Variant report

Variant	nsv899308
Chromosome Location	chr12:75385097-75479379
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:169)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:169 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:75471599-75471657	K562	blood:	n/a	n/a
2	BATF	chr12:75404925-75405209	GM12878	blood:	n/a	n/a
3	BCL11A	chr12:75404926-75405216	GM12878	blood:	n/a	n/a
4	BHLHE40	chr12:75446343-75446405	A549	lung:	n/a	n/a
5	BHLHE40	chr12:75442107-75442113	HepG2	liver:	n/a	n/a
6	CEBPB	chr12:75434399-75434463	HepG2	liver:	n/a	chr12:75434441-75434452
7	CEBPB	chr12:75436602-75436732	H1-hESC	embryonic stem cell:	n/a	chr12:75436637-75436650
8	CTCF	chr12:75452180-75452330	HMEC	breast:	n/a	chr12:75452181-75452197 chr12:75452185-75452193
9	CTCF	chr12:75452087-75452335	GM12878	blood:	n/a	chr12:75452181-75452197 chr12:75452175-75452196 chr12:75452185-75452193
10	CTCF	chr12:75452101-75452338	IMR90	lung:	n/a	chr12:75452181-75452197 chr12:75452175-75452196 chr12:75452185-75452193
11	CTCF	chr12:75452240-75452390	MCF-7	breast:	n/a	n/a
12	CTCF	chr12:75417300-75417450	HPAF	blood vessel:	n/a	n/a
13	CTCF	chr12:75452130-75452247	HepG2	liver:	n/a	chr12:75452181-75452197 chr12:75452175-75452196 chr12:75452185-75452193
14	CTCF	chr12:75452159-75452275	HUVEC	blood vessel:	n/a	chr12:75452181-75452197 chr12:75452175-75452196 chr12:75452185-75452193
15	CTCF	chr12:75452120-75452411	MCF-7	breast:	n/a	chr12:75452181-75452197 chr12:75452175-75452196 chr12:75452185-75452193
16	CTCF	chr12:75452140-75452290	RPTEC	kidney:	n/a	chr12:75452181-75452197 chr12:75452175-75452196 chr12:75452185-75452193
17	CTCF	chr12:75452280-75452430	MCF-7	breast:	n/a	n/a
18	CTCF	chr12:75407421-75407461	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr12:75452154-75452267	Hela-S3	cervix:	n/a	chr12:75452181-75452197 chr12:75452175-75452196 chr12:75452185-75452193
20	CTCF	chr12:75471998-75472046	GM20000	blood:	n/a	n/a
21	CTCF	chr12:75452010-75452495	HCT-116	colon:	n/a	chr12:75452181-75452197 chr12:75452175-75452196 chr12:75452185-75452193
22	CTCF	chr12:75452160-75452310	HRPEpiC	eye:	n/a	chr12:75452181-75452197 chr12:75452175-75452196 chr12:75452185-75452193
23	CTCF	chr12:75452100-75452250	HRE	kidney:	n/a	chr12:75452181-75452197 chr12:75452175-75452196 chr12:75452185-75452193
24	CTCF	chr12:75452020-75452170	HMEC	breast:	n/a	n/a
25	CTCF	chr12:75452114-75452409	MCF-7	breast:	n/a	chr12:75452181-75452197 chr12:75452175-75452196 chr12:75452185-75452193
26	CTCF	chr12:75407000-75407069	Lung_OC	lung:	n/a	n/a
27	CTCF	chr12:75452120-75452270	HCPEpiC	choroid plexus:	n/a	chr12:75452181-75452197 chr12:75452175-75452196 chr12:75452185-75452193
28	CTCF	chr12:75472720-75472870	GM06990	blood:	n/a	n/a
29	E2F4	chr12:75448685-75448690	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr12:75417902-75418066	MCF10A-Er-Src	breast:	n/a	n/a
31	EBF1	chr12:75442092-75442120	GM12878	blood:	n/a	n/a
32	EGR1	chr12:75404961-75405347	MCF-7	breast:	n/a	n/a
33	EP300	chr12:75440045-75440049	K562	blood:	n/a	n/a
34	EP300	chr12:75404921-75405208	GM12878	blood:	n/a	n/a
35	EP300	chr12:75405063-75405183	GM12878	blood:	n/a	n/a
36	EP300	chr12:75404740-75405303	MCF-7	breast:	n/a	n/a
37	EP300	chr12:75441537-75441549	GM12878	blood:	n/a	n/a
38	FAM48A	chr12:75445899-75445994	GM12878	blood:	n/a	n/a
39	FAM48A	chr12:75439051-75439158	GM12878	blood:	n/a	n/a
40	FOS	chr12:75404968-75405261	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr12:75405004-75405253	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr12:75405011-75405263	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr12:75404983-75405251	MCF10A-Er-Src	breast:	n/a	n/a
44	FOXP2	chr12:75404997-75405169	PFSK-1	brain:	n/a	n/a
45	FOXP2	chr12:75404957-75405195	SK-N-MC	brain:	n/a	n/a
46	GATA2	chr12:75477948-75478170	K562	blood:	n/a	n/a
47	GATA2	chr12:75422226-75422535	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr12:75422264-75422352	SH-SY5Y	brain:	n/a	n/a
49	IRF1	chr12:75416776-75416793	K562	blood:	n/a	n/a
50	KAP1	chr12:75413766-75414447	HEK293	kidney:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:75435362-75435412	PANC-1	pancreas:	n/a
2	chr12:75435362-75435412	HEK293	kidney:	embryo
3	chr12:75435362-75435412	SAEC	small airway:	n/a
4	chr12:75435362-75435412	Hela-S3	cervix:	n/a
5	chr12:75435362-75435412	AG09309	skin:	n/a
6	chr12:75435362-75435412	HUVEC	blood vessel:	n/a
7	chr12:75435362-75435412	NB4	blood:	n/a
8	chr12:75435362-75435412	AG04450	lung:	fetal
9	chr12:75435362-75435412	AG10803	skin:	n/a
10	chr12:75435362-75435412	GM12892	blood:	n/a
11	chr12:75435362-75435412	NHBE	bronchial:	n/a
12	chr12:75435362-75435412	ProgFib	skin:	n/a
13	chr12:75435362-75435412	LNCaP	prostate:	n/a
14	chr12:75435362-75435412	MCF-7	breast:	n/a
15	chr12:75435362-75435412	SK-N-SH	brain:	n/a
16	chr12:75435362-75435412	NHDF-neo	bronchial:	n/a
17	chr12:75435362-75435412	MCF10A-Er-Src	breast:	n/a
18	chr12:75435362-75435412	HCM	heart:	n/a
19	chr12:75435362-75435412	Hepatocyte	liver:	n/a
20	chr12:75435362-75435412	PrEC	prostate:	n/a
21	chr12:75435362-75435412	SK-N-MC	brain:	n/a
22	chr12:75435362-75435412	HCT-116	colon:	n/a
23	chr12:75435362-75435412	HIPEpiC	eye:	n/a
24	chr12:75435362-75435412	A549	lung:	n/a
25	chr12:75435362-75435412	BJ	skin:	n/a
26	chr12:75435362-75435412	RPTEC	kidney:	n/a
27	chr12:75435362-75435412	GM12891	blood:	n/a
28	chr12:75435362-75435412	NT2-D1	testis:	n/a
29	chr12:75435362-75435412	GM19239	blood:	n/a
30	chr12:75435362-75435412	SK-N-SH_RA	brain:	n/a
31	chr12:75435362-75435412	HCPEpiC	choroid plexus:	n/a
32	chr12:75435362-75435412	IMR90	lung:	fetal
33	chr12:75435362-75435412	HAEpiC	amniotic membrane:	n/a
34	chr12:75435362-75435412	AoSMC	blood vessel:	n/a
35	chr12:75435362-75435412	HRE	kidney:	n/a
36	chr12:75435362-75435412	HMEC	breast:	n/a
37	chr12:75435362-75435412	Caco-2	colon:	n/a
38	chr12:75435362-75435412	HL-60	blood:	n/a
39	chr12:75435362-75435412	ovcar-3	ovarian:	n/a
40	chr12:75435362-75435412	HepG2	liver:	n/a
41	chr12:75435362-75435412	PFSK-1	brain:	n/a
42	chr12:75435362-75435412	HRPEpiC	eye:	n/a
43	chr12:75435362-75435412	SKMC	muscle:	n/a
44	chr12:75435362-75435412	HPAEpiC	pulmonary alveolar:	n/a
45	chr12:75435362-75435412	HEEpiC	esophagus:	n/a
46	chr12:75435362-75435412	HCF	heart:	n/a
47	chr12:75435362-75435412	CMK	blood:	n/a
48	chr12:75435362-75435412	GM12878	blood:	n/a
49	chr12:75435362-75435412	AG04449	skin:	fetal
50	chr12:75435362-75435412	NH-A	brain:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:75450802..75452995-chr12:75458776..75460677,2	MCF-7	breast:
2	chr12:75413695..75414606-chr15:56538291..56538861,2	MCF-7	breast:
3	chr12:75443458..75445239-chr12:75448407..75451297,2	MCF-7	breast:
4	chr12:75472504..75474383-chr12:75575455..75577189,2	K562	blood:
5	chr12:75449527..75451079-chr12:75455433..75457461,2	MCF-7	breast:
6	chr12:75450802..75452995-chr12:75458776..75460677,2	MCF-7	breast:
7	chr12:75358040..75360198-chr12:75422290..75423830,2	MCF-7	breast:
8	chr12:75404209..75404838-chr20:39924998..39925789,2	MCF-7	breast:
9	chr12:75449527..75451079-chr12:75455433..75457461,2	MCF-7	breast:
10	chr12:75140910..75141773-chr12:75451603..75452321,3	MCF-7	breast:
11	chr12:75435528..75437912-chr12:75438665..75440854,2	K562	blood:
12	chr10:125205389..125206272-chr12:75451784..75452560,2	MCF-7	breast:
13	chr12:75082796..75083489-chr12:75451709..75452443,2	MCF-7	breast:
14	chr12:75435528..75437912-chr12:75438665..75440854,2	K562	blood:
15	chr12:75471106..75471647-chr12:75480652..75481167,2	MCF-7	breast:
16	chr12:75424336..75426758-chr12:75436388..75438151,2	K562	blood:
17	chr12:75424336..75426758-chr12:75436388..75438151,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLIPR1L1-2	chr12:75434738-75435132	NONHSAT029518
2	lnc-GLIPR1L1-2	chr12:75414749-75414864	ENSG00000257434.1
3	lnc-GLIPR1L1-2	chr12:75418854-75418965	ENSG00000257434.1
4	lnc-GLIPR1L1-4	chr12:75477807-75477928	l_680_chr12:75477806-75480269_testes
5	lnc-GLIPR1L1-2	chr12:75419767-75419984	ENSG00000257434.1
6	lnc-GLIPR1L1-2	chr12:75421835-75421869	NONHSAT029518
7	lnc-GLIPR1L1-2	chr12:75438258-75438573	ENSG00000257434.1
8	lnc-GLIPR1L1-2	chr12:75434738-75435052	ENSG00000257434.1
9	lnc-GLIPR1L1-2	chr12:75419754-75419984	ENSG00000257434.1
10	lnc-GLIPR1L1-2	chr12:75434738-75434922	ENSG00000257434.1
11	lnc-GLIPR1L1-4	chr12:75477994-75478144	l_680_chr12:75477806-75480269_testes
12	lnc-GLIPR1L1-2	chr12:75434738-75437150	ENSG00000257434.1

No data

Variant related genes	Relation type
KCNC2	TF binding region
ENSG00000257434	TF binding region
KCNC2	CpG island
ENSG00000257434	CpG island
ENSG00000166006	chromatin interactions

Extended variants
information (count: 1031 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1031 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538323974	chr12:75387629-75387630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs374704788	chr12:75387667-75387668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561791188	chr12:75387747-75387748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs145902272	chr12:75387761-75387762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7295795	chr12:75387765-75387766	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs564047936	chr12:75387766-75387767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181097167	chr12:75387792-75387793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7310132	chr12:75387793-75387794	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs553856944	chr12:75387803-75387804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563400558	chr12:75387805-75387806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs529427429	chr12:75387820-75387821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551597641	chr12:75387825-75387826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138712697	chr12:75387839-75387840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566190488	chr12:75387877-75387878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185554881	chr12:75387935-75387936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189573908	chr12:75387991-75387992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144020859	chr12:75388006-75388007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537071408	chr12:75388036-75388037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556986759	chr12:75388095-75388096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571389075	chr12:75388101-75388102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533748688	chr12:75388103-75388104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs182295803	chr12:75388190-75388191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs207473105	chr12:75388234-75388235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536385380	chr12:75388236-75388237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555532322	chr12:75388261-75388262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572174728	chr12:75388266-75388267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541316099	chr12:75388302-75388303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs186248686	chr12:75388303-75388304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577683122	chr12:75388307-75388308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs76221361	chr12:75388314-75388315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144350149	chr12:75388352-75388353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs79736804	chr12:75388355-75388356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs548834737	chr12:75388384-75388385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559883820	chr12:75388386-75388387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs528678448	chr12:75388430-75388431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs551633129	chr12:75388483-75388484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs116620907	chr12:75388486-75388487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191050151	chr12:75388495-75388496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs369272171	chr12:75388568-75388569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550940286	chr12:75388581-75388582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs371905776	chr12:75388585-75388586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs17114452	chr12:75388607-75388608	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs536725466	chr12:75388616-75388617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs1526807	chr12:75388623-75388624	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs565844434	chr12:75388628-75388629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573589051	chr12:75388631-75388632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs558037308	chr12:75388641-75388642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs117614894	chr12:75388719-75388720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs566854156	chr12:75388724-75388725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs61934780	chr12:75388731-75388732	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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
Colorectal cancer	16272173	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
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	17133270	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
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:75387600-75388600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:75387800-75388800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr12:75388000-75388800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr12:75391600-75391800	Enhancers	Liver	Liver
5	chr12:75391800-75392400	Weak transcription	Liver	Liver
6	chr12:75392400-75393000	Enhancers	Liver	Liver
7	chr12:75393000-75393600	Active TSS	Liver	Liver
8	chr12:75393200-75393600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
9	chr12:75393200-75394200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr12:75393600-75394600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr12:75404000-75406000	Enhancers	Fetal Kidney	kidney
12	chr12:75410400-75410800	ZNF genes & repeats	Adipose Nuclei	Adipose
13	chr12:75413000-75413200	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
14	chr12:75413800-75414400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
15	chr12:75413800-75414600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:75434600-75436400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr12:75435200-75435800	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr12:75435400-75436200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr12:75435600-75436000	Enhancers	Liver	Liver
20	chr12:75436400-75436600	Enhancers	Liver	Liver
21	chr12:75441600-75442000	Weak transcription	Pancreas	Pancrea
22	chr12:75442000-75442200	ZNF genes & repeats	Pancreas	Pancrea
23	chr12:75442400-75444000	Enhancers	Liver	Liver
24	chr12:75456000-75456400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr12:75456400-75456800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr12:75456800-75457600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr12:75457400-75457800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr12:75474000-75474600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr12:75474200-75474600	Enhancers	Rectal Smooth Muscle	rectum
30	chr12:75474200-75474800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr12:75474600-75480000	Weak transcription	Rectal Smooth Muscle	rectum
32	chr12:75478400-75480200	Enhancers	Colon Smooth Muscle	Colon
33	chr12:75479200-75480200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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