Variant report

Variant	nsv559693
Chromosome Location	chr12:87216285-87447757
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:87403863-87404208	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:87402568-87403105	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:87328246-87328300	K562	blood:	n/a	n/a
4	ATF1	chr12:87283289-87283337	K562	blood:	n/a	n/a
5	ATF1	chr12:87371930-87371953	K562	blood:	n/a	n/a
6	BCL3	chr12:87220989-87221712	A549	lung:	n/a	n/a
7	BHLHE40	chr12:87219939-87220108	A549	lung:	n/a	n/a
8	BHLHE40	chr12:87222440-87222493	GM12878	blood:	n/a	n/a
9	BRCA1	chr12:87280525-87280594	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr12:87340632-87340744	GM12878	blood:	n/a	n/a
11	BRCA1	chr12:87297594-87297609	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr12:87343121-87343160	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:87271066-87271372	K562	blood:	n/a	chr12:87271223-87271236 chr12:87271225-87271234 chr12:87271223-87271236 chr12:87271225-87271236 chr12:87271223-87271234
14	CEBPB	chr12:87342736-87342952	MCF-7	breast:	n/a	chr12:87342846-87342863 chr12:87342848-87342859
15	CEBPB	chr12:87308522-87308994	A549	lung:	n/a	chr12:87308753-87308764 chr12:87308557-87308568 chr12:87308751-87308764 chr12:87308753-87308764 chr12:87308713-87308726
16	CEBPB	chr12:87343873-87344183	A549	lung:	n/a	chr12:87344011-87344022
17	CEBPB	chr12:87342689-87343014	IMR90	lung:	n/a	chr12:87342846-87342863 chr12:87342848-87342859
18	CEBPB	chr12:87308435-87308759	HepG2	liver:	n/a	chr12:87308557-87308568 chr12:87308713-87308726
19	CEBPB	chr12:87343857-87344182	HepG2	liver:	n/a	chr12:87344011-87344022
20	CEBPB	chr12:87343848-87344183	IMR90	lung:	n/a	chr12:87344011-87344022
21	CEBPB	chr12:87308529-87308925	Hela-S3	cervix:	n/a	chr12:87308753-87308764 chr12:87308557-87308568 chr12:87308751-87308764 chr12:87308753-87308764 chr12:87308713-87308726
22	CEBPB	chr12:87271114-87271390	H1-hESC	embryonic stem cell:	n/a	chr12:87271223-87271236 chr12:87271225-87271234 chr12:87271223-87271236 chr12:87271225-87271236 chr12:87271223-87271234
23	CEBPB	chr12:87271059-87271363	A549	lung:	n/a	chr12:87271223-87271236 chr12:87271225-87271234 chr12:87271223-87271236 chr12:87271225-87271236 chr12:87271223-87271234
24	CEBPB	chr12:87402561-87402961	HepG2	liver:	n/a	n/a
25	CEBPB	chr12:87414555-87414783	A549	lung:	n/a	chr12:87414695-87414706
26	CEBPB	chr12:87356544-87356595	A549	lung:	n/a	n/a
27	CEBPB	chr12:87414578-87414822	HepG2	liver:	n/a	chr12:87414695-87414706
28	CEBPB	chr12:87343878-87344102	H1-hESC	embryonic stem cell:	n/a	chr12:87344011-87344022
29	CEBPB	chr12:87346005-87346080	A549	lung:	n/a	n/a
30	CEBPB	chr12:87271065-87271403	IMR90	lung:	n/a	chr12:87271223-87271236 chr12:87271225-87271234 chr12:87271223-87271236 chr12:87271225-87271236 chr12:87271223-87271234
31	CEBPB	chr12:87308490-87308930	MCF-7	breast:	n/a	chr12:87308753-87308764 chr12:87308557-87308568 chr12:87308751-87308764 chr12:87308753-87308764 chr12:87308713-87308726
32	CEBPB	chr12:87308499-87308893	IMR90	lung:	n/a	chr12:87308753-87308764 chr12:87308557-87308568 chr12:87308751-87308764 chr12:87308753-87308764 chr12:87308713-87308726
33	CEBPB	chr12:87308526-87308894	A549	lung:	n/a	chr12:87308753-87308764 chr12:87308557-87308568 chr12:87308751-87308764 chr12:87308753-87308764 chr12:87308713-87308726
34	CEBPB	chr12:87308591-87308638	K562	blood:	n/a	n/a
35	CEBPB	chr12:87308603-87308891	ECC-1	luminal epithelium:	n/a	chr12:87308753-87308764 chr12:87308751-87308764 chr12:87308753-87308764 chr12:87308713-87308726
36	CEBPB	chr12:87343856-87344158	Hela-S3	cervix:	n/a	chr12:87344011-87344022
37	CEBPB	chr12:87251221-87251487	HepG2	liver:	n/a	chr12:87251355-87251366
38	CEBPB	chr12:87308580-87308953	MCF-7	breast:	n/a	chr12:87308753-87308764 chr12:87308751-87308764 chr12:87308753-87308764 chr12:87308713-87308726
39	CEBPB	chr12:87271055-87271397	HepG2	liver:	n/a	chr12:87271223-87271236 chr12:87271225-87271234 chr12:87271223-87271236 chr12:87271225-87271236 chr12:87271223-87271234
40	CEBPB	chr12:87308518-87308856	H1-hESC	embryonic stem cell:	n/a	chr12:87308753-87308764 chr12:87308557-87308568 chr12:87308751-87308764 chr12:87308753-87308764 chr12:87308713-87308726
41	CEBPB	chr12:87342833-87343001	HepG2	liver:	n/a	chr12:87342846-87342863 chr12:87342848-87342859
42	CTCF	chr12:87308604-87308801	NHEK	skin:	n/a	chr12:87308679-87308697 chr12:87308674-87308695
43	CTCF	chr12:87308620-87308770	HA-sp	spinal cord:	n/a	chr12:87308679-87308697 chr12:87308674-87308695
44	CTCF	chr12:87232640-87232790	AG09319	gingival:	n/a	n/a
45	CTCF	chr12:87308600-87308750	AG09319	gingival:	n/a	chr12:87308679-87308697 chr12:87308674-87308695
46	CTCF	chr12:87257764-87257790	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr12:87308620-87308770	AoAF	blood vessel:	n/a	chr12:87308679-87308697 chr12:87308674-87308695
48	CTCF	chr12:87308678-87308694	K562	blood:	n/a	n/a
49	CTCF	chr12:87232700-87232850	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr12:87308600-87308750	Caco-2	colon:	n/a	chr12:87308679-87308697 chr12:87308674-87308695

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:87232692-87232742	HepG2	liver:	n/a
2	chr12:87232511-87232561	HNPCEpiC	eye:	n/a
3	chr12:87232692-87232742	NHBE	bronchial:	n/a
4	chr12:87232511-87232561	HIPEpiC	eye:	n/a
5	chr12:87232692-87232742	LNCaP	prostate:	n/a
6	chr12:87232511-87232561	NH-A	brain:	n/a
7	chr12:87232511-87232561	GM06990	blood:	n/a
8	chr12:87232821-87232871	HEEpiC	esophagus:	n/a
9	chr12:87232821-87232871	H1-hESC	embryonic stem cell:	embryo
10	chr12:87232692-87232742	HCPEpiC	choroid plexus:	n/a
11	chr12:87232692-87232742	GM19239	blood:	n/a
12	chr12:87232821-87232871	SK-N-MC	brain:	n/a
13	chr12:87232821-87232871	U87	brain:	n/a
14	chr12:87232511-87232561	K562	blood:	n/a
15	chr12:87232821-87232871	HMEC	breast:	n/a
16	chr12:87232511-87232561	HL-60	blood:	n/a
17	chr12:87232511-87232561	NHBE	bronchial:	n/a
18	chr12:87232821-87232871	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:87232692-87232742	HCF	heart:	n/a
20	chr12:87232511-87232561	HepG2	liver:	n/a
21	chr12:87232511-87232561	HCT-116	colon:	n/a
22	chr12:87232821-87232871	HIPEpiC	eye:	n/a
23	chr12:87232692-87232742	HUVEC	blood vessel:	n/a
24	chr12:87232511-87232561	HRPEpiC	eye:	n/a
25	chr12:87232511-87232561	HCM	heart:	n/a
26	chr12:87232511-87232561	GM19239	blood:	n/a
27	chr12:87232511-87232561	GM12892	blood:	n/a
28	chr12:87232692-87232742	NT2-D1	testis:	n/a
29	chr12:87232692-87232742	Hela-S3	cervix:	n/a
30	chr12:87232692-87232742	MCF-7	breast:	n/a
31	chr12:87232821-87232871	ProgFib	skin:	n/a
32	chr12:87232821-87232871	HCF	heart:	n/a
33	chr12:87232511-87232561	A549	lung:	n/a
34	chr12:87232511-87232561	NT2-D1	testis:	n/a
35	chr12:87232692-87232742	SK-N-MC	brain:	n/a
36	chr12:87232511-87232561	CMK	blood:	n/a
37	chr12:87232821-87232871	SK-N-SH	brain:	n/a
38	chr12:87232821-87232871	Jurkat	blood:	n/a
39	chr12:87232511-87232561	PANC-1	pancreas:	n/a
40	chr12:87232511-87232561	GM12878	blood:	n/a
41	chr12:87232692-87232742	HAEpiC	amniotic membrane:	n/a
42	chr12:87232821-87232871	HCPEpiC	choroid plexus:	n/a
43	chr12:87232511-87232561	PrEC	prostate:	n/a
44	chr12:87232821-87232871	T-47D	breast:	n/a
45	chr12:87232821-87232871	MCF10A-Er-Src	breast:	n/a
46	chr12:87232511-87232561	MCF-7	breast:	n/a
47	chr12:87232511-87232561	HPAEpiC	pulmonary alveolar:	n/a
48	chr12:87232821-87232871	AG09309	skin:	n/a
49	chr12:87232692-87232742	U87	brain:	n/a
50	chr12:87232821-87232871	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr12:87376736..87379148-chr12:87408006..87409813,2	K562	blood:
2	chr12:87386481..87388359-chr12:87403399..87406210,2	MCF-7	breast:
3	chr12:87386481..87388359-chr12:87403399..87406210,2	MCF-7	breast:
4	chr12:87376736..87379148-chr12:87408006..87409813,2	K562	blood:
5	chr12:87237467..87238342-chr7:40961627..40962369,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MGAT4C-1	chr12:87232443-87232905	ENSG00000258185
2	lnc-MGAT4C-1	chr12:87232443-87232775	ENSG00000258185
3	lnc-MGAT4C-3	chr12:87345415-87345519	NONHSAT029768
4	lnc-MGAT4C-1	chr12:87232443-87232681	NONHSAT029762
5	lnc-MGAT4C-3	chr12:87335669-87335818	NONHSAT029768

Variant related genes	Relation type
MGAT4C	TF binding region
ENSG00000258185	TF binding region
MGAT4C	CpG island
ENSG00000258185	CpG island

Extended variants
information (count: 4077 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:4077 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543864124	chr12:87220814-87220815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs368822598	chr12:87220815-87220816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs17310613	chr12:87220867-87220868	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs575545776	chr12:87220878-87220879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187514095	chr12:87220880-87220881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2035719	chr12:87220898-87220899	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs376902054	chr12:87220899-87220900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs193269919	chr12:87220923-87220924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs11831438	chr12:87220929-87220930	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs547111491	chr12:87220931-87220932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369054928	chr12:87220942-87220943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562038619	chr12:87220956-87220957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs34058511	chr12:87220978-87220979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529348121	chr12:87220979-87220980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551011148	chr12:87221069-87221070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs569248372	chr12:87221159-87221160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185050680	chr12:87221162-87221163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs551687479	chr12:87221175-87221176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs78849602	chr12:87221182-87221183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533748407	chr12:87221188-87221189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs73395150	chr12:87221193-87221194	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs567256544	chr12:87221194-87221195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs181762494	chr12:87221196-87221197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147590111	chr12:87221198-87221199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs577193920	chr12:87221239-87221240	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs546121172	chr12:87221246-87221247	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs76023612	chr12:87221278-87221279	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs184505963	chr12:87221282-87221283	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs540472111	chr12:87221298-87221299	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs141923589	chr12:87221367-87221368	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs113394073	chr12:87221378-87221379	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs544697740	chr12:87221385-87221386	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs78650852	chr12:87221395-87221396	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs181171418	chr12:87221396-87221397	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs551749005	chr12:87221410-87221411	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs566659736	chr12:87221424-87221425	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs527538028	chr12:87221473-87221474	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs373564648	chr12:87221592-87221593	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs548918607	chr12:87221609-87221610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs567424312	chr12:87221664-87221665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554249745	chr12:87221701-87221702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201798948	chr12:87221715-87221716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537575962	chr12:87221742-87221743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs375603715	chr12:87221766-87221767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572401020	chr12:87221774-87221775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs61949615	chr12:87226378-87226379	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs530229773	chr12:87226392-87226393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548329613	chr12:87226396-87226397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192432857	chr12:87226399-87226400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34570644	chr12:87226423-87226424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	17550852	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:205 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:87220800-87221200	Enhancers	A549	lung
2	chr12:87221200-87221600	Flanking Active TSS	A549	lung
3	chr12:87221600-87221800	Enhancers	A549	lung
4	chr12:87226200-87230200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr12:87228600-87230600	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr12:87229200-87229400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr12:87229200-87232800	Active TSS	Fetal Brain Female	brain
8	chr12:87229400-87230000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr12:87229400-87233200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr12:87230000-87232600	Active TSS	Fetal Brain Male	brain
11	chr12:87230000-87232800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr12:87230200-87230800	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr12:87230200-87232800	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr12:87230600-87231000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr12:87230600-87232600	Active TSS	Brain Anterior Caudate	brain
16	chr12:87230600-87232800	Active TSS	Brain Hippocampus Middle	brain
17	chr12:87230800-87231200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
18	chr12:87230800-87231200	Active TSS	Brain Germinal Matrix	brain
19	chr12:87230800-87231600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr12:87230800-87232800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr12:87230800-87232800	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr12:87231000-87231400	Active TSS	ES-I3 Cell Line	embryonic stem cell
23	chr12:87231000-87231400	Enhancers	Aorta	Aorta
24	chr12:87231000-87233000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
25	chr12:87231200-87232800	Active TSS	Brain Cingulate Gyrus	brain
26	chr12:87231200-87233000	Enhancers	H1 Cell Line	embryonic stem cell
27	chr12:87231400-87231800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
28	chr12:87231400-87232800	Active TSS	Brain Inferior Temporal Lobe	brain
29	chr12:87231600-87232800	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr12:87231800-87232400	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr12:87232200-87232800	Active TSS	Fetal Lung	lung
32	chr12:87232200-87232800	Active TSS	Fetal Muscle Leg	muscle
33	chr12:87232200-87232800	Active TSS	Right Atrium	heart
34	chr12:87232200-87233000	Active TSS	Brain Angular Gyrus	brain
35	chr12:87232400-87232800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
36	chr12:87232400-87232800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
37	chr12:87232600-87232800	Flanking Active TSS	Brain Anterior Caudate	brain
38	chr12:87232600-87233200	Weak transcription	Fetal Brain Male	brain
39	chr12:87232800-87233000	Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr12:87232800-87233000	Enhancers	Fetal Lung	lung
41	chr12:87233000-87234000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr12:87233200-87234000	Enhancers	Fetal Brain Male	brain
43	chr12:87234000-87234600	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr12:87263000-87263400	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr12:87286400-87286600	Enhancers	Gastric	stomach
46	chr12:87286600-87286800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr12:87286600-87286800	ZNF genes & repeats	Gastric	stomach
48	chr12:87297000-87297400	Enhancers	Fetal Brain Female	brain
49	chr12:87299600-87305800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr12:87305400-87307200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell

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