Variant report

Variant	nsv1052700
Chromosome Location	chr12:33542309-34078208
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2025)
CpG islands
(count:1160)
Chromatin interactive
region (count:218)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2025 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:33807257-33807627	K562	blood:	n/a	n/a
2	ARID3A	chr12:33806348-33806595	K562	blood:	n/a	n/a
3	ARID3A	chr12:33831095-33831857	K562	blood:	n/a	n/a
4	ARID3A	chr12:33905885-33906235	K562	blood:	n/a	n/a
5	ARID3A	chr12:33740984-33742025	K562	blood:	n/a	n/a
6	ATF1	chr12:33918231-33918238	K562	blood:	n/a	n/a
7	ATF1	chr12:33807257-33807582	K562	blood:	n/a	n/a
8	ATF1	chr12:33905799-33906217	K562	blood:	n/a	n/a
9	ATF1	chr12:33749134-33749614	K562	blood:	n/a	n/a
10	ATF1	chr12:33837952-33838076	K562	blood:	n/a	n/a
11	ATF1	chr12:33740996-33741606	K562	blood:	n/a	n/a
12	ATF1	chr12:33580111-33580282	K562	blood:	n/a	n/a
13	ATF1	chr12:33590564-33590891	K562	blood:	n/a	n/a
14	ATF1	chr12:33582476-33582638	K562	blood:	n/a	n/a
15	ATF2	chr12:33741735-33742256	GM12878	blood:	n/a	n/a
16	ATF2	chr12:33740950-33741433	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr12:33740922-33741468	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	chr12:33847319-33847363	K562	blood:	n/a	n/a
21	BACH1	chr12:33740516-33741383	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr12:33854735-33854758	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr12:33807354-33807505	K562	blood:	n/a	n/a
24	BACH1	chr12:33905912-33906117	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr12:33583365-33583487	K562	blood:	n/a	n/a
26	BACH1	chr12:33592008-33593130	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr12:33591361-33591590	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr12:33625286-33625549	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr12:33613710-33613715	K562	blood:	n/a	n/a
30	BACH1	chr12:33751125-33751167	K562	blood:	n/a	n/a
31	BACH1	chr12:33812366-33812495	K562	blood:	n/a	n/a
32	BATF	chr12:33741913-33742237	GM12878	blood:	n/a	n/a
33	BCL11A	chr12:33741023-33741182	H1-hESC	embryonic stem cell:	n/a	n/a
34	BCL11A	chr12:33802958-33803315	H1-hESC	embryonic stem cell:	n/a	chr12:33803028-33803037
35	BHLHE40	chr12:33905773-33906139	K562	blood:	n/a	n/a
36	BHLHE40	chr12:33697751-33697753	K562	blood:	n/a	n/a
37	BHLHE40	chr12:33591276-33591724	K562	blood:	n/a	n/a
38	BHLHE40	chr12:33759702-33760074	GM12878	blood:	n/a	n/a
39	BHLHE40	chr12:33741030-33741823	K562	blood:	n/a	n/a
40	BHLHE40	chr12:33592354-33592978	K562	blood:	n/a	n/a
41	BHLHE40	chr12:33867451-33867477	K562	blood:	n/a	n/a
42	BHLHE40	chr12:33759769-33760039	K562	blood:	n/a	n/a
43	BHLHE40	chr12:33734583-33735390	GM12878	blood:	n/a	n/a
44	BHLHE40	chr12:33806387-33806560	K562	blood:	n/a	n/a
45	BHLHE40	chr12:33741303-33741660	GM12878	blood:	n/a	n/a
46	BRCA1	chr12:34046005-34046050	Hela-S3	cervix:	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	CBX3	chr12:33715396-33715617	K562	blood:	n/a	n/a
50	CBX3	chr12:33740710-33741670	K562	blood:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:33590837-33590887	SKMC	muscle:	n/a
2	chr12:33590837-33590887	SKMC	muscle:	n/a
3	chr12:33593913-33593963	GM12878	blood:	n/a
4	chr12:34061681-34061731	HL-60	blood:	n/a
5	chr12:33591336-33591386	NH-A	brain:	n/a
6	chr12:34001319-34001369	ECC-1	luminal epithelium:	n/a
7	chr12:33592078-33592128	ovcar-3	ovarian:	n/a
8	chr12:33593913-33593963	PANC-1	pancreas:	n/a
9	chr12:33593913-33593963	SAEC	small airway:	n/a
10	chr12:33595118-33595168	Jurkat	blood:	n/a
11	chr12:33593004-33593054	ProgFib	skin:	n/a
12	chr12:33593049-33593099	A549	lung:	n/a
13	chr12:34001319-34001369	HRCEpiC	kidney:	n/a
14	chr12:33593177-33593227	HL-60	blood:	n/a
15	chr12:33592078-33592128	ECC-1	luminal epithelium:	n/a
16	chr12:33591336-33591386	HEK293	kidney:	embryo
17	chr12:34061681-34061731	HIPEpiC	eye:	n/a
18	chr12:33591336-33591386	CMK	blood:	n/a
19	chr12:33593049-33593099	HEEpiC	esophagus:	n/a
20	chr12:34061681-34061731	CMK	blood:	n/a
21	chr12:33591899-33591949	Caco-2	colon:	n/a
22	chr12:33593913-33593963	HEEpiC	esophagus:	n/a
23	chr12:33593177-33593227	U87	brain:	n/a
24	chr12:33595118-33595168	NB4	blood:	n/a
25	chr12:33592642-33592692	IMR90	lung:	fetal
26	chr12:33750494-33750544	AoSMC	blood vessel:	n/a
27	chr12:33750494-33750544	PANC-1	pancreas:	n/a
28	chr12:33592078-33592128	Hepatocyte	liver:	n/a
29	chr12:33592500-33592550	HepG2	liver:	n/a
30	chr12:33591899-33591949	AG10803	skin:	n/a
31	chr12:33593004-33593054	HUVEC	blood vessel:	n/a
32	chr12:33591505-33591555	IMR90	lung:	fetal
33	chr12:33595118-33595168	AG04450	lung:	fetal
34	chr12:33591336-33591386	T-47D	breast:	n/a
35	chr12:33591336-33591386	HAEpiC	amniotic membrane:	n/a
36	chr12:33592285-33592335	AG09309	skin:	n/a
37	chr12:33595118-33595168	HPAEpiC	pulmonary alveolar:	n/a
38	chr12:34061681-34061731	SAEC	small airway:	n/a
39	chr12:33750494-33750544	MCF-7	breast:	n/a
40	chr12:33592078-33592128	Jurkat	blood:	n/a
41	chr12:33593913-33593963	PrEC	prostate:	n/a
42	chr12:33787337-33787387	T-47D	breast:	n/a
43	chr12:34061681-34061731	AG04450	lung:	fetal
44	chr12:33593049-33593099	SK-N-SH	brain:	n/a
45	chr12:33593177-33593227	LNCaP	prostate:	n/a
46	chr12:33593913-33593963	T-47D	breast:	n/a
47	chr12:33591336-33591386	ProgFib	skin:	n/a
48	chr12:33593049-33593099	SK-N-SH_RA	brain:	n/a
49	chr12:33589594-33589644	AG04450	lung:	fetal
50	chr12:33750494-33750544	HEK293	kidney:	embryo

(count:218 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr12:33680785..33683680-chr12:33685838..33687484,3	MCF-7	breast:
2	chr12:33762584..33764416-chr12:33765590..33768500,2	MCF-7	breast:
3	chr12:33737757..33739747-chr12:33741389..33743027,2	MCF-7	breast:
4	chr12:33571037..33573922-chr12:33575969..33577746,2	MCF-7	breast:
5	chr12:33737682..33739227-chr12:33743519..33746177,2	K562	blood:
6	chr12:33581348..33583914-chr12:33584659..33586358,3	MCF-7	breast:
7	chr12:34053367..34054987-chr12:34055066..34057564,2	MCF-7	breast:
8	chr12:33615181..33617280-chr12:33622628..33625177,2	MCF-7	breast:
9	chr12:33762278..33765239-chr12:33769487..33771063,2	K562	blood:
10	chr12:33757088..33759339-chr12:33761312..33763614,2	K562	blood:
11	chr12:33753748..33755380-chr12:33758835..33761146,2	K562	blood:
12	chr12:33590728..33593622-chr12:33761421..33764471,4	MCF-7	breast:
13	chr12:33984638..33987420-chr12:33995374..33998517,3	MCF-7	breast:
14	chr12:33737757..33739747-chr12:33741389..33743027,2	MCF-7	breast:
15	chr12:33749299..33751532-chr12:33760036..33763741,3	MCF-7	breast:
16	chr12:33903835..33905859-chr12:33907919..33910698,2	MCF-7	breast:
17	chr12:33749840..33752814-chr12:33754848..33757190,2	K562	blood:
18	chr12:34009182..34012663-chr12:34013902..34015537,3	MCF-7	breast:
19	chr12:33575316..33578004-chr12:33579015..33581251,4	MCF-7	breast:
20	chr12:33673191..33674096-chr7:136092701..136093461,2	MCF-7	breast:
21	chr12:33571037..33573922-chr12:33575969..33577746,2	MCF-7	breast:
22	chr12:33740590..33741231-chr12:33762284..33763123,2	MCF-7	breast:
23	chr12:33807598..33810256-chr12:33811118..33813511,2	K562	blood:
24	chr12:33758071..33760342-chr12:33762792..33765785,2	MCF-7	breast:
25	chr12:33749943..33752525-chr12:33753325..33754973,2	MCF-7	breast:
26	chr12:33589747..33593267-chr12:33745774..33749514,5	MCF-7	breast:
27	chr12:33700293..33703250-chr12:33739121..33741427,2	K562	blood:
28	chr12:33586288..33588588-chr12:33738098..33741571,3	MCF-7	breast:
29	chr12:33851368..33853439-chr12:33854297..33856163,2	K562	blood:
30	chr12:33749840..33752814-chr12:33754848..33757190,2	K562	blood:
31	chr12:33734204..33736505-chr12:33740513..33742206,2	K562	blood:
32	chr12:33570058..33573036-chr12:33573431..33575463,2	MCF-7	breast:
33	chr12:33740467..33741676-chr12:33762290..33763074,5	MCF-7	breast:
34	chr12:33590911..33594784-chr12:33761182..33765828,4	MCF-7	breast:
35	chr12:34053367..34054987-chr12:34055066..34057564,2	MCF-7	breast:
36	chr12:33680785..33683680-chr12:33685838..33687484,3	MCF-7	breast:
37	chr12:34017264..34017766-chr13:48856661..48857204,2	MCF-7	breast:
38	chr12:33741049..33744622-chr12:33756451..33760061,5	MCF-7	breast:
39	chr12:33585883..33590144-chr12:33590166..33593632,7	K562	blood:
40	chr12:33990071..33993034-chr8:42750325..42752539,2	MCF-7	breast:
41	chr12:33636131..33639117-chr12:33639347..33641138,2	MCF-7	breast:
42	chr12:33601580..33602442-chr12:33758672..33759329,2	MCF-7	breast:
43	chr12:33807598..33810256-chr12:33811118..33813511,2	K562	blood:
44	chr12:33730883..33732707-chr12:33745155..33746710,2	MCF-7	breast:
45	chr12:33590760..33594067-chr12:33739942..33743332,4	K562	blood:
46	chr12:33762584..33764416-chr12:33765590..33768500,2	MCF-7	breast:
47	chr12:33983313..33984854-chr12:33986265..33988102,2	MCF-7	breast:
48	chr12:33785580..33788231-chr12:33795540..33797279,2	MCF-7	breast:
49	chr12:33590905..33594094-chr12:33596140..33600356,5	MCF-7	breast:
50	chr12:33817225..33819690-chr12:33823230..33824769,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PKP2-2	chr12:33560733-33561253	NONHSAT027643
2	lnc-PKP2-1	chr12:33557810-33558831	ENSG00000259937.1
3	lnc-ALG10-6	chr12:33870788-33871152	NONHSAT027645
4	lnc-PKP2-2	chr12:33579073-33579095	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
ENSG00000266044	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000139131	chromatin interactions
ENSG00000110975	chromatin interactions
ENSG00000212475	chromatin interactions
ENSG00000131931	chromatin interactions
ENSG00000168172	chromatin interactions
ENSG00000171148	chromatin interactions
ENSG00000006327	chromatin interactions
ENSG00000184697	chromatin interactions
ENSG00000120925	chromatin interactions
ENSG00000250151	chromatin interactions
ENSG00000241553	chromatin interactions

Extended variants
information (count: 8439 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:8439 , 50 per page) page: 1 2 3 4 5 6 7 ... 169

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528786840	chr12:33542616-33542617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548455873	chr12:33542661-33542662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568380914	chr12:33542684-33542685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530956085	chr12:33542747-33542748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184658878	chr12:33542851-33542852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187931086	chr12:33542903-33542904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539540662	chr12:33542932-33542933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11832934	chr12:33543018-33543019	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs77279125	chr12:33543020-33543021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12301124	chr12:33543024-33543025	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs554928405	chr12:33543087-33543088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73312108	chr12:33543092-33543093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs577135268	chr12:33543094-33543095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs74947066	chr12:33543122-33543123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs60642772	chr12:33543146-33543147	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs576919021	chr12:33543194-33543195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79237616	chr12:33543208-33543209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs1905416	chr12:33543220-33543221	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs528676483	chr12:33543233-33543234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541990201	chr12:33543238-33543239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376400038	chr12:33543245-33543246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560980420	chr12:33543340-33543341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562045728	chr12:33543361-33543362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs73312113	chr12:33543367-33543368	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs148664679	chr12:33543369-33543370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550991523	chr12:33543391-33543392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562344222	chr12:33543403-33543404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570752295	chr12:33543456-33543457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183739177	chr12:33543487-33543488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547134131	chr12:33543490-33543491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201830382	chr12:33543500-33543501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566946255	chr12:33543501-33543502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs3046350	chr12:33543503-33543504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11052673	chr12:33543512-33543513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35751457	chr12:33543514-33543515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs397749399	chr12:33543515-33543516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189465207	chr12:33543539-33543540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568384353	chr12:33543550-33543551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536945426	chr12:33543556-33543557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1905415	chr12:33543560-33543561	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs576746788	chr12:33543593-33543594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141814457	chr12:33543600-33543601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537103871	chr12:33543621-33543622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539011463	chr12:33543658-33543659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552671618	chr12:33543659-33543660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192923179	chr12:33543730-33543731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12579354	chr12:33543853-33543854	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs560955139	chr12:33543860-33543861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185020894	chr12:33543864-33543865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371227266	chr12:33543865-33543866	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
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:807 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:33542600-33543000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr12:33543000-33544400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr12:33544400-33545400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr12:33566400-33575400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr12:33570400-33575800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:33574000-33576200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr12:33575400-33577600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr12:33575800-33578200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:33576200-33577400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr12:33577400-33580400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr12:33577600-33578400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr12:33578200-33588400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr12:33578400-33579200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr12:33579200-33590600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr12:33586800-33589800	Weak transcription	K562	blood
16	chr12:33588200-33588400	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr12:33588400-33590000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:33589800-33595600	Active TSS	K562	blood
19	chr12:33590000-33590600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr12:33590200-33591200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr12:33590400-33590600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
22	chr12:33590400-33590600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:33590600-33590800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
24	chr12:33590600-33591000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:33590600-33591200	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr12:33590600-33591200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
27	chr12:33590600-33592000	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:33590600-33593200	Active TSS	Brain Anterior Caudate	brain
29	chr12:33590600-33593400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
30	chr12:33590800-33591000	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
31	chr12:33590800-33591000	Bivalent/Poised TSS	Brain Germinal Matrix	brain
32	chr12:33590800-33591000	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
33	chr12:33590800-33591000	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
34	chr12:33590800-33591200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
35	chr12:33590800-33591400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
36	chr12:33590800-33591600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
37	chr12:33590800-33592000	Bivalent/Poised TSS	Right Atrium	heart
38	chr12:33591000-33591200	Bivalent Enhancer	Brain Angular Gyrus	brain
39	chr12:33591000-33591200	Bivalent Enhancer	Fetal Brain Male	brain
40	chr12:33591000-33591200	Bivalent Enhancer	Fetal Brain Female	brain
41	chr12:33591000-33591200	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
42	chr12:33591000-33591200	Bivalent/Poised TSS	Fetal Stomach	stomach
43	chr12:33591000-33591400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr12:33591000-33591400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
45	chr12:33591000-33591400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr12:33591000-33591400	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
47	chr12:33591000-33591400	Bivalent Enhancer	Right Ventricle	heart
48	chr12:33591000-33591600	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr12:33591000-33591600	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
50	chr12:33591000-33591600	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain

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