Variant report

Variant	nsv932193
Chromosome Location	chr12:33545149-34096639
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2097)
CpG islands
(count:1159)
Chromatin interactive
region (count:219)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2097 , 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	chr12:33905885-33906235	K562	blood:	n/a	n/a
2	ARID3A	chr12:33806348-33806595	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	chr12:33807257-33807627	K562	blood:	n/a	n/a
6	ATF1	chr12:33580111-33580282	K562	blood:	n/a	n/a
7	ATF1	chr12:33590564-33590891	K562	blood:	n/a	n/a
8	ATF1	chr12:33837952-33838076	K562	blood:	n/a	n/a
9	ATF1	chr12:33582476-33582638	K562	blood:	n/a	n/a
10	ATF1	chr12:33905799-33906217	K562	blood:	n/a	n/a
11	ATF1	chr12:33740996-33741606	K562	blood:	n/a	n/a
12	ATF1	chr12:33918231-33918238	K562	blood:	n/a	n/a
13	ATF1	chr12:33807257-33807582	K562	blood:	n/a	n/a
14	ATF1	chr12:33749134-33749614	K562	blood:	n/a	n/a
15	ATF2	chr12:33740950-33741433	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr12:33740922-33741468	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr12:33741735-33742256	GM12878	blood:	n/a	n/a
18	ATF3	chr12:33806344-33806588	K562	blood:	n/a	n/a
19	ATF3	chr12:33740980-33741602	K562	blood:	n/a	n/a
20	BACH1	chr12:33847319-33847363	K562	blood:	n/a	n/a
21	BACH1	chr12:33751125-33751167	K562	blood:	n/a	n/a
22	BACH1	chr12:33613710-33613715	K562	blood:	n/a	n/a
23	BACH1	chr12:33905912-33906117	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr12:33591361-33591590	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr12:33854735-33854758	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr12:33625286-33625549	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr12:33592008-33593130	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr12:33583365-33583487	K562	blood:	n/a	n/a
29	BACH1	chr12:33812366-33812495	K562	blood:	n/a	n/a
30	BACH1	chr12:33807354-33807505	K562	blood:	n/a	n/a
31	BACH1	chr12:33740516-33741383	H1-hESC	embryonic stem cell:	n/a	n/a
32	BATF	chr12:33741913-33742237	GM12878	blood:	n/a	n/a
33	BCL11A	chr12:33802958-33803315	H1-hESC	embryonic stem cell:	n/a	chr12:33803028-33803037
34	BCL11A	chr12:33741023-33741182	H1-hESC	embryonic stem cell:	n/a	n/a
35	BHLHE40	chr12:33806387-33806560	K562	blood:	n/a	n/a
36	BHLHE40	chr12:33741303-33741660	GM12878	blood:	n/a	n/a
37	BHLHE40	chr12:33867451-33867477	K562	blood:	n/a	n/a
38	BHLHE40	chr12:33591276-33591724	K562	blood:	n/a	n/a
39	BHLHE40	chr12:33697751-33697753	K562	blood:	n/a	n/a
40	BHLHE40	chr12:33759702-33760074	GM12878	blood:	n/a	n/a
41	BHLHE40	chr12:33734583-33735390	GM12878	blood:	n/a	n/a
42	BHLHE40	chr12:33905773-33906139	K562	blood:	n/a	n/a
43	BHLHE40	chr12:33592354-33592978	K562	blood:	n/a	n/a
44	BHLHE40	chr12:33759769-33760039	K562	blood:	n/a	n/a
45	BHLHE40	chr12:33741030-33741823	K562	blood:	n/a	n/a
46	BRCA1	chr12:33740352-33740651	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr12:33713910-33713913	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr12:34046005-34046050	Hela-S3	cervix:	n/a	n/a
49	CBX3	chr12:33803718-33804191	K562	blood:	n/a	n/a
50	CBX3	chr12:33703185-33703489	K562	blood:	n/a	n/a

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:33592078-33592128	HCM	heart:	n/a
2	chr12:33590837-33590887	ECC-1	luminal epithelium:	n/a
3	chr12:33787337-33787387	Caco-2	colon:	n/a
4	chr12:33593049-33593099	SAEC	small airway:	n/a
5	chr12:34001319-34001369	CMK	blood:	n/a
6	chr12:33589385-33589435	SK-N-MC	brain:	n/a
7	chr12:34061681-34061731	SKMC	muscle:	n/a
8	chr12:33592285-33592335	HCM	heart:	n/a
9	chr12:34061681-34061731	AG09319	gingival:	n/a
10	chr12:33593049-33593099	HEK293	kidney:	embryo
11	chr12:33590837-33590887	GM12878	blood:	n/a
12	chr12:33593913-33593963	HRE	kidney:	n/a
13	chr12:33595118-33595168	Caco-2	colon:	n/a
14	chr12:33590837-33590887	MCF10A-Er-Src	breast:	n/a
15	chr12:33593004-33593054	AG04450	lung:	fetal
16	chr12:33595118-33595168	RPTEC	kidney:	n/a
17	chr12:33750494-33750544	Hepatocyte	liver:	n/a
18	chr12:34061681-34061731	AoSMC	blood vessel:	n/a
19	chr12:34061681-34061731	HNPCEpiC	eye:	n/a
20	chr12:34061681-34061731	AG04450	lung:	fetal
21	chr12:33591336-33591386	PrEC	prostate:	n/a
22	chr12:34061681-34061731	H1-hESC	embryonic stem cell:	embryo
23	chr12:33593913-33593963	HMEC	breast:	n/a
24	chr12:33593049-33593099	HNPCEpiC	eye:	n/a
25	chr12:33593004-33593054	HRE	kidney:	n/a
26	chr12:33592285-33592335	NHDF-neo	bronchial:	n/a
27	chr12:33593913-33593963	GM06990	blood:	n/a
28	chr12:34061681-34061731	SK-N-SH_RA	brain:	n/a
29	chr12:33589385-33589435	PFSK-1	brain:	n/a
30	chr12:33591505-33591555	HMEC	breast:	n/a
31	chr12:33591336-33591386	NB4	blood:	n/a
32	chr12:33592285-33592335	BJ	skin:	n/a
33	chr12:34061681-34061731	ECC-1	luminal epithelium:	n/a
34	chr12:33590837-33590887	HIPEpiC	eye:	n/a
35	chr12:33593177-33593227	PFSK-1	brain:	n/a
36	chr12:33592642-33592692	Jurkat	blood:	n/a
37	chr12:33589594-33589644	SK-N-SH_RA	brain:	n/a
38	chr12:33591505-33591555	GM19239	blood:	n/a
39	chr12:33591336-33591386	HPAEpiC	pulmonary alveolar:	n/a
40	chr12:33589594-33589644	SAEC	small airway:	n/a
41	chr12:33593913-33593963	HCM	heart:	n/a
42	chr12:33593049-33593099	Hepatocyte	liver:	n/a
43	chr12:33593049-33593099	HMEC	breast:	n/a
44	chr12:33589594-33589644	SKMC	muscle:	n/a
45	chr12:33593049-33593099	HRPEpiC	eye:	n/a
46	chr12:33590837-33590887	K562	blood:	n/a
47	chr12:33592285-33592335	MCF10A-Er-Src	breast:	n/a
48	chr12:33750494-33750544	GM12878	blood:	n/a
49	chr12:33592078-33592128	HMEC	breast:	n/a
50	chr12:33750494-33750544	AoSMC	blood vessel:	n/a

(count:219 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr12:33588584..33590612-chr12:33792019..33793766,2	K562	blood:
2	chr12:33694299..33696215-chr12:33697909..33700735,2	MCF-7	breast:
3	chr12:33585788..33587542-chr12:33741964..33743676,2	MCF-7	breast:
4	chr12:33796695..33799615-chr12:33802612..33805057,2	K562	blood:
5	chr12:33901002..33902516-chr12:33905016..33907291,2	MCF-7	breast:
6	chr12:33762278..33765239-chr12:33769487..33771063,2	K562	blood:
7	chr12:33615181..33617280-chr12:33622628..33625177,2	MCF-7	breast:
8	chr12:33762584..33764416-chr12:33765590..33768500,2	MCF-7	breast:
9	chr12:33586288..33588588-chr12:33738098..33741571,3	MCF-7	breast:
10	chr12:33752276..33753246-chr12:33762327..33763192,5	MCF-7	breast:
11	chr12:33555550..33557717-chr12:33560120..33561805,2	K562	blood:
12	chr12:33663952..33667378-chr12:33671771..33674594,3	MCF-7	breast:
13	chr12:33590684..33593436-chr12:33756476..33760229,4	MCF-7	breast:
14	chr12:33601474..33603509-chr12:33613032..33615014,2	K562	blood:
15	chr12:33652466..33655399-chr12:33657814..33659678,2	K562	blood:
16	chr12:33737757..33739747-chr12:33741389..33743027,2	MCF-7	breast:
17	chr12:33724218..33727073-chr12:33731146..33732945,2	MCF-7	breast:
18	chr12:33762272..33764150-chr8:42748547..42750407,2	MCF-7	breast:
19	chr12:33570058..33573036-chr12:33573431..33575463,2	MCF-7	breast:
20	chr12:33735767..33737470-chr12:33737741..33739409,2	K562	blood:
21	chr12:34053367..34054987-chr12:34055066..34057564,2	MCF-7	breast:
22	chr12:33582705..33584694-chr12:33588953..33591212,2	K562	blood:
23	chr12:33815236..33817568-chr12:33820316..33823181,2	K562	blood:
24	chr12:33582010..33584536-chr12:33585632..33588258,2	K562	blood:
25	chr12:33680785..33683680-chr12:33685838..33687484,3	MCF-7	breast:
26	chr12:32908104..32910738-chr12:33762406..33764699,2	MCF-7	breast:
27	chr12:33591186..33595243-chr12:33750295..33755472,6	MCF-7	breast:
28	chr12:33903835..33905859-chr12:33907919..33910698,2	MCF-7	breast:
29	chr12:33663952..33667378-chr12:33671771..33674594,3	MCF-7	breast:
30	chr10:58407921..58410026-chr12:33604212..33606934,2	MCF-7	breast:
31	chr12:33700293..33703250-chr12:33739121..33741427,2	K562	blood:
32	chr12:33673352..33675554-chr12:33738881..33741351,2	MCF-7	breast:
33	chr12:33404543..33406817-chr12:33570626..33572211,2	MCF-7	breast:
34	chr12:33737757..33739747-chr12:33741389..33743027,2	MCF-7	breast:
35	chr12:33579807..33580648-chr12:33758471..33759360,2	MCF-7	breast:
36	chr12:33815236..33817568-chr12:33820316..33823181,2	K562	blood:
37	chr12:33741049..33744622-chr12:33756451..33760061,5	MCF-7	breast:
38	chr12:33588056..33590356-chr12:33591232..33593129,2	K562	blood:
39	chr12:33632921..33635641-chr12:33638680..33640584,2	K562	blood:
40	chr12:33749943..33752525-chr12:33753325..33754973,2	MCF-7	breast:
41	chr12:33697913..33700088-chr12:33701563..33703139,2	K562	blood:
42	chr12:33711689..33714048-chr12:33717879..33720013,2	MCF-7	breast:
43	chr12:33730883..33732707-chr12:33745155..33746710,2	MCF-7	breast:
44	chr12:33916761..33918446-chr16:3069457..3072448,2	MCF-7	breast:
45	chr12:31834709..31836887-chr12:33736084..33739059,2	K562	blood:
46	chr12:33555550..33557717-chr12:33560120..33561805,2	K562	blood:
47	chr12:33720010..33722634-chr12:33727963..33730491,2	K562	blood:
48	chr12:33829191..33832015-chr12:33832800..33835417,2	K562	blood:
49	chr12:33758071..33760342-chr12:33762792..33765785,2	MCF-7	breast:
50	chr12:32908939..32909783-chr12:33758798..33759372,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 8610 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:8610 , 50 per page) page: 1 2 3 4 5 6 7 ... 173

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191817174	chr12:33545153-33545154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs531790075	chr12:33545199-33545200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544115878	chr12:33545230-33545231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564300008	chr12:33545271-33545272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562581524	chr12:33545277-33545278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546472140	chr12:33545310-33545311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566402743	chr12:33545328-33545329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143327333	chr12:33545337-33545338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1994170	chr12:33545355-33545356	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs182974811	chr12:33545356-33545357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs147924351	chr12:33545391-33545392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548487121	chr12:33557814-33557815	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs146313131	chr12:33557852-33557853	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs371214129	chr12:33557898-33557899	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs561605281	chr12:33557933-33557934	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs544950302	chr12:33557953-33557954	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs532578137	chr12:33557954-33557955	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs530436046	chr12:33557975-33557976	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs550149551	chr12:33558104-33558105	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs80106860	chr12:33558247-33558248	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs12313930	chr12:33558264-33558265	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs181019151	chr12:33558267-33558268	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs566767666	chr12:33558424-33558425	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs535644435	chr12:33558473-33558474	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs556098382	chr12:33558492-33558493	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs531385608	chr12:33558512-33558513	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs575967663	chr12:33558513-33558514	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs538289558	chr12:33558567-33558568	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs558163990	chr12:33558598-33558599	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs578062503	chr12:33558634-33558635	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs183901251	chr12:33558638-33558639	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs569944887	chr12:33558703-33558704	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs1905431	chr12:33558720-33558721	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs572999736	chr12:33558741-33558742	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs369977802	chr12:33558762-33558763	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs11052683	chr12:33558768-33558769	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs373960527	chr12:33558779-33558780	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs5797534	chr12:33558794-33558795	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs397703854	chr12:33558804-33558805	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs550186752	chr12:33559074-33559075	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs532944176	chr12:33559637-33559638	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs539804229	chr12:33559643-33559644	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs560234594	chr12:33559646-33559647	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs528959573	chr12:33559647-33559648	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs549633506	chr12:33559653-33559654	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs186865193	chr12:33559656-33559657	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs531915199	chr12:33559671-33559672	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs16920985	chr12:33559673-33559674	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs375766818	chr12:33559677-33559678	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs571810055	chr12:33559701-33559702	Inactive region	TF binding region	1 gene(s)	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
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	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:810 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:33544400-33545400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr12:33566400-33575400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr12:33570400-33575800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:33574000-33576200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr12:33575400-33577600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr12:33575800-33578200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:33576200-33577400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr12:33577400-33580400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr12:33577600-33578400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr12:33578200-33588400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr12:33578400-33579200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr12:33579200-33590600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr12:33586800-33589800	Weak transcription	K562	blood
14	chr12:33588200-33588400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr12:33588400-33590000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr12:33589800-33595600	Active TSS	K562	blood
17	chr12:33590000-33590600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:33590200-33591200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr12:33590400-33590600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
20	chr12:33590400-33590600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
21	chr12:33590600-33590800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
22	chr12:33590600-33591000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr12:33590600-33591200	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr12:33590600-33591200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
25	chr12:33590600-33592000	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:33590600-33593200	Active TSS	Brain Anterior Caudate	brain
27	chr12:33590600-33593400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
28	chr12:33590800-33591000	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
29	chr12:33590800-33591000	Bivalent/Poised TSS	Brain Germinal Matrix	brain
30	chr12:33590800-33591000	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
31	chr12:33590800-33591000	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
32	chr12:33590800-33591200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
33	chr12:33590800-33591400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
34	chr12:33590800-33591600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
35	chr12:33590800-33592000	Bivalent/Poised TSS	Right Atrium	heart
36	chr12:33591000-33591200	Bivalent Enhancer	Brain Angular Gyrus	brain
37	chr12:33591000-33591200	Bivalent Enhancer	Fetal Brain Male	brain
38	chr12:33591000-33591200	Bivalent Enhancer	Fetal Brain Female	brain
39	chr12:33591000-33591200	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
40	chr12:33591000-33591200	Bivalent/Poised TSS	Fetal Stomach	stomach
41	chr12:33591000-33591400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr12:33591000-33591400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
43	chr12:33591000-33591400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr12:33591000-33591400	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
45	chr12:33591000-33591400	Bivalent Enhancer	Right Ventricle	heart
46	chr12:33591000-33591600	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr12:33591000-33591600	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
48	chr12:33591000-33591600	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
49	chr12:33591000-33591800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
50	chr12:33591000-33591800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin

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