Variant report

Variant	nsv535640
Chromosome Location	chr2:35731937-36422991
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1625)
CpG islands
(count:244)
Chromatin interactive
region (count:29)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1625 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:36214717-36214956	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:36392370-36392619	HepG2	liver:	n/a	n/a
3	ATF2	chr2:36374728-36375202	GM12878	blood:	n/a	n/a
4	BACH1	chr2:36417402-36417520	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:36163349-36163414	K562	blood:	n/a	n/a
6	BACH1	chr2:36246312-36246349	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr2:36180017-36180019	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr2:36374889-36375165	GM12878	blood:	n/a	n/a
9	BATF	chr2:36374886-36375226	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:36374942-36375184	GM12878	blood:	n/a	chr2:36374970-36374979
11	BHLHE40	chr2:36214674-36215098	HepG2	liver:	n/a	n/a
12	BHLHE40	chr2:36115733-36115738	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:36411001-36411307	HepG2	liver:	n/a	n/a
14	BRCA1	chr2:36214839-36214902	HepG2	liver:	n/a	n/a
15	BRCA1	chr2:36285622-36285667	Hela-S3	cervix:	n/a	n/a
16	CCNT2	chr2:36229329-36229487	K562	blood:	n/a	n/a
17	CEBPB	chr2:35939944-35940305	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr2:35735382-35735623	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:36156290-36156470	A549	lung:	n/a	n/a
20	CEBPB	chr2:35844691-35844762	HepG2	liver:	n/a	chr2:35844710-35844721
21	CEBPB	chr2:36231732-36231912	HepG2	liver:	n/a	chr2:36231856-36231867
22	CEBPB	chr2:35748868-35749205	IMR90	lung:	n/a	chr2:35749027-35749038
23	CEBPB	chr2:36395475-36395510	IMR90	lung:	n/a	chr2:36395482-36395495 chr2:36395482-36395493 chr2:36395482-36395495 chr2:36395484-36395495 chr2:36395479-36395496
24	CEBPB	chr2:35939874-35940327	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:35966616-35966957	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr2:35913520-35913719	A549	lung:	n/a	n/a
27	CEBPB	chr2:36375180-36375486	A549	lung:	n/a	n/a
28	CEBPB	chr2:35931148-35931461	HepG2	liver:	n/a	chr2:35931306-35931319 chr2:35931306-35931317
29	CEBPB	chr2:36305807-36305895	HepG2	liver:	n/a	chr2:36305858-36305869
30	CEBPB	chr2:35848050-35848250	HepG2	liver:	n/a	chr2:35848175-35848184 chr2:35848174-35848185 chr2:35848173-35848184
31	CEBPB	chr2:35939980-35940327	K562	blood:	n/a	n/a
32	CEBPB	chr2:36156260-36156477	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:35884866-35884899	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:36022021-36022040	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:35748850-35749215	HepG2	liver:	n/a	chr2:35749027-35749038
36	CEBPB	chr2:35858519-35858578	K562	blood:	n/a	chr2:35858550-35858561
37	CEBPB	chr2:35933609-35933943	H1-hESC	embryonic stem cell:	n/a	chr2:35933776-35933785 chr2:35933774-35933785 chr2:35933776-35933787
38	CEBPB	chr2:35748851-35749208	A549	lung:	n/a	chr2:35749027-35749038
39	CEBPB	chr2:36420172-36420519	ECC-1	luminal epithelium:	n/a	chr2:36420312-36420325
40	CEBPB	chr2:36052197-36052252	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:36002964-36003212	HepG2	liver:	n/a	chr2:36003126-36003135 chr2:36003124-36003135 chr2:36003125-36003136
42	CEBPB	chr2:36068970-36069119	IMR90	lung:	n/a	chr2:36069021-36069032
43	CEBPB	chr2:36379331-36379617	A549	lung:	n/a	chr2:36379457-36379468
44	CEBPB	chr2:36380814-36381038	IMR90	lung:	n/a	chr2:36380974-36380985
45	CEBPB	chr2:35939882-35940380	A549	lung:	n/a	n/a
46	CEBPB	chr2:36137484-36137491	HepG2	liver:	n/a	n/a
47	CEBPB	chr2:36395379-36395613	A549	lung:	n/a	chr2:36395482-36395495 chr2:36395482-36395493 chr2:36395482-36395495 chr2:36395484-36395495 chr2:36395479-36395496
48	CEBPB	chr2:36000760-36001020	HepG2	liver:	n/a	chr2:36000859-36000870 chr2:36000860-36000871
49	CEBPB	chr2:36106593-36106880	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr2:36374813-36375491	IMR90	lung:	n/a	chr2:36374901-36374912 chr2:36374900-36374911

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:36049853-36049903	AoSMC	blood vessel:	n/a
2	chr2:36018275-36018325	MCF10A-Er-Src	breast:	n/a
3	chr2:36018275-36018325	H1-hESC	embryonic stem cell:	embryo
4	chr2:36157995-36158045	SK-N-SH_RA	brain:	n/a
5	chr2:36157995-36158045	HEK293	kidney:	embryo
6	chr2:36049853-36049903	HNPCEpiC	eye:	n/a
7	chr2:36049853-36049903	HAEpiC	amniotic membrane:	n/a
8	chr2:36157995-36158045	SKMC	muscle:	n/a
9	chr2:36018275-36018325	K562	blood:	n/a
10	chr2:36049853-36049903	RPTEC	kidney:	n/a
11	chr2:36157995-36158045	AG10803	skin:	n/a
12	chr2:36049853-36049903	GM19239	blood:	n/a
13	chr2:36157995-36158045	A549	lung:	n/a
14	chr2:36049853-36049903	Hela-S3	cervix:	n/a
15	chr2:36049853-36049903	LNCaP	prostate:	n/a
16	chr2:36406592-36406642	AG09319	gingival:	n/a
17	chr2:36406592-36406642	SKMC	muscle:	n/a
18	chr2:36018275-36018325	SK-N-SH_RA	brain:	n/a
19	chr2:36049853-36049903	AG04450	lung:	fetal
20	chr2:36049853-36049903	HIPEpiC	eye:	n/a
21	chr2:36018275-36018325	AG09309	skin:	n/a
22	chr2:36406592-36406642	HEK293	kidney:	embryo
23	chr2:36049853-36049903	GM12878	blood:	n/a
24	chr2:36157995-36158045	HRCEpiC	kidney:	n/a
25	chr2:36406592-36406642	IMR90	lung:	fetal
26	chr2:36049853-36049903	HCT-116	colon:	n/a
27	chr2:36406592-36406642	HNPCEpiC	eye:	n/a
28	chr2:36049853-36049903	HPAEpiC	pulmonary alveolar:	n/a
29	chr2:36018275-36018325	SK-N-SH	brain:	n/a
30	chr2:36157995-36158045	HEEpiC	esophagus:	n/a
31	chr2:36406592-36406642	SK-N-SH	brain:	n/a
32	chr2:36018275-36018325	HCM	heart:	n/a
33	chr2:36157995-36158045	HMEC	breast:	n/a
34	chr2:36018275-36018325	HCPEpiC	choroid plexus:	n/a
35	chr2:36406592-36406642	HL-60	blood:	n/a
36	chr2:36157995-36158045	GM06990	blood:	n/a
37	chr2:36018275-36018325	HCF	heart:	n/a
38	chr2:36049853-36049903	PANC-1	pancreas:	n/a
39	chr2:36049853-36049903	CMK	blood:	n/a
40	chr2:36049853-36049903	HepG2	liver:	n/a
41	chr2:36018275-36018325	IMR90	lung:	fetal
42	chr2:36018275-36018325	HL-60	blood:	n/a
43	chr2:36018275-36018325	NB4	blood:	n/a
44	chr2:36406592-36406642	AG10803	skin:	n/a
45	chr2:36406592-36406642	GM12892	blood:	n/a
46	chr2:36049853-36049903	NHDF-neo	bronchial:	n/a
47	chr2:36406592-36406642	Caco-2	colon:	n/a
48	chr2:36406592-36406642	SK-N-MC	brain:	n/a
49	chr2:36406592-36406642	K562	blood:	n/a
50	chr2:36018275-36018325	HMEC	breast:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:
2	chr2:36198079..36198752-chr2:36549195..36549978,3	MCF-7	breast:
3	chr2:35949877..35953265-chr2:35954228..35956588,3	MCF-7	breast:
4	chr2:35887668..35890004-chr2:35892119..35894663,2	K562	blood:
5	chr2:36208827..36211193-chr2:36213089..36216018,2	MCF-7	breast:
6	chr2:36262623..36264860-chr2:36265182..36267594,2	K562	blood:
7	chr2:36167966..36170859-chr2:36172337..36174849,2	MCF-7	breast:
8	chr2:35877173..35880679-chr2:35885712..35889508,3	MCF-7	breast:
9	chr2:35877173..35880679-chr2:35885712..35889508,3	MCF-7	breast:
10	chr2:36243496..36245168-chr2:36248339..36251225,2	K562	blood:
11	chr2:35878984..35880554-chr2:35880811..35883619,2	K562	blood:
12	chr2:36167966..36170859-chr2:36172337..36174849,2	MCF-7	breast:
13	chr2:36346980..36349018-chr2:36352266..36354440,2	K562	blood:
14	chr2:35847208..35849274-chr2:35852737..35854636,2	K562	blood:
15	chr2:36198095..36199022-chr2:36584804..36585700,2	MCF-7	breast:
16	chr2:36222475..36223224-chr6:31509383..31509944,2	MCF-7	breast:
17	chr2:35887668..35890004-chr2:35892119..35894663,2	K562	blood:
18	chr2:36346980..36349018-chr2:36352266..36354440,2	K562	blood:
19	chr2:35878984..35880554-chr2:35880811..35883619,2	K562	blood:
20	chr2:36262623..36264860-chr2:36265182..36267594,2	K562	blood:
21	chr2:35863760..35866047-chr2:35869717..35871925,2	MCF-7	breast:
22	chr2:36099243..36100067-chr2:36734209..36735134,2	MCF-7	breast:
23	chr2:36243496..36245168-chr2:36248339..36251225,2	K562	blood:
24	chr2:36026668..36029472-chr2:36034547..36037398,2	K562	blood:
25	chr2:36026668..36029472-chr2:36034547..36037398,2	K562	blood:
26	chr2:36208827..36211193-chr2:36213089..36216018,2	MCF-7	breast:
27	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:
28	chr2:35847208..35849274-chr2:35852737..35854636,2	K562	blood:
29	chr2:35863760..35866047-chr2:35869717..35871925,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC007401.2.1-6	chr2:35949825-35950208	NONHSAT070075

No data

Variant related genes	Relation type
MRPL50P1	TF binding region
MRPL50P1	CpG island
ENSG00000234587	chromatin interactions
ENSG00000198563	chromatin interactions

Extended variants
information (count: 16916 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:16916 , 50 per page) page: 1 2 3 4 5 6 7 ... 339

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76177534	chr2:35731947-35731948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189571615	chr2:35731958-35731959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551948281	chr2:35731981-35731982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs180759605	chr2:35731995-35731996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12712441	chr2:35732012-35732013	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs17016809	chr2:35732029-35732030	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs568296574	chr2:35732031-35732032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78673569	chr2:35732033-35732034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12712442	chr2:35732050-35732051	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs143147635	chr2:35732056-35732057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12712443	chr2:35732103-35732104	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs13023651	chr2:35732132-35732133	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs541288075	chr2:35732137-35732138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12712444	chr2:35732148-35732149	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs576475115	chr2:35732184-35732185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs149981514	chr2:35732204-35732205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577726345	chr2:35732216-35732217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573920733	chr2:35732251-35732252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541293237	chr2:35732265-35732266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559632383	chr2:35732270-35732271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11687904	chr2:35732277-35732278	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs112566920	chr2:35732287-35732288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563966635	chr2:35732289-35732290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs12477435	chr2:35732304-35732305	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs563606827	chr2:35732336-35732337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188414031	chr2:35732413-35732414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568232898	chr2:35732453-35732454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs66570353	chr2:35732461-35732462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs34965147	chr2:35732463-35732464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs398060083	chr2:35732466-35732467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200597661	chr2:35732467-35732468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs17016818	chr2:35732518-35732519	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs547673609	chr2:35732561-35732562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145214357	chr2:35732600-35732601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4567910	chr2:35732653-35732654	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs558120730	chr2:35732660-35732661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149213335	chr2:35732663-35732664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4312465	chr2:35732687-35732688	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs570847065	chr2:35732693-35732694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11682305	chr2:35732726-35732727	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs573858871	chr2:35732727-35732728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554107159	chr2:35732743-35732744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541231712	chr2:35732748-35732749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553198702	chr2:35732809-35732810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs578189283	chr2:35732811-35732812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181918531	chr2:35732853-35732854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564089046	chr2:35732929-35732930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373910426	chr2:35732960-35732961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531228471	chr2:35732997-35732998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565935385	chr2:35733032-35733033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:669 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:35730400-35733600	Weak transcription	HUVEC	blood vessel
2	chr2:35730400-35735600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:35730400-35735600	Weak transcription	HMEC	breast
4	chr2:35733600-35735600	Enhancers	HUVEC	blood vessel
5	chr2:35735600-35736200	Flanking Active TSS	HUVEC	blood vessel
6	chr2:35735600-35736400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:35735600-35736400	Enhancers	HMEC	breast
8	chr2:35735800-35736200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr2:35735800-35736200	Enhancers	Adipose Nuclei	Adipose
10	chr2:35735800-35736400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr2:35736200-35736800	Enhancers	HUVEC	blood vessel
12	chr2:35736400-35739800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr2:35739800-35740200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr2:35741000-35743000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr2:35743000-35743800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr2:35743800-35747600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr2:35743800-35754600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr2:35747000-35748000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr2:35747000-35748200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr2:35747000-35748200	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr2:35747200-35747800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr2:35747200-35748000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr2:35747600-35748000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr2:35747800-35748200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr2:35747800-35748400	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr2:35748200-35749000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr2:35754600-35755000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr2:35754600-35755000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
29	chr2:35755000-35757400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr2:35755800-35756200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr2:35764000-35764600	Enhancers	HMEC	breast
32	chr2:35764200-35764800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr2:35764600-35766400	Weak transcription	HMEC	breast
34	chr2:35766400-35766800	Enhancers	HMEC	breast
35	chr2:35771000-35771600	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr2:35781000-35781800	Enhancers	Pancreas	Pancrea
37	chr2:35794400-35795200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr2:35800000-35800800	Enhancers	Pancreas	Pancrea
39	chr2:35800200-35800600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr2:35800800-35803200	Weak transcription	Pancreas	Pancrea
41	chr2:35802800-35803600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:35803200-35803400	Enhancers	Pancreas	Pancrea
43	chr2:35803200-35803800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
44	chr2:35808000-35813400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr2:35820000-35821600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr2:35823200-35826000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr2:35823400-35825200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr2:35823400-35825200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr2:35823400-35825200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
50	chr2:35825000-35825200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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