Variant report

Variant	nsv877541
Chromosome Location	chr3:138645013-138673922
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1506)
CpG islands
(count:4153)
Chromatin interactive
region (count:48)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1506 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:138654213-138654525	K562	blood:	n/a	n/a
2	ARID3A	chr3:138665913-138665957	K562	blood:	n/a	n/a
3	ARID3A	chr3:138655258-138655397	HepG2	liver:	n/a	n/a
4	ATF1	chr3:138662703-138663024	K562	blood:	n/a	n/a
5	ATF1	chr3:138665829-138666172	K562	blood:	n/a	chr3:138666004-138666018
6	ATF2	chr3:138654987-138655420	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr3:138667972-138668305	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr3:138654999-138655324	K562	blood:	n/a	n/a
9	ATF3	chr3:138664245-138664490	K562	blood:	n/a	n/a
10	BACH1	chr3:138662124-138662317	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr3:138657914-138657946	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:138656997-138657451	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr3:138654800-138655472	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr3:138669003-138669174	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr3:138665821-138666009	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr3:138654403-138654576	K562	blood:	n/a	n/a
17	BACH1	chr3:138667987-138668254	H1-hESC	embryonic stem cell:	n/a	n/a
18	BHLHE40	chr3:138654553-138655485	K562	blood:	n/a	n/a
19	BHLHE40	chr3:138665062-138666787	K562	blood:	n/a	chr3:138665604-138665620
20	BHLHE40	chr3:138663796-138664347	K562	blood:	n/a	n/a
21	BHLHE40	chr3:138661979-138662213	K562	blood:	n/a	n/a
22	BHLHE40	chr3:138662779-138663033	K562	blood:	n/a	n/a
23	BHLHE40	chr3:138654973-138655324	HepG2	liver:	n/a	n/a
24	BHLHE40	chr3:138655066-138655361	GM12878	blood:	n/a	n/a
25	BRCA1	chr3:138665645-138665802	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr3:138658033-138658203	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr3:138665775-138666607	K562	blood:	n/a	n/a
28	CBX3	chr3:138660067-138660478	K562	blood:	n/a	n/a
29	CBX3	chr3:138663708-138664570	K562	blood:	n/a	n/a
30	CBX3	chr3:138654594-138655689	K562	blood:	n/a	n/a
31	CBX3	chr3:138665027-138665486	K562	blood:	n/a	n/a
32	CBX3	chr3:138655053-138655377	K562	blood:	n/a	n/a
33	CCNT2	chr3:138654711-138655373	K562	blood:	n/a	n/a
34	CCNT2	chr3:138663704-138666364	K562	blood:	n/a	chr3:138665889-138665898 chr3:138665882-138665891
35	CCNT2	chr3:138658351-138658505	K562	blood:	n/a	n/a
36	CEBPB	chr3:138654968-138655341	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr3:138665919-138666064	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr3:138662777-138663030	K562	blood:	n/a	n/a
39	CEBPB	chr3:138662241-138662299	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr3:138666552-138667023	K562	blood:	n/a	n/a
41	CEBPB	chr3:138665858-138666184	K562	blood:	n/a	n/a
42	CEBPB	chr3:138655064-138655255	K562	blood:	n/a	n/a
43	CEBPB	chr3:138667980-138668286	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr3:138665832-138666199	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr3:138657545-138657675	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr3:138654717-138655405	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr3:138654103-138654280	K562	blood:	n/a	n/a
48	CEBPB	chr3:138654989-138655187	A549	lung:	n/a	n/a
49	CHD1	chr3:138665004-138665161	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr3:138657111-138657428	H1-hESC	embryonic stem cell:	n/a	n/a

(count:4153 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:138661281-138661331	NHDF-neo	bronchial:	n/a
2	chr3:138666473-138666523	Hela-S3	cervix:	n/a
3	chr3:138669434-138669484	HCPEpiC	choroid plexus:	n/a
4	chr3:138655338-138655388	HMEC	breast:	n/a
5	chr3:138658704-138658754	CMK	blood:	n/a
6	chr3:138661281-138661331	NHDF-neo	bronchial:	n/a
7	chr3:138666473-138666523	Hela-S3	cervix:	n/a
8	chr3:138669434-138669484	HCPEpiC	choroid plexus:	n/a
9	chr3:138655338-138655388	HMEC	breast:	n/a
10	chr3:138658704-138658754	CMK	blood:	n/a
11	chr3:138648052-138648102	PFSK-1	brain:	n/a
12	chr3:138666885-138666935	HRCEpiC	kidney:	n/a
13	chr3:138661840-138661890	H1-hESC	embryonic stem cell:	embryo
14	chr3:138668832-138668882	CMK	blood:	n/a
15	chr3:138657541-138657591	HRE	kidney:	n/a
16	chr3:138656356-138656406	K562	blood:	n/a
17	chr3:138665006-138665056	GM12892	blood:	n/a
18	chr3:138666732-138666782	HEEpiC	esophagus:	n/a
19	chr3:138666054-138666104	HAEpiC	amniotic membrane:	n/a
20	chr3:138648284-138648334	SK-N-SH_RA	brain:	n/a
21	chr3:138648052-138648102	GM19239	blood:	n/a
22	chr3:138665006-138665056	HCM	heart:	n/a
23	chr3:138657774-138657824	GM12892	blood:	n/a
24	chr3:138658878-138658928	NB4	blood:	n/a
25	chr3:138655158-138655208	HepG2	liver:	n/a
26	chr3:138658704-138658754	SK-N-MC	brain:	n/a
27	chr3:138656471-138656521	HNPCEpiC	eye:	n/a
28	chr3:138657774-138657824	Jurkat	blood:	n/a
29	chr3:138655338-138655388	SK-N-MC	brain:	n/a
30	chr3:138654993-138655043	HUVEC	blood vessel:	n/a
31	chr3:138666040-138666090	HL-60	blood:	n/a
32	chr3:138648052-138648102	AG04449	skin:	fetal
33	chr3:138666048-138666098	SK-N-SH_RA	brain:	n/a
34	chr3:138666040-138666090	PANC-1	pancreas:	n/a
35	chr3:138648284-138648334	GM19239	blood:	n/a
36	chr3:138654993-138655043	HCF	heart:	n/a
37	chr3:138656356-138656406	LNCaP	prostate:	n/a
38	chr3:138665816-138665866	PFSK-1	brain:	n/a
39	chr3:138656471-138656521	SK-N-SH	brain:	n/a
40	chr3:138666118-138666168	HEK293	kidney:	embryo
41	chr3:138660387-138660437	HCT-116	colon:	n/a
42	chr3:138656042-138656092	SK-N-SH	brain:	n/a
43	chr3:138669434-138669484	GM06990	blood:	n/a
44	chr3:138658243-138658293	HCF	heart:	n/a
45	chr3:138665654-138665704	GM12891	blood:	n/a
46	chr3:138665984-138666034	PANC-1	pancreas:	n/a
47	chr3:138665930-138665980	ProgFib	skin:	n/a
48	chr3:138665984-138666034	ovcar-3	ovarian:	n/a
49	chr3:138667775-138667825	GM19239	blood:	n/a
50	chr3:138665930-138665980	GM19239	blood:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:138653172..138655075-chr3:138696943..138698906,2	K562	blood:
2	chr3:138659729..138660803-chr3:139047591..139048852,19	MCF-7	breast:
3	chr3:138654768..138655753-chr3:138698437..138699225,3	MCF-7	breast:
4	chr3:138369214..138371379-chr3:138655274..138656934,2	K562	blood:
5	chr3:138667185..138669200-chr3:139015942..139017731,2	K562	blood:
6	chr3:138662930..138665142-chr3:139048462..139050899,2	K562	blood:
7	chr3:138672783..138675327-chr3:138678243..138680215,2	K562	blood:
8	chr3:138655774..138657700-chr3:138692387..138694349,2	K562	blood:
9	chr3:138659826..138661110-chr3:138920916..138922197,6	MCF-7	breast:
10	chr3:138654852..138656122-chr3:139047855..139048698,3	MCF-7	breast:
11	chr3:138654619..138656713-chr3:138694256..138696204,2	K562	blood:
12	chr3:138659052..138660709-chr3:138693240..138696002,2	K562	blood:
13	chr3:138660095..138660771-chr3:138679788..138680398,3	K562	blood:
14	chr3:138654402..138658110-chr3:139047575..139051045,3	K562	blood:
15	chr3:138642228..138643880-chr3:138648374..138651238,2	K562	blood:
16	chr3:138648109..138650987-chr3:138654230..138656484,2	MCF-7	breast:
17	chr3:138552259..138555153-chr3:138660631..138662853,2	K562	blood:
18	chr3:138654813..138655512-chr3:138698389..138699485,6	MCF-7	breast:
19	chr3:138552293..138554429-chr3:138658908..138660505,2	K562	blood:
20	chr3:138654476..138656121-chr3:138659491..138661137,2	MCF-7	breast:
21	chr3:138671344..138677284-chr3:138678243..138683566,6	K562	blood:
22	chr3:138659804..138660791-chr3:138698304..138699362,13	MCF-7	breast:
23	chr3:138663376..138665458-chr3:138892996..138895666,2	K562	blood:
24	chr3:138552263..138555163-chr3:138665790..138667540,3	K562	blood:
25	chr3:138659358..138660755-chr3:139047481..139048803,7	MCF-7	breast:
26	chr3:138654739..138655701-chr3:138698189..138698792,4	K562	blood:
27	chr3:138654772..138655801-chr3:138680091..138680721,3	K562	blood:
28	chr3:138654781..138655716-chr3:139047822..139048838,5	MCF-7	breast:
29	chr3:138641635..138643731-chr3:138657597..138660077,2	K562	blood:
30	chr3:138654970..138655687-chr3:139047873..139048821,4	K562	blood:
31	chr3:138663277..138665291-chr3:138920079..138922965,2	K562	blood:
32	chr3:138660094..138660757-chr3:138920977..138921829,3	MCF-7	breast:
33	chr3:138655102..138656710-chr3:138945646..138947395,2	K562	blood:
34	chr3:138648109..138650987-chr3:138654230..138656484,2	MCF-7	breast:
35	chr3:138661994..138662559-chr3:138698351..138698972,2	K562	blood:
36	chr3:138552568..138555141-chr3:138666105..138668600,2	K562	blood:
37	chr3:138659931..138660808-chr3:138698430..138699219,3	K562	blood:
38	chr3:138661376..138665068-chr3:139062620..139064700,3	K562	blood:
39	chr3:138659869..138660701-chr3:139049015..139049692,2	MCF-7	breast:
40	chr3:138659774..138660703-chr3:138679825..138680699,2	MCF-7	breast:
41	chr3:138660233..138660820-chr3:139047905..139048802,2	K562	blood:
42	chr3:138660271..138660907-chr3:138754909..138755634,2	MCF-7	breast:
43	chr3:138654954..138655571-chr3:138920961..138921828,2	MCF-7	breast:
44	chr3:138655696..138657918-chr3:138697620..138699294,2	K562	blood:
45	chr3:138654476..138656121-chr3:138659491..138661137,2	MCF-7	breast:
46	chr3:138655209..138657640-chr3:138920861..138922707,2	MCF-7	breast:
47	chr3:138640908..138642658-chr3:138654077..138656499,2	K562	blood:
48	chr3:138350409..138353105-chr3:138651572..138653384,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXL2-1	chr3:138662808-138662845	ENSG00000244578
2	lnc-FOXL2-1	chr3:138659270-138659557	ENSG00000244578
3	lnc-FOXL2-1	chr3:138656750-138657278	ENSG00000244578
4	lnc-FOXL2-1	chr3:138661226-138661420	ENSG00000244578
5	lnc-MRPS22-3	chr3:138668354-138669670	NONHSAT092347
6	lnc-FOXL2-1	chr3:138661163-138661460	ENSG00000244578
7	lnc-MRPS22-3	chr3:138666454-138666849	NONHSAT092347

No data

Variant related genes	Relation type
ENSG00000244578	TF binding region
C3orf72	TF binding region
FOXL2	TF binding region
ENSG00000244578	CpG island
C3orf72	CpG island
FOXL2	CpG island
ENSG00000051382	chromatin interactions
ENSG00000175110	chromatin interactions

Extended variants
information (count: 1062 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1062 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9846784	chr3:138645013-138645014	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572375866	chr3:138645055-138645056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538983274	chr3:138645056-138645057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190480562	chr3:138645060-138645061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs75754513	chr3:138645124-138645125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs529894834	chr3:138645149-138645150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527571370	chr3:138645156-138645157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143251493	chr3:138645221-138645222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563609824	chr3:138645224-138645225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147086960	chr3:138645228-138645229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558680909	chr3:138645276-138645277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552475539	chr3:138645281-138645282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192521513	chr3:138645308-138645309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572516834	chr3:138645313-138645314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201103815	chr3:138645322-138645323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs13060060	chr3:138645326-138645327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7614807	chr3:138645327-138645328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562989270	chr3:138645328-138645329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs10537856	chr3:138645329-138645330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201114535	chr3:138645330-138645331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554936537	chr3:138645337-138645338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs58414375	chr3:138645353-138645354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183533108	chr3:138645433-138645434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188215927	chr3:138645438-138645439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs28525343	chr3:138645488-138645489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs180971888	chr3:138645508-138645509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538968412	chr3:138645509-138645510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs74665010	chr3:138645527-138645528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs75314977	chr3:138645528-138645529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs397965412	chr3:138645539-138645540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs73231640	chr3:138645554-138645555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572356484	chr3:138645567-138645568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs367993057	chr3:138645607-138645608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541368274	chr3:138645628-138645629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545930907	chr3:138645635-138645636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574862541	chr3:138645649-138645650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559077032	chr3:138645768-138645769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557222864	chr3:138645791-138645792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543670282	chr3:138645842-138645843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138232895	chr3:138645872-138645873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185383423	chr3:138645881-138645882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552512497	chr3:138645949-138645950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559554998	chr3:138645970-138645971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149580133	chr3:138645972-138645973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144246332	chr3:138645974-138645975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568095536	chr3:138646004-138646005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148705591	chr3:138646086-138646087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200571702	chr3:138646117-138646118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149707429	chr3:138646120-138646121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550231307	chr3:138646132-138646133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Disorders of sex development	22315593	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	21321671	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:1585 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:138635200-138652600	Weak transcription	Ovary	ovary
2	chr3:138635200-138654800	Weak transcription	Right Atrium	heart
3	chr3:138641200-138647000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr3:138642800-138647000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr3:138642800-138647200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr3:138647000-138647200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr3:138647000-138647200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr3:138647000-138648200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr3:138647200-138647400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr3:138647200-138651600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr3:138648200-138649000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr3:138649000-138649800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr3:138649400-138649600	Enhancers	H1 Cell Line	embryonic stem cell
14	chr3:138649400-138649600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr3:138649600-138651600	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr3:138649800-138651400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr3:138649800-138652000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr3:138651400-138653200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr3:138651600-138652400	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr3:138651600-138652400	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr3:138651600-138652600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr3:138651600-138652800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr3:138651600-138653000	Enhancers	H1 Cell Line	embryonic stem cell
24	chr3:138651800-138652000	Enhancers	H9 Cell Line	embryonic stem cell
25	chr3:138651800-138652400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
26	chr3:138652000-138652200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr3:138652000-138652600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr3:138652200-138652800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
29	chr3:138652200-138652800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr3:138652400-138652800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
31	chr3:138652400-138653200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
32	chr3:138652600-138652800	Enhancers	H9 Cell Line	embryonic stem cell
33	chr3:138652600-138652800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
34	chr3:138652600-138653600	Enhancers	Ovary	ovary
35	chr3:138652600-138654400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr3:138652800-138653000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr3:138653000-138653200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
38	chr3:138653000-138653200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr3:138653000-138653200	Bivalent Enhancer	HUVEC	blood vessel
40	chr3:138653000-138653600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr3:138653200-138653400	Bivalent Enhancer	Fetal Muscle Leg	muscle
42	chr3:138653200-138654600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr3:138653600-138654600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr3:138653600-138654600	Weak transcription	Ovary	ovary
45	chr3:138654200-138654400	Enhancers	K562	blood
46	chr3:138654400-138654600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
47	chr3:138654400-138654600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
48	chr3:138654400-138654600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
49	chr3:138654400-138654600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr3:138654400-138654600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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