Variant report

Variant	nsv876965
Chromosome Location	chr3:75222937-75294417
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:622)
CpG islands
(count:305)
Chromatin interactive
region (count:4)
LncRNA
region (count:9)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:622 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:75273635-75274085	K562	blood:	n/a	n/a
2	ATF2	chr3:75229570-75230214	GM12878	blood:	n/a	n/a
3	ATF2	chr3:75229597-75230101	GM12878	blood:	n/a	n/a
4	ATF2	chr3:75241228-75241540	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr3:75229707-75230159	GM12878	blood:	n/a	n/a
6	BCL11A	chr3:75229596-75230089	GM12878	blood:	n/a	n/a
7	BCL11A	chr3:75229688-75230088	GM12878	blood:	n/a	n/a
8	BCL3	chr3:75229695-75230085	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:75275145-75275162	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:75227294-75227303	GM12878	blood:	n/a	n/a
11	BHLHE40	chr3:75226190-75226494	GM12878	blood:	n/a	n/a
12	BHLHE40	chr3:75229629-75230115	GM12878	blood:	n/a	n/a
13	CEBPB	chr3:75273586-75274005	Hela-S3	cervix:	n/a	chr3:75273812-75273823
14	CEBPB	chr3:75242648-75242901	A549	lung:	n/a	chr3:75242773-75242784
15	CEBPB	chr3:75242621-75242943	IMR90	lung:	n/a	chr3:75242773-75242784
16	CEBPB	chr3:75242606-75242929	HepG2	liver:	n/a	chr3:75242773-75242784
17	CEBPB	chr3:75236311-75236614	IMR90	lung:	n/a	chr3:75236334-75236347
18	CEBPB	chr3:75273652-75273997	HepG2	liver:	n/a	chr3:75273812-75273823
19	CEBPB	chr3:75236445-75236543	K562	blood:	n/a	n/a
20	CEBPB	chr3:75235119-75235256	H1-hESC	embryonic stem cell:	n/a	chr3:75235211-75235224
21	CEBPB	chr3:75273634-75273992	A549	lung:	n/a	chr3:75273812-75273823
22	CEBPB	chr3:75224080-75224265	IMR90	lung:	n/a	chr3:75224186-75224195 chr3:75224184-75224195 chr3:75224186-75224195 chr3:75224184-75224197 chr3:75224186-75224195 chr3:75224186-75224195 chr3:75224184-75224197
23	CEBPB	chr3:75236452-75236563	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr3:75236305-75236610	HepG2	liver:	n/a	chr3:75236334-75236347
25	CEBPB	chr3:75223799-75223857	IMR90	lung:	n/a	n/a
26	CHD1	chr3:75274164-75274330	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr3:75229450-75230366	GM12878	blood:	n/a	n/a
28	CHD1	chr3:75227291-75227355	GM12878	blood:	n/a	n/a
29	CHD2	chr3:75229546-75230156	GM12878	blood:	n/a	n/a
30	CREB1	chr3:75270143-75270436	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr3:75241236-75241562	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr3:75273020-75273170	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr3:75241276-75241524	HepG2	liver:	n/a	n/a
34	CTCF	chr3:75241300-75241450	NHLF	lung:	n/a	n/a
35	CTCF	chr3:75241036-75241155	GM13977	blood:	n/a	n/a
36	CTCF	chr3:75241320-75241470	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr3:75241306-75241544	GM12892	blood:	n/a	n/a
38	CTCF	chr3:75241266-75241542	GM10248	blood:	n/a	n/a
39	CTCF	chr3:75241360-75241510	HFF	foreskin:	n/a	n/a
40	CTCF	chr3:75241880-75242030	GM12870	blood:	n/a	n/a
41	CTCF	chr3:75241320-75241470	AG04449	skin:	n/a	n/a
42	CTCF	chr3:75267865-75267927	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:75241320-75241470	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr3:75273040-75273190	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr3:75273000-75273150	HMF	breast:	n/a	n/a
46	CTCF	chr3:75241194-75241609	GM12878	blood:	n/a	n/a
47	CTCF	chr3:75271656-75271732	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr3:75240006-75240138	LNCaP	prostate:	n/a	n/a
49	CTCF	chr3:75267819-75267960	LNCaP	prostate:	n/a	n/a
50	CTCF	chr3:75272920-75273070	HPF	lung:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75263685-75263735	GM19239	blood:	n/a
2	chr3:75263619-75263669	ovcar-3	ovarian:	n/a
3	chr3:75263691-75263741	HCT-116	colon:	n/a
4	chr3:75263619-75263669	HRCEpiC	kidney:	n/a
5	chr3:75263685-75263735	ProgFib	skin:	n/a
6	chr3:75263685-75263735	SAEC	small airway:	n/a
7	chr3:75263619-75263669	PrEC	prostate:	n/a
8	chr3:75263641-75263691	GM12892	blood:	n/a
9	chr3:75263691-75263741	SK-N-SH_RA	brain:	n/a
10	chr3:75263685-75263735	PrEC	prostate:	n/a
11	chr3:75263685-75263735	HUVEC	blood vessel:	n/a
12	chr3:75263685-75263735	GM12892	blood:	n/a
13	chr3:75263691-75263741	ovcar-3	ovarian:	n/a
14	chr3:75263691-75263741	HEK293	kidney:	embryo
15	chr3:75263619-75263669	GM12891	blood:	n/a
16	chr3:75263691-75263741	GM12878	blood:	n/a
17	chr3:75263619-75263669	T-47D	breast:	n/a
18	chr3:75263691-75263741	ProgFib	skin:	n/a
19	chr3:75263626-75263676	HRCEpiC	kidney:	n/a
20	chr3:75263641-75263691	HRCEpiC	kidney:	n/a
21	chr3:75263641-75263691	AG04450	lung:	fetal
22	chr3:75263641-75263691	Jurkat	blood:	n/a
23	chr3:75263626-75263676	ovcar-3	ovarian:	n/a
24	chr3:75263685-75263735	SK-N-MC	brain:	n/a
25	chr3:75263691-75263741	GM12891	blood:	n/a
26	chr3:75263685-75263735	HCF	heart:	n/a
27	chr3:75263619-75263669	HRE	kidney:	n/a
28	chr3:75263626-75263676	HCF	heart:	n/a
29	chr3:75263626-75263676	HCM	heart:	n/a
30	chr3:75263626-75263676	HCPEpiC	choroid plexus:	n/a
31	chr3:75263619-75263669	PFSK-1	brain:	n/a
32	chr3:75263685-75263735	RPTEC	kidney:	n/a
33	chr3:75263641-75263691	GM12878	blood:	n/a
34	chr3:75263626-75263676	AG04450	lung:	fetal
35	chr3:75263691-75263741	PrEC	prostate:	n/a
36	chr3:75263619-75263669	NHDF-neo	bronchial:	n/a
37	chr3:75263691-75263741	PANC-1	pancreas:	n/a
38	chr3:75263685-75263735	T-47D	breast:	n/a
39	chr3:75263626-75263676	HIPEpiC	eye:	n/a
40	chr3:75263691-75263741	HCPEpiC	choroid plexus:	n/a
41	chr3:75263641-75263691	BE2_C	brain:	n/a
42	chr3:75263685-75263735	HMEC	breast:	n/a
43	chr3:75263685-75263735	NHBE	bronchial:	n/a
44	chr3:75263626-75263676	NT2-D1	testis:	n/a
45	chr3:75263685-75263735	HAEpiC	amniotic membrane:	n/a
46	chr3:75263641-75263691	HRE	kidney:	n/a
47	chr3:75263685-75263735	HL-60	blood:	n/a
48	chr3:75263641-75263691	HUVEC	blood vessel:	n/a
49	chr3:75263626-75263676	HPAEpiC	pulmonary alveolar:	n/a
50	chr3:75263641-75263691	SK-N-SH_RA	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:75248466..75250220-chr3:75254434..75257051,2	K562	blood:
2	chr3:75225822..75228445-chr3:75228843..75230349,2	MCF-7	breast:
3	chr3:75225822..75228445-chr3:75228843..75230349,2	MCF-7	breast:
4	chr3:75248466..75250220-chr3:75254434..75257051,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-4	chr3:75289122-75289170	NONHSAT090505
2	lnc-ZNF717-8	chr3:75231907-75232199	NONHSAT090502
3	lnc-ZNF717-7	chr3:75264616-75264635	NONHSAT090504
4	lnc-FRG2C-4	chr3:75289333-75289869	NONHSAT090505
5	lnc-FRG2C-4	chr3:75289336-75289618	XLOC_002709
6	lnc-ZNF717-7	chr3:75264310-75264481	NONHSAT090504
7	lnc-FRG2C-4	chr3:75273688-75273709	XLOC_002709
8	lnc-ZNF717-7	chr3:75264644-75264868	NONHSAT090504
9	lnc-FRG2C-4	chr3:75273648-75273709	NONHSAT090505

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4444	chr3:75263669-75263686	MIMAT0018962_1

No data

Variant related genes	Relation type
HNRNPA3P6	TF binding region
RN7SL294P	TF binding region
MIR4444-1	TF binding region
HNRNPA3P6	CpG island
RN7SL294P	CpG island
MIR4444-1	CpG island
FAM199X	miRNA target sites
FAM20C	miRNA target sites

Extended variants
information (count: 2197 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2197 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9810161	chr3:75222937-75222938	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs79830090	chr3:75222943-75222944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs71627411	chr3:75223041-75223042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545225213	chr3:75223042-75223043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs114897250	chr3:75223053-75223054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561933769	chr3:75223069-75223070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs370881589	chr3:75223111-75223112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549082726	chr3:75223169-75223170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114724289	chr3:75223173-75223174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6776740	chr3:75223185-75223186	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs114988675	chr3:75223191-75223192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571408000	chr3:75223241-75223242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs117784228	chr3:75223251-75223252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs6776847	chr3:75223308-75223309	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs181051757	chr3:75223318-75223319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534057003	chr3:75223335-75223336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146530403	chr3:75223356-75223357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6810317	chr3:75223412-75223413	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs145882509	chr3:75223464-75223465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138419097	chr3:75223475-75223476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374626936	chr3:75223477-75223478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs63048461	chr3:75223497-75223498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113106585	chr3:75223511-75223512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537814027	chr3:75223589-75223590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549862286	chr3:75223605-75223606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186037112	chr3:75223619-75223620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs578167885	chr3:75223625-75223626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6762105	chr3:75223643-75223644	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs151180657	chr3:75223651-75223652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79974762	chr3:75223660-75223661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572653331	chr3:75223673-75223674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190272142	chr3:75223703-75223704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542790307	chr3:75223714-75223715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs75895948	chr3:75223716-75223717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs75983857	chr3:75223783-75223784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531339244	chr3:75223807-75223808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547487307	chr3:75223822-75223823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570413153	chr3:75223850-75223851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549461565	chr3:75223894-75223895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539420140	chr3:75223914-75223915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575242683	chr3:75223917-75223918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374211553	chr3:75223959-75223960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565204415	chr3:75223981-75223982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6774966	chr3:75224006-75224007	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs77171472	chr3:75224036-75224037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200707037	chr3:75224070-75224071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565588299	chr3:75224077-75224078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs6775067	chr3:75224078-75224079	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs573030793	chr3:75224079-75224080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567378187	chr3:75224091-75224092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	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
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Autism	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75220800-75226000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr3:75222600-75224600	Weak transcription	Brain Germinal Matrix	brain
3	chr3:75224200-75225400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:75224600-75225200	Enhancers	Brain Germinal Matrix	brain
5	chr3:75225200-75228200	Weak transcription	Brain Germinal Matrix	brain
6	chr3:75226000-75226600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr3:75226000-75226800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr3:75226200-75226600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr3:75226200-75226600	Enhancers	H1 Cell Line	embryonic stem cell
10	chr3:75226200-75226600	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr3:75226200-75226600	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr3:75226200-75226800	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr3:75226600-75229200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr3:75227200-75227600	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr3:75228200-75228800	Enhancers	Brain Germinal Matrix	brain
16	chr3:75229200-75229400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr3:75229600-75230000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr3:75229600-75230400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr3:75230000-75230400	Enhancers	NH-A	brain
20	chr3:75234800-75235200	Enhancers	H9 Cell Line	embryonic stem cell
21	chr3:75235200-75237800	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr3:75235800-75236800	Enhancers	Brain Germinal Matrix	brain
23	chr3:75236600-75238400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:75236800-75237600	Weak transcription	Brain Germinal Matrix	brain
25	chr3:75237600-75239200	Enhancers	Brain Germinal Matrix	brain
26	chr3:75237800-75238200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr3:75237800-75238400	Enhancers	H9 Cell Line	embryonic stem cell
28	chr3:75238000-75238400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr3:75238000-75238800	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr3:75238200-75238400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr3:75238200-75239000	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr3:75238200-75240200	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr3:75238400-75239400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr3:75238400-75241600	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr3:75239000-75240000	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr3:75239400-75239800	Enhancers	H1 Cell Line	embryonic stem cell
37	chr3:75239400-75239800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr3:75240000-75240200	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr3:75240800-75244600	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr3:75241400-75241600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr3:75241400-75242000	Enhancers	HMEC	breast
42	chr3:75241600-75241800	Enhancers	H9 Cell Line	embryonic stem cell
43	chr3:75242600-75243600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr3:75250200-75250400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr3:75250400-75251800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr3:75250400-75257800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr3:75251400-75251800	Enhancers	Brain Germinal Matrix	brain
48	chr3:75257200-75257600	Weak transcription	Aorta	Aorta
49	chr3:75257600-75257800	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr3:75257600-75257800	ZNF genes & repeats	Aorta	Aorta

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