Variant report

Variant	nsv535643
Chromosome Location	chr2:36838387-37011384
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2565)
CpG islands
(count:793)
Chromatin interactive
region (count:75)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2565 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:36881088-36881859	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:36891203-36891741	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:36877205-36877537	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:36873379-36873727	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:36886856-36887693	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:36885441-36885931	HepG2	liver:	n/a	n/a
7	ATF1	chr2:36845544-36845891	K562	blood:	n/a	n/a
8	ATF1	chr2:36842472-36842776	K562	blood:	n/a	n/a
9	ATF1	chr2:36873395-36873735	K562	blood:	n/a	n/a
10	ATF1	chr2:37005015-37005196	K562	blood:	n/a	n/a
11	ATF2	chr2:36997856-36998247	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr2:36887032-36887548	GM12878	blood:	n/a	n/a
13	ATF2	chr2:36873297-36873747	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr2:36873285-36873766	GM12878	blood:	n/a	n/a
15	ATF2	chr2:36873274-36873760	GM12878	blood:	n/a	n/a
16	ATF2	chr2:36873300-36873758	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr2:36873306-36873764	K562	blood:	n/a	n/a
18	ATF3	chr2:36852471-36852899	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr2:36845443-36845940	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr2:36852467-36852862	A549	lung:	n/a	n/a
21	ATF3	chr2:36845443-36845844	GM12878	blood:	n/a	n/a
22	ATF3	chr2:36852451-36852883	HCT-116	colon:	n/a	n/a
23	ATF3	chr2:36845551-36845792	K562	blood:	n/a	n/a
24	ATF3	chr2:36852490-36852747	K562	blood:	n/a	n/a
25	ATF3	chr2:36852487-36852779	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF3	chr2:36845573-36845814	HepG2	liver:	n/a	n/a
27	ATF3	chr2:36961470-36961737	K562	blood:	n/a	n/a
28	ATF3	chr2:36877200-36877481	K562	blood:	n/a	n/a
29	ATF3	chr2:36845534-36845791	GM12878	blood:	n/a	n/a
30	BACH1	chr2:36842513-36842737	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr2:36997827-36998168	K562	blood:	n/a	n/a
32	BACH1	chr2:36989667-36989680	K562	blood:	n/a	n/a
33	BATF	chr2:36877282-36877486	GM12878	blood:	n/a	chr2:36877369-36877380
34	BATF	chr2:36887081-36887401	GM12878	blood:	n/a	n/a
35	BHLHE40	chr2:36863498-36863643	K562	blood:	n/a	chr2:36863550-36863563
36	BHLHE40	chr2:36997791-36998222	K562	blood:	n/a	n/a
37	BHLHE40	chr2:36934226-36934528	K562	blood:	n/a	n/a
38	BHLHE40	chr2:37007503-37007700	GM12878	blood:	n/a	n/a
39	BHLHE40	chr2:36980424-36980447	K562	blood:	n/a	n/a
40	BHLHE40	chr2:36845506-36845923	K562	blood:	n/a	n/a
41	BHLHE40	chr2:36944869-36944912	K562	blood:	n/a	n/a
42	BRCA1	chr2:36899038-36899637	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr2:36958934-36959934	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr2:36842363-36842751	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr2:36928364-36928913	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr2:36997868-36998219	H1-hESC	embryonic stem cell:	n/a	n/a
47	CBX3	chr2:36873371-36873771	K562	blood:	n/a	n/a
48	CBX3	chr2:36997838-36998291	K562	blood:	n/a	n/a
49	CBX3	chr2:36852533-36852784	K562	blood:	n/a	n/a
50	CBX3	chr2:36873308-36874078	HCT-116	colon:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:36905302-36905352	SK-N-SH	brain:	n/a
2	chr2:36964593-36964643	SK-N-SH	brain:	n/a
3	chr2:36877454-36877504	AG04449	skin:	fetal
4	chr2:36934773-36934823	GM19239	blood:	n/a
5	chr2:36934773-36934823	HIPEpiC	eye:	n/a
6	chr2:36923828-36923878	HepG2	liver:	n/a
7	chr2:36898641-36898691	A549	lung:	n/a
8	chr2:36922916-36922966	HNPCEpiC	eye:	n/a
9	chr2:36923086-36923136	HPAEpiC	pulmonary alveolar:	n/a
10	chr2:36905302-36905352	HL-60	blood:	n/a
11	chr2:36923828-36923878	NT2-D1	testis:	n/a
12	chr2:36842633-36842683	AG09309	skin:	n/a
13	chr2:36891490-36891540	HEEpiC	esophagus:	n/a
14	chr2:36898641-36898691	IMR90	lung:	fetal
15	chr2:36964593-36964643	AoSMC	blood vessel:	n/a
16	chr2:36923086-36923136	GM12878	blood:	n/a
17	chr2:36916346-36916396	HCM	heart:	n/a
18	chr2:36980923-36980973	SKMC	muscle:	n/a
19	chr2:36916346-36916396	AoSMC	blood vessel:	n/a
20	chr2:36922916-36922966	Hela-S3	cervix:	n/a
21	chr2:36923086-36923136	HMEC	breast:	n/a
22	chr2:36845361-36845411	HCPEpiC	choroid plexus:	n/a
23	chr2:36877454-36877504	MCF-7	breast:	n/a
24	chr2:36964593-36964643	BE2_C	brain:	n/a
25	chr2:36905302-36905352	HRCEpiC	kidney:	n/a
26	chr2:36980923-36980973	HCF	heart:	n/a
27	chr2:36905302-36905352	MCF-7	breast:	n/a
28	chr2:36905302-36905352	K562	blood:	n/a
29	chr2:36845361-36845411	BE2_C	brain:	n/a
30	chr2:36877454-36877504	BJ	skin:	n/a
31	chr2:36845361-36845411	HCT-116	colon:	n/a
32	chr2:36891490-36891540	AG04450	lung:	fetal
33	chr2:36980923-36980973	AG04450	lung:	fetal
34	chr2:36898641-36898691	HEK293	kidney:	embryo
35	chr2:36934773-36934823	GM12891	blood:	n/a
36	chr2:36898641-36898691	PrEC	prostate:	n/a
37	chr2:36964593-36964643	GM12892	blood:	n/a
38	chr2:36905302-36905352	RPTEC	kidney:	n/a
39	chr2:36845361-36845411	HAEpiC	amniotic membrane:	n/a
40	chr2:36842633-36842683	HIPEpiC	eye:	n/a
41	chr2:36905302-36905352	BE2_C	brain:	n/a
42	chr2:36964593-36964643	T-47D	breast:	n/a
43	chr2:36905302-36905352	NT2-D1	testis:	n/a
44	chr2:36923086-36923136	ECC-1	luminal epithelium:	n/a
45	chr2:36980923-36980973	NHBE	bronchial:	n/a
46	chr2:36923086-36923136	HepG2	liver:	n/a
47	chr2:36845361-36845411	AG09309	skin:	n/a
48	chr2:36898641-36898691	AG09309	skin:	n/a
49	chr2:36916346-36916396	CMK	blood:	n/a
50	chr2:36964593-36964643	GM12891	blood:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:37008165..37009704-chr2:37010243..37012241,2	MCF-7	breast:
2	chr2:36845094..36847827-chr2:36854780..36857434,2	K562	blood:
3	chr2:36579295..36579845-chr2:36891074..36891911,3	K562	blood:
4	chr2:36932681..36933457-chr2:36997721..36998478,3	MCF-7	breast:
5	chr2:36997788..36998511-chr2:37012444..37013096,2	K562	blood:
6	chr2:37005141..37008070-chr2:37014842..37017137,3	K562	blood:
7	chr2:37007149..37007661-chr2:37145609..37146127,2	MCF-7	breast:
8	chr2:36873347..36875175-chr2:36875195..36878718,3	MCF-7	breast:
9	chr2:36857170..36859524-chr2:36860213..36863125,2	K562	blood:
10	chr2:36963255..36965422-chr2:36965948..36967670,2	MCF-7	breast:
11	chr14:39344148..39344668-chr2:36899113..36899743,2	MCF-7	breast:
12	chr2:36928366..36930832-chr2:36932347..36935302,2	MCF-7	breast:
13	chr2:36932681..36933457-chr2:36997721..36998478,3	MCF-7	breast:
14	chr2:36981413..36983737-chr2:36983835..36986819,2	K562	blood:
15	chr2:37005478..37008643-chr2:37010810..37013126,3	MCF-7	breast:
16	chr2:36983691..36986604-chr2:36986917..36989477,2	MCF-7	breast:
17	chr2:36931946..36934651-chr2:36940635..36943330,2	K562	blood:
18	chr2:36826854..36828860-chr2:36842420..36843944,2	MCF-7	breast:
19	chr2:36823941..36826551-chr2:36849186..36851217,2	MCF-7	breast:
20	chr2:37006258..37010448-chr2:37010681..37014372,3	K562	blood:
21	chr2:37005478..37008643-chr2:37010810..37013126,3	MCF-7	breast:
22	chr2:36823336..36826112-chr2:36873879..36877943,4	MCF-7	breast:
23	chr2:36959452..36962419-chr2:36962892..36964794,2	K562	blood:
24	chr2:36823734..36826594-chr2:36851912..36854688,2	MCF-7	breast:
25	chr2:36907958..36910188-chr2:36910655..36912308,2	K562	blood:
26	chr2:37006258..37010448-chr2:37010681..37014372,3	K562	blood:
27	chr2:36857170..36859524-chr2:36860213..36863125,2	K562	blood:
28	chr2:36789668..36791996-chr2:37007136..37008825,2	K562	blood:
29	chr2:36961444..36963530-chr2:36969103..36971971,2	K562	blood:
30	chr2:36956863..36959854-chr2:36963372..36965753,3	MCF-7	breast:
31	chr2:36928051..36929243-chr2:36997518..36998542,3	MCF-7	breast:
32	chr2:37000302..37001833-chr2:37006942..37009260,2	K562	blood:
33	chr2:36922695..36923609-chr2:36997471..36998399,4	MCF-7	breast:
34	chr2:36983691..36986604-chr2:36986917..36989477,2	MCF-7	breast:
35	chr2:36578991..36579848-chr2:36873541..36874070,2	K562	blood:
36	chr2:36987514..36989270-chr2:36997117..36998900,2	K562	blood:
37	chr2:36846931..36849384-chr2:36851133..36853576,2	K562	blood:
38	chr2:36579120..36579851-chr2:36890803..36891518,3	MCF-7	breast:
39	chr2:36961444..36963530-chr2:36969103..36971971,2	K562	blood:
40	chr2:36824532..36826491-chr2:36885626..36887144,2	MCF-7	breast:
41	chr2:36907958..36910188-chr2:36910655..36912308,2	K562	blood:
42	chr2:36823509..36825415-chr2:36873494..36875458,2	K562	blood:
43	chr2:36997612..36998606-chr2:37012147..37012935,3	MCF-7	breast:
44	chr2:36987514..36989270-chr2:36997117..36998900,2	K562	blood:
45	chr2:37005040..37005587-chr2:37231880..37232793,2	MCF-7	breast:
46	chr2:36873347..36875175-chr2:36875195..36878718,3	MCF-7	breast:
47	chr2:36832118..36833779-chr2:36837070..36839522,2	K562	blood:
48	chr2:37011366..37014092-chr2:37310068..37313025,2	K562	blood:
49	chr2:36922543..36923508-chr2:37012076..37013001,3	MCF-7	breast:
50	chr2:36922695..36923609-chr2:36997471..36998399,4	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FEZ2-3	chr2:36925545-36925959	expReg_chr2_2324_-
2	lnc-FEZ2-4	chr2:36926267-36926537	expReg_chr2_2328_-
3	lnc-CRIM1-2	chr2:36991437-36993016	NONHSAT070090
4	lnc-FEZ2-5	chr2:36927423-36927967	expReg_chr2_2337_-
5	lnc-FEZ2-1	chr2:36883465-36884084	NONHSAT070089
6	lnc-FEZ2-2	chr2:36924810-36925173	expReg_chr2_2321_-

No data

Variant related genes	Relation type
VIT	TF binding region
ENSG00000270677	TF binding region
FEZ2	TF binding region
VIT	CpG island
ENSG00000270677	CpG island
FEZ2	CpG island
ENSG00000205221	chromatin interactions
ENSG00000152133	chromatin interactions
ENSG00000171055	chromatin interactions
ENSG00000008869	chromatin interactions

Extended variants
information (count: 7491 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:7491 , 50 per page) page: 1 2 3 4 5 6 7 ... 150

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575049276	chr2:36838391-36838392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs138803307	chr2:36838395-36838396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149437713	chr2:36838396-36838397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562108159	chr2:36838415-36838416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534434323	chr2:36838425-36838426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551537061	chr2:36838439-36838440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542515927	chr2:36838501-36838502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571158522	chr2:36838507-36838508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs529526244	chr2:36838514-36838515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs35792773	chr2:36838515-36838516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538207963	chr2:36838522-36838523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556532187	chr2:36838529-36838530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs144823371	chr2:36838575-36838576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148143434	chr2:36838580-36838581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs918066	chr2:36838600-36838601	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs79126621	chr2:36838614-36838615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs114170623	chr2:36838620-36838621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565337942	chr2:36838624-36838625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147298776	chr2:36838656-36838657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544663320	chr2:36838687-36838688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562847740	chr2:36838705-36838706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114760931	chr2:36838725-36838726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs562688226	chr2:36838766-36838767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566974112	chr2:36838774-36838775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376659522	chr2:36838811-36838812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs533145651	chr2:36838815-36838816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546387281	chr2:36838855-36838856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187169425	chr2:36838856-36838857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538346900	chr2:36838857-36838858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140445409	chr2:36838888-36838889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551319922	chr2:36838906-36838907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374820225	chr2:36838928-36838929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs536158666	chr2:36838988-36838989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554799780	chr2:36839002-36839003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572960646	chr2:36839030-36839031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191152571	chr2:36839171-36839172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558467174	chr2:36839201-36839202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144291658	chr2:36839222-36839223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544702026	chr2:36839227-36839228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562884493	chr2:36839241-36839242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377513069	chr2:36839258-36839259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542163673	chr2:36839304-36839305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560797958	chr2:36839319-36839320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546885641	chr2:36839396-36839397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552785974	chr2:36839404-36839405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564321692	chr2:36839494-36839495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555737706	chr2:36839546-36839547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182399528	chr2:36839602-36839603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs115317749	chr2:36839603-36839604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568514345	chr2:36839604-36839605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
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
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22737080	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1413 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:36835400-36842400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:36835800-36842000	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr2:36837000-36840600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr2:36837000-36841600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr2:36837400-36841200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:36837800-36839000	Enhancers	Placenta	Placenta
7	chr2:36838200-36838800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr2:36838400-36838600	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr2:36838400-36839000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr2:36838600-36842200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr2:36838800-36841200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr2:36839000-36841200	Weak transcription	Placenta	Placenta
13	chr2:36839600-36839800	Enhancers	H1 Cell Line	embryonic stem cell
14	chr2:36840200-36841400	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr2:36840600-36841800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr2:36840800-36842800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr2:36841000-36842000	Enhancers	Adipose Nuclei	Adipose
18	chr2:36841200-36841400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr2:36841200-36841400	Enhancers	Fetal Lung	lung
20	chr2:36841200-36841600	Enhancers	Fetal Kidney	kidney
21	chr2:36841200-36841600	Enhancers	Gastric	stomach
22	chr2:36841200-36842600	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr2:36841200-36842800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr2:36841200-36843000	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr2:36841200-36843000	Enhancers	Osteobl	bone
26	chr2:36841200-36843200	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr2:36841200-36844200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr2:36841200-36845200	Enhancers	Placenta	Placenta
29	chr2:36841400-36841600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr2:36841400-36842400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr2:36841400-36842600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr2:36841400-36842800	Enhancers	H1 Cell Line	embryonic stem cell
33	chr2:36841400-36842800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr2:36841400-36842800	Enhancers	Fetal Muscle Leg	muscle
35	chr2:36841400-36843200	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr2:36841400-36843200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr2:36841400-36843800	Weak transcription	Fetal Lung	lung
38	chr2:36841400-36844000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr2:36841600-36842200	Enhancers	Hela-S3	cervix
40	chr2:36841600-36842600	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr2:36841600-36844000	Weak transcription	Fetal Kidney	kidney
42	chr2:36841600-36844800	Enhancers	Placenta Amnion	Placenta Amnion
43	chr2:36841600-36846600	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr2:36841800-36842800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr2:36842000-36842200	Flanking Active TSS	Adipose Nuclei	Adipose
46	chr2:36842000-36842800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr2:36842000-36843000	Enhancers	NHDF-Ad	bronchial
48	chr2:36842000-36843000	Enhancers	NHLF	lung
49	chr2:36842000-36843400	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr2:36842200-36842400	Enhancers	Adipose Nuclei	Adipose

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