Variant report

Variant	nsv590641
Chromosome Location	chr3:75228373-75322243
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:806)
CpG islands
(count:306)
Chromatin interactive
region (count:7)
LncRNA
region (count:9)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:806 , 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	chr3:75308537-75308777	HepG2	liver:	n/a	n/a
2	ATF1	chr3:75273635-75274085	K562	blood:	n/a	n/a
3	ATF2	chr3:75229570-75230214	GM12878	blood:	n/a	n/a
4	ATF2	chr3:75229597-75230101	GM12878	blood:	n/a	n/a
5	ATF2	chr3:75241228-75241540	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr3:75229707-75230159	GM12878	blood:	n/a	n/a
7	BCL11A	chr3:75229688-75230088	GM12878	blood:	n/a	n/a
8	BCL11A	chr3:75229596-75230089	GM12878	blood:	n/a	n/a
9	BCL3	chr3:75229695-75230085	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:75275145-75275162	GM12878	blood:	n/a	n/a
11	BHLHE40	chr3:75229629-75230115	GM12878	blood:	n/a	n/a
12	CEBPB	chr3:75242621-75242943	IMR90	lung:	n/a	chr3:75242773-75242784
13	CEBPB	chr3:75235119-75235256	H1-hESC	embryonic stem cell:	n/a	chr3:75235211-75235224
14	CEBPB	chr3:75298607-75298890	HepG2	liver:	n/a	chr3:75298746-75298757
15	CEBPB	chr3:75273652-75273997	HepG2	liver:	n/a	chr3:75273812-75273823
16	CEBPB	chr3:75308543-75308721	HepG2	liver:	n/a	chr3:75308643-75308654
17	CEBPB	chr3:75304679-75304870	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr3:75308521-75308803	HepG2	liver:	n/a	chr3:75308643-75308654
19	CEBPB	chr3:75236311-75236614	IMR90	lung:	n/a	chr3:75236334-75236347
20	CEBPB	chr3:75236452-75236563	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr3:75273634-75273992	A549	lung:	n/a	chr3:75273812-75273823
22	CEBPB	chr3:75242648-75242901	A549	lung:	n/a	chr3:75242773-75242784
23	CEBPB	chr3:75242606-75242929	HepG2	liver:	n/a	chr3:75242773-75242784
24	CEBPB	chr3:75273586-75274005	Hela-S3	cervix:	n/a	chr3:75273812-75273823
25	CEBPB	chr3:75298676-75298908	IMR90	lung:	n/a	chr3:75298746-75298757
26	CEBPB	chr3:75236445-75236543	K562	blood:	n/a	n/a
27	CEBPB	chr3:75298279-75298413	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr3:75321899-75322205	IMR90	lung:	n/a	n/a
29	CEBPB	chr3:75236305-75236610	HepG2	liver:	n/a	chr3:75236334-75236347
30	CHD1	chr3:75274164-75274330	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr3:75229450-75230366	GM12878	blood:	n/a	n/a
32	CHD2	chr3:75303964-75304222	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr3:75229546-75230156	GM12878	blood:	n/a	n/a
34	CREB1	chr3:75270143-75270436	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr3:75308020-75308170	HFF	foreskin:	n/a	chr3:75308148-75308161 chr3:75308147-75308168 chr3:75308145-75308163
36	CTCF	chr3:75273520-75273670	AG04450	lung:	n/a	n/a
37	CTCF	chr3:75308020-75308170	NHDF-neo	bronchial:	n/a	chr3:75308148-75308161 chr3:75308147-75308168 chr3:75308145-75308163
38	CTCF	chr3:75241012-75241907	SK-N-SH	brain:	n/a	n/a
39	CTCF	chr3:75241340-75241490	GM12874	blood:	n/a	n/a
40	CTCF	chr3:75308060-75308210	HRPEpiC	eye:	n/a	chr3:75308148-75308161 chr3:75308147-75308168 chr3:75308145-75308163
41	CTCF	chr3:75241340-75241490	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr3:75308040-75308190	AG04450	lung:	n/a	chr3:75308148-75308161 chr3:75308147-75308168 chr3:75308145-75308163
43	CTCF	chr3:75241360-75241510	GM12872	blood:	n/a	n/a
44	CTCF	chr3:75308086-75308227	HepG2	liver:	n/a	chr3:75308148-75308161 chr3:75308147-75308168 chr3:75308145-75308163
45	CTCF	chr3:75309271-75309347	MCF-7	breast:	n/a	n/a
46	CTCF	chr3:75308069-75308259	Pancreas_OC	pancreas:	n/a	chr3:75308148-75308161 chr3:75308147-75308168 chr3:75308145-75308163
47	CTCF	chr3:75307919-75308299	MCF-7	breast:	n/a	chr3:75308148-75308161 chr3:75308147-75308168 chr3:75308145-75308163
48	CTCF	chr3:75308003-75308267	Medullo	brain:	n/a	chr3:75308148-75308161 chr3:75308147-75308168 chr3:75308145-75308163
49	CTCF	chr3:75241287-75241540	Fibrobl	skin:	n/a	n/a
50	CTCF	chr3:75273000-75273150	HMF	breast:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75263691-75263741	IMR90	lung:	fetal
2	chr3:75263691-75263741	IMR90	lung:	fetal
3	chr3:75263691-75263741	NHBE	bronchial:	n/a
4	chr3:75263619-75263669	HAEpiC	amniotic membrane:	n/a
5	chr3:75263641-75263691	GM12892	blood:	n/a
6	chr3:75263685-75263735	CMK	blood:	n/a
7	chr3:75263641-75263691	SAEC	small airway:	n/a
8	chr3:75263691-75263741	BJ	skin:	n/a
9	chr3:75263626-75263676	HRCEpiC	kidney:	n/a
10	chr3:75263641-75263691	NHBE	bronchial:	n/a
11	chr3:75263691-75263741	HepG2	liver:	n/a
12	chr3:75263685-75263735	HRE	kidney:	n/a
13	chr3:75263626-75263676	GM06990	blood:	n/a
14	chr3:75263685-75263735	NT2-D1	testis:	n/a
15	chr3:75263619-75263669	ECC-1	luminal epithelium:	n/a
16	chr3:75263685-75263735	SK-N-SH_RA	brain:	n/a
17	chr3:75263641-75263691	PrEC	prostate:	n/a
18	chr3:75263691-75263741	Hela-S3	cervix:	n/a
19	chr3:75263626-75263676	NT2-D1	testis:	n/a
20	chr3:75263619-75263669	CMK	blood:	n/a
21	chr3:75263626-75263676	AG09319	gingival:	n/a
22	chr3:75263626-75263676	HEEpiC	esophagus:	n/a
23	chr3:75263619-75263669	HPAEpiC	pulmonary alveolar:	n/a
24	chr3:75263685-75263735	SK-N-SH	brain:	n/a
25	chr3:75263685-75263735	GM06990	blood:	n/a
26	chr3:75263641-75263691	HAEpiC	amniotic membrane:	n/a
27	chr3:75263691-75263741	GM12878	blood:	n/a
28	chr3:75263685-75263735	GM12891	blood:	n/a
29	chr3:75263641-75263691	GM12878	blood:	n/a
30	chr3:75263641-75263691	HRPEpiC	eye:	n/a
31	chr3:75263626-75263676	BE2_C	brain:	n/a
32	chr3:75263626-75263676	Hela-S3	cervix:	n/a
33	chr3:75263626-75263676	PFSK-1	brain:	n/a
34	chr3:75263626-75263676	T-47D	breast:	n/a
35	chr3:75263619-75263669	HNPCEpiC	eye:	n/a
36	chr3:75263619-75263669	AG04450	lung:	fetal
37	chr3:75263619-75263669	A549	lung:	n/a
38	chr3:75263641-75263691	K562	blood:	n/a
39	chr3:75263685-75263735	RPTEC	kidney:	n/a
40	chr3:75263619-75263669	HRE	kidney:	n/a
41	chr3:75263641-75263691	MCF10A-Er-Src	breast:	n/a
42	chr3:75263691-75263741	SK-N-MC	brain:	n/a
43	chr3:75263626-75263676	AG04449	skin:	fetal
44	chr3:75263691-75263741	U87	brain:	n/a
45	chr3:75263691-75263741	GM12891	blood:	n/a
46	chr3:75263691-75263741	LNCaP	prostate:	n/a
47	chr3:75263685-75263735	NB4	blood:	n/a
48	chr3:75263626-75263676	AoSMC	blood vessel:	n/a
49	chr3:75263691-75263741	HCT-116	colon:	n/a
50	chr3:75263685-75263735	HNPCEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:75299981..75301854-chr3:75306203..75307918,2	MCF-7	breast:
2	chr3:75248466..75250220-chr3:75254434..75257051,2	K562	blood:
3	chr3:75225822..75228445-chr3:75228843..75230349,2	MCF-7	breast:
4	chr3:75248466..75250220-chr3:75254434..75257051,2	K562	blood:
5	chr3:75225822..75228445-chr3:75228843..75230349,2	MCF-7	breast:
6	chr3:75308414..75309217-chr3:75343438..75343942,2	MCF-7	breast:
7	chr3:75299981..75301854-chr3:75306203..75307918,2	MCF-7	breast:

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

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

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: 2899 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2899 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4076738	chr3:75228373-75228374	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573861415	chr3:75228411-75228412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs28454928	chr3:75228431-75228432	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs557167645	chr3:75228446-75228447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142229822	chr3:75228457-75228458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545829321	chr3:75228508-75228509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564460184	chr3:75228640-75228641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs151184361	chr3:75228656-75228657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540509519	chr3:75228660-75228661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568954060	chr3:75228697-75228698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185262297	chr3:75228728-75228729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs77515301	chr3:75228737-75228738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190540019	chr3:75228747-75228748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140297359	chr3:75228799-75228800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7630321	chr3:75228860-75228861	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs10222613	chr3:75228876-75228877	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs182218445	chr3:75228925-75228926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569376295	chr3:75228945-75228946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184350275	chr3:75228978-75228979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188184617	chr3:75228991-75228992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181336884	chr3:75229033-75229034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528866505	chr3:75229091-75229092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549299180	chr3:75229102-75229103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4078307	chr3:75229125-75229126	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs75204511	chr3:75229143-75229144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146955684	chr3:75229210-75229211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs185841967	chr3:75229235-75229236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539833286	chr3:75229272-75229273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs557761691	chr3:75229275-75229276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs572879483	chr3:75229366-75229367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540571043	chr3:75229374-75229375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs562033201	chr3:75229387-75229388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs141944593	chr3:75229608-75229609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs145797922	chr3:75229634-75229635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs564496986	chr3:75229646-75229647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs567403336	chr3:75229647-75229648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs538064907	chr3:75229663-75229664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs115565041	chr3:75229688-75229689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571401295	chr3:75229730-75229731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113320057	chr3:75229749-75229750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557826959	chr3:75229841-75229842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs574138015	chr3:75229843-75229844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138393431	chr3:75230005-75230006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533891573	chr3:75230014-75230015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556049544	chr3:75230070-75230071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs113842580	chr3:75230071-75230072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs4513474	chr3:75230116-75230117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs372695137	chr3:75230138-75230139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543092878	chr3:75230193-75230194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376968881	chr3:75230235-75230236	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Breast cancer	22522925	CNVD

Chromatin state (count:202 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75226600-75229200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr3:75228200-75228800	Enhancers	Brain Germinal Matrix	brain
3	chr3:75229200-75229400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr3:75229600-75230000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr3:75229600-75230400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr3:75230000-75230400	Enhancers	NH-A	brain
7	chr3:75234800-75235200	Enhancers	H9 Cell Line	embryonic stem cell
8	chr3:75235200-75237800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr3:75235800-75236800	Enhancers	Brain Germinal Matrix	brain
10	chr3:75236600-75238400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:75236800-75237600	Weak transcription	Brain Germinal Matrix	brain
12	chr3:75237600-75239200	Enhancers	Brain Germinal Matrix	brain
13	chr3:75237800-75238200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr3:75237800-75238400	Enhancers	H9 Cell Line	embryonic stem cell
15	chr3:75238000-75238400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr3:75238000-75238800	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr3:75238200-75238400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr3:75238200-75239000	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr3:75238200-75240200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr3:75238400-75239400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr3:75238400-75241600	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr3:75239000-75240000	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr3:75239400-75239800	Enhancers	H1 Cell Line	embryonic stem cell
24	chr3:75239400-75239800	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr3:75240000-75240200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr3:75240800-75244600	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr3:75241400-75241600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr3:75241400-75242000	Enhancers	HMEC	breast
29	chr3:75241600-75241800	Enhancers	H9 Cell Line	embryonic stem cell
30	chr3:75242600-75243600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr3:75250200-75250400	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr3:75250400-75251800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr3:75250400-75257800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr3:75251400-75251800	Enhancers	Brain Germinal Matrix	brain
35	chr3:75257200-75257600	Weak transcription	Aorta	Aorta
36	chr3:75257600-75257800	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr3:75257600-75257800	ZNF genes & repeats	Aorta	Aorta
38	chr3:75257600-75258400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr3:75257600-75259800	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr3:75257800-75258800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr3:75257800-75259600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr3:75257800-75259600	Weak transcription	Aorta	Aorta
43	chr3:75258000-75258800	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr3:75258800-75259400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr3:75258800-75259400	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr3:75259000-75259600	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr3:75259400-75259600	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr3:75259400-75259600	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr3:75259400-75259800	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr3:75259600-75260000	Enhancers	iPS-20b Cell Line	embryonic stem cell

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