Variant report

Variant	nsv874199
Chromosome Location	chr2:58031249-58161520
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:880)
CpG islands
(count:122)
Chromatin interactive
region (count:37)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:880 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:58133318-58133560	K562	blood:	n/a	n/a
2	ARID3A	chr2:58120865-58121650	HepG2	liver:	n/a	chr2:58120933-58120949
3	ARID3A	chr2:58109239-58109431	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:58110241-58110306	HepG2	liver:	n/a	n/a
5	ATF2	chr2:58135565-58136257	GM12878	blood:	n/a	n/a
6	ATF2	chr2:58036301-58036756	GM12878	blood:	n/a	n/a
7	ATF2	chr2:58036295-58036793	GM12878	blood:	n/a	n/a
8	ATF2	chr2:58103420-58103903	GM12878	blood:	n/a	n/a
9	ATF2	chr2:58117511-58118049	GM12878	blood:	n/a	n/a
10	ATF2	chr2:58135724-58136260	GM12878	blood:	n/a	n/a
11	ATF2	chr2:58119903-58120465	GM12878	blood:	n/a	n/a
12	ATF2	chr2:58119765-58120524	GM12878	blood:	n/a	n/a
13	ATF3	chr2:58113432-58113668	K562	blood:	n/a	n/a
14	ATF3	chr2:58108949-58109883	A549	lung:	n/a	n/a
15	ATF3	chr2:58108826-58109957	A549	lung:	n/a	n/a
16	BATF	chr2:58109338-58109594	GM12878	blood:	n/a	chr2:58109489-58109500
17	BATF	chr2:58103529-58103763	GM12878	blood:	n/a	n/a
18	BATF	chr2:58103513-58103804	GM12878	blood:	n/a	n/a
19	BATF	chr2:58117578-58117969	GM12878	blood:	n/a	chr2:58117780-58117791
20	BATF	chr2:58119946-58120342	GM12878	blood:	n/a	n/a
21	BATF	chr2:58117612-58117933	GM12878	blood:	n/a	chr2:58117780-58117791
22	BATF	chr2:58119970-58120390	GM12878	blood:	n/a	n/a
23	BCL11A	chr2:58069787-58069928	GM12878	blood:	n/a	n/a
24	BCL11A	chr2:58119906-58120406	GM12878	blood:	n/a	n/a
25	BCL3	chr2:58108414-58110314	A549	lung:	n/a	n/a
26	BCL3	chr2:58117504-58118039	GM12878	blood:	n/a	n/a
27	BCL3	chr2:58108514-58110446	A549	lung:	n/a	n/a
28	BCL3	chr2:58119962-58120440	GM12878	blood:	n/a	n/a
29	BCLAF1	chr2:58120008-58120402	GM12878	blood:	n/a	n/a
30	BCLAF1	chr2:58119888-58120533	GM12878	blood:	n/a	n/a
31	BCLAF1	chr2:58133272-58133611	GM12878	blood:	n/a	n/a
32	BCLAF1	chr2:58133225-58133655	GM12878	blood:	n/a	n/a
33	BCLAF1	chr2:58036584-58036924	GM12878	blood:	n/a	n/a
34	BHLHE40	chr2:58113306-58113616	GM12878	blood:	n/a	n/a
35	BHLHE40	chr2:58135826-58136451	GM12878	blood:	n/a	n/a
36	BHLHE40	chr2:58113487-58113591	K562	blood:	n/a	n/a
37	BHLHE40	chr2:58119898-58120467	GM12878	blood:	n/a	n/a
38	BRCA1	chr2:58104147-58104166	GM12878	blood:	n/a	n/a
39	BRCA1	chr2:58109764-58109960	GM12878	blood:	n/a	n/a
40	BRCA1	chr2:58109008-58109651	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr2:58148064-58148075	GM12878	blood:	n/a	n/a
42	CBX3	chr2:58155306-58155541	K562	blood:	n/a	n/a
43	CBX3	chr2:58155326-58155543	K562	blood:	n/a	n/a
44	CEBPB	chr2:58108913-58109691	A549	lung:	n/a	chr2:58109240-58109251
45	CEBPB	chr2:58140356-58140505	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr2:58119795-58120526	GM12878	blood:	n/a	chr2:58120292-58120303
47	CEBPB	chr2:58113439-58113597	K562	blood:	n/a	chr2:58113511-58113522
48	CEBPB	chr2:58113440-58113679	IMR90	lung:	n/a	chr2:58113511-58113522
49	CEBPB	chr2:58108988-58109639	Hela-S3	cervix:	n/a	chr2:58109240-58109251
50	CEBPB	chr2:58140266-58140472	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:58130074-58130124	HCM	heart:	n/a
2	chr2:58133858-58133908	HPAEpiC	pulmonary alveolar:	n/a
3	chr2:58130074-58130124	ProgFib	skin:	n/a
4	chr2:58130074-58130124	Hela-S3	cervix:	n/a
5	chr2:58130074-58130124	PFSK-1	brain:	n/a
6	chr2:58130074-58130124	HCT-116	colon:	n/a
7	chr2:58130074-58130124	K562	blood:	n/a
8	chr2:58133858-58133908	SAEC	small airway:	n/a
9	chr2:58130074-58130124	AoSMC	blood vessel:	n/a
10	chr2:58130074-58130124	AG10803	skin:	n/a
11	chr2:58130074-58130124	HL-60	blood:	n/a
12	chr2:58130074-58130124	NB4	blood:	n/a
13	chr2:58130074-58130124	SK-N-SH	brain:	n/a
14	chr2:58130074-58130124	GM12878	blood:	n/a
15	chr2:58130074-58130124	CMK	blood:	n/a
16	chr2:58133858-58133908	GM12878	blood:	n/a
17	chr2:58133858-58133908	HEK293	kidney:	embryo
18	chr2:58130074-58130124	HEK293	kidney:	embryo
19	chr2:58133858-58133908	HCT-116	colon:	n/a
20	chr2:58133858-58133908	HEEpiC	esophagus:	n/a
21	chr2:58133858-58133908	AG09309	skin:	n/a
22	chr2:58130074-58130124	NHBE	bronchial:	n/a
23	chr2:58133858-58133908	GM06990	blood:	n/a
24	chr2:58130074-58130124	Caco-2	colon:	n/a
25	chr2:58133858-58133908	T-47D	breast:	n/a
26	chr2:58130074-58130124	T-47D	breast:	n/a
27	chr2:58130074-58130124	HMEC	breast:	n/a
28	chr2:58130074-58130124	HCF	heart:	n/a
29	chr2:58133858-58133908	SK-N-SH_RA	brain:	n/a
30	chr2:58130074-58130124	MCF-7	breast:	n/a
31	chr2:58130074-58130124	ovcar-3	ovarian:	n/a
32	chr2:58133858-58133908	HCF	heart:	n/a
33	chr2:58133858-58133908	AG04449	skin:	fetal
34	chr2:58133858-58133908	MCF-7	breast:	n/a
35	chr2:58130074-58130124	HAEpiC	amniotic membrane:	n/a
36	chr2:58130074-58130124	HRPEpiC	eye:	n/a
37	chr2:58130074-58130124	A549	lung:	n/a
38	chr2:58133858-58133908	NB4	blood:	n/a
39	chr2:58133858-58133908	PrEC	prostate:	n/a
40	chr2:58130074-58130124	HNPCEpiC	eye:	n/a
41	chr2:58130074-58130124	GM19239	blood:	n/a
42	chr2:58130074-58130124	BE2_C	brain:	n/a
43	chr2:58130074-58130124	SK-N-MC	brain:	n/a
44	chr2:58130074-58130124	BJ	skin:	n/a
45	chr2:58130074-58130124	AG09319	gingival:	n/a
46	chr2:58130074-58130124	SAEC	small airway:	n/a
47	chr2:58133858-58133908	Hela-S3	cervix:	n/a
48	chr2:58130074-58130124	SK-N-SH_RA	brain:	n/a
49	chr2:58130074-58130124	GM12891	blood:	n/a
50	chr2:58130074-58130124	H1-hESC	embryonic stem cell:	embryo

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:58107882..58110920-chr2:58111613..58114646,4	MCF-7	breast:
2	chr2:58155866..58157650-chr2:58160702..58162361,2	MCF-7	breast:
3	chr2:58158038..58160729-chr2:58160739..58162666,2	MCF-7	breast:
4	chr2:58133060..58135151-chr2:58272508..58275235,2	MCF-7	breast:
5	chr2:58097977..58100316-chr2:58105031..58107914,3	K562	blood:
6	chr2:58085320..58088148-chr2:58088783..58090766,2	K562	blood:
7	chr2:58109065..58111032-chr2:58113088..58114709,2	MCF-7	breast:
8	chr2:58133383..58133906-chr2:58674883..58675813,3	K562	blood:
9	chr2:58067853..58070668-chr20:48552901..48554981,2	MCF-7	breast:
10	chr2:58092863..58095736-chr2:58103912..58105798,2	K562	blood:
11	chr2:58025264..58027443-chr2:58030430..58032051,2	MCF-7	breast:
12	chr2:58090841..58093056-chr2:58096618..58098915,2	K562	blood:
13	chr2:58108798..58111320-chr2:58112288..58115523,3	K562	blood:
14	chr2:58118375..58121623-chr2:58123563..58127574,4	K562	blood:
15	chr2:58096956..58099985-chr2:58100360..58105173,5	K562	blood:
16	chr2:58097977..58100316-chr2:58105031..58107914,3	K562	blood:
17	chr2:58133222..58134008-chr2:58674834..58675396,2	MCF-7	breast:
18	chr2:58092863..58095736-chr2:58103912..58105798,2	K562	blood:
19	chr2:58035263..58037581-chr2:58040221..58042453,2	K562	blood:
20	chr2:58155866..58157650-chr2:58160702..58162361,2	MCF-7	breast:
21	chr2:58096956..58099985-chr2:58100360..58105173,5	K562	blood:
22	chr2:58118375..58121623-chr2:58123563..58127574,4	K562	blood:
23	chr2:58109065..58111032-chr2:58113088..58114709,2	MCF-7	breast:
24	chr2:58094285..58096431-chr2:58101485..58103642,2	MCF-7	breast:
25	chr2:58137881..58138419-chr2:58675132..58675784,2	MCF-7	breast:
26	chr2:58131028..58133565-chr2:58275828..58277987,2	MCF-7	breast:
27	chr2:58085320..58088148-chr2:58088783..58090766,2	K562	blood:
28	chr2:58108798..58111320-chr2:58112288..58115523,3	K562	blood:
29	chr2:58132702..58133921-chr2:58674913..58675821,15	MCF-7	breast:
30	chr2:58107882..58110920-chr2:58111613..58114646,4	MCF-7	breast:
31	chr2:58133863..58138456-chr2:58272095..58275151,4	MCF-7	breast:
32	chr2:58035263..58037581-chr2:58040221..58042453,2	K562	blood:
33	chr2:58090841..58093056-chr2:58096618..58098915,2	K562	blood:
34	chr2:58110610..58113165-chr2:58114758..58117259,2	MCF-7	breast:
35	chr2:58110610..58113165-chr2:58114758..58117259,2	MCF-7	breast:
36	chr2:58094285..58096431-chr2:58101485..58103642,2	MCF-7	breast:
37	chr2:58158038..58160729-chr2:58160739..58162666,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC85A-6	chr2:58134787-58134974	NONHSAT070843
2	lnc-CCDC85A-6	chr2:58134791-58134974	NONHSAT070844

No data

Variant related genes	Relation type
VRK2	TF binding region
VRK2	CpG island
ENSG00000028116	chromatin interactions
ENSG00000124226	chromatin interactions

Extended variants
information (count: 3258 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3258 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370771374	chr2:58032235-58032236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs375043482	chr2:58032278-58032279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575531735	chr2:58032294-58032295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555130597	chr2:58032306-58032307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567044586	chr2:58032319-58032320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534398716	chr2:58032321-58032322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150019751	chr2:58032345-58032346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564688274	chr2:58032366-58032367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs184940136	chr2:58032367-58032368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559245464	chr2:58032403-58032404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550626825	chr2:58032429-58032430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76386882	chr2:58032459-58032460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs578086783	chr2:58032461-58032462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs13422790	chr2:58032468-58032469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570107452	chr2:58032481-58032482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189848814	chr2:58032485-58032486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575158554	chr2:58032495-58032496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2717075	chr2:58032530-58032531	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs2683620	chr2:58032553-58032554	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs566204270	chr2:58032572-58032573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182443869	chr2:58032642-58032643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540041259	chr2:58032675-58032676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs111407799	chr2:58032682-58032683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139666726	chr2:58032709-58032710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2683619	chr2:58032759-58032760	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs549387998	chr2:58032771-58032772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377054565	chr2:58032777-58032778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569215601	chr2:58032791-58032792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530064048	chr2:58032797-58032798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs142962337	chr2:58032805-58032806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368913211	chr2:58032817-58032818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528767268	chr2:58032841-58032842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534335116	chr2:58032866-58032867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562916694	chr2:58032906-58032907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530802290	chr2:58032923-58032924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372215505	chr2:58032945-58032946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575777961	chr2:58033021-58033022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570989021	chr2:58033086-58033087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34856986	chr2:58033121-58033122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375897305	chr2:58033122-58033123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556600354	chr2:58033158-58033159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146141618	chr2:58033165-58033166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542224270	chr2:58033188-58033189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187175787	chr2:58033205-58033206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572601608	chr2:58033218-58033219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139980195	chr2:58033227-58033228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565077005	chr2:58033248-58033249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532236629	chr2:58033255-58033256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544470238	chr2:58033270-58033271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562658553	chr2:58033282-58033283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	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	chr2:58032200-58032400	Enhancers	GM12878-XiMat	blood
2	chr2:58032400-58033600	Weak transcription	GM12878-XiMat	blood
3	chr2:58033600-58034000	Enhancers	GM12878-XiMat	blood
4	chr2:58034000-58036400	Weak transcription	GM12878-XiMat	blood
5	chr2:58036400-58037000	Enhancers	GM12878-XiMat	blood
6	chr2:58036600-58036800	Enhancers	A549	lung
7	chr2:58036800-58041600	Weak transcription	A549	lung
8	chr2:58041600-58042000	Enhancers	A549	lung
9	chr2:58042000-58043400	Weak transcription	A549	lung
10	chr2:58043400-58043800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr2:58043400-58044000	Enhancers	A549	lung
12	chr2:58051800-58052000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr2:58052000-58054600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr2:58054600-58055200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr2:58054800-58055800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr2:58069600-58070000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr2:58069600-58070400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr2:58069800-58070600	Enhancers	Pancreas	Pancrea
19	chr2:58069800-58070600	Bivalent Enhancer	Osteobl	bone
20	chr2:58070600-58073400	Weak transcription	Pancreas	Pancrea
21	chr2:58073400-58073800	ZNF genes & repeats	Pancreas	Pancrea
22	chr2:58073600-58073800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr2:58073600-58073800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr2:58073800-58074200	Weak transcription	Gastric	stomach
25	chr2:58073800-58076000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr2:58073800-58076000	Weak transcription	Pancreas	Pancrea
27	chr2:58076000-58076200	ZNF genes & repeats	Pancreas	Pancrea
28	chr2:58076000-58077400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr2:58076200-58077000	Weak transcription	Pancreas	Pancrea
30	chr2:58077000-58078000	ZNF genes & repeats	Pancreas	Pancrea
31	chr2:58077400-58077600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr2:58077400-58077800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr2:58077800-58078000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr2:58078000-58078200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr2:58088200-58089200	Enhancers	A549	lung
36	chr2:58089200-58090200	Flanking Active TSS	A549	lung
37	chr2:58089400-58090000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr2:58089400-58090200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr2:58089400-58090800	Enhancers	Muscle Satellite Cultured Cells	--
40	chr2:58090200-58091400	Enhancers	A549	lung
41	chr2:58090200-58104200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr2:58090800-58091400	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr2:58091400-58092400	Weak transcription	A549	lung
44	chr2:58091400-58093400	Enhancers	Muscle Satellite Cultured Cells	--
45	chr2:58091600-58093000	Enhancers	HUVEC	blood vessel
46	chr2:58092400-58092800	Enhancers	A549	lung
47	chr2:58092800-58095000	Weak transcription	A549	lung
48	chr2:58093400-58094800	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr2:58094800-58097400	Enhancers	Muscle Satellite Cultured Cells	--
50	chr2:58095000-58095200	Enhancers	Brain Substantia Nigra	brain

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