Variant report

Variant	nsv817840
Chromosome Location	chr2:47044218-47070827
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:129)
CpG islands
(count:490)
Chromatin interactive
region (count:13)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:129 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:47068922-47069122	K562	blood:	n/a	n/a
2	BACH1	chr2:47059112-47059135	K562	blood:	n/a	n/a
3	BCL3	chr2:47054377-47054680	GM12878	blood:	n/a	n/a
4	BCL3	chr2:47054381-47054719	GM12878	blood:	n/a	n/a
5	CEBPB	chr2:47058538-47058911	K562	blood:	n/a	n/a
6	CEBPB	chr2:47058215-47058840	A549	lung:	n/a	chr2:47058372-47058383
7	CEBPB	chr2:47053298-47053673	IMR90	lung:	n/a	n/a
8	CEBPB	chr2:47058192-47058976	Hela-S3	cervix:	n/a	chr2:47058372-47058383
9	CEBPB	chr2:47058234-47058909	HepG2	liver:	n/a	chr2:47058372-47058383
10	CEBPB	chr2:47058195-47058978	IMR90	lung:	n/a	chr2:47058372-47058383
11	CEBPB	chr2:47058194-47058986	A549	lung:	n/a	chr2:47058372-47058383
12	CTCF	chr2:47045920-47046070	HepG2	liver:	n/a	n/a
13	CTCF	chr2:47056720-47056870	HRPEpiC	eye:	n/a	chr2:47056819-47056832
14	CTCF	chr2:47060180-47060330	HMF	breast:	n/a	n/a
15	CTCF	chr2:47060220-47060370	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr2:47067380-47067530	GM12866	blood:	n/a	n/a
17	CTCF	chr2:47056720-47056870	HepG2	liver:	n/a	chr2:47056819-47056832
18	CTCF	chr2:47060280-47060430	HepG2	liver:	n/a	n/a
19	CTCF	chr2:47060260-47060410	HMF	breast:	n/a	n/a
20	CTCF	chr2:47058440-47058590	AG10803	skin:	n/a	n/a
21	CTCF	chr2:47063540-47063690	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr2:47053380-47053530	HBMEC	blood vessel:	n/a	n/a
23	EP300	chr2:47063284-47064041	SK-N-SH	brain:	n/a	n/a
24	EP300	chr2:47063381-47063854	SK-N-SH_RA	brain:	n/a	n/a
25	EP300	chr2:47058268-47058816	Hela-S3	cervix:	n/a	n/a
26	EP300	chr2:47060160-47060538	SK-N-SH_RA	brain:	n/a	n/a
27	EP300	chr2:47060143-47060513	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr2:47063352-47063877	SK-N-SH_RA	brain:	n/a	n/a
29	FOS	chr2:47053482-47053528	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr2:47054840-47054925	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr2:47054759-47055063	HUVEC	blood vessel:	n/a	n/a
32	FOS	chr2:47064003-47064008	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr2:47054792-47055026	MCF10A-Er-Src	breast:	n/a	n/a
34	GATA3	chr2:47061252-47061261	SH-SY5Y	brain:	n/a	n/a
35	HDAC2	chr2:47056242-47056537	HepG2	liver:	n/a	n/a
36	HMGN3	chr2:47066516-47066622	K562	blood:	n/a	n/a
37	IRF3	chr2:47060264-47060281	GM12878	blood:	n/a	n/a
38	JUN	chr2:47059945-47060058	K562	blood:	n/a	n/a
39	MAFF	chr2:47058697-47058910	HepG2	liver:	n/a	chr2:47058758-47058776
40	MAFF	chr2:47056476-47056601	HepG2	liver:	n/a	chr2:47056535-47056553
41	MAFF	chr2:47060699-47060866	HepG2	liver:	n/a	chr2:47060765-47060783
42	MAFK	chr2:47060686-47060804	Hela-S3	cervix:	n/a	n/a
43	MAFK	chr2:47056450-47056583	HepG2	liver:	n/a	chr2:47056537-47056553 chr2:47056538-47056549
44	MAFK	chr2:47058625-47058848	HepG2	liver:	n/a	n/a
45	MAFK	chr2:47058295-47058963	Hela-S3	cervix:	n/a	n/a
46	MAFK	chr2:47060381-47060855	HepG2	liver:	n/a	n/a
47	MAFK	chr2:47060604-47060932	HepG2	liver:	n/a	n/a
48	MAFK	chr2:47058414-47058940	IMR90	lung:	n/a	n/a
49	MAFK	chr2:47060738-47060970	IMR90	lung:	n/a	n/a
50	MAX	chr2:47052424-47052485	NB4	blood:	n/a	chr2:47052461-47052471

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:47058307-47058357	GM06990	blood:	n/a
2	chr2:47053870-47053920	HEEpiC	esophagus:	n/a
3	chr2:47058307-47058357	GM06990	blood:	n/a
4	chr2:47053870-47053920	HEEpiC	esophagus:	n/a
5	chr2:47053842-47053892	IMR90	lung:	fetal
6	chr2:47055138-47055188	NHDF-neo	bronchial:	n/a
7	chr2:47053870-47053920	SK-N-SH	brain:	n/a
8	chr2:47053842-47053892	SK-N-SH_RA	brain:	n/a
9	chr2:47054833-47054883	HRPEpiC	eye:	n/a
10	chr2:47054833-47054883	HCPEpiC	choroid plexus:	n/a
11	chr2:47053842-47053892	LNCaP	prostate:	n/a
12	chr2:47063626-47063676	NHBE	bronchial:	n/a
13	chr2:47055138-47055188	ProgFib	skin:	n/a
14	chr2:47058307-47058357	HNPCEpiC	eye:	n/a
15	chr2:47054833-47054883	BE2_C	brain:	n/a
16	chr2:47058307-47058357	HCF	heart:	n/a
17	chr2:47063626-47063676	AG09309	skin:	n/a
18	chr2:47058307-47058357	HEEpiC	esophagus:	n/a
19	chr2:47054833-47054883	SK-N-SH	brain:	n/a
20	chr2:47055138-47055188	MCF10A-Er-Src	breast:	n/a
21	chr2:47054963-47055013	AG04449	skin:	fetal
22	chr2:47053771-47053821	SAEC	small airway:	n/a
23	chr2:47054833-47054883	ECC-1	luminal epithelium:	n/a
24	chr2:47053842-47053892	HRE	kidney:	n/a
25	chr2:47054833-47054883	ProgFib	skin:	n/a
26	chr2:47054963-47055013	AG04450	lung:	fetal
27	chr2:47063626-47063676	HCPEpiC	choroid plexus:	n/a
28	chr2:47055138-47055188	GM12891	blood:	n/a
29	chr2:47055138-47055188	U87	brain:	n/a
30	chr2:47058307-47058357	RPTEC	kidney:	n/a
31	chr2:47058307-47058357	GM19239	blood:	n/a
32	chr2:47055138-47055188	GM12878	blood:	n/a
33	chr2:47053870-47053920	ovcar-3	ovarian:	n/a
34	chr2:47063626-47063676	HRPEpiC	eye:	n/a
35	chr2:47063626-47063676	RPTEC	kidney:	n/a
36	chr2:47054963-47055013	HEK293	kidney:	embryo
37	chr2:47063626-47063676	NH-A	brain:	n/a
38	chr2:47063626-47063676	BE2_C	brain:	n/a
39	chr2:47053842-47053892	PANC-1	pancreas:	n/a
40	chr2:47053771-47053821	HepG2	liver:	n/a
41	chr2:47054963-47055013	SKMC	muscle:	n/a
42	chr2:47063626-47063676	A549	lung:	n/a
43	chr2:47054963-47055013	HepG2	liver:	n/a
44	chr2:47054963-47055013	NHDF-neo	bronchial:	n/a
45	chr2:47054833-47054883	RPTEC	kidney:	n/a
46	chr2:47053870-47053920	PANC-1	pancreas:	n/a
47	chr2:47058307-47058357	HUVEC	blood vessel:	n/a
48	chr2:47063626-47063676	ovcar-3	ovarian:	n/a
49	chr2:47053870-47053920	AG09319	gingival:	n/a
50	chr2:47063626-47063676	AG10803	skin:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:47060025..47062821-chr2:47071667..47074428,2	MCF-7	breast:
2	chr2:47057725..47059943-chr2:47060673..47063152,2	MCF-7	breast:
3	chr2:47054203..47056588-chr2:47056736..47058616,2	K562	blood:
4	chr2:47050047..47052798-chr2:47110089..47111890,2	MCF-7	breast:
5	chr2:47051846..47053973-chr2:47059703..47062442,2	MCF-7	breast:
6	chr2:47044554..47046907-chr2:47075215..47076971,2	K562	blood:
7	chr2:47057725..47059943-chr2:47060673..47063152,2	MCF-7	breast:
8	chr2:47051846..47053973-chr2:47059703..47062442,2	MCF-7	breast:
9	chr2:47068428..47070813-chr2:47109229..47111715,2	K562	blood:
10	chr2:47038370..47041063-chr2:47049130..47051492,2	K562	blood:
11	chr2:47052966..47054812-chr2:47054856..47057996,3	MCF-7	breast:
12	chr2:47066380..47069019-chr2:47071701..47073820,2	K562	blood:
13	chr2:47061029..47062708-chr2:47100543..47102533,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SOCS5-2	chr2:47044387-47044452	XLOC_001459
2	lnc-SOCS5-2	chr2:47045319-47045370	NR_034099
3	lnc-SOCS5-2	chr2:47045319-47045370	XLOC_001459
4	lnc-SOCS5-2	chr2:47049240-47049799	NR_034099
5	lnc-SOCS5-2	chr2:47044387-47044572	NR_034099
6	lnc-SOCS5-2	chr2:47045319-47046597	NONHSAT070528
7	lnc-AC016722.1.1-1	chr2:47055003-47055223	XLOC_001458
8	lnc-SOCS5-2	chr2:47044387-47044572	XLOC_001459
9	lnc-AC016722.1.1-1	chr2:47055003-47055223	NONHSAT070529
10	lnc-SOCS5-2	chr2:47045319-47045370	XLOC_001459
11	lnc-SOCS5-2	chr2:47049240-47050498	XLOC_001459
12	lnc-SOCS5-2	chr2:47049240-47049798	XLOC_001459
13	lnc-SOCS5-2	chr2:47044509-47044572	NONHSAT070528

No data

Variant related genes	Relation type
LINC01119	TF binding region
LINC01119	CpG island
ENSG00000239332	chromatin interactions
SRSF9	miRNA target sites

Extended variants
information (count: 1254 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1254 , 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	rs2289929	chr2:47044218-47044219	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183861198	chr2:47044224-47044225	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs35601954	chr2:47044234-47044235	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs549454223	chr2:47044244-47044245	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs561253345	chr2:47044261-47044262	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs531918913	chr2:47044262-47044263	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs140474407	chr2:47044263-47044264	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs2289930	chr2:47044277-47044278	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs538898424	chr2:47044283-47044284	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs547693864	chr2:47044297-47044298	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs566453096	chr2:47044315-47044316	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs533596748	chr2:47044316-47044317	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs555416021	chr2:47044321-47044322	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs115839070	chr2:47044354-47044355	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs537953500	chr2:47044365-47044366	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs11682999	chr2:47044381-47044382	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs186267924	chr2:47044386-47044387	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs370012546	chr2:47044421-47044422	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
19	rs149454941	chr2:47044443-47044444	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
20	rs577923169	chr2:47044444-47044445	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
21	rs545315155	chr2:47044472-47044473	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
22	rs75614528	chr2:47044481-47044482	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
23	rs572383704	chr2:47044514-47044515	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
24	rs138141127	chr2:47044517-47044518	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
25	rs561350899	chr2:47044525-47044526	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
26	rs577524145	chr2:47044558-47044559	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
27	rs79892725	chr2:47044591-47044592	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs117837399	chr2:47044596-47044597	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs565094989	chr2:47044597-47044598	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs545003914	chr2:47044606-47044607	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs532608103	chr2:47044613-47044614	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs548065539	chr2:47044625-47044626	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs566269090	chr2:47044654-47044655	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs190593334	chr2:47044655-47044656	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs548666096	chr2:47044670-47044671	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs567274248	chr2:47044683-47044684	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs182802169	chr2:47044684-47044685	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs556336841	chr2:47044685-47044686	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs146110667	chr2:47044697-47044698	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs564830265	chr2:47044712-47044713	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs538867708	chr2:47044778-47044779	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs187086274	chr2:47044813-47044814	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs554019130	chr2:47044814-47044815	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs72804460	chr2:47044816-47044817	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs542932110	chr2:47044829-47044830	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs554619043	chr2:47044844-47044845	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs576036556	chr2:47044890-47044891	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs138897271	chr2:47044907-47044908	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs540655050	chr2:47044916-47044917	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs565083371	chr2:47044958-47044959	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
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
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Myelofibrosis	22110671	CNVD
Hypotonia	17579669	CNVD
Hypotonia-Cystinuria syndrome	16385448	CNVD
Glioblastoma multiforme	17002787	CNVD
Cystinuria	17625506	CNVD
Breast cancer	16272173	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:406 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:47031400-47052000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:47038600-47046400	Enhancers	Lung	lung
3	chr2:47038600-47046400	Enhancers	Right Atrium	heart
4	chr2:47038800-47046200	Enhancers	Right Ventricle	heart
5	chr2:47039800-47053800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr2:47040400-47045800	Weak transcription	HMEC	breast
7	chr2:47040600-47044800	Weak transcription	Brain Hippocampus Middle	brain
8	chr2:47040600-47045000	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr2:47040600-47045200	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr2:47040600-47045200	Weak transcription	HSMMtube	muscle
11	chr2:47042000-47044600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr2:47042200-47045000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr2:47042400-47044400	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr2:47042400-47044600	Weak transcription	Ovary	ovary
15	chr2:47042400-47044600	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr2:47042400-47045000	Weak transcription	Fetal Muscle Leg	muscle
17	chr2:47042400-47047000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr2:47042400-47048800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr2:47042600-47044600	Weak transcription	Rectal Smooth Muscle	rectum
20	chr2:47042600-47045000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr2:47042600-47045000	Weak transcription	NHDF-Ad	bronchial
22	chr2:47042800-47044400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr2:47042800-47044600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr2:47042800-47053400	Weak transcription	Fetal Lung	lung
25	chr2:47043400-47045000	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr2:47043800-47044600	Flanking Active TSS	Placenta	Placenta
27	chr2:47043800-47045000	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr2:47043800-47046400	Enhancers	Fetal Heart	heart
29	chr2:47043800-47046400	Enhancers	Left Ventricle	heart
30	chr2:47044000-47044400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr2:47044000-47044400	Enhancers	Stomach Smooth Muscle	stomach
32	chr2:47044000-47044400	Active TSS	Spleen	Spleen
33	chr2:47044000-47045000	Enhancers	Esophagus	oesophagus
34	chr2:47044000-47046000	Enhancers	Colon Smooth Muscle	Colon
35	chr2:47044000-47046200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr2:47044000-47046200	Enhancers	Psoas Muscle	Psoas
37	chr2:47044200-47044400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr2:47044200-47044400	Enhancers	Brain Cingulate Gyrus	brain
39	chr2:47044200-47044400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr2:47044200-47044600	Weak transcription	Aorta	Aorta
41	chr2:47044200-47044600	Weak transcription	Brain Anterior Caudate	brain
42	chr2:47044200-47046200	Enhancers	Adipose Nuclei	Adipose
43	chr2:47044400-47045200	Enhancers	Spleen	Spleen
44	chr2:47044400-47045400	Flanking Active TSS	Stomach Smooth Muscle	stomach
45	chr2:47044400-47045800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr2:47044400-47045800	Enhancers	Fetal Muscle Trunk	muscle
47	chr2:47044400-47046000	Enhancers	Duodenum Smooth Muscle	Duodenum
48	chr2:47044400-47046200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr2:47044600-47044800	Active TSS	Placenta	Placenta
50	chr2:47044600-47046000	Enhancers	Aorta	Aorta

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