Variant report

Variant	nsv1053849
Chromosome Location	chr12:33132909-33279169
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:356)
CpG islands
(count:428)
Chromatin interactive
region (count:23)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:356 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:33136348-33136356	K562	blood:	n/a	n/a
2	ARID3A	chr12:33137036-33137211	K562	blood:	n/a	n/a
3	BHLHE40	chr12:33143419-33143471	GM12878	blood:	n/a	n/a
4	CEBPB	chr12:33246489-33246818	K562	blood:	n/a	chr12:33246665-33246676
5	CEBPB	chr12:33213290-33213498	A549	lung:	n/a	n/a
6	CEBPB	chr12:33246484-33246860	HepG2	liver:	n/a	chr12:33246665-33246676
7	CEBPB	chr12:33263976-33264050	K562	blood:	n/a	chr12:33264032-33264045 chr12:33264032-33264043
8	CEBPB	chr12:33246415-33246913	MCF-7	breast:	n/a	chr12:33246665-33246676
9	CEBPB	chr12:33246511-33246844	Hela-S3	cervix:	n/a	chr12:33246665-33246676
10	CEBPB	chr12:33263916-33264115	H1-hESC	embryonic stem cell:	n/a	chr12:33264032-33264045 chr12:33264032-33264043
11	CEBPB	chr12:33174198-33174503	MCF-7	breast:	n/a	n/a
12	CEBPB	chr12:33246498-33246848	H1-hESC	embryonic stem cell:	n/a	chr12:33246665-33246676
13	CEBPB	chr12:33190883-33190925	K562	blood:	n/a	n/a
14	CEBPB	chr12:33246481-33246856	A549	lung:	n/a	chr12:33246665-33246676
15	CEBPB	chr12:33137260-33137263	K562	blood:	n/a	n/a
16	CEBPB	chr12:33263978-33264116	HepG2	liver:	n/a	chr12:33264032-33264045 chr12:33264032-33264043
17	CEBPB	chr12:33246399-33247204	MCF-7	breast:	n/a	chr12:33246665-33246676
18	CEBPB	chr12:33194962-33195281	HepG2	liver:	n/a	chr12:33195131-33195142
19	CEBPB	chr12:33246481-33246858	IMR90	lung:	n/a	chr12:33246665-33246676
20	CEBPB	chr12:33263970-33264148	A549	lung:	n/a	chr12:33264032-33264045 chr12:33264032-33264043
21	CEBPB	chr12:33140531-33140731	K562	blood:	n/a	n/a
22	CEBPB	chr12:33269265-33269603	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPD	chr12:33136200-33136745	K562	blood:	n/a	n/a
24	CTCF	chr12:33227251-33227316	GM13976	blood:	n/a	n/a
25	CTCF	chr12:33277180-33277330	MCF-7	breast:	n/a	n/a
26	CTCF	chr12:33170099-33170185	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr12:33176980-33177130	Caco-2	colon:	n/a	n/a
28	CTCF	chr12:33245380-33245530	GM12864	blood:	n/a	n/a
29	CTCF	chr12:33261279-33261290	MCF-7	breast:	n/a	n/a
30	CTCF	chr12:33133540-33133690	NB4	blood:	n/a	n/a
31	CTCF	chr12:33261214-33261268	MCF-7	breast:	n/a	n/a
32	CTCF	chr12:33181550-33181621	Lung_OC	lung:	n/a	n/a
33	CTCF	chr12:33180400-33180550	GM06990	blood:	n/a	n/a
34	CTCF	chr12:33277060-33277210	NHEK	skin:	n/a	n/a
35	CTCF	chr12:33209053-33209109	GM13976	blood:	n/a	n/a
36	CTCF	chr12:33276980-33277130	MCF-7	breast:	n/a	n/a
37	CTCF	chr12:33133443-33133746	MCF-7	breast:	n/a	n/a
38	CTCF	chr12:33133548-33133671	MCF-7	breast:	n/a	n/a
39	CTCF	chr12:33261225-33261249	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:33197384-33197438	Fibrobl	skin:	n/a	n/a
41	CTCF	chr12:33133524-33133636	LNCaP	prostate:	n/a	n/a
42	CTCF	chr12:33277080-33277230	HRE	kidney:	n/a	n/a
43	CUX1	chr12:33136461-33136528	K562	blood:	n/a	n/a
44	E2F4	chr12:33142485-33142735	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr12:33273116-33273297	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr12:33276720-33276827	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr12:33181983-33182142	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr12:33213706-33213815	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr12:33132931-33133024	MCF10A-Er-Src	breast:	n/a	n/a
50	ELF1	chr12:33246605-33246952	MCF-7	breast:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:33139395-33139445	NH-A	brain:	n/a
2	chr12:33139395-33139445	NH-A	brain:	n/a
3	chr12:33205702-33205752	MCF10A-Er-Src	breast:	n/a
4	chr12:33139435-33139485	BE2_C	brain:	n/a
5	chr12:33139395-33139445	ProgFib	skin:	n/a
6	chr12:33205862-33205912	HCM	heart:	n/a
7	chr12:33205862-33205912	ProgFib	skin:	n/a
8	chr12:33205429-33205479	HRCEpiC	kidney:	n/a
9	chr12:33205429-33205479	HL-60	blood:	n/a
10	chr12:33176381-33176431	T-47D	breast:	n/a
11	chr12:33139395-33139445	SK-N-MC	brain:	n/a
12	chr12:33205862-33205912	SK-N-SH_RA	brain:	n/a
13	chr12:33139395-33139445	AG09309	skin:	n/a
14	chr12:33139395-33139445	PANC-1	pancreas:	n/a
15	chr12:33139395-33139445	HRE	kidney:	n/a
16	chr12:33139435-33139485	HCT-116	colon:	n/a
17	chr12:33205862-33205912	PFSK-1	brain:	n/a
18	chr12:33205814-33205864	Caco-2	colon:	n/a
19	chr12:33139395-33139445	K562	blood:	n/a
20	chr12:33205702-33205752	U87	brain:	n/a
21	chr12:33205429-33205479	AG04450	lung:	fetal
22	chr12:33176381-33176431	HRE	kidney:	n/a
23	chr12:33139435-33139485	H1-hESC	embryonic stem cell:	embryo
24	chr12:33176381-33176431	HIPEpiC	eye:	n/a
25	chr12:33205429-33205479	Hela-S3	cervix:	n/a
26	chr12:33205429-33205479	MCF-7	breast:	n/a
27	chr12:33139435-33139485	HL-60	blood:	n/a
28	chr12:33139395-33139445	HCT-116	colon:	n/a
29	chr12:33205429-33205479	RPTEC	kidney:	n/a
30	chr12:33205814-33205864	T-47D	breast:	n/a
31	chr12:33205702-33205752	AG10803	skin:	n/a
32	chr12:33205702-33205752	Hepatocyte	liver:	n/a
33	chr12:33205814-33205864	ovcar-3	ovarian:	n/a
34	chr12:33205862-33205912	HepG2	liver:	n/a
35	chr12:33176381-33176431	GM19239	blood:	n/a
36	chr12:33139435-33139485	GM12891	blood:	n/a
37	chr12:33205814-33205864	Jurkat	blood:	n/a
38	chr12:33139435-33139485	HCM	heart:	n/a
39	chr12:33139395-33139445	T-47D	breast:	n/a
40	chr12:33139435-33139485	AG04450	lung:	fetal
41	chr12:33176381-33176431	PFSK-1	brain:	n/a
42	chr12:33205862-33205912	AG10803	skin:	n/a
43	chr12:33205702-33205752	HMEC	breast:	n/a
44	chr12:33205702-33205752	HCM	heart:	n/a
45	chr12:33176381-33176431	SKMC	muscle:	n/a
46	chr12:33205814-33205864	HepG2	liver:	n/a
47	chr12:33139395-33139445	BJ	skin:	n/a
48	chr12:33205429-33205479	T-47D	breast:	n/a
49	chr12:33139435-33139485	MCF-7	breast:	n/a
50	chr12:33176381-33176431	Hepatocyte	liver:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:33179128..33181931-chr12:33189282..33192289,3	MCF-7	breast:
2	chr12:33233492..33236424-chr12:33237163..33238890,2	MCF-7	breast:
3	chr12:33275813..33277341-chr12:33279661..33282309,2	K562	blood:
4	chr12:33233492..33236424-chr12:33237163..33238890,2	MCF-7	breast:
5	chr12:33245520..33247527-chr12:33268044..33270867,2	MCF-7	breast:
6	chr12:33166950..33169241-chr12:33179153..33181275,2	MCF-7	breast:
7	chr12:33134639..33136187-chr12:45734034..45735761,2	MCF-7	breast:
8	chr12:33097948..33099540-chr12:33236195..33238566,2	MCF-7	breast:
9	chr12:32908039..32910424-chr12:33136172..33137819,2	MCF-7	breast:
10	chr12:33132215..33134574-chr12:33135484..33138415,2	MCF-7	breast:
11	chr12:33267275..33267984-chr12:33276076..33276722,2	MCF-7	breast:
12	chr12:33189309..33192081-chr12:33194448..33196554,2	MCF-7	breast:
13	chr12:33267275..33267984-chr12:33276076..33276722,2	MCF-7	breast:
14	chr12:33126654..33128516-chr12:33135468..33137723,3	K562	blood:
15	chr12:33245520..33247527-chr12:33268044..33270867,2	MCF-7	breast:
16	chr12:33179128..33181931-chr12:33189282..33192289,3	MCF-7	breast:
17	chr12:33121116..33123367-chr12:33136089..33138096,2	MCF-7	breast:
18	chr12:33126037..33128154-chr12:33135286..33137644,2	K562	blood:
19	chr12:33166950..33169241-chr12:33179153..33181275,2	MCF-7	breast:
20	chr12:33137708..33139764-chr12:33142209..33143776,2	MCF-7	breast:
21	chr12:32907923..32910854-chr12:33249270..33250898,2	K562	blood:
22	chr12:33132215..33134574-chr12:33135484..33138415,2	MCF-7	breast:
23	chr12:33276474..33280086-chr12:33280622..33283450,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DNM1L-1	chr12:33146498-33146688	ENSG00000257435
2	lnc-DNM1L-1	chr12:33141697-33141825	ENSG00000257435

No data

Variant related genes	Relation type
ENSG00000257435	TF binding region
ENSG00000257316	TF binding region
ENSG00000238911	TF binding region
ENSG00000257435	CpG island
ENSG00000257316	CpG island
ENSG00000238911	CpG island
ENSG00000257316	chromatin interactions
ENSG00000139131	chromatin interactions
ENSG00000238911	chromatin interactions

Extended variants
information (count: 3557 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3557 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545365274	chr12:33132916-33132917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs565106747	chr12:33132922-33132923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527533873	chr12:33132945-33132946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188869756	chr12:33132995-33132996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541119706	chr12:33133032-33133033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs78752237	chr12:33133065-33133066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs59635494	chr12:33133078-33133079	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs148503414	chr12:33133138-33133139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375177712	chr12:33133229-33133230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs142878170	chr12:33133253-33133254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs151054962	chr12:33133276-33133277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551667696	chr12:33133318-33133319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571112659	chr12:33133479-33133480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537981262	chr12:33133482-33133483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547174382	chr12:33133486-33133487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567412087	chr12:33133495-33133496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536827007	chr12:33133498-33133499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556824597	chr12:33133511-33133512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549839424	chr12:33133576-33133577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181317535	chr12:33133652-33133653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538928891	chr12:33133705-33133706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559206971	chr12:33133724-33133725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560510469	chr12:33133733-33133734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368281445	chr12:33133749-33133750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185451484	chr12:33133794-33133795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs142169072	chr12:33133808-33133809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs74074827	chr12:33133846-33133847	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs189915693	chr12:33133870-33133871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs73092701	chr12:33133916-33133917	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs554092411	chr12:33133920-33133921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147822338	chr12:33134029-33134030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375211842	chr12:33134088-33134089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs117378789	chr12:33134100-33134101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544931657	chr12:33134229-33134230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs151098215	chr12:33134253-33134254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372336707	chr12:33134256-33134257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565232522	chr12:33134263-33134264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77757076	chr12:33134264-33134265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141491734	chr12:33134286-33134287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113742235	chr12:33134312-33134313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12230305	chr12:33134334-33134335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182884394	chr12:33134357-33134358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74074828	chr12:33134383-33134384	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs114642601	chr12:33134391-33134392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539268244	chr12:33134437-33134438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558977590	chr12:33134457-33134458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566396084	chr12:33134477-33134478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12827499	chr12:33134582-33134583	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs369936953	chr12:33134643-33134644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs137944093	chr12:33134654-33134655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
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	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21272361	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD
Alcoholism	22295116	CNVD
Intellectual disability	22045946	CNVD
Alcoholism	21790672	CNVD

Chromatin state (count:304 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:33131600-33136200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr12:33135200-33135600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr12:33135600-33135800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr12:33135800-33136200	Enhancers	K562	blood
5	chr12:33135800-33137000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr12:33136200-33136600	Flanking Active TSS	K562	blood
7	chr12:33136200-33137000	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr12:33136400-33137000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr12:33136400-33137000	Enhancers	Placenta Amnion	Placenta Amnion
10	chr12:33136400-33137200	Enhancers	Placenta	Placenta
11	chr12:33136600-33137600	Enhancers	K562	blood
12	chr12:33136800-33138800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr12:33137000-33141600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr12:33137000-33142200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr12:33137200-33141400	Weak transcription	Placenta	Placenta
16	chr12:33137200-33141600	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr12:33140200-33140400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr12:33140400-33140600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr12:33140400-33140600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:33140400-33144400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr12:33140600-33140800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr12:33140600-33140800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr12:33140600-33142000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:33140600-33164800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr12:33140800-33142000	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr12:33140800-33142200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr12:33141400-33141600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:33141400-33142200	Enhancers	Placenta	Placenta
29	chr12:33141600-33142400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr12:33141600-33142800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr12:33141600-33142800	Enhancers	Hela-S3	cervix
32	chr12:33141600-33143000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr12:33141600-33143200	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr12:33141600-33143800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr12:33141600-33147200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr12:33141800-33142200	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr12:33141800-33143600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr12:33142000-33143000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr12:33142000-33143000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr12:33142000-33143200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr12:33142000-33143200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr12:33142000-33143600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr12:33142000-33144400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr12:33142200-33143400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr12:33142200-33143400	Weak transcription	Placenta	Placenta
46	chr12:33142200-33144200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr12:33142400-33142800	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr12:33142800-33143000	Enhancers	H1 Cell Line	embryonic stem cell
49	chr12:33142800-33143000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr12:33142800-33144600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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