Variant report

Variant	nsv541461
Chromosome Location	chr12:33527371-34078208
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2056)
CpG islands
(count:1221)
Chromatin interactive
region (count:220)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2056 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:33806348-33806595	K562	blood:	n/a	n/a
2	ARID3A	chr12:33807257-33807627	K562	blood:	n/a	n/a
3	ARID3A	chr12:33740984-33742025	K562	blood:	n/a	n/a
4	ARID3A	chr12:33831095-33831857	K562	blood:	n/a	n/a
5	ARID3A	chr12:33905885-33906235	K562	blood:	n/a	n/a
6	ATF1	chr12:33580111-33580282	K562	blood:	n/a	n/a
7	ATF1	chr12:33582476-33582638	K562	blood:	n/a	n/a
8	ATF1	chr12:33590564-33590891	K562	blood:	n/a	n/a
9	ATF1	chr12:33837952-33838076	K562	blood:	n/a	n/a
10	ATF1	chr12:33807257-33807582	K562	blood:	n/a	n/a
11	ATF1	chr12:33905799-33906217	K562	blood:	n/a	n/a
12	ATF1	chr12:33740996-33741606	K562	blood:	n/a	n/a
13	ATF1	chr12:33749134-33749614	K562	blood:	n/a	n/a
14	ATF1	chr12:33918231-33918238	K562	blood:	n/a	n/a
15	ATF2	chr12:33740922-33741468	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr12:33741735-33742256	GM12878	blood:	n/a	n/a
17	ATF2	chr12:33740950-33741433	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr12:33740980-33741602	K562	blood:	n/a	n/a
19	ATF3	chr12:33806344-33806588	K562	blood:	n/a	n/a
20	BACH1	chr12:33536437-33536460	K562	blood:	n/a	n/a
21	BACH1	chr12:33625286-33625549	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr12:33812366-33812495	K562	blood:	n/a	n/a
23	BACH1	chr12:33751125-33751167	K562	blood:	n/a	n/a
24	BACH1	chr12:33854735-33854758	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr12:33591361-33591590	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr12:33592008-33593130	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr12:33583365-33583487	K562	blood:	n/a	n/a
28	BACH1	chr12:33905912-33906117	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr12:33847319-33847363	K562	blood:	n/a	n/a
30	BACH1	chr12:33740516-33741383	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr12:33807354-33807505	K562	blood:	n/a	n/a
32	BACH1	chr12:33613710-33613715	K562	blood:	n/a	n/a
33	BATF	chr12:33741913-33742237	GM12878	blood:	n/a	n/a
34	BCL11A	chr12:33741023-33741182	H1-hESC	embryonic stem cell:	n/a	n/a
35	BCL11A	chr12:33802958-33803315	H1-hESC	embryonic stem cell:	n/a	chr12:33803028-33803037
36	BHLHE40	chr12:33591276-33591724	K562	blood:	n/a	n/a
37	BHLHE40	chr12:33759769-33760039	K562	blood:	n/a	n/a
38	BHLHE40	chr12:33867451-33867477	K562	blood:	n/a	n/a
39	BHLHE40	chr12:33759702-33760074	GM12878	blood:	n/a	n/a
40	BHLHE40	chr12:33741030-33741823	K562	blood:	n/a	n/a
41	BHLHE40	chr12:33905773-33906139	K562	blood:	n/a	n/a
42	BHLHE40	chr12:33806387-33806560	K562	blood:	n/a	n/a
43	BHLHE40	chr12:33734583-33735390	GM12878	blood:	n/a	n/a
44	BHLHE40	chr12:33741303-33741660	GM12878	blood:	n/a	n/a
45	BHLHE40	chr12:33697751-33697753	K562	blood:	n/a	n/a
46	BHLHE40	chr12:33592354-33592978	K562	blood:	n/a	n/a
47	BRCA1	chr12:33740352-33740651	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr12:33713910-33713913	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr12:34046005-34046050	Hela-S3	cervix:	n/a	n/a
50	CBX3	chr12:33673832-33674319	K562	blood:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:33592285-33592335	AoSMC	blood vessel:	n/a
2	chr12:33592285-33592335	AoSMC	blood vessel:	n/a
3	chr12:33589385-33589435	CMK	blood:	n/a
4	chr12:33592642-33592692	HEK293	kidney:	embryo
5	chr12:33750494-33750544	U87	brain:	n/a
6	chr12:33528782-33528832	HRPEpiC	eye:	n/a
7	chr12:33787337-33787387	HepG2	liver:	n/a
8	chr12:34061681-34061731	AoSMC	blood vessel:	n/a
9	chr12:33593913-33593963	AG10803	skin:	n/a
10	chr12:33591899-33591949	A549	lung:	n/a
11	chr12:33589385-33589435	RPTEC	kidney:	n/a
12	chr12:33593913-33593963	PrEC	prostate:	n/a
13	chr12:33592285-33592335	HRCEpiC	kidney:	n/a
14	chr12:33593177-33593227	SK-N-SH	brain:	n/a
15	chr12:33787337-33787387	NH-A	brain:	n/a
16	chr12:33593004-33593054	HCF	heart:	n/a
17	chr12:33750494-33750544	HCM	heart:	n/a
18	chr12:33593004-33593054	HRCEpiC	kidney:	n/a
19	chr12:33592642-33592692	BJ	skin:	n/a
20	chr12:33593004-33593054	NB4	blood:	n/a
21	chr12:33595118-33595168	SK-N-SH	brain:	n/a
22	chr12:33590837-33590887	PrEC	prostate:	n/a
23	chr12:33592285-33592335	IMR90	lung:	fetal
24	chr12:33787337-33787387	HNPCEpiC	eye:	n/a
25	chr12:34061681-34061731	GM12891	blood:	n/a
26	chr12:33592642-33592692	RPTEC	kidney:	n/a
27	chr12:33591899-33591949	HRCEpiC	kidney:	n/a
28	chr12:33593004-33593054	HMEC	breast:	n/a
29	chr12:33787337-33787387	HUVEC	blood vessel:	n/a
30	chr12:33592500-33592550	HCPEpiC	choroid plexus:	n/a
31	chr12:33592500-33592550	Hela-S3	cervix:	n/a
32	chr12:33593177-33593227	HepG2	liver:	n/a
33	chr12:33787337-33787387	ovcar-3	ovarian:	n/a
34	chr12:33589385-33589435	HMEC	breast:	n/a
35	chr12:33590837-33590887	NHBE	bronchial:	n/a
36	chr12:33590837-33590887	MCF10A-Er-Src	breast:	n/a
37	chr12:33593177-33593227	SK-N-MC	brain:	n/a
38	chr12:33593004-33593054	PrEC	prostate:	n/a
39	chr12:33593177-33593227	HNPCEpiC	eye:	n/a
40	chr12:33592642-33592692	SK-N-SH_RA	brain:	n/a
41	chr12:33589594-33589644	MCF-7	breast:	n/a
42	chr12:33590837-33590887	SK-N-SH_RA	brain:	n/a
43	chr12:34001319-34001369	HEEpiC	esophagus:	n/a
44	chr12:33590837-33590887	RPTEC	kidney:	n/a
45	chr12:33592500-33592550	NH-A	brain:	n/a
46	chr12:33750494-33750544	SAEC	small airway:	n/a
47	chr12:33591505-33591555	MCF-7	breast:	n/a
48	chr12:34001319-34001369	AG10803	skin:	n/a
49	chr12:33787337-33787387	HEEpiC	esophagus:	n/a
50	chr12:33591505-33591555	A549	lung:	n/a

(count:220 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr12:33758791..33761325-chr12:33805781..33808679,2	K562	blood:
2	chr12:33570058..33573036-chr12:33573431..33575463,2	MCF-7	breast:
3	chr12:33585788..33587542-chr12:33741964..33743676,2	MCF-7	breast:
4	chr12:33590760..33594067-chr12:33739942..33743332,4	K562	blood:
5	chr12:33680785..33683680-chr12:33685838..33687484,3	MCF-7	breast:
6	chr12:33652466..33655399-chr12:33657814..33659678,2	K562	blood:
7	chr12:33580127..33582925-chr12:33586373..33588630,2	MCF-7	breast:
8	chr12:33719195..33722497-chr12:33723252..33727386,3	MCF-7	breast:
9	chr12:33796695..33799615-chr12:33802612..33805057,2	K562	blood:
10	chr12:33749840..33752814-chr12:33754848..33757190,2	K562	blood:
11	chr12:33735767..33737470-chr12:33737741..33739409,2	K562	blood:
12	chr12:33555550..33557717-chr12:33560120..33561805,2	K562	blood:
13	chr12:33740590..33741231-chr12:33762284..33763123,2	MCF-7	breast:
14	chr12:33694299..33696215-chr12:33697909..33700735,2	MCF-7	breast:
15	chr12:33593109..33594784-chr12:33753664..33755603,2	MCF-7	breast:
16	chr12:34053367..34054987-chr12:34055066..34057564,2	MCF-7	breast:
17	chr12:33538532..33540050-chr12:33561297..33564273,2	MCF-7	breast:
18	chr12:33101880..33104767-chr12:33761445..33763993,2	MCF-7	breast:
19	chr12:33721763..33724607-chr12:33725779..33728514,2	MCF-7	breast:
20	chr12:33588584..33590612-chr12:33792019..33793766,2	K562	blood:
21	chr12:33579807..33580648-chr12:33758471..33759360,2	MCF-7	breast:
22	chr12:33568450..33571114-chr12:33575254..33577909,2	K562	blood:
23	chr12:33724218..33727073-chr12:33731146..33732945,2	MCF-7	breast:
24	chr12:33830515..33832081-chr12:33832328..33834300,2	K562	blood:
25	chr12:33916761..33918446-chr16:3069457..3072448,2	MCF-7	breast:
26	chr12:33975803..33979098-chr12:33979674..33983619,4	MCF-7	breast:
27	chr12:33538532..33540050-chr12:33561297..33564273,2	MCF-7	breast:
28	chr12:33740467..33741676-chr12:33762290..33763074,5	MCF-7	breast:
29	chr12:33730883..33732707-chr12:33745155..33746710,2	MCF-7	breast:
30	chr12:33737757..33739747-chr12:33741389..33743027,2	MCF-7	breast:
31	chr12:33809313..33810966-chr12:33832220..33835115,2	K562	blood:
32	chr12:33762584..33764416-chr12:33765590..33768500,2	MCF-7	breast:
33	chr12:33749299..33751532-chr12:33760036..33763741,3	MCF-7	breast:
34	chr12:33580522..33582279-chr12:33590834..33593788,2	MCF-7	breast:
35	chr12:33984638..33987420-chr12:33995374..33998517,3	MCF-7	breast:
36	chr12:33636131..33639117-chr12:33639347..33641138,2	MCF-7	breast:
37	chr12:33734204..33736505-chr12:33740513..33742206,2	K562	blood:
38	chr12:33570058..33573036-chr12:33573431..33575463,2	MCF-7	breast:
39	chr12:33903835..33905859-chr12:33907919..33910698,2	MCF-7	breast:
40	chr12:33757088..33759339-chr12:33761312..33763614,2	K562	blood:
41	chr12:33589726..33596989-chr12:33737254..33743557,12	MCF-7	breast:
42	chr12:33785580..33788231-chr12:33795540..33797279,2	MCF-7	breast:
43	chr12:33631092..33633580-chr12:33640097..33642228,2	MCF-7	breast:
44	chr12:33592469..33594296-chr12:33715860..33717717,2	MCF-7	breast:
45	chr12:33762278..33765239-chr12:33769487..33771063,2	K562	blood:
46	chr12:33700293..33703250-chr12:33739121..33741427,2	K562	blood:
47	chr12:33749299..33751532-chr12:33760036..33763741,3	MCF-7	breast:
48	chr12:33667255..33668975-chr12:33733951..33735986,2	MCF-7	breast:
49	chr12:33593109..33594784-chr12:33753664..33755603,2	MCF-7	breast:
50	chr12:33752276..33753246-chr12:33762327..33763192,5	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALG10-6	chr12:33870788-33871152	NONHSAT027645
2	lnc-PKP2-2	chr12:33579073-33579095	NONHSAT027643
3	lnc-PKP2-1	chr12:33557810-33558831	ENSG00000259937.1
4	lnc-PKP2-2	chr12:33560733-33561253	NONHSAT027643

No data

Variant related genes	Relation type
SYT10	TF binding region
ENSG00000270807	TF binding region
ENSG00000265029	TF binding region
ENSG00000256070	TF binding region
RNU6-400P	TF binding region
ENSG00000259937	TF binding region
RNU6-472P	TF binding region
SYT10	CpG island
ENSG00000270807	CpG island
ENSG00000265029	CpG island
ENSG00000256070	CpG island
RNU6-400P	CpG island
ENSG00000259937	CpG island
RNU6-472P	CpG island
ENSG00000250151	chromatin interactions
ENSG00000168172	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000120925	chromatin interactions
ENSG00000006327	chromatin interactions
ENSG00000241553	chromatin interactions
ENSG00000171148	chromatin interactions
ENSG00000266044	chromatin interactions
ENSG00000110975	chromatin interactions
ENSG00000139131	chromatin interactions
ENSG00000184697	chromatin interactions
ENSG00000212475	chromatin interactions
ENSG00000131931	chromatin interactions

Extended variants
information (count: 8932 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:8932 , 50 per page) page: 1 2 3 4 5 6 7 ... 179

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563465188	chr12:33527430-33527431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs1947969	chr12:33527446-33527447	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs551170415	chr12:33527465-33527466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs137948037	chr12:33527480-33527481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527633167	chr12:33527489-33527490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533099301	chr12:33527506-33527507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181933524	chr12:33527632-33527633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568884048	chr12:33527662-33527663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545952056	chr12:33527668-33527669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549713750	chr12:33527719-33527720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569775947	chr12:33527722-33527723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79859072	chr12:33527725-33527726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559239363	chr12:33527736-33527737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34843302	chr12:33527780-33527781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143081085	chr12:33527820-33527821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535362797	chr12:33527873-33527874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112072044	chr12:33527899-33527900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575049792	chr12:33528000-33528001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566082344	chr12:33528073-33528074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543470187	chr12:33528076-33528077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370670749	chr12:33528112-33528113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373562674	chr12:33528134-33528135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12309785	chr12:33528143-33528144	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs148212936	chr12:33528178-33528179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545891687	chr12:33528205-33528206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566363841	chr12:33528209-33528210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375045419	chr12:33528212-33528213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533735202	chr12:33528259-33528260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs202091251	chr12:33528281-33528282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141953546	chr12:33528296-33528297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527481544	chr12:33528331-33528332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547700400	chr12:33528367-33528368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561040406	chr12:33528413-33528414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529957201	chr12:33528441-33528442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549802379	chr12:33528442-33528443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146134251	chr12:33528499-33528500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532285590	chr12:33528533-33528534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552284902	chr12:33528556-33528557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185922615	chr12:33528560-33528561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376432948	chr12:33528592-33528593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189139302	chr12:33528602-33528603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs397851168	chr12:33528609-33528610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369766108	chr12:33528628-33528629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568670452	chr12:33528658-33528659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555481335	chr12:33528674-33528675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537704685	chr12:33528712-33528713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567662758	chr12:33528729-33528730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140119098	chr12:33528772-33528773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576819055	chr12:33528783-33528784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538289005	chr12:33528793-33528794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chordoma	18071362	CNVD
Lung cancer	18438408	CNVD
Cancer	21272361	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
Tetralogy of Fallot	22912587	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:814 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:33525600-33534600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr12:33534600-33535400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr12:33535400-33536600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr12:33536600-33536800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr12:33536800-33537200	Enhancers	Brain Cingulate Gyrus	brain
6	chr12:33536800-33537600	Enhancers	Brain Germinal Matrix	brain
7	chr12:33537800-33540000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr12:33542600-33543000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr12:33543000-33544400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr12:33544400-33545400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr12:33566400-33575400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr12:33570400-33575800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr12:33574000-33576200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr12:33575400-33577600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr12:33575800-33578200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr12:33576200-33577400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr12:33577400-33580400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr12:33577600-33578400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr12:33578200-33588400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr12:33578400-33579200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr12:33579200-33590600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr12:33586800-33589800	Weak transcription	K562	blood
23	chr12:33588200-33588400	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr12:33588400-33590000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:33589800-33595600	Active TSS	K562	blood
26	chr12:33590000-33590600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr12:33590200-33591200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr12:33590400-33590600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
29	chr12:33590400-33590600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
30	chr12:33590600-33590800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
31	chr12:33590600-33591000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr12:33590600-33591200	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr12:33590600-33591200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
34	chr12:33590600-33592000	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
35	chr12:33590600-33593200	Active TSS	Brain Anterior Caudate	brain
36	chr12:33590600-33593400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
37	chr12:33590800-33591000	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
38	chr12:33590800-33591000	Bivalent/Poised TSS	Brain Germinal Matrix	brain
39	chr12:33590800-33591000	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
40	chr12:33590800-33591000	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
41	chr12:33590800-33591200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
42	chr12:33590800-33591400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
43	chr12:33590800-33591600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
44	chr12:33590800-33592000	Bivalent/Poised TSS	Right Atrium	heart
45	chr12:33591000-33591200	Bivalent Enhancer	Brain Angular Gyrus	brain
46	chr12:33591000-33591200	Bivalent Enhancer	Fetal Brain Male	brain
47	chr12:33591000-33591200	Bivalent Enhancer	Fetal Brain Female	brain
48	chr12:33591000-33591200	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
49	chr12:33591000-33591200	Bivalent/Poised TSS	Fetal Stomach	stomach
50	chr12:33591000-33591400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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