Variant report

Variant	nsv1008441
Chromosome Location	chr3:120730017-121102735
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:663)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:5)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:663 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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	chr3:120830894-120831105	K562	blood:	n/a	n/a
9	CEBPB	chr3:120730639-120730757	H1-hESC	embryonic stem cell:	n/a	chr3:120730725-120730736
10	CEBPB	chr3:121024511-121024633	H1-hESC	embryonic stem cell:	n/a	chr3:121024540-121024551
11	CEBPB	chr3:121038287-121038620	K562	blood:	n/a	n/a
12	CEBPB	chr3:121038397-121038535	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr3:120730551-120730896	HepG2	liver:	n/a	chr3:120730725-120730736
14	CEBPB	chr3:121030037-121030310	HepG2	liver:	n/a	chr3:121030079-121030090
15	CEBPB	chr3:120822664-120822845	HepG2	liver:	n/a	n/a
16	CEBPB	chr3:121014181-121015355	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr3:120830133-120830171	K562	blood:	n/a	chr3:120830133-120830144
18	CEBPB	chr3:121024454-121024688	A549	lung:	n/a	chr3:121024540-121024551
19	CEBPB	chr3:120830826-120831152	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr3:121024385-121024688	HepG2	liver:	n/a	chr3:121024540-121024551
21	CEBPB	chr3:120877260-120877460	K562	blood:	n/a	chr3:120877371-120877382
22	CEBPB	chr3:120830072-120830272	A549	lung:	n/a	chr3:120830133-120830144
23	CEBPB	chr3:120877238-120877488	HepG2	liver:	n/a	chr3:120877371-120877382
24	CEBPB	chr3:120730574-120730867	MCF-7	breast:	n/a	chr3:120730725-120730736
25	CEBPB	chr3:120829969-120830281	Hela-S3	cervix:	n/a	chr3:120830133-120830144
26	CEBPB	chr3:120730575-120730885	A549	lung:	n/a	chr3:120730725-120730736
27	CEBPB	chr3:120830064-120830248	ECC-1	luminal epithelium:	n/a	chr3:120830133-120830144
28	CEBPB	chr3:120877234-120877467	A549	lung:	n/a	chr3:120877371-120877382
29	CEBPB	chr3:120730564-120730863	IMR90	lung:	n/a	chr3:120730725-120730736
30	CEBPB	chr3:120830052-120830302	MCF-7	breast:	n/a	chr3:120830133-120830144
31	CEBPB	chr3:120892760-120892883	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr3:120845332-120845587	Hela-S3	cervix:	n/a	chr3:120845476-120845487
33	CEBPB	chr3:120959887-120959918	K562	blood:	n/a	n/a
34	CEBPB	chr3:121038299-121038614	A549	lung:	n/a	n/a
35	CEBPB	chr3:120830891-120831091	HepG2	liver:	n/a	n/a
36	CEBPB	chr3:120829975-120830303	HepG2	liver:	n/a	chr3:120830133-120830144
37	CEBPB	chr3:120730640-120730877	Hela-S3	cervix:	n/a	chr3:120730725-120730736
38	CEBPB	chr3:121024403-121024693	IMR90	lung:	n/a	chr3:121024540-121024551
39	CEBPB	chr3:121030012-121030161	K562	blood:	n/a	chr3:121030079-121030090
40	CEBPB	chr3:120845421-120845545	HepG2	liver:	n/a	chr3:120845476-120845487
41	CEBPB	chr3:120822725-120822791	IMR90	lung:	n/a	n/a
42	CEBPD	chr3:120886259-120886658	K562	blood:	n/a	n/a
43	CEBPD	chr3:120886293-120886675	K562	blood:	n/a	n/a
44	CHD2	chr3:120782613-120782867	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr3:120830930-120831060	HepG2	liver:	n/a	n/a
46	CTCF	chr3:120871600-120871750	HepG2	liver:	n/a	chr3:120871613-120871631 chr3:120871608-120871629
47	CTCF	chr3:120871619-120871704	Medullo	brain:	n/a	n/a
48	CTCF	chr3:120871567-120871722	MCF-7	breast:	n/a	chr3:120871613-120871631 chr3:120871608-120871629
49	CTCF	chr3:120838080-120838230	HCT-116	colon:	n/a	n/a
50	CTCF	chr3:120871480-120871630	GM12878	blood:	n/a	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	GM06990	blood:	n/a
2	chr3:120909792-120909842	AG09309	skin:	n/a
3	chr3:120909792-120909842	NT2-D1	testis:	n/a
4	chr3:121025407-121025457	HRCEpiC	kidney:	n/a
5	chr3:120909792-120909842	HEEpiC	esophagus:	n/a
6	chr3:121025407-121025457	BE2_C	brain:	n/a
7	chr3:121025407-121025457	NT2-D1	testis:	n/a
8	chr3:121025407-121025457	HUVEC	blood vessel:	n/a
9	chr3:121025407-121025457	HEK293	kidney:	embryo
10	chr3:121025407-121025457	HRE	kidney:	n/a
11	chr3:121025407-121025457	HPAEpiC	pulmonary alveolar:	n/a
12	chr3:121025407-121025457	RPTEC	kidney:	n/a
13	chr3:121025407-121025457	NB4	blood:	n/a
14	chr3:121025407-121025457	HCM	heart:	n/a
15	chr3:120909792-120909842	K562	blood:	n/a
16	chr3:121025407-121025457	GM12878	blood:	n/a
17	chr3:120909792-120909842	HPAEpiC	pulmonary alveolar:	n/a
18	chr3:121025407-121025457	Hepatocyte	liver:	n/a
19	chr3:120909792-120909842	HUVEC	blood vessel:	n/a
20	chr3:121025407-121025457	AG09319	gingival:	n/a
21	chr3:121025407-121025457	HNPCEpiC	eye:	n/a
22	chr3:120909792-120909842	AG04450	lung:	fetal
23	chr3:120909792-120909842	SK-N-MC	brain:	n/a
24	chr3:121025407-121025457	HL-60	blood:	n/a
25	chr3:120909792-120909842	MCF10A-Er-Src	breast:	n/a
26	chr3:121025407-121025457	SK-N-SH_RA	brain:	n/a
27	chr3:120909792-120909842	HRE	kidney:	n/a
28	chr3:120909792-120909842	NB4	blood:	n/a
29	chr3:120909792-120909842	HEK293	kidney:	embryo
30	chr3:120909792-120909842	IMR90	lung:	fetal
31	chr3:120909792-120909842	SK-N-SH_RA	brain:	n/a
32	chr3:121025407-121025457	HIPEpiC	eye:	n/a
33	chr3:121025407-121025457	SAEC	small airway:	n/a
34	chr3:120909792-120909842	HepG2	liver:	n/a
35	chr3:120909792-120909842	SKMC	muscle:	n/a
36	chr3:121025407-121025457	HRPEpiC	eye:	n/a
37	chr3:120909792-120909842	ECC-1	luminal epithelium:	n/a
38	chr3:121025407-121025457	GM12891	blood:	n/a
39	chr3:120909792-120909842	H1-hESC	embryonic stem cell:	embryo
40	chr3:121025407-121025457	NH-A	brain:	n/a
41	chr3:121025407-121025457	U87	brain:	n/a
42	chr3:121025407-121025457	MCF-7	breast:	n/a
43	chr3:121025407-121025457	HCF	heart:	n/a
44	chr3:121025407-121025457	CMK	blood:	n/a
45	chr3:120909792-120909842	HNPCEpiC	eye:	n/a
46	chr3:121025407-121025457	NHBE	bronchial:	n/a
47	chr3:121025407-121025457	GM19239	blood:	n/a
48	chr3:121025407-121025457	Caco-2	colon:	n/a
49	chr3:120909792-120909842	HRCEpiC	kidney:	n/a
50	chr3:120909792-120909842	HCM	heart:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:121047561..121048621-chr3:121247919..121248785,3	MCF-7	breast:
2	chr3:120860340..120860840-chr8:23021037..23021834,2	Hela-S3	cervix:
3	chr3:120850081..120852968-chr3:120854898..120857782,2	MCF-7	breast:
4	chr3:120841817..120844758-chr3:120846450..120848360,2	K562	blood:
5	chr3:121004364..121006948-chr3:121012227..121014018,2	MCF-7	breast:
6	chr3:120841817..120844758-chr3:120846450..120848360,2	K562	blood:
7	chr3:120875889..120878792-chr3:120892011..120893979,2	K562	blood:
8	chr3:120875889..120878792-chr3:120892011..120893979,2	K562	blood:
9	chr3:121004364..121006948-chr3:121012227..121014018,2	MCF-7	breast:
10	chr3:120279838..120280352-chr3:120871430..120872100,2	MCF-7	breast:
11	chr3:120850081..120852968-chr3:120854898..120857782,2	MCF-7	breast:
12	chr3:62626007..62626708-chr3:120837876..120838423,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POLQ-2	chr3:120873476-120873875	ucscGeneNc_uc003edb_1
2	lnc-ARGFX-1	chr3:121075838-121076787	NONHSAT091471
3	lnc-GTF2E1-4	chr3:120817955-120818621	NONHSAT091470
4	lnc-POLQ-2	chr3:120872301-120873382	ucscGeneNc_uc003edb_1
5	lnc-RABL3-5	chr3:120799296-120799541	predAs_chen_BG200968_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
ENSG00000242103	TF binding region
MIR5682	CpG island
ENSG00000243813	CpG island
ENSG00000242103	CpG island
ENSG00000173530	chromatin interactions

Extended variants
information (count: 10724 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:10724 , 50 per page) page: 1 2 3 4 5 6 7 ... 215

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376243381	chr3:120730020-120730021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs568894193	chr3:120730068-120730069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145781689	chr3:120730114-120730115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533620392	chr3:120730122-120730123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370313524	chr3:120730142-120730143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554240788	chr3:120730151-120730152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369107409	chr3:120730152-120730153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182674938	chr3:120730176-120730177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186998929	chr3:120730208-120730209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1688684	chr3:120730219-120730220	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs529474994	chr3:120730221-120730222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553655340	chr3:120730228-120730229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs73855303	chr3:120730242-120730243	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs548006653	chr3:120730253-120730254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545637443	chr3:120730267-120730268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115853048	chr3:120730277-120730278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376964060	chr3:120730284-120730285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs193164966	chr3:120730291-120730292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185040596	chr3:120730308-120730309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12494552	chr3:120730321-120730322	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs572405900	chr3:120730347-120730348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536660525	chr3:120730350-120730351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564809921	chr3:120730352-120730353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374183363	chr3:120730353-120730354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545368835	chr3:120730381-120730382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533550010	chr3:120730388-120730389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550426050	chr3:120730480-120730481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200667115	chr3:120730507-120730508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11921863	chr3:120730510-120730511	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs531275426	chr3:120730511-120730512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548277119	chr3:120730512-120730513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567919242	chr3:120730517-120730518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111346209	chr3:120730532-120730533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547283019	chr3:120730550-120730551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190722942	chr3:120730593-120730594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147766783	chr3:120730606-120730607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140628869	chr3:120730609-120730610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201669059	chr3:120730610-120730611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs193059538	chr3:120730628-120730629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570413621	chr3:120730685-120730686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs28751972	chr3:120730689-120730690	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs555874662	chr3:120730699-120730700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs34114855	chr3:120730726-120730727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572461841	chr3:120730734-120730735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541471358	chr3:120730745-120730746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564748437	chr3:120730749-120730750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370901776	chr3:120730771-120730772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552834693	chr3:120730778-120730779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544112168	chr3:120730801-120730802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563692182	chr3:120730897-120730898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Bipolar disorder	17953491	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Cancer	20164919	CNVD

Chromatin state (count:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:120720600-120737800	Weak transcription	Ovary	ovary
2	chr3:120737800-120738200	ZNF genes & repeats	Ovary	ovary
3	chr3:120737800-120738600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr3:120737800-120738600	Enhancers	HMEC	breast
5	chr3:120738000-120738400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr3:120738200-120738600	Weak transcription	Ovary	ovary
7	chr3:120746200-120746800	Enhancers	Brain Substantia Nigra	brain
8	chr3:120762800-120767600	Weak transcription	Ovary	ovary
9	chr3:120763200-120768400	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr3:120764200-120767400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
11	chr3:120766000-120767200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr3:120766600-120767000	ZNF genes & repeats	Brain Anterior Caudate	brain
13	chr3:120766800-120768200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr3:120767000-120768000	Weak transcription	Brain Anterior Caudate	brain
15	chr3:120767000-120769000	ZNF genes & repeats	Fetal Brain Female	brain
16	chr3:120767200-120768200	Weak transcription	Gastric	stomach
17	chr3:120767400-120769000	Strong transcription	Pancreatic Islets	Pancreatic Islet
18	chr3:120767600-120768200	Weak transcription	Brain Angular Gyrus	brain
19	chr3:120767600-120769000	Strong transcription	Ovary	ovary
20	chr3:120767600-120770200	Weak transcription	Brain Cingulate Gyrus	brain
21	chr3:120768000-120768400	Strong transcription	Brain Anterior Caudate	brain
22	chr3:120768200-120769000	ZNF genes & repeats	Brain Angular Gyrus	brain
23	chr3:120768200-120769000	ZNF genes & repeats	Brain Germinal Matrix	brain
24	chr3:120768200-120769000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr3:120768200-120769000	ZNF genes & repeats	Gastric	stomach
26	chr3:120768400-120768800	ZNF genes & repeats	Brain Anterior Caudate	brain
27	chr3:120768400-120768800	Strong transcription	Brain Inferior Temporal Lobe	brain
28	chr3:120768600-120769000	ZNF genes & repeats	Pancreas	Pancrea
29	chr3:120768800-120769000	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
30	chr3:120769000-120769200	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr3:120769000-120770600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr3:120769000-120777000	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr3:120769000-120791200	Weak transcription	Ovary	ovary
34	chr3:120777000-120777200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
35	chr3:120781400-120782200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr3:120781600-120790800	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr3:120782200-120782600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr3:120782200-120783200	Enhancers	H1 Cell Line	embryonic stem cell
39	chr3:120782200-120783200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr3:120782400-120783000	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr3:120782400-120783000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr3:120782400-120783200	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr3:120782600-120782800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr3:120782600-120782800	Enhancers	A549	lung
45	chr3:120782600-120783000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr3:120782600-120783200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr3:120782600-120783200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr3:120782800-120783200	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr3:120783000-120783400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr3:120783000-120789400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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