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs137972911	chr9:44116039-44116040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186706288	chr9:44116067-44116068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543750380	chr9:44116079-44116080	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
Schizophrenia	20967226	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:44114000-44115000	Enhancers	Liver	Liver
2	chr9:44115000-44118000	Weak transcription	Liver	Liver
3	chr9:44118000-44118200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:44118000-44118200	Active TSS	Primary T cells fromperipheralblood	blood
5	chr9:44118000-44118200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr9:44118000-44118200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr9:44118000-44118200	Active TSS	Right Ventricle	heart
8	chr9:44118000-44118400	Active TSS	Primary monocytes fromperipheralblood	blood
9	chr9:44118000-44118600	Active TSS	Breast Myoepithelial Primary Cells	Breast
10	chr9:44118000-44118600	Active TSS	Brain Hippocampus Middle	brain
11	chr9:44118000-44118800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr9:44118000-44118800	Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr9:44118000-44118800	Active TSS	Liver	Liver
14	chr9:44118000-44118800	Active TSS	NHEK	skin
15	chr9:44118000-44119000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr9:44118000-44119000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
17	chr9:44118000-44119000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr9:44118000-44119000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
19	chr9:44118000-44119000	Active TSS	Primary hematopoietic stem cells	blood
20	chr9:44118000-44119000	Active TSS	Primary hematopoietic stem cells short term culture	blood
21	chr9:44118000-44119000	Active TSS	Cortex derived primary cultured neurospheres	brain
22	chr9:44118000-44119000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr9:44118000-44119000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
24	chr9:44118000-44119000	Active TSS	Colon Smooth Muscle	Colon
25	chr9:44118000-44119000	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
26	chr9:44118000-44119000	Active TSS	Left Ventricle	heart
27	chr9:44118000-44119000	Active TSS	Rectal Mucosa Donor 31	rectum
28	chr9:44118000-44119000	Active TSS	A549	lung
29	chr9:44118000-44119000	Active TSS	Dnd41	blood
30	chr9:44118000-44119200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
31	chr9:44118000-44119200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
32	chr9:44118000-44119200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr9:44118000-44119200	Active TSS	Brain Angular Gyrus	brain
34	chr9:44118000-44119200	Active TSS	Brain Inferior Temporal Lobe	brain
35	chr9:44118000-44119200	Active TSS	HepG2	liver
36	chr9:44118000-44119400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr9:44118000-44119400	Active TSS	Adipose Nuclei	Adipose
38	chr9:44118000-44119400	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
39	chr9:44118000-44119400	ZNF genes & repeats	Fetal Intestine Large	intestine
40	chr9:44118000-44119400	Active TSS	Fetal Thymus	thymus
41	chr9:44118000-44119600	Active TSS	Brain Anterior Caudate	brain
42	chr9:44118000-44119600	Active TSS	Thymus	Thymus
43	chr9:44118000-44119800	Active TSS	Brain Germinal Matrix	brain
44	chr9:44118000-44120000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr9:44118000-44120000	Active TSS	Fetal Brain Female	brain
46	chr9:44118200-44118400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr9:44118200-44118400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr9:44118200-44118400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr9:44118200-44118400	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr9:44118200-44118400	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle

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