Variant report

Variant	nsv1007107
Chromosome Location	chr2:34563725-34664738
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	ATF2	chr2:34590863-34591498	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr2:34626250-34626627	GM12878	blood:	n/a	chr2:34626402-34626412 chr2:34626401-34626412
3	BATF	chr2:34626271-34626588	GM12878	blood:	n/a	chr2:34626402-34626412 chr2:34626401-34626412
4	BCL11A	chr2:34591088-34591422	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr2:34626351-34626529	GM12878	blood:	n/a	chr2:34626400-34626409 chr2:34626401-34626410
6	BCL3	chr2:34633212-34633509	GM12878	blood:	n/a	chr2:34633318-34633327 chr2:34633317-34633326
7	BCL3	chr2:34633202-34633571	GM12878	blood:	n/a	chr2:34633318-34633327 chr2:34633317-34633326
8	BHLHE40	chr2:34633159-34633448	GM12878	blood:	n/a	n/a
9	CCNT2	chr2:34623370-34623530	K562	blood:	n/a	n/a
10	CEBPB	chr2:34661633-34661923	HepG2	liver:	n/a	chr2:34661857-34661869
11	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
12	CEBPB	chr2:34610850-34611138	MCF-7	breast:	n/a	chr2:34610999-34611008 chr2:34611030-34611038 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610999-34611008 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610997-34611008 chr2:34610997-34611010 chr2:34610998-34611009 chr2:34610997-34611008
13	CEBPB	chr2:34651781-34652060	IMR90	lung:	n/a	chr2:34651953-34651964
14	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
15	CEBPB	chr2:34651815-34652025	H1-hESC	embryonic stem cell:	n/a	chr2:34651953-34651964
16	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
17	CEBPB	chr2:34610824-34611131	Hela-S3	cervix:	n/a	chr2:34610999-34611008 chr2:34611030-34611038 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610999-34611008 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610997-34611008 chr2:34610997-34611010 chr2:34610998-34611009 chr2:34610997-34611008
18	CEBPB	chr2:34651784-34652054	A549	lung:	n/a	chr2:34651953-34651964
19	CEBPB	chr2:34608697-34608972	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:34634613-34634777	A549	lung:	n/a	n/a
21	CEBPB	chr2:34610815-34611181	A549	lung:	n/a	chr2:34610999-34611008 chr2:34611030-34611038 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610999-34611008 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610997-34611008 chr2:34610997-34611010 chr2:34610998-34611009 chr2:34610997-34611008
22	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
23	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
24	CEBPB	chr2:34575982-34576211	HepG2	liver:	n/a	chr2:34576118-34576129
25	CEBPB	chr2:34633823-34633989	A549	lung:	n/a	chr2:34633880-34633891 chr2:34633878-34633891 chr2:34633878-34633889 chr2:34633878-34633891
26	CEBPB	chr2:34651788-34652080	HepG2	liver:	n/a	chr2:34651953-34651964
27	CEBPB	chr2:34633778-34633979	HepG2	liver:	n/a	chr2:34633880-34633891 chr2:34633878-34633891 chr2:34633878-34633889 chr2:34633878-34633891
28	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
29	CEBPB	chr2:34590884-34591363	H1-hESC	embryonic stem cell:	n/a	n/a
30	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
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	chr2:34651786-34652048	K562	blood:	n/a	chr2:34651953-34651964
33	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
34	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
35	CEBPB	chr2:34610823-34611180	IMR90	lung:	n/a	chr2:34610999-34611008 chr2:34611030-34611038 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610999-34611008 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610997-34611008 chr2:34610997-34611010 chr2:34610998-34611009 chr2:34610997-34611008
36	CEBPB	chr2:34610798-34611191	HepG2	liver:	n/a	chr2:34610999-34611008 chr2:34611030-34611038 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610999-34611008 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610997-34611008 chr2:34610997-34611010 chr2:34610998-34611009 chr2:34610997-34611008
37	CHD2	chr2:34590960-34591415	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr2:34632765-34632782	GM12878	blood:	n/a	n/a
39	CTCF	chr2:34591140-34591290	RPTEC	kidney:	n/a	chr2:34591235-34591243
40	CTCF	chr2:34578820-34578970	GM06990	blood:	n/a	chr2:34578939-34578960 chr2:34578949-34578957
41	CTCF	chr2:34591160-34591310	HRPEpiC	eye:	n/a	chr2:34591235-34591243
42	CTCF	chr2:34591200-34591350	HEK293	kidney:	n/a	chr2:34591235-34591243
43	CTCF	chr2:34644200-34644350	GM12864	blood:	n/a	n/a
44	CTCF	chr2:34591202-34591372	Medullo	brain:	n/a	chr2:34591235-34591243
45	CTCF	chr2:34578820-34578970	RPTEC	kidney:	n/a	chr2:34578939-34578960 chr2:34578949-34578957
46	CTCF	chr2:34578878-34579039	HUVEC	blood vessel:	n/a	chr2:34578939-34578960 chr2:34578949-34578957
47	CTCF	chr2:34591220-34591370	HRPEpiC	eye:	n/a	chr2:34591235-34591243
48	CTCF	chr2:34578840-34578990	HRE	kidney:	n/a	chr2:34578939-34578960 chr2:34578949-34578957
49	CTCF	chr2:34651013-34651114	Gliobla	brain:	n/a	n/a
50	CTCF	chr2:34578940-34579090	MCF-7	breast:	n/a	chr2:34578949-34578957

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:34633637-34633687	GM12891	blood:	n/a
2	chr2:34590591-34590641	A549	lung:	n/a
3	chr2:34633637-34633687	HRPEpiC	eye:	n/a
4	chr2:34590591-34590641	NHBE	bronchial:	n/a
5	chr2:34590591-34590641	GM12891	blood:	n/a
6	chr2:34590591-34590641	RPTEC	kidney:	n/a
7	chr2:34590591-34590641	HIPEpiC	eye:	n/a
8	chr2:34633637-34633687	PANC-1	pancreas:	n/a
9	chr2:34633637-34633687	HRE	kidney:	n/a
10	chr2:34590591-34590641	Hepatocyte	liver:	n/a
11	chr2:34590591-34590641	AG10803	skin:	n/a
12	chr2:34633637-34633687	H1-hESC	embryonic stem cell:	embryo
13	chr2:34590591-34590641	HCT-116	colon:	n/a
14	chr2:34590591-34590641	AG04450	lung:	fetal
15	chr2:34633637-34633687	NB4	blood:	n/a
16	chr2:34590591-34590641	GM06990	blood:	n/a
17	chr2:34590591-34590641	SAEC	small airway:	n/a
18	chr2:34590591-34590641	NH-A	brain:	n/a
19	chr2:34633637-34633687	NT2-D1	testis:	n/a
20	chr2:34590591-34590641	ovcar-3	ovarian:	n/a
21	chr2:34633637-34633687	RPTEC	kidney:	n/a
22	chr2:34633637-34633687	HIPEpiC	eye:	n/a
23	chr2:34590591-34590641	NHDF-neo	bronchial:	n/a
24	chr2:34633637-34633687	HepG2	liver:	n/a
25	chr2:34633637-34633687	Hela-S3	cervix:	n/a
26	chr2:34633637-34633687	IMR90	lung:	fetal
27	chr2:34590591-34590641	HMEC	breast:	n/a
28	chr2:34633637-34633687	HCM	heart:	n/a
29	chr2:34633637-34633687	ovcar-3	ovarian:	n/a
30	chr2:34590591-34590641	GM12878	blood:	n/a
31	chr2:34633637-34633687	HL-60	blood:	n/a
32	chr2:34633637-34633687	PFSK-1	brain:	n/a
33	chr2:34590591-34590641	SKMC	muscle:	n/a
34	chr2:34590591-34590641	CMK	blood:	n/a
35	chr2:34633637-34633687	HRCEpiC	kidney:	n/a
36	chr2:34590591-34590641	AoSMC	blood vessel:	n/a
37	chr2:34590591-34590641	AG09319	gingival:	n/a
38	chr2:34633637-34633687	SK-N-MC	brain:	n/a
39	chr2:34633637-34633687	GM12878	blood:	n/a
40	chr2:34590591-34590641	HAEpiC	amniotic membrane:	n/a
41	chr2:34633637-34633687	GM19239	blood:	n/a
42	chr2:34590591-34590641	HCPEpiC	choroid plexus:	n/a
43	chr2:34633637-34633687	BE2_C	brain:	n/a
44	chr2:34590591-34590641	Hela-S3	cervix:	n/a
45	chr2:34633637-34633687	HPAEpiC	pulmonary alveolar:	n/a
46	chr2:34590591-34590641	HRPEpiC	eye:	n/a
47	chr2:34633637-34633687	Caco-2	colon:	n/a
48	chr2:34590591-34590641	PFSK-1	brain:	n/a
49	chr2:34633637-34633687	HCT-116	colon:	n/a
50	chr2:34590591-34590641	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:34590795..34592507-chr2:34600278..34603033,2	K562	blood:
2	chr2:34636657..34638446-chr2:34644514..34646250,2	K562	blood:
3	chr17:41466170..41467868-chr2:34623111..34624611,2	MCF-7	breast:
4	chr2:34624209..34626557-chr2:34688886..34690644,2	K562	blood:
5	chr12:46765173..46767943-chr2:34590937..34593382,2	MCF-7	breast:
6	chr2:34590795..34592507-chr2:34600278..34603033,2	K562	blood:
7	chr2:34636657..34638446-chr2:34644514..34646250,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASGRP3-3	chr2:34608855-34609276	ENSG00000226785
2	lnc-RASGRP3-3	chr2:34609584-34609636	ENSG00000226785
3	lnc-RASGRP3-3	chr2:34609584-34609796	NONHSAT070034

Variant related genes	Relation type
ENSG00000212025	TF binding region
ENSG00000226785	TF binding region
ENSG00000212025	CpG island
ENSG00000226785	CpG island
ENSG00000188825	chromatin interactions
ENSG00000134294	chromatin interactions
ENSG00000258096	chromatin interactions

Extended variants
information (count: 1668 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1668 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566452773	chr2:34570200-34570201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs79377357	chr2:34570271-34570272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs74317201	chr2:34570283-34570284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575207470	chr2:34570309-34570310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187378531	chr2:34570327-34570328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs193291996	chr2:34570340-34570341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185538612	chr2:34570343-34570344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs546075848	chr2:34570366-34570367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs139010715	chr2:34570391-34570392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528782899	chr2:34570425-34570426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs75564716	chr2:34570438-34570439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541825999	chr2:34570453-34570454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562123588	chr2:34570498-34570499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530864011	chr2:34570525-34570526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs35119247	chr2:34570608-34570609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551101556	chr2:34570618-34570619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115242567	chr2:34570626-34570627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533190118	chr2:34570659-34570660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546837979	chr2:34570669-34570670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561425667	chr2:34570674-34570675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs377267460	chr2:34570675-34570676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143020471	chr2:34570688-34570689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535757332	chr2:34570692-34570693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs555014380	chr2:34570706-34570707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576698963	chr2:34570739-34570740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187976184	chr2:34570780-34570781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147526674	chr2:34570828-34570829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557866309	chr2:34570841-34570842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577004653	chr2:34570843-34570844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs34273550	chr2:34570887-34570888	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs553168222	chr2:34570897-34570898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs114453492	chr2:34570906-34570907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542514672	chr2:34570924-34570925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs6713718	chr2:34570926-34570927	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs575636165	chr2:34570932-34570933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs544365532	chr2:34570965-34570966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs547925616	chr2:34570996-34570997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566642588	chr2:34570997-34570998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543981269	chr2:34571021-34571022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534014482	chr2:34571086-34571087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574580340	chr2:34571088-34571089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs116794601	chr2:34571121-34571122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546776358	chr2:34571131-34571132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139413213	chr2:34571133-34571134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529170368	chr2:34571145-34571146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549296828	chr2:34571146-34571147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs568742799	chr2:34571168-34571169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs192254046	chr2:34571171-34571172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs7567813	chr2:34571172-34571173	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs555845472	chr2:34571176-34571177	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Incontinentia Pigmenti	22033527	CNVD
Alcoholism	22295116	CNVD
small cell lung cancer	20016488	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:147 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:34570200-34571000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:34570200-34571000	Enhancers	Fetal Brain Female	brain
3	chr2:34570400-34570600	Enhancers	Fetal Heart	heart
4	chr2:34570400-34571200	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr2:34571000-34571400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr2:34573400-34575400	Enhancers	Fetal Heart	heart
7	chr2:34578200-34579000	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr2:34578400-34579200	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr2:34578600-34579000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr2:34578600-34579400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr2:34578800-34579200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr2:34578800-34579200	Enhancers	Liver	Liver
13	chr2:34581600-34582000	Enhancers	Fetal Heart	heart
14	chr2:34584200-34584800	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr2:34587400-34591400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:34587800-34590000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr2:34587800-34590800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr2:34588000-34588600	Enhancers	Fetal Kidney	kidney
19	chr2:34588000-34590600	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr2:34588000-34590800	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr2:34588200-34588400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr2:34588200-34590800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr2:34588400-34589200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr2:34588600-34589000	Weak transcription	Fetal Kidney	kidney
25	chr2:34588800-34589000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr2:34588800-34589400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr2:34588800-34590800	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr2:34589000-34589200	Enhancers	Fetal Kidney	kidney
29	chr2:34589000-34589600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr2:34589000-34589800	Enhancers	Colon Smooth Muscle	Colon
31	chr2:34589000-34590200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr2:34589000-34590800	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr2:34589000-34592400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr2:34589200-34589400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr2:34589200-34589400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr2:34589200-34589600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr2:34589200-34590800	Weak transcription	Fetal Kidney	kidney
38	chr2:34589200-34591200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr2:34589400-34590800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr2:34589400-34590800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr2:34589600-34590000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr2:34589600-34590400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr2:34589600-34590800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:34590000-34590400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr2:34590000-34592600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr2:34590200-34591400	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr2:34590400-34590800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr2:34590400-34592200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr2:34590600-34590800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr2:34590800-34591000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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