Variant report

Variant	esv2829972
Chromosome Location	chr12:60079404-60111653
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:125)
CpG islands
(count:244)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:125 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:60086163-60086242	K562	blood:	n/a	n/a
2	CEBPB	chr12:60089199-60089549	IMR90	lung:	n/a	n/a
3	CEBPB	chr12:60093380-60093773	MCF-7	breast:	n/a	chr12:60093595-60093606
4	CEBPB	chr12:60107358-60107634	MCF-7	breast:	n/a	chr12:60107500-60107511 chr12:60107498-60107509
5	CEBPB	chr12:60093432-60093776	MCF-7	breast:	n/a	chr12:60093595-60093606
6	CEBPB	chr12:60107367-60107613	HepG2	liver:	n/a	chr12:60107500-60107511 chr12:60107498-60107509
7	CEBPB	chr12:60092466-60092741	A549	lung:	n/a	n/a
8	CEBPB	chr12:60093475-60093729	ECC-1	luminal epithelium:	n/a	chr12:60093595-60093606
9	CEBPB	chr12:60093373-60093796	Hela-S3	cervix:	n/a	chr12:60093595-60093606
10	CEBPB	chr12:60092391-60092810	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr12:60107344-60107645	H1-hESC	embryonic stem cell:	n/a	chr12:60107500-60107511 chr12:60107498-60107509
12	CEBPB	chr12:60103775-60104229	HepG2	liver:	n/a	chr12:60104182-60104193
13	CEBPB	chr12:60092223-60092841	IMR90	lung:	n/a	n/a
14	CEBPB	chr12:60093441-60093770	HepG2	liver:	n/a	chr12:60093595-60093606
15	CEBPB	chr12:60092476-60092745	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:60093364-60093972	IMR90	lung:	n/a	chr12:60093595-60093606
17	CEBPB	chr12:60089194-60089528	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr12:60092384-60092795	A549	lung:	n/a	n/a
19	CHD1	chr12:60093128-60093960	IMR90	lung:	n/a	n/a
20	CTCF	chr12:60089060-60089210	AG09309	skin:	n/a	n/a
21	CTCF	chr12:60089140-60089290	HMF	breast:	n/a	n/a
22	CTCF	chr12:60089180-60089330	NHLF	lung:	n/a	n/a
23	CTCF	chr12:60089180-60089330	HFF	foreskin:	n/a	n/a
24	CTCF	chr12:60089160-60089310	AG09309	skin:	n/a	n/a
25	CTCF	chr12:60089100-60089250	HMF	breast:	n/a	n/a
26	CTCF	chr12:60089200-60089350	SAEC	small airway:	n/a	n/a
27	CTCF	chr12:60089160-60089310	HMEC	breast:	n/a	n/a
28	CTCF	chr12:60089160-60089310	HCFaa	heart:	n/a	n/a
29	CTCF	chr12:60089120-60089270	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr12:60089080-60089230	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr12:60089120-60089270	BJ	skin:	n/a	n/a
32	CTCF	chr12:60089160-60089310	HEEpiC	esophagus:	n/a	n/a
33	CTCF	chr12:60089120-60089270	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr12:60089280-60089430	NHDF-neo	bronchial:	n/a	n/a
35	E2F4	chr12:60089287-60089576	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr12:60102012-60102212	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr12:60103308-60103391	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr12:60093340-60093706	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr12:60092521-60092939	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr12:60095156-60095529	MCF10A-Er-Src	breast:	n/a	n/a
41	EBF1	chr12:60106215-60106363	GM12878	blood:	n/a	chr12:60106273-60106284
42	EP300	chr12:60093375-60093749	Hela-S3	cervix:	n/a	n/a
43	EP300	chr12:60111542-60111548	GM12878	blood:	n/a	n/a
44	EP300	chr12:60092281-60092799	Hela-S3	cervix:	n/a	n/a
45	EP300	chr12:60082695-60082714	GM12878	blood:	n/a	n/a
46	FOS	chr12:60099331-60099592	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr12:60099331-60099464	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr12:60101836-60102533	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr12:60092206-60092809	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr12:60101832-60102532	MCF10A-Er-Src	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:60081776-60081826	PANC-1	pancreas:	n/a
2	chr12:60091171-60091221	PANC-1	pancreas:	n/a
3	chr12:60081776-60081826	HIPEpiC	eye:	n/a
4	chr12:60081776-60081826	HAEpiC	amniotic membrane:	n/a
5	chr12:60081776-60081826	AG09319	gingival:	n/a
6	chr12:60082038-60082088	CMK	blood:	n/a
7	chr12:60082038-60082088	NH-A	brain:	n/a
8	chr12:60081776-60081826	HRPEpiC	eye:	n/a
9	chr12:60091171-60091221	MCF-7	breast:	n/a
10	chr12:60082038-60082088	MCF-7	breast:	n/a
11	chr12:60083246-60083296	T-47D	breast:	n/a
12	chr12:60081776-60081826	LNCaP	prostate:	n/a
13	chr12:60083246-60083296	AG09309	skin:	n/a
14	chr12:60083246-60083296	HUVEC	blood vessel:	n/a
15	chr12:60081776-60081826	GM12878	blood:	n/a
16	chr12:60091171-60091221	IMR90	lung:	fetal
17	chr12:60091171-60091221	GM12878	blood:	n/a
18	chr12:60081776-60081826	NHBE	bronchial:	n/a
19	chr12:60082038-60082088	SAEC	small airway:	n/a
20	chr12:60082038-60082088	U87	brain:	n/a
21	chr12:60082038-60082088	HCF	heart:	n/a
22	chr12:60082038-60082088	NHDF-neo	bronchial:	n/a
23	chr12:60082038-60082088	ECC-1	luminal epithelium:	n/a
24	chr12:60082038-60082088	SKMC	muscle:	n/a
25	chr12:60082038-60082088	HRCEpiC	kidney:	n/a
26	chr12:60083246-60083296	MCF10A-Er-Src	breast:	n/a
27	chr12:60091171-60091221	NHDF-neo	bronchial:	n/a
28	chr12:60081776-60081826	U87	brain:	n/a
29	chr12:60081776-60081826	PFSK-1	brain:	n/a
30	chr12:60083246-60083296	Jurkat	blood:	n/a
31	chr12:60091171-60091221	AG09319	gingival:	n/a
32	chr12:60082038-60082088	HPAEpiC	pulmonary alveolar:	n/a
33	chr12:60083246-60083296	HMEC	breast:	n/a
34	chr12:60083246-60083296	ovcar-3	ovarian:	n/a
35	chr12:60091171-60091221	ovcar-3	ovarian:	n/a
36	chr12:60091171-60091221	T-47D	breast:	n/a
37	chr12:60091171-60091221	ECC-1	luminal epithelium:	n/a
38	chr12:60091171-60091221	HepG2	liver:	n/a
39	chr12:60082038-60082088	PFSK-1	brain:	n/a
40	chr12:60083246-60083296	GM19239	blood:	n/a
41	chr12:60081776-60081826	AG04449	skin:	fetal
42	chr12:60081776-60081826	BJ	skin:	n/a
43	chr12:60082038-60082088	SK-N-SH_RA	brain:	n/a
44	chr12:60082038-60082088	GM12891	blood:	n/a
45	chr12:60082038-60082088	HMEC	breast:	n/a
46	chr12:60091171-60091221	NT2-D1	testis:	n/a
47	chr12:60082038-60082088	AG04449	skin:	fetal
48	chr12:60091171-60091221	ProgFib	skin:	n/a
49	chr12:60081776-60081826	GM12891	blood:	n/a
50	chr12:60083246-60083296	GM12878	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:34097991..34100054-chr12:60091596..60093323,2	MCF-7	breast:
2	chr12:60097757..60100206-chr12:60101491..60103766,2	MCF-7	breast:
3	chr12:60017381..60019392-chr12:60100051..60102873,2	MCF-7	breast:
4	chr12:34098184..34100062-chr12:60091369..60093533,4	MCF-7	breast:
5	chr12:49657827..49660167-chr12:60098296..60100510,2	MCF-7	breast:
6	chr12:60097757..60100206-chr12:60101491..60103766,2	MCF-7	breast:
7	chr12:49657670..49659344-chr12:60094234..60097237,3	MCF-7	breast:
8	chr12:49658095..49659753-chr12:60101910..60104297,2	MCF-7	breast:

No data

Variant related genes	Relation type
SLC16A7	TF binding region
SLC16A7	CpG island
ENSG00000167553	chromatin interactions
ENSG00000258101	chromatin interactions

Extended variants
information (count: 1165 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1165 , 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	rs995342	chr12:60079404-60079405	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs546928082	chr12:60079406-60079407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543498255	chr12:60079516-60079517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566664746	chr12:60079563-60079564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563270053	chr12:60079566-60079567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs17122858	chr12:60079602-60079603	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs552103958	chr12:60079623-60079624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565613045	chr12:60079633-60079634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs113039077	chr12:60079637-60079638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528373679	chr12:60079648-60079649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs368508596	chr12:60079666-60079667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568104409	chr12:60079684-60079685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs34003318	chr12:60079720-60079721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141293640	chr12:60079777-60079778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542888292	chr12:60079781-60079782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559203802	chr12:60079819-60079820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375047787	chr12:60079852-60079853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12229478	chr12:60079855-60079856	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs553605934	chr12:60079870-60079871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376633320	chr12:60079875-60079876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572779305	chr12:60079877-60079878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572826511	chr12:60079881-60079882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573535929	chr12:60079897-60079898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369201254	chr12:60079907-60079908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544920772	chr12:60079914-60079915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564900878	chr12:60079921-60079922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556139357	chr12:60079922-60079923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs137982411	chr12:60079983-60079984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189626110	chr12:60080047-60080048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563363676	chr12:60080126-60080127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576889638	chr12:60080127-60080128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545937185	chr12:60080132-60080133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149040650	chr12:60080143-60080144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528310299	chr12:60080200-60080201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546570121	chr12:60080266-60080267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7342290	chr12:60080270-60080271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569287849	chr12:60080318-60080319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs143019609	chr12:60080319-60080320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs12309542	chr12:60080364-60080365	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs373489098	chr12:60080411-60080412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186696517	chr12:60080523-60080524	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs191059906	chr12:60080532-60080533	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs528629941	chr12:60080534-60080535	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs551460041	chr12:60080565-60080566	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs56848747	chr12:60080585-60080586	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs111261679	chr12:60080598-60080599	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs181582626	chr12:60080625-60080626	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs556082111	chr12:60080675-60080676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575867186	chr12:60080686-60080687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs59408837	chr12:60080742-60080743	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

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
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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	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
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
Schizophrenia	23813976	CNVD

Chromatin state (count:268 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:60026600-60089200	Weak transcription	Gastric	stomach
2	chr12:60045800-60085400	Weak transcription	NHDF-Ad	bronchial
3	chr12:60045800-60099800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr12:60050800-60098600	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr12:60058800-60080200	Weak transcription	Fetal Heart	heart
6	chr12:60062200-60085800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr12:60069600-60131400	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr12:60071600-60098600	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr12:60072200-60098600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr12:60072400-60085800	Weak transcription	Primary T cells from cord blood	blood
11	chr12:60072600-60085000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr12:60072800-60098000	Weak transcription	Primary B cells from peripheral blood	blood
13	chr12:60073000-60081000	Weak transcription	Ovary	ovary
14	chr12:60073000-60085000	Weak transcription	Primary B cells from cord blood	blood
15	chr12:60073000-60089000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr12:60073200-60081400	Weak transcription	Right Atrium	heart
17	chr12:60073200-60084400	Weak transcription	Primary hematopoietic stem cells	blood
18	chr12:60078600-60085200	Weak transcription	Left Ventricle	heart
19	chr12:60078600-60085800	Weak transcription	Aorta	Aorta
20	chr12:60080200-60080400	Enhancers	Fetal Heart	heart
21	chr12:60080400-60080800	Weak transcription	Fetal Heart	heart
22	chr12:60080800-60082400	Enhancers	Fetal Heart	heart
23	chr12:60081000-60081200	Enhancers	Ovary	ovary
24	chr12:60081400-60082200	Enhancers	Right Atrium	heart
25	chr12:60082400-60082800	Weak transcription	Fetal Heart	heart
26	chr12:60082800-60084400	Enhancers	Fetal Heart	heart
27	chr12:60083000-60083600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr12:60083600-60084000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr12:60083600-60084000	Enhancers	Osteobl	bone
30	chr12:60083800-60085800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr12:60084000-60084800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr12:60084400-60090800	Weak transcription	Fetal Heart	heart
33	chr12:60085000-60085200	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
34	chr12:60085000-60086200	Strong transcription	Primary B cells from cord blood	blood
35	chr12:60085200-60086200	ZNF genes & repeats	Left Ventricle	heart
36	chr12:60085200-60098600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr12:60085400-60086200	ZNF genes & repeats	NHDF-Ad	bronchial
38	chr12:60085600-60086200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr12:60085800-60086000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr12:60085800-60086000	ZNF genes & repeats	Primary T cells from cord blood	blood
41	chr12:60085800-60086200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr12:60085800-60086200	ZNF genes & repeats	Aorta	Aorta
43	chr12:60086000-60088200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr12:60086000-60102400	Weak transcription	Primary T cells from cord blood	blood
45	chr12:60086200-60087800	Weak transcription	NHDF-Ad	bronchial
46	chr12:60086200-60088800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr12:60086200-60089000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr12:60086200-60089000	Weak transcription	Left Ventricle	heart
49	chr12:60086200-60098400	Weak transcription	Primary B cells from cord blood	blood
50	chr12:60086200-60105200	Weak transcription	Aorta	Aorta

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