Variant report

Variant	nsv581508
Chromosome Location	chr2:40833142-40890416
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	CEBPB	chr2:40864774-40865035	IMR90	lung:	n/a	chr2:40864924-40864935
2	CEBPB	chr2:40853015-40853457	IMR90	lung:	n/a	n/a
3	CEBPB	chr2:40864914-40865021	A549	lung:	n/a	chr2:40864924-40864935
4	CTCF	chr2:40869840-40869990	BE2_C	brain:	n/a	n/a
5	CTCF	chr2:40869880-40870030	SK-N-SH_RA	brain:	n/a	chr2:40870000-40870021 chr2:40870001-40870010
6	CTCF	chr2:40835900-40836050	NHEK	skin:	n/a	n/a
7	CTCF	chr2:40869900-40870050	BE2_C	brain:	n/a	chr2:40870000-40870021 chr2:40870001-40870010
8	CTCF	chr2:40843055-40843124	Kidney_OC	kidney:	n/a	n/a
9	CTCF	chr2:40869900-40870050	HMF	breast:	n/a	chr2:40870000-40870021 chr2:40870001-40870010
10	E2F4	chr2:40881190-40881398	MCF10A-Er-Src	breast:	n/a	n/a
11	E2F4	chr2:40835780-40835952	MCF10A-Er-Src	breast:	n/a	n/a
12	EP300	chr2:40869404-40869688	SK-N-SH_RA	brain:	n/a	n/a
13	EP300	chr2:40888133-40888264	GM12878	blood:	n/a	n/a
14	EP300	chr2:40843652-40844316	SK-N-SH	brain:	n/a	n/a
15	EP300	chr2:40869459-40869676	SK-N-SH_RA	brain:	n/a	n/a
16	EP300	chr2:40853241-40853243	GM12878	blood:	n/a	n/a
17	FOS	chr2:40834167-40834274	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr2:40852959-40853404	MCF10A-Er-Src	breast:	n/a	chr2:40853169-40853180 chr2:40853215-40853227 chr2:40853217-40853225
19	FOS	chr2:40852992-40853476	MCF10A-Er-Src	breast:	n/a	chr2:40853169-40853180 chr2:40853215-40853227 chr2:40853217-40853225
20	FOS	chr2:40853018-40853306	HUVEC	blood vessel:	n/a	chr2:40853169-40853180 chr2:40853215-40853227 chr2:40853217-40853225
21	FOS	chr2:40880970-40881348	MCF10A-Er-Src	breast:	n/a	chr2:40881290-40881299
22	FOS	chr2:40880922-40881828	MCF10A-Er-Src	breast:	n/a	chr2:40881290-40881299
23	FOS	chr2:40852992-40853412	MCF10A-Er-Src	breast:	n/a	chr2:40853169-40853180 chr2:40853215-40853227 chr2:40853217-40853225
24	FOS	chr2:40880941-40881695	MCF10A-Er-Src	breast:	n/a	chr2:40881290-40881299
25	FOS	chr2:40853013-40853377	MCF10A-Er-Src	breast:	n/a	chr2:40853169-40853180 chr2:40853215-40853227 chr2:40853217-40853225
26	FOS	chr2:40880931-40881442	MCF10A-Er-Src	breast:	n/a	chr2:40881290-40881299
27	FOSL2	chr2:40880960-40881431	SK-N-SH	brain:	n/a	chr2:40881290-40881299
28	GATA2	chr2:40843913-40844188	SH-SY5Y	brain:	n/a	n/a
29	GATA3	chr2:40881833-40881852	SH-SY5Y	brain:	n/a	n/a
30	GATA3	chr2:40877872-40878261	SK-N-SH	brain:	n/a	n/a
31	GATA3	chr2:40834484-40834672	SH-SY5Y	brain:	n/a	n/a
32	GATA3	chr2:40843288-40843369	SH-SY5Y	brain:	n/a	n/a
33	GATA3	chr2:40869057-40869169	SH-SY5Y	brain:	n/a	n/a
34	GATA3	chr2:40843791-40844144	SH-SY5Y	brain:	n/a	chr2:40843893-40843902 chr2:40843892-40843902 chr2:40843893-40843900 chr2:40843893-40843900 chr2:40843886-40843907 chr2:40843893-40843900
35	GATA3	chr2:40877700-40878346	SH-SY5Y	brain:	n/a	n/a
36	GATA3	chr2:40877794-40878159	SK-N-SH	brain:	n/a	n/a
37	GATA3	chr2:40855903-40856186	SH-SY5Y	brain:	n/a	n/a
38	GATA3	chr2:40849087-40849399	SH-SY5Y	brain:	n/a	n/a
39	JUN	chr2:40864789-40864969	HepG2	liver:	n/a	chr2:40864922-40864935
40	JUN	chr2:40882850-40882970	K562	blood:	n/a	n/a
41	JUN	chr2:40862002-40862229	HepG2	liver:	n/a	chr2:40862166-40862175 chr2:40862111-40862124
42	JUND	chr2:40869275-40869388	HepG2	liver:	n/a	n/a
43	JUND	chr2:40875891-40876106	HepG2	liver:	n/a	n/a
44	JUND	chr2:40862001-40862227	HepG2	liver:	n/a	chr2:40862166-40862175
45	MAFF	chr2:40850298-40850584	HepG2	liver:	n/a	chr2:40850431-40850449
46	MAFF	chr2:40857232-40857538	HepG2	liver:	n/a	chr2:40857368-40857386
47	MAFF	chr2:40850367-40850522	K562	blood:	n/a	chr2:40850431-40850449
48	MAFK	chr2:40850300-40850592	HepG2	liver:	n/a	chr2:40850432-40850447
49	MAFK	chr2:40867749-40867797	H1-hESC	embryonic stem cell:	n/a	n/a
50	MAFK	chr2:40853083-40853339	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:40845989-40846039	HCPEpiC	choroid plexus:	n/a
2	chr2:40845989-40846039	HCM	heart:	n/a
3	chr2:40845989-40846039	HUVEC	blood vessel:	n/a
4	chr2:40845989-40846039	GM19239	blood:	n/a
5	chr2:40845989-40846039	HMEC	breast:	n/a
6	chr2:40845989-40846039	MCF10A-Er-Src	breast:	n/a
7	chr2:40845989-40846039	Hepatocyte	liver:	n/a
8	chr2:40845989-40846039	GM06990	blood:	n/a
9	chr2:40845989-40846039	MCF-7	breast:	n/a
10	chr2:40845989-40846039	AG04449	skin:	fetal
11	chr2:40845989-40846039	HPAEpiC	pulmonary alveolar:	n/a
12	chr2:40845989-40846039	PANC-1	pancreas:	n/a
13	chr2:40845989-40846039	ProgFib	skin:	n/a
14	chr2:40845989-40846039	K562	blood:	n/a
15	chr2:40845989-40846039	NHDF-neo	bronchial:	n/a
16	chr2:40845989-40846039	BJ	skin:	n/a
17	chr2:40845989-40846039	ECC-1	luminal epithelium:	n/a
18	chr2:40845989-40846039	NB4	blood:	n/a
19	chr2:40845989-40846039	BE2_C	brain:	n/a
20	chr2:40845989-40846039	HL-60	blood:	n/a
21	chr2:40845989-40846039	HEEpiC	esophagus:	n/a
22	chr2:40845989-40846039	NH-A	brain:	n/a
23	chr2:40845989-40846039	NT2-D1	testis:	n/a
24	chr2:40845989-40846039	IMR90	lung:	fetal
25	chr2:40845989-40846039	GM12892	blood:	n/a
26	chr2:40845989-40846039	SKMC	muscle:	n/a
27	chr2:40845989-40846039	HIPEpiC	eye:	n/a
28	chr2:40845989-40846039	CMK	blood:	n/a
29	chr2:40845989-40846039	H1-hESC	embryonic stem cell:	embryo
30	chr2:40845989-40846039	AG09309	skin:	n/a
31	chr2:40845989-40846039	RPTEC	kidney:	n/a
32	chr2:40845989-40846039	PFSK-1	brain:	n/a
33	chr2:40845989-40846039	AG04450	lung:	fetal
34	chr2:40845989-40846039	U87	brain:	n/a
35	chr2:40845989-40846039	GM12891	blood:	n/a
36	chr2:40845989-40846039	HAEpiC	amniotic membrane:	n/a
37	chr2:40845989-40846039	HRPEpiC	eye:	n/a
38	chr2:40845989-40846039	SAEC	small airway:	n/a
39	chr2:40845989-40846039	LNCaP	prostate:	n/a
40	chr2:40845989-40846039	SK-N-SH	brain:	n/a
41	chr2:40845989-40846039	HepG2	liver:	n/a
42	chr2:40845989-40846039	AG09319	gingival:	n/a
43	chr2:40845989-40846039	ovcar-3	ovarian:	n/a
44	chr2:40845989-40846039	HRCEpiC	kidney:	n/a
45	chr2:40845989-40846039	Caco-2	colon:	n/a
46	chr2:40845989-40846039	AG10803	skin:	n/a
47	chr2:40845989-40846039	HEK293	kidney:	embryo
48	chr2:40845989-40846039	Jurkat	blood:	n/a
49	chr2:40845989-40846039	T-47D	breast:	n/a
50	chr2:40845989-40846039	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:40868683..40869510-chr2:58548247..58548778,2	MCF-7	breast:
2	chr2:40863344..40866000-chr2:40868912..40871639,2	K562	blood:
3	chr2:40863344..40866000-chr2:40868912..40871639,2	K562	blood:
4	chr2:40869635..40872329-chr2:40880298..40882464,2	K562	blood:
5	chr2:40869635..40872329-chr2:40880298..40882464,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM178-7	chr2:40835782-40835863	NONHSAT070282
2	lnc-TMEM178-7	chr2:40835210-40835273	NONHSAT070282
3	lnc-TMEM178-7	chr2:40835782-40835863	l_1815_chr2:40835264-40838463_testes
4	lnc-TMEM178-7	chr2:40835265-40835273	l_1815_chr2:40835264-40838463_testes
5	lnc-TMEM178-7	chr2:40847860-40848096	NONHSAT070282
6	lnc-TMEM178-7	chr2:40838265-40838463	l_1815_chr2:40835264-40838463_testes

Variant related genes	Relation type
SLC8A1	TF binding region
SLC8A1	CpG island

Extended variants
information (count: 1288 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1288 , 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	rs544348308	chr2:40833607-40833608	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs369171187	chr2:40833626-40833627	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs75263099	chr2:40833634-40833635	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185643729	chr2:40833652-40833653	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7419294	chr2:40833664-40833665	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs149132163	chr2:40833707-40833708	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs569861268	chr2:40833729-40833730	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189271077	chr2:40833754-40833755	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113365802	chr2:40833756-40833757	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146451973	chr2:40833795-40833796	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550357064	chr2:40833801-40833802	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs374189666	chr2:40833866-40833867	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs12474948	chr2:40833893-40833894	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs370002079	chr2:40833898-40833899	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs112275704	chr2:40833899-40833900	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs535043272	chr2:40833906-40833907	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs181034737	chr2:40833930-40833931	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs112447715	chr2:40833959-40833960	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs374389330	chr2:40833984-40833985	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs559628315	chr2:40833994-40833995	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs571722585	chr2:40834043-40834044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539227293	chr2:40834055-40834056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs557163661	chr2:40834062-40834063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs74699869	chr2:40834076-40834077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186530643	chr2:40834077-40834078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs553631048	chr2:40834146-40834147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114444099	chr2:40834164-40834165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs116200878	chr2:40834165-40834166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs74653154	chr2:40834167-40834168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs77143225	chr2:40834227-40834228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs78571164	chr2:40834242-40834243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs111311922	chr2:40834249-40834250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376348179	chr2:40834281-40834282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs372095042	chr2:40834286-40834287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs373801304	chr2:40834317-40834318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs112121704	chr2:40834388-40834389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570416656	chr2:40834429-40834430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545899155	chr2:40834439-40834440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544437520	chr2:40834534-40834535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557533417	chr2:40834544-40834545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs562241744	chr2:40834616-40834617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529767690	chr2:40834631-40834632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112924892	chr2:40834699-40834700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs559687001	chr2:40834775-40834776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs189697870	chr2:40834788-40834789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573228313	chr2:40835237-40835238	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs534207181	chr2:40835256-40835257	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs368193031	chr2:40835261-40835262	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs201863823	chr2:40835805-40835806	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs13420501	chr2:40835808-40835809	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40833600-40834000	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
2	chr2:40833600-40834800	Enhancers	HMEC	breast
3	chr2:40833800-40834200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr2:40833800-40834200	Enhancers	NH-A	brain
5	chr2:40833800-40834600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr2:40833800-40834600	Enhancers	Osteobl	bone
7	chr2:40836200-40836600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr2:40843800-40844400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr2:40844400-40853000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr2:40852200-40853800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr2:40852400-40853200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr2:40852400-40853200	Enhancers	NHDF-Ad	bronchial
13	chr2:40852400-40854000	Enhancers	NHEK	skin
14	chr2:40852600-40853400	Enhancers	Muscle Satellite Cultured Cells	--
15	chr2:40852600-40853400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr2:40852800-40853600	Enhancers	Osteobl	bone
17	chr2:40853000-40854200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr2:40856800-40857200	Enhancers	Colon Smooth Muscle	Colon
19	chr2:40864200-40864400	Enhancers	Colon Smooth Muscle	Colon
20	chr2:40864400-40869200	Weak transcription	Colon Smooth Muscle	Colon
21	chr2:40866200-40867000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr2:40866200-40867400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr2:40866400-40867000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr2:40866600-40866800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr2:40866800-40867000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:40866800-40869000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr2:40867800-40869400	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr2:40868600-40869200	Enhancers	HUVEC	blood vessel
29	chr2:40869000-40871400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr2:40869200-40869600	Enhancers	Rectal Smooth Muscle	rectum
31	chr2:40869200-40870400	Enhancers	Colon Smooth Muscle	Colon
32	chr2:40871400-40875200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr2:40875200-40877000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr2:40876000-40876200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr2:40876400-40878200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr2:40877000-40878000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr2:40878000-40878200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr2:40878000-40878600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr2:40878200-40878600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr2:40878200-40878600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr2:40878600-40879600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr2:40878600-40879800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr2:40879800-40880000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr2:40879800-40880400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr2:40880000-40882200	Enhancers	NHEK	skin
46	chr2:40880400-40880800	Enhancers	HMEC	breast
47	chr2:40880400-40881200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr2:40880400-40882400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr2:40880800-40881800	Weak transcription	HMEC	breast
50	chr2:40880800-40883000	Enhancers	Muscle Satellite Cultured Cells	--

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