Variant report

Variant	nsv1000899
Chromosome Location	chr2:57537817-57694142
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:690)
CpG islands
(count:61)
Chromatin interactive
region (count:21)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:690 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:57677308-57677677	GM12878	blood:	n/a	n/a
2	ATF2	chr2:57677283-57677736	GM12878	blood:	n/a	n/a
3	ATF3	chr2:57600561-57601162	HCT-116	colon:	n/a	n/a
4	BACH1	chr2:57623493-57623938	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr2:57677301-57677735	GM12878	blood:	n/a	n/a
6	BATF	chr2:57677353-57677672	GM12878	blood:	n/a	n/a
7	BCL11A	chr2:57677351-57677642	GM12878	blood:	n/a	n/a
8	BCL11A	chr2:57677323-57677668	GM12878	blood:	n/a	n/a
9	BCL3	chr2:57677288-57677769	GM12878	blood:	n/a	n/a
10	BCL3	chr2:57656947-57657199	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:57540650-57541005	HepG2	liver:	n/a	n/a
12	BHLHE40	chr2:57677398-57677689	GM12878	blood:	n/a	n/a
13	BRCA1	chr2:57625938-57625986	GM12878	blood:	n/a	n/a
14	CBX3	chr2:57600551-57601256	HCT-116	colon:	n/a	n/a
15	CBX3	chr2:57570484-57570977	HCT-116	colon:	n/a	n/a
16	CEBPB	chr2:57541461-57541662	A549	lung:	n/a	chr2:57541545-57541556
17	CEBPB	chr2:57635068-57635356	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr2:57540913-57541201	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:57653300-57653715	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:57671275-57671658	A549	lung:	n/a	chr2:57671434-57671445
21	CEBPB	chr2:57560415-57560691	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr2:57686957-57687253	A549	lung:	n/a	chr2:57687072-57687083
23	CEBPB	chr2:57541450-57541674	HepG2	liver:	n/a	chr2:57541545-57541556
24	CEBPB	chr2:57560414-57560688	A549	lung:	n/a	n/a
25	CEBPB	chr2:57670883-57671690	HCT-116	colon:	n/a	chr2:57671434-57671445
26	CEBPB	chr2:57671281-57671572	HepG2	liver:	n/a	chr2:57671434-57671445
27	CEBPB	chr2:57542794-57543019	Hela-S3	cervix:	n/a	chr2:57542879-57542892 chr2:57542879-57542892
28	CEBPB	chr2:57560462-57560684	IMR90	lung:	n/a	n/a
29	CEBPB	chr2:57671064-57671644	HCT-116	colon:	n/a	chr2:57671434-57671445
30	CEBPB	chr2:57560455-57560691	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:57549134-57549362	A549	lung:	n/a	chr2:57549209-57549220
32	CEBPB	chr2:57677243-57677819	GM12878	blood:	n/a	n/a
33	CEBPB	chr2:57549106-57549358	HepG2	liver:	n/a	chr2:57549209-57549220
34	CEBPB	chr2:57584646-57584648	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:57595173-57595845	HCT-116	colon:	n/a	n/a
36	CEBPB	chr2:57671313-57671586	IMR90	lung:	n/a	chr2:57671434-57671445
37	CEBPB	chr2:57686952-57687247	HepG2	liver:	n/a	chr2:57687072-57687083
38	CEBPB	chr2:57671256-57671580	Hela-S3	cervix:	n/a	chr2:57671434-57671445
39	CEBPB	chr2:57595285-57595780	HCT-116	colon:	n/a	n/a
40	CEBPB	chr2:57548887-57549388	Hela-S3	cervix:	n/a	chr2:57549209-57549220
41	CEBPB	chr2:57644218-57644262	A549	lung:	n/a	n/a
42	CEBPB	chr2:57630938-57631021	A549	lung:	n/a	chr2:57630962-57630975
43	CHD2	chr2:57677410-57677610	GM12878	blood:	n/a	n/a
44	CREB1	chr2:57677261-57677817	GM12878	blood:	n/a	n/a
45	CTCF	chr2:57604229-57604389	LNCaP	prostate:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
46	CTCF	chr2:57604303-57604311	GM20000	blood:	n/a	n/a
47	CTCF	chr2:57604202-57604410	GM13977	blood:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
48	CTCF	chr2:57604280-57604430	HVMF	connective:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
49	CTCF	chr2:57681180-57681330	GM06990	blood:	n/a	n/a
50	CTCF	chr2:57681140-57681290	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:57634837-57634887	PrEC	prostate:	n/a
2	chr2:57634837-57634887	AoSMC	blood vessel:	n/a
3	chr2:57634837-57634887	HL-60	blood:	n/a
4	chr2:57634837-57634887	HAEpiC	amniotic membrane:	n/a
5	chr2:57634837-57634887	SAEC	small airway:	n/a
6	chr2:57634837-57634887	HIPEpiC	eye:	n/a
7	chr2:57634837-57634887	A549	lung:	n/a
8	chr2:57634837-57634887	ProgFib	skin:	n/a
9	chr2:57634837-57634887	CMK	blood:	n/a
10	chr2:57634837-57634887	HepG2	liver:	n/a
11	chr2:57634837-57634887	Hepatocyte	liver:	n/a
12	chr2:57634837-57634887	AG09309	skin:	n/a
13	chr2:57634837-57634887	HCPEpiC	choroid plexus:	n/a
14	chr2:57634837-57634887	U87	brain:	n/a
15	chr2:57634837-57634887	BE2_C	brain:	n/a
16	chr2:57634837-57634887	HNPCEpiC	eye:	n/a
17	chr2:57634837-57634887	HRCEpiC	kidney:	n/a
18	chr2:57634837-57634887	AG04449	skin:	fetal
19	chr2:57634837-57634887	K562	blood:	n/a
20	chr2:57634837-57634887	PFSK-1	brain:	n/a
21	chr2:57634837-57634887	GM12878	blood:	n/a
22	chr2:57634837-57634887	SK-N-MC	brain:	n/a
23	chr2:57634837-57634887	GM06990	blood:	n/a
24	chr2:57634837-57634887	HPAEpiC	pulmonary alveolar:	n/a
25	chr2:57634837-57634887	SKMC	muscle:	n/a
26	chr2:57634837-57634887	T-47D	breast:	n/a
27	chr2:57634837-57634887	PANC-1	pancreas:	n/a
28	chr2:57634837-57634887	Jurkat	blood:	n/a
29	chr2:57634837-57634887	AG10803	skin:	n/a
30	chr2:57634837-57634887	HCF	heart:	n/a
31	chr2:57634837-57634887	IMR90	lung:	fetal
32	chr2:57634837-57634887	HMEC	breast:	n/a
33	chr2:57634837-57634887	ECC-1	luminal epithelium:	n/a
34	chr2:57634837-57634887	LNCaP	prostate:	n/a
35	chr2:57634837-57634887	HCT-116	colon:	n/a
36	chr2:57634837-57634887	ovcar-3	ovarian:	n/a
37	chr2:57634837-57634887	AG04450	lung:	fetal
38	chr2:57634837-57634887	MCF-7	breast:	n/a
39	chr2:57634837-57634887	HCM	heart:	n/a
40	chr2:57634837-57634887	BJ	skin:	n/a
41	chr2:57634837-57634887	NH-A	brain:	n/a
42	chr2:57634837-57634887	RPTEC	kidney:	n/a
43	chr2:57634837-57634887	NT2-D1	testis:	n/a
44	chr2:57634837-57634887	Caco-2	colon:	n/a
45	chr2:57634837-57634887	NHDF-neo	bronchial:	n/a
46	chr2:57634837-57634887	AG09319	gingival:	n/a
47	chr2:57634837-57634887	NB4	blood:	n/a
48	chr2:57634837-57634887	GM12891	blood:	n/a
49	chr2:57634837-57634887	HRE	kidney:	n/a
50	chr2:57634837-57634887	GM19239	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:57011309..57011934-chr2:57604188..57604743,2	MCF-7	breast:
2	chr2:57670502..57672263-chr2:57675373..57678104,2	MCF-7	breast:
3	chr2:57603852..57604740-chr2:57724321..57725273,3	MCF-7	breast:
4	chr2:56412160..56413674-chr2:57559267..57562168,2	MCF-7	breast:
5	chr2:57633446..57635721-chr2:57643662..57645382,2	MCF-7	breast:
6	chr2:57602104..57602641-chr2:57724502..57725135,2	MCF-7	breast:
7	chr2:57631506..57633055-chr2:57645760..57647304,2	MCF-7	breast:
8	chr2:57603431..57604465-chr2:57724481..57725285,5	MCF-7	breast:
9	chr2:57627476..57629537-chr2:57644280..57646195,2	MCF-7	breast:
10	chr2:57670502..57672263-chr2:57675373..57678104,2	MCF-7	breast:
11	chr2:57584628..57586577-chr2:57587736..57590174,2	K562	blood:
12	chr2:57669021..57671005-chr2:57673900..57675904,2	K562	blood:
13	chr2:57540667..57542939-chr2:57544069..57546908,2	K562	blood:
14	chr2:57627476..57629537-chr2:57644280..57646195,2	MCF-7	breast:
15	chr2:57631506..57633055-chr2:57645760..57647304,2	MCF-7	breast:
16	chr2:57680802..57681722-chr2:57724395..57725159,3	MCF-7	breast:
17	chr2:57669021..57671005-chr2:57673900..57675904,2	K562	blood:
18	chr2:57633446..57635721-chr2:57643662..57645382,2	MCF-7	breast:
19	chr2:57540667..57542939-chr2:57544069..57546908,2	K562	blood:
20	chr2:57686552..57689405-chr2:57735534..57737911,2	K562	blood:
21	chr2:57584628..57586577-chr2:57587736..57590174,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCL-2	chr2:57541338-57541655	XLOC_002102
2	lnc-FANCL-8	chr2:57656683-57656947	NONHSAT070833
3	lnc-FANCL-8	chr2:57657781-57657828	NONHSAT070833
4	lnc-FANCL-8	chr2:57657275-57657340	NONHSAT070833
5	lnc-FANCL-2	chr2:57542598-57542640	NONHSAT070831
6	lnc-FANCL-2	chr2:57542599-57542640	XLOC_002102
7	lnc-FANCL-2	chr2:57541337-57541655	NONHSAT070831
8	lnc-VRK2-16	chr2:57672949-57673194	NONHSAT070834
9	lnc-VRK2-16	chr2:57659475-57659520	NONHSAT070834

No data

Variant related genes	Relation type
ENSG00000270569	TF binding region
ENSG00000270569	CpG island
ENSG00000233251	chromatin interactions
TSC1	miRNA target sites
SPRY4	miRNA target sites

Extended variants
information (count: 2585 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2585 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145225148	chr2:57539201-57539202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553621090	chr2:57539205-57539206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs17805484	chr2:57539209-57539210	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs540681701	chr2:57539223-57539224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs76605163	chr2:57539258-57539259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs80098883	chr2:57539301-57539302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543044686	chr2:57539339-57539340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542264899	chr2:57539343-57539344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562830967	chr2:57539352-57539353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs562619857	chr2:57539373-57539374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs149142172	chr2:57539398-57539399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551152010	chr2:57539415-57539416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564698720	chr2:57539427-57539428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182201214	chr2:57539438-57539439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547054688	chr2:57539471-57539472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10178543	chr2:57539475-57539476	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs1357378	chr2:57539489-57539490	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs549793577	chr2:57539499-57539500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569439762	chr2:57539504-57539505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542095024	chr2:57539524-57539525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538497483	chr2:57539526-57539527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs78134281	chr2:57539527-57539528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs578194664	chr2:57539531-57539532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545148740	chr2:57539549-57539550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78588593	chr2:57539560-57539561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76361044	chr2:57539590-57539591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376571274	chr2:57539609-57539610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187209174	chr2:57539629-57539630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs116481759	chr2:57539634-57539635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542654838	chr2:57539646-57539647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562942750	chr2:57539676-57539677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576038592	chr2:57539684-57539685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149275840	chr2:57539708-57539709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs199505177	chr2:57539709-57539710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540995189	chr2:57539720-57539721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201397291	chr2:57539722-57539723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564857926	chr2:57539727-57539728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527467934	chr2:57539777-57539778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547216757	chr2:57539933-57539934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77063340	chr2:57539954-57539955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376796822	chr2:57539962-57539963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529835484	chr2:57539997-57539998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112786631	chr2:57540026-57540027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190984849	chr2:57540032-57540033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538979317	chr2:57540039-57540040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538657299	chr2:57540040-57540041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563803218	chr2:57540071-57540072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572008005	chr2:57540133-57540134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530114250	chr2:57540154-57540155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113354936	chr2:57540182-57540183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:57539200-57539400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:57539400-57540400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:57540400-57541200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:57540400-57541200	Enhancers	HMEC	breast
5	chr2:57540400-57542800	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr2:57540600-57541200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr2:57557200-57557400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr2:57557200-57558200	Enhancers	Fetal Heart	heart
9	chr2:57557400-57558400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr2:57557600-57558200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr2:57557600-57558200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr2:57557600-57558200	Enhancers	NHEK	skin
13	chr2:57557600-57558400	Enhancers	HSMM	muscle
14	chr2:57558200-57559800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr2:57558400-57558800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr2:57559600-57560200	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr2:57559800-57560000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr2:57593600-57601000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr2:57595200-57595800	Enhancers	HMEC	breast
20	chr2:57595400-57595800	Enhancers	NHEK	skin
21	chr2:57595800-57599600	Weak transcription	NHEK	skin
22	chr2:57595800-57600000	Weak transcription	HMEC	breast
23	chr2:57596200-57596800	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr2:57598000-57598400	Enhancers	HSMMtube	muscle
25	chr2:57598200-57598400	Enhancers	HSMM	muscle
26	chr2:57598400-57599800	Weak transcription	HSMMtube	muscle
27	chr2:57598400-57602000	Enhancers	Muscle Satellite Cultured Cells	--
28	chr2:57598600-57599600	Weak transcription	HSMM	muscle
29	chr2:57599000-57601400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr2:57599400-57601400	Enhancers	HUVEC	blood vessel
31	chr2:57599600-57600200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr2:57599600-57601400	Enhancers	NHEK	skin
33	chr2:57599600-57601800	Enhancers	HSMM	muscle
34	chr2:57599600-57601800	Enhancers	NHDF-Ad	bronchial
35	chr2:57599800-57600000	Active TSS	A549	lung
36	chr2:57599800-57601400	Enhancers	HSMMtube	muscle
37	chr2:57600000-57600200	Flanking Active TSS	A549	lung
38	chr2:57600000-57601000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr2:57600000-57601200	Enhancers	NH-A	brain
40	chr2:57600000-57601400	Enhancers	HMEC	breast
41	chr2:57600200-57601800	Enhancers	A549	lung
42	chr2:57601000-57601200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr2:57605600-57606400	Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr2:57613400-57614000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr2:57623200-57624000	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr2:57623400-57623800	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr2:57623400-57624000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr2:57623400-57624200	Enhancers	H1 Cell Line	embryonic stem cell
49	chr2:57623400-57624200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr2:57623400-57624200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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