Variant report

Variant	nsv741
Chromosome Location	chr12:63038255-63064846
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:172)
CpG islands
(count:184)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:63047402-63047950	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr12:63047420-63047961	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr12:63053091-63053837	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr12:63044859-63045450	GM12878	blood:	n/a	n/a
5	ATF2	chr12:63053015-63053701	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr12:63044954-63045343	GM12878	blood:	n/a	chr12:63045180-63045189
7	BCL11A	chr12:63047505-63047835	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr12:63053189-63053425	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr12:63047511-63047850	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr12:63053116-63053944	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr12:63053150-63053633	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr12:63054449-63054961	IMR90	lung:	n/a	chr12:63054629-63054640 chr12:63054629-63054642 chr12:63054631-63054640
13	CEBPB	chr12:63054531-63054749	HepG2	liver:	n/a	chr12:63054629-63054640 chr12:63054629-63054642 chr12:63054631-63054640
14	CEBPB	chr12:63054489-63054781	A549	lung:	n/a	chr12:63054629-63054640 chr12:63054629-63054642 chr12:63054631-63054640
15	CHD1	chr12:63051910-63051930	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr12:63053131-63053695	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr12:63053083-63053696	H1-hESC	embryonic stem cell:	n/a	n/a
18	CREB1	chr12:63047355-63047966	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr12:63044843-63045260	GM12878	blood:	n/a	n/a
20	CREB1	chr12:63044766-63045405	GM12878	blood:	n/a	n/a
21	CTBP2	chr12:63052869-63053710	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr12:63049450-63050035	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTBP2	chr12:63047468-63048287	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr12:63039580-63039730	GM12864	blood:	n/a	n/a
25	CTCF	chr12:63050820-63050970	GM12872	blood:	n/a	n/a
26	E2F4	chr12:63041324-63041424	MCF10A-Er-Src	breast:	n/a	n/a
27	EBF1	chr12:63050888-63050914	GM12878	blood:	n/a	n/a
28	EGR1	chr12:63047374-63047865	H1-hESC	embryonic stem cell:	n/a	n/a
29	EGR1	chr12:63047407-63047867	H1-hESC	embryonic stem cell:	n/a	n/a
30	EP300	chr12:63053049-63053621	H1-hESC	embryonic stem cell:	n/a	chr12:63053391-63053405
31	EP300	chr12:63050870-63050904	GM12878	blood:	n/a	n/a
32	EP300	chr12:63053203-63053638	H1-hESC	embryonic stem cell:	n/a	chr12:63053391-63053405
33	EP300	chr12:63047492-63047901	H1-hESC	embryonic stem cell:	n/a	n/a
34	EP300	chr12:63047325-63048060	ECC-1	luminal epithelium:	n/a	n/a
35	EP300	chr12:63047361-63047965	H1-hESC	embryonic stem cell:	n/a	n/a
36	EP300	chr12:63061276-63061760	T-47D	breast:	n/a	n/a
37	FOS	chr12:63054530-63054882	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr12:63054543-63054868	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr12:63054540-63054913	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr12:63054511-63055101	HUVEC	blood vessel:	n/a	n/a
41	FOS	chr12:63054508-63054909	MCF10A-Er-Src	breast:	n/a	n/a
42	FOXA1	chr12:63061303-63061620	T-47D	breast:	n/a	n/a
43	FOXA1	chr12:63063180-63063373	T-47D	breast:	n/a	n/a
44	FOXA1	chr12:63063191-63063439	T-47D	breast:	n/a	n/a
45	FOXA2	chr12:63058077-63058508	A549	lung:	n/a	n/a
46	GATA2	chr12:63054581-63055036	HUVEC	blood vessel:	n/a	n/a
47	GATA3	chr12:63061282-63061686	T-47D	breast:	n/a	n/a
48	GATA3	chr12:63061320-63061699	T-47D	breast:	n/a	n/a
49	GTF2F1	chr12:63053305-63053672	H1-hESC	embryonic stem cell:	n/a	n/a
50	GTF2F1	chr12:63049843-63049906	H1-hESC	embryonic stem cell:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:63038420-63038470	NHBE	bronchial:	n/a
2	chr12:63038420-63038470	NHBE	bronchial:	n/a
3	chr12:63049980-63050030	H1-hESC	embryonic stem cell:	embryo
4	chr12:63039927-63039977	GM06990	blood:	n/a
5	chr12:63038420-63038470	HRCEpiC	kidney:	n/a
6	chr12:63039927-63039977	IMR90	lung:	fetal
7	chr12:63039927-63039977	ECC-1	luminal epithelium:	n/a
8	chr12:63049980-63050030	HEK293	kidney:	embryo
9	chr12:63039927-63039977	PFSK-1	brain:	n/a
10	chr12:63049980-63050030	HRCEpiC	kidney:	n/a
11	chr12:63049980-63050030	PANC-1	pancreas:	n/a
12	chr12:63049980-63050030	GM12892	blood:	n/a
13	chr12:63038420-63038470	AG04450	lung:	fetal
14	chr12:63038420-63038470	IMR90	lung:	fetal
15	chr12:63049980-63050030	Hepatocyte	liver:	n/a
16	chr12:63038420-63038470	HCF	heart:	n/a
17	chr12:63039927-63039977	HCPEpiC	choroid plexus:	n/a
18	chr12:63038420-63038470	SKMC	muscle:	n/a
19	chr12:63049980-63050030	Caco-2	colon:	n/a
20	chr12:63039927-63039977	GM19239	blood:	n/a
21	chr12:63038420-63038470	AG09309	skin:	n/a
22	chr12:63049980-63050030	RPTEC	kidney:	n/a
23	chr12:63038420-63038470	GM06990	blood:	n/a
24	chr12:63049980-63050030	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:63038420-63038470	SK-N-MC	brain:	n/a
26	chr12:63049980-63050030	ovcar-3	ovarian:	n/a
27	chr12:63038420-63038470	Caco-2	colon:	n/a
28	chr12:63049980-63050030	LNCaP	prostate:	n/a
29	chr12:63049980-63050030	AG09309	skin:	n/a
30	chr12:63049980-63050030	SKMC	muscle:	n/a
31	chr12:63039927-63039977	NH-A	brain:	n/a
32	chr12:63039927-63039977	SK-N-SH	brain:	n/a
33	chr12:63039927-63039977	HRCEpiC	kidney:	n/a
34	chr12:63039927-63039977	HEK293	kidney:	embryo
35	chr12:63038420-63038470	ovcar-3	ovarian:	n/a
36	chr12:63039927-63039977	HRE	kidney:	n/a
37	chr12:63038420-63038470	HCT-116	colon:	n/a
38	chr12:63049980-63050030	HCPEpiC	choroid plexus:	n/a
39	chr12:63049980-63050030	SK-N-MC	brain:	n/a
40	chr12:63038420-63038470	HCM	heart:	n/a
41	chr12:63039927-63039977	RPTEC	kidney:	n/a
42	chr12:63039927-63039977	PANC-1	pancreas:	n/a
43	chr12:63049980-63050030	HAEpiC	amniotic membrane:	n/a
44	chr12:63039927-63039977	HL-60	blood:	n/a
45	chr12:63039927-63039977	SK-N-SH_RA	brain:	n/a
46	chr12:63039927-63039977	SK-N-MC	brain:	n/a
47	chr12:63049980-63050030	HCM	heart:	n/a
48	chr12:63038420-63038470	HPAEpiC	pulmonary alveolar:	n/a
49	chr12:63038420-63038470	AG10803	skin:	n/a
50	chr12:63038420-63038470	GM19239	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:63060371..63062636-chr12:63063773..63065877,2	K562	blood:
2	chr12:63041505..63044112-chr12:63048353..63051271,2	K562	blood:
3	chr12:63034781..63036515-chr12:63038569..63040635,2	K562	blood:
4	chr12:63034717..63037649-chr12:63039194..63042442,3	MCF-7	breast:
5	chr12:63041505..63044112-chr12:63048353..63051271,2	K562	blood:
6	chr12:63034981..63038220-chr12:63040076..63042937,3	MCF-7	breast:
7	chr12:63045607..63047672-chr12:63047992..63050853,2	MCF-7	breast:
8	chr12:62994712..62998388-chr12:63040223..63045301,6	K562	blood:
9	chr12:62996652..62998554-chr12:63059242..63061234,2	MCF-7	breast:
10	chr12:63039398..63042181-chr12:63096184..63099134,2	MCF-7	breast:
11	chr12:63038732..63045047-chr12:63045521..63050769,8	MCF-7	breast:
12	chr12:63061475..63063114-chr12:63073758..63076546,2	MCF-7	breast:
13	chr12:63035839..63038546-chr12:63180946..63183735,2	MCF-7	breast:
14	chr12:63057019..63058905-chr12:63069466..63071487,2	MCF-7	breast:
15	chr12:62996374..62997985-chr12:63036259..63038918,2	MCF-7	breast:
16	chr12:62996006..62999301-chr12:63039821..63044054,4	MCF-7	breast:
17	chr12:63045607..63047672-chr12:63047992..63050853,2	MCF-7	breast:
18	chr12:63045714..63050618-chr12:63051733..63055030,6	MCF-7	breast:
19	chr12:63060371..63062636-chr12:63063773..63065877,2	K562	blood:
20	chr12:63033523..63036576-chr12:63048236..63051524,3	K562	blood:
21	chr12:63062986..63065767-chr12:63067965..63070685,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	PPM1H	hsa-miR-222-3p	chr12:63038265-63038285
2	PPM1H	hsa-miR-1	chr12:63041671-63041691
3	PPM1H	hsa-miR-125b-5p	chr12:63041793-63041787

Variant related genes	Relation type
RPL32P26	TF binding region
ENSG00000238475	TF binding region
RPL32P26	CpG island
ENSG00000238475	CpG island
ENSG00000238475	chromatin interactions
ENSG00000221949	chromatin interactions
ENSG00000241941	chromatin interactions
ENSG00000257354	chromatin interactions
ENSG00000111110	chromatin interactions
ENSG00000199179	chromatin interactions

Extended variants
information (count: 1168 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1168 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555416850	chr12:63038334-63038335	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs575490945	chr12:63038340-63038341	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs141527272	chr12:63038407-63038408	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs564269061	chr12:63038416-63038417	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs577830949	chr12:63038448-63038449	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs17098110	chr12:63038503-63038504	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs560265959	chr12:63038520-63038521	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs528928893	chr12:63038547-63038548	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs548988494	chr12:63038566-63038567	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs189824813	chr12:63038637-63038638	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs10877901	chr12:63038638-63038639	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs461461	chr12:63038646-63038647	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs574087490	chr12:63038650-63038651	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs558714588	chr12:63038696-63038697	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs3825305	chr12:63038698-63038699	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs150895751	chr12:63038709-63038710	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs534048461	chr12:63038751-63038752	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs61148406	chr12:63038765-63038766	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs539687735	chr12:63038794-63038795	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs112260231	chr12:63038795-63038796	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs568741180	chr12:63038815-63038816	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs181811531	chr12:63038817-63038818	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs74095836	chr12:63038844-63038845	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs77789187	chr12:63038874-63038875	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs573031654	chr12:63038879-63038880	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs575460751	chr12:63038888-63038889	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs538111989	chr12:63038889-63038890	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs557690788	chr12:63038920-63038921	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538485949	chr12:63038965-63038966	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577939259	chr12:63038987-63038988	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540410260	chr12:63039099-63039100	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530722045	chr12:63039129-63039130	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142327436	chr12:63039130-63039131	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542260101	chr12:63039153-63039154	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111609641	chr12:63039168-63039169	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs375565331	chr12:63039225-63039226	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573950275	chr12:63039269-63039270	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs145949867	chr12:63039308-63039309	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs111251534	chr12:63039352-63039353	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552022352	chr12:63039430-63039431	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550536828	chr12:63039447-63039448	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139860374	chr12:63039492-63039493	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527921424	chr12:63039506-63039507	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369907474	chr12:63039557-63039558	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184507362	chr12:63039583-63039584	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188460556	chr12:63039596-63039597	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181310000	chr12:63039601-63039602	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149704520	chr12:63039615-63039616	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570007558	chr12:63039639-63039640	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145512614	chr12:63039645-63039646	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Man infertility	21397064	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:568 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63026600-63049800	Weak transcription	Right Atrium	heart
2	chr12:63030000-63038400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr12:63030000-63040400	Weak transcription	Brain Hippocampus Middle	brain
4	chr12:63030000-63040800	Weak transcription	Brain Angular Gyrus	brain
5	chr12:63030400-63040200	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr12:63030400-63040600	Weak transcription	Brain Substantia Nigra	brain
7	chr12:63030400-63040800	Weak transcription	Brain Anterior Caudate	brain
8	chr12:63031600-63041000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr12:63031800-63040200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr12:63031800-63047000	Weak transcription	Liver	Liver
11	chr12:63032000-63038400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr12:63032000-63039000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:63034400-63041000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr12:63034400-63042000	Weak transcription	Gastric	stomach
15	chr12:63034400-63043200	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr12:63035000-63048000	Weak transcription	Primary hematopoietic stem cells	blood
17	chr12:63035200-63041400	Weak transcription	Adipose Nuclei	Adipose
18	chr12:63035200-63041400	Weak transcription	Osteobl	bone
19	chr12:63035200-63043200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr12:63035200-63048400	Weak transcription	Fetal Muscle Leg	muscle
21	chr12:63035200-63069800	Weak transcription	Left Ventricle	heart
22	chr12:63035400-63038400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr12:63035400-63038400	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr12:63035400-63038400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr12:63035400-63040600	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr12:63035600-63038400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr12:63035600-63038600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr12:63035600-63040400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr12:63035600-63041200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr12:63035600-63042200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr12:63035600-63043200	Weak transcription	A549	lung
32	chr12:63035600-63044200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr12:63036200-63038600	Weak transcription	HepG2	liver
34	chr12:63036200-63040800	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr12:63036400-63039200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr12:63036400-63044000	Weak transcription	Duodenum Mucosa	Duodenum
37	chr12:63036800-63039200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr12:63036800-63040400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr12:63037000-63038600	Strong transcription	Fetal Intestine Small	intestine
40	chr12:63037000-63039000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr12:63037200-63041600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr12:63037200-63050800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr12:63037200-63069600	Weak transcription	Fetal Intestine Large	intestine
44	chr12:63037400-63041400	Weak transcription	Fetal Muscle Trunk	muscle
45	chr12:63037600-63041200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr12:63038200-63038600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr12:63038200-63039200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr12:63038200-63039400	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr12:63038200-63043200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr12:63038400-63038600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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