Variant report

Variant	nsv874238
Chromosome Location	chr2:64575738-64614241
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:64581785-64582323	K562	blood:	n/a	n/a
2	BACH1	chr2:64613844-64614134	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr2:64602846-64603311	GM12878	blood:	n/a	n/a
4	BATF	chr2:64579517-64579737	GM12878	blood:	n/a	chr2:64579636-64579647
5	BHLHE40	chr2:64602809-64603396	HepG2	liver:	n/a	n/a
6	BHLHE40	chr2:64582263-64582567	A549	lung:	n/a	chr2:64582263-64582279
7	BHLHE40	chr2:64581902-64582467	K562	blood:	n/a	chr2:64582263-64582279
8	BHLHE40	chr2:64595332-64595346	A549	lung:	n/a	n/a
9	CCNT2	chr2:64581934-64582422	K562	blood:	n/a	n/a
10	CEBPB	chr2:64589488-64590049	MCF-7	breast:	n/a	n/a
11	CEBPB	chr2:64592272-64592592	A549	lung:	n/a	chr2:64592461-64592472
12	CEBPB	chr2:64592347-64592618	K562	blood:	n/a	chr2:64592461-64592472
13	CEBPB	chr2:64592302-64592616	HepG2	liver:	n/a	chr2:64592461-64592472
14	CEBPB	chr2:64592321-64592607	IMR90	lung:	n/a	chr2:64592461-64592472
15	CEBPB	chr2:64611636-64611727	A549	lung:	n/a	n/a
16	CEBPB	chr2:64589716-64590276	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr2:64579532-64579773	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:64602660-64603461	GM12878	blood:	n/a	n/a
19	CEBPD	chr2:64581834-64582402	K562	blood:	n/a	n/a
20	CEBPD	chr2:64581880-64582395	K562	blood:	n/a	n/a
21	CHD2	chr2:64587217-64587566	Hela-S3	cervix:	n/a	n/a
22	CREB1	chr2:64581859-64582376	K562	blood:	n/a	n/a
23	CREB1	chr2:64581769-64582376	K562	blood:	n/a	n/a
24	CTCF	chr2:64603333-64603380	GM19239	blood:	n/a	n/a
25	CTCF	chr2:64587551-64587652	A549	lung:	n/a	chr2:64587600-64587610 chr2:64587596-64587612 chr2:64587598-64587611 chr2:64587598-64587607 chr2:64587595-64587613
26	CTCF	chr2:64587540-64587690	HPAF	blood vessel:	n/a	chr2:64587600-64587610 chr2:64587596-64587612 chr2:64587598-64587611 chr2:64587598-64587607 chr2:64587595-64587613
27	CTCF	chr2:64576380-64576530	HCFaa	heart:	n/a	n/a
28	CTCF	chr2:64591070-64591192	H1-hESC	embryonic stem cell:	n/a	chr2:64591139-64591155
29	CTCF	chr2:64591040-64591190	HCPEpiC	choroid plexus:	n/a	chr2:64591139-64591155
30	CTCF	chr2:64591020-64591170	HMEC	breast:	n/a	chr2:64591139-64591155
31	CTCF	chr2:64587557-64587638	MCF-7	breast:	n/a	chr2:64587600-64587610 chr2:64587596-64587612 chr2:64587598-64587611 chr2:64587598-64587607 chr2:64587595-64587613
32	CTCF	chr2:64591040-64591190	HepG2	liver:	n/a	chr2:64591139-64591155
33	CTCF	chr2:64591160-64591310	HCT-116	colon:	n/a	chr2:64591281-64591294
34	CTCF	chr2:64603164-64603266	GM19239	blood:	n/a	n/a
35	CTCF	chr2:64587500-64587650	HFF-Myc	foreskin:	n/a	chr2:64587600-64587610 chr2:64587596-64587612 chr2:64587598-64587611 chr2:64587598-64587607 chr2:64587595-64587613
36	CTCF	chr2:64591080-64591230	HPAF	blood vessel:	n/a	chr2:64591139-64591155
37	CTCF	chr2:64603234-64603287	Lung_OC	lung:	n/a	n/a
38	CTCF	chr2:64587360-64587510	HFF	foreskin:	n/a	n/a
39	CTCF	chr2:64587580-64587730	SAEC	small airway:	n/a	chr2:64587600-64587610 chr2:64587596-64587612 chr2:64587598-64587611 chr2:64587598-64587607 chr2:64587595-64587613
40	CTCF	chr2:64587680-64587830	HCFaa	heart:	n/a	n/a
41	CTCF	chr2:64601140-64601290	HepG2	liver:	n/a	n/a
42	CTCF	chr2:64587313-64587850	MCF-7	breast:	n/a	chr2:64587600-64587610 chr2:64587596-64587612 chr2:64587598-64587611 chr2:64587598-64587607 chr2:64587595-64587613
43	CTCF	chr2:64587530-64587685	Medullo	brain:	n/a	chr2:64587600-64587610 chr2:64587596-64587612 chr2:64587598-64587611 chr2:64587598-64587607 chr2:64587595-64587613
44	CTCF	chr2:64591057-64591181	GM12891	blood:	n/a	chr2:64591139-64591155
45	CTCF	chr2:64591086-64591202	HepG2	liver:	n/a	chr2:64591139-64591155
46	CTCF	chr2:64587460-64587610	HRE	kidney:	n/a	chr2:64587600-64587610 chr2:64587598-64587607
47	CTCF	chr2:64587560-64587710	NHLF	lung:	n/a	chr2:64587600-64587610 chr2:64587596-64587612 chr2:64587598-64587611 chr2:64587598-64587607 chr2:64587595-64587613
48	CTCF	chr2:64591200-64591350	GM12874	blood:	n/a	chr2:64591281-64591294
49	CTCF	chr2:64579580-64579730	HEK293	kidney:	n/a	n/a
50	CTCF	chr2:64579620-64579770	HMEC	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:64588440-64588490	AG09309	skin:	n/a
2	chr2:64588128-64588178	AG04450	lung:	fetal
3	chr2:64588440-64588490	K562	blood:	n/a
4	chr2:64588128-64588178	RPTEC	kidney:	n/a
5	chr2:64588440-64588490	HNPCEpiC	eye:	n/a
6	chr2:64588128-64588178	HCT-116	colon:	n/a
7	chr2:64588128-64588178	HAEpiC	amniotic membrane:	n/a
8	chr2:64590619-64590669	Hepatocyte	liver:	n/a
9	chr2:64588128-64588178	A549	lung:	n/a
10	chr2:64590619-64590669	HCM	heart:	n/a
11	chr2:64588128-64588178	HRE	kidney:	n/a
12	chr2:64588440-64588490	HPAEpiC	pulmonary alveolar:	n/a
13	chr2:64590619-64590669	ProgFib	skin:	n/a
14	chr2:64588440-64588490	GM06990	blood:	n/a
15	chr2:64588440-64588490	HCM	heart:	n/a
16	chr2:64590619-64590669	HCT-116	colon:	n/a
17	chr2:64590619-64590669	Caco-2	colon:	n/a
18	chr2:64588128-64588178	HEEpiC	esophagus:	n/a
19	chr2:64588128-64588178	AG04449	skin:	fetal
20	chr2:64590619-64590669	BE2_C	brain:	n/a
21	chr2:64588440-64588490	HRE	kidney:	n/a
22	chr2:64588128-64588178	GM19239	blood:	n/a
23	chr2:64590619-64590669	GM12891	blood:	n/a
24	chr2:64588440-64588490	HEEpiC	esophagus:	n/a
25	chr2:64590619-64590669	MCF10A-Er-Src	breast:	n/a
26	chr2:64588440-64588490	HAEpiC	amniotic membrane:	n/a
27	chr2:64590619-64590669	MCF-7	breast:	n/a
28	chr2:64590619-64590669	NH-A	brain:	n/a
29	chr2:64590619-64590669	GM12892	blood:	n/a
30	chr2:64590619-64590669	A549	lung:	n/a
31	chr2:64590619-64590669	NB4	blood:	n/a
32	chr2:64588128-64588178	HEK293	kidney:	embryo
33	chr2:64590619-64590669	HCPEpiC	choroid plexus:	n/a
34	chr2:64590619-64590669	HIPEpiC	eye:	n/a
35	chr2:64588128-64588178	GM06990	blood:	n/a
36	chr2:64590619-64590669	AG09309	skin:	n/a
37	chr2:64590619-64590669	HL-60	blood:	n/a
38	chr2:64588128-64588178	AG10803	skin:	n/a
39	chr2:64590619-64590669	SK-N-SH_RA	brain:	n/a
40	chr2:64588128-64588178	Hepatocyte	liver:	n/a
41	chr2:64588440-64588490	HCPEpiC	choroid plexus:	n/a
42	chr2:64588440-64588490	NHBE	bronchial:	n/a
43	chr2:64588440-64588490	AoSMC	blood vessel:	n/a
44	chr2:64588440-64588490	T-47D	breast:	n/a
45	chr2:64588128-64588178	HIPEpiC	eye:	n/a
46	chr2:64588128-64588178	SK-N-MC	brain:	n/a
47	chr2:64590619-64590669	BJ	skin:	n/a
48	chr2:64588128-64588178	Caco-2	colon:	n/a
49	chr2:64588440-64588490	Hela-S3	cervix:	n/a
50	chr2:64588128-64588178	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:64603709..64605931-chr2:64609518..64611551,3	K562	blood:
2	chr2:64580653..64583828-chr2:64584436..64587337,3	MCF-7	breast:
3	chr2:64583701..64585384-chr2:64588386..64591287,2	MCF-7	breast:
4	chr2:64585285..64586792-chr2:64588668..64591328,2	MCF-7	breast:
5	chr2:64587180..64587751-chr2:64714896..64715586,2	MCF-7	breast:
6	chr2:64582213..64584164-chr2:64584374..64587054,2	K562	blood:
7	chr2:64595365..64597527-chr2:64680554..64682467,3	MCF-7	breast:
8	chr1:121484723..121485398-chr2:64585871..64586554,2	MCF-7	breast:
9	chr2:64585285..64586792-chr2:64588668..64591328,2	MCF-7	breast:
10	chr2:64583701..64585384-chr2:64588386..64591287,2	MCF-7	breast:
11	chr2:64587517..64589977-chr2:64675091..64677835,2	MCF-7	breast:
12	chr2:64582213..64584164-chr2:64584374..64587054,2	K562	blood:
13	chr2:64580653..64583828-chr2:64584436..64587337,3	MCF-7	breast:
14	chr2:64584849..64587757-chr2:64625757..64628031,2	MCF-7	breast:
15	chr2:64602910..64605138-chr2:64606085..64607679,2	MCF-7	breast:
16	chr2:64586053..64589004-chr2:64618647..64620148,2	MCF-7	breast:
17	chr2:64611244..64613848-chr2:64618868..64621387,2	K562	blood:
18	chr2:64557743..64558404-chr2:64600820..64601498,2	MCF-7	breast:
19	chr2:64586292..64588331-chr2:64589357..64592036,2	K562	blood:
20	chr2:64602910..64605138-chr2:64606085..64607679,2	MCF-7	breast:
21	chr2:64607740..64609976-chr2:64680582..64682718,2	MCF-7	breast:
22	chr2:64588315..64590489-chr2:64680621..64682875,2	MCF-7	breast:
23	chr2:64586292..64588331-chr2:64589357..64592036,2	K562	blood:
24	chr2:64603709..64605931-chr2:64609518..64611551,3	K562	blood:
25	chr2:64587206..64587798-chr2:64714856..64715793,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PELI1-9	chr2:64600929-64601022	l_1848_chr2:64600928-64604931_testes
2	lnc-PELI1-9	chr2:64603641-64604931	l_1848_chr2:64600928-64604931_testes
3	lnc-LGALSL-6	chr2:64581157-64581542	NONHSAT071111

Variant related genes	Relation type
ENSG00000236148	TF binding region
ENSG00000236148	CpG island
ENSG00000119862	chromatin interactions
ENSG00000237217	chromatin interactions
ENSG00000223935	chromatin interactions

Extended variants
information (count: 1471 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1471 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4671563	chr2:64575738-64575739	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561918230	chr2:64575805-64575806	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs143146746	chr2:64575822-64575823	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs551927053	chr2:64575875-64575876	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs547856054	chr2:64575996-64575997	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs186925015	chr2:64576008-64576009	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs560290861	chr2:64576015-64576016	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs533360446	chr2:64576037-64576038	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs559127794	chr2:64576039-64576040	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs115764358	chr2:64576088-64576089	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs77358716	chr2:64576089-64576090	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs148252727	chr2:64576099-64576100	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs537618502	chr2:64576124-64576125	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs62136483	chr2:64576232-64576233	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs79017078	chr2:64576256-64576257	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs141186286	chr2:64576356-64576357	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs146960388	chr2:64576507-64576508	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs538639421	chr2:64576562-64576563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552698254	chr2:64576588-64576589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs137861056	chr2:64576589-64576590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567546396	chr2:64576610-64576611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs371901988	chr2:64576626-64576627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191317591	chr2:64576718-64576719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78430838	chr2:64576733-64576734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs58527631	chr2:64576753-64576754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536675588	chr2:64576772-64576773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs143470946	chr2:64576789-64576790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567877576	chr2:64576806-64576807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35358047	chr2:64576883-64576884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541215731	chr2:64576896-64576897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35689281	chr2:64576927-64576928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs34724985	chr2:64576937-64576938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183182882	chr2:64577008-64577009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375050690	chr2:64577020-64577021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533226536	chr2:64577041-64577042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs34670260	chr2:64577044-64577045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550480223	chr2:64577169-64577170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570329999	chr2:64577198-64577199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs72812016	chr2:64577213-64577214	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs539361155	chr2:64577242-64577243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189752203	chr2:64577249-64577250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549282945	chr2:64577278-64577279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182055425	chr2:64577305-64577306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs367874944	chr2:64577319-64577320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559144999	chr2:64577335-64577336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187946227	chr2:64577348-64577349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572641754	chr2:64577364-64577365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534417849	chr2:64577438-64577439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190860192	chr2:64577446-64577447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544405467	chr2:64577460-64577461	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:463 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:64568400-64575800	Weak transcription	Fetal Muscle Leg	muscle
2	chr2:64572600-64581800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:64573800-64576000	Weak transcription	A549	lung
4	chr2:64575000-64576400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr2:64575200-64576600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr2:64575400-64576000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr2:64575400-64576000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr2:64575400-64576200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr2:64575400-64576200	Enhancers	NH-A	brain
10	chr2:64575400-64576400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr2:64575400-64576600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr2:64575400-64576800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr2:64575400-64576800	Enhancers	NHLF	lung
14	chr2:64575600-64576200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr2:64575600-64576400	Enhancers	Muscle Satellite Cultured Cells	--
16	chr2:64575600-64576600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr2:64575600-64576600	Enhancers	NHDF-Ad	bronchial
18	chr2:64575600-64576600	Enhancers	NHEK	skin
19	chr2:64575800-64576000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr2:64575800-64576000	Enhancers	Spleen	Spleen
21	chr2:64575800-64576200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr2:64575800-64576400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr2:64575800-64576400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr2:64575800-64576400	Enhancers	HMEC	breast
25	chr2:64575800-64576600	Enhancers	Fetal Muscle Leg	muscle
26	chr2:64576000-64576400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr2:64576000-64576400	Enhancers	A549	lung
28	chr2:64576000-64582200	Weak transcription	Spleen	Spleen
29	chr2:64576200-64579000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr2:64576400-64576800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr2:64576400-64581600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr2:64576400-64581600	Weak transcription	HMEC	breast
33	chr2:64576400-64581800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr2:64576400-64581800	Weak transcription	A549	lung
35	chr2:64576600-64579400	Weak transcription	NHEK	skin
36	chr2:64576600-64581600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr2:64576600-64581800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr2:64577600-64577800	Enhancers	Pancreas	Pancrea
39	chr2:64577800-64586600	Weak transcription	Pancreas	Pancrea
40	chr2:64578200-64578400	Enhancers	Lung	lung
41	chr2:64578200-64579400	Enhancers	Gastric	stomach
42	chr2:64578400-64579200	Weak transcription	Lung	lung
43	chr2:64578400-64579800	Enhancers	Stomach Mucosa	stomach
44	chr2:64579200-64579400	Enhancers	Lung	lung
45	chr2:64579200-64579800	Enhancers	Esophagus	oesophagus
46	chr2:64579400-64579800	Enhancers	NHEK	skin
47	chr2:64579400-64581800	Weak transcription	Lung	lung
48	chr2:64579800-64581600	Weak transcription	NHEK	skin
49	chr2:64579800-64582000	Weak transcription	Esophagus	oesophagus
50	chr2:64579800-64582000	Weak transcription	Stomach Mucosa	stomach

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