Variant report

Variant	nsv1003061
Chromosome Location	chr2:187950057-188282330
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1537)
CpG islands
(count:428)
Chromatin interactive
region (count:58)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1537 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:188082673-188083042	K562	blood:	n/a	chr2:188082805-188082821 chr2:188082806-188082822
2	ATF2	chr2:188128538-188128835	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr2:188033747-188034164	GM12878	blood:	n/a	n/a
4	ATF3	chr2:188075532-188075733	K562	blood:	n/a	n/a
5	BACH1	chr2:188268698-188269088	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:188190158-188190174	K562	blood:	n/a	n/a
7	BACH1	chr2:188208775-188208862	K562	blood:	n/a	n/a
8	BATF	chr2:188092264-188092475	GM12878	blood:	n/a	n/a
9	BCL11A	chr2:188089782-188090028	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr2:188268255-188268781	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:188268422-188268441	K562	blood:	n/a	n/a
12	BRCA1	chr2:187955611-187955635	H1-hESC	embryonic stem cell:	n/a	n/a
13	CBX3	chr2:188020298-188020615	HCT-116	colon:	n/a	n/a
14	CBX3	chr2:188193434-188193635	K562	blood:	n/a	n/a
15	CCNT2	chr2:188235207-188235395	K562	blood:	n/a	n/a
16	CCNT2	chr2:187972244-187972415	K562	blood:	n/a	n/a
17	CCNT2	chr2:187970957-187971070	K562	blood:	n/a	n/a
18	CEBPB	chr2:188161818-188162035	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:188075525-188075712	K562	blood:	n/a	chr2:188075578-188075589
20	CEBPB	chr2:187984174-187984487	IMR90	lung:	n/a	chr2:187984312-187984323
21	CEBPB	chr2:187984232-187984354	K562	blood:	n/a	chr2:187984312-187984323
22	CEBPB	chr2:188247829-188248047	IMR90	lung:	n/a	n/a
23	CEBPB	chr2:187995333-187995543	H1-hESC	embryonic stem cell:	n/a	chr2:187995431-187995442 chr2:187995433-187995442 chr2:187995433-187995442 chr2:187995431-187995444 chr2:187995433-187995442 chr2:187995431-187995444 chr2:187995433-187995442 chr2:187995433-187995444
24	CEBPB	chr2:188255544-188256024	A549	lung:	n/a	n/a
25	CEBPB	chr2:188064139-188064438	HepG2	liver:	n/a	chr2:188064300-188064311 chr2:188064301-188064312
26	CEBPB	chr2:188092236-188092435	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr2:187992438-187992790	HepG2	liver:	n/a	chr2:187992561-187992572 chr2:187992504-187992515
28	CEBPB	chr2:188107016-188107020	IMR90	lung:	n/a	n/a
29	CEBPB	chr2:188255557-188255969	IMR90	lung:	n/a	n/a
30	CEBPB	chr2:188246985-188247189	IMR90	lung:	n/a	chr2:188247056-188247067
31	CEBPB	chr2:187967067-187967329	HepG2	liver:	n/a	chr2:187967202-187967211
32	CEBPB	chr2:187980104-187980240	HepG2	liver:	n/a	chr2:187980172-187980185 chr2:187980172-187980183
33	CEBPB	chr2:188265611-188265953	HepG2	liver:	n/a	chr2:188265786-188265797
34	CEBPB	chr2:188224947-188225370	ECC-1	luminal epithelium:	n/a	chr2:188225170-188225187
35	CEBPB	chr2:187971749-187971925	HepG2	liver:	n/a	chr2:187971818-187971829
36	CEBPB	chr2:188064188-188064450	K562	blood:	n/a	chr2:188064300-188064311 chr2:188064301-188064312
37	CEBPB	chr2:188243537-188243874	HepG2	liver:	n/a	chr2:188243700-188243711
38	CEBPB	chr2:188011908-188012168	HepG2	liver:	n/a	chr2:188012053-188012064
39	CEBPB	chr2:188265688-188265928	Hela-S3	cervix:	n/a	chr2:188265786-188265797
40	CEBPB	chr2:187984157-187984487	HepG2	liver:	n/a	chr2:187984312-187984323
41	CEBPB	chr2:187967122-187967247	K562	blood:	n/a	chr2:187967202-187967211
42	CEBPB	chr2:188265642-188265965	A549	lung:	n/a	chr2:188265786-188265797
43	CEBPB	chr2:188243574-188243869	IMR90	lung:	n/a	chr2:188243700-188243711
44	CEBPB	chr2:188246914-188247199	K562	blood:	n/a	chr2:188247056-188247067
45	CEBPB	chr2:188075474-188075737	K562	blood:	n/a	chr2:188075578-188075589
46	CEBPB	chr2:188247909-188247932	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr2:188075457-188075812	Hela-S3	cervix:	n/a	chr2:188075578-188075589
48	CEBPB	chr2:188011965-188012105	A549	lung:	n/a	chr2:188012053-188012064
49	CEBPB	chr2:188166681-188166784	HepG2	liver:	n/a	n/a
50	CEBPB	chr2:187984178-187984438	A549	lung:	n/a	chr2:187984312-187984323

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:188093537-188093587	ovcar-3	ovarian:	n/a
2	chr2:188093537-188093587	ovcar-3	ovarian:	n/a
3	chr2:188093537-188093587	A549	lung:	n/a
4	chr2:188269443-188269493	ProgFib	skin:	n/a
5	chr2:188210673-188210723	K562	blood:	n/a
6	chr2:188269443-188269493	BJ	skin:	n/a
7	chr2:188093537-188093587	GM12891	blood:	n/a
8	chr2:188128809-188128859	LNCaP	prostate:	n/a
9	chr2:188274544-188274594	ECC-1	luminal epithelium:	n/a
10	chr2:188211981-188212031	HRCEpiC	kidney:	n/a
11	chr2:188210673-188210723	HCM	heart:	n/a
12	chr2:188274544-188274594	HRPEpiC	eye:	n/a
13	chr2:188274544-188274594	Caco-2	colon:	n/a
14	chr2:188274544-188274594	SK-N-MC	brain:	n/a
15	chr2:188093537-188093587	SKMC	muscle:	n/a
16	chr2:188274544-188274594	HUVEC	blood vessel:	n/a
17	chr2:188093537-188093587	NH-A	brain:	n/a
18	chr2:188211981-188212031	HL-60	blood:	n/a
19	chr2:188128809-188128859	PANC-1	pancreas:	n/a
20	chr2:188093537-188093587	GM19239	blood:	n/a
21	chr2:188269443-188269493	AG09319	gingival:	n/a
22	chr2:188211981-188212031	LNCaP	prostate:	n/a
23	chr2:188274544-188274594	NB4	blood:	n/a
24	chr2:188210673-188210723	H1-hESC	embryonic stem cell:	embryo
25	chr2:188210673-188210723	HAEpiC	amniotic membrane:	n/a
26	chr2:188128809-188128859	ECC-1	luminal epithelium:	n/a
27	chr2:188093537-188093587	PFSK-1	brain:	n/a
28	chr2:188210673-188210723	BJ	skin:	n/a
29	chr2:188269443-188269493	IMR90	lung:	fetal
30	chr2:188210673-188210723	GM19239	blood:	n/a
31	chr2:188169789-188169839	HCT-116	colon:	n/a
32	chr2:188169789-188169839	PFSK-1	brain:	n/a
33	chr2:188211981-188212031	H1-hESC	embryonic stem cell:	embryo
34	chr2:188211981-188212031	AG09309	skin:	n/a
35	chr2:188274544-188274594	GM12892	blood:	n/a
36	chr2:188093537-188093587	HMEC	breast:	n/a
37	chr2:188274544-188274594	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:188274544-188274594	ovcar-3	ovarian:	n/a
39	chr2:188274544-188274594	SK-N-SH	brain:	n/a
40	chr2:188274544-188274594	HL-60	blood:	n/a
41	chr2:188210673-188210723	AG10803	skin:	n/a
42	chr2:188269443-188269493	NH-A	brain:	n/a
43	chr2:188210673-188210723	LNCaP	prostate:	n/a
44	chr2:188210673-188210723	T-47D	breast:	n/a
45	chr2:188269443-188269493	HCF	heart:	n/a
46	chr2:188093537-188093587	NT2-D1	testis:	n/a
47	chr2:188211981-188212031	HIPEpiC	eye:	n/a
48	chr2:188210673-188210723	U87	brain:	n/a
49	chr2:188211981-188212031	Hela-S3	cervix:	n/a
50	chr2:188210673-188210723	HEEpiC	esophagus:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:188246636..188248522-chr2:188250885..188252795,2	K562	blood:
2	chr2:187968891..187971122-chr2:187972387..187974898,2	K562	blood:
3	chr2:188081497..188084400-chr2:188085542..188087074,2	K562	blood:
4	chr2:188276001..188278638-chr2:188296407..188297953,2	K562	blood:
5	chr2:188163616..188164504-chr2:188317553..188318396,2	MCF-7	breast:
6	chr2:188256239..188259274-chr2:188268273..188271204,3	K562	blood:
7	chr2:187976486..187978838-chr2:187984311..187986500,2	K562	blood:
8	chr2:187970999..187973523-chr2:187990145..187992171,2	MCF-7	breast:
9	chr2:188049075..188051640-chr2:188058153..188060182,2	K562	blood:
10	chr2:187950499..187953541-chr2:187954538..187958392,4	K562	blood:
11	chr2:188160492..188162802-chr2:188166384..188168217,2	K562	blood:
12	chr2:188256239..188259274-chr2:188268273..188271204,3	K562	blood:
13	chr2:188110055..188111838-chr2:188114697..188116780,2	K562	blood:
14	chr2:188082290..188085324-chr2:188088101..188090494,3	K562	blood:
15	chr2:188163672..188164442-chr2:188307237..188307741,2	MCF-7	breast:
16	chr2:188004807..188007406-chr2:188017789..188019661,2	K562	blood:
17	chr2:188163565..188166308-chr2:188168308..188169936,2	K562	blood:
18	chr2:188254302..188256367-chr2:188293903..188296593,2	MCF-7	breast:
19	chr2:187957403..187959802-chr2:187965098..187967313,2	K562	blood:
20	chr2:188115424..188118005-chr2:188119188..188121188,2	MCF-7	breast:
21	chr2:187950499..187953541-chr2:187954538..187958392,4	K562	blood:
22	chr2:188110055..188111838-chr2:188114697..188116780,2	K562	blood:
23	chr2:188108987..188110844-chr2:188112727..188114579,2	K562	blood:
24	chr2:188088219..188089827-chr2:188091606..188093417,2	K562	blood:
25	chr2:188241492..188244171-chr5:66176765..66178294,2	MCF-7	breast:
26	chr2:188000535..188003975-chr2:188004995..188007174,3	K562	blood:
27	chr2:188088219..188089827-chr2:188091606..188093417,2	K562	blood:
28	chr2:188265281..188268088-chr2:188269599..188271306,2	K562	blood:
29	chr2:188265281..188268088-chr2:188269599..188271306,2	K562	blood:
30	chr2:188179679..188182159-chr2:188184415..188186221,2	K562	blood:
31	chr2:188247827..188249573-chr2:188255118..188257406,2	K562	blood:
32	chr2:188000535..188003975-chr2:188004995..188007174,3	K562	blood:
33	chr2:187976486..187978838-chr2:187984311..187986500,2	K562	blood:
34	chr2:188081497..188084400-chr2:188085542..188087074,2	K562	blood:
35	chr2:187970999..187973523-chr2:187990145..187992171,2	MCF-7	breast:
36	chr2:188202421..188204619-chr2:188206871..188209816,3	K562	blood:
37	chr2:188160492..188162802-chr2:188166384..188168217,2	K562	blood:
38	chr2:188082290..188085324-chr2:188088101..188090494,3	K562	blood:
39	chr2:188179679..188182159-chr2:188184415..188186221,2	K562	blood:
40	chr2:187970958..187972570-chr2:188030940..188032958,2	K562	blood:
41	chr2:188108987..188110844-chr2:188112727..188114579,2	K562	blood:
42	chr2:188118124..188120319-chr2:188121977..188123485,2	MCF-7	breast:
43	chr2:188247827..188249573-chr2:188255118..188257406,2	K562	blood:
44	chr2:187989280..187992184-chr2:188006220..188008232,2	K562	blood:
45	chr2:188118124..188120319-chr2:188121977..188123485,2	MCF-7	breast:
46	chr2:187970958..187972570-chr2:188030940..188032958,2	K562	blood:
47	chr2:187868263..187869936-chr2:188017498..188019004,2	K562	blood:
48	chr2:187989280..187992184-chr2:188006220..188008232,2	K562	blood:
49	chr2:188049075..188051640-chr2:188058153..188060182,2	K562	blood:
50	chr2:188247022..188249051-chr2:188251094..188252795,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM171B-3	chr2:188176063-188176360	NONHSAT076014
2	lnc-TFPI-1	chr2:188252393-188252483	NONHSAT076017
3	lnc-TFPI-1	chr2:188252393-188252483	NONHSAT076015
4	lnc-CALCRL-3	chr2:187987289-187987588	NONHSAT076009
5	lnc-FAM171B-1	chr2:188056562-188056658	NONHSAT076011
6	lnc-TFPI-1	chr2:188252126-188252483	NONHSAT076016
7	lnc-TFPI-1	chr2:188252065-188252220	NONHSAT076015
8	lnc-FAM171B-1	chr2:188042973-188043244	NONHSAT076011
9	lnc-FAM171B-1	chr2:188060089-188060574	NONHSAT076011
10	lnc-FAM171B-3	chr2:188194854-188195100	NONHSAT076014

No data

Variant related genes	Relation type
RN7SKP42	TF binding region
GAPDHP59	TF binding region
RNU6-989P	TF binding region
RN7SKP42	CpG island
GAPDHP59	CpG island
RNU6-989P	CpG island

Extended variants
information (count: 6276 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:6276 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5837014	chr2:187957209-187957210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs369293289	chr2:187957211-187957212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs202146525	chr2:187957212-187957213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs368088418	chr2:187957213-187957214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs201201264	chr2:187957215-187957216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs13024632	chr2:187957266-187957267	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs536392628	chr2:187957316-187957317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs373997429	chr2:187957349-187957350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573949642	chr2:187957364-187957365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554532221	chr2:187957368-187957369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569577060	chr2:187957380-187957381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573246744	chr2:187959642-187959643	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs181058263	chr2:187959664-187959665	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs113076676	chr2:187959763-187959764	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs553263431	chr2:187959823-187959824	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs574680097	chr2:187959851-187959852	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs541657496	chr2:187959857-187959858	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs563541101	chr2:187959873-187959874	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs149123599	chr2:187959874-187959875	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs182947194	chr2:187959905-187959906	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs71432484	chr2:187959914-187959915	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs376711646	chr2:187959943-187959944	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs113489043	chr2:187959961-187959962	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs16828613	chr2:187959963-187959964	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs73045626	chr2:187967611-187967612	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs545525170	chr2:187967646-187967647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563864212	chr2:187967666-187967667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs139986748	chr2:187967720-187967721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546829062	chr2:187968046-187968047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184746718	chr2:187968051-187968052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189472934	chr2:187968132-187968133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542507087	chr2:187968141-187968142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376869162	chr2:187968153-187968154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192052420	chr2:187968187-187968188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs149813576	chr2:187968201-187968202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568339288	chr2:187968210-187968211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373576123	chr2:187968289-187968290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377011881	chr2:187968297-187968298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185355787	chr2:187968305-187968306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535386147	chr2:187968366-187968367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556719278	chr2:187968394-187968395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575058456	chr2:187968398-187968399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539255276	chr2:187968402-187968403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199535497	chr2:187968405-187968406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567031118	chr2:187968415-187968416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571807247	chr2:187968452-187968453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540222367	chr2:187968489-187968490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555098528	chr2:187968560-187968561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532720185	chr2:187968659-187968660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574259857	chr2:187968667-187968668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	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
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Urothelial carcinoma	21177765	CNVD
Bipolar disorder	19114987	CNVD
early-passage human iPS cells	21368824	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Tetralogy of Fallot	22912587	CNVD

Chromatin state (count:826 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:187957200-187957400	Enhancers	Fetal Lung	lung
2	chr2:187959600-187960000	Active TSS	HUVEC	blood vessel
3	chr2:187967600-187967800	Enhancers	Adipose Nuclei	Adipose
4	chr2:187968000-187969400	Weak transcription	Adipose Nuclei	Adipose
5	chr2:187969400-187970400	Enhancers	Adipose Nuclei	Adipose
6	chr2:187970400-187971400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:187971000-187971400	Enhancers	Fetal Lung	lung
8	chr2:187982400-187982800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:187986000-187986200	Enhancers	Esophagus	oesophagus
10	chr2:187987400-187987600	Bivalent Enhancer	Esophagus	oesophagus
11	chr2:187989400-187990000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:187990000-187991000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr2:187991200-187991400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr2:188000600-188004400	Enhancers	HUVEC	blood vessel
15	chr2:188001000-188001400	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr2:188001200-188001600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr2:188001400-188001800	Enhancers	Primary hematopoietic stem cells	blood
18	chr2:188014400-188015000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr2:188014600-188015200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr2:188014800-188015200	Enhancers	Ovary	ovary
21	chr2:188015600-188016200	Enhancers	Colon Smooth Muscle	Colon
22	chr2:188026400-188026800	Enhancers	Fetal Lung	lung
23	chr2:188030000-188030400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr2:188030400-188030800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr2:188030600-188031000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr2:188030600-188031800	Enhancers	GM12878-XiMat	blood
27	chr2:188030800-188031000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr2:188030800-188031200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr2:188030800-188035000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr2:188031000-188032800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr2:188031000-188034800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr2:188031800-188033000	Weak transcription	GM12878-XiMat	blood
33	chr2:188032800-188033200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr2:188033000-188033200	Enhancers	GM12878-XiMat	blood
35	chr2:188033000-188033400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr2:188033000-188035200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr2:188033200-188033600	Flanking Active TSS	GM12878-XiMat	blood
38	chr2:188033200-188033800	Enhancers	Fetal Kidney	kidney
39	chr2:188033200-188034400	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr2:188033200-188035000	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr2:188033200-188035000	Enhancers	Primary B cells from cord blood	blood
42	chr2:188033200-188035000	Enhancers	Primary hematopoietic stem cells	blood
43	chr2:188033400-188034400	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr2:188033400-188034400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr2:188033400-188034400	Enhancers	HUVEC	blood vessel
46	chr2:188033600-188036800	Enhancers	GM12878-XiMat	blood
47	chr2:188034200-188035200	Enhancers	Primary B cells from peripheral blood	blood
48	chr2:188034400-188034800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr2:188034400-188034800	Enhancers	Colon Smooth Muscle	Colon
50	chr2:188034800-188035000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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