Variant report

Variant	nsv873792
Chromosome Location	chr2:33682737-33715742
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:987)
CpG islands
(count:550)
Chromatin interactive
region (count:8)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:987 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:33704389-33704526	K562	blood:	n/a	n/a
2	ATF1	chr2:33702627-33703529	K562	blood:	n/a	n/a
3	ATF1	chr2:33683023-33683136	K562	blood:	n/a	n/a
4	ATF1	chr2:33700744-33701743	K562	blood:	n/a	n/a
5	ATF2	chr2:33713147-33714559	GM12878	blood:	n/a	n/a
6	ATF2	chr2:33703823-33704501	GM12878	blood:	n/a	n/a
7	ATF2	chr2:33713064-33714314	GM12878	blood:	n/a	n/a
8	ATF2	chr2:33700215-33702042	GM12878	blood:	n/a	n/a
9	ATF2	chr2:33700310-33703643	GM12878	blood:	n/a	n/a
10	ATF2	chr2:33702420-33703119	GM12878	blood:	n/a	n/a
11	ATF2	chr2:33708855-33709954	GM12878	blood:	n/a	n/a
12	ATF2	chr2:33708882-33709744	GM12878	blood:	n/a	n/a
13	ATF3	chr2:33702670-33702990	K562	blood:	n/a	chr2:33702817-33702830 chr2:33702818-33702828 chr2:33702820-33702828 chr2:33702817-33702828
14	ATF3	chr2:33682914-33683172	K562	blood:	n/a	chr2:33683049-33683062 chr2:33683049-33683062
15	BACH1	chr2:33700776-33701040	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr2:33713681-33714208	GM12878	blood:	n/a	n/a
17	BATF	chr2:33708823-33709684	GM12878	blood:	n/a	n/a
18	BATF	chr2:33708905-33709680	GM12878	blood:	n/a	n/a
19	BATF	chr2:33713236-33713664	GM12878	blood:	n/a	n/a
20	BATF	chr2:33700501-33701088	GM12878	blood:	n/a	n/a
21	BATF	chr2:33713218-33714227	GM12878	blood:	n/a	n/a
22	BATF	chr2:33701285-33701876	GM12878	blood:	n/a	chr2:33701358-33701366
23	BCL11A	chr2:33709353-33709721	GM12878	blood:	n/a	chr2:33709507-33709516
24	BCL11A	chr2:33708967-33709330	GM12878	blood:	n/a	n/a
25	BCL11A	chr2:33713714-33714167	GM12878	blood:	n/a	chr2:33713931-33713940
26	BCL3	chr2:33709272-33709694	GM12878	blood:	n/a	chr2:33709507-33709516
27	BCL3	chr2:33700583-33701667	A549	lung:	n/a	chr2:33701471-33701478
28	BCL3	chr2:33713210-33714444	GM12878	blood:	n/a	chr2:33713931-33713940
29	BCLAF1	chr2:33700472-33702155	GM12878	blood:	n/a	chr2:33701471-33701478
30	BCLAF1	chr2:33708967-33709959	GM12878	blood:	n/a	chr2:33709507-33709516
31	BCLAF1	chr2:33703642-33705098	GM12878	blood:	n/a	n/a
32	BCLAF1	chr2:33713169-33714182	GM12878	blood:	n/a	chr2:33713931-33713940
33	BCLAF1	chr2:33712759-33714256	GM12878	blood:	n/a	chr2:33713931-33713940
34	BCLAF1	chr2:33700411-33703583	GM12878	blood:	n/a	chr2:33703464-33703473 chr2:33701471-33701478
35	BHLHE40	chr2:33704570-33705069	GM12878	blood:	n/a	n/a
36	BHLHE40	chr2:33700770-33701939	K562	blood:	n/a	n/a
37	BHLHE40	chr2:33700260-33703171	GM12878	blood:	n/a	n/a
38	BHLHE40	chr2:33708935-33709967	GM12878	blood:	n/a	n/a
39	BHLHE40	chr2:33702594-33703371	K562	blood:	n/a	n/a
40	BHLHE40	chr2:33700735-33701143	HepG2	liver:	n/a	n/a
41	BHLHE40	chr2:33713084-33714178	GM12878	blood:	n/a	n/a
42	BRCA1	chr2:33701035-33701111	HepG2	liver:	n/a	n/a
43	BRCA1	chr2:33700830-33701106	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr2:33700700-33701174	K562	blood:	n/a	n/a
45	CBX3	chr2:33700552-33701985	HCT-116	colon:	n/a	n/a
46	CBX3	chr2:33702580-33703109	K562	blood:	n/a	n/a
47	CCNT2	chr2:33702867-33703405	K562	blood:	n/a	n/a
48	CCNT2	chr2:33700788-33701155	K562	blood:	n/a	n/a
49	CEBPB	chr2:33706497-33706795	HepG2	liver:	n/a	n/a
50	CEBPB	chr2:33686000-33686200	HepG2	liver:	n/a	chr2:33686060-33686071 chr2:33686058-33686075

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:33700849-33700899	MCF-7	breast:	n/a
2	chr2:33700849-33700899	MCF-7	breast:	n/a
3	chr2:33700871-33700921	GM06990	blood:	n/a
4	chr2:33701579-33701629	GM12892	blood:	n/a
5	chr2:33700871-33700921	HRE	kidney:	n/a
6	chr2:33700849-33700899	Hela-S3	cervix:	n/a
7	chr2:33701120-33701170	Hepatocyte	liver:	n/a
8	chr2:33701229-33701279	Hepatocyte	liver:	n/a
9	chr2:33701579-33701629	MCF10A-Er-Src	breast:	n/a
10	chr2:33701229-33701279	HRE	kidney:	n/a
11	chr2:33701120-33701170	T-47D	breast:	n/a
12	chr2:33701579-33701629	HRCEpiC	kidney:	n/a
13	chr2:33701285-33701335	HEEpiC	esophagus:	n/a
14	chr2:33700917-33700967	HNPCEpiC	eye:	n/a
15	chr2:33701285-33701335	AG09319	gingival:	n/a
16	chr2:33701705-33701755	H1-hESC	embryonic stem cell:	embryo
17	chr2:33700871-33700921	RPTEC	kidney:	n/a
18	chr2:33701120-33701170	ECC-1	luminal epithelium:	n/a
19	chr2:33701579-33701629	HIPEpiC	eye:	n/a
20	chr2:33701229-33701279	SK-N-SH	brain:	n/a
21	chr2:33700849-33700899	HEK293	kidney:	embryo
22	chr2:33701319-33701369	GM12891	blood:	n/a
23	chr2:33700871-33700921	SK-N-SH	brain:	n/a
24	chr2:33701319-33701369	SK-N-SH_RA	brain:	n/a
25	chr2:33701705-33701755	NH-A	brain:	n/a
26	chr2:33701705-33701755	ECC-1	luminal epithelium:	n/a
27	chr2:33701285-33701335	HUVEC	blood vessel:	n/a
28	chr2:33701705-33701755	HCM	heart:	n/a
29	chr2:33701120-33701170	HCPEpiC	choroid plexus:	n/a
30	chr2:33701705-33701755	HAEpiC	amniotic membrane:	n/a
31	chr2:33701120-33701170	PrEC	prostate:	n/a
32	chr2:33700849-33700899	AoSMC	blood vessel:	n/a
33	chr2:33701319-33701369	HIPEpiC	eye:	n/a
34	chr2:33701120-33701170	HCT-116	colon:	n/a
35	chr2:33700849-33700899	T-47D	breast:	n/a
36	chr2:33701705-33701755	AG09319	gingival:	n/a
37	chr2:33701579-33701629	K562	blood:	n/a
38	chr2:33700917-33700967	T-47D	breast:	n/a
39	chr2:33701579-33701629	Jurkat	blood:	n/a
40	chr2:33700849-33700899	HMEC	breast:	n/a
41	chr2:33701579-33701629	HRE	kidney:	n/a
42	chr2:33701285-33701335	HepG2	liver:	n/a
43	chr2:33700917-33700967	NHDF-neo	bronchial:	n/a
44	chr2:33701705-33701755	HPAEpiC	pulmonary alveolar:	n/a
45	chr2:33701229-33701279	HCF	heart:	n/a
46	chr2:33700849-33700899	LNCaP	prostate:	n/a
47	chr2:33701229-33701279	U87	brain:	n/a
48	chr2:33701229-33701279	NH-A	brain:	n/a
49	chr2:33701705-33701755	MCF10A-Er-Src	breast:	n/a
50	chr2:33701120-33701170	SAEC	small airway:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:33690962..33692571-chr2:33696512..33698027,2	K562	blood:
2	chr2:33708290..33711080-chr2:33714152..33717140,3	K562	blood:
3	chr2:33708290..33711080-chr2:33714152..33717140,3	K562	blood:
4	chr2:33689322..33690915-chr2:33701330..33704184,2	K562	blood:
5	chr2:33692695..33693460-chr2:33808050..33808892,2	K562	blood:
6	chr2:33702588..33705548-chr2:33744716..33747266,2	K562	blood:
7	chr2:33690962..33692571-chr2:33696512..33698027,2	K562	blood:
8	chr2:33700002..33701535-chr2:33708828..33711417,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LTBP1-1	chr2:33706250-33707081	NONHSAT070015
2	lnc-LTBP1-1	chr2:33706250-33708003	NONHSAT070011
3	lnc-LTBP1-1	chr2:33701732-33701774	NONHSAT070015
4	lnc-LTBP1-1	chr2:33706250-33706371	NONHSAT070012

No data

Variant related genes	Relation type
RASGRP3	TF binding region
RASGRP3	CpG island
ENSG00000152689	chromatin interactions

Extended variants
information (count: 1611 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1611 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2124437	chr2:33682737-33682738	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368054200	chr2:33682758-33682759	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs560155263	chr2:33682807-33682808	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs561065224	chr2:33682825-33682826	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs529869112	chr2:33682826-33682827	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs2124436	chr2:33682858-33682859	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs78456890	chr2:33682874-33682875	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs112146292	chr2:33682875-33682876	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs147659468	chr2:33682897-33682898	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs571267435	chr2:33682908-33682909	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs534032543	chr2:33683023-33683024	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs183788744	chr2:33683030-33683031	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs574169310	chr2:33683041-33683042	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs377368888	chr2:33683055-33683056	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs542601533	chr2:33683056-33683057	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs536840986	chr2:33683102-33683103	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs556608882	chr2:33683107-33683108	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs75966397	chr2:33683156-33683157	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188063376	chr2:33683162-33683163	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181414304	chr2:33683179-33683180	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572022704	chr2:33683183-33683184	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541147605	chr2:33683191-33683192	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560930469	chr2:33683216-33683217	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186365960	chr2:33683224-33683225	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528183974	chr2:33683236-33683237	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191676921	chr2:33683258-33683259	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112922447	chr2:33683287-33683288	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549946597	chr2:33683289-33683290	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148747304	chr2:33683379-33683380	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7578413	chr2:33683384-33683385	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs552006905	chr2:33683401-33683402	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs75909961	chr2:33683411-33683412	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181614300	chr2:33683449-33683450	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186470556	chr2:33683464-33683465	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567729631	chr2:33683472-33683473	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs199557233	chr2:33683477-33683478	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs75447223	chr2:33683481-33683482	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556705341	chr2:33683489-33683490	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576517561	chr2:33683542-33683543	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78487506	chr2:33683574-33683575	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs72802092	chr2:33683587-33683588	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs551018537	chr2:33683591-33683592	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73926659	chr2:33683619-33683620	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs191201003	chr2:33683681-33683682	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560993476	chr2:33683705-33683706	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142303509	chr2:33683716-33683717	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs6728969	chr2:33683727-33683728	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs62147120	chr2:33683730-33683731	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs375823940	chr2:33683741-33683742	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373850994	chr2:33683767-33683768	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
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
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
Pancreatic cancer	17952125	CNVD
Autism	22495309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:823 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33668800-33685200	Weak transcription	HUVEC	blood vessel
2	chr2:33682000-33682800	Enhancers	Primary hematopoietic stem cells	blood
3	chr2:33682000-33682800	Enhancers	Fetal Heart	heart
4	chr2:33682000-33683400	Enhancers	Left Ventricle	heart
5	chr2:33682400-33683200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr2:33682400-33683200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr2:33682400-33685200	Enhancers	Liver	Liver
8	chr2:33682600-33682800	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr2:33682600-33682800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
10	chr2:33682600-33683000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr2:33682600-33683200	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr2:33682600-33683200	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr2:33682600-33683400	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr2:33682600-33683800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
15	chr2:33682600-33683800	Enhancers	Adipose Nuclei	Adipose
16	chr2:33682600-33684000	Enhancers	Stomach Smooth Muscle	stomach
17	chr2:33682800-33683000	Flanking Active TSS	Primary hematopoietic stem cells	blood
18	chr2:33682800-33683000	Flanking Active TSS	Fetal Heart	heart
19	chr2:33682800-33683000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
20	chr2:33682800-33683000	Active TSS	Skeletal Muscle Female	skeletal muscle
21	chr2:33682800-33683200	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr2:33682800-33683200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr2:33682800-33683200	Enhancers	Colon Smooth Muscle	Colon
24	chr2:33682800-33683200	Enhancers	Duodenum Smooth Muscle	Duodenum
25	chr2:33682800-33683200	Enhancers	Rectal Smooth Muscle	rectum
26	chr2:33682800-33683400	Enhancers	Primary B cells from peripheral blood	blood
27	chr2:33682800-33683400	Enhancers	Fetal Intestine Small	intestine
28	chr2:33682800-33683800	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr2:33682800-33684000	Active TSS	Psoas Muscle	Psoas
30	chr2:33682800-33684000	Active TSS	Right Atrium	heart
31	chr2:33682800-33684000	Active TSS	Right Ventricle	heart
32	chr2:33682800-33685000	Enhancers	Fetal Stomach	stomach
33	chr2:33683000-33683200	Enhancers	Primary hematopoietic stem cells	blood
34	chr2:33683000-33683200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
35	chr2:33683000-33683400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:33683000-33683800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr2:33683000-33683800	Active TSS	Fetal Muscle Trunk	muscle
38	chr2:33683000-33683800	Enhancers	Ovary	ovary
39	chr2:33683000-33684000	Active TSS	Fetal Heart	heart
40	chr2:33683000-33684600	Active TSS	Skeletal Muscle Male	skeletal muscle
41	chr2:33683200-33683400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr2:33683200-33683800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr2:33683200-33684000	Active TSS	Fetal Muscle Leg	muscle
44	chr2:33683200-33685000	Active TSS	Skeletal Muscle Female	skeletal muscle
45	chr2:33683400-33684000	Active TSS	Left Ventricle	heart
46	chr2:33683800-33684000	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr2:33683800-33687200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr2:33684000-33684200	Weak transcription	Fetal Heart	heart
49	chr2:33684000-33684600	Weak transcription	Right Atrium	heart
50	chr2:33684000-33684800	Weak transcription	Left Ventricle	heart

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