Variant report

Variant	esv3395703
Chromosome Location	chr2:127309762-127404005
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:627)
CpG islands
(count:122)
Chromatin interactive
region (count:16)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:627 , 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	chr2:127391859-127392208	K562	blood:	n/a	n/a
2	ARID3A	chr2:127402147-127402563	K562	blood:	n/a	n/a
3	ARID3A	chr2:127395046-127395207	K562	blood:	n/a	n/a
4	ARID3A	chr2:127402808-127403349	K562	blood:	n/a	n/a
5	ARID3A	chr2:127403751-127404006	K562	blood:	n/a	n/a
6	ATF1	chr2:127402238-127403246	K562	blood:	n/a	n/a
7	ATF3	chr2:127337535-127337711	K562	blood:	n/a	n/a
8	BCLAF1	chr2:127402737-127403291	K562	blood:	n/a	n/a
9	BHLHE40	chr2:127337582-127337677	K562	blood:	n/a	n/a
10	BHLHE40	chr2:127391886-127392192	K562	blood:	n/a	n/a
11	BHLHE40	chr2:127395501-127395605	K562	blood:	n/a	n/a
12	BHLHE40	chr2:127402075-127403319	K562	blood:	n/a	n/a
13	BHLHE40	chr2:127401131-127401299	K562	blood:	n/a	n/a
14	BHLHE40	chr2:127374134-127374584	GM12878	blood:	n/a	n/a
15	BRCA1	chr2:127374645-127374751	GM12878	blood:	n/a	n/a
16	CBX3	chr2:127402806-127403242	K562	blood:	n/a	n/a
17	CBX3	chr2:127397315-127397708	K562	blood:	n/a	n/a
18	CBX3	chr2:127356681-127356963	K562	blood:	n/a	n/a
19	CBX3	chr2:127356722-127356910	K562	blood:	n/a	n/a
20	CBX3	chr2:127402156-127403276	K562	blood:	n/a	n/a
21	CCNT2	chr2:127402806-127403257	K562	blood:	n/a	n/a
22	CCNT2	chr2:127403754-127403815	K562	blood:	n/a	n/a
23	CEBPB	chr2:127384633-127384981	K562	blood:	n/a	n/a
24	CEBPB	chr2:127384690-127384916	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:127392931-127393291	HepG2	liver:	n/a	chr2:127393113-127393124 chr2:127393115-127393124 chr2:127393113-127393126
26	CEBPB	chr2:127397422-127397687	K562	blood:	n/a	chr2:127397567-127397578
27	CEBPB	chr2:127402676-127403131	K562	blood:	n/a	n/a
28	CEBPB	chr2:127375657-127375872	K562	blood:	n/a	n/a
29	CEBPB	chr2:127336681-127337005	HepG2	liver:	n/a	chr2:127336837-127336848 chr2:127336839-127336850 chr2:127336837-127336850
30	CEBPB	chr2:127392936-127393285	K562	blood:	n/a	chr2:127393113-127393124 chr2:127393115-127393124 chr2:127393113-127393126
31	CEBPB	chr2:127381224-127381340	K562	blood:	n/a	n/a
32	CEBPB	chr2:127336724-127336923	IMR90	lung:	n/a	chr2:127336837-127336848 chr2:127336839-127336850 chr2:127336837-127336850
33	CEBPB	chr2:127392972-127393153	H1-hESC	embryonic stem cell:	n/a	chr2:127393113-127393124 chr2:127393115-127393124 chr2:127393113-127393126
34	CEBPB	chr2:127355029-127355128	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:127323902-127324092	HepG2	liver:	n/a	chr2:127324046-127324057
36	CEBPB	chr2:127402584-127403241	K562	blood:	n/a	n/a
37	CEBPD	chr2:127402663-127403310	K562	blood:	n/a	n/a
38	CEBPD	chr2:127402715-127403272	K562	blood:	n/a	n/a
39	CHD2	chr2:127402032-127402168	GM12878	blood:	n/a	n/a
40	CHD2	chr2:127374246-127374667	GM12878	blood:	n/a	n/a
41	CTCF	chr2:127401249-127401331	K562	blood:	n/a	n/a
42	CTCF	chr2:127391900-127392050	GM12866	blood:	n/a	n/a
43	CTCF	chr2:127391881-127392164	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr2:127391960-127392110	GM12874	blood:	n/a	n/a
45	CTCF	chr2:127391805-127392281	K562	blood:	n/a	n/a
46	CTCF	chr2:127391865-127392157	GM10266	blood:	n/a	n/a
47	CTCF	chr2:127374586-127374650	K562	blood:	n/a	chr2:127374608-127374629
48	CTCF	chr2:127392009-127392089	GM12891	blood:	n/a	n/a
49	CTCF	chr2:127391940-127392090	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr2:127391960-127392110	HMF	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:127401321-127401371	MCF-7	breast:	n/a
2	chr2:127401321-127401371	GM12891	blood:	n/a
3	chr2:127315703-127315753	HEEpiC	esophagus:	n/a
4	chr2:127315703-127315753	AoSMC	blood vessel:	n/a
5	chr2:127315703-127315753	NHBE	bronchial:	n/a
6	chr2:127315703-127315753	NHDF-neo	bronchial:	n/a
7	chr2:127401321-127401371	Hepatocyte	liver:	n/a
8	chr2:127401321-127401371	T-47D	breast:	n/a
9	chr2:127401321-127401371	HPAEpiC	pulmonary alveolar:	n/a
10	chr2:127401321-127401371	RPTEC	kidney:	n/a
11	chr2:127401321-127401371	HL-60	blood:	n/a
12	chr2:127401321-127401371	ProgFib	skin:	n/a
13	chr2:127401321-127401371	BJ	skin:	n/a
14	chr2:127315703-127315753	HRE	kidney:	n/a
15	chr2:127401321-127401371	H1-hESC	embryonic stem cell:	embryo
16	chr2:127401321-127401371	Hela-S3	cervix:	n/a
17	chr2:127315703-127315753	IMR90	lung:	fetal
18	chr2:127401321-127401371	HIPEpiC	eye:	n/a
19	chr2:127401321-127401371	AG04449	skin:	fetal
20	chr2:127315703-127315753	HUVEC	blood vessel:	n/a
21	chr2:127401321-127401371	ovcar-3	ovarian:	n/a
22	chr2:127315703-127315753	AG04450	lung:	fetal
23	chr2:127315703-127315753	HCF	heart:	n/a
24	chr2:127315703-127315753	HL-60	blood:	n/a
25	chr2:127315703-127315753	SAEC	small airway:	n/a
26	chr2:127315703-127315753	MCF10A-Er-Src	breast:	n/a
27	chr2:127315703-127315753	GM12891	blood:	n/a
28	chr2:127315703-127315753	CMK	blood:	n/a
29	chr2:127315703-127315753	HIPEpiC	eye:	n/a
30	chr2:127315703-127315753	H1-hESC	embryonic stem cell:	embryo
31	chr2:127401321-127401371	MCF10A-Er-Src	breast:	n/a
32	chr2:127315703-127315753	AG09319	gingival:	n/a
33	chr2:127401321-127401371	HAEpiC	amniotic membrane:	n/a
34	chr2:127401321-127401371	HEEpiC	esophagus:	n/a
35	chr2:127315703-127315753	BJ	skin:	n/a
36	chr2:127315703-127315753	AG10803	skin:	n/a
37	chr2:127315703-127315753	HCM	heart:	n/a
38	chr2:127315703-127315753	Hepatocyte	liver:	n/a
39	chr2:127315703-127315753	GM12878	blood:	n/a
40	chr2:127315703-127315753	MCF-7	breast:	n/a
41	chr2:127401321-127401371	HRCEpiC	kidney:	n/a
42	chr2:127315703-127315753	HAEpiC	amniotic membrane:	n/a
43	chr2:127401321-127401371	NH-A	brain:	n/a
44	chr2:127401321-127401371	Jurkat	blood:	n/a
45	chr2:127315703-127315753	Jurkat	blood:	n/a
46	chr2:127315703-127315753	NH-A	brain:	n/a
47	chr2:127401321-127401371	NB4	blood:	n/a
48	chr2:127401321-127401371	A549	lung:	n/a
49	chr2:127401321-127401371	NHBE	bronchial:	n/a
50	chr2:127315703-127315753	RPTEC	kidney:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:127390524..127393916-chr2:127398705..127401575,5	K562	blood:
2	chr2:127301968..127303777-chr2:127308434..127310224,2	K562	blood:
3	chr1:115039483..115041308-chr2:127347462..127348962,2	MCF-7	breast:
4	chr2:127390524..127393916-chr2:127398705..127401575,4	K562	blood:
5	chr2:127395382..127399408-chr2:127400196..127404194,4	K562	blood:
6	chr2:127395011..127397551-chr2:127398537..127401253,2	K562	blood:
7	chr2:127395382..127399408-chr2:127400196..127404194,4	K562	blood:
8	chr2:127391584..127392574-chr2:127534356..127535586,7	MCF-7	breast:
9	chr2:127400846..127406536-chr2:127411242..127416959,8	K562	blood:
10	chr2:127330201..127332917-chr20:49407514..49409550,2	MCF-7	breast:
11	chr2:127392390..127395069-chr2:127405481..127407043,2	K562	blood:
12	chr2:127390524..127393916-chr2:127398705..127401575,5	K562	blood:
13	chr2:127401454..127404450-chr2:127413694..127415742,3	K562	blood:
14	chr2:127390524..127393916-chr2:127398705..127401575,4	K562	blood:
15	chr2:127395011..127397551-chr2:127398537..127401253,2	K562	blood:
16	chr2:127285684..127286286-chr2:127392233..127393052,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BIN1-7	chr2:127403608-127403745	NONHSAT074131
2	lnc-BIN1-7	chr2:127390520-127390640	NONHSAT074131

No data

Variant related genes	Relation type
YWHAZP2	TF binding region
YWHAZP2	CpG island
ENSG00000136732	chromatin interactions

Extended variants
information (count: 1704 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1704 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372002668	chr2:127315755-127315756	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs189931721	chr2:127315761-127315762	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs527673270	chr2:127315797-127315798	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs548019745	chr2:127315800-127315801	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs547888364	chr2:127315812-127315813	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs547183959	chr2:127315859-127315860	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs187457484	chr2:127317156-127317157	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs191476727	chr2:127317161-127317162	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs6748116	chr2:127317184-127317185	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs140417555	chr2:127317198-127317199	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs143828213	chr2:127317221-127317222	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs112403356	chr2:127318774-127318775	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs34806789	chr2:127318801-127318802	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs528720388	chr2:127318844-127318845	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs529655712	chr2:127319016-127319017	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs569876252	chr2:127320035-127320036	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs368052347	chr2:127320111-127320112	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs539168138	chr2:127320117-127320118	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs557777940	chr2:127324668-127324669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577963296	chr2:127324684-127324685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11902220	chr2:127324687-127324688	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs563755303	chr2:127324702-127324703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376193961	chr2:127324704-127324705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6758636	chr2:127324713-127324714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529559703	chr2:127324813-127324814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559969180	chr2:127324823-127324824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190368388	chr2:127324825-127324826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs144648419	chr2:127324863-127324864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564911464	chr2:127324902-127324903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs6758976	chr2:127324998-127324999	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs570554796	chr2:127324999-127325000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113922479	chr2:127325116-127325117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555770730	chr2:127325134-127325135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528193413	chr2:127325136-127325137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181612977	chr2:127325139-127325140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs377567183	chr2:127325165-127325166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79339952	chr2:127325186-127325187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77906233	chr2:127325187-127325188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546419120	chr2:127325195-127325196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566327637	chr2:127325231-127325232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538589523	chr2:127325262-127325263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186186062	chr2:127325294-127325295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577962348	chr2:127325307-127325308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537423806	chr2:127325327-127325328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557190314	chr2:127325328-127325329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574111191	chr2:127325403-127325404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543120973	chr2:127325428-127325429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566021218	chr2:127325431-127325432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560032650	chr2:127325472-127325473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372836979	chr2:127325525-127325526	Weak transcription	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	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD

Chromatin state (count:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:127324600-127333000	Weak transcription	Fetal Brain Male	brain
2	chr2:127326400-127327000	Enhancers	Primary B cells from peripheral blood	blood
3	chr2:127333000-127334200	Enhancers	Fetal Brain Male	brain
4	chr2:127334800-127335000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr2:127335000-127335800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr2:127335800-127336800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr2:127343400-127343600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr2:127352400-127352600	Enhancers	Pancreas	Pancrea
9	chr2:127354600-127354800	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr2:127355400-127355600	Enhancers	Skeletal Muscle Male	skeletal muscle
11	chr2:127366000-127366800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr2:127366200-127366600	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr2:127366200-127367000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr2:127366400-127366800	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr2:127371400-127373200	Enhancers	NHLF	lung
16	chr2:127371600-127372000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr2:127371600-127372600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr2:127371600-127372600	Enhancers	Fetal Lung	lung
19	chr2:127371800-127372600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr2:127371800-127372600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr2:127371800-127372800	Enhancers	Muscle Satellite Cultured Cells	--
22	chr2:127372000-127372200	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr2:127372000-127372400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr2:127372000-127372400	Enhancers	Fetal Brain Male	brain
25	chr2:127372000-127372600	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr2:127372000-127372600	Enhancers	Fetal Heart	heart
27	chr2:127372000-127372800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr2:127372000-127372800	Enhancers	Adipose Nuclei	Adipose
29	chr2:127372000-127373200	Enhancers	HSMM	muscle
30	chr2:127372200-127372600	Enhancers	H9 Cell Line	embryonic stem cell
31	chr2:127372200-127372800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr2:127372200-127372800	Enhancers	HSMMtube	muscle
33	chr2:127372400-127372600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr2:127372400-127373600	Weak transcription	Fetal Brain Male	brain
35	chr2:127372800-127373200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr2:127372800-127374000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:127373600-127374400	Enhancers	Primary B cells from cord blood	blood
38	chr2:127373800-127374000	Enhancers	Fetal Brain Male	brain
39	chr2:127373800-127374800	Enhancers	Primary B cells from peripheral blood	blood
40	chr2:127373800-127374800	Enhancers	GM12878-XiMat	blood
41	chr2:127374000-127374400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr2:127374000-127375000	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr2:127374200-127374600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr2:127374600-127374800	Enhancers	H9 Cell Line	embryonic stem cell
45	chr2:127374800-127377200	Weak transcription	Primary B cells from peripheral blood	blood
46	chr2:127375400-127375800	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr2:127375400-127376000	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr2:127376000-127377400	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr2:127377400-127377600	Enhancers	Primary B cells from peripheral blood	blood
50	chr2:127377400-127378200	Enhancers	Monocytes-CD14+_RO01746	blood

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