Variant report

Variant	nsv873789
Chromosome Location	chr2:33297967-33390188
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1001)
CpG islands
(count:794)
Chromatin interactive
region (count:70)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1001 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:33343824-33343996	K562	blood:	n/a	n/a
2	ARID3A	chr2:33333652-33334321	K562	blood:	n/a	n/a
3	ARID3A	chr2:33359413-33359619	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:33366668-33366820	K562	blood:	n/a	n/a
5	ATF1	chr2:33347733-33348203	K562	blood:	n/a	n/a
6	ATF1	chr2:33333227-33334393	K562	blood:	n/a	n/a
7	ATF3	chr2:33333639-33334249	K562	blood:	n/a	n/a
8	BACH1	chr2:33333738-33333858	K562	blood:	n/a	n/a
9	BACH1	chr2:33329593-33330080	H1-hESC	embryonic stem cell:	n/a	chr2:33329934-33329948
10	BACH1	chr2:33329783-33330049	K562	blood:	n/a	chr2:33329934-33329948
11	BHLHE40	chr2:33358791-33358805	K562	blood:	n/a	n/a
12	BHLHE40	chr2:33314483-33314612	K562	blood:	n/a	n/a
13	BHLHE40	chr2:33336056-33336315	HepG2	liver:	n/a	n/a
14	BHLHE40	chr2:33333586-33334367	K562	blood:	n/a	n/a
15	BRCA1	chr2:33318891-33319051	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr2:33315537-33315669	GM12878	blood:	n/a	n/a
17	CBX3	chr2:33333745-33334066	K562	blood:	n/a	n/a
18	CBX3	chr2:33366535-33366906	K562	blood:	n/a	n/a
19	CBX3	chr2:33329649-33330320	HCT-116	colon:	n/a	n/a
20	CBX3	chr2:33347614-33348187	K562	blood:	n/a	n/a
21	CBX3	chr2:33333483-33334470	K562	blood:	n/a	n/a
22	CCNT2	chr2:33373636-33373807	K562	blood:	n/a	n/a
23	CCNT2	chr2:33333652-33334227	K562	blood:	n/a	chr2:33333880-33333900
24	CCNT2	chr2:33347794-33348047	K562	blood:	n/a	n/a
25	CEBPB	chr2:33335923-33336422	A549	lung:	n/a	n/a
26	CEBPB	chr2:33354443-33354710	K562	blood:	n/a	chr2:33354581-33354592 chr2:33354594-33354605 chr2:33354583-33354594 chr2:33354593-33354606
27	CEBPB	chr2:33340314-33340668	IMR90	lung:	n/a	n/a
28	CEBPB	chr2:33333111-33333389	IMR90	lung:	n/a	n/a
29	CEBPB	chr2:33332735-33332744	A549	lung:	n/a	n/a
30	CEBPB	chr2:33335898-33336418	A549	lung:	n/a	n/a
31	CEBPB	chr2:33358980-33359846	IMR90	lung:	n/a	n/a
32	CEBPB	chr2:33333587-33334261	K562	blood:	n/a	n/a
33	CEBPB	chr2:33354447-33354752	HepG2	liver:	n/a	chr2:33354581-33354592 chr2:33354594-33354605 chr2:33354583-33354594 chr2:33354593-33354606
34	CEBPB	chr2:33348419-33348450	IMR90	lung:	n/a	n/a
35	CEBPB	chr2:33359130-33359547	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:33333772-33334163	IMR90	lung:	n/a	n/a
37	CEBPB	chr2:33389223-33389507	IMR90	lung:	n/a	n/a
38	CEBPB	chr2:33354448-33354711	IMR90	lung:	n/a	chr2:33354581-33354592 chr2:33354594-33354605 chr2:33354583-33354594 chr2:33354593-33354606
39	CEBPB	chr2:33366685-33366885	K562	blood:	n/a	n/a
40	CEBPB	chr2:33358399-33358754	K562	blood:	n/a	n/a
41	CEBPB	chr2:33383607-33384159	IMR90	lung:	n/a	n/a
42	CEBPB	chr2:33347789-33348162	K562	blood:	n/a	n/a
43	CEBPB	chr2:33333731-33334076	K562	blood:	n/a	n/a
44	CEBPB	chr2:33347821-33348163	K562	blood:	n/a	n/a
45	CEBPB	chr2:33319378-33319669	A549	lung:	n/a	n/a
46	CEBPB	chr2:33354462-33354692	A549	lung:	n/a	chr2:33354581-33354592 chr2:33354594-33354605 chr2:33354583-33354594 chr2:33354593-33354606
47	CEBPB	chr2:33366558-33366880	K562	blood:	n/a	n/a
48	CEBPB	chr2:33358429-33358768	K562	blood:	n/a	n/a
49	CEBPB	chr2:33358417-33358780	IMR90	lung:	n/a	n/a
50	CEBPB	chr2:33358491-33358702	K562	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:33359688-33359738	AG10803	skin:	n/a
2	chr2:33359688-33359738	AG10803	skin:	n/a
3	chr2:33384367-33384417	GM06990	blood:	n/a
4	chr2:33384367-33384417	HIPEpiC	eye:	n/a
5	chr2:33368461-33368511	HEK293	kidney:	embryo
6	chr2:33384367-33384417	NB4	blood:	n/a
7	chr2:33368461-33368511	HCF	heart:	n/a
8	chr2:33317174-33317224	Hepatocyte	liver:	n/a
9	chr2:33359550-33359600	HAEpiC	amniotic membrane:	n/a
10	chr2:33359550-33359600	HL-60	blood:	n/a
11	chr2:33311428-33311478	Caco-2	colon:	n/a
12	chr2:33359356-33359406	Hepatocyte	liver:	n/a
13	chr2:33384367-33384417	GM12878	blood:	n/a
14	chr2:33359529-33359579	SK-N-MC	brain:	n/a
15	chr2:33359688-33359738	MCF10A-Er-Src	breast:	n/a
16	chr2:33372733-33372783	SAEC	small airway:	n/a
17	chr2:33359356-33359406	NB4	blood:	n/a
18	chr2:33311428-33311478	AG10803	skin:	n/a
19	chr2:33311428-33311478	HNPCEpiC	eye:	n/a
20	chr2:33372733-33372783	AG09309	skin:	n/a
21	chr2:33359281-33359331	HCT-116	colon:	n/a
22	chr2:33359550-33359600	HRCEpiC	kidney:	n/a
23	chr2:33359550-33359600	ProgFib	skin:	n/a
24	chr2:33359198-33359248	PANC-1	pancreas:	n/a
25	chr2:33359198-33359248	Hela-S3	cervix:	n/a
26	chr2:33368461-33368511	MCF-7	breast:	n/a
27	chr2:33317174-33317224	HL-60	blood:	n/a
28	chr2:33368461-33368511	NB4	blood:	n/a
29	chr2:33368461-33368511	H1-hESC	embryonic stem cell:	embryo
30	chr2:33384367-33384417	PANC-1	pancreas:	n/a
31	chr2:33368461-33368511	MCF10A-Er-Src	breast:	n/a
32	chr2:33359688-33359738	HCM	heart:	n/a
33	chr2:33372733-33372783	SK-N-SH_RA	brain:	n/a
34	chr2:33359550-33359600	AG09319	gingival:	n/a
35	chr2:33359688-33359738	CMK	blood:	n/a
36	chr2:33359529-33359579	AG09319	gingival:	n/a
37	chr2:33311428-33311478	NHBE	bronchial:	n/a
38	chr2:33359529-33359579	SK-N-SH_RA	brain:	n/a
39	chr2:33359281-33359331	HEK293	kidney:	embryo
40	chr2:33359550-33359600	GM12892	blood:	n/a
41	chr2:33348262-33348312	HEK293	kidney:	embryo
42	chr2:33384367-33384417	PFSK-1	brain:	n/a
43	chr2:33359550-33359600	RPTEC	kidney:	n/a
44	chr2:33359529-33359579	HUVEC	blood vessel:	n/a
45	chr2:33384367-33384417	SAEC	small airway:	n/a
46	chr2:33368461-33368511	GM06990	blood:	n/a
47	chr2:33348262-33348312	AG04449	skin:	fetal
48	chr2:33359529-33359579	NB4	blood:	n/a
49	chr2:33359550-33359600	GM06990	blood:	n/a
50	chr2:33359198-33359248	IMR90	lung:	fetal

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:33383408..33387314-chr2:33391651..33394582,3	K562	blood:
2	chr2:33346676..33349370-chr2:33351753..33353323,2	MCF-7	breast:
3	chr2:33295214..33297626-chr2:33299821..33301525,2	K562	blood:
4	chr2:32997868..32998558-chr2:33311540..33312044,2	K562	blood:
5	chr2:33372580..33375286-chr2:33379288..33381912,2	MCF-7	breast:
6	chr2:33363634..33367831-chr2:33371387..33375003,3	K562	blood:
7	chr2:33332965..33336318-chr2:33345461..33348526,4	K562	blood:
8	chr2:33317907..33319908-chr2:33328771..33331730,2	K562	blood:
9	chr2:33325545..33328306-chr2:33331227..33333844,3	K562	blood:
10	chr2:33352861..33355600-chr2:33385791..33387865,2	MCF-7	breast:
11	chr2:33335855..33338715-chr2:33339721..33342037,2	K562	blood:
12	chr2:33315357..33320010-chr2:33321376..33324681,5	K562	blood:
13	chr2:33382825..33385246-chr2:33385612..33388538,2	K562	blood:
14	chr2:33360506..33363015-chr2:33369952..33372450,2	K562	blood:
15	chr2:33333082..33335535-chr2:33335888..33338274,2	K562	blood:
16	chr2:33347601..33349574-chr2:33351512..33354132,2	K562	blood:
17	chr2:33293451..33296755-chr2:33301954..33305143,4	MCF-7	breast:
18	chr2:33325612..33327794-chr2:33340279..33342950,2	MCF-7	breast:
19	chr2:33321965..33324050-chr2:33326516..33328893,2	K562	blood:
20	chr2:33355814..33359074-chr2:33359730..33364790,5	K562	blood:
21	chr2:33321965..33324050-chr2:33326516..33328893,2	K562	blood:
22	chr2:33342989..33344574-chr2:33349726..33351939,2	K562	blood:
23	chr2:33358329..33361000-chr2:33362823..33365595,2	MCF-7	breast:
24	chr2:33325664..33327642-chr2:33328388..33329926,2	K562	blood:
25	chr2:33292854..33294446-chr2:33300367..33303363,2	K562	blood:
26	chr2:33294735..33295846-chr2:33311218..33312090,8	MCF-7	breast:
27	chr2:33323744..33329444-chr2:33330202..33334725,9	K562	blood:
28	chr2:33387130..33389156-chr2:33413071..33415726,2	K562	blood:
29	chr2:33363634..33367831-chr2:33371387..33375003,3	K562	blood:
30	chr2:33319782..33321597-chr2:33324862..33327252,2	K562	blood:
31	chr2:33333082..33335535-chr2:33335888..33338274,2	K562	blood:
32	chr2:33360698..33363585-chr2:33365349..33368333,2	K562	blood:
33	chr2:33342989..33344574-chr2:33349726..33351939,2	K562	blood:
34	chr2:33320811..33323465-chr2:33327393..33329847,2	K562	blood:
35	chr2:33346676..33349370-chr2:33351753..33353323,2	MCF-7	breast:
36	chr2:33347601..33349574-chr2:33351512..33354132,2	K562	blood:
37	chr2:33357374..33360115-chr2:33361788..33364595,2	K562	blood:
38	chr2:33368241..33370517-chr2:33370553..33373234,2	K562	blood:
39	chr2:33332965..33336318-chr2:33345461..33348526,4	K562	blood:
40	chr2:33341850..33346633-chr2:33347912..33351586,5	K562	blood:
41	chr2:33319782..33321597-chr2:33324862..33327252,2	K562	blood:
42	chr2:33295981..33298155-chr2:33304588..33306275,2	K562	blood:
43	chr2:33352861..33355600-chr2:33385791..33387865,2	MCF-7	breast:
44	chr2:33360506..33363015-chr2:33369952..33372450,2	K562	blood:
45	chr2:33172001..33174458-chr2:33303500..33306499,2	MCF-7	breast:
46	chr2:33294735..33295813-chr2:33311218..33312090,5	MCF-7	breast:
47	chr2:33294964..33297126-chr2:33297596..33299242,2	MCF-7	breast:
48	chr2:32779080..32779581-chr2:33311536..33312319,2	K562	blood:
49	chr2:33359671..33361313-chr2:33368452..33370513,2	K562	blood:
50	chr2:33360698..33363585-chr2:33365349..33368333,2	K562	blood:

No data

Variant related genes	Relation type
LTBP1	TF binding region
LTBP1	CpG island
ENSG00000049323	chromatin interactions

Extended variants
information (count: 4022 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4022 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11885904	chr2:33297967-33297968	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs530916208	chr2:33297972-33297973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557460643	chr2:33297981-33297982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550663719	chr2:33297985-33297986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183229423	chr2:33297996-33297997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575625328	chr2:33298006-33298007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188639247	chr2:33298044-33298045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553512179	chr2:33298055-33298056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567058908	chr2:33298073-33298074	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373353576	chr2:33298099-33298100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs79145446	chr2:33298121-33298122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556003285	chr2:33298122-33298123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs575814306	chr2:33298127-33298128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192092644	chr2:33298134-33298135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546263926	chr2:33298145-33298146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557423326	chr2:33298186-33298187	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577229515	chr2:33298204-33298205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs72869686	chr2:33298205-33298206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs559863811	chr2:33298215-33298216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs117974711	chr2:33298232-33298233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs542493129	chr2:33298267-33298268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562716601	chr2:33298272-33298273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371108725	chr2:33298290-33298291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs448658	chr2:33298327-33298328	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs75979816	chr2:33298344-33298345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs80161869	chr2:33298345-33298346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs199859110	chr2:33298348-33298349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs199697981	chr2:33298352-33298353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs386644580	chr2:33298353-33298354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs533405279	chr2:33298354-33298355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547112033	chr2:33298355-33298356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs371296031	chr2:33298358-33298359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs11411636	chr2:33298359-33298360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566999239	chr2:33298453-33298454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs535970318	chr2:33298471-33298472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs549283862	chr2:33298520-33298521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs60610279	chr2:33298584-33298585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538117078	chr2:33298587-33298588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558472643	chr2:33298602-33298603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs577217397	chr2:33298642-33298643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183314029	chr2:33298681-33298682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372400679	chr2:33298703-33298704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533573871	chr2:33298758-33298759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs151053370	chr2:33298776-33298777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs573364608	chr2:33298780-33298781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542725973	chr2:33298851-33298852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs113037388	chr2:33298854-33298855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576192552	chr2:33298886-33298887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186900290	chr2:33298940-33298941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs149834977	chr2:33298949-33298950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	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	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1593 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33289600-33308200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:33292000-33298200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr2:33292000-33299200	Enhancers	HUVEC	blood vessel
4	chr2:33294200-33299600	Enhancers	Placenta	Placenta
5	chr2:33295600-33308800	Weak transcription	K562	blood
6	chr2:33295800-33298600	Enhancers	Muscle Satellite Cultured Cells	--
7	chr2:33295800-33308400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr2:33296000-33298000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr2:33296000-33298400	Enhancers	HMEC	breast
10	chr2:33296200-33298400	Enhancers	A549	lung
11	chr2:33296200-33302600	Weak transcription	Stomach Mucosa	stomach
12	chr2:33296400-33302800	Weak transcription	Fetal Stomach	stomach
13	chr2:33296400-33310800	Weak transcription	Esophagus	oesophagus
14	chr2:33296600-33302000	Weak transcription	Aorta	Aorta
15	chr2:33296600-33311000	Weak transcription	Stomach Smooth Muscle	stomach
16	chr2:33296800-33310000	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr2:33297000-33298000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr2:33297000-33302000	Weak transcription	Fetal Heart	heart
19	chr2:33297200-33302400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr2:33297400-33298200	Enhancers	NH-A	brain
21	chr2:33297400-33298800	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr2:33297600-33298000	Weak transcription	Psoas Muscle	Psoas
23	chr2:33297600-33298200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr2:33297600-33298400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr2:33297600-33298400	Enhancers	Osteobl	bone
26	chr2:33297600-33302400	Weak transcription	Left Ventricle	heart
27	chr2:33297600-33308400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr2:33297800-33298200	Enhancers	NHLF	lung
29	chr2:33297800-33298400	Enhancers	NHDF-Ad	bronchial
30	chr2:33297800-33298600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr2:33297800-33298600	Enhancers	NHEK	skin
32	chr2:33298000-33298200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr2:33298000-33298200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr2:33298000-33298200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr2:33298000-33298200	Enhancers	Psoas Muscle	Psoas
36	chr2:33298200-33310800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr2:33298200-33310800	Weak transcription	Psoas Muscle	Psoas
38	chr2:33298200-33311000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr2:33298400-33303000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr2:33298600-33302200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr2:33298800-33299400	Enhancers	Placenta Amnion	Placenta Amnion
42	chr2:33299200-33309400	Weak transcription	HUVEC	blood vessel
43	chr2:33301000-33301200	Enhancers	Fetal Kidney	kidney
44	chr2:33302000-33303400	Enhancers	Aorta	Aorta
45	chr2:33302000-33303600	Enhancers	Fetal Heart	heart
46	chr2:33302000-33312400	Enhancers	Primary B cells from cord blood	blood
47	chr2:33302200-33303200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr2:33302400-33303000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr2:33302400-33303200	Enhancers	Left Ventricle	heart
50	chr2:33302600-33303600	Enhancers	Stomach Mucosa	stomach

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