Variant report

Variant	nsv965397
Chromosome Location	chr3:145789376-145797057
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:49)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:49 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr3:145795862-145796117	GM12878	blood:	n/a	n/a
2	BRCA1	chr3:145789570-145789603	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr3:145789503-145789784	HepG2	liver:	n/a	chr3:145789595-145789607 chr3:145789682-145789693
4	CEBPB	chr3:145789496-145789808	A549	lung:	n/a	chr3:145789595-145789607 chr3:145789682-145789693
5	CEBPB	chr3:145789511-145789811	Hela-S3	cervix:	n/a	chr3:145789595-145789607 chr3:145789682-145789693
6	CTCF	chr3:145794181-145794274	Pancreas_OC	pancreas:	n/a	n/a
7	CTCF	chr3:145794236-145794267	GM13977	blood:	n/a	n/a
8	E2F4	chr3:145789160-145789716	MCF10A-Er-Src	breast:	n/a	n/a
9	FOS	chr3:145795059-145795353	HUVEC	blood vessel:	n/a	chr3:145795150-145795161
10	FOS	chr3:145790660-145790860	MCF10A-Er-Src	breast:	n/a	n/a
11	FOS	chr3:145789455-145789750	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr3:145795870-145796140	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr3:145795097-145795216	MCF10A-Er-Src	breast:	n/a	chr3:145795150-145795161
14	FOS	chr3:145795121-145795276	MCF10A-Er-Src	breast:	n/a	chr3:145795150-145795161
15	FOS	chr3:145795883-145796083	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr3:145789544-145789728	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr3:145789514-145789703	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr3:145795890-145796122	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr3:145795870-145796181	MCF10A-Er-Src	breast:	n/a	n/a
20	GATA3	chr3:145796896-145797372	MCF-7	breast:	n/a	n/a
21	JUN	chr3:145789756-145790164	HepG2	liver:	n/a	chr3:145790042-145790051
22	JUN	chr3:145790627-145790773	K562	blood:	n/a	n/a
23	JUND	chr3:145789919-145790121	H1-hESC	embryonic stem cell:	n/a	chr3:145790042-145790051
24	JUND	chr3:145789911-145790222	HepG2	liver:	n/a	chr3:145790042-145790051
25	JUND	chr3:145793060-145793139	H1-hESC	embryonic stem cell:	n/a	n/a
26	MAZ	chr3:145793345-145793401	HepG2	liver:	n/a	n/a
27	MAZ	chr3:145796478-145796480	HepG2	liver:	n/a	n/a
28	MXI1	chr3:145790529-145791226	IMR90	lung:	n/a	n/a
29	MYC	chr3:145790694-145790969	MCF10A-Er-Src	breast:	n/a	n/a
30	MYC	chr3:145790685-145790907	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr3:145789937-145790063	MCF10A-Er-Src	breast:	n/a	n/a
32	POLR2A	chr3:145793235-145793368	MCF10A-Er-Src	breast:	n/a	n/a
33	POLR2A	chr3:145788381-145790538	U87	brain:	n/a	n/a
34	POLR2A	chr3:145795845-145796204	U87	brain:	n/a	n/a
35	POLR2A	chr3:145793622-145794454	U87	brain:	n/a	n/a
36	POLR2A	chr3:145793622-145794403	U87	brain:	n/a	n/a
37	POLR2A	chr3:145792697-145793091	U87	brain:	n/a	n/a
38	POLR2A	chr3:145788806-145790500	HepG2	liver:	n/a	n/a
39	POLR2A	chr3:145788406-145790532	U87	brain:	n/a	n/a
40	POLR2A	chr3:145791243-145791350	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr3:145795640-145796205	U87	brain:	n/a	n/a
42	POLR2A	chr3:145792832-145793446	U87	brain:	n/a	n/a
43	POLR2A	chr3:145796878-145796918	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr3:145792447-145793452	U87	brain:	n/a	n/a
45	POLR2A	chr3:145790568-145790955	U87	brain:	n/a	n/a
46	POLR2A	chr3:145789480-145790473	A549	lung:	n/a	n/a
47	POLR2A	chr3:145795796-145796204	U87	brain:	n/a	n/a
48	STAT3	chr3:145789440-145789550	MCF10A-Er-Src	breast:	n/a	chr3:145789487-145789494
49	ZZZ3	chr3:145792776-145792962	Hela-S3	cervix:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:145790097-145790147	K562	blood:	n/a
2	chr3:145790097-145790147	NHDF-neo	bronchial:	n/a
3	chr3:145790097-145790147	HNPCEpiC	eye:	n/a
4	chr3:145790097-145790147	HAEpiC	amniotic membrane:	n/a
5	chr3:145790097-145790147	Caco-2	colon:	n/a
6	chr3:145790097-145790147	HIPEpiC	eye:	n/a
7	chr3:145790097-145790147	ovcar-3	ovarian:	n/a
8	chr3:145790097-145790147	A549	lung:	n/a
9	chr3:145790097-145790147	NH-A	brain:	n/a
10	chr3:145790097-145790147	GM19239	blood:	n/a
11	chr3:145790097-145790147	SAEC	small airway:	n/a
12	chr3:145790097-145790147	HPAEpiC	pulmonary alveolar:	n/a
13	chr3:145790097-145790147	GM12878	blood:	n/a
14	chr3:145790097-145790147	AoSMC	blood vessel:	n/a
15	chr3:145790097-145790147	H1-hESC	embryonic stem cell:	embryo
16	chr3:145790097-145790147	HCT-116	colon:	n/a
17	chr3:145790097-145790147	HUVEC	blood vessel:	n/a
18	chr3:145790097-145790147	NHBE	bronchial:	n/a
19	chr3:145790097-145790147	CMK	blood:	n/a
20	chr3:145790097-145790147	NB4	blood:	n/a
21	chr3:145790097-145790147	ProgFib	skin:	n/a
22	chr3:145790097-145790147	AG04449	skin:	fetal
23	chr3:145790097-145790147	SK-N-SH	brain:	n/a
24	chr3:145790097-145790147	AG04450	lung:	fetal
25	chr3:145790097-145790147	HMEC	breast:	n/a
26	chr3:145790097-145790147	PFSK-1	brain:	n/a
27	chr3:145790097-145790147	IMR90	lung:	fetal
28	chr3:145790097-145790147	HCM	heart:	n/a
29	chr3:145790097-145790147	AG09309	skin:	n/a
30	chr3:145790097-145790147	GM12892	blood:	n/a
31	chr3:145790097-145790147	SK-N-SH_RA	brain:	n/a
32	chr3:145790097-145790147	HEEpiC	esophagus:	n/a
33	chr3:145790097-145790147	Hepatocyte	liver:	n/a
34	chr3:145790097-145790147	RPTEC	kidney:	n/a
35	chr3:145790097-145790147	SK-N-MC	brain:	n/a
36	chr3:145790097-145790147	PANC-1	pancreas:	n/a
37	chr3:145790097-145790147	Jurkat	blood:	n/a
38	chr3:145790097-145790147	T-47D	breast:	n/a
39	chr3:145790097-145790147	HRCEpiC	kidney:	n/a
40	chr3:145790097-145790147	BJ	skin:	n/a
41	chr3:145790097-145790147	NT2-D1	testis:	n/a
42	chr3:145790097-145790147	HCPEpiC	choroid plexus:	n/a
43	chr3:145790097-145790147	HepG2	liver:	n/a
44	chr3:145790097-145790147	HCF	heart:	n/a
45	chr3:145790097-145790147	LNCaP	prostate:	n/a
46	chr3:145790097-145790147	MCF-7	breast:	n/a
47	chr3:145790097-145790147	HEK293	kidney:	embryo
48	chr3:145790097-145790147	HL-60	blood:	n/a
49	chr3:145790097-145790147	GM06990	blood:	n/a
50	chr3:145790097-145790147	SKMC	muscle:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:145783528..145785150-chr3:145794804..145797191,2	MCF-7	breast:
2	chr3:145787365..145792721-chr3:145875341..145880381,7	MCF-7	breast:
3	chr3:145791294..145794023-chr3:145794706..145796698,2	MCF-7	breast:
4	chr3:145795852..145797776-chr3:145810151..145811741,2	K562	blood:
5	chr3:145795863..145799081-chr3:145877263..145880316,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000240032	TF binding region
PLOD2	TF binding region
ENSG00000240032	CpG island
PLOD2	CpG island
ENSG00000152952	chromatin interactions

Extended variants
information (count: 292 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533273765	chr3:145789403-145789404	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs560299610	chr3:145789415-145789416	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs144751051	chr3:145789421-145789422	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs569995637	chr3:145789440-145789441	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs537342787	chr3:145789453-145789454	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs138775222	chr3:145789459-145789460	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs141837591	chr3:145789479-145789480	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs572347410	chr3:145789485-145789486	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs553214155	chr3:145789542-145789543	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs1375589	chr3:145789579-145789580	Enhancers Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs1375588	chr3:145789609-145789610	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs376779859	chr3:145789621-145789622	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs3792345	chr3:145789634-145789635	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs575168576	chr3:145789675-145789676	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs146315598	chr3:145789680-145789681	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs1375587	chr3:145789696-145789697	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs574007729	chr3:145789697-145789698	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs1375586	chr3:145789699-145789700	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs559522738	chr3:145789758-145789759	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs568927759	chr3:145789763-145789764	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs138148087	chr3:145789768-145789769	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs563683508	chr3:145789800-145789801	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs4681293	chr3:145789827-145789828	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs149551371	chr3:145789996-145789997	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs190112742	chr3:145790011-145790012	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs144294117	chr3:145790021-145790022	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs546815411	chr3:145790023-145790024	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs34106207	chr3:145790025-145790026	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs3804670	chr3:145790046-145790047	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs538714340	chr3:145790048-145790049	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs201942820	chr3:145790061-145790062	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs76344866	chr3:145790063-145790064	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs200597103	chr3:145790064-145790065	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs537951567	chr3:145790145-145790146	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs202042741	chr3:145790186-145790187	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs113195215	chr3:145790246-145790247	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs554151163	chr3:145790259-145790260	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs375912701	chr3:145790276-145790277	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs181264004	chr3:145790277-145790278	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs573947263	chr3:145790281-145790282	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs116355501	chr3:145790282-145790283	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs113550952	chr3:145790283-145790284	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs112122519	chr3:145790292-145790293	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs148735874	chr3:145790293-145790294	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs199938282	chr3:145790405-145790406	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs202110196	chr3:145790417-145790418	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs374567883	chr3:145790452-145790453	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs376704588	chr3:145790463-145790464	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs368810705	chr3:145790470-145790471	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs201071953	chr3:145790472-145790473	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	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
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
Basal cell lymphoma	21115979	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	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
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autism	21956041	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:204 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:145774600-145795400	Weak transcription	Aorta	Aorta
2	chr3:145777000-145819400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr3:145778200-145817200	Weak transcription	Fetal Stomach	stomach
4	chr3:145779000-145789600	Weak transcription	Fetal Heart	heart
5	chr3:145779600-145820600	Weak transcription	Fetal Kidney	kidney
6	chr3:145780000-145815600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr3:145780600-145820400	Weak transcription	Placenta	Placenta
8	chr3:145780800-145793800	Weak transcription	Ovary	ovary
9	chr3:145780800-145793800	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr3:145780800-145819800	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr3:145781800-145831800	Weak transcription	Psoas Muscle	Psoas
12	chr3:145782800-145843200	Weak transcription	Pancreas	Pancrea
13	chr3:145784000-145789400	Weak transcription	Colon Smooth Muscle	Colon
14	chr3:145784000-145811800	Weak transcription	Rectal Smooth Muscle	rectum
15	chr3:145784600-145790400	Weak transcription	NHLF	lung
16	chr3:145784600-145848800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr3:145784800-145789600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr3:145784800-145794000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr3:145785000-145789600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr3:145785200-145806400	Weak transcription	Colonic Mucosa	Colon
21	chr3:145785200-145819400	Weak transcription	Duodenum Mucosa	Duodenum
22	chr3:145785400-145789400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr3:145785400-145790400	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr3:145785400-145791800	Strong transcription	HSMM	muscle
25	chr3:145785400-145796800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr3:145785600-145790800	Strong transcription	Muscle Satellite Cultured Cells	--
27	chr3:145785600-145790800	Weak transcription	NHDF-Ad	bronchial
28	chr3:145785600-145798600	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr3:145785800-145789400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr3:145785800-145790000	Strong transcription	Osteobl	bone
31	chr3:145786000-145790800	Strong transcription	HUVEC	blood vessel
32	chr3:145786200-145789400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr3:145786200-145789600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr3:145786200-145789800	Strong transcription	Liver	Liver
35	chr3:145786400-145791000	Genic enhancers	A549	lung
36	chr3:145786600-145792800	Strong transcription	HepG2	liver
37	chr3:145786800-145789800	Weak transcription	HSMMtube	muscle
38	chr3:145786800-145793800	Weak transcription	Stomach Smooth Muscle	stomach
39	chr3:145787000-145789400	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr3:145787000-145807200	Weak transcription	Fetal Lung	lung
41	chr3:145787200-145789800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr3:145787200-145798400	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr3:145787400-145793200	Weak transcription	Brain Hippocampus Middle	brain
44	chr3:145787400-145793800	Weak transcription	Brain Anterior Caudate	brain
45	chr3:145787600-145798200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr3:145787800-145791200	Weak transcription	Small Intestine	intestine
47	chr3:145788400-145789600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr3:145788400-145789600	Strong transcription	Fetal Intestine Large	intestine
49	chr3:145788400-145789800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr3:145788400-145790400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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