Variant report

Variant	nsv541470
Chromosome Location	chr12:33797560-34078208
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:594)
CpG islands
(count:122)
Chromatin interactive
region (count:53)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	chr12:33831095-33831857	K562	blood:	n/a	n/a
3	ARID3A	chr12:33806348-33806595	K562	blood:	n/a	n/a
4	ARID3A	chr12:33807257-33807627	K562	blood:	n/a	n/a
5	ATF1	chr12:33807257-33807582	K562	blood:	n/a	n/a
6	ATF1	chr12:33837952-33838076	K562	blood:	n/a	n/a
7	ATF1	chr12:33918231-33918238	K562	blood:	n/a	n/a
8	ATF1	chr12:33905799-33906217	K562	blood:	n/a	n/a
9	ATF3	chr12:33806344-33806588	K562	blood:	n/a	n/a
10	BACH1	chr12:33807354-33807505	K562	blood:	n/a	n/a
11	BACH1	chr12:33812366-33812495	K562	blood:	n/a	n/a
12	BACH1	chr12:33905912-33906117	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr12:33847319-33847363	K562	blood:	n/a	n/a
14	BACH1	chr12:33854735-33854758	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr12:33802958-33803315	H1-hESC	embryonic stem cell:	n/a	chr12:33803028-33803037
16	BHLHE40	chr12:33905773-33906139	K562	blood:	n/a	n/a
17	BHLHE40	chr12:33867451-33867477	K562	blood:	n/a	n/a
18	BHLHE40	chr12:33806387-33806560	K562	blood:	n/a	n/a
19	BRCA1	chr12:34046005-34046050	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr12:33803718-33804191	K562	blood:	n/a	n/a
21	CBX3	chr12:33803725-33804117	K562	blood:	n/a	n/a
22	CBX3	chr12:33905727-33906205	K562	blood:	n/a	n/a
23	CEBPB	chr12:33859895-33860215	IMR90	lung:	n/a	n/a
24	CEBPB	chr12:33985877-33986165	H1-hESC	embryonic stem cell:	n/a	chr12:33986016-33986029 chr12:33986016-33986027 chr12:33986018-33986029
25	CEBPB	chr12:34035659-34035858	HepG2	liver:	n/a	n/a
26	CEBPB	chr12:34017562-34017665	A549	lung:	n/a	chr12:34017650-34017661
27	CEBPB	chr12:34035643-34035942	A549	lung:	n/a	n/a
28	CEBPB	chr12:33884502-33884721	HepG2	liver:	n/a	chr12:33884579-33884590
29	CEBPB	chr12:34075788-34076026	A549	lung:	n/a	chr12:34075905-34075916
30	CEBPB	chr12:34045415-34045716	H1-hESC	embryonic stem cell:	n/a	chr12:34045544-34045555
31	CEBPB	chr12:34017618-34017682	HepG2	liver:	n/a	chr12:34017650-34017661
32	CEBPB	chr12:34045370-34045733	IMR90	lung:	n/a	chr12:34045544-34045555
33	CEBPB	chr12:34045415-34045710	K562	blood:	n/a	chr12:34045544-34045555
34	CEBPB	chr12:33821454-33821714	HepG2	liver:	n/a	chr12:33821568-33821579
35	CEBPB	chr12:33805881-33806093	K562	blood:	n/a	n/a
36	CEBPB	chr12:33884519-33884734	IMR90	lung:	n/a	chr12:33884579-33884590
37	CEBPB	chr12:33939535-33939880	HepG2	liver:	n/a	chr12:33939709-33939720
38	CEBPB	chr12:33874543-33874787	Hela-S3	cervix:	n/a	chr12:33874667-33874676
39	CEBPB	chr12:34075757-34076029	HepG2	liver:	n/a	chr12:34075905-34075916
40	CEBPB	chr12:33859890-33860233	HepG2	liver:	n/a	n/a
41	CEBPB	chr12:33884520-33884677	K562	blood:	n/a	chr12:33884579-33884590
42	CEBPB	chr12:33901844-33902079	IMR90	lung:	n/a	n/a
43	CEBPB	chr12:33985858-33986203	K562	blood:	n/a	chr12:33986016-33986029 chr12:33986016-33986027 chr12:33986018-33986029
44	CEBPB	chr12:33843303-33843542	HepG2	liver:	n/a	chr12:33843373-33843384
45	CEBPB	chr12:33911471-33911677	HepG2	liver:	n/a	chr12:33911549-33911560 chr12:33911547-33911560 chr12:33911547-33911558 chr12:33911547-33911560
46	CEBPB	chr12:33802974-33803262	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr12:33869924-33870124	HepG2	liver:	n/a	chr12:33869980-33869991
48	CEBPB	chr12:33985871-33986186	A549	lung:	n/a	chr12:33986016-33986029 chr12:33986016-33986027 chr12:33986018-33986029
49	CEBPB	chr12:34045411-34045695	A549	lung:	n/a	chr12:34045544-34045555
50	CEBPB	chr12:34063911-34064203	HepG2	liver:	n/a	chr12:34064049-34064060

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:34061681-34061731	HL-60	blood:	n/a
2	chr12:34061681-34061731	SKMC	muscle:	n/a
3	chr12:34001319-34001369	AG04450	lung:	fetal
4	chr12:34001319-34001369	BJ	skin:	n/a
5	chr12:34061681-34061731	H1-hESC	embryonic stem cell:	embryo
6	chr12:34001319-34001369	HIPEpiC	eye:	n/a
7	chr12:34061681-34061731	K562	blood:	n/a
8	chr12:34001319-34001369	HCF	heart:	n/a
9	chr12:34001319-34001369	H1-hESC	embryonic stem cell:	embryo
10	chr12:34001319-34001369	HEK293	kidney:	embryo
11	chr12:34061681-34061731	AG04449	skin:	fetal
12	chr12:34061681-34061731	Hela-S3	cervix:	n/a
13	chr12:34001319-34001369	HMEC	breast:	n/a
14	chr12:34061681-34061731	Caco-2	colon:	n/a
15	chr12:34061681-34061731	HCM	heart:	n/a
16	chr12:34001319-34001369	MCF-7	breast:	n/a
17	chr12:34061681-34061731	GM12878	blood:	n/a
18	chr12:34001319-34001369	HNPCEpiC	eye:	n/a
19	chr12:34001319-34001369	HUVEC	blood vessel:	n/a
20	chr12:34061681-34061731	Hepatocyte	liver:	n/a
21	chr12:34061681-34061731	ovcar-3	ovarian:	n/a
22	chr12:34061681-34061731	LNCaP	prostate:	n/a
23	chr12:34001319-34001369	PFSK-1	brain:	n/a
24	chr12:34061681-34061731	HRE	kidney:	n/a
25	chr12:34001319-34001369	PrEC	prostate:	n/a
26	chr12:34061681-34061731	NHDF-neo	bronchial:	n/a
27	chr12:34001319-34001369	NB4	blood:	n/a
28	chr12:34061681-34061731	Jurkat	blood:	n/a
29	chr12:34001319-34001369	MCF10A-Er-Src	breast:	n/a
30	chr12:34001319-34001369	ProgFib	skin:	n/a
31	chr12:34061681-34061731	RPTEC	kidney:	n/a
32	chr12:34001319-34001369	K562	blood:	n/a
33	chr12:34061681-34061731	NH-A	brain:	n/a
34	chr12:34001319-34001369	AG04449	skin:	fetal
35	chr12:34061681-34061731	HCF	heart:	n/a
36	chr12:34001319-34001369	NHDF-neo	bronchial:	n/a
37	chr12:34061681-34061731	GM06990	blood:	n/a
38	chr12:34061681-34061731	PFSK-1	brain:	n/a
39	chr12:34061681-34061731	HepG2	liver:	n/a
40	chr12:34001319-34001369	GM19239	blood:	n/a
41	chr12:34001319-34001369	HRE	kidney:	n/a
42	chr12:34061681-34061731	GM19239	blood:	n/a
43	chr12:34061681-34061731	NT2-D1	testis:	n/a
44	chr12:34061681-34061731	GM12892	blood:	n/a
45	chr12:34061681-34061731	HIPEpiC	eye:	n/a
46	chr12:34001319-34001369	HPAEpiC	pulmonary alveolar:	n/a
47	chr12:34001319-34001369	SK-N-SH	brain:	n/a
48	chr12:34061681-34061731	GM12891	blood:	n/a
49	chr12:34001319-34001369	AoSMC	blood vessel:	n/a
50	chr12:34001319-34001369	GM06990	blood:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:33799617..33801183-chr8:42749699..42752602,2	MCF-7	breast:
2	chr12:33817225..33819690-chr12:33823230..33824769,2	MCF-7	breast:
3	chr12:33807598..33810256-chr12:33811118..33813511,2	K562	blood:
4	chr12:33817225..33819690-chr12:33823230..33824769,2	MCF-7	breast:
5	chr12:33984638..33987420-chr12:33995374..33998517,3	MCF-7	breast:
6	chr12:33916761..33918446-chr16:3069457..3072448,2	MCF-7	breast:
7	chr12:33831200..33833987-chr12:33837460..33839264,2	K562	blood:
8	chr12:33983313..33984854-chr12:33986265..33988102,2	MCF-7	breast:
9	chr12:33851368..33853439-chr12:33854297..33856163,2	K562	blood:
10	chr12:33828843..33831342-chr12:33831748..33833892,2	MCF-7	breast:
11	chr12:33851368..33853439-chr12:33854297..33856163,2	K562	blood:
12	chr12:33796695..33799615-chr12:33802612..33805057,2	K562	blood:
13	chr12:33830515..33832081-chr12:33832328..33834300,2	K562	blood:
14	chr12:33815236..33817568-chr12:33820316..33823181,2	K562	blood:
15	chr12:33828843..33831342-chr12:33831748..33833892,2	MCF-7	breast:
16	chr12:34053367..34054987-chr12:34055066..34057564,2	MCF-7	breast:
17	chr12:34009182..34012663-chr12:34013902..34015537,3	MCF-7	breast:
18	chr12:33801659..33804071-chr3:9833585..9835951,2	MCF-7	breast:
19	chr12:33795537..33797751-chr12:33801352..33803205,2	MCF-7	breast:
20	chr12:33831200..33833987-chr12:33837460..33839264,2	K562	blood:
21	chr12:33903835..33905859-chr12:33907919..33910698,2	MCF-7	breast:
22	chr12:33809313..33810966-chr12:33832220..33835115,2	K562	blood:
23	chr12:33984638..33987420-chr12:33995374..33998517,3	MCF-7	breast:
24	chr12:33796695..33799615-chr12:33802612..33805057,2	K562	blood:
25	chr12:33934409..33936900-chr12:33939410..33941605,3	K562	blood:
26	chr12:33807598..33810256-chr12:33811118..33813511,2	K562	blood:
27	chr12:33977547..33980480-chr12:33992605..33994282,2	K562	blood:
28	chr12:33809313..33810966-chr12:33832220..33835115,2	K562	blood:
29	chr12:33587036..33589098-chr12:33993044..33994546,2	MCF-7	breast:
30	chr12:33795771..33798343-chr12:33800787..33802349,2	K562	blood:
31	chr12:33983313..33984854-chr12:33986265..33988102,2	MCF-7	breast:
32	chr12:34009182..34012663-chr12:34013902..34015537,3	MCF-7	breast:
33	chr12:33975803..33979098-chr12:33979674..33983619,4	MCF-7	breast:
34	chr12:33795537..33797751-chr12:33801352..33803205,2	MCF-7	breast:
35	chr12:33829191..33832015-chr12:33832800..33835417,2	K562	blood:
36	chr12:33975803..33979098-chr12:33979674..33983619,4	MCF-7	breast:
37	chr12:33977547..33980480-chr12:33992605..33994282,2	K562	blood:
38	chr12:33901002..33902516-chr12:33905016..33907291,2	MCF-7	breast:
39	chr12:33990071..33993034-chr8:42750325..42752539,2	MCF-7	breast:
40	chr12:33795771..33798343-chr12:33800787..33802349,2	K562	blood:
41	chr12:33901002..33902516-chr12:33905016..33907291,2	MCF-7	breast:
42	chr12:33828756..33830899-chr12:33837528..33839909,2	MCF-7	breast:
43	chr12:33830515..33832081-chr12:33832328..33834300,2	K562	blood:
44	chr12:34008981..34009786-chr2:33211553..33212456,2	MCF-7	breast:
45	chr12:33815236..33817568-chr12:33820316..33823181,2	K562	blood:
46	chr12:33828756..33830899-chr12:33837528..33839909,2	MCF-7	breast:
47	chr12:34053367..34054987-chr12:34055066..34057564,2	MCF-7	breast:
48	chr12:34017264..34017766-chr13:48856661..48857204,2	MCF-7	breast:
49	chr12:33758791..33761325-chr12:33805781..33808679,2	K562	blood:
50	chr12:33825675..33828123-chr8:42750828..42752625,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALG10-6	chr12:33870788-33871152	NONHSAT027645

No data

Variant related genes	Relation type
ENSG00000270807	TF binding region
RNU6-472P	TF binding region
ENSG00000270807	CpG island
RNU6-472P	CpG island
ENSG00000171148	chromatin interactions
ENSG00000250151	chromatin interactions
ENSG00000168172	chromatin interactions
ENSG00000266044	chromatin interactions
ENSG00000006327	chromatin interactions
ENSG00000241553	chromatin interactions
ENSG00000184697	chromatin interactions
ENSG00000120925	chromatin interactions

Extended variants
information (count: 3074 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:3074 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533569059	chr12:33797598-33797599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553763809	chr12:33797635-33797636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113532221	chr12:33797641-33797642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372182587	chr12:33797652-33797653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372921753	chr12:33797721-33797722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543350711	chr12:33797734-33797735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113347658	chr12:33797739-33797740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576235722	chr12:33797877-33797878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116699861	chr12:33797882-33797883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565057008	chr12:33797896-33797897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148217011	chr12:33797906-33797907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541046395	chr12:33797913-33797914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs141970246	chr12:33797944-33797945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76884455	chr12:33798001-33798002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542942234	chr12:33798082-33798083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs16921189	chr12:33798101-33798102	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs186807756	chr12:33798107-33798108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531558415	chr12:33798118-33798119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs16921193	chr12:33798136-33798137	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs12829254	chr12:33798144-33798145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571348051	chr12:33798148-33798149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs71459511	chr12:33798154-33798155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533915152	chr12:33798257-33798258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150654412	chr12:33798318-33798319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190009934	chr12:33798371-33798372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11052815	chr12:33798546-33798547	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs182644126	chr12:33798551-33798552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375902503	chr12:33798559-33798560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs61932719	chr12:33798592-33798593	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs545185128	chr12:33798605-33798606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558756449	chr12:33798621-33798622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572446835	chr12:33798622-33798623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551471026	chr12:33798688-33798689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187249532	chr12:33798712-33798713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561087591	chr12:33798798-33798799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533751887	chr12:33798815-33798816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555738400	chr12:33798842-33798843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542529705	chr12:33798945-33798946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs17640757	chr12:33798989-33798990	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs141030486	chr12:33799055-33799056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551579003	chr12:33799088-33799089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192943084	chr12:33799140-33799141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556094455	chr12:33799144-33799145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577732116	chr12:33799170-33799171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527384211	chr12:33799175-33799176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547477166	chr12:33799186-33799187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374825263	chr12:33799256-33799257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143279858	chr12:33799263-33799264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185497031	chr12:33799310-33799311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs202193769	chr12:33799311-33799312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Tetralogy of Fallot	22912587	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:172 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:33794400-33801200	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr12:33796000-33801400	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr12:33797400-33797600	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr12:33797400-33797600	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr12:33797400-33801600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr12:33801200-33802200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
7	chr12:33801400-33802200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
8	chr12:33801600-33801800	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
9	chr12:33801600-33805200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
10	chr12:33801800-33802600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr12:33802200-33802400	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr12:33802200-33803600	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr12:33802400-33802600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
14	chr12:33802400-33803000	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr12:33802600-33802800	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr12:33802600-33803000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr12:33802600-33803000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr12:33802800-33803000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
19	chr12:33802800-33803800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr12:33803000-33803600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr12:33803600-33805400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
22	chr12:33803800-33804000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
23	chr12:33803800-33805400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
24	chr12:33804000-33805400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr12:33804600-33805200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
26	chr12:33805400-33810400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr12:33807200-33807600	Enhancers	K562	blood
28	chr12:33810000-33811000	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr12:33810200-33810800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr12:33810400-33811000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr12:33811000-33814000	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr12:33811000-33815600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr12:33812800-33813000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr12:33812800-33813000	Enhancers	Duodenum Mucosa	Duodenum
35	chr12:33812800-33813000	Active TSS	Fetal Muscle Trunk	muscle
36	chr12:33812800-33813000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
37	chr12:33813000-33816600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr12:33814000-33814400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr12:33814000-33814600	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr12:33814000-33814600	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr12:33814000-33814800	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr12:33814000-33814800	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr12:33814200-33814400	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr12:33814200-33814600	Enhancers	H1 Cell Line	embryonic stem cell
45	chr12:33814600-33815800	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr12:33814600-33820800	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr12:33814600-33821400	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr12:33814800-33821000	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr12:33815600-33816000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr12:33815800-33816000	Enhancers	H1 Cell Line	embryonic stem cell

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