Variant report

Variant	nsv558248
Chromosome Location	chr12:33524082-33714866
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:770)
CpG islands
(count:976)
Chromatin interactive
region (count:80)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:770 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:33590564-33590891	K562	blood:	n/a	n/a
2	ATF1	chr12:33580111-33580282	K562	blood:	n/a	n/a
3	ATF1	chr12:33582476-33582638	K562	blood:	n/a	n/a
4	BACH1	chr12:33592008-33593130	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr12:33583365-33583487	K562	blood:	n/a	n/a
6	BACH1	chr12:33625286-33625549	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr12:33591361-33591590	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr12:33613710-33613715	K562	blood:	n/a	n/a
9	BACH1	chr12:33536437-33536460	K562	blood:	n/a	n/a
10	BHLHE40	chr12:33591276-33591724	K562	blood:	n/a	n/a
11	BHLHE40	chr12:33592354-33592978	K562	blood:	n/a	n/a
12	BHLHE40	chr12:33697751-33697753	K562	blood:	n/a	n/a
13	BRCA1	chr12:33713910-33713913	H1-hESC	embryonic stem cell:	n/a	n/a
14	CBX3	chr12:33673832-33674319	K562	blood:	n/a	n/a
15	CBX3	chr12:33703953-33704297	K562	blood:	n/a	n/a
16	CBX3	chr12:33592581-33592968	K562	blood:	n/a	n/a
17	CBX3	chr12:33703185-33703489	K562	blood:	n/a	n/a
18	CCNT2	chr12:33591941-33592947	K562	blood:	n/a	chr12:33592759-33592768
19	CCNT2	chr12:33591404-33591604	K562	blood:	n/a	n/a
20	CEBPB	chr12:33578540-33578719	K562	blood:	n/a	chr12:33578619-33578630 chr12:33578620-33578631
21	CEBPB	chr12:33708093-33708429	K562	blood:	n/a	chr12:33708261-33708272 chr12:33708344-33708357
22	CEBPB	chr12:33524874-33525094	HepG2	liver:	n/a	chr12:33524963-33524974
23	CEBPB	chr12:33595143-33595398	K562	blood:	n/a	n/a
24	CEBPB	chr12:33529153-33529455	Hela-S3	cervix:	n/a	chr12:33529283-33529294
25	CEBPB	chr12:33704584-33704792	HepG2	liver:	n/a	chr12:33704654-33704665
26	CEBPB	chr12:33578485-33578778	HepG2	liver:	n/a	chr12:33578619-33578630 chr12:33578620-33578631
27	CEBPB	chr12:33704517-33704702	Hela-S3	cervix:	n/a	chr12:33704654-33704665
28	CEBPB	chr12:33712455-33712704	A549	lung:	n/a	chr12:33712545-33712556
29	CEBPB	chr12:33672207-33672491	HepG2	liver:	n/a	chr12:33672352-33672365 chr12:33672352-33672363 chr12:33672354-33672365
30	CEBPB	chr12:33578482-33578763	IMR90	lung:	n/a	chr12:33578619-33578630 chr12:33578620-33578631
31	CEBPB	chr12:33547502-33547698	A549	lung:	n/a	n/a
32	CEBPB	chr12:33547465-33547674	HepG2	liver:	n/a	n/a
33	CEBPB	chr12:33573243-33573258	K562	blood:	n/a	n/a
34	CEBPB	chr12:33529111-33529474	K562	blood:	n/a	chr12:33529283-33529294
35	CEBPB	chr12:33529126-33529471	ECC-1	luminal epithelium:	n/a	chr12:33529283-33529294
36	CEBPB	chr12:33673343-33673349	K562	blood:	n/a	n/a
37	CEBPB	chr12:33708080-33708415	HepG2	liver:	n/a	chr12:33708261-33708272 chr12:33708344-33708357
38	CEBPB	chr12:33648317-33648399	A549	lung:	n/a	n/a
39	CEBPB	chr12:33529107-33529534	IMR90	lung:	n/a	chr12:33529283-33529294
40	CEBPB	chr12:33532106-33532294	HepG2	liver:	n/a	chr12:33532186-33532197
41	CEBPB	chr12:33582542-33582742	K562	blood:	n/a	n/a
42	CEBPB	chr12:33640896-33641346	MCF-7	breast:	n/a	n/a
43	CEBPB	chr12:33712447-33712679	HepG2	liver:	n/a	chr12:33712545-33712556
44	CEBPB	chr12:33529072-33529512	MCF-7	breast:	n/a	chr12:33529283-33529294
45	CEBPB	chr12:33529114-33529466	H1-hESC	embryonic stem cell:	n/a	chr12:33529283-33529294
46	CEBPB	chr12:33608367-33608484	HepG2	liver:	n/a	n/a
47	CEBPB	chr12:33708119-33708382	A549	lung:	n/a	chr12:33708261-33708272 chr12:33708344-33708357
48	CEBPB	chr12:33529190-33529465	HepG2	liver:	n/a	chr12:33529283-33529294
49	CEBPB	chr12:33578486-33578753	A549	lung:	n/a	chr12:33578619-33578630 chr12:33578620-33578631
50	CEBPB	chr12:33670739-33670769	H1-hESC	embryonic stem cell:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:33591505-33591555	PANC-1	pancreas:	n/a
2	chr12:33528782-33528832	AG09309	skin:	n/a
3	chr12:33591336-33591386	NHBE	bronchial:	n/a
4	chr12:33589385-33589435	HepG2	liver:	n/a
5	chr12:33528782-33528832	HRPEpiC	eye:	n/a
6	chr12:33528782-33528832	ProgFib	skin:	n/a
7	chr12:33593177-33593227	CMK	blood:	n/a
8	chr12:33593004-33593054	AG04449	skin:	fetal
9	chr12:33593004-33593054	NH-A	brain:	n/a
10	chr12:33593177-33593227	HEEpiC	esophagus:	n/a
11	chr12:33591336-33591386	CMK	blood:	n/a
12	chr12:33593177-33593227	AG04450	lung:	fetal
13	chr12:33591899-33591949	SK-N-SH_RA	brain:	n/a
14	chr12:33590837-33590887	AoSMC	blood vessel:	n/a
15	chr12:33595118-33595168	HEEpiC	esophagus:	n/a
16	chr12:33592078-33592128	HCM	heart:	n/a
17	chr12:33593913-33593963	GM12892	blood:	n/a
18	chr12:33591899-33591949	HRE	kidney:	n/a
19	chr12:33591505-33591555	MCF10A-Er-Src	breast:	n/a
20	chr12:33593049-33593099	HCT-116	colon:	n/a
21	chr12:33593049-33593099	HepG2	liver:	n/a
22	chr12:33592500-33592550	SKMC	muscle:	n/a
23	chr12:33592285-33592335	HPAEpiC	pulmonary alveolar:	n/a
24	chr12:33589594-33589644	ProgFib	skin:	n/a
25	chr12:33593049-33593099	K562	blood:	n/a
26	chr12:33595118-33595168	U87	brain:	n/a
27	chr12:33528782-33528832	PrEC	prostate:	n/a
28	chr12:33592642-33592692	AG04449	skin:	fetal
29	chr12:33589594-33589644	AG04450	lung:	fetal
30	chr12:33593177-33593227	A549	lung:	n/a
31	chr12:33592500-33592550	MCF10A-Er-Src	breast:	n/a
32	chr12:33591336-33591386	HRPEpiC	eye:	n/a
33	chr12:33593913-33593963	T-47D	breast:	n/a
34	chr12:33592285-33592335	CMK	blood:	n/a
35	chr12:33595118-33595168	ECC-1	luminal epithelium:	n/a
36	chr12:33593177-33593227	BJ	skin:	n/a
37	chr12:33592078-33592128	ProgFib	skin:	n/a
38	chr12:33590837-33590887	AG10803	skin:	n/a
39	chr12:33590837-33590887	BJ	skin:	n/a
40	chr12:33589385-33589435	MCF10A-Er-Src	breast:	n/a
41	chr12:33592078-33592128	HMEC	breast:	n/a
42	chr12:33591336-33591386	K562	blood:	n/a
43	chr12:33592078-33592128	Hepatocyte	liver:	n/a
44	chr12:33591336-33591386	A549	lung:	n/a
45	chr12:33593004-33593054	BE2_C	brain:	n/a
46	chr12:33528782-33528832	Hepatocyte	liver:	n/a
47	chr12:33591899-33591949	AG09309	skin:	n/a
48	chr12:33593913-33593963	ovcar-3	ovarian:	n/a
49	chr12:33595118-33595168	HCM	heart:	n/a
50	chr12:33592285-33592335	IMR90	lung:	fetal

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:33587036..33589098-chr12:33993044..33994546,2	MCF-7	breast:
2	chr12:33615181..33617280-chr12:33622628..33625177,2	MCF-7	breast:
3	chr12:33591224..33595287-chr12:33601141..33606110,5	K562	blood:
4	chr12:33581348..33583914-chr12:33584659..33586358,3	MCF-7	breast:
5	chr12:33538532..33540050-chr12:33561297..33564273,2	MCF-7	breast:
6	chr12:33688358..33691054-chr12:33691826..33694361,2	K562	blood:
7	chr12:33581348..33583914-chr12:33584659..33586358,3	MCF-7	breast:
8	chr12:33636131..33639117-chr12:33639347..33641138,2	MCF-7	breast:
9	chr12:33580522..33582279-chr12:33590834..33593788,2	MCF-7	breast:
10	chr12:33585788..33587542-chr12:33741964..33743676,2	MCF-7	breast:
11	chr12:33570058..33573036-chr12:33573431..33575463,2	MCF-7	breast:
12	chr12:33588584..33590612-chr12:33792019..33793766,2	K562	blood:
13	chr12:33590681..33593666-chr12:33611371..33613830,2	K562	blood:
14	chr12:33673191..33674096-chr7:136092701..136093461,2	MCF-7	breast:
15	chr12:33601474..33603509-chr12:33613032..33615014,2	K562	blood:
16	chr12:33585883..33590144-chr12:33590166..33593632,7	K562	blood:
17	chr12:33593109..33594784-chr12:33753664..33755603,2	MCF-7	breast:
18	chr12:33704309..33707491-chr12:33710515..33713446,4	K562	blood:
19	chr12:33636131..33639117-chr12:33639347..33641138,2	MCF-7	breast:
20	chr12:33615181..33617280-chr12:33622628..33625177,2	MCF-7	breast:
21	chr12:33667255..33668975-chr12:33733951..33735986,2	MCF-7	breast:
22	chr12:33652466..33655399-chr12:33657814..33659678,2	K562	blood:
23	chr12:33575316..33578004-chr12:33579015..33581251,4	MCF-7	breast:
24	chr12:33590753..33592625-chr12:33706633..33709299,2	K562	blood:
25	chr12:33333640..33335661-chr12:33603103..33604823,2	MCF-7	breast:
26	chr12:33632921..33635641-chr12:33638680..33640584,2	K562	blood:
27	chr12:33601580..33602442-chr12:33758672..33759329,2	MCF-7	breast:
28	chr12:33579135..33582133-chr12:33592492..33594552,2	K562	blood:
29	chr12:33601474..33603509-chr12:33613032..33615014,2	K562	blood:
30	chr12:33538532..33540050-chr12:33561297..33564273,2	MCF-7	breast:
31	chr12:33592809..33594554-chr12:33758267..33760517,2	MCF-7	breast:
32	chr12:33694299..33696215-chr12:33697909..33700735,2	MCF-7	breast:
33	chr12:33631092..33633580-chr12:33640097..33642228,2	MCF-7	breast:
34	chr12:33578497..33581181-chr12:33582764..33584614,2	K562	blood:
35	chr12:33669502..33671895-chr12:33672073..33673805,2	MCF-7	breast:
36	chr12:32908013..32910248-chr12:33589503..33591482,2	K562	blood:
37	chr12:33700293..33703250-chr12:33739121..33741427,2	K562	blood:
38	chr12:33580127..33582925-chr12:33586373..33588630,2	MCF-7	breast:
39	chr12:33632921..33635641-chr12:33638680..33640584,2	K562	blood:
40	chr12:33697913..33700088-chr12:33701563..33703139,2	K562	blood:
41	chr12:33680785..33683680-chr12:33685838..33687484,3	MCF-7	breast:
42	chr12:33570058..33573036-chr12:33573431..33575463,2	MCF-7	breast:
43	chr12:33688358..33691054-chr12:33691826..33694361,2	K562	blood:
44	chr12:33669502..33671895-chr12:33672073..33673805,2	MCF-7	breast:
45	chr12:33582705..33584694-chr12:33588953..33591212,2	K562	blood:
46	chr12:33582010..33584536-chr12:33585632..33588258,2	K562	blood:
47	chr12:33704309..33707491-chr12:33710515..33713446,4	K562	blood:
48	chr12:33590785..33592619-chr12:33667736..33669567,2	MCF-7	breast:
49	chr10:58407921..58410026-chr12:33604212..33606934,2	MCF-7	breast:
50	chr12:33573643..33576869-chr12:33577917..33580501,4	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PKP2-2	chr12:33560733-33561253	NONHSAT027643
2	lnc-PKP2-2	chr12:33579073-33579095	NONHSAT027643
3	lnc-PKP2-1	chr12:33557810-33558831	ENSG00000259937.1

No data

Variant related genes	Relation type
ENSG00000265029	TF binding region
ENSG00000256070	TF binding region
ENSG00000259937	TF binding region
SYT10	TF binding region
ENSG00000265029	CpG island
ENSG00000256070	CpG island
ENSG00000259937	CpG island
SYT10	CpG island
ENSG00000168298	chromatin interactions
ENSG00000110975	chromatin interactions
ENSG00000139131	chromatin interactions

Extended variants
information (count: 4074 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:4074 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537699767	chr12:33525613-33525614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs557377219	chr12:33525624-33525625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192827619	chr12:33525676-33525677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539680427	chr12:33525718-33525719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557534979	chr12:33525726-33525727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539974230	chr12:33525780-33525781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75812790	chr12:33525788-33525789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184702637	chr12:33525815-33525816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7958976	chr12:33525835-33525836	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs562903097	chr12:33525836-33525837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532050419	chr12:33525877-33525878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188852890	chr12:33525892-33525893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565322145	chr12:33525893-33525894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527662244	chr12:33525968-33525969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374149545	chr12:33525973-33525974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547781979	chr12:33526032-33526033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs151053128	chr12:33526144-33526145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530096026	chr12:33526147-33526148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs74967183	chr12:33526208-33526209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568954539	chr12:33526292-33526293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537787967	chr12:33526293-33526294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148031558	chr12:33526349-33526350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs59499949	chr12:33526354-33526355	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs201901199	chr12:33526355-33526356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528829056	chr12:33526363-33526364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140840287	chr12:33526384-33526385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553455346	chr12:33526407-33526408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573690322	chr12:33526432-33526433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556480331	chr12:33526462-33526463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs58533538	chr12:33526465-33526466	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs556766561	chr12:33526597-33526598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540074430	chr12:33526657-33526658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546865788	chr12:33526694-33526695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145915096	chr12:33526702-33526703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565597689	chr12:33526704-33526705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12319793	chr12:33526742-33526743	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs541421504	chr12:33526761-33526762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192103441	chr12:33526805-33526806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138810711	chr12:33526815-33526816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10466764	chr12:33526822-33526823	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs560682193	chr12:33526835-33526836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs76452875	chr12:33526850-33526851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551135200	chr12:33526866-33526867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527869654	chr12:33526906-33526907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571224230	chr12:33526959-33526960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184606018	chr12:33526967-33526968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533797081	chr12:33526972-33526973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547375441	chr12:33527005-33527006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567150248	chr12:33527042-33527043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs16920890	chr12:33527078-33527079	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:57)

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

Chromatin state (count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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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