Variant report

Variant	nsv581746
Chromosome Location	chr2:46699145-46719922
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:369)
CpG islands
(count:732)
Chromatin interactive
region (count:20)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:46708723-46709083	K562	blood:	n/a	n/a
2	ATF1	chr2:46708665-46709104	K562	blood:	n/a	n/a
3	ATF2	chr2:46717670-46718108	GM12878	blood:	n/a	n/a
4	ATF3	chr2:46714867-46715087	K562	blood:	n/a	n/a
5	BHLHE40	chr2:46709062-46710009	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:46709622-46710013	HepG2	liver:	n/a	n/a
7	CBX3	chr2:46704602-46705028	K562	blood:	n/a	n/a
8	CEBPB	chr2:46708603-46709107	IMR90	lung:	n/a	n/a
9	CEBPB	chr2:46708640-46709211	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr2:46715203-46715515	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr2:46719420-46719542	K562	blood:	n/a	chr2:46719482-46719493
12	CEBPB	chr2:46698877-46699146	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:46719385-46719598	HepG2	liver:	n/a	chr2:46719482-46719493
14	CEBPB	chr2:46719420-46719560	IMR90	lung:	n/a	chr2:46719482-46719493
15	CHD2	chr2:46715159-46715485	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr2:46717740-46717940	K562	blood:	n/a	n/a
17	CTCF	chr2:46718120-46718270	GM12865	blood:	n/a	n/a
18	CTCF	chr2:46715620-46715770	HMF	breast:	n/a	n/a
19	CTCF	chr2:46717760-46717910	GM12869	blood:	n/a	n/a
20	CTCF	chr2:46715660-46715810	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr2:46715620-46715770	GM12878	blood:	n/a	n/a
22	CTCF	chr2:46717815-46717857	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr2:46715712-46715789	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr2:46715688-46715775	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr2:46715680-46715830	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr2:46715560-46715710	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr2:46715666-46715736	K562	blood:	n/a	n/a
28	CTCF	chr2:46713734-46714043	GM12878	blood:	n/a	n/a
29	CTCF	chr2:46715580-46715730	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr2:46715580-46715730	HVMF	connective:	n/a	n/a
31	CTCF	chr2:46715780-46715930	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr2:46715620-46715770	GM12873	blood:	n/a	n/a
33	CTCF	chr2:46718120-46718270	HEK293	kidney:	n/a	n/a
34	CTCF	chr2:46715440-46715590	NHLF	lung:	n/a	n/a
35	CTCF	chr2:46718120-46718270	HPF	lung:	n/a	n/a
36	CTCF	chr2:46715620-46715770	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr2:46717744-46717936	GM12892	blood:	n/a	n/a
38	CTCF	chr2:46718000-46718150	NHLF	lung:	n/a	n/a
39	CTCF	chr2:46713829-46713906	K562	blood:	n/a	n/a
40	CTCF	chr2:46718140-46718290	GM12873	blood:	n/a	n/a
41	CTCF	chr2:46718200-46718350	GM12868	blood:	n/a	n/a
42	CTCF	chr2:46715100-46715250	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr2:46715680-46715830	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr2:46717760-46717910	GM12878	blood:	n/a	n/a
45	CTCF	chr2:46718100-46718250	GM12872	blood:	n/a	n/a
46	CTCF	chr2:46717720-46717870	GM12866	blood:	n/a	n/a
47	CTCF	chr2:46715520-46715670	HRE	kidney:	n/a	n/a
48	CTCF	chr2:46715600-46715750	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr2:46718120-46718270	GM12872	blood:	n/a	n/a
50	CTCF	chr2:46718140-46718290	SK-N-SH_RA	brain:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:46705989-46706039	SKMC	muscle:	n/a
2	chr2:46706709-46706759	NHBE	bronchial:	n/a
3	chr2:46717839-46717889	AG04450	lung:	fetal
4	chr2:46715231-46715281	AG04450	lung:	fetal
5	chr2:46707678-46707728	GM06990	blood:	n/a
6	chr2:46706139-46706189	Jurkat	blood:	n/a
7	chr2:46707626-46707676	HAEpiC	amniotic membrane:	n/a
8	chr2:46717839-46717889	SKMC	muscle:	n/a
9	chr2:46706139-46706189	HEK293	kidney:	embryo
10	chr2:46706709-46706759	T-47D	breast:	n/a
11	chr2:46707626-46707676	HMEC	breast:	n/a
12	chr2:46711337-46711387	HEEpiC	esophagus:	n/a
13	chr2:46707773-46707823	ProgFib	skin:	n/a
14	chr2:46705350-46705400	PFSK-1	brain:	n/a
15	chr2:46717839-46717889	MCF-7	breast:	n/a
16	chr2:46707844-46707894	NT2-D1	testis:	n/a
17	chr2:46707773-46707823	AG10803	skin:	n/a
18	chr2:46717839-46717889	ovcar-3	ovarian:	n/a
19	chr2:46715231-46715281	PFSK-1	brain:	n/a
20	chr2:46717839-46717889	HRE	kidney:	n/a
21	chr2:46707626-46707676	SAEC	small airway:	n/a
22	chr2:46717839-46717889	HAEpiC	amniotic membrane:	n/a
23	chr2:46709125-46709175	HL-60	blood:	n/a
24	chr2:46706709-46706759	HUVEC	blood vessel:	n/a
25	chr2:46709125-46709175	GM06990	blood:	n/a
26	chr2:46711337-46711387	HUVEC	blood vessel:	n/a
27	chr2:46707773-46707823	AG09319	gingival:	n/a
28	chr2:46705350-46705400	AG10803	skin:	n/a
29	chr2:46705350-46705400	LNCaP	prostate:	n/a
30	chr2:46709125-46709175	SK-N-SH_RA	brain:	n/a
31	chr2:46707773-46707823	AG04449	skin:	fetal
32	chr2:46707626-46707676	AG04450	lung:	fetal
33	chr2:46707678-46707728	HUVEC	blood vessel:	n/a
34	chr2:46707844-46707894	AG09319	gingival:	n/a
35	chr2:46707678-46707728	ProgFib	skin:	n/a
36	chr2:46707773-46707823	HEK293	kidney:	embryo
37	chr2:46706139-46706189	BJ	skin:	n/a
38	chr2:46705350-46705400	HepG2	liver:	n/a
39	chr2:46709125-46709175	GM19239	blood:	n/a
40	chr2:46709125-46709175	HUVEC	blood vessel:	n/a
41	chr2:46707626-46707676	PFSK-1	brain:	n/a
42	chr2:46706139-46706189	HL-60	blood:	n/a
43	chr2:46706139-46706189	HCPEpiC	choroid plexus:	n/a
44	chr2:46707626-46707676	SK-N-SH_RA	brain:	n/a
45	chr2:46705989-46706039	K562	blood:	n/a
46	chr2:46715231-46715281	HEEpiC	esophagus:	n/a
47	chr2:46711337-46711387	SK-N-SH	brain:	n/a
48	chr2:46707678-46707728	SK-N-SH	brain:	n/a
49	chr2:46707678-46707728	HCM	heart:	n/a
50	chr2:46711337-46711387	AG09319	gingival:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:46693283..46695227-chr2:46712341..46714395,2	K562	blood:
2	chr2:46710065..46711846-chr2:46725513..46727572,2	MCF-7	breast:
3	chr2:46713674..46717376-chr2:46717590..46719594,3	K562	blood:
4	chr2:46713674..46716471-chr2:46717649..46719594,2	K562	blood:
5	chr2:46715260..46716783-chr2:46718663..46721578,2	MCF-7	breast:
6	chr2:46707494..46710484-chr2:46718946..46721502,2	K562	blood:
7	chr2:46656214..46657827-chr2:46704173..46707018,3	K562	blood:
8	chr2:46709342..46712080-chr2:46908104..46909816,2	K562	blood:
9	chr2:46704470..46707025-chr2:46769256..46770963,2	MCF-7	breast:
10	chr2:46716484..46718309-chr2:46842742..46845548,2	K562	blood:
11	chr2:46707494..46710484-chr2:46718946..46721502,2	K562	blood:
12	chr2:46715260..46716783-chr2:46718663..46721578,2	MCF-7	breast:
13	chr2:46714508..46716993-chr2:46724518..46727090,2	K562	blood:
14	chr2:46703332..46705552-chr2:46707048..46709063,2	K562	blood:
15	chr2:46713674..46717376-chr2:46717590..46719594,3	K562	blood:
16	chr2:46710349..46713099-chr2:46769270..46771905,2	MCF-7	breast:
17	chr2:46705265..46709008-chr2:46724758..46728950,5	K562	blood:
18	chr2:46703332..46705552-chr2:46707048..46709063,2	K562	blood:
19	chr2:46712457..46718126-chr2:46724421..46727428,6	K562	blood:
20	chr2:46713674..46716471-chr2:46717649..46719594,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V1E2-5	chr2:46717889-46717970	NONHSAT070501

No data

Variant related genes	Relation type
TMEM247	TF binding region
TMEM247	CpG island
ENSG00000250565	chromatin interactions
ENSG00000119729	chromatin interactions
ENSG00000119878	chromatin interactions
ENSG00000187600	chromatin interactions
ENSG00000151665	chromatin interactions
ENSG00000253515	chromatin interactions

Extended variants
information (count: 1038 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1451154	chr2:46699145-46699146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs559641082	chr2:46699162-46699163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528369148	chr2:46699193-46699194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs61693092	chr2:46699262-46699263	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs530590687	chr2:46699278-46699279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs59854247	chr2:46699302-46699303	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs567207220	chr2:46699303-46699304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190288613	chr2:46699334-46699335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182543524	chr2:46699341-46699342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186869285	chr2:46699346-46699347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535321654	chr2:46699357-46699358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558457499	chr2:46699362-46699363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571893865	chr2:46699385-46699386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs139366243	chr2:46699386-46699387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs144099212	chr2:46699399-46699400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs57258681	chr2:46699432-46699433	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs61093993	chr2:46699441-46699442	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs191527888	chr2:46699455-46699456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370839888	chr2:46699463-46699464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182758935	chr2:46699506-46699507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188937353	chr2:46699511-46699512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564790467	chr2:46699523-46699524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530625113	chr2:46699545-46699546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375241073	chr2:46699551-46699552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544065078	chr2:46699573-46699574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs61436327	chr2:46699587-46699588	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs145502126	chr2:46699617-46699618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs141178649	chr2:46699634-46699635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs58143719	chr2:46699639-46699640	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs532120393	chr2:46699647-46699648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs193249955	chr2:46699648-46699649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571928725	chr2:46699651-46699652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537691688	chr2:46699670-46699671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557270126	chr2:46699676-46699677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567777096	chr2:46699699-46699700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536361498	chr2:46699705-46699706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553020975	chr2:46699715-46699716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572904147	chr2:46699735-46699736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371326772	chr2:46699784-46699785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185179841	chr2:46699813-46699814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147957045	chr2:46699871-46699872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575444045	chr2:46699884-46699885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544421884	chr2:46699885-46699886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560909126	chr2:46699889-46699890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529864634	chr2:46699902-46699903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373863453	chr2:46699931-46699932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201044271	chr2:46699948-46699949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533722525	chr2:46699961-46699962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540351527	chr2:46699964-46699965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367827585	chr2:46700006-46700007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:46686400-46704400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr2:46689200-46704800	Weak transcription	Placenta	Placenta
3	chr2:46689200-46714800	Weak transcription	Right Atrium	heart
4	chr2:46692000-46702600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr2:46698600-46699200	Enhancers	Hela-S3	cervix
6	chr2:46700200-46714800	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr2:46702600-46702800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:46702800-46703200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr2:46703200-46703600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr2:46704000-46705800	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr2:46704200-46704400	Enhancers	Primary T cells from cord blood	blood
12	chr2:46704200-46704800	Enhancers	K562	blood
13	chr2:46704200-46705400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr2:46704200-46705600	Enhancers	Primary T cells fromperipheralblood	blood
15	chr2:46704200-46705600	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr2:46704200-46705800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr2:46704400-46704600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr2:46704400-46705000	Enhancers	Primary B cells from peripheral blood	blood
19	chr2:46704400-46705200	Enhancers	Primary T killer memory cells from peripheral blood	blood
20	chr2:46704400-46705400	Enhancers	Fetal Thymus	thymus
21	chr2:46704400-46705600	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr2:46704400-46705600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
23	chr2:46704400-46705600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr2:46704400-46705800	Enhancers	H9 Cell Line	embryonic stem cell
25	chr2:46704400-46705800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr2:46704400-46706000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr2:46704600-46705000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
28	chr2:46704800-46705000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr2:46704800-46705000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr2:46704800-46705000	Active TSS	iPS-15b Cell Line	embryonic stem cell
31	chr2:46704800-46705000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr2:46704800-46705000	Enhancers	Placenta	Placenta
33	chr2:46704800-46705400	Flanking Active TSS	K562	blood
34	chr2:46704800-46705600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr2:46705000-46705200	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr2:46705000-46705200	Enhancers	Primary T cells from cord blood	blood
37	chr2:46705000-46706000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
38	chr2:46705000-46707400	Weak transcription	Placenta	Placenta
39	chr2:46705000-46707600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr2:46705000-46716600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr2:46705200-46705600	Active TSS	iPS-15b Cell Line	embryonic stem cell
42	chr2:46705200-46705600	Active TSS	Primary T killer memory cells from peripheral blood	blood
43	chr2:46705400-46706000	Enhancers	K562	blood
44	chr2:46706600-46708400	Enhancers	Lung	lung
45	chr2:46707400-46708200	Enhancers	Placenta	Placenta
46	chr2:46707400-46709200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr2:46707400-46710000	Enhancers	Hela-S3	cervix
48	chr2:46707600-46709400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr2:46707800-46708400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr2:46707800-46708600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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