Variant report

Variant	esv3333990
Chromosome Location	chr3:145950303-145982133
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:145959778-145959950	K562	blood:	n/a	n/a
2	BACH1	chr3:145968459-145969085	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr3:145968815-145968925	K562	blood:	n/a	n/a
4	CCNT2	chr3:145968563-145969088	K562	blood:	n/a	n/a
5	CEBPB	chr3:145967646-145968183	A549	lung:	n/a	chr3:145968037-145968048 chr3:145968037-145968050 chr3:145968037-145968048
6	CEBPB	chr3:145967604-145968179	Hela-S3	cervix:	n/a	chr3:145968037-145968048 chr3:145968037-145968050 chr3:145968037-145968048
7	CEBPB	chr3:145968381-145969227	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr3:145968610-145968627	K562	blood:	n/a	n/a
9	CEBPB	chr3:145967647-145967801	K562	blood:	n/a	n/a
10	CEBPB	chr3:145967627-145968119	IMR90	lung:	n/a	chr3:145968037-145968048 chr3:145968037-145968050 chr3:145968037-145968048
11	CEBPB	chr3:145965734-145966053	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr3:145975222-145975278	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr3:145968318-145969145	Hela-S3	cervix:	n/a	n/a
14	CREB1	chr3:145968387-145969169	A549	lung:	n/a	n/a
15	CTBP2	chr3:145968207-145969151	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr3:145968681-145968685	MCF-7	breast:	n/a	n/a
17	CTCF	chr3:145968553-145968569	ProgFib	skin:	n/a	n/a
18	CTCF	chr3:145968520-145968670	SAEC	small airway:	n/a	n/a
19	CTCF	chr3:145968620-145968770	HBMEC	blood vessel:	n/a	n/a
20	CTCF	chr3:145968528-145968686	MCF-7	breast:	n/a	n/a
21	CTCF	chr3:145968530-145968678	MCF-7	breast:	n/a	n/a
22	E2F1	chr3:145968404-145969145	Hela-S3	cervix:	n/a	n/a
23	E2F4	chr3:145968380-145969194	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F6	chr3:145968313-145969008	H1-hESC	embryonic stem cell:	n/a	n/a
25	E2F6	chr3:145968385-145968815	H1-hESC	embryonic stem cell:	n/a	n/a
26	E2F6	chr3:145968442-145968748	K562	blood:	n/a	n/a
27	E2F6	chr3:145968584-145968762	K562	blood:	n/a	n/a
28	E2F6	chr3:145974628-145975362	H1-hESC	embryonic stem cell:	n/a	n/a
29	ELF1	chr3:145968894-145969096	K562	blood:	n/a	n/a
30	ELF1	chr3:145968886-145969158	K562	blood:	n/a	n/a
31	ELK1	chr3:145968358-145969012	Hela-S3	cervix:	n/a	n/a
32	EP300	chr3:145959774-145959950	K562	blood:	n/a	n/a
33	FOS	chr3:145972883-145973087	MCF10A-Er-Src	breast:	n/a	chr3:145972951-145972962 chr3:145972952-145972961 chr3:145972953-145972961 chr3:145972954-145972961
34	FOS	chr3:145972799-145973205	HUVEC	blood vessel:	n/a	chr3:145972951-145972962 chr3:145972952-145972961 chr3:145972953-145972961 chr3:145972954-145972961
35	FOS	chr3:145972787-145973095	MCF10A-Er-Src	breast:	n/a	chr3:145972951-145972962 chr3:145972952-145972961 chr3:145972953-145972961 chr3:145972954-145972961
36	FOS	chr3:145972775-145973084	MCF10A-Er-Src	breast:	n/a	chr3:145972951-145972962 chr3:145972952-145972961 chr3:145972953-145972961 chr3:145972954-145972961
37	FOS	chr3:145972784-145973096	MCF10A-Er-Src	breast:	n/a	chr3:145972951-145972962 chr3:145972952-145972961 chr3:145972953-145972961 chr3:145972954-145972961
38	FOXA1	chr3:145966359-145966655	HepG2	liver:	n/a	n/a
39	FOXP2	chr3:145959558-145960036	SK-N-MC	brain:	n/a	n/a
40	FOXP2	chr3:145968366-145968709	SK-N-MC	brain:	n/a	n/a
41	GATA1	chr3:145967865-145969597	PBDE	blood:	n/a	chr3:145968166-145968173 chr3:145968166-145968176 chr3:145968819-145968829 chr3:145968163-145968175
42	GATA2	chr3:145967908-145968768	HUVEC	blood vessel:	n/a	chr3:145968166-145968173 chr3:145968166-145968176 chr3:145968163-145968175
43	GATA3	chr3:145982043-145982247	MCF-7	breast:	n/a	chr3:145982128-145982135 chr3:145982126-145982136 chr3:145982123-145982139 chr3:145982128-145982135 chr3:145982121-145982142 chr3:145982128-145982138 chr3:145982128-145982135
44	GATA3	chr3:145982094-145982536	MCF-7	breast:	n/a	chr3:145982128-145982135 chr3:145982126-145982136 chr3:145982123-145982139 chr3:145982128-145982135 chr3:145982121-145982142 chr3:145982128-145982138 chr3:145982128-145982135
45	GATA3	chr3:145961433-145961633	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr3:145968214-145968924	MCF-7	breast:	n/a	chr3:145968819-145968829
47	GTF2F1	chr3:145968268-145969188	Hela-S3	cervix:	n/a	n/a
48	GTF2F1	chr3:145967772-145967870	H1-hESC	embryonic stem cell:	n/a	n/a
49	HA-E2F1	chr3:145968209-145969275	MCF-7	breast:	n/a	n/a
50	HA-E2F1	chr3:145968365-145969182	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:145968722-145968772	HCPEpiC	choroid plexus:	n/a
2	chr3:145969579-145969629	SKMC	muscle:	n/a
3	chr3:145968242-145968292	AG10803	skin:	n/a
4	chr3:145969625-145969675	GM12891	blood:	n/a
5	chr3:145969625-145969675	HRPEpiC	eye:	n/a
6	chr3:145969007-145969057	MCF10A-Er-Src	breast:	n/a
7	chr3:145968696-145968746	SKMC	muscle:	n/a
8	chr3:145968389-145968439	HL-60	blood:	n/a
9	chr3:145968620-145968670	HEK293	kidney:	embryo
10	chr3:145969718-145969768	HL-60	blood:	n/a
11	chr3:145969718-145969768	SK-N-SH	brain:	n/a
12	chr3:145968696-145968746	CMK	blood:	n/a
13	chr3:145968692-145968742	AG04449	skin:	fetal
14	chr3:145968389-145968439	HNPCEpiC	eye:	n/a
15	chr3:145968389-145968439	LNCaP	prostate:	n/a
16	chr3:145968700-145968750	AG04450	lung:	fetal
17	chr3:145969007-145969057	HUVEC	blood vessel:	n/a
18	chr3:145969007-145969057	NT2-D1	testis:	n/a
19	chr3:145968620-145968670	HPAEpiC	pulmonary alveolar:	n/a
20	chr3:145968696-145968746	BJ	skin:	n/a
21	chr3:145969625-145969675	ECC-1	luminal epithelium:	n/a
22	chr3:145968389-145968439	U87	brain:	n/a
23	chr3:145968389-145968439	CMK	blood:	n/a
24	chr3:145968389-145968439	HRCEpiC	kidney:	n/a
25	chr3:145969579-145969629	MCF-7	breast:	n/a
26	chr3:145970385-145970435	Hela-S3	cervix:	n/a
27	chr3:145968242-145968292	GM12892	blood:	n/a
28	chr3:145969625-145969675	HRE	kidney:	n/a
29	chr3:145969718-145969768	AG09309	skin:	n/a
30	chr3:145969007-145969057	ProgFib	skin:	n/a
31	chr3:145968389-145968439	A549	lung:	n/a
32	chr3:145968696-145968746	K562	blood:	n/a
33	chr3:145970385-145970435	LNCaP	prostate:	n/a
34	chr3:145968692-145968742	MCF10A-Er-Src	breast:	n/a
35	chr3:145968700-145968750	LNCaP	prostate:	n/a
36	chr3:145969579-145969629	GM12878	blood:	n/a
37	chr3:145969625-145969675	SK-N-SH	brain:	n/a
38	chr3:145968620-145968670	PANC-1	pancreas:	n/a
39	chr3:145969625-145969675	MCF-7	breast:	n/a
40	chr3:145968722-145968772	Hela-S3	cervix:	n/a
41	chr3:145968700-145968750	GM12891	blood:	n/a
42	chr3:145968700-145968750	ovcar-3	ovarian:	n/a
43	chr3:145969579-145969629	GM06990	blood:	n/a
44	chr3:145968620-145968670	AG09319	gingival:	n/a
45	chr3:145968692-145968742	AoSMC	blood vessel:	n/a
46	chr3:145968700-145968750	AG04449	skin:	fetal
47	chr3:145968242-145968292	MCF-7	breast:	n/a
48	chr3:145968620-145968670	MCF-7	breast:	n/a
49	chr3:145968726-145968776	GM12878	blood:	n/a
50	chr3:145968389-145968439	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:145979759..145981408-chr3:145991775..145993643,2	K562	blood:
2	chr3:145961600..145965107-chr3:145968575..145970473,3	K562	blood:
3	chr3:145956753..145960171-chr3:145962648..145965540,3	K562	blood:
4	chr3:145878599..145881384-chr3:145968449..145970595,2	MCF-7	breast:
5	chr3:145956753..145960171-chr3:145962648..145965540,3	K562	blood:

Variant related genes	Relation type
PLSCR4	TF binding region
PLSCR4	CpG island
ENSG00000152952	chromatin interactions
ENSG00000114698	chromatin interactions

Extended variants
information (count: 1296 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1296 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7614839	chr3:145950324-145950325	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs116487047	chr3:145950347-145950348	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs567888122	chr3:145950389-145950390	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs181622995	chr3:145950421-145950422	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs372984335	chr3:145950427-145950428	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs111851904	chr3:145950441-145950442	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs116303456	chr3:145950478-145950479	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs376447405	chr3:145950484-145950485	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs386666793	chr3:145950492-145950493	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs6440422	chr3:145950494-145950495	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs575159379	chr3:145950537-145950538	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs545409757	chr3:145950610-145950611	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs542532517	chr3:145950629-145950630	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs554319130	chr3:145950649-145950650	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs188518675	chr3:145950654-145950655	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs181362034	chr3:145950657-145950658	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs76165156	chr3:145950689-145950690	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs77157773	chr3:145950747-145950748	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs142019179	chr3:145950765-145950766	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs543827844	chr3:145950817-145950818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565912623	chr3:145950844-145950845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562489895	chr3:145950862-145950863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11915448	chr3:145950870-145950871	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs549733242	chr3:145950896-145950897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76696195	chr3:145950907-145950908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs79827091	chr3:145950911-145950912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547178635	chr3:145950951-145950952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185488032	chr3:145951006-145951007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539137006	chr3:145951064-145951065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547896483	chr3:145951071-145951072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550530348	chr3:145951079-145951080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs73865368	chr3:145951095-145951096	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs114080515	chr3:145951197-145951198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs116681522	chr3:145951218-145951219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190629350	chr3:145951225-145951226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs116386523	chr3:145951246-145951247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375785665	chr3:145951252-145951253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558724961	chr3:145951274-145951275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533332317	chr3:145951312-145951313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2055977	chr3:145951329-145951330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1512890	chr3:145951330-145951331	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs373319713	chr3:145951389-145951390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs76761605	chr3:145951454-145951455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76918098	chr3:145951503-145951504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570318872	chr3:145951505-145951506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574526077	chr3:145951516-145951517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543343067	chr3:145951522-145951523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149584864	chr3:145951544-145951545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182914686	chr3:145951571-145951572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528793691	chr3:145951684-145951685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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

Chromatin state (count:524 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:145925400-145952800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr3:145925600-145950800	Weak transcription	Fetal Kidney	kidney
3	chr3:145934600-145952200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr3:145940600-145953000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr3:145940600-145953600	Weak transcription	NHDF-Ad	bronchial
6	chr3:145941600-145952200	Weak transcription	Left Ventricle	heart
7	chr3:145941600-145952600	Weak transcription	Fetal Intestine Small	intestine
8	chr3:145941600-145954000	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr3:145942200-145953400	Weak transcription	HUVEC	blood vessel
10	chr3:145945200-145959800	Weak transcription	Ovary	ovary
11	chr3:145946000-145952400	Weak transcription	Fetal Stomach	stomach
12	chr3:145946200-145952600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr3:145946400-145953000	Weak transcription	Stomach Smooth Muscle	stomach
14	chr3:145947200-145953000	Weak transcription	Adipose Nuclei	Adipose
15	chr3:145947400-145953200	Weak transcription	Fetal Intestine Large	intestine
16	chr3:145948000-145967800	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr3:145948600-145952000	Weak transcription	Aorta	Aorta
18	chr3:145949400-145950800	ZNF genes & repeats	Fetal Lung	lung
19	chr3:145950200-145950600	Enhancers	Liver	Liver
20	chr3:145950600-145951600	Weak transcription	Liver	Liver
21	chr3:145950800-145953000	Weak transcription	Fetal Lung	lung
22	chr3:145951000-145953000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr3:145951600-145952200	Enhancers	Liver	Liver
24	chr3:145952000-145952400	Enhancers	Aorta	Aorta
25	chr3:145952200-145952400	ZNF genes & repeats	Left Ventricle	heart
26	chr3:145952200-145953000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr3:145952400-145952600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
28	chr3:145952400-145953000	Weak transcription	Aorta	Aorta
29	chr3:145952400-145953200	ZNF genes & repeats	Fetal Stomach	stomach
30	chr3:145952600-145954400	ZNF genes & repeats	Fetal Intestine Small	intestine
31	chr3:145952600-145955000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr3:145952600-145956200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr3:145952800-145953200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
34	chr3:145952800-145957200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr3:145953000-145953200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr3:145953000-145953200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr3:145953000-145953200	ZNF genes & repeats	Aorta	Aorta
38	chr3:145953000-145954000	ZNF genes & repeats	Adipose Nuclei	Adipose
39	chr3:145953000-145954200	ZNF genes & repeats	Stomach Smooth Muscle	stomach
40	chr3:145953000-145955200	ZNF genes & repeats	Fetal Lung	lung
41	chr3:145953200-145954000	ZNF genes & repeats	Fetal Intestine Large	intestine
42	chr3:145953200-145954200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr3:145953200-145968000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr3:145953400-145954800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
45	chr3:145953600-145954000	ZNF genes & repeats	NHDF-Ad	bronchial
46	chr3:145954000-145954400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr3:145954000-145955400	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
48	chr3:145954400-145954600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr3:145954600-145955000	ZNF genes & repeats	NHDF-Ad	bronchial
50	chr3:145954600-145962600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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