Variant report

Variant	nsv583214
Chromosome Location	chr2:142299923-142458316
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:142314780-142315309	GM12878	blood:	n/a	n/a
2	ATF2	chr2:142314848-142315209	GM12878	blood:	n/a	n/a
3	BRCA1	chr2:142312351-142312696	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr2:142346890-142347265	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr2:142301879-142302229	HepG2	liver:	n/a	chr2:142302051-142302062
6	CEBPB	chr2:142314951-142315151	A549	lung:	n/a	n/a
7	CEBPB	chr2:142301986-142302212	A549	lung:	n/a	chr2:142302051-142302062
8	CEBPB	chr2:142374350-142374784	MCF-7	breast:	n/a	n/a
9	CEBPB	chr2:142340629-142340928	IMR90	lung:	n/a	chr2:142340775-142340786 chr2:142340777-142340786
10	CEBPB	chr2:142457153-142457510	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:142314948-142315216	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr2:142320051-142320366	H1-hESC	embryonic stem cell:	n/a	chr2:142320205-142320216 chr2:142320207-142320216
13	CEBPB	chr2:142346438-142346646	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:142391093-142391444	HepG2	liver:	n/a	chr2:142391396-142391409 chr2:142391248-142391259 chr2:142391396-142391407
15	CEBPB	chr2:142374381-142374819	MCF-7	breast:	n/a	n/a
16	CEBPB	chr2:142391188-142391388	H1-hESC	embryonic stem cell:	n/a	chr2:142391248-142391259
17	CEBPB	chr2:142414267-142414467	A549	lung:	n/a	chr2:142414400-142414411 chr2:142414398-142414411 chr2:142414398-142414409 chr2:142414398-142414411
18	CEBPB	chr2:142340638-142340962	HepG2	liver:	n/a	chr2:142340775-142340786 chr2:142340777-142340786
19	CEBPB	chr2:142346903-142347248	A549	lung:	n/a	n/a
20	CEBPB	chr2:142340634-142340918	A549	lung:	n/a	chr2:142340775-142340786 chr2:142340777-142340786
21	CEBPB	chr2:142368691-142368945	IMR90	lung:	n/a	chr2:142368869-142368882
22	CEBPB	chr2:142346888-142347264	IMR90	lung:	n/a	n/a
23	CEBPB	chr2:142346857-142347357	A549	lung:	n/a	n/a
24	CEBPB	chr2:142414231-142414544	HepG2	liver:	n/a	chr2:142414400-142414411 chr2:142414398-142414411 chr2:142414398-142414409 chr2:142414398-142414411
25	CEBPB	chr2:142457238-142457398	HepG2	liver:	n/a	n/a
26	CEBPB	chr2:142346926-142347249	K562	blood:	n/a	n/a
27	CEBPB	chr2:142388316-142388330	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:142301944-142302196	IMR90	lung:	n/a	chr2:142302051-142302062
29	CEBPB	chr2:142368559-142369062	Hela-S3	cervix:	n/a	chr2:142368869-142368882
30	CEBPB	chr2:142346898-142347242	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr2:142301989-142302219	MCF-7	breast:	n/a	chr2:142302051-142302062
32	CEBPB	chr2:142320032-142320365	HepG2	liver:	n/a	chr2:142320205-142320216 chr2:142320207-142320216
33	CEBPB	chr2:142346890-142347263	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:142323048-142323653	MCF-7	breast:	n/a	n/a
35	CEBPB	chr2:142320153-142320282	K562	blood:	n/a	chr2:142320205-142320216 chr2:142320207-142320216
36	CEBPB	chr2:142314830-142315261	IMR90	lung:	n/a	n/a
37	CEBPB	chr2:142346893-142347268	A549	lung:	n/a	n/a
38	CEBPB	chr2:142323069-142323584	MCF-7	breast:	n/a	n/a
39	CEBPB	chr2:142398949-142399398	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr2:142346949-142347256	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr2:142319981-142320458	MCF-7	breast:	n/a	chr2:142320205-142320216 chr2:142320207-142320216
42	CEBPB	chr2:142431185-142431500	HepG2	liver:	n/a	chr2:142431361-142431372
43	CEBPB	chr2:142346952-142347268	MCF-7	breast:	n/a	n/a
44	CTCF	chr2:142312362-142312745	H1-hESC	embryonic stem cell:	n/a	chr2:142312554-142312575 chr2:142312560-142312576 chr2:142312559-142312577
45	CTCF	chr2:142312480-142312630	SAEC	small airway:	n/a	chr2:142312554-142312575 chr2:142312560-142312576 chr2:142312559-142312577
46	CTCF	chr2:142312480-142312630	AG09319	gingival:	n/a	chr2:142312554-142312575 chr2:142312560-142312576 chr2:142312559-142312577
47	CTCF	chr2:142312400-142312550	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr2:142312518-142312661	MCF-7	breast:	n/a	chr2:142312554-142312575 chr2:142312560-142312576 chr2:142312559-142312577
49	CTCF	chr2:142312500-142312650	HPAF	blood vessel:	n/a	chr2:142312554-142312575 chr2:142312560-142312576 chr2:142312559-142312577
50	CTCF	chr2:142312520-142312670	SK-N-SH_RA	brain:	n/a	chr2:142312554-142312575 chr2:142312560-142312576 chr2:142312559-142312577

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:142369345-142369395	RPTEC	kidney:	n/a
2	chr2:142338869-142338919	HUVEC	blood vessel:	n/a
3	chr2:142338869-142338919	HepG2	liver:	n/a
4	chr2:142338869-142338919	GM06990	blood:	n/a
5	chr2:142416800-142416850	A549	lung:	n/a
6	chr2:142369345-142369395	HMEC	breast:	n/a
7	chr2:142416800-142416850	CMK	blood:	n/a
8	chr2:142338869-142338919	HCM	heart:	n/a
9	chr2:142416800-142416850	SK-N-SH	brain:	n/a
10	chr2:142338869-142338919	SK-N-SH_RA	brain:	n/a
11	chr2:142416800-142416850	HRCEpiC	kidney:	n/a
12	chr2:142416800-142416850	HPAEpiC	pulmonary alveolar:	n/a
13	chr2:142416800-142416850	NB4	blood:	n/a
14	chr2:142416800-142416850	HUVEC	blood vessel:	n/a
15	chr2:142369345-142369395	H1-hESC	embryonic stem cell:	embryo
16	chr2:142416800-142416850	Hepatocyte	liver:	n/a
17	chr2:142416800-142416850	GM12891	blood:	n/a
18	chr2:142416800-142416850	MCF10A-Er-Src	breast:	n/a
19	chr2:142416800-142416850	GM12878	blood:	n/a
20	chr2:142338869-142338919	ProgFib	skin:	n/a
21	chr2:142338869-142338919	AG04449	skin:	fetal
22	chr2:142416800-142416850	ovcar-3	ovarian:	n/a
23	chr2:142369345-142369395	SK-N-SH	brain:	n/a
24	chr2:142369345-142369395	NH-A	brain:	n/a
25	chr2:142416800-142416850	PANC-1	pancreas:	n/a
26	chr2:142416800-142416850	AG09319	gingival:	n/a
27	chr2:142416800-142416850	GM19239	blood:	n/a
28	chr2:142338869-142338919	A549	lung:	n/a
29	chr2:142369345-142369395	A549	lung:	n/a
30	chr2:142369345-142369395	GM12891	blood:	n/a
31	chr2:142369345-142369395	NT2-D1	testis:	n/a
32	chr2:142416800-142416850	SAEC	small airway:	n/a
33	chr2:142416800-142416850	AoSMC	blood vessel:	n/a
34	chr2:142369345-142369395	GM19239	blood:	n/a
35	chr2:142338869-142338919	HAEpiC	amniotic membrane:	n/a
36	chr2:142416800-142416850	BJ	skin:	n/a
37	chr2:142416800-142416850	HCT-116	colon:	n/a
38	chr2:142416800-142416850	NHBE	bronchial:	n/a
39	chr2:142369345-142369395	NHBE	bronchial:	n/a
40	chr2:142338869-142338919	GM12878	blood:	n/a
41	chr2:142369345-142369395	BJ	skin:	n/a
42	chr2:142416800-142416850	HEK293	kidney:	embryo
43	chr2:142416800-142416850	HRPEpiC	eye:	n/a
44	chr2:142338869-142338919	MCF-7	breast:	n/a
45	chr2:142416800-142416850	GM12892	blood:	n/a
46	chr2:142369345-142369395	T-47D	breast:	n/a
47	chr2:142369345-142369395	AG10803	skin:	n/a
48	chr2:142369345-142369395	BE2_C	brain:	n/a
49	chr2:142416800-142416850	GM06990	blood:	n/a
50	chr2:142338869-142338919	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:142322809..142324424-chr2:142379273..142380846,2	MCF-7	breast:
2	chr2:142435826..142437412-chr2:142439074..142441235,2	MCF-7	breast:
3	chr2:142363098..142365424-chr2:142366631..142368354,2	MCF-7	breast:
4	chr2:142398871..142401024-chr2:142404435..142406777,2	MCF-7	breast:
5	chr2:142317711..142321512-chr2:142324977..142327310,3	MCF-7	breast:
6	chr2:142435826..142437412-chr2:142439074..142441235,2	MCF-7	breast:
7	chr2:142267530..142270120-chr2:142367084..142369508,2	MCF-7	breast:
8	chr2:142308972..142312076-chr2:142313360..142316898,3	K562	blood:
9	chr2:142386784..142389689-chr2:142401427..142404139,2	MCF-7	breast:
10	chr2:142299065..142301455-chr2:142302719..142305386,2	MCF-7	breast:
11	chr2:142399092..142400937-chr2:142401190..142403149,2	MCF-7	breast:
12	chr2:142299065..142301455-chr2:142302719..142305386,2	MCF-7	breast:
13	chr2:142303735..142305902-chr2:142307985..142310549,2	K562	blood:
14	chr2:142303735..142305902-chr2:142307985..142310549,2	K562	blood:
15	chr2:142399092..142400937-chr2:142401190..142403149,2	MCF-7	breast:
16	chr2:142432833..142434470-chr2:142438511..142441100,3	K562	blood:
17	chr2:142399705..142402607-chr2:142407743..142409987,2	MCF-7	breast:
18	chr2:142348226..142350841-chr2:142353391..142355433,2	MCF-7	breast:
19	chr2:142320561..142322150-chr2:142885194..142887458,2	MCF-7	breast:
20	chr2:142432833..142434470-chr2:142438511..142441100,3	K562	blood:
21	chr2:142399705..142402607-chr2:142407743..142409987,2	MCF-7	breast:
22	chr2:142317711..142321512-chr2:142324977..142327310,3	MCF-7	breast:
23	chr2:142259500..142260427-chr2:142322823..142323400,2	MCF-7	breast:
24	chr2:142348226..142350841-chr2:142353391..142355433,2	MCF-7	breast:
25	chr2:142398871..142401024-chr2:142404435..142406777,2	MCF-7	breast:
26	chr2:142322809..142324424-chr2:142379273..142380846,2	MCF-7	breast:
27	chr2:142308972..142312076-chr2:142313360..142316898,3	K562	blood:
28	chr2:142386784..142389689-chr2:142401427..142404139,2	MCF-7	breast:
29	chr2:142363098..142365424-chr2:142366631..142368354,2	MCF-7	breast:
30	chr2:129063359..129065202-chr2:142304288..142305941,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000265224	TF binding region
ENSG00000265224	CpG island

Extended variants
information (count: 3270 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:3270 , 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	rs531975659	chr2:142303807-142303808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs551782152	chr2:142303836-142303837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs139449848	chr2:142303898-142303899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs10190973	chr2:142303919-142303920	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs144976450	chr2:142303920-142303921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185331179	chr2:142303938-142303939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567860820	chr2:142303953-142303954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147564609	chr2:142304044-142304045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556616507	chr2:142304057-142304058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs75614752	chr2:142304061-142304062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs62169788	chr2:142304102-142304103	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs559006833	chr2:142304129-142304130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190091135	chr2:142304155-142304156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs572340541	chr2:142304185-142304186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs182656719	chr2:142304274-142304275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554426781	chr2:142304329-142304330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185896134	chr2:142304360-142304361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs140864857	chr2:142304383-142304384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150172367	chr2:142304392-142304393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs71417148	chr2:142304396-142304397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191762225	chr2:142304405-142304406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs10170114	chr2:142304490-142304491	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs545367812	chr2:142304513-142304514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs558928242	chr2:142304531-142304532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs145553499	chr2:142304550-142304551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs548063117	chr2:142304559-142304560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs561473086	chr2:142304576-142304577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76504749	chr2:142304577-142304578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550143033	chr2:142304608-142304609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs148886116	chr2:142304639-142304640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539156096	chr2:142304643-142304644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540868182	chr2:142304665-142304666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs183488313	chr2:142304666-142304667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs552558826	chr2:142304677-142304678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566087535	chr2:142304688-142304689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs368558169	chr2:142304709-142304710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs72853562	chr2:142304762-142304763	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs574572259	chr2:142304778-142304779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574669676	chr2:142304792-142304793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541964745	chr2:142304815-142304816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs373752807	chr2:142304849-142304850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563238041	chr2:142304853-142304854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs78762504	chr2:142304855-142304856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188935263	chr2:142304879-142304880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs367941468	chr2:142304913-142304914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs114100477	chr2:142304917-142304918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541489218	chr2:142304929-142304930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs564621021	chr2:142304943-142304944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145687090	chr2:142304950-142304951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs193098441	chr2:142304951-142304952	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:280 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:142303800-142304800	Enhancers	Brain Inferior Temporal Lobe	brain
2	chr2:142303800-142305200	Enhancers	Brain Anterior Caudate	brain
3	chr2:142304200-142304400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:142304200-142304600	Enhancers	Brain Substantia Nigra	brain
5	chr2:142304200-142304800	Enhancers	Brain Hippocampus Middle	brain
6	chr2:142304400-142305600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:142304600-142305800	Weak transcription	Brain Substantia Nigra	brain
8	chr2:142304800-142305800	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr2:142305600-142306200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr2:142305800-142306200	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr2:142305800-142306400	Enhancers	Brain Substantia Nigra	brain
12	chr2:142306200-142312200	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr2:142306400-142312200	Weak transcription	Brain Substantia Nigra	brain
14	chr2:142312200-142313000	Enhancers	Brain Anterior Caudate	brain
15	chr2:142312200-142313000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
16	chr2:142312200-142313000	Enhancers	Dnd41	blood
17	chr2:142312200-142313600	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr2:142312200-142314600	Enhancers	Brain Substantia Nigra	brain
19	chr2:142312400-142312600	Enhancers	NH-A	brain
20	chr2:142312400-142312800	Enhancers	Brain Angular Gyrus	brain
21	chr2:142312600-142312800	Enhancers	Brain Cingulate Gyrus	brain
22	chr2:142312600-142313600	Weak transcription	NH-A	brain
23	chr2:142312600-142314000	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr2:142312600-142314000	Enhancers	Brain Hippocampus Middle	brain
25	chr2:142312800-142313800	Weak transcription	Brain Angular Gyrus	brain
26	chr2:142313000-142313400	Weak transcription	Brain Anterior Caudate	brain
27	chr2:142313000-142313400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr2:142313400-142313600	Enhancers	Brain Anterior Caudate	brain
29	chr2:142313400-142313800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr2:142313400-142313800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr2:142313600-142313800	Active TSS	Brain Cingulate Gyrus	brain
32	chr2:142313600-142314000	Flanking Active TSS	Brain Anterior Caudate	brain
33	chr2:142313600-142314200	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr2:142313600-142314400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr2:142313600-142315800	Enhancers	NH-A	brain
36	chr2:142313600-142316000	Enhancers	Muscle Satellite Cultured Cells	--
37	chr2:142313800-142314000	Enhancers	Brain Angular Gyrus	brain
38	chr2:142313800-142314000	Flanking Active TSS	Brain Cingulate Gyrus	brain
39	chr2:142313800-142314400	Enhancers	Fetal Stomach	stomach
40	chr2:142313800-142315800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr2:142313800-142316000	Enhancers	HMEC	breast
42	chr2:142314000-142314200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr2:142314000-142315000	Weak transcription	Brain Hippocampus Middle	brain
44	chr2:142314200-142314800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr2:142314200-142315200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr2:142314200-142315200	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr2:142314200-142315800	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr2:142314200-142316000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr2:142314400-142316000	Enhancers	Primary hematopoietic stem cells	blood
50	chr2:142314800-142315000	Enhancers	HUES64 Cell Line	embryonic stem cell

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