Variant report

Variant	nsv874995
Chromosome Location	chr2:126802800-127044904
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:600)
CpG islands
(count:62)
Chromatin interactive
region (count:26)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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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	chr2:127033610-127033850	K562	blood:	n/a	n/a
3	BHLHE40	chr2:126814395-126814436	GM12878	blood:	n/a	n/a
4	CCNT2	chr2:126979227-126979431	K562	blood:	n/a	n/a
5	CEBPB	chr2:127032787-127033015	A549	lung:	n/a	n/a
6	CEBPB	chr2:126867460-126867667	HepG2	liver:	n/a	n/a
7	CEBPB	chr2:127032720-127033055	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:126894293-126894471	K562	blood:	n/a	chr2:126894387-126894398
9	CEBPB	chr2:126965984-126966195	K562	blood:	n/a	chr2:126966076-126966087
10	CEBPB	chr2:126832450-126832523	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:127032653-127033111	K562	blood:	n/a	n/a
12	CEBPB	chr2:126812345-126812628	IMR90	lung:	n/a	n/a
13	CEBPB	chr2:127038381-127038408	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr2:127026003-127026347	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr2:126817998-126818291	HepG2	liver:	n/a	chr2:126818138-126818149
16	CEBPB	chr2:127030099-127030156	HepG2	liver:	n/a	chr2:127030107-127030119
17	CEBPB	chr2:126894239-126894498	HepG2	liver:	n/a	chr2:126894387-126894398
18	CEBPB	chr2:127020627-127020908	HepG2	liver:	n/a	chr2:127020777-127020788
19	CEBPB	chr2:127032739-127032956	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr2:126965925-126966248	HepG2	liver:	n/a	chr2:126966076-126966087
21	CEBPB	chr2:127032728-127033056	K562	blood:	n/a	n/a
22	CEBPB	chr2:126965950-126966118	H1-hESC	embryonic stem cell:	n/a	chr2:126966076-126966087
23	CEBPB	chr2:126972867-126972872	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:127032685-127033063	K562	blood:	n/a	n/a
25	CEBPB	chr2:126894241-126894539	IMR90	lung:	n/a	chr2:126894387-126894398
26	CEBPB	chr2:126818093-126818256	H1-hESC	embryonic stem cell:	n/a	chr2:126818138-126818149
27	CEBPD	chr2:126979063-126979398	K562	blood:	n/a	n/a
28	CEBPD	chr2:127032778-127033087	K562	blood:	n/a	n/a
29	CEBPD	chr2:126979021-126979484	K562	blood:	n/a	n/a
30	CEBPZ	chr2:126985079-126985087	HepG2	liver:	n/a	n/a
31	CHD1	chr2:126963599-126963613	GM12878	blood:	n/a	n/a
32	CHD2	chr2:127002698-127002740	HepG2	liver:	n/a	n/a
33	CTCF	chr2:127002476-127002907	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr2:126984860-126985010	GM12873	blood:	n/a	n/a
35	CTCF	chr2:126984915-126985084	MCF-7	breast:	n/a	n/a
36	CTCF	chr2:127002599-127002836	GM19238	blood:	n/a	n/a
37	CTCF	chr2:126984940-126985090	GM12878	blood:	n/a	n/a
38	CTCF	chr2:126984960-126985110	HepG2	liver:	n/a	n/a
39	CTCF	chr2:127002605-127002851	MCF-7	breast:	n/a	n/a
40	CTCF	chr2:127002626-127002783	Lung_OC	lung:	n/a	n/a
41	CTCF	chr2:127002614-127002803	GM10266	blood:	n/a	n/a
42	CTCF	chr2:126863737-126863749	Fibrobl	skin:	n/a	n/a
43	CTCF	chr2:127002624-127002841	MCF-7	breast:	n/a	n/a
44	CTCF	chr2:127002640-127002790	GM12868	blood:	n/a	n/a
45	CTCF	chr2:126984900-126985050	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr2:127002660-127002810	AG04449	skin:	n/a	n/a
47	CTCF	chr2:127002622-127002812	ECC-1	luminal epithelium:	n/a	n/a
48	CTCF	chr2:126984860-126985010	BE2_C	brain:	n/a	n/a
49	CTCF	chr2:127002660-127002810	HRE	kidney:	n/a	n/a
50	CTCF	chr2:127002638-127002848	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:126874175-126874225	SAEC	small airway:	n/a
2	chr2:126874175-126874225	SAEC	small airway:	n/a
3	chr2:126874175-126874225	SK-N-MC	brain:	n/a
4	chr2:126874175-126874225	SK-N-SH_RA	brain:	n/a
5	chr2:126874175-126874225	AG04449	skin:	fetal
6	chr2:126874175-126874225	ProgFib	skin:	n/a
7	chr2:126874175-126874225	GM12878	blood:	n/a
8	chr2:126874175-126874225	HMEC	breast:	n/a
9	chr2:126874175-126874225	GM12891	blood:	n/a
10	chr2:126874175-126874225	SK-N-SH	brain:	n/a
11	chr2:126874175-126874225	AoSMC	blood vessel:	n/a
12	chr2:126874175-126874225	AG09309	skin:	n/a
13	chr2:126874175-126874225	HAEpiC	amniotic membrane:	n/a
14	chr2:126874175-126874225	K562	blood:	n/a
15	chr2:126874175-126874225	GM12892	blood:	n/a
16	chr2:126874175-126874225	HepG2	liver:	n/a
17	chr2:126874175-126874225	AG09319	gingival:	n/a
18	chr2:126874175-126874225	NT2-D1	testis:	n/a
19	chr2:126874175-126874225	BJ	skin:	n/a
20	chr2:126874175-126874225	Hela-S3	cervix:	n/a
21	chr2:126874175-126874225	HIPEpiC	eye:	n/a
22	chr2:126874175-126874225	HEK293	kidney:	embryo
23	chr2:126874175-126874225	MCF-7	breast:	n/a
24	chr2:126874175-126874225	Caco-2	colon:	n/a
25	chr2:126874175-126874225	BE2_C	brain:	n/a
26	chr2:126874175-126874225	U87	brain:	n/a
27	chr2:126874175-126874225	SKMC	muscle:	n/a
28	chr2:126874175-126874225	CMK	blood:	n/a
29	chr2:126874175-126874225	PANC-1	pancreas:	n/a
30	chr2:126874175-126874225	HCM	heart:	n/a
31	chr2:126874175-126874225	AG04450	lung:	fetal
32	chr2:126874175-126874225	HPAEpiC	pulmonary alveolar:	n/a
33	chr2:126874175-126874225	IMR90	lung:	fetal
34	chr2:126874175-126874225	ovcar-3	ovarian:	n/a
35	chr2:126874175-126874225	NHBE	bronchial:	n/a
36	chr2:126874175-126874225	Jurkat	blood:	n/a
37	chr2:126874175-126874225	PFSK-1	brain:	n/a
38	chr2:126874175-126874225	Hepatocyte	liver:	n/a
39	chr2:126874175-126874225	NHDF-neo	bronchial:	n/a
40	chr2:126874175-126874225	GM06990	blood:	n/a
41	chr2:126874175-126874225	AG10803	skin:	n/a
42	chr2:126874175-126874225	HCT-116	colon:	n/a
43	chr2:126874175-126874225	MCF10A-Er-Src	breast:	n/a
44	chr2:126874175-126874225	HRPEpiC	eye:	n/a
45	chr2:126874175-126874225	NH-A	brain:	n/a
46	chr2:126874175-126874225	HRE	kidney:	n/a
47	chr2:126874175-126874225	HUVEC	blood vessel:	n/a
48	chr2:126874175-126874225	HRCEpiC	kidney:	n/a
49	chr2:126874175-126874225	PrEC	prostate:	n/a
50	chr2:126874175-126874225	ECC-1	luminal epithelium:	n/a

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No.	Distal block	Cell Line	Cell type
1	chr2:127005924..127008963-chr2:127010494..127013764,3	K562	blood:
2	chr1:112162320..112163164-chr2:126989298..126989817,2	Hela-S3	cervix:
3	chr2:127027458..127030124-chr2:127074150..127076122,2	K562	blood:
4	chr2:127009698..127011900-chr2:127012722..127015678,2	MCF-7	breast:
5	chr2:127002261..127003206-chr2:127534544..127535568,4	MCF-7	breast:
6	chr2:127000756..127002293-chr2:127004018..127005768,2	MCF-7	breast:
7	chr2:126944838..126946720-chr2:126951819..126954117,2	K562	blood:
8	chr2:127002488..127003146-chr2:127240428..127241073,2	K562	blood:
9	chr2:126943914..126946210-chr2:126970364..126971921,2	K562	blood:
10	chr2:127027671..127029245-chr2:127034455..127036337,2	K562	blood:
11	chr2:127002510..127003198-chr2:127534689..127535540,2	MCF-7	breast:
12	chr2:127027819..127029825-chr2:127044636..127047534,2	K562	blood:
13	chr2:127000756..127002293-chr2:127004018..127005768,2	MCF-7	breast:
14	chr2:127005924..127008963-chr2:127010494..127013764,3	K562	blood:
15	chr2:126952183..126952703-chr9:94896143..94896774,2	MCF-7	breast:
16	chr2:127005363..127007196-chr2:127065380..127068265,2	K562	blood:
17	chr2:127027671..127029245-chr2:127034455..127036337,2	K562	blood:
18	chr2:127002328..127003186-chr2:127807433..127808421,2	K562	blood:
19	chr2:127009698..127011900-chr2:127012722..127015678,2	MCF-7	breast:
20	chr2:127040484..127043318-chr2:127048128..127049666,2	K562	blood:
21	chr2:127027819..127029825-chr2:127044636..127047534,2	K562	blood:
22	chr2:127022733..127024721-chr2:127064398..127066092,2	K562	blood:
23	chr2:126944838..126946720-chr2:126951819..126954117,2	K562	blood:
24	chr2:126943914..126946210-chr2:126970364..126971921,2	K562	blood:
25	chr2:127041438..127045671-chr2:127046702..127049174,3	K562	blood:
26	chr2:126502797..126503723-chr2:127002290..127003108,2	MCF-7	breast:

(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	chr2:126870510-126870747	XLOC_002308
3	lnc-BIN1-2	chr2:126867676-126867887	XLOC_002308
4	lnc-BIN1-2	chr2:126875500-126875562	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: 3364 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:3364 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567999066	chr2:126806487-126806488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs189656467	chr2:126806624-126806625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs72862455	chr2:126806663-126806664	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs537498906	chr2:126806672-126806673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs13030845	chr2:126806674-126806675	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs116460503	chr2:126806707-126806708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs13007279	chr2:126806753-126806754	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs560816455	chr2:126806766-126806767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs207462347	chr2:126806788-126806789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577398270	chr2:126806852-126806853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs78746389	chr2:126806907-126806908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs62158079	chr2:126806931-126806932	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs538410817	chr2:126806936-126806937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531847562	chr2:126806942-126806943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548664580	chr2:126806954-126806955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142395508	chr2:126806964-126806965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs73956279	chr2:126806980-126806981	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs535761365	chr2:126806986-126806987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs116012399	chr2:126806992-126806993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146835837	chr2:126807010-126807011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs181745441	chr2:126807028-126807029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568669140	chr2:126807090-126807091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373025055	chr2:126807124-126807125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535365588	chr2:126807140-126807141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs554214694	chr2:126807163-126807164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs369451234	chr2:126807173-126807174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114779478	chr2:126807217-126807218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533766467	chr2:126807259-126807260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554209967	chr2:126807261-126807262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553969296	chr2:126807283-126807284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577463991	chr2:126807286-126807287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555232709	chr2:126807299-126807300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs77410313	chr2:126807300-126807301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575100596	chr2:126807301-126807302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12617965	chr2:126807357-126807358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186831218	chr2:126807372-126807373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190468701	chr2:126807468-126807469	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs542366618	chr2:126807471-126807472	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs12987423	chr2:126807480-126807481	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs140674495	chr2:126807508-126807509	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs145848792	chr2:126807513-126807514	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs146638012	chr2:126807517-126807518	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs372742833	chr2:126807539-126807540	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs558133689	chr2:126807569-126807570	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs115802569	chr2:126807571-126807572	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs55946722	chr2:126807589-126807590	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs532444110	chr2:126807603-126807604	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs552150889	chr2:126807607-126807608	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs181847454	chr2:126807662-126807663	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs76506871	chr2:126807757-126807758	ZNF genes & repeats	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:155 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:126806400-126807200	Enhancers	Liver	Liver
2	chr2:126807200-126807400	Weak transcription	Liver	Liver
3	chr2:126807400-126809800	ZNF genes & repeats	Liver	Liver
4	chr2:126816400-126817200	Enhancers	H9 Cell Line	embryonic stem cell
5	chr2:126816400-126817200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr2:126816400-126817400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr2:126816400-126817400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr2:126816400-126817400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr2:126816400-126817800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr2:126816600-126818000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr2:126816800-126817200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr2:126816800-126817800	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr2:126817000-126817400	Enhancers	H1 Cell Line	embryonic stem cell
14	chr2:126817200-126821800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr2:126817400-126817800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr2:126817400-126821400	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr2:126817800-126818600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr2:126821400-126821600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
19	chr2:126821800-126822000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr2:126821800-126822000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
21	chr2:126829600-126830000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr2:126834800-126835800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr2:126839000-126850400	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr2:126842400-126842800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr2:126842400-126843000	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr2:126842600-126843000	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr2:126855000-126855400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr2:126863400-126863800	ZNF genes & repeats	Pancreas	Pancrea
29	chr2:126863600-126863800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr2:126863600-126863800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr2:126873000-126874200	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr2:126873200-126874000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr2:126873200-126874200	Enhancers	H9 Cell Line	embryonic stem cell
34	chr2:126873200-126874200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr2:126873200-126874200	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr2:126873400-126874000	Enhancers	H1 Cell Line	embryonic stem cell
37	chr2:126873400-126874000	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr2:126873400-126874000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr2:126873400-126874200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr2:126873400-126874200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr2:126873600-126874000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr2:126873600-126874600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr2:126873600-126874600	Enhancers	Brain Germinal Matrix	brain
44	chr2:126883400-126883800	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr2:126883400-126884000	Enhancers	Brain Substantia Nigra	brain
46	chr2:126883400-126884200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr2:126883400-126884600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr2:126883800-126884400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr2:126884400-126884600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr2:126884400-126885400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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