Variant report

Variant	nsv1046614
Chromosome Location	chr9:104492314-104686326
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:842)
CpG islands
(count:427)
Chromatin interactive
region (count:30)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:842 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:104604440-104604568	K562	blood:	n/a	n/a
2	ARID3A	chr9:104602870-104603634	K562	blood:	n/a	n/a
3	ARID3A	chr9:104603974-104604201	K562	blood:	n/a	n/a
4	ARID3A	chr9:104656203-104656979	K562	blood:	n/a	n/a
5	ARID3A	chr9:104604790-104605089	K562	blood:	n/a	n/a
6	ATF1	chr9:104602937-104603620	K562	blood:	n/a	n/a
7	ATF1	chr9:104667150-104667409	K562	blood:	n/a	n/a
8	ATF2	chr9:104499005-104499385	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr9:104602886-104603521	K562	blood:	n/a	n/a
10	BACH1	chr9:104666707-104666740	K562	blood:	n/a	n/a
11	BACH1	chr9:104500655-104501144	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr9:104603020-104603535	K562	blood:	n/a	n/a
13	BCLAF1	chr9:104602989-104603485	K562	blood:	n/a	n/a
14	BHLHE40	chr9:104602981-104603519	K562	blood:	n/a	n/a
15	BHLHE40	chr9:104641860-104641886	GM12878	blood:	n/a	n/a
16	BHLHE40	chr9:104656000-104656660	K562	blood:	n/a	n/a
17	BHLHE40	chr9:104603872-104603981	K562	blood:	n/a	n/a
18	BHLHE40	chr9:104629233-104629302	K562	blood:	n/a	n/a
19	BRCA1	chr9:104525751-104525924	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr9:104601296-104601594	K562	blood:	n/a	n/a
21	CBX3	chr9:104602902-104603580	K562	blood:	n/a	n/a
22	CBX3	chr9:104656265-104656906	K562	blood:	n/a	n/a
23	CBX3	chr9:104602864-104603528	K562	blood:	n/a	n/a
24	CCNT2	chr9:104656253-104656608	K562	blood:	n/a	n/a
25	CCNT2	chr9:104602949-104603796	K562	blood:	n/a	n/a
26	CEBPB	chr9:104652997-104653341	K562	blood:	n/a	chr9:104653155-104653166 chr9:104653155-104653168
27	CEBPB	chr9:104557426-104557815	K562	blood:	n/a	chr9:104557616-104557627
28	CEBPB	chr9:104653098-104653298	HepG2	liver:	n/a	chr9:104653155-104653166 chr9:104653155-104653168
29	CEBPB	chr9:104684397-104684686	IMR90	lung:	n/a	chr9:104684525-104684534 chr9:104684523-104684536
30	CEBPB	chr9:104643934-104644220	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr9:104657056-104657181	K562	blood:	n/a	n/a
32	CEBPB	chr9:104557424-104557737	A549	lung:	n/a	chr9:104557616-104557627
33	CEBPB	chr9:104684384-104684709	K562	blood:	n/a	chr9:104684525-104684534 chr9:104684523-104684536
34	CEBPB	chr9:104557478-104557775	K562	blood:	n/a	chr9:104557616-104557627
35	CEBPB	chr9:104643971-104644157	K562	blood:	n/a	n/a
36	CEBPB	chr9:104553838-104554309	HepG2	liver:	n/a	n/a
37	CEBPB	chr9:104586855-104587085	K562	blood:	n/a	chr9:104587024-104587035 chr9:104587023-104587034 chr9:104587023-104587034
38	CEBPB	chr9:104500497-104500505	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr9:104553821-104554141	A549	lung:	n/a	n/a
40	CEBPB	chr9:104586973-104587159	HepG2	liver:	n/a	chr9:104587024-104587035 chr9:104587023-104587034 chr9:104587023-104587034
41	CEBPB	chr9:104603213-104603499	K562	blood:	n/a	n/a
42	CEBPB	chr9:104557453-104557803	HepG2	liver:	n/a	chr9:104557616-104557627
43	CEBPB	chr9:104571492-104571600	HepG2	liver:	n/a	chr9:104571514-104571525
44	CEBPB	chr9:104684467-104684629	H1-hESC	embryonic stem cell:	n/a	chr9:104684525-104684534 chr9:104684523-104684536
45	CEBPB	chr9:104596347-104596651	HepG2	liver:	n/a	chr9:104596523-104596534
46	CEBPB	chr9:104520633-104520833	A549	lung:	n/a	chr9:104520734-104520745 chr9:104520733-104520744
47	CEBPB	chr9:104597034-104597167	HepG2	liver:	n/a	chr9:104597125-104597136
48	CEBPB	chr9:104553848-104554426	K562	blood:	n/a	n/a
49	CEBPB	chr9:104520587-104520900	HepG2	liver:	n/a	chr9:104520734-104520745 chr9:104520733-104520744
50	CEBPB	chr9:104557455-104557771	Hela-S3	cervix:	n/a	chr9:104557616-104557627

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:104500729-104500779	NT2-D1	testis:	n/a
2	chr9:104500954-104501004	HPAEpiC	pulmonary alveolar:	n/a
3	chr9:104499850-104499900	HCF	heart:	n/a
4	chr9:104500958-104501008	HPAEpiC	pulmonary alveolar:	n/a
5	chr9:104499850-104499900	BJ	skin:	n/a
6	chr9:104499850-104499900	PrEC	prostate:	n/a
7	chr9:104501030-104501080	Caco-2	colon:	n/a
8	chr9:104500322-104500372	HRE	kidney:	n/a
9	chr9:104499700-104499750	HPAEpiC	pulmonary alveolar:	n/a
10	chr9:104499700-104499750	LNCaP	prostate:	n/a
11	chr9:104500958-104501008	NHDF-neo	bronchial:	n/a
12	chr9:104499850-104499900	HEEpiC	esophagus:	n/a
13	chr9:104501030-104501080	HCT-116	colon:	n/a
14	chr9:104500958-104501008	HCPEpiC	choroid plexus:	n/a
15	chr9:104500954-104501004	HAEpiC	amniotic membrane:	n/a
16	chr9:104501030-104501080	ECC-1	luminal epithelium:	n/a
17	chr9:104500954-104501004	HCM	heart:	n/a
18	chr9:104499700-104499750	T-47D	breast:	n/a
19	chr9:104500322-104500372	HL-60	blood:	n/a
20	chr9:104500322-104500372	HNPCEpiC	eye:	n/a
21	chr9:104500729-104500779	NHBE	bronchial:	n/a
22	chr9:104499850-104499900	AG04449	skin:	fetal
23	chr9:104500954-104501004	Jurkat	blood:	n/a
24	chr9:104499700-104499750	HIPEpiC	eye:	n/a
25	chr9:104499850-104499900	ProgFib	skin:	n/a
26	chr9:104501030-104501080	BE2_C	brain:	n/a
27	chr9:104501030-104501080	NHBE	bronchial:	n/a
28	chr9:104499700-104499750	GM12878	blood:	n/a
29	chr9:104500322-104500372	NH-A	brain:	n/a
30	chr9:104501030-104501080	GM06990	blood:	n/a
31	chr9:104499850-104499900	Hela-S3	cervix:	n/a
32	chr9:104500729-104500779	HUVEC	blood vessel:	n/a
33	chr9:104500322-104500372	T-47D	breast:	n/a
34	chr9:104499850-104499900	SAEC	small airway:	n/a
35	chr9:104499850-104499900	HEK293	kidney:	embryo
36	chr9:104499700-104499750	AG04449	skin:	fetal
37	chr9:104500958-104501008	U87	brain:	n/a
38	chr9:104501030-104501080	HEEpiC	esophagus:	n/a
39	chr9:104499700-104499750	IMR90	lung:	fetal
40	chr9:104499700-104499750	ECC-1	luminal epithelium:	n/a
41	chr9:104500322-104500372	HRPEpiC	eye:	n/a
42	chr9:104500729-104500779	GM12891	blood:	n/a
43	chr9:104499700-104499750	AoSMC	blood vessel:	n/a
44	chr9:104499850-104499900	GM19239	blood:	n/a
45	chr9:104499700-104499750	AG09309	skin:	n/a
46	chr9:104500322-104500372	HCT-116	colon:	n/a
47	chr9:104499850-104499900	NB4	blood:	n/a
48	chr9:104500958-104501008	MCF10A-Er-Src	breast:	n/a
49	chr9:104500729-104500779	H1-hESC	embryonic stem cell:	embryo
50	chr9:104500322-104500372	SK-N-SH	brain:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:104602976..104605098-chr9:104654861..104656583,2	K562	blood:
2	chr10:86116689..86117545-chr9:104638316..104638864,2	MCF-7	breast:
3	chr9:104658581..104661092-chr9:104661771..104663841,2	K562	blood:
4	chr9:104594444..104596154-chr9:104597009..104599073,2	MCF-7	breast:
5	chr9:104651692..104653674-chr9:104654831..104656536,3	K562	blood:
6	chr9:104534684..104536933-chr9:104538278..104540964,2	K562	blood:
7	chr9:104554048..104554859-chr9:104734774..104735456,4	MCF-7	breast:
8	chr9:104534684..104536933-chr9:104538278..104540964,2	K562	blood:
9	chr9:104554304..104554879-chr9:107148429..107149219,2	MCF-7	breast:
10	chr9:104594444..104596154-chr9:104597009..104599073,2	MCF-7	breast:
11	chr9:104529138..104530867-chr9:104533732..104536723,2	K562	blood:
12	chr10:26587616..26588136-chr9:104616741..104617261,2	MCF-7	breast:
13	chr9:104656494..104659292-chr9:104659378..104660947,2	K562	blood:
14	chr9:104529138..104530867-chr9:104533732..104536723,2	K562	blood:
15	chr9:104628351..104631183-chr9:104634996..104637004,2	K562	blood:
16	chr9:104626627..104628605-chr9:104630406..104631919,2	K562	blood:
17	chr9:104658581..104661092-chr9:104661771..104663841,2	K562	blood:
18	chr9:104600370..104602657-chr9:104607856..104609607,2	K562	blood:
19	chr9:104618154..104619898-chr9:104623303..104626288,2	K562	blood:
20	chr9:104626627..104628605-chr9:104630406..104631919,2	K562	blood:
21	chr9:104493214..104495968-chr9:104498085..104500159,2	K562	blood:
22	chr9:104662236..104665131-chr9:104665548..104668439,2	K562	blood:
23	chr9:104656494..104659292-chr9:104659378..104660947,2	K562	blood:
24	chr9:104651692..104653674-chr9:104654831..104656536,3	K562	blood:
25	chr9:104618154..104619898-chr9:104623303..104626288,2	K562	blood:
26	chr9:104602976..104605098-chr9:104654861..104656583,2	K562	blood:
27	chr9:104493214..104495968-chr9:104498085..104500159,2	K562	blood:
28	chr9:104628351..104631183-chr9:104634996..104637004,2	K562	blood:
29	chr9:104600370..104602657-chr9:104607856..104609607,2	K562	blood:
30	chr9:104662236..104665131-chr9:104665548..104668439,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF20-4	chr9:104567769-104567808	NONHSAT133752
2	lnc-RNF20-2	chr9:104652669-104652689	XLOC_007493
3	lnc-RNF20-2	chr9:104654473-104654712	XLOC_007493
4	lnc-RNF20-4	chr9:104567913-104568131	NONHSAT133752

No data

Variant related genes	Relation type
MTND3P4	TF binding region
GRIN3A	TF binding region
MTND3P4	CpG island
GRIN3A	CpG island

Extended variants
information (count: 3742 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3742 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569733654	chr9:104492392-104492393	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs538851733	chr9:104492396-104492397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558493179	chr9:104492437-104492438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572267534	chr9:104492455-104492456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534928013	chr9:104492474-104492475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114588659	chr9:104492475-104492476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574132078	chr9:104492493-104492494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73504933	chr9:104492495-104492496	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs191220822	chr9:104492563-104492564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183728407	chr9:104492577-104492578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7041051	chr9:104492591-104492592	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs565353699	chr9:104492636-104492637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373517868	chr9:104492641-104492642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559472484	chr9:104492655-104492656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568590031	chr9:104492660-104492661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs137915772	chr9:104492663-104492664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs58033393	chr9:104492675-104492676	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs560537358	chr9:104492696-104492697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs55732995	chr9:104492712-104492713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149489386	chr9:104492724-104492725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549440649	chr9:104492727-104492728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143966395	chr9:104492776-104492777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148660302	chr9:104492785-104492786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554510408	chr9:104492794-104492795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182446075	chr9:104492817-104492818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565742685	chr9:104492828-104492829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113808443	chr9:104492897-104492898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377584775	chr9:104492920-104492921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534915146	chr9:104492937-104492938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554946927	chr9:104492959-104492960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185004737	chr9:104492962-104492963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190251270	chr9:104492972-104492973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556305249	chr9:104492990-104492991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35020776	chr9:104493053-104493054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181901167	chr9:104493070-104493071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370912028	chr9:104493073-104493074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545182213	chr9:104493126-104493127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559102595	chr9:104493173-104493174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572343680	chr9:104493179-104493180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185656134	chr9:104493213-104493214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572991441	chr9:104493223-104493224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541309112	chr9:104493252-104493253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561272459	chr9:104493272-104493273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530345515	chr9:104493308-104493309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375801915	chr9:104493360-104493361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533703112	chr9:104493377-104493378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190371660	chr9:104493399-104493400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs180778991	chr9:104493427-104493428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552034384	chr9:104493521-104493522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565861223	chr9:104493536-104493537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Mantle cell lymphoma	19029149	CNVD
Intracranial aneurysm	16715129	CNVD
Neuroblastoma	20406844	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104490600-104495000	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr9:104490600-104496000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr9:104491400-104492400	Strong transcription	Liver	Liver
4	chr9:104492400-104493800	Weak transcription	Liver	Liver
5	chr9:104493800-104494200	Enhancers	Liver	Liver
6	chr9:104494200-104499600	Weak transcription	Liver	Liver
7	chr9:104495000-104496000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr9:104495600-104495800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
9	chr9:104496000-104496200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr9:104497800-104500000	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
11	chr9:104497800-104501200	Active TSS	Pancreatic Islets	Pancreatic Islet
12	chr9:104498600-104499600	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
13	chr9:104498800-104499200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
14	chr9:104498800-104499600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
15	chr9:104499000-104499200	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
16	chr9:104499000-104499400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
17	chr9:104499000-104499400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
18	chr9:104499000-104499400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
19	chr9:104499000-104499600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
20	chr9:104499000-104499600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
21	chr9:104499000-104499600	Bivalent/Poised TSS	Left Ventricle	heart
22	chr9:104499000-104499600	Bivalent/Poised TSS	Right Ventricle	heart
23	chr9:104499000-104500200	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
24	chr9:104499000-104501200	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
25	chr9:104499200-104499400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
26	chr9:104499200-104499600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
27	chr9:104499200-104501000	Bivalent/Poised TSS	Brain Angular Gyrus	brain
28	chr9:104499200-104501000	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
29	chr9:104499400-104499600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
30	chr9:104499400-104499600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr9:104499400-104499600	Bivalent Enhancer	Brain Anterior Caudate	brain
32	chr9:104499400-104499600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
33	chr9:104499400-104499600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
34	chr9:104499400-104499600	Flanking Bivalent TSS/Enh	Fetal Heart	heart
35	chr9:104499400-104499600	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
36	chr9:104499400-104500000	Enhancers	Pancreas	Pancrea
37	chr9:104499400-104500200	Bivalent Enhancer	Fetal Muscle Leg	muscle
38	chr9:104499400-104500200	Flanking Active TSS	Ovary	ovary
39	chr9:104499400-104500400	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
40	chr9:104499400-104500600	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
41	chr9:104499400-104500600	Bivalent Enhancer	Fetal Brain Male	brain
42	chr9:104499400-104501000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
43	chr9:104499400-104501600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
44	chr9:104499600-104499800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
45	chr9:104499600-104499800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
46	chr9:104499600-104499800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr9:104499600-104499800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
48	chr9:104499600-104499800	Flanking Bivalent TSS/Enh	Brain Anterior Caudate	brain
49	chr9:104499600-104499800	Flanking Bivalent TSS/Enh	Brain Substantia Nigra	brain
50	chr9:104499600-104499800	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum

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