Variant report

Variant	nsv899078
Chromosome Location	chr12:51213433-51286750
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:548)
CpG islands
(count:610)
Chromatin interactive
region (count:41)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:51219106-51219568	HepG2	liver:	n/a	chr12:51219307-51219323
2	ARID3A	chr12:51218888-51219408	K562	blood:	n/a	chr12:51219307-51219323
3	ARID3A	chr12:51256210-51256365	K562	blood:	n/a	n/a
4	ARID3A	chr12:51251123-51251484	K562	blood:	n/a	n/a
5	ATF1	chr12:51235600-51235867	K562	blood:	n/a	n/a
6	ATF1	chr12:51219091-51219440	K562	blood:	n/a	n/a
7	ATF2	chr12:51219047-51219483	GM12878	blood:	n/a	n/a
8	ATF2	chr12:51218941-51219468	GM12878	blood:	n/a	n/a
9	ATF3	chr12:51219020-51219519	K562	blood:	n/a	n/a
10	BACH1	chr12:51256241-51256441	K562	blood:	n/a	chr12:51256281-51256295
11	BHLHE40	chr12:51253476-51253632	HepG2	liver:	n/a	n/a
12	BHLHE40	chr12:51235528-51235762	K562	blood:	n/a	n/a
13	BHLHE40	chr12:51219184-51219333	K562	blood:	n/a	n/a
14	CBX3	chr12:51234635-51234882	K562	blood:	n/a	n/a
15	CBX3	chr12:51227572-51227831	K562	blood:	n/a	n/a
16	CBX3	chr12:51227866-51228082	K562	blood:	n/a	n/a
17	CBX3	chr12:51259038-51259381	K562	blood:	n/a	n/a
18	CBX3	chr12:51258986-51259407	K562	blood:	n/a	n/a
19	CBX3	chr12:51227564-51228181	K562	blood:	n/a	n/a
20	CBX3	chr12:51234543-51234979	K562	blood:	n/a	n/a
21	CCNT2	chr12:51251132-51251337	K562	blood:	n/a	n/a
22	CEBPB	chr12:51222028-51222137	HepG2	liver:	n/a	chr12:51222032-51222043
23	CEBPB	chr12:51218833-51219480	H1-hESC	embryonic stem cell:	n/a	chr12:51219272-51219283
24	CEBPB	chr12:51255537-51255569	IMR90	lung:	n/a	n/a
25	CEBPB	chr12:51215881-51216284	A549	lung:	n/a	chr12:51216072-51216083
26	CEBPB	chr12:51278890-51279051	K562	blood:	n/a	n/a
27	CEBPB	chr12:51219133-51219387	HepG2	liver:	n/a	chr12:51219272-51219283
28	CEBPB	chr12:51253456-51253671	K562	blood:	n/a	chr12:51253626-51253637 chr12:51253613-51253624
29	CEBPB	chr12:51253461-51253746	HepG2	liver:	n/a	chr12:51253626-51253637 chr12:51253613-51253624
30	CEBPB	chr12:51251191-51251316	K562	blood:	n/a	n/a
31	CEBPB	chr12:51218919-51219550	ECC-1	luminal epithelium:	n/a	chr12:51219272-51219283
32	CEBPB	chr12:51219010-51219514	ECC-1	luminal epithelium:	n/a	chr12:51219272-51219283
33	CEBPB	chr12:51253443-51253777	K562	blood:	n/a	chr12:51253626-51253637 chr12:51253613-51253624
34	CEBPB	chr12:51218870-51219607	HCT-116	colon:	n/a	chr12:51219272-51219283
35	CEBPB	chr12:51219075-51219491	IMR90	lung:	n/a	chr12:51219272-51219283
36	CEBPB	chr12:51218867-51219643	A549	lung:	n/a	chr12:51219272-51219283
37	CEBPB	chr12:51219061-51219523	MCF-7	breast:	n/a	chr12:51219272-51219283
38	CEBPB	chr12:51215897-51216262	K562	blood:	n/a	chr12:51216072-51216083
39	CEBPB	chr12:51218830-51219508	K562	blood:	n/a	chr12:51219272-51219283
40	CEBPB	chr12:51215859-51216212	K562	blood:	n/a	chr12:51216072-51216083
41	CEBPB	chr12:51218989-51219525	A549	lung:	n/a	chr12:51219272-51219283
42	CEBPB	chr12:51215859-51216303	MCF-7	breast:	n/a	chr12:51216072-51216083
43	CEBPB	chr12:51215904-51216244	ECC-1	luminal epithelium:	n/a	chr12:51216072-51216083
44	CEBPB	chr12:51219089-51219477	HepG2	liver:	n/a	chr12:51219272-51219283
45	CEBPB	chr12:51218928-51219567	Hela-S3	cervix:	n/a	chr12:51219272-51219283
46	CEBPB	chr12:51219085-51219481	A549	lung:	n/a	chr12:51219272-51219283
47	CEBPB	chr12:51215895-51216226	HepG2	liver:	n/a	chr12:51216072-51216083
48	CEBPB	chr12:51215895-51216260	Hela-S3	cervix:	n/a	chr12:51216072-51216083
49	CEBPB	chr12:51253478-51253738	A549	lung:	n/a	chr12:51253626-51253637 chr12:51253613-51253624
50	CEBPB	chr12:51219106-51219458	K562	blood:	n/a	chr12:51219272-51219283

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:51233392-51233442	HRE	kidney:	n/a
2	chr12:51236768-51236818	AG04450	lung:	fetal
3	chr12:51236704-51236754	HCM	heart:	n/a
4	chr12:51236768-51236818	ovcar-3	ovarian:	n/a
5	chr12:51236634-51236684	HCF	heart:	n/a
6	chr12:51213748-51213798	HL-60	blood:	n/a
7	chr12:51219239-51219289	SK-N-SH_RA	brain:	n/a
8	chr12:51236693-51236743	HIPEpiC	eye:	n/a
9	chr12:51236059-51236109	HEEpiC	esophagus:	n/a
10	chr12:51219239-51219289	HUVEC	blood vessel:	n/a
11	chr12:51236704-51236754	IMR90	lung:	fetal
12	chr12:51236634-51236684	HNPCEpiC	eye:	n/a
13	chr12:51219239-51219289	AG09319	gingival:	n/a
14	chr12:51236634-51236684	HCT-116	colon:	n/a
15	chr12:51236634-51236684	Hepatocyte	liver:	n/a
16	chr12:51219239-51219289	AoSMC	blood vessel:	n/a
17	chr12:51213748-51213798	HAEpiC	amniotic membrane:	n/a
18	chr12:51236704-51236754	SK-N-MC	brain:	n/a
19	chr12:51236582-51236632	BJ	skin:	n/a
20	chr12:51236059-51236109	K562	blood:	n/a
21	chr12:51236582-51236632	A549	lung:	n/a
22	chr12:51219239-51219289	Jurkat	blood:	n/a
23	chr12:51236638-51236688	SK-N-SH_RA	brain:	n/a
24	chr12:51236059-51236109	Hepatocyte	liver:	n/a
25	chr12:51233392-51233442	GM12878	blood:	n/a
26	chr12:51236638-51236688	HCF	heart:	n/a
27	chr12:51236768-51236818	AoSMC	blood vessel:	n/a
28	chr12:51219239-51219289	IMR90	lung:	fetal
29	chr12:51236582-51236632	HCM	heart:	n/a
30	chr12:51236638-51236688	IMR90	lung:	fetal
31	chr12:51236768-51236818	SAEC	small airway:	n/a
32	chr12:51213748-51213798	MCF10A-Er-Src	breast:	n/a
33	chr12:51236704-51236754	HRPEpiC	eye:	n/a
34	chr12:51236634-51236684	SK-N-SH_RA	brain:	n/a
35	chr12:51233392-51233442	HUVEC	blood vessel:	n/a
36	chr12:51236582-51236632	HAEpiC	amniotic membrane:	n/a
37	chr12:51236704-51236754	HMEC	breast:	n/a
38	chr12:51236582-51236632	HMEC	breast:	n/a
39	chr12:51233392-51233442	AG04450	lung:	fetal
40	chr12:51236768-51236818	NHDF-neo	bronchial:	n/a
41	chr12:51236768-51236818	HEEpiC	esophagus:	n/a
42	chr12:51236059-51236109	HCF	heart:	n/a
43	chr12:51233392-51233442	HAEpiC	amniotic membrane:	n/a
44	chr12:51236693-51236743	Hela-S3	cervix:	n/a
45	chr12:51236704-51236754	SK-N-SH	brain:	n/a
46	chr12:51236059-51236109	HPAEpiC	pulmonary alveolar:	n/a
47	chr12:51219239-51219289	Hepatocyte	liver:	n/a
48	chr12:51236582-51236632	HepG2	liver:	n/a
49	chr12:51236059-51236109	SKMC	muscle:	n/a
50	chr12:51219239-51219289	HIPEpiC	eye:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:51233571..51235108-chr12:51328091..51331063,2	K562	blood:
2	chr12:50793039..50794712-chr12:51216768..51219272,2	K562	blood:
3	chr12:51157232..51159790-chr12:51217662..51220370,4	MCF-7	breast:
4	chr12:51230523..51233092-chr12:51235059..51236989,2	MCF-7	breast:
5	chr12:51229364..51231906-chr12:51476163..51477901,2	MCF-7	breast:
6	chr12:51194188..51196779-chr12:51231539..51234008,2	MCF-7	breast:
7	chr12:51230105..51232434-chr12:51237161..51239319,2	MCF-7	breast:
8	chr12:51156562..51158962-chr12:51222268..51224971,2	K562	blood:
9	chr12:51212755..51215653-chr12:51225131..51226878,2	K562	blood:
10	chr12:51219096..51220890-chr12:51222074..51224257,2	MCF-7	breast:
11	chr12:51212786..51214358-chr12:51219133..51221117,2	K562	blood:
12	chr12:51220629..51223236-chr12:51418576..51421161,3	MCF-7	breast:
13	chr12:51230105..51232434-chr12:51237161..51239319,2	MCF-7	breast:
14	chr12:51218193..51220790-chr12:51416290..51419028,2	K562	blood:
15	chr12:51274420..51277137-chr12:51281604..51283969,2	K562	blood:
16	chr12:51218257..51221554-chr12:51475850..51478812,3	MCF-7	breast:
17	chr12:51285941..51288769-chr12:51333436..51336349,2	MCF-7	breast:
18	chr12:51184951..51187491-chr12:51218198..51219760,2	MCF-7	breast:
19	chr12:51216774..51221510-chr12:51379576..51384198,5	MCF-7	breast:
20	chr12:51158475..51160420-chr12:51281763..51283394,2	K562	blood:
21	chr12:51212755..51215653-chr12:51225131..51226878,2	K562	blood:
22	chr12:51155993..51157542-chr12:51233838..51236379,2	MCF-7	breast:
23	chr12:51218097..51220673-chr12:51419291..51422139,4	MCF-7	breast:
24	chr12:51219278..51219813-chr12:51735276..51735836,2	K562	blood:
25	chr12:51215681..51217224-chr12:51232031..51234390,2	K562	blood:
26	chr12:51216775..51221102-chr12:51419333..51421670,3	K562	blood:
27	chr12:51206635..51209642-chr12:51213405..51216758,3	K562	blood:
28	chr12:51274420..51277137-chr12:51281604..51283969,2	K562	blood:
29	chr12:51215681..51217224-chr12:51232031..51234390,2	K562	blood:
30	chr12:51207076..51210339-chr12:51211809..51214905,4	K562	blood:
31	chr12:51271631..51273564-chr12:51476067..51478746,2	MCF-7	breast:
32	chr12:51219096..51220890-chr12:51222074..51224257,2	MCF-7	breast:
33	chr12:51212786..51214358-chr12:51219133..51221117,2	K562	blood:
34	chr12:51219126..51219822-chr12:51379841..51381362,5	MCF-7	breast:
35	chr12:51218827..51219730-chr12:51421603..51422600,3	MCF-7	breast:
36	chr12:51157606..51159711-chr12:51223429..51225922,2	MCF-7	breast:
37	chr12:51218890..51219846-chr12:51380451..51381461,7	MCF-7	breast:
38	chr12:51234605..51237036-chr12:51237344..51239459,2	K562	blood:
39	chr12:51156191..51157743-chr12:51230542..51233377,2	MCF-7	breast:
40	chr12:51213097..51215653-chr12:51224289..51226631,2	K562	blood:
41	chr12:51213097..51215653-chr12:51224289..51226631,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC11A2-3	chr12:51241708-51242095	NONHSAT028217
2	lnc-SLC11A2-4	chr12:51235283-51235612	NONHSAT028216

No data

Variant related genes	Relation type
ENSG00000271621	TF binding region
RN7SL519P	TF binding region
TMPRSS12	TF binding region
ENSG00000271621	CpG island
RN7SL519P	CpG island
TMPRSS12	CpG island
ENSG00000110911	chromatin interactions
ENSG00000110925	chromatin interactions
ENSG00000243075	chromatin interactions
ENSG00000186452	chromatin interactions
ENSG00000199740	chromatin interactions
ENSG00000123268	chromatin interactions
ENSG00000161813	chromatin interactions

Extended variants
information (count: 1751 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1751 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17291650	chr12:51213433-51213434	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance disease
2	rs545666741	chr12:51213463-51213464	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565435031	chr12:51213515-51213516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189980785	chr12:51213587-51213588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181447737	chr12:51213604-51213605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560961637	chr12:51213661-51213662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563409143	chr12:51213665-51213666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184951419	chr12:51213744-51213745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs11169571	chr12:51213765-51213766	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs189354008	chr12:51213775-51213776	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532269819	chr12:51213814-51213815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372971600	chr12:51213817-51213818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551955436	chr12:51213824-51213825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550467653	chr12:51213883-51213884	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568669177	chr12:51213891-51213892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537161616	chr12:51213909-51213910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs180970190	chr12:51213940-51213941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567724058	chr12:51213957-51213958	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377030140	chr12:51213958-51213959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150963409	chr12:51213974-51213975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536292618	chr12:51214003-51214004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35199663	chr12:51214082-51214083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146985068	chr12:51214099-51214100	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145093086	chr12:51214102-51214103	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553331268	chr12:51214223-51214224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542687732	chr12:51214233-51214234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573463564	chr12:51214241-51214242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545678746	chr12:51214253-51214254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs76618993	chr12:51214267-51214268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs829125	chr12:51214327-51214328	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs544798225	chr12:51214380-51214381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560854108	chr12:51214396-51214397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529786358	chr12:51214420-51214421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539895051	chr12:51214440-51214441	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551254271	chr12:51214530-51214531	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560045868	chr12:51214542-51214543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532282226	chr12:51214546-51214547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552016824	chr12:51214594-51214595	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568731286	chr12:51214599-51214600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575996276	chr12:51214611-51214612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185888477	chr12:51214619-51214620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143593869	chr12:51214627-51214628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567703604	chr12:51214682-51214683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552427114	chr12:51214686-51214687	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148067084	chr12:51214758-51214759	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376720445	chr12:51214770-51214771	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546687900	chr12:51214855-51214856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142345757	chr12:51214923-51214924	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12305727	chr12:51215038-51215039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191579597	chr12:51215050-51215051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Seminomas	18059402	CNVD
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
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Cancer	17160897	CNVD
Breast cancer	21858162	CNVD
Urothelial carcinoma	21177765	CNVD
Schizophrenia	23813976	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:51190200-51215200	Weak transcription	Pancreas	Pancrea
2	chr12:51194600-51214600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:51198600-51215400	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr12:51200600-51222200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr12:51201400-51213800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr12:51201800-51213800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:51202200-51213800	Strong transcription	Fetal Thymus	thymus
8	chr12:51202200-51214200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr12:51202600-51213800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr12:51202600-51214400	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr12:51202800-51213600	Strong transcription	Primary neutrophils fromperipheralblood	blood
12	chr12:51202800-51214000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr12:51202800-51215000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr12:51203200-51213800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
15	chr12:51203200-51213800	Strong transcription	Primary T helper cells fromperipheralblood	blood
16	chr12:51203200-51213800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr12:51203200-51213800	Strong transcription	Adipose Nuclei	Adipose
18	chr12:51203200-51213800	Strong transcription	Rectal Mucosa Donor 29	rectum
19	chr12:51203200-51214000	Strong transcription	Primary T cells fromperipheralblood	blood
20	chr12:51203200-51214000	Strong transcription	Duodenum Mucosa	Duodenum
21	chr12:51203200-51214200	Strong transcription	HUES64 Cell Line	embryonic stem cell
22	chr12:51203200-51214200	Strong transcription	Primary T helper cells PMA-I stimulated	--
23	chr12:51203400-51213600	Strong transcription	Primary B cells from peripheral blood	blood
24	chr12:51203400-51213800	Strong transcription	Skeletal Muscle Female	skeletal muscle
25	chr12:51203800-51214000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr12:51204400-51213600	Strong transcription	Primary T cells from cord blood	blood
27	chr12:51204400-51215400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr12:51205000-51228200	Weak transcription	Gastric	stomach
29	chr12:51205200-51217600	Weak transcription	Psoas Muscle	Psoas
30	chr12:51207400-51214000	Strong transcription	Liver	Liver
31	chr12:51207400-51214000	Strong transcription	Dnd41	blood
32	chr12:51207400-51215000	Strong transcription	HUES48 Cell Line	embryonic stem cell
33	chr12:51207600-51214000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr12:51207600-51214000	Strong transcription	Duodenum Smooth Muscle	Duodenum
35	chr12:51207600-51214000	Strong transcription	NHDF-Ad	bronchial
36	chr12:51207800-51213800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
37	chr12:51207800-51213800	Strong transcription	Left Ventricle	heart
38	chr12:51207800-51214200	Strong transcription	Osteobl	bone
39	chr12:51208000-51213600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr12:51208000-51213600	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr12:51208000-51213800	Strong transcription	HUVEC	blood vessel
42	chr12:51208000-51219000	Weak transcription	Stomach Mucosa	stomach
43	chr12:51208400-51216600	Weak transcription	GM12878-XiMat	blood
44	chr12:51208400-51218800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr12:51208400-51219000	Weak transcription	HSMMtube	muscle
46	chr12:51208400-51219000	Weak transcription	NHLF	lung
47	chr12:51208600-51219000	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr12:51208800-51215200	Weak transcription	Small Intestine	intestine
49	chr12:51209400-51215400	Strong transcription	Hela-S3	cervix
50	chr12:51209800-51219000	Weak transcription	Fetal Kidney	kidney

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