Variant report

Variant	nsv834393
Chromosome Location	chr2:142256714-142431564
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:964)
CpG islands
(count:183)
Chromatin interactive
region (count:58)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:964 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:142275467-142275803	HepG2	liver:	n/a	n/a
2	ATF2	chr2:142271286-142271988	GM12878	blood:	n/a	n/a
3	ATF2	chr2:142292012-142292986	GM12878	blood:	n/a	n/a
4	ATF2	chr2:142280345-142281185	GM12878	blood:	n/a	n/a
5	ATF2	chr2:142286538-142287000	GM12878	blood:	n/a	n/a
6	ATF2	chr2:142314848-142315209	GM12878	blood:	n/a	n/a
7	ATF2	chr2:142314780-142315309	GM12878	blood:	n/a	n/a
8	ATF2	chr2:142292160-142292927	GM12878	blood:	n/a	n/a
9	ATF2	chr2:142280682-142281081	GM12878	blood:	n/a	n/a
10	ATF2	chr2:142286459-142287141	GM12878	blood:	n/a	n/a
11	ATF2	chr2:142287179-142287676	GM12878	blood:	n/a	n/a
12	ATF2	chr2:142279523-142280059	GM12878	blood:	n/a	n/a
13	ATF2	chr2:142271278-142271897	GM12878	blood:	n/a	n/a
14	BATF	chr2:142287304-142287606	GM12878	blood:	n/a	chr2:142287363-142287372
15	BATF	chr2:142271394-142271777	GM12878	blood:	n/a	n/a
16	BATF	chr2:142279582-142279974	GM12878	blood:	n/a	chr2:142279817-142279828 chr2:142279822-142279832
17	BATF	chr2:142271332-142271941	GM12878	blood:	n/a	n/a
18	BATF	chr2:142292183-142292719	GM12878	blood:	n/a	n/a
19	BATF	chr2:142280726-142281108	GM12878	blood:	n/a	n/a
20	BCL11A	chr2:142271335-142271881	GM12878	blood:	n/a	n/a
21	BCL11A	chr2:142271441-142271781	GM12878	blood:	n/a	n/a
22	BCL11A	chr2:142280773-142281125	GM12878	blood:	n/a	n/a
23	BCL11A	chr2:142292285-142292686	GM12878	blood:	n/a	n/a
24	BCL3	chr2:142271339-142271801	GM12878	blood:	n/a	n/a
25	BCL3	chr2:142271369-142271816	GM12878	blood:	n/a	n/a
26	BCLAF1	chr2:142286470-142287030	GM12878	blood:	n/a	n/a
27	BCLAF1	chr2:142292162-142292828	GM12878	blood:	n/a	n/a
28	BCLAF1	chr2:142271310-142271907	GM12878	blood:	n/a	n/a
29	BCLAF1	chr2:142271413-142271849	GM12878	blood:	n/a	n/a
30	BHLHE40	chr2:142271474-142271776	GM12878	blood:	n/a	n/a
31	BHLHE40	chr2:142292484-142292504	GM12878	blood:	n/a	n/a
32	BHLHE40	chr2:142275239-142275266	HepG2	liver:	n/a	n/a
33	BRCA1	chr2:142312351-142312696	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr2:142301989-142302219	MCF-7	breast:	n/a	chr2:142302051-142302062
35	CEBPB	chr2:142268629-142269158	MCF-7	breast:	n/a	chr2:142268857-142268870 chr2:142268859-142268870
36	CEBPB	chr2:142346888-142347264	IMR90	lung:	n/a	n/a
37	CEBPB	chr2:142340629-142340928	IMR90	lung:	n/a	chr2:142340775-142340786 chr2:142340777-142340786
38	CEBPB	chr2:142319981-142320458	MCF-7	breast:	n/a	chr2:142320205-142320216 chr2:142320207-142320216
39	CEBPB	chr2:142320153-142320282	K562	blood:	n/a	chr2:142320205-142320216 chr2:142320207-142320216
40	CEBPB	chr2:142374350-142374784	MCF-7	breast:	n/a	n/a
41	CEBPB	chr2:142398949-142399398	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr2:142301944-142302196	IMR90	lung:	n/a	chr2:142302051-142302062
43	CEBPB	chr2:142299437-142299612	HepG2	liver:	n/a	chr2:142299470-142299483 chr2:142299467-142299484 chr2:142299456-142299469 chr2:142299470-142299481
44	CEBPB	chr2:142346903-142347248	A549	lung:	n/a	n/a
45	CEBPB	chr2:142346926-142347249	K562	blood:	n/a	n/a
46	CEBPB	chr2:142275553-142275739	HepG2	liver:	n/a	chr2:142275671-142275682 chr2:142275671-142275684
47	CEBPB	chr2:142368691-142368945	IMR90	lung:	n/a	chr2:142368869-142368882
48	CEBPB	chr2:142388316-142388330	HepG2	liver:	n/a	n/a
49	CEBPB	chr2:142414231-142414544	HepG2	liver:	n/a	chr2:142414400-142414411 chr2:142414398-142414411 chr2:142414398-142414409 chr2:142414398-142414411
50	CEBPB	chr2:142275316-142275852	A549	lung:	n/a	chr2:142275671-142275682 chr2:142275671-142275684

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:142416800-142416850	PFSK-1	brain:	n/a
2	chr2:142338869-142338919	HNPCEpiC	eye:	n/a
3	chr2:142338869-142338919	RPTEC	kidney:	n/a
4	chr2:142416800-142416850	NHDF-neo	bronchial:	n/a
5	chr2:142369345-142369395	LNCaP	prostate:	n/a
6	chr2:142416800-142416850	AG09309	skin:	n/a
7	chr2:142416800-142416850	HEEpiC	esophagus:	n/a
8	chr2:142416800-142416850	AG10803	skin:	n/a
9	chr2:142416800-142416850	HRPEpiC	eye:	n/a
10	chr2:142416800-142416850	HPAEpiC	pulmonary alveolar:	n/a
11	chr2:142369345-142369395	GM12891	blood:	n/a
12	chr2:142338869-142338919	BJ	skin:	n/a
13	chr2:142369345-142369395	ovcar-3	ovarian:	n/a
14	chr2:142369345-142369395	MCF10A-Er-Src	breast:	n/a
15	chr2:142416800-142416850	GM12878	blood:	n/a
16	chr2:142369345-142369395	ProgFib	skin:	n/a
17	chr2:142416800-142416850	ovcar-3	ovarian:	n/a
18	chr2:142416800-142416850	GM19239	blood:	n/a
19	chr2:142416800-142416850	CMK	blood:	n/a
20	chr2:142369345-142369395	HL-60	blood:	n/a
21	chr2:142369345-142369395	PFSK-1	brain:	n/a
22	chr2:142338869-142338919	HepG2	liver:	n/a
23	chr2:142369345-142369395	H1-hESC	embryonic stem cell:	embryo
24	chr2:142338869-142338919	AG09309	skin:	n/a
25	chr2:142338869-142338919	HRPEpiC	eye:	n/a
26	chr2:142369345-142369395	MCF-7	breast:	n/a
27	chr2:142338869-142338919	Hela-S3	cervix:	n/a
28	chr2:142416800-142416850	AG09319	gingival:	n/a
29	chr2:142338869-142338919	HMEC	breast:	n/a
30	chr2:142416800-142416850	Hela-S3	cervix:	n/a
31	chr2:142416800-142416850	SK-N-SH	brain:	n/a
32	chr2:142416800-142416850	HNPCEpiC	eye:	n/a
33	chr2:142338869-142338919	GM12892	blood:	n/a
34	chr2:142338869-142338919	GM19239	blood:	n/a
35	chr2:142416800-142416850	MCF10A-Er-Src	breast:	n/a
36	chr2:142338869-142338919	NB4	blood:	n/a
37	chr2:142369345-142369395	AG04450	lung:	fetal
38	chr2:142338869-142338919	CMK	blood:	n/a
39	chr2:142416800-142416850	Hepatocyte	liver:	n/a
40	chr2:142369345-142369395	GM06990	blood:	n/a
41	chr2:142369345-142369395	GM12892	blood:	n/a
42	chr2:142416800-142416850	SK-N-MC	brain:	n/a
43	chr2:142369345-142369395	HCM	heart:	n/a
44	chr2:142338869-142338919	T-47D	breast:	n/a
45	chr2:142416800-142416850	NB4	blood:	n/a
46	chr2:142416800-142416850	HL-60	blood:	n/a
47	chr2:142338869-142338919	K562	blood:	n/a
48	chr2:142416800-142416850	HCT-116	colon:	n/a
49	chr2:142369345-142369395	SK-N-SH_RA	brain:	n/a
50	chr2:142369345-142369395	BE2_C	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:142291504..142294290-chr2:142295014..142296558,2	MCF-7	breast:
2	chr2:142241833..142244486-chr2:142265674..142268047,2	MCF-7	breast:
3	chr2:142260948..142262730-chr2:142271665..142273452,2	MCF-7	breast:
4	chr2:142317711..142321512-chr2:142324977..142327310,3	MCF-7	breast:
5	chr2:142259500..142260427-chr2:142322823..142323400,2	MCF-7	breast:
6	chr2:142225007..142227143-chr2:142273674..142276575,2	MCF-7	breast:
7	chr2:142317711..142321512-chr2:142324977..142327310,3	MCF-7	breast:
8	chr2:142303735..142305902-chr2:142307985..142310549,2	K562	blood:
9	chr2:142308972..142312076-chr2:142313360..142316898,3	K562	blood:
10	chr2:142265321..142267918-chr2:142664161..142666622,2	MCF-7	breast:
11	chr2:142308972..142312076-chr2:142313360..142316898,3	K562	blood:
12	chr2:142348226..142350841-chr2:142353391..142355433,2	MCF-7	breast:
13	chr2:142322809..142324424-chr2:142379273..142380846,2	MCF-7	breast:
14	chr2:142320561..142322150-chr2:142885194..142887458,2	MCF-7	breast:
15	chr2:142259654..142261746-chr2:142265611..142267711,3	MCF-7	breast:
16	chr2:142285408..142288288-chr2:142294613..142297064,2	MCF-7	breast:
17	chr2:142257639..142260616-chr2:142261708..142263676,2	MCF-7	breast:
18	chr2:142263240..142267352-chr2:142886657..142889435,3	MCF-7	breast:
19	chr2:142288498..142290059-chr2:142292199..142295076,2	MCF-7	breast:
20	chr2:142265220..142267079-chr2:142275773..142278354,2	MCF-7	breast:
21	chr2:142291504..142294290-chr2:142295014..142296558,2	MCF-7	breast:
22	chr2:142399705..142402607-chr2:142407743..142409987,2	MCF-7	breast:
23	chr2:142299065..142301455-chr2:142302719..142305386,2	MCF-7	breast:
24	chr2:142399092..142400937-chr2:142401190..142403149,2	MCF-7	breast:
25	chr2:142259654..142261746-chr2:142265611..142267711,3	MCF-7	breast:
26	chr2:142303735..142305902-chr2:142307985..142310549,2	K562	blood:
27	chr2:142267530..142270120-chr2:142367084..142369508,2	MCF-7	breast:
28	chr2:142322809..142324424-chr2:142379273..142380846,2	MCF-7	breast:
29	chr2:142348226..142350841-chr2:142353391..142355433,2	MCF-7	breast:
30	chr2:142223533..142226548-chr2:142266133..142269163,3	MCF-7	breast:
31	chr2:142363098..142365424-chr2:142366631..142368354,2	MCF-7	breast:
32	chr2:142259034..142262033-chr2:142268324..142270584,3	MCF-7	breast:
33	chr2:142399705..142402607-chr2:142407743..142409987,2	MCF-7	breast:
34	chr2:142259034..142262033-chr2:142268324..142270584,3	MCF-7	breast:
35	chr2:142259500..142260427-chr2:142322823..142323400,2	MCF-7	breast:
36	chr2:129063359..129065202-chr2:142304288..142305941,2	MCF-7	breast:
37	chr2:142386784..142389689-chr2:142401427..142404139,2	MCF-7	breast:
38	chr2:142267758..142272921-chr2:142273064..142275767,4	MCF-7	breast:
39	chr2:142363098..142365424-chr2:142366631..142368354,2	MCF-7	breast:
40	chr2:142248367..142251172-chr2:142262537..142266743,4	MCF-7	breast:
41	chr2:142260948..142262730-chr2:142271665..142273452,2	MCF-7	breast:
42	chr2:142285408..142288288-chr2:142294613..142297064,2	MCF-7	breast:
43	chr2:142267530..142270120-chr2:142367084..142369508,2	MCF-7	breast:
44	chr2:142398871..142401024-chr2:142404435..142406777,2	MCF-7	breast:
45	chr2:142267758..142272921-chr2:142273064..142275767,4	MCF-7	breast:
46	chr2:142386784..142389689-chr2:142401427..142404139,2	MCF-7	breast:
47	chr2:142257639..142260616-chr2:142261708..142263676,2	MCF-7	breast:
48	chr2:142261934..142264280-chr2:142265309..142267485,3	MCF-7	breast:
49	chr2:142265220..142267079-chr2:142275773..142278354,2	MCF-7	breast:
50	chr2:142399092..142400937-chr2:142401190..142403149,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000265224	TF binding region
ENSG00000265224	CpG island
ENSG00000168702	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 4547 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:4547 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544342915	chr2:142256714-142256715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs72851323	chr2:142256740-142256741	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs147182082	chr2:142256772-142256773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546067842	chr2:142256778-142256779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201337357	chr2:142256783-142256784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs72851325	chr2:142256806-142256807	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs552193013	chr2:142256810-142256811	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548506834	chr2:142256837-142256838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562164083	chr2:142256878-142256879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs530903032	chr2:142256880-142256881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551091547	chr2:142256940-142256941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570842940	chr2:142256954-142256955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139576230	chr2:142256965-142256966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546884735	chr2:142256966-142256967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375598407	chr2:142256975-142256976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187851913	chr2:142256978-142256979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs149369063	chr2:142256990-142256991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200483549	chr2:142256998-142256999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192956146	chr2:142257101-142257102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7572480	chr2:142257127-142257128	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs574435614	chr2:142257131-142257132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577191594	chr2:142257173-142257174	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539856332	chr2:142257188-142257189	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553209059	chr2:142257199-142257200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112724294	chr2:142257267-142257268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566641323	chr2:142257349-142257350	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542555869	chr2:142257350-142257351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184988192	chr2:142257352-142257353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531166027	chr2:142257356-142257357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532367659	chr2:142257360-142257361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553649314	chr2:142257404-142257405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544356770	chr2:142257431-142257432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74810497	chr2:142257434-142257435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs367833128	chr2:142257458-142257459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189120573	chr2:142257462-142257463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566921633	chr2:142257512-142257513	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557130944	chr2:142257527-142257528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529168904	chr2:142257540-142257541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549294698	chr2:142257591-142257592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575692902	chr2:142257610-142257611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568936752	chr2:142257676-142257677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538067132	chr2:142257685-142257686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557398329	chr2:142257715-142257716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs35703162	chr2:142257720-142257721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs34050146	chr2:142257738-142257739	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs533498011	chr2:142257764-142257765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553348297	chr2:142257768-142257769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573619062	chr2:142257776-142257777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542141221	chr2:142257777-142257778	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192326095	chr2:142257813-142257814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	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
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma	21080181	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Autism	22543975	CNVD
Cancer	20164920	CNVD
Hypertension	22686481	CNVD
Hypospadia	22686481	CNVD
Intellectual disability	22686481	CNVD
Omphalocele	22686481	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:441 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:142247800-142266200	Weak transcription	Brain Anterior Caudate	brain
2	chr2:142249600-142257600	Weak transcription	Brain Substantia Nigra	brain
3	chr2:142254800-142257800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr2:142255000-142256800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr2:142255600-142257000	Enhancers	NH-A	brain
6	chr2:142256000-142257000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr2:142256000-142257800	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr2:142256000-142257800	Enhancers	Fetal Heart	heart
9	chr2:142256000-142258800	Weak transcription	Dnd41	blood
10	chr2:142256400-142257200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr2:142256400-142263600	Weak transcription	Brain Hippocampus Middle	brain
12	chr2:142256800-142257000	Enhancers	Primary hematopoietic stem cells	blood
13	chr2:142257400-142257800	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr2:142257600-142258000	Enhancers	Brain Substantia Nigra	brain
15	chr2:142257600-142258200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr2:142257800-142259200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr2:142257800-142265800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr2:142258000-142265800	Weak transcription	Brain Substantia Nigra	brain
19	chr2:142258800-142260200	Enhancers	Dnd41	blood
20	chr2:142259000-142259600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:142259000-142259800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr2:142259000-142260200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr2:142259200-142259800	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr2:142259600-142259800	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr2:142259600-142259800	Enhancers	Fetal Brain Male	brain
26	chr2:142259800-142261000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr2:142259800-142262600	Weak transcription	Fetal Brain Male	brain
28	chr2:142260000-142261000	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr2:142260200-142263400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr2:142261000-142261600	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr2:142261000-142261800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr2:142261200-142261400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr2:142261600-142263400	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr2:142262600-142264200	Enhancers	Fetal Brain Male	brain
35	chr2:142263400-142264000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr2:142263400-142264200	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr2:142263600-142264000	Enhancers	Brain Hippocampus Middle	brain
38	chr2:142263600-142264000	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr2:142264000-142265800	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr2:142264000-142266600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr2:142264000-142268000	Weak transcription	Brain Hippocampus Middle	brain
42	chr2:142264200-142266600	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr2:142265800-142266600	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr2:142265800-142266600	Enhancers	Brain Substantia Nigra	brain
45	chr2:142265800-142266800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr2:142266000-142267200	Enhancers	A549	lung
47	chr2:142266200-142267600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr2:142266200-142267600	Enhancers	Brain Anterior Caudate	brain
49	chr2:142266400-142267200	Enhancers	Brain Cingulate Gyrus	brain
50	chr2:142266600-142266800	Enhancers	Cortex derived primary cultured neurospheres	brain

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