Variant report

Variant	nsv1004166
Chromosome Location	chr2:127634679-127672143
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:347)
CpG islands
(count:855)
Chromatin interactive
region (count:17)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:127643415-127643737	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr2:127643943-127644143	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr2:127642374-127642673	GM12878	blood:	n/a	n/a
4	BHLHE40	chr2:127643972-127644158	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:127643957-127644268	K562	blood:	n/a	n/a
6	BHLHE40	chr2:127662893-127663051	HepG2	liver:	n/a	n/a
7	BRCA1	chr2:127643891-127644233	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr2:127660620-127660631	HepG2	liver:	n/a	n/a
9	CBX3	chr2:127643885-127644225	K562	blood:	n/a	n/a
10	CCNT2	chr2:127643925-127644205	K562	blood:	n/a	n/a
11	CEBPB	chr2:127648711-127648871	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:127638939-127639165	IMR90	lung:	n/a	chr2:127639023-127639034
13	CEBPB	chr2:127638911-127639100	K562	blood:	n/a	chr2:127639023-127639034
14	CEBPB	chr2:127638898-127639131	A549	lung:	n/a	chr2:127639023-127639034
15	CEBPB	chr2:127638886-127639127	HepG2	liver:	n/a	chr2:127639023-127639034
16	CHD2	chr2:127643846-127644233	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr2:127643900-127644213	HepG2	liver:	n/a	n/a
18	CHD2	chr2:127643866-127644214	K562	blood:	n/a	n/a
19	CHD2	chr2:127644016-127644130	GM12878	blood:	n/a	n/a
20	CREB1	chr2:127643827-127644286	A549	lung:	n/a	n/a
21	CTCF	chr2:127643980-127644130	HCM	heart:	n/a	chr2:127644059-127644075
22	CTCF	chr2:127644000-127644150	HVMF	connective:	n/a	chr2:127644059-127644075
23	CTCF	chr2:127643926-127644200	ProgFib	skin:	n/a	chr2:127644059-127644075
24	CTCF	chr2:127643980-127644130	GM12870	blood:	n/a	chr2:127644059-127644075
25	CTCF	chr2:127643901-127644121	A549	lung:	n/a	chr2:127644059-127644075
26	CTCF	chr2:127644020-127644170	HPAF	blood vessel:	n/a	chr2:127644059-127644075
27	CTCF	chr2:127643837-127644276	K562	blood:	n/a	chr2:127644059-127644075
28	CTCF	chr2:127643980-127644130	HRPEpiC	eye:	n/a	chr2:127644059-127644075
29	CTCF	chr2:127644340-127644490	HVMF	connective:	n/a	n/a
30	CTCF	chr2:127644040-127644190	HMF	breast:	n/a	chr2:127644059-127644075
31	CTCF	chr2:127643980-127644130	GM12868	blood:	n/a	chr2:127644059-127644075
32	CTCF	chr2:127643940-127644090	AG09309	skin:	n/a	chr2:127644059-127644075
33	CTCF	chr2:127644020-127644170	HBMEC	blood vessel:	n/a	chr2:127644059-127644075
34	CTCF	chr2:127643960-127644110	SAEC	small airway:	n/a	chr2:127644059-127644075
35	CTCF	chr2:127643980-127644130	MCF-7	breast:	n/a	chr2:127644059-127644075
36	CTCF	chr2:127644000-127644150	GM12878	blood:	n/a	chr2:127644059-127644075
37	CTCF	chr2:127643894-127644225	MCF-7	breast:	n/a	chr2:127644059-127644075
38	CTCF	chr2:127643957-127644189	GM13976	blood:	n/a	chr2:127644059-127644075
39	CTCF	chr2:127644000-127644150	GM12867	blood:	n/a	chr2:127644059-127644075
40	CTCF	chr2:127643940-127644090	GM12875	blood:	n/a	chr2:127644059-127644075
41	CTCF	chr2:127644000-127644150	GM12866	blood:	n/a	chr2:127644059-127644075
42	CTCF	chr2:127644020-127644170	GM12869	blood:	n/a	chr2:127644059-127644075
43	CTCF	chr2:127643969-127644182	A549	lung:	n/a	chr2:127644059-127644075
44	CTCF	chr2:127643978-127644155	HUVEC	blood vessel:	n/a	chr2:127644059-127644075
45	CTCF	chr2:127637244-127637351	GM19239	blood:	n/a	n/a
46	CTCF	chr2:127644000-127644150	AG10803	skin:	n/a	chr2:127644059-127644075
47	CTCF	chr2:127643931-127644214	A549	lung:	n/a	chr2:127644059-127644075
48	CTCF	chr2:127637375-127637428	GM19239	blood:	n/a	n/a
49	CTCF	chr2:127644040-127644190	HCFaa	heart:	n/a	chr2:127644059-127644075
50	CTCF	chr2:127643940-127644090	HRE	kidney:	n/a	chr2:127644059-127644075

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:127634784-127634834	T-47D	breast:	n/a
2	chr2:127634784-127634834	T-47D	breast:	n/a
3	chr2:127640322-127640372	CMK	blood:	n/a
4	chr2:127646404-127646454	Caco-2	colon:	n/a
5	chr2:127635678-127635728	AG04449	skin:	fetal
6	chr2:127635678-127635728	HRE	kidney:	n/a
7	chr2:127643971-127644021	AoSMC	blood vessel:	n/a
8	chr2:127635678-127635728	HepG2	liver:	n/a
9	chr2:127640322-127640372	HEEpiC	esophagus:	n/a
10	chr2:127643360-127643410	HPAEpiC	pulmonary alveolar:	n/a
11	chr2:127642574-127642624	HUVEC	blood vessel:	n/a
12	chr2:127635644-127635694	GM12892	blood:	n/a
13	chr2:127634784-127634834	LNCaP	prostate:	n/a
14	chr2:127644612-127644662	HEK293	kidney:	embryo
15	chr2:127635644-127635694	HRPEpiC	eye:	n/a
16	chr2:127644612-127644662	Hela-S3	cervix:	n/a
17	chr2:127640322-127640372	ProgFib	skin:	n/a
18	chr2:127644612-127644662	HUVEC	blood vessel:	n/a
19	chr2:127644075-127644125	AG04450	lung:	fetal
20	chr2:127646592-127646642	CMK	blood:	n/a
21	chr2:127646404-127646454	AG10803	skin:	n/a
22	chr2:127643858-127643908	LNCaP	prostate:	n/a
23	chr2:127640322-127640372	HL-60	blood:	n/a
24	chr2:127646404-127646454	AG04449	skin:	fetal
25	chr2:127643971-127644021	HEEpiC	esophagus:	n/a
26	chr2:127643360-127643410	GM19239	blood:	n/a
27	chr2:127640322-127640372	HCT-116	colon:	n/a
28	chr2:127635678-127635728	HCF	heart:	n/a
29	chr2:127643360-127643410	H1-hESC	embryonic stem cell:	embryo
30	chr2:127646592-127646642	AG04449	skin:	fetal
31	chr2:127635614-127635664	HCT-116	colon:	n/a
32	chr2:127644612-127644662	HCM	heart:	n/a
33	chr2:127634784-127634834	Jurkat	blood:	n/a
34	chr2:127644612-127644662	A549	lung:	n/a
35	chr2:127642574-127642624	BJ	skin:	n/a
36	chr2:127643360-127643410	A549	lung:	n/a
37	chr2:127634784-127634834	SAEC	small airway:	n/a
38	chr2:127643858-127643908	NHBE	bronchial:	n/a
39	chr2:127635614-127635664	HRE	kidney:	n/a
40	chr2:127642574-127642624	HMEC	breast:	n/a
41	chr2:127635678-127635728	AG04450	lung:	fetal
42	chr2:127644075-127644125	HEK293	kidney:	embryo
43	chr2:127634784-127634834	HEK293	kidney:	embryo
44	chr2:127644075-127644125	GM12891	blood:	n/a
45	chr2:127635279-127635329	HRCEpiC	kidney:	n/a
46	chr2:127635279-127635329	BJ	skin:	n/a
47	chr2:127635279-127635329	AG10803	skin:	n/a
48	chr2:127644612-127644662	MCF-7	breast:	n/a
49	chr2:127644075-127644125	HUVEC	blood vessel:	n/a
50	chr2:127644075-127644125	Caco-2	colon:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:127662850..127664564-chr2:127666506..127668375,2	K562	blood:
2	chr2:127621673..127623605-chr2:127639820..127641552,2	K562	blood:
3	chr2:127645857..127648098-chr2:127650154..127652226,2	MCF-7	breast:
4	chr2:127645857..127648098-chr2:127650154..127652226,2	MCF-7	breast:
5	chr2:127663020..127665879-chr2:127676391..127678881,2	MCF-7	breast:
6	chr2:127640855..127642848-chr2:127645832..127648441,2	K562	blood:
7	chr2:127643258..127645447-chr2:127648554..127651485,2	MCF-7	breast:
8	chr2:127643178..127645880-chr2:127648030..127650091,2	K562	blood:
9	chr2:127643515..127644193-chr2:127729132..127729892,3	MCF-7	breast:
10	chr2:127643258..127645447-chr2:127648554..127651485,2	MCF-7	breast:
11	chr2:127643679..127644563-chr2:127807789..127808402,4	MCF-7	breast:
12	chr2:127556385..127559250-chr2:127644550..127646479,2	K562	blood:
13	chr2:127534763..127535468-chr2:127643597..127644526,2	MCF-7	breast:
14	chr2:127643178..127645880-chr2:127648030..127650091,2	K562	blood:
15	chr2:127643808..127644560-chr2:127807706..127808371,2	K562	blood:
16	chr2:127640855..127642848-chr2:127645832..127648441,2	K562	blood:
17	chr2:127662850..127664564-chr2:127666506..127668375,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC114783.1.1-1	chr2:127657098-127657188	ENSG00000237524
2	lnc-AC114783.1.1-1	chr2:127658786-127658858	ENSG00000237524
3	lnc-AC114783.1.1-1	chr2:127659445-127659673	ENSG00000237524
4	lnc-AC114783.1.1-1	chr2:127659445-127659673	ENSG00000237524
5	lnc-AC114783.1.1-1	chr2:127656793-127657003	ENSG00000237524
6	lnc-AC114783.1.1-1	chr2:127657412-127657429	ENSG00000237524
7	lnc-AC114783.1.1-1	chr2:127658786-127658854	ENSG00000237524
8	lnc-AC114783.1.1-1	chr2:127656795-127656867	ENSG00000237524
9	lnc-AC114783.1.1-1	chr2:127656510-127656693	ENSG00000237524
10	lnc-AC114783.1.1-1	chr2:127657099-127657188	ENSG00000237524

No data

Variant related genes	Relation type
ENSG00000237524	TF binding region
ENSG00000237524	CpG island

Extended variants
information (count: 1565 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1565 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6431194	chr2:127634679-127634680	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555651286	chr2:127634691-127634692	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs377013624	chr2:127634740-127634741	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs574794045	chr2:127634748-127634749	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs185538490	chr2:127634762-127634763	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs564289700	chr2:127634782-127634783	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs74559799	chr2:127634784-127634785	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs545865115	chr2:127634785-127634786	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs557165396	chr2:127634810-127634811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs562659827	chr2:127634868-127634869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567571605	chr2:127634871-127634872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs115568350	chr2:127634894-127634895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532532652	chr2:127634903-127634904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs115909316	chr2:127634925-127634926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs55843005	chr2:127635054-127635055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368148214	chr2:127635055-127635056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs77730187	chr2:127635064-127635065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs397985816	chr2:127635065-127635066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs56768908	chr2:127635066-127635067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536510903	chr2:127635172-127635173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545977783	chr2:127635203-127635204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73956115	chr2:127635246-127635247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368614758	chr2:127635261-127635262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553223034	chr2:127635270-127635271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547813021	chr2:127635280-127635281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570993530	chr2:127635293-127635294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533690691	chr2:127635410-127635411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540051002	chr2:127635447-127635448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556251242	chr2:127635486-127635487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77953063	chr2:127635501-127635502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371376301	chr2:127635533-127635534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535589975	chr2:127635537-127635538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7425789	chr2:127635553-127635554	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs571980917	chr2:127635585-127635586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368221138	chr2:127635590-127635591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372295784	chr2:127635604-127635605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541296184	chr2:127635615-127635616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs75453956	chr2:127635636-127635637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143150102	chr2:127635660-127635661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189623382	chr2:127635697-127635698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs60825457	chr2:127635712-127635713	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs531690919	chr2:127635859-127635860	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541963264	chr2:127635877-127635878	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs114447509	chr2:127635879-127635880	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs527715847	chr2:127635970-127635971	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558405823	chr2:127636096-127636097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571063962	chr2:127636117-127636118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181472791	chr2:127636137-127636138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186110187	chr2:127636226-127636227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs188568273	chr2:127636230-127636231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:127634200-127635000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:127634400-127634800	Enhancers	H1 Cell Line	embryonic stem cell
3	chr2:127634400-127634800	Enhancers	H9 Cell Line	embryonic stem cell
4	chr2:127634400-127634800	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr2:127634400-127634800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr2:127634600-127634800	ZNF genes & repeats	Gastric	stomach
7	chr2:127634600-127637000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr2:127634800-127635800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr2:127634800-127636800	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr2:127634800-127637200	Weak transcription	Gastric	stomach
11	chr2:127634800-127637400	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr2:127635800-127636000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr2:127635800-127636600	Enhancers	Fetal Kidney	kidney
14	chr2:127636000-127637000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr2:127636400-127643800	Weak transcription	Right Atrium	heart
16	chr2:127636600-127636800	Weak transcription	Fetal Kidney	kidney
17	chr2:127636600-127637200	ZNF genes & repeats	Pancreas	Pancrea
18	chr2:127636800-127637600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
19	chr2:127636800-127637600	ZNF genes & repeats	Fetal Kidney	kidney
20	chr2:127636800-127637800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr2:127636800-127637800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr2:127637000-127637400	Transcr. at gene 5' and 3'	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr2:127637000-127637600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr2:127637200-127637600	Active TSS	Fetal Lung	lung
25	chr2:127637200-127637600	Enhancers	Gastric	stomach
26	chr2:127637400-127637600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr2:127637400-127638400	Enhancers	H1 Cell Line	embryonic stem cell
28	chr2:127637600-127638000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr2:127637600-127643000	Weak transcription	Fetal Kidney	kidney
30	chr2:127637600-127643600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr2:127637600-127643800	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr2:127637600-127643800	Weak transcription	Gastric	stomach
33	chr2:127637800-127638400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr2:127637800-127643800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr2:127638000-127638400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr2:127638400-127638600	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr2:127638400-127643000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr2:127638400-127643200	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr2:127638600-127639200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr2:127638800-127639600	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr2:127639000-127639400	Enhancers	Fetal Muscle Leg	muscle
42	chr2:127639200-127639600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
43	chr2:127639200-127639600	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr2:127639400-127639600	Bivalent Enhancer	Fetal Muscle Leg	muscle
45	chr2:127639600-127643000	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr2:127639600-127643400	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr2:127639800-127641400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr2:127640000-127641400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:127640400-127640600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
50	chr2:127640600-127641000	Enhancers	Fetal Muscle Trunk	muscle

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