Variant report

Variant	nsv875590
Chromosome Location	chr2:188471271-188690187
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:821)
CpG islands
(count:244)
Chromatin interactive
region (count:44)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:821 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:188684551-188684613	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:188513230-188513415	K562	blood:	n/a	n/a
3	ATF1	chr2:188633855-188634067	K562	blood:	n/a	n/a
4	ATF1	chr2:188551050-188551187	K562	blood:	n/a	n/a
5	ATF1	chr2:188558759-188558891	K562	blood:	n/a	n/a
6	BACH1	chr2:188689902-188690134	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr2:188647107-188647253	K562	blood:	n/a	n/a
8	BHLHE40	chr2:188521903-188522037	K562	blood:	n/a	n/a
9	BHLHE40	chr2:188639528-188639589	GM12878	blood:	n/a	n/a
10	CBX3	chr2:188505670-188506206	K562	blood:	n/a	n/a
11	CCNT2	chr2:188671617-188671704	K562	blood:	n/a	n/a
12	CCNT2	chr2:188505985-188506183	K562	blood:	n/a	n/a
13	CEBPB	chr2:188648876-188649229	IMR90	lung:	n/a	chr2:188649052-188649063
14	CEBPB	chr2:188479434-188479634	A549	lung:	n/a	n/a
15	CEBPB	chr2:188648988-188649117	Hela-S3	cervix:	n/a	chr2:188649052-188649063
16	CEBPB	chr2:188481819-188482019	IMR90	lung:	n/a	n/a
17	CEBPB	chr2:188581048-188581245	A549	lung:	n/a	n/a
18	CEBPB	chr2:188659234-188659471	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:188608641-188608753	K562	blood:	n/a	chr2:188608676-188608687
20	CEBPB	chr2:188473851-188474022	A549	lung:	n/a	n/a
21	CEBPB	chr2:188626594-188626733	A549	lung:	n/a	n/a
22	CEBPB	chr2:188480117-188480126	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:188481870-188482145	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr2:188553978-188554022	A549	lung:	n/a	n/a
25	CEBPB	chr2:188608570-188608763	IMR90	lung:	n/a	chr2:188608676-188608687
26	CEBPB	chr2:188648982-188649119	K562	blood:	n/a	chr2:188649052-188649063
27	CEBPB	chr2:188481903-188482085	K562	blood:	n/a	n/a
28	CEBPB	chr2:188479419-188479729	IMR90	lung:	n/a	n/a
29	CEBPB	chr2:188649012-188649117	H1-hESC	embryonic stem cell:	n/a	chr2:188649052-188649063
30	CEBPB	chr2:188648874-188649234	HepG2	liver:	n/a	chr2:188649052-188649063
31	CEBPB	chr2:188656420-188656432	HepG2	liver:	n/a	n/a
32	CEBPB	chr2:188683622-188683880	HepG2	liver:	n/a	chr2:188683751-188683762
33	CEBPB	chr2:188608563-188608828	HepG2	liver:	n/a	chr2:188608676-188608687
34	CEBPB	chr2:188659239-188659491	A549	lung:	n/a	n/a
35	CEBPB	chr2:188659268-188659401	K562	blood:	n/a	n/a
36	CEBPB	chr2:188657288-188657534	HepG2	liver:	n/a	chr2:188657412-188657423
37	CEBPB	chr2:188648886-188649231	A549	lung:	n/a	chr2:188649052-188649063
38	CEBPB	chr2:188481857-188482003	A549	lung:	n/a	n/a
39	CEBPB	chr2:188479419-188479749	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr2:188523720-188523870	GM12865	blood:	n/a	n/a
41	CTCF	chr2:188648260-188648410	AG04449	skin:	n/a	n/a
42	CTCF	chr2:188523703-188524040	Gliobla	brain:	n/a	n/a
43	CTCF	chr2:188648300-188648450	MCF-7	breast:	n/a	n/a
44	CTCF	chr2:188523800-188523950	GM12868	blood:	n/a	n/a
45	CTCF	chr2:188480229-188480317	GM19239	blood:	n/a	n/a
46	CTCF	chr2:188523760-188523910	HCFaa	heart:	n/a	n/a
47	CTCF	chr2:188523760-188523910	GM12875	blood:	n/a	n/a
48	CTCF	chr2:188523740-188523890	GM12872	blood:	n/a	n/a
49	CTCF	chr2:188648338-188648408	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr2:188648290-188648449	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:188583082-188583132	HCF	heart:	n/a
2	chr2:188583082-188583132	AG04449	skin:	fetal
3	chr2:188481707-188481757	HCPEpiC	choroid plexus:	n/a
4	chr2:188689981-188690031	AG04450	lung:	fetal
5	chr2:188483530-188483580	SK-N-MC	brain:	n/a
6	chr2:188583082-188583132	HCT-116	colon:	n/a
7	chr2:188689981-188690031	HEK293	kidney:	embryo
8	chr2:188689981-188690031	LNCaP	prostate:	n/a
9	chr2:188481707-188481757	HEK293	kidney:	embryo
10	chr2:188481707-188481757	H1-hESC	embryonic stem cell:	embryo
11	chr2:188583082-188583132	PFSK-1	brain:	n/a
12	chr2:188481707-188481757	ovcar-3	ovarian:	n/a
13	chr2:188583082-188583132	NB4	blood:	n/a
14	chr2:188483530-188483580	ProgFib	skin:	n/a
15	chr2:188689981-188690031	AG04449	skin:	fetal
16	chr2:188481707-188481757	MCF-7	breast:	n/a
17	chr2:188481707-188481757	NHDF-neo	bronchial:	n/a
18	chr2:188481707-188481757	IMR90	lung:	fetal
19	chr2:188481707-188481757	A549	lung:	n/a
20	chr2:188481707-188481757	BE2_C	brain:	n/a
21	chr2:188689981-188690031	MCF10A-Er-Src	breast:	n/a
22	chr2:188689981-188690031	ProgFib	skin:	n/a
23	chr2:188583082-188583132	MCF10A-Er-Src	breast:	n/a
24	chr2:188481707-188481757	BJ	skin:	n/a
25	chr2:188481707-188481757	AG09309	skin:	n/a
26	chr2:188689981-188690031	MCF-7	breast:	n/a
27	chr2:188583082-188583132	HCM	heart:	n/a
28	chr2:188583082-188583132	HPAEpiC	pulmonary alveolar:	n/a
29	chr2:188583082-188583132	GM12892	blood:	n/a
30	chr2:188481707-188481757	Hepatocyte	liver:	n/a
31	chr2:188689981-188690031	HCF	heart:	n/a
32	chr2:188583082-188583132	AG04450	lung:	fetal
33	chr2:188483530-188483580	AG04449	skin:	fetal
34	chr2:188689981-188690031	PrEC	prostate:	n/a
35	chr2:188481707-188481757	U87	brain:	n/a
36	chr2:188583082-188583132	AG09319	gingival:	n/a
37	chr2:188481707-188481757	GM12878	blood:	n/a
38	chr2:188689981-188690031	RPTEC	kidney:	n/a
39	chr2:188483530-188483580	HPAEpiC	pulmonary alveolar:	n/a
40	chr2:188481707-188481757	GM19239	blood:	n/a
41	chr2:188689981-188690031	HNPCEpiC	eye:	n/a
42	chr2:188481707-188481757	SKMC	muscle:	n/a
43	chr2:188481707-188481757	HL-60	blood:	n/a
44	chr2:188583082-188583132	ovcar-3	ovarian:	n/a
45	chr2:188483530-188483580	HRPEpiC	eye:	n/a
46	chr2:188689981-188690031	HCPEpiC	choroid plexus:	n/a
47	chr2:188689981-188690031	GM19239	blood:	n/a
48	chr2:188583082-188583132	AoSMC	blood vessel:	n/a
49	chr2:188483530-188483580	HCPEpiC	choroid plexus:	n/a
50	chr2:188481707-188481757	PrEC	prostate:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:188506449..188508323-chr2:188511407..188513734,2	K562	blood:
2	chr2:188544173..188545945-chr2:188547538..188549082,2	K562	blood:
3	chr2:188668614..188671113-chr2:188671408..188674313,2	K562	blood:
4	chr2:188601766..188603906-chr2:188606320..188608826,2	K562	blood:
5	chr2:188473583..188475657-chr2:188480041..188481763,2	K562	blood:
6	chr2:188523368..188524314-chr2:188579524..188580267,2	K562	blood:
7	chr2:188581473..188583744-chr2:188592833..188595412,2	MCF-7	breast:
8	chr2:188478443..188481336-chr2:188482033..188484662,2	K562	blood:
9	chr2:188506449..188508323-chr2:188511407..188513734,2	K562	blood:
10	chr2:188467603..188470192-chr2:188473529..188476139,3	K562	blood:
11	chr2:188480199..188482146-chr2:188486058..188487606,2	K562	blood:
12	chr2:188478443..188481336-chr2:188482033..188484662,2	K562	blood:
13	chr2:188604449..188606812-chr2:188608184..188609837,2	K562	blood:
14	chr2:188480221..188482587-chr2:188496790..188498507,2	K562	blood:
15	chr2:188549053..188550995-chr2:188552944..188555111,2	K562	blood:
16	chr2:188473165..188475172-chr2:188477640..188480014,2	K562	blood:
17	chr2:188601026..188603906-chr2:188607326..188609061,2	K562	blood:
18	chr2:188473583..188475657-chr2:188480041..188481763,2	K562	blood:
19	chr2:188523368..188524314-chr2:188579524..188580267,2	K562	blood:
20	chr2:188460269..188463083-chr2:188643990..188646491,2	K562	blood:
21	chr2:188478254..188481614-chr2:188483978..188486883,3	K562	blood:
22	chr2:188630653..188632661-chr2:188633986..188636856,2	K562	blood:
23	chr2:188478254..188481614-chr2:188483978..188486883,3	K562	blood:
24	chr2:188560452..188562867-chr2:188563141..188566315,4	K562	blood:
25	chr2:188480199..188482146-chr2:188486058..188487606,2	K562	blood:
26	chr2:188302851..188305687-chr2:188602438..188604231,2	K562	blood:
27	chr2:188549053..188550995-chr2:188552944..188555111,2	K562	blood:
28	chr2:188554226..188556067-chr2:188557220..188559283,2	K562	blood:
29	chr2:188668614..188671113-chr2:188671408..188674313,2	K562	blood:
30	chr2:188506973..188509886-chr2:188511524..188513522,2	MCF-7	breast:
31	chr2:188554226..188556067-chr2:188557220..188559283,2	K562	blood:
32	chr2:188506973..188509886-chr2:188511524..188513522,2	MCF-7	breast:
33	chr2:188634121..188636479-chr2:188637228..188640007,2	K562	blood:
34	chr2:188581473..188583744-chr2:188592833..188595412,2	MCF-7	breast:
35	chr2:188634121..188636479-chr2:188637228..188640007,2	K562	blood:
36	chr2:188544173..188545945-chr2:188547538..188549082,2	K562	blood:
37	chr2:188480221..188482587-chr2:188496790..188498507,2	K562	blood:
38	chr2:188473165..188475172-chr2:188477640..188480014,2	K562	blood:
39	chr2:188523465..188524329-chr2:188707490..188708173,2	MCF-7	breast:
40	chr2:188591288..188593045-chr2:188603697..188606410,2	K562	blood:
41	chr2:188560452..188562867-chr2:188563141..188566315,4	K562	blood:
42	chr2:188591288..188593045-chr2:188603697..188606410,2	K562	blood:
43	chr2:188630653..188632661-chr2:188633986..188636856,2	K562	blood:
44	chr2:188604449..188606812-chr2:188608184..188609837,2	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
ENSG00000252004	chromatin interactions

Extended variants
information (count: 5883 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:5883 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561786618	chr2:188478001-188478002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs114287770	chr2:188478021-188478022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141857571	chr2:188478032-188478033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs13013074	chr2:188478070-188478071	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs533724948	chr2:188478078-188478079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551797607	chr2:188478103-188478104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566220882	chr2:188478115-188478116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs567106795	chr2:188478116-188478117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368345484	chr2:188478118-188478119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527903305	chr2:188478147-188478148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549132442	chr2:188478193-188478194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs184028950	chr2:188478239-188478240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372075160	chr2:188478278-188478279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78400784	chr2:188478338-188478339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs533785461	chr2:188478343-188478344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556185212	chr2:188478391-188478392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571541998	chr2:188478392-188478393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs367986382	chr2:188478498-188478499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187975468	chr2:188478527-188478528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558720703	chr2:188478556-188478557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549590461	chr2:188478598-188478599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201477194	chr2:188478610-188478611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140302201	chr2:188478612-188478613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs77746473	chr2:188478613-188478614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs67999212	chr2:188478614-188478615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538161070	chr2:188478651-188478652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528110333	chr2:188478680-188478681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573062925	chr2:188478692-188478693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540440894	chr2:188478809-188478810	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375178282	chr2:188478855-188478856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10191560	chr2:188478906-188478907	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs573829007	chr2:188478943-188478944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181017852	chr2:188478950-188478951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186223235	chr2:188478961-188478962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10167734	chr2:188479037-188479038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561698069	chr2:188479089-188479090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574916390	chr2:188479168-188479169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532793466	chr2:188479202-188479203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190775946	chr2:188479250-188479251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116320938	chr2:188479293-188479294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538326213	chr2:188479302-188479303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs76111464	chr2:188479303-188479304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549191747	chr2:188479307-188479308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs143748506	chr2:188479312-188479313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545899817	chr2:188479414-188479415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs151093867	chr2:188479444-188479445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs549870019	chr2:188479456-188479457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181654961	chr2:188479489-188479490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186852369	chr2:188479529-188479530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545933577	chr2:188479552-188479553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

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	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:188478000-188478200	Enhancers	Muscle Satellite Cultured Cells	--
2	chr2:188478200-188479400	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr2:188478800-188479200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:188479200-188482800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:188479400-188480000	Enhancers	Muscle Satellite Cultured Cells	--
6	chr2:188479400-188480000	Enhancers	Fetal Lung	lung
7	chr2:188479400-188480200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr2:188479400-188480400	Enhancers	HSMM	muscle
9	chr2:188479400-188480600	Enhancers	HSMMtube	muscle
10	chr2:188479400-188484200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr2:188479400-188485200	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr2:188479400-188485400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr2:188479600-188480200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr2:188479600-188480400	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr2:188479800-188480200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr2:188479800-188480600	Enhancers	Fetal Kidney	kidney
17	chr2:188479800-188483600	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr2:188480000-188480400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr2:188480000-188480400	Enhancers	Ovary	ovary
20	chr2:188480000-188480800	Enhancers	H9 Cell Line	embryonic stem cell
21	chr2:188480000-188480800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr2:188480000-188481000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr2:188480000-188482600	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr2:188480200-188481000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr2:188480200-188481200	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr2:188480200-188483400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr2:188480200-188484200	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr2:188480400-188480600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr2:188480400-188482000	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr2:188480400-188482200	Weak transcription	HSMM	muscle
31	chr2:188480400-188482600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr2:188480400-188483200	Weak transcription	Ovary	ovary
33	chr2:188480400-188484400	Enhancers	Brain Germinal Matrix	brain
34	chr2:188480600-188482600	Weak transcription	HSMMtube	muscle
35	chr2:188480600-188483800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr2:188480800-188481000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr2:188480800-188481800	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr2:188480800-188482200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr2:188481000-188482000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr2:188481000-188482200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr2:188481000-188482800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr2:188481200-188481600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr2:188481600-188484600	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr2:188481800-188483000	Enhancers	H9 Cell Line	embryonic stem cell
45	chr2:188481800-188483200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr2:188482000-188483000	Enhancers	H1 Cell Line	embryonic stem cell
47	chr2:188482000-188483000	Enhancers	Brain Cingulate Gyrus	brain
48	chr2:188482000-188483000	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr2:188482000-188483400	Enhancers	Brain Angular Gyrus	brain
50	chr2:188482000-188483400	Enhancers	Brain Inferior Temporal Lobe	brain

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