Variant report

Variant	nsv899406
Chromosome Location	chr12:87233995-87528020
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	chr12:87402568-87403105	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:87328246-87328300	K562	blood:	n/a	n/a
3	ARID3A	chr12:87403863-87404208	HepG2	liver:	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	BATF	chr12:87507875-87508091	GM12878	blood:	n/a	n/a
7	BHLHE40	chr12:87507928-87508017	GM12878	blood:	n/a	n/a
8	BRCA1	chr12:87280525-87280594	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr12:87343121-87343160	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	CEBPB	chr12:87479846-87480160	Hela-S3	cervix:	n/a	chr12:87479982-87479995
13	CEBPB	chr12:87308603-87308891	ECC-1	luminal epithelium:	n/a	chr12:87308753-87308764 chr12:87308751-87308764 chr12:87308753-87308764 chr12:87308713-87308726
14	CEBPB	chr12:87271066-87271372	K562	blood:	n/a	chr12:87271223-87271236 chr12:87271225-87271234 chr12:87271223-87271236 chr12:87271225-87271236 chr12:87271223-87271234
15	CEBPB	chr12:87343856-87344158	Hela-S3	cervix:	n/a	chr12:87344011-87344022
16	CEBPB	chr12:87308529-87308925	Hela-S3	cervix:	n/a	chr12:87308753-87308764 chr12:87308557-87308568 chr12:87308751-87308764 chr12:87308753-87308764 chr12:87308713-87308726
17	CEBPB	chr12:87342833-87343001	HepG2	liver:	n/a	chr12:87342846-87342863 chr12:87342848-87342859
18	CEBPB	chr12:87271055-87271397	HepG2	liver:	n/a	chr12:87271223-87271236 chr12:87271225-87271234 chr12:87271223-87271236 chr12:87271225-87271236 chr12:87271223-87271234
19	CEBPB	chr12:87308591-87308638	K562	blood:	n/a	n/a
20	CEBPB	chr12:87308580-87308953	MCF-7	breast:	n/a	chr12:87308753-87308764 chr12:87308751-87308764 chr12:87308753-87308764 chr12:87308713-87308726
21	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
22	CEBPB	chr12:87308522-87308994	A549	lung:	n/a	chr12:87308753-87308764 chr12:87308557-87308568 chr12:87308751-87308764 chr12:87308753-87308764 chr12:87308713-87308726
23	CEBPB	chr12:87271065-87271403	IMR90	lung:	n/a	chr12:87271223-87271236 chr12:87271225-87271234 chr12:87271223-87271236 chr12:87271225-87271236 chr12:87271223-87271234
24	CEBPB	chr12:87343878-87344102	H1-hESC	embryonic stem cell:	n/a	chr12:87344011-87344022
25	CEBPB	chr12:87503739-87503919	A549	lung:	n/a	n/a
26	CEBPB	chr12:87342736-87342952	MCF-7	breast:	n/a	chr12:87342846-87342863 chr12:87342848-87342859
27	CEBPB	chr12:87271059-87271363	A549	lung:	n/a	chr12:87271223-87271236 chr12:87271225-87271234 chr12:87271223-87271236 chr12:87271225-87271236 chr12:87271223-87271234
28	CEBPB	chr12:87476656-87476858	IMR90	lung:	n/a	n/a
29	CEBPB	chr12:87414578-87414822	HepG2	liver:	n/a	chr12:87414695-87414706
30	CEBPB	chr12:87476530-87476879	MCF-7	breast:	n/a	n/a
31	CEBPB	chr12:87308526-87308894	A549	lung:	n/a	chr12:87308753-87308764 chr12:87308557-87308568 chr12:87308751-87308764 chr12:87308753-87308764 chr12:87308713-87308726
32	CEBPB	chr12:87356544-87356595	A549	lung:	n/a	n/a
33	CEBPB	chr12:87308435-87308759	HepG2	liver:	n/a	chr12:87308557-87308568 chr12:87308713-87308726
34	CEBPB	chr12:87476697-87476906	A549	lung:	n/a	n/a
35	CEBPB	chr12:87515638-87516023	Hela-S3	cervix:	n/a	n/a
36	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
37	CEBPB	chr12:87510465-87510747	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr12:87342689-87343014	IMR90	lung:	n/a	chr12:87342846-87342863 chr12:87342848-87342859
39	CEBPB	chr12:87343873-87344183	A549	lung:	n/a	chr12:87344011-87344022
40	CEBPB	chr12:87343857-87344182	HepG2	liver:	n/a	chr12:87344011-87344022
41	CEBPB	chr12:87402561-87402961	HepG2	liver:	n/a	n/a
42	CEBPB	chr12:87346005-87346080	A549	lung:	n/a	n/a
43	CEBPB	chr12:87480282-87480669	MCF-7	breast:	n/a	n/a
44	CEBPB	chr12:87308499-87308893	IMR90	lung:	n/a	chr12:87308753-87308764 chr12:87308557-87308568 chr12:87308751-87308764 chr12:87308753-87308764 chr12:87308713-87308726
45	CEBPB	chr12:87343848-87344183	IMR90	lung:	n/a	chr12:87344011-87344022
46	CEBPB	chr12:87251221-87251487	HepG2	liver:	n/a	chr12:87251355-87251366
47	CEBPB	chr12:87308490-87308930	MCF-7	breast:	n/a	chr12:87308753-87308764 chr12:87308557-87308568 chr12:87308751-87308764 chr12:87308753-87308764 chr12:87308713-87308726
48	CEBPB	chr12:87476604-87476893	MCF-7	breast:	n/a	n/a
49	CEBPB	chr12:87414555-87414783	A549	lung:	n/a	chr12:87414695-87414706
50	CHD2	chr12:87508072-87508272	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:87510712-87510762	NT2-D1	testis:	n/a
2	chr12:87510712-87510762	SK-N-SH	brain:	n/a
3	chr12:87510712-87510762	MCF-7	breast:	n/a
4	chr12:87510712-87510762	HIPEpiC	eye:	n/a
5	chr12:87510712-87510762	SK-N-SH_RA	brain:	n/a
6	chr12:87510712-87510762	T-47D	breast:	n/a
7	chr12:87510712-87510762	HEK293	kidney:	embryo
8	chr12:87510712-87510762	HL-60	blood:	n/a
9	chr12:87510712-87510762	AoSMC	blood vessel:	n/a
10	chr12:87510712-87510762	HRE	kidney:	n/a
11	chr12:87510712-87510762	PrEC	prostate:	n/a
12	chr12:87510712-87510762	K562	blood:	n/a
13	chr12:87510712-87510762	A549	lung:	n/a
14	chr12:87510712-87510762	GM06990	blood:	n/a
15	chr12:87510712-87510762	AG04449	skin:	fetal
16	chr12:87510712-87510762	HMEC	breast:	n/a
17	chr12:87510712-87510762	HRCEpiC	kidney:	n/a
18	chr12:87510712-87510762	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:87510712-87510762	AG09309	skin:	n/a
20	chr12:87510712-87510762	SKMC	muscle:	n/a
21	chr12:87510712-87510762	MCF10A-Er-Src	breast:	n/a
22	chr12:87510712-87510762	HCPEpiC	choroid plexus:	n/a
23	chr12:87510712-87510762	GM12891	blood:	n/a
24	chr12:87510712-87510762	AG04450	lung:	fetal
25	chr12:87510712-87510762	PFSK-1	brain:	n/a
26	chr12:87510712-87510762	BJ	skin:	n/a
27	chr12:87510712-87510762	ovcar-3	ovarian:	n/a
28	chr12:87510712-87510762	GM12878	blood:	n/a
29	chr12:87510712-87510762	Hepatocyte	liver:	n/a
30	chr12:87510712-87510762	Hela-S3	cervix:	n/a
31	chr12:87510712-87510762	HUVEC	blood vessel:	n/a
32	chr12:87510712-87510762	ECC-1	luminal epithelium:	n/a
33	chr12:87510712-87510762	HNPCEpiC	eye:	n/a
34	chr12:87510712-87510762	HAEpiC	amniotic membrane:	n/a
35	chr12:87510712-87510762	HEEpiC	esophagus:	n/a
36	chr12:87510712-87510762	Jurkat	blood:	n/a
37	chr12:87510712-87510762	H1-hESC	embryonic stem cell:	embryo
38	chr12:87510712-87510762	CMK	blood:	n/a
39	chr12:87510712-87510762	U87	brain:	n/a
40	chr12:87510712-87510762	AG09319	gingival:	n/a
41	chr12:87510712-87510762	IMR90	lung:	fetal
42	chr12:87510712-87510762	HRPEpiC	eye:	n/a
43	chr12:87510712-87510762	GM19239	blood:	n/a
44	chr12:87510712-87510762	BE2_C	brain:	n/a
45	chr12:87510712-87510762	HCM	heart:	n/a
46	chr12:87510712-87510762	LNCaP	prostate:	n/a
47	chr12:87510712-87510762	HCT-116	colon:	n/a
48	chr12:87510712-87510762	AG10803	skin:	n/a
49	chr12:87510712-87510762	RPTEC	kidney:	n/a
50	chr12:87510712-87510762	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:87523604..87525877-chr12:87529351..87531918,2	MCF-7	breast:
2	chr12:87237467..87238342-chr7:40961627..40962369,2	MCF-7	breast:
3	chr12:87376736..87379148-chr12:87408006..87409813,2	K562	blood:
4	chr12:87512654..87515691-chr12:87528653..87530382,3	MCF-7	breast:
5	chr12:87513960..87515515-chr12:87520858..87523427,2	MCF-7	breast:
6	chr12:87386481..87388359-chr12:87403399..87406210,2	MCF-7	breast:
7	chr12:87507574..87509719-chr12:87517143..87519195,2	MCF-7	breast:
8	chr12:87513960..87515515-chr12:87520858..87523427,2	MCF-7	breast:
9	chr12:87512190..87514558-chr12:87523597..87525941,2	K562	blood:
10	chr12:87512190..87514558-chr12:87523597..87525941,2	K562	blood:
11	chr12:87376736..87379148-chr12:87408006..87409813,2	K562	blood:
12	chr12:87386481..87388359-chr12:87403399..87406210,2	MCF-7	breast:
13	chr12:87507574..87509719-chr12:87517143..87519195,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MGAT4C-3	chr12:87345415-87345519	NONHSAT029768
2	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: 5162 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:5162 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12812815	chr12:87233995-87233996	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559559923	chr12:87233998-87233999	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs563548431	chr12:87234069-87234070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530227513	chr12:87234099-87234100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139088026	chr12:87234119-87234120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs144068592	chr12:87234127-87234128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs80176323	chr12:87234141-87234142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552308256	chr12:87234171-87234172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570805854	chr12:87234180-87234181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528412788	chr12:87234188-87234189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs12317790	chr12:87234207-87234208	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs568310672	chr12:87234244-87234245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535650965	chr12:87234265-87234266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs578181579	chr12:87234292-87234293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs191742728	chr12:87234293-87234294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184115582	chr12:87234309-87234310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557502832	chr12:87234314-87234315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572786489	chr12:87234318-87234319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541371572	chr12:87234341-87234342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs74442645	chr12:87234423-87234424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs377687113	chr12:87234496-87234497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs77215834	chr12:87234500-87234501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371230294	chr12:87234510-87234511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149471332	chr12:87234514-87234515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528576710	chr12:87234521-87234522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs146416094	chr12:87234550-87234551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563875560	chr12:87234590-87234591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs10858501	chr12:87234655-87234656	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs546970631	chr12:87234678-87234679	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs561974096	chr12:87234698-87234699	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs543810186	chr12:87234818-87234819	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs538618119	chr12:87234841-87234842	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs188466411	chr12:87234851-87234852	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs557246255	chr12:87234897-87234898	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs191466429	chr12:87234927-87234928	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs184435383	chr12:87234929-87234930	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs181525235	chr12:87235963-87235964	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs370073669	chr12:87236030-87236031	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs371766668	chr12:87236068-87236069	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs535788875	chr12:87236092-87236093	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs577737418	chr12:87236099-87236100	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs185873144	chr12:87236121-87236122	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs190198833	chr12:87236127-87236128	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs148866389	chr12:87236148-87236149	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs12314448	chr12:87236159-87236160	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs566011880	chr12:87236214-87236215	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs150996739	chr12:87236788-87236789	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs11104124	chr12:87236802-87236803	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs190614132	chr12:87236828-87236829	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs55789636	chr12:87236845-87236846	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:70)

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
Urothelial cell carcinoma	18451213	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute lymphoblastic leukemia	17443227	CNVD

Chromatin state (count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:87233000-87234000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr12:87233200-87234000	Enhancers	Fetal Brain Male	brain
3	chr12:87234000-87234600	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr12:87263000-87263400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr12:87286400-87286600	Enhancers	Gastric	stomach
6	chr12:87286600-87286800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr12:87286600-87286800	ZNF genes & repeats	Gastric	stomach
8	chr12:87297000-87297400	Enhancers	Fetal Brain Female	brain
9	chr12:87299600-87305800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr12:87305400-87307200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
11	chr12:87305800-87306200	Enhancers	H1 Cell Line	embryonic stem cell
12	chr12:87305800-87306400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:87306000-87306400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr12:87306200-87307600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
15	chr12:87306400-87306600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:87306600-87307200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
17	chr12:87306600-87309000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr12:87307200-87310800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr12:87307600-87311000	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr12:87308600-87309200	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr12:87309000-87309200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr12:87310800-87311400	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr12:87311000-87311200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr12:87311000-87311200	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr12:87318600-87319200	Enhancers	Fetal Heart	heart
26	chr12:87318800-87319800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr12:87325600-87326000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr12:87327200-87327400	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr12:87327400-87330600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr12:87328800-87329400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr12:87329000-87329200	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr12:87329000-87329400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr12:87329200-87330400	Active TSS	HUES6 Cell Line	embryonic stem cell
34	chr12:87329400-87331800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr12:87329400-87337800	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr12:87330400-87331200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
37	chr12:87330600-87330800	Active TSS	ES-I3 Cell Line	embryonic stem cell
38	chr12:87330600-87332000	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr12:87330800-87331200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr12:87330800-87331200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr12:87331200-87331600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr12:87331200-87331800	Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr12:87331200-87338600	Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr12:87331600-87332400	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr12:87331800-87332400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr12:87331800-87332400	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr12:87332000-87332400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
48	chr12:87332200-87332400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr12:87332400-87333400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr12:87332400-87336600	Active TSS	iPS-15b Cell Line	embryonic stem cell

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