Variant report

Variant	nsv833725
Chromosome Location	chr2:34618928-34787991
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	BATF	chr2:34626250-34626627	GM12878	blood:	n/a	chr2:34626402-34626412 chr2:34626401-34626412
2	BATF	chr2:34626271-34626588	GM12878	blood:	n/a	chr2:34626402-34626412 chr2:34626401-34626412
3	BCL11A	chr2:34626351-34626529	GM12878	blood:	n/a	chr2:34626400-34626409 chr2:34626401-34626410
4	BCL3	chr2:34633202-34633571	GM12878	blood:	n/a	chr2:34633318-34633327 chr2:34633317-34633326
5	BCL3	chr2:34633212-34633509	GM12878	blood:	n/a	chr2:34633318-34633327 chr2:34633317-34633326
6	BHLHE40	chr2:34633159-34633448	GM12878	blood:	n/a	n/a
7	CBX3	chr2:34744823-34745018	K562	blood:	n/a	n/a
8	CCNT2	chr2:34623370-34623530	K562	blood:	n/a	n/a
9	CEBPB	chr2:34651788-34652080	HepG2	liver:	n/a	chr2:34651953-34651964
10	CEBPB	chr2:34634613-34634777	A549	lung:	n/a	n/a
11	CEBPB	chr2:34661633-34661923	HepG2	liver:	n/a	chr2:34661857-34661869
12	CEBPB	chr2:34717914-34718139	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:34637610-34637983	IMR90	lung:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
14	CEBPB	chr2:34706655-34707006	MCF-7	breast:	n/a	chr2:34706794-34706805
15	CEBPB	chr2:34633823-34633989	A549	lung:	n/a	chr2:34633880-34633891 chr2:34633878-34633891 chr2:34633878-34633889 chr2:34633878-34633891
16	CEBPB	chr2:34637705-34637966	MCF-7	breast:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
17	CEBPB	chr2:34637636-34637968	Hela-S3	cervix:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
18	CEBPB	chr2:34651781-34652060	IMR90	lung:	n/a	chr2:34651953-34651964
19	CEBPB	chr2:34759033-34759047	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:34706625-34706972	K562	blood:	n/a	chr2:34706794-34706805
21	CEBPB	chr2:34651786-34652048	K562	blood:	n/a	chr2:34651953-34651964
22	CEBPB	chr2:34633778-34633979	HepG2	liver:	n/a	chr2:34633880-34633891 chr2:34633878-34633891 chr2:34633878-34633889 chr2:34633878-34633891
23	CEBPB	chr2:34651815-34652025	H1-hESC	embryonic stem cell:	n/a	chr2:34651953-34651964
24	CEBPB	chr2:34637703-34637950	MCF-7	breast:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
25	CEBPB	chr2:34706608-34706989	HepG2	liver:	n/a	chr2:34706794-34706805
26	CEBPB	chr2:34706730-34706928	H1-hESC	embryonic stem cell:	n/a	chr2:34706794-34706805
27	CEBPB	chr2:34637693-34638019	A549	lung:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
28	CEBPB	chr2:34717910-34718155	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr2:34759877-34760165	K562	blood:	n/a	chr2:34759972-34759985
30	CEBPB	chr2:34706676-34706941	A549	lung:	n/a	chr2:34706794-34706805
31	CEBPB	chr2:34637607-34637980	HepG2	liver:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
32	CEBPB	chr2:34706631-34706981	IMR90	lung:	n/a	chr2:34706794-34706805
33	CEBPB	chr2:34637613-34637978	K562	blood:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
34	CEBPB	chr2:34759749-34759988	HepG2	liver:	n/a	chr2:34759832-34759845 chr2:34759832-34759843 chr2:34759972-34759985
35	CEBPB	chr2:34637621-34637979	H1-hESC	embryonic stem cell:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
36	CEBPB	chr2:34736004-34736033	HepG2	liver:	n/a	chr2:34736017-34736028
37	CEBPB	chr2:34759886-34760188	MCF-7	breast:	n/a	chr2:34759972-34759985
38	CEBPB	chr2:34637625-34637979	A549	lung:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
39	CEBPB	chr2:34637712-34637983	ECC-1	luminal epithelium:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
40	CEBPB	chr2:34651784-34652054	A549	lung:	n/a	chr2:34651953-34651964
41	CHD2	chr2:34632765-34632782	GM12878	blood:	n/a	n/a
42	CHD2	chr2:34672099-34672569	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr2:34773140-34773290	GM12873	blood:	n/a	n/a
44	CTCF	chr2:34772500-34772650	GM12872	blood:	n/a	n/a
45	CTCF	chr2:34772598-34772612	GM19238	blood:	n/a	n/a
46	CTCF	chr2:34773205-34773235	NHEK	skin:	n/a	n/a
47	CTCF	chr2:34772535-34772743	GM12878	blood:	n/a	n/a
48	CTCF	chr2:34772520-34772670	RPTEC	kidney:	n/a	n/a
49	CTCF	chr2:34712260-34712410	RPTEC	kidney:	n/a	n/a
50	CTCF	chr2:34772480-34772630	GM12874	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:34719565-34719615	NHBE	bronchial:	n/a
2	chr2:34720275-34720325	HNPCEpiC	eye:	n/a
3	chr2:34719565-34719615	NT2-D1	testis:	n/a
4	chr2:34719719-34719769	AG04449	skin:	fetal
5	chr2:34719719-34719769	PrEC	prostate:	n/a
6	chr2:34719565-34719615	A549	lung:	n/a
7	chr2:34719565-34719615	AG09309	skin:	n/a
8	chr2:34719565-34719615	BE2_C	brain:	n/a
9	chr2:34719565-34719615	HUVEC	blood vessel:	n/a
10	chr2:34719565-34719615	HPAEpiC	pulmonary alveolar:	n/a
11	chr2:34719719-34719769	A549	lung:	n/a
12	chr2:34719719-34719769	LNCaP	prostate:	n/a
13	chr2:34720275-34720325	BE2_C	brain:	n/a
14	chr2:34720275-34720325	ProgFib	skin:	n/a
15	chr2:34633637-34633687	SKMC	muscle:	n/a
16	chr2:34720275-34720325	T-47D	breast:	n/a
17	chr2:34720275-34720325	IMR90	lung:	fetal
18	chr2:34633637-34633687	HRE	kidney:	n/a
19	chr2:34633637-34633687	HRCEpiC	kidney:	n/a
20	chr2:34719565-34719615	GM12892	blood:	n/a
21	chr2:34719719-34719769	AG09319	gingival:	n/a
22	chr2:34720275-34720325	HRPEpiC	eye:	n/a
23	chr2:34720275-34720325	AG04450	lung:	fetal
24	chr2:34720275-34720325	Hela-S3	cervix:	n/a
25	chr2:34719565-34719615	Caco-2	colon:	n/a
26	chr2:34719565-34719615	Jurkat	blood:	n/a
27	chr2:34719719-34719769	HNPCEpiC	eye:	n/a
28	chr2:34633637-34633687	SK-N-SH_RA	brain:	n/a
29	chr2:34720275-34720325	Hepatocyte	liver:	n/a
30	chr2:34633637-34633687	HIPEpiC	eye:	n/a
31	chr2:34719565-34719615	HCM	heart:	n/a
32	chr2:34633637-34633687	H1-hESC	embryonic stem cell:	embryo
33	chr2:34719719-34719769	MCF-7	breast:	n/a
34	chr2:34633637-34633687	RPTEC	kidney:	n/a
35	chr2:34719565-34719615	Hela-S3	cervix:	n/a
36	chr2:34720275-34720325	MCF-7	breast:	n/a
37	chr2:34633637-34633687	Caco-2	colon:	n/a
38	chr2:34720275-34720325	RPTEC	kidney:	n/a
39	chr2:34719565-34719615	LNCaP	prostate:	n/a
40	chr2:34633637-34633687	NHBE	bronchial:	n/a
41	chr2:34719565-34719615	GM12878	blood:	n/a
42	chr2:34633637-34633687	HCF	heart:	n/a
43	chr2:34633637-34633687	IMR90	lung:	fetal
44	chr2:34719719-34719769	BE2_C	brain:	n/a
45	chr2:34719719-34719769	HUVEC	blood vessel:	n/a
46	chr2:34720275-34720325	HAEpiC	amniotic membrane:	n/a
47	chr2:34720275-34720325	NH-A	brain:	n/a
48	chr2:34719719-34719769	CMK	blood:	n/a
49	chr2:34719565-34719615	HEK293	kidney:	embryo
50	chr2:34633637-34633687	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:57969237..57970939-chr2:34675539..34678526,2	MCF-7	breast:
2	chr17:76778253..76778888-chr2:34769758..34770277,2	MCF-7	breast:
3	chr2:34321239..34322372-chr2:34772370..34773083,4	MCF-7	breast:
4	chr2:34624209..34626557-chr2:34688886..34690644,2	K562	blood:
5	chr2:34636657..34638446-chr2:34644514..34646250,2	K562	blood:
6	chr2:34707651..34709954-chr2:34710435..34712219,2	MCF-7	breast:
7	chr2:34707651..34709954-chr2:34710435..34712219,2	MCF-7	breast:
8	chr2:34624209..34626557-chr2:34688886..34690644,2	K562	blood:
9	chr2:34636657..34638446-chr2:34644514..34646250,2	K562	blood:
10	chr17:41466170..41467868-chr2:34623111..34624611,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASGRP3-13	chr2:34713820-34713911	NONHSAT070033
2	lnc-FAM98A-7	chr2:34787656-34787849	NONHSAT070038
3	lnc-RASGRP3-14	chr2:34756150-34756498	NONHSAT070037

Variant related genes	Relation type
ENSG00000212025	TF binding region
ENSG00000212025	CpG island
ENSG00000108423	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000108669	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 3160 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3160 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs151083249	chr2:34618936-34618937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs569825148	chr2:34618940-34618941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568320680	chr2:34618982-34618983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182916648	chr2:34618988-34618989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558889940	chr2:34619000-34619001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190138949	chr2:34623113-34623114	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs183708982	chr2:34623114-34623115	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs112980181	chr2:34623132-34623133	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs58869142	chr2:34623164-34623165	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs150156842	chr2:34623267-34623268	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs2060397	chr2:34623277-34623278	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs116306436	chr2:34623305-34623306	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs186710029	chr2:34623343-34623344	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs533796515	chr2:34623369-34623370	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs112755551	chr2:34623393-34623394	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs569089081	chr2:34623421-34623422	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs573888279	chr2:34623487-34623488	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs542963934	chr2:34623508-34623509	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs562418922	chr2:34623588-34623589	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs11693585	chr2:34623598-34623599	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs551325311	chr2:34623666-34623667	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs545112376	chr2:34623680-34623681	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs35315038	chr2:34623745-34623746	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs71909816	chr2:34623746-34623747	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs566368150	chr2:34623752-34623753	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs71870334	chr2:34623755-34623756	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs533548603	chr2:34623760-34623761	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs397825628	chr2:34623765-34623766	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs73928321	chr2:34623766-34623767	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs74848506	chr2:34623788-34623789	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs560751137	chr2:34623795-34623796	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs12465811	chr2:34623796-34623797	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs549269346	chr2:34623801-34623802	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs62163257	chr2:34623826-34623827	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs531638542	chr2:34623859-34623860	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs551852254	chr2:34623869-34623870	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs538002755	chr2:34623953-34623954	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs551453772	chr2:34623954-34623955	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs149335968	chr2:34623972-34623973	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs74863879	chr2:34624006-34624007	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs567470051	chr2:34624045-34624046	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs536507174	chr2:34624063-34624064	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs556534831	chr2:34624116-34624117	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs12712385	chr2:34624135-34624136	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs545049922	chr2:34624149-34624150	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs534886460	chr2:34624155-34624156	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs572009448	chr2:34624164-34624165	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs541143860	chr2:34624168-34624169	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs560435976	chr2:34624180-34624181	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs529455731	chr2:34624193-34624194	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
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
Breast cancer	21785460	CNVD
Lung cancer	18438408	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
Autism	22495309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:130 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:34618800-34619000	Enhancers	Fetal Brain Female	brain
2	chr2:34626400-34627000	Enhancers	NH-A	brain
3	chr2:34627200-34628400	Enhancers	Fetal Brain Male	brain
4	chr2:34627600-34628200	Enhancers	Fetal Brain Female	brain
5	chr2:34631400-34633600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr2:34632400-34633800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr2:34632600-34633600	Enhancers	H9 Cell Line	embryonic stem cell
8	chr2:34632600-34634000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr2:34632600-34634000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr2:34632600-34634200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr2:34632800-34633800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr2:34633200-34633400	Enhancers	Brain Hippocampus Middle	brain
13	chr2:34633200-34633800	Enhancers	Brain Anterior Caudate	brain
14	chr2:34633200-34634000	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr2:34633200-34634400	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr2:34633400-34633800	Flanking Active TSS	Brain Hippocampus Middle	brain
17	chr2:34633400-34633800	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr2:34633400-34634000	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr2:34633600-34634000	Enhancers	Brain Substantia Nigra	brain
20	chr2:34633800-34634000	Enhancers	Brain Hippocampus Middle	brain
21	chr2:34636400-34636800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr2:34636800-34641800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr2:34638800-34640400	Enhancers	Brain Germinal Matrix	brain
24	chr2:34639200-34640800	Enhancers	Fetal Brain Female	brain
25	chr2:34639400-34642800	Enhancers	Fetal Brain Male	brain
26	chr2:34640800-34642000	Weak transcription	Fetal Brain Female	brain
27	chr2:34641200-34642000	Enhancers	Colon Smooth Muscle	Colon
28	chr2:34642000-34642200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr2:34642400-34642600	Enhancers	Fetal Brain Female	brain
30	chr2:34644400-34645000	Active TSS	Aorta	Aorta
31	chr2:34646600-34650000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr2:34648200-34648400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
33	chr2:34648200-34648400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
34	chr2:34649400-34650200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
35	chr2:34650800-34651200	Active TSS	Hela-S3	cervix
36	chr2:34652400-34654400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr2:34659600-34660200	Enhancers	Gastric	stomach
38	chr2:34665800-34666400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr2:34666400-34667800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr2:34667400-34671200	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr2:34667800-34668200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:34667800-34668200	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr2:34668200-34670400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr2:34668800-34669000	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr2:34668800-34669000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr2:34669000-34670800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr2:34670400-34673800	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr2:34670600-34673800	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr2:34670800-34671400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr2:34670800-34671800	Enhancers	iPS-20b Cell Line	embryonic stem cell

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