Variant report

Variant	nsv1007922
Chromosome Location	chr2:35447551-35582768
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:468)
CpG islands
(count:62)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:468 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:35494699-35494878	K562	blood:	n/a	n/a
2	ATF1	chr2:35541934-35542123	K562	blood:	n/a	n/a
3	BHLHE40	chr2:35582544-35582658	A549	lung:	n/a	n/a
4	CEBPB	chr2:35580058-35580433	MCF-7	breast:	n/a	n/a
5	CEBPB	chr2:35580165-35580349	K562	blood:	n/a	n/a
6	CEBPB	chr2:35552875-35553037	A549	lung:	n/a	chr2:35552925-35552936
7	CEBPB	chr2:35536549-35536754	HepG2	liver:	n/a	chr2:35536636-35536647
8	CEBPB	chr2:35522431-35522932	MCF-7	breast:	n/a	n/a
9	CEBPB	chr2:35580075-35580424	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr2:35579289-35579503	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:35580077-35580330	A549	lung:	n/a	n/a
12	CEBPB	chr2:35574533-35574820	HepG2	liver:	n/a	chr2:35574649-35574660
13	CEBPB	chr2:35513131-35513454	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:35580076-35580399	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:35523567-35524007	MCF-7	breast:	n/a	n/a
16	CEBPB	chr2:35574544-35574831	A549	lung:	n/a	chr2:35574649-35574660
17	CEBPB	chr2:35574532-35574904	IMR90	lung:	n/a	chr2:35574649-35574660
18	CEBPB	chr2:35573952-35574195	A549	lung:	n/a	n/a
19	CEBPB	chr2:35580086-35580411	IMR90	lung:	n/a	n/a
20	CEBPB	chr2:35522459-35522928	MCF-7	breast:	n/a	n/a
21	CEBPB	chr2:35574542-35574834	H1-hESC	embryonic stem cell:	n/a	chr2:35574649-35574660
22	CEBPB	chr2:35552817-35553093	HepG2	liver:	n/a	chr2:35552925-35552936
23	CEBPB	chr2:35451298-35451471	HepG2	liver:	n/a	chr2:35451382-35451393
24	CHD2	chr2:35453824-35453831	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr2:35505168-35505188	GM20000	blood:	n/a	n/a
26	CTCF	chr2:35568301-35568509	HepG2	liver:	n/a	n/a
27	CTCF	chr2:35568340-35568490	HRE	kidney:	n/a	n/a
28	CTCF	chr2:35568380-35568530	HVMF	connective:	n/a	n/a
29	CTCF	chr2:35568320-35568470	GM12867	blood:	n/a	n/a
30	CTCF	chr2:35568080-35568230	GM12869	blood:	n/a	n/a
31	CTCF	chr2:35517252-35517320	MCF-7	breast:	n/a	n/a
32	CTCF	chr2:35568976-35569015	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr2:35568320-35568470	HepG2	liver:	n/a	n/a
34	CTCF	chr2:35568360-35568510	RPTEC	kidney:	n/a	n/a
35	CTCF	chr2:35568323-35568530	LNCaP	prostate:	n/a	n/a
36	CTCF	chr2:35568322-35568505	K562	blood:	n/a	n/a
37	CTCF	chr2:35568186-35568573	A549	lung:	n/a	n/a
38	CTCF	chr2:35568225-35568588	GM12878	blood:	n/a	n/a
39	CTCF	chr2:35568300-35568450	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr2:35568320-35568470	GM12868	blood:	n/a	n/a
41	CTCF	chr2:35568280-35568430	GM12865	blood:	n/a	n/a
42	CTCF	chr2:35568151-35568523	MCF-7	breast:	n/a	n/a
43	CTCF	chr2:35568360-35568510	GM12865	blood:	n/a	n/a
44	CTCF	chr2:35568340-35568490	BE2_C	brain:	n/a	n/a
45	CTCF	chr2:35568175-35568527	MCF-7	breast:	n/a	n/a
46	CTCF	chr2:35568300-35568450	A549	lung:	n/a	n/a
47	CTCF	chr2:35477538-35477582	GM13976	blood:	n/a	n/a
48	CTCF	chr2:35568380-35568530	Caco-2	colon:	n/a	n/a
49	CTCF	chr2:35568300-35568450	MCF-7	breast:	n/a	n/a
50	CTCF	chr2:35568306-35568515	HUVEC	blood vessel:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:35518097-35518147	NHBE	bronchial:	n/a
2	chr2:35518097-35518147	NHBE	bronchial:	n/a
3	chr2:35518097-35518147	K562	blood:	n/a
4	chr2:35518097-35518147	PANC-1	pancreas:	n/a
5	chr2:35518097-35518147	SK-N-MC	brain:	n/a
6	chr2:35518097-35518147	SAEC	small airway:	n/a
7	chr2:35518097-35518147	ECC-1	luminal epithelium:	n/a
8	chr2:35518097-35518147	HEK293	kidney:	embryo
9	chr2:35518097-35518147	HRPEpiC	eye:	n/a
10	chr2:35518097-35518147	GM19239	blood:	n/a
11	chr2:35518097-35518147	HAEpiC	amniotic membrane:	n/a
12	chr2:35518097-35518147	SK-N-SH_RA	brain:	n/a
13	chr2:35518097-35518147	HRCEpiC	kidney:	n/a
14	chr2:35518097-35518147	GM06990	blood:	n/a
15	chr2:35518097-35518147	GM12891	blood:	n/a
16	chr2:35518097-35518147	Hela-S3	cervix:	n/a
17	chr2:35518097-35518147	AG09319	gingival:	n/a
18	chr2:35518097-35518147	Jurkat	blood:	n/a
19	chr2:35518097-35518147	GM12892	blood:	n/a
20	chr2:35518097-35518147	Hepatocyte	liver:	n/a
21	chr2:35518097-35518147	HUVEC	blood vessel:	n/a
22	chr2:35518097-35518147	PrEC	prostate:	n/a
23	chr2:35518097-35518147	SK-N-SH	brain:	n/a
24	chr2:35518097-35518147	HEEpiC	esophagus:	n/a
25	chr2:35518097-35518147	U87	brain:	n/a
26	chr2:35518097-35518147	BE2_C	brain:	n/a
27	chr2:35518097-35518147	MCF-7	breast:	n/a
28	chr2:35518097-35518147	CMK	blood:	n/a
29	chr2:35518097-35518147	GM12878	blood:	n/a
30	chr2:35518097-35518147	AG09309	skin:	n/a
31	chr2:35518097-35518147	HCT-116	colon:	n/a
32	chr2:35518097-35518147	HIPEpiC	eye:	n/a
33	chr2:35518097-35518147	NB4	blood:	n/a
34	chr2:35518097-35518147	HCF	heart:	n/a
35	chr2:35518097-35518147	AoSMC	blood vessel:	n/a
36	chr2:35518097-35518147	IMR90	lung:	fetal
37	chr2:35518097-35518147	BJ	skin:	n/a
38	chr2:35518097-35518147	PFSK-1	brain:	n/a
39	chr2:35518097-35518147	HCPEpiC	choroid plexus:	n/a
40	chr2:35518097-35518147	H1-hESC	embryonic stem cell:	embryo
41	chr2:35518097-35518147	HCM	heart:	n/a
42	chr2:35518097-35518147	NHDF-neo	bronchial:	n/a
43	chr2:35518097-35518147	SKMC	muscle:	n/a
44	chr2:35518097-35518147	ovcar-3	ovarian:	n/a
45	chr2:35518097-35518147	MCF10A-Er-Src	breast:	n/a
46	chr2:35518097-35518147	T-47D	breast:	n/a
47	chr2:35518097-35518147	NH-A	brain:	n/a
48	chr2:35518097-35518147	Caco-2	colon:	n/a
49	chr2:35518097-35518147	HepG2	liver:	n/a
50	chr2:35518097-35518147	RPTEC	kidney:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:35494459..35497337-chr2:35509045..35511917,2	MCF-7	breast:
2	chr2:35524345..35526725-chr2:35531053..35532688,2	MCF-7	breast:
3	chr2:35534253..35536153-chr2:35536523..35538995,2	MCF-7	breast:
4	chr2:35419204..35420824-chr2:35561387..35563219,2	MCF-7	breast:
5	chr2:35494459..35497337-chr2:35509045..35511917,2	MCF-7	breast:
6	chr2:35438569..35439074-chr2:35522272..35523184,2	MCF-7	breast:
7	chr2:35508463..35510186-chr2:35510352..35512886,2	K562	blood:
8	chr2:35508463..35510186-chr2:35510352..35512886,2	K562	blood:
9	chr2:35522554..35524084-chr2:35594104..35596851,2	MCF-7	breast:
10	chr2:35392713..35393658-chr2:35567942..35568821,2	MCF-7	breast:
11	chr2:35393099..35394069-chr2:35567966..35568823,5	MCF-7	breast:
12	chr2:35534253..35536153-chr2:35536523..35538995,2	MCF-7	breast:
13	chr2:35523124..35525670-chr2:35529266..35531418,2	MCF-7	breast:
14	chr2:35555522..35558497-chr2:35583892..35586551,2	MCF-7	breast:
15	chr2:35523124..35525670-chr2:35529266..35531418,2	MCF-7	breast:
16	chr2:35515834..35519983-chr2:35520328..35526264,11	MCF-7	breast:
17	chr2:35524345..35526725-chr2:35531053..35532688,2	MCF-7	breast:
18	chr2:35515834..35519983-chr2:35520328..35526264,11	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000196085	TF binding region
ENSG00000196085	CpG island

Extended variants
information (count: 1757 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1757 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs137989589	chr2:35447552-35447553	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs116515881	chr2:35447554-35447555	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs565098224	chr2:35447568-35447569	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs368520933	chr2:35447582-35447583	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs527523346	chr2:35447593-35447594	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs538265149	chr2:35447599-35447600	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs6707443	chr2:35447634-35447635	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs374162763	chr2:35447651-35447652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567053425	chr2:35447661-35447662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529726788	chr2:35447670-35447671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372868503	chr2:35447677-35447678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569501417	chr2:35447686-35447687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538537761	chr2:35447732-35447733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12621205	chr2:35447736-35447737	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs113944390	chr2:35447743-35447744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369925389	chr2:35447766-35447767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181068029	chr2:35447788-35447789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574195550	chr2:35447797-35447798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531011948	chr2:35448230-35448231	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs4144053	chr2:35448243-35448244	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs534459781	chr2:35448265-35448266	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs189525248	chr2:35448279-35448280	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs565101384	chr2:35448294-35448295	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs567814910	chr2:35448316-35448317	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs12468540	chr2:35448317-35448318	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs541097256	chr2:35448363-35448364	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs559697834	chr2:35448366-35448367	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs180869036	chr2:35448371-35448372	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs17327201	chr2:35448384-35448385	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs565957316	chr2:35448396-35448397	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs375695980	chr2:35448401-35448402	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs572027014	chr2:35448460-35448461	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs529703668	chr2:35448535-35448536	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs540879020	chr2:35448599-35448600	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs558552518	chr2:35448975-35448976	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs572066135	chr2:35449016-35449017	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs555916126	chr2:35449026-35449027	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs4670456	chr2:35449028-35449029	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs554486764	chr2:35449044-35449045	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs371494888	chr2:35449051-35449052	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs11885727	chr2:35449053-35449054	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs547121204	chr2:35449113-35449114	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs72872610	chr2:35449115-35449116	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs563462010	chr2:35449153-35449154	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs558201605	chr2:35449158-35449159	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs576885900	chr2:35449190-35449191	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs374787969	chr2:35449207-35449208	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs545835004	chr2:35449219-35449220	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs143865575	chr2:35449223-35449224	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs567798476	chr2:35449231-35449232	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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	21293372	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:35445800-35447800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:35452200-35452400	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr2:35452200-35452600	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr2:35452200-35454800	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr2:35452400-35453400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr2:35452400-35454800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr2:35452600-35453000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr2:35452600-35454600	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr2:35453000-35453400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr2:35453000-35454000	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr2:35453200-35453800	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr2:35453200-35454400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr2:35453400-35453600	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr2:35453400-35453600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr2:35453400-35454000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
16	chr2:35453600-35453800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr2:35453600-35454000	Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr2:35453800-35454000	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr2:35453800-35454200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
20	chr2:35454000-35454200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr2:35454000-35454400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr2:35454000-35454400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr2:35454000-35454400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr2:35454000-35457400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr2:35454200-35455200	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr2:35454200-35455600	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr2:35454400-35454600	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr2:35454800-35455800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr2:35455600-35458000	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr2:35456000-35456200	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr2:35456000-35456200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr2:35457400-35458600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr2:35457600-35458000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr2:35472200-35474600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr2:35499000-35499200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr2:35510200-35511400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:35517200-35518200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr2:35517400-35517800	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr2:35517800-35518000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr2:35517800-35518200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr2:35517800-35518600	Enhancers	H1 Cell Line	embryonic stem cell
42	chr2:35517800-35518600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr2:35517800-35518600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr2:35518000-35518200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr2:35518000-35518400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr2:35518000-35518800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr2:35518200-35518400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr2:35518200-35518800	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr2:35518200-35519000	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr2:35518200-35519400	Enhancers	HUES48 Cell Line	embryonic stem cell

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