Variant report

Variant	nsv1005525
Chromosome Location	chr3:120749594-121027161
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:535)
CpG islands
(count:122)
Chromatin interactive
region (count:11)
LncRNA
region (count:4)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:535 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:120782469-120782845	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr3:120872687-120873031	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr3:120789742-120789992	GM12878	blood:	n/a	n/a
4	BHLHE40	chr3:120784878-120785113	GM12878	blood:	n/a	n/a
5	BRCA1	chr3:121014343-121015554	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr3:120883994-120884728	HCT-116	colon:	n/a	n/a
7	CCNT2	chr3:120886331-120886573	K562	blood:	n/a	n/a
8	CEBPB	chr3:120829969-120830281	Hela-S3	cervix:	n/a	chr3:120830133-120830144
9	CEBPB	chr3:121024511-121024633	H1-hESC	embryonic stem cell:	n/a	chr3:121024540-121024551
10	CEBPB	chr3:120877234-120877467	A549	lung:	n/a	chr3:120877371-120877382
11	CEBPB	chr3:121024403-121024693	IMR90	lung:	n/a	chr3:121024540-121024551
12	CEBPB	chr3:120877260-120877460	K562	blood:	n/a	chr3:120877371-120877382
13	CEBPB	chr3:120845332-120845587	Hela-S3	cervix:	n/a	chr3:120845476-120845487
14	CEBPB	chr3:120822664-120822845	HepG2	liver:	n/a	n/a
15	CEBPB	chr3:120830064-120830248	ECC-1	luminal epithelium:	n/a	chr3:120830133-120830144
16	CEBPB	chr3:121024385-121024688	HepG2	liver:	n/a	chr3:121024540-121024551
17	CEBPB	chr3:120959887-120959918	K562	blood:	n/a	n/a
18	CEBPB	chr3:120822725-120822791	IMR90	lung:	n/a	n/a
19	CEBPB	chr3:120830826-120831152	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr3:120830891-120831091	HepG2	liver:	n/a	n/a
21	CEBPB	chr3:120877238-120877488	HepG2	liver:	n/a	chr3:120877371-120877382
22	CEBPB	chr3:121024454-121024688	A549	lung:	n/a	chr3:121024540-121024551
23	CEBPB	chr3:120830133-120830171	K562	blood:	n/a	chr3:120830133-120830144
24	CEBPB	chr3:121014181-121015355	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr3:120830072-120830272	A549	lung:	n/a	chr3:120830133-120830144
26	CEBPB	chr3:120830894-120831105	K562	blood:	n/a	n/a
27	CEBPB	chr3:120892760-120892883	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr3:120845421-120845545	HepG2	liver:	n/a	chr3:120845476-120845487
29	CEBPB	chr3:120830052-120830302	MCF-7	breast:	n/a	chr3:120830133-120830144
30	CEBPB	chr3:120829975-120830303	HepG2	liver:	n/a	chr3:120830133-120830144
31	CEBPD	chr3:120886293-120886675	K562	blood:	n/a	n/a
32	CEBPD	chr3:120886259-120886658	K562	blood:	n/a	n/a
33	CHD2	chr3:120782613-120782867	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr3:120830930-120831060	HepG2	liver:	n/a	n/a
35	CTCF	chr3:120871520-120871670	RPTEC	kidney:	n/a	chr3:120871613-120871631 chr3:120871608-120871629
36	CTCF	chr3:121008180-121008330	GM12866	blood:	n/a	n/a
37	CTCF	chr3:120830842-120831043	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr3:121008200-121008350	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr3:120871520-120871670	HMF	breast:	n/a	chr3:120871613-120871631 chr3:120871608-120871629
40	CTCF	chr3:120795200-120795350	GM12875	blood:	n/a	n/a
41	CTCF	chr3:120951100-120951250	HEK293	kidney:	n/a	chr3:120951139-120951160
42	CTCF	chr3:120871600-120871750	RPTEC	kidney:	n/a	chr3:120871613-120871631 chr3:120871608-120871629
43	CTCF	chr3:120838060-120838210	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr3:120871580-120871730	SK-N-SH_RA	brain:	n/a	chr3:120871613-120871631 chr3:120871608-120871629
45	CTCF	chr3:120871523-120871709	HUVEC	blood vessel:	n/a	chr3:120871613-120871631 chr3:120871608-120871629
46	CTCF	chr3:120871595-120871662	GM20000	blood:	n/a	chr3:120871613-120871631 chr3:120871608-120871629
47	CTCF	chr3:120871583-120871703	K562	blood:	n/a	chr3:120871613-120871631 chr3:120871608-120871629
48	CTCF	chr3:120871619-120871704	Medullo	brain:	n/a	n/a
49	CTCF	chr3:120830860-120831010	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr3:120871600-120871750	SAEC	small airway:	n/a	chr3:120871613-120871631 chr3:120871608-120871629

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:121025407-121025457	HRCEpiC	kidney:	n/a
2	chr3:121025407-121025457	MCF-7	breast:	n/a
3	chr3:120909792-120909842	AG09309	skin:	n/a
4	chr3:121025407-121025457	PrEC	prostate:	n/a
5	chr3:120909792-120909842	NHDF-neo	bronchial:	n/a
6	chr3:120909792-120909842	SK-N-SH_RA	brain:	n/a
7	chr3:120909792-120909842	HL-60	blood:	n/a
8	chr3:121025407-121025457	Caco-2	colon:	n/a
9	chr3:121025407-121025457	HCPEpiC	choroid plexus:	n/a
10	chr3:120909792-120909842	HepG2	liver:	n/a
11	chr3:121025407-121025457	HCT-116	colon:	n/a
12	chr3:121025407-121025457	SKMC	muscle:	n/a
13	chr3:120909792-120909842	HEK293	kidney:	embryo
14	chr3:121025407-121025457	T-47D	breast:	n/a
15	chr3:120909792-120909842	HNPCEpiC	eye:	n/a
16	chr3:120909792-120909842	GM19239	blood:	n/a
17	chr3:121025407-121025457	ECC-1	luminal epithelium:	n/a
18	chr3:120909792-120909842	MCF10A-Er-Src	breast:	n/a
19	chr3:121025407-121025457	HAEpiC	amniotic membrane:	n/a
20	chr3:120909792-120909842	HMEC	breast:	n/a
21	chr3:120909792-120909842	U87	brain:	n/a
22	chr3:121025407-121025457	CMK	blood:	n/a
23	chr3:121025407-121025457	HEK293	kidney:	embryo
24	chr3:121025407-121025457	AG09309	skin:	n/a
25	chr3:121025407-121025457	H1-hESC	embryonic stem cell:	embryo
26	chr3:121025407-121025457	SAEC	small airway:	n/a
27	chr3:120909792-120909842	IMR90	lung:	fetal
28	chr3:120909792-120909842	T-47D	breast:	n/a
29	chr3:121025407-121025457	NHDF-neo	bronchial:	n/a
30	chr3:120909792-120909842	SK-N-MC	brain:	n/a
31	chr3:120909792-120909842	AG04449	skin:	fetal
32	chr3:121025407-121025457	GM06990	blood:	n/a
33	chr3:120909792-120909842	Hepatocyte	liver:	n/a
34	chr3:120909792-120909842	HRE	kidney:	n/a
35	chr3:120909792-120909842	HUVEC	blood vessel:	n/a
36	chr3:121025407-121025457	HEEpiC	esophagus:	n/a
37	chr3:120909792-120909842	K562	blood:	n/a
38	chr3:120909792-120909842	HIPEpiC	eye:	n/a
39	chr3:121025407-121025457	ovcar-3	ovarian:	n/a
40	chr3:120909792-120909842	Hela-S3	cervix:	n/a
41	chr3:121025407-121025457	HIPEpiC	eye:	n/a
42	chr3:120909792-120909842	RPTEC	kidney:	n/a
43	chr3:121025407-121025457	NB4	blood:	n/a
44	chr3:121025407-121025457	HMEC	breast:	n/a
45	chr3:121025407-121025457	HRE	kidney:	n/a
46	chr3:120909792-120909842	BJ	skin:	n/a
47	chr3:120909792-120909842	ProgFib	skin:	n/a
48	chr3:121025407-121025457	SK-N-SH_RA	brain:	n/a
49	chr3:120909792-120909842	MCF-7	breast:	n/a
50	chr3:121025407-121025457	PANC-1	pancreas:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:120841817..120844758-chr3:120846450..120848360,2	K562	blood:
2	chr3:120850081..120852968-chr3:120854898..120857782,2	MCF-7	breast:
3	chr3:62626007..62626708-chr3:120837876..120838423,2	MCF-7	breast:
4	chr3:120875889..120878792-chr3:120892011..120893979,2	K562	blood:
5	chr3:120279838..120280352-chr3:120871430..120872100,2	MCF-7	breast:
6	chr3:121004364..121006948-chr3:121012227..121014018,2	MCF-7	breast:
7	chr3:120875889..120878792-chr3:120892011..120893979,2	K562	blood:
8	chr3:121004364..121006948-chr3:121012227..121014018,2	MCF-7	breast:
9	chr3:120850081..120852968-chr3:120854898..120857782,2	MCF-7	breast:
10	chr3:120860340..120860840-chr8:23021037..23021834,2	Hela-S3	cervix:
11	chr3:120841817..120844758-chr3:120846450..120848360,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RABL3-5	chr3:120799296-120799541	predAs_chen_BG200968_1
2	lnc-POLQ-2	chr3:120873476-120873875	ucscGeneNc_uc003edb_1
3	lnc-GTF2E1-4	chr3:120817955-120818621	NONHSAT091470
4	lnc-POLQ-2	chr3:120872301-120873382	ucscGeneNc_uc003edb_1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5682	chr3:120768531-120768552	MIMAT0022470

No data

Variant related genes	Relation type
MIR5682	TF binding region
ENSG00000243813	TF binding region
MIR5682	CpG island
ENSG00000243813	CpG island
ENSG00000173530	chromatin interactions

Extended variants
information (count: 8839 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:8839 , 50 per page) page: 1 2 3 4 5 6 7 ... 177

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79419720	chr3:120762801-120762802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73187437	chr3:120762814-120762815	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs376969654	chr3:120762874-120762875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567045612	chr3:120762894-120762895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185826829	chr3:120762896-120762897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143750376	chr3:120762908-120762909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545276111	chr3:120762933-120762934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544840170	chr3:120762940-120762941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536815435	chr3:120762961-120762962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191071814	chr3:120762985-120762986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9840595	chr3:120763002-120763003	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs542249490	chr3:120763003-120763004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs78875022	chr3:120763033-120763034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577218788	chr3:120763037-120763038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545978294	chr3:120763072-120763073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573030777	chr3:120763081-120763082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs67659681	chr3:120763085-120763086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544937151	chr3:120763106-120763107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564853554	chr3:120763111-120763112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146068852	chr3:120763124-120763125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35920898	chr3:120763139-120763140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs183244418	chr3:120763215-120763216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187558097	chr3:120763257-120763258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs5852259	chr3:120763261-120763262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11720216	chr3:120763269-120763270	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs34331676	chr3:120763285-120763286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192373991	chr3:120763309-120763310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140023403	chr3:120763323-120763324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs57774720	chr3:120763334-120763335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566888522	chr3:120763341-120763342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182691588	chr3:120763342-120763343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562335542	chr3:120763358-120763359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs73187495	chr3:120763361-120763362	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs375402421	chr3:120763375-120763376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73187496	chr3:120763387-120763388	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs564521729	chr3:120763409-120763410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569571359	chr3:120763435-120763436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538397972	chr3:120763440-120763441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555185070	chr3:120763463-120763464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188084148	chr3:120763464-120763465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573650777	chr3:120763478-120763479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536373974	chr3:120763512-120763513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192886148	chr3:120763517-120763518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184700246	chr3:120763543-120763544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs9841743	chr3:120763552-120763553	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs564790597	chr3:120763608-120763609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575183429	chr3:120763613-120763614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369357056	chr3:120763616-120763617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543996019	chr3:120763633-120763634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561186757	chr3:120763637-120763638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	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
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	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
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	22241247	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:192 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:120762800-120767600	Weak transcription	Ovary	ovary
2	chr3:120763200-120768400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr3:120764200-120767400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
4	chr3:120766000-120767200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr3:120766600-120767000	ZNF genes & repeats	Brain Anterior Caudate	brain
6	chr3:120766800-120768200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr3:120767000-120768000	Weak transcription	Brain Anterior Caudate	brain
8	chr3:120767000-120769000	ZNF genes & repeats	Fetal Brain Female	brain
9	chr3:120767200-120768200	Weak transcription	Gastric	stomach
10	chr3:120767400-120769000	Strong transcription	Pancreatic Islets	Pancreatic Islet
11	chr3:120767600-120768200	Weak transcription	Brain Angular Gyrus	brain
12	chr3:120767600-120769000	Strong transcription	Ovary	ovary
13	chr3:120767600-120770200	Weak transcription	Brain Cingulate Gyrus	brain
14	chr3:120768000-120768400	Strong transcription	Brain Anterior Caudate	brain
15	chr3:120768200-120769000	ZNF genes & repeats	Brain Angular Gyrus	brain
16	chr3:120768200-120769000	ZNF genes & repeats	Brain Germinal Matrix	brain
17	chr3:120768200-120769000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr3:120768200-120769000	ZNF genes & repeats	Gastric	stomach
19	chr3:120768400-120768800	ZNF genes & repeats	Brain Anterior Caudate	brain
20	chr3:120768400-120768800	Strong transcription	Brain Inferior Temporal Lobe	brain
21	chr3:120768600-120769000	ZNF genes & repeats	Pancreas	Pancrea
22	chr3:120768800-120769000	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
23	chr3:120769000-120769200	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr3:120769000-120770600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr3:120769000-120777000	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr3:120769000-120791200	Weak transcription	Ovary	ovary
27	chr3:120777000-120777200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
28	chr3:120781400-120782200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr3:120781600-120790800	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr3:120782200-120782600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr3:120782200-120783200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr3:120782200-120783200	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr3:120782400-120783000	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr3:120782400-120783000	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr3:120782400-120783200	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr3:120782600-120782800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr3:120782600-120782800	Enhancers	A549	lung
38	chr3:120782600-120783000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr3:120782600-120783200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr3:120782600-120783200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr3:120782800-120783200	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr3:120783000-120783400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr3:120783000-120789400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr3:120789400-120789600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr3:120789600-120790200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr3:120790200-120790400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr3:120790200-120790800	Enhancers	Aorta	Aorta
48	chr3:120790200-120791400	Enhancers	Placenta	Placenta
49	chr3:120790400-120792600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr3:120790800-120791000	Enhancers	Pancreatic Islets	Pancreatic Islet

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