Variant report

Variant	nsv874994
Chromosome Location	chr2:126794403-127056534
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:643)
CpG islands
(count:61)
Chromatin interactive
region (count:37)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:643 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:126988167-126988210	K562	blood:	n/a	n/a
2	BHLHE40	chr2:126814395-126814436	GM12878	blood:	n/a	n/a
3	BHLHE40	chr2:127033610-127033850	K562	blood:	n/a	n/a
4	CCNT2	chr2:126979227-126979431	K562	blood:	n/a	n/a
5	CCNT2	chr2:126799836-126800164	K562	blood:	n/a	n/a
6	CEBPB	chr2:127032685-127033063	K562	blood:	n/a	n/a
7	CEBPB	chr2:126832450-126832523	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:126965984-126966195	K562	blood:	n/a	chr2:126966076-126966087
9	CEBPB	chr2:127020627-127020908	HepG2	liver:	n/a	chr2:127020777-127020788
10	CEBPB	chr2:126965925-126966248	HepG2	liver:	n/a	chr2:126966076-126966087
11	CEBPB	chr2:127032720-127033055	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:126972867-126972872	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:126818093-126818256	H1-hESC	embryonic stem cell:	n/a	chr2:126818138-126818149
14	CEBPB	chr2:127030099-127030156	HepG2	liver:	n/a	chr2:127030107-127030119
15	CEBPB	chr2:127032739-127032956	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr2:127032653-127033111	K562	blood:	n/a	n/a
17	CEBPB	chr2:127026003-127026347	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr2:127032728-127033056	K562	blood:	n/a	n/a
19	CEBPB	chr2:127038381-127038408	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr2:126867460-126867667	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:126894241-126894539	IMR90	lung:	n/a	chr2:126894387-126894398
22	CEBPB	chr2:126812345-126812628	IMR90	lung:	n/a	n/a
23	CEBPB	chr2:126894239-126894498	HepG2	liver:	n/a	chr2:126894387-126894398
24	CEBPB	chr2:126894293-126894471	K562	blood:	n/a	chr2:126894387-126894398
25	CEBPB	chr2:126817998-126818291	HepG2	liver:	n/a	chr2:126818138-126818149
26	CEBPB	chr2:127032787-127033015	A549	lung:	n/a	n/a
27	CEBPB	chr2:126965950-126966118	H1-hESC	embryonic stem cell:	n/a	chr2:126966076-126966087
28	CEBPD	chr2:126979063-126979398	K562	blood:	n/a	n/a
29	CEBPD	chr2:127032778-127033087	K562	blood:	n/a	n/a
30	CEBPD	chr2:126979021-126979484	K562	blood:	n/a	n/a
31	CEBPZ	chr2:126985079-126985087	HepG2	liver:	n/a	n/a
32	CHD1	chr2:126963599-126963613	GM12878	blood:	n/a	n/a
33	CHD2	chr2:127002698-127002740	HepG2	liver:	n/a	n/a
34	CTCF	chr2:127002605-127002851	MCF-7	breast:	n/a	n/a
35	CTCF	chr2:126984920-126985070	Caco-2	colon:	n/a	n/a
36	CTCF	chr2:126984900-126985050	K562	blood:	n/a	n/a
37	CTCF	chr2:126881595-126881728	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr2:126984940-126985090	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr2:126984920-126985070	HepG2	liver:	n/a	n/a
40	CTCF	chr2:126984900-126985050	GM12866	blood:	n/a	n/a
41	CTCF	chr2:127002680-127002830	HCT-116	colon:	n/a	n/a
42	CTCF	chr2:126841580-126841730	WI-38	lung:	n/a	n/a
43	CTCF	chr2:127002620-127002770	A549	lung:	n/a	n/a
44	CTCF	chr2:126863737-126863749	Fibrobl	skin:	n/a	n/a
45	CTCF	chr2:126984920-126985070	HVMF	connective:	n/a	n/a
46	CTCF	chr2:126984940-126985090	GM12867	blood:	n/a	n/a
47	CTCF	chr2:127002535-127002877	K562	blood:	n/a	n/a
48	CTCF	chr2:126984920-126985070	GM12871	blood:	n/a	n/a
49	CTCF	chr2:126984940-126985090	GM12868	blood:	n/a	n/a
50	CTCF	chr2:126984940-126985090	WERI-Rb-1	eye:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:126874175-126874225	SK-N-SH	brain:	n/a
2	chr2:126874175-126874225	HEK293	kidney:	embryo
3	chr2:126874175-126874225	SAEC	small airway:	n/a
4	chr2:126874175-126874225	GM12891	blood:	n/a
5	chr2:126874175-126874225	NHDF-neo	bronchial:	n/a
6	chr2:126874175-126874225	T-47D	breast:	n/a
7	chr2:126874175-126874225	NHBE	bronchial:	n/a
8	chr2:126874175-126874225	AG04450	lung:	fetal
9	chr2:126874175-126874225	PrEC	prostate:	n/a
10	chr2:126874175-126874225	HEEpiC	esophagus:	n/a
11	chr2:126874175-126874225	ProgFib	skin:	n/a
12	chr2:126874175-126874225	HCPEpiC	choroid plexus:	n/a
13	chr2:126874175-126874225	MCF-7	breast:	n/a
14	chr2:126874175-126874225	CMK	blood:	n/a
15	chr2:126874175-126874225	K562	blood:	n/a
16	chr2:126874175-126874225	LNCaP	prostate:	n/a
17	chr2:126874175-126874225	AG10803	skin:	n/a
18	chr2:126874175-126874225	HL-60	blood:	n/a
19	chr2:126874175-126874225	HUVEC	blood vessel:	n/a
20	chr2:126874175-126874225	HRE	kidney:	n/a
21	chr2:126874175-126874225	PANC-1	pancreas:	n/a
22	chr2:126874175-126874225	HCM	heart:	n/a
23	chr2:126874175-126874225	Hela-S3	cervix:	n/a
24	chr2:126874175-126874225	Hepatocyte	liver:	n/a
25	chr2:126874175-126874225	H1-hESC	embryonic stem cell:	embryo
26	chr2:126874175-126874225	HCT-116	colon:	n/a
27	chr2:126874175-126874225	Caco-2	colon:	n/a
28	chr2:126874175-126874225	AG09319	gingival:	n/a
29	chr2:126874175-126874225	A549	lung:	n/a
30	chr2:126874175-126874225	HAEpiC	amniotic membrane:	n/a
31	chr2:126874175-126874225	HRCEpiC	kidney:	n/a
32	chr2:126874175-126874225	GM12892	blood:	n/a
33	chr2:126874175-126874225	GM12878	blood:	n/a
34	chr2:126874175-126874225	NT2-D1	testis:	n/a
35	chr2:126874175-126874225	SK-N-MC	brain:	n/a
36	chr2:126874175-126874225	HPAEpiC	pulmonary alveolar:	n/a
37	chr2:126874175-126874225	SK-N-SH_RA	brain:	n/a
38	chr2:126874175-126874225	HIPEpiC	eye:	n/a
39	chr2:126874175-126874225	SKMC	muscle:	n/a
40	chr2:126874175-126874225	HepG2	liver:	n/a
41	chr2:126874175-126874225	GM06990	blood:	n/a
42	chr2:126874175-126874225	HRPEpiC	eye:	n/a
43	chr2:126874175-126874225	PFSK-1	brain:	n/a
44	chr2:126874175-126874225	MCF10A-Er-Src	breast:	n/a
45	chr2:126874175-126874225	BE2_C	brain:	n/a
46	chr2:126874175-126874225	HNPCEpiC	eye:	n/a
47	chr2:126874175-126874225	ovcar-3	ovarian:	n/a
48	chr2:126874175-126874225	NH-A	brain:	n/a
49	chr2:126874175-126874225	NB4	blood:	n/a
50	chr2:126874175-126874225	GM19239	blood:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:127002488..127003146-chr2:127240428..127241073,2	K562	blood:
2	chr2:127047489..127050410-chr2:127061477..127063111,3	K562	blood:
3	chr2:127027671..127029245-chr2:127034455..127036337,2	K562	blood:
4	chr2:127047834..127050586-chr2:127064392..127067288,3	K562	blood:
5	chr2:127048911..127050723-chr2:127064487..127067288,2	K562	blood:
6	chr2:126952183..126952703-chr9:94896143..94896774,2	MCF-7	breast:
7	chr2:126502797..126503723-chr2:127002290..127003108,2	MCF-7	breast:
8	chr2:127005924..127008963-chr2:127010494..127013764,3	K562	blood:
9	chr2:127049240..127051434-chr2:127053138..127056030,2	K562	blood:
10	chr2:127027819..127029825-chr2:127044636..127047534,2	K562	blood:
11	chr2:127022733..127024721-chr2:127064398..127066092,2	K562	blood:
12	chr2:126943914..126946210-chr2:126970364..126971921,2	K562	blood:
13	chr2:127000756..127002293-chr2:127004018..127005768,2	MCF-7	breast:
14	chr2:127027458..127030124-chr2:127074150..127076122,2	K562	blood:
15	chr2:127040484..127043318-chr2:127048128..127049666,2	K562	blood:
16	chr2:126943914..126946210-chr2:126970364..126971921,2	K562	blood:
17	chr2:127041438..127045671-chr2:127046702..127049174,3	K562	blood:
18	chr2:126944838..126946720-chr2:126951819..126954117,2	K562	blood:
19	chr2:126944838..126946720-chr2:126951819..126954117,2	K562	blood:
20	chr2:127002510..127003198-chr2:127534689..127535540,2	MCF-7	breast:
21	chr2:127047421..127050381-chr2:127057655..127059904,2	K562	blood:
22	chr2:127005924..127008963-chr2:127010494..127013764,3	K562	blood:
23	chr2:127005363..127007196-chr2:127065380..127068265,2	K562	blood:
24	chr2:127041438..127045671-chr2:127046702..127049174,3	K562	blood:
25	chr2:127002261..127003206-chr2:127534544..127535568,4	MCF-7	breast:
26	chr2:127009698..127011900-chr2:127012722..127015678,2	MCF-7	breast:
27	chr2:126788578..126790549-chr2:126792869..126795586,2	K562	blood:
28	chr2:127027671..127029245-chr2:127034455..127036337,2	K562	blood:
29	chr2:127002328..127003186-chr2:127807433..127808421,2	K562	blood:
30	chr2:127000756..127002293-chr2:127004018..127005768,2	MCF-7	breast:
31	chr2:127027819..127029825-chr2:127044636..127047534,2	K562	blood:
32	chr1:112162320..112163164-chr2:126989298..126989817,2	Hela-S3	cervix:
33	chr2:127049240..127051434-chr2:127053138..127056030,2	K562	blood:
34	chr2:127048776..127051434-chr2:127053138..127055273,2	K562	blood:
35	chr2:127048776..127051434-chr2:127053138..127055273,2	K562	blood:
36	chr2:127009698..127011900-chr2:127012722..127015678,2	MCF-7	breast:
37	chr2:127040484..127043318-chr2:127048128..127049666,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BIN1-2	chr2:126871594-126871704	XLOC_002308
2	lnc-BIN1-2	chr2:126875500-126875562	XLOC_002308
3	lnc-BIN1-2	chr2:126870510-126870747	XLOC_002308
4	lnc-BIN1-2	chr2:126867676-126867887	XLOC_002308

No data

Variant related genes	Relation type
ENSG00000226813	TF binding region
ENSG00000226813	CpG island
ENSG00000235774	chromatin interactions
ENSG00000116473	chromatin interactions

Extended variants
information (count: 3992 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:3992 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7581039	chr2:126794403-126794404	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372489545	chr2:126794430-126794431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576517016	chr2:126794797-126794798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545434187	chr2:126794840-126794841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs114683654	chr2:126794843-126794844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs180928770	chr2:126794865-126794866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542169770	chr2:126794886-126794887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562377012	chr2:126794891-126794892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527914687	chr2:126794896-126794897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138056798	chr2:126794915-126794916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376763527	chr2:126794943-126794944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575287100	chr2:126794970-126794971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564610084	chr2:126794974-126794975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141750174	chr2:126794986-126794987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545007206	chr2:126795005-126795006	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550199255	chr2:126795021-126795022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554921651	chr2:126795037-126795038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574814642	chr2:126795056-126795057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569957789	chr2:126795063-126795064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529251220	chr2:126795081-126795082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548211987	chr2:126795082-126795083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568325322	chr2:126795142-126795143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185812051	chr2:126795143-126795144	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553544215	chr2:126795150-126795151	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570259663	chr2:126795200-126795201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191503319	chr2:126795250-126795251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371075994	chr2:126795353-126795354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147096239	chr2:126795356-126795357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs575968690	chr2:126795381-126795382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs72862434	chr2:126795393-126795394	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs148162935	chr2:126795398-126795399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530550955	chr2:126795415-126795416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs17695513	chr2:126795430-126795431	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs377378584	chr2:126795551-126795552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs141982292	chr2:126795583-126795584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150698944	chr2:126795643-126795644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138677486	chr2:126795666-126795667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs141964820	chr2:126795667-126795668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182895835	chr2:126795673-126795674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549346002	chr2:126795680-126795681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561690250	chr2:126795707-126795708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529454482	chr2:126795735-126795736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185998950	chr2:126795740-126795741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190463648	chr2:126795788-126795789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs72862436	chr2:126795789-126795790	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs541775268	chr2:126795790-126795791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146329844	chr2:126795872-126795873	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs532346909	chr2:126795888-126795889	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544377479	chr2:126795889-126795890	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139649977	chr2:126795900-126795901	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Mental retardation	17621639	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Medulloblastoma	16968546	CNVD
Neurocytoma	17123091	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:178 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:126794000-126795200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr2:126794400-126795800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr2:126794800-126795800	Enhancers	Primary hematopoietic stem cells	blood
4	chr2:126795200-126797400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr2:126795600-126796200	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr2:126795800-126796200	Flanking Active TSS	Primary hematopoietic stem cells	blood
7	chr2:126795800-126796400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr2:126795800-126797400	Enhancers	Fetal Heart	heart
9	chr2:126796000-126797200	Enhancers	Primary B cells from cord blood	blood
10	chr2:126796200-126797200	Enhancers	Primary B cells from peripheral blood	blood
11	chr2:126796200-126797200	Enhancers	Primary hematopoietic stem cells	blood
12	chr2:126796400-126797200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr2:126797200-126798400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr2:126797400-126799000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr2:126798400-126800000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr2:126799000-126799400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr2:126799000-126799400	Enhancers	Brain Germinal Matrix	brain
18	chr2:126799000-126800000	Enhancers	Liver	Liver
19	chr2:126806400-126807200	Enhancers	Liver	Liver
20	chr2:126807200-126807400	Weak transcription	Liver	Liver
21	chr2:126807400-126809800	ZNF genes & repeats	Liver	Liver
22	chr2:126816400-126817200	Enhancers	H9 Cell Line	embryonic stem cell
23	chr2:126816400-126817200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr2:126816400-126817400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr2:126816400-126817400	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr2:126816400-126817400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr2:126816400-126817800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr2:126816600-126818000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr2:126816800-126817200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr2:126816800-126817800	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr2:126817000-126817400	Enhancers	H1 Cell Line	embryonic stem cell
32	chr2:126817200-126821800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr2:126817400-126817800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr2:126817400-126821400	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr2:126817800-126818600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr2:126821400-126821600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
37	chr2:126821800-126822000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr2:126821800-126822000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
39	chr2:126829600-126830000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr2:126834800-126835800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr2:126839000-126850400	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr2:126842400-126842800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr2:126842400-126843000	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr2:126842600-126843000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr2:126855000-126855400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr2:126863400-126863800	ZNF genes & repeats	Pancreas	Pancrea
47	chr2:126863600-126863800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr2:126863600-126863800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
49	chr2:126873000-126874200	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr2:126873200-126874000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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