Variant report

Variant	nsv530516
Chromosome Location	chr2:56447922-56633505
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	BACH1	chr2:56609888-56609893	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr2:56503402-56503656	GM12878	blood:	n/a	n/a
3	BCL11A	chr2:56545320-56545591	GM12878	blood:	n/a	n/a
4	BHLHE40	chr2:56545340-56545585	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:56565371-56565964	GM12878	blood:	n/a	n/a
6	BRCA1	chr2:56457381-56457608	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr2:56519048-56519209	K562	blood:	n/a	chr2:56519176-56519187
8	CEBPB	chr2:56519071-56519313	IMR90	lung:	n/a	chr2:56519176-56519187
9	CEBPB	chr2:56532868-56533008	K562	blood:	n/a	chr2:56532962-56532971 chr2:56532961-56532972 chr2:56532960-56532971
10	CEBPB	chr2:56576216-56576333	IMR90	lung:	n/a	chr2:56576268-56576279 chr2:56576266-56576277 chr2:56576266-56576279 chr2:56576268-56576277
11	CEBPB	chr2:56457272-56457434	A549	lung:	n/a	chr2:56457333-56457346 chr2:56457335-56457346
12	CEBPB	chr2:56521073-56521330	HepG2	liver:	n/a	chr2:56521230-56521241
13	CEBPB	chr2:56613769-56614063	HepG2	liver:	n/a	chr2:56613909-56613920 chr2:56613909-56613922
14	CEBPB	chr2:56576147-56576382	HepG2	liver:	n/a	chr2:56576268-56576279 chr2:56576266-56576277 chr2:56576266-56576279 chr2:56576268-56576277
15	CEBPB	chr2:56558025-56558191	HepG2	liver:	n/a	chr2:56558074-56558085
16	CEBPB	chr2:56454989-56455254	HepG2	liver:	n/a	chr2:56455023-56455036 chr2:56455122-56455133
17	CEBPB	chr2:56521071-56521415	A549	lung:	n/a	chr2:56521230-56521241
18	CEBPB	chr2:56457088-56457680	Hela-S3	cervix:	n/a	chr2:56457235-56457246 chr2:56457333-56457346 chr2:56457335-56457346
19	CEBPB	chr2:56532812-56533144	HepG2	liver:	n/a	chr2:56532860-56532868 chr2:56532962-56532971 chr2:56532961-56532972 chr2:56532960-56532971
20	CEBPB	chr2:56538411-56538449	Hela-S3	cervix:	n/a	chr2:56538420-56538433 chr2:56538420-56538433 chr2:56538422-56538433 chr2:56538422-56538433 chr2:56538420-56538433
21	CEBPB	chr2:56504115-56504425	HepG2	liver:	n/a	chr2:56504248-56504259
22	CEBPB	chr2:56502650-56502969	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:56532812-56533081	A549	lung:	n/a	chr2:56532860-56532868 chr2:56532962-56532971 chr2:56532961-56532972 chr2:56532960-56532971
24	CEBPB	chr2:56457185-56457759	HCT-116	colon:	n/a	chr2:56457235-56457246 chr2:56457333-56457346 chr2:56457335-56457346
25	CEBPB	chr2:56521152-56521352	IMR90	lung:	n/a	chr2:56521230-56521241
26	CEBPB	chr2:56504242-56504294	IMR90	lung:	n/a	chr2:56504248-56504259
27	CEBPB	chr2:56532836-56533117	IMR90	lung:	n/a	chr2:56532860-56532868 chr2:56532962-56532971 chr2:56532961-56532972 chr2:56532960-56532971
28	CEBPB	chr2:56532896-56532979	Hela-S3	cervix:	n/a	chr2:56532962-56532971 chr2:56532961-56532972 chr2:56532960-56532971
29	CEBPB	chr2:56561220-56561603	Hela-S3	cervix:	n/a	chr2:56561477-56561489
30	CEBPB	chr2:56538314-56538571	H1-hESC	embryonic stem cell:	n/a	chr2:56538420-56538433 chr2:56538420-56538433 chr2:56538422-56538433 chr2:56538422-56538433 chr2:56538420-56538433
31	CEBPB	chr2:56519004-56519311	HepG2	liver:	n/a	chr2:56519176-56519187
32	CHD2	chr2:56620059-56620080	HepG2	liver:	n/a	n/a
33	CHD2	chr2:56565525-56565608	GM12878	blood:	n/a	n/a
34	CHD2	chr2:56536851-56536867	GM12878	blood:	n/a	n/a
35	CHD2	chr2:56545326-56545640	GM12878	blood:	n/a	n/a
36	CTCF	chr2:56516380-56516530	GM12878	blood:	n/a	n/a
37	CTCF	chr2:56498994-56499084	Lung_OC	lung:	n/a	n/a
38	CTCF	chr2:56516420-56516570	GM12873	blood:	n/a	n/a
39	CTCF	chr2:56516380-56516530	GM12872	blood:	n/a	n/a
40	CTCF	chr2:56516380-56516530	GM12871	blood:	n/a	n/a
41	CTCF	chr2:56516480-56516630	NHEK	skin:	n/a	n/a
42	CTCF	chr2:56516360-56516510	MCF-7	breast:	n/a	n/a
43	CTCF	chr2:56516400-56516550	HEK293	kidney:	n/a	n/a
44	CTCF	chr2:56516461-56516533	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr2:56516473-56516594	NHEK	skin:	n/a	n/a
46	CTCF	chr2:56516380-56516530	BJ	skin:	n/a	n/a
47	CTCF	chr2:56516343-56516745	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:56516446-56516548	LNCaP	prostate:	n/a	n/a
49	CTCF	chr2:56604267-56604363	ProgFib	skin:	n/a	n/a
50	CTCF	chr2:56516200-56516350	GM12865	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:56574420-56574470	HCPEpiC	choroid plexus:	n/a
2	chr2:56574420-56574470	ProgFib	skin:	n/a
3	chr2:56461845-56461895	HRCEpiC	kidney:	n/a
4	chr2:56461845-56461895	K562	blood:	n/a
5	chr2:56574420-56574470	LNCaP	prostate:	n/a
6	chr2:56461845-56461895	SKMC	muscle:	n/a
7	chr2:56461845-56461895	MCF-7	breast:	n/a
8	chr2:56461845-56461895	SK-N-SH	brain:	n/a
9	chr2:56461845-56461895	HL-60	blood:	n/a
10	chr2:56461845-56461895	NHBE	bronchial:	n/a
11	chr2:56461845-56461895	CMK	blood:	n/a
12	chr2:56461845-56461895	HCF	heart:	n/a
13	chr2:56574420-56574470	HL-60	blood:	n/a
14	chr2:56574420-56574470	PrEC	prostate:	n/a
15	chr2:56461845-56461895	GM12878	blood:	n/a
16	chr2:56461845-56461895	U87	brain:	n/a
17	chr2:56574420-56574470	HCT-116	colon:	n/a
18	chr2:56574420-56574470	NT2-D1	testis:	n/a
19	chr2:56574420-56574470	SK-N-MC	brain:	n/a
20	chr2:56574420-56574470	Hela-S3	cervix:	n/a
21	chr2:56574420-56574470	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:56574420-56574470	HEK293	kidney:	embryo
23	chr2:56461845-56461895	HEK293	kidney:	embryo
24	chr2:56574420-56574470	HRCEpiC	kidney:	n/a
25	chr2:56461845-56461895	Caco-2	colon:	n/a
26	chr2:56574420-56574470	SKMC	muscle:	n/a
27	chr2:56574420-56574470	HUVEC	blood vessel:	n/a
28	chr2:56574420-56574470	HNPCEpiC	eye:	n/a
29	chr2:56461845-56461895	NT2-D1	testis:	n/a
30	chr2:56461845-56461895	Hela-S3	cervix:	n/a
31	chr2:56461845-56461895	GM12891	blood:	n/a
32	chr2:56574420-56574470	BJ	skin:	n/a
33	chr2:56574420-56574470	PANC-1	pancreas:	n/a
34	chr2:56574420-56574470	T-47D	breast:	n/a
35	chr2:56574420-56574470	ovcar-3	ovarian:	n/a
36	chr2:56461845-56461895	H1-hESC	embryonic stem cell:	embryo
37	chr2:56574420-56574470	U87	brain:	n/a
38	chr2:56461845-56461895	SK-N-MC	brain:	n/a
39	chr2:56574420-56574470	GM19239	blood:	n/a
40	chr2:56574420-56574470	IMR90	lung:	fetal
41	chr2:56574420-56574470	SK-N-SH	brain:	n/a
42	chr2:56461845-56461895	HUVEC	blood vessel:	n/a
43	chr2:56461845-56461895	Jurkat	blood:	n/a
44	chr2:56574420-56574470	Hepatocyte	liver:	n/a
45	chr2:56461845-56461895	HCPEpiC	choroid plexus:	n/a
46	chr2:56574420-56574470	HCM	heart:	n/a
47	chr2:56574420-56574470	HepG2	liver:	n/a
48	chr2:56574420-56574470	NH-A	brain:	n/a
49	chr2:56461845-56461895	AG10803	skin:	n/a
50	chr2:56461845-56461895	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:56535064..56538835-chr2:56538969..56542795,4	K562	blood:
2	chr2:56618904..56620543-chr2:56628115..56630656,2	K562	blood:
3	chr2:56455869..56458402-chr2:56460925..56463383,2	K562	blood:
4	chr2:56584362..56587143-chr2:56589529..56592392,2	K562	blood:
5	chr2:56495147..56497223-chr2:56498821..56501572,2	K562	blood:
6	chr2:56501627..56504616-chr2:56522910..56525116,2	K562	blood:
7	chr2:56493299..56495631-chr2:56495862..56498685,2	K562	blood:
8	chr2:56496763..56498267-chr2:56498962..56500465,2	K562	blood:
9	chr2:56464641..56466230-chr2:56471449..56473593,2	K562	blood:
10	chr2:56618904..56620543-chr2:56628115..56630656,2	K562	blood:
11	chr11:78431114..78431635-chr2:56568356..56568877,2	MCF-7	breast:
12	chr2:56496763..56498267-chr2:56498962..56500465,2	K562	blood:
13	chr2:56497998..56500277-chr2:56521559..56523561,2	MCF-7	breast:
14	chr2:56591468..56594426-chr2:56642626..56645610,2	MCF-7	breast:
15	chr2:56464641..56466230-chr2:56471449..56473593,2	K562	blood:
16	chr2:56456139..56458402-chr2:56461204..56463383,2	K562	blood:
17	chr2:56497998..56500277-chr2:56521559..56523561,2	MCF-7	breast:
18	chr2:56495147..56497223-chr2:56498821..56501572,2	K562	blood:
19	chr2:56501627..56504616-chr2:56522910..56525116,2	K562	blood:
20	chr2:56493299..56495631-chr2:56495862..56498685,2	K562	blood:
21	chr2:56535064..56538835-chr2:56538969..56542795,4	K562	blood:
22	chr2:56492076..56493596-chr6:44214720..44217244,2	K562	blood:
23	chr2:56542595..56543142-chr4:88834329..88835129,2	MCF-7	breast:
24	chr2:56584362..56587143-chr2:56589529..56592392,2	K562	blood:

Variant related genes	Relation type
RNA5SP93	TF binding region
RNA5SP93	CpG island
ENSG00000199395	chromatin interactions
ENSG00000096384	chromatin interactions

Extended variants
information (count: 7445 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:7445 , 50 per page) page: 1 2 3 4 5 6 7 ... 149

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560241726	chr2:56447957-56447958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs182593478	chr2:56447983-56447984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542634748	chr2:56448017-56448018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188326652	chr2:56448072-56448073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113894979	chr2:56448073-56448074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531484725	chr2:56448101-56448102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551623896	chr2:56448104-56448105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150091061	chr2:56448110-56448111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527443229	chr2:56448115-56448116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532906571	chr2:56448155-56448156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191418408	chr2:56448175-56448176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541080508	chr2:56448184-56448185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs78334090	chr2:56448214-56448215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10490395	chr2:56448266-56448267	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs548944488	chr2:56448279-56448280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183697746	chr2:56448293-56448294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188567682	chr2:56448347-56448348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374491640	chr2:56448374-56448375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558391308	chr2:56448376-56448377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs578110096	chr2:56448408-56448409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192463840	chr2:56448411-56448412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566563207	chr2:56448441-56448442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184826161	chr2:56448446-56448447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563321717	chr2:56448504-56448505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186589820	chr2:56448528-56448529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191376982	chr2:56448590-56448591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542671730	chr2:56448591-56448592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562365059	chr2:56448610-56448611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575958653	chr2:56448734-56448735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138357654	chr2:56448759-56448760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565183637	chr2:56448861-56448862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369058584	chr2:56448899-56448900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs527523340	chr2:56448924-56448925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529559860	chr2:56448965-56448966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184598916	chr2:56448967-56448968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560241652	chr2:56448992-56448993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529370115	chr2:56449019-56449020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs149336978	chr2:56449031-56449032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189869714	chr2:56449054-56449055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549553745	chr2:56449056-56449057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538194555	chr2:56449074-56449075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192806673	chr2:56449092-56449093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368650182	chr2:56449101-56449102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144602289	chr2:56449156-56449157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185262296	chr2:56449179-56449180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116247157	chr2:56449210-56449211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536368336	chr2:56449244-56449245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs72801191	chr2:56449261-56449262	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs558058641	chr2:56449370-56449371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557891364	chr2:56449375-56449376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
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
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
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Mental retardation	19951919	CNVD
Myelofibrosis	22110671	CNVD
Microcephaly	20799320	CNVD
camptodactyly	20799320	CNVD
cognitive delay	20799320	CNVD
prenatal and postnatal growth deficiency	20799320	CNVD
ptosis of eyelids	20799320	CNVD
Maculopathy	20981449	CNVD
2p16.1 microdeletion syndrome	22283845	CNVD
Autism	22579565	CNVD
Autism	16963482	CNVD
Autism	21750575	CNVD
idiopathic intellectual disability	16963482	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Multiple myeloma	16616336	CNVD
Follicular lymphoma	17699855	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:558 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:56439600-56451000	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr2:56446800-56454600	Weak transcription	HSMM	muscle
3	chr2:56451000-56451400	Enhancers	Muscle Satellite Cultured Cells	--
4	chr2:56451200-56452000	Enhancers	HUVEC	blood vessel
5	chr2:56451400-56451600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
6	chr2:56451600-56452000	Enhancers	Muscle Satellite Cultured Cells	--
7	chr2:56452000-56453000	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr2:56452000-56454400	Weak transcription	HUVEC	blood vessel
9	chr2:56453000-56454800	Enhancers	Muscle Satellite Cultured Cells	--
10	chr2:56454400-56457000	Enhancers	HUVEC	blood vessel
11	chr2:56454600-56455200	Enhancers	HSMM	muscle
12	chr2:56454800-56455400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
13	chr2:56454800-56455400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr2:56454800-56455600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr2:56455200-56455400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr2:56455200-56456800	Weak transcription	HSMM	muscle
17	chr2:56455400-56456000	Enhancers	Muscle Satellite Cultured Cells	--
18	chr2:56455600-56456000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr2:56455600-56457000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr2:56456000-56456200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
21	chr2:56456000-56456400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr2:56456000-56458200	Enhancers	HMEC	breast
23	chr2:56456000-56458600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr2:56456200-56456600	Enhancers	Muscle Satellite Cultured Cells	--
25	chr2:56456200-56457800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr2:56456200-56457800	Enhancers	Hela-S3	cervix
27	chr2:56456200-56458200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr2:56456400-56456800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr2:56456600-56457400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
30	chr2:56456800-56457400	Enhancers	HSMMtube	muscle
31	chr2:56456800-56457800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr2:56456800-56458600	Enhancers	HSMM	muscle
33	chr2:56457000-56457200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr2:56457000-56457800	Flanking Active TSS	HUVEC	blood vessel
35	chr2:56457000-56457800	Enhancers	NHEK	skin
36	chr2:56457000-56458400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr2:56457200-56457600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr2:56457200-56457800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr2:56457400-56457600	Enhancers	Muscle Satellite Cultured Cells	--
40	chr2:56457400-56461000	Weak transcription	HSMMtube	muscle
41	chr2:56457600-56458000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
42	chr2:56457600-56458600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr2:56457800-56458600	Enhancers	HUVEC	blood vessel
44	chr2:56458000-56458400	Enhancers	Muscle Satellite Cultured Cells	--
45	chr2:56458200-56466000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr2:56458400-56458600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
47	chr2:56458600-56459000	Enhancers	Muscle Satellite Cultured Cells	--
48	chr2:56458600-56461000	Weak transcription	HSMM	muscle
49	chr2:56459000-56459200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
50	chr2:56459200-56461200	Enhancers	Muscle Satellite Cultured Cells	--

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