Variant report

Variant	nsv536086
Chromosome Location	chr2:188574612-188758772
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:713)
CpG islands
(count:183)
Chromatin interactive
region (count:39)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:713 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:188707985-188708297	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:188729881-188730106	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:188684551-188684613	HepG2	liver:	n/a	n/a
4	ATF1	chr2:188633855-188634067	K562	blood:	n/a	n/a
5	BACH1	chr2:188689902-188690134	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:188647107-188647253	K562	blood:	n/a	n/a
7	BATF	chr2:188733916-188734173	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:188639528-188639589	GM12878	blood:	n/a	n/a
9	CCNT2	chr2:188671617-188671704	K562	blood:	n/a	n/a
10	CEBPB	chr2:188657288-188657534	HepG2	liver:	n/a	chr2:188657412-188657423
11	CEBPB	chr2:188659239-188659491	A549	lung:	n/a	n/a
12	CEBPB	chr2:188724170-188724362	HepG2	liver:	n/a	chr2:188724258-188724269
13	CEBPB	chr2:188626594-188626733	A549	lung:	n/a	n/a
14	CEBPB	chr2:188697541-188697879	K562	blood:	n/a	chr2:188697730-188697739 chr2:188697728-188697741 chr2:188697728-188697739
15	CEBPB	chr2:188648876-188649229	IMR90	lung:	n/a	chr2:188649052-188649063
16	CEBPB	chr2:188683622-188683880	HepG2	liver:	n/a	chr2:188683751-188683762
17	CEBPB	chr2:188608563-188608828	HepG2	liver:	n/a	chr2:188608676-188608687
18	CEBPB	chr2:188648874-188649234	HepG2	liver:	n/a	chr2:188649052-188649063
19	CEBPB	chr2:188691096-188691299	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr2:188659234-188659471	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:188697226-188697904	HepG2	liver:	n/a	chr2:188697730-188697739 chr2:188697728-188697741 chr2:188697728-188697739
22	CEBPB	chr2:188697561-188697865	IMR90	lung:	n/a	chr2:188697730-188697739 chr2:188697728-188697741 chr2:188697728-188697739
23	CEBPB	chr2:188649012-188649117	H1-hESC	embryonic stem cell:	n/a	chr2:188649052-188649063
24	CEBPB	chr2:188648982-188649119	K562	blood:	n/a	chr2:188649052-188649063
25	CEBPB	chr2:188581048-188581245	A549	lung:	n/a	n/a
26	CEBPB	chr2:188608570-188608763	IMR90	lung:	n/a	chr2:188608676-188608687
27	CEBPB	chr2:188608641-188608753	K562	blood:	n/a	chr2:188608676-188608687
28	CEBPB	chr2:188705494-188705694	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:188656420-188656432	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:188648886-188649231	A549	lung:	n/a	chr2:188649052-188649063
31	CEBPB	chr2:188659268-188659401	K562	blood:	n/a	n/a
32	CEBPB	chr2:188648988-188649117	Hela-S3	cervix:	n/a	chr2:188649052-188649063
33	CHD1	chr2:188707846-188708434	IMR90	lung:	n/a	n/a
34	CTCF	chr2:188708080-188708230	GM12873	blood:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
35	CTCF	chr2:188708080-188708230	HRE	kidney:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
36	CTCF	chr2:188708140-188708290	BE2_C	brain:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
37	CTCF	chr2:188648280-188648430	HAc	cerebellar:	n/a	n/a
38	CTCF	chr2:188617140-188617290	GM12865	blood:	n/a	n/a
39	CTCF	chr2:188708100-188708250	AG04450	lung:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
40	CTCF	chr2:188707961-188708338	K562	blood:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
41	CTCF	chr2:188708060-188708210	RPTEC	kidney:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
42	CTCF	chr2:188648300-188648450	SAEC	small airway:	n/a	n/a
43	CTCF	chr2:188707912-188708266	A549	lung:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
44	CTCF	chr2:188708021-188708188	SK-N-SH_RA	brain:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
45	CTCF	chr2:188648080-188648230	RPTEC	kidney:	n/a	n/a
46	CTCF	chr2:188708020-188708170	RPTEC	kidney:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
47	CTCF	chr2:188708400-188708550	GM12873	blood:	n/a	n/a
48	CTCF	chr2:188708040-188708190	NHLF	lung:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
49	CTCF	chr2:188648338-188648408	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr2:188648280-188648430	HCPEpiC	choroid plexus:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:188754840-188754890	HMEC	breast:	n/a
2	chr2:188689981-188690031	Hela-S3	cervix:	n/a
3	chr2:188754840-188754890	ECC-1	luminal epithelium:	n/a
4	chr2:188754840-188754890	HCF	heart:	n/a
5	chr2:188754840-188754890	GM06990	blood:	n/a
6	chr2:188754840-188754890	NHDF-neo	bronchial:	n/a
7	chr2:188689981-188690031	HAEpiC	amniotic membrane:	n/a
8	chr2:188583082-188583132	HNPCEpiC	eye:	n/a
9	chr2:188754840-188754890	HCT-116	colon:	n/a
10	chr2:188689981-188690031	PFSK-1	brain:	n/a
11	chr2:188689981-188690031	HUVEC	blood vessel:	n/a
12	chr2:188583082-188583132	PrEC	prostate:	n/a
13	chr2:188583082-188583132	T-47D	breast:	n/a
14	chr2:188689981-188690031	HL-60	blood:	n/a
15	chr2:188583082-188583132	PFSK-1	brain:	n/a
16	chr2:188689981-188690031	LNCaP	prostate:	n/a
17	chr2:188583082-188583132	HCPEpiC	choroid plexus:	n/a
18	chr2:188689981-188690031	AG04449	skin:	fetal
19	chr2:188583082-188583132	HepG2	liver:	n/a
20	chr2:188583082-188583132	LNCaP	prostate:	n/a
21	chr2:188583082-188583132	IMR90	lung:	fetal
22	chr2:188583082-188583132	AG09309	skin:	n/a
23	chr2:188689981-188690031	SK-N-SH	brain:	n/a
24	chr2:188583082-188583132	A549	lung:	n/a
25	chr2:188583082-188583132	NHDF-neo	bronchial:	n/a
26	chr2:188754840-188754890	HCPEpiC	choroid plexus:	n/a
27	chr2:188689981-188690031	AoSMC	blood vessel:	n/a
28	chr2:188754840-188754890	HEK293	kidney:	embryo
29	chr2:188583082-188583132	CMK	blood:	n/a
30	chr2:188754840-188754890	HNPCEpiC	eye:	n/a
31	chr2:188754840-188754890	AG10803	skin:	n/a
32	chr2:188583082-188583132	SKMC	muscle:	n/a
33	chr2:188754840-188754890	MCF-7	breast:	n/a
34	chr2:188754840-188754890	A549	lung:	n/a
35	chr2:188583082-188583132	GM12891	blood:	n/a
36	chr2:188583082-188583132	HRPEpiC	eye:	n/a
37	chr2:188583082-188583132	SK-N-SH	brain:	n/a
38	chr2:188754840-188754890	T-47D	breast:	n/a
39	chr2:188754840-188754890	ovcar-3	ovarian:	n/a
40	chr2:188689981-188690031	HRCEpiC	kidney:	n/a
41	chr2:188583082-188583132	Hepatocyte	liver:	n/a
42	chr2:188689981-188690031	AG04450	lung:	fetal
43	chr2:188689981-188690031	HCT-116	colon:	n/a
44	chr2:188754840-188754890	NH-A	brain:	n/a
45	chr2:188754840-188754890	CMK	blood:	n/a
46	chr2:188689981-188690031	SKMC	muscle:	n/a
47	chr2:188754840-188754890	BE2_C	brain:	n/a
48	chr2:188689981-188690031	HCF	heart:	n/a
49	chr2:188754840-188754890	Caco-2	colon:	n/a
50	chr2:188754840-188754890	U87	brain:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:188591288..188593045-chr2:188603697..188606410,2	K562	blood:
2	chr2:188707924..188708424-chr2:189233846..189234774,2	MCF-7	breast:
3	chr2:188634121..188636479-chr2:188637228..188640007,2	K562	blood:
4	chr2:188604449..188606812-chr2:188608184..188609837,2	K562	blood:
5	chr2:188717832..188720223-chr2:188721480..188723340,2	K562	blood:
6	chr2:188523465..188524329-chr2:188707490..188708173,2	MCF-7	breast:
7	chr2:188581473..188583744-chr2:188592833..188595412,2	MCF-7	breast:
8	chr2:188630653..188632661-chr2:188633986..188636856,2	K562	blood:
9	chr2:188604449..188606812-chr2:188608184..188609837,2	K562	blood:
10	chr2:188460269..188463083-chr2:188643990..188646491,2	K562	blood:
11	chr2:188717832..188720223-chr2:188721480..188723340,2	K562	blood:
12	chr2:188712201..188714788-chr2:189156773..189159131,2	MCF-7	breast:
13	chr2:188591288..188593045-chr2:188603697..188606410,2	K562	blood:
14	chr2:188630653..188632661-chr2:188633986..188636856,2	K562	blood:
15	chr2:188695020..188696926-chr2:188699233..188701652,2	K562	blood:
16	chr2:188668614..188671113-chr2:188671408..188674313,2	K562	blood:
17	chr2:188711161..188713691-chr2:188716532..188718506,2	MCF-7	breast:
18	chr2:188581473..188583744-chr2:188592833..188595412,2	MCF-7	breast:
19	chr2:188695020..188696926-chr2:188699233..188701652,2	K562	blood:
20	chr10:79342547..79345269-chr2:188716021..188718292,2	MCF-7	breast:
21	chr2:188704815..188707426-chr2:188716735..188719605,2	MCF-7	breast:
22	chr2:188601766..188603906-chr2:188606320..188608826,2	K562	blood:
23	chr2:188302851..188305687-chr2:188602438..188604231,2	K562	blood:
24	chr2:188711161..188713691-chr2:188716532..188718506,2	MCF-7	breast:
25	chr2:188445739..188446515-chr2:188708197..188708735,2	MCF-7	breast:
26	chr2:188523368..188524314-chr2:188579524..188580267,2	K562	blood:
27	chr2:188710121..188711814-chr2:188979120..188982025,2	MCF-7	breast:
28	chr2:188668614..188671113-chr2:188671408..188674313,2	K562	blood:
29	chr2:188364379..188365187-chr2:188708060..188708991,2	MCF-7	breast:
30	chr2:188704815..188707426-chr2:188716735..188719605,2	MCF-7	breast:
31	chr2:188747783..188749370-chr2:188752482..188755177,2	K562	blood:
32	chr2:188445783..188446859-chr2:188707667..188708674,8	MCF-7	breast:
33	chr2:188634121..188636479-chr2:188637228..188640007,2	K562	blood:
34	chr2:188364448..188365318-chr2:188707678..188708407,3	K562	blood:
35	chr2:188601026..188603906-chr2:188607326..188609061,2	K562	blood:
36	chr2:188736660..188738467-chr2:188741573..188744493,2	MCF-7	breast:
37	chr2:188707921..188708505-chr2:189376811..189377638,2	MCF-7	breast:
38	chr2:188736660..188738467-chr2:188741573..188744493,2	MCF-7	breast:
39	chr2:188747783..188749370-chr2:188752482..188755177,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DIRC1-2	chr2:188577543-188577606	ENSG00000231689

No data

Variant related genes	Relation type
ST13P2	TF binding region
ENSG00000252004	TF binding region
ST13P2	CpG island
ENSG00000252004	CpG island
ENSG00000144366	chromatin interactions
ENSG00000252004	chromatin interactions

Extended variants
information (count: 4352 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:4352 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561201575	chr2:188574626-188574627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs531746233	chr2:188574690-188574691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550250919	chr2:188574704-188574705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571645981	chr2:188574717-188574718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532678214	chr2:188574719-188574720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547657765	chr2:188574735-188574736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566289414	chr2:188574737-188574738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs57995758	chr2:188574778-188574779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs113855487	chr2:188574857-188574858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34679983	chr2:188574882-188574883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs79095137	chr2:188574920-188574921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554854689	chr2:188574969-188574970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370777385	chr2:188575022-188575023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201220197	chr2:188575031-188575032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139678004	chr2:188575032-188575033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183049419	chr2:188575048-188575049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75166436	chr2:188575055-188575056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76526961	chr2:188575056-188575057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532890060	chr2:188575091-188575092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541150008	chr2:188575108-188575109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs59373669	chr2:188575113-188575114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs114222043	chr2:188575146-188575147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79305570	chr2:188575289-188575290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542105389	chr2:188575365-188575366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563577283	chr2:188575387-188575388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530873063	chr2:188575418-188575419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201653599	chr2:188575446-188575447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543827280	chr2:188575451-188575452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200058642	chr2:188575484-188575485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369632456	chr2:188575486-188575487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565313595	chr2:188575598-188575599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532476626	chr2:188575603-188575604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547888707	chr2:188575646-188575647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187695968	chr2:188575747-188575748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547306055	chr2:188575765-188575766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530237618	chr2:188575798-188575799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548423520	chr2:188575832-188575833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs569544115	chr2:188575908-188575909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs147312669	chr2:188575916-188575917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375377721	chr2:188575953-188575954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs112174303	chr2:188575982-188575983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs149818377	chr2:188576024-188576025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369890494	chr2:188576028-188576029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570450154	chr2:188576043-188576044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs530564984	chr2:188576066-188576067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374252268	chr2:188576086-188576087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548845688	chr2:188576099-188576100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs111631253	chr2:188576161-188576162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs574500335	chr2:188576198-188576199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs10931304	chr2:188576211-188576212	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Urothelial carcinoma	21177765	CNVD
Intellectual disability	22102821	CNVD
Tetralogy of Fallot	22912587	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:188566200-188586000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:188567600-188577600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr2:188570000-188575600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr2:188574200-188579800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr2:188575600-188576200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr2:188575600-188576800	Enhancers	Fetal Lung	lung
7	chr2:188575800-188576000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr2:188576000-188577800	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr2:188576200-188577600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr2:188577400-188578000	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr2:188577600-188577800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr2:188577600-188578000	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr2:188577600-188578000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr2:188577800-188578000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr2:188577800-188578400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr2:188578000-188579800	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr2:188578000-188580000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr2:188578400-188579400	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr2:188579400-188580000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
20	chr2:188579800-188580400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
21	chr2:188579800-188580600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
22	chr2:188580000-188580600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
23	chr2:188580000-188581000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
24	chr2:188580400-188581000	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr2:188580400-188585000	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr2:188580600-188581200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr2:188580600-188582800	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr2:188580800-188581200	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr2:188581000-188581600	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr2:188581000-188583000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr2:188581000-188583400	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr2:188581200-188582000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr2:188581200-188582400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr2:188581600-188582000	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr2:188582000-188583000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr2:188582000-188584400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:188582000-188585000	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr2:188582200-188583400	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr2:188582400-188582800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr2:188582800-188583000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr2:188582800-188583400	Enhancers	H1 Cell Line	embryonic stem cell
42	chr2:188582800-188583400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr2:188583000-188583200	Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr2:188583000-188583400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr2:188583400-188584200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr2:188583400-188584400	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr2:188583400-188584400	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr2:188583400-188584400	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr2:188583400-188584600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr2:188584400-188584600	Enhancers	H1 Cell Line	embryonic stem cell

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